Ligand source activities (1 row/activity)





Ligands Receptor Assay information Chemical information
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name
GPCRdb ID #Vendors Reference
ligand
Fold selectivity
(Potency)
# tested GPCRs
(Potency)
Species p-value
(-log)
Type Activity
Relation
Activity
Value
Assay Type Assay Description Source Mol
weight
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H don H acc LogP Smiles DOI
16133225 415 47 None -5 4 Human 9.3 pEC50 = 9.3 Functional
Agonist activity at human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ assessed as induction of intracellular Ca2+ mobilization by bioluminescence assayAgonist activity at human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ assessed as induction of intracellular Ca2+ mobilization by bioluminescence assay
ChEMBL None None None None 10.1021/acs.jmedchem.5b01495
172198 415 47 None -5 4 Human 9.3 pEC50 = 9.3 Functional
Agonist activity at human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ assessed as induction of intracellular Ca2+ mobilization by bioluminescence assayAgonist activity at human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ assessed as induction of intracellular Ca2+ mobilization by bioluminescence assay
ChEMBL None None None None 10.1021/acs.jmedchem.5b01495
2504 415 47 None -5 4 Human 9.3 pEC50 = 9.3 Functional
Agonist activity at human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ assessed as induction of intracellular Ca2+ mobilization by bioluminescence assayAgonist activity at human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ assessed as induction of intracellular Ca2+ mobilization by bioluminescence assay
ChEMBL None None None None 10.1021/acs.jmedchem.5b01495
45266664 415 47 None -5 4 Human 9.3 pEC50 = 9.3 Functional
Agonist activity at human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ assessed as induction of intracellular Ca2+ mobilization by bioluminescence assayAgonist activity at human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ assessed as induction of intracellular Ca2+ mobilization by bioluminescence assay
ChEMBL None None None None 10.1021/acs.jmedchem.5b01495
5272 415 47 None -5 4 Human 9.3 pEC50 = 9.3 Functional
Agonist activity at human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ assessed as induction of intracellular Ca2+ mobilization by bioluminescence assayAgonist activity at human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ assessed as induction of intracellular Ca2+ mobilization by bioluminescence assay
ChEMBL None None None None 10.1021/acs.jmedchem.5b01495
CHEMBL408403 415 47 None -5 4 Human 9.3 pEC50 = 9.3 Functional
Agonist activity at human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ assessed as induction of intracellular Ca2+ mobilization by bioluminescence assayAgonist activity at human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ assessed as induction of intracellular Ca2+ mobilization by bioluminescence assay
ChEMBL None None None None 10.1021/acs.jmedchem.5b01495
DB11842 415 47 None -5 4 Human 9.3 pEC50 = 9.3 Functional
Agonist activity at human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ assessed as induction of intracellular Ca2+ mobilization by bioluminescence assayAgonist activity at human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ assessed as induction of intracellular Ca2+ mobilization by bioluminescence assay
ChEMBL None None None None 10.1021/acs.jmedchem.5b01495
16133225 415 47 None -5 4 Human 9.3 pEC50 = 9.3 Functional
Agonist activity at human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ assessed as induction of intracellular Ca2+ mobilization by bioluminescence assayAgonist activity at human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ assessed as induction of intracellular Ca2+ mobilization by bioluminescence assay
ChEMBL None None None None 10.1021/acs.jmedchem.5b01495
172198 415 47 None -5 4 Human 9.3 pEC50 = 9.3 Functional
Agonist activity at human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ assessed as induction of intracellular Ca2+ mobilization by bioluminescence assayAgonist activity at human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ assessed as induction of intracellular Ca2+ mobilization by bioluminescence assay
ChEMBL None None None None 10.1021/acs.jmedchem.5b01495
2504 415 47 None -5 4 Human 9.3 pEC50 = 9.3 Functional
Agonist activity at human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ assessed as induction of intracellular Ca2+ mobilization by bioluminescence assayAgonist activity at human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ assessed as induction of intracellular Ca2+ mobilization by bioluminescence assay
ChEMBL None None None None 10.1021/acs.jmedchem.5b01495
45266664 415 47 None -5 4 Human 9.3 pEC50 = 9.3 Functional
Agonist activity at human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ assessed as induction of intracellular Ca2+ mobilization by bioluminescence assayAgonist activity at human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ assessed as induction of intracellular Ca2+ mobilization by bioluminescence assay
ChEMBL None None None None 10.1021/acs.jmedchem.5b01495
5272 415 47 None -5 4 Human 9.3 pEC50 = 9.3 Functional
Agonist activity at human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ assessed as induction of intracellular Ca2+ mobilization by bioluminescence assayAgonist activity at human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ assessed as induction of intracellular Ca2+ mobilization by bioluminescence assay
ChEMBL None None None None 10.1021/acs.jmedchem.5b01495
CHEMBL408403 415 47 None -5 4 Human 9.3 pEC50 = 9.3 Functional
Agonist activity at human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ assessed as induction of intracellular Ca2+ mobilization by bioluminescence assayAgonist activity at human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ assessed as induction of intracellular Ca2+ mobilization by bioluminescence assay
ChEMBL None None None None 10.1021/acs.jmedchem.5b01495
DB11842 415 47 None -5 4 Human 9.3 pEC50 = 9.3 Functional
Agonist activity at human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ assessed as induction of intracellular Ca2+ mobilization by bioluminescence assayAgonist activity at human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ assessed as induction of intracellular Ca2+ mobilization by bioluminescence assay
ChEMBL None None None None 10.1021/acs.jmedchem.5b01495
127030943 138652 0 None - 1 Human 9.0 pEC50 = 9.0 Functional
Agonist activity at human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ assessed as induction of intracellular Ca2+ mobilization by bioluminescence assayAgonist activity at human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ assessed as induction of intracellular Ca2+ mobilization by bioluminescence assay
ChEMBL 1216 35 15 14 -0.7 CCC(=O)NCCCCNC(=O)/N=C(\N)NCCC[C@H](NC(=O)[C@@H](N)CC(=O)O)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O)[C@@H](C)CC)C(C)C 10.1021/acs.jmedchem.5b01495
CHEMBL3787243 138652 0 None - 1 Human 9.0 pEC50 = 9.0 Functional
Agonist activity at human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ assessed as induction of intracellular Ca2+ mobilization by bioluminescence assayAgonist activity at human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ assessed as induction of intracellular Ca2+ mobilization by bioluminescence assay
ChEMBL 1216 35 15 14 -0.7 CCC(=O)NCCCCNC(=O)/N=C(\N)NCCC[C@H](NC(=O)[C@@H](N)CC(=O)O)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O)[C@@H](C)CC)C(C)C 10.1021/acs.jmedchem.5b01495
CHEMBL3787375 138652 0 None - 1 Human 9.0 pEC50 = 9.0 Functional
Agonist activity at human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ assessed as induction of intracellular Ca2+ mobilization by bioluminescence assayAgonist activity at human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ assessed as induction of intracellular Ca2+ mobilization by bioluminescence assay
ChEMBL 1216 35 15 14 -0.7 CCC(=O)NCCCCNC(=O)/N=C(\N)NCCC[C@H](NC(=O)[C@@H](N)CC(=O)O)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O)[C@@H](C)CC)C(C)C 10.1021/acs.jmedchem.5b01495
CHEMBL3787700 138652 0 None - 1 Human 9.0 pEC50 = 9.0 Functional
Agonist activity at human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ assessed as induction of intracellular Ca2+ mobilization by bioluminescence assayAgonist activity at human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ assessed as induction of intracellular Ca2+ mobilization by bioluminescence assay
ChEMBL 1216 35 15 14 -0.7 CCC(=O)NCCCCNC(=O)/N=C(\N)NCCC[C@H](NC(=O)[C@@H](N)CC(=O)O)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O)[C@@H](C)CC)C(C)C 10.1021/acs.jmedchem.5b01495
127030943 138652 0 None - 1 Human 9.0 pEC50 = 9.0 Functional
Agonist activity at human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ assessed as induction of intracellular Ca2+ mobilization by bioluminescence assayAgonist activity at human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ assessed as induction of intracellular Ca2+ mobilization by bioluminescence assay
ChEMBL 1216 35 15 14 -0.7 CCC(=O)NCCCCNC(=O)/N=C(\N)NCCC[C@H](NC(=O)[C@@H](N)CC(=O)O)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O)[C@@H](C)CC)C(C)C 10.1021/acs.jmedchem.5b01495
CHEMBL3787243 138652 0 None - 1 Human 9.0 pEC50 = 9.0 Functional
Agonist activity at human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ assessed as induction of intracellular Ca2+ mobilization by bioluminescence assayAgonist activity at human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ assessed as induction of intracellular Ca2+ mobilization by bioluminescence assay
ChEMBL 1216 35 15 14 -0.7 CCC(=O)NCCCCNC(=O)/N=C(\N)NCCC[C@H](NC(=O)[C@@H](N)CC(=O)O)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O)[C@@H](C)CC)C(C)C 10.1021/acs.jmedchem.5b01495
CHEMBL3787375 138652 0 None - 1 Human 9.0 pEC50 = 9.0 Functional
Agonist activity at human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ assessed as induction of intracellular Ca2+ mobilization by bioluminescence assayAgonist activity at human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ assessed as induction of intracellular Ca2+ mobilization by bioluminescence assay
ChEMBL 1216 35 15 14 -0.7 CCC(=O)NCCCCNC(=O)/N=C(\N)NCCC[C@H](NC(=O)[C@@H](N)CC(=O)O)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O)[C@@H](C)CC)C(C)C 10.1021/acs.jmedchem.5b01495
CHEMBL3787700 138652 0 None - 1 Human 9.0 pEC50 = 9.0 Functional
Agonist activity at human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ assessed as induction of intracellular Ca2+ mobilization by bioluminescence assayAgonist activity at human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ assessed as induction of intracellular Ca2+ mobilization by bioluminescence assay
ChEMBL 1216 35 15 14 -0.7 CCC(=O)NCCCCNC(=O)/N=C(\N)NCCC[C@H](NC(=O)[C@@H](N)CC(=O)O)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O)[C@@H](C)CC)C(C)C 10.1021/acs.jmedchem.5b01495
16133225 415 47 None -6 4 Rat 8.9 pEC50 = 8.9 Functional
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL None None None None nan
172198 415 47 None -6 4 Rat 8.9 pEC50 = 8.9 Functional
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL None None None None nan
2504 415 47 None -6 4 Rat 8.9 pEC50 = 8.9 Functional
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL None None None None nan
45266664 415 47 None -6 4 Rat 8.9 pEC50 = 8.9 Functional
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL None None None None nan
5272 415 47 None -6 4 Rat 8.9 pEC50 = 8.9 Functional
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL None None None None nan
CHEMBL408403 415 47 None -6 4 Rat 8.9 pEC50 = 8.9 Functional
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL None None None None nan
DB11842 415 47 None -6 4 Rat 8.9 pEC50 = 8.9 Functional
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL None None None None nan
127029976 138674 0 None - 1 Human 8.9 pEC50 = 8.9 Functional
Agonist activity at human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ assessed as induction of intracellular Ca2+ mobilization by bioluminescence assayAgonist activity at human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ assessed as induction of intracellular Ca2+ mobilization by bioluminescence assay
ChEMBL 1160 33 15 14 -1.2 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCN/C(N)=N/C(=O)NCCCCN)NC(=O)[C@@H](N)CC(=O)O)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O 10.1021/acs.jmedchem.5b01495
CHEMBL3786145 138674 0 None - 1 Human 8.9 pEC50 = 8.9 Functional
Agonist activity at human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ assessed as induction of intracellular Ca2+ mobilization by bioluminescence assayAgonist activity at human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ assessed as induction of intracellular Ca2+ mobilization by bioluminescence assay
ChEMBL 1160 33 15 14 -1.2 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCN/C(N)=N/C(=O)NCCCCN)NC(=O)[C@@H](N)CC(=O)O)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O 10.1021/acs.jmedchem.5b01495
CHEMBL3787767 138674 0 None - 1 Human 8.9 pEC50 = 8.9 Functional
Agonist activity at human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ assessed as induction of intracellular Ca2+ mobilization by bioluminescence assayAgonist activity at human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ assessed as induction of intracellular Ca2+ mobilization by bioluminescence assay
ChEMBL 1160 33 15 14 -1.2 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCN/C(N)=N/C(=O)NCCCCN)NC(=O)[C@@H](N)CC(=O)O)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O 10.1021/acs.jmedchem.5b01495
127029976 138674 0 None - 1 Human 8.9 pEC50 = 8.9 Functional
Agonist activity at human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ assessed as induction of intracellular Ca2+ mobilization by bioluminescence assayAgonist activity at human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ assessed as induction of intracellular Ca2+ mobilization by bioluminescence assay
ChEMBL 1160 33 15 14 -1.2 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCN/C(N)=N/C(=O)NCCCCN)NC(=O)[C@@H](N)CC(=O)O)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O 10.1021/acs.jmedchem.5b01495
CHEMBL3786145 138674 0 None - 1 Human 8.9 pEC50 = 8.9 Functional
Agonist activity at human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ assessed as induction of intracellular Ca2+ mobilization by bioluminescence assayAgonist activity at human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ assessed as induction of intracellular Ca2+ mobilization by bioluminescence assay
ChEMBL 1160 33 15 14 -1.2 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCN/C(N)=N/C(=O)NCCCCN)NC(=O)[C@@H](N)CC(=O)O)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O 10.1021/acs.jmedchem.5b01495
CHEMBL3787767 138674 0 None - 1 Human 8.9 pEC50 = 8.9 Functional
Agonist activity at human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ assessed as induction of intracellular Ca2+ mobilization by bioluminescence assayAgonist activity at human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ assessed as induction of intracellular Ca2+ mobilization by bioluminescence assay
ChEMBL 1160 33 15 14 -1.2 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCN/C(N)=N/C(=O)NCCCCN)NC(=O)[C@@H](N)CC(=O)O)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O 10.1021/acs.jmedchem.5b01495
155564502 174678 0 None 2 2 Rat 7.0 pEC50 = 7 Functional
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL 2296 33 30 27 -2.1 CC[C@H](C)[C@@H]1NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](C(C)C)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H]2CCCN2C(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@H]([C@@H](C)CC)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](C(C)C)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H]2CCCN2C(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@H]([C@@H](C)CC)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](C(C)C)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H]2CCCN2C(=O)[C@H](Cc2cnc[nH]2)NC1=O nan
CHEMBL4572408 174678 0 None 2 2 Rat 7.0 pEC50 = 7 Functional
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL 2296 33 30 27 -2.1 CC[C@H](C)[C@@H]1NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](C(C)C)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H]2CCCN2C(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@H]([C@@H](C)CC)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](C(C)C)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H]2CCCN2C(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@H]([C@@H](C)CC)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](C(C)C)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H]2CCCN2C(=O)[C@H](Cc2cnc[nH]2)NC1=O nan
11943 3802 0 None 14 2 Rat 8.0 pEC50 = 8.0 Functional
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL None None None None nan
145925549 3802 0 None 14 2 Rat 8.0 pEC50 = 8.0 Functional
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL None None None None nan
CHEMBL4438122 3802 0 None 14 2 Rat 8.0 pEC50 = 8.0 Functional
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL None None None None nan
155558059 174101 0 None -5 2 Human 7.0 pEC50 = 7.0 Functional
Agonist activity at human AT1R expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL 790 23 12 11 -4.6 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)NCC(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)NCC(N)=O)C(C)C)C(C)C nan
CHEMBL4559239 174101 0 None -5 2 Human 7.0 pEC50 = 7.0 Functional
Agonist activity at human AT1R expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL 790 23 12 11 -4.6 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)NCC(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)NCC(N)=O)C(C)C)C(C)C nan
155541440 172440 0 None -1 2 Rat 7.9 pEC50 = 7.9 Functional
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL 954 28 13 12 -1.1 CCC[C@H](NC(=O)[C@@H]1CCCN1C(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)[C@@H](C)CC)C(=O)O nan
CHEMBL4518530 172440 0 None -1 2 Rat 7.9 pEC50 = 7.9 Functional
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL 954 28 13 12 -1.1 CCC[C@H](NC(=O)[C@@H]1CCCN1C(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)[C@@H](C)CC)C(=O)O nan
155541295 172432 0 None 4 2 Rat 7.9 pEC50 = 7.9 Functional
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL 926 25 12 12 -2.0 CC(C)[C@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CN(C)C)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O)C(C)C nan
CHEMBL4518318 172432 0 None 4 2 Rat 7.9 pEC50 = 7.9 Functional
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL 926 25 12 12 -2.0 CC(C)[C@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CN(C)C)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O)C(C)C nan
155540639 172354 0 None -1 2 Rat 5.9 pEC50 = 5.9 Functional
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL 947 25 14 13 -2.5 CC(C)[C@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](N)CC(=O)O)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(N)=O nan
CHEMBL4516768 172354 0 None -1 2 Rat 5.9 pEC50 = 5.9 Functional
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL 947 25 14 13 -2.5 CC(C)[C@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](N)CC(=O)O)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(N)=O nan
CHEMBL2028943 207381 0 None -1 2 Human 6.8 pEC50 = 6.8 Functional
Agonist activity at human AT1R expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@@H]1CCCN1C(=O)[C@H](Cc1c[nH]cn1)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCN=C(N)N)NC(=O)CNC)C(C)C)C(=O)O nan
155553930 174858 0 None -1 2 Rat 4.8 pEC50 = 4.8 Functional
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL 1177 26 13 12 -0.7 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1cc(I)c(O)c(I)c1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
CHEMBL4576650 174858 0 None -1 2 Rat 4.8 pEC50 = 4.8 Functional
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL 1177 26 13 12 -0.7 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1cc(I)c(O)c(I)c1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
155540033 172311 0 None -2 2 Human 6.7 pEC50 = 6.7 Functional
Agonist activity at human AT1R expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL 953 27 13 12 -1.9 CC[C@H](C)[C@H](NC(=O)[C@@H]1CCCN1C(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(C)C)C(N)=O nan
CHEMBL4515768 172311 0 None -2 2 Human 6.7 pEC50 = 6.7 Functional
Agonist activity at human AT1R expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL 953 27 13 12 -1.9 CC[C@H](C)[C@H](NC(=O)[C@@H]1CCCN1C(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(C)C)C(N)=O nan
127029977 138675 0 None - 1 Human 8.7 pEC50 = 8.7 Functional
Agonist activity at human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ assessed as induction of intracellular Ca2+ mobilization by bioluminescence assayAgonist activity at human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ assessed as induction of intracellular Ca2+ mobilization by bioluminescence assay
ChEMBL 1220 37 15 16 -2.0 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCN/C(N)=N/C(=O)NCCOCCOCCN)NC(=O)[C@@H](N)CC(=O)O)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O 10.1021/acs.jmedchem.5b01495
CHEMBL3786986 138675 0 None - 1 Human 8.7 pEC50 = 8.7 Functional
Agonist activity at human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ assessed as induction of intracellular Ca2+ mobilization by bioluminescence assayAgonist activity at human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ assessed as induction of intracellular Ca2+ mobilization by bioluminescence assay
ChEMBL 1220 37 15 16 -2.0 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCN/C(N)=N/C(=O)NCCOCCOCCN)NC(=O)[C@@H](N)CC(=O)O)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O 10.1021/acs.jmedchem.5b01495
CHEMBL3787768 138675 0 None - 1 Human 8.7 pEC50 = 8.7 Functional
Agonist activity at human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ assessed as induction of intracellular Ca2+ mobilization by bioluminescence assayAgonist activity at human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ assessed as induction of intracellular Ca2+ mobilization by bioluminescence assay
ChEMBL 1220 37 15 16 -2.0 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCN/C(N)=N/C(=O)NCCOCCOCCN)NC(=O)[C@@H](N)CC(=O)O)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O 10.1021/acs.jmedchem.5b01495
127029977 138675 0 None - 1 Human 8.7 pEC50 = 8.7 Functional
Agonist activity at human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ assessed as induction of intracellular Ca2+ mobilization by bioluminescence assayAgonist activity at human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ assessed as induction of intracellular Ca2+ mobilization by bioluminescence assay
ChEMBL 1220 37 15 16 -2.0 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCN/C(N)=N/C(=O)NCCOCCOCCN)NC(=O)[C@@H](N)CC(=O)O)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O 10.1021/acs.jmedchem.5b01495
CHEMBL3786986 138675 0 None - 1 Human 8.7 pEC50 = 8.7 Functional
Agonist activity at human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ assessed as induction of intracellular Ca2+ mobilization by bioluminescence assayAgonist activity at human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ assessed as induction of intracellular Ca2+ mobilization by bioluminescence assay
ChEMBL 1220 37 15 16 -2.0 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCN/C(N)=N/C(=O)NCCOCCOCCN)NC(=O)[C@@H](N)CC(=O)O)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O 10.1021/acs.jmedchem.5b01495
CHEMBL3787768 138675 0 None - 1 Human 8.7 pEC50 = 8.7 Functional
Agonist activity at human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ assessed as induction of intracellular Ca2+ mobilization by bioluminescence assayAgonist activity at human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ assessed as induction of intracellular Ca2+ mobilization by bioluminescence assay
ChEMBL 1220 37 15 16 -2.0 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCN/C(N)=N/C(=O)NCCOCCOCCN)NC(=O)[C@@H](N)CC(=O)O)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O 10.1021/acs.jmedchem.5b01495
127031545 138653 0 None - 1 Human 8.6 pEC50 = 8.6 Functional
Agonist activity at human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ assessed as induction of intracellular Ca2+ mobilization by bioluminescence assayAgonist activity at human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ assessed as induction of intracellular Ca2+ mobilization by bioluminescence assay
ChEMBL 1276 39 15 16 -1.4 CCC(=O)NCCOCCOCCNC(=O)/N=C(\N)NCCC[C@H](NC(=O)[C@@H](N)CC(=O)O)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O)[C@@H](C)CC)C(C)C 10.1021/acs.jmedchem.5b01495
CHEMBL3787379 138653 0 None - 1 Human 8.6 pEC50 = 8.6 Functional
Agonist activity at human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ assessed as induction of intracellular Ca2+ mobilization by bioluminescence assayAgonist activity at human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ assessed as induction of intracellular Ca2+ mobilization by bioluminescence assay
ChEMBL 1276 39 15 16 -1.4 CCC(=O)NCCOCCOCCNC(=O)/N=C(\N)NCCC[C@H](NC(=O)[C@@H](N)CC(=O)O)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O)[C@@H](C)CC)C(C)C 10.1021/acs.jmedchem.5b01495
CHEMBL3787701 138653 0 None - 1 Human 8.6 pEC50 = 8.6 Functional
Agonist activity at human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ assessed as induction of intracellular Ca2+ mobilization by bioluminescence assayAgonist activity at human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ assessed as induction of intracellular Ca2+ mobilization by bioluminescence assay
ChEMBL 1276 39 15 16 -1.4 CCC(=O)NCCOCCOCCNC(=O)/N=C(\N)NCCC[C@H](NC(=O)[C@@H](N)CC(=O)O)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O)[C@@H](C)CC)C(C)C 10.1021/acs.jmedchem.5b01495
127031545 138653 0 None - 1 Human 8.6 pEC50 = 8.6 Functional
Agonist activity at human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ assessed as induction of intracellular Ca2+ mobilization by bioluminescence assayAgonist activity at human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ assessed as induction of intracellular Ca2+ mobilization by bioluminescence assay
ChEMBL 1276 39 15 16 -1.4 CCC(=O)NCCOCCOCCNC(=O)/N=C(\N)NCCC[C@H](NC(=O)[C@@H](N)CC(=O)O)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O)[C@@H](C)CC)C(C)C 10.1021/acs.jmedchem.5b01495
CHEMBL3787379 138653 0 None - 1 Human 8.6 pEC50 = 8.6 Functional
Agonist activity at human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ assessed as induction of intracellular Ca2+ mobilization by bioluminescence assayAgonist activity at human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ assessed as induction of intracellular Ca2+ mobilization by bioluminescence assay
ChEMBL 1276 39 15 16 -1.4 CCC(=O)NCCOCCOCCNC(=O)/N=C(\N)NCCC[C@H](NC(=O)[C@@H](N)CC(=O)O)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O)[C@@H](C)CC)C(C)C 10.1021/acs.jmedchem.5b01495
CHEMBL3787701 138653 0 None - 1 Human 8.6 pEC50 = 8.6 Functional
Agonist activity at human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ assessed as induction of intracellular Ca2+ mobilization by bioluminescence assayAgonist activity at human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ assessed as induction of intracellular Ca2+ mobilization by bioluminescence assay
ChEMBL 1276 39 15 16 -1.4 CCC(=O)NCCOCCOCCNC(=O)/N=C(\N)NCCC[C@H](NC(=O)[C@@H](N)CC(=O)O)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O)[C@@H](C)CC)C(C)C 10.1021/acs.jmedchem.5b01495
16133225 415 47 None -5 4 Human 8.6 pEC50 = 8.6 Functional
Agonist activity at human AT1R expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL None None None None nan
172198 415 47 None -5 4 Human 8.6 pEC50 = 8.6 Functional
Agonist activity at human AT1R expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL None None None None nan
2504 415 47 None -5 4 Human 8.6 pEC50 = 8.6 Functional
Agonist activity at human AT1R expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL None None None None nan
45266664 415 47 None -5 4 Human 8.6 pEC50 = 8.6 Functional
Agonist activity at human AT1R expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL None None None None nan
5272 415 47 None -5 4 Human 8.6 pEC50 = 8.6 Functional
Agonist activity at human AT1R expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL None None None None nan
CHEMBL408403 415 47 None -5 4 Human 8.6 pEC50 = 8.6 Functional
Agonist activity at human AT1R expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL None None None None nan
DB11842 415 47 None -5 4 Human 8.6 pEC50 = 8.6 Functional
Agonist activity at human AT1R expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL None None None None nan
155541440 172440 0 None 1 2 Human 8.6 pEC50 = 8.6 Functional
Agonist activity at human AT1R expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL 954 28 13 12 -1.1 CCC[C@H](NC(=O)[C@@H]1CCCN1C(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)[C@@H](C)CC)C(=O)O nan
CHEMBL4518530 172440 0 None 1 2 Human 8.6 pEC50 = 8.6 Functional
Agonist activity at human AT1R expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL 954 28 13 12 -1.1 CCC[C@H](NC(=O)[C@@H]1CCCN1C(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)[C@@H](C)CC)C(=O)O nan
10533900 175386 5 None 10 2 Rat 7.7 pEC50 = 7.7 Functional
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL 955 27 14 13 -2.7 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H](N)CC(=O)O)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)NCC(=O)O nan
CHEMBL4588454 175386 5 None 10 2 Rat 7.7 pEC50 = 7.7 Functional
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL 955 27 14 13 -2.7 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H](N)CC(=O)O)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)NCC(=O)O nan
155556507 173904 0 None 2 2 Rat 6.7 pEC50 = 6.7 Functional
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL 910 26 12 11 -1.6 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
CHEMBL4554466 173904 0 None 2 2 Rat 6.7 pEC50 = 6.7 Functional
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL 910 26 12 11 -1.6 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
155563538 174718 0 None -1 2 Rat 6.7 pEC50 = 6.7 Functional
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL 925 26 13 12 -2.5 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(N)=O nan
CHEMBL4573250 174718 0 None -1 2 Rat 6.7 pEC50 = 6.7 Functional
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL 925 26 13 12 -2.5 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(N)=O nan
155559104 174224 0 None 2 2 Rat 7.6 pEC50 = 7.6 Functional
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL 940 26 12 12 -1.6 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CN(C)C)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O nan
CHEMBL4562270 174224 0 None 2 2 Rat 7.6 pEC50 = 7.6 Functional
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL 940 26 12 12 -1.6 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CN(C)C)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O nan
155554865 173772 0 None 2 2 Rat 6.6 pEC50 = 6.6 Functional
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL 2269 27 21 24 3.8 CC[C@H](C)[C@@H]1NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](C(C)C)NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@@H]2CCCN2C(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@H]([C@@H](C)CC)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](C(C)C)NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@@H]2CCCN2C(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@H]([C@@H](C)CC)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](C(C)C)NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@@H]2CCCN2C(=O)[C@H](Cc2cnc[nH]2)NC1=O nan
CHEMBL4551317 173772 0 None 2 2 Rat 6.6 pEC50 = 6.6 Functional
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL 2269 27 21 24 3.8 CC[C@H](C)[C@@H]1NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](C(C)C)NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@@H]2CCCN2C(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@H]([C@@H](C)CC)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](C(C)C)NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@@H]2CCCN2C(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@H]([C@@H](C)CC)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](C(C)C)NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@@H]2CCCN2C(=O)[C@H](Cc2cnc[nH]2)NC1=O nan
155540328 172322 0 None -3 2 Human 6.6 pEC50 = 6.6 Functional
Agonist activity at human AT1R expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL 1017 28 14 13 -1.6 CC[C@H](C)[C@H](NC(=O)[C@@H]1CCCN1C(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(N)=O nan
CHEMBL4516066 172322 0 None -3 2 Human 6.6 pEC50 = 6.6 Functional
Agonist activity at human AT1R expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL 1017 28 14 13 -1.6 CC[C@H](C)[C@H](NC(=O)[C@@H]1CCCN1C(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(N)=O nan
155553479 173596 0 None 3 2 Rat 6.6 pEC50 = 6.6 Functional
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL 949 26 14 13 -3.0 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O)C(C)C nan
CHEMBL4547423 173596 0 None 3 2 Rat 6.6 pEC50 = 6.6 Functional
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL 949 26 14 13 -3.0 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O)C(C)C nan
155558003 174111 0 None 1 2 Rat 5.6 pEC50 = 5.6 Functional
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL 1015 28 13 16 -2.1 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1cc([N+](=O)[O-])c(O)c([N+](=O)[O-])c1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
CHEMBL4559421 174111 0 None 1 2 Rat 5.6 pEC50 = 5.6 Functional
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL 1015 28 13 16 -2.1 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1cc([N+](=O)[O-])c(O)c([N+](=O)[O-])c1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
155547428 173033 0 None -22 2 Rat 4.6 pEC50 = 4.6 Functional
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL 959 26 13 12 -1.3 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)c(Cl)c1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
CHEMBL4533618 173033 0 None -22 2 Rat 4.6 pEC50 = 4.6 Functional
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL 959 26 13 12 -1.3 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)c(Cl)c1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
155566196 175163 0 None -5 2 Rat 4.6 pEC50 = 4.6 Functional
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL 954 26 13 12 -1.3 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1c(C)cc(O)cc1C)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
CHEMBL4583284 175163 0 None -5 2 Rat 4.6 pEC50 = 4.6 Functional
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL 954 26 13 12 -1.3 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1c(C)cc(O)cc1C)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
155558428 174147 0 None 1 2 Rat 7.6 pEC50 = 7.6 Functional
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL 897 26 15 12 -3.8 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(N)=O)C(C)C nan
CHEMBL4560224 174147 0 None 1 2 Rat 7.6 pEC50 = 7.6 Functional
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL 897 26 15 12 -3.8 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(N)=O)C(C)C nan
11944 3803 0 None 4 2 Rat 6.6 pEC50 = 6.6 Functional
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL None None None None nan
155552190 3803 0 None 4 2 Rat 6.6 pEC50 = 6.6 Functional
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL None None None None nan
CHEMBL4544228 3803 0 None 4 2 Rat 6.6 pEC50 = 6.6 Functional
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL None None None None nan
CHEMBL77838 214091 3 None -1 2 Rat 8.5 pEC50 = 8.5 Functional
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@@H]1CCCN1C(=O)[C@H](Cc1c[nH]cn1)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCN=C(N)N)NC(=O)CNC)C(C)C)C(C)C)C(=O)O nan
155552475 173470 0 None 9 2 Human 8.4 pEC50 = 8.4 Functional
Agonist activity at human AT1R expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL 947 25 14 13 -2.5 CC(C)[C@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H](N)CC(=O)O)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(N)=O nan
CHEMBL4543860 173470 0 None 9 2 Human 8.4 pEC50 = 8.4 Functional
Agonist activity at human AT1R expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL 947 25 14 13 -2.5 CC(C)[C@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H](N)CC(=O)O)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(N)=O nan
155542907 172596 0 None 3 2 Rat 6.5 pEC50 = 6.5 Functional
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL 904 24 13 12 -1.5 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)O)C(C)C nan
CHEMBL4522038 172596 0 None 3 2 Rat 6.5 pEC50 = 6.5 Functional
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL 904 24 13 12 -1.5 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)O)C(C)C nan
CHEMBL2028943 207381 0 None 1 2 Rat 7.5 pEC50 = 7.5 Functional
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@@H]1CCCN1C(=O)[C@H](Cc1c[nH]cn1)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCN=C(N)N)NC(=O)CNC)C(C)C)C(=O)O nan
155552475 173470 0 None -9 2 Rat 6.5 pEC50 = 6.5 Functional
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL 947 25 14 13 -2.5 CC(C)[C@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H](N)CC(=O)O)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(N)=O nan
CHEMBL4543860 173470 0 None -9 2 Rat 6.5 pEC50 = 6.5 Functional
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL 947 25 14 13 -2.5 CC(C)[C@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H](N)CC(=O)O)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(N)=O nan
155556530 173929 0 None 2 2 Rat 7.5 pEC50 = 7.5 Functional
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL 911 25 13 12 -2.9 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(N)=O)C(C)C)C(C)C nan
CHEMBL4555119 173929 0 None 2 2 Rat 7.5 pEC50 = 7.5 Functional
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL 911 25 13 12 -2.9 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(N)=O)C(C)C)C(C)C nan
155561376 175092 0 None 12 2 Rat 6.4 pEC50 = 6.4 Functional
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL 917 28 12 11 -1.4 CC[C@H](C)[C@H](NC(=O)[C@@H]1CCCN1C(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)[C@@H](C)CC)[C@@H](C)CC)C(N)=O nan
CHEMBL4581718 175092 0 None 12 2 Rat 6.4 pEC50 = 6.4 Functional
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL 917 28 12 11 -1.4 CC[C@H](C)[C@H](NC(=O)[C@@H]1CCCN1C(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)[C@@H](C)CC)[C@@H](C)CC)C(N)=O nan
155541125 172386 0 None 6 2 Rat 7.4 pEC50 = 7.4 Functional
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL 904 27 12 11 -1.2 CC[C@H](C)[C@H](NC(=O)[C@@H]1CCCN1C(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)[C@@H](C)CC)C(C)C)C(=O)O nan
CHEMBL4517561 172386 0 None 6 2 Rat 7.4 pEC50 = 7.4 Functional
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL 904 27 12 11 -1.2 CC[C@H](C)[C@H](NC(=O)[C@@H]1CCCN1C(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)[C@@H](C)CC)C(C)C)C(=O)O nan
24892627 55349 4 None -5 2 Human 4.2 pEC50 = 4.2 Functional
PUBCHEM_BIOASSAY: Dose Response screen for agonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule agonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays (depositor defined):AID2520, AID2580]PUBCHEM_BIOASSAY: Dose Response screen for agonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule agonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays (depositor defined):AID2520, AID2580]
ChEMBL 548 8 0 6 5.0 Cc1ccc2nc(N(CCCN(C)C)C(=O)c3ccc(S(=O)(=O)N4CCc5ccccc5C4)cc3)sc2c1 nan
CHEMBL1460676 55349 4 None -5 2 Human 4.2 pEC50 = 4.2 Functional
PUBCHEM_BIOASSAY: Dose Response screen for agonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule agonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays (depositor defined):AID2520, AID2580]PUBCHEM_BIOASSAY: Dose Response screen for agonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule agonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays (depositor defined):AID2520, AID2580]
ChEMBL 548 8 0 6 5.0 Cc1ccc2nc(N(CCCN(C)C)C(=O)c3ccc(S(=O)(=O)N4CCc5ccccc5C4)cc3)sc2c1 nan
CHEMBL1621632 55349 4 None -5 2 Human 4.2 pEC50 = 4.2 Functional
PUBCHEM_BIOASSAY: Dose Response screen for agonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule agonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays (depositor defined):AID2520, AID2580]PUBCHEM_BIOASSAY: Dose Response screen for agonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule agonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays (depositor defined):AID2520, AID2580]
ChEMBL 548 8 0 6 5.0 Cc1ccc2nc(N(CCCN(C)C)C(=O)c3ccc(S(=O)(=O)N4CCc5ccccc5C4)cc3)sc2c1 nan
155558059 174101 0 None 5 2 Rat 7.2 pEC50 = 7.2 Functional
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL 790 23 12 11 -4.6 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)NCC(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)NCC(N)=O)C(C)C)C(C)C nan
CHEMBL4559239 174101 0 None 5 2 Rat 7.2 pEC50 = 7.2 Functional
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL 790 23 12 11 -4.6 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)NCC(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)NCC(N)=O)C(C)C)C(C)C nan
CHEMBL938 214120 24 None -10 4 Rat 8.2 pEC50 = 8.2 Functional
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL None None None CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O)C(C)C)C(C)C nan
CHEMBL312754 209354 16 None 1 2 Rat 8.2 pEC50 = 8.2 Functional
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCN=C(N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O nan
154573825 175406 6 None 8 2 Rat 8.2 pEC50 = 8.2 Functional
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL 742 22 12 10 -2.4 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(N)=O)C(C)C)C(C)C nan
CHEMBL4588946 175406 6 None 8 2 Rat 8.2 pEC50 = 8.2 Functional
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL 742 22 12 10 -2.4 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(N)=O)C(C)C)C(C)C nan
155560463 174458 0 None -1 2 Rat 7.2 pEC50 = 7.2 Functional
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL 1052 28 14 13 -0.8 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](Cc1ccccc1)C(=O)O)C(C)C nan
CHEMBL4567667 174458 0 None -1 2 Rat 7.2 pEC50 = 7.2 Functional
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL 1052 28 14 13 -0.8 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](Cc1ccccc1)C(=O)O)C(C)C nan
155553003 173494 0 None 1 2 Human 7.2 pEC50 = 7.2 Functional
Agonist activity at human AT1R expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL 791 23 12 11 -4.0 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)NCC(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)NCC(=O)O)C(C)C)C(C)C nan
CHEMBL4544308 173494 0 None 1 2 Human 7.2 pEC50 = 7.2 Functional
Agonist activity at human AT1R expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL 791 23 12 11 -4.0 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)NCC(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)NCC(=O)O)C(C)C)C(C)C nan
10533900 175386 5 None -10 2 Human 6.2 pEC50 = 6.2 Functional
Agonist activity at human AT1R expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL 955 27 14 13 -2.7 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H](N)CC(=O)O)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)NCC(=O)O nan
CHEMBL4588454 175386 5 None -10 2 Human 6.2 pEC50 = 6.2 Functional
Agonist activity at human AT1R expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL 955 27 14 13 -2.7 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H](N)CC(=O)O)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)NCC(=O)O nan
CHEMBL2392353 208659 6 None -50 3 Rat 8.1 pEC50 = 8.1 Functional
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL None None None None nan
155553098 173528 0 None 22 2 Rat 8.1 pEC50 = 8.1 Functional
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL 969 28 16 13 -3.7 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O)C(C)C nan
CHEMBL4545153 173528 0 None 22 2 Rat 8.1 pEC50 = 8.1 Functional
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL 969 28 16 13 -3.7 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O)C(C)C nan
1588251 58950 10 None - 1 Human 5.1 pEC50 = 5.1 Functional
PUBCHEM_BIOASSAY: Dose Response screen for agonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule agonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays (depositor defined):AID2520, AID2580]PUBCHEM_BIOASSAY: Dose Response screen for agonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule agonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays (depositor defined):AID2520, AID2580]
ChEMBL 436 4 0 5 5.8 CCN1C(c2ccccc2)=C(c2ccccc2)S/C1=C\C=C1/SC(=S)N(C)C1=O nan
CHEMBL1704271 58950 10 None - 1 Human 5.1 pEC50 = 5.1 Functional
PUBCHEM_BIOASSAY: Dose Response screen for agonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule agonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays (depositor defined):AID2520, AID2580]PUBCHEM_BIOASSAY: Dose Response screen for agonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule agonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays (depositor defined):AID2520, AID2580]
ChEMBL 436 4 0 5 5.8 CCN1C(c2ccccc2)=C(c2ccccc2)S/C1=C\C=C1/SC(=S)N(C)C1=O nan
155540328 172322 0 None 3 2 Rat 7.1 pEC50 = 7.1 Functional
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL 1017 28 14 13 -1.6 CC[C@H](C)[C@H](NC(=O)[C@@H]1CCCN1C(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(N)=O nan
CHEMBL4516066 172322 0 None 3 2 Rat 7.1 pEC50 = 7.1 Functional
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL 1017 28 14 13 -1.6 CC[C@H](C)[C@H](NC(=O)[C@@H]1CCCN1C(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(N)=O nan
155540033 172311 0 None 2 2 Rat 7.1 pEC50 = 7.1 Functional
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL 953 27 13 12 -1.9 CC[C@H](C)[C@H](NC(=O)[C@@H]1CCCN1C(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(C)C)C(N)=O nan
CHEMBL4515768 172311 0 None 2 2 Rat 7.1 pEC50 = 7.1 Functional
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL 953 27 13 12 -1.9 CC[C@H](C)[C@H](NC(=O)[C@@H]1CCCN1C(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(C)C)C(N)=O nan
155539838 172316 0 None 1 2 Rat 8.1 pEC50 = 8.1 Functional
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL 940 26 13 12 -1.5 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](C)NC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
CHEMBL4515848 172316 0 None 1 2 Rat 8.1 pEC50 = 8.1 Functional
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL 940 26 13 12 -1.5 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](C)NC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
CHEMBL2370909 208193 0 None 7 2 Rat 7.0 pEC50 = 7.0 Functional
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@@H]1CCCN1C(=O)[C@H](Cc1c[nH]cn1)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCN=C(N)N)NC(=O)CNC)C(C)C)C(=O)O nan
155558784 174194 0 None -2 2 Rat 6.0 pEC50 = 6.0 Functional
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL 756 9 7 8 1.3 CC[C@H](C)[C@@H]1NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](C(C)C)NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@@H]2CCCN2C(=O)[C@H](Cc2cnc[nH]2)NC1=O nan
CHEMBL4561366 174194 0 None -2 2 Rat 6.0 pEC50 = 6.0 Functional
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL 756 9 7 8 1.3 CC[C@H](C)[C@@H]1NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](C(C)C)NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@@H]2CCCN2C(=O)[C@H](Cc2cnc[nH]2)NC1=O nan
154573825 175406 6 None -8 2 Human 7.0 pEC50 = 7.0 Functional
Agonist activity at human AT1R expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL 742 22 12 10 -2.4 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(N)=O)C(C)C)C(C)C nan
CHEMBL4588946 175406 6 None -8 2 Human 7.0 pEC50 = 7.0 Functional
Agonist activity at human AT1R expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL 742 22 12 10 -2.4 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(N)=O)C(C)C)C(C)C nan
155553003 173494 0 None -1 2 Rat 7.0 pEC50 = 7.0 Functional
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL 791 23 12 11 -4.0 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)NCC(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)NCC(=O)O)C(C)C)C(C)C nan
CHEMBL4544308 173494 0 None -1 2 Rat 7.0 pEC50 = 7.0 Functional
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 30 mins by IP1 accumulation assay
ChEMBL 791 23 12 11 -4.0 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)NCC(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)NCC(=O)O)C(C)C)C(C)C nan
3025727 183488 10 None 10000 2 Rabbit 10.3 pIC50 = 10.3 Functional
Antagonist activity at angiotensin AT1 receptor in rabbit aortic strip assessed as inhibition of angiotensin 2-induced contractile responseAntagonist activity at angiotensin AT1 receptor in rabbit aortic strip assessed as inhibition of angiotensin 2-induced contractile response
ChEMBL 452 8 2 6 5.0 CCCCc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.bmc.2010.10.043
CHEMBL48242 183488 10 None 10000 2 Rabbit 10.3 pIC50 = 10.3 Functional
Antagonist activity at angiotensin AT1 receptor in rabbit aortic strip assessed as inhibition of angiotensin 2-induced contractile responseAntagonist activity at angiotensin AT1 receptor in rabbit aortic strip assessed as inhibition of angiotensin 2-induced contractile response
ChEMBL 452 8 2 6 5.0 CCCCc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.bmc.2010.10.043
14971704 111879 0 None - 1 Rabbit 9.7 pIC50 = 9.7 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 546 9 2 6 6.7 CCCCc1nn(-c2c(Cl)cccc2Cl)c(C(=O)O)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
CHEMBL329616 111879 0 None - 1 Rabbit 9.7 pIC50 = 9.7 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 546 9 2 6 6.7 CCCCc1nn(-c2c(Cl)cccc2Cl)c(C(=O)O)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
133031 100379 16 None 1 3 Human 9.7 pIC50 = 9.7 Functional
Antagonist activity at angiotensin 1 receptorAntagonist activity at angiotensin 1 receptor
ChEMBL 524 7 1 6 5.4 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1021/jm1013693
CHEMBL293511 100379 16 None 1 3 Human 9.7 pIC50 = 9.7 Functional
Antagonist activity at angiotensin 1 receptorAntagonist activity at angiotensin 1 receptor
ChEMBL 524 7 1 6 5.4 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1021/jm1013693
9892554 99718 4 None - 1 Rabbit 9.7 pIC50 = 9.7 Functional
Antagonist activity at angiotensin AT1 receptor in rabbit aortaAntagonist activity at angiotensin AT1 receptor in rabbit aorta
ChEMBL 510 9 1 8 3.5 CCCCc1nc2ccn(CC(=O)N(C)C)c(=O)c2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmc.2010.10.043
CHEMBL288246 99718 4 None - 1 Rabbit 9.7 pIC50 = 9.7 Functional
Antagonist activity at angiotensin AT1 receptor in rabbit aortaAntagonist activity at angiotensin AT1 receptor in rabbit aorta
ChEMBL 510 9 1 8 3.5 CCCCc1nc2ccn(CC(=O)N(C)C)c(=O)c2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmc.2010.10.043
14971715 167662 0 None - 1 Rabbit 9.7 pIC50 = 9.7 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 492 10 2 6 5.4 CCCCc1nn(Cc2ccccc2)c(C(=O)O)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
CHEMBL433646 167662 0 None - 1 Rabbit 9.7 pIC50 = 9.7 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 492 10 2 6 5.4 CCCCc1nn(Cc2ccccc2)c(C(=O)O)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
14971716 14340 0 None - 1 Rabbit 9.6 pIC50 = 9.6 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 506 11 2 6 5.6 CCCCc1nn(CCc2ccccc2)c(C(=O)O)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
CHEMBL120199 14340 0 None - 1 Rabbit 9.6 pIC50 = 9.6 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 506 11 2 6 5.6 CCCCc1nn(CCc2ccccc2)c(C(=O)O)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
14971706 205470 0 None - 1 Rabbit 9.6 pIC50 = 9.6 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 546 9 2 6 6.4 CCCCc1nn(-c2ccccc2C(F)(F)F)c(C(=O)O)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
CHEMBL92654 205470 0 None - 1 Rabbit 9.6 pIC50 = 9.6 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 546 9 2 6 6.4 CCCCc1nn(-c2ccccc2C(F)(F)F)c(C(=O)O)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
183134 203126 13 None -4 7 Human 9.5 pIC50 = 9.5 Functional
Antagonist activity at angiotensin 1 receptorAntagonist activity at angiotensin 1 receptor
ChEMBL 409 5 1 6 4.5 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm1013693
CHEMBL7550 203126 13 None -4 7 Human 9.5 pIC50 = 9.5 Functional
Antagonist activity at angiotensin 1 receptorAntagonist activity at angiotensin 1 receptor
ChEMBL 409 5 1 6 4.5 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm1013693
14971698 205552 0 None - 1 Rabbit 9.5 pIC50 = 9.5 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 512 9 2 6 6.0 CCCCc1nn(-c2ccccc2Cl)c(C(=O)O)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
CHEMBL93226 205552 0 None - 1 Rabbit 9.5 pIC50 = 9.5 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 512 9 2 6 6.0 CCCCc1nn(-c2ccccc2Cl)c(C(=O)O)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
9827346 99263 1 None 1 2 Human 9.4 pIC50 = 9.4 Functional
Antagonist activity at angiotensin AT1 receptorAntagonist activity at angiotensin AT1 receptor
ChEMBL 501 7 2 8 3.4 CCc1nn(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/c(=N/C(=O)C2=C(C(=O)O)CCC2)s1 10.1016/j.bmc.2010.10.043
CHEMBL284918 99263 1 None 1 2 Human 9.4 pIC50 = 9.4 Functional
Antagonist activity at angiotensin AT1 receptorAntagonist activity at angiotensin AT1 receptor
ChEMBL 501 7 2 8 3.4 CCc1nn(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/c(=N/C(=O)C2=C(C(=O)O)CCC2)s1 10.1016/j.bmc.2010.10.043
CHEMBL34866 99263 1 None 1 2 Human 9.4 pIC50 = 9.4 Functional
Antagonist activity at angiotensin AT1 receptorAntagonist activity at angiotensin AT1 receptor
ChEMBL 501 7 2 8 3.4 CCc1nn(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/c(=N/C(=O)C2=C(C(=O)O)CCC2)s1 10.1016/j.bmc.2010.10.043
9870652 70533 68 None 15 2 Rabbit 9.4 pIC50 = 9.4 Functional
Antagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challengeAntagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challenge
ChEMBL 501 9 1 7 4.2 CCCCc1nc(C)c(CC(=S)N(C)C)c(=O)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2011.12.116
CHEMBL1951143 70533 68 None 15 2 Rabbit 9.4 pIC50 = 9.4 Functional
Antagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challengeAntagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challenge
ChEMBL 501 9 1 7 4.2 CCCCc1nc(C)c(CC(=S)N(C)C)c(=O)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2011.12.116
14971720 114311 0 None - 1 Rabbit 9.4 pIC50 = 9.4 Functional
Antagonist activity at angiotensin AT1 receptor in rabbit aortaAntagonist activity at angiotensin AT1 receptor in rabbit aorta
ChEMBL 478 9 2 6 5.0 CCCc1nn(Cc2ccccc2)c(C(=O)O)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.bmc.2010.10.043
CHEMBL334145 114311 0 None - 1 Rabbit 9.4 pIC50 = 9.4 Functional
Antagonist activity at angiotensin AT1 receptor in rabbit aortaAntagonist activity at angiotensin AT1 receptor in rabbit aorta
ChEMBL 478 9 2 6 5.0 CCCc1nn(Cc2ccccc2)c(C(=O)O)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.bmc.2010.10.043
14971720 114311 0 None - 1 Rabbit 9.4 pIC50 = 9.4 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 478 9 2 6 5.0 CCCc1nn(Cc2ccccc2)c(C(=O)O)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
CHEMBL334145 114311 0 None - 1 Rabbit 9.4 pIC50 = 9.4 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 478 9 2 6 5.0 CCCc1nn(Cc2ccccc2)c(C(=O)O)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
14971705 205012 0 None - 1 Rabbit 9.3 pIC50 = 9.3 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 492 9 2 6 5.7 CCCCc1nn(-c2ccccc2C)c(C(=O)O)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
CHEMBL90011 205012 0 None - 1 Rabbit 9.3 pIC50 = 9.3 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 492 9 2 6 5.7 CCCCc1nn(-c2ccccc2C)c(C(=O)O)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
10325927 205149 0 None - 1 Rabbit 9.3 pIC50 = 9.3 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 580 9 2 6 7.3 CCCCc1nn(-c2c(Cl)cc(Cl)cc2Cl)c(C(=O)O)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
CHEMBL90774 205149 0 None - 1 Rabbit 9.3 pIC50 = 9.3 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 580 9 2 6 7.3 CCCCc1nn(-c2c(Cl)cc(Cl)cc2Cl)c(C(=O)O)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
14971714 98720 0 None - 1 Rabbit 9.3 pIC50 = 9.3 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 484 9 2 6 4.9 CCCCc1nn(CC(F)(F)F)c(C(=O)O)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
CHEMBL281386 98720 0 None - 1 Rabbit 9.3 pIC50 = 9.3 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 484 9 2 6 4.9 CCCCc1nn(CC(F)(F)F)c(C(=O)O)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
183134 203126 13 None -2 7 Rabbit 9.3 pIC50 = 9.3 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 409 5 1 6 4.5 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00078a013
183134 203126 13 None -2 7 Rabbit 9.3 pIC50 = 9.3 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 409 5 1 6 4.5 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00078a014
CHEMBL7550 203126 13 None -2 7 Rabbit 9.3 pIC50 = 9.3 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 409 5 1 6 4.5 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00078a013
CHEMBL7550 203126 13 None -2 7 Rabbit 9.3 pIC50 = 9.3 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 409 5 1 6 4.5 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00078a014
14971639 113620 0 None - 1 Rabbit 9.3 pIC50 = 9.3 Functional
Antagonist activity at angiotensin AT1 receptor in rabbit aorta assessed as reduction of angiotensin 2-induced contractile responseAntagonist activity at angiotensin AT1 receptor in rabbit aorta assessed as reduction of angiotensin 2-induced contractile response
ChEMBL 512 9 2 6 6.1 CCCCc1nc(-c2ccccc2Cl)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.bmc.2010.10.043
CHEMBL332897 113620 0 None - 1 Rabbit 9.3 pIC50 = 9.3 Functional
Antagonist activity at angiotensin AT1 receptor in rabbit aorta assessed as reduction of angiotensin 2-induced contractile responseAntagonist activity at angiotensin AT1 receptor in rabbit aorta assessed as reduction of angiotensin 2-induced contractile response
ChEMBL 512 9 2 6 6.1 CCCCc1nc(-c2ccccc2Cl)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.bmc.2010.10.043
14971639 113620 0 None - 1 Rabbit 9.3 pIC50 = 9.3 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 512 9 2 6 6.1 CCCCc1nc(-c2ccccc2Cl)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
CHEMBL332897 113620 0 None - 1 Rabbit 9.3 pIC50 = 9.3 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 512 9 2 6 6.1 CCCCc1nc(-c2ccccc2Cl)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
14971702 205440 0 None - 1 Rabbit 9.2 pIC50 = 9.2 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 546 9 2 6 6.7 CCCCc1nn(-c2ccc(Cl)cc2Cl)c(C(=O)O)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
CHEMBL92472 205440 0 None - 1 Rabbit 9.2 pIC50 = 9.2 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 546 9 2 6 6.7 CCCCc1nn(-c2ccc(Cl)cc2Cl)c(C(=O)O)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
14971710 205656 0 None - 1 Rabbit 9.2 pIC50 = 9.2 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 554 10 2 6 7.0 CCCCc1nn(-c2ccccc2-c2ccccc2)c(C(=O)O)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
CHEMBL93886 205656 0 None - 1 Rabbit 9.2 pIC50 = 9.2 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 554 10 2 6 7.0 CCCCc1nn(-c2ccccc2-c2ccccc2)c(C(=O)O)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
14971717 14398 0 None - 1 Rabbit 9.2 pIC50 = 9.2 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 532 8 2 6 6.0 CCCc1nn(-c2ccccc2C(F)(F)F)c(C(=O)O)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
CHEMBL120457 14398 0 None - 1 Rabbit 9.2 pIC50 = 9.2 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 532 8 2 6 6.0 CCCc1nn(-c2ccccc2C(F)(F)F)c(C(=O)O)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
10369813 116466 0 None - 1 Rabbit 9.2 pIC50 = 9.2 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 532 8 2 6 6.3 CCCc1nn(-c2c(Cl)cccc2Cl)c(C(=O)O)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
CHEMBL338740 116466 0 None - 1 Rabbit 9.2 pIC50 = 9.2 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 532 8 2 6 6.3 CCCc1nn(-c2c(Cl)cccc2Cl)c(C(=O)O)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
142534045 165914 0 None - 1 Human 9.2 pIC50 = 9.2 Functional
Antagonist activity at type-1 angiotensin 2 receptor (unknown origin) by calcium mobilizing assayAntagonist activity at type-1 angiotensin 2 receptor (unknown origin) by calcium mobilizing assay
ChEMBL 543 9 1 7 4.9 CCCCc1nc(C)c(CC(=S)N2CCCC2)c(=O)n1Cc1ccc(-c2ccccc2-c2noc(=O)[nH]2)cc1 10.1016/j.bmcl.2018.08.036
CHEMBL4278280 165914 0 None - 1 Human 9.2 pIC50 = 9.2 Functional
Antagonist activity at type-1 angiotensin 2 receptor (unknown origin) by calcium mobilizing assayAntagonist activity at type-1 angiotensin 2 receptor (unknown origin) by calcium mobilizing assay
ChEMBL 543 9 1 7 4.9 CCCCc1nc(C)c(CC(=S)N2CCCC2)c(=O)n1Cc1ccc(-c2ccccc2-c2noc(=O)[nH]2)cc1 10.1016/j.bmcl.2018.08.036
14956763 162833 0 None - 1 Rabbit 9.1 pIC50 = 9.1 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 526 10 1 10 4.2 CCCCc1nn(-c2ccc(OC)cc2[N+](=O)[O-])c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL419483 162833 0 None - 1 Rabbit 9.1 pIC50 = 9.1 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 526 10 1 10 4.2 CCCCc1nn(-c2ccc(OC)cc2[N+](=O)[O-])c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
14971701 205676 0 None - 1 Rabbit 9.1 pIC50 = 9.1 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 546 9 2 6 6.7 CCCCc1nn(-c2cccc(Cl)c2Cl)c(C(=O)O)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
CHEMBL94002 205676 0 None - 1 Rabbit 9.1 pIC50 = 9.1 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 546 9 2 6 6.7 CCCCc1nn(-c2cccc(Cl)c2Cl)c(C(=O)O)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
14971708 114083 0 None - 1 Rabbit 9.1 pIC50 = 9.1 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 508 10 2 7 5.4 CCCCc1nn(-c2ccc(OC)cc2)c(C(=O)O)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
CHEMBL333800 114083 0 None - 1 Rabbit 9.1 pIC50 = 9.1 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 508 10 2 7 5.4 CCCCc1nn(-c2ccc(OC)cc2)c(C(=O)O)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
10393717 115586 0 None 524 2 Rabbit 9.1 pIC50 = 9.1 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 595 11 1 7 6.1 CCCN(c1ccc(Cn2c(CC)nc3c(C)cc(C)nc32)cc1)C(C(=O)NS(=O)(=O)c1ccccc1)c1ccccc1 10.1021/jm00078a014
CHEMBL335722 115586 0 None 524 2 Rabbit 9.1 pIC50 = 9.1 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 595 11 1 7 6.1 CCCN(c1ccc(Cn2c(CC)nc3c(C)cc(C)nc32)cc1)C(C(=O)NS(=O)(=O)c1ccccc1)c1ccccc1 10.1021/jm00078a014
9914666 116157 0 None 3388 2 Rabbit 9.1 pIC50 = 9.1 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 520 5 1 6 6.3 CCc1nc2c(C)cc(C)nc2n1Cc1ccc2c(ccn2C(=O)c2c(Cl)ccc(Cl)c2C(=O)O)c1 10.1021/jm00078a013
CHEMBL337086 116157 0 None 3388 2 Rabbit 9.1 pIC50 = 9.1 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 520 5 1 6 6.3 CCc1nc2c(C)cc(C)nc2n1Cc1ccc2c(ccn2C(=O)c2c(Cl)ccc(Cl)c2C(=O)O)c1 10.1021/jm00078a013
14956739 204569 0 None - 1 Rabbit 9.1 pIC50 = 9.1 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 496 9 1 9 4.2 CCCCc1nn(-c2ccccc2[N+](=O)[O-])c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL87074 204569 0 None - 1 Rabbit 9.1 pIC50 = 9.1 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 496 9 1 9 4.2 CCCCc1nn(-c2ccccc2[N+](=O)[O-])c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
192567 116139 6 None 223 2 Rabbit 9.1 pIC50 = 9.1 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 581 10 1 7 5.7 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(N(CC)C(C(=O)NS(=O)(=O)c2ccccc2)c2ccccc2)cc1 10.1021/jm00078a014
CHEMBL337007 116139 6 None 223 2 Rabbit 9.1 pIC50 = 9.1 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 581 10 1 7 5.7 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(N(CC)C(C(=O)NS(=O)(=O)c2ccccc2)c2ccccc2)cc1 10.1021/jm00078a014
10140613 105603 0 None 3 2 Rabbit 9.1 pIC50 = 9.1 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 479 10 1 7 4.5 CCCCc1nn(CCc2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL313371 105603 0 None 3 2 Rabbit 9.1 pIC50 = 9.1 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 479 10 1 7 4.5 CCCCc1nn(CCc2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
14956772 105454 0 None - 1 Rabbit 9.0 pIC50 = 9.0 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 510 10 1 9 4.6 CCCCCc1nn(-c2ccccc2[N+](=O)[O-])c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL312913 105454 0 None - 1 Rabbit 9.0 pIC50 = 9.0 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 510 10 1 9 4.6 CCCCCc1nn(-c2ccccc2[N+](=O)[O-])c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
192345 26016 6 None 12022 2 Rabbit 9.0 pIC50 = 9 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 496 6 1 7 5.5 CCc1nc2c(C)cc(C)nc2n1Cc1ccc2c(ccn2Cc2c(Cl)cccc2-c2nn[nH]n2)c1 10.1021/jm00078a013
CHEMBL135775 26016 6 None 12022 2 Rabbit 9.0 pIC50 = 9 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 496 6 1 7 5.5 CCc1nc2c(C)cc(C)nc2n1Cc1ccc2c(ccn2Cc2c(Cl)cccc2-c2nn[nH]n2)c1 10.1021/jm00078a013
10326140 116138 0 None 2884 2 Rabbit 9.0 pIC50 = 9 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 593 11 1 7 5.9 C=CCN(c1ccc(Cn2c(CC)nc3c(C)cc(C)nc32)cc1)C(C(=O)NS(=O)(=O)c1ccccc1)c1ccccc1 10.1021/jm00078a014
CHEMBL337006 116138 0 None 2884 2 Rabbit 9.0 pIC50 = 9 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 593 11 1 7 5.9 C=CCN(c1ccc(Cn2c(CC)nc3c(C)cc(C)nc32)cc1)C(C(=O)NS(=O)(=O)c1ccccc1)c1ccccc1 10.1021/jm00078a014
9807766 70525 0 None - 1 Rabbit 9.0 pIC50 = 9.0 Functional
Antagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challengeAntagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challenge
ChEMBL 555 9 1 8 4.0 CCCCc1nc(C)c(CC(=O)N2CC(C)OC(C)C2)c(=O)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2011.12.116
CHEMBL1951136 70525 0 None - 1 Rabbit 9.0 pIC50 = 9.0 Functional
Antagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challengeAntagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challenge
ChEMBL 555 9 1 8 4.0 CCCCc1nc(C)c(CC(=O)N2CC(C)OC(C)C2)c(=O)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2011.12.116
60770 168921 13 None - 1 Rabbit 9.0 pIC50 = 9.0 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 506 8 2 6 5.1 CCCc1nc(C(F)(F)C(F)(F)F)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
CHEMBL443269 168921 13 None - 1 Rabbit 9.0 pIC50 = 9.0 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 506 8 2 6 5.1 CCCc1nc(C(F)(F)C(F)(F)F)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
142534141 166613 0 None - 1 Human 8.9 pIC50 = 8.9 Functional
Antagonist activity at type-1 angiotensin 2 receptor (unknown origin) by calcium mobilizing assayAntagonist activity at type-1 angiotensin 2 receptor (unknown origin) by calcium mobilizing assay
ChEMBL 557 9 1 7 5.3 CCCCc1nc(C)c(CC(=S)N2CCCC2C)c(=O)n1Cc1ccc(-c2ccccc2-c2noc(=O)[nH]2)cc1 10.1016/j.bmcl.2018.08.036
CHEMBL4291216 166613 0 None - 1 Human 8.9 pIC50 = 8.9 Functional
Antagonist activity at type-1 angiotensin 2 receptor (unknown origin) by calcium mobilizing assayAntagonist activity at type-1 angiotensin 2 receptor (unknown origin) by calcium mobilizing assay
ChEMBL 557 9 1 7 5.3 CCCCc1nc(C)c(CC(=S)N2CCCC2C)c(=O)n1Cc1ccc(-c2ccccc2-c2noc(=O)[nH]2)cc1 10.1016/j.bmcl.2018.08.036
14956757 67236 0 None 831 2 Rabbit 8.9 pIC50 = 8.9 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 519 8 1 7 5.3 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL19018 67236 0 None 831 2 Rabbit 8.9 pIC50 = 8.9 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 519 8 1 7 5.3 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
14971700 205714 0 None - 1 Rabbit 8.9 pIC50 = 8.9 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 512 9 2 6 6.0 CCCCc1nn(-c2ccc(Cl)cc2)c(C(=O)O)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
CHEMBL94221 205714 0 None - 1 Rabbit 8.9 pIC50 = 8.9 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 512 9 2 6 6.0 CCCCc1nn(-c2ccc(Cl)cc2)c(C(=O)O)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
9871638 70534 0 None - 1 Rabbit 8.9 pIC50 = 8.9 Functional
Antagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challengeAntagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challenge
ChEMBL 529 11 1 7 5.0 CCCCc1nc(C)c(CC(=S)N(CC)CC)c(=O)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2011.12.116
CHEMBL1951144 70534 0 None - 1 Rabbit 8.9 pIC50 = 8.9 Functional
Antagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challengeAntagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challenge
ChEMBL 529 11 1 7 5.0 CCCCc1nc(C)c(CC(=S)N(CC)CC)c(=O)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2011.12.116
44320012 167349 0 None - 1 Rabbit 8.9 pIC50 = 8.9 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 493 9 1 7 5.4 CCCCc1nn(-c2ccccc2C(C)C)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL431411 167349 0 None - 1 Rabbit 8.9 pIC50 = 8.9 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 493 9 1 7 5.4 CCCCc1nn(-c2ccccc2C(C)C)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
155542482 172546 0 None - 1 Human 8.8 pIC50 = 8.8 Functional
Antagonist activity at type-1 angiotensin 2 receptor (unknown origin) by calcium mobilizing assayAntagonist activity at type-1 angiotensin 2 receptor (unknown origin) by calcium mobilizing assay
ChEMBL 487 9 1 6 5.5 CCCCC1=NC(C)=C(CC(=S)N(C)C)CN1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2018.12.043
CHEMBL4520827 172546 0 None - 1 Human 8.8 pIC50 = 8.8 Functional
Antagonist activity at type-1 angiotensin 2 receptor (unknown origin) by calcium mobilizing assayAntagonist activity at type-1 angiotensin 2 receptor (unknown origin) by calcium mobilizing assay
ChEMBL 487 9 1 6 5.5 CCCCC1=NC(C)=C(CC(=S)N(C)C)CN1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2018.12.043
44213341 70518 0 None - 1 Rabbit 8.8 pIC50 = 8.8 Functional
Antagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challengeAntagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challenge
ChEMBL 511 9 1 7 4.0 CCCCc1nc(C)c(CC(=O)N2CCCC2)c(=O)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2011.12.116
CHEMBL1951129 70518 0 None - 1 Rabbit 8.8 pIC50 = 8.8 Functional
Antagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challengeAntagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challenge
ChEMBL 511 9 1 7 4.0 CCCCc1nc(C)c(CC(=O)N2CCCC2)c(=O)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2011.12.116
137532858 166526 0 None - 1 Human 8.8 pIC50 = 8.8 Functional
Antagonist activity at type-1 angiotensin 2 receptor (unknown origin) by calcium mobilizing assayAntagonist activity at type-1 angiotensin 2 receptor (unknown origin) by calcium mobilizing assay
ChEMBL 517 9 1 7 4.4 CCCCc1nc(C)c(CC(=S)N(C)C)c(=O)n1Cc1ccc(-c2ccccc2-c2noc(=O)[nH]2)cc1 10.1016/j.bmcl.2018.08.036
CHEMBL4289788 166526 0 None - 1 Human 8.8 pIC50 = 8.8 Functional
Antagonist activity at type-1 angiotensin 2 receptor (unknown origin) by calcium mobilizing assayAntagonist activity at type-1 angiotensin 2 receptor (unknown origin) by calcium mobilizing assay
ChEMBL 517 9 1 7 4.4 CCCCc1nc(C)c(CC(=S)N(C)C)c(=O)n1Cc1ccc(-c2ccccc2-c2noc(=O)[nH]2)cc1 10.1016/j.bmcl.2018.08.036
14971719 114281 0 None - 1 Rabbit 8.8 pIC50 = 8.8 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 470 8 2 6 4.5 CCCc1nn(CC(F)(F)F)c(C(=O)O)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
CHEMBL333978 114281 0 None - 1 Rabbit 8.8 pIC50 = 8.8 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 470 8 2 6 4.5 CCCc1nn(CC(F)(F)F)c(C(=O)O)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
14971711 16362 0 None - 1 Rabbit 8.8 pIC50 = 8.8 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 479 9 2 7 4.7 CCCCc1nn(-c2ccccn2)c(C(=O)O)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
CHEMBL123767 16362 0 None - 1 Rabbit 8.8 pIC50 = 8.8 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 479 9 2 7 4.7 CCCCc1nn(-c2ccccn2)c(C(=O)O)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
14971707 205595 0 None - 1 Rabbit 8.8 pIC50 = 8.8 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 523 10 2 8 5.3 CCCCc1nn(-c2ccccc2[N+](=O)[O-])c(C(=O)O)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
CHEMBL93547 205595 0 None - 1 Rabbit 8.8 pIC50 = 8.8 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 523 10 2 8 5.3 CCCCc1nn(-c2ccccc2[N+](=O)[O-])c(C(=O)O)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
44213349 70524 0 None - 1 Rabbit 8.8 pIC50 = 8.8 Functional
Antagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challengeAntagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challenge
ChEMBL 527 9 1 8 3.2 CCCCc1nc(C)c(CC(=O)N2CCOCC2)c(=O)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2011.12.116
CHEMBL1951135 70524 0 None - 1 Rabbit 8.8 pIC50 = 8.8 Functional
Antagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challengeAntagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challenge
ChEMBL 527 9 1 8 3.2 CCCCc1nc(C)c(CC(=O)N2CCOCC2)c(=O)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2011.12.116
20081627 91724 0 None 1 2 Human 8.7 pIC50 = 8.7 Functional
Antagonist activity at angiotensin AT1 receptorAntagonist activity at angiotensin AT1 receptor
ChEMBL 502 6 2 7 4.7 CC1CC(=O)NN=C1c1ccc2nc(C3CC3)n(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c2c1 10.1016/j.bmc.2010.10.043
CHEMBL24224 91724 0 None 1 2 Human 8.7 pIC50 = 8.7 Functional
Antagonist activity at angiotensin AT1 receptorAntagonist activity at angiotensin AT1 receptor
ChEMBL 502 6 2 7 4.7 CC1CC(=O)NN=C1c1ccc2nc(C3CC3)n(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c2c1 10.1016/j.bmc.2010.10.043
145981239 166045 0 None - 1 Human 8.7 pIC50 = 8.7 Functional
Antagonist activity at type-1 angiotensin 2 receptor (unknown origin) by calcium mobilizing assayAntagonist activity at type-1 angiotensin 2 receptor (unknown origin) by calcium mobilizing assay
ChEMBL 571 9 1 7 5.7 CCCCc1nc(C)c(CC(=S)N2[C@H](C)CC[C@H]2C)c(=O)n1Cc1ccc(-c2ccccc2-c2noc(=O)[nH]2)cc1 10.1016/j.bmcl.2018.08.036
CHEMBL4280574 166045 0 None - 1 Human 8.7 pIC50 = 8.7 Functional
Antagonist activity at type-1 angiotensin 2 receptor (unknown origin) by calcium mobilizing assayAntagonist activity at type-1 angiotensin 2 receptor (unknown origin) by calcium mobilizing assay
ChEMBL 571 9 1 7 5.7 CCCCc1nc(C)c(CC(=S)N2[C@H](C)CC[C@H]2C)c(=O)n1Cc1ccc(-c2ccccc2-c2noc(=O)[nH]2)cc1 10.1016/j.bmcl.2018.08.036
131654 204667 10 None 1 2 Rabbit 8.7 pIC50 = 8.7 Functional
In vitro antagonistic activity for AT1 receptor by displacing 125I[Sar, ILe8]AII radioligand in rabbit aorta membrane using 0.2% bovine serum albumin (BSA)In vitro antagonistic activity for AT1 receptor by displacing 125I[Sar, ILe8]AII radioligand in rabbit aorta membrane using 0.2% bovine serum albumin (BSA)
ChEMBL 431 10 1 7 4.1 CCCCc1nn(CCCC)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL87778 204667 10 None 1 2 Rabbit 8.7 pIC50 = 8.7 Functional
In vitro antagonistic activity for AT1 receptor by displacing 125I[Sar, ILe8]AII radioligand in rabbit aorta membrane using 0.2% bovine serum albumin (BSA)In vitro antagonistic activity for AT1 receptor by displacing 125I[Sar, ILe8]AII radioligand in rabbit aorta membrane using 0.2% bovine serum albumin (BSA)
ChEMBL 431 10 1 7 4.1 CCCCc1nn(CCCC)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
14956781 204443 0 None - 1 Rabbit 8.7 pIC50 = 8.7 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 443 8 1 7 4.4 CCCCc1nn(C2CCCC2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL86314 204443 0 None - 1 Rabbit 8.7 pIC50 = 8.7 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 443 8 1 7 4.4 CCCCc1nn(C2CCCC2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
9845644 204697 0 None 5 2 Rabbit 8.7 pIC50 = 8.7 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 431 9 1 7 4.3 CCCCc1nn(C(C)CC)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL87964 204697 0 None 5 2 Rabbit 8.7 pIC50 = 8.7 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 431 9 1 7 4.3 CCCCc1nn(C(C)CC)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
1610 2305 89 None -2 9 Rabbit 8.0 pIC50 = 8 Functional
Antagonist activity against AT1 receptor assessed as inhibition of Ang2-induced rabbit aortic strip contractionAntagonist activity against AT1 receptor assessed as inhibition of Ang2-induced rabbit aortic strip contraction
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm0603163
3941 2305 89 None -2 9 Rabbit 8.0 pIC50 = 8 Functional
Antagonist activity against AT1 receptor assessed as inhibition of Ang2-induced rabbit aortic strip contractionAntagonist activity against AT1 receptor assessed as inhibition of Ang2-induced rabbit aortic strip contraction
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm0603163
3961 2305 89 None -2 9 Rabbit 8.0 pIC50 = 8 Functional
Antagonist activity against AT1 receptor assessed as inhibition of Ang2-induced rabbit aortic strip contractionAntagonist activity against AT1 receptor assessed as inhibition of Ang2-induced rabbit aortic strip contraction
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm0603163
590 2305 89 None -2 9 Rabbit 8.0 pIC50 = 8 Functional
Antagonist activity against AT1 receptor assessed as inhibition of Ang2-induced rabbit aortic strip contractionAntagonist activity against AT1 receptor assessed as inhibition of Ang2-induced rabbit aortic strip contraction
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm0603163
CHEMBL191 2305 89 None -2 9 Rabbit 8.0 pIC50 = 8 Functional
Antagonist activity against AT1 receptor assessed as inhibition of Ang2-induced rabbit aortic strip contractionAntagonist activity against AT1 receptor assessed as inhibition of Ang2-induced rabbit aortic strip contraction
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm0603163
DB00678 2305 89 None -2 9 Rabbit 8.0 pIC50 = 8 Functional
Antagonist activity against AT1 receptor assessed as inhibition of Ang2-induced rabbit aortic strip contractionAntagonist activity against AT1 receptor assessed as inhibition of Ang2-induced rabbit aortic strip contraction
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm0603163
10095589 115007 0 None 851 2 Rabbit 8.0 pIC50 = 8 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 456 8 1 5 5.6 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(N(CC)C(C(=O)O)c2ccccc2)c(C)c1 10.1021/jm00078a014
CHEMBL335289 115007 0 None 851 2 Rabbit 8.0 pIC50 = 8 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 456 8 1 5 5.6 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(N(CC)C(C(=O)O)c2ccccc2)c(C)c1 10.1021/jm00078a014
19939399 105671 0 None - 1 Rabbit 8.0 pIC50 = 8 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 609 11 2 10 5.2 CCCCc1nn(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL313696 105671 0 None - 1 Rabbit 8.0 pIC50 = 8 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 609 11 2 10 5.2 CCCCc1nn(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
10222835 204415 0 None 2 2 Rabbit 8.0 pIC50 = 8 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 403 8 1 7 3.3 CCCCc1nn(CC)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL86084 204415 0 None 2 2 Rabbit 8.0 pIC50 = 8 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 403 8 1 7 3.3 CCCCc1nn(CC)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
142533975 166484 0 None - 1 Human 8.0 pIC50 = 8.0 Functional
Antagonist activity at type-1 angiotensin 2 receptor (unknown origin) by beta-arrestin recruitment assayAntagonist activity at type-1 angiotensin 2 receptor (unknown origin) by beta-arrestin recruitment assay
ChEMBL 571 10 1 7 5.7 CCCCc1nc(C(C)C)c(CC(=S)N2CCCC2)c(=O)n1Cc1ccc(-c2ccccc2-c2noc(=O)[nH]2)cc1 10.1016/j.bmcl.2018.08.036
CHEMBL4288964 166484 0 None - 1 Human 8.0 pIC50 = 8.0 Functional
Antagonist activity at type-1 angiotensin 2 receptor (unknown origin) by beta-arrestin recruitment assayAntagonist activity at type-1 angiotensin 2 receptor (unknown origin) by beta-arrestin recruitment assay
ChEMBL 571 10 1 7 5.7 CCCCc1nc(C(C)C)c(CC(=S)N2CCCC2)c(=O)n1Cc1ccc(-c2ccccc2-c2noc(=O)[nH]2)cc1 10.1016/j.bmcl.2018.08.036
44348352 16336 0 None 1 2 Rabbit 7.0 pIC50 = 7 Functional
Antagonist activity at angiotensin AT1 receptor in rabbit adrenal cortex assessed as inhibition of angiotensin 2-induced contractile responseAntagonist activity at angiotensin AT1 receptor in rabbit adrenal cortex assessed as inhibition of angiotensin 2-induced contractile response
ChEMBL 459 8 1 6 4.5 CCOC(=O)/C=C1\N(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)C(=O)CC1(CC)CC 10.1016/j.bmc.2010.10.043
CHEMBL123713 16336 0 None 1 2 Rabbit 7.0 pIC50 = 7 Functional
Antagonist activity at angiotensin AT1 receptor in rabbit adrenal cortex assessed as inhibition of angiotensin 2-induced contractile responseAntagonist activity at angiotensin AT1 receptor in rabbit adrenal cortex assessed as inhibition of angiotensin 2-induced contractile response
ChEMBL 459 8 1 6 4.5 CCOC(=O)/C=C1\N(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)C(=O)CC1(CC)CC 10.1016/j.bmc.2010.10.043
14971675 205231 0 None - 1 Rabbit 7.0 pIC50 = 7 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 540 10 1 7 6.5 CCCCc1nn(-c2ccc(Cl)cc2)c(C(=O)OCC)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
CHEMBL91287 205231 0 None - 1 Rabbit 7.0 pIC50 = 7 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 540 10 1 7 6.5 CCCCc1nn(-c2ccc(Cl)cc2)c(C(=O)OCC)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
10048220 25969 0 None 109 2 Rabbit 7.0 pIC50 = 7 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 428 7 2 5 5.2 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(NC(C(=O)O)c2ccccc2)c(C)c1 10.1021/jm00078a014
CHEMBL135704 25969 0 None 109 2 Rabbit 7.0 pIC50 = 7 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 428 7 2 5 5.2 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(NC(C(=O)O)c2ccccc2)c(C)c1 10.1021/jm00078a014
14956760 164937 0 None - 1 Rabbit 7.0 pIC50 = 7 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 466 8 2 8 3.9 CCCCc1nn(-c2ccccc2N)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL424053 164937 0 None - 1 Rabbit 7.0 pIC50 = 7 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 466 8 2 8 3.9 CCCCc1nn(-c2ccccc2N)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
14956777 204596 0 None - 1 Rabbit 7.0 pIC50 = 7 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 415 8 1 7 3.6 CCCCc1nn(C2CC2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL87276 204596 0 None - 1 Rabbit 7.0 pIC50 = 7 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 415 8 1 7 3.6 CCCCc1nn(C2CC2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
164611301 184425 0 None -1 2 Human 5.0 pIC50 = 5 Functional
Antagonist activity at human AT1 overexpressed in CHO-K1 cells in presence of 10 nM [Val5-angiotensin II measured after 90 mins by HTRF based IP-one assayAntagonist activity at human AT1 overexpressed in CHO-K1 cells in presence of 10 nM [Val5-angiotensin II measured after 90 mins by HTRF based IP-one assay
ChEMBL 416 7 1 5 3.9 CCCC[C@H]1N(Cc2ccc(-c3ccccc3-c3nnn[nH]3)cc2)C(=O)[C@H]2CCCN21 10.1021/acsmedchemlett.1c00240
CHEMBL4854916 184425 0 None -1 2 Human 5.0 pIC50 = 5 Functional
Antagonist activity at human AT1 overexpressed in CHO-K1 cells in presence of 10 nM [Val5-angiotensin II measured after 90 mins by HTRF based IP-one assayAntagonist activity at human AT1 overexpressed in CHO-K1 cells in presence of 10 nM [Val5-angiotensin II measured after 90 mins by HTRF based IP-one assay
ChEMBL 416 7 1 5 3.9 CCCC[C@H]1N(Cc2ccc(-c3ccccc3-c3nnn[nH]3)cc2)C(=O)[C@H]2CCCN21 10.1021/acsmedchemlett.1c00240
1240113 29242 8 None -3 3 Human 5.0 pIC50 = 5 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 265 3 0 2 4.8 Cc1cccc(CSc2cccc3cccnc23)c1 nan
CHEMBL1384550 29242 8 None -3 3 Human 5.0 pIC50 = 5 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 265 3 0 2 4.8 Cc1cccc(CSc2cccc3cccnc23)c1 nan
164622816 185282 0 None - 1 Human 6.0 pIC50 = 6 Functional
Antagonist activity at human AT1 overexpressed in CHO-K1 cells in presence of 10 nM [Val5-angiotensin II measured after 90 mins by HTRF based IP-one assayAntagonist activity at human AT1 overexpressed in CHO-K1 cells in presence of 10 nM [Val5-angiotensin II measured after 90 mins by HTRF based IP-one assay
ChEMBL 416 7 1 5 3.9 CCCC[C@@H]1N(Cc2ccc(-c3ccccc3-c3nnn[nH]3)cc2)C(=O)[C@@H]2CCCN21 10.1021/acsmedchemlett.1c00240
CHEMBL4868159 185282 0 None - 1 Human 6.0 pIC50 = 6 Functional
Antagonist activity at human AT1 overexpressed in CHO-K1 cells in presence of 10 nM [Val5-angiotensin II measured after 90 mins by HTRF based IP-one assayAntagonist activity at human AT1 overexpressed in CHO-K1 cells in presence of 10 nM [Val5-angiotensin II measured after 90 mins by HTRF based IP-one assay
ChEMBL 416 7 1 5 3.9 CCCC[C@@H]1N(Cc2ccc(-c3ccccc3-c3nnn[nH]3)cc2)C(=O)[C@@H]2CCCN21 10.1021/acsmedchemlett.1c00240
5411796 71568 9 None - 1 Human 5.0 pIC50 = 5.0 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 335 4 1 3 3.9 O=C(N/N=C(\c1ccccc1)c1ccccn1)c1ccccc1Cl nan
CHEMBL1972216 71568 9 None - 1 Human 5.0 pIC50 = 5.0 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 335 4 1 3 3.9 O=C(N/N=C(\c1ccccc1)c1ccccn1)c1ccccc1Cl nan
5740287 39940 8 None -1 2 Human 5.0 pIC50 = 5.0 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 394 6 0 7 4.3 COc1cc(/C=C/c2ccc3cccc(OC)c3n2)c(OC(C)=O)c([N+](=O)[O-])c1 nan
CHEMBL1480264 39940 8 None -1 2 Human 5.0 pIC50 = 5.0 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 394 6 0 7 4.3 COc1cc(/C=C/c2ccc3cccc(OC)c3n2)c(OC(C)=O)c([N+](=O)[O-])c1 nan
5738419 48175 13 None - 1 Human 5.0 pIC50 = 5.0 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 253 2 1 3 4.2 Oc1cccc2ccc(/C=C/c3cccs3)nc12 nan
CHEMBL1555793 48175 13 None - 1 Human 5.0 pIC50 = 5.0 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 253 2 1 3 4.2 Oc1cccc2ccc(/C=C/c3cccs3)nc12 nan
659124 38186 8 None -1 2 Human 5.0 pIC50 = 5.0 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 406 7 1 7 4.4 CCCCn1c(NC(=O)c2ccco2)c(C(=O)OCC)c2nc3ccccc3nc21 nan
CHEMBL1463829 38186 8 None -1 2 Human 5.0 pIC50 = 5.0 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 406 7 1 7 4.4 CCCCn1c(NC(=O)c2ccco2)c(C(=O)OCC)c2nc3ccccc3nc21 nan
1183382 23287 14 None - 1 Human 5.0 pIC50 = 5.0 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 367 5 0 7 3.3 COc1cc(/C=C/[N+](=O)[O-])ccc1OC(=O)c1cc2ccccc2oc1=O nan
CHEMBL1333737 23287 14 None - 1 Human 5.0 pIC50 = 5.0 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 367 5 0 7 3.3 COc1cc(/C=C/[N+](=O)[O-])ccc1OC(=O)c1cc2ccccc2oc1=O nan
1334532 36680 7 None - 1 Human 5.0 pIC50 = 5.0 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 365 2 3 4 3.0 Cc1cc(O)ccc1NC(=S)NC(=O)c1cncc(Br)c1 nan
CHEMBL1451169 36680 7 None - 1 Human 5.0 pIC50 = 5.0 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 365 2 3 4 3.0 Cc1cc(O)ccc1NC(=S)NC(=O)c1cncc(Br)c1 nan
10257526 111866 0 None - 1 Rabbit 7.0 pIC50 = 7.0 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 574 10 1 7 7.1 CCCCc1nn(-c2cc(Cl)ccc2Cl)c(C(=O)OCC)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
CHEMBL329541 111866 0 None - 1 Rabbit 7.0 pIC50 = 7.0 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 574 10 1 7 7.1 CCCCc1nn(-c2cc(Cl)ccc2Cl)c(C(=O)OCC)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
5952109 71687 8 None -1 2 Human 5.0 pIC50 = 5.0 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 389 4 1 5 5.6 CC(=O)/C(=N\Nc1ccc(Cl)cc1Cl)Sc1cccc2cccnc12 nan
CHEMBL1976317 71687 8 None -1 2 Human 5.0 pIC50 = 5.0 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 389 4 1 5 5.6 CC(=O)/C(=N\Nc1ccc(Cl)cc1Cl)Sc1cccc2cccnc12 nan
2236648 28478 11 None - 1 Human 5.0 pIC50 = 5.0 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 355 2 3 3 3.0 CC(C)(C)C(=O)NC(=S)NNC(=O)c1ccc(-c2ccccc2)cc1 nan
CHEMBL1377849 28478 11 None - 1 Human 5.0 pIC50 = 5.0 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 355 2 3 3 3.0 CC(C)(C)C(=O)NC(=S)NNC(=O)c1ccc(-c2ccccc2)cc1 nan
6154033 107982 5 None 1 2 Human 5.0 pIC50 = 5.0 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 319 4 1 3 3.4 O=C(N/N=C(\c1ccccc1)c1cccnc1)c1cccc(F)c1 nan
CHEMBL3199403 107982 5 None 1 2 Human 5.0 pIC50 = 5.0 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 319 4 1 3 3.4 O=C(N/N=C(\c1ccccc1)c1cccnc1)c1cccc(F)c1 nan
4116022 50707 6 None - 1 Human 5.0 pIC50 = 5.0 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 368 10 1 9 3.4 CCCSc1cc(NCCOC(=O)CCC)c([N+](=O)[O-])c2nonc12 nan
CHEMBL1578324 50707 6 None - 1 Human 5.0 pIC50 = 5.0 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 368 10 1 9 3.4 CCCSc1cc(NCCOC(=O)CCC)c([N+](=O)[O-])c2nonc12 nan
19939367 105457 0 None - 1 Rabbit 8.0 pIC50 = 8.0 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 523 10 1 9 4.1 CCCCc1nn(Cc2ccccc2C(=O)OC)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL312921 105457 0 None - 1 Rabbit 8.0 pIC50 = 8.0 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 523 10 1 9 4.1 CCCCc1nn(Cc2ccccc2C(=O)OC)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
14956804 105506 0 None 1 2 Rabbit 8.0 pIC50 = 8.0 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 493 11 1 7 4.9 CCCCc1nn(CCCc2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL313222 105506 0 None 1 2 Rabbit 8.0 pIC50 = 8.0 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 493 11 1 7 4.9 CCCCc1nn(CCCc2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
14956792 106270 0 None - 1 Rabbit 8.0 pIC50 = 8.0 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 479 9 1 7 4.6 CCCCc1nn(Cc2ccccc2C)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL314447 106270 0 None - 1 Rabbit 8.0 pIC50 = 8.0 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 479 9 1 7 4.6 CCCCc1nn(Cc2ccccc2C)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
14956754 156831 0 None - 1 Rabbit 8.0 pIC50 = 8.0 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 541 10 1 7 5.9 CCCCc1nn(-c2ccccc2Cc2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL407827 156831 0 None - 1 Rabbit 8.0 pIC50 = 8.0 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 541 10 1 7 5.9 CCCCc1nn(-c2ccccc2Cc2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
14956787 204614 0 None - 1 Rabbit 8.0 pIC50 = 8.0 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 461 9 1 9 3.0 CCCCc1nn(C(C)C(=O)OC)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL87363 204614 0 None - 1 Rabbit 8.0 pIC50 = 8.0 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 461 9 1 9 3.0 CCCCc1nn(C(C)C(=O)OC)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
44373246 167693 0 None - 1 Bovine 8.0 pIC50 = 8.0 Functional
In vitro antagonistic potency against Angiotensin II receptor, type 1 in rat adrenal cortexIn vitro antagonistic potency against Angiotensin II receptor, type 1 in rat adrenal cortex
ChEMBL 435 5 1 6 4.5 CCc1nc2c(C)cc(C)nc2n1Cc1ccc2c(c1)C(Cc1nnn[nH]1)c1ccccc1-2 10.1021/jm9504722
CHEMBL433895 167693 0 None - 1 Bovine 8.0 pIC50 = 8.0 Functional
In vitro antagonistic potency against Angiotensin II receptor, type 1 in rat adrenal cortexIn vitro antagonistic potency against Angiotensin II receptor, type 1 in rat adrenal cortex
ChEMBL 435 5 1 6 4.5 CCc1nc2c(C)cc(C)nc2n1Cc1ccc2c(c1)C(Cc1nnn[nH]1)c1ccccc1-2 10.1021/jm9504722
14956796 204075 0 None - 1 Rabbit 7.0 pIC50 = 7.0 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 523 10 1 9 4.1 CCCCc1nn(Cc2cccc(C(=O)OC)c2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL83182 204075 0 None - 1 Rabbit 7.0 pIC50 = 7.0 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 523 10 1 9 4.1 CCCCc1nn(Cc2cccc(C(=O)OC)c2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
10094520 24539 0 None 11 2 Rabbit 6.0 pIC50 = 6.0 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 435 5 0 5 5.6 CCc1nc2c(C)cc(C)nc2n1Cc1ccc2c(c1)CCN2C(C#N)c1ccccc1C 10.1021/jm00078a013
CHEMBL134433 24539 0 None 11 2 Rabbit 6.0 pIC50 = 6.0 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 435 5 0 5 5.6 CCc1nc2c(C)cc(C)nc2n1Cc1ccc2c(c1)CCN2C(C#N)c1ccccc1C 10.1021/jm00078a013
3504072 33394 11 None 1 2 Human 5.0 pIC50 = 5.0 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 299 2 2 3 2.1 O=C(NNC(=O)C12CC3CC(CC(C3)C1)C2)c1ccccn1 nan
CHEMBL1421427 33394 11 None 1 2 Human 5.0 pIC50 = 5.0 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 299 2 2 3 2.1 O=C(NNC(=O)C12CC3CC(CC(C3)C1)C2)c1ccccn1 nan
869765 38337 7 None - 1 Human 5.0 pIC50 = 5.0 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 322 5 2 6 3.1 COc1ccc(-c2cc(-c3ccccc3)nc(NN)n2)cc1OC nan
CHEMBL1464917 38337 7 None - 1 Human 5.0 pIC50 = 5.0 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 322 5 2 6 3.1 COc1ccc(-c2cc(-c3ccccc3)nc(NN)n2)cc1OC nan
16446215 47328 9 None - 1 Human 5.0 pIC50 = 5.0 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 467 7 1 6 4.3 Cc1ccc(CS(=O)(=O)c2ncc(Cl)c(C(=O)Nc3ccc(OC(F)F)cc3)n2)cc1 nan
CHEMBL1546607 47328 9 None - 1 Human 5.0 pIC50 = 5.0 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 467 7 1 6 4.3 Cc1ccc(CS(=O)(=O)c2ncc(Cl)c(C(=O)Nc3ccc(OC(F)F)cc3)n2)cc1 nan
5295671 35273 10 None - 1 Human 5.0 pIC50 = 5.0 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 314 2 0 6 2.1 CC(=O)C1=C(c2ccccc2)N(C(C)=O)n2c(C)nnc2S1 nan
CHEMBL1438779 35273 10 None - 1 Human 5.0 pIC50 = 5.0 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 314 2 0 6 2.1 CC(=O)C1=C(c2ccccc2)N(C(C)=O)n2c(C)nnc2S1 nan
1653161 40069 13 None - 1 Human 5.0 pIC50 = 5.0 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 319 3 3 5 1.2 COc1ccccc1C(=O)NNC(=S)NC(=O)c1ccco1 nan
CHEMBL1481281 40069 13 None - 1 Human 5.0 pIC50 = 5.0 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 319 3 3 5 1.2 COc1ccccc1C(=O)NNC(=S)NC(=O)c1ccco1 nan
14956759 204372 0 None - 1 Rabbit 6.9 pIC50 = 6.9 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 495 9 2 8 4.0 CCCCc1nn(-c2ccccc2C(=O)O)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL85704 204372 0 None - 1 Rabbit 6.9 pIC50 = 6.9 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 495 9 2 8 4.0 CCCCc1nn(-c2ccccc2C(=O)O)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
5335659 107964 7 None - 1 Human 4.9 pIC50 = 4.9 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 257 3 1 3 2.4 C/C(=N\NC(=O)c1ccccc1F)c1ccccn1 nan
CHEMBL3199216 107964 7 None - 1 Human 4.9 pIC50 = 4.9 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 257 3 1 3 2.4 C/C(=N\NC(=O)c1ccccc1F)c1ccccn1 nan
16446684 42734 9 None - 1 Human 4.9 pIC50 = 4.9 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 405 5 1 5 3.5 O=C(Nc1ccc(F)cc1)c1nc(S(=O)(=O)Cc2ccccc2)ncc1Cl nan
CHEMBL1504077 42734 9 None - 1 Human 4.9 pIC50 = 4.9 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 405 5 1 5 3.5 O=C(Nc1ccc(F)cc1)c1nc(S(=O)(=O)Cc2ccccc2)ncc1Cl nan
2426231 37874 6 None - 1 Human 4.9 pIC50 = 4.9 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 394 3 3 3 5.3 Cc1c(Cl)cccc1N=C(S)NNc1ncc(C(F)(F)F)cc1Cl nan
CHEMBL1461119 37874 6 None - 1 Human 4.9 pIC50 = 4.9 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 394 3 3 3 5.3 Cc1c(Cl)cccc1N=C(S)NNc1ncc(C(F)(F)F)cc1Cl nan
53319274 57280 0 None - 1 Human 7.9 pIC50 = 7.9 Functional
Antagonist activity at angiotensin AT1 receptor in human PLC-PRF5 cellsAntagonist activity at angiotensin AT1 receptor in human PLC-PRF5 cells
ChEMBL 559 9 1 7 4.2 CCCCN1CC2(CN1Cc1ccc(-c3ccccc3S(=O)(=O)NC(=O)c3ccccc3)cc1)C(=O)CCC2=O 10.1016/j.bmc.2010.10.043
CHEMBL1668000 57280 0 None - 1 Human 7.9 pIC50 = 7.9 Functional
Antagonist activity at angiotensin AT1 receptor in human PLC-PRF5 cellsAntagonist activity at angiotensin AT1 receptor in human PLC-PRF5 cells
ChEMBL 559 9 1 7 4.2 CCCCN1CC2(CN1Cc1ccc(-c3ccccc3S(=O)(=O)NC(=O)c3ccccc3)cc1)C(=O)CCC2=O 10.1016/j.bmc.2010.10.043
10027714 114925 0 None 398 2 Rabbit 7.9 pIC50 = 7.9 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 470 9 1 5 6.0 CCCN(c1ccc(Cn2c(CC)nc3c(C)cc(C)nc32)cc1C)C(C(=O)O)c1ccccc1 10.1021/jm00078a014
CHEMBL335066 114925 0 None 398 2 Rabbit 7.9 pIC50 = 7.9 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 470 9 1 5 6.0 CCCN(c1ccc(Cn2c(CC)nc3c(C)cc(C)nc32)cc1C)C(C(=O)O)c1ccccc1 10.1021/jm00078a014
14956793 204575 0 None - 1 Rabbit 7.9 pIC50 = 7.9 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 479 9 1 7 4.6 CCCCc1nn(Cc2cccc(C)c2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL87129 204575 0 None - 1 Rabbit 7.9 pIC50 = 7.9 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 479 9 1 7 4.6 CCCCc1nn(Cc2cccc(C)c2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
14956791 204608 0 None - 1 Rabbit 7.9 pIC50 = 7.9 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 459 8 2 8 3.4 CCCCc1nn(C2CCCC2O)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL87341 204608 0 None - 1 Rabbit 7.9 pIC50 = 7.9 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 459 8 2 8 3.4 CCCCc1nn(C2CCCC2O)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
14956798 204673 0 None - 1 Rabbit 7.9 pIC50 = 7.9 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 523 10 1 9 4.0 CCCCc1nn(C(C(=O)OC)c2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL87798 204673 0 None - 1 Rabbit 7.9 pIC50 = 7.9 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 523 10 1 9 4.0 CCCCc1nn(C(C(=O)OC)c2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
14951059 204693 0 None -1 2 Rabbit 7.9 pIC50 = 7.9 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 493 10 1 8 4.2 CCCCc1nn(CC(=O)c2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL87942 204693 0 None -1 2 Rabbit 7.9 pIC50 = 7.9 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 493 10 1 8 4.2 CCCCc1nn(CC(=O)c2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
11744670 114742 0 None - 1 Rabbit 6.9 pIC50 = 6.9 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 453 5 0 5 6.2 CCc1nc2c(C)cc(C)nc2n1Cc1ccc2c(ccn2Cc2c(Cl)cccc2C#N)c1 10.1021/jm00078a013
CHEMBL334775 114742 0 None - 1 Rabbit 6.9 pIC50 = 6.9 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 453 5 0 5 6.2 CCc1nc2c(C)cc(C)nc2n1Cc1ccc2c(ccn2Cc2c(Cl)cccc2C#N)c1 10.1021/jm00078a013
14956742 204595 0 None - 1 Rabbit 6.9 pIC50 = 6.9 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 485 8 1 7 4.9 CCCCc1nn(-c2cccc(Cl)c2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL87275 204595 0 None - 1 Rabbit 6.9 pIC50 = 6.9 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 485 8 1 7 4.9 CCCCc1nn(-c2cccc(Cl)c2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
5187118 51570 7 None -5 4 Human 4.9 pIC50 = 4.9 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 338 3 1 3 4.8 Oc1c(C(c2ccccc2Cl)N2CCCC2)ccc2cccnc12 nan
CHEMBL1585527 51570 7 None -5 4 Human 4.9 pIC50 = 4.9 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 338 3 1 3 4.8 Oc1c(C(c2ccccc2Cl)N2CCCC2)ccc2cccnc12 nan
2313746 51826 1 None - 1 Human 4.9 pIC50 = 4.9 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 333 4 4 7 0.6 O=C1OCC(CO)(CO)N=C1NNc1cc(Cl)ccc1Cl nan
CHEMBL1587672 51826 1 None - 1 Human 4.9 pIC50 = 4.9 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 333 4 4 7 0.6 O=C1OCC(CO)(CO)N=C1NNc1cc(Cl)ccc1Cl nan
6917582 45402 1 None - 1 Human 4.9 pIC50 = 4.9 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 378 3 1 5 3.1 COc1ccc2c(c1)C(=O)[C@H](O)[C@@H](c1ccc(OC)c(Br)c1)O2 nan
CHEMBL1529805 45402 1 None - 1 Human 4.9 pIC50 = 4.9 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 378 3 1 5 3.1 COc1ccc2c(c1)C(=O)[C@H](O)[C@@H](c1ccc(OC)c(Br)c1)O2 nan
665535 44725 6 None -1 3 Human 4.9 pIC50 = 4.9 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 425 7 1 9 1.8 COC(=O)CS(=O)(=O)c1nnc([C@H](Cc2ccccc2)NC(=O)OC(C)(C)C)o1 nan
CHEMBL1523699 44725 6 None -1 3 Human 4.9 pIC50 = 4.9 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 425 7 1 9 1.8 COC(=O)CS(=O)(=O)c1nnc([C@H](Cc2ccccc2)NC(=O)OC(C)(C)C)o1 nan
2812568 36961 5 None - 1 Human 4.9 pIC50 = 4.9 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 286 3 2 3 3.8 O=C(NNc1ccc(Cl)cc1)c1sccc1Cl nan
CHEMBL1453309 36961 5 None - 1 Human 4.9 pIC50 = 4.9 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 286 3 2 3 3.8 O=C(NNc1ccc(Cl)cc1)c1sccc1Cl nan
921731 51882 7 None - 1 Human 4.9 pIC50 = 4.9 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 321 5 0 7 2.1 O=C(COC(=O)c1cnccn1)c1ccc(Cl)c([N+](=O)[O-])c1 nan
CHEMBL1588194 51882 7 None - 1 Human 4.9 pIC50 = 4.9 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 321 5 0 7 2.1 O=C(COC(=O)c1cnccn1)c1ccc(Cl)c([N+](=O)[O-])c1 nan
6173110 107661 4 None 1 3 Human 4.9 pIC50 = 4.9 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 331 5 1 4 3.3 COc1cccc(C(=O)N/N=C(/c2ccccc2)c2ccccn2)c1 nan
CHEMBL3196139 107661 4 None 1 3 Human 4.9 pIC50 = 4.9 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 331 5 1 4 3.3 COc1cccc(C(=O)N/N=C(/c2ccccc2)c2ccccn2)c1 nan
2351493 49501 3 None - 1 Human 4.9 pIC50 = 4.9 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 301 4 1 3 3.3 O=C(NN=C(c1ccccc1)c1ccccn1)c1ccccc1 nan
CHEMBL1567294 49501 3 None - 1 Human 4.9 pIC50 = 4.9 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 301 4 1 3 3.3 O=C(NN=C(c1ccccc1)c1ccccn1)c1ccccc1 nan
11467216 122074 0 None - 1 Rabbit 5.9 pIC50 = 5.9 Functional
Vasorelaxing potency was determinedVasorelaxing potency was determined
ChEMBL 567 15 1 10 5.2 CCCCc1nc(Cl)c(COC(=O)CCCCO[N+](=O)[O-])n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm049681p
CHEMBL360220 122074 0 None - 1 Rabbit 5.9 pIC50 = 5.9 Functional
Vasorelaxing potency was determinedVasorelaxing potency was determined
ChEMBL 567 15 1 10 5.2 CCCCc1nc(Cl)c(COC(=O)CCCCO[N+](=O)[O-])n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm049681p
135457059 50727 21 None -2 2 Human 4.9 pIC50 = 4.9 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 329 4 1 5 4.2 Oc1cc(CSc2ccc(Cl)cc2)nc(-c2ccccn2)n1 nan
CHEMBL1578482 50727 21 None -2 2 Human 4.9 pIC50 = 4.9 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 329 4 1 5 4.2 Oc1cc(CSc2ccc(Cl)cc2)nc(-c2ccccn2)n1 nan
2303647 28199 10 None - 1 Human 4.9 pIC50 = 4.9 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 262 3 2 4 3.1 NNc1nc(-c2ccccc2)cc(-c2ccccc2)n1 nan
CHEMBL1375248 28199 10 None - 1 Human 4.9 pIC50 = 4.9 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 262 3 2 4 3.1 NNc1nc(-c2ccccc2)cc(-c2ccccc2)n1 nan
11328757 204241 0 None -1 2 Rabbit 7.9 pIC50 = 7.9 Functional
Antagonist activity against AT1 receptor assessed as inhibition of Ang2-induced rabbit aortic strip contractionAntagonist activity against AT1 receptor assessed as inhibition of Ang2-induced rabbit aortic strip contraction
ChEMBL 464 6 1 5 6.3 CCCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2c(C(=O)O)c(C)nc3ccccc23)cc1 10.1021/jm0603163
CHEMBL84573 204241 0 None -1 2 Rabbit 7.9 pIC50 = 7.9 Functional
Antagonist activity against AT1 receptor assessed as inhibition of Ang2-induced rabbit aortic strip contractionAntagonist activity against AT1 receptor assessed as inhibition of Ang2-induced rabbit aortic strip contraction
ChEMBL 464 6 1 5 6.3 CCCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2c(C(=O)O)c(C)nc3ccccc23)cc1 10.1021/jm0603163
9896251 98305 0 None 1 3 Human 7.9 pIC50 = 7.9 Functional
Antagonist activity at type 1 angiotensin 2 receptorAntagonist activity at type 1 angiotensin 2 receptor
ChEMBL 682 12 1 9 7.1 CCCc1cc(Cn2c(CC)nc3c(C)cc(C)nc32)ccc1OC(C(=O)NS(=O)(=O)c1ccc(C(C)C)cc1)c1ccc2c(c1)OCO2 10.1016/j.bmc.2012.06.011
CHEMBL278176 98305 0 None 1 3 Human 7.9 pIC50 = 7.9 Functional
Antagonist activity at type 1 angiotensin 2 receptorAntagonist activity at type 1 angiotensin 2 receptor
ChEMBL 682 12 1 9 7.1 CCCc1cc(Cn2c(CC)nc3c(C)cc(C)nc32)ccc1OC(C(=O)NS(=O)(=O)c1ccc(C(C)C)cc1)c1ccc2c(c1)OCO2 10.1016/j.bmc.2012.06.011
9958963 205492 0 None - 1 Rabbit 7.9 pIC50 = 7.9 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 540 10 1 7 6.5 CCCCc1nn(-c2ccccc2Cl)c(C(=O)OCC)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
CHEMBL92821 205492 0 None - 1 Rabbit 7.9 pIC50 = 7.9 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 540 10 1 7 6.5 CCCCc1nn(-c2ccccc2Cl)c(C(=O)OCC)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
14971680 205629 0 None - 1 Rabbit 7.9 pIC50 = 7.9 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 520 10 1 7 6.1 CCCCc1nn(-c2ccccc2C)c(C(=O)OCC)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
CHEMBL93735 205629 0 None - 1 Rabbit 7.9 pIC50 = 7.9 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 520 10 1 7 6.1 CCCCc1nn(-c2ccccc2C)c(C(=O)OCC)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
57391456 70532 0 None - 1 Rabbit 7.9 pIC50 = 7.9 Functional
Antagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challengeAntagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challenge
ChEMBL 569 10 1 8 4.4 CCCCc1nc(C)c(CCC(=O)N2CC(C)OC(C)C2)c(=O)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2011.12.116
CHEMBL1951142 70532 0 None - 1 Rabbit 7.9 pIC50 = 7.9 Functional
Antagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challengeAntagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challenge
ChEMBL 569 10 1 8 4.4 CCCCc1nc(C)c(CCC(=O)N2CC(C)OC(C)C2)c(=O)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2011.12.116
14971687 14629 0 None - 1 Rabbit 6.9 pIC50 = 6.9 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 430 9 2 6 4.4 CCCCc1n[nH]c(C(=O)OCC)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
CHEMBL120716 14629 0 None - 1 Rabbit 6.9 pIC50 = 6.9 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 430 9 2 6 4.4 CCCCc1n[nH]c(C(=O)OCC)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
14956812 106177 0 None - 1 Rabbit 6.9 pIC50 = 6.9 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 463 8 1 7 4.1 O=c1n(CCc2ccccc2)nc(C2CC2)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL314333 106177 0 None - 1 Rabbit 6.9 pIC50 = 6.9 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 463 8 1 7 4.1 O=c1n(CCc2ccccc2)nc(C2CC2)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
793621 26360 8 None 1 2 Human 4.9 pIC50 = 4.9 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 281 1 1 5 3.3 CC1=NC(Nc2nc(C)c3ccccc3n2)=NC(C)(C)C1 nan
CHEMBL1361034 26360 8 None 1 2 Human 4.9 pIC50 = 4.9 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 281 1 1 5 3.3 CC1=NC(Nc2nc(C)c3ccccc3n2)=NC(C)(C)C1 nan
2420694 32816 6 None - 1 Human 4.9 pIC50 = 4.9 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 360 3 3 3 4.8 Cc1cccc(NC(S)=NNc2ncc(C(F)(F)F)cc2Cl)c1 nan
CHEMBL1416497 32816 6 None - 1 Human 4.9 pIC50 = 4.9 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 360 3 3 3 4.8 Cc1cccc(NC(S)=NNc2ncc(C(F)(F)F)cc2Cl)c1 nan
1477595 44392 27 None - 1 Human 4.9 pIC50 = 4.9 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 264 3 0 5 1.8 O=[N+]([O-])c1ccc(S(=O)(=O)c2ccccc2)nc1 nan
CHEMBL1520753 44392 27 None - 1 Human 4.9 pIC50 = 4.9 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 264 3 0 5 1.8 O=[N+]([O-])c1ccc(S(=O)(=O)c2ccccc2)nc1 nan
1336836 32775 10 None -1 2 Human 4.9 pIC50 = 4.9 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 398 5 0 6 4.5 Cc1ccc2nc(C)cc(C(=O)OCC(=O)c3ccc(Cl)c([N+](=O)[O-])c3)c2c1 nan
CHEMBL1416155 32775 10 None -1 2 Human 4.9 pIC50 = 4.9 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 398 5 0 6 4.5 Cc1ccc2nc(C)cc(C(=O)OCC(=O)c3ccc(Cl)c([N+](=O)[O-])c3)c2c1 nan
135489943 107367 3 None - 1 Human 4.9 pIC50 = 4.9 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 387 9 2 5 4.0 CCCCN(CCCC)C(=S)N/N=C/c1c(C)nn(-c2ccccc2)c1O nan
CHEMBL3192625 107367 3 None - 1 Human 4.9 pIC50 = 4.9 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 387 9 2 5 4.0 CCCCN(CCCC)C(=S)N/N=C/c1c(C)nn(-c2ccccc2)c1O nan
1139588 38111 11 None - 1 Human 4.9 pIC50 = 4.9 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 363 5 0 6 3.2 O=C(Cn1nnc2ccccc21)OCC(=O)c1ccc(Cl)c(Cl)c1 nan
CHEMBL1463168 38111 11 None - 1 Human 4.9 pIC50 = 4.9 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 363 5 0 6 3.2 O=C(Cn1nnc2ccccc21)OCC(=O)c1ccc(Cl)c(Cl)c1 nan
6873170 107966 8 None - 1 Human 4.9 pIC50 = 4.9 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 249 2 1 3 1.2 S=C(N/N=C/c1ccccc1)N1CCOCC1 nan
CHEMBL3199234 107966 8 None - 1 Human 4.9 pIC50 = 4.9 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 249 2 1 3 1.2 S=C(N/N=C/c1ccccc1)N1CCOCC1 nan
804442 53529 53 None - 1 Human 4.9 pIC50 = 4.9 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 289 4 1 2 3.7 O=C(CNc1ccc(Br)cc1)c1ccccc1 nan
CHEMBL1604367 53529 53 None - 1 Human 4.9 pIC50 = 4.9 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 289 4 1 2 3.7 O=C(CNc1ccc(Br)cc1)c1ccccc1 nan
929469 46284 9 None - 1 Human 4.9 pIC50 = 4.9 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 287 5 0 7 1.4 O=C(COC(=O)c1cnccn1)c1cccc([N+](=O)[O-])c1 nan
CHEMBL1537991 46284 9 None - 1 Human 4.9 pIC50 = 4.9 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 287 5 0 7 1.4 O=C(COC(=O)c1cnccn1)c1cccc([N+](=O)[O-])c1 nan
3244543 197805 24 None -3 2 Human 4.9 pIC50 = 4.9 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 188 0 2 3 2.1 Cc1cc(C)c2ccc(N)nc2c1O nan
CHEMBL591834 197805 24 None -3 2 Human 4.9 pIC50 = 4.9 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 188 0 2 3 2.1 Cc1cc(C)c2ccc(N)nc2c1O nan
43001 52490 25 None - 1 Human 4.9 pIC50 = 4.9 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 230 1 1 4 2.0 Nc1c(N2CCCC2)c2ccccc2oc1=O nan
CHEMBL1594894 52490 25 None - 1 Human 4.9 pIC50 = 4.9 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 230 1 1 4 2.0 Nc1c(N2CCCC2)c2ccccc2oc1=O nan
788616 52779 9 None - 1 Human 4.9 pIC50 = 4.9 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 269 5 1 4 2.8 COC(=O)c1ccc(NCC(=O)c2ccccc2)cc1 nan
CHEMBL1597563 52779 9 None - 1 Human 4.9 pIC50 = 4.9 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 269 5 1 4 2.8 COC(=O)c1ccc(NCC(=O)c2ccccc2)cc1 nan
2998385 24935 1 None - 1 Human 4.9 pIC50 = 4.9 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 381 8 1 6 2.7 CC(NC(=O)COc1ccccc1)C(=O)OCC(=O)c1cc2ccccc2o1 nan
CHEMBL1347643 24935 1 None - 1 Human 4.9 pIC50 = 4.9 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 381 8 1 6 2.7 CC(NC(=O)COc1ccccc1)C(=O)OCC(=O)c1cc2ccccc2o1 nan
9549748 23021 8 None - 1 Human 4.9 pIC50 = 4.9 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 287 1 1 1 4.4 SC1=NCCc2ccccc2C1c1ccccc1Cl nan
CHEMBL1331656 23021 8 None - 1 Human 4.9 pIC50 = 4.9 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 287 1 1 1 4.4 SC1=NCCc2ccccc2C1c1ccccc1Cl nan
2939261 21900 6 None - 1 Human 4.9 pIC50 = 4.9 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 329 4 3 4 3.4 CCC(C)c1ccc(O)c(NC(=S)NC(=O)c2cccnc2)c1 nan
CHEMBL1322052 21900 6 None - 1 Human 4.9 pIC50 = 4.9 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 329 4 3 4 3.4 CCC(C)c1ccc(O)c(NC(=S)NC(=O)c2cccnc2)c1 nan
14956799 106403 0 None - 1 Rabbit 7.9 pIC50 = 7.9 Functional
In vitro antagonistic activity for AT1 receptor by displacing 125I[Sar, ILe8]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for AT1 receptor by displacing 125I[Sar, ILe8]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 509 10 2 8 4.0 CCCCc1nn(Cc2ccccc2C(=O)O)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL314590 106403 0 None - 1 Rabbit 7.9 pIC50 = 7.9 Functional
In vitro antagonistic activity for AT1 receptor by displacing 125I[Sar, ILe8]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for AT1 receptor by displacing 125I[Sar, ILe8]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 509 10 2 8 4.0 CCCCc1nn(Cc2ccccc2C(=O)O)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
14956766 106483 0 None - 1 Rabbit 7.9 pIC50 = 7.9 Functional
In vitro antagonistic activity for AT1 receptor by displacing 125I[Sar, ILe8]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for AT1 receptor by displacing 125I[Sar, ILe8]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 471 7 1 7 4.5 CCCc1nn(-c2ccccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL315128 106483 0 None - 1 Rabbit 7.9 pIC50 = 7.9 Functional
In vitro antagonistic activity for AT1 receptor by displacing 125I[Sar, ILe8]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for AT1 receptor by displacing 125I[Sar, ILe8]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 471 7 1 7 4.5 CCCc1nn(-c2ccccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
14956813 204606 0 None - 1 Rabbit 7.9 pIC50 = 7.9 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 477 9 1 7 4.1 O=c1n(CCc2ccccc2)nc(CC2CC2)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL87330 204606 0 None - 1 Rabbit 7.9 pIC50 = 7.9 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 477 9 1 7 4.1 O=c1n(CCc2ccccc2)nc(CC2CC2)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
44211606 100730 0 None - 1 Bovine 6.9 pIC50 = 6.9 Functional
In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.
ChEMBL 591 10 1 10 5.2 CCCCc1nc2ccc(C3(C)CC(C(=O)OCC)=NO3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80365-0
CHEMBL295905 100730 0 None - 1 Bovine 6.9 pIC50 = 6.9 Functional
In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.
ChEMBL 591 10 1 10 5.2 CCCCc1nc2ccc(C3(C)CC(C(=O)OCC)=NO3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80365-0
44246747 55532 0 None - 1 Human 4.9 pIC50 = 4.9 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 429 3 2 5 3.2 O=C1/C(=C/c2ccccc2)C[C@@]2(O)[C@H]3Cc4ccc(O)c5c4[C@@]2(CCN3CC2CC2)C1O5 nan
CHEMBL1521291 55532 0 None - 1 Human 4.9 pIC50 = 4.9 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 429 3 2 5 3.2 O=C1/C(=C/c2ccccc2)C[C@@]2(O)[C@H]3Cc4ccc(O)c5c4[C@@]2(CCN3CC2CC2)C1O5 nan
CHEMBL1623128 55532 0 None - 1 Human 4.9 pIC50 = 4.9 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 429 3 2 5 3.2 O=C1/C(=C/c2ccccc2)C[C@@]2(O)[C@H]3Cc4ccc(O)c5c4[C@@]2(CCN3CC2CC2)C1O5 nan
135501733 36814 14 None -1 2 Human 4.9 pIC50 = 4.9 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 336 3 2 5 2.4 Cc1nc(-n2nc3c(c2O)CCCC3)[nH]c(=O)c1Cc1ccccc1 nan
CHEMBL1452116 36814 14 None -1 2 Human 4.9 pIC50 = 4.9 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 336 3 2 5 2.4 Cc1nc(-n2nc3c(c2O)CCCC3)[nH]c(=O)c1Cc1ccccc1 nan
2898747 36520 11 None - 1 Human 4.8 pIC50 = 4.8 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 418 6 0 7 1.8 O=C(CN1C(=O)C2C3C=CC(C3)C2C1=O)OCC(=O)c1ccc(Cl)c([N+](=O)[O-])c1 nan
CHEMBL1449757 36520 11 None - 1 Human 4.8 pIC50 = 4.8 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 418 6 0 7 1.8 O=C(CN1C(=O)C2C3C=CC(C3)C2C1=O)OCC(=O)c1ccc(Cl)c([N+](=O)[O-])c1 nan
788619 45296 10 None - 1 Human 4.8 pIC50 = 4.8 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 273 4 1 2 4.3 Cc1ccc(C)c(NCC(=O)c2ccc(Cl)cc2)c1 nan
CHEMBL1528883 45296 10 None - 1 Human 4.8 pIC50 = 4.8 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 273 4 1 2 4.3 Cc1ccc(C)c(NCC(=O)c2ccc(Cl)cc2)c1 nan
3648468 51217 8 None - 1 Human 4.8 pIC50 = 4.8 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 373 4 1 3 4.6 O=C(CNc1ccc(Br)cc1)c1ccc(Br)s1 nan
CHEMBL1582697 51217 8 None - 1 Human 4.8 pIC50 = 4.8 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 373 4 1 3 4.6 O=C(CNc1ccc(Br)cc1)c1ccc(Br)s1 nan
135419079 29997 8 None -1 4 Human 4.8 pIC50 = 4.8 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 340 2 2 5 4.0 Cc1[nH]c2ccccc2c1/C=C1\SC(=N)N(c2nccs2)C1=O nan
CHEMBL1390716 29997 8 None -1 4 Human 4.8 pIC50 = 4.8 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 340 2 2 5 4.0 Cc1[nH]c2ccccc2c1/C=C1\SC(=N)N(c2nccs2)C1=O nan
877472 36431 8 None - 1 Human 4.8 pIC50 = 4.8 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 323 4 1 2 4.4 O=C(CNc1cccc(Cl)c1)c1ccc(Br)cc1 nan
CHEMBL1449035 36431 8 None - 1 Human 4.8 pIC50 = 4.8 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 323 4 1 2 4.4 O=C(CNc1cccc(Cl)c1)c1ccc(Br)cc1 nan
902793 42952 17 None - 1 Human 4.8 pIC50 = 4.8 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 309 4 0 4 3.4 O=C(COC(=O)c1ccncc1)c1ccc(Cl)c(Cl)c1 nan
CHEMBL1505893 42952 17 None - 1 Human 4.8 pIC50 = 4.8 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 309 4 0 4 3.4 O=C(COC(=O)c1ccncc1)c1ccc(Cl)c(Cl)c1 nan
67903280 185610 0 None 4 2 Human 7.8 pIC50 = 7.8 Functional
Antagonist activity at human AT1 overexpressed in CHO-K1 cells in presence of 10 nM [Val5-angiotensin II measured after 90 mins by HTRF based IP-one assayAntagonist activity at human AT1 overexpressed in CHO-K1 cells in presence of 10 nM [Val5-angiotensin II measured after 90 mins by HTRF based IP-one assay
ChEMBL 430 8 1 5 4.9 CCCCC1=NC(C)(C(C)C)C(=O)N1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1021/acsmedchemlett.1c00240
CHEMBL4872989 185610 0 None 4 2 Human 7.8 pIC50 = 7.8 Functional
Antagonist activity at human AT1 overexpressed in CHO-K1 cells in presence of 10 nM [Val5-angiotensin II measured after 90 mins by HTRF based IP-one assayAntagonist activity at human AT1 overexpressed in CHO-K1 cells in presence of 10 nM [Val5-angiotensin II measured after 90 mins by HTRF based IP-one assay
ChEMBL 430 8 1 5 4.9 CCCCC1=NC(C)(C(C)C)C(=O)N1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1021/acsmedchemlett.1c00240
44355662 26243 0 None 125 2 Rabbit 7.8 pIC50 = 7.8 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 506 6 1 5 6.7 CCc1nc2c(C)cc(C)nc2n1Cc1ccc2c(ccn2Cc2cc(Cl)c(Cl)cc2C(=O)O)c1 10.1021/jm00078a013
CHEMBL135999 26243 0 None 125 2 Rabbit 7.8 pIC50 = 7.8 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 506 6 1 5 6.7 CCc1nc2c(C)cc(C)nc2n1Cc1ccc2c(ccn2Cc2cc(Cl)c(Cl)cc2C(=O)O)c1 10.1021/jm00078a013
10004013 116180 0 None - 1 Rabbit 7.8 pIC50 = 7.8 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 452 7 1 7 4.4 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(N(C)C(c2ccccc2)c2nnn[nH]2)cc1 10.1021/jm00078a014
CHEMBL337217 116180 0 None - 1 Rabbit 7.8 pIC50 = 7.8 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 452 7 1 7 4.4 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(N(C)C(c2ccccc2)c2nnn[nH]2)cc1 10.1021/jm00078a014
14956744 204433 0 None - 1 Rabbit 7.8 pIC50 = 7.8 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 481 9 1 8 4.3 CCCCc1nn(-c2cccc(OC)c2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL86255 204433 0 None - 1 Rabbit 7.8 pIC50 = 7.8 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 481 9 1 8 4.3 CCCCc1nn(-c2cccc(OC)c2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
1726745 23711 11 None - 1 Human 4.8 pIC50 = 4.8 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 390 8 1 6 3.4 O=C(CCC(=O)OCC(=O)c1cccc([N+](=O)[O-])c1)Nc1ccccc1Cl nan
CHEMBL1337184 23711 11 None - 1 Human 4.8 pIC50 = 4.8 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 390 8 1 6 3.4 O=C(CCC(=O)OCC(=O)c1cccc([N+](=O)[O-])c1)Nc1ccccc1Cl nan
5731702 186060 10 None - 1 Human 4.8 pIC50 = 4.8 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 277 3 1 3 4.1 COc1cccc(/C=C/c2ccc3cccc(O)c3n2)c1 nan
CHEMBL488140 186060 10 None - 1 Human 4.8 pIC50 = 4.8 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 277 3 1 3 4.1 COc1cccc(/C=C/c2ccc3cccc(O)c3n2)c1 nan
2476054 47618 2 None - 1 Human 4.8 pIC50 = 4.8 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 347 3 3 4 3.9 FC(F)(F)c1cnc(NN=C(S)Nc2cccnc2)c(Cl)c1 nan
CHEMBL1549272 47618 2 None - 1 Human 4.8 pIC50 = 4.8 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 347 3 3 4 3.9 FC(F)(F)c1cnc(NN=C(S)Nc2cccnc2)c(Cl)c1 nan
2458676 31180 5 None - 1 Human 4.8 pIC50 = 4.8 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 373 6 1 6 2.4 CNS(=O)(=O)c1cccc(C(=O)OCC(=O)c2cc3ccccc3o2)c1 nan
CHEMBL1402558 31180 5 None - 1 Human 4.8 pIC50 = 4.8 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 373 6 1 6 2.4 CNS(=O)(=O)c1cccc(C(=O)OCC(=O)c2cc3ccccc3o2)c1 nan
2221657 34277 11 None -3 2 Human 4.8 pIC50 = 4.8 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 353 2 0 5 3.6 O=C1c2cccc3c([N+](=O)[O-])ccc(c23)C(=O)N1c1ccc(Cl)cn1 nan
CHEMBL1428950 34277 11 None -3 2 Human 4.8 pIC50 = 4.8 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 353 2 0 5 3.6 O=C1c2cccc3c([N+](=O)[O-])ccc(c23)C(=O)N1c1ccc(Cl)cn1 nan
44342039 10181 0 None -21 3 Human 6.8 pIC50 = 6.8 Functional
Antagonist activity at human AT1 overexpressed in CHO-K1 cells in presence of 10 nM [Val5-angiotensin II measured after 90 mins by HTRF based IP-one assayAntagonist activity at human AT1 overexpressed in CHO-K1 cells in presence of 10 nM [Val5-angiotensin II measured after 90 mins by HTRF based IP-one assay
ChEMBL 418 7 1 3 5.7 CCCCC1=NC2(CCCCC2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/acsmedchemlett.1c00240
CHEMBL116170 10181 0 None -21 3 Human 6.8 pIC50 = 6.8 Functional
Antagonist activity at human AT1 overexpressed in CHO-K1 cells in presence of 10 nM [Val5-angiotensin II measured after 90 mins by HTRF based IP-one assayAntagonist activity at human AT1 overexpressed in CHO-K1 cells in presence of 10 nM [Val5-angiotensin II measured after 90 mins by HTRF based IP-one assay
ChEMBL 418 7 1 3 5.7 CCCCC1=NC2(CCCCC2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/acsmedchemlett.1c00240
2426360 46609 6 None -8 2 Human 4.8 pIC50 = 4.8 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 382 3 3 3 4.6 Fc1ccc(N=C(S)NNc2ncc(C(F)(F)F)cc2Cl)c(F)c1 nan
CHEMBL1540808 46609 6 None -8 2 Human 4.8 pIC50 = 4.8 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 382 3 3 3 4.6 Fc1ccc(N=C(S)NNc2ncc(C(F)(F)F)cc2Cl)c(F)c1 nan
9653239 107149 4 None - 1 Human 5.8 pIC50 = 5.8 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 291 3 2 4 2.7 O=C(N/N=C/c1cccc2cccnc12)c1ccccc1O nan
CHEMBL3190198 107149 4 None - 1 Human 5.8 pIC50 = 5.8 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 291 3 2 4 2.7 O=C(N/N=C/c1cccc2cccnc12)c1ccccc1O nan
5730138 34555 11 None - 1 Human 4.8 pIC50 = 4.8 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 307 4 1 4 4.1 COc1cccc(/C=C/c2ccc3cccc(O)c3n2)c1OC nan
CHEMBL1431014 34555 11 None - 1 Human 4.8 pIC50 = 4.8 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 307 4 1 4 4.1 COc1cccc(/C=C/c2ccc3cccc(O)c3n2)c1OC nan
12005285 52769 6 None 3 2 Human 5.8 pIC50 = 5.8 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 402 8 1 9 4.0 CC(=O)OCCCNc1cc(Sc2ccc(C)cc2)c2nonc2c1[N+](=O)[O-] nan
CHEMBL1597454 52769 6 None 3 2 Human 5.8 pIC50 = 5.8 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 402 8 1 9 4.0 CC(=O)OCCCNc1cc(Sc2ccc(C)cc2)c2nonc2c1[N+](=O)[O-] nan
1767917 31006 10 None -3 2 Human 4.8 pIC50 = 4.8 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 375 5 3 4 2.2 Cc1nn(CCC(=O)NNC(S)=NCC(C)C)c(C)c1Br nan
CHEMBL1401122 31006 10 None -3 2 Human 4.8 pIC50 = 4.8 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 375 5 3 4 2.2 Cc1nn(CCC(=O)NNC(S)=NCC(C)C)c(C)c1Br nan
14956806 106434 0 None - 1 Rabbit 7.8 pIC50 = 7.8 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 497 10 1 8 5.0 CCCCc1nn(CSc2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL314810 106434 0 None - 1 Rabbit 7.8 pIC50 = 7.8 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 497 10 1 8 5.0 CCCCc1nn(CSc2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
14956768 106475 0 None - 1 Rabbit 7.8 pIC50 = 7.8 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 499 8 1 7 5.2 CC(C)CCc1nn(-c2ccccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL315077 106475 0 None - 1 Rabbit 7.8 pIC50 = 7.8 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 499 8 1 7 5.2 CC(C)CCc1nn(-c2ccccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
14956745 204536 0 None - 1 Rabbit 7.8 pIC50 = 7.8 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 465 8 1 7 4.6 CCCCc1nn(-c2ccc(C)cc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL86906 204536 0 None - 1 Rabbit 7.8 pIC50 = 7.8 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 465 8 1 7 4.6 CCCCc1nn(-c2ccc(C)cc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
14951062 204656 0 None -1 2 Rabbit 7.8 pIC50 = 7.8 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 429 9 1 7 3.7 CCCCc1nn(CC2CC2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL87669 204656 0 None -1 2 Rabbit 7.8 pIC50 = 7.8 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 429 9 1 7 3.7 CCCCc1nn(CC2CC2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
14971694 14508 0 None - 1 Rabbit 6.8 pIC50 = 6.8 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 416 8 2 6 4.0 CCCc1n[nH]c(C(=O)OCC)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
CHEMBL120605 14508 0 None - 1 Rabbit 6.8 pIC50 = 6.8 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 416 8 2 6 4.0 CCCc1n[nH]c(C(=O)OCC)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
44355660 21342 0 None 89 2 Rabbit 6.8 pIC50 = 6.8 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 483 7 1 7 5.3 CCc1nc2c(C)cc(C)nc2n1Cc1ccc2c(ccn2Cc2cccc([N+](=O)[O-])c2C(=O)O)c1 10.1021/jm00078a013
CHEMBL131676 21342 0 None 89 2 Rabbit 6.8 pIC50 = 6.8 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 483 7 1 7 5.3 CCc1nc2c(C)cc(C)nc2n1Cc1ccc2c(ccn2Cc2cccc([N+](=O)[O-])c2C(=O)O)c1 10.1021/jm00078a013
10410730 24399 0 None 6 2 Rabbit 5.8 pIC50 = 5.8 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 435 5 0 5 5.6 CCc1nc2c(C)cc(C)nc2n1Cc1ccc2c(c1)CCN2C(C#N)c1cccc(C)c1 10.1021/jm00078a013
CHEMBL134307 24399 0 None 6 2 Rabbit 5.8 pIC50 = 5.8 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 435 5 0 5 5.6 CCc1nc2c(C)cc(C)nc2n1Cc1ccc2c(c1)CCN2C(C#N)c1cccc(C)c1 10.1021/jm00078a013
2898434 53570 9 None - 1 Human 4.8 pIC50 = 4.8 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 406 6 0 7 1.9 O=C(CN1C(=O)C2CC=CCC2C1=O)OCC(=O)c1ccc(Cl)c([N+](=O)[O-])c1 nan
CHEMBL1604741 53570 9 None - 1 Human 4.8 pIC50 = 4.8 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 406 6 0 7 1.9 O=C(CN1C(=O)C2CC=CCC2C1=O)OCC(=O)c1ccc(Cl)c([N+](=O)[O-])c1 nan
3532334 42092 7 None - 1 Human 4.8 pIC50 = 4.8 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 303 2 1 4 3.2 O=c1c2cc(Cl)ccc2[nH]c(=S)n1Cc1ccccn1 nan
CHEMBL1498428 42092 7 None - 1 Human 4.8 pIC50 = 4.8 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 303 2 1 4 3.2 O=c1c2cc(Cl)ccc2[nH]c(=S)n1Cc1ccccn1 nan
2640418 21933 8 None - 1 Human 4.8 pIC50 = 4.8 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 377 6 0 6 2.5 O=C(COC(=O)c1ccco1)c1ccc(S(=O)(=O)N2CCCCC2)cc1 nan
CHEMBL1322344 21933 8 None - 1 Human 4.8 pIC50 = 4.8 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 377 6 0 6 2.5 O=C(COC(=O)c1ccco1)c1ccc(S(=O)(=O)N2CCCCC2)cc1 nan
5687785 107905 2 None - 1 Human 4.8 pIC50 = 4.8 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 346 5 1 5 3.2 O=C(N/N=C(\c1ccccc1)c1ccccn1)c1cccc([N+](=O)[O-])c1 nan
CHEMBL3198576 107905 2 None - 1 Human 4.8 pIC50 = 4.8 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 346 5 1 5 3.2 O=C(N/N=C(\c1ccccc1)c1ccccn1)c1cccc([N+](=O)[O-])c1 nan
5735740 41394 10 None - 1 Human 4.8 pIC50 = 4.8 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 321 5 1 4 4.5 CCOc1cccc(/C=C/c2ccc3cccc(O)c3n2)c1OC nan
CHEMBL1491932 41394 10 None - 1 Human 4.8 pIC50 = 4.8 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 321 5 1 4 4.5 CCOc1cccc(/C=C/c2ccc3cccc(O)c3n2)c1OC nan
2320855 36307 5 None - 1 Human 4.8 pIC50 = 4.8 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 333 4 4 7 0.6 O=C1OCC(CO)(CO)N=C1NNc1ccc(Cl)c(Cl)c1 nan
CHEMBL1448161 36307 5 None - 1 Human 4.8 pIC50 = 4.8 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 333 4 4 7 0.6 O=C1OCC(CO)(CO)N=C1NNc1ccc(Cl)c(Cl)c1 nan
5091521 25076 7 None - 1 Human 4.8 pIC50 = 4.8 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 402 2 2 9 2.9 CC1(C)Cc2c(c(N3CCOCC3)nc3sc4c(NN)ncnc4c23)CS1 nan
CHEMBL1348954 25076 7 None - 1 Human 4.8 pIC50 = 4.8 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 402 2 2 9 2.9 CC1(C)Cc2c(c(N3CCOCC3)nc3sc4c(NN)ncnc4c23)CS1 nan
2121806 41805 6 None - 1 Human 4.8 pIC50 = 4.8 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 266 4 1 6 2.3 CCSc1nnc(NC(=O)c2ccccn2)s1 nan
CHEMBL1495849 41805 6 None - 1 Human 4.8 pIC50 = 4.8 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 266 4 1 6 2.3 CCSc1nnc(NC(=O)c2ccccn2)s1 nan
2733001 29069 4 None -1 2 Human 4.8 pIC50 = 4.8 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 288 5 1 4 3.7 Cc1ccc(C(C[N+](=O)[O-])Sc2ccc(N)cc2)cc1 nan
CHEMBL1382939 29069 4 None -1 2 Human 4.8 pIC50 = 4.8 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 288 5 1 4 3.7 Cc1ccc(C(C[N+](=O)[O-])Sc2ccc(N)cc2)cc1 nan
25162518 39597 6 None - 1 Human 4.8 pIC50 = 4.8 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 417 8 0 6 2.7 O=C(COc1ccccc1)OCC(=O)c1ccc(S(=O)(=O)N2CCCCC2)cc1 nan
CHEMBL1477291 39597 6 None - 1 Human 4.8 pIC50 = 4.8 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 417 8 0 6 2.7 O=C(COc1ccccc1)OCC(=O)c1ccc(S(=O)(=O)N2CCCCC2)cc1 nan
14956784 106062 0 None - 1 Rabbit 7.8 pIC50 = 7.8 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 447 9 1 9 2.5 CCCCc1nn(CC(=O)OC)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL314179 106062 0 None - 1 Rabbit 7.8 pIC50 = 7.8 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 447 9 1 9 2.5 CCCCc1nn(CC(=O)OC)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
14956764 204347 0 None - 1 Rabbit 7.8 pIC50 = 7.8 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 541 8 1 7 5.0 CCCCc1nn(-c2c(F)c(F)c(F)c(F)c2F)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL85541 204347 0 None - 1 Rabbit 7.8 pIC50 = 7.8 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 541 8 1 7 5.0 CCCCc1nn(-c2c(F)c(F)c(F)c(F)c2F)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
44355628 24687 0 None 5 2 Rabbit 6.8 pIC50 = 6.8 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 508 6 1 5 6.2 CCc1nc2c(C)cc(C)nc2n1Cc1ccc2c(c1)CCN2Cc1cc(Cl)c(Cl)cc1C(=O)O 10.1021/jm00078a013
CHEMBL134567 24687 0 None 5 2 Rabbit 6.8 pIC50 = 6.8 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 508 6 1 5 6.2 CCc1nc2c(C)cc(C)nc2n1Cc1ccc2c(c1)CCN2Cc1cc(Cl)c(Cl)cc1C(=O)O 10.1021/jm00078a013
10095493 25828 0 None 93 2 Rabbit 6.8 pIC50 = 6.8 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 454 6 0 6 4.9 CCc1nc2c(C)cc(C)nc2n1Cc1ccc2c(c1)CCN2C(C(=O)OC)c1ccccc1 10.1021/jm00078a013
CHEMBL135521 25828 0 None 93 2 Rabbit 6.8 pIC50 = 6.8 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 454 6 0 6 4.9 CCc1nc2c(C)cc(C)nc2n1Cc1ccc2c(c1)CCN2C(C(=O)OC)c1ccccc1 10.1021/jm00078a013
1336623 38037 19 None - 1 Human 4.8 pIC50 = 4.8 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 350 5 0 6 3.5 Cc1cc(C(=O)OCC(=O)c2cccc([N+](=O)[O-])c2)c2ccccc2n1 nan
CHEMBL1462517 38037 19 None - 1 Human 4.8 pIC50 = 4.8 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 350 5 0 6 3.5 Cc1cc(C(=O)OCC(=O)c2cccc([N+](=O)[O-])c2)c2ccccc2n1 nan
2165745 34442 9 None - 1 Human 4.8 pIC50 = 4.8 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 425 8 1 8 0.7 O=C(CN1C(=O)c2ccccc2C1=O)NCC(=O)OCC(=O)c1cccc([N+](=O)[O-])c1 nan
CHEMBL1430172 34442 9 None - 1 Human 4.8 pIC50 = 4.8 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 425 8 1 8 0.7 O=C(CN1C(=O)c2ccccc2C1=O)NCC(=O)OCC(=O)c1cccc([N+](=O)[O-])c1 nan
659805 21751 6 None -2 2 Human 4.8 pIC50 = 4.8 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 302 1 2 4 3.7 ON1C(c2ccc(Cl)cc2Cl)N(O)[C@@H]2CCCC[C@@H]21 nan
CHEMBL1320678 21751 6 None -2 2 Human 4.8 pIC50 = 4.8 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 302 1 2 4 3.7 ON1C(c2ccc(Cl)cc2Cl)N(O)[C@@H]2CCCC[C@@H]21 nan
135415440 197362 8 None -10 5 Human 5.8 pIC50 = 5.8 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 295 3 2 6 3.0 Cc1ccc(Nc2cc(C)nn2-c2nc(C)cc(O)n2)cc1 nan
CHEMBL586135 197362 8 None -10 5 Human 5.8 pIC50 = 5.8 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 295 3 2 6 3.0 Cc1ccc(Nc2cc(C)nn2-c2nc(C)cc(O)n2)cc1 nan
579121 48852 12 None -1 2 Human 4.8 pIC50 = 4.8 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 377 4 1 4 4.7 COc1ccc(NC2(c3ccc(Cl)cc3)C(=O)c3ccccc3C2=O)cc1 nan
CHEMBL1561907 48852 12 None -1 2 Human 4.8 pIC50 = 4.8 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 377 4 1 4 4.7 COc1ccc(NC2(c3ccc(Cl)cc3)C(=O)c3ccccc3C2=O)cc1 nan
24983202 27591 6 None - 1 Human 4.8 pIC50 = 4.8 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 444 7 1 6 2.9 CC(=O)Nc1cccc(C(=O)OCC(=O)c2ccc(S(=O)(=O)N3CCCCC3)cc2)c1 nan
CHEMBL1371002 27591 6 None - 1 Human 4.8 pIC50 = 4.8 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 444 7 1 6 2.9 CC(=O)Nc1cccc(C(=O)OCC(=O)c2ccc(S(=O)(=O)N3CCCCC3)cc2)c1 nan
14971686 15065 0 None - 1 Rabbit 7.8 pIC50 = 7.8 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 507 10 1 8 5.2 CCCCc1nn(-c2ccccn2)c(C(=O)OCC)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
CHEMBL121125 15065 0 None - 1 Rabbit 7.8 pIC50 = 7.8 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 507 10 1 8 5.2 CCCCc1nn(-c2ccccn2)c(C(=O)OCC)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
10414429 115484 0 None 363 2 Rabbit 7.8 pIC50 = 7.8 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 522 5 1 5 5.9 CCc1nc2c(C)cc(C)nc2n1Cc1ccc2c(c1)CCN2C(=O)c1c(Cl)ccc(Cl)c1C(=O)O 10.1021/jm00078a013
CHEMBL335535 115484 0 None 363 2 Rabbit 7.8 pIC50 = 7.8 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 522 5 1 5 5.9 CCc1nc2c(C)cc(C)nc2n1Cc1ccc2c(c1)CCN2C(=O)c1c(Cl)ccc(Cl)c1C(=O)O 10.1021/jm00078a013
10322211 168894 0 None - 1 Rabbit 7.8 pIC50 = 7.8 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 464 6 1 7 4.3 CCc1nc2c(C)cc(C)nc2n1Cc1ccc2c(c1)CCN2C(c1ccccc1)c1nnn[nH]1 10.1021/jm00078a013
CHEMBL442963 168894 0 None - 1 Rabbit 7.8 pIC50 = 7.8 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 464 6 1 7 4.3 CCc1nc2c(C)cc(C)nc2n1Cc1ccc2c(c1)CCN2C(c1ccccc1)c1nnn[nH]1 10.1021/jm00078a013
14956741 106558 0 None - 1 Rabbit 7.8 pIC50 = 7.8 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 465 8 1 7 4.6 CCCCc1nn(-c2cccc(C)c2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL315615 106558 0 None - 1 Rabbit 7.8 pIC50 = 7.8 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 465 8 1 7 4.6 CCCCc1nn(-c2cccc(C)c2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
44292094 100961 0 None - 1 Bovine 6.8 pIC50 = 6.8 Functional
In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.
ChEMBL 585 9 1 9 6.4 CCCCc1nc2ccc(C3CC(c4cc(C)co4)=NO3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80365-0
CHEMBL297583 100961 0 None - 1 Bovine 6.8 pIC50 = 6.8 Functional
In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.
ChEMBL 585 9 1 9 6.4 CCCCc1nc2ccc(C3CC(c4cc(C)co4)=NO3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80365-0
23205 116407 35 None -7 2 Human 4.7 pIC50 = 4.7 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 262 0 1 4 1.2 C=C1C(=O)O[C@@H]2C[C@@H](C)[C@@H]3C=CC(=O)[C@@]3(C)[C@@H](O)[C@H]12 nan
CHEMBL338474 116407 35 None -7 2 Human 4.7 pIC50 = 4.7 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 262 0 1 4 1.2 C=C1C(=O)O[C@@H]2C[C@@H](C)[C@@H]3C=CC(=O)[C@@]3(C)[C@@H](O)[C@H]12 nan
24981067 44933 6 None - 1 Human 4.7 pIC50 = 4.7 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 480 8 1 7 1.8 CNS(=O)(=O)c1cccc(C(=O)OCC(=O)c2ccc(S(=O)(=O)N3CCCCC3)cc2)c1 nan
CHEMBL1525764 44933 6 None - 1 Human 4.7 pIC50 = 4.7 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 480 8 1 7 1.8 CNS(=O)(=O)c1cccc(C(=O)OCC(=O)c2ccc(S(=O)(=O)N3CCCCC3)cc2)c1 nan
768473 49686 6 None - 1 Human 4.7 pIC50 = 4.7 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 267 6 0 2 3.9 CCN(CC)CC(=O)c1ccc(-c2ccccc2)cc1 nan
CHEMBL1568922 49686 6 None - 1 Human 4.7 pIC50 = 4.7 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 267 6 0 2 3.9 CCN(CC)CC(=O)c1ccc(-c2ccccc2)cc1 nan
4799115 24311 8 None - 1 Human 4.7 pIC50 = 4.7 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 332 3 2 4 4.1 O=C(Nc1nc(-c2ccccn2)cs1)Nc1ccc(F)cc1F nan
CHEMBL1342423 24311 8 None - 1 Human 4.7 pIC50 = 4.7 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 332 3 2 4 4.1 O=C(Nc1nc(-c2ccccn2)cs1)Nc1ccc(F)cc1F nan
11957260 32779 6 None 5 2 Human 5.7 pIC50 = 5.7 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 389 6 2 10 3.3 O=[N+]([O-])c1c(NCCO)cc(Sc2nc3ccccc3s2)c2nonc12 nan
CHEMBL1416184 32779 6 None 5 2 Human 5.7 pIC50 = 5.7 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 389 6 2 10 3.3 O=[N+]([O-])c1c(NCCO)cc(Sc2nc3ccccc3s2)c2nonc12 nan
1610 2305 89 None -2 9 Rat 7.7 pIC50 = 7.7 Functional
In vitro antagonistic activity by displacement of [125I]-Sar1-Ile8-A II at the rat adrenal cortical aorta Angiotensin II receptor, type 1In vitro antagonistic activity by displacement of [125I]-Sar1-Ile8-A II at the rat adrenal cortical aorta Angiotensin II receptor, type 1
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00057a009
3941 2305 89 None -2 9 Rat 7.7 pIC50 = 7.7 Functional
In vitro antagonistic activity by displacement of [125I]-Sar1-Ile8-A II at the rat adrenal cortical aorta Angiotensin II receptor, type 1In vitro antagonistic activity by displacement of [125I]-Sar1-Ile8-A II at the rat adrenal cortical aorta Angiotensin II receptor, type 1
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00057a009
3961 2305 89 None -2 9 Rat 7.7 pIC50 = 7.7 Functional
In vitro antagonistic activity by displacement of [125I]-Sar1-Ile8-A II at the rat adrenal cortical aorta Angiotensin II receptor, type 1In vitro antagonistic activity by displacement of [125I]-Sar1-Ile8-A II at the rat adrenal cortical aorta Angiotensin II receptor, type 1
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00057a009
590 2305 89 None -2 9 Rat 7.7 pIC50 = 7.7 Functional
In vitro antagonistic activity by displacement of [125I]-Sar1-Ile8-A II at the rat adrenal cortical aorta Angiotensin II receptor, type 1In vitro antagonistic activity by displacement of [125I]-Sar1-Ile8-A II at the rat adrenal cortical aorta Angiotensin II receptor, type 1
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00057a009
CHEMBL191 2305 89 None -2 9 Rat 7.7 pIC50 = 7.7 Functional
In vitro antagonistic activity by displacement of [125I]-Sar1-Ile8-A II at the rat adrenal cortical aorta Angiotensin II receptor, type 1In vitro antagonistic activity by displacement of [125I]-Sar1-Ile8-A II at the rat adrenal cortical aorta Angiotensin II receptor, type 1
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00057a009
DB00678 2305 89 None -2 9 Rat 7.7 pIC50 = 7.7 Functional
In vitro antagonistic activity by displacement of [125I]-Sar1-Ile8-A II at the rat adrenal cortical aorta Angiotensin II receptor, type 1In vitro antagonistic activity by displacement of [125I]-Sar1-Ile8-A II at the rat adrenal cortical aorta Angiotensin II receptor, type 1
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00057a009
1610 2305 89 None -2 9 Rabbit 7.7 pIC50 = 7.7 Functional
In vitro antagonistic activity for AT1 receptor by displacing 125I[Sar, ILe8]AII radioligand in rabbit aorta membrane using 0.2% bovine serum albumin (BSA)In vitro antagonistic activity for AT1 receptor by displacing 125I[Sar, ILe8]AII radioligand in rabbit aorta membrane using 0.2% bovine serum albumin (BSA)
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00069a015
3941 2305 89 None -2 9 Rabbit 7.7 pIC50 = 7.7 Functional
In vitro antagonistic activity for AT1 receptor by displacing 125I[Sar, ILe8]AII radioligand in rabbit aorta membrane using 0.2% bovine serum albumin (BSA)In vitro antagonistic activity for AT1 receptor by displacing 125I[Sar, ILe8]AII radioligand in rabbit aorta membrane using 0.2% bovine serum albumin (BSA)
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00069a015
3961 2305 89 None -2 9 Rabbit 7.7 pIC50 = 7.7 Functional
In vitro antagonistic activity for AT1 receptor by displacing 125I[Sar, ILe8]AII radioligand in rabbit aorta membrane using 0.2% bovine serum albumin (BSA)In vitro antagonistic activity for AT1 receptor by displacing 125I[Sar, ILe8]AII radioligand in rabbit aorta membrane using 0.2% bovine serum albumin (BSA)
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00069a015
590 2305 89 None -2 9 Rabbit 7.7 pIC50 = 7.7 Functional
In vitro antagonistic activity for AT1 receptor by displacing 125I[Sar, ILe8]AII radioligand in rabbit aorta membrane using 0.2% bovine serum albumin (BSA)In vitro antagonistic activity for AT1 receptor by displacing 125I[Sar, ILe8]AII radioligand in rabbit aorta membrane using 0.2% bovine serum albumin (BSA)
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00069a015
CHEMBL191 2305 89 None -2 9 Rabbit 7.7 pIC50 = 7.7 Functional
In vitro antagonistic activity for AT1 receptor by displacing 125I[Sar, ILe8]AII radioligand in rabbit aorta membrane using 0.2% bovine serum albumin (BSA)In vitro antagonistic activity for AT1 receptor by displacing 125I[Sar, ILe8]AII radioligand in rabbit aorta membrane using 0.2% bovine serum albumin (BSA)
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00069a015
DB00678 2305 89 None -2 9 Rabbit 7.7 pIC50 = 7.7 Functional
In vitro antagonistic activity for AT1 receptor by displacing 125I[Sar, ILe8]AII radioligand in rabbit aorta membrane using 0.2% bovine serum albumin (BSA)In vitro antagonistic activity for AT1 receptor by displacing 125I[Sar, ILe8]AII radioligand in rabbit aorta membrane using 0.2% bovine serum albumin (BSA)
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00069a015
10069786 168524 0 None -19 3 Human 6.7 pIC50 = 6.7 Functional
Antagonist activity at human AT1 overexpressed in CHO-K1 cells in presence of 10 nM [Val5-angiotensin II measured after 90 mins by HTRF based IP-one assayAntagonist activity at human AT1 overexpressed in CHO-K1 cells in presence of 10 nM [Val5-angiotensin II measured after 90 mins by HTRF based IP-one assay
ChEMBL 404 7 1 3 5.3 CCCCC1=NC2(CCCC2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/acsmedchemlett.1c00240
CHEMBL439968 168524 0 None -19 3 Human 6.7 pIC50 = 6.7 Functional
Antagonist activity at human AT1 overexpressed in CHO-K1 cells in presence of 10 nM [Val5-angiotensin II measured after 90 mins by HTRF based IP-one assayAntagonist activity at human AT1 overexpressed in CHO-K1 cells in presence of 10 nM [Val5-angiotensin II measured after 90 mins by HTRF based IP-one assay
ChEMBL 404 7 1 3 5.3 CCCCC1=NC2(CCCC2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/acsmedchemlett.1c00240
10393397 22582 0 None 6 2 Rabbit 5.7 pIC50 = 5.7 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 578 8 1 5 7.3 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(N(CC)C(C(=O)O)c2cc(C(F)(F)F)cc(C(F)(F)F)c2)cc1 10.1021/jm00078a014
CHEMBL132807 22582 0 None 6 2 Rabbit 5.7 pIC50 = 5.7 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 578 8 1 5 7.3 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(N(CC)C(C(=O)O)c2cc(C(F)(F)F)cc(C(F)(F)F)c2)cc1 10.1021/jm00078a014
568849 31491 11 None - 1 Human 4.7 pIC50 = 4.7 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 313 7 0 5 3.0 O=C(CCc1ccccc1)OCC(=O)c1cccc([N+](=O)[O-])c1 nan
CHEMBL1405657 31491 11 None - 1 Human 4.7 pIC50 = 4.7 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 313 7 0 5 3.0 O=C(CCc1ccccc1)OCC(=O)c1cccc([N+](=O)[O-])c1 nan
5720743 107751 7 None - 1 Human 5.7 pIC50 = 5.7 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 257 3 1 3 2.4 C/C(=N\NC(=O)c1ccc(F)cc1)c1ccccn1 nan
CHEMBL3197070 107751 7 None - 1 Human 5.7 pIC50 = 5.7 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 257 3 1 3 2.4 C/C(=N\NC(=O)c1ccc(F)cc1)c1ccccn1 nan
761850 38543 10 None - 1 Human 4.7 pIC50 = 4.7 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 300 5 0 6 2.3 Cc1ccc(C(=O)COC(=O)c2ccncc2)cc1[N+](=O)[O-] nan
CHEMBL1466556 38543 10 None - 1 Human 4.7 pIC50 = 4.7 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 300 5 0 6 2.3 Cc1ccc(C(=O)COC(=O)c2ccncc2)cc1[N+](=O)[O-] nan
142534050 166402 0 None - 1 Human 8.7 pIC50 = 8.7 Functional
Antagonist activity at type-1 angiotensin 2 receptor (unknown origin) by calcium mobilizing assayAntagonist activity at type-1 angiotensin 2 receptor (unknown origin) by calcium mobilizing assay
ChEMBL 545 11 1 7 5.2 CCCCc1nc(C)c(CC(=S)N(CC)CC)c(=O)n1Cc1ccc(-c2ccccc2-c2noc(=O)[nH]2)cc1 10.1016/j.bmcl.2018.08.036
CHEMBL4287379 166402 0 None - 1 Human 8.7 pIC50 = 8.7 Functional
Antagonist activity at type-1 angiotensin 2 receptor (unknown origin) by calcium mobilizing assayAntagonist activity at type-1 angiotensin 2 receptor (unknown origin) by calcium mobilizing assay
ChEMBL 545 11 1 7 5.2 CCCCc1nc(C)c(CC(=S)N(CC)CC)c(=O)n1Cc1ccc(-c2ccccc2-c2noc(=O)[nH]2)cc1 10.1016/j.bmcl.2018.08.036
14971712 99129 0 None - 1 Rabbit 8.7 pIC50 = 8.7 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 402 8 3 5 3.9 CCCCc1n[nH]c(C(=O)O)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
CHEMBL283975 99129 0 None - 1 Rabbit 8.7 pIC50 = 8.7 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 402 8 3 5 3.9 CCCCc1n[nH]c(C(=O)O)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
14956756 204637 0 None - 1 Rabbit 8.7 pIC50 = 8.7 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 529 8 1 7 5.0 CCCCc1nn(-c2ccccc2Br)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL87513 204637 0 None - 1 Rabbit 8.7 pIC50 = 8.7 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 529 8 1 7 5.0 CCCCc1nn(-c2ccccc2Br)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
20081627 91724 0 None -1 2 Rabbit 8.7 pIC50 = 8.7 Functional
Inhibitory activity against Angiotensin II receptor, type 1 induced contractions in isolated rabbit aortic ringsInhibitory activity against Angiotensin II receptor, type 1 induced contractions in isolated rabbit aortic rings
ChEMBL 502 6 2 7 4.7 CC1CC(=O)NN=C1c1ccc2nc(C3CC3)n(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c2c1 10.1016/S0960-894X(01)80348-6
CHEMBL24224 91724 0 None -1 2 Rabbit 8.7 pIC50 = 8.7 Functional
Inhibitory activity against Angiotensin II receptor, type 1 induced contractions in isolated rabbit aortic ringsInhibitory activity against Angiotensin II receptor, type 1 induced contractions in isolated rabbit aortic rings
ChEMBL 502 6 2 7 4.7 CC1CC(=O)NN=C1c1ccc2nc(C3CC3)n(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c2c1 10.1016/S0960-894X(01)80348-6
44459871 92084 0 None - 1 Rabbit 8.7 pIC50 = 8.7 Functional
Inhibitory activity against Angiotensin II receptor, type 1 induced contractions in isolated rabbit aortic ringsInhibitory activity against Angiotensin II receptor, type 1 induced contractions in isolated rabbit aortic rings
ChEMBL 573 8 1 8 4.2 CN(C)C(=O)CN1N=C(c2ccc3nc(C4CC4)n(Cc4ccc(-c5ccccc5-c5nn[nH]n5)cc4)c3c2)CCC1=O 10.1016/S0960-894X(01)80348-6
CHEMBL2079791 92084 0 None - 1 Rabbit 8.7 pIC50 = 8.7 Functional
Inhibitory activity against Angiotensin II receptor, type 1 induced contractions in isolated rabbit aortic ringsInhibitory activity against Angiotensin II receptor, type 1 induced contractions in isolated rabbit aortic rings
ChEMBL 573 8 1 8 4.2 CN(C)C(=O)CN1N=C(c2ccc3nc(C4CC4)n(Cc4ccc(-c5ccccc5-c5nn[nH]n5)cc4)c3c2)CCC1=O 10.1016/S0960-894X(01)80348-6
CHEMBL24319 92084 0 None - 1 Rabbit 8.7 pIC50 = 8.7 Functional
Inhibitory activity against Angiotensin II receptor, type 1 induced contractions in isolated rabbit aortic ringsInhibitory activity against Angiotensin II receptor, type 1 induced contractions in isolated rabbit aortic rings
ChEMBL 573 8 1 8 4.2 CN(C)C(=O)CN1N=C(c2ccc3nc(C4CC4)n(Cc4ccc(-c5ccccc5-c5nn[nH]n5)cc4)c3c2)CCC1=O 10.1016/S0960-894X(01)80348-6
44459655 92780 0 None - 1 Rabbit 8.7 pIC50 = 8.7 Functional
Inhibitory activity against Angiotensin II receptor, type 1 induced contractions in isolated rabbit aortic ringsInhibitory activity against Angiotensin II receptor, type 1 induced contractions in isolated rabbit aortic rings
ChEMBL 575 9 1 8 4.3 CCCc1nc2ccc(C3=NN(CC(=O)N(C)C)C(=O)CC3)cc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80348-6
CHEMBL2079788 92780 0 None - 1 Rabbit 8.7 pIC50 = 8.7 Functional
Inhibitory activity against Angiotensin II receptor, type 1 induced contractions in isolated rabbit aortic ringsInhibitory activity against Angiotensin II receptor, type 1 induced contractions in isolated rabbit aortic rings
ChEMBL 575 9 1 8 4.3 CCCc1nc2ccc(C3=NN(CC(=O)N(C)C)C(=O)CC3)cc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80348-6
CHEMBL24478 92780 0 None - 1 Rabbit 8.7 pIC50 = 8.7 Functional
Inhibitory activity against Angiotensin II receptor, type 1 induced contractions in isolated rabbit aortic ringsInhibitory activity against Angiotensin II receptor, type 1 induced contractions in isolated rabbit aortic rings
ChEMBL 575 9 1 8 4.3 CCCc1nc2ccc(C3=NN(CC(=O)N(C)C)C(=O)CC3)cc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80348-6
44459835 167465 0 None - 1 Rabbit 8.7 pIC50 = 8.7 Functional
Inhibitory activity against Angiotensin II receptor, type 1 induced contractions in isolated rabbit aortic ringsInhibitory activity against Angiotensin II receptor, type 1 induced contractions in isolated rabbit aortic rings
ChEMBL 587 8 1 8 4.5 CC1CC(=O)N(CC(=O)N(C)C)N=C1c1ccc2nc(C3CC3)n(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c2c1 10.1016/S0960-894X(01)80348-6
CHEMBL2079790 167465 0 None - 1 Rabbit 8.7 pIC50 = 8.7 Functional
Inhibitory activity against Angiotensin II receptor, type 1 induced contractions in isolated rabbit aortic ringsInhibitory activity against Angiotensin II receptor, type 1 induced contractions in isolated rabbit aortic rings
ChEMBL 587 8 1 8 4.5 CC1CC(=O)N(CC(=O)N(C)C)N=C1c1ccc2nc(C3CC3)n(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c2c1 10.1016/S0960-894X(01)80348-6
CHEMBL432271 167465 0 None - 1 Rabbit 8.7 pIC50 = 8.7 Functional
Inhibitory activity against Angiotensin II receptor, type 1 induced contractions in isolated rabbit aortic ringsInhibitory activity against Angiotensin II receptor, type 1 induced contractions in isolated rabbit aortic rings
ChEMBL 587 8 1 8 4.5 CC1CC(=O)N(CC(=O)N(C)C)N=C1c1ccc2nc(C3CC3)n(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c2c1 10.1016/S0960-894X(01)80348-6
44459654 167536 0 None - 1 Rabbit 8.7 pIC50 = 8.7 Functional
Inhibitory activity against Angiotensin II receptor, type 1 induced contractions in isolated rabbit aortic ringsInhibitory activity against Angiotensin II receptor, type 1 induced contractions in isolated rabbit aortic rings
ChEMBL 601 8 1 8 4.9 CN(C)C(=O)CN1N=C(c2ccc3nc(C4CC4)n(Cc4ccc(-c5ccccc5-c5nn[nH]n5)cc4)c3c2)C(C)(C)CC1=O 10.1016/S0960-894X(01)80348-6
CHEMBL2079787 167536 0 None - 1 Rabbit 8.7 pIC50 = 8.7 Functional
Inhibitory activity against Angiotensin II receptor, type 1 induced contractions in isolated rabbit aortic ringsInhibitory activity against Angiotensin II receptor, type 1 induced contractions in isolated rabbit aortic rings
ChEMBL 601 8 1 8 4.9 CN(C)C(=O)CN1N=C(c2ccc3nc(C4CC4)n(Cc4ccc(-c5ccccc5-c5nn[nH]n5)cc4)c3c2)C(C)(C)CC1=O 10.1016/S0960-894X(01)80348-6
CHEMBL432847 167536 0 None - 1 Rabbit 8.7 pIC50 = 8.7 Functional
Inhibitory activity against Angiotensin II receptor, type 1 induced contractions in isolated rabbit aortic ringsInhibitory activity against Angiotensin II receptor, type 1 induced contractions in isolated rabbit aortic rings
ChEMBL 601 8 1 8 4.9 CN(C)C(=O)CN1N=C(c2ccc3nc(C4CC4)n(Cc4ccc(-c5ccccc5-c5nn[nH]n5)cc4)c3c2)C(C)(C)CC1=O 10.1016/S0960-894X(01)80348-6
22942227 70519 0 None - 1 Rabbit 8.7 pIC50 = 8.7 Functional
Antagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challengeAntagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challenge
ChEMBL 569 10 1 9 3.5 CCCCc1nc(C)c(CC(=O)N2CCC[C@H]2C(=O)OC)c(=O)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2011.12.116
CHEMBL1951130 70519 0 None - 1 Rabbit 8.7 pIC50 = 8.7 Functional
Antagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challengeAntagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challenge
ChEMBL 569 10 1 9 3.5 CCCCc1nc(C)c(CC(=O)N2CCC[C@H]2C(=O)OC)c(=O)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2011.12.116
22942226 70520 0 None - 1 Rabbit 8.7 pIC50 = 8.7 Functional
Antagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challengeAntagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challenge
ChEMBL 554 10 2 8 2.8 CCCCc1nc(C)c(CC(=O)N2CCC[C@H]2C(N)=O)c(=O)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2011.12.116
CHEMBL1951131 70520 0 None - 1 Rabbit 8.7 pIC50 = 8.7 Functional
Antagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challengeAntagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challenge
ChEMBL 554 10 2 8 2.8 CCCCc1nc(C)c(CC(=O)N2CCC[C@H]2C(N)=O)c(=O)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2011.12.116
142534121 166157 0 None - 1 Human 8.7 pIC50 = 8.7 Functional
Antagonist activity at type-1 angiotensin 2 receptor (unknown origin) by calcium mobilizing assayAntagonist activity at type-1 angiotensin 2 receptor (unknown origin) by calcium mobilizing assay
ChEMBL 559 11 1 7 5.4 CCCCc1nc(C)c(CC(=S)N(C)CC(C)C)c(=O)n1Cc1ccc(-c2ccccc2-c2noc(=O)[nH]2)cc1 10.1016/j.bmcl.2018.08.036
CHEMBL4282931 166157 0 None - 1 Human 8.7 pIC50 = 8.7 Functional
Antagonist activity at type-1 angiotensin 2 receptor (unknown origin) by calcium mobilizing assayAntagonist activity at type-1 angiotensin 2 receptor (unknown origin) by calcium mobilizing assay
ChEMBL 559 11 1 7 5.4 CCCCc1nc(C)c(CC(=S)N(C)CC(C)C)c(=O)n1Cc1ccc(-c2ccccc2-c2noc(=O)[nH]2)cc1 10.1016/j.bmcl.2018.08.036
14971638 114364 0 None - 1 Rabbit 8.7 pIC50 = 8.7 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 478 9 2 6 5.5 CCCCc1nc(-c2ccccc2)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
CHEMBL334192 114364 0 None - 1 Rabbit 8.7 pIC50 = 8.7 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 478 9 2 6 5.5 CCCCc1nc(-c2ccccc2)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
9845644 204697 0 None 5 2 Rabbit 8.7 pIC50 = 8.7 Functional
In vitro antagonistic activity for AT1 receptor by displacing 125I[Sar, ILe8]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for AT1 receptor by displacing 125I[Sar, ILe8]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 431 9 1 7 4.3 CCCCc1nn(C(C)CC)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL87964 204697 0 None 5 2 Rabbit 8.7 pIC50 = 8.7 Functional
In vitro antagonistic activity for AT1 receptor by displacing 125I[Sar, ILe8]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for AT1 receptor by displacing 125I[Sar, ILe8]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 431 9 1 7 4.3 CCCCc1nn(C(C)CC)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
14956779 68306 0 None - 1 Rabbit 8.7 pIC50 = 8.7 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 445 8 1 7 4.3 CCCCc1nn(CC(C)(C)C)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL19202 68306 0 None - 1 Rabbit 8.7 pIC50 = 8.7 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 445 8 1 7 4.3 CCCCc1nn(CC(C)(C)C)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
142533975 166484 0 None - 1 Human 8.7 pIC50 = 8.7 Functional
Antagonist activity at type-1 angiotensin 2 receptor (unknown origin) by calcium mobilizing assayAntagonist activity at type-1 angiotensin 2 receptor (unknown origin) by calcium mobilizing assay
ChEMBL 571 10 1 7 5.7 CCCCc1nc(C(C)C)c(CC(=S)N2CCCC2)c(=O)n1Cc1ccc(-c2ccccc2-c2noc(=O)[nH]2)cc1 10.1016/j.bmcl.2018.08.036
CHEMBL4288964 166484 0 None - 1 Human 8.7 pIC50 = 8.7 Functional
Antagonist activity at type-1 angiotensin 2 receptor (unknown origin) by calcium mobilizing assayAntagonist activity at type-1 angiotensin 2 receptor (unknown origin) by calcium mobilizing assay
ChEMBL 571 10 1 7 5.7 CCCCc1nc(C(C)C)c(CC(=S)N2CCCC2)c(=O)n1Cc1ccc(-c2ccccc2-c2noc(=O)[nH]2)cc1 10.1016/j.bmcl.2018.08.036
155517399 169603 0 None - 1 Human 8.7 pIC50 = 8.7 Functional
Antagonist activity at type-1 angiotensin 2 receptor (unknown origin) by calcium mobilizing assayAntagonist activity at type-1 angiotensin 2 receptor (unknown origin) by calcium mobilizing assay
ChEMBL 557 10 1 6 6.8 CCCCC1=NC(C(C)C)=C(CC(=S)N2CCCC2)CN1Cc1ccc(-c2ccccc2-c2noc(=O)[nH]2)cc1 10.1016/j.bmcl.2018.12.043
CHEMBL4444760 169603 0 None - 1 Human 8.7 pIC50 = 8.7 Functional
Antagonist activity at type-1 angiotensin 2 receptor (unknown origin) by calcium mobilizing assayAntagonist activity at type-1 angiotensin 2 receptor (unknown origin) by calcium mobilizing assay
ChEMBL 557 10 1 6 6.8 CCCCC1=NC(C(C)C)=C(CC(=S)N2CCCC2)CN1Cc1ccc(-c2ccccc2-c2noc(=O)[nH]2)cc1 10.1016/j.bmcl.2018.12.043
14971699 112273 0 None - 1 Rabbit 8.6 pIC50 = 8.6 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 512 9 2 6 6.0 CCCCc1nn(-c2cccc(Cl)c2)c(C(=O)O)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
CHEMBL330571 112273 0 None - 1 Rabbit 8.6 pIC50 = 8.6 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 512 9 2 6 6.0 CCCCc1nn(-c2cccc(Cl)c2)c(C(=O)O)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
44213343 70515 22 None - 1 Rabbit 8.6 pIC50 = 8.6 Functional
Antagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challengeAntagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challenge
ChEMBL 485 9 1 7 3.4 CCCCc1nc(C)c(CC(=O)N(C)C)c(=O)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2011.12.116
CHEMBL1951126 70515 22 None - 1 Rabbit 8.6 pIC50 = 8.6 Functional
Antagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challengeAntagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challenge
ChEMBL 485 9 1 7 3.4 CCCCc1nc(C)c(CC(=O)N(C)C)c(=O)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2011.12.116
9935106 64936 0 None - 1 Rabbit 8.6 pIC50 = 8.6 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 485 8 1 7 4.9 CCCCc1nn(-c2ccccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL18287 64936 0 None - 1 Rabbit 8.6 pIC50 = 8.6 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 485 8 1 7 4.9 CCCCc1nn(-c2ccccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
44213346 70521 0 None - 1 Rabbit 8.6 pIC50 = 8.6 Functional
Antagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challengeAntagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challenge
ChEMBL 525 9 1 7 4.3 CCCCc1nc(C)c(CC(=O)N2CCCCC2)c(=O)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2011.12.116
CHEMBL1951132 70521 0 None - 1 Rabbit 8.6 pIC50 = 8.6 Functional
Antagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challengeAntagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challenge
ChEMBL 525 9 1 7 4.3 CCCCc1nc(C)c(CC(=O)N2CCCCC2)c(=O)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2011.12.116
14971709 15159 0 None - 1 Rabbit 8.6 pIC50 = 8.6 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 553 11 2 9 5.3 CCCCc1nn(-c2ccc(OC)cc2[N+](=O)[O-])c(C(=O)O)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
CHEMBL121416 15159 0 None - 1 Rabbit 8.6 pIC50 = 8.6 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 553 11 2 9 5.3 CCCCc1nn(-c2ccc(OC)cc2[N+](=O)[O-])c(C(=O)O)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
57401930 70509 0 None - 1 Rabbit 8.6 pIC50 = 8.6 Functional
Antagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challengeAntagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challenge
ChEMBL 500 11 1 8 4.3 CCCCc1nc(C)c(CCC(=O)OCC)c(=O)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2011.12.116
CHEMBL1951120 70509 0 None - 1 Rabbit 8.6 pIC50 = 8.6 Functional
Antagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challengeAntagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challenge
ChEMBL 500 11 1 8 4.3 CCCCc1nc(C)c(CCC(=O)OCC)c(=O)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2011.12.116
44213342 70512 11 None - 1 Rabbit 8.6 pIC50 = 8.6 Functional
Antagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challengeAntagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challenge
ChEMBL 458 9 2 7 3.4 CCCCc1nc(C)c(CC(=O)O)c(=O)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2011.12.116
CHEMBL1951123 70512 11 None - 1 Rabbit 8.6 pIC50 = 8.6 Functional
Antagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challengeAntagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challenge
ChEMBL 458 9 2 7 3.4 CCCCc1nc(C)c(CC(=O)O)c(=O)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2011.12.116
14971713 167409 0 None - 1 Rabbit 8.6 pIC50 = 8.6 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 430 9 2 6 4.4 CCCCc1nn(CC)c(C(=O)O)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
CHEMBL431887 167409 0 None - 1 Rabbit 8.6 pIC50 = 8.6 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 430 9 2 6 4.4 CCCCc1nn(CC)c(C(=O)O)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
57393227 70523 0 None - 1 Rabbit 8.6 pIC50 = 8.6 Functional
Antagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challengeAntagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challenge
ChEMBL 543 9 1 8 3.9 CCCCc1nc(C)c(CC(=O)N2CCSCC2)c(=O)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2011.12.116
CHEMBL1951134 70523 0 None - 1 Rabbit 8.6 pIC50 = 8.6 Functional
Antagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challengeAntagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challenge
ChEMBL 543 9 1 8 3.9 CCCCc1nc(C)c(CC(=O)N2CCSCC2)c(=O)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2011.12.116
108185 1578 71 None -3 5 Rabbit 8.6 pIC50 = 8.6 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 436 8 2 6 4.5 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)C(=O)O)Cl 10.1021/jm00075a014
586 1578 71 None -3 5 Rabbit 8.6 pIC50 = 8.6 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 436 8 2 6 4.5 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)C(=O)O)Cl 10.1021/jm00075a014
CHEMBL907 1578 71 None -3 5 Rabbit 8.6 pIC50 = 8.6 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 436 8 2 6 4.5 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)C(=O)O)Cl 10.1021/jm00075a014
14971697 111040 0 None - 1 Rabbit 8.5 pIC50 = 8.5 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 478 9 2 6 5.4 CCCCc1nn(-c2ccccc2)c(C(=O)O)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
CHEMBL327982 111040 0 None - 1 Rabbit 8.5 pIC50 = 8.5 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 478 9 2 6 5.4 CCCCc1nn(-c2ccccc2)c(C(=O)O)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
10298977 204590 0 None - 1 Rabbit 8.5 pIC50 = 8.5 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 471 9 1 7 4.9 CCCCc1nn(CC2CCCCC2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL87239 204590 0 None - 1 Rabbit 8.5 pIC50 = 8.5 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 471 9 1 7 4.9 CCCCc1nn(CC2CCCCC2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
131654 204667 10 None 1 2 Rabbit 8.5 pIC50 = 8.5 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 431 10 1 7 4.1 CCCCc1nn(CCCC)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL87778 204667 10 None 1 2 Rabbit 8.5 pIC50 = 8.5 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 431 10 1 7 4.1 CCCCc1nn(CCCC)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
14971683 14678 0 None - 1 Rabbit 7.7 pIC50 = 7.7 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 536 11 1 8 5.8 CCCCc1nn(-c2ccc(OC)cc2)c(C(=O)OCC)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
CHEMBL120750 14678 0 None - 1 Rabbit 7.7 pIC50 = 7.7 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 536 11 1 8 5.8 CCCCc1nn(-c2ccc(OC)cc2)c(C(=O)OCC)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
14971692 112441 0 None - 1 Rabbit 7.7 pIC50 = 7.7 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 560 9 1 7 6.7 CCCc1nn(-c2c(Cl)cccc2Cl)c(C(=O)OCC)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
CHEMBL331078 112441 0 None - 1 Rabbit 7.7 pIC50 = 7.7 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 560 9 1 7 6.7 CCCc1nn(-c2c(Cl)cccc2Cl)c(C(=O)OCC)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
10026868 23640 0 None 331 2 Rabbit 7.7 pIC50 = 7.7 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 452 5 1 6 5.0 CCc1nc2c(C)cc(C)nc2n1Cc1ccc2c(ccn2C(=O)c2ccccc2C(=O)O)c1 10.1021/jm00078a013
CHEMBL133653 23640 0 None 331 2 Rabbit 7.7 pIC50 = 7.7 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 452 5 1 6 5.0 CCc1nc2c(C)cc(C)nc2n1Cc1ccc2c(ccn2C(=O)c2ccccc2C(=O)O)c1 10.1021/jm00078a013
14956766 106483 0 None - 1 Rabbit 7.7 pIC50 = 7.7 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 471 7 1 7 4.5 CCCc1nn(-c2ccccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL315128 106483 0 None - 1 Rabbit 7.7 pIC50 = 7.7 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 471 7 1 7 4.5 CCCc1nn(-c2ccccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
2540 4320 102 None -28 3 Rabbit 6.7 pIC50 = 6.7 Functional
Antagonist activity at angiotensin AT1 receptor in rabbit aortic strip assessed as inhibition of angiotensin 2-induced contractile responseAntagonist activity at angiotensin AT1 receptor in rabbit aortic strip assessed as inhibition of angiotensin 2-induced contractile response
ChEMBL 610 10 1 11 6.3 CCOc1nc2cccc(C(=O)OC(C)OC(=O)OC3CCCCC3)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.bmc.2010.10.043
CHEMBL1014 4320 102 None -28 3 Rabbit 6.7 pIC50 = 6.7 Functional
Antagonist activity at angiotensin AT1 receptor in rabbit aortic strip assessed as inhibition of angiotensin 2-induced contractile responseAntagonist activity at angiotensin AT1 receptor in rabbit aortic strip assessed as inhibition of angiotensin 2-induced contractile response
ChEMBL 610 10 1 11 6.3 CCOc1nc2cccc(C(=O)OC(C)OC(=O)OC3CCCCC3)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.bmc.2010.10.043
10409549 115465 0 None 104 2 Rabbit 6.7 pIC50 = 6.7 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 414 7 2 5 4.9 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(NC(C(=O)O)c2ccccc2)cc1 10.1021/jm00078a014
CHEMBL335514 115465 0 None 104 2 Rabbit 6.7 pIC50 = 6.7 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 414 7 2 5 4.9 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(NC(C(=O)O)c2ccccc2)cc1 10.1021/jm00078a014
10345459 116257 0 None 43 2 Rabbit 6.7 pIC50 = 6.7 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 490 9 1 5 5.8 C=CCN(c1ccc(Cn2c(CC)nc3c(C)cc(C)nc32)cc1)C(C(=O)O)c1cc(F)ccc1F 10.1021/jm00078a014
CHEMBL337663 116257 0 None 43 2 Rabbit 6.7 pIC50 = 6.7 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 490 9 1 5 5.8 C=CCN(c1ccc(Cn2c(CC)nc3c(C)cc(C)nc32)cc1)C(C(=O)O)c1cc(F)ccc1F 10.1021/jm00078a014
25163176 43827 6 None - 1 Human 4.7 pIC50 = 4.7 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 431 8 0 6 2.8 COc1ccc(CC(=O)OCC(=O)c2ccc(S(=O)(=O)N3CCCCC3)cc2)cc1 nan
CHEMBL1514866 43827 6 None - 1 Human 4.7 pIC50 = 4.7 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 431 8 0 6 2.8 COc1ccc(CC(=O)OCC(=O)c2ccc(S(=O)(=O)N3CCCCC3)cc2)cc1 nan
3116640 20192 11 None - 1 Human 4.7 pIC50 = 4.7 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 542 6 0 7 2.1 O=C(CN1C(=O)C2C3CC(C(Br)C3Br)C2C1=O)OCC(=O)c1cccc([N+](=O)[O-])c1 nan
CHEMBL1306605 20192 11 None - 1 Human 4.7 pIC50 = 4.7 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 542 6 0 7 2.1 O=C(CN1C(=O)C2C3CC(C(Br)C3Br)C2C1=O)OCC(=O)c1cccc([N+](=O)[O-])c1 nan
1653162 49712 11 None - 1 Human 4.7 pIC50 = 4.7 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 335 3 3 5 1.7 COc1ccccc1C(=O)NNC(=S)NC(=O)c1cccs1 nan
CHEMBL1569107 49712 11 None - 1 Human 4.7 pIC50 = 4.7 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 335 3 3 5 1.7 COc1ccccc1C(=O)NNC(=S)NC(=O)c1cccs1 nan
11957180 22528 6 None 6 2 Human 5.7 pIC50 = 5.7 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 403 7 2 10 3.7 O=[N+]([O-])c1c(NCCCO)cc(Sc2nc3ccccc3s2)c2nonc12 nan
CHEMBL1327721 22528 6 None 6 2 Human 5.7 pIC50 = 5.7 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 403 7 2 10 3.7 O=[N+]([O-])c1c(NCCCO)cc(Sc2nc3ccccc3s2)c2nonc12 nan
11957209 42773 6 None 6 2 Human 5.7 pIC50 = 5.7 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 445 8 1 11 4.3 CC(=O)OCCCNc1cc(Sc2nc3ccccc3s2)c2nonc2c1[N+](=O)[O-] nan
CHEMBL1504429 42773 6 None 6 2 Human 5.7 pIC50 = 5.7 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 445 8 1 11 4.3 CC(=O)OCCCNc1cc(Sc2nc3ccccc3s2)c2nonc2c1[N+](=O)[O-] nan
9550611 49480 6 None - 1 Human 5.7 pIC50 = 5.7 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 403 6 1 10 3.3 CN(CCO)c1cc(Sc2nc3ccccc3s2)c2nonc2c1[N+](=O)[O-] nan
CHEMBL1567159 49480 6 None - 1 Human 5.7 pIC50 = 5.7 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 403 6 1 10 3.3 CN(CCO)c1cc(Sc2nc3ccccc3s2)c2nonc2c1[N+](=O)[O-] nan
780302 31652 7 None - 1 Human 5.7 pIC50 = 5.7 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 340 3 2 4 3.9 NNc1nc(-c2ccccc2)cc(-c2ccc(Br)cc2)n1 nan
CHEMBL1407100 31652 7 None - 1 Human 5.7 pIC50 = 5.7 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 340 3 2 4 3.9 NNc1nc(-c2ccccc2)cc(-c2ccc(Br)cc2)n1 nan
14971681 111019 0 None - 1 Rabbit 7.7 pIC50 = 7.7 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 574 10 1 7 6.8 CCCCc1nn(-c2ccccc2C(F)(F)F)c(C(=O)OCC)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
CHEMBL327862 111019 0 None - 1 Rabbit 7.7 pIC50 = 7.7 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 574 10 1 7 6.8 CCCCc1nn(-c2ccccc2C(F)(F)F)c(C(=O)OCC)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
14956771 204620 0 None - 1 Rabbit 7.7 pIC50 = 7.7 Functional
In vitro antagonistic activity for AT1 receptor by displacing 125I[Sar, ILe8]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for AT1 receptor by displacing 125I[Sar, ILe8]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 482 8 1 9 3.8 CCCc1nn(-c2ccccc2[N+](=O)[O-])c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL87392 204620 0 None - 1 Rabbit 7.7 pIC50 = 7.7 Functional
In vitro antagonistic activity for AT1 receptor by displacing 125I[Sar, ILe8]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for AT1 receptor by displacing 125I[Sar, ILe8]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 482 8 1 9 3.8 CCCc1nn(-c2ccccc2[N+](=O)[O-])c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
14956750 204355 0 None - 1 Rabbit 7.7 pIC50 = 7.7 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 469 8 1 7 4.4 CCCCc1nn(-c2ccc(F)cc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL85596 204355 0 None - 1 Rabbit 7.7 pIC50 = 7.7 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 469 8 1 7 4.4 CCCCc1nn(-c2ccc(F)cc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
2412928 21502 8 None - 1 Human 4.7 pIC50 = 4.7 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 500 7 1 11 1.5 Cn1c(N)c(C(=O)COC(=O)c2ccccc2C(=O)c2ccc(Cl)c([N+](=O)[O-])c2)c(=O)n(C)c1=O nan
CHEMBL1318653 21502 8 None - 1 Human 4.7 pIC50 = 4.7 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 500 7 1 11 1.5 Cn1c(N)c(C(=O)COC(=O)c2ccccc2C(=O)c2ccc(Cl)c([N+](=O)[O-])c2)c(=O)n(C)c1=O nan
6418891 22599 11 None -1 2 Human 4.7 pIC50 = 4.7 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 401 3 0 4 5.7 FC(F)(F)c1cccc(Sc2nc(-c3ccccc3)nnc2C(F)(F)F)c1 nan
CHEMBL1328168 22599 11 None -1 2 Human 4.7 pIC50 = 4.7 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 401 3 0 4 5.7 FC(F)(F)c1cccc(Sc2nc(-c3ccccc3)nnc2C(F)(F)F)c1 nan
2815589 41416 5 None - 1 Human 4.7 pIC50 = 4.7 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 272 5 2 3 2.2 NC(=O)c1ccccc1NCC(=O)c1ccc(F)cc1 nan
CHEMBL1492089 41416 5 None - 1 Human 4.7 pIC50 = 4.7 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 272 5 2 3 2.2 NC(=O)c1ccccc1NCC(=O)c1ccc(F)cc1 nan
16436605 38209 9 None - 1 Human 5.7 pIC50 = 5.7 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 486 6 1 7 2.6 CCS(=O)(=O)c1ncc(Cl)c(C(=O)Nc2ccc(S(=O)(=O)N3CCCC(C)C3)cc2)n1 nan
CHEMBL1464024 38209 9 None - 1 Human 5.7 pIC50 = 5.7 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 486 6 1 7 2.6 CCS(=O)(=O)c1ncc(Cl)c(C(=O)Nc2ccc(S(=O)(=O)N3CCCC(C)C3)cc2)n1 nan
11159916 123320 6 None - 1 Rabbit 4.7 pIC50 = 4.7 Functional
Vasorelaxing potency was determinedVasorelaxing potency was determined
ChEMBL 197 4 1 4 1.1 O=C(O)c1cccc(CO[N+](=O)[O-])c1 10.1021/jm049681p
CHEMBL362550 123320 6 None - 1 Rabbit 4.7 pIC50 = 4.7 Functional
Vasorelaxing potency was determinedVasorelaxing potency was determined
ChEMBL 197 4 1 4 1.1 O=C(O)c1cccc(CO[N+](=O)[O-])c1 10.1021/jm049681p
442142 184878 11 None -4 2 Human 4.7 pIC50 = 4.7 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 304 1 0 5 1.8 C=C1C(=O)O[C@@H]2C[C@@H](C)[C@@H]3C=CC(=O)[C@@]3(C)[C@@H](OC(C)=O)[C@H]12 nan
CHEMBL486196 184878 11 None -4 2 Human 4.7 pIC50 = 4.7 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 304 1 0 5 1.8 C=C1C(=O)O[C@@H]2C[C@@H](C)[C@@H]3C=CC(=O)[C@@]3(C)[C@@H](OC(C)=O)[C@H]12 nan
53317942 57279 0 None - 1 Human 7.7 pIC50 = 7.7 Functional
Antagonist activity at angiotensin AT1 receptor in human PLC-PRF5 cellsAntagonist activity at angiotensin AT1 receptor in human PLC-PRF5 cells
ChEMBL 444 7 1 7 3.3 CCCCN1CC2(CN1Cc1ccc(-c3ccccc3-c3nnn[nH]3)cc1)C(=O)CCC2=O 10.1016/j.bmc.2010.10.043
CHEMBL1667999 57279 0 None - 1 Human 7.7 pIC50 = 7.7 Functional
Antagonist activity at angiotensin AT1 receptor in human PLC-PRF5 cellsAntagonist activity at angiotensin AT1 receptor in human PLC-PRF5 cells
ChEMBL 444 7 1 7 3.3 CCCCN1CC2(CN1Cc1ccc(-c3ccccc3-c3nnn[nH]3)cc1)C(=O)CCC2=O 10.1016/j.bmc.2010.10.043
14971695 14687 0 None - 1 Rabbit 7.7 pIC50 = 7.7 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 506 10 1 7 5.5 CCCc1nn(Cc2ccccc2)c(C(=O)OCC)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
CHEMBL120762 14687 0 None - 1 Rabbit 7.7 pIC50 = 7.7 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 506 10 1 7 5.5 CCCc1nn(Cc2ccccc2)c(C(=O)OCC)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
44292181 100682 0 None - 1 Bovine 7.7 pIC50 = 7.7 Functional
In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.
ChEMBL 575 8 1 8 6.0 CCCCc1nc2ccc([C@@]3(C)C[C@H]4CCCCN4O3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80365-0
CHEMBL295529 100682 0 None - 1 Bovine 7.7 pIC50 = 7.7 Functional
In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.
ChEMBL 575 8 1 8 6.0 CCCCc1nc2ccc([C@@]3(C)C[C@H]4CCCCN4O3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80365-0
9982177 26279 0 None - 1 Rabbit 7.7 pIC50 = 7.7 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 470 9 1 5 5.9 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(N(CC(C)C)C(C(=O)O)c2ccccc2)cc1 10.1021/jm00078a014
CHEMBL136028 26279 0 None - 1 Rabbit 7.7 pIC50 = 7.7 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 470 9 1 5 5.9 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(N(CC(C)C)C(C(=O)O)c2ccccc2)cc1 10.1021/jm00078a014
10275744 204388 0 None 2 2 Rabbit 7.7 pIC50 = 7.7 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 451 8 1 7 4.3 CCCCc1nn(-c2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL85876 204388 0 None 2 2 Rabbit 7.7 pIC50 = 7.7 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 451 8 1 7 4.3 CCCCc1nn(-c2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
2939837 37026 7 None -4 2 Human 4.7 pIC50 = 4.7 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 363 2 3 4 3.9 CC(C)(C)c1cc(Cl)c(O)c(NC(=S)NC(=O)c2cccnc2)c1 nan
CHEMBL1453857 37026 7 None -4 2 Human 4.7 pIC50 = 4.7 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 363 2 3 4 3.9 CC(C)(C)c1cc(Cl)c(O)c(NC(=S)NC(=O)c2cccnc2)c1 nan
800048 24266 25 None 1 2 Human 5.7 pIC50 = 5.7 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 252 2 0 4 2.6 CCn1c(=O)c([N+](=O)[O-])c(Cl)c2ccccc21 nan
CHEMBL1342053 24266 25 None 1 2 Human 5.7 pIC50 = 5.7 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 252 2 0 4 2.6 CCn1c(=O)c([N+](=O)[O-])c(Cl)c2ccccc21 nan
972880 192915 10 None -6 3 Human 5.7 pIC50 = 5.7 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 268 3 1 5 3.7 Cc1cccnc1Nc1nc(-c2ccccn2)cs1 nan
CHEMBL528694 192915 10 None -6 3 Human 5.7 pIC50 = 5.7 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 268 3 1 5 3.7 Cc1cccnc1Nc1nc(-c2ccccn2)cs1 nan
9660957 72396 11 None -1 5 Human 5.7 pIC50 = 5.7 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 330 4 0 5 2.3 CCn1c(Cl)c(C=O)s/c1=N\S(=O)(=O)c1ccccc1 nan
CHEMBL1999049 72396 11 None -1 5 Human 5.7 pIC50 = 5.7 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 330 4 0 5 2.3 CCn1c(Cl)c(C=O)s/c1=N\S(=O)(=O)c1ccccc1 nan
1472225 24525 10 None -5 7 Human 5.7 pIC50 = 5.7 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 398 6 1 4 3.9 COc1ccc(NC(=O)/C(Cl)=C(/Cl)[S+]([O-])Cc2ccc(C)cc2)cn1 nan
CHEMBL1344225 24525 10 None -5 7 Human 5.7 pIC50 = 5.7 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 398 6 1 4 3.9 COc1ccc(NC(=O)/C(Cl)=C(/Cl)[S+]([O-])Cc2ccc(C)cc2)cn1 nan
3734285 46336 15 None -2 2 Human 4.7 pIC50 = 4.7 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 399 7 1 4 4.8 CN(C)CCCNC(=O)c1ccc(-c2nc(-c3ccc(Cl)cc3)cs2)cc1 nan
CHEMBL1538399 46336 15 None -2 2 Human 4.7 pIC50 = 4.7 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 399 7 1 4 4.8 CN(C)CCCNC(=O)c1ccc(-c2nc(-c3ccc(Cl)cc3)cs2)cc1 nan
5335941 107410 8 None -1 2 Human 4.7 pIC50 = 4.7 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 279 2 2 2 3.4 CC1CC2=C(CC1/C=N/NC(N)=S)C(C)(C)CCC2 nan
CHEMBL3193181 107410 8 None -1 2 Human 4.7 pIC50 = 4.7 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 279 2 2 2 3.4 CC1CC2=C(CC1/C=N/NC(N)=S)C(C)(C)CCC2 nan
9590741 107349 5 None -2 2 Human 5.6 pIC50 = 5.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 273 3 1 3 2.9 C/C(=N\NC(=O)c1ccc(Cl)cc1)c1ccccn1 nan
CHEMBL3192432 107349 5 None -2 2 Human 5.6 pIC50 = 5.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 273 3 1 3 2.9 C/C(=N\NC(=O)c1ccc(Cl)cc1)c1ccccn1 nan
2539399 39634 6 None - 1 Human 4.6 pIC50 = 4.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 392 4 2 5 2.4 Cc1cc(C)nc(NNS(=O)(=O)c2c(F)cc(F)cc2Br)n1 nan
CHEMBL1477553 39634 6 None - 1 Human 4.6 pIC50 = 4.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 392 4 2 5 2.4 Cc1cc(C)nc(NNS(=O)(=O)c2c(F)cc(F)cc2Br)n1 nan
11159916 123320 6 None - 1 Rabbit 4.6 pIC50 = 4.6 Functional
Vasorelaxing potency in the presence of eserin was determinedVasorelaxing potency in the presence of eserin was determined
ChEMBL 197 4 1 4 1.1 O=C(O)c1cccc(CO[N+](=O)[O-])c1 10.1021/jm049681p
CHEMBL362550 123320 6 None - 1 Rabbit 4.6 pIC50 = 4.6 Functional
Vasorelaxing potency in the presence of eserin was determinedVasorelaxing potency in the presence of eserin was determined
ChEMBL 197 4 1 4 1.1 O=C(O)c1cccc(CO[N+](=O)[O-])c1 10.1021/jm049681p
2283939 44148 10 None - 1 Human 4.6 pIC50 = 4.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 404 8 1 6 3.7 Cc1ccc(C(=O)COC(=O)CCC(=O)Nc2ccccc2Cl)cc1[N+](=O)[O-] nan
CHEMBL1518619 44148 10 None - 1 Human 4.6 pIC50 = 4.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 404 8 1 6 3.7 Cc1ccc(C(=O)COC(=O)CCC(=O)Nc2ccccc2Cl)cc1[N+](=O)[O-] nan
14971685 155966 0 None - 1 Rabbit 7.6 pIC50 = 7.6 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 582 11 1 7 7.5 CCCCc1nn(-c2ccccc2-c2ccccc2)c(C(=O)OCC)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
CHEMBL406791 155966 0 None - 1 Rabbit 7.6 pIC50 = 7.6 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 582 11 1 7 7.5 CCCCc1nn(-c2ccccc2-c2ccccc2)c(C(=O)OCC)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
10113613 106264 0 None - 1 Rabbit 7.6 pIC50 = 7.6 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 431 7 1 7 4.0 CCCCc1nn(C(C)(C)C)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL314436 106264 0 None - 1 Rabbit 7.6 pIC50 = 7.6 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 431 7 1 7 4.0 CCCCc1nn(C(C)(C)C)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
14956797 204683 0 None - 1 Rabbit 7.6 pIC50 = 7.6 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 523 10 1 9 4.1 CCCCc1nn(Cc2ccc(C(=O)OC)cc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL87885 204683 0 None - 1 Rabbit 7.6 pIC50 = 7.6 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 523 10 1 9 4.1 CCCCc1nn(Cc2ccc(C(=O)OC)cc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
10048776 114710 0 None - 1 Rabbit 6.6 pIC50 = 6.6 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 438 6 1 5 5.4 CCc1nc2c(C)cc(C)nc2n1Cc1ccc2c(ccn2Cc2ccccc2C(=O)O)c1 10.1021/jm00078a013
CHEMBL334622 114710 0 None - 1 Rabbit 6.6 pIC50 = 6.6 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 438 6 1 5 5.4 CCc1nc2c(C)cc(C)nc2n1Cc1ccc2c(ccn2Cc2ccccc2C(=O)O)c1 10.1021/jm00078a013
1096078 49338 5 None - 1 Human 4.6 pIC50 = 4.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 364 4 1 4 4.2 COc1ccc(NS(=O)(=O)c2ccc3ccccc3c2)c2ncccc12 nan
CHEMBL1566084 49338 5 None - 1 Human 4.6 pIC50 = 4.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 364 4 1 4 4.2 COc1ccc(NS(=O)(=O)c2ccc3ccccc3c2)c2ncccc12 nan
2645512 32229 7 None - 1 Human 4.6 pIC50 = 4.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 455 6 0 6 3.3 O=C(COC(=O)c1ccc(Br)o1)c1ccc(S(=O)(=O)N2CCCCC2)cc1 nan
CHEMBL1411597 32229 7 None - 1 Human 4.6 pIC50 = 4.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 455 6 0 6 3.3 O=C(COC(=O)c1ccc(Br)o1)c1ccc(S(=O)(=O)N2CCCCC2)cc1 nan
2171031 38921 10 None - 1 Human 4.6 pIC50 = 4.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 356 8 1 6 1.7 O=C(Cc1ccccc1)NCC(=O)OCC(=O)c1cccc([N+](=O)[O-])c1 nan
CHEMBL1469682 38921 10 None - 1 Human 4.6 pIC50 = 4.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 356 8 1 6 1.7 O=C(Cc1ccccc1)NCC(=O)OCC(=O)c1cccc([N+](=O)[O-])c1 nan
889369 54186 7 None - 1 Human 4.6 pIC50 = 4.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 315 3 3 4 3.0 CC(C)c1ccc(O)c(NC(=S)NC(=O)c2cccnc2)c1 nan
CHEMBL1609718 54186 7 None - 1 Human 4.6 pIC50 = 4.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 315 3 3 4 3.0 CC(C)c1ccc(O)c(NC(=S)NC(=O)c2cccnc2)c1 nan
2905495 19805 13 None 1 4 Human 5.6 pIC50 = 5.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 400 4 1 9 3.3 Cc1c(Nc2cc(Cl)c3nonc3c2[N+](=O)[O-])c(=O)n(-c2ccccc2)n1C nan
CHEMBL1303426 19805 13 None 1 4 Human 5.6 pIC50 = 5.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 400 4 1 9 3.3 Cc1c(Nc2cc(Cl)c3nonc3c2[N+](=O)[O-])c(=O)n(-c2ccccc2)n1C nan
3239204 53717 11 None - 1 Human 4.6 pIC50 = 4.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 319 4 1 7 4.0 COc1cccc2sc(Nc3nc(C)c(C(C)=O)s3)nc12 nan
CHEMBL1605977 53717 11 None - 1 Human 4.6 pIC50 = 4.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 319 4 1 7 4.0 COc1cccc2sc(Nc3nc(C)c(C(C)=O)s3)nc12 nan
2848041 21867 7 None - 1 Human 5.6 pIC50 = 5.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 298 3 1 3 3.3 Cc1ccc2cccc(NS(=O)(=O)c3ccccc3)c2n1 nan
CHEMBL1321754 21867 7 None - 1 Human 5.6 pIC50 = 5.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 298 3 1 3 3.3 Cc1ccc2cccc(NS(=O)(=O)c3ccccc3)c2n1 nan
1472220 41636 10 None 3 3 Human 5.6 pIC50 = 5.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 418 6 1 4 4.3 COc1ccc(NC(=O)/C(Cl)=C(/Cl)[S+]([O-])Cc2ccc(Cl)cc2)cn1 nan
CHEMBL1494120 41636 10 None 3 3 Human 5.6 pIC50 = 5.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 418 6 1 4 4.3 COc1ccc(NC(=O)/C(Cl)=C(/Cl)[S+]([O-])Cc2ccc(Cl)cc2)cn1 nan
135636104 43810 9 None - 1 Human 4.6 pIC50 = 4.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 217 3 1 5 2.7 O=[N+]([O-])c1ccc(N=Nc2ncc[nH]2)cc1 nan
CHEMBL1514691 43810 9 None - 1 Human 4.6 pIC50 = 4.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 217 3 1 5 2.7 O=[N+]([O-])c1ccc(N=Nc2ncc[nH]2)cc1 nan
936147 52375 8 None - 1 Human 4.6 pIC50 = 4.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 306 6 0 4 4.3 CCCN(CCC)c1nc(-c2ccccn2)nc2ccccc12 nan
CHEMBL1593888 52375 8 None - 1 Human 4.6 pIC50 = 4.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 306 6 0 4 4.3 CCCN(CCC)c1nc(-c2ccccn2)nc2ccccc12 nan
8480343 43646 7 None - 1 Human 4.6 pIC50 = 4.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 330 4 2 5 2.2 Cc1cc(C)nc(NNS(=O)(=O)c2ccc(F)c(Cl)c2)n1 nan
CHEMBL1512236 43646 7 None - 1 Human 4.6 pIC50 = 4.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 330 4 2 5 2.2 Cc1cc(C)nc(NNS(=O)(=O)c2ccc(F)c(Cl)c2)n1 nan
2632794 22545 6 None - 1 Human 4.6 pIC50 = 4.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 312 5 0 4 3.5 O=C(Cc1ccc(F)cc1)OCC(=O)c1cc2ccccc2o1 nan
CHEMBL1327815 22545 6 None - 1 Human 4.6 pIC50 = 4.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 312 5 0 4 3.5 O=C(Cc1ccc(F)cc1)OCC(=O)c1cc2ccccc2o1 nan
14956786 106469 0 None - 1 Rabbit 7.6 pIC50 = 7.6 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 433 9 2 8 2.8 CCCCc1nn(C(C)CO)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL315012 106469 0 None - 1 Rabbit 7.6 pIC50 = 7.6 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 433 9 2 8 2.8 CCCCc1nn(C(C)CO)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
10250898 117971 0 None 37 2 Rabbit 6.6 pIC50 = 6.6 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 408 4 0 5 5.3 CCc1nc2c(C)cc(C)nc2n1Cc1ccc2c(ccn2C(=O)c2ccccc2)c1 10.1021/jm00078a013
CHEMBL341407 117971 0 None 37 2 Rabbit 6.6 pIC50 = 6.6 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 408 4 0 5 5.3 CCc1nc2c(C)cc(C)nc2n1Cc1ccc2c(ccn2C(=O)c2ccccc2)c1 10.1021/jm00078a013
6908540 107249 18 None - 1 Human 4.6 pIC50 = 4.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 305 5 1 5 1.9 O=[N+]([O-])c1cccc(/C=N/NS(=O)(=O)c2ccccc2)c1 nan
CHEMBL3191392 107249 18 None - 1 Human 4.6 pIC50 = 4.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 305 5 1 5 1.9 O=[N+]([O-])c1cccc(/C=N/NS(=O)(=O)c2ccccc2)c1 nan
2739277 29463 5 None - 1 Human 5.6 pIC50 = 5.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 364 4 2 5 4.3 O=C(NNc1ccc(-c2csnn2)cc1)c1cc(Cl)cc(Cl)c1 nan
CHEMBL1386393 29463 5 None - 1 Human 5.6 pIC50 = 5.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 364 4 2 5 4.3 O=C(NNc1ccc(-c2csnn2)cc1)c1cc(Cl)cc(Cl)c1 nan
135478724 34890 32 None - 1 Human 4.6 pIC50 = 4.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 240 1 1 2 2.9 O=C1Nc2ccccc2C1=Nc1ccc(F)cc1 nan
CHEMBL1434292 34890 32 None - 1 Human 4.6 pIC50 = 4.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 240 1 1 2 2.9 O=C1Nc2ccccc2C1=Nc1ccc(F)cc1 nan
3118020 47207 13 None - 1 Human 4.6 pIC50 = 4.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 400 6 0 7 1.7 CC(C(=O)OCC(=O)c1cccc([N+](=O)[O-])c1)N1C(=O)C2C3CCC(C3)C2C1=O nan
CHEMBL1545561 47207 13 None - 1 Human 4.6 pIC50 = 4.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 400 6 0 7 1.7 CC(C(=O)OCC(=O)c1cccc([N+](=O)[O-])c1)N1C(=O)C2C3CCC(C3)C2C1=O nan
164613537 184533 0 None 21 2 Human 7.6 pIC50 = 7.6 Functional
Antagonist activity at human AT1 overexpressed in CHO-K1 cells in presence of 10 nM [Val5-angiotensin II measured after 90 mins by HTRF based IP-one assayAntagonist activity at human AT1 overexpressed in CHO-K1 cells in presence of 10 nM [Val5-angiotensin II measured after 90 mins by HTRF based IP-one assay
ChEMBL 464 8 1 5 5.4 CCCCC1=NC(C)(c2ccccc2)C(=O)N1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1021/acsmedchemlett.1c00240
CHEMBL4856425 184533 0 None 21 2 Human 7.6 pIC50 = 7.6 Functional
Antagonist activity at human AT1 overexpressed in CHO-K1 cells in presence of 10 nM [Val5-angiotensin II measured after 90 mins by HTRF based IP-one assayAntagonist activity at human AT1 overexpressed in CHO-K1 cells in presence of 10 nM [Val5-angiotensin II measured after 90 mins by HTRF based IP-one assay
ChEMBL 464 8 1 5 5.4 CCCCC1=NC(C)(c2ccccc2)C(=O)N1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1021/acsmedchemlett.1c00240
10025873 115022 0 None - 1 Rabbit 6.6 pIC50 = 6.6 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 433 4 0 6 5.2 CCc1nc2c(C)cc(C)nc2n1Cc1ccc2c(ccn2C(=O)c2ccccc2C#N)c1 10.1021/jm00078a013
CHEMBL335323 115022 0 None - 1 Rabbit 6.6 pIC50 = 6.6 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 433 4 0 6 5.2 CCc1nc2c(C)cc(C)nc2n1Cc1ccc2c(ccn2C(=O)c2ccccc2C#N)c1 10.1021/jm00078a013
14956765 204686 0 None - 1 Rabbit 6.6 pIC50 = 6.6 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 469 6 1 7 4.5 O=c1n(-c2ccccc2Cl)nc(C2CC2)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL87890 204686 0 None - 1 Rabbit 6.6 pIC50 = 6.6 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 469 6 1 7 4.5 O=c1n(-c2ccccc2Cl)nc(C2CC2)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
773605 44908 18 None - 1 Human 4.6 pIC50 = 4.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 253 2 2 3 3.3 Fc1ccc(NC(S)=Nc2nccs2)cc1 nan
CHEMBL1525546 44908 18 None - 1 Human 4.6 pIC50 = 4.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 253 2 2 3 3.3 Fc1ccc(NC(S)=Nc2nccs2)cc1 nan
3754656 47653 8 None - 1 Human 4.6 pIC50 = 4.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 362 8 1 6 2.6 O=C(CCC(=O)OCC(=O)c1cccc([N+](=O)[O-])c1)NC1CCCCC1 nan
CHEMBL1549587 47653 8 None - 1 Human 4.6 pIC50 = 4.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 362 8 1 6 2.6 O=C(CCC(=O)OCC(=O)c1cccc([N+](=O)[O-])c1)NC1CCCCC1 nan
933895 22502 30 None - 1 Human 4.6 pIC50 = 4.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 166 2 2 5 1.0 CC(C)c1nc(C#N)c(NN)o1 nan
CHEMBL1327546 22502 30 None - 1 Human 4.6 pIC50 = 4.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 166 2 2 5 1.0 CC(C)c1nc(C#N)c(NN)o1 nan
42600949 54086 0 None - 1 Human 4.6 pIC50 = 4.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 385 4 1 5 3.9 CCC1Nc2ncnc(N3CCCCC3)c2N(Cc2ccc(Cl)cc2)C1=O nan
CHEMBL1608922 54086 0 None - 1 Human 4.6 pIC50 = 4.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 385 4 1 5 3.9 CCC1Nc2ncnc(N3CCCCC3)c2N(Cc2ccc(Cl)cc2)C1=O nan
CHEMBL2131333 54086 0 None - 1 Human 4.6 pIC50 = 4.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 385 4 1 5 3.9 CCC1Nc2ncnc(N3CCCCC3)c2N(Cc2ccc(Cl)cc2)C1=O nan
2811327 34086 5 None - 1 Human 5.6 pIC50 = 5.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 288 4 2 2 4.0 CCc1ccc(C(=O)NNc2ccc(C)c(Cl)c2)cc1 nan
CHEMBL1427235 34086 5 None - 1 Human 5.6 pIC50 = 5.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 288 4 2 2 4.0 CCc1ccc(C(=O)NNc2ccc(C)c(Cl)c2)cc1 nan
2896074 45389 7 None - 1 Human 4.6 pIC50 = 4.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 491 3 2 7 5.2 O=C1Nc2ccc(F)cc2C12Nc1ccccc1-c1nnc(SCc3ccccc3Cl)nc1O2 nan
CHEMBL1529705 45389 7 None - 1 Human 4.6 pIC50 = 4.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 491 3 2 7 5.2 O=C1Nc2ccc(F)cc2C12Nc1ccccc1-c1nnc(SCc3ccccc3Cl)nc1O2 nan
2813088 48267 5 None - 1 Human 5.6 pIC50 = 5.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 290 3 2 5 2.9 Cc1nnsc1C(=O)NNc1ccc(C(C)(C)C)cc1 nan
CHEMBL1556712 48267 5 None - 1 Human 5.6 pIC50 = 5.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 290 3 2 5 2.9 Cc1nnsc1C(=O)NNc1ccc(C(C)(C)C)cc1 nan
6887818 107638 5 None 1 2 Human 5.6 pIC50 = 5.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 430 4 1 4 4.8 O=C(N/N=C/c1ccccn1)c1cc(-c2ccc(Br)cc2)nc2ccccc12 nan
CHEMBL3195898 107638 5 None 1 2 Human 5.6 pIC50 = 5.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 430 4 1 4 4.8 O=C(N/N=C/c1ccccn1)c1cc(-c2ccc(Br)cc2)nc2ccccc12 nan
2883150 50660 14 None - 1 Human 4.6 pIC50 = 4.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 413 9 2 7 2.7 CC(=O)Nc1ccc(NC(=O)CCC(=O)OCC(=O)c2cccc([N+](=O)[O-])c2)cc1 nan
CHEMBL1577988 50660 14 None - 1 Human 4.6 pIC50 = 4.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 413 9 2 7 2.7 CC(=O)Nc1ccc(NC(=O)CCC(=O)OCC(=O)c2cccc([N+](=O)[O-])c2)cc1 nan
14956788 106534 0 None - 1 Rabbit 7.6 pIC50 = 7.6 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 447 9 2 8 2.9 CCCCc1nn(C(C)C(=O)O)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL315469 106534 0 None - 1 Rabbit 7.6 pIC50 = 7.6 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 447 9 2 8 2.9 CCCCc1nn(C(C)C(=O)O)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
2321121 55151 3 None - 1 Human 4.6 pIC50 = 4.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 557 7 1 5 6.3 O=C(C[n+]1ccc(-c2cc(C(=O)Nc3cccc(C(F)(F)F)c3)c3ccccc3n2)cc1)c1cccc([N+](=O)[O-])c1 nan
CHEMBL1412385 55151 3 None - 1 Human 4.6 pIC50 = 4.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 557 7 1 5 6.3 O=C(C[n+]1ccc(-c2cc(C(=O)Nc3cccc(C(F)(F)F)c3)c3ccccc3n2)cc1)c1cccc([N+](=O)[O-])c1 nan
CHEMBL1619819 55151 3 None - 1 Human 4.6 pIC50 = 4.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 557 7 1 5 6.3 O=C(C[n+]1ccc(-c2cc(C(=O)Nc3cccc(C(F)(F)F)c3)c3ccccc3n2)cc1)c1cccc([N+](=O)[O-])c1 nan
2378336 35879 2 None - 1 Human 4.6 pIC50 = 4.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 271 6 2 4 2.5 COc1ccc(C(=O)CNc2ccccc2CO)cc1 nan
CHEMBL1444275 35879 2 None - 1 Human 4.6 pIC50 = 4.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 271 6 2 4 2.5 COc1ccc(C(=O)CNc2ccccc2CO)cc1 nan
3118009 44378 10 None - 1 Human 4.6 pIC50 = 4.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 386 6 0 7 1.4 O=C(CN1C(=O)C2C3CCC(C3)C2C1=O)OCC(=O)c1cccc([N+](=O)[O-])c1 nan
CHEMBL1520643 44378 10 None - 1 Human 4.6 pIC50 = 4.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 386 6 0 7 1.4 O=C(CN1C(=O)C2C3CCC(C3)C2C1=O)OCC(=O)c1cccc([N+](=O)[O-])c1 nan
135492609 107757 5 None - 1 Human 4.6 pIC50 = 4.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 521 2 1 7 3.6 CN1/C(=c2/s/c(=C3/C(=O)N(c4ccccc4)N=C3Nc3ccccc3)n(C)c2=O)C(C)(C)c2ccccc21 nan
CHEMBL3197135 107757 5 None - 1 Human 4.6 pIC50 = 4.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 521 2 1 7 3.6 CN1/C(=c2/s/c(=C3/C(=O)N(c4ccccc4)N=C3Nc3ccccc3)n(C)c2=O)C(C)(C)c2ccccc21 nan
183134 203126 13 None -134 7 Bovine 7.6 pIC50 = 7.6 Functional
Compound was tested for in vitro for AII receptor antagonistic activity in bovine adrenal cortex.Compound was tested for in vitro for AII receptor antagonistic activity in bovine adrenal cortex.
ChEMBL 409 5 1 6 4.5 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80366-2
CHEMBL7550 203126 13 None -134 7 Bovine 7.6 pIC50 = 7.6 Functional
Compound was tested for in vitro for AII receptor antagonistic activity in bovine adrenal cortex.Compound was tested for in vitro for AII receptor antagonistic activity in bovine adrenal cortex.
ChEMBL 409 5 1 6 4.5 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80366-2
11527144 178516 0 None - 1 Bovine 7.6 pIC50 = 7.6 Functional
In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.
ChEMBL 561 8 1 8 5.6 CCCCc1nc2ccc([C@]3(C)C[C@H]4CCCN4O3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80365-0
CHEMBL297425 178516 0 None - 1 Bovine 7.6 pIC50 = 7.6 Functional
In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.
ChEMBL 561 8 1 8 5.6 CCCCc1nc2ccc([C@]3(C)C[C@H]4CCCN4O3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80365-0
CHEMBL47177 178516 0 None - 1 Bovine 7.6 pIC50 = 7.6 Functional
In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.
ChEMBL 561 8 1 8 5.6 CCCCc1nc2ccc([C@]3(C)C[C@H]4CCCN4O3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80365-0
14956749 204486 0 None - 1 Rabbit 7.6 pIC50 = 7.6 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 479 9 1 7 4.8 CCCCc1nn(-c2ccc(CC)cc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL86613 204486 0 None - 1 Rabbit 7.6 pIC50 = 7.6 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 479 9 1 7 4.8 CCCCc1nn(-c2ccc(CC)cc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
14956803 204552 0 None 10 2 Rabbit 7.6 pIC50 = 7.6 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 515 9 1 7 5.5 CCCCc1nn(Cc2ccc3ccccc3c2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL86986 204552 0 None 10 2 Rabbit 7.6 pIC50 = 7.6 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 515 9 1 7 5.5 CCCCc1nn(Cc2ccc3ccccc3c2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
14956767 204652 0 None - 1 Rabbit 7.6 pIC50 = 7.6 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 483 7 1 7 4.5 O=c1n(-c2ccccc2Cl)nc(CC2CC2)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL87650 204652 0 None - 1 Rabbit 7.6 pIC50 = 7.6 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 483 7 1 7 4.5 O=c1n(-c2ccccc2Cl)nc(CC2CC2)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
54500223 70513 0 None - 1 Rabbit 7.6 pIC50 = 7.6 Functional
Antagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challengeAntagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challenge
ChEMBL 444 8 2 7 3.0 CCCc1nc(C)c(CC(=O)O)c(=O)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2011.12.116
CHEMBL1951124 70513 0 None - 1 Rabbit 7.6 pIC50 = 7.6 Functional
Antagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challengeAntagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challenge
ChEMBL 444 8 2 7 3.0 CCCc1nc(C)c(CC(=O)O)c(=O)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2011.12.116
324450 40659 22 None - 1 Human 5.6 pIC50 = 5.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 219 3 2 3 1.4 O=C(CCl)NNc1cccc(Cl)n1 nan
CHEMBL1486528 40659 22 None - 1 Human 5.6 pIC50 = 5.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 219 3 2 3 1.4 O=C(CCl)NNc1cccc(Cl)n1 nan
3103390 44571 11 None - 1 Human 4.6 pIC50 = 4.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 410 7 1 7 2.1 O=C(CNC(=O)c1ccc(Br)o1)OCC(=O)c1cccc([N+](=O)[O-])c1 nan
CHEMBL1522230 44571 11 None - 1 Human 4.6 pIC50 = 4.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 410 7 1 7 2.1 O=C(CNC(=O)c1ccc(Br)o1)OCC(=O)c1cccc([N+](=O)[O-])c1 nan
1231596 35607 12 None - 1 Human 4.6 pIC50 = 4.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 406 4 1 7 4.2 COc1cc(/C=C2\SC(=O)N(c3cccc(Cl)c3)C2=O)cc([N+](=O)[O-])c1O nan
CHEMBL1441794 35607 12 None - 1 Human 4.6 pIC50 = 4.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 406 4 1 7 4.2 COc1cc(/C=C2\SC(=O)N(c3cccc(Cl)c3)C2=O)cc([N+](=O)[O-])c1O nan
9653430 71388 2 None -3 2 Human 4.6 pIC50 = 4.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 331 3 2 3 4.2 COc1cccc(NC(=S)N/N=C2\CC3CCC2(C)C3(C)C)c1 nan
CHEMBL1966283 71388 2 None -3 2 Human 4.6 pIC50 = 4.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 331 3 2 3 4.2 COc1cccc(NC(=S)N/N=C2\CC3CCC2(C)C3(C)C)c1 nan
161167 95034 35 None - 1 Human 5.6 pIC50 = 5.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 284 3 1 3 3.0 O=S(=O)(Nc1cccc2cccnc12)c1ccccc1 nan
CHEMBL257286 95034 35 None - 1 Human 5.6 pIC50 = 5.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 284 3 1 3 3.0 O=S(=O)(Nc1cccc2cccnc12)c1ccccc1 nan
3235730 51847 12 None -2 3 Human 4.6 pIC50 = 4.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 432 8 1 9 3.4 CCSC1(SCC)N=C(N)C2(C#N)C(c3ccc(OC)c(OC)c3OC)C12C#N nan
CHEMBL1587831 51847 12 None -2 3 Human 4.6 pIC50 = 4.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 432 8 1 9 3.4 CCSC1(SCC)N=C(N)C2(C#N)C(c3ccc(OC)c(OC)c3OC)C12C#N nan
793994 107203 7 None -1 2 Human 5.6 pIC50 = 5.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 304 2 1 4 4.9 Oc1c(/C=N/c2cccc3cccnc23)sc2ccccc12 nan
CHEMBL3190827 107203 7 None -1 2 Human 5.6 pIC50 = 5.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 304 2 1 4 4.9 Oc1c(/C=N/c2cccc3cccnc23)sc2ccccc12 nan
135444079 38891 14 None - 1 Human 4.6 pIC50 = 4.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 270 1 1 2 3.7 Cc1cccc2c1NC(=O)C2=Nc1ccc(Cl)cc1 nan
CHEMBL1469448 38891 14 None - 1 Human 4.6 pIC50 = 4.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 270 1 1 2 3.7 Cc1cccc2c1NC(=O)C2=Nc1ccc(Cl)cc1 nan
2412176 54605 7 None - 1 Human 4.6 pIC50 = 4.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 259 5 1 3 3.1 COc1ccc(C(=O)CNc2cccc(F)c2)cc1 nan
CHEMBL1613520 54605 7 None - 1 Human 4.6 pIC50 = 4.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 259 5 1 3 3.1 COc1ccc(C(=O)CNc2cccc(F)c2)cc1 nan
10411101 165102 0 None 676 2 Rabbit 7.6 pIC50 = 7.6 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 442 7 2 5 5.5 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(NC(C(=O)O)c2ccccc2C)c(C)c1 10.1021/jm00078a014
CHEMBL424465 165102 0 None 676 2 Rabbit 7.6 pIC50 = 7.6 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 442 7 2 5 5.5 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(NC(C(=O)O)c2ccccc2C)c(C)c1 10.1021/jm00078a014
10371403 66573 12 None - 1 Rabbit 5.6 pIC50 = 5.6 Functional
Vasorelaxing potency was determinedVasorelaxing potency was determined
ChEMBL 601 13 1 10 5.8 CCCCc1nc(Cl)c(COC(=O)c2cccc(CO[N+](=O)[O-])c2)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm049681p
CHEMBL186572 66573 12 None - 1 Rabbit 5.6 pIC50 = 5.6 Functional
Vasorelaxing potency was determinedVasorelaxing potency was determined
ChEMBL 601 13 1 10 5.8 CCCCc1nc(Cl)c(COC(=O)c2cccc(CO[N+](=O)[O-])c2)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm049681p
3119388 47057 11 None - 1 Human 4.6 pIC50 = 4.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 556 7 0 7 2.5 O=C(CCN1C(=O)C2C3CC(C(Br)C3Br)C2C1=O)OCC(=O)c1cccc([N+](=O)[O-])c1 nan
CHEMBL1544373 47057 11 None - 1 Human 4.6 pIC50 = 4.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 556 7 0 7 2.5 O=C(CCN1C(=O)C2C3CC(C(Br)C3Br)C2C1=O)OCC(=O)c1cccc([N+](=O)[O-])c1 nan
4691872 46979 1 None - 1 Human 4.6 pIC50 = 4.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 372 5 1 6 2.8 COC(=O)C1NN=C(C(=O)c2ccc(Cl)cc2)C1c1ccc(OC)cc1 nan
CHEMBL1543866 46979 1 None - 1 Human 4.6 pIC50 = 4.6 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 372 5 1 6 2.8 COC(=O)C1NN=C(C(=O)c2ccc(Cl)cc2)C1c1ccc(OC)cc1 nan
135557876 107756 4 None - 1 Human 4.5 pIC50 = 4.5 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 326 4 3 6 2.4 Cc1ncc(CO)c(/C=N/Nc2ccc(C(F)(F)F)cn2)c1O nan
CHEMBL3197126 107756 4 None - 1 Human 4.5 pIC50 = 4.5 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 326 4 3 6 2.4 Cc1ncc(CO)c(/C=N/Nc2ccc(C(F)(F)F)cn2)c1O nan
2767330 95914 23 None 1 2 Human 5.5 pIC50 = 5.5 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 272 1 0 3 3.7 Cc1ccc(-c2cc3c(nn2)-c2ccccc2C3=O)cc1 nan
CHEMBL261693 95914 23 None 1 2 Human 5.5 pIC50 = 5.5 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 272 1 0 3 3.7 Cc1ccc(-c2cc3c(nn2)-c2ccccc2C3=O)cc1 nan
852940 49556 13 None - 1 Human 5.5 pIC50 = 5.5 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 257 2 1 5 3.0 CCc1cc2c(O)nc(-c3ccccn3)nc2s1 nan
CHEMBL1567827 49556 13 None - 1 Human 5.5 pIC50 = 5.5 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 257 2 1 5 3.0 CCc1cc2c(O)nc(-c3ccccn3)nc2s1 nan
3138587 34281 4 None 1 2 Human 4.5 pIC50 = 4.5 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 391 6 5 10 -2.3 CN(C)c1ccc2nc3c(=O)[nH]c(=O)nc-3n(CC(O)C(O)C(O)CO)c2c1 nan
CHEMBL1428985 34281 4 None 1 2 Human 4.5 pIC50 = 4.5 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 391 6 5 10 -2.3 CN(C)c1ccc2nc3c(=O)[nH]c(=O)nc-3n(CC(O)C(O)C(O)CO)c2c1 nan
1472222 28463 10 None 1 3 Human 5.5 pIC50 = 5.5 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 414 7 1 5 3.6 COc1ccc(C[S+]([O-])/C(Cl)=C(/Cl)C(=O)Nc2ccc(OC)nc2)cc1 nan
CHEMBL1377737 28463 10 None 1 3 Human 5.5 pIC50 = 5.5 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 414 7 1 5 3.6 COc1ccc(C[S+]([O-])/C(Cl)=C(/Cl)C(=O)Nc2ccc(OC)nc2)cc1 nan
135443160 31487 5 None - 1 Human 4.5 pIC50 = 4.5 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 435 2 1 5 4.5 O=C1Nc2ccc(Br)cc2C1=Nc1ccc(-c2nnc3n2CCCCC3)cc1 nan
CHEMBL1405610 31487 5 None - 1 Human 4.5 pIC50 = 4.5 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 435 2 1 5 4.5 O=C1Nc2ccc(Br)cc2C1=Nc1ccc(-c2nnc3n2CCCCC3)cc1 nan
2920316 37426 9 None - 1 Human 4.5 pIC50 = 4.5 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 446 9 1 6 3.6 Cc1ccc(C(=O)COC(=O)CNC(=O)C(c2ccccc2)c2ccccc2)cc1[N+](=O)[O-] nan
CHEMBL1457414 37426 9 None - 1 Human 4.5 pIC50 = 4.5 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 446 9 1 6 3.6 Cc1ccc(C(=O)COC(=O)CNC(=O)C(c2ccccc2)c2ccccc2)cc1[N+](=O)[O-] nan
4146306 25000 3 None - 1 Human 4.5 pIC50 = 4.5 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 347 2 1 4 3.3 O=c1c2cc(Br)ccc2[nH]c(=S)n1Cc1ccccn1 nan
CHEMBL1348215 25000 3 None - 1 Human 4.5 pIC50 = 4.5 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 347 2 1 4 3.3 O=c1c2cc(Br)ccc2[nH]c(=S)n1Cc1ccccn1 nan
1610 2305 89 None -2 9 Rabbit 8.5 pIC50 = 8.5 Functional
Inhibitory activity against Angiotensin II receptor, type 1 induced contractions in isolated rabbit aortic ringsInhibitory activity against Angiotensin II receptor, type 1 induced contractions in isolated rabbit aortic rings
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(01)80348-6
3941 2305 89 None -2 9 Rabbit 8.5 pIC50 = 8.5 Functional
Inhibitory activity against Angiotensin II receptor, type 1 induced contractions in isolated rabbit aortic ringsInhibitory activity against Angiotensin II receptor, type 1 induced contractions in isolated rabbit aortic rings
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(01)80348-6
3961 2305 89 None -2 9 Rabbit 8.5 pIC50 = 8.5 Functional
Inhibitory activity against Angiotensin II receptor, type 1 induced contractions in isolated rabbit aortic ringsInhibitory activity against Angiotensin II receptor, type 1 induced contractions in isolated rabbit aortic rings
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(01)80348-6
590 2305 89 None -2 9 Rabbit 8.5 pIC50 = 8.5 Functional
Inhibitory activity against Angiotensin II receptor, type 1 induced contractions in isolated rabbit aortic ringsInhibitory activity against Angiotensin II receptor, type 1 induced contractions in isolated rabbit aortic rings
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(01)80348-6
CHEMBL191 2305 89 None -2 9 Rabbit 8.5 pIC50 = 8.5 Functional
Inhibitory activity against Angiotensin II receptor, type 1 induced contractions in isolated rabbit aortic ringsInhibitory activity against Angiotensin II receptor, type 1 induced contractions in isolated rabbit aortic rings
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(01)80348-6
DB00678 2305 89 None -2 9 Rabbit 8.5 pIC50 = 8.5 Functional
Inhibitory activity against Angiotensin II receptor, type 1 induced contractions in isolated rabbit aortic ringsInhibitory activity against Angiotensin II receptor, type 1 induced contractions in isolated rabbit aortic rings
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(01)80348-6
20081616 91794 0 None - 1 Rabbit 8.5 pIC50 = 8.5 Functional
Inhibitory activity against Angiotensin II receptor, type 1 induced contractions in isolated rabbit aortic ringsInhibitory activity against Angiotensin II receptor, type 1 induced contractions in isolated rabbit aortic rings
ChEMBL 500 6 2 8 5.3 Cc1cc(O)nnc1-c1ccc2nc(C3CC3)n(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c2c1 10.1016/S0960-894X(01)80348-6
CHEMBL24266 91794 0 None - 1 Rabbit 8.5 pIC50 = 8.5 Functional
Inhibitory activity against Angiotensin II receptor, type 1 induced contractions in isolated rabbit aortic ringsInhibitory activity against Angiotensin II receptor, type 1 induced contractions in isolated rabbit aortic rings
ChEMBL 500 6 2 8 5.3 Cc1cc(O)nnc1-c1ccc2nc(C3CC3)n(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c2c1 10.1016/S0960-894X(01)80348-6
44459656 99152 0 None - 1 Rabbit 8.5 pIC50 = 8.5 Functional
Inhibitory activity against Angiotensin II receptor, type 1 induced contractions in isolated rabbit aortic ringsInhibitory activity against Angiotensin II receptor, type 1 induced contractions in isolated rabbit aortic rings
ChEMBL 561 8 1 8 3.9 CCc1nc2ccc(C3=NN(CC(=O)N(C)C)C(=O)CC3)cc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80348-6
CHEMBL2079789 99152 0 None - 1 Rabbit 8.5 pIC50 = 8.5 Functional
Inhibitory activity against Angiotensin II receptor, type 1 induced contractions in isolated rabbit aortic ringsInhibitory activity against Angiotensin II receptor, type 1 induced contractions in isolated rabbit aortic rings
ChEMBL 561 8 1 8 3.9 CCc1nc2ccc(C3=NN(CC(=O)N(C)C)C(=O)CC3)cc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80348-6
CHEMBL284140 99152 0 None - 1 Rabbit 8.5 pIC50 = 8.5 Functional
Inhibitory activity against Angiotensin II receptor, type 1 induced contractions in isolated rabbit aortic ringsInhibitory activity against Angiotensin II receptor, type 1 induced contractions in isolated rabbit aortic rings
ChEMBL 561 8 1 8 3.9 CCc1nc2ccc(C3=NN(CC(=O)N(C)C)C(=O)CC3)cc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80348-6
14956814 204076 0 None - 1 Rabbit 8.5 pIC50 = 8.5 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 493 10 1 7 4.8 CC(C)CCc1nn(CCc2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL83194 204076 0 None - 1 Rabbit 8.5 pIC50 = 8.5 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 493 10 1 7 4.8 CC(C)CCc1nn(CCc2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
14971703 106591 0 None - 1 Rabbit 8.5 pIC50 = 8.5 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 546 9 2 6 6.7 CCCCc1nn(-c2cc(Cl)ccc2Cl)c(C(=O)O)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
CHEMBL315878 106591 0 None - 1 Rabbit 8.5 pIC50 = 8.5 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 546 9 2 6 6.7 CCCCc1nn(-c2cc(Cl)ccc2Cl)c(C(=O)O)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
14956761 105478 0 None - 1 Rabbit 8.5 pIC50 = 8.5 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 494 9 1 8 4.3 CCCCc1nn(-c2ccccc2N(C)C)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL313025 105478 0 None - 1 Rabbit 8.5 pIC50 = 8.5 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 494 9 1 8 4.3 CCCCc1nn(-c2ccccc2N(C)C)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
14956778 204560 0 None - 1 Rabbit 8.5 pIC50 = 8.5 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 431 9 1 7 3.9 CCCCc1nn(CC(C)C)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL87057 204560 0 None - 1 Rabbit 8.5 pIC50 = 8.5 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 431 9 1 7 3.9 CCCCc1nn(CC(C)C)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
44320509 204605 0 None 1 2 Rabbit 8.5 pIC50 = 8.5 Functional
Antagonist activity against AT1 receptor assessed as inhibition of Ang2-induced rabbit aortic strip contractionAntagonist activity against AT1 receptor assessed as inhibition of Ang2-induced rabbit aortic strip contraction
ChEMBL 465 6 2 6 5.5 CCCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2c(C(=O)O)c(N)nc3ccccc23)cc1 10.1021/jm0603163
CHEMBL87327 204605 0 None 1 2 Rabbit 8.5 pIC50 = 8.5 Functional
Antagonist activity against AT1 receptor assessed as inhibition of Ang2-induced rabbit aortic strip contractionAntagonist activity against AT1 receptor assessed as inhibition of Ang2-induced rabbit aortic strip contraction
ChEMBL 465 6 2 6 5.5 CCCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2c(C(=O)O)c(N)nc3ccccc23)cc1 10.1021/jm0603163
22942224 70526 0 None - 1 Rabbit 8.5 pIC50 = 8.5 Functional
Antagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challengeAntagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challenge
ChEMBL 583 11 1 9 3.9 CCCCc1nc(C)c(CCC(=O)N2CCC[C@H]2C(=O)OC)c(=O)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2011.12.116
CHEMBL1951137 70526 0 None - 1 Rabbit 8.5 pIC50 = 8.5 Functional
Antagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challengeAntagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challenge
ChEMBL 583 11 1 9 3.9 CCCCc1nc(C)c(CCC(=O)N2CCC[C@H]2C(=O)OC)c(=O)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2011.12.116
44292471 156998 0 None - 1 Bovine 8.5 pIC50 = 8.5 Functional
Compound was tested for in vitro for AII receptor antagonistic activity in bovine adrenal cortex.Compound was tested for in vitro for AII receptor antagonistic activity in bovine adrenal cortex.
ChEMBL 563 10 3 8 5.0 CCCCc1nc2ccc(C(C)(O)C[C@H]3CCCN3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80366-2
CHEMBL408033 156998 0 None - 1 Bovine 8.5 pIC50 = 8.5 Functional
Compound was tested for in vitro for AII receptor antagonistic activity in bovine adrenal cortex.Compound was tested for in vitro for AII receptor antagonistic activity in bovine adrenal cortex.
ChEMBL 563 10 3 8 5.0 CCCCc1nc2ccc(C(C)(O)C[C@H]3CCCN3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80366-2
54277224 70522 0 None - 1 Rabbit 8.5 pIC50 = 8.5 Functional
Antagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challengeAntagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challenge
ChEMBL 540 9 1 8 3.1 CCCCc1nc(C)c(CC(=O)N2CCN(C)CC2)c(=O)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2011.12.116
CHEMBL1951133 70522 0 None - 1 Rabbit 8.5 pIC50 = 8.5 Functional
Antagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challengeAntagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challenge
ChEMBL 540 9 1 8 3.1 CCCCc1nc(C)c(CC(=O)N2CCN(C)CC2)c(=O)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2011.12.116
14971718 15342 0 None - 1 Rabbit 8.4 pIC50 = 8.4 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 388 7 3 5 3.5 CCCc1n[nH]c(C(=O)O)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
CHEMBL121847 15342 0 None - 1 Rabbit 8.4 pIC50 = 8.4 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 388 7 3 5 3.5 CCCc1n[nH]c(C(=O)O)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
14956753 106574 0 None - 1 Rabbit 8.4 pIC50 = 8.4 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 527 9 1 7 5.9 CCCCc1nn(-c2ccccc2-c2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL315776 106574 0 None - 1 Rabbit 8.4 pIC50 = 8.4 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 527 9 1 7 5.9 CCCCc1nn(-c2ccccc2-c2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
14971721 112671 0 None - 1 Rabbit 8.4 pIC50 = 8.4 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 544 8 2 6 6.3 O=C(O)c1c(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c(CC2CC2)nn1-c1c(Cl)cccc1Cl 10.1021/jm00075a014
CHEMBL331475 112671 0 None - 1 Rabbit 8.4 pIC50 = 8.4 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 544 8 2 6 6.3 O=C(O)c1c(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c(CC2CC2)nn1-c1c(Cl)cccc1Cl 10.1021/jm00075a014
4673492 4061 5 None 5248 2 Guinea pig 8.4 pIC50 = 8.4 Functional
In vitro antagonistic potency against Angiotensin II receptor, type 1 in guinea pig adrenal membraneIn vitro antagonistic potency against Angiotensin II receptor, type 1 in guinea pig adrenal membrane
ChEMBL 438 6 1 5 4.5 CCc1nc(CC)c2c(c1)N(Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)C(=O)CC2 10.1021/jm9504722
8324 4061 5 None 5248 2 Guinea pig 8.4 pIC50 = 8.4 Functional
In vitro antagonistic potency against Angiotensin II receptor, type 1 in guinea pig adrenal membraneIn vitro antagonistic potency against Angiotensin II receptor, type 1 in guinea pig adrenal membrane
ChEMBL 438 6 1 5 4.5 CCc1nc(CC)c2c(c1)N(Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)C(=O)CC2 10.1021/jm9504722
CHEMBL159096 4061 5 None 5248 2 Guinea pig 8.4 pIC50 = 8.4 Functional
In vitro antagonistic potency against Angiotensin II receptor, type 1 in guinea pig adrenal membraneIn vitro antagonistic potency against Angiotensin II receptor, type 1 in guinea pig adrenal membrane
ChEMBL 438 6 1 5 4.5 CCc1nc(CC)c2c(c1)N(Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)C(=O)CC2 10.1021/jm9504722
14971689 12087 0 None - 1 Rabbit 7.5 pIC50 = 7.5 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 512 10 1 7 5.4 CCCCc1nn(CC(F)(F)F)c(C(=O)OCC)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
CHEMBL118431 12087 0 None - 1 Rabbit 7.5 pIC50 = 7.5 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 512 10 1 7 5.4 CCCCc1nn(CC(F)(F)F)c(C(=O)OCC)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
44211605 170183 0 None - 1 Bovine 7.5 pIC50 = 7.5 Functional
In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.
ChEMBL 577 10 1 10 5.0 CCCCc1nc2ccc(C3CC(C(=O)OCC)=NO3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80365-0
CHEMBL44526 170183 0 None - 1 Bovine 7.5 pIC50 = 7.5 Functional
In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.
ChEMBL 577 10 1 10 5.0 CCCCc1nc2ccc(C3CC(C(=O)OCC)=NO3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80365-0
14956809 105698 0 None - 1 Rabbit 7.5 pIC50 = 7.5 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 656 15 1 9 6.5 CCCCc1nn(CCCN(Cc2ccccc2)C(=O)OCc2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL313837 105698 0 None - 1 Rabbit 7.5 pIC50 = 7.5 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 656 15 1 9 6.5 CCCCc1nn(CCCN(Cc2ccccc2)C(=O)OCc2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
132562 99209 3 None - 1 Guinea pig 7.5 pIC50 = 7.5 Functional
In vitro antagonistic potency against Angiotensin II receptor, type 1 in guinea pig adrenal membraneIn vitro antagonistic potency against Angiotensin II receptor, type 1 in guinea pig adrenal membrane
ChEMBL 407 6 1 5 5.2 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2ccccc2n1 10.1021/jm9504722
CHEMBL284536 99209 3 None - 1 Guinea pig 7.5 pIC50 = 7.5 Functional
In vitro antagonistic potency against Angiotensin II receptor, type 1 in guinea pig adrenal membraneIn vitro antagonistic potency against Angiotensin II receptor, type 1 in guinea pig adrenal membrane
ChEMBL 407 6 1 5 5.2 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2ccccc2n1 10.1021/jm9504722
57403666 70511 0 None - 1 Rabbit 7.5 pIC50 = 7.5 Functional
Antagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challengeAntagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challenge
ChEMBL 472 9 1 8 3.5 CCOC(=O)CCc1c(C)nc(CC)n(Cc2ccc(-c3ccccc3-c3nnn[nH]3)cc2)c1=O 10.1016/j.bmcl.2011.12.116
CHEMBL1951122 70511 0 None - 1 Rabbit 7.5 pIC50 = 7.5 Functional
Antagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challengeAntagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challenge
ChEMBL 472 9 1 8 3.5 CCOC(=O)CCc1c(C)nc(CC)n(Cc2ccc(-c3ccccc3-c3nnn[nH]3)cc2)c1=O 10.1016/j.bmcl.2011.12.116
57396698 70516 0 None - 1 Rabbit 7.5 pIC50 = 7.5 Functional
Antagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challengeAntagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challenge
ChEMBL 513 11 1 7 4.2 CCCCc1nc(C)c(CC(=O)N(CC)CC)c(=O)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2011.12.116
CHEMBL1951127 70516 0 None - 1 Rabbit 7.5 pIC50 = 7.5 Functional
Antagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challengeAntagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challenge
ChEMBL 513 11 1 7 4.2 CCCCc1nc(C)c(CC(=O)N(CC)CC)c(=O)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2011.12.116
6918269 98005 8 None -5 2 Bovine 7.5 pIC50 = 7.5 Functional
In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.
ChEMBL 508 9 1 7 5.5 CCCCc1nc2ccc(C(C)(C)OC)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80365-0
CHEMBL275875 98005 8 None -5 2 Bovine 7.5 pIC50 = 7.5 Functional
In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.
ChEMBL 508 9 1 7 5.5 CCCCc1nc2ccc(C(C)(C)OC)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80365-0
CHEMBL295959 98005 8 None -5 2 Bovine 7.5 pIC50 = 7.5 Functional
In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.
ChEMBL 508 9 1 7 5.5 CCCCc1nc2ccc(C(C)(C)OC)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80365-0
10027636 24375 0 None 70 2 Rabbit 7.5 pIC50 = 7.5 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 468 9 1 5 5.7 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(N(CC2CC2)C(C(=O)O)c2ccccc2)cc1 10.1021/jm00078a014
CHEMBL134286 24375 0 None 70 2 Rabbit 7.5 pIC50 = 7.5 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 468 9 1 5 5.7 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(N(CC2CC2)C(C(=O)O)c2ccccc2)cc1 10.1021/jm00078a014
135406019 23814 15 None - 1 Human 5.5 pIC50 = 5.5 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 264 2 1 3 3.0 CC(=O)c1ccc(N=C2C(=O)Nc3ccccc32)cc1 nan
CHEMBL1338100 23814 15 None - 1 Human 5.5 pIC50 = 5.5 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 264 2 1 3 3.0 CC(=O)c1ccc(N=C2C(=O)Nc3ccccc32)cc1 nan
3395163 29608 6 None - 1 Human 4.5 pIC50 = 4.5 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 441 11 1 7 3.5 CSCCC(NC(=O)COc1ccccc1)C(=O)OCC(=O)c1cc2ccccc2o1 nan
CHEMBL1387520 29608 6 None - 1 Human 4.5 pIC50 = 4.5 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 441 11 1 7 3.5 CSCCC(NC(=O)COc1ccccc1)C(=O)OCC(=O)c1cc2ccccc2o1 nan
16012865 23123 9 None - 1 Human 5.5 pIC50 = 5.5 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 480 6 1 7 2.6 CN(c1ccccc1)S(=O)(=O)c1ccc(NC(=O)c2nc(S(C)(=O)=O)ncc2Cl)cc1 nan
CHEMBL1332454 23123 9 None - 1 Human 5.5 pIC50 = 5.5 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 480 6 1 7 2.6 CN(c1ccccc1)S(=O)(=O)c1ccc(NC(=O)c2nc(S(C)(=O)=O)ncc2Cl)cc1 nan
67903275 185931 2 None 257 2 Human 7.5 pIC50 = 7.5 Functional
Antagonist activity at human AT1 overexpressed in CHO-K1 cells in presence of 10 nM [Val5-angiotensin II measured after 90 mins by HTRF based IP-one assayAntagonist activity at human AT1 overexpressed in CHO-K1 cells in presence of 10 nM [Val5-angiotensin II measured after 90 mins by HTRF based IP-one assay
ChEMBL 402 7 1 5 4.2 CCCCC1=NC(C)(C)C(=O)N1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1021/acsmedchemlett.1c00240
CHEMBL4877651 185931 2 None 257 2 Human 7.5 pIC50 = 7.5 Functional
Antagonist activity at human AT1 overexpressed in CHO-K1 cells in presence of 10 nM [Val5-angiotensin II measured after 90 mins by HTRF based IP-one assayAntagonist activity at human AT1 overexpressed in CHO-K1 cells in presence of 10 nM [Val5-angiotensin II measured after 90 mins by HTRF based IP-one assay
ChEMBL 402 7 1 5 4.2 CCCCC1=NC(C)(C)C(=O)N1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1021/acsmedchemlett.1c00240
142534170 166240 0 None - 1 Human 7.5 pIC50 = 7.5 Functional
Antagonist activity at type-1 angiotensin 2 receptor (unknown origin) by calcium mobilizing assayAntagonist activity at type-1 angiotensin 2 receptor (unknown origin) by calcium mobilizing assay
ChEMBL 591 9 1 7 5.8 CCCCc1nc(C)c(CC(=S)N2Cc3ccccc3C2)c(=O)n1Cc1ccc(-c2ccccc2-c2noc(=O)[nH]2)cc1 10.1016/j.bmcl.2018.08.036
CHEMBL4284403 166240 0 None - 1 Human 7.5 pIC50 = 7.5 Functional
Antagonist activity at type-1 angiotensin 2 receptor (unknown origin) by calcium mobilizing assayAntagonist activity at type-1 angiotensin 2 receptor (unknown origin) by calcium mobilizing assay
ChEMBL 591 9 1 7 5.8 CCCCc1nc(C)c(CC(=S)N2Cc3ccccc3C2)c(=O)n1Cc1ccc(-c2ccccc2-c2noc(=O)[nH]2)cc1 10.1016/j.bmcl.2018.08.036
44292039 181501 1 None - 1 Bovine 7.5 pIC50 = 7.5 Functional
In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.
ChEMBL 547 8 1 8 5.5 CCCCc1nc2ccc([C@@H]3C[C@H]4CCCN4O3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80365-0
CHEMBL47817 181501 1 None - 1 Bovine 7.5 pIC50 = 7.5 Functional
In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.
ChEMBL 547 8 1 8 5.5 CCCCc1nc2ccc([C@@H]3C[C@H]4CCCN4O3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80365-0
14956801 204380 0 None - 1 Rabbit 7.5 pIC50 = 7.5 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 555 9 1 7 5.0 CCCCc1nn(Cc2c(F)c(F)c(F)c(F)c2F)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL85765 204380 0 None - 1 Rabbit 7.5 pIC50 = 7.5 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 555 9 1 7 5.0 CCCCc1nn(Cc2c(F)c(F)c(F)c(F)c2F)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
10251520 98352 0 None - 1 Rabbit 6.5 pIC50 = 6.5 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 419 5 0 5 5.5 CCc1nc2c(C)cc(C)nc2n1Cc1ccc2c(ccn2Cc2ccccc2C#N)c1 10.1021/jm00078a013
CHEMBL278656 98352 0 None - 1 Rabbit 6.5 pIC50 = 6.5 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 419 5 0 5 5.5 CCc1nc2c(C)cc(C)nc2n1Cc1ccc2c(ccn2Cc2ccccc2C#N)c1 10.1021/jm00078a013
5731496 52888 9 None - 1 Human 4.5 pIC50 = 4.5 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 281 2 1 2 4.8 Oc1cccc2ccc(/C=C/c3ccccc3Cl)nc12 nan
CHEMBL1598569 52888 9 None - 1 Human 4.5 pIC50 = 4.5 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 281 2 1 2 4.8 Oc1cccc2ccc(/C=C/c3ccccc3Cl)nc12 nan
1613606 47744 12 None - 1 Human 4.5 pIC50 = 4.5 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 392 8 1 7 1.6 Cc1ccc(C(=O)COC(=O)CNS(=O)(=O)c2ccccc2)cc1[N+](=O)[O-] nan
CHEMBL1550301 47744 12 None - 1 Human 4.5 pIC50 = 4.5 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 392 8 1 7 1.6 Cc1ccc(C(=O)COC(=O)CNS(=O)(=O)c2ccccc2)cc1[N+](=O)[O-] nan
44417426 141032 0 None - 1 Rabbit 7.5 pIC50 = 7.5 Functional
Antagonist activity against AT1 receptor assessed as inhibition of Ang2-induced rabbit aortic strip contractionAntagonist activity against AT1 receptor assessed as inhibition of Ang2-induced rabbit aortic strip contraction
ChEMBL 469 6 2 5 5.1 CCCc1nc2c(C)cc(C)nc2n1Cc1ccc(C2c3ccccc3C(C)(O)C2C(=O)O)cc1 10.1021/jm0603163
CHEMBL384936 141032 0 None - 1 Rabbit 7.5 pIC50 = 7.5 Functional
Antagonist activity against AT1 receptor assessed as inhibition of Ang2-induced rabbit aortic strip contractionAntagonist activity against AT1 receptor assessed as inhibition of Ang2-induced rabbit aortic strip contraction
ChEMBL 469 6 2 5 5.1 CCCc1nc2c(C)cc(C)nc2n1Cc1ccc(C2c3ccccc3C(C)(O)C2C(=O)O)cc1 10.1021/jm0603163
14956751 204568 0 None - 1 Rabbit 7.5 pIC50 = 7.5 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 509 9 1 9 4.1 CCCCc1nn(-c2ccc(C(=O)OC)cc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL87073 204568 0 None - 1 Rabbit 7.5 pIC50 = 7.5 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 509 9 1 9 4.1 CCCCc1nn(-c2ccc(C(=O)OC)cc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
14956802 204582 0 None 1 2 Rabbit 7.5 pIC50 = 7.5 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 515 9 1 7 5.5 CCCCc1nn(Cc2cccc3ccccc23)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL87184 204582 0 None 1 2 Rabbit 7.5 pIC50 = 7.5 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 515 9 1 7 5.5 CCCCc1nn(Cc2cccc3ccccc23)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
1610 2305 89 None -14 9 Bovine 6.5 pIC50 = 6.5 Functional
In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(00)80365-0
3941 2305 89 None -14 9 Bovine 6.5 pIC50 = 6.5 Functional
In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(00)80365-0
3961 2305 89 None -14 9 Bovine 6.5 pIC50 = 6.5 Functional
In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(00)80365-0
590 2305 89 None -14 9 Bovine 6.5 pIC50 = 6.5 Functional
In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(00)80365-0
CHEMBL191 2305 89 None -14 9 Bovine 6.5 pIC50 = 6.5 Functional
In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(00)80365-0
DB00678 2305 89 None -14 9 Bovine 6.5 pIC50 = 6.5 Functional
In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(00)80365-0
44355656 115571 0 None - 1 Rabbit 5.5 pIC50 = 5.5 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 467 6 1 6 5.8 CCc1nc2c(C)cc(C)nc2n1Cc1ccc2c(ccn2Cc2ccccc2NC(=O)OC)c1 10.1021/jm00078a013
CHEMBL335680 115571 0 None - 1 Rabbit 5.5 pIC50 = 5.5 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 467 6 1 6 5.8 CCc1nc2c(C)cc(C)nc2n1Cc1ccc2c(ccn2Cc2ccccc2NC(=O)OC)c1 10.1021/jm00078a013
44202070 39365 0 None - 1 Human 4.5 pIC50 = 4.5 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 271 1 0 2 3.5 Cc1ccc2c(c1)C(=O)C(=O)N2c1ccc(Cl)cc1 nan
CHEMBL1474191 39365 0 None - 1 Human 4.5 pIC50 = 4.5 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 271 1 0 2 3.5 Cc1ccc2c(c1)C(=O)C(=O)N2c1ccc(Cl)cc1 nan
1730709 23821 12 None - 1 Human 4.5 pIC50 = 4.5 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 370 8 1 6 3.0 Cc1ccccc1NC(=O)CCC(=O)OCC(=O)c1cccc([N+](=O)[O-])c1 nan
CHEMBL1338165 23821 12 None - 1 Human 4.5 pIC50 = 4.5 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 370 8 1 6 3.0 Cc1ccccc1NC(=O)CCC(=O)OCC(=O)c1cccc([N+](=O)[O-])c1 nan
2899190 52256 9 None - 1 Human 4.5 pIC50 = 4.5 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 386 6 0 7 1.6 Cc1ccc(C(=O)COC(=O)CN2C(=O)C3CC=CCC3C2=O)cc1[N+](=O)[O-] nan
CHEMBL1592181 52256 9 None - 1 Human 4.5 pIC50 = 4.5 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 386 6 0 7 1.6 Cc1ccc(C(=O)COC(=O)CN2C(=O)C3CC=CCC3C2=O)cc1[N+](=O)[O-] nan
2285607 38310 10 None - 1 Human 4.5 pIC50 = 4.5 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 400 9 1 7 3.1 COc1ccccc1NC(=O)CCC(=O)OCC(=O)c1ccc(C)c([N+](=O)[O-])c1 nan
CHEMBL1464749 38310 10 None - 1 Human 4.5 pIC50 = 4.5 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 400 9 1 7 3.1 COc1ccccc1NC(=O)CCC(=O)OCC(=O)c1ccc(C)c([N+](=O)[O-])c1 nan
44201736 27240 0 None - 1 Human 4.5 pIC50 = 4.5 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 586 9 2 5 5.2 O=C1NC[C@H](c2ccccc2)OC(=O)[C@@H](Cc2ccc(F)cc2)CC/C=C/C[C@@H]1CC(=O)N(CCO)Cc1ccccc1 nan
CHEMBL1368499 27240 0 None - 1 Human 4.5 pIC50 = 4.5 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 586 9 2 5 5.2 O=C1NC[C@H](c2ccccc2)OC(=O)[C@@H](Cc2ccc(F)cc2)CC/C=C/C[C@@H]1CC(=O)N(CCO)Cc1ccccc1 nan
16195321 50754 4 None - 1 Human 4.5 pIC50 = 4.5 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 413 6 0 5 4.9 CN(C)CCN(Cc1ccco1)C(=O)c1cc2c(Cl)nc3ccccc3c2s1 nan
CHEMBL1578651 50754 4 None - 1 Human 4.5 pIC50 = 4.5 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 413 6 0 5 4.9 CN(C)CCN(Cc1ccco1)C(=O)c1cc2c(Cl)nc3ccccc3c2s1 nan
10344571 116101 0 None 125 2 Rabbit 7.5 pIC50 = 7.5 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 468 9 1 5 5.8 C=CCN(c1ccc(Cn2c(CC)nc3c(C)cc(C)nc32)cc1C)C(C(=O)O)c1ccccc1 10.1021/jm00078a014
CHEMBL336773 116101 0 None 125 2 Rabbit 7.5 pIC50 = 7.5 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 468 9 1 5 5.8 C=CCN(c1ccc(Cn2c(CC)nc3c(C)cc(C)nc32)cc1C)C(C(=O)O)c1ccccc1 10.1021/jm00078a014
4210369 42170 12 None - 1 Human 4.5 pIC50 = 4.5 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 424 8 1 6 4.0 O=C(CCC(=O)OCC(=O)c1cccc([N+](=O)[O-])c1)Nc1cccc(Cl)c1Cl nan
CHEMBL1499072 42170 12 None - 1 Human 4.5 pIC50 = 4.5 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 424 8 1 6 4.0 O=C(CCC(=O)OCC(=O)c1cccc([N+](=O)[O-])c1)Nc1cccc(Cl)c1Cl nan
1726742 33161 13 None - 1 Human 4.5 pIC50 = 4.5 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 398 9 1 7 2.9 CC(=O)c1ccc(NC(=O)CCC(=O)OCC(=O)c2cccc([N+](=O)[O-])c2)cc1 nan
CHEMBL1419495 33161 13 None - 1 Human 4.5 pIC50 = 4.5 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 398 9 1 7 2.9 CC(=O)c1ccc(NC(=O)CCC(=O)OCC(=O)c2cccc([N+](=O)[O-])c2)cc1 nan
9548123 47485 0 None - 1 Human 4.5 pIC50 = 4.5 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 378 3 1 5 3.1 COc1ccc2c(c1)C(=O)[C@@H](O)[C@H](c1ccc(OC)c(Br)c1)O2 nan
CHEMBL1548173 47485 0 None - 1 Human 4.5 pIC50 = 4.5 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 378 3 1 5 3.1 COc1ccc2c(c1)C(=O)[C@@H](O)[C@H](c1ccc(OC)c(Br)c1)O2 nan
5416363 107684 3 None - 1 Human 5.5 pIC50 = 5.5 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 295 3 1 3 3.5 C/C(=N/NC(=O)c1ccc(C(C)(C)C)cc1)c1ccccn1 nan
CHEMBL3196324 107684 3 None - 1 Human 5.5 pIC50 = 5.5 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 295 3 1 3 3.5 C/C(=N/NC(=O)c1ccc(C(C)(C)C)cc1)c1ccccn1 nan
44292214 175307 0 None - 1 Bovine 7.5 pIC50 = 7.5 Functional
In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.
ChEMBL 577 9 2 9 4.6 CCCCc1nc2ccc([C@]3(CO)C[C@H]4CCCN4O3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80365-0
CHEMBL45864 175307 0 None - 1 Bovine 7.5 pIC50 = 7.5 Functional
In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.
ChEMBL 577 9 2 9 4.6 CCCCc1nc2ccc([C@]3(CO)C[C@H]4CCCN4O3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80365-0
10364891 26025 0 None 33 2 Rabbit 6.5 pIC50 = 6.5 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 421 5 0 5 5.3 CCc1nc2c(C)cc(C)nc2n1Cc1ccc2c(c1)CCN2C(C#N)c1ccccc1 10.1021/jm00078a013
CHEMBL135792 26025 0 None 33 2 Rabbit 6.5 pIC50 = 6.5 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 421 5 0 5 5.3 CCc1nc2c(C)cc(C)nc2n1Cc1ccc2c(c1)CCN2C(C#N)c1ccccc1 10.1021/jm00078a013
9550553 54221 6 None 2 3 Human 5.5 pIC50 = 5.5 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 445 8 1 11 4.3 CCC(=O)OCCNc1cc(Sc2nc3ccccc3s2)c2nonc2c1[N+](=O)[O-] nan
CHEMBL1610025 54221 6 None 2 3 Human 5.5 pIC50 = 5.5 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 445 8 1 11 4.3 CCC(=O)OCCNc1cc(Sc2nc3ccccc3s2)c2nonc2c1[N+](=O)[O-] nan
1266032 40622 7 None 3 2 Human 5.5 pIC50 = 5.5 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 343 2 0 3 4.9 O=C(Sc1cccc2cccnc12)c1ccccc1Br nan
CHEMBL1486214 40622 7 None 3 2 Human 5.5 pIC50 = 5.5 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 343 2 0 3 4.9 O=C(Sc1cccc2cccnc12)c1ccccc1Br nan
9608279 107291 6 None - 1 Human 5.5 pIC50 = 5.5 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 366 6 1 8 3.1 COc1ccc(/C=N/Nc2cc(C)nc(-n3nc(C)cc3C)n2)c(OC)c1 nan
CHEMBL3191846 107291 6 None - 1 Human 5.5 pIC50 = 5.5 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 366 6 1 8 3.1 COc1ccc(/C=N/Nc2cc(C)nc(-n3nc(C)cc3C)n2)c(OC)c1 nan
5341487 71991 8 None -1 2 Human 5.5 pIC50 = 5.5 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 317 3 1 3 3.0 C/C(=N\NC(=O)c1cccc(Br)c1)c1ccccn1 nan
CHEMBL1984876 71991 8 None -1 2 Human 5.5 pIC50 = 5.5 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 317 3 1 3 3.0 C/C(=N\NC(=O)c1cccc(Br)c1)c1ccccn1 nan
11100 125422 74 None - 1 Human 4.5 pIC50 = 4.5 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 192 3 1 4 1.8 O=C(c1ccco1)C(O)c1ccco1 nan
CHEMBL364893 125422 74 None - 1 Human 4.5 pIC50 = 4.5 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 192 3 1 4 1.8 O=C(c1ccco1)C(O)c1ccco1 nan
135472780 28219 6 None - 1 Human 4.5 pIC50 = 4.5 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 277 2 1 4 5.0 Cc1ccc(N=Nc2ccc(O)c3ncccc23)cc1C nan
CHEMBL1375373 28219 6 None - 1 Human 4.5 pIC50 = 4.5 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 277 2 1 4 5.0 Cc1ccc(N=Nc2ccc(O)c3ncccc23)cc1C nan
2360979 38699 7 None - 1 Human 4.5 pIC50 = 4.5 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 275 5 1 3 3.6 COc1ccccc1NCC(=O)c1ccc(Cl)cc1 nan
CHEMBL1467838 38699 7 None - 1 Human 4.5 pIC50 = 4.5 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 275 5 1 3 3.6 COc1ccccc1NCC(=O)c1ccc(Cl)cc1 nan
3106500 24570 8 None -1 2 Human 4.5 pIC50 = 4.5 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 306 3 1 7 1.5 CC1=NN(C(N)=S)C(=O)C1N=Nc1ccc([N+](=O)[O-])cc1 nan
CHEMBL1344603 24570 8 None -1 2 Human 4.5 pIC50 = 4.5 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 306 3 1 7 1.5 CC1=NN(C(N)=S)C(=O)C1N=Nc1ccc([N+](=O)[O-])cc1 nan
2431535 38672 7 None - 1 Human 4.5 pIC50 = 4.5 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 343 4 0 4 4.1 O=C(COC(=O)c1cccnc1Cl)c1ccc(Cl)cc1Cl nan
CHEMBL1467556 38672 7 None - 1 Human 4.5 pIC50 = 4.5 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 343 4 0 4 4.1 O=C(COC(=O)c1cccnc1Cl)c1ccc(Cl)cc1Cl nan
2324620 24680 14 None - 1 Human 4.5 pIC50 = 4.5 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 455 4 4 4 4.3 CC(C)(C)c1cc(CCC(=O)NNC(=S)NC(=O)c2ccccc2)cc(C(C)(C)C)c1O nan
CHEMBL1345564 24680 14 None - 1 Human 4.5 pIC50 = 4.5 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 455 4 4 4 4.3 CC(C)(C)c1cc(CCC(=O)NNC(=S)NC(=O)c2ccccc2)cc(C(C)(C)C)c1O nan
1875884 24285 7 None - 1 Human 4.5 pIC50 = 4.5 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 436 5 3 6 3.0 COc1ccc(/C=C/C(=O)NC(=S)NNC(=O)c2c(-c3ccccc3)noc2C)cc1 nan
CHEMBL1342221 24285 7 None - 1 Human 4.5 pIC50 = 4.5 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 436 5 3 6 3.0 COc1ccc(/C=C/C(=O)NC(=S)NNC(=O)c2c(-c3ccccc3)noc2C)cc1 nan
16012896 32765 10 None 1 3 Human 5.5 pIC50 = 5.5 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 494 7 1 7 3.0 CCS(=O)(=O)c1ncc(Cl)c(C(=O)Nc2ccc(S(=O)(=O)N(C)c3ccccc3)cc2)n1 nan
CHEMBL1416089 32765 10 None 1 3 Human 5.5 pIC50 = 5.5 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 494 7 1 7 3.0 CCS(=O)(=O)c1ncc(Cl)c(C(=O)Nc2ccc(S(=O)(=O)N(C)c3ccccc3)cc2)n1 nan
2352555 52078 7 None - 1 Human 4.5 pIC50 = 4.5 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 309 4 0 4 3.4 O=C(OCC(=O)c1ccc(Cl)cc1Cl)c1ccccn1 nan
CHEMBL1589900 52078 7 None - 1 Human 4.5 pIC50 = 4.5 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 309 4 0 4 3.4 O=C(OCC(=O)c1ccc(Cl)cc1Cl)c1ccccn1 nan
3146836 107159 9 None - 1 Human 4.4 pIC50 = 4.4 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 399 4 1 6 5.6 CCOC(=O)C1=C(C)N=C2CC(c3cccs3)CC(O)=C2C1c1cccs1 nan
CHEMBL3190347 107159 9 None - 1 Human 4.4 pIC50 = 4.4 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 399 4 1 6 5.6 CCOC(=O)C1=C(C)N=C2CC(c3cccs3)CC(O)=C2C1c1cccs1 nan
135400342 39513 7 None - 1 Human 5.4 pIC50 = 5.4 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 293 4 2 7 2.2 O=[N+]([O-])c1ccc(O)c(/C=N/Nc2ccc(Cl)nn2)c1 nan
CHEMBL1476264 39513 7 None - 1 Human 5.4 pIC50 = 5.4 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 293 4 2 7 2.2 O=[N+]([O-])c1ccc(O)c(/C=N/Nc2ccc(Cl)nn2)c1 nan
1612942 40580 9 None - 1 Human 4.4 pIC50 = 4.4 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 370 7 1 6 2.4 Cc1ccc(C(=O)NCC(=O)OCC(=O)c2ccc(C)c([N+](=O)[O-])c2)cc1 nan
CHEMBL1485784 40580 9 None - 1 Human 4.4 pIC50 = 4.4 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 370 7 1 6 2.4 Cc1ccc(C(=O)NCC(=O)OCC(=O)c2ccc(C)c([N+](=O)[O-])c2)cc1 nan
24818379 40842 5 None - 1 Human 4.4 pIC50 = 4.4 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 353 6 2 8 1.3 COc1ccc(S(=O)(=O)NNc2nc(C)cc(C)n2)cc1[N+](=O)[O-] nan
CHEMBL1487991 40842 5 None - 1 Human 4.4 pIC50 = 4.4 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 353 6 2 8 1.3 COc1ccc(S(=O)(=O)NNc2nc(C)cc(C)n2)cc1[N+](=O)[O-] nan
82533 40788 63 None -6 5 Human 5.4 pIC50 = 5.4 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 298 3 1 3 3.3 Cc1ccc(S(=O)(=O)Nc2cccc3cccnc23)cc1 nan
CHEMBL1487635 40788 63 None -6 5 Human 5.4 pIC50 = 5.4 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 298 3 1 3 3.3 Cc1ccc(S(=O)(=O)Nc2cccc3cccnc23)cc1 nan
5286934 49021 8 None -2 5 Human 5.4 pIC50 = 5.4 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 294 9 0 4 2.4 CCCCS(=O)(=O)/C=C\C=C/S(=O)(=O)CCCC nan
CHEMBL1563483 49021 8 None -2 5 Human 5.4 pIC50 = 5.4 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 294 9 0 4 2.4 CCCCS(=O)(=O)/C=C\C=C/S(=O)(=O)CCCC nan
930382 33772 12 None - 1 Human 4.4 pIC50 = 4.4 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 309 4 0 4 3.4 O=C(COC(=O)c1cccnc1)c1ccc(Cl)c(Cl)c1 nan
CHEMBL1424582 33772 12 None - 1 Human 4.4 pIC50 = 4.4 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 309 4 0 4 3.4 O=C(COC(=O)c1cccnc1)c1ccc(Cl)c(Cl)c1 nan
2811457 34183 5 None - 1 Human 5.4 pIC50 = 5.4 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 273 4 2 4 3.2 Cc1noc(C)c1C(=O)NNc1ccc(C(C)C)cc1 nan
CHEMBL1428121 34183 5 None - 1 Human 5.4 pIC50 = 5.4 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 273 4 2 4 3.2 Cc1noc(C)c1C(=O)NNc1ccc(C(C)C)cc1 nan
14971679 111147 0 None - 1 Rabbit 7.4 pIC50 = 7.4 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 608 10 1 7 7.8 CCCCc1nn(-c2c(Cl)cc(Cl)cc2Cl)c(C(=O)OCC)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
CHEMBL328598 111147 0 None - 1 Rabbit 7.4 pIC50 = 7.4 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 608 10 1 7 7.8 CCCCc1nn(-c2c(Cl)cc(Cl)cc2Cl)c(C(=O)OCC)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
108185 1578 71 None -3 5 Rat 7.4 pIC50 = 7.4 Functional
In vitro antagonistic activity by displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta Angiotensin II receptor, type 1In vitro antagonistic activity by displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 436 8 2 6 4.5 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)C(=O)O)Cl 10.1021/jm00057a009
586 1578 71 None -3 5 Rat 7.4 pIC50 = 7.4 Functional
In vitro antagonistic activity by displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta Angiotensin II receptor, type 1In vitro antagonistic activity by displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 436 8 2 6 4.5 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)C(=O)O)Cl 10.1021/jm00057a009
CHEMBL907 1578 71 None -3 5 Rat 7.4 pIC50 = 7.4 Functional
In vitro antagonistic activity by displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta Angiotensin II receptor, type 1In vitro antagonistic activity by displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 436 8 2 6 4.5 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)C(=O)O)Cl 10.1021/jm00057a009
108185 1578 71 None -3 5 Rabbit 7.4 pIC50 = 7.4 Functional
In vitro antagonistic activity for AT1 receptor by displacing 125I[Sar, ILe8]AII radioligand in rabbit aorta membrane using 0.2% bovine serum albumin (BSA)In vitro antagonistic activity for AT1 receptor by displacing 125I[Sar, ILe8]AII radioligand in rabbit aorta membrane using 0.2% bovine serum albumin (BSA)
ChEMBL 436 8 2 6 4.5 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)C(=O)O)Cl 10.1021/jm00069a015
586 1578 71 None -3 5 Rabbit 7.4 pIC50 = 7.4 Functional
In vitro antagonistic activity for AT1 receptor by displacing 125I[Sar, ILe8]AII radioligand in rabbit aorta membrane using 0.2% bovine serum albumin (BSA)In vitro antagonistic activity for AT1 receptor by displacing 125I[Sar, ILe8]AII radioligand in rabbit aorta membrane using 0.2% bovine serum albumin (BSA)
ChEMBL 436 8 2 6 4.5 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)C(=O)O)Cl 10.1021/jm00069a015
CHEMBL907 1578 71 None -3 5 Rabbit 7.4 pIC50 = 7.4 Functional
In vitro antagonistic activity for AT1 receptor by displacing 125I[Sar, ILe8]AII radioligand in rabbit aorta membrane using 0.2% bovine serum albumin (BSA)In vitro antagonistic activity for AT1 receptor by displacing 125I[Sar, ILe8]AII radioligand in rabbit aorta membrane using 0.2% bovine serum albumin (BSA)
ChEMBL 436 8 2 6 4.5 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)C(=O)O)Cl 10.1021/jm00069a015
14956783 204052 0 None - 1 Rabbit 7.4 pIC50 = 7.4 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 414 8 1 8 2.8 CCCCc1nn(CC#N)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL82920 204052 0 None - 1 Rabbit 7.4 pIC50 = 7.4 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 414 8 1 8 2.8 CCCCc1nn(CC#N)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
9612783 107425 3 None 2 2 Human 5.4 pIC50 = 5.4 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 345 6 1 4 3.7 C/C(=N\NC(=O)COc1ccccc1-c1ccccc1)c1ccccn1 nan
CHEMBL3193378 107425 3 None 2 2 Human 5.4 pIC50 = 5.4 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 345 6 1 4 3.7 C/C(=N\NC(=O)COc1ccccc1-c1ccccc1)c1ccccn1 nan
142534004 166793 0 None - 1 Human 7.4 pIC50 = 7.4 Functional
Antagonist activity at type-1 angiotensin 2 receptor (unknown origin) by calcium mobilizing assayAntagonist activity at type-1 angiotensin 2 receptor (unknown origin) by calcium mobilizing assay
ChEMBL 557 9 1 7 5.3 CCCCc1nc(C)c(CC(=S)N2CCCCC2)c(=O)n1Cc1ccc(-c2ccccc2-c2noc(=O)[nH]2)cc1 10.1016/j.bmcl.2018.08.036
CHEMBL4294618 166793 0 None - 1 Human 7.4 pIC50 = 7.4 Functional
Antagonist activity at type-1 angiotensin 2 receptor (unknown origin) by calcium mobilizing assayAntagonist activity at type-1 angiotensin 2 receptor (unknown origin) by calcium mobilizing assay
ChEMBL 557 9 1 7 5.3 CCCCc1nc(C)c(CC(=S)N2CCCCC2)c(=O)n1Cc1ccc(-c2ccccc2-c2noc(=O)[nH]2)cc1 10.1016/j.bmcl.2018.08.036
15229102 100709 0 None - 1 Bovine 7.4 pIC50 = 7.4 Functional
In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.
ChEMBL 561 8 1 8 5.9 CCCCc1nc2ccc([C@@H]3C[C@H]4CCCCN4O3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80365-0
CHEMBL295695 100709 0 None - 1 Bovine 7.4 pIC50 = 7.4 Functional
In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.
ChEMBL 561 8 1 8 5.9 CCCCc1nc2ccc([C@@H]3C[C@H]4CCCCN4O3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80365-0
9982458 26289 0 None - 1 Rabbit 6.4 pIC50 = 6.4 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 476 8 1 5 6.0 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(N(CC)C(C(=O)O)c2ccccc2Cl)cc1 10.1021/jm00078a014
CHEMBL136034 26289 0 None - 1 Rabbit 6.4 pIC50 = 6.4 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 476 8 1 5 6.0 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(N(CC)C(C(=O)O)c2ccccc2Cl)cc1 10.1021/jm00078a014
1720698 19324 12 None - 1 Human 4.4 pIC50 = 4.4 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 378 8 1 7 1.3 O=C(CNS(=O)(=O)c1ccccc1)OCC(=O)c1cccc([N+](=O)[O-])c1 nan
CHEMBL1299557 19324 12 None - 1 Human 4.4 pIC50 = 4.4 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 378 8 1 7 1.3 O=C(CNS(=O)(=O)c1ccccc1)OCC(=O)c1cccc([N+](=O)[O-])c1 nan
2812498 43381 5 None 2 2 Human 5.4 pIC50 = 5.4 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 362 5 2 4 4.3 Cc1ccc(NNC(=O)c2cc(C(C)(C)C)nn2Cc2ccccc2)cc1 nan
CHEMBL1509694 43381 5 None 2 2 Human 5.4 pIC50 = 5.4 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 362 5 2 4 4.3 Cc1ccc(NNC(=O)c2cc(C(C)(C)C)nn2Cc2ccccc2)cc1 nan
888488 50411 11 None - 1 Human 4.4 pIC50 = 4.4 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 301 5 0 7 1.7 Cc1ccc(C(=O)COC(=O)c2cnccn2)cc1[N+](=O)[O-] nan
CHEMBL1575784 50411 11 None - 1 Human 4.4 pIC50 = 4.4 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 301 5 0 7 1.7 Cc1ccc(C(=O)COC(=O)c2cnccn2)cc1[N+](=O)[O-] nan
2766929 50024 24 None -20 4 Human 4.4 pIC50 = 4.4 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 287 1 0 4 3.1 CC(C)(C)c1ccc(-n2nc(C#N)c(Cl)cc2=O)cc1 nan
CHEMBL1572001 50024 24 None -20 4 Human 4.4 pIC50 = 4.4 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 287 1 0 4 3.1 CC(C)(C)c1ccc(-n2nc(C#N)c(Cl)cc2=O)cc1 nan
130606 36026 48 None 1 3 Human 5.4 pIC50 = 5.4 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 328 4 1 4 3.4 COc1cc(NS(=O)(=O)c2ccc(C)cc2)c2ncccc2c1 nan
CHEMBL1445650 36026 48 None 1 3 Human 5.4 pIC50 = 5.4 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 328 4 1 4 3.4 COc1cc(NS(=O)(=O)c2ccc(C)cc2)c2ncccc2c1 nan
44292173 171876 0 None - 1 Bovine 7.4 pIC50 = 7.4 Functional
In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.
ChEMBL 575 8 1 8 6.3 CCCCc1nc2ccc([C@@H]3C[C@H]4CCC(C)(C)N4O3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80365-0
CHEMBL44798 171876 0 None - 1 Bovine 7.4 pIC50 = 7.4 Functional
In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.
ChEMBL 575 8 1 8 6.3 CCCCc1nc2ccc([C@@H]3C[C@H]4CCC(C)(C)N4O3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80365-0
164616479 184724 0 None 16 2 Human 6.4 pIC50 = 6.4 Functional
Antagonist activity at human AT1 overexpressed in CHO-K1 cells in presence of 10 nM [Val5-angiotensin II measured after 90 mins by HTRF based IP-one assayAntagonist activity at human AT1 overexpressed in CHO-K1 cells in presence of 10 nM [Val5-angiotensin II measured after 90 mins by HTRF based IP-one assay
ChEMBL 404 7 2 5 3.8 CCCCC1NC(C)(C)C(=O)N1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1021/acsmedchemlett.1c00240
CHEMBL4859498 184724 0 None 16 2 Human 6.4 pIC50 = 6.4 Functional
Antagonist activity at human AT1 overexpressed in CHO-K1 cells in presence of 10 nM [Val5-angiotensin II measured after 90 mins by HTRF based IP-one assayAntagonist activity at human AT1 overexpressed in CHO-K1 cells in presence of 10 nM [Val5-angiotensin II measured after 90 mins by HTRF based IP-one assay
ChEMBL 404 7 2 5 3.8 CCCCC1NC(C)(C)C(=O)N1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1021/acsmedchemlett.1c00240
2426323 37323 6 None - 1 Human 4.4 pIC50 = 4.4 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 360 3 3 3 4.6 Cc1ccccc1N=C(S)NNc1ncc(C(F)(F)F)cc1Cl nan
CHEMBL1456428 37323 6 None - 1 Human 4.4 pIC50 = 4.4 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 360 3 3 3 4.6 Cc1ccccc1N=C(S)NNc1ncc(C(F)(F)F)cc1Cl nan
1472216 50327 11 None -3 4 Human 5.4 pIC50 = 5.4 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 384 6 1 4 3.6 COc1ccc(NC(=O)/C(Cl)=C(/Cl)[S+]([O-])Cc2ccccc2)cn1 nan
CHEMBL1574879 50327 11 None -3 4 Human 5.4 pIC50 = 5.4 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 384 6 1 4 3.6 COc1ccc(NC(=O)/C(Cl)=C(/Cl)[S+]([O-])Cc2ccccc2)cn1 nan
135421501 49545 16 None - 1 Human 5.4 pIC50 = 5.4 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 344 2 1 3 3.8 COc1ccc(N=C2C(=O)Nc3ccc(C)c(Br)c32)cc1 nan
CHEMBL1567702 49545 16 None - 1 Human 5.4 pIC50 = 5.4 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 344 2 1 3 3.8 COc1ccc(N=C2C(=O)Nc3ccc(C)c(Br)c32)cc1 nan
16193016 55822 4 None - 1 Human 4.4 pIC50 = 4.4 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 354 4 0 2 3.4 O=C(C[N+]1(CC#Cc2ccccc2)CCOCC1)c1ccc(Cl)cc1 nan
CHEMBL1602056 55822 4 None - 1 Human 4.4 pIC50 = 4.4 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 354 4 0 2 3.4 O=C(C[N+]1(CC#Cc2ccccc2)CCOCC1)c1ccc(Cl)cc1 nan
CHEMBL1625597 55822 4 None - 1 Human 4.4 pIC50 = 4.4 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 354 4 0 2 3.4 O=C(C[N+]1(CC#Cc2ccccc2)CCOCC1)c1ccc(Cl)cc1 nan
3368605 19606 9 None - 1 Human 4.4 pIC50 = 4.4 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 504 5 0 6 5.4 O=C(OCC(=O)c1ccc(Cl)cc1Cl)c1ccc2c(c1)C(=O)N(c1cccc3ncccc13)C2=O nan
CHEMBL1301939 19606 9 None - 1 Human 4.4 pIC50 = 4.4 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 504 5 0 6 5.4 O=C(OCC(=O)c1ccc(Cl)cc1Cl)c1ccc2c(c1)C(=O)N(c1cccc3ncccc13)C2=O nan
2114872 20568 7 None 1 2 Human 5.4 pIC50 = 5.4 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 273 2 1 4 3.1 O=C(Nc1nc2ccc(F)cc2s1)c1ccccn1 nan
CHEMBL1309573 20568 7 None 1 2 Human 5.4 pIC50 = 5.4 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 273 2 1 4 3.1 O=C(Nc1nc2ccc(F)cc2s1)c1ccccn1 nan
2928370 45196 8 None - 1 Human 4.4 pIC50 = 4.4 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 356 5 1 5 3.2 CCOC(=O)C1=NNC(C(=O)c2ccc(Cl)cc2)C1c1ccccc1 nan
CHEMBL1528033 45196 8 None - 1 Human 4.4 pIC50 = 4.4 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 356 5 1 5 3.2 CCOC(=O)C1=NNC(C(=O)c2ccc(Cl)cc2)C1c1ccccc1 nan
135426090 34108 12 None 3 2 Human 5.4 pIC50 = 5.4 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 318 3 2 6 4.0 Cc1ccc2oc(Nc3nc(O)cc(-c4ccccc4)n3)nc2c1 nan
CHEMBL1427431 34108 12 None 3 2 Human 5.4 pIC50 = 5.4 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 318 3 2 6 4.0 Cc1ccc2oc(Nc3nc(O)cc(-c4ccccc4)n3)nc2c1 nan
135632169 51378 8 None - 1 Human 4.4 pIC50 = 4.4 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 419 5 2 7 2.4 O=C1N=C(NS(=O)(=O)Cc2ccccc2)S/C1=C/c1cc([N+](=O)[O-])ccc1O nan
136087362 51378 8 None - 1 Human 4.4 pIC50 = 4.4 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 419 5 2 7 2.4 O=C1N=C(NS(=O)(=O)Cc2ccccc2)S/C1=C/c1cc([N+](=O)[O-])ccc1O nan
CHEMBL1583998 51378 8 None - 1 Human 4.4 pIC50 = 4.4 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 419 5 2 7 2.4 O=C1N=C(NS(=O)(=O)Cc2ccccc2)S/C1=C/c1cc([N+](=O)[O-])ccc1O nan
10456041 25636 0 None 186 2 Rabbit 8.4 pIC50 = 8.4 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 442 8 1 5 5.3 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(N(CC)C(C(=O)O)c2ccccc2)cc1 10.1021/jm00078a014
CHEMBL135346 25636 0 None 186 2 Rabbit 8.4 pIC50 = 8.4 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 442 8 1 5 5.3 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(N(CC)C(C(=O)O)c2ccccc2)cc1 10.1021/jm00078a014
44459595 98985 0 None - 1 Rabbit 8.4 pIC50 = 8.4 Functional
Inhibitory activity against Angiotensin II receptor, type 1 induced contractions in isolated rabbit aortic ringsInhibitory activity against Angiotensin II receptor, type 1 induced contractions in isolated rabbit aortic rings
ChEMBL 516 6 2 7 5.1 CC1(C)CC(=O)NN=C1c1ccc2nc(C3CC3)n(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c2c1 10.1016/S0960-894X(01)80348-6
CHEMBL2079785 98985 0 None - 1 Rabbit 8.4 pIC50 = 8.4 Functional
Inhibitory activity against Angiotensin II receptor, type 1 induced contractions in isolated rabbit aortic ringsInhibitory activity against Angiotensin II receptor, type 1 induced contractions in isolated rabbit aortic rings
ChEMBL 516 6 2 7 5.1 CC1(C)CC(=O)NN=C1c1ccc2nc(C3CC3)n(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c2c1 10.1016/S0960-894X(01)80348-6
CHEMBL283055 98985 0 None - 1 Rabbit 8.4 pIC50 = 8.4 Functional
Inhibitory activity against Angiotensin II receptor, type 1 induced contractions in isolated rabbit aortic ringsInhibitory activity against Angiotensin II receptor, type 1 induced contractions in isolated rabbit aortic rings
ChEMBL 516 6 2 7 5.1 CC1(C)CC(=O)NN=C1c1ccc2nc(C3CC3)n(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c2c1 10.1016/S0960-894X(01)80348-6
44459878 99233 0 None - 1 Rabbit 8.4 pIC50 = 8.4 Functional
Inhibitory activity against Angiotensin II receptor, type 1 induced contractions in isolated rabbit aortic ringsInhibitory activity against Angiotensin II receptor, type 1 induced contractions in isolated rabbit aortic rings
ChEMBL 574 8 1 9 4.6 COC(=O)CN1N=C(c2ccc3nc(C4CC4)n(Cc4ccc(-c5ccccc5-c5nn[nH]n5)cc4)c3c2)C(C)CC1=O 10.1016/S0960-894X(01)80348-6
CHEMBL284704 99233 0 None - 1 Rabbit 8.4 pIC50 = 8.4 Functional
Inhibitory activity against Angiotensin II receptor, type 1 induced contractions in isolated rabbit aortic ringsInhibitory activity against Angiotensin II receptor, type 1 induced contractions in isolated rabbit aortic rings
ChEMBL 574 8 1 9 4.6 COC(=O)CN1N=C(c2ccc3nc(C4CC4)n(Cc4ccc(-c5ccccc5-c5nn[nH]n5)cc4)c3c2)C(C)CC1=O 10.1016/S0960-894X(01)80348-6
53657506 70527 0 None - 1 Rabbit 8.4 pIC50 = 8.4 Functional
Antagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challengeAntagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challenge
ChEMBL 557 10 1 8 4.3 CCCCc1nc(C)c(CCC(=O)N2CCSCC2)c(=O)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2011.12.116
CHEMBL1951138 70527 0 None - 1 Rabbit 8.4 pIC50 = 8.4 Functional
Antagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challengeAntagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challenge
ChEMBL 557 10 1 8 4.3 CCCCc1nc(C)c(CCC(=O)N2CCSCC2)c(=O)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2011.12.116
14956738 204074 0 None - 1 Rabbit 8.4 pIC50 = 8.4 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 465 8 1 7 4.6 CCCCc1nn(-c2ccccc2C)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL83180 204074 0 None - 1 Rabbit 8.4 pIC50 = 8.4 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 465 8 1 7 4.6 CCCCc1nn(-c2ccccc2C)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
9870652 70533 68 None -15 2 Human 8.4 pIC50 = 8.4 Functional
Antagonist activity at type-1 angiotensin 2 receptor (unknown origin) by calcium mobilizing assayAntagonist activity at type-1 angiotensin 2 receptor (unknown origin) by calcium mobilizing assay
ChEMBL 501 9 1 7 4.2 CCCCc1nc(C)c(CC(=S)N(C)C)c(=O)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2018.08.036
CHEMBL1951143 70533 68 None -15 2 Human 8.4 pIC50 = 8.4 Functional
Antagonist activity at type-1 angiotensin 2 receptor (unknown origin) by calcium mobilizing assayAntagonist activity at type-1 angiotensin 2 receptor (unknown origin) by calcium mobilizing assay
ChEMBL 501 9 1 7 4.2 CCCCc1nc(C)c(CC(=S)N(C)C)c(=O)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2018.08.036
11974939 81713 0 None - 1 Rabbit 8.3 pIC50 = 8.3 Functional
Antagonist activity against AT1 receptor assessed as inhibition of Ang2-induced rabbit aortic strip contractionAntagonist activity against AT1 receptor assessed as inhibition of Ang2-induced rabbit aortic strip contraction
ChEMBL 466 5 1 6 4.9 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2c(C(=O)O)n(C)c(=O)c3ccccc23)cc1 10.1021/jm0603163
CHEMBL216747 81713 0 None - 1 Rabbit 8.3 pIC50 = 8.3 Functional
Antagonist activity against AT1 receptor assessed as inhibition of Ang2-induced rabbit aortic strip contractionAntagonist activity against AT1 receptor assessed as inhibition of Ang2-induced rabbit aortic strip contraction
ChEMBL 466 5 1 6 4.9 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2c(C(=O)O)n(C)c(=O)c3ccccc23)cc1 10.1021/jm0603163
10183373 164447 0 None 3 2 Rabbit 8.3 pIC50 = 8.3 Functional
In vitro antagonistic activity for AT1 receptor by displacing 125I[Sar, ILe8]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for AT1 receptor by displacing 125I[Sar, ILe8]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 465 9 1 7 4.3 CCCCc1nn(Cc2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL422593 164447 0 None 3 2 Rabbit 8.3 pIC50 = 8.3 Functional
In vitro antagonistic activity for AT1 receptor by displacing 125I[Sar, ILe8]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for AT1 receptor by displacing 125I[Sar, ILe8]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 465 9 1 7 4.3 CCCCc1nn(Cc2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
10183373 164447 0 None 3 2 Rabbit 8.3 pIC50 = 8.3 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 465 9 1 7 4.3 CCCCc1nn(Cc2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL422593 164447 0 None 3 2 Rabbit 8.3 pIC50 = 8.3 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 465 9 1 7 4.3 CCCCc1nn(Cc2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
54199501 70508 0 None - 1 Rabbit 8.3 pIC50 = 8.3 Functional
Antagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challengeAntagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challenge
ChEMBL 486 10 1 8 3.9 CCCCc1nc(C)c(CC(=O)OCC)c(=O)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2011.12.116
CHEMBL1951119 70508 0 None - 1 Rabbit 8.3 pIC50 = 8.3 Functional
Antagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challengeAntagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challenge
ChEMBL 486 10 1 8 3.9 CCCCc1nc(C)c(CC(=O)OCC)c(=O)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2011.12.116
54558598 70517 0 None - 1 Rabbit 8.3 pIC50 = 8.3 Functional
Antagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challengeAntagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challenge
ChEMBL 499 10 1 7 3.8 CCCc1nc(C)c(CC(=O)N(CC)CC)c(=O)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2011.12.116
CHEMBL1951128 70517 0 None - 1 Rabbit 8.3 pIC50 = 8.3 Functional
Antagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challengeAntagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challenge
ChEMBL 499 10 1 7 3.8 CCCc1nc(C)c(CC(=O)N(CC)CC)c(=O)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2011.12.116
142534183 166705 0 None - 1 Human 8.3 pIC50 = 8.3 Functional
Antagonist activity at type-1 angiotensin 2 receptor (unknown origin) by calcium mobilizing assayAntagonist activity at type-1 angiotensin 2 receptor (unknown origin) by calcium mobilizing assay
ChEMBL 503 8 1 7 4.0 CCCc1nc(C)c(CC(=S)N(C)C)c(=O)n1Cc1ccc(-c2ccccc2-c2noc(=O)[nH]2)cc1 10.1016/j.bmcl.2018.08.036
CHEMBL4293170 166705 0 None - 1 Human 8.3 pIC50 = 8.3 Functional
Antagonist activity at type-1 angiotensin 2 receptor (unknown origin) by calcium mobilizing assayAntagonist activity at type-1 angiotensin 2 receptor (unknown origin) by calcium mobilizing assay
ChEMBL 503 8 1 7 4.0 CCCc1nc(C)c(CC(=S)N(C)C)c(=O)n1Cc1ccc(-c2ccccc2-c2noc(=O)[nH]2)cc1 10.1016/j.bmcl.2018.08.036
14956794 204348 0 None - 1 Rabbit 8.3 pIC50 = 8.3 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 479 9 1 7 4.9 CCCCc1nn(C(C)c2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL85545 204348 0 None - 1 Rabbit 8.3 pIC50 = 8.3 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 479 9 1 7 4.9 CCCCc1nn(C(C)c2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
1610 2305 89 None -2 9 Rabbit 7.4 pIC50 = 7.4 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00075a014
3941 2305 89 None -2 9 Rabbit 7.4 pIC50 = 7.4 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00075a014
3961 2305 89 None -2 9 Rabbit 7.4 pIC50 = 7.4 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00075a014
590 2305 89 None -2 9 Rabbit 7.4 pIC50 = 7.4 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00075a014
CHEMBL191 2305 89 None -2 9 Rabbit 7.4 pIC50 = 7.4 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00075a014
DB00678 2305 89 None -2 9 Rabbit 7.4 pIC50 = 7.4 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00075a014
5335625 108193 9 None - 1 Human 5.4 pIC50 = 5.4 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 293 3 1 3 3.2 O=C(N/N=C/c1ccccn1)c1ccc(Cl)c(Cl)c1 nan
CHEMBL3208035 108193 9 None - 1 Human 5.4 pIC50 = 5.4 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 293 3 1 3 3.2 O=C(N/N=C/c1ccccn1)c1ccc(Cl)c(Cl)c1 nan
46495021 107329 4 None 1 2 Human 5.4 pIC50 = 5.4 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 315 5 1 7 1.7 O=C(N/N=C/c1ccccn1)c1cc([N+](=O)[O-])cc([N+](=O)[O-])c1 nan
CHEMBL3192235 107329 4 None 1 2 Human 5.4 pIC50 = 5.4 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 315 5 1 7 1.7 O=C(N/N=C/c1ccccn1)c1cc([N+](=O)[O-])cc([N+](=O)[O-])c1 nan
14971636 114302 0 None - 1 Rabbit 7.4 pIC50 = 7.4 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 506 10 1 7 6.0 CCCCc1nc(-c2ccccc2)c(C(=O)OCC)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
CHEMBL334083 114302 0 None - 1 Rabbit 7.4 pIC50 = 7.4 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 506 10 1 7 6.0 CCCCc1nc(-c2ccccc2)c(C(=O)OCC)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
44292040 100653 0 None - 1 Bovine 6.4 pIC50 = 6.4 Functional
In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.
ChEMBL 601 9 1 9 6.9 CCCCc1nc2ccc(C3CC(c4cc(C)cs4)=NO3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80365-0
CHEMBL295279 100653 0 None - 1 Bovine 6.4 pIC50 = 6.4 Functional
In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.
ChEMBL 601 9 1 9 6.9 CCCCc1nc2ccc(C3CC(c4cc(C)cs4)=NO3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80365-0
5759185 38426 3 None -5 5 Human 5.4 pIC50 = 5.4 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 300 4 0 6 2.8 CC(C)(C)C(=O)/C(=C\c1cccc([N+](=O)[O-])c1)n1cncn1 nan
CHEMBL1465592 38426 3 None -5 5 Human 5.4 pIC50 = 5.4 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 300 4 0 6 2.8 CC(C)(C)C(=O)/C(=C\c1cccc([N+](=O)[O-])c1)n1cncn1 nan
5217512 42140 5 None -1 2 Human 5.4 pIC50 = 5.4 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 278 3 3 5 2.8 NNc1nc(-c2ccccc2)cc(-c2ccccc2O)n1 nan
CHEMBL1498886 42140 5 None -1 2 Human 5.4 pIC50 = 5.4 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 278 3 3 5 2.8 NNc1nc(-c2ccccc2)cc(-c2ccccc2O)n1 nan
10371403 66573 12 None - 1 Rabbit 5.4 pIC50 = 5.4 Functional
Vasorelaxing potency in the presence of eserin was determinedVasorelaxing potency in the presence of eserin was determined
ChEMBL 601 13 1 10 5.8 CCCCc1nc(Cl)c(COC(=O)c2cccc(CO[N+](=O)[O-])c2)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm049681p
CHEMBL186572 66573 12 None - 1 Rabbit 5.4 pIC50 = 5.4 Functional
Vasorelaxing potency in the presence of eserin was determinedVasorelaxing potency in the presence of eserin was determined
ChEMBL 601 13 1 10 5.8 CCCCc1nc(Cl)c(COC(=O)c2cccc(CO[N+](=O)[O-])c2)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm049681p
14956743 163542 0 None - 1 Rabbit 7.4 pIC50 = 7.4 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 496 9 1 9 4.2 CCCCc1nn(-c2cccc([N+](=O)[O-])c2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL420970 163542 0 None - 1 Rabbit 7.4 pIC50 = 7.4 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 496 9 1 9 4.2 CCCCc1nn(-c2cccc([N+](=O)[O-])c2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
56991879 70510 0 None - 1 Rabbit 7.4 pIC50 = 7.4 Functional
Antagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challengeAntagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challenge
ChEMBL 528 13 1 8 4.9 CCCCc1nc(CCC)c(CCC(=O)OCC)c(=O)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2011.12.116
CHEMBL1951121 70510 0 None - 1 Rabbit 7.4 pIC50 = 7.4 Functional
Antagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challengeAntagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challenge
ChEMBL 528 13 1 8 4.9 CCCCc1nc(CCC)c(CCC(=O)OCC)c(=O)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2011.12.116
9618012 77550 4 None - 1 Human 5.3 pIC50 = 5.3 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 289 3 1 3 3.4 C/C(=N\NC(=O)c1cccc2ccccc12)c1ccccn1 nan
CHEMBL2094484 77550 4 None - 1 Human 5.3 pIC50 = 5.3 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 289 3 1 3 3.4 C/C(=N\NC(=O)c1cccc2ccccc12)c1ccccn1 nan
1475345 29008 10 None -1 3 Human 5.3 pIC50 = 5.3 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 418 6 1 4 4.3 COc1ccc(NC(=O)/C(Cl)=C(/Cl)[S+]([O-])Cc2ccccc2Cl)cn1 nan
CHEMBL1382438 29008 10 None -1 3 Human 5.3 pIC50 = 5.3 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 418 6 1 4 4.3 COc1ccc(NC(=O)/C(Cl)=C(/Cl)[S+]([O-])Cc2ccccc2Cl)cn1 nan
18666499 175036 0 None - 1 Bovine 7.3 pIC50 = 7.3 Functional
In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.
ChEMBL 591 9 2 9 4.7 CCCCc1nc2ccc([C@]3(C(=O)O)C[C@H]4CCCN4O3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80365-0
CHEMBL45805 175036 0 None - 1 Bovine 7.3 pIC50 = 7.3 Functional
In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.
ChEMBL 591 9 2 9 4.7 CCCCc1nc2ccc([C@]3(C(=O)O)C[C@H]4CCCN4O3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80365-0
11743704 114986 0 None 3 2 Rabbit 5.3 pIC50 = 5.3 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 435 5 0 5 5.6 CCc1nc2c(C)cc(C)nc2n1Cc1ccc2c(c1)CCN2C(C#N)c1ccc(C)cc1 10.1021/jm00078a013
CHEMBL335179 114986 0 None 3 2 Rabbit 5.3 pIC50 = 5.3 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 435 5 0 5 5.6 CCc1nc2c(C)cc(C)nc2n1Cc1ccc2c(c1)CCN2C(C#N)c1ccc(C)cc1 10.1021/jm00078a013
44292038 181943 0 None - 1 Bovine 7.3 pIC50 = 7.3 Functional
In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.
ChEMBL 575 8 1 8 6.0 CCCCc1nc2ccc([C@]3(C)C[C@H]4CCCCN4O3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80365-0
CHEMBL47873 181943 0 None - 1 Bovine 7.3 pIC50 = 7.3 Functional
In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.
ChEMBL 575 8 1 8 6.0 CCCCc1nc2ccc([C@]3(C)C[C@H]4CCCCN4O3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80365-0
5218417 24595 6 None - 1 Human 5.3 pIC50 = 5.3 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 285 3 0 2 3.9 CC1CCCN(CC(=O)c2ccc(Cl)c(Cl)c2)C1 nan
CHEMBL1344824 24595 6 None - 1 Human 5.3 pIC50 = 5.3 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 285 3 0 2 3.9 CC1CCCN(CC(=O)c2ccc(Cl)c(Cl)c2)C1 nan
10411653 24205 0 None 208 2 Rabbit 7.3 pIC50 = 7.3 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 454 5 1 5 4.6 CCc1nc2c(C)cc(C)nc2n1Cc1ccc2c(c1)CCN2C(=O)c1ccccc1C(=O)O 10.1021/jm00078a013
CHEMBL134151 24205 0 None 208 2 Rabbit 7.3 pIC50 = 7.3 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 454 5 1 5 4.6 CCc1nc2c(C)cc(C)nc2n1Cc1ccc2c(c1)CCN2C(=O)c1ccccc1C(=O)O 10.1021/jm00078a013
14956799 106403 0 None - 1 Rabbit 6.3 pIC50 = 6.3 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 509 10 2 8 4.0 CCCCc1nn(Cc2ccccc2C(=O)O)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL314590 106403 0 None - 1 Rabbit 6.3 pIC50 = 6.3 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 509 10 2 8 4.0 CCCCc1nn(Cc2ccccc2C(=O)O)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
6873617 72057 5 None -3 2 Human 5.3 pIC50 = 5.3 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 386 4 1 4 4.7 O=C(N/N=C/c1ccccn1)c1cc(-c2ccc(Cl)cc2)nc2ccccc12 nan
CHEMBL1987579 72057 5 None -3 2 Human 5.3 pIC50 = 5.3 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 386 4 1 4 4.7 O=C(N/N=C/c1ccccn1)c1cc(-c2ccc(Cl)cc2)nc2ccccc12 nan
10367704 22128 0 None 25 2 Rabbit 8.3 pIC50 = 8.3 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 476 5 1 8 4.5 CCc1nc2c(C)cc(C)nc2n1Cc1ccc2c(ccn2C(=O)c2ccccc2-c2nn[nH]n2)c1 10.1021/jm00078a013
CHEMBL132408 22128 0 None 25 2 Rabbit 8.3 pIC50 = 8.3 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 476 5 1 8 4.5 CCc1nc2c(C)cc(C)nc2n1Cc1ccc2c(ccn2C(=O)c2ccccc2-c2nn[nH]n2)c1 10.1021/jm00078a013
131654 204667 10 None 1 2 Rabbit 8.3 pIC50 = 8.3 Functional
In vitro antagonistic activity for AT1 receptor by displacing 125I[Sar, ILe8]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for AT1 receptor by displacing 125I[Sar, ILe8]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 431 10 1 7 4.1 CCCCc1nn(CCCC)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL87778 204667 10 None 1 2 Rabbit 8.3 pIC50 = 8.3 Functional
In vitro antagonistic activity for AT1 receptor by displacing 125I[Sar, ILe8]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for AT1 receptor by displacing 125I[Sar, ILe8]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 431 10 1 7 4.1 CCCCc1nn(CCCC)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
14956748 204246 0 None - 1 Rabbit 8.3 pIC50 = 8.3 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 481 9 1 8 4.3 CCCCc1nn(-c2ccc(OC)cc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL84627 204246 0 None - 1 Rabbit 8.3 pIC50 = 8.3 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 481 9 1 8 4.3 CCCCc1nn(-c2ccc(OC)cc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
9887844 162637 1 None - 1 Guinea pig 8.3 pIC50 = 8.3 Functional
In vitro antagonistic potency against Angiotensin II receptor, type 1 in guinea pig adrenal membraneIn vitro antagonistic potency against Angiotensin II receptor, type 1 in guinea pig adrenal membrane
ChEMBL 411 6 1 5 4.9 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2c(n1)CCCC2 10.1021/jm9504722
CHEMBL418226 162637 1 None - 1 Guinea pig 8.3 pIC50 = 8.3 Functional
In vitro antagonistic potency against Angiotensin II receptor, type 1 in guinea pig adrenal membraneIn vitro antagonistic potency against Angiotensin II receptor, type 1 in guinea pig adrenal membrane
ChEMBL 411 6 1 5 4.9 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2c(n1)CCCC2 10.1021/jm9504722
54393565 70528 0 None - 1 Rabbit 8.3 pIC50 = 8.3 Functional
Antagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challengeAntagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challenge
ChEMBL 541 10 1 8 3.6 CCCCc1nc(C)c(CCC(=O)N2CCOCC2)c(=O)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2011.12.116
CHEMBL1951139 70528 0 None - 1 Rabbit 8.3 pIC50 = 8.3 Functional
Antagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challengeAntagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challenge
ChEMBL 541 10 1 8 3.6 CCCCc1nc(C)c(CCC(=O)N2CCOCC2)c(=O)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2011.12.116
10004112 25311 0 None 93 2 Rabbit 8.3 pIC50 = 8.3 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 454 9 1 5 5.5 C=CCN(c1ccc(Cn2c(CC)nc3c(C)cc(C)nc32)cc1)C(C(=O)O)c1ccccc1 10.1021/jm00078a014
CHEMBL135089 25311 0 None 93 2 Rabbit 8.3 pIC50 = 8.3 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 454 9 1 5 5.5 C=CCN(c1ccc(Cn2c(CC)nc3c(C)cc(C)nc32)cc1)C(C(=O)O)c1ccccc1 10.1021/jm00078a014
10344052 116094 0 None 107 2 Rabbit 8.3 pIC50 = 8.3 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 456 9 1 5 5.7 CCCN(c1ccc(Cn2c(CC)nc3c(C)cc(C)nc32)cc1)C(C(=O)O)c1ccccc1 10.1021/jm00078a014
CHEMBL336738 116094 0 None 107 2 Rabbit 8.3 pIC50 = 8.3 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 456 9 1 5 5.7 CCCN(c1ccc(Cn2c(CC)nc3c(C)cc(C)nc32)cc1)C(C(=O)O)c1ccccc1 10.1021/jm00078a014
142534191 166219 0 None - 1 Human 8.3 pIC50 = 8.3 Functional
Antagonist activity at type-1 angiotensin 2 receptor (unknown origin) by calcium mobilizing assayAntagonist activity at type-1 angiotensin 2 receptor (unknown origin) by calcium mobilizing assay
ChEMBL 559 9 1 8 4.2 CCCCc1nc(C)c(CC(=S)N2CCOCC2)c(=O)n1Cc1ccc(-c2ccccc2-c2noc(=O)[nH]2)cc1 10.1016/j.bmcl.2018.08.036
CHEMBL4284022 166219 0 None - 1 Human 8.3 pIC50 = 8.3 Functional
Antagonist activity at type-1 angiotensin 2 receptor (unknown origin) by calcium mobilizing assayAntagonist activity at type-1 angiotensin 2 receptor (unknown origin) by calcium mobilizing assay
ChEMBL 559 9 1 8 4.2 CCCCc1nc(C)c(CC(=S)N2CCOCC2)c(=O)n1Cc1ccc(-c2ccccc2-c2noc(=O)[nH]2)cc1 10.1016/j.bmcl.2018.08.036
14956758 106036 0 None - 1 Rabbit 8.3 pIC50 = 8.3 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 509 9 1 9 4.1 CCCCc1nn(-c2ccccc2C(=O)OC)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL314042 106036 0 None - 1 Rabbit 8.3 pIC50 = 8.3 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 509 9 1 9 4.1 CCCCc1nn(-c2ccccc2C(=O)OC)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
14956769 106619 0 None - 1 Rabbit 8.2 pIC50 = 8.2 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 499 9 1 7 5.3 CCCCCc1nn(-c2ccccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL316052 106619 0 None - 1 Rabbit 8.2 pIC50 = 8.2 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 499 9 1 7 5.3 CCCCCc1nn(-c2ccccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
14956762 98361 0 None - 1 Rabbit 8.2 pIC50 = 8.2 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 519 8 1 7 5.6 CCCCc1nn(-c2c(Cl)cccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL278741 98361 0 None - 1 Rabbit 8.2 pIC50 = 8.2 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 519 8 1 7 5.6 CCCCc1nn(-c2c(Cl)cccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
54479908 70530 0 None - 1 Rabbit 8.2 pIC50 = 8.2 Functional
Antagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challengeAntagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challenge
ChEMBL 525 10 1 7 4.3 CCCCc1nc(C)c(CCC(=O)N2CCCC2)c(=O)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2011.12.116
CHEMBL1951140 70530 0 None - 1 Rabbit 8.2 pIC50 = 8.2 Functional
Antagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challengeAntagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challenge
ChEMBL 525 10 1 7 4.3 CCCCc1nc(C)c(CCC(=O)N2CCCC2)c(=O)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2011.12.116
14956759 204372 0 None - 1 Rabbit 7.3 pIC50 = 7.3 Functional
In vitro antagonistic activity for AT1 receptor by displacing 125I[Sar, ILe8]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for AT1 receptor by displacing 125I[Sar, ILe8]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 495 9 2 8 4.0 CCCCc1nn(-c2ccccc2C(=O)O)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL85704 204372 0 None - 1 Rabbit 7.3 pIC50 = 7.3 Functional
In vitro antagonistic activity for AT1 receptor by displacing 125I[Sar, ILe8]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for AT1 receptor by displacing 125I[Sar, ILe8]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 495 9 2 8 4.0 CCCCc1nn(-c2ccccc2C(=O)O)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
14956800 204420 0 None - 1 Rabbit 7.3 pIC50 = 7.3 Functional
In vitro antagonistic activity for AT1 receptor by displacing 125I[Sar, ILe8]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for AT1 receptor by displacing 125I[Sar, ILe8]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 509 10 2 8 4.0 CCCCc1nn(C(C(=O)O)c2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL86143 204420 0 None - 1 Rabbit 7.3 pIC50 = 7.3 Functional
In vitro antagonistic activity for AT1 receptor by displacing 125I[Sar, ILe8]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for AT1 receptor by displacing 125I[Sar, ILe8]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 509 10 2 8 4.0 CCCCc1nn(C(C(=O)O)c2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
1610 2305 89 None -2 9 Rabbit 7.3 pIC50 = 7.3 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00069a015
3941 2305 89 None -2 9 Rabbit 7.3 pIC50 = 7.3 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00069a015
3961 2305 89 None -2 9 Rabbit 7.3 pIC50 = 7.3 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00069a015
590 2305 89 None -2 9 Rabbit 7.3 pIC50 = 7.3 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00069a015
CHEMBL191 2305 89 None -2 9 Rabbit 7.3 pIC50 = 7.3 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00069a015
DB00678 2305 89 None -2 9 Rabbit 7.3 pIC50 = 7.3 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00069a015
14956805 204611 0 None - 1 Rabbit 7.3 pIC50 = 7.3 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 515 10 1 8 5.0 CCCCc1nn(COc2ccc(Cl)cc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL87354 204611 0 None - 1 Rabbit 7.3 pIC50 = 7.3 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 515 10 1 8 5.0 CCCCc1nn(COc2ccc(Cl)cc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
9893748 181932 0 None - 1 Bovine 6.3 pIC50 = 6.3 Functional
In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.
ChEMBL 549 9 2 9 4.5 CCCCc1nc2ccc(C3CC(C(=O)O)=NO3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80365-0
CHEMBL47872 181932 0 None - 1 Bovine 6.3 pIC50 = 6.3 Functional
In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.
ChEMBL 549 9 2 9 4.5 CCCCc1nc2ccc(C3CC(C(=O)O)=NO3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80365-0
742856 53472 21 None - 1 Human 5.3 pIC50 = 5.3 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 279 4 1 2 4.3 O=C(CNc1cccc(Cl)c1)c1ccc(Cl)cc1 nan
CHEMBL1603871 53472 21 None - 1 Human 5.3 pIC50 = 5.3 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 279 4 1 2 4.3 O=C(CNc1cccc(Cl)c1)c1ccc(Cl)cc1 nan
14956789 204703 0 None - 1 Rabbit 7.3 pIC50 = 7.3 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 489 10 1 9 3.7 CCCCc1nn(C(C(=O)OC)C(C)C)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL88002 204703 0 None - 1 Rabbit 7.3 pIC50 = 7.3 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 489 10 1 9 3.7 CCCCc1nn(C(C(=O)OC)C(C)C)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
2811329 28425 5 None - 1 Human 5.3 pIC50 = 5.3 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 279 3 2 4 3.0 Cc1ccc(NNC(=O)c2c(C)noc2C)cc1Cl nan
CHEMBL1377329 28425 5 None - 1 Human 5.3 pIC50 = 5.3 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 279 3 2 4 3.0 Cc1ccc(NNC(=O)c2c(C)noc2C)cc1Cl nan
4328866 19278 3 None - 1 Human 5.3 pIC50 = 5.3 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 247 3 0 4 1.2 CC(C)OC(=O)CN1C(=O)C(=O)c2ccccc21 nan
CHEMBL1299266 19278 3 None - 1 Human 5.3 pIC50 = 5.3 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 247 3 0 4 1.2 CC(C)OC(=O)CN1C(=O)C(=O)c2ccccc21 nan
5770964 26236 2 None 1 2 Human 5.3 pIC50 = 5.3 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 444 9 2 6 2.6 COc1ccc(C(=O)/C=C/C(=O)N(CC(=O)NC2CCCCC2)CC2CCCO2)c(O)c1 nan
CHEMBL1359902 26236 2 None 1 2 Human 5.3 pIC50 = 5.3 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 444 9 2 6 2.6 COc1ccc(C(=O)/C=C/C(=O)N(CC(=O)NC2CCCCC2)CC2CCCO2)c(O)c1 nan
2744279 26439 3 None - 1 Human 5.3 pIC50 = 5.3 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 351 5 0 10 2.5 CCn1nc(C)cc1-c1nnc(Sc2ncc([N+](=O)[O-])s2)n1C nan
CHEMBL1361740 26439 3 None - 1 Human 5.3 pIC50 = 5.3 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 351 5 0 10 2.5 CCn1nc(C)cc1-c1nnc(Sc2ncc([N+](=O)[O-])s2)n1C nan
4068403 20507 11 None - 1 Human 5.3 pIC50 = 5.3 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 360 4 1 6 4.0 O=C(Nc1nc(-c2ccccn2)cs1)c1cc(Cl)ccc1[N+](=O)[O-] nan
CHEMBL1309127 20507 11 None - 1 Human 5.3 pIC50 = 5.3 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 360 4 1 6 4.0 O=C(Nc1nc(-c2ccccn2)cs1)c1cc(Cl)ccc1[N+](=O)[O-] nan
1610 2305 89 None -2 9 Rabbit 7.3 pIC50 = 7.3 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00078a013
1610 2305 89 None -2 9 Rabbit 7.3 pIC50 = 7.3 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00078a014
3941 2305 89 None -2 9 Rabbit 7.3 pIC50 = 7.3 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00078a013
3941 2305 89 None -2 9 Rabbit 7.3 pIC50 = 7.3 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00078a014
3961 2305 89 None -2 9 Rabbit 7.3 pIC50 = 7.3 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00078a013
3961 2305 89 None -2 9 Rabbit 7.3 pIC50 = 7.3 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00078a014
590 2305 89 None -2 9 Rabbit 7.3 pIC50 = 7.3 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00078a013
590 2305 89 None -2 9 Rabbit 7.3 pIC50 = 7.3 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00078a014
CHEMBL191 2305 89 None -2 9 Rabbit 7.3 pIC50 = 7.3 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00078a013
CHEMBL191 2305 89 None -2 9 Rabbit 7.3 pIC50 = 7.3 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00078a014
DB00678 2305 89 None -2 9 Rabbit 7.3 pIC50 = 7.3 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00078a013
DB00678 2305 89 None -2 9 Rabbit 7.3 pIC50 = 7.3 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00078a014
788411 27148 13 None - 1 Human 5.3 pIC50 = 5.3 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 273 4 1 2 4.3 Cc1ccc(C(=O)CNc2ccc(C)c(Cl)c2)cc1 nan
CHEMBL1367827 27148 13 None - 1 Human 5.3 pIC50 = 5.3 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 273 4 1 2 4.3 Cc1ccc(C(=O)CNc2ccc(C)c(Cl)c2)cc1 nan
14971674 205559 0 None - 1 Rabbit 7.3 pIC50 = 7.3 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 540 10 1 7 6.5 CCCCc1nn(-c2cccc(Cl)c2)c(C(=O)OCC)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
CHEMBL93289 205559 0 None - 1 Rabbit 7.3 pIC50 = 7.3 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 540 10 1 7 6.5 CCCCc1nn(-c2cccc(Cl)c2)c(C(=O)OCC)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
15233933 100683 0 None - 1 Bovine 7.3 pIC50 = 7.3 Functional
In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.
ChEMBL 561 8 1 8 5.6 CCCCc1nc2ccc([C@@]3(C)C[C@H]4CCCN4O3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80365-0
CHEMBL295532 100683 0 None - 1 Bovine 7.3 pIC50 = 7.3 Functional
In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.
ChEMBL 561 8 1 8 5.6 CCCCc1nc2ccc([C@@]3(C)C[C@H]4CCCN4O3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80365-0
14971693 112399 0 None - 1 Rabbit 7.3 pIC50 = 7.3 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 560 9 1 7 6.5 CCCc1nn(-c2ccccc2C(F)(F)F)c(C(=O)OCC)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
CHEMBL331063 112399 0 None - 1 Rabbit 7.3 pIC50 = 7.3 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 560 9 1 7 6.5 CCCc1nn(-c2ccccc2C(F)(F)F)c(C(=O)OCC)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
18655851 100818 0 None - 1 Bovine 7.3 pIC50 = 7.3 Functional
In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.
ChEMBL 623 9 1 8 6.7 CCCCc1nc2ccc([C@]3(c4ccccc4)C[C@H]4CCCN4O3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80365-0
CHEMBL296519 100818 0 None - 1 Bovine 7.3 pIC50 = 7.3 Functional
In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.
ChEMBL 623 9 1 8 6.7 CCCCc1nc2ccc([C@]3(c4ccccc4)C[C@H]4CCCN4O3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80365-0
100520 32491 5 None -4 4 Human 5.3 pIC50 = 5.3 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 240 3 0 7 2.0 O=[N+]([O-])c1cnc(Sc2ccncn2)s1 nan
CHEMBL1413680 32491 5 None -4 4 Human 5.3 pIC50 = 5.3 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 240 3 0 7 2.0 O=[N+]([O-])c1cnc(Sc2ccncn2)s1 nan
788410 20952 14 None - 1 Human 5.2 pIC50 = 5.2 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 259 4 1 2 3.9 Cc1ccc(NCC(=O)c2ccccc2)cc1Cl nan
CHEMBL1312651 20952 14 None - 1 Human 5.2 pIC50 = 5.2 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 259 4 1 2 3.9 Cc1ccc(NCC(=O)c2ccccc2)cc1Cl nan
44292072 100817 0 None - 1 Bovine 7.2 pIC50 = 7.2 Functional
In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.
ChEMBL 618 9 1 9 4.7 CCCCc1nc2ccc([C@]3(C(=O)N(C)C)C[C@H]4CCCN4O3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80365-0
CHEMBL296518 100817 0 None - 1 Bovine 7.2 pIC50 = 7.2 Functional
In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.
ChEMBL 618 9 1 9 4.7 CCCCc1nc2ccc([C@]3(C(=O)N(C)C)C[C@H]4CCCN4O3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80365-0
14956773 204365 0 None - 1 Rabbit 6.2 pIC50 = 6.2 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 504 9 2 6 5.0 CCCCc1nn(-c2ccccc2Cl)c(=O)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00069a015
CHEMBL85659 204365 0 None - 1 Rabbit 6.2 pIC50 = 6.2 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 504 9 2 6 5.0 CCCCc1nn(-c2ccccc2Cl)c(=O)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00069a015
44292162 171715 0 None - 1 Bovine 7.2 pIC50 = 7.2 Functional
In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.
ChEMBL 575 9 1 8 6.0 CCCCc1nc2ccc([C@@]3(CC)C[C@H]4CCCN4O3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80365-0
CHEMBL44749 171715 0 None - 1 Bovine 7.2 pIC50 = 7.2 Functional
In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.
ChEMBL 575 9 1 8 6.0 CCCCc1nc2ccc([C@@]3(CC)C[C@H]4CCCN4O3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80365-0
16446380 31392 9 None - 1 Human 5.2 pIC50 = 5.2 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 447 7 1 7 3.4 COc1ccc(OC)c(NC(=O)c2nc(S(=O)(=O)Cc3ccccc3)ncc2Cl)c1 nan
CHEMBL1404578 31392 9 None - 1 Human 5.2 pIC50 = 5.2 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 447 7 1 7 3.4 COc1ccc(OC)c(NC(=O)c2nc(S(=O)(=O)Cc3ccccc3)ncc2Cl)c1 nan
718402 33651 15 None - 1 Human 5.2 pIC50 = 5.2 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 300 5 0 6 2.6 COc1cc(/C=C/[N+](=O)[O-])ccc1OC(=O)c1cccnc1 nan
CHEMBL1423567 33651 15 None - 1 Human 5.2 pIC50 = 5.2 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 300 5 0 6 2.6 COc1cc(/C=C/[N+](=O)[O-])ccc1OC(=O)c1cccnc1 nan
16437205 31772 9 None -5 3 Human 5.2 pIC50 = 5.2 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 486 6 1 7 2.7 CCC1CCCCN1S(=O)(=O)c1ccc(NC(=O)c2nc(S(C)(=O)=O)ncc2Cl)cc1 nan
CHEMBL1407961 31772 9 None -5 3 Human 5.2 pIC50 = 5.2 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 486 6 1 7 2.7 CCC1CCCCN1S(=O)(=O)c1ccc(NC(=O)c2nc(S(C)(=O)=O)ncc2Cl)cc1 nan
6873485 107079 8 None 1 2 Human 5.2 pIC50 = 5.2 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 410 7 1 5 4.9 CCCOc1cccc(-c2cc(C(=O)N/N=C/c3ccccn3)c3ccccc3n2)c1 nan
CHEMBL3189289 107079 8 None 1 2 Human 5.2 pIC50 = 5.2 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 410 7 1 5 4.9 CCCOc1cccc(-c2cc(C(=O)N/N=C/c3ccccn3)c3ccccc3n2)c1 nan
9569064 71891 2 None - 1 Human 5.2 pIC50 = 5.2 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 363 6 1 4 4.0 C/C(=N\NC(=O)c1ccccc1OCc1ccc(F)cc1)c1ccccn1 nan
CHEMBL1981898 71891 2 None - 1 Human 5.2 pIC50 = 5.2 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 363 6 1 4 4.0 C/C(=N\NC(=O)c1ccccc1OCc1ccc(F)cc1)c1ccccn1 nan
1481 2027 109 None -6 4 Human 8.2 pIC50 = 8.2 Functional
Antagonist activity at human AT1 overexpressed in CHO-K1 cells in presence of 10 nM [Val5-angiotensin II measured after 90 mins by HTRF based IP-one assayAntagonist activity at human AT1 overexpressed in CHO-K1 cells in presence of 10 nM [Val5-angiotensin II measured after 90 mins by HTRF based IP-one assay
ChEMBL 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 10.1021/acsmedchemlett.1c00240
3749 2027 109 None -6 4 Human 8.2 pIC50 = 8.2 Functional
Antagonist activity at human AT1 overexpressed in CHO-K1 cells in presence of 10 nM [Val5-angiotensin II measured after 90 mins by HTRF based IP-one assayAntagonist activity at human AT1 overexpressed in CHO-K1 cells in presence of 10 nM [Val5-angiotensin II measured after 90 mins by HTRF based IP-one assay
ChEMBL 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 10.1021/acsmedchemlett.1c00240
589 2027 109 None -6 4 Human 8.2 pIC50 = 8.2 Functional
Antagonist activity at human AT1 overexpressed in CHO-K1 cells in presence of 10 nM [Val5-angiotensin II measured after 90 mins by HTRF based IP-one assayAntagonist activity at human AT1 overexpressed in CHO-K1 cells in presence of 10 nM [Val5-angiotensin II measured after 90 mins by HTRF based IP-one assay
ChEMBL 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 10.1021/acsmedchemlett.1c00240
6908 2027 109 None -6 4 Human 8.2 pIC50 = 8.2 Functional
Antagonist activity at human AT1 overexpressed in CHO-K1 cells in presence of 10 nM [Val5-angiotensin II measured after 90 mins by HTRF based IP-one assayAntagonist activity at human AT1 overexpressed in CHO-K1 cells in presence of 10 nM [Val5-angiotensin II measured after 90 mins by HTRF based IP-one assay
ChEMBL 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 10.1021/acsmedchemlett.1c00240
CHEMBL1513 2027 109 None -6 4 Human 8.2 pIC50 = 8.2 Functional
Antagonist activity at human AT1 overexpressed in CHO-K1 cells in presence of 10 nM [Val5-angiotensin II measured after 90 mins by HTRF based IP-one assayAntagonist activity at human AT1 overexpressed in CHO-K1 cells in presence of 10 nM [Val5-angiotensin II measured after 90 mins by HTRF based IP-one assay
ChEMBL 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 10.1021/acsmedchemlett.1c00240
DB01029 2027 109 None -6 4 Human 8.2 pIC50 = 8.2 Functional
Antagonist activity at human AT1 overexpressed in CHO-K1 cells in presence of 10 nM [Val5-angiotensin II measured after 90 mins by HTRF based IP-one assayAntagonist activity at human AT1 overexpressed in CHO-K1 cells in presence of 10 nM [Val5-angiotensin II measured after 90 mins by HTRF based IP-one assay
ChEMBL 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 10.1021/acsmedchemlett.1c00240
108185 1578 71 None -3 5 Rabbit 8.2 pIC50 = 8.2 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 436 8 2 6 4.5 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)C(=O)O)Cl 10.1021/jm00069a015
586 1578 71 None -3 5 Rabbit 8.2 pIC50 = 8.2 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 436 8 2 6 4.5 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)C(=O)O)Cl 10.1021/jm00069a015
CHEMBL907 1578 71 None -3 5 Rabbit 8.2 pIC50 = 8.2 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 436 8 2 6 4.5 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)C(=O)O)Cl 10.1021/jm00069a015
57393229 70535 0 None - 1 Rabbit 8.2 pIC50 = 8.2 Functional
Antagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challengeAntagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challenge
ChEMBL 555 9 1 7 5.5 CCCCc1nc(C)c(CC(=S)N2CCCCCC2)c(=O)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2011.12.116
CHEMBL1951145 70535 0 None - 1 Rabbit 8.2 pIC50 = 8.2 Functional
Antagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challengeAntagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challenge
ChEMBL 555 9 1 7 5.5 CCCCc1nc(C)c(CC(=S)N2CCCCCC2)c(=O)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2011.12.116
14956740 204084 0 None - 1 Rabbit 8.2 pIC50 = 8.2 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 481 9 1 8 4.3 CCCCc1nn(-c2ccccc2OC)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL83248 204084 0 None - 1 Rabbit 8.2 pIC50 = 8.2 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 481 9 1 8 4.3 CCCCc1nn(-c2ccccc2OC)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
14971677 111010 0 None - 1 Rabbit 8.2 pIC50 = 8.2 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 574 10 1 7 7.1 CCCCc1nn(-c2ccc(Cl)cc2Cl)c(C(=O)OCC)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
CHEMBL327837 111010 0 None - 1 Rabbit 8.2 pIC50 = 8.2 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 574 10 1 7 7.1 CCCCc1nn(-c2ccc(Cl)cc2Cl)c(C(=O)OCC)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
14956775 202274 0 None -1 2 Rabbit 7.2 pIC50 = 7.2 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 375 7 2 7 3.2 CCCCc1nnc(O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL69508 202274 0 None -1 2 Rabbit 7.2 pIC50 = 7.2 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 375 7 2 7 3.2 CCCCc1nnc(O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
14956808 204695 0 None - 1 Rabbit 7.2 pIC50 = 7.2 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 580 13 1 9 4.9 CCCCc1nn(CCCN(C)C(=O)OCc2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL87957 204695 0 None - 1 Rabbit 7.2 pIC50 = 7.2 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 580 13 1 9 4.9 CCCCc1nn(CCCN(C)C(=O)OCc2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
330973 49406 3 None -16 4 Human 5.2 pIC50 = 5.2 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 592 4 0 10 3.0 C=C1C(=O)O[C@@H]2C[C@@H](C)[C@@H]3C=CC(=O)[C@@]3(C)[C@@H](OC(=O)CC(=O)O[C@H]3[C@@H]4C(=C)C(=O)O[C@@H]4C[C@@H](C)[C@@H]4C=CC(=O)[C@@]34C)[C@H]12 nan
CHEMBL1566610 49406 3 None -16 4 Human 5.2 pIC50 = 5.2 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 592 4 0 10 3.0 C=C1C(=O)O[C@@H]2C[C@@H](C)[C@@H]3C=CC(=O)[C@@]3(C)[C@@H](OC(=O)CC(=O)O[C@H]3[C@@H]4C(=C)C(=O)O[C@@H]4C[C@@H](C)[C@@H]4C=CC(=O)[C@@]34C)[C@H]12 nan
2812572 24805 5 None - 1 Human 5.2 pIC50 = 5.2 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 274 4 2 2 3.7 CCc1ccc(C(=O)NNc2ccc(Cl)cc2)cc1 nan
CHEMBL1346661 24805 5 None - 1 Human 5.2 pIC50 = 5.2 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 274 4 2 2 3.7 CCc1ccc(C(=O)NNc2ccc(Cl)cc2)cc1 nan
890649 53333 14 None 1 2 Human 5.2 pIC50 = 5.2 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 342 3 0 6 3.6 O=S1(=O)C=C(Sc2nnc(-c3ccccc3)o2)c2ccccc21 nan
CHEMBL1602759 53333 14 None 1 2 Human 5.2 pIC50 = 5.2 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 342 3 0 6 3.6 O=S1(=O)C=C(Sc2nnc(-c3ccccc3)o2)c2ccccc21 nan
44292456 100680 0 None - 1 Bovine 7.2 pIC50 = 7.2 Functional
In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.
ChEMBL 658 9 1 9 5.6 CCCCc1nc2ccc(C3(C(=O)N4CCCCC4)C[C@H]4CCCN4O3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80365-0
CHEMBL295514 100680 0 None - 1 Bovine 7.2 pIC50 = 7.2 Functional
In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.
ChEMBL 658 9 1 9 5.6 CCCCc1nc2ccc(C3(C(=O)N4CCCCC4)C[C@H]4CCCN4O3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80365-0
1610 2305 89 None -2 9 Rabbit 7.2 pIC50 = 7.2 Functional
Antagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challengeAntagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challenge
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmcl.2011.12.116
3941 2305 89 None -2 9 Rabbit 7.2 pIC50 = 7.2 Functional
Antagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challengeAntagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challenge
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmcl.2011.12.116
3961 2305 89 None -2 9 Rabbit 7.2 pIC50 = 7.2 Functional
Antagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challengeAntagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challenge
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmcl.2011.12.116
590 2305 89 None -2 9 Rabbit 7.2 pIC50 = 7.2 Functional
Antagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challengeAntagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challenge
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmcl.2011.12.116
CHEMBL191 2305 89 None -2 9 Rabbit 7.2 pIC50 = 7.2 Functional
Antagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challengeAntagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challenge
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmcl.2011.12.116
DB00678 2305 89 None -2 9 Rabbit 7.2 pIC50 = 7.2 Functional
Antagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challengeAntagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challenge
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmcl.2011.12.116
16436607 23846 10 None - 1 Human 5.2 pIC50 = 5.2 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 486 6 1 7 2.6 CCS(=O)(=O)c1ncc(Cl)c(C(=O)Nc2ccc(S(=O)(=O)N3CCC(C)CC3)cc2)n1 nan
CHEMBL1338304 23846 10 None - 1 Human 5.2 pIC50 = 5.2 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 486 6 1 7 2.6 CCS(=O)(=O)c1ncc(Cl)c(C(=O)Nc2ccc(S(=O)(=O)N3CCC(C)CC3)cc2)n1 nan
9619214 107578 6 None -2 3 Human 5.2 pIC50 = 5.2 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 351 5 1 8 2.9 Cc1cc(N/N=C/c2ccccc2[N+](=O)[O-])nc(-n2nc(C)cc2C)n1 nan
CHEMBL3195226 107578 6 None -2 3 Human 5.2 pIC50 = 5.2 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 351 5 1 8 2.9 Cc1cc(N/N=C/c2ccccc2[N+](=O)[O-])nc(-n2nc(C)cc2C)n1 nan
11744592 114991 0 None 33 2 Rabbit 6.2 pIC50 = 6.2 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 452 6 0 6 5.4 CCc1nc2c(C)cc(C)nc2n1Cc1ccc2c(ccn2Cc2ccccc2C(=O)OC)c1 10.1021/jm00078a013
CHEMBL335228 114991 0 None 33 2 Rabbit 6.2 pIC50 = 6.2 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 452 6 0 6 5.4 CCc1nc2c(C)cc(C)nc2n1Cc1ccc2c(ccn2Cc2ccccc2C(=O)OC)c1 10.1021/jm00078a013
6091989 49567 8 None - 1 Human 5.2 pIC50 = 5.2 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 337 5 1 5 4.1 COc1cc(/C=C/c2ccc3cccc(O)c3n2)cc(OC)c1OC nan
CHEMBL1567899 49567 8 None - 1 Human 5.2 pIC50 = 5.2 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 337 5 1 5 4.1 COc1cc(/C=C/c2ccc3cccc(O)c3n2)cc(OC)c1OC nan
44292070 171278 0 None - 1 Bovine 7.2 pIC50 = 7.2 Functional
In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.
ChEMBL 589 8 1 8 6.4 CCCCc1nc2ccc([C@]3(C)C[C@H]4CCC(C)(C)N4O3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80365-0
CHEMBL44690 171278 0 None - 1 Bovine 7.2 pIC50 = 7.2 Functional
In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.
ChEMBL 589 8 1 8 6.4 CCCCc1nc2ccc([C@]3(C)C[C@H]4CCC(C)(C)N4O3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80365-0
44292342 176675 0 None - 1 Bovine 7.2 pIC50 = 7.2 Functional
In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.
ChEMBL 575 8 1 8 6.3 CCCCc1nc2ccc([C@@H]3C[C@@]4(C)CCCCN4O3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80365-0
CHEMBL46361 176675 0 None - 1 Bovine 7.2 pIC50 = 7.2 Functional
In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.
ChEMBL 575 8 1 8 6.3 CCCCc1nc2ccc([C@@H]3C[C@@]4(C)CCCCN4O3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80365-0
6883924 71332 8 None 1 2 Human 5.2 pIC50 = 5.2 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 315 3 1 4 3.7 O=C(N/N=C/c1ccccn1)c1sc2ccccc2c1Cl nan
CHEMBL1964873 71332 8 None 1 2 Human 5.2 pIC50 = 5.2 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 315 3 1 4 3.7 O=C(N/N=C/c1ccccn1)c1sc2ccccc2c1Cl nan
10366811 24607 0 None 31 2 Rabbit 7.2 pIC50 = 7.2 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 456 8 1 5 5.6 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(N(CC)C(C(=O)O)c2cccc(C)c2)cc1 10.1021/jm00078a014
CHEMBL134491 24607 0 None 31 2 Rabbit 7.2 pIC50 = 7.2 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 456 8 1 5 5.6 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(N(CC)C(C(=O)O)c2cccc(C)c2)cc1 10.1021/jm00078a014
3117 206096 100 None -18 20 Human 5.2 pIC50 = 5.2 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 296 4 0 4 3.6 CCN(CC)C(=S)SSC(=S)N(CC)CC nan
CHEMBL964 206096 100 None -18 20 Human 5.2 pIC50 = 5.2 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 296 4 0 4 3.6 CCN(CC)C(=S)SSC(=S)N(CC)CC nan
780062 28719 7 None - 1 Human 5.2 pIC50 = 5.2 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 276 3 2 4 3.4 Cc1ccc(-c2cc(-c3ccccc3)nc(NN)n2)cc1 nan
CHEMBL1380035 28719 7 None - 1 Human 5.2 pIC50 = 5.2 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 276 3 2 4 3.4 Cc1ccc(-c2cc(-c3ccccc3)nc(NN)n2)cc1 nan
10048602 25830 0 None 37 2 Rabbit 6.2 pIC50 = 6.2 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 435 4 0 5 4.7 CCc1nc2c(C)cc(C)nc2n1Cc1ccc2c(c1)CCN2C(=O)c1ccccc1C#N 10.1021/jm00078a013
CHEMBL135522 25830 0 None 37 2 Rabbit 6.2 pIC50 = 6.2 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 435 4 0 5 4.7 CCc1nc2c(C)cc(C)nc2n1Cc1ccc2c(c1)CCN2C(=O)c1ccccc1C#N 10.1021/jm00078a013
9556585 154361 8 None - 1 Human 5.2 pIC50 = 5.2 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 303 3 1 3 2.6 O=C(N/N=C/c1ccccn1)c1ccc(Br)cc1 nan
CHEMBL400912 154361 8 None - 1 Human 5.2 pIC50 = 5.2 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 303 3 1 3 2.6 O=C(N/N=C/c1ccccn1)c1ccc(Br)cc1 nan
14956800 204420 0 None - 1 Rabbit 7.2 pIC50 = 7.2 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 509 10 2 8 4.0 CCCCc1nn(C(C(=O)O)c2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL86143 204420 0 None - 1 Rabbit 7.2 pIC50 = 7.2 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 509 10 2 8 4.0 CCCCc1nn(C(C(=O)O)c2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
14956810 204429 0 None - 1 Rabbit 6.2 pIC50 = 6.2 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 566 10 1 8 5.9 CCCCc1nn(Cc2ccc(-c3ccccc3C#N)cc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL86232 204429 0 None - 1 Rabbit 6.2 pIC50 = 6.2 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 566 10 1 8 5.9 CCCCc1nn(Cc2ccc(-c3ccccc3C#N)cc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
135449568 41405 4 None 1 2 Human 5.2 pIC50 = 5.2 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 286 4 2 7 2.5 COCc1cc(O)nc(Nc2nc3ccc(C)cc3o2)n1 nan
CHEMBL1492017 41405 4 None 1 2 Human 5.2 pIC50 = 5.2 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 286 4 2 7 2.5 COCc1cc(O)nc(Nc2nc3ccc(C)cc3o2)n1 nan
44292428 100612 0 None - 1 Bovine 7.2 pIC50 = 7.2 Functional
In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.
ChEMBL 644 9 1 9 5.3 CCCCc1nc2ccc(C3(C(=O)N4CCCC4)C[C@H]4CCCN4O3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80365-0
CHEMBL294992 100612 0 None - 1 Bovine 7.2 pIC50 = 7.2 Functional
In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.
ChEMBL 644 9 1 9 5.3 CCCCc1nc2ccc(C3(C(=O)N4CCCC4)C[C@H]4CCCN4O3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80365-0
44291956 170698 0 None - 1 Bovine 7.2 pIC50 = 7.2 Functional
In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.
ChEMBL 619 10 1 10 5.3 CCCCc1nc2ccc([C@H]3ON4CCCC4C3C(=O)OCC)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80365-0
CHEMBL44605 170698 0 None - 1 Bovine 7.2 pIC50 = 7.2 Functional
In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.
ChEMBL 619 10 1 10 5.3 CCCCc1nc2ccc([C@H]3ON4CCCC4C3C(=O)OCC)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80365-0
14956746 204463 0 None - 1 Rabbit 7.2 pIC50 = 7.2 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 485 8 1 7 4.9 CCCCc1nn(-c2ccc(Cl)cc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL86440 204463 0 None - 1 Rabbit 7.2 pIC50 = 7.2 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 485 8 1 7 4.9 CCCCc1nn(-c2ccc(Cl)cc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
379338 16694 24 None - 1 Human 5.2 pIC50 = 5.2 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 288 2 0 4 3.4 COc1ccc(-c2cc3c(nn2)-c2ccccc2C3=O)cc1 nan
CHEMBL125044 16694 24 None - 1 Human 5.2 pIC50 = 5.2 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 288 2 0 4 3.4 COc1ccc(-c2cc3c(nn2)-c2ccccc2C3=O)cc1 nan
14956807 105631 0 None - 1 Rabbit 8.1 pIC50 = 8.1 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 566 12 1 9 4.9 CCCCc1nn(CCCOC(=O)N(C)c2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL313435 105631 0 None - 1 Rabbit 8.1 pIC50 = 8.1 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 566 12 1 9 4.9 CCCCc1nn(CCCOC(=O)N(C)c2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
14956755 105656 0 None - 1 Rabbit 8.1 pIC50 = 8.1 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 469 8 1 7 4.4 CCCCc1nn(-c2ccccc2F)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL313579 105656 0 None - 1 Rabbit 8.1 pIC50 = 8.1 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 469 8 1 7 4.4 CCCCc1nn(-c2ccccc2F)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
10202093 204699 0 None 2 2 Rabbit 8.1 pIC50 = 8.1 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 417 8 1 7 3.9 CCCCc1nn(C(C)C)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL87985 204699 0 None 2 2 Rabbit 8.1 pIC50 = 8.1 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 417 8 1 7 3.9 CCCCc1nn(C(C)C)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
145987183 166668 0 None - 1 Human 7.2 pIC50 = 7.2 Functional
Antagonist activity at type-1 angiotensin 2 receptor (unknown origin) by calcium mobilizing assayAntagonist activity at type-1 angiotensin 2 receptor (unknown origin) by calcium mobilizing assay
ChEMBL 597 9 1 7 6.1 CCCCc1nc(C)c(CC(=S)N2CC[C@@H]3CCCC[C@H]32)c(=O)n1Cc1ccc(-c2ccccc2-c2noc(=O)[nH]2)cc1 10.1016/j.bmcl.2018.08.036
CHEMBL4292297 166668 0 None - 1 Human 7.2 pIC50 = 7.2 Functional
Antagonist activity at type-1 angiotensin 2 receptor (unknown origin) by calcium mobilizing assayAntagonist activity at type-1 angiotensin 2 receptor (unknown origin) by calcium mobilizing assay
ChEMBL 597 9 1 7 6.1 CCCCc1nc(C)c(CC(=S)N2CC[C@@H]3CCCC[C@H]32)c(=O)n1Cc1ccc(-c2ccccc2-c2noc(=O)[nH]2)cc1 10.1016/j.bmcl.2018.08.036
44291955 96165 0 None - 1 Bovine 7.2 pIC50 = 7.2 Functional
In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.
ChEMBL 589 8 1 8 6.4 CCCCc1nc2ccc([C@@]3(C)C[C@H]4CCC(C)(C)N4O3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80365-0
CHEMBL263471 96165 0 None - 1 Bovine 7.2 pIC50 = 7.2 Functional
In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.
ChEMBL 589 8 1 8 6.4 CCCCc1nc2ccc([C@@]3(C)C[C@H]4CCC(C)(C)N4O3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80365-0
18942289 100847 0 None - 1 Bovine 7.2 pIC50 = 7.2 Functional
In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.
ChEMBL 595 9 1 8 6.8 CCCCc1nc2ccc(C3CC(c4ccc(C)cc4)=NO3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80365-0
CHEMBL296719 100847 0 None - 1 Bovine 7.2 pIC50 = 7.2 Functional
In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.
ChEMBL 595 9 1 8 6.8 CCCCc1nc2ccc(C3CC(c4ccc(C)cc4)=NO3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80365-0
10003482 165179 0 None 158 2 Rabbit 7.2 pIC50 = 7.2 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 442 7 1 5 5.2 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(N(C)C(C(=O)O)c2ccccc2)c(C)c1 10.1021/jm00078a014
CHEMBL424643 165179 0 None 158 2 Rabbit 7.2 pIC50 = 7.2 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 442 7 1 5 5.2 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(N(C)C(C(=O)O)c2ccccc2)c(C)c1 10.1021/jm00078a014
14956776 105475 0 None - 1 Rabbit 7.2 pIC50 = 7.2 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 389 7 1 7 2.8 CCCCc1nn(C)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL313017 105475 0 None - 1 Rabbit 7.2 pIC50 = 7.2 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 389 7 1 7 2.8 CCCCc1nn(C)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
14956790 170774 0 None - 1 Rabbit 7.2 pIC50 = 7.2 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 475 10 2 8 3.6 CCCCc1nn(C(C(=O)O)C(C)C)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL446152 170774 0 None - 1 Rabbit 7.2 pIC50 = 7.2 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 475 10 2 8 3.6 CCCCc1nn(C(C(=O)O)C(C)C)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
851388 54925 12 None - 1 Human 5.2 pIC50 = 5.2 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 229 4 1 2 3.1 O=C(CNc1ccc(F)cc1)c1ccccc1 nan
CHEMBL1328306 54925 12 None - 1 Human 5.2 pIC50 = 5.2 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 229 4 1 2 3.1 O=C(CNc1ccc(F)cc1)c1ccccc1 nan
CHEMBL1617841 54925 12 None - 1 Human 5.2 pIC50 = 5.2 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 229 4 1 2 3.1 O=C(CNc1ccc(F)cc1)c1ccccc1 nan
1728272 44567 12 None 1 2 Human 5.2 pIC50 = 5.2 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 309 5 3 4 1.5 CCCOc1ccc(C(=O)NNC(=S)NC(=O)CC)cc1 nan
CHEMBL1522211 44567 12 None 1 2 Human 5.2 pIC50 = 5.2 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 309 5 3 4 1.5 CCCOc1ccc(C(=O)NNC(=S)NC(=O)CC)cc1 nan
135411933 40961 21 None - 1 Human 5.1 pIC50 = 5.1 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 300 1 1 2 3.5 O=C1Nc2ccccc2C1=Nc1ccc(Br)cc1 nan
CHEMBL1488802 40961 21 None - 1 Human 5.1 pIC50 = 5.1 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 300 1 1 2 3.5 O=C1Nc2ccccc2C1=Nc1ccc(Br)cc1 nan
2796987 23155 5 None - 1 Human 5.1 pIC50 = 5.1 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 288 5 2 3 2.7 NC(=O)c1ccccc1NCC(=O)c1ccc(Cl)cc1 nan
CHEMBL1332717 23155 5 None - 1 Human 5.1 pIC50 = 5.1 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 288 5 2 3 2.7 NC(=O)c1ccccc1NCC(=O)c1ccc(Cl)cc1 nan
379337 163644 25 None - 1 Human 5.1 pIC50 = 5.1 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 258 1 0 3 3.4 O=C1c2ccccc2-c2nnc(-c3ccccc3)cc21 nan
CHEMBL421088 163644 25 None - 1 Human 5.1 pIC50 = 5.1 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 258 1 0 3 3.4 O=C1c2ccccc2-c2nnc(-c3ccccc3)cc21 nan
788612 52032 9 None - 1 Human 5.1 pIC50 = 5.1 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 303 4 1 2 4.1 Cc1ccc(C(=O)CNc2ccc(Br)cc2)cc1 nan
CHEMBL1589540 52032 9 None - 1 Human 5.1 pIC50 = 5.1 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 303 4 1 2 4.1 Cc1ccc(C(=O)CNc2ccc(Br)cc2)cc1 nan
583493 42474 11 None - 1 Human 5.1 pIC50 = 5.1 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 255 5 2 3 2.7 O=C(CNc1ccccc1C(=O)O)c1ccccc1 nan
CHEMBL1501792 42474 11 None - 1 Human 5.1 pIC50 = 5.1 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 255 5 2 3 2.7 O=C(CNc1ccccc1C(=O)O)c1ccccc1 nan
1593681 30136 8 None - 1 Human 5.1 pIC50 = 5.1 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 423 9 2 8 1.1 O=C(CNC(=O)c1ccco1)NCC(=O)OCC(=O)c1ccc(Cl)c([N+](=O)[O-])c1 nan
CHEMBL1391919 30136 8 None - 1 Human 5.1 pIC50 = 5.1 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 423 9 2 8 1.1 O=C(CNC(=O)c1ccco1)NCC(=O)OCC(=O)c1ccc(Cl)c([N+](=O)[O-])c1 nan
10258828 14475 0 None - 1 Rabbit 7.1 pIC50 = 7.1 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 498 9 1 7 5.0 CCCc1nn(CC(F)(F)F)c(C(=O)OCC)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
CHEMBL120549 14475 0 None - 1 Rabbit 7.1 pIC50 = 7.1 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 498 9 1 7 5.0 CCCc1nn(CC(F)(F)F)c(C(=O)OCC)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
14971696 112916 0 None - 1 Rabbit 7.1 pIC50 = 7.1 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 572 9 1 7 6.7 CCOC(=O)c1c(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c(CC2CC2)nn1-c1c(Cl)cccc1Cl 10.1021/jm00075a014
CHEMBL331886 112916 0 None - 1 Rabbit 7.1 pIC50 = 7.1 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 572 9 1 7 6.7 CCOC(=O)c1c(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c(CC2CC2)nn1-c1c(Cl)cccc1Cl 10.1021/jm00075a014
14956782 204669 0 None - 1 Rabbit 7.1 pIC50 = 7.1 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 457 8 1 7 3.8 CCCCc1nn(CC(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL87780 204669 0 None - 1 Rabbit 7.1 pIC50 = 7.1 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 457 8 1 7 3.8 CCCCc1nn(CC(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
44341650 169309 0 None -2 3 Human 5.1 pIC50 = 5.1 Functional
Antagonist activity at human AT1 overexpressed in CHO-K1 cells in presence of 10 nM [Val5-angiotensin II measured after 90 mins by HTRF based IP-one assayAntagonist activity at human AT1 overexpressed in CHO-K1 cells in presence of 10 nM [Val5-angiotensin II measured after 90 mins by HTRF based IP-one assay
ChEMBL 406 7 2 3 4.8 CCCCC1NC(=O)C2(CCCC2)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/acsmedchemlett.1c00240
CHEMBL444060 169309 0 None -2 3 Human 5.1 pIC50 = 5.1 Functional
Antagonist activity at human AT1 overexpressed in CHO-K1 cells in presence of 10 nM [Val5-angiotensin II measured after 90 mins by HTRF based IP-one assayAntagonist activity at human AT1 overexpressed in CHO-K1 cells in presence of 10 nM [Val5-angiotensin II measured after 90 mins by HTRF based IP-one assay
ChEMBL 406 7 2 3 4.8 CCCCC1NC(=O)C2(CCCC2)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/acsmedchemlett.1c00240
135400371 53004 20 None - 1 Human 5.1 pIC50 = 5.1 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 314 1 1 2 3.8 Cc1ccc(N=C2C(=O)Nc3ccc(Br)cc32)cc1 nan
CHEMBL1599499 53004 20 None - 1 Human 5.1 pIC50 = 5.1 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 314 1 1 2 3.8 Cc1ccc(N=C2C(=O)Nc3ccc(Br)cc32)cc1 nan
135403068 23285 14 None - 1 Human 5.1 pIC50 = 5.1 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 358 3 1 3 4.2 CCOc1ccc(N=C2C(=O)Nc3ccc(C)c(Br)c32)cc1 nan
CHEMBL1333730 23285 14 None - 1 Human 5.1 pIC50 = 5.1 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 358 3 1 3 4.2 CCOc1ccc(N=C2C(=O)Nc3ccc(C)c(Br)c32)cc1 nan
6884203 107745 10 None -1 2 Human 5.1 pIC50 = 5.1 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 352 4 1 4 4.1 O=C(N/N=C/c1ccccn1)c1cc(-c2ccccc2)nc2ccccc12 nan
CHEMBL3197021 107745 10 None -1 2 Human 5.1 pIC50 = 5.1 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 352 4 1 4 4.1 O=C(N/N=C/c1ccccn1)c1cc(-c2ccccc2)nc2ccccc12 nan
2989697 48469 17 None - 1 Human 5.1 pIC50 = 5.1 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 377 5 1 6 2.4 CS(=O)(=O)c1ncc(Cl)c(C(=O)Nc2ccc(OC(F)F)cc2)n1 nan
CHEMBL1558462 48469 17 None - 1 Human 5.1 pIC50 = 5.1 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 377 5 1 6 2.4 CS(=O)(=O)c1ncc(Cl)c(C(=O)Nc2ccc(OC(F)F)cc2)n1 nan
10435200 23644 0 None - 1 Rabbit 6.1 pIC50 = 6.1 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 478 5 1 7 4.0 CCc1nc2c(C)cc(C)nc2n1Cc1ccc2c(c1)CCN2C(=O)c1ccccc1-c1nn[nH]n1 10.1021/jm00078a013
CHEMBL133654 23644 0 None - 1 Rabbit 6.1 pIC50 = 6.1 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 478 5 1 7 4.0 CCc1nc2c(C)cc(C)nc2n1Cc1ccc2c(c1)CCN2C(=O)c1ccccc1-c1nn[nH]n1 10.1021/jm00078a013
5953874 40846 5 None -1 2 Human 5.1 pIC50 = 5.1 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 277 2 1 6 2.8 N=C1S/C(=C\c2ccco2)C(=O)N1c1nccs1 nan
CHEMBL1488024 40846 5 None -1 2 Human 5.1 pIC50 = 5.1 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 277 2 1 6 2.8 N=C1S/C(=C\c2ccco2)C(=O)N1c1nccs1 nan
9675542 107310 4 None - 1 Human 5.1 pIC50 = 5.1 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 273 3 1 3 2.8 Cc1cccc(/C=N/NC(=O)c2cccc(Cl)c2)n1 nan
CHEMBL3191999 107310 4 None - 1 Human 5.1 pIC50 = 5.1 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 273 3 1 3 2.8 Cc1cccc(/C=N/NC(=O)c2cccc(Cl)c2)n1 nan
44292215 174857 0 None - 1 Bovine 7.1 pIC50 = 7.1 Functional
In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.
ChEMBL 605 9 1 10 4.8 CCCCc1nc2ccc([C@]3(C(=O)OC)C[C@H]4CCCN4O3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80365-0
CHEMBL45766 174857 0 None - 1 Bovine 7.1 pIC50 = 7.1 Functional
In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.
ChEMBL 605 9 1 10 4.8 CCCCc1nc2ccc([C@]3(C(=O)OC)C[C@H]4CCCN4O3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80365-0
14956774 204505 0 None - 1 Rabbit 7.1 pIC50 = 7.1 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 452 8 1 8 3.7 CCCCc1nn(-c2ccccn2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL86741 204505 0 None - 1 Rabbit 7.1 pIC50 = 7.1 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 452 8 1 8 3.7 CCCCc1nn(-c2ccccn2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
6873171 108224 5 None - 1 Human 5.1 pIC50 = 5.1 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 283 2 1 3 1.9 S=C(N/N=C/c1ccc(Cl)cc1)N1CCOCC1 nan
CHEMBL3208447 108224 5 None - 1 Human 5.1 pIC50 = 5.1 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 283 2 1 3 1.9 S=C(N/N=C/c1ccc(Cl)cc1)N1CCOCC1 nan
14971678 14361 0 None - 1 Rabbit 8.1 pIC50 = 8.1 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 574 10 1 7 7.1 CCCCc1nn(-c2c(Cl)cccc2Cl)c(C(=O)OCC)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
CHEMBL120290 14361 0 None - 1 Rabbit 8.1 pIC50 = 8.1 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 574 10 1 7 7.1 CCCCc1nn(-c2c(Cl)cccc2Cl)c(C(=O)OCC)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
10365283 25634 0 None 416 2 Rabbit 8.1 pIC50 = 8.1 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 428 7 1 5 4.9 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(N(C)C(C(=O)O)c2ccccc2)cc1 10.1021/jm00078a014
CHEMBL135345 25634 0 None 416 2 Rabbit 8.1 pIC50 = 8.1 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 428 7 1 5 4.9 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(N(C)C(C(=O)O)c2ccccc2)cc1 10.1021/jm00078a014
10223724 204033 0 None 1 2 Rabbit 8.1 pIC50 = 8.1 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 417 9 1 7 3.7 CCCCc1nn(CCC)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL82797 204033 0 None 1 2 Rabbit 8.1 pIC50 = 8.1 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 417 9 1 7 3.7 CCCCc1nn(CCC)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
10479472 114713 0 None - 1 Rabbit 8.1 pIC50 = 8.1 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 462 6 1 7 4.8 CCc1nc2c(C)cc(C)nc2n1Cc1ccc2c(ccn2Cc2ccccc2-c2nn[nH]n2)c1 10.1021/jm00078a013
CHEMBL334660 114713 0 None - 1 Rabbit 8.1 pIC50 = 8.1 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 462 6 1 7 4.8 CCc1nc2c(C)cc(C)nc2n1Cc1ccc2c(ccn2Cc2ccccc2-c2nn[nH]n2)c1 10.1021/jm00078a013
10344235 204430 0 None -1 3 Rabbit 8.1 pIC50 = 8.1 Functional
Antagonist activity against AT1 receptor assessed as inhibition of Ang2-induced rabbit aortic strip contractionAntagonist activity against AT1 receptor assessed as inhibition of Ang2-induced rabbit aortic strip contraction
ChEMBL 460 5 1 7 5.1 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2c(-c3nn[nH]n3)cnc3ccccc23)cc1 10.1021/jm0603163
CHEMBL86247 204430 0 None -1 3 Rabbit 8.1 pIC50 = 8.1 Functional
Antagonist activity against AT1 receptor assessed as inhibition of Ang2-induced rabbit aortic strip contractionAntagonist activity against AT1 receptor assessed as inhibition of Ang2-induced rabbit aortic strip contraction
ChEMBL 460 5 1 7 5.1 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2c(-c3nn[nH]n3)cnc3ccccc23)cc1 10.1021/jm0603163
10322504 26163 0 None 19 2 Rabbit 7.1 pIC50 = 7.1 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 470 9 1 5 6.1 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(N(C(C)CC)C(C(=O)O)c2ccccc2)cc1 10.1021/jm00078a014
CHEMBL135929 26163 0 None 19 2 Rabbit 7.1 pIC50 = 7.1 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 470 9 1 5 6.1 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(N(C(C)CC)C(C(=O)O)c2ccccc2)cc1 10.1021/jm00078a014
14956747 204247 0 None - 1 Rabbit 7.1 pIC50 = 7.1 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 496 9 1 9 4.2 CCCCc1nn(-c2ccc([N+](=O)[O-])cc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL84630 204247 0 None - 1 Rabbit 7.1 pIC50 = 7.1 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 496 9 1 9 4.2 CCCCc1nn(-c2ccc([N+](=O)[O-])cc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
14971673 111855 0 None - 1 Rabbit 7.1 pIC50 = 7.1 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 506 10 1 7 5.8 CCCCc1nn(-c2ccccc2)c(C(=O)OCC)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
CHEMBL329466 111855 0 None - 1 Rabbit 7.1 pIC50 = 7.1 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 506 10 1 7 5.8 CCCCc1nn(-c2ccccc2)c(C(=O)OCC)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
5339648 72591 12 None 1 2 Human 5.1 pIC50 = 5.1 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 270 4 1 5 1.8 O=C(N/N=C/c1ccccn1)c1cccc([N+](=O)[O-])c1 nan
CHEMBL2005961 72591 12 None 1 2 Human 5.1 pIC50 = 5.1 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 270 4 1 5 1.8 O=C(N/N=C/c1ccccn1)c1cccc([N+](=O)[O-])c1 nan
10322995 114751 0 None 134 2 Rabbit 7.1 pIC50 = 7.1 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 482 9 1 5 6.1 C=CCN(c1ccc(Cn2c(CC)nc3c(C)cc(C)nc32)cc1C)C(C(=O)O)c1ccccc1C 10.1021/jm00078a014
CHEMBL334832 114751 0 None 134 2 Rabbit 7.1 pIC50 = 7.1 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 482 9 1 5 6.1 C=CCN(c1ccc(Cn2c(CC)nc3c(C)cc(C)nc32)cc1C)C(C(=O)O)c1ccccc1C 10.1021/jm00078a014
10026268 116417 0 None 173 2 Rabbit 7.1 pIC50 = 7.1 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 440 6 1 5 4.8 CCc1nc2c(C)cc(C)nc2n1Cc1ccc2c(c1)CCN2C(C(=O)O)c1ccccc1 10.1021/jm00078a013
CHEMBL338505 116417 0 None 173 2 Rabbit 7.1 pIC50 = 7.1 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 440 6 1 5 4.8 CCc1nc2c(C)cc(C)nc2n1Cc1ccc2c(c1)CCN2C(C(=O)O)c1ccccc1 10.1021/jm00078a013
854200 35788 9 None - 1 Human 5.1 pIC50 = 5.1 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 239 4 1 2 3.6 Cc1ccc(C(=O)CNc2ccccc2C)cc1 nan
CHEMBL1443417 35788 9 None - 1 Human 5.1 pIC50 = 5.1 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 239 4 1 2 3.6 Cc1ccc(C(=O)CNc2ccccc2C)cc1 nan
973504 94765 9 None -1 2 Human 5.1 pIC50 = 5.1 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 343 4 1 5 3.3 Cc1ccc(S(=O)(=O)Nc2cccc3cccnc23)c([N+](=O)[O-])c1 nan
CHEMBL256042 94765 9 None -1 2 Human 5.1 pIC50 = 5.1 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 343 4 1 5 3.3 Cc1ccc(S(=O)(=O)Nc2cccc3cccnc23)c([N+](=O)[O-])c1 nan
44292180 180356 0 None - 1 Bovine 7.1 pIC50 = 7.1 Functional
In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.
ChEMBL 575 9 1 8 6.0 CCCCc1nc2ccc([C@]3(CC)C[C@H]4CCCN4O3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80365-0
CHEMBL47583 180356 0 None - 1 Bovine 7.1 pIC50 = 7.1 Functional
In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.In vitro Angiotensin II receptor antagonism in bovine adrenal cortex tissue.
ChEMBL 575 9 1 8 6.0 CCCCc1nc2ccc([C@]3(CC)C[C@H]4CCCN4O3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80365-0
200953 45565 7 None - 1 Human 5.1 pIC50 = 5.1 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 196 1 0 2 2.5 O=C(C#Cc1ccccc1)c1ccco1 nan
CHEMBL1531308 45565 7 None - 1 Human 5.1 pIC50 = 5.1 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 196 1 0 2 2.5 O=C(C#Cc1ccccc1)c1ccco1 nan
2812483 43322 5 None - 1 Human 5.1 pIC50 = 5.1 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 245 3 2 4 2.4 Cc1cc(C(=O)NNc2ccc(C)c(C)c2)no1 nan
CHEMBL1509162 43322 5 None - 1 Human 5.1 pIC50 = 5.1 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 245 3 2 4 2.4 Cc1cc(C(=O)NNc2ccc(C)c(C)c2)no1 nan
6873172 108582 11 None - 1 Human 5.1 pIC50 = 5.1 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 263 2 1 3 1.5 Cc1ccc(/C=N/NC(=S)N2CCOCC2)cc1 nan
CHEMBL3213140 108582 11 None - 1 Human 5.1 pIC50 = 5.1 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 263 2 1 3 1.5 Cc1ccc(/C=N/NC(=S)N2CCOCC2)cc1 nan
10437543 26047 0 None 7 2 Rabbit 6.1 pIC50 = 6.1 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 550 7 2 5 6.9 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(NC(C(=O)O)c2cc(C(F)(F)F)cc(C(F)(F)F)c2)cc1 10.1021/jm00078a014
CHEMBL135819 26047 0 None 7 2 Rabbit 6.1 pIC50 = 6.1 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 550 7 2 5 6.9 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(NC(C(=O)O)c2cc(C(F)(F)F)cc(C(F)(F)F)c2)cc1 10.1021/jm00078a014
878879 37935 10 None - 1 Human 5.1 pIC50 = 5.1 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 303 4 1 2 4.1 Cc1ccccc1NCC(=O)c1ccc(Br)cc1 nan
CHEMBL1461745 37935 10 None - 1 Human 5.1 pIC50 = 5.1 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 303 4 1 2 4.1 Cc1ccccc1NCC(=O)c1ccc(Br)cc1 nan
44341785 10037 0 None -3 3 Human 5.1 pIC50 = 5.1 Functional
Antagonist activity at human AT1 overexpressed in CHO-K1 cells in presence of 10 nM [Val5-angiotensin II measured after 90 mins by HTRF based IP-one assayAntagonist activity at human AT1 overexpressed in CHO-K1 cells in presence of 10 nM [Val5-angiotensin II measured after 90 mins by HTRF based IP-one assay
ChEMBL 438 6 1 3 5.3 O=C(O)c1ccccc1-c1ccc(CN2C(=O)C3(CCCC3)N=C2Cc2ccccc2)cc1 10.1021/acsmedchemlett.1c00240
CHEMBL115771 10037 0 None -3 3 Human 5.1 pIC50 = 5.1 Functional
Antagonist activity at human AT1 overexpressed in CHO-K1 cells in presence of 10 nM [Val5-angiotensin II measured after 90 mins by HTRF based IP-one assayAntagonist activity at human AT1 overexpressed in CHO-K1 cells in presence of 10 nM [Val5-angiotensin II measured after 90 mins by HTRF based IP-one assay
ChEMBL 438 6 1 3 5.3 O=C(O)c1ccccc1-c1ccc(CN2C(=O)C3(CCCC3)N=C2Cc2ccccc2)cc1 10.1021/acsmedchemlett.1c00240
6792924 107489 10 None 1 2 Human 5.1 pIC50 = 5.1 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 259 3 1 3 2.5 O=C(N/N=C/c1ccccn1)c1ccc(Cl)cc1 nan
CHEMBL3194040 107489 10 None 1 2 Human 5.1 pIC50 = 5.1 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 259 3 1 3 2.5 O=C(N/N=C/c1ccccn1)c1ccc(Cl)cc1 nan
1511959 20910 10 None - 1 Human 5.1 pIC50 = 5.1 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 359 3 0 8 2.0 CC(=O)C1=C(c2cccc([N+](=O)[O-])c2)N(C(C)=O)n2c(C)nnc2S1 nan
CHEMBL1312377 20910 10 None - 1 Human 5.1 pIC50 = 5.1 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 359 3 0 8 2.0 CC(=O)C1=C(c2cccc([N+](=O)[O-])c2)N(C(C)=O)n2c(C)nnc2S1 nan
10050755 114999 0 None - 1 Rabbit 7.1 pIC50 = 7.1 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 478 8 1 5 5.6 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(N(CC)C(C(=O)O)c2cc(F)ccc2F)cc1 10.1021/jm00078a014
CHEMBL335276 114999 0 None - 1 Rabbit 7.1 pIC50 = 7.1 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 478 8 1 5 5.6 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(N(CC)C(C(=O)O)c2cc(F)ccc2F)cc1 10.1021/jm00078a014
54508770 70514 0 None - 1 Rabbit 8.0 pIC50 = 8.0 Functional
Antagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challengeAntagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challenge
ChEMBL 472 10 2 7 3.8 CCCCc1nc(C)c(CCC(=O)O)c(=O)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2011.12.116
CHEMBL1951125 70514 0 None - 1 Rabbit 8.0 pIC50 = 8.0 Functional
Antagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challengeAntagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challenge
ChEMBL 472 10 2 7 3.8 CCCCc1nc(C)c(CCC(=O)O)c(=O)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2011.12.116
14971682 110986 0 None - 1 Rabbit 8.0 pIC50 = 8.0 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 551 11 1 9 5.7 CCCCc1nn(-c2ccccc2[N+](=O)[O-])c(C(=O)OCC)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
CHEMBL327718 110986 0 None - 1 Rabbit 8.0 pIC50 = 8.0 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 551 11 1 9 5.7 CCCCc1nn(-c2ccccc2[N+](=O)[O-])c(C(=O)OCC)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
14956771 204620 0 None - 1 Rabbit 8.0 pIC50 = 8.0 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 482 8 1 9 3.8 CCCc1nn(-c2ccccc2[N+](=O)[O-])c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL87392 204620 0 None - 1 Rabbit 8.0 pIC50 = 8.0 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 482 8 1 9 3.8 CCCc1nn(-c2ccccc2[N+](=O)[O-])c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
57393228 70531 0 None - 1 Rabbit 8.0 pIC50 = 8.0 Functional
Antagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challengeAntagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challenge
ChEMBL 539 10 1 7 4.7 CCCCc1nc(C)c(CCC(=O)N2CCCCC2)c(=O)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2011.12.116
CHEMBL1951141 70531 0 None - 1 Rabbit 8.0 pIC50 = 8.0 Functional
Antagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challengeAntagonist activity at angiotensin 2 receptor type 1 in New Zealand White rabbit descending thoracic aorta rings assessed as inhibition of angiotensin 2-induced contraction preincubated for 30 mins prior angiotensin 2 challenge
ChEMBL 539 10 1 7 4.7 CCCCc1nc(C)c(CCC(=O)N2CCCCC2)c(=O)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2011.12.116
14971676 162810 0 None - 1 Rabbit 7.1 pIC50 = 7.1 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 574 10 1 7 7.1 CCCCc1nn(-c2cccc(Cl)c2Cl)c(C(=O)OCC)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
CHEMBL419321 162810 0 None - 1 Rabbit 7.1 pIC50 = 7.1 Functional
Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1Evaluation of Angiotensin II antagonistic activity by displacement of [125I]-Sar Ile-AII at the rabbit aorta Angiotensin II receptor, type 1
ChEMBL 574 10 1 7 7.1 CCCCc1nn(-c2cccc(Cl)c2Cl)c(C(=O)OCC)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a014
14956776 105475 0 None - 1 Rabbit 7.1 pIC50 = 7.1 Functional
In vitro antagonistic activity for AT1 receptor by displacing 125I[Sar, ILe8]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for AT1 receptor by displacing 125I[Sar, ILe8]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 389 7 1 7 2.8 CCCCc1nn(C)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL313017 105475 0 None - 1 Rabbit 7.1 pIC50 = 7.1 Functional
In vitro antagonistic activity for AT1 receptor by displacing 125I[Sar, ILe8]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for AT1 receptor by displacing 125I[Sar, ILe8]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 389 7 1 7 2.8 CCCCc1nn(C)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
824082 26261 10 None - 1 Human 5.0 pIC50 = 5.0 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 326 5 0 5 2.6 Cc1ccc(OCCN2C(=O)c3ccccc3C2=O)c([N+](=O)[O-])c1 nan
CHEMBL1360149 26261 10 None - 1 Human 5.0 pIC50 = 5.0 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 326 5 0 5 2.6 Cc1ccc(OCCN2C(=O)c3ccccc3C2=O)c([N+](=O)[O-])c1 nan
2564786 44433 7 None - 1 Human 5.0 pIC50 = 5.0 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 225 4 1 2 3.3 Cc1ccc(C(=O)CNc2ccccc2)cc1 nan
CHEMBL1521054 44433 7 None - 1 Human 5.0 pIC50 = 5.0 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 225 4 1 2 3.3 Cc1ccc(C(=O)CNc2ccccc2)cc1 nan
11754335 25084 0 None 186 2 Rabbit 7.0 pIC50 = 7.0 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 467 5 2 6 5.4 CCc1nc2c(C)cc(C)nc2n1Cc1ccc2c(ccn2C(=O)c2ccccc2NC(=O)O)c1 10.1021/jm00078a013
CHEMBL134901 25084 0 None 186 2 Rabbit 7.0 pIC50 = 7.0 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 467 5 2 6 5.4 CCc1nc2c(C)cc(C)nc2n1Cc1ccc2c(ccn2C(=O)c2ccccc2NC(=O)O)c1 10.1021/jm00078a013
1625575 53985 10 None 1 2 Human 5.0 pIC50 = 5.0 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 297 5 1 5 1.5 CCOC(=O)/C=C/S(=O)(=O)c1ccc(NC(C)=O)cc1 nan
CHEMBL1608078 53985 10 None 1 2 Human 5.0 pIC50 = 5.0 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 297 5 1 5 1.5 CCOC(=O)/C=C/S(=O)(=O)c1ccc(NC(C)=O)cc1 nan
5680364 54604 5 None - 1 Human 5.0 pIC50 = 5.0 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 272 2 1 4 0.9 CCOC(=O)C1=C2NC(=O)c3ccccc3N2C(=O)C1 nan
CHEMBL1613515 54604 5 None - 1 Human 5.0 pIC50 = 5.0 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 272 2 1 4 0.9 CCOC(=O)C1=C2NC(=O)c3ccccc3N2C(=O)C1 nan
2411934 55147 3 None - 1 Human 5.0 pIC50 = 5.0 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 451 10 2 6 4.3 CCOC(=O)c1c(-c2ccc(-c3ccccc3)cc2)csc1NC(=O)CNCCN(C)C nan
CHEMBL1409219 55147 3 None - 1 Human 5.0 pIC50 = 5.0 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 451 10 2 6 4.3 CCOC(=O)c1c(-c2ccc(-c3ccccc3)cc2)csc1NC(=O)CNCCN(C)C nan
CHEMBL1619798 55147 3 None - 1 Human 5.0 pIC50 = 5.0 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 451 10 2 6 4.3 CCOC(=O)c1c(-c2ccc(-c3ccccc3)cc2)csc1NC(=O)CNCCN(C)C nan
2170433 45915 10 None - 1 Human 5.0 pIC50 = 5.0 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 390 8 1 6 2.3 O=C(Cc1ccccc1)NCC(=O)OCC(=O)c1ccc(Cl)c([N+](=O)[O-])c1 nan
CHEMBL1534477 45915 10 None - 1 Human 5.0 pIC50 = 5.0 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 390 8 1 6 2.3 O=C(Cc1ccccc1)NCC(=O)OCC(=O)c1ccc(Cl)c([N+](=O)[O-])c1 nan
9590742 107074 3 None -1 2 Human 5.0 pIC50 = 5.0 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 273 3 1 3 2.9 C/C(=N\NC(=O)c1ccccc1Cl)c1ccccn1 nan
CHEMBL3189245 107074 3 None -1 2 Human 5.0 pIC50 = 5.0 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 273 3 1 3 2.9 C/C(=N\NC(=O)c1ccccc1Cl)c1ccccn1 nan
10434876 116105 0 None 7 2 Rabbit 7.0 pIC50 = 7.0 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 470 10 1 5 6.1 CCCCN(c1ccc(Cn2c(CC)nc3c(C)cc(C)nc32)cc1)C(C(=O)O)c1ccccc1 10.1021/jm00078a014
CHEMBL336808 116105 0 None 7 2 Rabbit 7.0 pIC50 = 7.0 Functional
In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.In vitro antagonist activity against angiotensin II receptor type 1 in rabbit aorta using [125I]-Sar, Ile AII.
ChEMBL 470 10 1 5 6.1 CCCCN(c1ccc(Cn2c(CC)nc3c(C)cc(C)nc32)cc1)C(C(=O)O)c1ccccc1 10.1021/jm00078a014
2474590 42905 4 None -1 2 Human 5.0 pIC50 = 5.0 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 291 2 1 4 3.2 O=C(Nc1nc2c(F)cc(F)cc2s1)c1ccccn1 nan
CHEMBL1505604 42905 4 None -1 2 Human 5.0 pIC50 = 5.0 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 291 2 1 4 3.2 O=C(Nc1nc2c(F)cc(F)cc2s1)c1ccccn1 nan
9667523 108350 8 None -3 2 Human 5.0 pIC50 = 5.0 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 328 6 1 6 2.3 C/C(=N\NC(=O)C(C)Oc1ccc([N+](=O)[O-])cc1)c1ccccn1 nan
CHEMBL3210072 108350 8 None -3 2 Human 5.0 pIC50 = 5.0 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 328 6 1 6 2.3 C/C(=N\NC(=O)C(C)Oc1ccc([N+](=O)[O-])cc1)c1ccccn1 nan
14956770 204524 0 None - 1 Rabbit 7.0 pIC50 = 7.0 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 480 7 1 9 3.7 O=c1n(-c2ccccc2[N+](=O)[O-])nc(C2CC2)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL86853 204524 0 None - 1 Rabbit 7.0 pIC50 = 7.0 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 480 7 1 9 3.7 O=c1n(-c2ccccc2[N+](=O)[O-])nc(C2CC2)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
14956785 204657 0 None - 1 Rabbit 7.0 pIC50 = 7.0 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 460 9 2 8 2.6 CCCCc1nn(C(C)C(=O)NC)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
CHEMBL87682 204657 0 None - 1 Rabbit 7.0 pIC50 = 7.0 Functional
In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)In vitro antagonistic activity for angiotensin II receptor, type 1 by displacing 125I[Sar, ILe8 ]AII radioligand in rabbit aorta membrane without using bovine serum albumin (BSA)
ChEMBL 460 9 2 8 2.6 CCCCc1nn(C(C)C(=O)NC)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00069a015
1487013 51672 14 None 1 3 Human 5.0 pIC50 = 5.0 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 317 3 1 6 1.4 CNC(=O)c1nnsc1S(=O)(=O)c1ccc(Cl)cc1 nan
CHEMBL1586425 51672 14 None 1 3 Human 5.0 pIC50 = 5.0 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 317 3 1 6 1.4 CNC(=O)c1nnsc1S(=O)(=O)c1ccc(Cl)cc1 nan
5337284 45435 6 None - 1 Human 5.0 pIC50 = 5.0 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 342 5 1 3 4.5 Cc1cccc(C(=O)Nc2ccc(C(=O)/C=C/c3ccncc3)cc2)c1 nan
CHEMBL1530173 45435 6 None - 1 Human 5.0 pIC50 = 5.0 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 342 5 1 3 4.5 Cc1cccc(C(=O)Nc2ccc(C(=O)/C=C/c3ccncc3)cc2)c1 nan
991372 53552 30 None 1 2 Human 5.0 pIC50 = 5.0 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 382 1 2 5 4.5 CC1(C)CC(=O)C2=C(C1)OC1=C(C(=O)CC(C)(C)C1)C2c1ccc(O)cc1O nan
CHEMBL1604546 53552 30 None 1 2 Human 5.0 pIC50 = 5.0 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 382 1 2 5 4.5 CC1(C)CC(=O)C2=C(C1)OC1=C(C(=O)CC(C)(C)C1)C2c1ccc(O)cc1O nan
135472791 22120 6 None - 1 Human 5.0 pIC50 = 5.0 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 277 2 1 4 5.0 Cc1ccc(C)c(N=Nc2ccc(O)c3ncccc23)c1 nan
CHEMBL1324011 22120 6 None - 1 Human 5.0 pIC50 = 5.0 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 277 2 1 4 5.0 Cc1ccc(C)c(N=Nc2ccc(O)c3ncccc23)c1 nan
788618 19789 10 None - 1 Human 5.0 pIC50 = 5.0 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 253 4 1 2 3.9 Cc1ccc(C(=O)CNc2cc(C)ccc2C)cc1 nan
CHEMBL1303334 19789 10 None - 1 Human 5.0 pIC50 = 5.0 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 253 4 1 2 3.9 Cc1ccc(C(=O)CNc2cc(C)ccc2C)cc1 nan
788408 43284 13 None - 1 Human 5.0 pIC50 = 5 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 259 4 1 2 3.9 Cc1ccc(C(=O)CNc2cccc(Cl)c2)cc1 nan
CHEMBL1508797 43284 13 None - 1 Human 5.0 pIC50 = 5 Functional
PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]PUBCHEM_BIOASSAY: Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor. (Class of assay: confirmatory) [Related pubchem assays: 2569, 2521 ]
ChEMBL 259 4 1 2 3.9 Cc1ccc(C(=O)CNc2cccc(Cl)c2)cc1 nan
6918269 98005 8 None 5 2 Human 10.9 pKd = 10.9 Functional
Antagonist activity at angiotensin AT1 receptorAntagonist activity at angiotensin AT1 receptor
ChEMBL 508 9 1 7 5.5 CCCCc1nc2ccc(C(C)(C)OC)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.bmc.2010.10.043
CHEMBL275875 98005 8 None 5 2 Human 10.9 pKd = 10.9 Functional
Antagonist activity at angiotensin AT1 receptorAntagonist activity at angiotensin AT1 receptor
ChEMBL 508 9 1 7 5.5 CCCCc1nc2ccc(C(C)(C)OC)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.bmc.2010.10.043
CHEMBL295959 98005 8 None 5 2 Human 10.9 pKd = 10.9 Functional
Antagonist activity at angiotensin AT1 receptorAntagonist activity at angiotensin AT1 receptor
ChEMBL 508 9 1 7 5.5 CCCCc1nc2ccc(C(C)(C)OC)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.bmc.2010.10.043
11527144 178516 0 None - 1 Human 10.9 pKd = 10.9 Functional
Antagonist activity at angiotensin AT1 receptorAntagonist activity at angiotensin AT1 receptor
ChEMBL 561 8 1 8 5.6 CCCCc1nc2ccc([C@]3(C)C[C@H]4CCCN4O3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.bmc.2010.10.043
CHEMBL297425 178516 0 None - 1 Human 10.9 pKd = 10.9 Functional
Antagonist activity at angiotensin AT1 receptorAntagonist activity at angiotensin AT1 receptor
ChEMBL 561 8 1 8 5.6 CCCCc1nc2ccc([C@]3(C)C[C@H]4CCCN4O3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.bmc.2010.10.043
CHEMBL47177 178516 0 None - 1 Human 10.9 pKd = 10.9 Functional
Antagonist activity at angiotensin AT1 receptorAntagonist activity at angiotensin AT1 receptor
ChEMBL 561 8 1 8 5.6 CCCCc1nc2ccc([C@]3(C)C[C@H]4CCCN4O3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.bmc.2010.10.043
133031 100379 16 None -1 3 Rabbit 10.3 pKd = 10.3 Functional
Antagonist activity at angiotensin AT1 receptor in rabbit aortaAntagonist activity at angiotensin AT1 receptor in rabbit aorta
ChEMBL 524 7 1 6 5.4 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/j.bmc.2010.10.043
CHEMBL293511 100379 16 None -1 3 Rabbit 10.3 pKd = 10.3 Functional
Antagonist activity at angiotensin AT1 receptor in rabbit aortaAntagonist activity at angiotensin AT1 receptor in rabbit aorta
ChEMBL 524 7 1 6 5.4 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/j.bmc.2010.10.043
9887844 162637 1 None - 1 Rabbit 10.3 pKd = 10.3 Functional
Antagonist activity at angiotensin AT1 receptor in rabbit aortaAntagonist activity at angiotensin AT1 receptor in rabbit aorta
ChEMBL 411 6 1 5 4.9 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2c(n1)CCCC2 10.1016/j.bmc.2010.10.043
CHEMBL418226 162637 1 None - 1 Rabbit 10.3 pKd = 10.3 Functional
Antagonist activity at angiotensin AT1 receptor in rabbit aortaAntagonist activity at angiotensin AT1 receptor in rabbit aorta
ChEMBL 411 6 1 5 4.9 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2c(n1)CCCC2 10.1016/j.bmc.2010.10.043
9911332 44434 1 None - 0 Rabbit 10.2 pKd = 10.2 Functional
Antagonism against Angiotensin II receptor, type 1 in rabbit aortaAntagonism against Angiotensin II receptor, type 1 in rabbit aorta
ChEMBL 444 7 2 6 4.7 CCCn1nc(C(C)(C)C)c(C(=O)O)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm9604383
CHEMBL152106 44434 1 None - 0 Rabbit 10.2 pKd = 10.2 Functional
Antagonism against Angiotensin II receptor, type 1 in rabbit aortaAntagonism against Angiotensin II receptor, type 1 in rabbit aorta
ChEMBL 444 7 2 6 4.7 CCCn1nc(C(C)(C)C)c(C(=O)O)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm9604383
132387 161772 18 None - 0 Rabbit 10.1 pKd = 10.1 Functional
Antagonist activity at angiotensin AT1 receptor in rabbit aortaAntagonist activity at angiotensin AT1 receptor in rabbit aorta
ChEMBL 414 8 2 6 4.0 CCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1ncccc1C(=O)O 10.1016/j.bmc.2010.10.043
CHEMBL416477 161772 18 None - 0 Rabbit 10.1 pKd = 10.1 Functional
Antagonist activity at angiotensin AT1 receptor in rabbit aortaAntagonist activity at angiotensin AT1 receptor in rabbit aorta
ChEMBL 414 8 2 6 4.0 CCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1ncccc1C(=O)O 10.1016/j.bmc.2010.10.043
108185 1578 71 None -3 5 Rabbit 10.1 pKd = 10.1 Functional
Antagonist activity at angiotensin AT1 receptor in rabbit aorta assessed as reduction of angiotensin 2-induced contractile responseAntagonist activity at angiotensin AT1 receptor in rabbit aorta assessed as reduction of angiotensin 2-induced contractile response
ChEMBL 436 8 2 6 4.5 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)C(=O)O)Cl 10.1016/j.bmc.2010.10.043
586 1578 71 None -3 5 Rabbit 10.1 pKd = 10.1 Functional
Antagonist activity at angiotensin AT1 receptor in rabbit aorta assessed as reduction of angiotensin 2-induced contractile responseAntagonist activity at angiotensin AT1 receptor in rabbit aorta assessed as reduction of angiotensin 2-induced contractile response
ChEMBL 436 8 2 6 4.5 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)C(=O)O)Cl 10.1016/j.bmc.2010.10.043
CHEMBL907 1578 71 None -3 5 Rabbit 10.1 pKd = 10.1 Functional
Antagonist activity at angiotensin AT1 receptor in rabbit aorta assessed as reduction of angiotensin 2-induced contractile responseAntagonist activity at angiotensin AT1 receptor in rabbit aorta assessed as reduction of angiotensin 2-induced contractile response
ChEMBL 436 8 2 6 4.5 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)C(=O)O)Cl 10.1016/j.bmc.2010.10.043
9802561 160692 19 None - 0 Rabbit 10.0 pKd = 10.0 Functional
Antagonist activity at angiotensin AT1 receptor in rabbit aortaAntagonist activity at angiotensin AT1 receptor in rabbit aorta
ChEMBL 426 6 1 6 4.6 CCCc1nc2c(n1Cc1ccc(-c3ccccc3-c3nn[nH]n3)cc1)C(=O)CCCC2 10.1016/j.bmc.2010.10.043
CHEMBL41194 160692 19 None - 0 Rabbit 10.0 pKd = 10.0 Functional
Antagonist activity at angiotensin AT1 receptor in rabbit aortaAntagonist activity at angiotensin AT1 receptor in rabbit aorta
ChEMBL 426 6 1 6 4.6 CCCc1nc2c(n1Cc1ccc(-c3ccccc3-c3nn[nH]n3)cc1)C(=O)CCCC2 10.1016/j.bmc.2010.10.043
19890807 111033 0 None - 0 Rabbit 10.0 pKd = 10 Functional
Antagonistic ability of angiotensin II to contract rabbit aortaAntagonistic ability of angiotensin II to contract rabbit aorta
ChEMBL 466 8 1 7 5.4 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2nc(OC(C)C)ccc2n1 10.1021/jm00070a012
CHEMBL327932 111033 0 None - 0 Rabbit 10.0 pKd = 10 Functional
Antagonistic ability of angiotensin II to contract rabbit aortaAntagonistic ability of angiotensin II to contract rabbit aorta
ChEMBL 466 8 1 7 5.4 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2nc(OC(C)C)ccc2n1 10.1021/jm00070a012
15657904 186889 4 None - 0 Rabbit 9.9 pKd = 9.9 Functional
Antagonist activity at angiotensin AT1 receptor in rabbit aortaAntagonist activity at angiotensin AT1 receptor in rabbit aorta
ChEMBL 415 8 2 7 3.4 CCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1ncncc1C(=O)O 10.1016/j.bmc.2010.10.043
CHEMBL49410 186889 4 None - 0 Rabbit 9.9 pKd = 9.9 Functional
Antagonist activity at angiotensin AT1 receptor in rabbit aortaAntagonist activity at angiotensin AT1 receptor in rabbit aorta
ChEMBL 415 8 2 7 3.4 CCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1ncncc1C(=O)O 10.1016/j.bmc.2010.10.043
19017678 175569 0 None - 0 Human 9.3 pKd = 9.3 Functional
Antagonist activity at angiotensin AT1 receptorAntagonist activity at angiotensin AT1 receptor
ChEMBL 474 11 2 8 4.3 CCCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1nnn(CC(C)C)c1C(=O)O 10.1016/j.bmc.2010.10.043
CHEMBL45927 175569 0 None - 0 Human 9.3 pKd = 9.3 Functional
Antagonist activity at angiotensin AT1 receptorAntagonist activity at angiotensin AT1 receptor
ChEMBL 474 11 2 8 4.3 CCCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1nnn(CC(C)C)c1C(=O)O 10.1016/j.bmc.2010.10.043
9935096 206026 0 None - 1 Human 9.3 pKd = 9.3 Functional
Antagonist activity at angiotensin AT1 receptorAntagonist activity at angiotensin AT1 receptor
ChEMBL 485 8 1 7 5.3 CCCCc1cn([C@@H]2[C@@H](C)CCC[C@H]2C)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)nc1 10.1016/j.bmc.2010.10.043
CHEMBL9599 206026 0 None - 1 Human 9.3 pKd = 9.3 Functional
Antagonist activity at angiotensin AT1 receptorAntagonist activity at angiotensin AT1 receptor
ChEMBL 485 8 1 7 5.3 CCCCc1cn([C@@H]2[C@@H](C)CCC[C@H]2C)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)nc1 10.1016/j.bmc.2010.10.043
44373246 167693 0 None - 1 Rabbit 9.2 pKd = 9.2 Functional
Antagonist activity at angiotensin AT1 receptor in rabbit aortic strip assessed as inhibition of angiotensin 2-induced contractile responseAntagonist activity at angiotensin AT1 receptor in rabbit aortic strip assessed as inhibition of angiotensin 2-induced contractile response
ChEMBL 435 5 1 6 4.5 CCc1nc2c(C)cc(C)nc2n1Cc1ccc2c(c1)C(Cc1nnn[nH]1)c1ccccc1-2 10.1016/j.bmc.2010.10.043
CHEMBL433895 167693 0 None - 1 Rabbit 9.2 pKd = 9.2 Functional
Antagonist activity at angiotensin AT1 receptor in rabbit aortic strip assessed as inhibition of angiotensin 2-induced contractile responseAntagonist activity at angiotensin AT1 receptor in rabbit aortic strip assessed as inhibition of angiotensin 2-induced contractile response
ChEMBL 435 5 1 6 4.5 CCc1nc2c(C)cc(C)nc2n1Cc1ccc2c(c1)C(Cc1nnn[nH]1)c1ccccc1-2 10.1016/j.bmc.2010.10.043
CHEMBL2373017 208599 0 None - 0 Rat 9.1 pKd = 9.1 Functional
pA2 value for Angiotensin II receptorpA2 value for Angiotensin II receptor
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@@H]1CCCN1C(=O)[C@H](Cc1c[nH]cn1)NC(=O)[C@@H]1CCSSCC[C@H](NC(=O)[C@H](CCCN=C(N)N)NC(=O)CNC)C(=O)N[C@@H](Cc2ccc(O)cc2)C(=O)N1)C(=O)O 10.1021/jm00169a019
9912059 184764 0 None - 1 Rabbit 9.0 pKd = 9 Functional
Antagonist activity at angiotensin AT1 receptor in rabbit aortaAntagonist activity at angiotensin AT1 receptor in rabbit aorta
ChEMBL 459 7 1 6 4.5 CCOC(=O)/C=C1\CC(C)(CC)CC(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.bmc.2010.10.043
CHEMBL48602 184764 0 None - 1 Rabbit 9.0 pKd = 9 Functional
Antagonist activity at angiotensin AT1 receptor in rabbit aortaAntagonist activity at angiotensin AT1 receptor in rabbit aorta
ChEMBL 459 7 1 6 4.5 CCOC(=O)/C=C1\CC(C)(CC)CC(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.bmc.2010.10.043
131654 204667 10 None 1 2 Rabbit 8.9 pKd = 8.9 Functional
Antagonist activity at angiotensin AT1 receptor in rabbit aorta assessed as reduction of angiotensin 2-induced contractile responseAntagonist activity at angiotensin AT1 receptor in rabbit aorta assessed as reduction of angiotensin 2-induced contractile response
ChEMBL 431 10 1 7 4.1 CCCCc1nn(CCCC)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.bmc.2010.10.043
CHEMBL87778 204667 10 None 1 2 Rabbit 8.9 pKd = 8.9 Functional
Antagonist activity at angiotensin AT1 receptor in rabbit aorta assessed as reduction of angiotensin 2-induced contractile responseAntagonist activity at angiotensin AT1 receptor in rabbit aorta assessed as reduction of angiotensin 2-induced contractile response
ChEMBL 431 10 1 7 4.1 CCCCc1nn(CCCC)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.bmc.2010.10.043
9801006 119211 0 None - 1 Rabbit 8.8 pKd = 8.8 Functional
Antagonist activity at angiotensin AT1 receptor in rabbit aortaAntagonist activity at angiotensin AT1 receptor in rabbit aorta
ChEMBL 398 6 1 7 3.6 CCc1nc2c(CC)cn(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)n2n1 10.1016/j.bmc.2010.10.043
CHEMBL347610 119211 0 None - 1 Rabbit 8.8 pKd = 8.8 Functional
Antagonist activity at angiotensin AT1 receptor in rabbit aortaAntagonist activity at angiotensin AT1 receptor in rabbit aorta
ChEMBL 398 6 1 7 3.6 CCc1nc2c(CC)cn(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)n2n1 10.1016/j.bmc.2010.10.043
178553 119726 10 None - 0 Rabbit 8.8 pKd = 8.8 Functional
Antagonist activity at angiotensin AT1 receptor in rabbit aorta assessed as reduction of angiotensin 2-induced contractile responseAntagonist activity at angiotensin AT1 receptor in rabbit aorta assessed as reduction of angiotensin 2-induced contractile response
ChEMBL 387 6 1 6 4.1 COc1c(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)cc(C)nc1C 10.1016/j.bmc.2010.10.043
CHEMBL352257 119726 10 None - 0 Rabbit 8.8 pKd = 8.8 Functional
Antagonist activity at angiotensin AT1 receptor in rabbit aorta assessed as reduction of angiotensin 2-induced contractile responseAntagonist activity at angiotensin AT1 receptor in rabbit aorta assessed as reduction of angiotensin 2-induced contractile response
ChEMBL 387 6 1 6 4.1 COc1c(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)cc(C)nc1C 10.1016/j.bmc.2010.10.043
70682146 75963 0 None - 1 Rabbit 8.8 pKd = 8.8 Functional
Antagonist activity at AT1 receptor in Japanese white rabbit thoracic aorta assessed as inhibition of KCl-induced contraction incubated 30 mins post KCl-induction for 1 hrAntagonist activity at AT1 receptor in Japanese white rabbit thoracic aorta assessed as inhibition of KCl-induced contraction incubated 30 mins post KCl-induction for 1 hr
ChEMBL 569 10 2 6 6.7 CCCc1nc2c(C)cc(C(=O)NCC(C)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmc.2012.05.056
CHEMBL2058860 75963 0 None - 1 Rabbit 8.8 pKd = 8.8 Functional
Antagonist activity at AT1 receptor in Japanese white rabbit thoracic aorta assessed as inhibition of KCl-induced contraction incubated 30 mins post KCl-induction for 1 hrAntagonist activity at AT1 receptor in Japanese white rabbit thoracic aorta assessed as inhibition of KCl-induced contraction incubated 30 mins post KCl-induction for 1 hr
ChEMBL 569 10 2 6 6.7 CCCc1nc2c(C)cc(C(=O)NCC(C)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmc.2012.05.056
46910493 75967 0 None - 1 Rabbit 8.7 pKd = 8.7 Functional
Antagonist activity at AT1 receptor in Japanese white rabbit thoracic aorta assessed as inhibition of KCl-induced contraction incubated 30 mins post KCl-induction for 1 hrAntagonist activity at AT1 receptor in Japanese white rabbit thoracic aorta assessed as inhibition of KCl-induced contraction incubated 30 mins post KCl-induction for 1 hr
ChEMBL 615 12 2 8 6.2 CCCc1nc2c(C)cc(C(=O)NCCc3ccc(OC)c(OC)c3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmc.2012.05.056
CHEMBL2058864 75967 0 None - 1 Rabbit 8.7 pKd = 8.7 Functional
Antagonist activity at AT1 receptor in Japanese white rabbit thoracic aorta assessed as inhibition of KCl-induced contraction incubated 30 mins post KCl-induction for 1 hrAntagonist activity at AT1 receptor in Japanese white rabbit thoracic aorta assessed as inhibition of KCl-induced contraction incubated 30 mins post KCl-induction for 1 hr
ChEMBL 615 12 2 8 6.2 CCCc1nc2c(C)cc(C(=O)NCCc3ccc(OC)c(OC)c3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmc.2012.05.056
9931685 204354 0 None 1 2 Human 8.7 pKd = 8.7 Functional
Antagonist activity at angiotensin AT1 receptorAntagonist activity at angiotensin AT1 receptor
ChEMBL 415 10 1 6 4.9 CCCCc1nc(CCCC)n(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)n1 10.1016/j.bmc.2010.10.043
CHEMBL85595 204354 0 None 1 2 Human 8.7 pKd = 8.7 Functional
Antagonist activity at angiotensin AT1 receptorAntagonist activity at angiotensin AT1 receptor
ChEMBL 415 10 1 6 4.9 CCCCc1nc(CCCC)n(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)n1 10.1016/j.bmc.2010.10.043
131857 202547 16 None - 0 Rabbit 8.7 pKd = 8.7 Functional
Antagonist activity at angiotensin AT1 receptor in rabbit aortaAntagonist activity at angiotensin AT1 receptor in rabbit aorta
ChEMBL 383 5 1 4 5.0 Cc1ccnc2c1nc(C1CC1)n2Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.bmc.2010.10.043
CHEMBL71162 202547 16 None - 0 Rabbit 8.7 pKd = 8.7 Functional
Antagonist activity at angiotensin AT1 receptor in rabbit aortaAntagonist activity at angiotensin AT1 receptor in rabbit aorta
ChEMBL 383 5 1 4 5.0 Cc1ccnc2c1nc(C1CC1)n2Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.bmc.2010.10.043
44438885 90509 0 None - 1 Rabbit 8.0 pKd = 8 Functional
Antagonist activity at AT1 receptor assessed inhibition of angiotensin-2-induced contraction of rabbit thoracic aortic ringsAntagonist activity at AT1 receptor assessed inhibition of angiotensin-2-induced contraction of rabbit thoracic aortic rings
ChEMBL 417 8 2 5 4.6 CCCCc1nc2cccc(C(=O)O)c2n1Cc1ccc(-n2cccc2C(=O)O)cc1 10.1016/j.bmcl.2007.02.042
CHEMBL239378 90509 0 None - 1 Rabbit 8.0 pKd = 8 Functional
Antagonist activity at AT1 receptor assessed inhibition of angiotensin-2-induced contraction of rabbit thoracic aortic ringsAntagonist activity at AT1 receptor assessed inhibition of angiotensin-2-induced contraction of rabbit thoracic aortic rings
ChEMBL 417 8 2 5 4.6 CCCCc1nc2cccc(C(=O)O)c2n1Cc1ccc(-n2cccc2C(=O)O)cc1 10.1016/j.bmcl.2007.02.042
2541 772 113 None - 7 Rat 8.0 pKd = 8 Functional
Antagonist activity at AT1 receptor in rat aortaAntagonist activity at AT1 receptor in rat aorta
ChEMBL 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10.1016/j.ejmech.2007.11.008
587 772 113 None - 7 Rat 8.0 pKd = 8 Functional
Antagonist activity at AT1 receptor in rat aortaAntagonist activity at AT1 receptor in rat aorta
ChEMBL 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10.1016/j.ejmech.2007.11.008
6907 772 113 None - 7 Rat 8.0 pKd = 8 Functional
Antagonist activity at AT1 receptor in rat aortaAntagonist activity at AT1 receptor in rat aorta
ChEMBL 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10.1016/j.ejmech.2007.11.008
CHEMBL1016 772 113 None - 7 Rat 8.0 pKd = 8 Functional
Antagonist activity at AT1 receptor in rat aortaAntagonist activity at AT1 receptor in rat aorta
ChEMBL 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10.1016/j.ejmech.2007.11.008
DB00796 772 113 None - 7 Rat 8.0 pKd = 8 Functional
Antagonist activity at AT1 receptor in rat aortaAntagonist activity at AT1 receptor in rat aorta
ChEMBL 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10.1016/j.ejmech.2007.11.008
DB13919 772 113 None - 7 Rat 8.0 pKd = 8 Functional
Antagonist activity at AT1 receptor in rat aortaAntagonist activity at AT1 receptor in rat aorta
ChEMBL 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10.1016/j.ejmech.2007.11.008
10094851 21082 0 None - 1 Rat 8.0 pKd = 8 Functional
Antagonist activity at AT1 receptor in rat aortaAntagonist activity at AT1 receptor in rat aorta
ChEMBL 441 8 2 4 5.8 CCCCc1nc2cc(NC(C)=O)ccc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2007.11.008
CHEMBL131365 21082 0 None - 1 Rat 8.0 pKd = 8 Functional
Antagonist activity at AT1 receptor in rat aortaAntagonist activity at AT1 receptor in rat aorta
ChEMBL 441 8 2 4 5.8 CCCCc1nc2cc(NC(C)=O)ccc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2007.11.008
1610 2305 89 None 1 9 Rat 8.0 pKd = 8 Functional
Antagonist activity at AT1 receptor in rat aortic ringsAntagonist activity at AT1 receptor in rat aortic rings
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmc.2008.10.056
3941 2305 89 None 1 9 Rat 8.0 pKd = 8 Functional
Antagonist activity at AT1 receptor in rat aortic ringsAntagonist activity at AT1 receptor in rat aortic rings
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmc.2008.10.056
3961 2305 89 None 1 9 Rat 8.0 pKd = 8 Functional
Antagonist activity at AT1 receptor in rat aortic ringsAntagonist activity at AT1 receptor in rat aortic rings
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmc.2008.10.056
590 2305 89 None 1 9 Rat 8.0 pKd = 8 Functional
Antagonist activity at AT1 receptor in rat aortic ringsAntagonist activity at AT1 receptor in rat aortic rings
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmc.2008.10.056
CHEMBL191 2305 89 None 1 9 Rat 8.0 pKd = 8 Functional
Antagonist activity at AT1 receptor in rat aortic ringsAntagonist activity at AT1 receptor in rat aortic rings
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmc.2008.10.056
DB00678 2305 89 None 1 9 Rat 8.0 pKd = 8 Functional
Antagonist activity at AT1 receptor in rat aortic ringsAntagonist activity at AT1 receptor in rat aortic rings
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmc.2008.10.056
24827770 95423 0 None - 1 Rabbit 8.0 pKd = 8.0 Functional
Antagonist activity at AT1 receptor in KCl-contracted rabbit aortic strips after 60 minsAntagonist activity at AT1 receptor in KCl-contracted rabbit aortic strips after 60 mins
ChEMBL 425 7 1 7 3.9 CCCCn1c(=O)c2cccnc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm7011563
CHEMBL259114 95423 0 None - 1 Rabbit 8.0 pKd = 8.0 Functional
Antagonist activity at AT1 receptor in KCl-contracted rabbit aortic strips after 60 minsAntagonist activity at AT1 receptor in KCl-contracted rabbit aortic strips after 60 mins
ChEMBL 425 7 1 7 3.9 CCCCn1c(=O)c2cccnc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm7011563
44438869 145790 0 None - 1 Rabbit 7.0 pKd = 7 Functional
Antagonist activity at AT1 receptor assessed inhibition of angiotensin-2-induced contraction of rabbit thoracic aortic ringsAntagonist activity at AT1 receptor assessed inhibition of angiotensin-2-induced contraction of rabbit thoracic aortic rings
ChEMBL 413 5 1 8 3.2 COC(=O)c1cccc2nc(C)n(Cc3ccc(-n4cccc4-c4nnn[nH]4)cc3)c12 10.1016/j.bmcl.2007.02.042
CHEMBL392118 145790 0 None - 1 Rabbit 7.0 pKd = 7 Functional
Antagonist activity at AT1 receptor assessed inhibition of angiotensin-2-induced contraction of rabbit thoracic aortic ringsAntagonist activity at AT1 receptor assessed inhibition of angiotensin-2-induced contraction of rabbit thoracic aortic rings
ChEMBL 413 5 1 8 3.2 COC(=O)c1cccc2nc(C)n(Cc3ccc(-n4cccc4-c4nnn[nH]4)cc3)c12 10.1016/j.bmcl.2007.02.042
44438900 147303 0 None - 1 Rabbit 7.0 pKd = 7 Functional
Antagonist activity at AT1 receptor assessed inhibition of angiotensin-2-induced contraction of rabbit thoracic aortic ringsAntagonist activity at AT1 receptor assessed inhibition of angiotensin-2-induced contraction of rabbit thoracic aortic rings
ChEMBL 403 7 2 5 4.2 CCCc1nc2cccc(C(=O)O)c2n1Cc1ccc(-n2cccc2C(=O)O)cc1 10.1016/j.bmcl.2007.02.042
CHEMBL393305 147303 0 None - 1 Rabbit 7.0 pKd = 7 Functional
Antagonist activity at AT1 receptor assessed inhibition of angiotensin-2-induced contraction of rabbit thoracic aortic ringsAntagonist activity at AT1 receptor assessed inhibition of angiotensin-2-induced contraction of rabbit thoracic aortic rings
ChEMBL 403 7 2 5 4.2 CCCc1nc2cccc(C(=O)O)c2n1Cc1ccc(-n2cccc2C(=O)O)cc1 10.1016/j.bmcl.2007.02.042
44570265 177824 0 None - 0 Rat 7.0 pKd = 7 Functional
Antagonist activity at AT1 receptor in rat aortic ringsAntagonist activity at AT1 receptor in rat aortic rings
ChEMBL 519 12 2 5 5.9 CCCCNS(=O)(=O)c1ccc2c(c1)nc(CCCC)n2Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.bmc.2008.10.056
CHEMBL465929 177824 0 None - 0 Rat 7.0 pKd = 7 Functional
Antagonist activity at AT1 receptor in rat aortic ringsAntagonist activity at AT1 receptor in rat aortic rings
ChEMBL 519 12 2 5 5.9 CCCCNS(=O)(=O)c1ccc2c(c1)nc(CCCC)n2Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.bmc.2008.10.056
19351553 118180 0 None - 0 Rabbit 7.0 pKd = 7 Functional
Antagonist activity at angiotensin AT1 receptor in rabbit aortaAntagonist activity at angiotensin AT1 receptor in rabbit aorta
ChEMBL 389 10 4 6 3.1 CCCCCCC(C(=O)O)n1cnc(NC(=O)c2cccc(O)c2C(=O)O)c1 10.1016/j.bmc.2010.10.043
CHEMBL341716 118180 0 None - 0 Rabbit 7.0 pKd = 7 Functional
Antagonist activity at angiotensin AT1 receptor in rabbit aortaAntagonist activity at angiotensin AT1 receptor in rabbit aorta
ChEMBL 389 10 4 6 3.1 CCCCCCC(C(=O)O)n1cnc(NC(=O)c2cccc(O)c2C(=O)O)c1 10.1016/j.bmc.2010.10.043
CHEMBL264230 208854 0 None - 0 Rabbit 7.0 pKd = 7.0 Functional
Negative log of the dose of antagonist (compound) that reduces response of a double dose of Angiotensin II receptor, type 1 to that of a single dose, on rabbit aortaNegative log of the dose of antagonist (compound) that reduces response of a double dose of Angiotensin II receptor, type 1 to that of a single dose, on rabbit aorta
ChEMBL None None None CC(=O)N[C@@H](CO)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)N1CCC[C@H]1C(=O)N[C@H](Cc1cccc2ccccc12)C(=O)O)C(C)C)C(C)C 10.1021/jm9608669
CHEMBL384349 210566 0 None - 0 Rabbit 7.0 pKd = 7.0 Functional
Negative log of the dose of antagonist (compound) that reduces response of a double dose of Angiotensin II receptor, type 1 to that of a single dose, on rabbit aortaNegative log of the dose of antagonist (compound) that reduces response of a double dose of Angiotensin II receptor, type 1 to that of a single dose, on rabbit aorta
ChEMBL None None None CCCCCCCCCCCCCCCC(=O)Oc1ccc(C[C@H](NC(=O)[C@@H](NC(=O)[C@H](CCCN=C(N)N)NC(=O)CNC)C(C)C)C(=O)N[C@H](C(=O)N[C@@H](Cc2c[nH]cn2)C(=O)N2CCC[C@H]2C(=O)N[C@H](Cc2ccc3ccccc3c2)C(=O)O)C(C)C)cc1 10.1021/jm9608669
1610 2305 89 None -2 9 Rabbit 7.9 pKd = 7.9 Functional
Antagonist activity at AT1 receptor assessed inhibition of angiotensin-2-induced contraction of rabbit thoracic aortic ringsAntagonist activity at AT1 receptor assessed inhibition of angiotensin-2-induced contraction of rabbit thoracic aortic rings
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmcl.2007.02.042
3941 2305 89 None -2 9 Rabbit 7.9 pKd = 7.9 Functional
Antagonist activity at AT1 receptor assessed inhibition of angiotensin-2-induced contraction of rabbit thoracic aortic ringsAntagonist activity at AT1 receptor assessed inhibition of angiotensin-2-induced contraction of rabbit thoracic aortic rings
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmcl.2007.02.042
3961 2305 89 None -2 9 Rabbit 7.9 pKd = 7.9 Functional
Antagonist activity at AT1 receptor assessed inhibition of angiotensin-2-induced contraction of rabbit thoracic aortic ringsAntagonist activity at AT1 receptor assessed inhibition of angiotensin-2-induced contraction of rabbit thoracic aortic rings
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmcl.2007.02.042
590 2305 89 None -2 9 Rabbit 7.9 pKd = 7.9 Functional
Antagonist activity at AT1 receptor assessed inhibition of angiotensin-2-induced contraction of rabbit thoracic aortic ringsAntagonist activity at AT1 receptor assessed inhibition of angiotensin-2-induced contraction of rabbit thoracic aortic rings
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmcl.2007.02.042
CHEMBL191 2305 89 None -2 9 Rabbit 7.9 pKd = 7.9 Functional
Antagonist activity at AT1 receptor assessed inhibition of angiotensin-2-induced contraction of rabbit thoracic aortic ringsAntagonist activity at AT1 receptor assessed inhibition of angiotensin-2-induced contraction of rabbit thoracic aortic rings
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmcl.2007.02.042
DB00678 2305 89 None -2 9 Rabbit 7.9 pKd = 7.9 Functional
Antagonist activity at AT1 receptor assessed inhibition of angiotensin-2-induced contraction of rabbit thoracic aortic ringsAntagonist activity at AT1 receptor assessed inhibition of angiotensin-2-induced contraction of rabbit thoracic aortic rings
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmcl.2007.02.042
44438865 92930 0 None - 1 Rabbit 7.9 pKd = 7.9 Functional
Antagonist activity at AT1 receptor assessed inhibition of angiotensin-2-induced contraction of rabbit thoracic aortic ringsAntagonist activity at AT1 receptor assessed inhibition of angiotensin-2-induced contraction of rabbit thoracic aortic rings
ChEMBL 441 7 1 8 3.8 CCCc1nc2cccc(C(=O)OC)c2n1Cc1ccc(-n2cccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2007.02.042
CHEMBL245644 92930 0 None - 1 Rabbit 7.9 pKd = 7.9 Functional
Antagonist activity at AT1 receptor assessed inhibition of angiotensin-2-induced contraction of rabbit thoracic aortic ringsAntagonist activity at AT1 receptor assessed inhibition of angiotensin-2-induced contraction of rabbit thoracic aortic rings
ChEMBL 441 7 1 8 3.8 CCCc1nc2cccc(C(=O)OC)c2n1Cc1ccc(-n2cccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2007.02.042
1610 2305 89 None -2 9 Rabbit 7.9 pKd = 7.9 Functional
Antagonist activity at AT1 receptor in Japanese white rabbit thoracic aorta assessed as inhibition of KCl-induced contraction incubated 30 mins post KCl-induction for 1 hrAntagonist activity at AT1 receptor in Japanese white rabbit thoracic aorta assessed as inhibition of KCl-induced contraction incubated 30 mins post KCl-induction for 1 hr
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmc.2012.05.056
3941 2305 89 None -2 9 Rabbit 7.9 pKd = 7.9 Functional
Antagonist activity at AT1 receptor in Japanese white rabbit thoracic aorta assessed as inhibition of KCl-induced contraction incubated 30 mins post KCl-induction for 1 hrAntagonist activity at AT1 receptor in Japanese white rabbit thoracic aorta assessed as inhibition of KCl-induced contraction incubated 30 mins post KCl-induction for 1 hr
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmc.2012.05.056
3961 2305 89 None -2 9 Rabbit 7.9 pKd = 7.9 Functional
Antagonist activity at AT1 receptor in Japanese white rabbit thoracic aorta assessed as inhibition of KCl-induced contraction incubated 30 mins post KCl-induction for 1 hrAntagonist activity at AT1 receptor in Japanese white rabbit thoracic aorta assessed as inhibition of KCl-induced contraction incubated 30 mins post KCl-induction for 1 hr
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmc.2012.05.056
590 2305 89 None -2 9 Rabbit 7.9 pKd = 7.9 Functional
Antagonist activity at AT1 receptor in Japanese white rabbit thoracic aorta assessed as inhibition of KCl-induced contraction incubated 30 mins post KCl-induction for 1 hrAntagonist activity at AT1 receptor in Japanese white rabbit thoracic aorta assessed as inhibition of KCl-induced contraction incubated 30 mins post KCl-induction for 1 hr
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmc.2012.05.056
CHEMBL191 2305 89 None -2 9 Rabbit 7.9 pKd = 7.9 Functional
Antagonist activity at AT1 receptor in Japanese white rabbit thoracic aorta assessed as inhibition of KCl-induced contraction incubated 30 mins post KCl-induction for 1 hrAntagonist activity at AT1 receptor in Japanese white rabbit thoracic aorta assessed as inhibition of KCl-induced contraction incubated 30 mins post KCl-induction for 1 hr
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmc.2012.05.056
DB00678 2305 89 None -2 9 Rabbit 7.9 pKd = 7.9 Functional
Antagonist activity at AT1 receptor in Japanese white rabbit thoracic aorta assessed as inhibition of KCl-induced contraction incubated 30 mins post KCl-induction for 1 hrAntagonist activity at AT1 receptor in Japanese white rabbit thoracic aorta assessed as inhibition of KCl-induced contraction incubated 30 mins post KCl-induction for 1 hr
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmc.2012.05.056
44570305 189714 0 None - 0 Rat 7.9 pKd = 7.9 Functional
Antagonist activity at AT1 receptor in rat aortic ringsAntagonist activity at AT1 receptor in rat aortic rings
ChEMBL 545 10 2 5 6.4 CCCCc1nc2cc(S(=O)(=O)NC3CCCCC3)ccc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.bmc.2008.10.056
CHEMBL517626 189714 0 None - 0 Rat 7.9 pKd = 7.9 Functional
Antagonist activity at AT1 receptor in rat aortic ringsAntagonist activity at AT1 receptor in rat aortic rings
ChEMBL 545 10 2 5 6.4 CCCCc1nc2cc(S(=O)(=O)NC3CCCCC3)ccc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.bmc.2008.10.056
1610 2305 89 None -2 9 Rabbit 7.9 pKd = 7.9 Functional
Antagonist activity at angiotensin 2 AT1 receptor in Japanese White rabbits thoracic aorta assessed as inhibition of KCl-indcuced contraction after 60 minsAntagonist activity at angiotensin 2 AT1 receptor in Japanese White rabbits thoracic aorta assessed as inhibition of KCl-indcuced contraction after 60 mins
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.ejmech.2012.01.009
3941 2305 89 None -2 9 Rabbit 7.9 pKd = 7.9 Functional
Antagonist activity at angiotensin 2 AT1 receptor in Japanese White rabbits thoracic aorta assessed as inhibition of KCl-indcuced contraction after 60 minsAntagonist activity at angiotensin 2 AT1 receptor in Japanese White rabbits thoracic aorta assessed as inhibition of KCl-indcuced contraction after 60 mins
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.ejmech.2012.01.009
3961 2305 89 None -2 9 Rabbit 7.9 pKd = 7.9 Functional
Antagonist activity at angiotensin 2 AT1 receptor in Japanese White rabbits thoracic aorta assessed as inhibition of KCl-indcuced contraction after 60 minsAntagonist activity at angiotensin 2 AT1 receptor in Japanese White rabbits thoracic aorta assessed as inhibition of KCl-indcuced contraction after 60 mins
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.ejmech.2012.01.009
590 2305 89 None -2 9 Rabbit 7.9 pKd = 7.9 Functional
Antagonist activity at angiotensin 2 AT1 receptor in Japanese White rabbits thoracic aorta assessed as inhibition of KCl-indcuced contraction after 60 minsAntagonist activity at angiotensin 2 AT1 receptor in Japanese White rabbits thoracic aorta assessed as inhibition of KCl-indcuced contraction after 60 mins
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.ejmech.2012.01.009
CHEMBL191 2305 89 None -2 9 Rabbit 7.9 pKd = 7.9 Functional
Antagonist activity at angiotensin 2 AT1 receptor in Japanese White rabbits thoracic aorta assessed as inhibition of KCl-indcuced contraction after 60 minsAntagonist activity at angiotensin 2 AT1 receptor in Japanese White rabbits thoracic aorta assessed as inhibition of KCl-indcuced contraction after 60 mins
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.ejmech.2012.01.009
DB00678 2305 89 None -2 9 Rabbit 7.9 pKd = 7.9 Functional
Antagonist activity at angiotensin 2 AT1 receptor in Japanese White rabbits thoracic aorta assessed as inhibition of KCl-indcuced contraction after 60 minsAntagonist activity at angiotensin 2 AT1 receptor in Japanese White rabbits thoracic aorta assessed as inhibition of KCl-indcuced contraction after 60 mins
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.ejmech.2012.01.009
44348352 16336 0 None 1 2 Rabbit 7.9 pKd = 7.9 Functional
Antagonist activity at angiotensin AT1 receptor in rabbit aortic strip assessed as inhibition of angiotensin 2-induced contractile responseAntagonist activity at angiotensin AT1 receptor in rabbit aortic strip assessed as inhibition of angiotensin 2-induced contractile response
ChEMBL 459 8 1 6 4.5 CCOC(=O)/C=C1\N(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)C(=O)CC1(CC)CC 10.1016/j.bmc.2010.10.043
CHEMBL123713 16336 0 None 1 2 Rabbit 7.9 pKd = 7.9 Functional
Antagonist activity at angiotensin AT1 receptor in rabbit aortic strip assessed as inhibition of angiotensin 2-induced contractile responseAntagonist activity at angiotensin AT1 receptor in rabbit aortic strip assessed as inhibition of angiotensin 2-induced contractile response
ChEMBL 459 8 1 6 4.5 CCOC(=O)/C=C1\N(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)C(=O)CC1(CC)CC 10.1016/j.bmc.2010.10.043
1610 2305 89 None -2 9 Rabbit 7.9 pKd = 7.9 Functional
Antagonist activity at angiotensin AT1 receptor in rabbit thoracic aortic ringsAntagonist activity at angiotensin AT1 receptor in rabbit thoracic aortic rings
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmc.2010.10.043
3941 2305 89 None -2 9 Rabbit 7.9 pKd = 7.9 Functional
Antagonist activity at angiotensin AT1 receptor in rabbit thoracic aortic ringsAntagonist activity at angiotensin AT1 receptor in rabbit thoracic aortic rings
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmc.2010.10.043
3961 2305 89 None -2 9 Rabbit 7.9 pKd = 7.9 Functional
Antagonist activity at angiotensin AT1 receptor in rabbit thoracic aortic ringsAntagonist activity at angiotensin AT1 receptor in rabbit thoracic aortic rings
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmc.2010.10.043
590 2305 89 None -2 9 Rabbit 7.9 pKd = 7.9 Functional
Antagonist activity at angiotensin AT1 receptor in rabbit thoracic aortic ringsAntagonist activity at angiotensin AT1 receptor in rabbit thoracic aortic rings
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmc.2010.10.043
CHEMBL191 2305 89 None -2 9 Rabbit 7.9 pKd = 7.9 Functional
Antagonist activity at angiotensin AT1 receptor in rabbit thoracic aortic ringsAntagonist activity at angiotensin AT1 receptor in rabbit thoracic aortic rings
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmc.2010.10.043
DB00678 2305 89 None -2 9 Rabbit 7.9 pKd = 7.9 Functional
Antagonist activity at angiotensin AT1 receptor in rabbit thoracic aortic ringsAntagonist activity at angiotensin AT1 receptor in rabbit thoracic aortic rings
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmc.2010.10.043
44570215 182959 0 None - 0 Rat 6.9 pKd = 6.9 Functional
Antagonist activity at AT1 receptor in rat aortic ringsAntagonist activity at AT1 receptor in rat aortic rings
ChEMBL 477 9 2 5 4.7 CCCCc1nc2cc(S(=O)(=O)NC)ccc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.bmc.2008.10.056
CHEMBL480018 182959 0 None - 0 Rat 6.9 pKd = 6.9 Functional
Antagonist activity at AT1 receptor in rat aortic ringsAntagonist activity at AT1 receptor in rat aortic rings
ChEMBL 477 9 2 5 4.7 CCCCc1nc2cc(S(=O)(=O)NC)ccc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.bmc.2008.10.056
9906367 51855 0 None - 0 Human 6.9 pKd = 6.9 Functional
Antagonist activity at angiotensin AT1 receptorAntagonist activity at angiotensin AT1 receptor
ChEMBL 349 4 1 5 3.1 C[C@H]1CN(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)C[C@@H](C)O1 10.1016/j.bmc.2010.10.043
CHEMBL158794 51855 0 None - 0 Human 6.9 pKd = 6.9 Functional
Antagonist activity at angiotensin AT1 receptorAntagonist activity at angiotensin AT1 receptor
ChEMBL 349 4 1 5 3.1 C[C@H]1CN(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)C[C@@H](C)O1 10.1016/j.bmc.2010.10.043
44438902 168819 0 None - 1 Rabbit 5.9 pKd = 5.9 Functional
Antagonist activity at AT1 receptor assessed inhibition of angiotensin-2-induced contraction of rabbit thoracic aortic ringsAntagonist activity at AT1 receptor assessed inhibition of angiotensin-2-induced contraction of rabbit thoracic aortic rings
ChEMBL 375 5 2 5 3.6 Cc1nc2cccc(C(=O)O)c2n1Cc1ccc(-n2cccc2C(=O)O)cc1 10.1016/j.bmcl.2007.02.042
CHEMBL442251 168819 0 None - 1 Rabbit 5.9 pKd = 5.9 Functional
Antagonist activity at AT1 receptor assessed inhibition of angiotensin-2-induced contraction of rabbit thoracic aortic ringsAntagonist activity at AT1 receptor assessed inhibition of angiotensin-2-induced contraction of rabbit thoracic aortic rings
ChEMBL 375 5 2 5 3.6 Cc1nc2cccc(C(=O)O)c2n1Cc1ccc(-n2cccc2C(=O)O)cc1 10.1016/j.bmcl.2007.02.042
46910495 75964 0 None - 1 Rabbit 7.8 pKd = 7.8 Functional
Antagonist activity at AT1 receptor in Japanese white rabbit thoracic aorta assessed as inhibition of KCl-induced contraction incubated 30 mins post KCl-induction for 1 hrAntagonist activity at AT1 receptor in Japanese white rabbit thoracic aorta assessed as inhibition of KCl-induced contraction incubated 30 mins post KCl-induction for 1 hr
ChEMBL 585 11 2 7 6.2 CCCc1nc2c(C)cc(C(=O)NCCc3cccc(OC)c3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmc.2012.05.056
CHEMBL2058861 75964 0 None - 1 Rabbit 7.8 pKd = 7.8 Functional
Antagonist activity at AT1 receptor in Japanese white rabbit thoracic aorta assessed as inhibition of KCl-induced contraction incubated 30 mins post KCl-induction for 1 hrAntagonist activity at AT1 receptor in Japanese white rabbit thoracic aorta assessed as inhibition of KCl-induced contraction incubated 30 mins post KCl-induction for 1 hr
ChEMBL 585 11 2 7 6.2 CCCc1nc2c(C)cc(C(=O)NCCc3cccc(OC)c3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmc.2012.05.056
24828707 95478 0 None - 1 Rabbit 7.8 pKd = 7.8 Functional
Antagonist activity at AT1 receptor in KCl-contracted rabbit aortic strips after 60 minsAntagonist activity at AT1 receptor in KCl-contracted rabbit aortic strips after 60 mins
ChEMBL 425 7 1 7 3.9 CCCCn1c2ncccc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm7011563
CHEMBL259353 95478 0 None - 1 Rabbit 7.8 pKd = 7.8 Functional
Antagonist activity at AT1 receptor in KCl-contracted rabbit aortic strips after 60 minsAntagonist activity at AT1 receptor in KCl-contracted rabbit aortic strips after 60 mins
ChEMBL 425 7 1 7 3.9 CCCCn1c2ncccc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm7011563
44438870 91559 0 None - 1 Rabbit 7.8 pKd = 7.8 Functional
Antagonist activity at AT1 receptor assessed inhibition of angiotensin-2-induced contraction of rabbit thoracic aortic ringsAntagonist activity at AT1 receptor assessed inhibition of angiotensin-2-induced contraction of rabbit thoracic aortic rings
ChEMBL 469 9 1 8 4.6 CCCCc1nc2cccc(C(=O)OCC)c2n1Cc1ccc(-n2cccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2007.02.042
CHEMBL241685 91559 0 None - 1 Rabbit 7.8 pKd = 7.8 Functional
Antagonist activity at AT1 receptor assessed inhibition of angiotensin-2-induced contraction of rabbit thoracic aortic ringsAntagonist activity at AT1 receptor assessed inhibition of angiotensin-2-induced contraction of rabbit thoracic aortic rings
ChEMBL 469 9 1 8 4.6 CCCCc1nc2cccc(C(=O)OCC)c2n1Cc1ccc(-n2cccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2007.02.042
10250336 18683 0 None - 1 Rat 7.8 pKd = 7.8 Functional
Antagonist activity at AT1 receptor in rat aortaAntagonist activity at AT1 receptor in rat aorta
ChEMBL 399 7 2 4 5.4 CCCCc1nc2cc(N)ccc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2007.11.008
CHEMBL128318 18683 0 None - 1 Rat 7.8 pKd = 7.8 Functional
Antagonist activity at AT1 receptor in rat aortaAntagonist activity at AT1 receptor in rat aorta
ChEMBL 399 7 2 4 5.4 CCCCc1nc2cc(N)ccc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2007.11.008
53323218 59921 0 None - 0 Guinea pig 7.8 pKd = 7.8 Functional
Antagonist activity at angiotensin AT1 receptor in guinea pig ileumAntagonist activity at angiotensin AT1 receptor in guinea pig ileum
ChEMBL 417 7 2 5 4.5 CCCc1nc2cc(C(=O)OC)[nH]c2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.bmc.2010.10.043
CHEMBL1668010 59921 0 None - 0 Guinea pig 7.8 pKd = 7.8 Functional
Antagonist activity at angiotensin AT1 receptor in guinea pig ileumAntagonist activity at angiotensin AT1 receptor in guinea pig ileum
ChEMBL 417 7 2 5 4.5 CCCc1nc2cc(C(=O)OC)[nH]c2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.bmc.2010.10.043
CHEMBL1741079 59921 0 None - 0 Guinea pig 7.8 pKd = 7.8 Functional
Antagonist activity at angiotensin AT1 receptor in guinea pig ileumAntagonist activity at angiotensin AT1 receptor in guinea pig ileum
ChEMBL 417 7 2 5 4.5 CCCc1nc2cc(C(=O)OC)[nH]c2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.bmc.2010.10.043
25110812 178451 0 None - 0 Rat 7.7 pKd = 7.7 Functional
Antagonist activity at AT1 receptor in rat aortaAntagonist activity at AT1 receptor in rat aorta
ChEMBL 455 9 2 4 6.1 CCCCc1nc2cc(NC(=O)CC)ccc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2007.11.008
CHEMBL471334 178451 0 None - 0 Rat 7.7 pKd = 7.7 Functional
Antagonist activity at AT1 receptor in rat aortaAntagonist activity at AT1 receptor in rat aorta
ChEMBL 455 9 2 4 6.1 CCCCc1nc2cc(NC(=O)CC)ccc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2007.11.008
1610 2305 89 None -2 9 Rabbit 6.7 pKd = 6.7 Functional
Antagonist activity at AT1 receptor in KCl-contracted rabbit aortic strips after 60 minsAntagonist activity at AT1 receptor in KCl-contracted rabbit aortic strips after 60 mins
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm7011563
3941 2305 89 None -2 9 Rabbit 6.7 pKd = 6.7 Functional
Antagonist activity at AT1 receptor in KCl-contracted rabbit aortic strips after 60 minsAntagonist activity at AT1 receptor in KCl-contracted rabbit aortic strips after 60 mins
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm7011563
3961 2305 89 None -2 9 Rabbit 6.7 pKd = 6.7 Functional
Antagonist activity at AT1 receptor in KCl-contracted rabbit aortic strips after 60 minsAntagonist activity at AT1 receptor in KCl-contracted rabbit aortic strips after 60 mins
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm7011563
590 2305 89 None -2 9 Rabbit 6.7 pKd = 6.7 Functional
Antagonist activity at AT1 receptor in KCl-contracted rabbit aortic strips after 60 minsAntagonist activity at AT1 receptor in KCl-contracted rabbit aortic strips after 60 mins
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm7011563
CHEMBL191 2305 89 None -2 9 Rabbit 6.7 pKd = 6.7 Functional
Antagonist activity at AT1 receptor in KCl-contracted rabbit aortic strips after 60 minsAntagonist activity at AT1 receptor in KCl-contracted rabbit aortic strips after 60 mins
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm7011563
DB00678 2305 89 None -2 9 Rabbit 6.7 pKd = 6.7 Functional
Antagonist activity at AT1 receptor in KCl-contracted rabbit aortic strips after 60 minsAntagonist activity at AT1 receptor in KCl-contracted rabbit aortic strips after 60 mins
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm7011563
44570214 182958 0 None - 0 Rat 6.7 pKd = 6.7 Functional
Antagonist activity at AT1 receptor in rat aortic ringsAntagonist activity at AT1 receptor in rat aortic rings
ChEMBL 463 8 2 5 4.4 CCCCc1nc2cc(S(N)(=O)=O)ccc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.bmc.2008.10.056
CHEMBL480017 182958 0 None - 0 Rat 6.7 pKd = 6.7 Functional
Antagonist activity at AT1 receptor in rat aortic ringsAntagonist activity at AT1 receptor in rat aortic rings
ChEMBL 463 8 2 5 4.4 CCCCc1nc2cc(S(N)(=O)=O)ccc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.bmc.2008.10.056
9932483 206098 0 None - 1 Human 8.7 pKd = 8.7 Functional
Antagonist activity at angiotensin AT1 receptorAntagonist activity at angiotensin AT1 receptor
ChEMBL 431 10 1 7 4.1 CCCCc1cn(CCCC)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)nc1 10.1016/j.bmc.2010.10.043
CHEMBL9642 206098 0 None - 1 Human 8.7 pKd = 8.7 Functional
Antagonist activity at angiotensin AT1 receptorAntagonist activity at angiotensin AT1 receptor
ChEMBL 431 10 1 7 4.1 CCCCc1cn(CCCC)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)nc1 10.1016/j.bmc.2010.10.043
9954408 206218 0 None - 1 Human 8.7 pKd = 8.7 Functional
Antagonist activity at angiotensin AT1 receptorAntagonist activity at angiotensin AT1 receptor
ChEMBL 430 10 1 6 4.7 CCCCc1cn(CCCC)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.bmc.2010.10.043
CHEMBL9714 206218 0 None - 1 Human 8.7 pKd = 8.7 Functional
Antagonist activity at angiotensin AT1 receptorAntagonist activity at angiotensin AT1 receptor
ChEMBL 430 10 1 6 4.7 CCCCc1cn(CCCC)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.bmc.2010.10.043
25112615 185299 0 None - 0 Rat 6.6 pKd = 6.6 Functional
Antagonist activity at AT1 receptor in rat aortaAntagonist activity at AT1 receptor in rat aorta
ChEMBL 503 9 2 4 7.0 CCCCc1nc2cc(NC(=O)c3ccccc3)ccc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2007.11.008
CHEMBL486847 185299 0 None - 0 Rat 6.6 pKd = 6.6 Functional
Antagonist activity at AT1 receptor in rat aortaAntagonist activity at AT1 receptor in rat aorta
ChEMBL 503 9 2 4 7.0 CCCCc1nc2cc(NC(=O)c3ccccc3)ccc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2007.11.008
44570306 177712 0 None - 0 Rat 6.6 pKd = 6.6 Functional
Antagonist activity at AT1 receptor in rat aortic ringsAntagonist activity at AT1 receptor in rat aortic rings
ChEMBL 464 8 2 5 5.0 CCCCc1nc2cc(S(=O)(=O)O)ccc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.bmc.2008.10.056
CHEMBL465097 177712 0 None - 0 Rat 6.6 pKd = 6.6 Functional
Antagonist activity at AT1 receptor in rat aortic ringsAntagonist activity at AT1 receptor in rat aortic rings
ChEMBL 464 8 2 5 5.0 CCCCc1nc2cc(S(=O)(=O)O)ccc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.bmc.2008.10.056
15224471 154283 0 None - 1 Rabbit 8.5 pKd = 8.5 Functional
Antagonist activity at AT1 receptor assessed inhibition of angiotensin-2-induced contraction of rabbit thoracic aortic ringsAntagonist activity at AT1 receptor assessed inhibition of angiotensin-2-induced contraction of rabbit thoracic aortic rings
ChEMBL 441 8 2 7 4.1 CCCCc1nc2cccc(C(=O)O)c2n1Cc1ccc(-n2cccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2007.02.042
CHEMBL400424 154283 0 None - 1 Rabbit 8.5 pKd = 8.5 Functional
Antagonist activity at AT1 receptor assessed inhibition of angiotensin-2-induced contraction of rabbit thoracic aortic ringsAntagonist activity at AT1 receptor assessed inhibition of angiotensin-2-induced contraction of rabbit thoracic aortic rings
ChEMBL 441 8 2 7 4.1 CCCCc1nc2cccc(C(=O)O)c2n1Cc1ccc(-n2cccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2007.02.042
2541 772 113 None - 7 Rat 8.5 pKd = 8.5 Functional
Antagonist activity at AT1 receptor in rat aortic ringsAntagonist activity at AT1 receptor in rat aortic rings
ChEMBL 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10.1016/j.bmc.2008.10.056
587 772 113 None - 7 Rat 8.5 pKd = 8.5 Functional
Antagonist activity at AT1 receptor in rat aortic ringsAntagonist activity at AT1 receptor in rat aortic rings
ChEMBL 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10.1016/j.bmc.2008.10.056
6907 772 113 None - 7 Rat 8.5 pKd = 8.5 Functional
Antagonist activity at AT1 receptor in rat aortic ringsAntagonist activity at AT1 receptor in rat aortic rings
ChEMBL 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10.1016/j.bmc.2008.10.056
CHEMBL1016 772 113 None - 7 Rat 8.5 pKd = 8.5 Functional
Antagonist activity at AT1 receptor in rat aortic ringsAntagonist activity at AT1 receptor in rat aortic rings
ChEMBL 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10.1016/j.bmc.2008.10.056
DB00796 772 113 None - 7 Rat 8.5 pKd = 8.5 Functional
Antagonist activity at AT1 receptor in rat aortic ringsAntagonist activity at AT1 receptor in rat aortic rings
ChEMBL 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10.1016/j.bmc.2008.10.056
DB13919 772 113 None - 7 Rat 8.5 pKd = 8.5 Functional
Antagonist activity at AT1 receptor in rat aortic ringsAntagonist activity at AT1 receptor in rat aortic rings
ChEMBL 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10.1016/j.bmc.2008.10.056
4110026 203217 1 None - 2 Rat 8.5 pKd = 8.5 Functional
Antagonist activity at AT1 receptor in rat aortic ringsAntagonist activity at AT1 receptor in rat aortic rings
ChEMBL 384 7 1 3 5.8 CCCCc1nc2ccccc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.bmc.2008.10.056
CHEMBL7632 203217 1 None - 2 Rat 8.5 pKd = 8.5 Functional
Antagonist activity at AT1 receptor in rat aortic ringsAntagonist activity at AT1 receptor in rat aortic rings
ChEMBL 384 7 1 3 5.8 CCCCc1nc2ccccc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.bmc.2008.10.056
57380647 69996 0 None - 2 Rabbit 8.5 pKd = 8.5 Functional
Antagonist activity at angiotensin 2 AT1 receptor in Japanese White rabbits thoracic aorta assessed as inhibition of KCl-indcuced contraction after 60 minsAntagonist activity at angiotensin 2 AT1 receptor in Japanese White rabbits thoracic aorta assessed as inhibition of KCl-indcuced contraction after 60 mins
ChEMBL 591 12 2 6 6.7 CCCc1nc2c(C)cc(C(=O)NCCc3cc(OC)ccc3OC)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2012.01.009
CHEMBL1945010 69996 0 None - 2 Rabbit 8.5 pKd = 8.5 Functional
Antagonist activity at angiotensin 2 AT1 receptor in Japanese White rabbits thoracic aorta assessed as inhibition of KCl-indcuced contraction after 60 minsAntagonist activity at angiotensin 2 AT1 receptor in Japanese White rabbits thoracic aorta assessed as inhibition of KCl-indcuced contraction after 60 mins
ChEMBL 591 12 2 6 6.7 CCCc1nc2c(C)cc(C(=O)NCCc3cc(OC)ccc3OC)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2012.01.009
9823146 19150 0 None - 1 Human 8.5 pKd = 8.5 Functional
Antagonist activity at angiotensin AT1 receptorAntagonist activity at angiotensin AT1 receptor
ChEMBL 415 10 1 6 4.9 CCCCc1nc(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)n(CCCC)n1 10.1016/j.bmc.2010.10.043
CHEMBL12909 19150 0 None - 1 Human 8.5 pKd = 8.5 Functional
Antagonist activity at angiotensin AT1 receptorAntagonist activity at angiotensin AT1 receptor
ChEMBL 415 10 1 6 4.9 CCCCc1nc(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)n(CCCC)n1 10.1016/j.bmc.2010.10.043
1610 2305 89 None -1 9 Human 8.5 pKd = 8.5 Functional
Antagonist activity at angiotensin AT1 receptorAntagonist activity at angiotensin AT1 receptor
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmc.2010.10.043
3941 2305 89 None -1 9 Human 8.5 pKd = 8.5 Functional
Antagonist activity at angiotensin AT1 receptorAntagonist activity at angiotensin AT1 receptor
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmc.2010.10.043
3961 2305 89 None -1 9 Human 8.5 pKd = 8.5 Functional
Antagonist activity at angiotensin AT1 receptorAntagonist activity at angiotensin AT1 receptor
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmc.2010.10.043
590 2305 89 None -1 9 Human 8.5 pKd = 8.5 Functional
Antagonist activity at angiotensin AT1 receptorAntagonist activity at angiotensin AT1 receptor
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmc.2010.10.043
CHEMBL191 2305 89 None -1 9 Human 8.5 pKd = 8.5 Functional
Antagonist activity at angiotensin AT1 receptorAntagonist activity at angiotensin AT1 receptor
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmc.2010.10.043
DB00678 2305 89 None -1 9 Human 8.5 pKd = 8.5 Functional
Antagonist activity at angiotensin AT1 receptorAntagonist activity at angiotensin AT1 receptor
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmc.2010.10.043
9801627 51768 11 None - 0 Rabbit 8.5 pKd = 8.5 Functional
Antagonist activity at angiotensin AT1 receptor in rabbit aortaAntagonist activity at angiotensin AT1 receptor in rabbit aorta
ChEMBL 409 7 1 6 4.7 CCCCc1nc2cccnc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmc.2010.10.043
CHEMBL158725 51768 11 None - 0 Rabbit 8.5 pKd = 8.5 Functional
Antagonist activity at angiotensin AT1 receptor in rabbit aortaAntagonist activity at angiotensin AT1 receptor in rabbit aorta
ChEMBL 409 7 1 6 4.7 CCCCc1nc2cccnc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmc.2010.10.043
17748251 92902 0 None - 1 Rabbit 8.4 pKd = 8.4 Functional
Antagonist activity at AT1 receptor assessed inhibition of angiotensin-2-induced contraction of rabbit thoracic aortic ringsAntagonist activity at AT1 receptor assessed inhibition of angiotensin-2-induced contraction of rabbit thoracic aortic rings
ChEMBL 455 8 1 8 4.2 CCCCc1nc2cccc(C(=O)OC)c2n1Cc1ccc(-n2cccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2007.02.042
CHEMBL245444 92902 0 None - 1 Rabbit 8.4 pKd = 8.4 Functional
Antagonist activity at AT1 receptor assessed inhibition of angiotensin-2-induced contraction of rabbit thoracic aortic ringsAntagonist activity at AT1 receptor assessed inhibition of angiotensin-2-induced contraction of rabbit thoracic aortic rings
ChEMBL 455 8 1 8 4.2 CCCCc1nc2cccc(C(=O)OC)c2n1Cc1ccc(-n2cccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2007.02.042
44570266 190211 0 None - 0 Rat 8.4 pKd = 8.4 Functional
Antagonist activity at AT1 receptor in rat aortic ringsAntagonist activity at AT1 receptor in rat aortic rings
ChEMBL 519 9 2 5 5.9 CCCCc1nc2cc(S(=O)(=O)NC(C)(C)C)ccc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.bmc.2008.10.056
CHEMBL518388 190211 0 None - 0 Rat 8.4 pKd = 8.4 Functional
Antagonist activity at AT1 receptor in rat aortic ringsAntagonist activity at AT1 receptor in rat aortic rings
ChEMBL 519 9 2 5 5.9 CCCCc1nc2cc(S(=O)(=O)NC(C)(C)C)ccc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.bmc.2008.10.056
9938452 117399 0 None - 0 Rabbit 8.4 pKd = 8.4 Functional
Antagonist activity at angiotensin AT1 receptor in rabbit aorta assessed as reduction of angiotensin 2-induced contractile responseAntagonist activity at angiotensin AT1 receptor in rabbit aorta assessed as reduction of angiotensin 2-induced contractile response
ChEMBL 591 13 2 6 8.1 CCCCCc1nc(SCc2ccc(-c3ccccc3C(=O)O)cc2)nn1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.bmc.2010.10.043
CHEMBL340315 117399 0 None - 0 Rabbit 8.4 pKd = 8.4 Functional
Antagonist activity at angiotensin AT1 receptor in rabbit aorta assessed as reduction of angiotensin 2-induced contractile responseAntagonist activity at angiotensin AT1 receptor in rabbit aorta assessed as reduction of angiotensin 2-induced contractile response
ChEMBL 591 13 2 6 8.1 CCCCCc1nc(SCc2ccc(-c3ccccc3C(=O)O)cc2)nn1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.bmc.2010.10.043
17748251 92902 0 None - 1 Rabbit 8.4 pKd = 8.4 Functional
Antagonist activity at angiotensin AT1 receptor in rabbit thoracic aortic ringsAntagonist activity at angiotensin AT1 receptor in rabbit thoracic aortic rings
ChEMBL 455 8 1 8 4.2 CCCCc1nc2cccc(C(=O)OC)c2n1Cc1ccc(-n2cccc2-c2nnn[nH]2)cc1 10.1016/j.bmc.2010.10.043
CHEMBL245444 92902 0 None - 1 Rabbit 8.4 pKd = 8.4 Functional
Antagonist activity at angiotensin AT1 receptor in rabbit thoracic aortic ringsAntagonist activity at angiotensin AT1 receptor in rabbit thoracic aortic rings
ChEMBL 455 8 1 8 4.2 CCCCc1nc2cccc(C(=O)OC)c2n1Cc1ccc(-n2cccc2-c2nnn[nH]2)cc1 10.1016/j.bmc.2010.10.043
44438868 91558 0 None - 1 Rabbit 7.5 pKd = 7.5 Functional
Antagonist activity at AT1 receptor assessed inhibition of angiotensin-2-induced contraction of rabbit thoracic aortic ringsAntagonist activity at AT1 receptor assessed inhibition of angiotensin-2-induced contraction of rabbit thoracic aortic rings
ChEMBL 427 6 1 8 3.4 CCc1nc2cccc(C(=O)OC)c2n1Cc1ccc(-n2cccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2007.02.042
CHEMBL241684 91558 0 None - 1 Rabbit 7.5 pKd = 7.5 Functional
Antagonist activity at AT1 receptor assessed inhibition of angiotensin-2-induced contraction of rabbit thoracic aortic ringsAntagonist activity at AT1 receptor assessed inhibition of angiotensin-2-induced contraction of rabbit thoracic aortic rings
ChEMBL 427 6 1 8 3.4 CCc1nc2cccc(C(=O)OC)c2n1Cc1ccc(-n2cccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2007.02.042
44438901 91541 0 None - 1 Rabbit 6.5 pKd = 6.5 Functional
Antagonist activity at AT1 receptor assessed inhibition of angiotensin-2-induced contraction of rabbit thoracic aortic ringsAntagonist activity at AT1 receptor assessed inhibition of angiotensin-2-induced contraction of rabbit thoracic aortic rings
ChEMBL 389 6 2 5 3.8 CCc1nc2cccc(C(=O)O)c2n1Cc1ccc(-n2cccc2C(=O)O)cc1 10.1016/j.bmcl.2007.02.042
CHEMBL241529 91541 0 None - 1 Rabbit 6.5 pKd = 6.5 Functional
Antagonist activity at AT1 receptor assessed inhibition of angiotensin-2-induced contraction of rabbit thoracic aortic ringsAntagonist activity at AT1 receptor assessed inhibition of angiotensin-2-induced contraction of rabbit thoracic aortic rings
ChEMBL 389 6 2 5 3.8 CCc1nc2cccc(C(=O)O)c2n1Cc1ccc(-n2cccc2C(=O)O)cc1 10.1016/j.bmcl.2007.02.042
25112616 185300 0 None - 0 Rat 6.5 pKd = 6.5 Functional
Antagonist activity at AT1 receptor in rat aortaAntagonist activity at AT1 receptor in rat aorta
ChEMBL 537 9 2 4 7.7 CCCCc1nc2cc(NC(=O)c3ccccc3Cl)ccc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2007.11.008
CHEMBL486848 185300 0 None - 0 Rat 6.5 pKd = 6.5 Functional
Antagonist activity at AT1 receptor in rat aortaAntagonist activity at AT1 receptor in rat aorta
ChEMBL 537 9 2 4 7.7 CCCCc1nc2cc(NC(=O)c3ccccc3Cl)ccc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2007.11.008
CHEMBL415157 211416 0 None - 0 Rabbit 7.4 pKd = 7.4 Functional
Negative log of the dose of antagonist (compound) that reduces response of a double dose of Angiotensin II receptor, type 1 to that of a single dose, on rabbit aortaNegative log of the dose of antagonist (compound) that reduces response of a double dose of Angiotensin II receptor, type 1 to that of a single dose, on rabbit aorta
ChEMBL None None None CCCCCCCCCCCCCCCC(=O)Oc1ccc(C[C@H](NC(=O)[C@@H](NC(=O)[C@H](CCCN=C(N)N)NC(=O)CNC)C(C)C)C(=O)N[C@H](C(=O)N[C@@H](Cc2c[nH]cn2)C(=O)N2CCC[C@H]2C(=O)N[C@H](Cc2ccccc2)C(=O)O)C(C)C)cc1 10.1021/jm9608669
1610 2305 89 None 1 9 Rat 7.4 pKd = 7.4 Functional
Antagonist activity at AT1 receptor in rat aortaAntagonist activity at AT1 receptor in rat aorta
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.ejmech.2007.11.008
3941 2305 89 None 1 9 Rat 7.4 pKd = 7.4 Functional
Antagonist activity at AT1 receptor in rat aortaAntagonist activity at AT1 receptor in rat aorta
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.ejmech.2007.11.008
3961 2305 89 None 1 9 Rat 7.4 pKd = 7.4 Functional
Antagonist activity at AT1 receptor in rat aortaAntagonist activity at AT1 receptor in rat aorta
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.ejmech.2007.11.008
590 2305 89 None 1 9 Rat 7.4 pKd = 7.4 Functional
Antagonist activity at AT1 receptor in rat aortaAntagonist activity at AT1 receptor in rat aorta
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.ejmech.2007.11.008
CHEMBL191 2305 89 None 1 9 Rat 7.4 pKd = 7.4 Functional
Antagonist activity at AT1 receptor in rat aortaAntagonist activity at AT1 receptor in rat aorta
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.ejmech.2007.11.008
DB00678 2305 89 None 1 9 Rat 7.4 pKd = 7.4 Functional
Antagonist activity at AT1 receptor in rat aortaAntagonist activity at AT1 receptor in rat aorta
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.ejmech.2007.11.008
25112614 191017 0 None - 0 Rat 6.4 pKd = 6.4 Functional
Antagonist activity at AT1 receptor in rat aortaAntagonist activity at AT1 receptor in rat aorta
ChEMBL 483 11 2 4 6.9 CCCCC(=O)Nc1ccc2c(c1)nc(CCCC)n2Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2007.11.008
CHEMBL519564 191017 0 None - 0 Rat 6.4 pKd = 6.4 Functional
Antagonist activity at AT1 receptor in rat aortaAntagonist activity at AT1 receptor in rat aorta
ChEMBL 483 11 2 4 6.9 CCCCC(=O)Nc1ccc2c(c1)nc(CCCC)n2Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2007.11.008
70686410 75962 0 None - 1 Rabbit 8.3 pKd = 8.3 Functional
Antagonist activity at AT1 receptor in Japanese white rabbit thoracic aorta assessed as inhibition of KCl-induced contraction incubated 30 mins post KCl-induction for 1 hrAntagonist activity at AT1 receptor in Japanese white rabbit thoracic aorta assessed as inhibition of KCl-induced contraction incubated 30 mins post KCl-induction for 1 hr
ChEMBL 555 10 2 6 6.2 CCCc1nc2c(C)cc(C(=O)NCCc3ccccc3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmc.2012.05.056
CHEMBL2058859 75962 0 None - 1 Rabbit 8.3 pKd = 8.3 Functional
Antagonist activity at AT1 receptor in Japanese white rabbit thoracic aorta assessed as inhibition of KCl-induced contraction incubated 30 mins post KCl-induction for 1 hrAntagonist activity at AT1 receptor in Japanese white rabbit thoracic aorta assessed as inhibition of KCl-induced contraction incubated 30 mins post KCl-induction for 1 hr
ChEMBL 555 10 2 6 6.2 CCCc1nc2c(C)cc(C(=O)NCCc3ccccc3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmc.2012.05.056
57380414 70171 0 None - 2 Rabbit 8.3 pKd = 8.3 Functional
Antagonist activity at angiotensin 2 AT1 receptor in Japanese White rabbits thoracic aorta assessed as inhibition of KCl-indcuced contraction after 60 minsAntagonist activity at angiotensin 2 AT1 receptor in Japanese White rabbits thoracic aorta assessed as inhibition of KCl-indcuced contraction after 60 mins
ChEMBL 547 10 2 5 6.6 CCCc1nc2c(C)cc(C(=O)NCc3ccc(OC)cc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2012.01.009
CHEMBL1947131 70171 0 None - 2 Rabbit 8.3 pKd = 8.3 Functional
Antagonist activity at angiotensin 2 AT1 receptor in Japanese White rabbits thoracic aorta assessed as inhibition of KCl-indcuced contraction after 60 minsAntagonist activity at angiotensin 2 AT1 receptor in Japanese White rabbits thoracic aorta assessed as inhibition of KCl-indcuced contraction after 60 mins
ChEMBL 547 10 2 5 6.6 CCCc1nc2c(C)cc(C(=O)NCc3ccc(OC)cc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2012.01.009
44339988 160448 0 None - 0 Rabbit 5.3 pKd = 5.3 Functional
Negative log of the dose of antagonist (compound) that reduces response of a double dose of Angiotensin II receptor, type 1 to that of a single dose, on rabbit aortaNegative log of the dose of antagonist (compound) that reduces response of a double dose of Angiotensin II receptor, type 1 to that of a single dose, on rabbit aorta
ChEMBL 989 27 12 12 -1.1 CC(C)[C@H](NC(=O)[C@H](CCCN=C(N)N)NC(=O)CCO)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)N1CCC[C@H]1C(=O)N[C@H](Cc1ccccc1)C(=O)O)C(C)C 10.1021/jm9608669
CHEMBL411624 160448 0 None - 0 Rabbit 5.3 pKd = 5.3 Functional
Negative log of the dose of antagonist (compound) that reduces response of a double dose of Angiotensin II receptor, type 1 to that of a single dose, on rabbit aortaNegative log of the dose of antagonist (compound) that reduces response of a double dose of Angiotensin II receptor, type 1 to that of a single dose, on rabbit aorta
ChEMBL 989 27 12 12 -1.1 CC(C)[C@H](NC(=O)[C@H](CCCN=C(N)N)NC(=O)CCO)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)N1CCC[C@H]1C(=O)N[C@H](Cc1ccccc1)C(=O)O)C(C)C 10.1021/jm9608669
132562 99209 3 None - 1 Rabbit 8.3 pKd = 8.3 Functional
Antagonist activity at angiotensin AT1 receptor in rabbit aortaAntagonist activity at angiotensin AT1 receptor in rabbit aorta
ChEMBL 407 6 1 5 5.2 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2ccccc2n1 10.1016/j.bmc.2010.10.043
CHEMBL284536 99209 3 None - 1 Rabbit 8.3 pKd = 8.3 Functional
Antagonist activity at angiotensin AT1 receptor in rabbit aortaAntagonist activity at angiotensin AT1 receptor in rabbit aorta
ChEMBL 407 6 1 5 5.2 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2ccccc2n1 10.1016/j.bmc.2010.10.043
53325868 57281 0 None - 0 Rabbit 8.3 pKd = 8.3 Functional
Antagonist activity at angiotensin AT1 receptor in rabbit thoracic aortic ringsAntagonist activity at angiotensin AT1 receptor in rabbit thoracic aortic rings
ChEMBL 515 12 2 6 5.8 CCCCc1nc2cc(OC)cc(C(=O)O)c2n1Cc1ccc(N(CC)C(C(=O)O)c2ccccc2)cc1 10.1016/j.bmc.2010.10.043
CHEMBL1668002 57281 0 None - 0 Rabbit 8.3 pKd = 8.3 Functional
Antagonist activity at angiotensin AT1 receptor in rabbit thoracic aortic ringsAntagonist activity at angiotensin AT1 receptor in rabbit thoracic aortic rings
ChEMBL 515 12 2 6 5.8 CCCCc1nc2cc(OC)cc(C(=O)O)c2n1Cc1ccc(N(CC)C(C(=O)O)c2ccccc2)cc1 10.1016/j.bmc.2010.10.043
44438880 91540 0 None - 1 Rabbit 8.2 pKd = 8.2 Functional
Antagonist activity at AT1 receptor assessed inhibition of angiotensin-2-induced contraction of rabbit thoracic aortic ringsAntagonist activity at AT1 receptor assessed inhibition of angiotensin-2-induced contraction of rabbit thoracic aortic rings
ChEMBL 427 7 2 7 3.7 CCCc1nc2cccc(C(=O)O)c2n1Cc1ccc(-n2cccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2007.02.042
CHEMBL241523 91540 0 None - 1 Rabbit 8.2 pKd = 8.2 Functional
Antagonist activity at AT1 receptor assessed inhibition of angiotensin-2-induced contraction of rabbit thoracic aortic ringsAntagonist activity at AT1 receptor assessed inhibition of angiotensin-2-induced contraction of rabbit thoracic aortic rings
ChEMBL 427 7 2 7 3.7 CCCc1nc2cccc(C(=O)O)c2n1Cc1ccc(-n2cccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2007.02.042
132706 1638 19 None -1 2 Human 8.2 pKd = 8.2 Functional
Antagonist activity at angiotensin AT1 receptorAntagonist activity at angiotensin AT1 receptor
ChEMBL 416 10 1 7 4.3 CCCCc1nc(nn1Cc1ccc(nc1)c1ccccc1c1n[nH]nn1)CCCC 10.1016/j.bmc.2010.10.043
6896 1638 19 None -1 2 Human 8.2 pKd = 8.2 Functional
Antagonist activity at angiotensin AT1 receptorAntagonist activity at angiotensin AT1 receptor
ChEMBL 416 10 1 7 4.3 CCCCc1nc(nn1Cc1ccc(nc1)c1ccccc1c1n[nH]nn1)CCCC 10.1016/j.bmc.2010.10.043
CHEMBL315021 1638 19 None -1 2 Human 8.2 pKd = 8.2 Functional
Antagonist activity at angiotensin AT1 receptorAntagonist activity at angiotensin AT1 receptor
ChEMBL 416 10 1 7 4.3 CCCCc1nc(nn1Cc1ccc(nc1)c1ccccc1c1n[nH]nn1)CCCC 10.1016/j.bmc.2010.10.043
DB01342 1638 19 None -1 2 Human 8.2 pKd = 8.2 Functional
Antagonist activity at angiotensin AT1 receptorAntagonist activity at angiotensin AT1 receptor
ChEMBL 416 10 1 7 4.3 CCCCc1nc(nn1Cc1ccc(nc1)c1ccccc1c1n[nH]nn1)CCCC 10.1016/j.bmc.2010.10.043
57380412 70169 0 None - 2 Rabbit 8.2 pKd = 8.2 Functional
Antagonist activity at angiotensin 2 AT1 receptor in Japanese White rabbits thoracic aorta assessed as inhibition of KCl-indcuced contraction after 60 minsAntagonist activity at angiotensin 2 AT1 receptor in Japanese White rabbits thoracic aorta assessed as inhibition of KCl-indcuced contraction after 60 mins
ChEMBL 547 10 2 5 6.6 CCCc1nc2c(C)cc(C(=O)NCc3ccccc3OC)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2012.01.009
CHEMBL1947129 70169 0 None - 2 Rabbit 8.2 pKd = 8.2 Functional
Antagonist activity at angiotensin 2 AT1 receptor in Japanese White rabbits thoracic aorta assessed as inhibition of KCl-indcuced contraction after 60 minsAntagonist activity at angiotensin 2 AT1 receptor in Japanese White rabbits thoracic aorta assessed as inhibition of KCl-indcuced contraction after 60 mins
ChEMBL 547 10 2 5 6.6 CCCc1nc2c(C)cc(C(=O)NCc3ccccc3OC)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2012.01.009
44570264 190103 0 None - 0 Rat 7.2 pKd = 7.2 Functional
Antagonist activity at AT1 receptor in rat aortic ringsAntagonist activity at AT1 receptor in rat aortic rings
ChEMBL 505 10 2 5 5.5 CCCCc1nc2cc(S(=O)(=O)NC(C)C)ccc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.bmc.2008.10.056
CHEMBL518230 190103 0 None - 0 Rat 7.2 pKd = 7.2 Functional
Antagonist activity at AT1 receptor in rat aortic ringsAntagonist activity at AT1 receptor in rat aortic rings
ChEMBL 505 10 2 5 5.5 CCCCc1nc2cc(S(=O)(=O)NC(C)C)ccc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.bmc.2008.10.056
25112617 186165 0 None - 0 Rat 6.2 pKd = 6.2 Functional
Antagonist activity at AT1 receptor in rat aortaAntagonist activity at AT1 receptor in rat aorta
ChEMBL 537 9 2 4 7.7 CCCCc1nc2cc(NC(=O)c3ccc(Cl)cc3)ccc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2007.11.008
CHEMBL488883 186165 0 None - 0 Rat 6.2 pKd = 6.2 Functional
Antagonist activity at AT1 receptor in rat aortaAntagonist activity at AT1 receptor in rat aorta
ChEMBL 537 9 2 4 7.7 CCCCc1nc2cc(NC(=O)c3ccc(Cl)cc3)ccc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2007.11.008
CHEMBL268804 209009 0 None - 0 Rabbit 8.1 pKd = 8.1 Functional
Negative log of the dose of antagonist (compound) that reduces response of a double dose of Angiotensin II receptor, type 1 to that of a single dose, on rabbit aortaNegative log of the dose of antagonist (compound) that reduces response of a double dose of Angiotensin II receptor, type 1 to that of a single dose, on rabbit aorta
ChEMBL None None None CNCC(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)N1CCC[C@H]1C(=O)N[C@H](Cc1ccc2ccccc2c1)C(=O)O)C(C)C)C(C)C 10.1021/jm9608669
44438872 168529 0 None - 1 Rabbit 7.1 pKd = 7.1 Functional
Antagonist activity at AT1 receptor assessed inhibition of angiotensin-2-induced contraction of rabbit thoracic aortic ringsAntagonist activity at AT1 receptor assessed inhibition of angiotensin-2-induced contraction of rabbit thoracic aortic rings
ChEMBL 455 8 1 8 4.2 CCCc1nc2cccc(C(=O)OCC)c2n1Cc1ccc(-n2cccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2007.02.042
CHEMBL440051 168529 0 None - 1 Rabbit 7.1 pKd = 7.1 Functional
Antagonist activity at AT1 receptor assessed inhibition of angiotensin-2-induced contraction of rabbit thoracic aortic ringsAntagonist activity at AT1 receptor assessed inhibition of angiotensin-2-induced contraction of rabbit thoracic aortic rings
ChEMBL 455 8 1 8 4.2 CCCc1nc2cccc(C(=O)OCC)c2n1Cc1ccc(-n2cccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2007.02.042
15069306 178474 0 None - 0 Rat 7.1 pKd = 7.1 Functional
Antagonist activity at AT1 receptor in rat aortaAntagonist activity at AT1 receptor in rat aorta
ChEMBL 469 10 2 4 6.5 CCCCc1nc2cc(NC(=O)CCC)ccc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2007.11.008
CHEMBL471505 178474 0 None - 0 Rat 7.1 pKd = 7.1 Functional
Antagonist activity at AT1 receptor in rat aortaAntagonist activity at AT1 receptor in rat aorta
ChEMBL 469 10 2 4 6.5 CCCCc1nc2cc(NC(=O)CCC)ccc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2007.11.008
44570217 182642 0 None - 0 Rat 7.1 pKd = 7.1 Functional
Antagonist activity at AT1 receptor in rat aortic ringsAntagonist activity at AT1 receptor in rat aortic rings
ChEMBL 505 11 2 5 5.5 CCCCc1nc2cc(S(=O)(=O)NCCC)ccc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.bmc.2008.10.056
CHEMBL479626 182642 0 None - 0 Rat 7.1 pKd = 7.1 Functional
Antagonist activity at AT1 receptor in rat aortic ringsAntagonist activity at AT1 receptor in rat aortic rings
ChEMBL 505 11 2 5 5.5 CCCCc1nc2cc(S(=O)(=O)NCCC)ccc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.bmc.2008.10.056
44570216 189454 0 None - 0 Rat 7.1 pKd = 7.1 Functional
Antagonist activity at AT1 receptor in rat aortic ringsAntagonist activity at AT1 receptor in rat aortic rings
ChEMBL 491 10 2 5 5.1 CCCCc1nc2cc(S(=O)(=O)NCC)ccc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.bmc.2008.10.056
CHEMBL517230 189454 0 None - 0 Rat 7.1 pKd = 7.1 Functional
Antagonist activity at AT1 receptor in rat aortic ringsAntagonist activity at AT1 receptor in rat aortic rings
ChEMBL 491 10 2 5 5.1 CCCCc1nc2cc(S(=O)(=O)NCC)ccc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.bmc.2008.10.056
6918269 98005 8 None - 2 Rabbit 8.0 pKd = 8.0 Functional
Antagonist activity at angiotensin AT1 receptor in rabbit aortaAntagonist activity at angiotensin AT1 receptor in rabbit aorta
ChEMBL 508 9 1 7 5.5 CCCCc1nc2ccc(C(C)(C)OC)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.bmc.2010.10.043
CHEMBL275875 98005 8 None - 2 Rabbit 8.0 pKd = 8.0 Functional
Antagonist activity at angiotensin AT1 receptor in rabbit aortaAntagonist activity at angiotensin AT1 receptor in rabbit aorta
ChEMBL 508 9 1 7 5.5 CCCCc1nc2ccc(C(C)(C)OC)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.bmc.2010.10.043
CHEMBL295959 98005 8 None - 2 Rabbit 8.0 pKd = 8.0 Functional
Antagonist activity at angiotensin AT1 receptor in rabbit aortaAntagonist activity at angiotensin AT1 receptor in rabbit aorta
ChEMBL 508 9 1 7 5.5 CCCCc1nc2ccc(C(C)(C)OC)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.bmc.2010.10.043
1610 2305 89 None -2 9 Rat 8.1 pKi = 8.1 Functional
In vitro antagonistic potency against angiotensin II receptor using [125I]- Sar,Ile8-angiotensin II as the radioligand in rat adrenal cortical membranesIn vitro antagonistic potency against angiotensin II receptor using [125I]- Sar,Ile8-angiotensin II as the radioligand in rat adrenal cortical membranes
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00103a014
3941 2305 89 None -2 9 Rat 8.1 pKi = 8.1 Functional
In vitro antagonistic potency against angiotensin II receptor using [125I]- Sar,Ile8-angiotensin II as the radioligand in rat adrenal cortical membranesIn vitro antagonistic potency against angiotensin II receptor using [125I]- Sar,Ile8-angiotensin II as the radioligand in rat adrenal cortical membranes
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00103a014
3961 2305 89 None -2 9 Rat 8.1 pKi = 8.1 Functional
In vitro antagonistic potency against angiotensin II receptor using [125I]- Sar,Ile8-angiotensin II as the radioligand in rat adrenal cortical membranesIn vitro antagonistic potency against angiotensin II receptor using [125I]- Sar,Ile8-angiotensin II as the radioligand in rat adrenal cortical membranes
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00103a014
590 2305 89 None -2 9 Rat 8.1 pKi = 8.1 Functional
In vitro antagonistic potency against angiotensin II receptor using [125I]- Sar,Ile8-angiotensin II as the radioligand in rat adrenal cortical membranesIn vitro antagonistic potency against angiotensin II receptor using [125I]- Sar,Ile8-angiotensin II as the radioligand in rat adrenal cortical membranes
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00103a014
CHEMBL191 2305 89 None -2 9 Rat 8.1 pKi = 8.1 Functional
In vitro antagonistic potency against angiotensin II receptor using [125I]- Sar,Ile8-angiotensin II as the radioligand in rat adrenal cortical membranesIn vitro antagonistic potency against angiotensin II receptor using [125I]- Sar,Ile8-angiotensin II as the radioligand in rat adrenal cortical membranes
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00103a014
DB00678 2305 89 None -2 9 Rat 8.1 pKi = 8.1 Functional
In vitro antagonistic potency against angiotensin II receptor using [125I]- Sar,Ile8-angiotensin II as the radioligand in rat adrenal cortical membranesIn vitro antagonistic potency against angiotensin II receptor using [125I]- Sar,Ile8-angiotensin II as the radioligand in rat adrenal cortical membranes
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00103a014
1610 2305 89 None -2 9 Rat 7.0 pKi = 7.0 Functional
In vitro antagonistic potency against angiotensin II receptor using [125I]- Sar,Ile8-angiotensin II as the radioligand in rat adrenal cortical membranesIn vitro antagonistic potency against angiotensin II receptor using [125I]- Sar,Ile8-angiotensin II as the radioligand in rat adrenal cortical membranes
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00103a014
3941 2305 89 None -2 9 Rat 7.0 pKi = 7.0 Functional
In vitro antagonistic potency against angiotensin II receptor using [125I]- Sar,Ile8-angiotensin II as the radioligand in rat adrenal cortical membranesIn vitro antagonistic potency against angiotensin II receptor using [125I]- Sar,Ile8-angiotensin II as the radioligand in rat adrenal cortical membranes
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00103a014
3961 2305 89 None -2 9 Rat 7.0 pKi = 7.0 Functional
In vitro antagonistic potency against angiotensin II receptor using [125I]- Sar,Ile8-angiotensin II as the radioligand in rat adrenal cortical membranesIn vitro antagonistic potency against angiotensin II receptor using [125I]- Sar,Ile8-angiotensin II as the radioligand in rat adrenal cortical membranes
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00103a014
590 2305 89 None -2 9 Rat 7.0 pKi = 7.0 Functional
In vitro antagonistic potency against angiotensin II receptor using [125I]- Sar,Ile8-angiotensin II as the radioligand in rat adrenal cortical membranesIn vitro antagonistic potency against angiotensin II receptor using [125I]- Sar,Ile8-angiotensin II as the radioligand in rat adrenal cortical membranes
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00103a014
CHEMBL191 2305 89 None -2 9 Rat 7.0 pKi = 7.0 Functional
In vitro antagonistic potency against angiotensin II receptor using [125I]- Sar,Ile8-angiotensin II as the radioligand in rat adrenal cortical membranesIn vitro antagonistic potency against angiotensin II receptor using [125I]- Sar,Ile8-angiotensin II as the radioligand in rat adrenal cortical membranes
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00103a014
DB00678 2305 89 None -2 9 Rat 7.0 pKi = 7.0 Functional
In vitro antagonistic potency against angiotensin II receptor using [125I]- Sar,Ile8-angiotensin II as the radioligand in rat adrenal cortical membranesIn vitro antagonistic potency against angiotensin II receptor using [125I]- Sar,Ile8-angiotensin II as the radioligand in rat adrenal cortical membranes
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00103a014
6917 132 0 None - 1 Human 7.8 pA2 = 7.8 Functional
UnclassifiedUnclassified
Guide to Pharmacology 348 7 1 3 4.9 CCCCc1cnc(n1Cc1ccc(cc1)c1ccccc1C)C(=O)O 22889560
73755250 132 0 None - 1 Human 7.8 pA2 = 7.8 Functional
UnclassifiedUnclassified
Guide to Pharmacology 348 7 1 3 4.9 CCCCc1cnc(n1Cc1ccc(cc1)c1ccccc1C)C(=O)O 22889560
11943 3802 0 None -14 2 Human 5.7 pEC50 = 5.7 Functional
β-arrestin recruitment assayβ-arrestin recruitment assay
Guide to Pharmacology None None None None None
145925549 3802 0 None -14 2 Human 5.7 pEC50 = 5.7 Functional
β-arrestin recruitment assayβ-arrestin recruitment assay
Guide to Pharmacology None None None None None
CHEMBL4438122 3802 0 None -14 2 Human 5.7 pEC50 = 5.7 Functional
β-arrestin recruitment assayβ-arrestin recruitment assay
Guide to Pharmacology None None None None None
123814 417 26 None - 1 Human 5.9 pEC50 = 5.9 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 12006574
5368 417 26 None - 1 Human 5.9 pEC50 = 5.9 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 12006574
CHEMBL261120 417 26 None - 1 Human 5.9 pEC50 = 5.9 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 12006574
6894 414 0 None -56 3 Human 8.2 pEC50 = 8.2 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 21464395
91691124 414 0 None -56 3 Human 8.2 pEC50 = 8.2 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 21464395
6905 3416 0 None - 1 Rat 8.8 pEC50 = 8.8 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 7499361
135409642 216004 0 None 1 2 Bovine 8.2 pIC50 = 8.2 Functional
NoneNone
Drug Central 568 9 1 11 4.7 CCOC1=NC2=CC=CC(C(=O)OCC3=C(C)OC(=O)O3)=C2N1CC1=CC=C(C=C1)C1=C(C=CC=C1)C1=NOC(=O)N1 None
2540 4320 102 None 1 3 Bovine 8.2 pIC50 = 8.2 Functional
NoneNone
Drug Central 610 10 1 11 6.3 CCOc1nc2cccc(C(=O)OC(C)OC(=O)OC3CCCCC3)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 None
CHEMBL1014 4320 102 None 1 3 Bovine 8.2 pIC50 = 8.2 Functional
NoneNone
Drug Central 610 10 1 11 6.3 CCOc1nc2cccc(C(=O)OC(C)OC(=O)OC3CCCCC3)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 None
3839 3688 78 None - 1 Human 8.1 pIC50 = 8.1 Functional
Compound was tested for inhibition against Angiotensin II receptor, type 1Compound was tested for inhibition against Angiotensin II receptor, type 1
Drug Central 411 4 1 6 3.4 Cc1nc(C)c2c(n1)N(Cc1ccc(cc1)c1ccccc1c1nn[nH]n1)C(=O)CC2 None
60919 3688 78 None - 1 Human 8.1 pIC50 = 8.1 Functional
Compound was tested for inhibition against Angiotensin II receptor, type 1Compound was tested for inhibition against Angiotensin II receptor, type 1
Drug Central 411 4 1 6 3.4 Cc1nc(C)c2c(n1)N(Cc1ccc(cc1)c1ccccc1c1nn[nH]n1)C(=O)CC2 None
6898 3688 78 None - 1 Human 8.1 pIC50 = 8.1 Functional
Compound was tested for inhibition against Angiotensin II receptor, type 1Compound was tested for inhibition against Angiotensin II receptor, type 1
Drug Central 411 4 1 6 3.4 Cc1nc(C)c2c(n1)N(Cc1ccc(cc1)c1ccccc1c1nn[nH]n1)C(=O)CC2 None
CHEMBL432162 3688 78 None - 1 Human 8.1 pIC50 = 8.1 Functional
Compound was tested for inhibition against Angiotensin II receptor, type 1Compound was tested for inhibition against Angiotensin II receptor, type 1
Drug Central 411 4 1 6 3.4 Cc1nc(C)c2c(n1)N(Cc1ccc(cc1)c1ccccc1c1nn[nH]n1)C(=O)CC2 None
DB01349 3688 78 None - 1 Human 8.1 pIC50 = 8.1 Functional
Compound was tested for inhibition against Angiotensin II receptor, type 1Compound was tested for inhibition against Angiotensin II receptor, type 1
Drug Central 411 4 1 6 3.4 Cc1nc(C)c2c(n1)N(Cc1ccc(cc1)c1ccccc1c1nn[nH]n1)C(=O)CC2 None
130881 2865 0 None -1 2 Bovine 8.1 pIC50 = 8.1 Functional
NoneNone
Drug Central 558 10 2 11 4.2 CCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1nnn[nH]1)C(=O)OCc1oc(=O)oc1C)C(O)(C)C None
1985 2865 0 None -1 2 Bovine 8.1 pIC50 = 8.1 Functional
NoneNone
Drug Central 558 10 2 11 4.2 CCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1nnn[nH]1)C(=O)OCc1oc(=O)oc1C)C(O)(C)C None
591 2865 0 None -1 2 Bovine 8.1 pIC50 = 8.1 Functional
NoneNone
Drug Central 558 10 2 11 4.2 CCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1nnn[nH]1)C(=O)OCc1oc(=O)oc1C)C(O)(C)C None
CHEMBL1200692 2865 0 None -1 2 Bovine 8.1 pIC50 = 8.1 Functional
NoneNone
Drug Central 558 10 2 11 4.2 CCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1nnn[nH]1)C(=O)OCc1oc(=O)oc1C)C(O)(C)C None
DB00275 2865 0 None -1 2 Bovine 8.1 pIC50 = 8.1 Functional
NoneNone
Drug Central 558 10 2 11 4.2 CCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1nnn[nH]1)C(=O)OCc1oc(=O)oc1C)C(O)(C)C None
130881 2865 0 None 1 2 Human 8.1 pIC50 = 8.1 Functional
NoneNone
Drug Central 558 10 2 11 4.2 CCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1nnn[nH]1)C(=O)OCc1oc(=O)oc1C)C(O)(C)C None
1985 2865 0 None 1 2 Human 8.1 pIC50 = 8.1 Functional
NoneNone
Drug Central 558 10 2 11 4.2 CCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1nnn[nH]1)C(=O)OCc1oc(=O)oc1C)C(O)(C)C None
591 2865 0 None 1 2 Human 8.1 pIC50 = 8.1 Functional
NoneNone
Drug Central 558 10 2 11 4.2 CCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1nnn[nH]1)C(=O)OCc1oc(=O)oc1C)C(O)(C)C None
CHEMBL1200692 2865 0 None 1 2 Human 8.1 pIC50 = 8.1 Functional
NoneNone
Drug Central 558 10 2 11 4.2 CCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1nnn[nH]1)C(=O)OCc1oc(=O)oc1C)C(O)(C)C None
DB00275 2865 0 None 1 2 Human 8.1 pIC50 = 8.1 Functional
NoneNone
Drug Central 558 10 2 11 4.2 CCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1nnn[nH]1)C(=O)OCc1oc(=O)oc1C)C(O)(C)C None
135409642 216004 0 None -1 2 Human 8.1 pIC50 = 8.1 Functional
NoneNone
Drug Central 568 9 1 11 4.7 CCOC1=NC2=CC=CC(C(=O)OCC3=C(C)OC(=O)O3)=C2N1CC1=CC=C(C=C1)C1=C(C=CC=C1)C1=NOC(=O)N1 None
16133225 415 47 None -5 4 Human 8.0 pIC50 = 8.0 Functional
NoneNone
Drug Central None None None None None
172198 415 47 None -5 4 Human 8.0 pIC50 = 8.0 Functional
NoneNone
Drug Central None None None None None
2504 415 47 None -5 4 Human 8.0 pIC50 = 8.0 Functional
NoneNone
Drug Central None None None None None
45266664 415 47 None -5 4 Human 8.0 pIC50 = 8.0 Functional
NoneNone
Drug Central None None None None None
5272 415 47 None -5 4 Human 8.0 pIC50 = 8.0 Functional
NoneNone
Drug Central None None None None None
CHEMBL408403 415 47 None -5 4 Human 8.0 pIC50 = 8.0 Functional
NoneNone
Drug Central None None None None None
DB11842 415 47 None -5 4 Human 8.0 pIC50 = 8.0 Functional
NoneNone
Drug Central None None None None None
9870652 70533 68 None -15 2 Human 8.0 pIC50 = 8.0 Functional
antagonism of angiotensin II induced contractionantagonism of angiotensin II induced contraction
Drug Central 501 9 1 7 4.2 CCCCc1nc(C)c(CC(=S)N(C)C)c(=O)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 None
CHEMBL1951143 70533 68 None -15 2 Human 8.0 pIC50 = 8.0 Functional
antagonism of angiotensin II induced contractionantagonism of angiotensin II induced contraction
Drug Central 501 9 1 7 4.2 CCCCc1nc(C)c(CC(=S)N(C)C)c(=O)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 None
1610 2305 89 None -1 9 Human 8.0 pIC50 = 8.0 Functional
Inhibition of angiotensin AT1 receptorInhibition of angiotensin AT1 receptor
Drug Central 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl None
3941 2305 89 None -1 9 Human 8.0 pIC50 = 8.0 Functional
Inhibition of angiotensin AT1 receptorInhibition of angiotensin AT1 receptor
Drug Central 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl None
3961 2305 89 None -1 9 Human 8.0 pIC50 = 8.0 Functional
Inhibition of angiotensin AT1 receptorInhibition of angiotensin AT1 receptor
Drug Central 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl None
590 2305 89 None -1 9 Human 8.0 pIC50 = 8.0 Functional
Inhibition of angiotensin AT1 receptorInhibition of angiotensin AT1 receptor
Drug Central 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl None
CHEMBL191 2305 89 None -1 9 Human 8.0 pIC50 = 8.0 Functional
Inhibition of angiotensin AT1 receptorInhibition of angiotensin AT1 receptor
Drug Central 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl None
DB00678 2305 89 None -1 9 Human 8.0 pIC50 = 8.0 Functional
Inhibition of angiotensin AT1 receptorInhibition of angiotensin AT1 receptor
Drug Central 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl None
3936 2171 28 None -1 6 Human 7.9 pIC50 = 7.9 Functional
UnclassifiedUnclassified
Guide to Pharmacology 582 11 1 8 6.8 CCCCOC(=O)NS(=O)(=O)c1sc(cc1c1ccc(cc1)Cn1c(CC)nc2c1nc(C)cc2C)CC(C)C 7829475
6603900 2171 28 None -1 6 Human 7.9 pIC50 = 7.9 Functional
UnclassifiedUnclassified
Guide to Pharmacology 582 11 1 8 6.8 CCCCOC(=O)NS(=O)(=O)c1sc(cc1c1ccc(cc1)Cn1c(CC)nc2c1nc(C)cc2C)CC(C)C 7829475
CHEMBL288174 2171 28 None -1 6 Human 7.9 pIC50 = 7.9 Functional
UnclassifiedUnclassified
Guide to Pharmacology 582 11 1 8 6.8 CCCCOC(=O)NS(=O)(=O)c1sc(cc1c1ccc(cc1)Cn1c(CC)nc2c1nc(C)cc2C)CC(C)C 7829475
6895 2172 0 None - 1 Human 7.9 pIC50 = 7.9 Functional
UnclassifiedUnclassified
Guide to Pharmacology 580 9 1 6 6.6 CCc1nc2c(n1Cc1ccc(cc1)c1cc(ccc1S(=O)(=O)NC(=O)c1ccccc1)CC(C)C)nc(cc2C)C 9383393
73755245 2172 0 None - 1 Human 7.9 pIC50 = 7.9 Functional
UnclassifiedUnclassified
Guide to Pharmacology 580 9 1 6 6.6 CCc1nc2c(n1Cc1ccc(cc1)c1cc(ccc1S(=O)(=O)NC(=O)c1ccccc1)CC(C)C)nc(cc2C)C 9383393
1610 2305 89 None -1 9 Human 8.1 pIC50 = 8.1 Functional
UnclassifiedUnclassified
Guide to Pharmacology 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 8372104
3941 2305 89 None -1 9 Human 8.1 pIC50 = 8.1 Functional
UnclassifiedUnclassified
Guide to Pharmacology 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 8372104
3961 2305 89 None -1 9 Human 8.1 pIC50 = 8.1 Functional
UnclassifiedUnclassified
Guide to Pharmacology 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 8372104
590 2305 89 None -1 9 Human 8.1 pIC50 = 8.1 Functional
UnclassifiedUnclassified
Guide to Pharmacology 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 8372104
CHEMBL191 2305 89 None -1 9 Human 8.1 pIC50 = 8.1 Functional
UnclassifiedUnclassified
Guide to Pharmacology 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 8372104
DB00678 2305 89 None -1 9 Human 8.1 pIC50 = 8.1 Functional
UnclassifiedUnclassified
Guide to Pharmacology 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 8372104
139031070 2786 0 None - 1 Human 8.1 pIC50 = 8.1 Functional
UnclassifiedUnclassified
Guide to Pharmacology 714 11 0 10 2.6 CCCCc1n([c+]nc1Cc1ccc(cc1)c1ccccc1c1nnn(n1)[Na])Cc1ccc(cc1)c1ccccc1c1nnn(n1)[Na].[Br-] 23376252
6911 2786 0 None - 1 Human 8.1 pIC50 = 8.1 Functional
UnclassifiedUnclassified
Guide to Pharmacology 714 11 0 10 2.6 CCCCc1n([c+]nc1Cc1ccc(cc1)c1ccccc1c1nnn(n1)[Na])Cc1ccc(cc1)c1ccccc1c1nnn(n1)[Na].[Br-] 23376252
73755247 2786 0 None - 1 Human 8.1 pIC50 = 8.1 Functional
UnclassifiedUnclassified
Guide to Pharmacology 714 11 0 10 2.6 CCCCc1n([c+]nc1Cc1ccc(cc1)c1ccccc1c1nnn(n1)[Na])Cc1ccc(cc1)c1ccccc1c1nnn(n1)[Na].[Br-] 23376252
130881 2865 0 None 1 2 Human 8.1 pIC50 = 8.1 Functional
UnclassifiedUnclassified
Guide to Pharmacology 558 10 2 11 4.2 CCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1nnn[nH]1)C(=O)OCc1oc(=O)oc1C)C(O)(C)C 11451212
1985 2865 0 None 1 2 Human 8.1 pIC50 = 8.1 Functional
UnclassifiedUnclassified
Guide to Pharmacology 558 10 2 11 4.2 CCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1nnn[nH]1)C(=O)OCc1oc(=O)oc1C)C(O)(C)C 11451212
591 2865 0 None 1 2 Human 8.1 pIC50 = 8.1 Functional
UnclassifiedUnclassified
Guide to Pharmacology 558 10 2 11 4.2 CCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1nnn[nH]1)C(=O)OCc1oc(=O)oc1C)C(O)(C)C 11451212
CHEMBL1200692 2865 0 None 1 2 Human 8.1 pIC50 = 8.1 Functional
UnclassifiedUnclassified
Guide to Pharmacology 558 10 2 11 4.2 CCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1nnn[nH]1)C(=O)OCc1oc(=O)oc1C)C(O)(C)C 11451212
DB00275 2865 0 None 1 2 Human 8.1 pIC50 = 8.1 Functional
UnclassifiedUnclassified
Guide to Pharmacology 558 10 2 11 4.2 CCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1nnn[nH]1)C(=O)OCc1oc(=O)oc1C)C(O)(C)C 11451212
135415867 554 89 None 53 2 Human 8.1 pIC50 = 8.1 Functional
UnclassifiedUnclassified
Guide to Pharmacology 456 7 2 7 4.2 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1[nH]oc(=O)n1)c(ccc2)C(=O)O 24739538
135415867 554 89 None 53 2 Human 8.1 pIC50 = 8.1 Functional
UnclassifiedUnclassified
Guide to Pharmacology 456 7 2 7 4.2 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1[nH]oc(=O)n1)c(ccc2)C(=O)O 24742498
6901 554 89 None 53 2 Human 8.1 pIC50 = 8.1 Functional
UnclassifiedUnclassified
Guide to Pharmacology 456 7 2 7 4.2 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1[nH]oc(=O)n1)c(ccc2)C(=O)O 24739538
6901 554 89 None 53 2 Human 8.1 pIC50 = 8.1 Functional
UnclassifiedUnclassified
Guide to Pharmacology 456 7 2 7 4.2 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1[nH]oc(=O)n1)c(ccc2)C(=O)O 24742498
CHEMBL57242 554 89 None 53 2 Human 8.1 pIC50 = 8.1 Functional
UnclassifiedUnclassified
Guide to Pharmacology 456 7 2 7 4.2 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1[nH]oc(=O)n1)c(ccc2)C(=O)O 24739538
CHEMBL57242 554 89 None 53 2 Human 8.1 pIC50 = 8.1 Functional
UnclassifiedUnclassified
Guide to Pharmacology 456 7 2 7 4.2 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1[nH]oc(=O)n1)c(ccc2)C(=O)O 24742498
6909 2366 0 None - 1 Human 8.2 pIC50 = 8.2 Functional
UnclassifiedUnclassified
Guide to Pharmacology 642 14 4 9 3.7 CCCCCC[C@@H](C(=O)N1C[C@H](C[C@H]1C(=O)O)Oc1ccc(cc1)C(=O)O)n1cnc(c1)NC(=O)c1ccccc1S(=O)(=O)O 11303957
73755246 2366 0 None - 1 Human 8.2 pIC50 = 8.2 Functional
UnclassifiedUnclassified
Guide to Pharmacology 642 14 4 9 3.7 CCCCCC[C@@H](C(=O)N1C[C@H](C[C@H]1C(=O)O)Oc1ccc(cc1)C(=O)O)n1cnc(c1)NC(=O)c1ccccc1S(=O)(=O)O 11303957
10416728 2367 0 None - 1 Human 8.3 pIC50 = 8.3 Functional
UnclassifiedUnclassified
Guide to Pharmacology 642 14 4 9 3.7 CCCCCC[C@H](C(=O)N1C[C@H](C[C@H]1C(=O)O)Oc1ccc(cc1)C(=O)O)n1cnc(c1)NC(=O)c1ccccc1S(=O)(=O)O 11303957
6910 2367 0 None - 1 Human 8.3 pIC50 = 8.3 Functional
UnclassifiedUnclassified
Guide to Pharmacology 642 14 4 9 3.7 CCCCCC[C@H](C(=O)N1C[C@H](C[C@H]1C(=O)O)Oc1ccc(cc1)C(=O)O)n1cnc(c1)NC(=O)c1ccccc1S(=O)(=O)O 11303957
CHEMBL344662 2367 0 None - 1 Human 8.3 pIC50 = 8.3 Functional
UnclassifiedUnclassified
Guide to Pharmacology 642 14 4 9 3.7 CCCCCC[C@H](C(=O)N1C[C@H](C[C@H]1C(=O)O)Oc1ccc(cc1)C(=O)O)n1cnc(c1)NC(=O)c1ccccc1S(=O)(=O)O 11303957
132706 1638 19 None 1 2 Rat 8.4 pIC50 = 8.4 Functional
UnclassifiedUnclassified
Guide to Pharmacology 416 10 1 7 4.3 CCCCc1nc(nn1Cc1ccc(nc1)c1ccccc1c1n[nH]nn1)CCCC 7505365
6896 1638 19 None 1 2 Rat 8.4 pIC50 = 8.4 Functional
UnclassifiedUnclassified
Guide to Pharmacology 416 10 1 7 4.3 CCCCc1nc(nn1Cc1ccc(nc1)c1ccccc1c1n[nH]nn1)CCCC 7505365
CHEMBL315021 1638 19 None 1 2 Rat 8.4 pIC50 = 8.4 Functional
UnclassifiedUnclassified
Guide to Pharmacology 416 10 1 7 4.3 CCCCc1nc(nn1Cc1ccc(nc1)c1ccccc1c1n[nH]nn1)CCCC 7505365
DB01342 1638 19 None 1 2 Rat 8.4 pIC50 = 8.4 Functional
UnclassifiedUnclassified
Guide to Pharmacology 416 10 1 7 4.3 CCCCc1nc(nn1Cc1ccc(nc1)c1ccccc1c1n[nH]nn1)CCCC 7505365
2583 3705 115 None -2 4 Human 8.4 pIC50 = 8.4 Functional
UnclassifiedUnclassified
Guide to Pharmacology 514 7 1 5 7.3 CCCc1nc2c(n1Cc1ccc(cc1)c1ccccc1C(=O)O)cc(cc2C)c1nc2c(n1C)cccc2 9878991
592 3705 115 None -2 4 Human 8.4 pIC50 = 8.4 Functional
UnclassifiedUnclassified
Guide to Pharmacology 514 7 1 5 7.3 CCCc1nc2c(n1Cc1ccc(cc1)c1ccccc1C(=O)O)cc(cc2C)c1nc2c(n1C)cccc2 9878991
65999 3705 115 None -2 4 Human 8.4 pIC50 = 8.4 Functional
UnclassifiedUnclassified
Guide to Pharmacology 514 7 1 5 7.3 CCCc1nc2c(n1Cc1ccc(cc1)c1ccccc1C(=O)O)cc(cc2C)c1nc2c(n1C)cccc2 9878991
CHEMBL1017 3705 115 None -2 4 Human 8.4 pIC50 = 8.4 Functional
UnclassifiedUnclassified
Guide to Pharmacology 514 7 1 5 7.3 CCCc1nc2c(n1Cc1ccc(cc1)c1ccccc1C(=O)O)cc(cc2C)c1nc2c(n1C)cccc2 9878991
DB00966 3705 115 None -2 4 Human 8.4 pIC50 = 8.4 Functional
UnclassifiedUnclassified
Guide to Pharmacology 514 7 1 5 7.3 CCCc1nc2c(n1Cc1ccc(cc1)c1ccccc1C(=O)O)cc(cc2C)c1nc2c(n1C)cccc2 9878991
4673492 4061 5 None 5248 2 Guinea pig 8.4 pIC50 = 8.4 Functional
UnclassifiedUnclassified
Guide to Pharmacology 438 6 1 5 4.5 CCc1nc(CC)c2c(c1)N(Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)C(=O)CC2 8576904
8324 4061 5 None 5248 2 Guinea pig 8.4 pIC50 = 8.4 Functional
UnclassifiedUnclassified
Guide to Pharmacology 438 6 1 5 4.5 CCc1nc(CC)c2c(c1)N(Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)C(=O)CC2 8576904
CHEMBL159096 4061 5 None 5248 2 Guinea pig 8.4 pIC50 = 8.4 Functional
UnclassifiedUnclassified
Guide to Pharmacology 438 6 1 5 4.5 CCc1nc(CC)c2c(c1)N(Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)C(=O)CC2 8576904
108185 1578 71 None 3 5 Human 8.4 pIC50 = 8.4 Functional
UnclassifiedUnclassified
Guide to Pharmacology 436 8 2 6 4.5 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)C(=O)O)Cl 10193788
108185 1578 71 None 3 5 Human 8.4 pIC50 = 8.4 Functional
UnclassifiedUnclassified
Guide to Pharmacology 436 8 2 6 4.5 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)C(=O)O)Cl 8372104
586 1578 71 None 3 5 Human 8.4 pIC50 = 8.4 Functional
UnclassifiedUnclassified
Guide to Pharmacology 436 8 2 6 4.5 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)C(=O)O)Cl 10193788
586 1578 71 None 3 5 Human 8.4 pIC50 = 8.4 Functional
UnclassifiedUnclassified
Guide to Pharmacology 436 8 2 6 4.5 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)C(=O)O)Cl 8372104
CHEMBL907 1578 71 None 3 5 Human 8.4 pIC50 = 8.4 Functional
UnclassifiedUnclassified
Guide to Pharmacology 436 8 2 6 4.5 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)C(=O)O)Cl 10193788
CHEMBL907 1578 71 None 3 5 Human 8.4 pIC50 = 8.4 Functional
UnclassifiedUnclassified
Guide to Pharmacology 436 8 2 6 4.5 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)C(=O)O)Cl 8372104
44299731 416 0 None -2 2 Human 8.5 pIC50 = 8.5 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None None
585 416 0 None -2 2 Human 8.5 pIC50 = 8.5 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None None
CHEMBL56448 416 0 None -2 2 Human 8.5 pIC50 = 8.5 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None None
6917 132 0 None - 1 Human 8.5 pIC50 = 8.5 Functional
UnclassifiedUnclassified
Guide to Pharmacology 348 7 1 3 4.9 CCCCc1cnc(n1Cc1ccc(cc1)c1ccccc1C)C(=O)O 22889560
73755250 132 0 None - 1 Human 8.5 pIC50 = 8.5 Functional
UnclassifiedUnclassified
Guide to Pharmacology 348 7 1 3 4.9 CCCCc1cnc(n1Cc1ccc(cc1)c1ccccc1C)C(=O)O 22889560
1037 1542 65 None -1 3 Human 8.6 pIC50 = 8.6 Functional
UnclassifiedUnclassified
Guide to Pharmacology 424 10 2 5 4.7 CCCCc1ncc(n1Cc1ccc(cc1)C(=O)O)/C=C(/C(=O)O)\Cc1cccs1 1309870
3940 1542 65 None -1 3 Human 8.6 pIC50 = 8.6 Functional
UnclassifiedUnclassified
Guide to Pharmacology 424 10 2 5 4.7 CCCCc1ncc(n1Cc1ccc(cc1)C(=O)O)/C=C(/C(=O)O)\Cc1cccs1 1309870
5281037 1542 65 None -1 3 Human 8.6 pIC50 = 8.6 Functional
UnclassifiedUnclassified
Guide to Pharmacology 424 10 2 5 4.7 CCCCc1ncc(n1Cc1ccc(cc1)C(=O)O)/C=C(/C(=O)O)\Cc1cccs1 1309870
588 1542 65 None -1 3 Human 8.6 pIC50 = 8.6 Functional
UnclassifiedUnclassified
Guide to Pharmacology 424 10 2 5 4.7 CCCCc1ncc(n1Cc1ccc(cc1)C(=O)O)/C=C(/C(=O)O)\Cc1cccs1 1309870
CHEMBL813 1542 65 None -1 3 Human 8.6 pIC50 = 8.6 Functional
UnclassifiedUnclassified
Guide to Pharmacology 424 10 2 5 4.7 CCCCc1ncc(n1Cc1ccc(cc1)C(=O)O)/C=C(/C(=O)O)\Cc1cccs1 1309870
DB00876 1542 65 None -1 3 Human 8.6 pIC50 = 8.6 Functional
UnclassifiedUnclassified
Guide to Pharmacology 424 10 2 5 4.7 CCCCc1ncc(n1Cc1ccc(cc1)C(=O)O)/C=C(/C(=O)O)\Cc1cccs1 1309870
2806 3894 109 None 1 4 Human 8.6 pIC50 = 8.6 Functional
UnclassifiedUnclassified
Guide to Pharmacology 435 10 2 5 4.2 CCCCC(=O)N([C@H](C(=O)O)C(C)C)Cc1ccc(cc1)c1ccccc1c1nnn[nH]1 8577935
3937 3894 109 None 1 4 Human 8.6 pIC50 = 8.6 Functional
UnclassifiedUnclassified
Guide to Pharmacology 435 10 2 5 4.2 CCCCC(=O)N([C@H](C(=O)O)C(C)C)Cc1ccc(cc1)c1ccccc1c1nnn[nH]1 8577935
593 3894 109 None 1 4 Human 8.6 pIC50 = 8.6 Functional
UnclassifiedUnclassified
Guide to Pharmacology 435 10 2 5 4.2 CCCCC(=O)N([C@H](C(=O)O)C(C)C)Cc1ccc(cc1)c1ccccc1c1nnn[nH]1 8577935
60846 3894 109 None 1 4 Human 8.6 pIC50 = 8.6 Functional
UnclassifiedUnclassified
Guide to Pharmacology 435 10 2 5 4.2 CCCCC(=O)N([C@H](C(=O)O)C(C)C)Cc1ccc(cc1)c1ccccc1c1nnn[nH]1 8577935
CHEMBL1069 3894 109 None 1 4 Human 8.6 pIC50 = 8.6 Functional
UnclassifiedUnclassified
Guide to Pharmacology 435 10 2 5 4.2 CCCCC(=O)N([C@H](C(=O)O)C(C)C)Cc1ccc(cc1)c1ccccc1c1nnn[nH]1 8577935
DB00177 3894 109 None 1 4 Human 8.6 pIC50 = 8.6 Functional
UnclassifiedUnclassified
Guide to Pharmacology 435 10 2 5 4.2 CCCCC(=O)N([C@H](C(=O)O)C(C)C)Cc1ccc(cc1)c1ccccc1c1nnn[nH]1 8577935
1481 2027 109 None -6 4 Human 8.8 pIC50 = 8.8 Functional
UnclassifiedUnclassified
Guide to Pharmacology 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 10193788
3749 2027 109 None -6 4 Human 8.8 pIC50 = 8.8 Functional
UnclassifiedUnclassified
Guide to Pharmacology 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 10193788
589 2027 109 None -6 4 Human 8.8 pIC50 = 8.8 Functional
UnclassifiedUnclassified
Guide to Pharmacology 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 10193788
6908 2027 109 None -6 4 Human 8.8 pIC50 = 8.8 Functional
UnclassifiedUnclassified
Guide to Pharmacology 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 10193788
CHEMBL1513 2027 109 None -6 4 Human 8.8 pIC50 = 8.8 Functional
UnclassifiedUnclassified
Guide to Pharmacology 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 10193788
DB01029 2027 109 None -6 4 Human 8.8 pIC50 = 8.8 Functional
UnclassifiedUnclassified
Guide to Pharmacology 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 10193788
136218976 150 0 None - 1 Rat 8.8 pIC50 = 8.8 Functional
UnclassifiedUnclassified
Guide to Pharmacology 423 9 2 5 3.7 CCC[C@H](N(C(=O)CC)Cc1ccc(cc1)c1ccccc1c1noc(=O)[nH]1)C(=O)O 22410249
6913 150 0 None - 1 Rat 8.8 pIC50 = 8.8 Functional
UnclassifiedUnclassified
Guide to Pharmacology 423 9 2 5 3.7 CCC[C@H](N(C(=O)CC)Cc1ccc(cc1)c1ccccc1c1noc(=O)[nH]1)C(=O)O 22410249
2806 3894 109 None 1 4 Human 8.9 pIC50 = 8.9 Functional
UnclassifiedUnclassified
Guide to Pharmacology 435 10 2 5 4.2 CCCCC(=O)N([C@H](C(=O)O)C(C)C)Cc1ccc(cc1)c1ccccc1c1nnn[nH]1 11206708
3937 3894 109 None 1 4 Human 8.9 pIC50 = 8.9 Functional
UnclassifiedUnclassified
Guide to Pharmacology 435 10 2 5 4.2 CCCCC(=O)N([C@H](C(=O)O)C(C)C)Cc1ccc(cc1)c1ccccc1c1nnn[nH]1 11206708
593 3894 109 None 1 4 Human 8.9 pIC50 = 8.9 Functional
UnclassifiedUnclassified
Guide to Pharmacology 435 10 2 5 4.2 CCCCC(=O)N([C@H](C(=O)O)C(C)C)Cc1ccc(cc1)c1ccccc1c1nnn[nH]1 11206708
60846 3894 109 None 1 4 Human 8.9 pIC50 = 8.9 Functional
UnclassifiedUnclassified
Guide to Pharmacology 435 10 2 5 4.2 CCCCC(=O)N([C@H](C(=O)O)C(C)C)Cc1ccc(cc1)c1ccccc1c1nnn[nH]1 11206708
CHEMBL1069 3894 109 None 1 4 Human 8.9 pIC50 = 8.9 Functional
UnclassifiedUnclassified
Guide to Pharmacology 435 10 2 5 4.2 CCCCC(=O)N([C@H](C(=O)O)C(C)C)Cc1ccc(cc1)c1ccccc1c1nnn[nH]1 11206708
DB00177 3894 109 None 1 4 Human 8.9 pIC50 = 8.9 Functional
UnclassifiedUnclassified
Guide to Pharmacology 435 10 2 5 4.2 CCCCC(=O)N([C@H](C(=O)O)C(C)C)Cc1ccc(cc1)c1ccccc1c1nnn[nH]1 11206708
3839 3688 78 None - 1 Human 8.9 pIC50 = 8.9 Functional
UnclassifiedUnclassified
Guide to Pharmacology 411 4 1 6 3.4 Cc1nc(C)c2c(n1)N(Cc1ccc(cc1)c1ccccc1c1nn[nH]n1)C(=O)CC2 11046101
60919 3688 78 None - 1 Human 8.9 pIC50 = 8.9 Functional
UnclassifiedUnclassified
Guide to Pharmacology 411 4 1 6 3.4 Cc1nc(C)c2c(n1)N(Cc1ccc(cc1)c1ccccc1c1nn[nH]n1)C(=O)CC2 11046101
6898 3688 78 None - 1 Human 8.9 pIC50 = 8.9 Functional
UnclassifiedUnclassified
Guide to Pharmacology 411 4 1 6 3.4 Cc1nc(C)c2c(n1)N(Cc1ccc(cc1)c1ccccc1c1nn[nH]n1)C(=O)CC2 11046101
CHEMBL432162 3688 78 None - 1 Human 8.9 pIC50 = 8.9 Functional
UnclassifiedUnclassified
Guide to Pharmacology 411 4 1 6 3.4 Cc1nc(C)c2c(n1)N(Cc1ccc(cc1)c1ccccc1c1nn[nH]n1)C(=O)CC2 11046101
DB01349 3688 78 None - 1 Human 8.9 pIC50 = 8.9 Functional
UnclassifiedUnclassified
Guide to Pharmacology 411 4 1 6 3.4 Cc1nc(C)c2c(n1)N(Cc1ccc(cc1)c1ccccc1c1nn[nH]n1)C(=O)CC2 11046101
16133225 415 47 None -5 4 Human 9.2 pIC50 = 9.2 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 10193788
172198 415 47 None -5 4 Human 9.2 pIC50 = 9.2 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 10193788
2504 415 47 None -5 4 Human 9.2 pIC50 = 9.2 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 10193788
45266664 415 47 None -5 4 Human 9.2 pIC50 = 9.2 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 10193788
5272 415 47 None -5 4 Human 9.2 pIC50 = 9.2 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 10193788
CHEMBL408403 415 47 None -5 4 Human 9.2 pIC50 = 9.2 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 10193788
DB11842 415 47 None -5 4 Human 9.2 pIC50 = 9.2 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 10193788
6894 414 0 None -2 3 Rat 9.5 pIC50 = 9.5 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 17138938
91691124 414 0 None -2 3 Rat 9.5 pIC50 = 9.5 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 17138938
2541 772 113 None 7 7 Human 9.6 pIC50 = 9.6 Functional
UnclassifiedUnclassified
Guide to Pharmacology 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10193788
587 772 113 None 7 7 Human 9.6 pIC50 = 9.6 Functional
UnclassifiedUnclassified
Guide to Pharmacology 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10193788
6907 772 113 None 7 7 Human 9.6 pIC50 = 9.6 Functional
UnclassifiedUnclassified
Guide to Pharmacology 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10193788
CHEMBL1016 772 113 None 7 7 Human 9.6 pIC50 = 9.6 Functional
UnclassifiedUnclassified
Guide to Pharmacology 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10193788
DB00796 772 113 None 7 7 Human 9.6 pIC50 = 9.6 Functional
UnclassifiedUnclassified
Guide to Pharmacology 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10193788
DB13919 772 113 None 7 7 Human 9.6 pIC50 = 9.6 Functional
UnclassifiedUnclassified
Guide to Pharmacology 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10193788




Ligands Receptor Assay information Chemical information
Sel. page Common
name
GPCRdb ID #Vendors Reference
ligand
Fold selectivity
(Affinity)
# tested GPCRs
(Affinity)
Species p-value
(-log)
Type Activity
Relation
Activity
Value
Assay Type Assay Description Source Mol
weight
Rot
Bonds
H don H acc LogP Smiles DOI
155540547 171944 0 None - 0 Human 8.0 pEC50 = 8 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 945 26 13 13 -2.8 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)c(F)c1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O)[C@@H](C)OC)C(C)C nan
CHEMBL4483576 171944 0 None - 0 Human 8.0 pEC50 = 8 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 945 26 13 13 -2.8 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)c(F)c1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O)[C@@H](C)OC)C(C)C nan
155539027 172245 0 None - 0 Rat 8.0 pEC50 = 8 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 944 26 13 12 -1.8 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)c(F)c1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
CHEMBL4514079 172245 0 None - 0 Rat 8.0 pEC50 = 8 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 944 26 13 12 -1.8 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)c(F)c1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
155541295 172432 0 None - 0 Human 7.0 pEC50 = 7 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 926 25 12 12 -2.0 CC(C)[C@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CN(C)C)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O)C(C)C nan
CHEMBL4518318 172432 0 None - 0 Human 7.0 pEC50 = 7 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 926 25 12 12 -2.0 CC(C)[C@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CN(C)C)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O)C(C)C nan
155547844 173116 0 None - 0 Human 7.0 pEC50 = 7 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 942 26 14 13 -2.2 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)c(O)c1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
CHEMBL4535678 173116 0 None - 0 Human 7.0 pEC50 = 7 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 942 26 14 13 -2.2 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)c(O)c1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
155565112 174916 0 None - 0 Rat 7.0 pEC50 = 7 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 1081 26 13 12 -0.4 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1cc(Br)c(O)c(Br)c1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
CHEMBL4577692 174916 0 None - 0 Rat 7.0 pEC50 = 7 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 1081 26 13 12 -0.4 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1cc(Br)c(O)c(Br)c1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
155546362 172969 0 None - 0 Human 6.0 pEC50 = 6 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 966 26 12 12 -1.0 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CN1CCCC1)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
CHEMBL4532075 172969 0 None - 0 Human 6.0 pEC50 = 6 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 966 26 12 12 -1.0 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CN1CCCC1)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
155568289 175543 0 None - 0 Human 6.0 pEC50 = 6 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 898 26 11 12 -1.0 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCCN)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
CHEMBL4592000 175543 0 None - 0 Human 6.0 pEC50 = 6 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 898 26 11 12 -1.0 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCCN)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
155557139 173962 0 None - 0 Human 5.0 pEC50 = 5 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 980 26 12 12 -0.6 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CN1CCCCC1)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
CHEMBL4556070 173962 0 None - 0 Human 5.0 pEC50 = 5 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 980 26 12 12 -0.6 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CN1CCCCC1)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
155520024 172665 0 None - 0 Rat 5.0 pEC50 = 5 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 959 27 13 12 -1.6 CN[C@@H](CCC(=O)O)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(N)=O)C(C)C nan
CHEMBL4524570 172665 0 None - 0 Rat 5.0 pEC50 = 5 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 959 27 13 12 -1.6 CN[C@@H](CCC(=O)O)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(N)=O)C(C)C nan
155557139 173962 0 None - 0 Rat 5.0 pEC50 = 5 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 980 26 12 12 -0.6 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CN1CCCCC1)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
CHEMBL4556070 173962 0 None - 0 Rat 5.0 pEC50 = 5 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 980 26 12 12 -0.6 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CN1CCCCC1)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
CHEMBL938 214120 24 None 1 2 Human 8.0 pEC50 = 8.0 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL None None None CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O)C(C)C)C(C)C nan
155544988 172860 0 None - 0 Rat 7.0 pEC50 = 7.0 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 853 24 12 11 -2.0 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@@H]1C(N)=O nan
CHEMBL4529051 172860 0 None - 0 Rat 7.0 pEC50 = 7.0 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 853 24 12 11 -2.0 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@@H]1C(N)=O nan
155541440 172440 0 None - 0 Human 7.9 pEC50 = 7.9 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 954 28 13 12 -1.1 CCC[C@H](NC(=O)[C@@H]1CCCN1C(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)[C@@H](C)CC)C(=O)O nan
CHEMBL4518530 172440 0 None - 0 Human 7.9 pEC50 = 7.9 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 954 28 13 12 -1.1 CCC[C@H](NC(=O)[C@@H]1CCCN1C(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)[C@@H](C)CC)C(=O)O nan
155540033 172311 0 None - 0 Rat 6.9 pEC50 = 6.9 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 953 27 13 12 -1.9 CC[C@H](C)[C@H](NC(=O)[C@@H]1CCCN1C(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(C)C)C(N)=O nan
CHEMBL4515768 172311 0 None - 0 Rat 6.9 pEC50 = 6.9 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 953 27 13 12 -1.9 CC[C@H](C)[C@H](NC(=O)[C@@H]1CCCN1C(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(C)C)C(N)=O nan
155541125 172386 0 None - 1 Rat 6.9 pEC50 = 6.9 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 904 27 12 11 -1.2 CC[C@H](C)[C@H](NC(=O)[C@@H]1CCCN1C(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)[C@@H](C)CC)C(C)C)C(=O)O nan
CHEMBL4517561 172386 0 None - 1 Rat 6.9 pEC50 = 6.9 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 904 27 12 11 -1.2 CC[C@H](C)[C@H](NC(=O)[C@@H]1CCCN1C(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)[C@@H](C)CC)C(C)C)C(=O)O nan
155540470 171899 0 None - 0 Human 5.9 pEC50 = 5.9 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 961 26 14 13 -2.3 CN[C@@H](CC(=O)O)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(N)=O)C(C)C nan
CHEMBL4482867 171899 0 None - 0 Human 5.9 pEC50 = 5.9 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 961 26 14 13 -2.3 CN[C@@H](CC(=O)O)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(N)=O)C(C)C nan
155559120 174204 0 None - 0 Human 5.9 pEC50 = 5.9 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 945 26 13 12 -1.8 CC(C)[C@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H](N)CCC(=O)O)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(N)=O nan
CHEMBL4561769 174204 0 None - 0 Human 5.9 pEC50 = 5.9 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 945 26 13 12 -1.8 CC(C)[C@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H](N)CCC(=O)O)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(N)=O nan
155564502 174678 0 None - 0 Human 5.9 pEC50 = 5.9 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 2296 33 30 27 -2.1 CC[C@H](C)[C@@H]1NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](C(C)C)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H]2CCCN2C(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@H]([C@@H](C)CC)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](C(C)C)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H]2CCCN2C(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@H]([C@@H](C)CC)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](C(C)C)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H]2CCCN2C(=O)[C@H](Cc2cnc[nH]2)NC1=O nan
CHEMBL4572408 174678 0 None - 0 Human 5.9 pEC50 = 5.9 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 2296 33 30 27 -2.1 CC[C@H](C)[C@@H]1NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](C(C)C)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H]2CCCN2C(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@H]([C@@H](C)CC)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](C(C)C)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H]2CCCN2C(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@H]([C@@H](C)CC)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](C(C)C)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H]2CCCN2C(=O)[C@H](Cc2cnc[nH]2)NC1=O nan
54696627 97881 0 None - 0 Bovine 5.9 pEC50 = 5.9 Binding
Inhibition of [125I]AII binding to angiotensin II receptor of bovine adrenal cortexInhibition of [125I]AII binding to angiotensin II receptor of bovine adrenal cortex
ChEMBL 486 5 2 7 5.0 Cc1ccc2c(O)c(-c3ccccc3)c(=O)n(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c2n1 10.1016/S0960-894X(01)81134-3
CHEMBL27511 97881 0 None - 0 Bovine 5.9 pEC50 = 5.9 Binding
Inhibition of [125I]AII binding to angiotensin II receptor of bovine adrenal cortexInhibition of [125I]AII binding to angiotensin II receptor of bovine adrenal cortex
ChEMBL 486 5 2 7 5.0 Cc1ccc2c(O)c(-c3ccccc3)c(=O)n(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c2n1 10.1016/S0960-894X(01)81134-3
54726669 98800 0 None - 0 Bovine 5.9 pEC50 = 5.9 Binding
Inhibition of [125I]AII binding to angiotensin II receptor of bovine adrenal cortexInhibition of [125I]AII binding to angiotensin II receptor of bovine adrenal cortex
ChEMBL 461 5 2 6 4.6 O=c1c(-c2ccccc2)c(O)c2c(n1Cc1ccc(-c3ccccc3-c3nn[nH]n3)cc1)CCC2 10.1016/S0960-894X(01)81134-3
CHEMBL281887 98800 0 None - 0 Bovine 5.9 pEC50 = 5.9 Binding
Inhibition of [125I]AII binding to angiotensin II receptor of bovine adrenal cortexInhibition of [125I]AII binding to angiotensin II receptor of bovine adrenal cortex
ChEMBL 461 5 2 6 4.6 O=c1c(-c2ccccc2)c(O)c2c(n1Cc1ccc(-c3ccccc3-c3nn[nH]n3)cc1)CCC2 10.1016/S0960-894X(01)81134-3
155539027 172245 0 None - 0 Human 7.9 pEC50 = 7.9 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 944 26 13 12 -1.8 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)c(F)c1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
CHEMBL4514079 172245 0 None - 0 Human 7.9 pEC50 = 7.9 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 944 26 13 12 -1.8 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)c(F)c1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
155547428 173033 0 None - 0 Rat 7.9 pEC50 = 7.9 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 959 26 13 12 -1.3 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)c(Cl)c1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
CHEMBL4533618 173033 0 None - 0 Rat 7.9 pEC50 = 7.9 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 959 26 13 12 -1.3 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)c(Cl)c1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
155550799 173692 0 None - 0 Rat 7.9 pEC50 = 7.9 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 959 26 13 12 -1.7 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O)C(C)C nan
CHEMBL4549405 173692 0 None - 0 Rat 7.9 pEC50 = 7.9 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 959 26 13 12 -1.7 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O)C(C)C nan
155543091 172599 0 None - 0 Rat 6.9 pEC50 = 6.9 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 940 26 13 12 -1.5 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H](C)NC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
CHEMBL4522246 172599 0 None - 0 Rat 6.9 pEC50 = 6.9 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 940 26 13 12 -1.5 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H](C)NC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
155520014 172655 0 None - 0 Human 5.9 pEC50 = 5.9 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 975 27 14 13 -1.9 CN[C@@H](CCC(=O)O)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(N)=O)C(C)C nan
CHEMBL4524300 172655 0 None - 0 Human 5.9 pEC50 = 5.9 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 975 27 14 13 -1.9 CN[C@@H](CCC(=O)O)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(N)=O)C(C)C nan
CHEMBL2028943 207381 0 None - 0 Rat 7.9 pEC50 = 7.9 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@@H]1CCCN1C(=O)[C@H](Cc1c[nH]cn1)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCN=C(N)N)NC(=O)CNC)C(C)C)C(=O)O nan
CHEMBL2370909 208193 0 None - 0 Rat 6.9 pEC50 = 6.9 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@@H]1CCCN1C(=O)[C@H](Cc1c[nH]cn1)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCN=C(N)N)NC(=O)CNC)C(C)C)C(=O)O nan
155542907 172596 0 None - 0 Human 5.9 pEC50 = 5.9 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 904 24 13 12 -1.5 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)O)C(C)C nan
CHEMBL4522038 172596 0 None - 0 Human 5.9 pEC50 = 5.9 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 904 24 13 12 -1.5 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)O)C(C)C nan
155563676 174762 0 None - 0 Human 5.9 pEC50 = 5.9 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 961 26 14 13 -2.1 CC(C)[C@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H](N)CCC(=O)O)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(N)=O nan
CHEMBL4574199 174762 0 None - 0 Human 5.9 pEC50 = 5.9 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 961 26 14 13 -2.1 CC(C)[C@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H](N)CCC(=O)O)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(N)=O nan
CHEMBL2392353 208659 6 None - 1 Rat 7.8 pEC50 = 7.8 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL None None None None nan
3082475 3804 9 None - 1 Rat 7.8 pEC50 = 7.8 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL None None None None nan
6902 3804 9 None - 1 Rat 7.8 pEC50 = 7.8 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL None None None None nan
CHEMBL4297447 3804 9 None - 1 Rat 7.8 pEC50 = 7.8 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL None None None None nan
DB12199 3804 9 None - 1 Rat 7.8 pEC50 = 7.8 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL None None None None nan
155568804 175536 0 None - 0 Rat 7.8 pEC50 = 7.8 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 927 26 13 13 -2.9 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O)[C@@H](C)OC)C(C)C nan
CHEMBL4591857 175536 0 None - 0 Rat 7.8 pEC50 = 7.8 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 927 26 13 13 -2.9 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O)[C@@H](C)OC)C(C)C nan
155541240 172437 0 None - 0 Human 6.8 pEC50 = 6.8 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 928 26 12 11 -1.5 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(F)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
CHEMBL4518420 172437 0 None - 0 Human 6.8 pEC50 = 6.8 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 928 26 12 11 -1.5 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(F)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
155563538 174718 0 None - 0 Human 6.8 pEC50 = 6.8 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 925 26 13 12 -2.5 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(N)=O nan
CHEMBL4573250 174718 0 None - 0 Human 6.8 pEC50 = 6.8 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 925 26 13 12 -2.5 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(N)=O nan
155554529 174051 0 None - 0 Rat 6.8 pEC50 = 6.8 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 961 26 13 12 -1.6 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1c(F)cc(O)cc1F)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
CHEMBL4557984 174051 0 None - 0 Rat 6.8 pEC50 = 6.8 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 961 26 13 12 -1.6 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1c(F)cc(O)cc1F)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
10533900 175386 5 None - 0 Rat 6.8 pEC50 = 6.8 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 955 27 14 13 -2.7 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H](N)CC(=O)O)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)NCC(=O)O nan
CHEMBL4588454 175386 5 None - 0 Rat 6.8 pEC50 = 6.8 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 955 27 14 13 -2.7 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H](N)CC(=O)O)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)NCC(=O)O nan
155544246 172784 0 None - 0 Human 5.8 pEC50 = 5.8 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 887 24 12 11 -1.8 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(N)=O)C(C)C nan
CHEMBL4527484 172784 0 None - 0 Human 5.8 pEC50 = 5.8 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 887 24 12 11 -1.8 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(N)=O)C(C)C nan
155553003 173494 0 None - 0 Human 5.8 pEC50 = 5.8 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 791 23 12 11 -4.0 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)NCC(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)NCC(=O)O)C(C)C)C(C)C nan
CHEMBL4544308 173494 0 None - 0 Human 5.8 pEC50 = 5.8 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 791 23 12 11 -4.0 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)NCC(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)NCC(=O)O)C(C)C)C(C)C nan
155561477 174610 0 None - 0 Human 5.8 pEC50 = 5.8 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 811 22 12 11 -3.0 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(N)=O)C(C)C nan
CHEMBL4570840 174610 0 None - 0 Human 5.8 pEC50 = 5.8 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 811 22 12 11 -3.0 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(N)=O)C(C)C nan
155562469 174639 0 None - 0 Human 5.8 pEC50 = 5.8 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 966 29 12 12 -1.1 C=CCOc1ccc(C[C@H](NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@H](C(=O)N[C@@H](Cc2cnc[nH]2)C(=O)N2CCC[C@H]2C(=O)N[C@H](C)C(=O)O)[C@@H](C)CC)cc1 nan
CHEMBL4571382 174639 0 None - 0 Human 5.8 pEC50 = 5.8 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 966 29 12 12 -1.1 C=CCOc1ccc(C[C@H](NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@H](C(=O)N[C@@H](Cc2cnc[nH]2)C(=O)N2CCC[C@H]2C(=O)N[C@H](C)C(=O)O)[C@@H](C)CC)cc1 nan
155553930 174858 0 None - 0 Human 5.8 pEC50 = 5.8 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 1177 26 13 12 -0.7 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1cc(I)c(O)c(I)c1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
CHEMBL4576650 174858 0 None - 0 Human 5.8 pEC50 = 5.8 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 1177 26 13 12 -0.7 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1cc(I)c(O)c(I)c1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
155551279 173405 0 None - 0 Human 7.8 pEC50 = 7.8 Binding
Agonist activity at human AT1 receptor assessed as increase in beta-arrestin recruitment by chemiluminescent assayAgonist activity at human AT1 receptor assessed as increase in beta-arrestin recruitment by chemiluminescent assay
ChEMBL 877 29 13 12 -2.3 CC[C@H](C)[C@H](NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](CCCCN)CN[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O 10.1021/acs.jmedchem.8b00435
CHEMBL4542269 173405 0 None - 0 Human 7.8 pEC50 = 7.8 Binding
Agonist activity at human AT1 receptor assessed as increase in beta-arrestin recruitment by chemiluminescent assayAgonist activity at human AT1 receptor assessed as increase in beta-arrestin recruitment by chemiluminescent assay
ChEMBL 877 29 13 12 -2.3 CC[C@H](C)[C@H](NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](CCCCN)CN[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O 10.1021/acs.jmedchem.8b00435
3082475 3804 9 None - 1 Human 7.8 pEC50 = 7.8 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL None None None None nan
6902 3804 9 None - 1 Human 7.8 pEC50 = 7.8 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL None None None None nan
CHEMBL4297447 3804 9 None - 1 Human 7.8 pEC50 = 7.8 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL None None None None nan
DB12199 3804 9 None - 1 Human 7.8 pEC50 = 7.8 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL None None None None nan
70538373 174915 0 None - 0 Rat 7.8 pEC50 = 7.8 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 840 23 12 11 -1.8 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)O)C(C)C)C(C)C nan
CHEMBL4577691 174915 0 None - 0 Rat 7.8 pEC50 = 7.8 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 840 23 12 11 -1.8 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)O)C(C)C)C(C)C nan
155554865 173772 0 None - 0 Human 5.8 pEC50 = 5.8 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 2269 27 21 24 3.8 CC[C@H](C)[C@@H]1NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](C(C)C)NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@@H]2CCCN2C(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@H]([C@@H](C)CC)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](C(C)C)NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@@H]2CCCN2C(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@H]([C@@H](C)CC)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](C(C)C)NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@@H]2CCCN2C(=O)[C@H](Cc2cnc[nH]2)NC1=O nan
CHEMBL4551317 173772 0 None - 0 Human 5.8 pEC50 = 5.8 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 2269 27 21 24 3.8 CC[C@H](C)[C@@H]1NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](C(C)C)NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@@H]2CCCN2C(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@H]([C@@H](C)CC)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](C(C)C)NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@@H]2CCCN2C(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@H]([C@@H](C)CC)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](C(C)C)NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@@H]2CCCN2C(=O)[C@H](Cc2cnc[nH]2)NC1=O nan
54726671 94173 0 None - 0 Bovine 5.8 pEC50 = 5.8 Binding
Inhibition of [125I]AII binding to angiotensin II receptor of bovine adrenal cortexInhibition of [125I]AII binding to angiotensin II receptor of bovine adrenal cortex
ChEMBL 471 5 2 6 5.3 O=c1c(-c2ccccc2)c(O)c2ccccc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81134-3
CHEMBL25226 94173 0 None - 0 Bovine 5.8 pEC50 = 5.8 Binding
Inhibition of [125I]AII binding to angiotensin II receptor of bovine adrenal cortexInhibition of [125I]AII binding to angiotensin II receptor of bovine adrenal cortex
ChEMBL 471 5 2 6 5.3 O=c1c(-c2ccccc2)c(O)c2ccccc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81134-3
155560095 174340 0 None - 0 Rat 7.8 pEC50 = 7.8 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 975 26 14 13 -2.0 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O)C(C)C nan
CHEMBL4564950 174340 0 None - 0 Rat 7.8 pEC50 = 7.8 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 975 26 14 13 -2.0 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O)C(C)C nan
155563538 174718 0 None - 0 Rat 6.8 pEC50 = 6.8 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 925 26 13 12 -2.5 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(N)=O nan
CHEMBL4573250 174718 0 None - 0 Rat 6.8 pEC50 = 6.8 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 925 26 13 12 -2.5 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(N)=O nan
155565687 175000 0 None - 0 Rat 6.8 pEC50 = 6.8 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 961 26 14 13 -2.1 CC(C)[C@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](N)CCC(=O)O)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(N)=O nan
CHEMBL4579604 175000 0 None - 0 Rat 6.8 pEC50 = 6.8 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 961 26 14 13 -2.1 CC(C)[C@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](N)CCC(=O)O)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(N)=O nan
155556507 173904 0 None - 0 Human 5.8 pEC50 = 5.8 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 910 26 12 11 -1.6 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
CHEMBL4554466 173904 0 None - 0 Human 5.8 pEC50 = 5.8 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 910 26 12 11 -1.6 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
54726670 93517 0 None - 0 Bovine 5.8 pEC50 = 5.8 Binding
Inhibition of [125I]AII binding to angiotensin II receptor of bovine adrenal cortexInhibition of [125I]AII binding to angiotensin II receptor of bovine adrenal cortex
ChEMBL 491 7 2 5 6.2 CCOc1ccc2c(O)c(-c3ccccc3)c(=O)n(Cc3ccc(-c4ccccc4C(=O)O)cc3)c2c1 10.1016/S0960-894X(01)81134-3
CHEMBL24842 93517 0 None - 0 Bovine 5.8 pEC50 = 5.8 Binding
Inhibition of [125I]AII binding to angiotensin II receptor of bovine adrenal cortexInhibition of [125I]AII binding to angiotensin II receptor of bovine adrenal cortex
ChEMBL 491 7 2 5 6.2 CCOc1ccc2c(O)c(-c3ccccc3)c(=O)n(Cc3ccc(-c4ccccc4C(=O)O)cc3)c2c1 10.1016/S0960-894X(01)81134-3
155560463 174458 0 None - 0 Rat 7.7 pEC50 = 7.7 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 1052 28 14 13 -0.8 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](Cc1ccccc1)C(=O)O)C(C)C nan
CHEMBL4567667 174458 0 None - 0 Rat 7.7 pEC50 = 7.7 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 1052 28 14 13 -0.8 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](Cc1ccccc1)C(=O)O)C(C)C nan
155553003 173494 0 None - 0 Rat 5.7 pEC50 = 5.7 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 791 23 12 11 -4.0 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)NCC(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)NCC(=O)O)C(C)C)C(C)C nan
CHEMBL4544308 173494 0 None - 0 Rat 5.7 pEC50 = 5.7 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 791 23 12 11 -4.0 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)NCC(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)NCC(=O)O)C(C)C)C(C)C nan
155554865 173772 0 None - 0 Rat 5.7 pEC50 = 5.7 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 2269 27 21 24 3.8 CC[C@H](C)[C@@H]1NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](C(C)C)NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@@H]2CCCN2C(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@H]([C@@H](C)CC)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](C(C)C)NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@@H]2CCCN2C(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@H]([C@@H](C)CC)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](C(C)C)NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@@H]2CCCN2C(=O)[C@H](Cc2cnc[nH]2)NC1=O nan
CHEMBL4551317 173772 0 None - 0 Rat 5.7 pEC50 = 5.7 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 2269 27 21 24 3.8 CC[C@H](C)[C@@H]1NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](C(C)C)NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@@H]2CCCN2C(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@H]([C@@H](C)CC)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](C(C)C)NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@@H]2CCCN2C(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@H]([C@@H](C)CC)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](C(C)C)NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@@H]2CCCN2C(=O)[C@H](Cc2cnc[nH]2)NC1=O nan
155564502 174678 0 None - 0 Rat 5.7 pEC50 = 5.7 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 2296 33 30 27 -2.1 CC[C@H](C)[C@@H]1NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](C(C)C)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H]2CCCN2C(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@H]([C@@H](C)CC)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](C(C)C)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H]2CCCN2C(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@H]([C@@H](C)CC)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](C(C)C)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H]2CCCN2C(=O)[C@H](Cc2cnc[nH]2)NC1=O nan
CHEMBL4572408 174678 0 None - 0 Rat 5.7 pEC50 = 5.7 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 2296 33 30 27 -2.1 CC[C@H](C)[C@@H]1NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](C(C)C)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H]2CCCN2C(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@H]([C@@H](C)CC)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](C(C)C)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H]2CCCN2C(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@H]([C@@H](C)CC)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](C(C)C)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H]2CCCN2C(=O)[C@H](Cc2cnc[nH]2)NC1=O nan
155560463 174458 0 None - 0 Human 7.7 pEC50 = 7.7 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 1052 28 14 13 -0.8 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](Cc1ccccc1)C(=O)O)C(C)C nan
CHEMBL4567667 174458 0 None - 0 Human 7.7 pEC50 = 7.7 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 1052 28 14 13 -0.8 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](Cc1ccccc1)C(=O)O)C(C)C nan
155551762 173428 0 None - 0 Human 6.7 pEC50 = 6.7 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 911 26 13 12 -2.2 CCC[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
CHEMBL4542709 173428 0 None - 0 Human 6.7 pEC50 = 6.7 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 911 26 13 12 -2.2 CCC[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
155552995 173530 0 None - 0 Rat 6.7 pEC50 = 6.7 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 940 27 12 12 -1.6 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(OC)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O nan
CHEMBL4545399 173530 0 None - 0 Rat 6.7 pEC50 = 6.7 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 940 27 12 12 -1.6 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(OC)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O nan
155556530 173929 0 None - 0 Rat 6.7 pEC50 = 6.7 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 911 25 13 12 -2.9 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(N)=O)C(C)C)C(C)C nan
CHEMBL4555119 173929 0 None - 0 Rat 6.7 pEC50 = 6.7 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 911 25 13 12 -2.9 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(N)=O)C(C)C)C(C)C nan
155568109 175455 0 None - 0 Human 5.7 pEC50 = 5.7 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 945 26 13 12 -2.0 CN[C@@H](CC(=O)O)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(N)=O)C(C)C nan
CHEMBL4590381 175455 0 None - 0 Human 5.7 pEC50 = 5.7 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 945 26 13 12 -2.0 CN[C@@H](CC(=O)O)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(N)=O)C(C)C nan
CHEMBL2392353 208659 6 None - 1 Human 7.7 pEC50 = 7.7 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL None None None None nan
155556530 173929 0 None - 0 Human 6.7 pEC50 = 6.7 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 911 25 13 12 -2.9 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(N)=O)C(C)C)C(C)C nan
CHEMBL4555119 173929 0 None - 0 Human 6.7 pEC50 = 6.7 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 911 25 13 12 -2.9 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(N)=O)C(C)C)C(C)C nan
11944 3803 0 None - 1 Human 5.7 pEC50 = 5.7 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL None None None None nan
155552190 3803 0 None - 1 Human 5.7 pEC50 = 5.7 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL None None None None nan
CHEMBL4544228 3803 0 None - 1 Human 5.7 pEC50 = 5.7 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL None None None None nan
155540470 171899 0 None - 0 Rat 5.7 pEC50 = 5.7 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 961 26 14 13 -2.3 CN[C@@H](CC(=O)O)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(N)=O)C(C)C nan
CHEMBL4482867 171899 0 None - 0 Rat 5.7 pEC50 = 5.7 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 961 26 14 13 -2.3 CN[C@@H](CC(=O)O)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(N)=O)C(C)C nan
155553311 173551 0 None - 0 Rat 5.7 pEC50 = 5.7 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 940 26 13 12 -1.5 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H](C)NC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O nan
CHEMBL4546162 173551 0 None - 0 Rat 5.7 pEC50 = 5.7 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 940 26 13 12 -1.5 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H](C)NC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O nan
154573825 175406 6 None - 0 Human 6.7 pEC50 = 6.7 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 742 22 12 10 -2.4 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(N)=O)C(C)C)C(C)C nan
CHEMBL4588946 175406 6 None - 0 Human 6.7 pEC50 = 6.7 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 742 22 12 10 -2.4 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(N)=O)C(C)C)C(C)C nan
54726676 98757 0 None - 0 Bovine 5.7 pEC50 = 5.7 Binding
Inhibition of [125I]AII binding to angiotensin II receptor of bovine adrenal cortexInhibition of [125I]AII binding to angiotensin II receptor of bovine adrenal cortex
ChEMBL 501 6 2 7 5.3 COc1ccc2c(O)c(-c3ccccc3)c(=O)n(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c2c1 10.1016/S0960-894X(01)81134-3
CHEMBL28162 98757 0 None - 0 Bovine 5.7 pEC50 = 5.7 Binding
Inhibition of [125I]AII binding to angiotensin II receptor of bovine adrenal cortexInhibition of [125I]AII binding to angiotensin II receptor of bovine adrenal cortex
ChEMBL 501 6 2 7 5.3 COc1ccc2c(O)c(-c3ccccc3)c(=O)n(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c2c1 10.1016/S0960-894X(01)81134-3
155540328 172322 0 None - 0 Rat 6.6 pEC50 = 6.6 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 1017 28 14 13 -1.6 CC[C@H](C)[C@H](NC(=O)[C@@H]1CCCN1C(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(N)=O nan
CHEMBL4516066 172322 0 None - 0 Rat 6.6 pEC50 = 6.6 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 1017 28 14 13 -1.6 CC[C@H](C)[C@H](NC(=O)[C@@H]1CCCN1C(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(N)=O nan
155547428 173033 0 None - 0 Human 7.6 pEC50 = 7.6 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 959 26 13 12 -1.3 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)c(Cl)c1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
CHEMBL4533618 173033 0 None - 0 Human 7.6 pEC50 = 7.6 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 959 26 13 12 -1.3 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)c(Cl)c1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
155568318 175518 0 None - 0 Human 7.6 pEC50 = 7.6 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 940 26 13 12 -1.5 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](C)NC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O nan
CHEMBL4591448 175518 0 None - 0 Human 7.6 pEC50 = 7.6 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 940 26 13 12 -1.5 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](C)NC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O nan
155559827 174333 0 None - 0 Rat 7.6 pEC50 = 7.6 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 970 27 13 14 -2.0 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)c([N+](=O)[O-])c1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
CHEMBL4564617 174333 0 None - 0 Rat 7.6 pEC50 = 7.6 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 970 27 13 14 -2.0 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)c([N+](=O)[O-])c1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
155565112 174916 0 None - 0 Human 6.6 pEC50 = 6.6 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 1081 26 13 12 -0.4 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1cc(Br)c(O)c(Br)c1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
CHEMBL4577692 174916 0 None - 0 Human 6.6 pEC50 = 6.6 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 1081 26 13 12 -0.4 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1cc(Br)c(O)c(Br)c1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
155558784 174194 0 None - 0 Rat 5.6 pEC50 = 5.6 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 756 9 7 8 1.3 CC[C@H](C)[C@@H]1NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](C(C)C)NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@@H]2CCCN2C(=O)[C@H](Cc2cnc[nH]2)NC1=O nan
CHEMBL4561366 174194 0 None - 0 Rat 5.6 pEC50 = 5.6 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 756 9 7 8 1.3 CC[C@H](C)[C@@H]1NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](C(C)C)NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@@H]2CCCN2C(=O)[C@H](Cc2cnc[nH]2)NC1=O nan
155540639 172354 0 None - 0 Rat 6.6 pEC50 = 6.6 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 947 25 14 13 -2.5 CC(C)[C@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](N)CC(=O)O)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(N)=O nan
CHEMBL4516768 172354 0 None - 0 Rat 6.6 pEC50 = 6.6 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 947 25 14 13 -2.5 CC(C)[C@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](N)CC(=O)O)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(N)=O nan
155553479 173596 0 None - 0 Rat 7.6 pEC50 = 7.6 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 949 26 14 13 -3.0 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O)C(C)C nan
CHEMBL4547423 173596 0 None - 0 Rat 7.6 pEC50 = 7.6 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 949 26 14 13 -3.0 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O)C(C)C nan
155558428 174147 0 None - 0 Rat 7.6 pEC50 = 7.6 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 897 26 15 12 -3.8 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(N)=O)C(C)C nan
CHEMBL4560224 174147 0 None - 0 Rat 7.6 pEC50 = 7.6 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 897 26 15 12 -3.8 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(N)=O)C(C)C nan
155553479 173596 0 None - 0 Human 6.6 pEC50 = 6.6 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 949 26 14 13 -3.0 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O)C(C)C nan
CHEMBL4547423 173596 0 None - 0 Human 6.6 pEC50 = 6.6 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 949 26 14 13 -3.0 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O)C(C)C nan
155543972 174433 0 None - 0 Rat 6.6 pEC50 = 6.6 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 917 28 13 12 -1.7 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](CCCCN)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
CHEMBL4567103 174433 0 None - 0 Rat 6.6 pEC50 = 6.6 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 917 28 13 12 -1.7 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](CCCCN)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
155567790 175469 0 None - 0 Rat 6.6 pEC50 = 6.6 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 877 24 13 12 -3.1 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(N)=O)C(C)C nan
CHEMBL4590589 175469 0 None - 0 Rat 6.6 pEC50 = 6.6 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 877 24 13 12 -3.1 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(N)=O)C(C)C nan
155556507 173904 0 None - 0 Rat 5.6 pEC50 = 5.6 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 910 26 12 11 -1.6 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
CHEMBL4554466 173904 0 None - 0 Rat 5.6 pEC50 = 5.6 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 910 26 12 11 -1.6 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
130762 97782 9 None - 0 Bovine 5.6 pEC50 = 5.6 Binding
Inhibition of [125I]AII binding to angiotensin II receptor of bovine adrenal cortexInhibition of [125I]AII binding to angiotensin II receptor of bovine adrenal cortex
ChEMBL 398 8 2 4 4.8 CCCCc1nc(Cl)c(CO)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/S0960-894X(01)81134-3
CHEMBL274447 97782 9 None - 0 Bovine 5.6 pEC50 = 5.6 Binding
Inhibition of [125I]AII binding to angiotensin II receptor of bovine adrenal cortexInhibition of [125I]AII binding to angiotensin II receptor of bovine adrenal cortex
ChEMBL 398 8 2 4 4.8 CCCCc1nc(Cl)c(CO)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/S0960-894X(01)81134-3
155568109 175455 0 None - 0 Rat 5.6 pEC50 = 5.6 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 945 26 13 12 -2.0 CN[C@@H](CC(=O)O)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(N)=O)C(C)C nan
CHEMBL4590381 175455 0 None - 0 Rat 5.6 pEC50 = 5.6 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 945 26 13 12 -2.0 CN[C@@H](CC(=O)O)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(N)=O)C(C)C nan
CHEMBL77838 214091 3 None - 0 Human 8.5 pEC50 = 8.5 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@@H]1CCCN1C(=O)[C@H](Cc1c[nH]cn1)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCN=C(N)N)NC(=O)CNC)C(C)C)C(C)C)C(=O)O nan
155558428 174147 0 None - 0 Human 7.5 pEC50 = 7.5 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 897 26 15 12 -3.8 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(N)=O)C(C)C nan
CHEMBL4560224 174147 0 None - 0 Human 7.5 pEC50 = 7.5 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 897 26 15 12 -3.8 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(N)=O)C(C)C nan
155560095 174340 0 None - 0 Human 7.5 pEC50 = 7.5 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 975 26 14 13 -2.0 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O)C(C)C nan
CHEMBL4564950 174340 0 None - 0 Human 7.5 pEC50 = 7.5 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 975 26 14 13 -2.0 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O)C(C)C nan
155548506 173172 0 None - 0 Rat 7.5 pEC50 = 7.5 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 926 25 13 12 -1.9 CN[C@@H](C)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O)C(C)C)C(C)C nan
CHEMBL4536886 173172 0 None - 0 Rat 7.5 pEC50 = 7.5 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 926 25 13 12 -1.9 CN[C@@H](C)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O)C(C)C)C(C)C nan
155569246 175599 0 None - 0 Rat 7.5 pEC50 = 7.5 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 869 25 13 12 -3.2 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(N)=O)C(C)C nan
CHEMBL4593310 175599 0 None - 0 Rat 7.5 pEC50 = 7.5 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 869 25 13 12 -3.2 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(N)=O)C(C)C nan
155568804 175536 0 None - 0 Human 7.5 pEC50 = 7.5 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 927 26 13 13 -2.9 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O)[C@@H](C)OC)C(C)C nan
CHEMBL4591857 175536 0 None - 0 Human 7.5 pEC50 = 7.5 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 927 26 13 13 -2.9 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O)[C@@H](C)OC)C(C)C nan
155568318 175518 0 None - 0 Rat 7.5 pEC50 = 7.5 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 940 26 13 12 -1.5 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](C)NC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O nan
CHEMBL4591448 175518 0 None - 0 Rat 7.5 pEC50 = 7.5 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 940 26 13 12 -1.5 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](C)NC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O nan
155543091 172599 0 None - 0 Human 6.5 pEC50 = 6.5 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 940 26 13 12 -1.5 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H](C)NC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
CHEMBL4522246 172599 0 None - 0 Human 6.5 pEC50 = 6.5 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 940 26 13 12 -1.5 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H](C)NC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
155550799 173692 0 None - 0 Human 7.5 pEC50 = 7.5 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 959 26 13 12 -1.7 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O)C(C)C nan
CHEMBL4549405 173692 0 None - 0 Human 7.5 pEC50 = 7.5 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 959 26 13 12 -1.7 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O)C(C)C nan
155540639 172354 0 None - 0 Human 6.5 pEC50 = 6.5 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 947 25 14 13 -2.5 CC(C)[C@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](N)CC(=O)O)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(N)=O nan
CHEMBL4516768 172354 0 None - 0 Human 6.5 pEC50 = 6.5 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 947 25 14 13 -2.5 CC(C)[C@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](N)CC(=O)O)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(N)=O nan
155544988 172860 0 None - 0 Human 6.5 pEC50 = 6.5 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 853 24 12 11 -2.0 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@@H]1C(N)=O nan
CHEMBL4529051 172860 0 None - 0 Human 6.5 pEC50 = 6.5 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 853 24 12 11 -2.0 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@@H]1C(N)=O nan
155565687 175000 0 None - 0 Human 6.5 pEC50 = 6.5 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 961 26 14 13 -2.1 CC(C)[C@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](N)CCC(=O)O)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(N)=O nan
CHEMBL4579604 175000 0 None - 0 Human 6.5 pEC50 = 6.5 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 961 26 14 13 -2.1 CC(C)[C@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](N)CCC(=O)O)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(N)=O nan
1610 2305 89 None - 4 Bovine 6.5 pEC50 = 6.5 Binding
Inhibition of [125I]AII binding to angiotensin II receptor of bovine adrenal cortexInhibition of [125I]AII binding to angiotensin II receptor of bovine adrenal cortex
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(01)81134-3
3941 2305 89 None - 4 Bovine 6.5 pEC50 = 6.5 Binding
Inhibition of [125I]AII binding to angiotensin II receptor of bovine adrenal cortexInhibition of [125I]AII binding to angiotensin II receptor of bovine adrenal cortex
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(01)81134-3
3961 2305 89 None - 4 Bovine 6.5 pEC50 = 6.5 Binding
Inhibition of [125I]AII binding to angiotensin II receptor of bovine adrenal cortexInhibition of [125I]AII binding to angiotensin II receptor of bovine adrenal cortex
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(01)81134-3
590 2305 89 None - 4 Bovine 6.5 pEC50 = 6.5 Binding
Inhibition of [125I]AII binding to angiotensin II receptor of bovine adrenal cortexInhibition of [125I]AII binding to angiotensin II receptor of bovine adrenal cortex
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(01)81134-3
CHEMBL191 2305 89 None - 4 Bovine 6.5 pEC50 = 6.5 Binding
Inhibition of [125I]AII binding to angiotensin II receptor of bovine adrenal cortexInhibition of [125I]AII binding to angiotensin II receptor of bovine adrenal cortex
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(01)81134-3
DB00678 2305 89 None - 4 Bovine 6.5 pEC50 = 6.5 Binding
Inhibition of [125I]AII binding to angiotensin II receptor of bovine adrenal cortexInhibition of [125I]AII binding to angiotensin II receptor of bovine adrenal cortex
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(01)81134-3
155563973 174779 0 None - 0 Rat 5.4 pEC50 = 5.4 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 941 27 14 13 -3.1 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O)C(C)C nan
CHEMBL4574655 174779 0 None - 0 Rat 5.4 pEC50 = 5.4 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 941 27 14 13 -3.1 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O)C(C)C nan
155541295 172432 0 None - 0 Rat 7.4 pEC50 = 7.4 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 926 25 12 12 -2.0 CC(C)[C@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CN(C)C)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O)C(C)C nan
CHEMBL4518318 172432 0 None - 0 Rat 7.4 pEC50 = 7.4 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 926 25 12 12 -2.0 CC(C)[C@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CN(C)C)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O)C(C)C nan
145925550 174889 0 None - 0 Rat 7.4 pEC50 = 7.4 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 903 24 13 12 -2.1 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(N)=O)C(C)C nan
CHEMBL4577270 174889 0 None - 0 Rat 7.4 pEC50 = 7.4 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 903 24 13 12 -2.1 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(N)=O)C(C)C nan
155539838 172316 0 None - 0 Human 7.4 pEC50 = 7.4 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 940 26 13 12 -1.5 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](C)NC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
CHEMBL4515848 172316 0 None - 0 Human 7.4 pEC50 = 7.4 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 940 26 13 12 -1.5 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](C)NC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
11943 3802 0 None - 1 Rat 7.4 pEC50 = 7.4 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL None None None None nan
145925549 3802 0 None - 1 Rat 7.4 pEC50 = 7.4 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL None None None None nan
CHEMBL4438122 3802 0 None - 1 Rat 7.4 pEC50 = 7.4 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL None None None None nan
155540033 172311 0 None - 0 Human 6.4 pEC50 = 6.4 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 953 27 13 12 -1.9 CC[C@H](C)[C@H](NC(=O)[C@@H]1CCCN1C(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(C)C)C(N)=O nan
CHEMBL4515768 172311 0 None - 0 Human 6.4 pEC50 = 6.4 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 953 27 13 12 -1.9 CC[C@H](C)[C@H](NC(=O)[C@@H]1CCCN1C(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(C)C)C(N)=O nan
155520014 172655 0 None - 0 Rat 5.4 pEC50 = 5.4 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 975 27 14 13 -1.9 CN[C@@H](CCC(=O)O)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(N)=O)C(C)C nan
CHEMBL4524300 172655 0 None - 0 Rat 5.4 pEC50 = 5.4 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 975 27 14 13 -1.9 CN[C@@H](CCC(=O)O)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(N)=O)C(C)C nan
CHEMBL312754 209354 16 None - 0 Rat 8.3 pEC50 = 8.3 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCN=C(N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O nan
155548506 173172 0 None - 0 Human 7.4 pEC50 = 7.4 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 926 25 13 12 -1.9 CN[C@@H](C)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O)C(C)C)C(C)C nan
CHEMBL4536886 173172 0 None - 0 Human 7.4 pEC50 = 7.4 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 926 25 13 12 -1.9 CN[C@@H](C)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O)C(C)C)C(C)C nan
155548148 173133 0 None - 0 Rat 7.4 pEC50 = 7.4 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 943 26 14 14 -3.2 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)c(O)c1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O)[C@@H](C)OC)C(C)C nan
CHEMBL4535997 173133 0 None - 0 Rat 7.4 pEC50 = 7.4 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 943 26 14 14 -3.2 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)c(O)c1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O)[C@@H](C)OC)C(C)C nan
155554529 174051 0 None - 0 Human 6.4 pEC50 = 6.4 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 961 26 13 12 -1.6 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1c(F)cc(O)cc1F)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
CHEMBL4557984 174051 0 None - 0 Human 6.4 pEC50 = 6.4 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 961 26 13 12 -1.6 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1c(F)cc(O)cc1F)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
155566196 175163 0 None - 0 Rat 6.4 pEC50 = 6.4 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 954 26 13 12 -1.3 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1c(C)cc(O)cc1C)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
CHEMBL4583284 175163 0 None - 0 Rat 6.4 pEC50 = 6.4 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 954 26 13 12 -1.3 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1c(C)cc(O)cc1C)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
155558003 174111 0 None - 0 Rat 5.4 pEC50 = 5.4 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 1015 28 13 16 -2.1 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1cc([N+](=O)[O-])c(O)c([N+](=O)[O-])c1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
CHEMBL4559421 174111 0 None - 0 Rat 5.4 pEC50 = 5.4 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 1015 28 13 16 -2.1 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1cc([N+](=O)[O-])c(O)c([N+](=O)[O-])c1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
70538373 174915 0 None - 0 Human 7.4 pEC50 = 7.4 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 840 23 12 11 -1.8 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)O)C(C)C)C(C)C nan
CHEMBL4577691 174915 0 None - 0 Human 7.4 pEC50 = 7.4 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 840 23 12 11 -1.8 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)O)C(C)C)C(C)C nan
154573825 175406 6 None - 0 Rat 7.4 pEC50 = 7.4 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 742 22 12 10 -2.4 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(N)=O)C(C)C)C(C)C nan
CHEMBL4588946 175406 6 None - 0 Rat 7.4 pEC50 = 7.4 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 742 22 12 10 -2.4 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(N)=O)C(C)C)C(C)C nan
155561477 174610 0 None - 0 Rat 6.4 pEC50 = 6.4 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 811 22 12 11 -3.0 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(N)=O)C(C)C nan
CHEMBL4570840 174610 0 None - 0 Rat 6.4 pEC50 = 6.4 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 811 22 12 11 -3.0 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(N)=O)C(C)C nan
155559104 174224 0 None - 0 Rat 7.4 pEC50 = 7.4 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 940 26 12 12 -1.6 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CN(C)C)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O nan
CHEMBL4562270 174224 0 None - 0 Rat 7.4 pEC50 = 7.4 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 940 26 12 12 -1.6 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CN(C)C)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O nan
155552475 173470 0 None - 0 Human 6.4 pEC50 = 6.4 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 947 25 14 13 -2.5 CC(C)[C@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H](N)CC(=O)O)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(N)=O nan
CHEMBL4543860 173470 0 None - 0 Human 6.4 pEC50 = 6.4 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 947 25 14 13 -2.5 CC(C)[C@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H](N)CC(=O)O)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(N)=O nan
155560024 174308 0 None - 0 Rat 4.4 pEC50 = 4.4 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 782 21 11 10 -1.4 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@@H](N)CCCNC(=N)N)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(N)=O nan
CHEMBL4564094 174308 0 None - 0 Rat 4.4 pEC50 = 4.4 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 782 21 11 10 -1.4 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@@H](N)CCCNC(=N)N)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(N)=O nan
11943 3802 0 None - 1 Human 7.4 pEC50 = 7.4 Binding
Agonist activity at human AT1 receptor assessed as increase in beta-arrestin recruitment by chemiluminescent assayAgonist activity at human AT1 receptor assessed as increase in beta-arrestin recruitment by chemiluminescent assay
ChEMBL None None None None 10.1021/acs.jmedchem.8b00435
145925549 3802 0 None - 1 Human 7.4 pEC50 = 7.4 Binding
Agonist activity at human AT1 receptor assessed as increase in beta-arrestin recruitment by chemiluminescent assayAgonist activity at human AT1 receptor assessed as increase in beta-arrestin recruitment by chemiluminescent assay
ChEMBL None None None None 10.1021/acs.jmedchem.8b00435
CHEMBL4438122 3802 0 None - 1 Human 7.4 pEC50 = 7.4 Binding
Agonist activity at human AT1 receptor assessed as increase in beta-arrestin recruitment by chemiluminescent assayAgonist activity at human AT1 receptor assessed as increase in beta-arrestin recruitment by chemiluminescent assay
ChEMBL None None None None 10.1021/acs.jmedchem.8b00435
11943 3802 0 None - 1 Human 7.4 pEC50 = 7.4 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL None None None None nan
145925549 3802 0 None - 1 Human 7.4 pEC50 = 7.4 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL None None None None nan
CHEMBL4438122 3802 0 None - 1 Human 7.4 pEC50 = 7.4 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL None None None None nan
155542907 172596 0 None - 0 Rat 6.4 pEC50 = 6.4 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 904 24 13 12 -1.5 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)O)C(C)C nan
CHEMBL4522038 172596 0 None - 0 Rat 6.4 pEC50 = 6.4 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 904 24 13 12 -1.5 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)O)C(C)C nan
155541125 172386 0 None - 1 Human 6.4 pEC50 = 6.4 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 904 27 12 11 -1.2 CC[C@H](C)[C@H](NC(=O)[C@@H]1CCCN1C(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)[C@@H](C)CC)C(C)C)C(=O)O nan
CHEMBL4517561 172386 0 None - 1 Human 6.4 pEC50 = 6.4 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 904 27 12 11 -1.2 CC[C@H](C)[C@H](NC(=O)[C@@H]1CCCN1C(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)[C@@H](C)CC)C(C)C)C(=O)O nan
155552475 173470 0 None - 0 Rat 6.4 pEC50 = 6.4 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 947 25 14 13 -2.5 CC(C)[C@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H](N)CC(=O)O)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(N)=O nan
CHEMBL4543860 173470 0 None - 0 Rat 6.4 pEC50 = 6.4 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 947 25 14 13 -2.5 CC(C)[C@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H](N)CC(=O)O)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(N)=O nan
155561376 175092 0 None - 0 Human 5.4 pEC50 = 5.4 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 917 28 12 11 -1.4 CC[C@H](C)[C@H](NC(=O)[C@@H]1CCCN1C(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)[C@@H](C)CC)[C@@H](C)CC)C(N)=O nan
CHEMBL4581718 175092 0 None - 0 Human 5.4 pEC50 = 5.4 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 917 28 12 11 -1.4 CC[C@H](C)[C@H](NC(=O)[C@@H]1CCCN1C(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)[C@@H](C)CC)[C@@H](C)CC)C(N)=O nan
155560024 174308 0 None - 0 Human 5.3 pEC50 = 5.3 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 782 21 11 10 -1.4 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@@H](N)CCCNC(=N)N)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(N)=O nan
CHEMBL4564094 174308 0 None - 0 Human 5.3 pEC50 = 5.3 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 782 21 11 10 -1.4 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@@H](N)CCCNC(=N)N)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(N)=O nan
155553098 173528 0 None - 0 Human 6.3 pEC50 = 6.3 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 969 28 16 13 -3.7 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O)C(C)C nan
CHEMBL4545153 173528 0 None - 0 Human 6.3 pEC50 = 6.3 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 969 28 16 13 -3.7 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O)C(C)C nan
155553311 173551 0 None - 0 Human 5.3 pEC50 = 5.3 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 940 26 13 12 -1.5 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H](C)NC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O nan
CHEMBL4546162 173551 0 None - 0 Human 5.3 pEC50 = 5.3 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 940 26 13 12 -1.5 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H](C)NC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O nan
155540547 171944 0 None - 0 Rat 8.3 pEC50 = 8.3 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 945 26 13 13 -2.8 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)c(F)c1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O)[C@@H](C)OC)C(C)C nan
CHEMBL4483576 171944 0 None - 0 Rat 8.3 pEC50 = 8.3 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 945 26 13 13 -2.8 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)c(F)c1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O)[C@@H](C)OC)C(C)C nan
155548148 173133 0 None - 0 Human 7.3 pEC50 = 7.3 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 943 26 14 14 -3.2 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)c(O)c1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O)[C@@H](C)OC)C(C)C nan
CHEMBL4535997 173133 0 None - 0 Human 7.3 pEC50 = 7.3 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 943 26 14 14 -3.2 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)c(O)c1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O)[C@@H](C)OC)C(C)C nan
155551762 173428 0 None - 0 Rat 7.3 pEC50 = 7.3 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 911 26 13 12 -2.2 CCC[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
CHEMBL4542709 173428 0 None - 0 Rat 7.3 pEC50 = 7.3 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 911 26 13 12 -2.2 CCC[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
155546362 172969 0 None - 0 Rat 6.3 pEC50 = 6.3 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 966 26 12 12 -1.0 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CN1CCCC1)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
CHEMBL4532075 172969 0 None - 0 Rat 6.3 pEC50 = 6.3 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 966 26 12 12 -1.0 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CN1CCCC1)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
155553930 174858 0 None - 0 Rat 6.3 pEC50 = 6.3 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 1177 26 13 12 -0.7 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1cc(I)c(O)c(I)c1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
CHEMBL4576650 174858 0 None - 0 Rat 6.3 pEC50 = 6.3 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 1177 26 13 12 -0.7 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1cc(I)c(O)c(I)c1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
54726675 98902 0 None - 0 Bovine 6.3 pEC50 = 6.3 Binding
Inhibition of [125I]AII binding to angiotensin II receptor of bovine adrenal cortexInhibition of [125I]AII binding to angiotensin II receptor of bovine adrenal cortex
ChEMBL 515 7 2 7 5.7 CCOc1ccc2c(O)c(-c3ccccc3)c(=O)n(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c2c1 10.1016/S0960-894X(01)81134-3
CHEMBL282566 98902 0 None - 0 Bovine 6.3 pEC50 = 6.3 Binding
Inhibition of [125I]AII binding to angiotensin II receptor of bovine adrenal cortexInhibition of [125I]AII binding to angiotensin II receptor of bovine adrenal cortex
ChEMBL 515 7 2 7 5.7 CCOc1ccc2c(O)c(-c3ccccc3)c(=O)n(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c2c1 10.1016/S0960-894X(01)81134-3
155558003 174111 0 None - 0 Human 5.3 pEC50 = 5.3 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 1015 28 13 16 -2.1 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1cc([N+](=O)[O-])c(O)c([N+](=O)[O-])c1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
CHEMBL4559421 174111 0 None - 0 Human 5.3 pEC50 = 5.3 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 1015 28 13 16 -2.1 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1cc([N+](=O)[O-])c(O)c([N+](=O)[O-])c1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
86727577 115463 0 None - 0 Human 5.3 pEC50 = 5.3 Binding
Agonist activity at AT1 receptor (unknown origin)Agonist activity at AT1 receptor (unknown origin)
ChEMBL 422 2 1 5 3.6 C[C@H]1CN(C)CC[C@H]1c1cc2c(cc1-c1ccccc1F)OCC1=NNC(=O)[C@@H](C)N12 10.1021/jm5013006
CHEMBL3355127 115463 0 None - 0 Human 5.3 pEC50 = 5.3 Binding
Agonist activity at AT1 receptor (unknown origin)Agonist activity at AT1 receptor (unknown origin)
ChEMBL 422 2 1 5 3.6 C[C@H]1CN(C)CC[C@H]1c1cc2c(cc1-c1ccccc1F)OCC1=NNC(=O)[C@@H](C)N12 10.1021/jm5013006
155555310 173777 0 None - 0 Human 6.3 pEC50 = 6.3 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 931 25 13 12 -2.2 CC(C)[C@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H](N)CC(=O)O)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(N)=O nan
CHEMBL4551431 173777 0 None - 0 Human 6.3 pEC50 = 6.3 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 931 25 13 12 -2.2 CC(C)[C@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H](N)CC(=O)O)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(N)=O nan
155555310 173777 0 None - 0 Rat 6.3 pEC50 = 6.3 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 931 25 13 12 -2.2 CC(C)[C@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H](N)CC(=O)O)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(N)=O nan
CHEMBL4551431 173777 0 None - 0 Rat 6.3 pEC50 = 6.3 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 931 25 13 12 -2.2 CC(C)[C@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H](N)CC(=O)O)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(N)=O nan
10533900 175386 5 None - 0 Human 6.3 pEC50 = 6.3 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 955 27 14 13 -2.7 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H](N)CC(=O)O)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)NCC(=O)O nan
CHEMBL4588454 175386 5 None - 0 Human 6.3 pEC50 = 6.3 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 955 27 14 13 -2.7 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H](N)CC(=O)O)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)NCC(=O)O nan
90219582 115464 0 None - 0 Human 5.3 pEC50 = 5.3 Binding
Agonist activity at AT1 receptor (unknown origin)Agonist activity at AT1 receptor (unknown origin)
ChEMBL 436 2 1 5 3.9 Cc1ccc(-c2cc3c(cc2[C@@H]2CCN(C)C[C@@H]2C)N2C(=NNC(=O)[C@H]2C)CO3)c(F)c1 10.1021/jm5013006
CHEMBL3355137 115464 0 None - 0 Human 5.3 pEC50 = 5.3 Binding
Agonist activity at AT1 receptor (unknown origin)Agonist activity at AT1 receptor (unknown origin)
ChEMBL 436 2 1 5 3.9 Cc1ccc(-c2cc3c(cc2[C@@H]2CCN(C)C[C@@H]2C)N2C(=NNC(=O)[C@H]2C)CO3)c(F)c1 10.1021/jm5013006
155552995 173530 0 None - 0 Human 6.2 pEC50 = 6.2 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 940 27 12 12 -1.6 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(OC)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O nan
CHEMBL4545399 173530 0 None - 0 Human 6.2 pEC50 = 6.2 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 940 27 12 12 -1.6 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(OC)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O nan
CHEMBL77838 214091 3 None - 0 Rat 8.2 pEC50 = 8.2 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@@H]1CCCN1C(=O)[C@H](Cc1c[nH]cn1)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCN=C(N)N)NC(=O)CNC)C(C)C)C(C)C)C(=O)O nan
16133225 415 47 None -4 6 Rat 8.2 pEC50 = 8.2 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL None None None None nan
172198 415 47 None -4 6 Rat 8.2 pEC50 = 8.2 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL None None None None nan
2504 415 47 None -4 6 Rat 8.2 pEC50 = 8.2 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL None None None None nan
45266664 415 47 None -4 6 Rat 8.2 pEC50 = 8.2 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL None None None None nan
5272 415 47 None -4 6 Rat 8.2 pEC50 = 8.2 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL None None None None nan
CHEMBL408403 415 47 None -4 6 Rat 8.2 pEC50 = 8.2 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL None None None None nan
DB11842 415 47 None -4 6 Rat 8.2 pEC50 = 8.2 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL None None None None nan
54726672 98837 0 None - 0 Bovine 6.2 pEC50 = 6.2 Binding
Inhibition of [125I]AII binding to angiotensin II receptor of bovine adrenal cortexInhibition of [125I]AII binding to angiotensin II receptor of bovine adrenal cortex
ChEMBL 517 6 2 7 6.0 CSc1ccc2c(O)c(-c3ccccc3)c(=O)n(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c2c1 10.1016/S0960-894X(01)81134-3
CHEMBL282082 98837 0 None - 0 Bovine 6.2 pEC50 = 6.2 Binding
Inhibition of [125I]AII binding to angiotensin II receptor of bovine adrenal cortexInhibition of [125I]AII binding to angiotensin II receptor of bovine adrenal cortex
ChEMBL 517 6 2 7 6.0 CSc1ccc2c(O)c(-c3ccccc3)c(=O)n(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c2c1 10.1016/S0960-894X(01)81134-3
54726668 96783 0 None - 0 Bovine 5.2 pEC50 = 5.2 Binding
Inhibition of [125I]AII binding to angiotensin II receptor of bovine adrenal cortexInhibition of [125I]AII binding to angiotensin II receptor of bovine adrenal cortex
ChEMBL 477 5 2 7 5.3 O=c1c(-c2ccccc2)c(O)c2sccc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81134-3
CHEMBL26875 96783 0 None - 0 Bovine 5.2 pEC50 = 5.2 Binding
Inhibition of [125I]AII binding to angiotensin II receptor of bovine adrenal cortexInhibition of [125I]AII binding to angiotensin II receptor of bovine adrenal cortex
ChEMBL 477 5 2 7 5.3 O=c1c(-c2ccccc2)c(O)c2sccc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81134-3
155559827 174333 0 None - 0 Human 7.2 pEC50 = 7.2 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 970 27 13 14 -2.0 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)c([N+](=O)[O-])c1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
CHEMBL4564617 174333 0 None - 0 Human 7.2 pEC50 = 7.2 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 970 27 13 14 -2.0 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)c([N+](=O)[O-])c1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
155539838 172316 0 None - 0 Rat 7.2 pEC50 = 7.2 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 940 26 13 12 -1.5 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](C)NC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
CHEMBL4515848 172316 0 None - 0 Rat 7.2 pEC50 = 7.2 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 940 26 13 12 -1.5 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](C)NC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
155547844 173116 0 None - 0 Rat 7.2 pEC50 = 7.2 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 942 26 14 13 -2.2 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)c(O)c1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
CHEMBL4535678 173116 0 None - 0 Rat 7.2 pEC50 = 7.2 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 942 26 14 13 -2.2 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)c(O)c1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
155553098 173528 0 None - 0 Rat 7.2 pEC50 = 7.2 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 969 28 16 13 -3.7 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O)C(C)C nan
CHEMBL4545153 173528 0 None - 0 Rat 7.2 pEC50 = 7.2 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 969 28 16 13 -3.7 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O)C(C)C nan
155566196 175163 0 None - 0 Human 6.2 pEC50 = 6.2 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 954 26 13 12 -1.3 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1c(C)cc(O)cc1C)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
CHEMBL4583284 175163 0 None - 0 Human 6.2 pEC50 = 6.2 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 954 26 13 12 -1.3 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1c(C)cc(O)cc1C)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
155567790 175469 0 None - 0 Human 6.2 pEC50 = 6.2 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 877 24 13 12 -3.1 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(N)=O)C(C)C nan
CHEMBL4590589 175469 0 None - 0 Human 6.2 pEC50 = 6.2 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 877 24 13 12 -3.1 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(N)=O)C(C)C nan
155562469 174639 0 None - 0 Rat 6.2 pEC50 = 6.2 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 966 29 12 12 -1.1 C=CCOc1ccc(C[C@H](NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@H](C(=O)N[C@@H](Cc2cnc[nH]2)C(=O)N2CCC[C@H]2C(=O)N[C@H](C)C(=O)O)[C@@H](C)CC)cc1 nan
CHEMBL4571382 174639 0 None - 0 Rat 6.2 pEC50 = 6.2 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 966 29 12 12 -1.1 C=CCOc1ccc(C[C@H](NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@H](C(=O)N[C@@H](Cc2cnc[nH]2)C(=O)N2CCC[C@H]2C(=O)N[C@H](C)C(=O)O)[C@@H](C)CC)cc1 nan
155568289 175543 0 None - 0 Rat 6.2 pEC50 = 6.2 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 898 26 11 12 -1.0 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCCN)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
CHEMBL4592000 175543 0 None - 0 Rat 6.2 pEC50 = 6.2 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 898 26 11 12 -1.0 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCCN)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
155544246 172784 0 None - 0 Rat 6.2 pEC50 = 6.2 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 887 24 12 11 -1.8 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(N)=O)C(C)C nan
CHEMBL4527484 172784 0 None - 0 Rat 6.2 pEC50 = 6.2 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 887 24 12 11 -1.8 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(N)=O)C(C)C nan
155520024 172665 0 None - 0 Human 5.2 pEC50 = 5.2 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 959 27 13 12 -1.6 CN[C@@H](CCC(=O)O)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(N)=O)C(C)C nan
CHEMBL4524570 172665 0 None - 0 Human 5.2 pEC50 = 5.2 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 959 27 13 12 -1.6 CN[C@@H](CCC(=O)O)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(N)=O)C(C)C nan
155558784 174194 0 None - 0 Human 6.2 pEC50 = 6.2 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 756 9 7 8 1.3 CC[C@H](C)[C@@H]1NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](C(C)C)NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@@H]2CCCN2C(=O)[C@H](Cc2cnc[nH]2)NC1=O nan
CHEMBL4561366 174194 0 None - 0 Human 6.2 pEC50 = 6.2 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 756 9 7 8 1.3 CC[C@H](C)[C@@H]1NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](C(C)C)NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@@H]2CCCN2C(=O)[C@H](Cc2cnc[nH]2)NC1=O nan
155543972 174433 0 None - 0 Human 6.2 pEC50 = 6.2 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 917 28 13 12 -1.7 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](CCCCN)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
CHEMBL4567103 174433 0 None - 0 Human 6.2 pEC50 = 6.2 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 917 28 13 12 -1.7 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](CCCCN)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
CHEMBL938 214120 24 None - 2 Rat 8.1 pEC50 = 8.1 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL None None None CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O)C(C)C)C(C)C nan
155552886 173514 0 None - 0 Human 8.1 pEC50 = 8.1 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 961 26 13 13 -2.3 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)c(Cl)c1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O)[C@@H](C)OC)C(C)C nan
CHEMBL4544902 173514 0 None - 0 Human 8.1 pEC50 = 8.1 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 961 26 13 13 -2.3 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)c(Cl)c1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O)[C@@H](C)OC)C(C)C nan
155552886 173514 0 None - 0 Rat 8.1 pEC50 = 8.1 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 961 26 13 13 -2.3 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)c(Cl)c1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O)[C@@H](C)OC)C(C)C nan
CHEMBL4544902 173514 0 None - 0 Rat 8.1 pEC50 = 8.1 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 961 26 13 13 -2.3 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)c(Cl)c1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O)[C@@H](C)OC)C(C)C nan
145925550 174889 0 None - 0 Human 7.1 pEC50 = 7.1 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 903 24 13 12 -2.1 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(N)=O)C(C)C nan
CHEMBL4577270 174889 0 None - 0 Human 7.1 pEC50 = 7.1 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 903 24 13 12 -2.1 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(N)=O)C(C)C nan
155559104 174224 0 None - 0 Human 7.1 pEC50 = 7.1 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 940 26 12 12 -1.6 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CN(C)C)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O nan
CHEMBL4562270 174224 0 None - 0 Human 7.1 pEC50 = 7.1 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 940 26 12 12 -1.6 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CN(C)C)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O nan
155541240 172437 0 None - 0 Rat 7.1 pEC50 = 7.1 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 928 26 12 11 -1.5 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(F)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
CHEMBL4518420 172437 0 None - 0 Rat 7.1 pEC50 = 7.1 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 928 26 12 11 -1.5 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(F)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(=O)O nan
CHEMBL2028943 207381 0 None - 0 Human 8.1 pEC50 = 8.1 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@@H]1CCCN1C(=O)[C@H](Cc1c[nH]cn1)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCN=C(N)N)NC(=O)CNC)C(C)C)C(=O)O nan
155552429 173575 0 None - 0 Rat 8.1 pEC50 = 8.1 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 927 26 13 13 -2.9 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O)[C@@H](C)OC)C(C)C nan
CHEMBL4546799 173575 0 None - 0 Rat 8.1 pEC50 = 8.1 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 927 26 13 13 -2.9 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O)[C@@H](C)OC)C(C)C nan
155540328 172322 0 None - 0 Human 6.1 pEC50 = 6.1 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 1017 28 14 13 -1.6 CC[C@H](C)[C@H](NC(=O)[C@@H]1CCCN1C(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(N)=O nan
CHEMBL4516066 172322 0 None - 0 Human 6.1 pEC50 = 6.1 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 1017 28 14 13 -1.6 CC[C@H](C)[C@H](NC(=O)[C@@H]1CCCN1C(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(N)=O nan
155563676 174762 0 None - 0 Rat 6.1 pEC50 = 6.1 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 961 26 14 13 -2.1 CC(C)[C@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H](N)CCC(=O)O)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(N)=O nan
CHEMBL4574199 174762 0 None - 0 Rat 6.1 pEC50 = 6.1 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 961 26 14 13 -2.1 CC(C)[C@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H](N)CCC(=O)O)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(N)=O nan
155559120 174204 0 None - 0 Rat 6.1 pEC50 = 6.1 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 945 26 13 12 -1.8 CC(C)[C@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H](N)CCC(=O)O)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(N)=O nan
CHEMBL4561769 174204 0 None - 0 Rat 6.1 pEC50 = 6.1 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 945 26 13 12 -1.8 CC(C)[C@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H](N)CCC(=O)O)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(N)=O nan
CHEMBL2370909 208193 0 None - 0 Human 6.1 pEC50 = 6.1 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@@H]1CCCN1C(=O)[C@H](Cc1c[nH]cn1)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCN=C(N)N)NC(=O)CNC)C(C)C)C(=O)O nan
155552429 173575 0 None - 0 Human 8.0 pEC50 = 8.0 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 927 26 13 13 -2.9 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O)[C@@H](C)OC)C(C)C nan
CHEMBL4546799 173575 0 None - 0 Human 8.0 pEC50 = 8.0 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 927 26 13 13 -2.9 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O)[C@@H](C)OC)C(C)C nan
CHEMBL312754 209354 16 None - 0 Human 8.0 pEC50 = 8.0 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCN=C(N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O nan
155541440 172440 0 None - 0 Rat 8.0 pEC50 = 8.0 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 954 28 13 12 -1.1 CCC[C@H](NC(=O)[C@@H]1CCCN1C(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)[C@@H](C)CC)C(=O)O nan
CHEMBL4518530 172440 0 None - 0 Rat 8.0 pEC50 = 8.0 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 954 28 13 12 -1.1 CCC[C@H](NC(=O)[C@@H]1CCCN1C(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)[C@@H](C)CC)C(=O)O nan
16133225 415 47 None -2 6 Human 8.0 pEC50 = 8.0 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL None None None None nan
172198 415 47 None -2 6 Human 8.0 pEC50 = 8.0 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL None None None None nan
2504 415 47 None -2 6 Human 8.0 pEC50 = 8.0 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL None None None None nan
45266664 415 47 None -2 6 Human 8.0 pEC50 = 8.0 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL None None None None nan
5272 415 47 None -2 6 Human 8.0 pEC50 = 8.0 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL None None None None nan
CHEMBL408403 415 47 None -2 6 Human 8.0 pEC50 = 8.0 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL None None None None nan
DB11842 415 47 None -2 6 Human 8.0 pEC50 = 8.0 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL None None None None nan
54726674 99256 0 None - 0 Bovine 7.1 pEC50 = 7.1 Binding
Inhibition of [125I]AII binding to angiotensin II receptor of bovine adrenal cortexInhibition of [125I]AII binding to angiotensin II receptor of bovine adrenal cortex
ChEMBL 505 6 2 7 5.9 CCc1cc2c(O)c(-c3ccccc3)c(=O)n(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c2s1 10.1016/S0960-894X(01)81134-3
CHEMBL284877 99256 0 None - 0 Bovine 7.1 pEC50 = 7.1 Binding
Inhibition of [125I]AII binding to angiotensin II receptor of bovine adrenal cortexInhibition of [125I]AII binding to angiotensin II receptor of bovine adrenal cortex
ChEMBL 505 6 2 7 5.9 CCc1cc2c(O)c(-c3ccccc3)c(=O)n(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c2s1 10.1016/S0960-894X(01)81134-3
11944 3803 0 None - 1 Rat 6.0 pEC50 = 6.0 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL None None None None nan
155552190 3803 0 None - 1 Rat 6.0 pEC50 = 6.0 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL None None None None nan
CHEMBL4544228 3803 0 None - 1 Rat 6.0 pEC50 = 6.0 Binding
Agonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at rat AT1aR expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL None None None None nan
155558059 174101 0 None - 0 Human 6.0 pEC50 = 6.0 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 790 23 12 11 -4.6 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)NCC(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)NCC(N)=O)C(C)C)C(C)C nan
CHEMBL4559239 174101 0 None - 0 Human 6.0 pEC50 = 6.0 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 790 23 12 11 -4.6 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)NCC(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)NCC(N)=O)C(C)C)C(C)C nan
155569246 175599 0 None - 0 Human 7.0 pEC50 = 7.0 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 869 25 13 12 -3.2 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(N)=O)C(C)C nan
CHEMBL4593310 175599 0 None - 0 Human 7.0 pEC50 = 7.0 Binding
Agonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assayAgonist activity at human AT1R expressed in HEK293 cells incubated for 60 mins by luminescence based beta-arrestin recruitment assay
ChEMBL 869 25 13 12 -3.2 CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(N)=O)C(C)C nan
54726673 98753 0 None - 0 Bovine 5.0 pEC50 = 5.0 Binding
Inhibition of [125I]AII binding to angiotensin II receptor of bovine adrenal cortexInhibition of [125I]AII binding to angiotensin II receptor of bovine adrenal cortex
ChEMBL 477 6 2 5 5.8 COc1ccc2c(O)c(-c3ccccc3)c(=O)n(Cc3ccc(-c4ccccc4C(=O)O)cc3)c2c1 10.1016/S0960-894X(01)81134-3
CHEMBL28160 98753 0 None - 0 Bovine 5.0 pEC50 = 5.0 Binding
Inhibition of [125I]AII binding to angiotensin II receptor of bovine adrenal cortexInhibition of [125I]AII binding to angiotensin II receptor of bovine adrenal cortex
ChEMBL 477 6 2 5 5.8 COc1ccc2c(O)c(-c3ccccc3)c(=O)n(Cc3ccc(-c4ccccc4C(=O)O)cc3)c2c1 10.1016/S0960-894X(01)81134-3
10032858 29533 0 None - 0 Rabbit 10.4 pIC50 = 10.4 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 729 12 2 9 7.1 CCCCc1nn(-c2cc(NC(=O)CC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2occ(Cl)c2Cl)cc1 10.1007/s00044-013-0831-x
CHEMBL138690 29533 0 None - 0 Rabbit 10.4 pIC50 = 10.4 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 729 12 2 9 7.1 CCCCc1nn(-c2cc(NC(=O)CC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2occ(Cl)c2Cl)cc1 10.1007/s00044-013-0831-x
10032858 29533 0 None - 0 Rabbit 10.4 pIC50 = 10.4 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 729 12 2 9 7.1 CCCCc1nn(-c2cc(NC(=O)CC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2occ(Cl)c2Cl)cc1 10.1021/jm00052a006
CHEMBL138690 29533 0 None - 0 Rabbit 10.4 pIC50 = 10.4 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 729 12 2 9 7.1 CCCCc1nn(-c2cc(NC(=O)CC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2occ(Cl)c2Cl)cc1 10.1021/jm00052a006
9895212 119122 0 None - 0 Human 10.3 pIC50 = 10.3 Binding
Inhibition of Angiotensin II receptor, type 1Inhibition of Angiotensin II receptor, type 1
ChEMBL 614 9 1 6 7.0 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)C(c2ccccc2)c2ccccc2)cc1 10.1021/jm9504722
CHEMBL346728 119122 0 None - 0 Human 10.3 pIC50 = 10.3 Binding
Inhibition of Angiotensin II receptor, type 1Inhibition of Angiotensin II receptor, type 1
ChEMBL 614 9 1 6 7.0 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)C(c2ccccc2)c2ccccc2)cc1 10.1021/jm9504722
10417251 96444 0 None - 0 Rabbit 10.3 pIC50 = 10.3 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 691 11 2 8 6.5 CCCCc1nn(-c2cc(NC(C)=O)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1007/s00044-013-0831-x
CHEMBL265797 96444 0 None - 0 Rabbit 10.3 pIC50 = 10.3 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 691 11 2 8 6.5 CCCCc1nn(-c2cc(NC(C)=O)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1007/s00044-013-0831-x
10417251 96444 0 None - 0 Rabbit 10.3 pIC50 = 10.3 Binding
In vitro ability to inhibit the binding of radioligand 125I[Sar1,IIe8]AII to AT1 receptor from rabbit aortaIn vitro ability to inhibit the binding of radioligand 125I[Sar1,IIe8]AII to AT1 receptor from rabbit aorta
ChEMBL 691 11 2 8 6.5 CCCCc1nn(-c2cc(NC(C)=O)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1016/S0960-894X(01)80595-3
CHEMBL265797 96444 0 None - 0 Rabbit 10.3 pIC50 = 10.3 Binding
In vitro ability to inhibit the binding of radioligand 125I[Sar1,IIe8]AII to AT1 receptor from rabbit aortaIn vitro ability to inhibit the binding of radioligand 125I[Sar1,IIe8]AII to AT1 receptor from rabbit aorta
ChEMBL 691 11 2 8 6.5 CCCCc1nn(-c2cc(NC(C)=O)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1016/S0960-894X(01)80595-3
10417251 96444 0 None - 0 Rabbit 10.3 pIC50 = 10.3 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 691 11 2 8 6.5 CCCCc1nn(-c2cc(NC(C)=O)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1021/jm00052a006
CHEMBL265797 96444 0 None - 0 Rabbit 10.3 pIC50 = 10.3 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 691 11 2 8 6.5 CCCCc1nn(-c2cc(NC(C)=O)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1021/jm00052a006
10349732 118235 0 None - 0 Rabbit 10.1 pIC50 = 10.1 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 695 13 2 9 7.1 CCCCC(=O)Nc1ccc(Cl)c(-n2nc(CCCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3)c2=O)c1 10.1007/s00044-013-0831-x
CHEMBL341828 118235 0 None - 0 Rabbit 10.1 pIC50 = 10.1 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 695 13 2 9 7.1 CCCCC(=O)Nc1ccc(Cl)c(-n2nc(CCCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3)c2=O)c1 10.1007/s00044-013-0831-x
10032820 116788 0 None - 0 Rabbit 10.1 pIC50 = 10.1 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 723 12 2 8 7.0 CCCCc1nn(-c2cc(NC(=O)CC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1F 10.1007/s00044-011-9815-x
CHEMBL339672 116788 0 None - 0 Rabbit 10.1 pIC50 = 10.1 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 723 12 2 8 7.0 CCCCc1nn(-c2cc(NC(=O)CC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1F 10.1007/s00044-011-9815-x
10032820 116788 0 None - 0 Rabbit 10.1 pIC50 = 10.1 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 723 12 2 8 7.0 CCCCc1nn(-c2cc(NC(=O)CC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1F 10.1021/jm00019a004
CHEMBL339672 116788 0 None - 0 Rabbit 10.1 pIC50 = 10.1 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 723 12 2 8 7.0 CCCCc1nn(-c2cc(NC(=O)CC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1F 10.1021/jm00019a004
10349732 118235 0 None - 0 Rabbit 10.1 pIC50 = 10.1 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 695 13 2 9 7.1 CCCCC(=O)Nc1ccc(Cl)c(-n2nc(CCCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3)c2=O)c1 10.1021/jm00052a006
CHEMBL341828 118235 0 None - 0 Rabbit 10.1 pIC50 = 10.1 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 695 13 2 9 7.1 CCCCC(=O)Nc1ccc(Cl)c(-n2nc(CCCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3)c2=O)c1 10.1021/jm00052a006
10032820 116788 0 None - 0 Rabbit 10.1 pIC50 = 10.1 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 723 12 2 8 7.0 CCCCc1nn(-c2cc(NC(=O)CC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1F 10.1007/s00044-011-9815-x
CHEMBL339672 116788 0 None - 0 Rabbit 10.1 pIC50 = 10.1 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 723 12 2 8 7.0 CCCCc1nn(-c2cc(NC(=O)CC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1F 10.1007/s00044-011-9815-x
10439848 118692 0 None - 0 Rabbit 10.1 pIC50 = 10.1 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 717 12 2 8 6.9 CCCCc1nn(-c2cc(NC(=O)C3CC3)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1007/s00044-013-0831-x
CHEMBL343309 118692 0 None - 0 Rabbit 10.1 pIC50 = 10.1 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 717 12 2 8 6.9 CCCCc1nn(-c2cc(NC(=O)C3CC3)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1007/s00044-013-0831-x
10439848 118692 0 None - 0 Rabbit 10.1 pIC50 = 10.1 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 717 12 2 8 6.9 CCCCc1nn(-c2cc(NC(=O)C3CC3)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1021/jm00052a006
CHEMBL343309 118692 0 None - 0 Rabbit 10.1 pIC50 = 10.1 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 717 12 2 8 6.9 CCCCc1nn(-c2cc(NC(=O)C3CC3)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1021/jm00052a006
10010071 116833 0 None - 0 Rabbit 10.0 pIC50 = 10 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 715 13 2 10 6.1 CCCCc1nn(-c2cc(NC(=O)COCC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1007/s00044-011-9815-x
CHEMBL339722 116833 0 None - 0 Rabbit 10.0 pIC50 = 10 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 715 13 2 10 6.1 CCCCc1nn(-c2cc(NC(=O)COCC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1007/s00044-011-9815-x
9829012 92110 0 None - 0 Rabbit 10.0 pIC50 = 10 Binding
Binding affinity against AT-1 receptor from rabbit aorta using [125I]-Sar1-Ile8-Ang II without BSABinding affinity against AT-1 receptor from rabbit aorta using [125I]-Sar1-Ile8-Ang II without BSA
ChEMBL 550 9 2 7 5.5 CCCCc1nc2ccc(NC(=O)N(C)C(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00073a024
CHEMBL24322 92110 0 None - 0 Rabbit 10.0 pIC50 = 10 Binding
Binding affinity against AT-1 receptor from rabbit aorta using [125I]-Sar1-Ile8-Ang II without BSABinding affinity against AT-1 receptor from rabbit aorta using [125I]-Sar1-Ile8-Ang II without BSA
ChEMBL 550 9 2 7 5.5 CCCCc1nc2ccc(NC(=O)N(C)C(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00073a024
44311455 102258 0 None - 0 Human 10.0 pIC50 = 10 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 782 17 1 9 8.2 CCCc1nc(CC)c(C(=O)OCCN(C(=O)c2ccccc2)c2ccccc2)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/S0960-894X(00)80077-3
CHEMBL305017 102258 0 None - 0 Human 10.0 pIC50 = 10 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 782 17 1 9 8.2 CCCc1nc(CC)c(C(=O)OCCN(C(=O)c2ccccc2)c2ccccc2)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/S0960-894X(00)80077-3
44311580 102293 0 None - 0 Human 10.0 pIC50 = 10 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 706 16 2 9 6.9 CCCc1nc(CC)c(C(=O)OCCC(=O)Nc2ccccc2)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/S0960-894X(00)80077-3
CHEMBL305238 102293 0 None - 0 Human 10.0 pIC50 = 10 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 706 16 2 9 6.9 CCCc1nc(CC)c(C(=O)OCCC(=O)Nc2ccccc2)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/S0960-894X(00)80077-3
44311676 102574 0 None - 0 Human 10.0 pIC50 = 10 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 706 17 2 9 7.0 CCCCCOC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCC)nc(CC)c2C(=O)OCCC(=O)Nc2ccccc2)c(F)c1 10.1016/S0960-894X(00)80077-3
CHEMBL307318 102574 0 None - 0 Human 10.0 pIC50 = 10 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 706 17 2 9 7.0 CCCCCOC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCC)nc(CC)c2C(=O)OCCC(=O)Nc2ccccc2)c(F)c1 10.1016/S0960-894X(00)80077-3
44311435 202315 0 None - 0 Human 10.0 pIC50 = 10 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 693 17 1 9 7.3 CCCc1nc(CC)c(C(=O)OCCCOc2ccccc2)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/S0960-894X(00)80077-3
CHEMBL69721 202315 0 None - 0 Human 10.0 pIC50 = 10 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 693 17 1 9 7.3 CCCc1nc(CC)c(C(=O)OCCCOc2ccccc2)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/S0960-894X(00)80077-3
44311415 202377 0 None - 0 Human 10.0 pIC50 = 10 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 705 17 1 9 7.5 CCCc1nc(CC)c(C(=O)OCCCC(=O)c2ccccc2)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/S0960-894X(00)80077-3
CHEMBL70161 202377 0 None - 0 Human 10.0 pIC50 = 10 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 705 17 1 9 7.5 CCCc1nc(CC)c(C(=O)OCCCC(=O)c2ccccc2)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/S0960-894X(00)80077-3
44311434 202415 0 None - 0 Human 10.0 pIC50 = 10 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 707 18 1 9 7.5 CCCc1nc(CC)c(C(=O)OCCCOCc2ccccc2)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/S0960-894X(00)80077-3
CHEMBL70370 202415 0 None - 0 Human 10.0 pIC50 = 10 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 707 18 1 9 7.5 CCCc1nc(CC)c(C(=O)OCCCOCc2ccccc2)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/S0960-894X(00)80077-3
44311072 202476 0 None - 0 Human 10.0 pIC50 = 10 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 679 15 1 9 7.1 CCCc1nc(CC)c(C(=O)OCc2ccccc2OC)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/S0960-894X(00)80077-3
CHEMBL70789 202476 0 None - 0 Human 10.0 pIC50 = 10 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 679 15 1 9 7.1 CCCc1nc(CC)c(C(=O)OCc2ccccc2OC)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/S0960-894X(00)80077-3
44311073 202490 0 None - 0 Human 10.0 pIC50 = 10 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 746 16 1 10 6.6 CCCc1nc(CC)c(C(=O)OCCCN2C(=O)c3ccccc3C2=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/S0960-894X(00)80077-3
CHEMBL70843 202490 0 None - 0 Human 10.0 pIC50 = 10 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 746 16 1 10 6.6 CCCc1nc(CC)c(C(=O)OCCCN2C(=O)c3ccccc3C2=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/S0960-894X(00)80077-3
44311414 202513 0 None - 0 Human 10.0 pIC50 = 10 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 677 15 1 9 6.8 CCCc1nc(CC)c(C(=O)OCC(=O)c2ccccc2)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/S0960-894X(00)80077-3
CHEMBL70935 202513 0 None - 0 Human 10.0 pIC50 = 10 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 677 15 1 9 6.8 CCCc1nc(CC)c(C(=O)OCC(=O)c2ccccc2)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/S0960-894X(00)80077-3
9829012 92110 0 None - 0 Rabbit 10.0 pIC50 = 10 Binding
Displacement of [125 I]Sar1Ile8-AII from type 1 Angiotensin II receptor of rabbit aorta membraneDisplacement of [125 I]Sar1Ile8-AII from type 1 Angiotensin II receptor of rabbit aorta membrane
ChEMBL 550 9 2 7 5.5 CCCCc1nc2ccc(NC(=O)N(C)C(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80517-5
CHEMBL24322 92110 0 None - 0 Rabbit 10.0 pIC50 = 10 Binding
Displacement of [125 I]Sar1Ile8-AII from type 1 Angiotensin II receptor of rabbit aorta membraneDisplacement of [125 I]Sar1Ile8-AII from type 1 Angiotensin II receptor of rabbit aorta membrane
ChEMBL 550 9 2 7 5.5 CCCCc1nc2ccc(NC(=O)N(C)C(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80517-5
73347893 92180 0 None - 0 Human 10.0 pIC50 = 10 Binding
Displacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysisDisplacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysis
ChEMBL 531 10 2 4 7.3 CCCc1nc2c(C)cc(NC(=O)CCc3ccccc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2013.08.014
CHEMBL2435828 92180 0 None - 0 Human 10.0 pIC50 = 10 Binding
Displacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysisDisplacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysis
ChEMBL 531 10 2 4 7.3 CCCc1nc2c(C)cc(NC(=O)CCc3ccccc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2013.08.014
9829012 92110 0 None - 0 Rabbit 10.0 pIC50 = 10 Binding
Displacement of [125I]Sar1-Ile8-AII (without BSA) from type 1 Angiotensin II receptor of rabbit aortaDisplacement of [125I]Sar1-Ile8-AII (without BSA) from type 1 Angiotensin II receptor of rabbit aorta
ChEMBL 550 9 2 7 5.5 CCCCc1nc2ccc(NC(=O)N(C)C(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80335-2
CHEMBL24322 92110 0 None - 0 Rabbit 10.0 pIC50 = 10 Binding
Displacement of [125I]Sar1-Ile8-AII (without BSA) from type 1 Angiotensin II receptor of rabbit aortaDisplacement of [125I]Sar1-Ile8-AII (without BSA) from type 1 Angiotensin II receptor of rabbit aorta
ChEMBL 550 9 2 7 5.5 CCCCc1nc2ccc(NC(=O)N(C)C(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80335-2
19754061 102248 0 None - 0 Rabbit 10.0 pIC50 = 10 Binding
In vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranesIn vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranes
ChEMBL 657 15 2 7 7.7 CCCCC(=O)Nc1cc2nc(CCCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)CCC4CCCC4)cc3)c2nc1C 10.1016/S0960-894X(01)81115-X
CHEMBL304947 102248 0 None - 0 Rabbit 10.0 pIC50 = 10 Binding
In vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranesIn vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranes
ChEMBL 657 15 2 7 7.7 CCCCC(=O)Nc1cc2nc(CCCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)CCC4CCCC4)cc3)c2nc1C 10.1016/S0960-894X(01)81115-X
44309719 202147 0 None - 0 Rabbit 10.0 pIC50 = 10 Binding
In vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranesIn vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranes
ChEMBL 544 9 1 6 6.1 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)CCC2CCCC2)cc1 10.1016/S0960-894X(01)81115-X
CHEMBL68638 202147 0 None - 0 Rabbit 10.0 pIC50 = 10 Binding
In vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranesIn vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranes
ChEMBL 544 9 1 6 6.1 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)CCC2CCCC2)cc1 10.1016/S0960-894X(01)81115-X
10010071 116833 0 None - 0 Rabbit 10.0 pIC50 = 10 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 715 13 2 10 6.1 CCCCc1nn(-c2cc(NC(=O)COCC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1021/jm00019a004
CHEMBL339722 116833 0 None - 0 Rabbit 10.0 pIC50 = 10 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 715 13 2 10 6.1 CCCCc1nn(-c2cc(NC(=O)COCC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1021/jm00019a004
9829012 92110 0 None - 0 Rabbit 10.0 pIC50 = 10 Binding
Inhibitory activity was evaluated against Angiotensin II receptor, type 1 in rabbit aortaInhibitory activity was evaluated against Angiotensin II receptor, type 1 in rabbit aorta
ChEMBL 550 9 2 7 5.5 CCCCc1nc2ccc(NC(=O)N(C)C(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm9504722
CHEMBL24322 92110 0 None - 0 Rabbit 10.0 pIC50 = 10 Binding
Inhibitory activity was evaluated against Angiotensin II receptor, type 1 in rabbit aortaInhibitory activity was evaluated against Angiotensin II receptor, type 1 in rabbit aorta
ChEMBL 550 9 2 7 5.5 CCCCc1nc2ccc(NC(=O)N(C)C(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm9504722
9829012 92110 0 None - 0 Human 10.0 pIC50 = 10 Binding
Inhibitory concentration against angiotensin II receptor, type 1Inhibitory concentration against angiotensin II receptor, type 1
ChEMBL 550 9 2 7 5.5 CCCCc1nc2ccc(NC(=O)N(C)C(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm058225d
CHEMBL24322 92110 0 None - 0 Human 10.0 pIC50 = 10 Binding
Inhibitory concentration against angiotensin II receptor, type 1Inhibitory concentration against angiotensin II receptor, type 1
ChEMBL 550 9 2 7 5.5 CCCCc1nc2ccc(NC(=O)N(C)C(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm058225d
9809961 106664 2 None - 0 Rabbit 10.0 pIC50 = 10.0 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 668 10 1 7 6.9 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1007/s00044-013-0831-x
CHEMBL316300 106664 2 None - 0 Rabbit 10.0 pIC50 = 10.0 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 668 10 1 7 6.9 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1007/s00044-013-0831-x
10439862 118254 0 None - 0 Rabbit 10.0 pIC50 = 10.0 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 719 13 2 8 7.3 CCCCc1nn(-c2cc(NC(=O)CCC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1007/s00044-013-0831-x
CHEMBL341934 118254 0 None - 0 Rabbit 10.0 pIC50 = 10.0 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 719 13 2 8 7.3 CCCCc1nn(-c2cc(NC(=O)CCC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1007/s00044-013-0831-x
10010195 118666 0 None - 0 Rabbit 10.0 pIC50 = 10.0 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 733 13 2 8 7.5 CCCCc1nn(-c2cc(NC(=O)CC(C)C)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1007/s00044-013-0831-x
CHEMBL343142 118666 0 None - 0 Rabbit 10.0 pIC50 = 10.0 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 733 13 2 8 7.5 CCCCc1nn(-c2cc(NC(=O)CC(C)C)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1007/s00044-013-0831-x
9809961 106664 2 None - 0 Rabbit 10.0 pIC50 = 10.0 Binding
In vitro ability to inhibit the binding of radioligand 125I[Sar1,IIe8]AII to AT1 receptor from rabbit aortaIn vitro ability to inhibit the binding of radioligand 125I[Sar1,IIe8]AII to AT1 receptor from rabbit aorta
ChEMBL 668 10 1 7 6.9 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1016/S0960-894X(01)80595-3
CHEMBL316300 106664 2 None - 0 Rabbit 10.0 pIC50 = 10.0 Binding
In vitro ability to inhibit the binding of radioligand 125I[Sar1,IIe8]AII to AT1 receptor from rabbit aortaIn vitro ability to inhibit the binding of radioligand 125I[Sar1,IIe8]AII to AT1 receptor from rabbit aorta
ChEMBL 668 10 1 7 6.9 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1016/S0960-894X(01)80595-3
9917295 102472 13 None - 0 Rabbit 10.0 pIC50 = 10.0 Binding
In vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranesIn vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranes
ChEMBL 633 15 2 8 7.1 CCCCOC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCCC)nc3cc(NC(=O)CCCC)c(C)nc32)cc1 10.1016/S0960-894X(01)81115-X
CHEMBL306407 102472 13 None - 0 Rabbit 10.0 pIC50 = 10.0 Binding
In vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranesIn vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranes
ChEMBL 633 15 2 8 7.1 CCCCOC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCCC)nc3cc(NC(=O)CCCC)c(C)nc32)cc1 10.1016/S0960-894X(01)81115-X
9809961 106664 2 None - 0 Rabbit 10.0 pIC50 = 10.0 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 668 10 1 7 6.9 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1021/jm00043a020
CHEMBL316300 106664 2 None - 0 Rabbit 10.0 pIC50 = 10.0 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 668 10 1 7 6.9 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1021/jm00043a020
9809961 106664 2 None - 0 Rabbit 10.0 pIC50 = 10.0 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 668 10 1 7 6.9 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1021/jm00052a006
CHEMBL316300 106664 2 None - 0 Rabbit 10.0 pIC50 = 10.0 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 668 10 1 7 6.9 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1021/jm00052a006
10439862 118254 0 None - 0 Rabbit 10.0 pIC50 = 10.0 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 719 13 2 8 7.3 CCCCc1nn(-c2cc(NC(=O)CCC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1021/jm00052a006
CHEMBL341934 118254 0 None - 0 Rabbit 10.0 pIC50 = 10.0 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 719 13 2 8 7.3 CCCCc1nn(-c2cc(NC(=O)CCC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1021/jm00052a006
10010195 118666 0 None - 0 Rabbit 10.0 pIC50 = 10.0 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 733 13 2 8 7.5 CCCCc1nn(-c2cc(NC(=O)CC(C)C)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1021/jm00052a006
CHEMBL343142 118666 0 None - 0 Rabbit 10.0 pIC50 = 10.0 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 733 13 2 8 7.5 CCCCc1nn(-c2cc(NC(=O)CC(C)C)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1021/jm00052a006
10395394 31649 0 None - 0 Rabbit 9.9 pIC50 = 9.9 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 767 13 2 8 7.7 CCCCc1nn(-c2cc(NC(=O)Cc3ccccc3)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1007/s00044-013-0831-x
CHEMBL140708 31649 0 None - 0 Rabbit 9.9 pIC50 = 9.9 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 767 13 2 8 7.7 CCCCc1nn(-c2cc(NC(=O)Cc3ccccc3)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1007/s00044-013-0831-x
10032851 16641 0 None - 0 Rabbit 9.9 pIC50 = 9.9 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 729 11 2 9 6.6 CCCCc1nn(-c2cc(NC(=O)CC)ccc2Br)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1007/s00044-011-9815-x
CHEMBL124771 16641 0 None - 0 Rabbit 9.9 pIC50 = 9.9 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 729 11 2 9 6.6 CCCCc1nn(-c2cc(NC(=O)CC)ccc2Br)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1007/s00044-011-9815-x
9809637 202145 0 None - 0 Rabbit 9.9 pIC50 = 9.9 Binding
In vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranesIn vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranes
ChEMBL 643 15 2 7 7.4 CCCCC(=O)Nc1cnc2c(c1)nc(CCCC)n2Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)CCC2CCCC2)cc1 10.1016/S0960-894X(01)81115-X
CHEMBL68618 202145 0 None - 0 Rabbit 9.9 pIC50 = 9.9 Binding
In vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranesIn vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranes
ChEMBL 643 15 2 7 7.4 CCCCC(=O)Nc1cnc2c(c1)nc(CCCC)n2Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)CCC2CCCC2)cc1 10.1016/S0960-894X(01)81115-X
10032851 16641 0 None - 0 Rabbit 9.9 pIC50 = 9.9 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 729 11 2 9 6.6 CCCCc1nn(-c2cc(NC(=O)CC)ccc2Br)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1021/jm00019a004
CHEMBL124771 16641 0 None - 0 Rabbit 9.9 pIC50 = 9.9 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 729 11 2 9 6.6 CCCCc1nn(-c2cc(NC(=O)CC)ccc2Br)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1021/jm00019a004
10395394 31649 0 None - 0 Rabbit 9.9 pIC50 = 9.9 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 767 13 2 8 7.7 CCCCc1nn(-c2cc(NC(=O)Cc3ccccc3)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1021/jm00052a006
CHEMBL140708 31649 0 None - 0 Rabbit 9.9 pIC50 = 9.9 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 767 13 2 8 7.7 CCCCc1nn(-c2cc(NC(=O)Cc3ccccc3)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1021/jm00052a006
44210588 119826 0 None - 0 Rabbit 9.9 pIC50 = 9.9 Binding
Tested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membraneTested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membrane
ChEMBL 633 12 3 8 5.8 CCCCOC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCC)nc3ccc(NC(=O)NC(C)C)cc3c2=O)cc1 10.1016/S0960-894X(01)81126-4
CHEMBL353037 119826 0 None - 0 Rabbit 9.9 pIC50 = 9.9 Binding
Tested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membraneTested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membrane
ChEMBL 633 12 3 8 5.8 CCCCOC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCC)nc3ccc(NC(=O)NC(C)C)cc3c2=O)cc1 10.1016/S0960-894X(01)81126-4
10032851 16641 0 None - 0 Rabbit 9.9 pIC50 = 9.9 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 729 11 2 9 6.6 CCCCc1nn(-c2cc(NC(=O)CC)ccc2Br)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1007/s00044-011-9815-x
CHEMBL124771 16641 0 None - 0 Rabbit 9.9 pIC50 = 9.9 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 729 11 2 9 6.6 CCCCc1nn(-c2cc(NC(=O)CC)ccc2Br)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1007/s00044-011-9815-x
10327309 113379 0 None - 0 Rabbit 9.9 pIC50 = 9.9 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 691 12 2 9 6.0 CCCCc1nn(-c2cc(NC(=O)CC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCC)cc1F 10.1007/s00044-011-9815-x
CHEMBL332576 113379 0 None - 0 Rabbit 9.9 pIC50 = 9.9 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 691 12 2 9 6.0 CCCCc1nn(-c2cc(NC(=O)CC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCC)cc1F 10.1007/s00044-011-9815-x
10395335 116568 0 None - 0 Rabbit 9.9 pIC50 = 9.9 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 757 12 2 8 7.4 CCCCc1nn(-c2cc(NC(=O)CC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1F 10.1007/s00044-011-9815-x
CHEMBL339256 116568 0 None - 0 Rabbit 9.9 pIC50 = 9.9 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 757 12 2 8 7.4 CCCCc1nn(-c2cc(NC(=O)CC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1F 10.1007/s00044-011-9815-x
10372451 116778 0 None - 0 Rabbit 9.9 pIC50 = 9.9 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 685 11 2 9 6.4 CCCCc1nn(-c2cc(NC(=O)CC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1007/s00044-011-9815-x
CHEMBL339605 116778 0 None - 0 Rabbit 9.9 pIC50 = 9.9 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 685 11 2 9 6.4 CCCCc1nn(-c2cc(NC(=O)CC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1007/s00044-011-9815-x
10327309 113379 0 None - 0 Rabbit 9.9 pIC50 = 9.9 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 691 12 2 9 6.0 CCCCc1nn(-c2cc(NC(=O)CC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCC)cc1F 10.1021/jm00019a004
CHEMBL332576 113379 0 None - 0 Rabbit 9.9 pIC50 = 9.9 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 691 12 2 9 6.0 CCCCc1nn(-c2cc(NC(=O)CC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCC)cc1F 10.1021/jm00019a004
10395335 116568 0 None - 0 Rabbit 9.9 pIC50 = 9.9 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 757 12 2 8 7.4 CCCCc1nn(-c2cc(NC(=O)CC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1F 10.1021/jm00019a004
CHEMBL339256 116568 0 None - 0 Rabbit 9.9 pIC50 = 9.9 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 757 12 2 8 7.4 CCCCc1nn(-c2cc(NC(=O)CC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1F 10.1021/jm00019a004
10372451 116778 0 None - 0 Rabbit 9.9 pIC50 = 9.9 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 685 11 2 9 6.4 CCCCc1nn(-c2cc(NC(=O)CC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1021/jm00019a004
CHEMBL339605 116778 0 None - 0 Rabbit 9.9 pIC50 = 9.9 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 685 11 2 9 6.4 CCCCc1nn(-c2cc(NC(=O)CC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1021/jm00019a004
10372093 112252 0 None - 0 Rabbit 9.9 pIC50 = 9.9 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 652 10 1 7 6.4 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2F)cc1 10.1021/jm00043a020
CHEMBL330533 112252 0 None - 0 Rabbit 9.9 pIC50 = 9.9 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 652 10 1 7 6.4 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2F)cc1 10.1021/jm00043a020
44314822 102463 0 None - 0 Rabbit 9.9 pIC50 = 9.9 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membrane
ChEMBL 691 13 2 8 6.7 CCCCc1nc2ccc(NC(=O)N(C)C(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC2CC2)cc1F 10.1016/0960-894X(94)85036-4
CHEMBL306362 102463 0 None - 0 Rabbit 9.9 pIC50 = 9.9 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membrane
ChEMBL 691 13 2 8 6.7 CCCCc1nc2ccc(NC(=O)N(C)C(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC2CC2)cc1F 10.1016/0960-894X(94)85036-4
10259411 30428 0 None - 0 Rabbit 9.9 pIC50 = 9.9 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 734 13 3 8 7.0 CCCCc1nn(-c2cc(NC(=O)NCCC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1007/s00044-013-0831-x
CHEMBL139452 30428 0 None - 0 Rabbit 9.9 pIC50 = 9.9 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 734 13 3 8 7.0 CCCCc1nn(-c2cc(NC(=O)NCCC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1007/s00044-013-0831-x
10485116 116340 0 None - 0 Rabbit 9.9 pIC50 = 9.9 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 733 14 2 8 7.0 CCCCNC(=O)c1ccc(Cl)c(-n2nc(CCCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)c4ccccc4Cl)cc3)c2=O)c1 10.1007/s00044-013-0831-x
CHEMBL338101 116340 0 None - 0 Rabbit 9.9 pIC50 = 9.9 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 733 14 2 8 7.0 CCCCNC(=O)c1ccc(Cl)c(-n2nc(CCCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)c4ccccc4Cl)cc3)c2=O)c1 10.1007/s00044-013-0831-x
10462598 113624 0 None - 0 Rabbit 9.9 pIC50 = 9.9 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 723 12 2 8 6.7 CCCCc1nn(-c2cc(NC(=O)CC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1F 10.1007/s00044-011-9815-x
CHEMBL332909 113624 0 None - 0 Rabbit 9.9 pIC50 = 9.9 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 723 12 2 8 6.7 CCCCc1nn(-c2cc(NC(=O)CC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1F 10.1007/s00044-011-9815-x
10485116 116340 0 None - 0 Rabbit 9.9 pIC50 = 9.9 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 733 14 2 8 7.0 CCCCNC(=O)c1ccc(Cl)c(-n2nc(CCCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)c4ccccc4Cl)cc3)c2=O)c1 10.1007/s00044-011-9815-x
CHEMBL338101 116340 0 None - 0 Rabbit 9.9 pIC50 = 9.9 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 733 14 2 8 7.0 CCCCNC(=O)c1ccc(Cl)c(-n2nc(CCCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)c4ccccc4Cl)cc3)c2=O)c1 10.1007/s00044-011-9815-x
10395076 168000 0 None - 0 Rabbit 9.9 pIC50 = 9.9 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 715 13 2 10 6.1 CCCCc1nn(-c2cc(NC(=O)CCOC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1007/s00044-011-9815-x
CHEMBL435811 168000 0 None - 0 Rabbit 9.9 pIC50 = 9.9 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 715 13 2 10 6.1 CCCCc1nn(-c2cc(NC(=O)CCOC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1007/s00044-011-9815-x
10462598 113624 0 None - 0 Rabbit 9.9 pIC50 = 9.9 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 723 12 2 8 6.7 CCCCc1nn(-c2cc(NC(=O)CC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1F 10.1021/jm00019a004
CHEMBL332909 113624 0 None - 0 Rabbit 9.9 pIC50 = 9.9 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 723 12 2 8 6.7 CCCCc1nn(-c2cc(NC(=O)CC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1F 10.1021/jm00019a004
10485116 116340 0 None - 0 Rabbit 9.9 pIC50 = 9.9 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 733 14 2 8 7.0 CCCCNC(=O)c1ccc(Cl)c(-n2nc(CCCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)c4ccccc4Cl)cc3)c2=O)c1 10.1021/jm00019a004
CHEMBL338101 116340 0 None - 0 Rabbit 9.9 pIC50 = 9.9 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 733 14 2 8 7.0 CCCCNC(=O)c1ccc(Cl)c(-n2nc(CCCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)c4ccccc4Cl)cc3)c2=O)c1 10.1021/jm00019a004
10395076 168000 0 None - 0 Rabbit 9.9 pIC50 = 9.9 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 715 13 2 10 6.1 CCCCc1nn(-c2cc(NC(=O)CCOC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1021/jm00019a004
CHEMBL435811 168000 0 None - 0 Rabbit 9.9 pIC50 = 9.9 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 715 13 2 10 6.1 CCCCc1nn(-c2cc(NC(=O)CCOC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1021/jm00019a004
10395076 168000 0 None - 0 Human 9.9 pIC50 = 9.9 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 715 13 2 10 6.1 CCCCc1nn(-c2cc(NC(=O)CCOC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1021/jm00019a004
CHEMBL435811 168000 0 None - 0 Human 9.9 pIC50 = 9.9 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 715 13 2 10 6.1 CCCCc1nn(-c2cc(NC(=O)CCOC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1021/jm00019a004
10259411 30428 0 None - 0 Rabbit 9.9 pIC50 = 9.9 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 734 13 3 8 7.0 CCCCc1nn(-c2cc(NC(=O)NCCC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1021/jm00052a006
CHEMBL139452 30428 0 None - 0 Rabbit 9.9 pIC50 = 9.9 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 734 13 3 8 7.0 CCCCc1nn(-c2cc(NC(=O)NCCC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1021/jm00052a006
10485116 116340 0 None - 0 Rabbit 9.9 pIC50 = 9.9 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 733 14 2 8 7.0 CCCCNC(=O)c1ccc(Cl)c(-n2nc(CCCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)c4ccccc4Cl)cc3)c2=O)c1 10.1021/jm00052a006
CHEMBL338101 116340 0 None - 0 Rabbit 9.9 pIC50 = 9.9 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 733 14 2 8 7.0 CCCCNC(=O)c1ccc(Cl)c(-n2nc(CCCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)c4ccccc4Cl)cc3)c2=O)c1 10.1021/jm00052a006
10462598 113624 0 None - 0 Rabbit 9.9 pIC50 = 9.9 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 723 12 2 8 6.7 CCCCc1nn(-c2cc(NC(=O)CC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1F 10.1007/s00044-011-9815-x
CHEMBL332909 113624 0 None - 0 Rabbit 9.9 pIC50 = 9.9 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 723 12 2 8 6.7 CCCCc1nn(-c2cc(NC(=O)CC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1F 10.1007/s00044-011-9815-x
10485116 116340 0 None - 0 Rabbit 9.9 pIC50 = 9.9 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 733 14 2 8 7.0 CCCCNC(=O)c1ccc(Cl)c(-n2nc(CCCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)c4ccccc4Cl)cc3)c2=O)c1 10.1007/s00044-011-9815-x
CHEMBL338101 116340 0 None - 0 Rabbit 9.9 pIC50 = 9.9 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 733 14 2 8 7.0 CCCCNC(=O)c1ccc(Cl)c(-n2nc(CCCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)c4ccccc4Cl)cc3)c2=O)c1 10.1007/s00044-011-9815-x
10395076 168000 0 None - 0 Rabbit 9.9 pIC50 = 9.9 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 715 13 2 10 6.1 CCCCc1nn(-c2cc(NC(=O)CCOC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1007/s00044-011-9815-x
CHEMBL435811 168000 0 None - 0 Rabbit 9.9 pIC50 = 9.9 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 715 13 2 10 6.1 CCCCc1nn(-c2cc(NC(=O)CCOC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1007/s00044-011-9815-x
19939453 111885 0 None - 0 Rabbit 9.8 pIC50 = 9.8 Binding
In vitro ability to inhibit the binding of radioligand 125I[Sar1,IIe8]AII to AT1 receptor from rabbit aortaIn vitro ability to inhibit the binding of radioligand 125I[Sar1,IIe8]AII to AT1 receptor from rabbit aorta
ChEMBL 686 10 1 7 7.0 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1F 10.1016/S0960-894X(01)80595-3
CHEMBL329679 111885 0 None - 0 Rabbit 9.8 pIC50 = 9.8 Binding
In vitro ability to inhibit the binding of radioligand 125I[Sar1,IIe8]AII to AT1 receptor from rabbit aortaIn vitro ability to inhibit the binding of radioligand 125I[Sar1,IIe8]AII to AT1 receptor from rabbit aorta
ChEMBL 686 10 1 7 7.0 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1F 10.1016/S0960-894X(01)80595-3
10326797 205830 0 None - 0 Rabbit 9.8 pIC50 = 9.8 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 640 10 1 7 6.5 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)C2CCCCC2)cc1 10.1021/jm00043a020
CHEMBL94905 205830 0 None - 0 Rabbit 9.8 pIC50 = 9.8 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 640 10 1 7 6.5 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)C2CCCCC2)cc1 10.1021/jm00043a020
44381724 119789 0 None - 0 Rabbit 9.8 pIC50 = 9.8 Binding
Tested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membraneTested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membrane
ChEMBL 651 11 3 7 6.1 CCCCc1nc2ccc(NC(=O)NC(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/S0960-894X(01)81126-4
CHEMBL352771 119789 0 None - 0 Rabbit 9.8 pIC50 = 9.8 Binding
Tested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membraneTested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membrane
ChEMBL 651 11 3 7 6.1 CCCCc1nc2ccc(NC(=O)NC(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/S0960-894X(01)81126-4
44381671 119908 0 None - 0 Rabbit 9.8 pIC50 = 9.8 Binding
Tested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membraneTested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membrane
ChEMBL 647 13 3 8 6.2 CCCCOC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCCC)nc3ccc(NC(=O)NC(C)C)cc3c2=O)cc1 10.1016/S0960-894X(01)81126-4
CHEMBL353800 119908 0 None - 0 Rabbit 9.8 pIC50 = 9.8 Binding
Tested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membraneTested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membrane
ChEMBL 647 13 3 8 6.2 CCCCOC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCCC)nc3ccc(NC(=O)NC(C)C)cc3c2=O)cc1 10.1016/S0960-894X(01)81126-4
10259395 26774 0 None - 0 Rabbit 9.8 pIC50 = 9.8 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 733 11 2 8 7.5 CCCCc1nn(-c2cc(NC(=O)C(C)(C)C)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1007/s00044-013-0831-x
CHEMBL136465 26774 0 None - 0 Rabbit 9.8 pIC50 = 9.8 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 733 11 2 8 7.5 CCCCc1nn(-c2cc(NC(=O)C(C)(C)C)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1007/s00044-013-0831-x
10078663 206042 0 None - 0 Rabbit 9.8 pIC50 = 9.8 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 733 14 2 8 7.6 CCCCC(=O)Nc1ccc(Cl)c(-n2nc(CCCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)c4ccccc4Cl)cc3)c2=O)c1 10.1007/s00044-013-0831-x
CHEMBL96075 206042 0 None - 0 Rabbit 9.8 pIC50 = 9.8 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 733 14 2 8 7.6 CCCCC(=O)Nc1ccc(Cl)c(-n2nc(CCCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)c4ccccc4Cl)cc3)c2=O)c1 10.1007/s00044-013-0831-x
9853391 116326 1 None - 0 Rabbit 9.8 pIC50 = 9.8 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 729 11 2 9 6.6 CCCCC(=O)Nc1ccc(Br)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1007/s00044-011-9815-x
CHEMBL338027 116326 1 None - 0 Rabbit 9.8 pIC50 = 9.8 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 729 11 2 9 6.6 CCCCC(=O)Nc1ccc(Br)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1007/s00044-011-9815-x
10101608 116515 0 None - 0 Rabbit 9.8 pIC50 = 9.8 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 751 14 2 8 7.2 CCCCNC(=O)c1ccc(Cl)c(-n2nc(CCCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)c4ccccc4Cl)cc3F)c2=O)c1 10.1007/s00044-011-9815-x
CHEMBL339004 116515 0 None - 0 Rabbit 9.8 pIC50 = 9.8 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 751 14 2 8 7.2 CCCCNC(=O)c1ccc(Cl)c(-n2nc(CCCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)c4ccccc4Cl)cc3F)c2=O)c1 10.1007/s00044-011-9815-x
10078663 206042 0 None - 0 Rabbit 9.8 pIC50 = 9.8 Binding
In vitro ability to inhibit the binding of radioligand 125I[Sar1,IIe8]AII to AT1 receptor from rabbit aortaIn vitro ability to inhibit the binding of radioligand 125I[Sar1,IIe8]AII to AT1 receptor from rabbit aorta
ChEMBL 733 14 2 8 7.6 CCCCC(=O)Nc1ccc(Cl)c(-n2nc(CCCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)c4ccccc4Cl)cc3)c2=O)c1 10.1016/S0960-894X(01)80595-3
CHEMBL96075 206042 0 None - 0 Rabbit 9.8 pIC50 = 9.8 Binding
In vitro ability to inhibit the binding of radioligand 125I[Sar1,IIe8]AII to AT1 receptor from rabbit aortaIn vitro ability to inhibit the binding of radioligand 125I[Sar1,IIe8]AII to AT1 receptor from rabbit aorta
ChEMBL 733 14 2 8 7.6 CCCCC(=O)Nc1ccc(Cl)c(-n2nc(CCCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)c4ccccc4Cl)cc3)c2=O)c1 10.1016/S0960-894X(01)80595-3
9853391 116326 1 None - 0 Rabbit 9.8 pIC50 = 9.8 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 729 11 2 9 6.6 CCCCC(=O)Nc1ccc(Br)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1021/jm00019a004
CHEMBL338027 116326 1 None - 0 Rabbit 9.8 pIC50 = 9.8 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 729 11 2 9 6.6 CCCCC(=O)Nc1ccc(Br)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1021/jm00019a004
10101608 116515 0 None - 0 Rabbit 9.8 pIC50 = 9.8 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 751 14 2 8 7.2 CCCCNC(=O)c1ccc(Cl)c(-n2nc(CCCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)c4ccccc4Cl)cc3F)c2=O)c1 10.1021/jm00019a004
CHEMBL339004 116515 0 None - 0 Rabbit 9.8 pIC50 = 9.8 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 751 14 2 8 7.2 CCCCNC(=O)c1ccc(Cl)c(-n2nc(CCCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)c4ccccc4Cl)cc3F)c2=O)c1 10.1021/jm00019a004
10009273 106728 0 None - 0 Rabbit 9.8 pIC50 = 9.8 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 636 11 1 8 5.1 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NS(=O)(=O)C(C)C)cc1 10.1021/jm00043a020
CHEMBL316706 106728 0 None - 0 Rabbit 9.8 pIC50 = 9.8 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 636 11 1 8 5.1 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NS(=O)(=O)C(C)C)cc1 10.1021/jm00043a020
10259395 26774 0 None - 0 Rabbit 9.8 pIC50 = 9.8 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 733 11 2 8 7.5 CCCCc1nn(-c2cc(NC(=O)C(C)(C)C)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1021/jm00052a006
CHEMBL136465 26774 0 None - 0 Rabbit 9.8 pIC50 = 9.8 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 733 11 2 8 7.5 CCCCc1nn(-c2cc(NC(=O)C(C)(C)C)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1021/jm00052a006
10078663 206042 0 None - 0 Rabbit 9.8 pIC50 = 9.8 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 733 14 2 8 7.6 CCCCC(=O)Nc1ccc(Cl)c(-n2nc(CCCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)c4ccccc4Cl)cc3)c2=O)c1 10.1021/jm00052a006
CHEMBL96075 206042 0 None - 0 Rabbit 9.8 pIC50 = 9.8 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 733 14 2 8 7.6 CCCCC(=O)Nc1ccc(Cl)c(-n2nc(CCCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)c4ccccc4Cl)cc3)c2=O)c1 10.1021/jm00052a006
44327716 106817 0 None - 0 Rat 9.8 pIC50 = 9.8 Binding
Tested for inhibition of [125I]- AII specific binding to rat mesenteric arteries, expressed as IC50Tested for inhibition of [125I]- AII specific binding to rat mesenteric arteries, expressed as IC50
ChEMBL 492 10 2 5 6.1 CCCCc1ncc(/C=C(\Cc2cccs2)C(=O)O)n1Cc1ccc(C(=O)O)c(Cl)c1Cl 10.1016/S0960-894X(01)81116-1
CHEMBL317343 106817 0 None - 0 Rat 9.8 pIC50 = 9.8 Binding
Tested for inhibition of [125I]- AII specific binding to rat mesenteric arteries, expressed as IC50Tested for inhibition of [125I]- AII specific binding to rat mesenteric arteries, expressed as IC50
ChEMBL 492 10 2 5 6.1 CCCCc1ncc(/C=C(\Cc2cccs2)C(=O)O)n1Cc1ccc(C(=O)O)c(Cl)c1Cl 10.1016/S0960-894X(01)81116-1
9853391 116326 1 None - 0 Rabbit 9.8 pIC50 = 9.8 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 729 11 2 9 6.6 CCCCC(=O)Nc1ccc(Br)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1007/s00044-011-9815-x
CHEMBL338027 116326 1 None - 0 Rabbit 9.8 pIC50 = 9.8 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 729 11 2 9 6.6 CCCCC(=O)Nc1ccc(Br)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1007/s00044-011-9815-x
10101608 116515 0 None - 0 Rabbit 9.8 pIC50 = 9.8 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 751 14 2 8 7.2 CCCCNC(=O)c1ccc(Cl)c(-n2nc(CCCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)c4ccccc4Cl)cc3F)c2=O)c1 10.1007/s00044-011-9815-x
CHEMBL339004 116515 0 None - 0 Rabbit 9.8 pIC50 = 9.8 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 751 14 2 8 7.2 CCCCNC(=O)c1ccc(Cl)c(-n2nc(CCCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)c4ccccc4Cl)cc3F)c2=O)c1 10.1007/s00044-011-9815-x
10101284 205659 0 None - 0 Rabbit 9.8 pIC50 = 9.8 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 705 12 2 8 6.9 CCCCc1nn(-c2cc(NC(=O)CC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1007/s00044-013-0831-x
CHEMBL93907 205659 0 None - 0 Rabbit 9.8 pIC50 = 9.8 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 705 12 2 8 6.9 CCCCc1nn(-c2cc(NC(=O)CC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1007/s00044-013-0831-x
10372659 117574 0 None - 0 Rabbit 9.8 pIC50 = 9.8 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 713 13 2 9 6.6 CCCCNC(=O)c1ccc(Cl)c(-n2nc(CCCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1007/s00044-011-9815-x
CHEMBL340632 117574 0 None - 0 Rabbit 9.8 pIC50 = 9.8 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 713 13 2 9 6.6 CCCCNC(=O)c1ccc(Cl)c(-n2nc(CCCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1007/s00044-011-9815-x
10101284 205659 0 None - 0 Rabbit 9.8 pIC50 = 9.8 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 705 12 2 8 6.9 CCCCc1nn(-c2cc(NC(=O)CC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1007/s00044-011-9815-x
CHEMBL93907 205659 0 None - 0 Rabbit 9.8 pIC50 = 9.8 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 705 12 2 8 6.9 CCCCc1nn(-c2cc(NC(=O)CC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1007/s00044-011-9815-x
54693559 202825 0 None - 0 Human 9.8 pIC50 = 9.8 Binding
Compound was tested for inhibition against Angiotensin II receptor, type 1Compound was tested for inhibition against Angiotensin II receptor, type 1
ChEMBL 425 4 2 8 3.0 Cc1nc(C)c2c(O)cc(=O)n(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c2n1 10.1021/jm0204237
CHEMBL72838 202825 0 None - 0 Human 9.8 pIC50 = 9.8 Binding
Compound was tested for inhibition against Angiotensin II receptor, type 1Compound was tested for inhibition against Angiotensin II receptor, type 1
ChEMBL 425 4 2 8 3.0 Cc1nc(C)c2c(O)cc(=O)n(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c2n1 10.1021/jm0204237
10101284 205659 0 None - 0 Rabbit 9.8 pIC50 = 9.8 Binding
In vitro ability to inhibit the binding of radioligand 125I[Sar1,IIe8]AII to AT1 receptor from rabbit aortaIn vitro ability to inhibit the binding of radioligand 125I[Sar1,IIe8]AII to AT1 receptor from rabbit aorta
ChEMBL 705 12 2 8 6.9 CCCCc1nn(-c2cc(NC(=O)CC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1016/S0960-894X(01)80595-3
CHEMBL93907 205659 0 None - 0 Rabbit 9.8 pIC50 = 9.8 Binding
In vitro ability to inhibit the binding of radioligand 125I[Sar1,IIe8]AII to AT1 receptor from rabbit aortaIn vitro ability to inhibit the binding of radioligand 125I[Sar1,IIe8]AII to AT1 receptor from rabbit aorta
ChEMBL 705 12 2 8 6.9 CCCCc1nn(-c2cc(NC(=O)CC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1016/S0960-894X(01)80595-3
10372659 117574 0 None - 0 Rabbit 9.8 pIC50 = 9.8 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 713 13 2 9 6.6 CCCCNC(=O)c1ccc(Cl)c(-n2nc(CCCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1021/jm00019a004
CHEMBL340632 117574 0 None - 0 Rabbit 9.8 pIC50 = 9.8 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 713 13 2 9 6.6 CCCCNC(=O)c1ccc(Cl)c(-n2nc(CCCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1021/jm00019a004
10101284 205659 0 None - 0 Rabbit 9.8 pIC50 = 9.8 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 705 12 2 8 6.9 CCCCc1nn(-c2cc(NC(=O)CC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1021/jm00019a004
CHEMBL93907 205659 0 None - 0 Rabbit 9.8 pIC50 = 9.8 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 705 12 2 8 6.9 CCCCc1nn(-c2cc(NC(=O)CC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1021/jm00019a004
10417351 206209 0 None - 0 Rabbit 9.8 pIC50 = 9.8 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 706 10 1 8 7.2 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2cc(C)oc2C(F)(F)F)cc1 10.1021/jm00043a020
CHEMBL97075 206209 0 None - 0 Rabbit 9.8 pIC50 = 9.8 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 706 10 1 8 7.2 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2cc(C)oc2C(F)(F)F)cc1 10.1021/jm00043a020
44327912 206384 0 None - 0 Rabbit 9.8 pIC50 = 9.8 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 748 12 1 9 8.0 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2cc3ccccc3o2)cc1.CCOCC 10.1021/jm00043a020
CHEMBL98068 206384 0 None - 0 Rabbit 9.8 pIC50 = 9.8 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 748 12 1 9 8.0 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2cc3ccccc3o2)cc1.CCOCC 10.1021/jm00043a020
10101284 205659 0 None - 0 Rabbit 9.8 pIC50 = 9.8 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 705 12 2 8 6.9 CCCCc1nn(-c2cc(NC(=O)CC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1021/jm00052a006
CHEMBL93907 205659 0 None - 0 Rabbit 9.8 pIC50 = 9.8 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 705 12 2 8 6.9 CCCCc1nn(-c2cc(NC(=O)CC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1021/jm00052a006
44381413 120197 0 None - 0 Rabbit 9.8 pIC50 = 9.8 Binding
Tested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membraneTested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membrane
ChEMBL 661 14 3 8 6.6 CCCCCOC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCCC)nc3ccc(NC(=O)NC(C)C)cc3c2=O)cc1 10.1016/S0960-894X(01)81126-4
CHEMBL354779 120197 0 None - 0 Rabbit 9.8 pIC50 = 9.8 Binding
Tested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membraneTested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membrane
ChEMBL 661 14 3 8 6.6 CCCCCOC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCCC)nc3ccc(NC(=O)NC(C)C)cc3c2=O)cc1 10.1016/S0960-894X(01)81126-4
10101284 205659 0 None - 0 Rabbit 9.8 pIC50 = 9.8 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 705 12 2 8 6.9 CCCCc1nn(-c2cc(NC(=O)CC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1007/s00044-011-9815-x
CHEMBL93907 205659 0 None - 0 Rabbit 9.8 pIC50 = 9.8 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 705 12 2 8 6.9 CCCCc1nn(-c2cc(NC(=O)CC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1007/s00044-011-9815-x
10372659 117574 0 None - 0 Rabbit 9.8 pIC50 = 9.8 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 713 13 2 9 6.6 CCCCNC(=O)c1ccc(Cl)c(-n2nc(CCCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1007/s00044-011-9815-x
CHEMBL340632 117574 0 None - 0 Rabbit 9.8 pIC50 = 9.8 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 713 13 2 9 6.6 CCCCNC(=O)c1ccc(Cl)c(-n2nc(CCCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1007/s00044-011-9815-x
10327537 116164 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 719 12 2 8 7.1 CCCCc1nn(-c2cc(NC(=O)C(C)C)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1007/s00044-013-0831-x
CHEMBL337118 116164 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 719 12 2 8 7.1 CCCCc1nn(-c2cc(NC(=O)C(C)C)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1007/s00044-013-0831-x
10327537 116164 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 719 12 2 8 7.1 CCCCc1nn(-c2cc(NC(=O)C(C)C)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1021/jm00052a006
CHEMBL337118 116164 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 719 12 2 8 7.1 CCCCc1nn(-c2cc(NC(=O)C(C)C)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1021/jm00052a006
44210586 58688 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
Tested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membraneTested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membrane
ChEMBL 619 12 3 8 5.4 CCCCOC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCC)nc3ccc(NC(=O)NCC)cc3c2=O)cc1 10.1016/S0960-894X(01)81126-4
CHEMBL169221 58688 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
Tested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membraneTested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membrane
ChEMBL 619 12 3 8 5.4 CCCCOC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCC)nc3ccc(NC(=O)NCC)cc3c2=O)cc1 10.1016/S0960-894X(01)81126-4
44381527 58750 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
Tested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membraneTested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membrane
ChEMBL 633 13 3 8 5.8 CCCCOC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCC)nc3ccc(NC(=O)NCCC)cc3c2=O)cc1 10.1016/S0960-894X(01)81126-4
CHEMBL169568 58750 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
Tested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membraneTested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membrane
ChEMBL 633 13 3 8 5.8 CCCCOC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCC)nc3ccc(NC(=O)NCCC)cc3c2=O)cc1 10.1016/S0960-894X(01)81126-4
10462933 16687 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 777 11 2 9 7.5 CCCCc1nn(-c2cc(NC(=O)c3ccccc3)ccc2Br)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1007/s00044-011-9815-x
CHEMBL125008 16687 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 777 11 2 9 7.5 CCCCc1nn(-c2cc(NC(=O)c3ccccc3)ccc2Br)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1007/s00044-011-9815-x
76333473 84467 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 771 13 2 8 8.0 CCCCC(=O)Nc1ccc(Cl)c(-n2nc(CCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)c4cc(Cl)ccc4Cl)cc3F)c2=O)c1 10.1007/s00044-011-9815-x
CHEMBL2236976 84467 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 771 13 2 8 8.0 CCCCC(=O)Nc1ccc(Cl)c(-n2nc(CCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)c4cc(Cl)ccc4Cl)cc3F)c2=O)c1 10.1007/s00044-011-9815-x
10462933 16687 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 777 11 2 9 7.5 CCCCc1nn(-c2cc(NC(=O)c3ccccc3)ccc2Br)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1021/jm00019a004
CHEMBL125008 16687 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 777 11 2 9 7.5 CCCCc1nn(-c2cc(NC(=O)c3ccccc3)ccc2Br)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1021/jm00019a004
44348523 112667 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 723 12 2 8 6.1 CCCNC(=O)c1ccc(C(F)(F)F)c(-n2nc(CCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)c4ccccc4)cc3F)c2=O)c1 10.1021/jm00019a004
CHEMBL331450 112667 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 723 12 2 8 6.1 CCCNC(=O)c1ccc(C(F)(F)F)c(-n2nc(CCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)c4ccccc4)cc3F)c2=O)c1 10.1021/jm00019a004
10078397 11988 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 692 10 1 8 7.1 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2occ(Cl)c2Cl)cc1 10.1021/jm00043a020
CHEMBL1184032 11988 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 692 10 1 8 7.1 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2occ(Cl)c2Cl)cc1 10.1021/jm00043a020
CHEMBL329290 11988 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 692 10 1 8 7.1 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2occ(Cl)c2Cl)cc1 10.1021/jm00043a020
44315351 104393 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membrane
ChEMBL 687 10 3 7 6.2 CCc1ccc(C(=O)NS(=O)(=O)c2ccccc2-c2ccc(Cn3c(CC)nc4ccc(NC(=O)NC(C)C)cc4c3=O)c(F)c2)c(F)c1 10.1016/0960-894X(94)85036-4
CHEMBL311160 104393 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membrane
ChEMBL 687 10 3 7 6.2 CCc1ccc(C(=O)NS(=O)(=O)c2ccccc2-c2ccc(Cn3c(CC)nc4ccc(NC(=O)NC(C)C)cc4c3=O)c(F)c2)c(F)c1 10.1016/0960-894X(94)85036-4
44314823 161326 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membrane
ChEMBL 679 13 2 8 6.7 CCCCOC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCCC)nc3ccc(NC(=O)N(C)C(C)C)cc3c2=O)c(F)c1 10.1016/0960-894X(94)85036-4
CHEMBL415073 161326 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membrane
ChEMBL 679 13 2 8 6.7 CCCCOC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCCC)nc3ccc(NC(=O)N(C)C(C)C)cc3c2=O)c(F)c1 10.1016/0960-894X(94)85036-4
44381427 119754 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
Tested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membraneTested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membrane
ChEMBL 632 14 2 8 6.4 CCCCOC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCC)nc3ccc(NC(=O)CCCC)cc3c2=O)cc1 10.1016/S0960-894X(01)81126-4
CHEMBL352503 119754 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
Tested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membraneTested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membrane
ChEMBL 632 14 2 8 6.4 CCCCOC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCC)nc3ccc(NC(=O)CCCC)cc3c2=O)cc1 10.1016/S0960-894X(01)81126-4
10462933 16687 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 777 11 2 9 7.5 CCCCc1nn(-c2cc(NC(=O)c3ccccc3)ccc2Br)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1007/s00044-011-9815-x
CHEMBL125008 16687 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 777 11 2 9 7.5 CCCCc1nn(-c2cc(NC(=O)c3ccccc3)ccc2Br)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1007/s00044-011-9815-x
76333473 84467 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 771 13 2 8 8.0 CCCCC(=O)Nc1ccc(Cl)c(-n2nc(CCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)c4cc(Cl)ccc4Cl)cc3F)c2=O)c1 10.1007/s00044-011-9815-x
CHEMBL2236976 84467 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 771 13 2 8 8.0 CCCCC(=O)Nc1ccc(Cl)c(-n2nc(CCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)c4cc(Cl)ccc4Cl)cc3F)c2=O)c1 10.1007/s00044-011-9815-x
10439837 16162 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 717 12 2 8 6.8 CCCCc1nn(-c2cc(NC(=O)CC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)CC(C)(C)C)cc1F 10.1007/s00044-011-9815-x
CHEMBL122917 16162 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 717 12 2 8 6.8 CCCCc1nn(-c2cc(NC(=O)CC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)CC(C)(C)C)cc1F 10.1007/s00044-011-9815-x
10462683 112770 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 735 12 2 10 6.0 CCCc1nn(-c2cc(NC(=O)COCC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1007/s00044-011-9815-x
CHEMBL331507 112770 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 735 12 2 10 6.0 CCCc1nn(-c2cc(NC(=O)COCC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1007/s00044-011-9815-x
44311289 101742 0 None - 0 Human 9.7 pIC50 = 9.7 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 707 18 1 9 7.7 CCCc1nc(CC)c(C(=O)OCCCCOc2ccccc2)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/S0960-894X(00)80077-3
CHEMBL302964 101742 0 None - 0 Human 9.7 pIC50 = 9.7 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 707 18 1 9 7.7 CCCc1nc(CC)c(C(=O)OCCCCOc2ccccc2)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/S0960-894X(00)80077-3
44311456 101815 0 None - 0 Human 9.7 pIC50 = 9.7 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 792 19 1 10 8.6 CCCc1nc(CC)c(C(=O)OCCN(C(=O)OCCC(C)C)c2ccccc2)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/S0960-894X(00)80077-3
CHEMBL303427 101815 0 None - 0 Human 9.7 pIC50 = 9.7 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 792 19 1 10 8.6 CCCc1nc(CC)c(C(=O)OCCN(C(=O)OCCC(C)C)c2ccccc2)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/S0960-894X(00)80077-3
44311715 102708 0 None - 0 Human 9.7 pIC50 = 9.7 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 741 17 1 10 6.7 CCCc1nc(CC)c(C(=O)OCCCS(=O)(=O)c2ccccc2)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/S0960-894X(00)80077-3
CHEMBL308323 102708 0 None - 0 Human 9.7 pIC50 = 9.7 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 741 17 1 10 6.7 CCCc1nc(CC)c(C(=O)OCCCS(=O)(=O)c2ccccc2)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/S0960-894X(00)80077-3
44311074 104408 0 None - 0 Human 9.7 pIC50 = 9.7 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 732 15 1 10 6.2 CCCc1nc(CC)c(C(=O)OCCN2C(=O)c3ccccc3C2=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/S0960-894X(00)80077-3
CHEMBL311253 104408 0 None - 0 Human 9.7 pIC50 = 9.7 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 732 15 1 10 6.2 CCCc1nc(CC)c(C(=O)OCCN2C(=O)c3ccccc3C2=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/S0960-894X(00)80077-3
44311412 104837 0 None - 0 Human 9.7 pIC50 = 9.7 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 725 17 1 9 7.1 CCCc1nc(CC)c(C(=O)OCCC[S+]([O-])c2ccccc2)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/S0960-894X(00)80077-3
CHEMBL311625 104837 0 None - 0 Human 9.7 pIC50 = 9.7 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 725 17 1 9 7.1 CCCc1nc(CC)c(C(=O)OCCC[S+]([O-])c2ccccc2)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/S0960-894X(00)80077-3
44311581 167259 0 None - 0 Human 9.7 pIC50 = 9.7 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 720 17 2 9 7.3 CCCc1nc(CC)c(C(=O)OCCCC(=O)Nc2ccccc2)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/S0960-894X(00)80077-3
CHEMBL430792 167259 0 None - 0 Human 9.7 pIC50 = 9.7 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 720 17 2 9 7.3 CCCc1nc(CC)c(C(=O)OCCCC(=O)Nc2ccccc2)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/S0960-894X(00)80077-3
44311582 202498 0 None - 0 Human 9.7 pIC50 = 9.7 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 790 21 1 9 8.5 CCCCN(Cc1ccccc1)C(=O)CCCOC(=O)c1c(CC)nc(CCC)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/S0960-894X(00)80077-3
CHEMBL70868 202498 0 None - 0 Human 9.7 pIC50 = 9.7 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 790 21 1 9 8.5 CCCCN(Cc1ccccc1)C(=O)CCCOC(=O)c1c(CC)nc(CCC)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/S0960-894X(00)80077-3
9918412 202550 0 None - 0 Human 9.7 pIC50 = 9.7 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 739 16 1 9 8.1 CCCCOC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCC)nc(CC)c2C(=O)OCc2ccccc2C(=O)c2ccccc2)c(F)c1 10.1016/S0960-894X(00)80077-3
CHEMBL71172 202550 0 None - 0 Human 9.7 pIC50 = 9.7 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 739 16 1 9 8.1 CCCCOC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCC)nc(CC)c2C(=O)OCc2ccccc2C(=O)c2ccccc2)c(F)c1 10.1016/S0960-894X(00)80077-3
44311413 202638 0 None - 0 Human 9.7 pIC50 = 9.7 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 709 17 1 9 8.1 CCCc1nc(CC)c(C(=O)OCCCSc2ccccc2)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/S0960-894X(00)80077-3
CHEMBL71639 202638 0 None - 0 Human 9.7 pIC50 = 9.7 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 709 17 1 9 8.1 CCCc1nc(CC)c(C(=O)OCCCSc2ccccc2)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/S0960-894X(00)80077-3
44311753 202895 0 None - 0 Human 9.7 pIC50 = 9.7 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 773 16 1 9 8.2 CCCc1nc(CC)c(C(=O)OCc2ccccc2[S+]([O-])c2ccccc2)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/S0960-894X(00)80077-3
CHEMBL73283 202895 0 None - 0 Human 9.7 pIC50 = 9.7 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 773 16 1 9 8.2 CCCc1nc(CC)c(C(=O)OCc2ccccc2[S+]([O-])c2ccccc2)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/S0960-894X(00)80077-3
133031 100379 16 None - 1 Rabbit 9.7 pIC50 = 9.7 Binding
Binding affinity to angiotensin AT1 receptor in rabbit aortic ringsBinding affinity to angiotensin AT1 receptor in rabbit aortic rings
ChEMBL 524 7 1 6 5.4 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/j.bmc.2010.10.043
CHEMBL293511 100379 16 None - 1 Rabbit 9.7 pIC50 = 9.7 Binding
Binding affinity to angiotensin AT1 receptor in rabbit aortic ringsBinding affinity to angiotensin AT1 receptor in rabbit aortic rings
ChEMBL 524 7 1 6 5.4 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/j.bmc.2010.10.043
19939756 4954 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
Compound was evaluated for inhibition of 125I[Sar1,Ile8] all binding to rabbit aorta Angiotensin II receptor, type 1Compound was evaluated for inhibition of 125I[Sar1,Ile8] all binding to rabbit aorta Angiotensin II receptor, type 1
ChEMBL 534 9 1 7 5.8 CCCCOC(=O)NS(=O)(=O)c1ccc(C)cc1-c1ccc(Cn2c(CC)nc3c(C)cc(C)nc32)cc1 10.1016/0960-894X(96)00017-0
CHEMBL105199 4954 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
Compound was evaluated for inhibition of 125I[Sar1,Ile8] all binding to rabbit aorta Angiotensin II receptor, type 1Compound was evaluated for inhibition of 125I[Sar1,Ile8] all binding to rabbit aorta Angiotensin II receptor, type 1
ChEMBL 534 9 1 7 5.8 CCCCOC(=O)NS(=O)(=O)c1ccc(C)cc1-c1ccc(Cn2c(CC)nc3c(C)cc(C)nc32)cc1 10.1016/0960-894X(96)00017-0
133031 100379 16 None - 1 Rabbit 9.7 pIC50 = 9.7 Binding
Compound was evaluated for inhibition of 125I[Sar1,Ile8] all binding to rabbit aorta Angiotensin II receptor, type 1Compound was evaluated for inhibition of 125I[Sar1,Ile8] all binding to rabbit aorta Angiotensin II receptor, type 1
ChEMBL 524 7 1 6 5.4 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/0960-894X(96)00017-0
CHEMBL293511 100379 16 None - 1 Rabbit 9.7 pIC50 = 9.7 Binding
Compound was evaluated for inhibition of 125I[Sar1,Ile8] all binding to rabbit aorta Angiotensin II receptor, type 1Compound was evaluated for inhibition of 125I[Sar1,Ile8] all binding to rabbit aorta Angiotensin II receptor, type 1
ChEMBL 524 7 1 6 5.4 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/0960-894X(96)00017-0
44335530 107010 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
Compound was evaluated for inhibition of 125I[Sar1,Ile8] all binding to rabbit aorta Angiotensin II receptor, type 1Compound was evaluated for inhibition of 125I[Sar1,Ile8] all binding to rabbit aorta Angiotensin II receptor, type 1
ChEMBL 520 9 1 7 5.5 CCCCOC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CC)nc3c(C)cc(C)nc32)cc1 10.1016/0960-894X(96)00017-0
CHEMBL318605 107010 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
Compound was evaluated for inhibition of 125I[Sar1,Ile8] all binding to rabbit aorta Angiotensin II receptor, type 1Compound was evaluated for inhibition of 125I[Sar1,Ile8] all binding to rabbit aorta Angiotensin II receptor, type 1
ChEMBL 520 9 1 7 5.5 CCCCOC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CC)nc3c(C)cc(C)nc32)cc1 10.1016/0960-894X(96)00017-0
133031 100379 16 None - 1 Rabbit 9.7 pIC50 = 9.7 Binding
In vitro binding affinity for angiotensin II AT1 receptor in rabbit aortaIn vitro binding affinity for angiotensin II AT1 receptor in rabbit aorta
ChEMBL 524 7 1 6 5.4 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1021/jm00050a002
CHEMBL293511 100379 16 None - 1 Rabbit 9.7 pIC50 = 9.7 Binding
In vitro binding affinity for angiotensin II AT1 receptor in rabbit aortaIn vitro binding affinity for angiotensin II AT1 receptor in rabbit aorta
ChEMBL 524 7 1 6 5.4 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1021/jm00050a002
10439837 16162 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 717 12 2 8 6.8 CCCCc1nn(-c2cc(NC(=O)CC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)CC(C)(C)C)cc1F 10.1021/jm00019a004
CHEMBL122917 16162 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 717 12 2 8 6.8 CCCCc1nn(-c2cc(NC(=O)CC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)CC(C)(C)C)cc1F 10.1021/jm00019a004
10462683 112770 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 735 12 2 10 6.0 CCCc1nn(-c2cc(NC(=O)COCC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1021/jm00019a004
CHEMBL331507 112770 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 735 12 2 10 6.0 CCCc1nn(-c2cc(NC(=O)COCC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1021/jm00019a004
44377058 119488 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aortaIn vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aorta
ChEMBL 554 16 3 6 5.8 CCCCCCCC(=O)NS(=O)(=O)Nc1ccccc1-c1ccc(Cn2c(C(=O)O)cnc2CCCC)cc1 10.1016/S0960-894X(01)81124-0
CHEMBL350121 119488 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aortaIn vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aorta
ChEMBL 554 16 3 6 5.8 CCCCCCCC(=O)NS(=O)(=O)Nc1ccccc1-c1ccc(Cn2c(C(=O)O)cnc2CCCC)cc1 10.1016/S0960-894X(01)81124-0
10349512 206257 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 670 11 1 8 5.8 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NS(=O)(=O)c2ccccc2)cc1 10.1021/jm00043a020
CHEMBL97332 206257 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 670 11 1 8 5.8 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NS(=O)(=O)c2ccccc2)cc1 10.1021/jm00043a020
44314761 102368 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membrane
ChEMBL 701 11 3 7 6.6 CCCc1nc2ccc(NC(=O)NC(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccc(CC)cc2F)cc1F 10.1016/0960-894X(94)85036-4
CHEMBL305647 102368 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membrane
ChEMBL 701 11 3 7 6.6 CCCc1nc2ccc(NC(=O)NC(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccc(CC)cc2F)cc1F 10.1016/0960-894X(94)85036-4
9853391 116326 1 None - 0 Human 9.7 pIC50 = 9.7 Binding
Inhibition of Angiotensin II receptor, type 1Inhibition of Angiotensin II receptor, type 1
ChEMBL 729 11 2 9 6.6 CCCCC(=O)Nc1ccc(Br)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1021/jm9504722
CHEMBL338027 116326 1 None - 0 Human 9.7 pIC50 = 9.7 Binding
Inhibition of Angiotensin II receptor, type 1Inhibition of Angiotensin II receptor, type 1
ChEMBL 729 11 2 9 6.6 CCCCC(=O)Nc1ccc(Br)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1021/jm9504722
133031 100379 16 None - 1 Rabbit 9.7 pIC50 = 9.7 Binding
Inhibitory activity was evaluated against Angiotensin II receptor, type 1 in rabbit aortaInhibitory activity was evaluated against Angiotensin II receptor, type 1 in rabbit aorta
ChEMBL 524 7 1 6 5.4 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1021/jm9504722
CHEMBL293511 100379 16 None - 1 Rabbit 9.7 pIC50 = 9.7 Binding
Inhibitory activity was evaluated against Angiotensin II receptor, type 1 in rabbit aortaInhibitory activity was evaluated against Angiotensin II receptor, type 1 in rabbit aorta
ChEMBL 524 7 1 6 5.4 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1021/jm9504722
10439837 16162 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 717 12 2 8 6.8 CCCCc1nn(-c2cc(NC(=O)CC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)CC(C)(C)C)cc1F 10.1007/s00044-011-9815-x
CHEMBL122917 16162 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 717 12 2 8 6.8 CCCCc1nn(-c2cc(NC(=O)CC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)CC(C)(C)C)cc1F 10.1007/s00044-011-9815-x
10462683 112770 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 735 12 2 10 6.0 CCCc1nn(-c2cc(NC(=O)COCC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1007/s00044-011-9815-x
CHEMBL331507 112770 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 735 12 2 10 6.0 CCCc1nn(-c2cc(NC(=O)COCC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1007/s00044-011-9815-x
10010234 97962 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 739 12 2 8 7.2 CCCCc1nn(-c2cc(NC(=O)CC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1007/s00044-013-0831-x
CHEMBL275552 97962 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 739 12 2 8 7.2 CCCCc1nn(-c2cc(NC(=O)CC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1007/s00044-013-0831-x
10100951 114533 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 667 11 2 9 6.3 CCCCc1nn(-c2cc(NC(=O)CC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1 10.1007/s00044-013-0831-x
CHEMBL334300 114533 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 667 11 2 9 6.3 CCCCc1nn(-c2cc(NC(=O)CC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1 10.1007/s00044-013-0831-x
9987614 167997 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 747 12 2 8 7.9 CCCCc1nn(-c2cc(NC(=O)CC(C)(C)C)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1007/s00044-013-0831-x
CHEMBL435792 167997 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 747 12 2 8 7.9 CCCCc1nn(-c2cc(NC(=O)CC(C)(C)C)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1007/s00044-013-0831-x
10100951 114533 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 667 11 2 9 6.3 CCCCc1nn(-c2cc(NC(=O)CC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1 10.1007/s00044-011-9815-x
CHEMBL334300 114533 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 667 11 2 9 6.3 CCCCc1nn(-c2cc(NC(=O)CC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1 10.1007/s00044-011-9815-x
10259468 117964 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 743 12 2 9 6.9 CCCCC(=O)Nc1ccc(Br)c(-n2nc(CCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1007/s00044-011-9815-x
CHEMBL341369 117964 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 743 12 2 9 6.9 CCCCC(=O)Nc1ccc(Br)c(-n2nc(CCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1007/s00044-011-9815-x
10390872 115633 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
In vitro binding affinity for angiotensin II AT1 receptor in rabbit aortaIn vitro binding affinity for angiotensin II AT1 receptor in rabbit aorta
ChEMBL 490 7 1 6 4.8 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)C(C)C)cc1 10.1021/jm00050a002
CHEMBL335778 115633 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
In vitro binding affinity for angiotensin II AT1 receptor in rabbit aortaIn vitro binding affinity for angiotensin II AT1 receptor in rabbit aorta
ChEMBL 490 7 1 6 4.8 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)C(C)C)cc1 10.1021/jm00050a002
10100951 114533 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 667 11 2 9 6.3 CCCCc1nn(-c2cc(NC(=O)CC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1 10.1021/jm00019a004
CHEMBL334300 114533 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 667 11 2 9 6.3 CCCCc1nn(-c2cc(NC(=O)CC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1 10.1021/jm00019a004
10259468 117964 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 743 12 2 9 6.9 CCCCC(=O)Nc1ccc(Br)c(-n2nc(CCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1021/jm00019a004
CHEMBL341369 117964 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 743 12 2 9 6.9 CCCCC(=O)Nc1ccc(Br)c(-n2nc(CCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1021/jm00019a004
9895635 111518 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 638 10 1 8 6.1 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2occc2C)cc1 10.1021/jm00043a020
CHEMBL328941 111518 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 638 10 1 8 6.1 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2occc2C)cc1 10.1021/jm00043a020
10010234 97962 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 739 12 2 8 7.2 CCCCc1nn(-c2cc(NC(=O)CC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1021/jm00052a006
CHEMBL275552 97962 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 739 12 2 8 7.2 CCCCc1nn(-c2cc(NC(=O)CC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1021/jm00052a006
10100951 114533 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 667 11 2 9 6.3 CCCCc1nn(-c2cc(NC(=O)CC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1 10.1021/jm00052a006
CHEMBL334300 114533 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 667 11 2 9 6.3 CCCCc1nn(-c2cc(NC(=O)CC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1 10.1021/jm00052a006
9987614 167997 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 747 12 2 8 7.9 CCCCc1nn(-c2cc(NC(=O)CC(C)(C)C)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1021/jm00052a006
CHEMBL435792 167997 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 747 12 2 8 7.9 CCCCc1nn(-c2cc(NC(=O)CC(C)(C)C)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1021/jm00052a006
44381402 58838 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
Tested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membraneTested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membrane
ChEMBL 647 12 2 8 6.2 CCCCOC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCC)nc3ccc(NC(=O)N(C)C(C)C)cc3c2=O)cc1 10.1016/S0960-894X(01)81126-4
CHEMBL169967 58838 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
Tested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membraneTested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membrane
ChEMBL 647 12 2 8 6.2 CCCCOC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCC)nc3ccc(NC(=O)N(C)C(C)C)cc3c2=O)cc1 10.1016/S0960-894X(01)81126-4
10100951 114533 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 667 11 2 9 6.3 CCCCc1nn(-c2cc(NC(=O)CC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1 10.1007/s00044-011-9815-x
CHEMBL334300 114533 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 667 11 2 9 6.3 CCCCc1nn(-c2cc(NC(=O)CC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1 10.1007/s00044-011-9815-x
10259468 117964 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 743 12 2 9 6.9 CCCCC(=O)Nc1ccc(Br)c(-n2nc(CCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1007/s00044-011-9815-x
CHEMBL341369 117964 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 743 12 2 9 6.9 CCCCC(=O)Nc1ccc(Br)c(-n2nc(CCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1007/s00044-011-9815-x
10101606 15580 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 751 12 2 8 6.6 CCCCC(=O)Nc1ccc(Br)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)c4ccccc4F)cc3F)c2=O)c1 10.1007/s00044-011-9815-x
CHEMBL122273 15580 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 751 12 2 8 6.6 CCCCC(=O)Nc1ccc(Br)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)c4ccccc4F)cc3F)c2=O)c1 10.1007/s00044-011-9815-x
10259447 16732 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 741 12 2 8 6.9 CCCCc1nn(-c2cc(NC(=O)CC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2F)cc1F 10.1007/s00044-011-9815-x
CHEMBL125280 16732 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 741 12 2 8 6.9 CCCCc1nn(-c2cc(NC(=O)CC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2F)cc1F 10.1007/s00044-011-9815-x
10101606 15580 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 751 12 2 8 6.6 CCCCC(=O)Nc1ccc(Br)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)c4ccccc4F)cc3F)c2=O)c1 10.1021/jm00019a004
CHEMBL122273 15580 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 751 12 2 8 6.6 CCCCC(=O)Nc1ccc(Br)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)c4ccccc4F)cc3F)c2=O)c1 10.1021/jm00019a004
10259447 16732 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 741 12 2 8 6.9 CCCCc1nn(-c2cc(NC(=O)CC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2F)cc1F 10.1021/jm00019a004
CHEMBL125280 16732 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 741 12 2 8 6.9 CCCCc1nn(-c2cc(NC(=O)CC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2F)cc1F 10.1021/jm00019a004
10326942 111888 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 652 10 1 8 6.4 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2oc(C)cc2C)cc1 10.1021/jm00043a020
CHEMBL329693 111888 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 652 10 1 8 6.4 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2oc(C)cc2C)cc1 10.1021/jm00043a020
10417102 205703 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 676 10 1 9 6.1 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)C2(C)SCCS2)cc1 10.1021/jm00043a020
CHEMBL94145 205703 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 676 10 1 9 6.1 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)C2(C)SCCS2)cc1 10.1021/jm00043a020
10101606 15580 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 751 12 2 8 6.6 CCCCC(=O)Nc1ccc(Br)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)c4ccccc4F)cc3F)c2=O)c1 10.1007/s00044-011-9815-x
CHEMBL122273 15580 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 751 12 2 8 6.6 CCCCC(=O)Nc1ccc(Br)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)c4ccccc4F)cc3F)c2=O)c1 10.1007/s00044-011-9815-x
10259447 16732 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 741 12 2 8 6.9 CCCCc1nn(-c2cc(NC(=O)CC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2F)cc1F 10.1007/s00044-011-9815-x
CHEMBL125280 16732 0 None - 0 Rabbit 9.7 pIC50 = 9.7 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 741 12 2 8 6.9 CCCCc1nn(-c2cc(NC(=O)CC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2F)cc1F 10.1007/s00044-011-9815-x
10033136 15882 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 769 12 2 8 6.7 CCCCC(=O)Nc1ccc(Br)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)c4cc(F)ccc4F)cc3F)c2=O)c1 10.1007/s00044-011-9815-x
CHEMBL122380 15882 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 769 12 2 8 6.7 CCCCC(=O)Nc1ccc(Br)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)c4cc(F)ccc4F)cc3F)c2=O)c1 10.1007/s00044-011-9815-x
10033136 15882 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 769 12 2 8 6.7 CCCCC(=O)Nc1ccc(Br)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)c4cc(F)ccc4F)cc3F)c2=O)c1 10.1021/jm00019a004
CHEMBL122380 15882 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 769 12 2 8 6.7 CCCCC(=O)Nc1ccc(Br)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)c4cc(F)ccc4F)cc3F)c2=O)c1 10.1021/jm00019a004
44315078 203038 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membrane
ChEMBL 693 13 2 8 6.9 CCCCc1nc2ccc(NC(=O)N(C)C(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/0960-894X(94)85036-4
CHEMBL74556 203038 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membrane
ChEMBL 693 13 2 8 6.9 CCCCc1nc2ccc(NC(=O)N(C)C(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/0960-894X(94)85036-4
10033136 15882 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 769 12 2 8 6.7 CCCCC(=O)Nc1ccc(Br)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)c4cc(F)ccc4F)cc3F)c2=O)c1 10.1007/s00044-011-9815-x
CHEMBL122380 15882 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 769 12 2 8 6.7 CCCCC(=O)Nc1ccc(Br)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)c4cc(F)ccc4F)cc3F)c2=O)c1 10.1007/s00044-011-9815-x
10009984 112668 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 705 12 2 9 6.4 CCCCc1nn(-c2cc(NC(=O)CC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)C)cc1F 10.1007/s00044-011-9815-x
CHEMBL331455 112668 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 705 12 2 9 6.4 CCCCc1nn(-c2cc(NC(=O)CC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)C)cc1F 10.1007/s00044-011-9815-x
10440144 116381 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 763 10 2 9 7.1 CCCc1nn(-c2cc(NC(=O)c3ccccc3)ccc2Br)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1007/s00044-011-9815-x
CHEMBL338342 116381 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 763 10 2 9 7.1 CCCc1nn(-c2cc(NC(=O)c3ccccc3)ccc2Br)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1007/s00044-011-9815-x
10009984 112668 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 705 12 2 9 6.4 CCCCc1nn(-c2cc(NC(=O)CC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)C)cc1F 10.1021/jm00019a004
CHEMBL331455 112668 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 705 12 2 9 6.4 CCCCc1nn(-c2cc(NC(=O)CC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)C)cc1F 10.1021/jm00019a004
10440144 116381 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 763 10 2 9 7.1 CCCc1nn(-c2cc(NC(=O)c3ccccc3)ccc2Br)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1021/jm00019a004
CHEMBL338342 116381 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 763 10 2 9 7.1 CCCc1nn(-c2cc(NC(=O)c3ccccc3)ccc2Br)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1021/jm00019a004
15292113 95574 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membrane
ChEMBL 693 11 2 9 5.5 CCCc1nc2ccc(NC(=O)N3CCOCC3)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/0960-894X(94)85036-4
CHEMBL259843 95574 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membrane
ChEMBL 693 11 2 9 5.5 CCCc1nc2ccc(NC(=O)N3CCOCC3)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/0960-894X(94)85036-4
9895984 203031 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membrane
ChEMBL 661 13 2 8 6.5 CCCCOC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCCC)nc3ccc(NC(=O)N(C)C(C)C)cc3c2=O)cc1 10.1016/0960-894X(94)85036-4
CHEMBL74476 203031 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membrane
ChEMBL 661 13 2 8 6.5 CCCCOC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCCC)nc3ccc(NC(=O)N(C)C(C)C)cc3c2=O)cc1 10.1016/0960-894X(94)85036-4
9895984 203031 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
Inhibition of Angiotensin II receptor, type 1Inhibition of Angiotensin II receptor, type 1
ChEMBL 661 13 2 8 6.5 CCCCOC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCCC)nc3ccc(NC(=O)N(C)C(C)C)cc3c2=O)cc1 10.1021/jm9504722
CHEMBL74476 203031 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
Inhibition of Angiotensin II receptor, type 1Inhibition of Angiotensin II receptor, type 1
ChEMBL 661 13 2 8 6.5 CCCCOC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCCC)nc3ccc(NC(=O)N(C)C(C)C)cc3c2=O)cc1 10.1021/jm9504722
44381657 58734 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
Tested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membraneTested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membrane
ChEMBL 633 13 3 8 5.8 CCCCOC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCCC)nc3ccc(NC(=O)NCC)cc3c2=O)cc1 10.1016/S0960-894X(01)81126-4
CHEMBL169488 58734 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
Tested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membraneTested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membrane
ChEMBL 633 13 3 8 5.8 CCCCOC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCCC)nc3ccc(NC(=O)NCC)cc3c2=O)cc1 10.1016/S0960-894X(01)81126-4
9895984 203031 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
Tested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membraneTested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membrane
ChEMBL 661 13 2 8 6.5 CCCCOC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCCC)nc3ccc(NC(=O)N(C)C(C)C)cc3c2=O)cc1 10.1016/S0960-894X(01)81126-4
CHEMBL74476 203031 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
Tested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membraneTested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membrane
ChEMBL 661 13 2 8 6.5 CCCCOC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCCC)nc3ccc(NC(=O)N(C)C(C)C)cc3c2=O)cc1 10.1016/S0960-894X(01)81126-4
10009984 112668 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 705 12 2 9 6.4 CCCCc1nn(-c2cc(NC(=O)CC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)C)cc1F 10.1007/s00044-011-9815-x
CHEMBL331455 112668 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 705 12 2 9 6.4 CCCCc1nn(-c2cc(NC(=O)CC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)C)cc1F 10.1007/s00044-011-9815-x
10440144 116381 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 763 10 2 9 7.1 CCCc1nn(-c2cc(NC(=O)c3ccccc3)ccc2Br)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1007/s00044-011-9815-x
CHEMBL338342 116381 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 763 10 2 9 7.1 CCCc1nn(-c2cc(NC(=O)c3ccccc3)ccc2Br)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1007/s00044-011-9815-x
10372497 118228 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 692 11 1 9 6.3 CCCCc1nn(-c2cc(C(=O)OC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1007/s00044-013-0831-x
CHEMBL341783 118228 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 692 11 1 9 6.3 CCCCc1nn(-c2cc(C(=O)OC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1007/s00044-013-0831-x
10259657 118875 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 781 14 2 8 8.1 CCCCc1nn(-c2cc(NC(=O)CCc3ccccc3)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1007/s00044-013-0831-x
CHEMBL344597 118875 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 781 14 2 8 8.1 CCCCc1nn(-c2cc(NC(=O)CCc3ccccc3)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1007/s00044-013-0831-x
10259489 16722 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 745 11 2 9 7.1 CCCCc1nn(-c2cc(NC(=O)CC)ccc2Br)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1Cl 10.1007/s00044-011-9815-x
CHEMBL125231 16722 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 745 11 2 9 7.1 CCCCc1nn(-c2cc(NC(=O)CC)ccc2Br)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1Cl 10.1007/s00044-011-9815-x
19939418 107771 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
In vitro ability to inhibit the binding of radioligand 125I[Sar1,IIe8]AII to AT1 receptor from rabbit aortaIn vitro ability to inhibit the binding of radioligand 125I[Sar1,IIe8]AII to AT1 receptor from rabbit aorta
ChEMBL 733 13 2 8 7.4 CCCCc1nn(-c2cc(NC(=O)CC)ccc2Cl)c(=O)n1Cc1ccc(-c2cc(CC)ccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1016/S0960-894X(01)80595-3
CHEMBL319730 107771 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
In vitro ability to inhibit the binding of radioligand 125I[Sar1,IIe8]AII to AT1 receptor from rabbit aortaIn vitro ability to inhibit the binding of radioligand 125I[Sar1,IIe8]AII to AT1 receptor from rabbit aorta
ChEMBL 733 13 2 8 7.4 CCCCc1nn(-c2cc(NC(=O)CC)ccc2Cl)c(=O)n1Cc1ccc(-c2cc(CC)ccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1016/S0960-894X(01)80595-3
10395335 116568 0 None - 0 Human 9.6 pIC50 = 9.6 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in human adrenal membrane preparations. For this assay, only 0.02%BSA was present in the assay mixture.In vitro inhibitory activity against Angiotensin II receptor, type 1 in human adrenal membrane preparations. For this assay, only 0.02%BSA was present in the assay mixture.
ChEMBL 757 12 2 8 7.4 CCCCc1nn(-c2cc(NC(=O)CC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1F 10.1021/jm00019a004
CHEMBL339256 116568 0 None - 0 Human 9.6 pIC50 = 9.6 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in human adrenal membrane preparations. For this assay, only 0.02%BSA was present in the assay mixture.In vitro inhibitory activity against Angiotensin II receptor, type 1 in human adrenal membrane preparations. For this assay, only 0.02%BSA was present in the assay mixture.
ChEMBL 757 12 2 8 7.4 CCCCc1nn(-c2cc(NC(=O)CC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1F 10.1021/jm00019a004
10259489 16722 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 745 11 2 9 7.1 CCCCc1nn(-c2cc(NC(=O)CC)ccc2Br)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1Cl 10.1021/jm00019a004
CHEMBL125231 16722 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 745 11 2 9 7.1 CCCCc1nn(-c2cc(NC(=O)CC)ccc2Br)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1Cl 10.1021/jm00019a004
10372497 118228 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 692 11 1 9 6.3 CCCCc1nn(-c2cc(C(=O)OC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1021/jm00052a006
CHEMBL341783 118228 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 692 11 1 9 6.3 CCCCc1nn(-c2cc(C(=O)OC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1021/jm00052a006
10259657 118875 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 781 14 2 8 8.1 CCCCc1nn(-c2cc(NC(=O)CCc3ccccc3)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1021/jm00052a006
CHEMBL344597 118875 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 781 14 2 8 8.1 CCCCc1nn(-c2cc(NC(=O)CCc3ccccc3)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1021/jm00052a006
44210589 58273 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
Tested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membraneTested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membrane
ChEMBL 619 11 3 8 5.4 CCCOC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCC)nc3ccc(NC(=O)NC(C)C)cc3c2=O)cc1 10.1016/S0960-894X(01)81126-4
CHEMBL168413 58273 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
Tested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membraneTested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membrane
ChEMBL 619 11 3 8 5.4 CCCOC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCC)nc3ccc(NC(=O)NC(C)C)cc3c2=O)cc1 10.1016/S0960-894X(01)81126-4
44381403 58839 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
Tested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membraneTested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membrane
ChEMBL 675 11 2 9 5.4 CCCc1nc2ccc(NC(=O)N3CCOCC3)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1 10.1016/S0960-894X(01)81126-4
CHEMBL169968 58839 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
Tested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membraneTested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membrane
ChEMBL 675 11 2 9 5.4 CCCc1nc2ccc(NC(=O)N3CCOCC3)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1 10.1016/S0960-894X(01)81126-4
44210585 119888 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
Tested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membraneTested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membrane
ChEMBL 647 14 3 8 6.2 CCCCNC(=O)Nc1ccc2nc(CCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OCCCC)cc3)c(=O)c2c1 10.1016/S0960-894X(01)81126-4
CHEMBL353615 119888 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
Tested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membraneTested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membrane
ChEMBL 647 14 3 8 6.2 CCCCNC(=O)Nc1ccc2nc(CCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OCCCC)cc3)c(=O)c2c1 10.1016/S0960-894X(01)81126-4
10010207 29966 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 735 13 2 9 7.5 CCCCc1nn(-c2cc(NC(=O)OCCC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1007/s00044-013-0831-x
CHEMBL139041 29966 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 735 13 2 9 7.5 CCCCc1nn(-c2cc(NC(=O)OCCC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1007/s00044-013-0831-x
10078780 116403 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 749 13 2 10 6.4 CCCCc1nn(-c2cc(NC(=O)COCC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1007/s00044-011-9815-x
CHEMBL338433 116403 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 749 13 2 10 6.4 CCCCc1nn(-c2cc(NC(=O)COCC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1007/s00044-011-9815-x
10439819 169311 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 715 13 2 10 5.5 CCCCc1nn(-c2cc(C(=O)NCCOC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1007/s00044-011-9815-x
CHEMBL444065 169311 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 715 13 2 10 5.5 CCCCc1nn(-c2cc(C(=O)NCCOC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1007/s00044-011-9815-x
19754068 102247 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
In vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranesIn vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranes
ChEMBL 643 13 2 7 7.2 CCCC(=O)Nc1c(C)nc2c(nc(CCC)n2Cc2ccc(-c3ccccc3S(=O)(=O)NC(=O)CCC3CCCC3)cc2)c1C 10.1016/S0960-894X(01)81115-X
CHEMBL304946 102247 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
In vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranesIn vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranes
ChEMBL 643 13 2 7 7.2 CCCC(=O)Nc1c(C)nc2c(nc(CCC)n2Cc2ccc(-c3ccccc3S(=O)(=O)NC(=O)CCC3CCCC3)cc2)c1C 10.1016/S0960-894X(01)81115-X
10078780 116403 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 749 13 2 10 6.4 CCCCc1nn(-c2cc(NC(=O)COCC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1021/jm00019a004
CHEMBL338433 116403 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 749 13 2 10 6.4 CCCCc1nn(-c2cc(NC(=O)COCC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1021/jm00019a004
10439819 169311 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 715 13 2 10 5.5 CCCCc1nn(-c2cc(C(=O)NCCOC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1021/jm00019a004
CHEMBL444065 169311 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 715 13 2 10 5.5 CCCCc1nn(-c2cc(C(=O)NCCOC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1021/jm00019a004
10416475 205960 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 624 10 1 8 5.8 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccco2)cc1 10.1021/jm00043a020
CHEMBL95579 205960 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 624 10 1 8 5.8 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccco2)cc1 10.1021/jm00043a020
10010207 29966 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 735 13 2 9 7.5 CCCCc1nn(-c2cc(NC(=O)OCCC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1021/jm00052a006
CHEMBL139041 29966 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 735 13 2 9 7.5 CCCCc1nn(-c2cc(NC(=O)OCCC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1021/jm00052a006
44210590 58391 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
Tested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membraneTested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membrane
ChEMBL 605 11 3 8 5.0 CCCCOC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCC)nc3ccc(NC(=O)NC)cc3c2=O)cc1 10.1016/S0960-894X(01)81126-4
CHEMBL168490 58391 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
Tested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membraneTested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membrane
ChEMBL 605 11 3 8 5.0 CCCCOC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCC)nc3ccc(NC(=O)NC)cc3c2=O)cc1 10.1016/S0960-894X(01)81126-4
10439715 116521 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 699 12 2 9 6.2 CCCCc1nn(-c2cc(C(=O)NCCC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1007/s00044-011-9815-x
CHEMBL339040 116521 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 699 12 2 9 6.2 CCCCc1nn(-c2cc(C(=O)NCCC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1007/s00044-011-9815-x
44309938 202587 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
In vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranesIn vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranes
ChEMBL 619 14 2 8 6.8 CCCCOC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCC)nc3c(C)c(NC(=O)CCCC)cnc32)cc1 10.1016/S0960-894X(01)81115-X
CHEMBL71388 202587 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
In vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranesIn vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranes
ChEMBL 619 14 2 8 6.8 CCCCOC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCC)nc3c(C)c(NC(=O)CCCC)cnc32)cc1 10.1016/S0960-894X(01)81115-X
10028545 20790 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
In vitro binding affinity for angiotensin II AT1 receptor in rabbit aortaIn vitro binding affinity for angiotensin II AT1 receptor in rabbit aorta
ChEMBL 490 8 1 6 4.9 CCCC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CC)nc3c(C)cc(C)nc32)cc1 10.1021/jm00050a002
CHEMBL131156 20790 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
In vitro binding affinity for angiotensin II AT1 receptor in rabbit aortaIn vitro binding affinity for angiotensin II AT1 receptor in rabbit aorta
ChEMBL 490 8 1 6 4.9 CCCC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CC)nc3c(C)cc(C)nc32)cc1 10.1021/jm00050a002
10439715 116521 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 699 12 2 9 6.2 CCCCc1nn(-c2cc(C(=O)NCCC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1021/jm00019a004
CHEMBL339040 116521 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 699 12 2 9 6.2 CCCCc1nn(-c2cc(C(=O)NCCC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1021/jm00019a004
10055534 156907 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 702 10 1 7 7.2 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2C(F)(F)F)cc1 10.1021/jm00043a020
CHEMBL407919 156907 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 702 10 1 7 7.2 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2C(F)(F)F)cc1 10.1021/jm00043a020
9875044 206279 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 674 10 1 8 6.9 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2sccc2Cl)cc1 10.1021/jm00043a020
CHEMBL97446 206279 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 674 10 1 8 6.9 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2sccc2Cl)cc1 10.1021/jm00043a020
10439715 116521 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 699 12 2 9 6.2 CCCCc1nn(-c2cc(C(=O)NCCC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1007/s00044-011-9815-x
CHEMBL339040 116521 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 699 12 2 9 6.2 CCCCc1nn(-c2cc(C(=O)NCCC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1007/s00044-011-9815-x
11765560 15347 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 743 12 2 9 6.3 CCCCNC(=O)c1ccc(Br)c(-n2nc(CCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1007/s00044-011-9815-x
CHEMBL121872 15347 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 743 12 2 9 6.3 CCCCNC(=O)c1ccc(Br)c(-n2nc(CCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1007/s00044-011-9815-x
9987414 116535 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 719 11 2 9 6.8 CCCCc1nn(-c2cc(NC(=O)CC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1007/s00044-011-9815-x
CHEMBL339113 116535 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 719 11 2 9 6.8 CCCCc1nn(-c2cc(NC(=O)CC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1007/s00044-011-9815-x
19430442 202465 0 None - 0 Human 9.6 pIC50 = 9.6 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 725 15 1 9 7.7 CCCOC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCC)nc(CC)c2C(=O)OCc2ccccc2C(=O)c2ccccc2)c(F)c1 10.1016/S0960-894X(00)80077-3
CHEMBL70726 202465 0 None - 0 Human 9.6 pIC50 = 9.6 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 725 15 1 9 7.7 CCCOC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCC)nc(CC)c2C(=O)OCc2ccccc2C(=O)c2ccccc2)c(F)c1 10.1016/S0960-894X(00)80077-3
11765560 15347 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 743 12 2 9 6.3 CCCCNC(=O)c1ccc(Br)c(-n2nc(CCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1021/jm00019a004
CHEMBL121872 15347 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 743 12 2 9 6.3 CCCCNC(=O)c1ccc(Br)c(-n2nc(CCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1021/jm00019a004
9987414 116535 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 719 11 2 9 6.8 CCCCc1nn(-c2cc(NC(=O)CC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1021/jm00019a004
CHEMBL339113 116535 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 719 11 2 9 6.8 CCCCc1nn(-c2cc(NC(=O)CC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1021/jm00019a004
10100951 114533 0 None - 0 Human 9.6 pIC50 = 9.6 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 667 11 2 9 6.3 CCCCc1nn(-c2cc(NC(=O)CC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1 10.1021/jm00019a004
CHEMBL334300 114533 0 None - 0 Human 9.6 pIC50 = 9.6 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 667 11 2 9 6.3 CCCCc1nn(-c2cc(NC(=O)CC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1 10.1021/jm00019a004
11765560 15347 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 743 12 2 9 6.3 CCCCNC(=O)c1ccc(Br)c(-n2nc(CCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1007/s00044-011-9815-x
CHEMBL121872 15347 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 743 12 2 9 6.3 CCCCNC(=O)c1ccc(Br)c(-n2nc(CCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1007/s00044-011-9815-x
9987414 116535 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 719 11 2 9 6.8 CCCCc1nn(-c2cc(NC(=O)CC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1007/s00044-011-9815-x
CHEMBL339113 116535 0 None - 0 Rabbit 9.6 pIC50 = 9.6 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 719 11 2 9 6.8 CCCCc1nn(-c2cc(NC(=O)CC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1007/s00044-011-9815-x
9810305 98107 0 None - 0 Rabbit 9.5 pIC50 = 9.5 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 701 11 2 9 6.7 CCCCc1nn(-c2cc(NC(=O)CC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1 10.1007/s00044-013-0831-x
CHEMBL276674 98107 0 None - 0 Rabbit 9.5 pIC50 = 9.5 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 701 11 2 9 6.7 CCCCc1nn(-c2cc(NC(=O)CC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1 10.1007/s00044-013-0831-x
9810305 98107 0 None - 0 Rabbit 9.5 pIC50 = 9.5 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 701 11 2 9 6.7 CCCCc1nn(-c2cc(NC(=O)CC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1 10.1007/s00044-011-9815-x
CHEMBL276674 98107 0 None - 0 Rabbit 9.5 pIC50 = 9.5 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 701 11 2 9 6.7 CCCCc1nn(-c2cc(NC(=O)CC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1 10.1007/s00044-011-9815-x
9810305 98107 0 None - 0 Rabbit 9.5 pIC50 = 9.5 Binding
In vitro ability to inhibit the binding of radioligand 125I[Sar1,IIe8]AII to AT1 receptor from rabbit aortaIn vitro ability to inhibit the binding of radioligand 125I[Sar1,IIe8]AII to AT1 receptor from rabbit aorta
ChEMBL 701 11 2 9 6.7 CCCCc1nn(-c2cc(NC(=O)CC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1 10.1016/S0960-894X(01)80595-3
CHEMBL276674 98107 0 None - 0 Rabbit 9.5 pIC50 = 9.5 Binding
In vitro ability to inhibit the binding of radioligand 125I[Sar1,IIe8]AII to AT1 receptor from rabbit aortaIn vitro ability to inhibit the binding of radioligand 125I[Sar1,IIe8]AII to AT1 receptor from rabbit aorta
ChEMBL 701 11 2 9 6.7 CCCCc1nn(-c2cc(NC(=O)CC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1 10.1016/S0960-894X(01)80595-3
9810305 98107 0 None - 0 Rabbit 9.5 pIC50 = 9.5 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 701 11 2 9 6.7 CCCCc1nn(-c2cc(NC(=O)CC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1 10.1021/jm00019a004
CHEMBL276674 98107 0 None - 0 Rabbit 9.5 pIC50 = 9.5 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 701 11 2 9 6.7 CCCCc1nn(-c2cc(NC(=O)CC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1 10.1021/jm00019a004
9810305 98107 0 None - 0 Rabbit 9.5 pIC50 = 9.5 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 701 11 2 9 6.7 CCCCc1nn(-c2cc(NC(=O)CC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1 10.1021/jm00052a006
CHEMBL276674 98107 0 None - 0 Rabbit 9.5 pIC50 = 9.5 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 701 11 2 9 6.7 CCCCc1nn(-c2cc(NC(=O)CC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1 10.1021/jm00052a006
9810305 98107 0 None - 0 Rabbit 9.5 pIC50 = 9.5 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 701 11 2 9 6.7 CCCCc1nn(-c2cc(NC(=O)CC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1 10.1007/s00044-011-9815-x
CHEMBL276674 98107 0 None - 0 Rabbit 9.5 pIC50 = 9.5 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 701 11 2 9 6.7 CCCCc1nn(-c2cc(NC(=O)CC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1 10.1007/s00044-011-9815-x
10439993 118738 0 None - 0 Rabbit 9.5 pIC50 = 9.5 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 739 13 2 8 8.1 CCCCc1nn(-c2cc(NCc3ccccc3)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1007/s00044-013-0831-x
CHEMBL343634 118738 0 None - 0 Rabbit 9.5 pIC50 = 9.5 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 739 13 2 8 8.1 CCCCc1nn(-c2cc(NCc3ccccc3)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1007/s00044-013-0831-x
183134 203126 13 None - 1 Rabbit 9.5 pIC50 = 9.5 Binding
Binding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membraneBinding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane
ChEMBL 409 5 1 6 4.5 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81148-3
CHEMBL7550 203126 13 None - 1 Rabbit 9.5 pIC50 = 9.5 Binding
Binding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membraneBinding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane
ChEMBL 409 5 1 6 4.5 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81148-3
44311675 101671 0 None - 0 Human 9.5 pIC50 = 9.5 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 768 16 2 9 8.3 CCCc1nc(CC)c(C(=O)OCc2ccccc2NC(=O)c2ccccc2)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/S0960-894X(00)80077-3
CHEMBL302579 101671 0 None - 0 Human 9.5 pIC50 = 9.5 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 768 16 2 9 8.3 CCCc1nc(CC)c(C(=O)OCc2ccccc2NC(=O)c2ccccc2)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/S0960-894X(00)80077-3
44311537 101849 0 None - 0 Human 9.5 pIC50 = 9.5 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 726 15 1 9 8.1 CCCc1nc(CC)c(C(=O)OCc2ccccc2-c2ccccn2)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/S0960-894X(00)80077-3
CHEMBL303647 101849 0 None - 0 Human 9.5 pIC50 = 9.5 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 726 15 1 9 8.1 CCCc1nc(CC)c(C(=O)OCc2ccccc2-c2ccccn2)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/S0960-894X(00)80077-3
44311454 102459 0 None - 0 Human 9.5 pIC50 = 9.5 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 692 17 2 8 6.9 CCCc1nc(CC)c(C(=O)NCCCOc2ccccc2)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/S0960-894X(00)80077-3
CHEMBL306340 102459 0 None - 0 Human 9.5 pIC50 = 9.5 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 692 17 2 8 6.9 CCCc1nc(CC)c(C(=O)NCCCOc2ccccc2)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/S0960-894X(00)80077-3
44311185 103701 0 None - 0 Human 9.5 pIC50 = 9.5 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 733 15 1 9 8.3 CCCc1nc(CC)c(C(=O)OCc2ccccc2C(=O)C(C)(C)C)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/S0960-894X(00)80077-3
CHEMBL309790 103701 0 None - 0 Human 9.5 pIC50 = 9.5 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 733 15 1 9 8.3 CCCc1nc(CC)c(C(=O)OCc2ccccc2C(=O)C(C)(C)C)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/S0960-894X(00)80077-3
44311752 104373 0 None - 0 Human 9.5 pIC50 = 9.5 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 725 15 1 9 7.7 CCCOC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCC)nc(CC)c2C(=O)OCc2cccc(C(=O)c3ccccc3)c2)c(F)c1 10.1016/S0960-894X(00)80077-3
CHEMBL311018 104373 0 None - 0 Human 9.5 pIC50 = 9.5 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 725 15 1 9 7.7 CCCOC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCC)nc(CC)c2C(=O)OCc2cccc(C(=O)c3ccccc3)c2)c(F)c1 10.1016/S0960-894X(00)80077-3
44311736 202497 0 None - 0 Human 9.5 pIC50 = 9.5 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 768 16 2 9 8.3 CCCc1nc(CC)c(C(=O)OCc2ccccc2C(=O)Nc2ccccc2)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/S0960-894X(00)80077-3
CHEMBL70867 202497 0 None - 0 Human 9.5 pIC50 = 9.5 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 768 16 2 9 8.3 CCCc1nc(CC)c(C(=O)OCc2ccccc2C(=O)Nc2ccccc2)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/S0960-894X(00)80077-3
44311557 202571 0 None - 0 Human 9.5 pIC50 = 9.5 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 703 14 1 9 8.2 CCCOC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCC)nc(CC)c2C(=O)OCc2ccccc2-c2ccsc2)c(F)c1 10.1016/S0960-894X(00)80077-3
CHEMBL71286 202571 0 None - 0 Human 9.5 pIC50 = 9.5 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 703 14 1 9 8.2 CCCOC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCC)nc(CC)c2C(=O)OCc2ccccc2-c2ccsc2)c(F)c1 10.1016/S0960-894X(00)80077-3
183134 203126 13 None - 1 Rabbit 9.5 pIC50 = 9.5 Binding
Binding affinity to angiotensin AT1 receptor in rabbit aortic ringsBinding affinity to angiotensin AT1 receptor in rabbit aortic rings
ChEMBL 409 5 1 6 4.5 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.bmc.2010.10.043
CHEMBL7550 203126 13 None - 1 Rabbit 9.5 pIC50 = 9.5 Binding
Binding affinity to angiotensin AT1 receptor in rabbit aortic ringsBinding affinity to angiotensin AT1 receptor in rabbit aortic rings
ChEMBL 409 5 1 6 4.5 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.bmc.2010.10.043
183134 203126 13 None - 1 Rabbit 9.5 pIC50 = 9.5 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 409 5 1 6 4.5 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
CHEMBL7550 203126 13 None - 1 Rabbit 9.5 pIC50 = 9.5 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 409 5 1 6 4.5 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
73353934 92176 0 None - 0 Human 9.5 pIC50 = 9.5 Binding
Displacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysisDisplacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysis
ChEMBL 469 9 2 4 6.4 CCCC(=O)Nc1cc(C)c2nc(CCC)n(Cc3ccc(-c4ccccc4C(=O)O)cc3)c2c1 10.1016/j.ejmech.2013.08.014
CHEMBL2435824 92176 0 None - 0 Human 9.5 pIC50 = 9.5 Binding
Displacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysisDisplacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysis
ChEMBL 469 9 2 4 6.4 CCCC(=O)Nc1cc(C)c2nc(CCC)n(Cc3ccc(-c4ccccc4C(=O)O)cc3)c2c1 10.1016/j.ejmech.2013.08.014
183134 203126 13 None - 1 Rabbit 9.5 pIC50 = 9.5 Binding
Displacement of the specific binding ligand [125I]Sar1,Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane.Displacement of the specific binding ligand [125I]Sar1,Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane.
ChEMBL 409 5 1 6 4.5 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81119-7
CHEMBL7550 203126 13 None - 1 Rabbit 9.5 pIC50 = 9.5 Binding
Displacement of the specific binding ligand [125I]Sar1,Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane.Displacement of the specific binding ligand [125I]Sar1,Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane.
ChEMBL 409 5 1 6 4.5 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81119-7
183134 203126 13 None - 1 Rabbit 9.5 pIC50 = 9.5 Binding
In vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranesIn vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranes
ChEMBL 409 5 1 6 4.5 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81115-X
CHEMBL7550 203126 13 None - 1 Rabbit 9.5 pIC50 = 9.5 Binding
In vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranesIn vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranes
ChEMBL 409 5 1 6 4.5 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81115-X
183134 203126 13 None - 1 Rabbit 9.5 pIC50 = 9.5 Binding
In vitro binding affinity for angiotensin II AT1 receptor in rabbit aortaIn vitro binding affinity for angiotensin II AT1 receptor in rabbit aorta
ChEMBL 409 5 1 6 4.5 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00050a002
CHEMBL7550 203126 13 None - 1 Rabbit 9.5 pIC50 = 9.5 Binding
In vitro binding affinity for angiotensin II AT1 receptor in rabbit aortaIn vitro binding affinity for angiotensin II AT1 receptor in rabbit aorta
ChEMBL 409 5 1 6 4.5 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00050a002
10326972 111756 0 None - 0 Rabbit 9.5 pIC50 = 9.5 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 654 10 1 7 6.9 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)C2CCCCCC2)cc1 10.1021/jm00043a020
CHEMBL329099 111756 0 None - 0 Rabbit 9.5 pIC50 = 9.5 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 654 10 1 7 6.9 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)C2CCCCCC2)cc1 10.1021/jm00043a020
133031 100379 16 None - 1 Rabbit 9.5 pIC50 = 9.5 Binding
Inhibition of Angiotensin II receptor type 1 in rabbit aorta binding assayInhibition of Angiotensin II receptor type 1 in rabbit aorta binding assay
ChEMBL 524 7 1 6 5.4 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/S0960-894X(01)81145-8
CHEMBL293511 100379 16 None - 1 Rabbit 9.5 pIC50 = 9.5 Binding
Inhibition of Angiotensin II receptor type 1 in rabbit aorta binding assayInhibition of Angiotensin II receptor type 1 in rabbit aorta binding assay
ChEMBL 524 7 1 6 5.4 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/S0960-894X(01)81145-8
44300826 197051 0 None - 0 Rabbit 9.5 pIC50 = 9.5 Binding
Inhibition of Angiotensin II receptor type 1 in rabbit aorta binding assayInhibition of Angiotensin II receptor type 1 in rabbit aorta binding assay
ChEMBL 544 7 1 7 5.8 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2cc(C)sc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/S0960-894X(01)81145-8
CHEMBL58291 197051 0 None - 0 Rabbit 9.5 pIC50 = 9.5 Binding
Inhibition of Angiotensin II receptor type 1 in rabbit aorta binding assayInhibition of Angiotensin II receptor type 1 in rabbit aorta binding assay
ChEMBL 544 7 1 7 5.8 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2cc(C)sc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/S0960-894X(01)81145-8
44372744 51857 0 None - 0 Rabbit 9.5 pIC50 = 9.5 Binding
Inhibition of Angiotensin II receptor, type 1Inhibition of Angiotensin II receptor, type 1
ChEMBL 451 7 1 6 5.5 CCCc1ccc(-c2nn[nH]n2)c(-c2ccc(Cn3c(CC)nc4c(C)cc(C)nc43)cc2)c1 10.1021/jm9504722
CHEMBL158795 51857 0 None - 0 Rabbit 9.5 pIC50 = 9.5 Binding
Inhibition of Angiotensin II receptor, type 1Inhibition of Angiotensin II receptor, type 1
ChEMBL 451 7 1 6 5.5 CCCc1ccc(-c2nn[nH]n2)c(-c2ccc(Cn3c(CC)nc4c(C)cc(C)nc43)cc2)c1 10.1021/jm9504722
9807029 201406 0 None - 0 Human 9.5 pIC50 = 9.5 Binding
Inhibition of Angiotensin II receptor, type 1Inhibition of Angiotensin II receptor, type 1
ChEMBL 530 11 3 7 4.4 CCCNC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCC)nc(SC)c2C(=O)O)cc1 10.1021/jm9504722
CHEMBL63998 201406 0 None - 0 Human 9.5 pIC50 = 9.5 Binding
Inhibition of Angiotensin II receptor, type 1Inhibition of Angiotensin II receptor, type 1
ChEMBL 530 11 3 7 4.4 CCCNC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCC)nc(SC)c2C(=O)O)cc1 10.1021/jm9504722
183134 203126 13 None - 1 Rabbit 9.5 pIC50 = 9.5 Binding
Inhibition of Angiotensin II receptor, type 1Inhibition of Angiotensin II receptor, type 1
ChEMBL 409 5 1 6 4.5 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a001
CHEMBL7550 203126 13 None - 1 Rabbit 9.5 pIC50 = 9.5 Binding
Inhibition of Angiotensin II receptor, type 1Inhibition of Angiotensin II receptor, type 1
ChEMBL 409 5 1 6 4.5 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a001
44384389 129302 0 None - 0 Rabbit 9.5 pIC50 = 9.5 Binding
Inhibition of [125I]-Sar1-Ile8-Ang II binding to Angiotensin II receptor type 1 from rabbit aortaInhibition of [125I]-Sar1-Ile8-Ang II binding to Angiotensin II receptor type 1 from rabbit aorta
ChEMBL 572 2 2 7 5.6 CCCc1nc2ccc3cc2c(=O)n1Cc1ccc(cc1)-c1ccccc1S(=O)(=O)NC(=O)CCCCCCCN3 10.1016/0960-894X(96)00116-3
CHEMBL367569 129302 0 None - 0 Rabbit 9.5 pIC50 = 9.5 Binding
Inhibition of [125I]-Sar1-Ile8-Ang II binding to Angiotensin II receptor type 1 from rabbit aortaInhibition of [125I]-Sar1-Ile8-Ang II binding to Angiotensin II receptor type 1 from rabbit aorta
ChEMBL 572 2 2 7 5.6 CCCc1nc2ccc3cc2c(=O)n1Cc1ccc(cc1)-c1ccccc1S(=O)(=O)NC(=O)CCCCCCCN3 10.1016/0960-894X(96)00116-3
183134 203126 13 None - 1 Rabbit 9.5 pIC50 = 9.5 Binding
Inhibitory activity was evaluated against Angiotensin II receptor, type 1 in rabbit aortaInhibitory activity was evaluated against Angiotensin II receptor, type 1 in rabbit aorta
ChEMBL 409 5 1 6 4.5 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm9504722
CHEMBL7550 203126 13 None - 1 Rabbit 9.5 pIC50 = 9.5 Binding
Inhibitory activity was evaluated against Angiotensin II receptor, type 1 in rabbit aortaInhibitory activity was evaluated against Angiotensin II receptor, type 1 in rabbit aorta
ChEMBL 409 5 1 6 4.5 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm9504722
10439993 118738 0 None - 0 Rabbit 9.5 pIC50 = 9.5 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 739 13 2 8 8.1 CCCCc1nn(-c2cc(NCc3ccccc3)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1021/jm00052a006
CHEMBL343634 118738 0 None - 0 Rabbit 9.5 pIC50 = 9.5 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 739 13 2 8 8.1 CCCCc1nn(-c2cc(NCc3ccccc3)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1021/jm00052a006
19102786 205450 0 None - 0 Rabbit 9.5 pIC50 = 9.5 Binding
In vitro ability to inhibit the binding of radioligand 125I[Sar1,IIe8]AII to AT1 receptor from rabbit aortaIn vitro ability to inhibit the binding of radioligand 125I[Sar1,IIe8]AII to AT1 receptor from rabbit aorta
ChEMBL 648 9 1 8 6.5 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1016/S0960-894X(01)80595-3
CHEMBL92533 205450 0 None - 0 Rabbit 9.5 pIC50 = 9.5 Binding
In vitro ability to inhibit the binding of radioligand 125I[Sar1,IIe8]AII to AT1 receptor from rabbit aortaIn vitro ability to inhibit the binding of radioligand 125I[Sar1,IIe8]AII to AT1 receptor from rabbit aorta
ChEMBL 648 9 1 8 6.5 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1016/S0960-894X(01)80595-3
9939191 98476 1 None - 1 Rat 9.5 pIC50 = 9.5 Binding
In vitro binding affinity towards Angiotensin II receptor, type 1 to displace 125I[Sar,Ile] from rat brain tissue preparationIn vitro binding affinity towards Angiotensin II receptor, type 1 to displace 125I[Sar,Ile] from rat brain tissue preparation
ChEMBL 634 10 1 7 6.2 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/S0960-894X(01)81132-X
CHEMBL279629 98476 1 None - 1 Rat 9.5 pIC50 = 9.5 Binding
In vitro binding affinity towards Angiotensin II receptor, type 1 to displace 125I[Sar,Ile] from rat brain tissue preparationIn vitro binding affinity towards Angiotensin II receptor, type 1 to displace 125I[Sar,Ile] from rat brain tissue preparation
ChEMBL 634 10 1 7 6.2 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/S0960-894X(01)81132-X
CHEMBL97539 98476 1 None - 1 Rat 9.5 pIC50 = 9.5 Binding
In vitro binding affinity towards Angiotensin II receptor, type 1 to displace 125I[Sar,Ile] from rat brain tissue preparationIn vitro binding affinity towards Angiotensin II receptor, type 1 to displace 125I[Sar,Ile] from rat brain tissue preparation
ChEMBL 634 10 1 7 6.2 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/S0960-894X(01)81132-X
10032583 12228 0 None - 0 Rabbit 9.5 pIC50 = 9.5 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 690 10 1 8 7.4 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2cc3ccccc3s2)cc1 10.1021/jm00043a020
CHEMBL1185398 12228 0 None - 0 Rabbit 9.5 pIC50 = 9.5 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 690 10 1 8 7.4 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2cc3ccccc3s2)cc1 10.1021/jm00043a020
CHEMBL411487 12228 0 None - 0 Rabbit 9.5 pIC50 = 9.5 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 690 10 1 8 7.4 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2cc3ccccc3s2)cc1 10.1021/jm00043a020
10054708 106657 0 None - 0 Rabbit 9.5 pIC50 = 9.5 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 626 10 1 7 6.1 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)C2CCCC2)cc1 10.1021/jm00043a020
CHEMBL316273 106657 0 None - 0 Rabbit 9.5 pIC50 = 9.5 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 626 10 1 7 6.1 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)C2CCCC2)cc1 10.1021/jm00043a020
10462598 113624 0 None - 0 Human 9.5 pIC50 = 9.5 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 723 12 2 8 6.7 CCCCc1nn(-c2cc(NC(=O)CC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1F 10.1021/jm00019a004
CHEMBL332909 113624 0 None - 0 Human 9.5 pIC50 = 9.5 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 723 12 2 8 6.7 CCCCc1nn(-c2cc(NC(=O)CC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1F 10.1021/jm00019a004
10032820 116788 0 None - 0 Human 9.5 pIC50 = 9.5 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 723 12 2 8 7.0 CCCCc1nn(-c2cc(NC(=O)CC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1F 10.1021/jm00019a004
CHEMBL339672 116788 0 None - 0 Human 9.5 pIC50 = 9.5 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 723 12 2 8 7.0 CCCCc1nn(-c2cc(NC(=O)CC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1F 10.1021/jm00019a004
44381552 119768 0 None - 0 Rabbit 9.5 pIC50 = 9.5 Binding
Tested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membraneTested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membrane
ChEMBL 649 13 3 9 5.0 CCCCc1nc2ccc(NC(=O)NC(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCOC)cc1 10.1016/S0960-894X(01)81126-4
CHEMBL352629 119768 0 None - 0 Rabbit 9.5 pIC50 = 9.5 Binding
Tested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membraneTested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membrane
ChEMBL 649 13 3 9 5.0 CCCCc1nc2ccc(NC(=O)NC(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCOC)cc1 10.1016/S0960-894X(01)81126-4
9917399 101663 0 None - 0 Rabbit 9.5 pIC50 = 9.5 Binding
In vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranesIn vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranes
ChEMBL 639 12 2 8 6.8 CCCC(=O)Nc1cnc2c(nc(CCC)n2Cc2ccc(-c3ccccc3S(=O)(=O)NC(=O)OCc3ccccc3)cc2)c1C 10.1016/S0960-894X(01)81115-X
CHEMBL302519 101663 0 None - 0 Rabbit 9.5 pIC50 = 9.5 Binding
In vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranesIn vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranes
ChEMBL 639 12 2 8 6.8 CCCC(=O)Nc1cnc2c(nc(CCC)n2Cc2ccc(-c3ccccc3S(=O)(=O)NC(=O)OCc3ccccc3)cc2)c1C 10.1016/S0960-894X(01)81115-X
9939191 98476 1 None - 1 Rat 9.5 pIC50 = 9.5 Binding
In vitro binding affinity towards Angiotensin II receptor, type 1 to displace 125I[Sar,Ile] from rat adrenal tissue preparationIn vitro binding affinity towards Angiotensin II receptor, type 1 to displace 125I[Sar,Ile] from rat adrenal tissue preparation
ChEMBL 634 10 1 7 6.2 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/S0960-894X(01)81132-X
CHEMBL279629 98476 1 None - 1 Rat 9.5 pIC50 = 9.5 Binding
In vitro binding affinity towards Angiotensin II receptor, type 1 to displace 125I[Sar,Ile] from rat adrenal tissue preparationIn vitro binding affinity towards Angiotensin II receptor, type 1 to displace 125I[Sar,Ile] from rat adrenal tissue preparation
ChEMBL 634 10 1 7 6.2 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/S0960-894X(01)81132-X
CHEMBL97539 98476 1 None - 1 Rat 9.5 pIC50 = 9.5 Binding
In vitro binding affinity towards Angiotensin II receptor, type 1 to displace 125I[Sar,Ile] from rat adrenal tissue preparationIn vitro binding affinity towards Angiotensin II receptor, type 1 to displace 125I[Sar,Ile] from rat adrenal tissue preparation
ChEMBL 634 10 1 7 6.2 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/S0960-894X(01)81132-X
9917399 101663 0 None - 0 Rabbit 9.5 pIC50 = 9.5 Binding
Inhibition of Angiotensin II receptor, type 1Inhibition of Angiotensin II receptor, type 1
ChEMBL 639 12 2 8 6.8 CCCC(=O)Nc1cnc2c(nc(CCC)n2Cc2ccc(-c3ccccc3S(=O)(=O)NC(=O)OCc3ccccc3)cc2)c1C 10.1021/jm9504722
CHEMBL302519 101663 0 None - 0 Rabbit 9.5 pIC50 = 9.5 Binding
Inhibition of Angiotensin II receptor, type 1Inhibition of Angiotensin II receptor, type 1
ChEMBL 639 12 2 8 6.8 CCCC(=O)Nc1cnc2c(nc(CCC)n2Cc2ccc(-c3ccccc3S(=O)(=O)NC(=O)OCc3ccccc3)cc2)c1C 10.1021/jm9504722
1610 2305 89 None 1 4 Human 9.5 pIC50 = 9.5 Binding
Inhibition of angiotensin AT1 receptorInhibition of angiotensin AT1 receptor
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmc.2012.05.056
3941 2305 89 None 1 4 Human 9.5 pIC50 = 9.5 Binding
Inhibition of angiotensin AT1 receptorInhibition of angiotensin AT1 receptor
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmc.2012.05.056
3961 2305 89 None 1 4 Human 9.5 pIC50 = 9.5 Binding
Inhibition of angiotensin AT1 receptorInhibition of angiotensin AT1 receptor
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmc.2012.05.056
590 2305 89 None 1 4 Human 9.5 pIC50 = 9.5 Binding
Inhibition of angiotensin AT1 receptorInhibition of angiotensin AT1 receptor
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmc.2012.05.056
CHEMBL191 2305 89 None 1 4 Human 9.5 pIC50 = 9.5 Binding
Inhibition of angiotensin AT1 receptorInhibition of angiotensin AT1 receptor
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmc.2012.05.056
DB00678 2305 89 None 1 4 Human 9.5 pIC50 = 9.5 Binding
Inhibition of angiotensin AT1 receptorInhibition of angiotensin AT1 receptor
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmc.2012.05.056
44381553 119817 0 None - 0 Rabbit 9.5 pIC50 = 9.5 Binding
Tested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membraneTested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membrane
ChEMBL 675 13 2 8 6.8 CCCCc1nc2ccc(NC(=O)N(C)C(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1 10.1016/S0960-894X(01)81126-4
CHEMBL352947 119817 0 None - 0 Rabbit 9.5 pIC50 = 9.5 Binding
Tested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membraneTested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membrane
ChEMBL 675 13 2 8 6.8 CCCCc1nc2ccc(NC(=O)N(C)C(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1 10.1016/S0960-894X(01)81126-4
136052288 123951 0 None - 0 Human 9.5 pIC50 = 9.5 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 568 8 1 8 5.2 CCc1cc2c(=O)n(CCc3ccc(F)cc3)c(=O)n(Cc3ccc(-c4ccccc4-c4nc(=O)o[nH]4)cc3)c2s1 nan
CHEMBL3640122 123951 0 None - 0 Human 9.5 pIC50 = 9.5 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 568 8 1 8 5.2 CCc1cc2c(=O)n(CCc3ccc(F)cc3)c(=O)n(Cc3ccc(-c4ccccc4-c4nc(=O)o[nH]4)cc3)c2s1 nan
10101351 168088 0 None - 0 Human 9.5 pIC50 = 9.5 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 715 10 2 9 6.2 CCCc1nn(-c2cc(NC(=O)CC)ccc2Br)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1021/jm00019a004
CHEMBL436396 168088 0 None - 0 Human 9.5 pIC50 = 9.5 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 715 10 2 9 6.2 CCCc1nn(-c2cc(NC(=O)CC)ccc2Br)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1021/jm00019a004
71652854 88712 0 None - 0 Human 9.5 pIC50 = 9.5 Binding
Displacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysisDisplacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysis
ChEMBL 593 11 2 7 5.9 CCCCc1c[n+](Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)cn1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.ejmech.2012.12.044
CHEMBL2337686 88712 0 None - 0 Human 9.5 pIC50 = 9.5 Binding
Displacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysisDisplacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysis
ChEMBL 593 11 2 7 5.9 CCCCc1c[n+](Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)cn1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.ejmech.2012.12.044
CHEMBL2366020 88712 0 None - 0 Human 9.5 pIC50 = 9.5 Binding
Displacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysisDisplacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysis
ChEMBL 593 11 2 7 5.9 CCCCc1c[n+](Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)cn1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.ejmech.2012.12.044
10101351 168088 0 None - 0 Rabbit 9.5 pIC50 = 9.5 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 715 10 2 9 6.2 CCCc1nn(-c2cc(NC(=O)CC)ccc2Br)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1007/s00044-011-9815-x
CHEMBL436396 168088 0 None - 0 Rabbit 9.5 pIC50 = 9.5 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 715 10 2 9 6.2 CCCc1nn(-c2cc(NC(=O)CC)ccc2Br)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1007/s00044-011-9815-x
19430462 102498 0 None - 0 Human 9.5 pIC50 = 9.5 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 735 16 1 9 8.2 CCCc1nc(CC)c(C(=O)OCc2ccccc2C(=O)c2ccccc2)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1 10.1016/S0960-894X(00)80077-3
CHEMBL306638 102498 0 None - 0 Human 9.5 pIC50 = 9.5 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 735 16 1 9 8.2 CCCc1nc(CC)c(C(=O)OCc2ccccc2C(=O)c2ccccc2)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1 10.1016/S0960-894X(00)80077-3
CHEMBL938 214120 24 None 1 2 Human 9.5 pIC50 = 9.5 Binding
Binding affinity to human AT1 receptor by radioligand displacement assayBinding affinity to human AT1 receptor by radioligand displacement assay
ChEMBL None None None CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O)C(C)C)C(C)C 10.1016/j.ejmech.2013.01.044
14971698 205552 0 None - 0 Rabbit 9.5 pIC50 = 9.5 Binding
Displacement of [125I]Sar1,I1e8-AII from AT1 receptor in rabbit aorta membraneDisplacement of [125I]Sar1,I1e8-AII from AT1 receptor in rabbit aorta membrane
ChEMBL 512 9 2 6 6.0 CCCCc1nn(-c2ccccc2Cl)c(C(=O)O)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1039/d2md00206j
CHEMBL93226 205552 0 None - 0 Rabbit 9.5 pIC50 = 9.5 Binding
Displacement of [125I]Sar1,I1e8-AII from AT1 receptor in rabbit aorta membraneDisplacement of [125I]Sar1,I1e8-AII from AT1 receptor in rabbit aorta membrane
ChEMBL 512 9 2 6 6.0 CCCCc1nn(-c2ccccc2Cl)c(C(=O)O)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1039/d2md00206j
10101351 168088 0 None - 0 Rabbit 9.5 pIC50 = 9.5 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 715 10 2 9 6.2 CCCc1nn(-c2cc(NC(=O)CC)ccc2Br)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1021/jm00019a004
CHEMBL436396 168088 0 None - 0 Rabbit 9.5 pIC50 = 9.5 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 715 10 2 9 6.2 CCCc1nn(-c2cc(NC(=O)CC)ccc2Br)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1021/jm00019a004
10032342 206272 0 None - 0 Rabbit 9.5 pIC50 = 9.5 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 662 10 1 9 5.7 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)C2SCCS2)cc1 10.1021/jm00043a020
CHEMBL97394 206272 0 None - 0 Rabbit 9.5 pIC50 = 9.5 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 662 10 1 9 5.7 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)C2SCCS2)cc1 10.1021/jm00043a020
44381426 119753 0 None - 0 Rabbit 9.5 pIC50 = 9.5 Binding
Tested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membraneTested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membrane
ChEMBL 666 12 2 8 6.8 CCCc1nc2ccc(NC(=O)c3ccccc3)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1 10.1016/S0960-894X(01)81126-4
CHEMBL352502 119753 0 None - 0 Rabbit 9.5 pIC50 = 9.5 Binding
Tested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membraneTested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membrane
ChEMBL 666 12 2 8 6.8 CCCc1nc2ccc(NC(=O)c3ccccc3)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1 10.1016/S0960-894X(01)81126-4
10101351 168088 0 None - 0 Rabbit 9.5 pIC50 = 9.5 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 715 10 2 9 6.2 CCCc1nn(-c2cc(NC(=O)CC)ccc2Br)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1007/s00044-011-9815-x
CHEMBL436396 168088 0 None - 0 Rabbit 9.5 pIC50 = 9.5 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 715 10 2 9 6.2 CCCc1nn(-c2cc(NC(=O)CC)ccc2Br)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1007/s00044-011-9815-x
10373120 117085 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 791 12 2 8 8.0 CCCCc1nn(-c2cc(NC(=O)CC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2cc(Cl)ccc2Cl)cc1F 10.1007/s00044-011-9815-x
CHEMBL340078 117085 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 791 12 2 8 8.0 CCCCc1nn(-c2cc(NC(=O)CC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2cc(Cl)ccc2Cl)cc1F 10.1007/s00044-011-9815-x
10373120 117085 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 791 12 2 8 8.0 CCCCc1nn(-c2cc(NC(=O)CC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2cc(Cl)ccc2Cl)cc1F 10.1021/jm00019a004
CHEMBL340078 117085 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 791 12 2 8 8.0 CCCCc1nn(-c2cc(NC(=O)CC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2cc(Cl)ccc2Cl)cc1F 10.1021/jm00019a004
19939398 106837 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 626 10 1 7 6.0 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)C2CC2(C)C)cc1 10.1021/jm00043a020
CHEMBL317547 106837 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 626 10 1 7 6.0 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)C2CC2(C)C)cc1 10.1021/jm00043a020
10372718 108057 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 722 10 1 7 7.4 O=C(NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCCC(F)(F)F)nn(-c3ccccc3C(F)(F)F)c2=O)cc1)c1ccccc1Cl 10.1021/jm00043a020
CHEMBL320222 108057 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 722 10 1 7 7.4 O=C(NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCCC(F)(F)F)nn(-c3ccccc3C(F)(F)F)c2=O)cc1)c1ccccc1Cl 10.1021/jm00043a020
10259447 16732 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 741 12 2 8 6.9 CCCCc1nn(-c2cc(NC(=O)CC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2F)cc1F 10.1021/jm00019a004
CHEMBL125280 16732 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 741 12 2 8 6.9 CCCCc1nn(-c2cc(NC(=O)CC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2F)cc1F 10.1021/jm00019a004
44381656 119749 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
Tested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membraneTested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membrane
ChEMBL 656 12 2 9 6.4 CCCc1nc2ccc(NC(=O)c3ccco3)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1 10.1016/S0960-894X(01)81126-4
CHEMBL352458 119749 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
Tested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membraneTested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membrane
ChEMBL 656 12 2 9 6.4 CCCc1nc2ccc(NC(=O)c3ccco3)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1 10.1016/S0960-894X(01)81126-4
10373120 117085 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 791 12 2 8 8.0 CCCCc1nn(-c2cc(NC(=O)CC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2cc(Cl)ccc2Cl)cc1F 10.1007/s00044-011-9815-x
CHEMBL340078 117085 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 791 12 2 8 8.0 CCCCc1nn(-c2cc(NC(=O)CC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2cc(Cl)ccc2Cl)cc1F 10.1007/s00044-011-9815-x
10440203 118469 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 773 13 2 8 8.5 CCCCc1nn(-c2ccc(NCc3ccccc3)cc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1007/s00044-013-0831-x
CHEMBL342492 118469 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 773 13 2 8 8.5 CCCCc1nn(-c2ccc(NCc3ccccc3)cc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1007/s00044-013-0831-x
11765454 117552 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 723 11 2 10 6.9 CCCCc1nn(-c2cc(NC(=O)c3ccco3)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1007/s00044-011-9815-x
CHEMBL340473 117552 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 723 11 2 10 6.9 CCCCc1nn(-c2cc(NC(=O)c3ccco3)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1007/s00044-011-9815-x
44310069 202034 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
In vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranesIn vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranes
ChEMBL 617 16 2 7 7.0 CCCCCC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCCC)nc3cc(NC(=O)CCCC)cnc32)cc1 10.1016/S0960-894X(01)81115-X
CHEMBL67801 202034 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
In vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranesIn vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranes
ChEMBL 617 16 2 7 7.0 CCCCCC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCCC)nc3cc(NC(=O)CCCC)cnc32)cc1 10.1016/S0960-894X(01)81115-X
11765454 117552 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 723 11 2 10 6.9 CCCCc1nn(-c2cc(NC(=O)c3ccco3)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1021/jm00019a004
CHEMBL340473 117552 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 723 11 2 10 6.9 CCCCc1nn(-c2cc(NC(=O)c3ccco3)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1021/jm00019a004
10349597 111115 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 680 10 1 7 6.5 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)C2(C)CC2(Cl)Cl)cc1 10.1021/jm00043a020
CHEMBL328434 111115 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 680 10 1 7 6.5 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)C2(C)CC2(Cl)Cl)cc1 10.1021/jm00043a020
10440203 118469 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 773 13 2 8 8.5 CCCCc1nn(-c2ccc(NCc3ccccc3)cc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1021/jm00052a006
CHEMBL342492 118469 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 773 13 2 8 8.5 CCCCc1nn(-c2ccc(NCc3ccccc3)cc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1021/jm00052a006
11765454 117552 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 723 11 2 10 6.9 CCCCc1nn(-c2cc(NC(=O)c3ccco3)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1007/s00044-011-9815-x
CHEMBL340473 117552 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 723 11 2 10 6.9 CCCCc1nn(-c2cc(NC(=O)c3ccco3)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1007/s00044-011-9815-x
10259525 15428 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 753 10 2 9 7.3 CCCc1nn(-c2cc(NC(=O)c3ccccc3)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1007/s00044-011-9815-x
CHEMBL122158 15428 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 753 10 2 9 7.3 CCCc1nn(-c2cc(NC(=O)c3ccccc3)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1007/s00044-011-9815-x
10349897 113916 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 715 10 2 9 6.3 CCCCC(=O)Nc1ccc(Br)c(-n2nc(C)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1007/s00044-011-9815-x
CHEMBL333224 113916 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 715 10 2 9 6.3 CCCCC(=O)Nc1ccc(Br)c(-n2nc(C)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1007/s00044-011-9815-x
10101690 116348 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 767 11 2 9 7.7 CCCCc1nn(-c2cc(NC(=O)c3ccccc3)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1007/s00044-011-9815-x
CHEMBL338137 116348 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 767 11 2 9 7.7 CCCCc1nn(-c2cc(NC(=O)c3ccccc3)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1007/s00044-011-9815-x
10010071 116833 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in human adrenal membrane preparations. For this assay, only 0.02%BSA was present in the assay mixture.In vitro inhibitory activity against Angiotensin II receptor, type 1 in human adrenal membrane preparations. For this assay, only 0.02%BSA was present in the assay mixture.
ChEMBL 715 13 2 10 6.1 CCCCc1nn(-c2cc(NC(=O)COCC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1021/jm00019a004
CHEMBL339722 116833 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in human adrenal membrane preparations. For this assay, only 0.02%BSA was present in the assay mixture.In vitro inhibitory activity against Angiotensin II receptor, type 1 in human adrenal membrane preparations. For this assay, only 0.02%BSA was present in the assay mixture.
ChEMBL 715 13 2 10 6.1 CCCCc1nn(-c2cc(NC(=O)COCC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1021/jm00019a004
10259525 15428 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 753 10 2 9 7.3 CCCc1nn(-c2cc(NC(=O)c3ccccc3)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1021/jm00019a004
CHEMBL122158 15428 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 753 10 2 9 7.3 CCCc1nn(-c2cc(NC(=O)c3ccccc3)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1021/jm00019a004
10349897 113916 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 715 10 2 9 6.3 CCCCC(=O)Nc1ccc(Br)c(-n2nc(C)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1021/jm00019a004
CHEMBL333224 113916 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 715 10 2 9 6.3 CCCCC(=O)Nc1ccc(Br)c(-n2nc(C)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1021/jm00019a004
10101690 116348 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 767 11 2 9 7.7 CCCCc1nn(-c2cc(NC(=O)c3ccccc3)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1021/jm00019a004
CHEMBL338137 116348 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 767 11 2 9 7.7 CCCCc1nn(-c2cc(NC(=O)c3ccccc3)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1021/jm00019a004
10259525 15428 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 753 10 2 9 7.3 CCCc1nn(-c2cc(NC(=O)c3ccccc3)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1007/s00044-011-9815-x
CHEMBL122158 15428 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 753 10 2 9 7.3 CCCc1nn(-c2cc(NC(=O)c3ccccc3)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1007/s00044-011-9815-x
10349897 113916 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 715 10 2 9 6.3 CCCCC(=O)Nc1ccc(Br)c(-n2nc(C)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1007/s00044-011-9815-x
CHEMBL333224 113916 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 715 10 2 9 6.3 CCCCC(=O)Nc1ccc(Br)c(-n2nc(C)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1007/s00044-011-9815-x
10101690 116348 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 767 11 2 9 7.7 CCCCc1nn(-c2cc(NC(=O)c3ccccc3)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1007/s00044-011-9815-x
CHEMBL338137 116348 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 767 11 2 9 7.7 CCCCc1nn(-c2cc(NC(=O)c3ccccc3)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1007/s00044-011-9815-x
44328276 112217 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 664 10 1 7 6.5 C=C1C2CCC(C2)C1C(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCCC)nn(-c3ccccc3C(F)(F)F)c2=O)cc1 10.1021/jm00043a020
CHEMBL330464 112217 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 664 10 1 7 6.5 C=C1C2CCC(C2)C1C(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCCC)nn(-c3ccccc3C(F)(F)F)c2=O)cc1 10.1021/jm00043a020
44381622 58697 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
Tested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membraneTested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membrane
ChEMBL 689 12 2 9 5.8 CCCc1nc2ccc(NC(=O)N3CCOCC3)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCCC(C)C)cc1 10.1016/S0960-894X(01)81126-4
CHEMBL169279 58697 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
Tested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membraneTested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membrane
ChEMBL 689 12 2 9 5.8 CCCc1nc2ccc(NC(=O)N3CCOCC3)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCCC(C)C)cc1 10.1016/S0960-894X(01)81126-4
44311619 102583 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 756 16 2 8 8.8 CCCc1nc(CC)c(C(=O)NCc2ccccc2Sc2ccccc2)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/S0960-894X(00)80077-3
CHEMBL307359 102583 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 756 16 2 8 8.8 CCCc1nc(CC)c(C(=O)NCc2ccccc2Sc2ccccc2)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/S0960-894X(00)80077-3
44311683 105126 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 789 16 1 10 7.9 CCCc1nc(CC)c(C(=O)OCc2ccccc2S(=O)(=O)c2ccccc2)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/S0960-894X(00)80077-3
CHEMBL312301 105126 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 789 16 1 10 7.9 CCCc1nc(CC)c(C(=O)OCc2ccccc2S(=O)(=O)c2ccccc2)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/S0960-894X(00)80077-3
44311453 202330 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 678 17 2 8 6.7 CCCCOC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCC)nc(CC)c2C(=O)NCCCOc2ccccc2)c(F)c1 10.1016/S0960-894X(00)80077-3
CHEMBL69839 202330 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 678 17 2 8 6.7 CCCCOC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCC)nc(CC)c2C(=O)NCCCOc2ccccc2)c(F)c1 10.1016/S0960-894X(00)80077-3
16133225 415 47 None -7 6 Rat 9.4 pIC50 = 9.4 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL None None None None 10.1021/jm031100t
172198 415 47 None -7 6 Rat 9.4 pIC50 = 9.4 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL None None None None 10.1021/jm031100t
2504 415 47 None -7 6 Rat 9.4 pIC50 = 9.4 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL None None None None 10.1021/jm031100t
45266664 415 47 None -7 6 Rat 9.4 pIC50 = 9.4 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL None None None None 10.1021/jm031100t
5272 415 47 None -7 6 Rat 9.4 pIC50 = 9.4 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL None None None None 10.1021/jm031100t
CHEMBL408403 415 47 None -7 6 Rat 9.4 pIC50 = 9.4 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL None None None None 10.1021/jm031100t
DB11842 415 47 None -7 6 Rat 9.4 pIC50 = 9.4 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL None None None None 10.1021/jm031100t
183134 203126 13 None - 1 Rat 9.4 pIC50 = 9.4 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 409 5 1 6 4.5 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm031100t
CHEMBL7550 203126 13 None - 1 Rat 9.4 pIC50 = 9.4 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 409 5 1 6 4.5 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm031100t
73347892 92175 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
Displacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysisDisplacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysis
ChEMBL 455 8 2 4 6.1 CCCc1nc2c(C)cc(NC(=O)CC)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2013.08.014
CHEMBL2435823 92175 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
Displacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysisDisplacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysis
ChEMBL 455 8 2 4 6.1 CCCc1nc2c(C)cc(NC(=O)CC)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2013.08.014
16133225 415 47 None -4 6 Rat 9.4 pIC50 = 9.4 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
ChEMBL None None None None 10.1021/jm7011563
172198 415 47 None -4 6 Rat 9.4 pIC50 = 9.4 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
ChEMBL None None None None 10.1021/jm7011563
2504 415 47 None -4 6 Rat 9.4 pIC50 = 9.4 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
ChEMBL None None None None 10.1021/jm7011563
45266664 415 47 None -4 6 Rat 9.4 pIC50 = 9.4 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
ChEMBL None None None None 10.1021/jm7011563
5272 415 47 None -4 6 Rat 9.4 pIC50 = 9.4 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
ChEMBL None None None None 10.1021/jm7011563
CHEMBL408403 415 47 None -4 6 Rat 9.4 pIC50 = 9.4 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
ChEMBL None None None None 10.1021/jm7011563
DB11842 415 47 None -4 6 Rat 9.4 pIC50 = 9.4 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
ChEMBL None None None None 10.1021/jm7011563
183134 203126 13 None - 1 Rat 9.4 pIC50 = 9.4 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
ChEMBL 409 5 1 6 4.5 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm7011563
CHEMBL7550 203126 13 None - 1 Rat 9.4 pIC50 = 9.4 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
ChEMBL 409 5 1 6 4.5 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm7011563
CHEMBL938 214120 24 None 1 2 Human 9.4 pIC50 = 9.4 Binding
Displacement of [125I][Sar, Ile]-ATII from human recombinant AT1 receptor expressed in HEK293 cellsDisplacement of [125I][Sar, Ile]-ATII from human recombinant AT1 receptor expressed in HEK293 cells
ChEMBL None None None CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O)C(C)C)C(C)C 10.1016/j.bmc.2016.03.006
CHEMBL938 214120 24 None 1 2 Human 9.4 pIC50 = 9.4 Binding
Displacement of [125I][Sar1,Ile8]-AT2 from human recombinant AT1 receptor expressed in HEK293 cells measured after 120 mins by scintillation counting methodDisplacement of [125I][Sar1,Ile8]-AT2 from human recombinant AT1 receptor expressed in HEK293 cells measured after 120 mins by scintillation counting method
ChEMBL None None None CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O)C(C)C)C(C)C 10.1016/j.bmc.2016.11.014
10394995 110893 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 702 10 1 8 6.6 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccc(Br)o2)cc1 10.1021/jm00043a020
CHEMBL327191 110893 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 702 10 1 8 6.6 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccc(Br)o2)cc1 10.1021/jm00043a020
10326775 111734 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 638 10 1 8 6.1 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccc(C)o2)cc1 10.1021/jm00043a020
CHEMBL329089 111734 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 638 10 1 8 6.1 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccc(C)o2)cc1 10.1021/jm00043a020
10010047 206202 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 712 10 1 7 7.0 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Br)cc1 10.1021/jm00043a020
CHEMBL97020 206202 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 712 10 1 7 7.0 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Br)cc1 10.1021/jm00043a020
10439819 169311 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 715 13 2 10 5.5 CCCCc1nn(-c2cc(C(=O)NCCOC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1021/jm00019a004
CHEMBL444065 169311 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 715 13 2 10 5.5 CCCCc1nn(-c2cc(C(=O)NCCOC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1021/jm00019a004
44384870 59716 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
Inhibition of [125I]-Sar1-Ile8-Ang II binding to Angiotensin II receptor type 1 from rabbit aortaInhibition of [125I]-Sar1-Ile8-Ang II binding to Angiotensin II receptor type 1 from rabbit aorta
ChEMBL 541 8 2 7 5.5 CCCc1nc2ccc(NC(=O)c3ccccc3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/0960-894X(96)00116-3
CHEMBL173643 59716 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
Inhibition of [125I]-Sar1-Ile8-Ang II binding to Angiotensin II receptor type 1 from rabbit aortaInhibition of [125I]-Sar1-Ile8-Ang II binding to Angiotensin II receptor type 1 from rabbit aorta
ChEMBL 541 8 2 7 5.5 CCCc1nc2ccc(NC(=O)c3ccccc3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/0960-894X(96)00116-3
10010311 30297 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 753 12 2 8 7.8 CCCCc1nn(-c2cc(NC(=O)c3ccccc3)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1007/s00044-013-0831-x
CHEMBL139325 30297 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 753 12 2 8 7.8 CCCCc1nn(-c2cc(NC(=O)c3ccccc3)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1007/s00044-013-0831-x
10417144 32746 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 679 11 1 9 6.4 CCCCc1nn(-c2cc([N+](=O)[O-])ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1007/s00044-013-0831-x
CHEMBL141592 32746 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 679 11 1 9 6.4 CCCCc1nn(-c2cc([N+](=O)[O-])ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1007/s00044-013-0831-x
10462573 116495 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 719 11 2 9 6.8 CCCCC(=O)Nc1ccc(C(F)(F)F)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1007/s00044-011-9815-x
CHEMBL338889 116495 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 719 11 2 9 6.8 CCCCC(=O)Nc1ccc(C(F)(F)F)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1007/s00044-011-9815-x
10032988 116404 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in human adrenal membrane preparations. For this assay, only 0.02%BSA was present in the assay mixture.In vitro inhibitory activity against Angiotensin II receptor, type 1 in human adrenal membrane preparations. For this assay, only 0.02%BSA was present in the assay mixture.
ChEMBL 747 13 2 9 7.6 CCCCC(=O)Nc1ccc(C(F)(F)F)c(-n2nc(CCCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1021/jm00019a004
CHEMBL338434 116404 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in human adrenal membrane preparations. For this assay, only 0.02%BSA was present in the assay mixture.In vitro inhibitory activity against Angiotensin II receptor, type 1 in human adrenal membrane preparations. For this assay, only 0.02%BSA was present in the assay mixture.
ChEMBL 747 13 2 9 7.6 CCCCC(=O)Nc1ccc(C(F)(F)F)c(-n2nc(CCCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1021/jm00019a004
10462573 116495 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 719 11 2 9 6.8 CCCCC(=O)Nc1ccc(C(F)(F)F)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1021/jm00019a004
CHEMBL338889 116495 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 719 11 2 9 6.8 CCCCC(=O)Nc1ccc(C(F)(F)F)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1021/jm00019a004
10078132 106754 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 664 11 1 8 6.2 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2OC)cc1 10.1021/jm00043a020
CHEMBL316904 106754 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 664 11 1 8 6.2 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2OC)cc1 10.1021/jm00043a020
10010311 30297 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 753 12 2 8 7.8 CCCCc1nn(-c2cc(NC(=O)c3ccccc3)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1021/jm00052a006
CHEMBL139325 30297 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 753 12 2 8 7.8 CCCCc1nn(-c2cc(NC(=O)c3ccccc3)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1021/jm00052a006
10417144 32746 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 679 11 1 9 6.4 CCCCc1nn(-c2cc([N+](=O)[O-])ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1021/jm00052a006
CHEMBL141592 32746 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 679 11 1 9 6.4 CCCCc1nn(-c2cc([N+](=O)[O-])ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1021/jm00052a006
10462573 116495 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 719 11 2 9 6.8 CCCCC(=O)Nc1ccc(C(F)(F)F)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1007/s00044-011-9815-x
CHEMBL338889 116495 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 719 11 2 9 6.8 CCCCC(=O)Nc1ccc(C(F)(F)F)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1007/s00044-011-9815-x
11765541 118490 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 739 12 2 8 7.2 CCCCc1nn(-c2ccc(NC(=O)CC)cc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1007/s00044-013-0831-x
CHEMBL342605 118490 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 739 12 2 8 7.2 CCCCc1nn(-c2ccc(NC(=O)CC)cc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1007/s00044-013-0831-x
10032988 116404 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 747 13 2 9 7.6 CCCCC(=O)Nc1ccc(C(F)(F)F)c(-n2nc(CCCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1007/s00044-011-9815-x
CHEMBL338434 116404 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 747 13 2 9 7.6 CCCCC(=O)Nc1ccc(C(F)(F)F)c(-n2nc(CCCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1007/s00044-011-9815-x
10032988 116404 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 747 13 2 9 7.6 CCCCC(=O)Nc1ccc(C(F)(F)F)c(-n2nc(CCCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1021/jm00019a004
CHEMBL338434 116404 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 747 13 2 9 7.6 CCCCC(=O)Nc1ccc(C(F)(F)F)c(-n2nc(CCCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1021/jm00019a004
10077743 206208 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 630 11 1 8 6.2 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCC(C)C)cc1 10.1021/jm00043a020
CHEMBL97068 206208 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 630 11 1 8 6.2 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCC(C)C)cc1 10.1021/jm00043a020
11765541 118490 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 739 12 2 8 7.2 CCCCc1nn(-c2ccc(NC(=O)CC)cc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1021/jm00052a006
CHEMBL342605 118490 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 739 12 2 8 7.2 CCCCc1nn(-c2ccc(NC(=O)CC)cc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1021/jm00052a006
10032988 116404 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 747 13 2 9 7.6 CCCCC(=O)Nc1ccc(C(F)(F)F)c(-n2nc(CCCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1007/s00044-011-9815-x
CHEMBL338434 116404 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 747 13 2 9 7.6 CCCCC(=O)Nc1ccc(C(F)(F)F)c(-n2nc(CCCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1007/s00044-011-9815-x
9939191 98476 1 None - 1 Rabbit 9.4 pIC50 = 9.4 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 634 10 1 7 6.2 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1007/s00044-013-0831-x
CHEMBL279629 98476 1 None - 1 Rabbit 9.4 pIC50 = 9.4 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 634 10 1 7 6.2 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1007/s00044-013-0831-x
CHEMBL97539 98476 1 None - 1 Rabbit 9.4 pIC50 = 9.4 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 634 10 1 7 6.2 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1007/s00044-013-0831-x
9939191 98476 1 None - 1 Rabbit 9.4 pIC50 = 9.4 Binding
Displacement of 125I[Sar,Ile] from rabbit aorta membrane Angiotensin II receptor type 1Displacement of 125I[Sar,Ile] from rabbit aorta membrane Angiotensin II receptor type 1
ChEMBL 634 10 1 7 6.2 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/S0960-894X(01)81132-X
CHEMBL279629 98476 1 None - 1 Rabbit 9.4 pIC50 = 9.4 Binding
Displacement of 125I[Sar,Ile] from rabbit aorta membrane Angiotensin II receptor type 1Displacement of 125I[Sar,Ile] from rabbit aorta membrane Angiotensin II receptor type 1
ChEMBL 634 10 1 7 6.2 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/S0960-894X(01)81132-X
CHEMBL97539 98476 1 None - 1 Rabbit 9.4 pIC50 = 9.4 Binding
Displacement of 125I[Sar,Ile] from rabbit aorta membrane Angiotensin II receptor type 1Displacement of 125I[Sar,Ile] from rabbit aorta membrane Angiotensin II receptor type 1
ChEMBL 634 10 1 7 6.2 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/S0960-894X(01)81132-X
9939191 98476 1 None - 1 Rabbit 9.4 pIC50 = 9.4 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 634 10 1 7 6.2 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1021/jm00019a004
CHEMBL279629 98476 1 None - 1 Rabbit 9.4 pIC50 = 9.4 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 634 10 1 7 6.2 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1021/jm00019a004
CHEMBL97539 98476 1 None - 1 Rabbit 9.4 pIC50 = 9.4 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 634 10 1 7 6.2 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1021/jm00019a004
9939191 98476 1 None - 1 Rabbit 9.4 pIC50 = 9.4 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 634 10 1 7 6.2 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1021/jm00043a020
CHEMBL279629 98476 1 None - 1 Rabbit 9.4 pIC50 = 9.4 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 634 10 1 7 6.2 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1021/jm00043a020
CHEMBL97539 98476 1 None - 1 Rabbit 9.4 pIC50 = 9.4 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 634 10 1 7 6.2 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1021/jm00043a020
10349659 111042 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 688 10 1 8 7.3 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2oc3ccccc3c2C)cc1 10.1021/jm00043a020
CHEMBL327988 111042 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 688 10 1 8 7.3 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2oc3ccccc3c2C)cc1 10.1021/jm00043a020
10395335 116568 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 757 12 2 8 7.4 CCCCc1nn(-c2cc(NC(=O)CC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1F 10.1021/jm00019a004
CHEMBL339256 116568 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 757 12 2 8 7.4 CCCCc1nn(-c2cc(NC(=O)CC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1F 10.1021/jm00019a004
10259468 117964 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 743 12 2 9 6.9 CCCCC(=O)Nc1ccc(Br)c(-n2nc(CCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1021/jm00019a004
CHEMBL341369 117964 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 743 12 2 9 6.9 CCCCC(=O)Nc1ccc(Br)c(-n2nc(CCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1021/jm00019a004
9939191 98476 1 None - 1 Rabbit 9.4 pIC50 = 9.4 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 634 10 1 7 6.2 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1021/jm00052a006
CHEMBL279629 98476 1 None - 1 Rabbit 9.4 pIC50 = 9.4 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 634 10 1 7 6.2 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1021/jm00052a006
CHEMBL97539 98476 1 None - 1 Rabbit 9.4 pIC50 = 9.4 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 634 10 1 7 6.2 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1021/jm00052a006
9852499 119944 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
Tested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membraneTested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membrane
ChEMBL 647 11 3 8 6.1 CCCc1nc2ccc(NC(=O)NCC)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)(C)C)cc1 10.1016/S0960-894X(01)81126-4
CHEMBL354080 119944 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
Tested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membraneTested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membrane
ChEMBL 647 11 3 8 6.1 CCCc1nc2ccc(NC(=O)NCC)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)(C)C)cc1 10.1016/S0960-894X(01)81126-4
10032877 15359 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 733 12 2 9 6.6 CCCCNC(=O)c1ccc(C(F)(F)F)c(-n2nc(CCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1007/s00044-011-9815-x
CHEMBL121907 15359 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 733 12 2 9 6.6 CCCCNC(=O)c1ccc(C(F)(F)F)c(-n2nc(CCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1007/s00044-011-9815-x
10259841 15967 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 815 13 2 8 7.6 CCCCNC(=O)c1ccc(Br)c(-n2nc(CCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)c4cc(Cl)ccc4Cl)cc3F)c2=O)c1 10.1007/s00044-011-9815-x
CHEMBL122401 15967 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 815 13 2 8 7.6 CCCCNC(=O)c1ccc(Br)c(-n2nc(CCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)c4cc(Cl)ccc4Cl)cc3F)c2=O)c1 10.1007/s00044-011-9815-x
9827346 99263 1 None - 0 Rat 9.4 pIC50 = 9.4 Binding
In vitro ability to displace the specific binding of [125I]-A II from receptors in rat liver membrane(type 1 receptor)In vitro ability to displace the specific binding of [125I]-A II from receptors in rat liver membrane(type 1 receptor)
ChEMBL 501 7 2 8 3.4 CCc1nn(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/c(=N/C(=O)C2=C(C(=O)O)CCC2)s1 10.1016/S0960-894X(96)00250-8
CHEMBL284918 99263 1 None - 0 Rat 9.4 pIC50 = 9.4 Binding
In vitro ability to displace the specific binding of [125I]-A II from receptors in rat liver membrane(type 1 receptor)In vitro ability to displace the specific binding of [125I]-A II from receptors in rat liver membrane(type 1 receptor)
ChEMBL 501 7 2 8 3.4 CCc1nn(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/c(=N/C(=O)C2=C(C(=O)O)CCC2)s1 10.1016/S0960-894X(96)00250-8
CHEMBL34866 99263 1 None - 0 Rat 9.4 pIC50 = 9.4 Binding
In vitro ability to displace the specific binding of [125I]-A II from receptors in rat liver membrane(type 1 receptor)In vitro ability to displace the specific binding of [125I]-A II from receptors in rat liver membrane(type 1 receptor)
ChEMBL 501 7 2 8 3.4 CCc1nn(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/c(=N/C(=O)C2=C(C(=O)O)CCC2)s1 10.1016/S0960-894X(96)00250-8
10032877 15359 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 733 12 2 9 6.6 CCCCNC(=O)c1ccc(C(F)(F)F)c(-n2nc(CCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1021/jm00019a004
CHEMBL121907 15359 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 733 12 2 9 6.6 CCCCNC(=O)c1ccc(C(F)(F)F)c(-n2nc(CCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1021/jm00019a004
10259841 15967 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 815 13 2 8 7.6 CCCCNC(=O)c1ccc(Br)c(-n2nc(CCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)c4cc(Cl)ccc4Cl)cc3F)c2=O)c1 10.1021/jm00019a004
CHEMBL122401 15967 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 815 13 2 8 7.6 CCCCNC(=O)c1ccc(Br)c(-n2nc(CCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)c4cc(Cl)ccc4Cl)cc3F)c2=O)c1 10.1021/jm00019a004
10372451 116778 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 685 11 2 9 6.4 CCCCc1nn(-c2cc(NC(=O)CC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1021/jm00019a004
CHEMBL339605 116778 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 685 11 2 9 6.4 CCCCc1nn(-c2cc(NC(=O)CC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1021/jm00019a004
10032877 15359 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 733 12 2 9 6.6 CCCCNC(=O)c1ccc(C(F)(F)F)c(-n2nc(CCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1007/s00044-011-9815-x
CHEMBL121907 15359 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 733 12 2 9 6.6 CCCCNC(=O)c1ccc(C(F)(F)F)c(-n2nc(CCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1007/s00044-011-9815-x
10259841 15967 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 815 13 2 8 7.6 CCCCNC(=O)c1ccc(Br)c(-n2nc(CCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)c4cc(Cl)ccc4Cl)cc3F)c2=O)c1 10.1007/s00044-011-9815-x
CHEMBL122401 15967 0 None - 0 Rabbit 9.4 pIC50 = 9.4 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 815 13 2 8 7.6 CCCCNC(=O)c1ccc(Br)c(-n2nc(CCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)c4cc(Cl)ccc4Cl)cc3F)c2=O)c1 10.1007/s00044-011-9815-x
9830680 100163 0 None - 1 Rabbit 9.4 pIC50 = 9.4 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 630 9 1 8 6.3 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1 10.1007/s00044-013-0831-x
CHEMBL292150 100163 0 None - 1 Rabbit 9.4 pIC50 = 9.4 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 630 9 1 8 6.3 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1 10.1007/s00044-013-0831-x
9830680 100163 0 None - 1 Rabbit 9.4 pIC50 = 9.4 Binding
In vitro ability to inhibit the binding of radioligand 125I[Sar1,IIe8]AII to AT1 receptor from rabbit aortaIn vitro ability to inhibit the binding of radioligand 125I[Sar1,IIe8]AII to AT1 receptor from rabbit aorta
ChEMBL 630 9 1 8 6.3 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1 10.1016/S0960-894X(01)80595-3
CHEMBL292150 100163 0 None - 1 Rabbit 9.4 pIC50 = 9.4 Binding
In vitro ability to inhibit the binding of radioligand 125I[Sar1,IIe8]AII to AT1 receptor from rabbit aortaIn vitro ability to inhibit the binding of radioligand 125I[Sar1,IIe8]AII to AT1 receptor from rabbit aorta
ChEMBL 630 9 1 8 6.3 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1 10.1016/S0960-894X(01)80595-3
9830680 100163 0 None - 1 Rabbit 9.4 pIC50 = 9.4 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 630 9 1 8 6.3 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1 10.1021/jm00043a020
CHEMBL292150 100163 0 None - 1 Rabbit 9.4 pIC50 = 9.4 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 630 9 1 8 6.3 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1 10.1021/jm00043a020
10009984 112668 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 705 12 2 9 6.4 CCCCc1nn(-c2cc(NC(=O)CC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)C)cc1F 10.1021/jm00019a004
CHEMBL331455 112668 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 705 12 2 9 6.4 CCCCc1nn(-c2cc(NC(=O)CC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)C)cc1F 10.1021/jm00019a004
9830680 100163 0 None - 1 Rabbit 9.4 pIC50 = 9.4 Binding
Inhibition of Angiotensin II receptor, type 1Inhibition of Angiotensin II receptor, type 1
ChEMBL 630 9 1 8 6.3 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1 10.1021/jm9504722
CHEMBL292150 100163 0 None - 1 Rabbit 9.4 pIC50 = 9.4 Binding
Inhibition of Angiotensin II receptor, type 1Inhibition of Angiotensin II receptor, type 1
ChEMBL 630 9 1 8 6.3 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1 10.1021/jm9504722
9830680 100163 0 None - 1 Rabbit 9.4 pIC50 = 9.4 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 630 9 1 8 6.3 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1 10.1021/jm00052a006
CHEMBL292150 100163 0 None - 1 Rabbit 9.4 pIC50 = 9.4 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 630 9 1 8 6.3 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1 10.1021/jm00052a006
44312565 203053 0 None - 1 Human 9.3 pIC50 = 9.3 Binding
Compound was tested for inhibition against Angiotensin II receptor, type 1Compound was tested for inhibition against Angiotensin II receptor, type 1
ChEMBL 437 9 3 6 3.1 CC(O)CCC(=O)N(c1ccc(-c2ccccc2-c2nn[nH]n2)cc1)[C@H](C(=O)O)C(C)C 10.1021/jm0204237
CHEMBL74767 203053 0 None - 1 Human 9.3 pIC50 = 9.3 Binding
Compound was tested for inhibition against Angiotensin II receptor, type 1Compound was tested for inhibition against Angiotensin II receptor, type 1
ChEMBL 437 9 3 6 3.1 CC(O)CCC(=O)N(c1ccc(-c2ccccc2-c2nn[nH]n2)cc1)[C@H](C(=O)O)C(C)C 10.1021/jm0204237
44348153 117454 0 None - 0 Rabbit 9.3 pIC50 = 9.3 Binding
Displacement of [1251][Sar1,IIe8]AII from rabbit aorta Angiotensin II receptor, type 1Displacement of [1251][Sar1,IIe8]AII from rabbit aorta Angiotensin II receptor, type 1
ChEMBL 591 13 1 6 8.6 CCCc1cc(Cn2c(CC)nc3c(C)cc(C)nc32)cc(CCC)c1OC(C(=O)O)c1cccc(Oc2ccccc2)c1 10.1021/jm00075a033
CHEMBL340367 117454 0 None - 0 Rabbit 9.3 pIC50 = 9.3 Binding
Displacement of [1251][Sar1,IIe8]AII from rabbit aorta Angiotensin II receptor, type 1Displacement of [1251][Sar1,IIe8]AII from rabbit aorta Angiotensin II receptor, type 1
ChEMBL 591 13 1 6 8.6 CCCc1cc(Cn2c(CC)nc3c(C)cc(C)nc32)cc(CCC)c1OC(C(=O)O)c1cccc(Oc2ccccc2)c1 10.1021/jm00075a033
72548703 161007 0 None - 0 Human 9.3 pIC50 = 9.3 Binding
Displacement of [125I][Sar1,Ile8]-AT-II from human recombinant AT1 receptor after 120 mins by scintillation counting analysisDisplacement of [125I][Sar1,Ile8]-AT-II from human recombinant AT1 receptor after 120 mins by scintillation counting analysis
ChEMBL 583 8 3 6 5.8 CC(C)(C)NS(=O)(=O)c1ccc(-c2sc(C(=O)N[C@H]3C[C@H](C(=O)O)C3)nc2CC2CCCCC2)c2ccccc12 10.1016/j.bmcl.2018.03.093
CHEMBL4128926 161007 0 None - 0 Human 9.3 pIC50 = 9.3 Binding
Displacement of [125I][Sar1,Ile8]-AT-II from human recombinant AT1 receptor after 120 mins by scintillation counting analysisDisplacement of [125I][Sar1,Ile8]-AT-II from human recombinant AT1 receptor after 120 mins by scintillation counting analysis
ChEMBL 583 8 3 6 5.8 CC(C)(C)NS(=O)(=O)c1ccc(-c2sc(C(=O)N[C@H]3C[C@H](C(=O)O)C3)nc2CC2CCCCC2)c2ccccc12 10.1016/j.bmcl.2018.03.093
10009968 112042 0 None - 0 Rabbit 9.3 pIC50 = 9.3 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 702 10 1 7 7.5 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2cc(Cl)ccc2Cl)cc1 10.1021/jm00043a020
CHEMBL329942 112042 0 None - 0 Rabbit 9.3 pIC50 = 9.3 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 702 10 1 7 7.5 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2cc(Cl)ccc2Cl)cc1 10.1021/jm00043a020
2583 3705 115 None - 1 Human 9.3 pIC50 = 9.3 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor afterDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after
ChEMBL 514 7 1 5 7.3 CCCc1nc2c(n1Cc1ccc(cc1)c1ccccc1C(=O)O)cc(cc2C)c1nc2c(n1C)cccc2 10.1016/j.bmcl.2012.11.088
592 3705 115 None - 1 Human 9.3 pIC50 = 9.3 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor afterDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after
ChEMBL 514 7 1 5 7.3 CCCc1nc2c(n1Cc1ccc(cc1)c1ccccc1C(=O)O)cc(cc2C)c1nc2c(n1C)cccc2 10.1016/j.bmcl.2012.11.088
65999 3705 115 None - 1 Human 9.3 pIC50 = 9.3 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor afterDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after
ChEMBL 514 7 1 5 7.3 CCCc1nc2c(n1Cc1ccc(cc1)c1ccccc1C(=O)O)cc(cc2C)c1nc2c(n1C)cccc2 10.1016/j.bmcl.2012.11.088
CHEMBL1017 3705 115 None - 1 Human 9.3 pIC50 = 9.3 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor afterDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after
ChEMBL 514 7 1 5 7.3 CCCc1nc2c(n1Cc1ccc(cc1)c1ccccc1C(=O)O)cc(cc2C)c1nc2c(n1C)cccc2 10.1016/j.bmcl.2012.11.088
DB00966 3705 115 None - 1 Human 9.3 pIC50 = 9.3 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor afterDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after
ChEMBL 514 7 1 5 7.3 CCCc1nc2c(n1Cc1ccc(cc1)c1ccccc1C(=O)O)cc(cc2C)c1nc2c(n1C)cccc2 10.1016/j.bmcl.2012.11.088
2583 3705 115 None - 1 Human 9.3 pIC50 = 9.3 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation countingDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation counting
ChEMBL 514 7 1 5 7.3 CCCc1nc2c(n1Cc1ccc(cc1)c1ccccc1C(=O)O)cc(cc2C)c1nc2c(n1C)cccc2 10.1021/jm200409s
592 3705 115 None - 1 Human 9.3 pIC50 = 9.3 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation countingDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation counting
ChEMBL 514 7 1 5 7.3 CCCc1nc2c(n1Cc1ccc(cc1)c1ccccc1C(=O)O)cc(cc2C)c1nc2c(n1C)cccc2 10.1021/jm200409s
65999 3705 115 None - 1 Human 9.3 pIC50 = 9.3 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation countingDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation counting
ChEMBL 514 7 1 5 7.3 CCCc1nc2c(n1Cc1ccc(cc1)c1ccccc1C(=O)O)cc(cc2C)c1nc2c(n1C)cccc2 10.1021/jm200409s
CHEMBL1017 3705 115 None - 1 Human 9.3 pIC50 = 9.3 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation countingDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation counting
ChEMBL 514 7 1 5 7.3 CCCc1nc2c(n1Cc1ccc(cc1)c1ccccc1C(=O)O)cc(cc2C)c1nc2c(n1C)cccc2 10.1021/jm200409s
DB00966 3705 115 None - 1 Human 9.3 pIC50 = 9.3 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation countingDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation counting
ChEMBL 514 7 1 5 7.3 CCCc1nc2c(n1Cc1ccc(cc1)c1ccccc1C(=O)O)cc(cc2C)c1nc2c(n1C)cccc2 10.1021/jm200409s
10480309 16186 0 None - 0 Human 9.3 pIC50 = 9.3 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 480 13 1 5 5.2 CCCCc1ncc(/C=C2\C(=O)N(CCCC)C(=O)N2CCCC)n1Cc1ccc(C(=O)O)cc1 10.1007/s00044-009-9205-9
CHEMBL122969 16186 0 None - 0 Human 9.3 pIC50 = 9.3 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 480 13 1 5 5.2 CCCCc1ncc(/C=C2\C(=O)N(CCCC)C(=O)N2CCCC)n1Cc1ccc(C(=O)O)cc1 10.1007/s00044-009-9205-9
10007362 17120 0 None - 0 Human 9.3 pIC50 = 9.3 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 536 12 2 8 4.6 CCCCc1ncc(/C=C2\C(=O)N(CCCC)C(=O)N2Cc2csc(N)n2)n1Cc1ccc(C(=O)O)cc1 10.1007/s00044-009-9205-9
CHEMBL125725 17120 0 None - 0 Human 9.3 pIC50 = 9.3 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 536 12 2 8 4.6 CCCCc1ncc(/C=C2\C(=O)N(CCCC)C(=O)N2Cc2csc(N)n2)n1Cc1ccc(C(=O)O)cc1 10.1007/s00044-009-9205-9
44311182 102540 0 None - 0 Human 9.3 pIC50 = 9.3 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 703 14 1 9 8.2 CCCOC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCC)nc(CC)c2C(=O)OCc2ccccc2-c2cccs2)c(F)c1 10.1016/S0960-894X(00)80077-3
CHEMBL307008 102540 0 None - 0 Human 9.3 pIC50 = 9.3 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 703 14 1 9 8.2 CCCOC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCC)nc(CC)c2C(=O)OCc2ccccc2-c2cccs2)c(F)c1 10.1016/S0960-894X(00)80077-3
44311452 202790 0 None - 0 Human 9.3 pIC50 = 9.3 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 739 15 1 9 7.9 CCCc1nc(CC)c(C(=O)OCc2ccccc2C(=O)c2ccccc2)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCC(C)C)cc1F 10.1016/S0960-894X(00)80077-3
CHEMBL72595 202790 0 None - 0 Human 9.3 pIC50 = 9.3 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 739 15 1 9 7.9 CCCc1nc(CC)c(C(=O)OCc2ccccc2C(=O)c2ccccc2)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCC(C)C)cc1F 10.1016/S0960-894X(00)80077-3
9940350 203040 0 None - 0 Human 9.3 pIC50 = 9.3 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 753 16 1 9 8.3 CCCc1nc(CC)c(C(=O)OCc2ccccc2C(=O)c2ccccc2)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/S0960-894X(00)80077-3
CHEMBL74573 203040 0 None - 0 Human 9.3 pIC50 = 9.3 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 753 16 1 9 8.3 CCCc1nc(CC)c(C(=O)OCc2ccccc2C(=O)c2ccccc2)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/S0960-894X(00)80077-3
44275095 94721 0 None - 0 Rabbit 9.3 pIC50 = 9.3 Binding
Displacement of [125I]Sar1-Ile8-AII (without BSA) from type 1 Angiotensin II receptor of rabbit aortaDisplacement of [125I]Sar1-Ile8-AII (without BSA) from type 1 Angiotensin II receptor of rabbit aorta
ChEMBL 536 9 3 7 5.2 CCCCc1nc2ccc(NC(=O)NC(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80335-2
CHEMBL25585 94721 0 None - 0 Rabbit 9.3 pIC50 = 9.3 Binding
Displacement of [125I]Sar1-Ile8-AII (without BSA) from type 1 Angiotensin II receptor of rabbit aortaDisplacement of [125I]Sar1-Ile8-AII (without BSA) from type 1 Angiotensin II receptor of rabbit aorta
ChEMBL 536 9 3 7 5.2 CCCCc1nc2ccc(NC(=O)NC(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80335-2
44309704 202566 0 None - 0 Rabbit 9.3 pIC50 = 9.3 Binding
In vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranesIn vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranes
ChEMBL 612 13 1 7 7.7 CCCCC(=O)N(Cc1ccccc1)c1cc2nc(CCCC)n(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c2nc1C 10.1016/S0960-894X(01)81115-X
CHEMBL71253 202566 0 None - 0 Rabbit 9.3 pIC50 = 9.3 Binding
In vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranesIn vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranes
ChEMBL 612 13 1 7 7.7 CCCCC(=O)N(Cc1ccccc1)c1cc2nc(CCCC)n(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c2nc1C 10.1016/S0960-894X(01)81115-X
183134 203126 13 None - 1 Rabbit 9.3 pIC50 = 9.3 Binding
In vitro binding affinity towards Angiotensin II type 1-AT1 receptor determined as its ability to displace 125I-Sarl,Ile8-AII from the receptor expressed in rabbit aorta membrane.In vitro binding affinity towards Angiotensin II type 1-AT1 receptor determined as its ability to displace 125I-Sarl,Ile8-AII from the receptor expressed in rabbit aorta membrane.
ChEMBL 409 5 1 6 4.5 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80044-X
CHEMBL7550 203126 13 None - 1 Rabbit 9.3 pIC50 = 9.3 Binding
In vitro binding affinity towards Angiotensin II type 1-AT1 receptor determined as its ability to displace 125I-Sarl,Ile8-AII from the receptor expressed in rabbit aorta membrane.In vitro binding affinity towards Angiotensin II type 1-AT1 receptor determined as its ability to displace 125I-Sarl,Ile8-AII from the receptor expressed in rabbit aorta membrane.
ChEMBL 409 5 1 6 4.5 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80044-X
9939191 98476 1 None - 1 Rabbit 9.3 pIC50 = 9.3 Binding
In vitro binding affinity towards angiotensin-1 receptor to displace 125I[Sar,Ile] from rabbit adrenal tissue preparationIn vitro binding affinity towards angiotensin-1 receptor to displace 125I[Sar,Ile] from rabbit adrenal tissue preparation
ChEMBL 634 10 1 7 6.2 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/S0960-894X(01)81132-X
CHEMBL279629 98476 1 None - 1 Rabbit 9.3 pIC50 = 9.3 Binding
In vitro binding affinity towards angiotensin-1 receptor to displace 125I[Sar,Ile] from rabbit adrenal tissue preparationIn vitro binding affinity towards angiotensin-1 receptor to displace 125I[Sar,Ile] from rabbit adrenal tissue preparation
ChEMBL 634 10 1 7 6.2 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/S0960-894X(01)81132-X
CHEMBL97539 98476 1 None - 1 Rabbit 9.3 pIC50 = 9.3 Binding
In vitro binding affinity towards angiotensin-1 receptor to displace 125I[Sar,Ile] from rabbit adrenal tissue preparationIn vitro binding affinity towards angiotensin-1 receptor to displace 125I[Sar,Ile] from rabbit adrenal tissue preparation
ChEMBL 634 10 1 7 6.2 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/S0960-894X(01)81132-X
44379268 119536 0 None - 0 Rabbit 9.3 pIC50 = 9.3 Binding
In vitro displacement of 125I-[Sar1, Ile8] from AT1 receptors in rabbit aorta membraneIn vitro displacement of 125I-[Sar1, Ile8] from AT1 receptors in rabbit aorta membrane
ChEMBL 666 11 1 8 6.4 CCCc1nc2ccc(N(C)C(=O)OCC(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/S0960-894X(01)81125-2
CHEMBL350554 119536 0 None - 0 Rabbit 9.3 pIC50 = 9.3 Binding
In vitro displacement of 125I-[Sar1, Ile8] from AT1 receptors in rabbit aorta membraneIn vitro displacement of 125I-[Sar1, Ile8] from AT1 receptors in rabbit aorta membrane
ChEMBL 666 11 1 8 6.4 CCCc1nc2ccc(N(C)C(=O)OCC(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/S0960-894X(01)81125-2
44377125 55335 0 None - 0 Rabbit 9.3 pIC50 = 9.3 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aortaIn vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aorta
ChEMBL 545 10 1 7 5.0 CCCc1nc(CC)c(C(=O)OC)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/S0960-894X(01)81124-0
CHEMBL162148 55335 0 None - 0 Rabbit 9.3 pIC50 = 9.3 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aortaIn vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aorta
ChEMBL 545 10 1 7 5.0 CCCc1nc(CC)c(C(=O)OC)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/S0960-894X(01)81124-0
10032851 16641 0 None - 0 Human 9.3 pIC50 = 9.3 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 729 11 2 9 6.6 CCCCc1nn(-c2cc(NC(=O)CC)ccc2Br)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1021/jm00019a004
CHEMBL124771 16641 0 None - 0 Human 9.3 pIC50 = 9.3 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 729 11 2 9 6.6 CCCCc1nn(-c2cc(NC(=O)CC)ccc2Br)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1021/jm00019a004
11765177 116494 0 None - 0 Rabbit 9.3 pIC50 = 9.3 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 685 11 2 9 6.4 CCCCC(=O)Nc1ccc(Cl)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1007/s00044-011-9815-x
CHEMBL338888 116494 0 None - 0 Rabbit 9.3 pIC50 = 9.3 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 685 11 2 9 6.4 CCCCC(=O)Nc1ccc(Cl)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1007/s00044-011-9815-x
19939753 202050 0 None - 0 Rabbit 9.3 pIC50 = 9.3 Binding
In vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranesIn vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranes
ChEMBL 605 13 2 8 6.4 CCCCOC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCC)nc3c(C)c(NC(=O)CCC)cnc32)cc1 10.1016/S0960-894X(01)81115-X
CHEMBL67921 202050 0 None - 0 Rabbit 9.3 pIC50 = 9.3 Binding
In vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranesIn vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranes
ChEMBL 605 13 2 8 6.4 CCCCOC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCC)nc3c(C)c(NC(=O)CCC)cnc32)cc1 10.1016/S0960-894X(01)81115-X
11765177 116494 0 None - 0 Rabbit 9.3 pIC50 = 9.3 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 685 11 2 9 6.4 CCCCC(=O)Nc1ccc(Cl)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1021/jm00019a004
CHEMBL338888 116494 0 None - 0 Rabbit 9.3 pIC50 = 9.3 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 685 11 2 9 6.4 CCCCC(=O)Nc1ccc(Cl)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1021/jm00019a004
11765177 116494 0 None - 0 Rabbit 9.3 pIC50 = 9.3 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 685 11 2 9 6.4 CCCCC(=O)Nc1ccc(Cl)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1007/s00044-011-9815-x
CHEMBL338888 116494 0 None - 0 Rabbit 9.3 pIC50 = 9.3 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 685 11 2 9 6.4 CCCCC(=O)Nc1ccc(Cl)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1007/s00044-011-9815-x
44315144 96131 0 None - 0 Rabbit 9.3 pIC50 = 9.3 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membrane
ChEMBL 665 13 3 8 5.2 CCCc1nc2ccc(NC(=O)NC(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)COCC(C)C)cc1F 10.1016/0960-894X(94)85036-4
CHEMBL263191 96131 0 None - 0 Rabbit 9.3 pIC50 = 9.3 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membrane
ChEMBL 665 13 3 8 5.2 CCCc1nc2ccc(NC(=O)NC(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)COCC(C)C)cc1F 10.1016/0960-894X(94)85036-4
10439858 16667 0 None - 0 Rabbit 9.3 pIC50 = 9.3 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 719 11 2 9 6.2 CCCCNC(=O)c1ccc(C(F)(F)F)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1007/s00044-011-9815-x
CHEMBL124903 16667 0 None - 0 Rabbit 9.3 pIC50 = 9.3 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 719 11 2 9 6.2 CCCCNC(=O)c1ccc(C(F)(F)F)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1007/s00044-011-9815-x
18950609 16213 0 None - 0 Rabbit 9.3 pIC50 = 9.3 Binding
Displacement of [1251][Sar1,IIe8]AII from rabbit aorta Angiotensin II receptor, type 1Displacement of [1251][Sar1,IIe8]AII from rabbit aorta Angiotensin II receptor, type 1
ChEMBL 533 11 1 5 7.4 CCCc1cc(Cn2c(CC)nc3c(C)cc(C)nc32)cc(CCC)c1OC(C(=O)O)c1ccccc1Cl 10.1021/jm00075a033
CHEMBL123084 16213 0 None - 0 Rabbit 9.3 pIC50 = 9.3 Binding
Displacement of [1251][Sar1,IIe8]AII from rabbit aorta Angiotensin II receptor, type 1Displacement of [1251][Sar1,IIe8]AII from rabbit aorta Angiotensin II receptor, type 1
ChEMBL 533 11 1 5 7.4 CCCc1cc(Cn2c(CC)nc3c(C)cc(C)nc32)cc(CCC)c1OC(C(=O)O)c1ccccc1Cl 10.1021/jm00075a033
10439858 16667 0 None - 0 Rabbit 9.3 pIC50 = 9.3 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 719 11 2 9 6.2 CCCCNC(=O)c1ccc(C(F)(F)F)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1021/jm00019a004
CHEMBL124903 16667 0 None - 0 Rabbit 9.3 pIC50 = 9.3 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 719 11 2 9 6.2 CCCCNC(=O)c1ccc(C(F)(F)F)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1021/jm00019a004
10439858 16667 0 None - 0 Rabbit 9.3 pIC50 = 9.3 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 719 11 2 9 6.2 CCCCNC(=O)c1ccc(C(F)(F)F)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1007/s00044-011-9815-x
CHEMBL124903 16667 0 None - 0 Rabbit 9.3 pIC50 = 9.3 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 719 11 2 9 6.2 CCCCNC(=O)c1ccc(C(F)(F)F)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1007/s00044-011-9815-x
183134 203126 13 None - 1 Rabbit 9.3 pIC50 = 9.3 Binding
Displacement of [1251][Sar1,IIe8]AII from rabbit aorta Angiotensin II receptor, type 1Displacement of [1251][Sar1,IIe8]AII from rabbit aorta Angiotensin II receptor, type 1
ChEMBL 409 5 1 6 4.5 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a033
CHEMBL7550 203126 13 None - 1 Rabbit 9.3 pIC50 = 9.3 Binding
Displacement of [1251][Sar1,IIe8]AII from rabbit aorta Angiotensin II receptor, type 1Displacement of [1251][Sar1,IIe8]AII from rabbit aorta Angiotensin II receptor, type 1
ChEMBL 409 5 1 6 4.5 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00075a033
44315282 96163 0 None - 0 Rabbit 9.3 pIC50 = 9.3 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membrane
ChEMBL 683 10 2 7 6.4 CCc1ccc(C(=O)NS(=O)(=O)c2ccccc2-c2ccc(Cn3c(CC)nc4ccc(NC(=O)N(C)C(C)C)cc4c3=O)c(F)c2)cc1 10.1016/0960-894X(94)85036-4
CHEMBL263452 96163 0 None - 0 Rabbit 9.3 pIC50 = 9.3 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membrane
ChEMBL 683 10 2 7 6.4 CCc1ccc(C(=O)NS(=O)(=O)c2ccccc2-c2ccc(Cn3c(CC)nc4ccc(NC(=O)N(C)C(C)C)cc4c3=O)c(F)c2)cc1 10.1016/0960-894X(94)85036-4
14971639 113620 0 None - 0 Rabbit 9.3 pIC50 = 9.3 Binding
Displacement of [125I]Sar1,I1e8-AII from AT1 receptor in rabbit aorta membraneDisplacement of [125I]Sar1,I1e8-AII from AT1 receptor in rabbit aorta membrane
ChEMBL 512 9 2 6 6.1 CCCCc1nc(-c2ccccc2Cl)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1039/d2md00206j
CHEMBL332897 113620 0 None - 0 Rabbit 9.3 pIC50 = 9.3 Binding
Displacement of [125I]Sar1,I1e8-AII from AT1 receptor in rabbit aorta membraneDisplacement of [125I]Sar1,I1e8-AII from AT1 receptor in rabbit aorta membrane
ChEMBL 512 9 2 6 6.1 CCCCc1nc(-c2ccccc2Cl)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1039/d2md00206j
9939191 98476 1 None - 1 Rabbit 9.3 pIC50 = 9.3 Binding
In vitro binding affinity towards angiotensin-1 receptor to displace 125I[Sar,Ile] from rabbit brain tissue preparationIn vitro binding affinity towards angiotensin-1 receptor to displace 125I[Sar,Ile] from rabbit brain tissue preparation
ChEMBL 634 10 1 7 6.2 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/S0960-894X(01)81132-X
CHEMBL279629 98476 1 None - 1 Rabbit 9.3 pIC50 = 9.3 Binding
In vitro binding affinity towards angiotensin-1 receptor to displace 125I[Sar,Ile] from rabbit brain tissue preparationIn vitro binding affinity towards angiotensin-1 receptor to displace 125I[Sar,Ile] from rabbit brain tissue preparation
ChEMBL 634 10 1 7 6.2 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/S0960-894X(01)81132-X
CHEMBL97539 98476 1 None - 1 Rabbit 9.3 pIC50 = 9.3 Binding
In vitro binding affinity towards angiotensin-1 receptor to displace 125I[Sar,Ile] from rabbit brain tissue preparationIn vitro binding affinity towards angiotensin-1 receptor to displace 125I[Sar,Ile] from rabbit brain tissue preparation
ChEMBL 634 10 1 7 6.2 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/S0960-894X(01)81132-X
10101608 116515 0 None - 0 Human 9.3 pIC50 = 9.3 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 751 14 2 8 7.2 CCCCNC(=O)c1ccc(Cl)c(-n2nc(CCCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)c4ccccc4Cl)cc3F)c2=O)c1 10.1021/jm00019a004
CHEMBL339004 116515 0 None - 0 Human 9.3 pIC50 = 9.3 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 751 14 2 8 7.2 CCCCNC(=O)c1ccc(Cl)c(-n2nc(CCCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)c4ccccc4Cl)cc3F)c2=O)c1 10.1021/jm00019a004
44381425 119935 0 None - 0 Rabbit 9.3 pIC50 = 9.3 Binding
Tested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membraneTested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membrane
ChEMBL 681 12 3 8 7.2 CCCc1nc2ccc(NC(=O)Nc3ccccc3)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1 10.1016/S0960-894X(01)81126-4
CHEMBL353980 119935 0 None - 0 Rabbit 9.3 pIC50 = 9.3 Binding
Tested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membraneTested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membrane
ChEMBL 681 12 3 8 7.2 CCCc1nc2ccc(NC(=O)Nc3ccccc3)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1 10.1016/S0960-894X(01)81126-4
10032193 118627 0 None - 0 Rabbit 9.3 pIC50 = 9.3 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 649 10 2 8 6.1 CCCCc1nn(-c2cc(N)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1007/s00044-013-0831-x
CHEMBL342843 118627 0 None - 0 Rabbit 9.3 pIC50 = 9.3 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 649 10 2 8 6.1 CCCCc1nn(-c2cc(N)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1007/s00044-013-0831-x
10394829 118842 0 None - 0 Rabbit 9.3 pIC50 = 9.3 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 683 10 2 8 6.5 CCCCc1nn(-c2ccc(N)cc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1007/s00044-013-0831-x
CHEMBL344387 118842 0 None - 0 Rabbit 9.3 pIC50 = 9.3 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 683 10 2 8 6.5 CCCCc1nn(-c2ccc(N)cc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1007/s00044-013-0831-x
10417321 15427 0 None - 0 Rabbit 9.3 pIC50 = 9.3 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 701 9 2 9 5.8 CCC(=O)Nc1ccc(Br)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1007/s00044-011-9815-x
CHEMBL122157 15427 0 None - 0 Rabbit 9.3 pIC50 = 9.3 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 701 9 2 9 5.8 CCC(=O)Nc1ccc(Br)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1007/s00044-011-9815-x
10417321 15427 0 None - 0 Rabbit 9.3 pIC50 = 9.3 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 701 9 2 9 5.8 CCC(=O)Nc1ccc(Br)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1021/jm00019a004
CHEMBL122157 15427 0 None - 0 Rabbit 9.3 pIC50 = 9.3 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 701 9 2 9 5.8 CCC(=O)Nc1ccc(Br)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1021/jm00019a004
10438745 106719 0 None - 0 Rabbit 9.3 pIC50 = 9.3 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 612 10 1 7 5.6 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)C2CC2C)cc1 10.1021/jm00043a020
CHEMBL316655 106719 0 None - 0 Rabbit 9.3 pIC50 = 9.3 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 612 10 1 7 5.6 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)C2CC2C)cc1 10.1021/jm00043a020
10258694 112079 0 None - 0 Rabbit 9.3 pIC50 = 9.3 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 648 10 1 7 6.5 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2C)cc1 10.1021/jm00043a020
CHEMBL330165 112079 0 None - 0 Rabbit 9.3 pIC50 = 9.3 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 648 10 1 7 6.5 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2C)cc1 10.1021/jm00043a020
10010071 116833 0 None - 0 Human 9.3 pIC50 = 9.3 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 715 13 2 10 6.1 CCCCc1nn(-c2cc(NC(=O)COCC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1021/jm00019a004
CHEMBL339722 116833 0 None - 0 Human 9.3 pIC50 = 9.3 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 715 13 2 10 6.1 CCCCc1nn(-c2cc(NC(=O)COCC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1021/jm00019a004
10032193 118627 0 None - 0 Rabbit 9.3 pIC50 = 9.3 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 649 10 2 8 6.1 CCCCc1nn(-c2cc(N)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1021/jm00052a006
CHEMBL342843 118627 0 None - 0 Rabbit 9.3 pIC50 = 9.3 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 649 10 2 8 6.1 CCCCc1nn(-c2cc(N)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1021/jm00052a006
10394829 118842 0 None - 0 Rabbit 9.3 pIC50 = 9.3 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 683 10 2 8 6.5 CCCCc1nn(-c2ccc(N)cc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1021/jm00052a006
CHEMBL344387 118842 0 None - 0 Rabbit 9.3 pIC50 = 9.3 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 683 10 2 8 6.5 CCCCc1nn(-c2ccc(N)cc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1021/jm00052a006
10417321 15427 0 None - 0 Rabbit 9.3 pIC50 = 9.3 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 701 9 2 9 5.8 CCC(=O)Nc1ccc(Br)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1007/s00044-011-9815-x
CHEMBL122157 15427 0 None - 0 Rabbit 9.3 pIC50 = 9.3 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 701 9 2 9 5.8 CCC(=O)Nc1ccc(Br)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1007/s00044-011-9815-x
19430475 202540 0 None - 0 Human 9.2 pIC50 = 9.2 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 787 16 1 9 8.5 CCCc1nc(CC)c(C(=O)OCc2ccccc2C(=O)c2ccccc2)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCc2ccccc2)cc1F 10.1016/S0960-894X(00)80077-3
CHEMBL71125 202540 0 None - 0 Human 9.2 pIC50 = 9.2 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 787 16 1 9 8.5 CCCc1nc(CC)c(C(=O)OCc2ccccc2C(=O)c2ccccc2)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCc2ccccc2)cc1F 10.1016/S0960-894X(00)80077-3
9874508 202964 0 None - 0 Rabbit 9.2 pIC50 = 9.2 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membrane
ChEMBL 663 11 2 8 5.9 CCc1nc2ccc(NC(=O)N(C)C(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC2CC2)cc1F 10.1016/0960-894X(94)85036-4
CHEMBL73876 202964 0 None - 0 Rabbit 9.2 pIC50 = 9.2 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membrane
ChEMBL 663 11 2 8 5.9 CCc1nc2ccc(NC(=O)N(C)C(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC2CC2)cc1F 10.1016/0960-894X(94)85036-4
9874508 202964 0 None - 0 Rabbit 9.2 pIC50 = 9.2 Binding
Inhibition of Angiotensin II receptor, type 1Inhibition of Angiotensin II receptor, type 1
ChEMBL 663 11 2 8 5.9 CCc1nc2ccc(NC(=O)N(C)C(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC2CC2)cc1F 10.1021/jm9504722
CHEMBL73876 202964 0 None - 0 Rabbit 9.2 pIC50 = 9.2 Binding
Inhibition of Angiotensin II receptor, type 1Inhibition of Angiotensin II receptor, type 1
ChEMBL 663 11 2 8 5.9 CCc1nc2ccc(NC(=O)N(C)C(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC2CC2)cc1F 10.1021/jm9504722
CHEMBL938 214120 24 None 1 2 Human 9.2 pIC50 = 9.2 Binding
Inhibition of human angiotensin II AT1 receptorInhibition of human angiotensin II AT1 receptor
ChEMBL None None None CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O)C(C)C)C(C)C 10.1016/j.bmc.2010.07.034
44274855 96481 0 None - 0 Rabbit 9.2 pIC50 = 9.2 Binding
Displacement of [125I]Sar1-Ile8-AII (without BSA) from type 1 Angiotensin II receptor of rabbit aortaDisplacement of [125I]Sar1-Ile8-AII (without BSA) from type 1 Angiotensin II receptor of rabbit aorta
ChEMBL 564 9 1 7 5.5 CCCCc1nc2ccc(N(C)C(=O)N(C)C(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80335-2
CHEMBL26614 96481 0 None - 0 Rabbit 9.2 pIC50 = 9.2 Binding
Displacement of [125I]Sar1-Ile8-AII (without BSA) from type 1 Angiotensin II receptor of rabbit aortaDisplacement of [125I]Sar1-Ile8-AII (without BSA) from type 1 Angiotensin II receptor of rabbit aorta
ChEMBL 564 9 1 7 5.5 CCCCc1nc2ccc(N(C)C(=O)N(C)C(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80335-2
9960852 106685 0 None - 0 Rabbit 9.2 pIC50 = 9.2 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 630 12 1 8 6.3 CCCCOC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCCC)nn(-c3ccccc3C(F)(F)F)c2=O)cc1 10.1021/jm00043a020
CHEMBL316482 106685 0 None - 0 Rabbit 9.2 pIC50 = 9.2 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 630 12 1 8 6.3 CCCCOC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCCC)nn(-c3ccccc3C(F)(F)F)c2=O)cc1 10.1021/jm00043a020
10030110 16059 0 None - 0 Human 9.2 pIC50 = 9.2 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 536 12 2 8 4.6 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2Cc2csc(N)n2)n1Cc1ccc(C(=O)O)cc1 10.1007/s00044-009-9205-9
CHEMBL122443 16059 0 None - 0 Human 9.2 pIC50 = 9.2 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 536 12 2 8 4.6 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2Cc2csc(N)n2)n1Cc1ccc(C(=O)O)cc1 10.1007/s00044-009-9205-9
10256602 16672 0 None - 0 Human 9.2 pIC50 = 9.2 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 534 12 1 6 5.9 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2Cc2ccc(C)s2)n1Cc1ccc(C(=O)O)cc1 10.1007/s00044-009-9205-9
CHEMBL124925 16672 0 None - 0 Human 9.2 pIC50 = 9.2 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 534 12 1 6 5.9 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2Cc2ccc(C)s2)n1Cc1ccc(C(=O)O)cc1 10.1007/s00044-009-9205-9
10052399 117951 0 None - 0 Human 9.2 pIC50 = 9.2 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 520 12 1 6 5.6 CCCCc1ncc(/C=C2\C(=O)N(CCCC)C(=O)N2Cc2cccs2)n1Cc1ccc(C(=O)O)cc1 10.1007/s00044-009-9205-9
CHEMBL341295 117951 0 None - 0 Human 9.2 pIC50 = 9.2 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 520 12 1 6 5.6 CCCCc1ncc(/C=C2\C(=O)N(CCCC)C(=O)N2Cc2cccs2)n1Cc1ccc(C(=O)O)cc1 10.1007/s00044-009-9205-9
44311617 102053 0 None - 0 Human 9.2 pIC50 = 9.2 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 679 13 1 9 6.7 CCCc1nc(CC)c(C(=O)OCc2ccccc2C(=O)c2ccccc2)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC)cc1 10.1016/S0960-894X(00)80077-3
CHEMBL304065 102053 0 None - 0 Human 9.2 pIC50 = 9.2 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 679 13 1 9 6.7 CCCc1nc(CC)c(C(=O)OCc2ccccc2C(=O)c2ccccc2)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC)cc1 10.1016/S0960-894X(00)80077-3
44311618 162773 0 None - 0 Human 9.2 pIC50 = 9.2 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 772 16 2 8 7.8 CCCc1nc(CC)c(C(=O)NCc2ccccc2[S+]([O-])c2ccccc2)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/S0960-894X(00)80077-3
CHEMBL419073 162773 0 None - 0 Human 9.2 pIC50 = 9.2 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 772 16 2 8 7.8 CCCc1nc(CC)c(C(=O)NCc2ccccc2[S+]([O-])c2ccccc2)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/S0960-894X(00)80077-3
19430479 202557 0 None - 0 Human 9.2 pIC50 = 9.2 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 753 16 1 9 8.3 CCCc1nc(CC)c(C(=O)OCc2cccc(C(=O)c3ccccc3)c2)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/S0960-894X(00)80077-3
CHEMBL71220 202557 0 None - 0 Human 9.2 pIC50 = 9.2 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 753 16 1 9 8.3 CCCc1nc(CC)c(C(=O)OCc2cccc(C(=O)c3ccccc3)c2)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/S0960-894X(00)80077-3
44311184 202706 0 None - 0 Human 9.2 pIC50 = 9.2 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 727 16 1 9 8.6 CCCCOC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCC)nc(CC)c2C(=O)OCc2ccccc2Oc2ccccc2)c(F)c1 10.1016/S0960-894X(00)80077-3
CHEMBL72099 202706 0 None - 0 Human 9.2 pIC50 = 9.2 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 727 16 1 9 8.6 CCCCOC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCC)nc(CC)c2C(=O)OCc2ccccc2Oc2ccccc2)c(F)c1 10.1016/S0960-894X(00)80077-3
44311558 203005 0 None - 0 Human 9.2 pIC50 = 9.2 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 731 15 1 9 8.8 CCCc1nc(CC)c(C(=O)OCc2ccccc2-c2ccsc2)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/S0960-894X(00)80077-3
CHEMBL74236 203005 0 None - 0 Human 9.2 pIC50 = 9.2 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 731 15 1 9 8.8 CCCc1nc(CC)c(C(=O)OCc2ccccc2-c2ccsc2)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/S0960-894X(00)80077-3
CHEMBL938 214120 24 None 1 2 Human 9.2 pIC50 = 9.2 Binding
Binding affinity to human angiotensin AT1 receptor by radioligand displacement assayBinding affinity to human angiotensin AT1 receptor by radioligand displacement assay
ChEMBL None None None CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O)C(C)C)C(C)C 10.1016/j.bmc.2013.03.016
44309902 102629 0 None - 0 Rabbit 9.2 pIC50 = 9.2 Binding
In vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranesIn vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranes
ChEMBL 598 12 1 7 7.4 CCCCc1nc2c(C)c(N(CCCC)C(=O)c3ccccc3)cnc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81115-X
CHEMBL307757 102629 0 None - 0 Rabbit 9.2 pIC50 = 9.2 Binding
In vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranesIn vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranes
ChEMBL 598 12 1 7 7.4 CCCCc1nc2c(C)c(N(CCCC)C(=O)c3ccccc3)cnc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81115-X
44309703 171976 0 None - 0 Rabbit 9.2 pIC50 = 9.2 Binding
In vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranesIn vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranes
ChEMBL 633 10 2 7 8.3 CCCCc1nc2cc(NC(=O)N(c3ccccc3)c3ccccc3)c(C)nc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81115-X
CHEMBL448476 171976 0 None - 0 Rabbit 9.2 pIC50 = 9.2 Binding
In vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranesIn vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranes
ChEMBL 633 10 2 7 8.3 CCCCc1nc2cc(NC(=O)N(c3ccccc3)c3ccccc3)c(C)nc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81115-X
44309903 202679 0 None - 0 Rabbit 9.2 pIC50 = 9.2 Binding
In vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranesIn vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranes
ChEMBL 633 10 2 7 8.3 CCCCc1nc2c(C)c(NC(=O)N(c3ccccc3)c3ccccc3)cnc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81115-X
CHEMBL71925 202679 0 None - 0 Rabbit 9.2 pIC50 = 9.2 Binding
In vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranesIn vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranes
ChEMBL 633 10 2 7 8.3 CCCCc1nc2c(C)c(NC(=O)N(c3ccccc3)c3ccccc3)cnc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81115-X
10010027 206282 0 None - 0 Rabbit 9.2 pIC50 = 9.2 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 710 11 1 7 7.9 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2-c2ccccc2)cc1 10.1021/jm00043a020
CHEMBL97465 206282 0 None - 0 Rabbit 9.2 pIC50 = 9.2 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 710 11 1 7 7.9 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2-c2ccccc2)cc1 10.1021/jm00043a020
44309903 202679 0 None - 0 Rabbit 9.2 pIC50 = 9.2 Binding
Inhibition of Angiotensin II receptor, type 1Inhibition of Angiotensin II receptor, type 1
ChEMBL 633 10 2 7 8.3 CCCCc1nc2c(C)c(NC(=O)N(c3ccccc3)c3ccccc3)cnc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm9504722
CHEMBL71925 202679 0 None - 0 Rabbit 9.2 pIC50 = 9.2 Binding
Inhibition of Angiotensin II receptor, type 1Inhibition of Angiotensin II receptor, type 1
ChEMBL 633 10 2 7 8.3 CCCCc1nc2c(C)c(NC(=O)N(c3ccccc3)c3ccccc3)cnc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm9504722
10372810 105708 0 None - 0 Rabbit 9.2 pIC50 = 9.2 Binding
In vitro ability to inhibit the binding of radioligand 125I[Sar1,IIe8]AII to AT1 receptor from rabbit aortaIn vitro ability to inhibit the binding of radioligand 125I[Sar1,IIe8]AII to AT1 receptor from rabbit aorta
ChEMBL 735 13 2 8 7.1 CCCCc1nn(-c2cc(NC(C)=O)ccc2Cl)c(=O)n1Cc1ccc(-c2cc(CCC)ccc2S(=O)(=O)NC(=O)c2ccccc2F)cc1F 10.1016/S0960-894X(01)80595-3
CHEMBL313868 105708 0 None - 0 Rabbit 9.2 pIC50 = 9.2 Binding
In vitro ability to inhibit the binding of radioligand 125I[Sar1,IIe8]AII to AT1 receptor from rabbit aortaIn vitro ability to inhibit the binding of radioligand 125I[Sar1,IIe8]AII to AT1 receptor from rabbit aorta
ChEMBL 735 13 2 8 7.1 CCCCc1nn(-c2cc(NC(C)=O)ccc2Cl)c(=O)n1Cc1ccc(-c2cc(CCC)ccc2S(=O)(=O)NC(=O)c2ccccc2F)cc1F 10.1016/S0960-894X(01)80595-3
15292111 203027 0 None - 0 Rabbit 9.2 pIC50 = 9.2 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membrane
ChEMBL 665 11 2 8 6.1 CCc1nc2ccc(NC(=O)N(C)C(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/0960-894X(94)85036-4
CHEMBL74442 203027 0 None - 0 Rabbit 9.2 pIC50 = 9.2 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membrane
ChEMBL 665 11 2 8 6.1 CCc1nc2ccc(NC(=O)N(C)C(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/0960-894X(94)85036-4
10485202 118902 0 None - 0 Rabbit 9.2 pIC50 = 9.2 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 747 14 1 8 7.4 CCCCc1nn(-c2cc(C(=O)N(C)CCCC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1007/s00044-013-0831-x
CHEMBL344811 118902 0 None - 0 Rabbit 9.2 pIC50 = 9.2 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 747 14 1 8 7.4 CCCCc1nn(-c2cc(C(=O)N(C)CCCC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1007/s00044-013-0831-x
10485202 118902 0 None - 0 Rabbit 9.2 pIC50 = 9.2 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 747 14 1 8 7.4 CCCCc1nn(-c2cc(C(=O)N(C)CCCC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1021/jm00052a006
CHEMBL344811 118902 0 None - 0 Rabbit 9.2 pIC50 = 9.2 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 747 14 1 8 7.4 CCCCc1nn(-c2cc(C(=O)N(C)CCCC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1021/jm00052a006
1952 2170 3 None - 2 Rabbit 9.2 pIC50 = 9.2 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 654 10 1 8 6.6 CCCCc1nn(c(=O)n1Cc1ccc(cc1)c1ccccc1S(=O)(=O)NC(=O)c1ccc(s1)C)c1ccccc1C(F)(F)F 10.1021/jm00043a020
5312129 2170 3 None - 2 Rabbit 9.2 pIC50 = 9.2 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 654 10 1 8 6.6 CCCCc1nn(c(=O)n1Cc1ccc(cc1)c1ccccc1S(=O)(=O)NC(=O)c1ccc(s1)C)c1ccccc1C(F)(F)F 10.1021/jm00043a020
CHEMBL1182768 2170 3 None - 2 Rabbit 9.2 pIC50 = 9.2 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 654 10 1 8 6.6 CCCCc1nn(c(=O)n1Cc1ccc(cc1)c1ccccc1S(=O)(=O)NC(=O)c1ccc(s1)C)c1ccccc1C(F)(F)F 10.1021/jm00043a020
9874086 108613 0 None - 0 Rabbit 9.2 pIC50 = 9.2 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 634 10 1 7 5.6 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)C2CC2(F)F)cc1 10.1021/jm00043a020
CHEMBL321367 108613 0 None - 0 Rabbit 9.2 pIC50 = 9.2 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 634 10 1 7 5.6 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)C2CC2(F)F)cc1 10.1021/jm00043a020
10439715 116521 0 None - 0 Human 9.2 pIC50 = 9.2 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 699 12 2 9 6.2 CCCCc1nn(-c2cc(C(=O)NCCC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1021/jm00019a004
CHEMBL339040 116521 0 None - 0 Human 9.2 pIC50 = 9.2 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 699 12 2 9 6.2 CCCCc1nn(-c2cc(C(=O)NCCC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1021/jm00019a004
10457566 201105 0 None - 0 Rat 9.2 pIC50 = 9.2 Binding
Tested for binding affinity against angiotensin II receptor in rat adrenal cortexTested for binding affinity against angiotensin II receptor in rat adrenal cortex
ChEMBL 473 8 1 8 1.9 CCCc1cc(=O)n(CC(=O)N(C)C)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/0960-894X(95)00370-9
CHEMBL62269 201105 0 None - 0 Rat 9.2 pIC50 = 9.2 Binding
Tested for binding affinity against angiotensin II receptor in rat adrenal cortexTested for binding affinity against angiotensin II receptor in rat adrenal cortex
ChEMBL 473 8 1 8 1.9 CCCc1cc(=O)n(CC(=O)N(C)C)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/0960-894X(95)00370-9
44282952 119910 0 None - 1 Rat 9.2 pIC50 = 9.2 Binding
In vitro ability to displace the specific binding of [125I]-A II from receptors in rat liver membrane(type 1 receptor)In vitro ability to displace the specific binding of [125I]-A II from receptors in rat liver membrane(type 1 receptor)
ChEMBL 511 7 2 8 3.8 CCc1nn(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/c(=N/C(=O)c2ccccc2C(=O)O)s1 10.1016/S0960-894X(96)00250-8
CHEMBL35381 119910 0 None - 1 Rat 9.2 pIC50 = 9.2 Binding
In vitro ability to displace the specific binding of [125I]-A II from receptors in rat liver membrane(type 1 receptor)In vitro ability to displace the specific binding of [125I]-A II from receptors in rat liver membrane(type 1 receptor)
ChEMBL 511 7 2 8 3.8 CCc1nn(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/c(=N/C(=O)c2ccccc2C(=O)O)s1 10.1016/S0960-894X(96)00250-8
CHEMBL938 214120 24 None 1 2 Human 9.2 pIC50 = 9.2 Binding
Displacement of radiolabeled saralasin from human AT1 receptorDisplacement of radiolabeled saralasin from human AT1 receptor
ChEMBL None None None CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O)C(C)C)C(C)C 10.1021/jm8007618
10350378 206448 0 None - 0 Rabbit 9.2 pIC50 = 9.2 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 796 10 1 8 7.8 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2cc(Br)sc2Br)cc1 10.1021/jm00043a020
CHEMBL98453 206448 0 None - 0 Rabbit 9.2 pIC50 = 9.2 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 796 10 1 8 7.8 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2cc(Br)sc2Br)cc1 10.1021/jm00043a020
10028460 116008 0 None - 0 Rabbit 9.2 pIC50 = 9.2 Binding
In vitro binding affinity for angiotensin II AT1 receptor in rabbit aortaIn vitro binding affinity for angiotensin II AT1 receptor in rabbit aorta
ChEMBL 488 7 1 6 4.5 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)C2CC2)cc1 10.1021/jm00050a002
CHEMBL336180 116008 0 None - 0 Rabbit 9.2 pIC50 = 9.2 Binding
In vitro binding affinity for angiotensin II AT1 receptor in rabbit aortaIn vitro binding affinity for angiotensin II AT1 receptor in rabbit aorta
ChEMBL 488 7 1 6 4.5 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)C2CC2)cc1 10.1021/jm00050a002
10009478 111967 0 None - 0 Rabbit 9.2 pIC50 = 9.2 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 652 10 1 7 6.4 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccc(F)cc2)cc1 10.1021/jm00043a020
CHEMBL329858 111967 0 None - 0 Rabbit 9.2 pIC50 = 9.2 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 652 10 1 7 6.4 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccc(F)cc2)cc1 10.1021/jm00043a020
2541 772 113 None -1 6 Human 9.2 pIC50 = 9.2 Binding
Displacement of [3H]-Angiotensin 2 from human AT1 receptor transfected in CHOK1 cells preincubated for 30 mins with bovine serum albumin followed by radioligand addition by liquid scintillation countingDisplacement of [3H]-Angiotensin 2 from human AT1 receptor transfected in CHOK1 cells preincubated for 30 mins with bovine serum albumin followed by radioligand addition by liquid scintillation counting
ChEMBL 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10.1021/acs.jmedchem.5b01495
587 772 113 None -1 6 Human 9.2 pIC50 = 9.2 Binding
Displacement of [3H]-Angiotensin 2 from human AT1 receptor transfected in CHOK1 cells preincubated for 30 mins with bovine serum albumin followed by radioligand addition by liquid scintillation countingDisplacement of [3H]-Angiotensin 2 from human AT1 receptor transfected in CHOK1 cells preincubated for 30 mins with bovine serum albumin followed by radioligand addition by liquid scintillation counting
ChEMBL 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10.1021/acs.jmedchem.5b01495
6907 772 113 None -1 6 Human 9.2 pIC50 = 9.2 Binding
Displacement of [3H]-Angiotensin 2 from human AT1 receptor transfected in CHOK1 cells preincubated for 30 mins with bovine serum albumin followed by radioligand addition by liquid scintillation countingDisplacement of [3H]-Angiotensin 2 from human AT1 receptor transfected in CHOK1 cells preincubated for 30 mins with bovine serum albumin followed by radioligand addition by liquid scintillation counting
ChEMBL 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10.1021/acs.jmedchem.5b01495
CHEMBL1016 772 113 None -1 6 Human 9.2 pIC50 = 9.2 Binding
Displacement of [3H]-Angiotensin 2 from human AT1 receptor transfected in CHOK1 cells preincubated for 30 mins with bovine serum albumin followed by radioligand addition by liquid scintillation countingDisplacement of [3H]-Angiotensin 2 from human AT1 receptor transfected in CHOK1 cells preincubated for 30 mins with bovine serum albumin followed by radioligand addition by liquid scintillation counting
ChEMBL 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10.1021/acs.jmedchem.5b01495
DB00796 772 113 None -1 6 Human 9.2 pIC50 = 9.2 Binding
Displacement of [3H]-Angiotensin 2 from human AT1 receptor transfected in CHOK1 cells preincubated for 30 mins with bovine serum albumin followed by radioligand addition by liquid scintillation countingDisplacement of [3H]-Angiotensin 2 from human AT1 receptor transfected in CHOK1 cells preincubated for 30 mins with bovine serum albumin followed by radioligand addition by liquid scintillation counting
ChEMBL 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10.1021/acs.jmedchem.5b01495
DB13919 772 113 None -1 6 Human 9.2 pIC50 = 9.2 Binding
Displacement of [3H]-Angiotensin 2 from human AT1 receptor transfected in CHOK1 cells preincubated for 30 mins with bovine serum albumin followed by radioligand addition by liquid scintillation countingDisplacement of [3H]-Angiotensin 2 from human AT1 receptor transfected in CHOK1 cells preincubated for 30 mins with bovine serum albumin followed by radioligand addition by liquid scintillation counting
ChEMBL 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10.1021/acs.jmedchem.5b01495
10414338 17766 0 None - 0 Human 9.2 pIC50 = 9.2 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 520 12 1 6 5.6 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2Cc2cccs2)n1Cc1ccc(C(=O)O)cc1 10.1007/s00044-009-9205-9
CHEMBL126111 17766 0 None - 0 Human 9.2 pIC50 = 9.2 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 520 12 1 6 5.6 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2Cc2cccs2)n1Cc1ccc(C(=O)O)cc1 10.1007/s00044-009-9205-9
9824776 118847 0 None - 0 Rabbit 9.2 pIC50 = 9.2 Binding
Binding affinity to angiotensin AT1 receptor in rabbit aortic ringsBinding affinity to angiotensin AT1 receptor in rabbit aortic rings
ChEMBL 445 5 1 6 4.2 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2C2=NOS(=O)N2)cc1 10.1016/j.bmc.2010.10.043
CHEMBL344407 118847 0 None - 0 Rabbit 9.2 pIC50 = 9.2 Binding
Binding affinity to angiotensin AT1 receptor in rabbit aortic ringsBinding affinity to angiotensin AT1 receptor in rabbit aortic rings
ChEMBL 445 5 1 6 4.2 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2C2=NOS(=O)N2)cc1 10.1016/j.bmc.2010.10.043
60148656 92181 0 None - 0 Human 9.2 pIC50 = 9.2 Binding
Displacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysisDisplacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysis
ChEMBL 457 7 2 5 5.9 CCCc1nc2c(C)cc(NC(=O)OC)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2013.08.014
CHEMBL2435829 92181 0 None - 0 Human 9.2 pIC50 = 9.2 Binding
Displacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysisDisplacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysis
ChEMBL 457 7 2 5 5.9 CCCc1nc2c(C)cc(NC(=O)OC)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2013.08.014
9824776 118847 0 None - 0 Rabbit 9.2 pIC50 = 9.2 Binding
Displacement of the specific binding ligand [125I]Sar1,Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane.Displacement of the specific binding ligand [125I]Sar1,Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane.
ChEMBL 445 5 1 6 4.2 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2C2=NOS(=O)N2)cc1 10.1016/S0960-894X(01)81119-7
CHEMBL344407 118847 0 None - 0 Rabbit 9.2 pIC50 = 9.2 Binding
Displacement of the specific binding ligand [125I]Sar1,Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane.Displacement of the specific binding ligand [125I]Sar1,Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane.
ChEMBL 445 5 1 6 4.2 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2C2=NOS(=O)N2)cc1 10.1016/S0960-894X(01)81119-7
15292113 95574 0 None - 0 Human 9.2 pIC50 = 9.2 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membrane
ChEMBL 693 11 2 9 5.5 CCCc1nc2ccc(NC(=O)N3CCOCC3)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/0960-894X(94)85036-4
CHEMBL259843 95574 0 None - 0 Human 9.2 pIC50 = 9.2 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membrane
ChEMBL 693 11 2 9 5.5 CCCc1nc2ccc(NC(=O)N3CCOCC3)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/0960-894X(94)85036-4
10349801 107439 0 None - 0 Rabbit 9.1 pIC50 = 9.1 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 702 10 1 7 7.5 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2cccc(Cl)c2Cl)cc1 10.1021/jm00043a020
CHEMBL319353 107439 0 None - 0 Rabbit 9.1 pIC50 = 9.1 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 702 10 1 7 7.5 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2cccc(Cl)c2Cl)cc1 10.1021/jm00043a020
10417431 108608 0 None - 0 Rabbit 9.1 pIC50 = 9.1 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 718 10 1 8 7.1 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2sccc2Br)cc1 10.1021/jm00043a020
CHEMBL321363 108608 0 None - 0 Rabbit 9.1 pIC50 = 9.1 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 718 10 1 8 7.1 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2sccc2Br)cc1 10.1021/jm00043a020
10101606 15580 0 None - 0 Human 9.1 pIC50 = 9.1 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 751 12 2 8 6.6 CCCCC(=O)Nc1ccc(Br)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)c4ccccc4F)cc3F)c2=O)c1 10.1021/jm00019a004
CHEMBL122273 15580 0 None - 0 Human 9.1 pIC50 = 9.1 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 751 12 2 8 6.6 CCCCC(=O)Nc1ccc(Br)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)c4ccccc4F)cc3F)c2=O)c1 10.1021/jm00019a004
16133225 415 47 None -2 6 Human 9.1 pIC50 = 9.1 Binding
Displacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation countingDisplacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation counting
ChEMBL None None None None 10.1021/acs.jmedchem.5b01495
172198 415 47 None -2 6 Human 9.1 pIC50 = 9.1 Binding
Displacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation countingDisplacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation counting
ChEMBL None None None None 10.1021/acs.jmedchem.5b01495
2504 415 47 None -2 6 Human 9.1 pIC50 = 9.1 Binding
Displacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation countingDisplacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation counting
ChEMBL None None None None 10.1021/acs.jmedchem.5b01495
45266664 415 47 None -2 6 Human 9.1 pIC50 = 9.1 Binding
Displacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation countingDisplacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation counting
ChEMBL None None None None 10.1021/acs.jmedchem.5b01495
5272 415 47 None -2 6 Human 9.1 pIC50 = 9.1 Binding
Displacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation countingDisplacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation counting
ChEMBL None None None None 10.1021/acs.jmedchem.5b01495
CHEMBL408403 415 47 None -2 6 Human 9.1 pIC50 = 9.1 Binding
Displacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation countingDisplacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation counting
ChEMBL None None None None 10.1021/acs.jmedchem.5b01495
DB11842 415 47 None -2 6 Human 9.1 pIC50 = 9.1 Binding
Displacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation countingDisplacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation counting
ChEMBL None None None None 10.1021/acs.jmedchem.5b01495
15292112 102462 0 None - 0 Rabbit 9.1 pIC50 = 9.1 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membrane
ChEMBL 635 11 3 8 5.2 CCNC(=O)Nc1ccc2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OCCC4CC4)cc3F)c(=O)c2c1 10.1016/0960-894X(94)85036-4
CHEMBL306361 102462 0 None - 0 Rabbit 9.1 pIC50 = 9.1 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membrane
ChEMBL 635 11 3 8 5.2 CCNC(=O)Nc1ccc2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OCCC4CC4)cc3F)c(=O)c2c1 10.1016/0960-894X(94)85036-4
14956763 162833 0 None - 0 Rabbit 9.1 pIC50 = 9.1 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 526 10 1 10 4.2 CCCCc1nn(-c2ccc(OC)cc2[N+](=O)[O-])c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
CHEMBL419483 162833 0 None - 0 Rabbit 9.1 pIC50 = 9.1 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 526 10 1 10 4.2 CCCCc1nn(-c2ccc(OC)cc2[N+](=O)[O-])c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
19430458 202366 0 None - 0 Human 9.1 pIC50 = 9.1 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 769 16 1 9 8.4 CCCc1nc(CC)c(C(=O)OCc2ccccc2C(=O)c2ccccc2)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCc2ccccc2)cc1 10.1016/S0960-894X(00)80077-3
CHEMBL70100 202366 0 None - 0 Human 9.1 pIC50 = 9.1 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 769 16 1 9 8.4 CCCc1nc(CC)c(C(=O)OCc2ccccc2C(=O)c2ccccc2)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCc2ccccc2)cc1 10.1016/S0960-894X(00)80077-3
18950608 15480 0 None - 0 Rabbit 9.1 pIC50 = 9.1 Binding
Displacement of [1251][Sar1,IIe8]AII from rabbit aorta Angiotensin II receptor, type 1Displacement of [1251][Sar1,IIe8]AII from rabbit aorta Angiotensin II receptor, type 1
ChEMBL 513 11 1 5 7.1 CCCc1cc(Cn2c(CC)nc3c(C)cc(C)nc32)cc(CCC)c1OC(C(=O)O)c1cccc(C)c1 10.1021/jm00075a033
CHEMBL122224 15480 0 None - 0 Rabbit 9.1 pIC50 = 9.1 Binding
Displacement of [1251][Sar1,IIe8]AII from rabbit aorta Angiotensin II receptor, type 1Displacement of [1251][Sar1,IIe8]AII from rabbit aorta Angiotensin II receptor, type 1
ChEMBL 513 11 1 5 7.1 CCCc1cc(Cn2c(CC)nc3c(C)cc(C)nc32)cc(CCC)c1OC(C(=O)O)c1cccc(C)c1 10.1021/jm00075a033
10032361 112216 0 None - 0 Rabbit 9.1 pIC50 = 9.1 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 664 11 1 8 6.2 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccc(OC)cc2)cc1 10.1021/jm00043a020
CHEMBL330463 112216 0 None - 0 Rabbit 9.1 pIC50 = 9.1 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 664 11 1 8 6.2 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccc(OC)cc2)cc1 10.1021/jm00043a020
9987414 116535 0 None - 0 Human 9.1 pIC50 = 9.1 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 719 11 2 9 6.8 CCCCc1nn(-c2cc(NC(=O)CC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1021/jm00019a004
CHEMBL339113 116535 0 None - 0 Human 9.1 pIC50 = 9.1 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 719 11 2 9 6.8 CCCCc1nn(-c2cc(NC(=O)CC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1021/jm00019a004
44275095 94721 0 None - 0 Rabbit 9.1 pIC50 = 9.1 Binding
Ability to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitroAbility to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitro
ChEMBL 536 9 3 7 5.2 CCCCc1nc2ccc(NC(=O)NC(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80335-2
CHEMBL25585 94721 0 None - 0 Rabbit 9.1 pIC50 = 9.1 Binding
Ability to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitroAbility to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitro
ChEMBL 536 9 3 7 5.2 CCCCc1nc2ccc(NC(=O)NC(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80335-2
18950586 15373 0 None - 0 Rabbit 9.1 pIC50 = 9.1 Binding
Displacement of [1251][Sar1,IIe8]AII from rabbit aorta Angiotensin II receptor, type 1Displacement of [1251][Sar1,IIe8]AII from rabbit aorta Angiotensin II receptor, type 1
ChEMBL 533 11 1 5 7.4 CCCc1cc(Cn2c(CC)nc3c(C)cc(C)nc32)cc(CCC)c1OC(C(=O)O)c1cccc(Cl)c1 10.1021/jm00075a033
CHEMBL122017 15373 0 None - 0 Rabbit 9.1 pIC50 = 9.1 Binding
Displacement of [1251][Sar1,IIe8]AII from rabbit aorta Angiotensin II receptor, type 1Displacement of [1251][Sar1,IIe8]AII from rabbit aorta Angiotensin II receptor, type 1
ChEMBL 533 11 1 5 7.4 CCCc1cc(Cn2c(CC)nc3c(C)cc(C)nc32)cc(CCC)c1OC(C(=O)O)c1cccc(Cl)c1 10.1021/jm00075a033
9986299 157893 0 None - 0 Rabbit 9.1 pIC50 = 9.1 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 616 12 1 8 5.0 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)COCC)cc1 10.1021/jm00043a020
CHEMBL409058 157893 0 None - 0 Rabbit 9.1 pIC50 = 9.1 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 616 12 1 8 5.0 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)COCC)cc1 10.1021/jm00043a020
10349392 206300 0 None - 0 Rabbit 9.1 pIC50 = 9.1 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 659 10 1 8 6.1 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccc(C#N)cc2)cc1 10.1021/jm00043a020
CHEMBL97557 206300 0 None - 0 Rabbit 9.1 pIC50 = 9.1 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 659 10 1 8 6.1 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccc(C#N)cc2)cc1 10.1021/jm00043a020
10372659 117574 0 None - 0 Human 9.1 pIC50 = 9.1 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 713 13 2 9 6.6 CCCCNC(=O)c1ccc(Cl)c(-n2nc(CCCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1021/jm00019a004
CHEMBL340632 117574 0 None - 0 Human 9.1 pIC50 = 9.1 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 713 13 2 9 6.6 CCCCNC(=O)c1ccc(Cl)c(-n2nc(CCCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1021/jm00019a004
135955119 123958 0 None - 0 Human 9.1 pIC50 = 9.1 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 612 9 1 10 4.9 CCc1cc2c(=O)n(CC(=O)c3ccc(OC)cc3)c(=O)n(Cc3ccc(-c4ccccc4-c4nc(=O)o[nH]4)cc3F)c2s1 nan
CHEMBL3640129 123958 0 None - 0 Human 9.1 pIC50 = 9.1 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 612 9 1 10 4.9 CCc1cc2c(=O)n(CC(=O)c3ccc(OC)cc3)c(=O)n(Cc3ccc(-c4ccccc4-c4nc(=O)o[nH]4)cc3F)c2s1 nan
53321879 57278 0 None - 0 Rabbit 9.1 pIC50 = 9.1 Binding
Binding affinity to angiotensin AT1 receptor in rabbit aortic ringsBinding affinity to angiotensin AT1 receptor in rabbit aortic rings
ChEMBL 470 8 1 5 5.8 CCCCC1=N[C@](C)(C2CCCCC2)C(=O)N1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmc.2010.10.043
CHEMBL1667998 57278 0 None - 0 Rabbit 9.1 pIC50 = 9.1 Binding
Binding affinity to angiotensin AT1 receptor in rabbit aortic ringsBinding affinity to angiotensin AT1 receptor in rabbit aortic rings
ChEMBL 470 8 1 5 5.8 CCCCC1=N[C@](C)(C2CCCCC2)C(=O)N1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmc.2010.10.043
44315304 203291 0 None - 0 Rabbit 9.1 pIC50 = 9.1 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membrane
ChEMBL 663 10 2 8 6.1 CCc1nc2ccc(NC(=O)N(C)C(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCC=C(C)C)cc1F 10.1016/0960-894X(94)85036-4
CHEMBL76821 203291 0 None - 0 Rabbit 9.1 pIC50 = 9.1 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membrane
ChEMBL 663 10 2 8 6.1 CCc1nc2ccc(NC(=O)N(C)C(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCC=C(C)C)cc1F 10.1016/0960-894X(94)85036-4
73349224 91747 0 None - 0 Rabbit 9.1 pIC50 = 9.1 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 626 9 1 11 4.0 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)n2cnnn2)cc1 10.1007/s00044-013-0831-x
CHEMBL2425239 91747 0 None - 0 Rabbit 9.1 pIC50 = 9.1 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 626 9 1 11 4.0 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)n2cnnn2)cc1 10.1007/s00044-013-0831-x
14956757 67236 0 None - 1 Rabbit 9.1 pIC50 = 9.1 Binding
Displacement of 125I[Sar,Ile] from rabbit aorta membrane Angiotensin II receptor type 1Displacement of 125I[Sar,Ile] from rabbit aorta membrane Angiotensin II receptor type 1
ChEMBL 519 8 1 7 5.3 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81132-X
CHEMBL19018 67236 0 None - 1 Rabbit 9.1 pIC50 = 9.1 Binding
Displacement of 125I[Sar,Ile] from rabbit aorta membrane Angiotensin II receptor type 1Displacement of 125I[Sar,Ile] from rabbit aorta membrane Angiotensin II receptor type 1
ChEMBL 519 8 1 7 5.3 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81132-X
14956757 67236 0 None - 1 Rabbit 9.1 pIC50 = 9.1 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 519 8 1 7 5.3 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00043a020
CHEMBL19018 67236 0 None - 1 Rabbit 9.1 pIC50 = 9.1 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 519 8 1 7 5.3 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00043a020
14956757 67236 0 None - 1 Rabbit 9.1 pIC50 = 9.1 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 519 8 1 7 5.3 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00052a006
CHEMBL19018 67236 0 None - 1 Rabbit 9.1 pIC50 = 9.1 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 519 8 1 7 5.3 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00052a006
44311538 102477 0 None - 0 Human 9.1 pIC50 = 9.1 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 699 14 1 10 6.9 CCCOC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCC)nc(CC)c2C(=O)OCc2ccccc2-c2cncnc2)c(F)c1 10.1016/S0960-894X(00)80077-3
CHEMBL306435 102477 0 None - 0 Human 9.1 pIC50 = 9.1 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 699 14 1 10 6.9 CCCOC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCC)nc(CC)c2C(=O)OCc2ccccc2-c2cncnc2)c(F)c1 10.1016/S0960-894X(00)80077-3
44311183 202984 0 None - 0 Human 9.1 pIC50 = 9.1 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 731 15 1 9 8.8 CCCc1nc(CC)c(C(=O)OCc2ccccc2-c2cccs2)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/S0960-894X(00)80077-3
CHEMBL74069 202984 0 None - 0 Human 9.1 pIC50 = 9.1 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 731 15 1 9 8.8 CCCc1nc(CC)c(C(=O)OCc2ccccc2-c2cccs2)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/S0960-894X(00)80077-3
44311735 203034 0 None - 0 Human 9.1 pIC50 = 9.1 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 753 16 1 9 8.5 CCCc1nc(CC)c(C(=O)OC(C(=O)c2ccccc2)c2ccccc2)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/S0960-894X(00)80077-3
CHEMBL74514 203034 0 None - 0 Human 9.1 pIC50 = 9.1 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 753 16 1 9 8.5 CCCc1nc(CC)c(C(=O)OC(C(=O)c2ccccc2)c2ccccc2)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/S0960-894X(00)80077-3
15076146 106480 0 None - 0 Rat 9.1 pIC50 = 9.1 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 423 6 1 6 4.9 CCCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm031100t
CHEMBL315104 106480 0 None - 0 Rat 9.1 pIC50 = 9.1 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 423 6 1 6 4.9 CCCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm031100t
9914666 116157 0 None - 0 Rabbit 9.1 pIC50 = 9.1 Binding
Binding affinity to angiotensin AT1 receptor in rabbit aortic ringsBinding affinity to angiotensin AT1 receptor in rabbit aortic rings
ChEMBL 520 5 1 6 6.3 CCc1nc2c(C)cc(C)nc2n1Cc1ccc2c(ccn2C(=O)c2c(Cl)ccc(Cl)c2C(=O)O)c1 10.1016/j.bmc.2010.10.043
CHEMBL337086 116157 0 None - 0 Rabbit 9.1 pIC50 = 9.1 Binding
Binding affinity to angiotensin AT1 receptor in rabbit aortic ringsBinding affinity to angiotensin AT1 receptor in rabbit aortic rings
ChEMBL 520 5 1 6 6.3 CCc1nc2c(C)cc(C)nc2n1Cc1ccc2c(ccn2C(=O)c2c(Cl)ccc(Cl)c2C(=O)O)c1 10.1016/j.bmc.2010.10.043
44272246 98320 0 None - 0 Rabbit 9.1 pIC50 = 9.1 Binding
Displacement of 125I[Sar,Ile] from rabbit aorta membrane Angiotensin II receptor type 1Displacement of 125I[Sar,Ile] from rabbit aorta membrane Angiotensin II receptor type 1
ChEMBL 628 11 1 8 5.1 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)C(=O)C(C)C)cc1 10.1016/S0960-894X(01)81132-X
CHEMBL278305 98320 0 None - 0 Rabbit 9.1 pIC50 = 9.1 Binding
Displacement of 125I[Sar,Ile] from rabbit aorta membrane Angiotensin II receptor type 1Displacement of 125I[Sar,Ile] from rabbit aorta membrane Angiotensin II receptor type 1
ChEMBL 628 11 1 8 5.1 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)C(=O)C(C)C)cc1 10.1016/S0960-894X(01)81132-X
44272247 98394 0 None - 0 Rabbit 9.1 pIC50 = 9.1 Binding
Displacement of 125I[Sar,Ile] from rabbit aorta membrane Angiotensin II receptor type 1Displacement of 125I[Sar,Ile] from rabbit aorta membrane Angiotensin II receptor type 1
ChEMBL 654 10 1 8 5.0 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)C(=O)C(F)(F)F)cc1 10.1016/S0960-894X(01)81132-X
CHEMBL278977 98394 0 None - 0 Rabbit 9.1 pIC50 = 9.1 Binding
Displacement of 125I[Sar,Ile] from rabbit aorta membrane Angiotensin II receptor type 1Displacement of 125I[Sar,Ile] from rabbit aorta membrane Angiotensin II receptor type 1
ChEMBL 654 10 1 8 5.0 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)C(=O)C(F)(F)F)cc1 10.1016/S0960-894X(01)81132-X
15076146 106480 0 None - 0 Rat 9.1 pIC50 = 9.1 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
ChEMBL 423 6 1 6 4.9 CCCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm7011563
CHEMBL315104 106480 0 None - 0 Rat 9.1 pIC50 = 9.1 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
ChEMBL 423 6 1 6 4.9 CCCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm7011563
44310586 172068 0 None - 0 Rabbit 9.1 pIC50 = 9.1 Binding
In vitro binding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membraneIn vitro binding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane
ChEMBL 524 7 1 6 5.3 CCc1nc2c(C)cc(C)nn2c1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/S0960-894X(01)81150-1
CHEMBL449648 172068 0 None - 0 Rabbit 9.1 pIC50 = 9.1 Binding
In vitro binding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membraneIn vitro binding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane
ChEMBL 524 7 1 6 5.3 CCc1nc2c(C)cc(C)nn2c1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/S0960-894X(01)81150-1
10483888 110954 0 None - 0 Rabbit 9.1 pIC50 = 9.1 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 612 10 1 7 5.7 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)C2(C)CC2)cc1 10.1021/jm00043a020
CHEMBL327563 110954 0 None - 0 Rabbit 9.1 pIC50 = 9.1 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 612 10 1 7 5.7 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)C2(C)CC2)cc1 10.1021/jm00043a020
10416501 111904 0 None - 0 Rabbit 9.1 pIC50 = 9.1 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 626 9 1 7 5.5 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)C(F)(F)F)cc1 10.1021/jm00043a020
CHEMBL329759 111904 0 None - 0 Rabbit 9.1 pIC50 = 9.1 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 626 9 1 7 5.5 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)C(F)(F)F)cc1 10.1021/jm00043a020
10483726 205832 0 None - 0 Rabbit 9.1 pIC50 = 9.1 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 600 10 1 7 5.6 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)C(C)C)cc1 10.1021/jm00043a020
CHEMBL94910 205832 0 None - 0 Rabbit 9.1 pIC50 = 9.1 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 600 10 1 7 5.6 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)C(C)C)cc1 10.1021/jm00043a020
183134 203126 13 None - 1 Rabbit 9.1 pIC50 = 9.1 Binding
Inhibition of Angiotensin II receptor type 1 in rabbit aorta binding assayInhibition of Angiotensin II receptor type 1 in rabbit aorta binding assay
ChEMBL 409 5 1 6 4.5 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81145-8
CHEMBL7550 203126 13 None - 1 Rabbit 9.1 pIC50 = 9.1 Binding
Inhibition of Angiotensin II receptor type 1 in rabbit aorta binding assayInhibition of Angiotensin II receptor type 1 in rabbit aorta binding assay
ChEMBL 409 5 1 6 4.5 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81145-8
9961192 11246 34 None - 0 Rabbit 9.1 pIC50 = 9.1 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 654 10 1 8 6.6 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2sccc2C)cc1 10.1021/jm00043a020
CHEMBL1179743 11246 34 None - 0 Rabbit 9.1 pIC50 = 9.1 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 654 10 1 8 6.6 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2sccc2C)cc1 10.1021/jm00043a020
CHEMBL97688 11246 34 None - 0 Rabbit 9.1 pIC50 = 9.1 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 654 10 1 8 6.6 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2sccc2C)cc1 10.1021/jm00043a020
10078554 116454 0 None - 0 Rabbit 9.1 pIC50 = 9.1 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 715 12 2 9 6.2 CCCCC(=O)Nc1ccc(Br)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)C)cc3F)c2=O)c1 10.1007/s00044-011-9815-x
CHEMBL338687 116454 0 None - 0 Rabbit 9.1 pIC50 = 9.1 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 715 12 2 9 6.2 CCCCC(=O)Nc1ccc(Br)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)C)cc3F)c2=O)c1 10.1007/s00044-011-9815-x
10078554 116454 0 None - 0 Rabbit 9.1 pIC50 = 9.1 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 715 12 2 9 6.2 CCCCC(=O)Nc1ccc(Br)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)C)cc3F)c2=O)c1 10.1021/jm00019a004
CHEMBL338687 116454 0 None - 0 Rabbit 9.1 pIC50 = 9.1 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 715 12 2 9 6.2 CCCCC(=O)Nc1ccc(Br)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)C)cc3F)c2=O)c1 10.1021/jm00019a004
10010125 206281 0 None - 0 Rabbit 9.1 pIC50 = 9.1 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 724 12 1 7 7.8 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cc2ccccc2)cc1 10.1021/jm00043a020
CHEMBL97464 206281 0 None - 0 Rabbit 9.1 pIC50 = 9.1 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 724 12 1 7 7.8 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cc2ccccc2)cc1 10.1021/jm00043a020
10078554 116454 0 None - 0 Rabbit 9.1 pIC50 = 9.1 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 715 12 2 9 6.2 CCCCC(=O)Nc1ccc(Br)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)C)cc3F)c2=O)c1 10.1007/s00044-011-9815-x
CHEMBL338687 116454 0 None - 0 Rabbit 9.1 pIC50 = 9.1 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 715 12 2 9 6.2 CCCCC(=O)Nc1ccc(Br)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)C)cc3F)c2=O)c1 10.1007/s00044-011-9815-x
44275096 94304 0 None - 0 Rabbit 9.1 pIC50 = 9.1 Binding
Ability to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitroAbility to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitro
ChEMBL 599 10 1 8 6.4 CCCCc1nc2ccc(N(C)C(=O)OCc3ccccc3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80335-2
CHEMBL25315 94304 0 None - 0 Rabbit 9.1 pIC50 = 9.1 Binding
Ability to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitroAbility to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitro
ChEMBL 599 10 1 8 6.4 CCCCc1nc2ccc(N(C)C(=O)OCc3ccccc3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80335-2
10259265 109541 0 None - 0 Rabbit 9.1 pIC50 = 9.1 Binding
In vitro ability to inhibit the binding of radioligand 125I[Sar1,IIe8]AII to AT1 receptor from rabbit aortaIn vitro ability to inhibit the binding of radioligand 125I[Sar1,IIe8]AII to AT1 receptor from rabbit aorta
ChEMBL 713 12 2 9 7.0 CCCCc1nn(-c2cc(NC(C)=O)ccc2Cl)c(=O)n1Cc1ccc(-c2cc(CCC)ccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1016/S0960-894X(01)80595-3
CHEMBL323506 109541 0 None - 0 Rabbit 9.1 pIC50 = 9.1 Binding
In vitro ability to inhibit the binding of radioligand 125I[Sar1,IIe8]AII to AT1 receptor from rabbit aortaIn vitro ability to inhibit the binding of radioligand 125I[Sar1,IIe8]AII to AT1 receptor from rabbit aorta
ChEMBL 713 12 2 9 7.0 CCCCc1nn(-c2cc(NC(C)=O)ccc2Cl)c(=O)n1Cc1ccc(-c2cc(CCC)ccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1016/S0960-894X(01)80595-3
10259265 109541 0 None - 0 Rabbit 9.1 pIC50 = 9.1 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 713 12 2 9 7.0 CCCCc1nn(-c2cc(NC(C)=O)ccc2Cl)c(=O)n1Cc1ccc(-c2cc(CCC)ccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1021/jm00019a004
CHEMBL323506 109541 0 None - 0 Rabbit 9.1 pIC50 = 9.1 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 713 12 2 9 7.0 CCCCc1nn(-c2cc(NC(C)=O)ccc2Cl)c(=O)n1Cc1ccc(-c2cc(CCC)ccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1021/jm00019a004
10077497 11249 0 None - 0 Rabbit 9.1 pIC50 = 9.1 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 612 10 1 7 5.7 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)C2CCC2)cc1 10.1021/jm00043a020
CHEMBL1179757 11249 0 None - 0 Rabbit 9.1 pIC50 = 9.1 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 612 10 1 7 5.7 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)C2CCC2)cc1 10.1021/jm00043a020
CHEMBL98426 11249 0 None - 0 Rabbit 9.1 pIC50 = 9.1 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 612 10 1 7 5.7 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)C2CCC2)cc1 10.1021/jm00043a020
11765560 15347 0 None - 0 Human 9.1 pIC50 = 9.1 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 743 12 2 9 6.3 CCCCNC(=O)c1ccc(Br)c(-n2nc(CCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1021/jm00019a004
CHEMBL121872 15347 0 None - 0 Human 9.1 pIC50 = 9.1 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 743 12 2 9 6.3 CCCCNC(=O)c1ccc(Br)c(-n2nc(CCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1021/jm00019a004
44314761 102368 0 None - 0 Human 9.1 pIC50 = 9.1 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membrane
ChEMBL 701 11 3 7 6.6 CCCc1nc2ccc(NC(=O)NC(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccc(CC)cc2F)cc1F 10.1016/0960-894X(94)85036-4
CHEMBL305647 102368 0 None - 0 Human 9.1 pIC50 = 9.1 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membrane
ChEMBL 701 11 3 7 6.6 CCCc1nc2ccc(NC(=O)NC(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccc(CC)cc2F)cc1F 10.1016/0960-894X(94)85036-4
10394712 118859 0 None - 0 Rabbit 9.1 pIC50 = 9.1 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 671 12 2 8 6.2 CCCCc1nn(-c2cccc(NC(=O)CC)c2)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1007/s00044-013-0831-x
CHEMBL344467 118859 0 None - 0 Rabbit 9.1 pIC50 = 9.1 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 671 12 2 8 6.2 CCCCc1nn(-c2cccc(NC(=O)CC)c2)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1007/s00044-013-0831-x
14956739 204569 0 None - 1 Rabbit 9.1 pIC50 = 9.1 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 496 9 1 9 4.2 CCCCc1nn(-c2ccccc2[N+](=O)[O-])c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
CHEMBL87074 204569 0 None - 1 Rabbit 9.1 pIC50 = 9.1 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 496 9 1 9 4.2 CCCCc1nn(-c2ccccc2[N+](=O)[O-])c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
10394712 118859 0 None - 0 Rabbit 9.1 pIC50 = 9.1 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 671 12 2 8 6.2 CCCCc1nn(-c2cccc(NC(=O)CC)c2)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1021/jm00052a006
CHEMBL344467 118859 0 None - 0 Rabbit 9.1 pIC50 = 9.1 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 671 12 2 8 6.2 CCCCc1nn(-c2cccc(NC(=O)CC)c2)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1021/jm00052a006
44381528 58669 0 None - 0 Rabbit 9.1 pIC50 = 9.1 Binding
Tested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membraneTested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membrane
ChEMBL 548 10 2 8 4.9 CCCCOC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCC)nc3ccc(N)cc3c2=O)cc1 10.1016/S0960-894X(01)81126-4
CHEMBL169009 58669 0 None - 0 Rabbit 9.1 pIC50 = 9.1 Binding
Tested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membraneTested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membrane
ChEMBL 548 10 2 8 4.9 CCCCOC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCC)nc3ccc(N)cc3c2=O)cc1 10.1016/S0960-894X(01)81126-4
10032877 15359 0 None - 0 Human 9.1 pIC50 = 9.1 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 733 12 2 9 6.6 CCCCNC(=O)c1ccc(C(F)(F)F)c(-n2nc(CCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1021/jm00019a004
CHEMBL121907 15359 0 None - 0 Human 9.1 pIC50 = 9.1 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 733 12 2 9 6.6 CCCCNC(=O)c1ccc(C(F)(F)F)c(-n2nc(CCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1021/jm00019a004
44314823 161326 0 None - 0 Human 9.1 pIC50 = 9.1 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membrane
ChEMBL 679 13 2 8 6.7 CCCCOC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCCC)nc3ccc(NC(=O)N(C)C(C)C)cc3c2=O)c(F)c1 10.1016/0960-894X(94)85036-4
CHEMBL415073 161326 0 None - 0 Human 9.1 pIC50 = 9.1 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membrane
ChEMBL 679 13 2 8 6.7 CCCCOC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCCC)nc3ccc(NC(=O)N(C)C(C)C)cc3c2=O)c(F)c1 10.1016/0960-894X(94)85036-4
10484866 31554 0 None - 0 Rabbit 9.1 pIC50 = 9.1 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 699 14 2 8 7.0 CCCCC(=O)Nc1cccc(-n2nc(CCCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)c4ccccc4Cl)cc3)c2=O)c1 10.1007/s00044-013-0831-x
CHEMBL140619 31554 0 None - 0 Rabbit 9.1 pIC50 = 9.1 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 699 14 2 8 7.0 CCCCC(=O)Nc1cccc(-n2nc(CCCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)c4ccccc4Cl)cc3)c2=O)c1 10.1007/s00044-013-0831-x
9984181 117931 0 None - 0 Human 9.1 pIC50 = 9.1 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 520 12 1 6 5.6 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2Cc2ccsc2)n1Cc1ccc(C(=O)O)cc1 10.1007/s00044-009-9205-9
CHEMBL341131 117931 0 None - 0 Human 9.1 pIC50 = 9.1 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 520 12 1 6 5.6 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2Cc2ccsc2)n1Cc1ccc(C(=O)O)cc1 10.1007/s00044-009-9205-9
44277573 99067 0 None - 0 Human 9.1 pIC50 = 9.1 Binding
Binding affinity against AT1 receptor in human adrenal tissueBinding affinity against AT1 receptor in human adrenal tissue
ChEMBL 604 8 0 9 5.5 Cn1nnnc1-c1ccccc1-c1ccc(Cn2cnc3ccc(N(Cc4cccnc4)C(=O)c4ccccc4)cc3c2=O)cc1 10.1016/0960-894X(95)00224-H
CHEMBL283495 99067 0 None - 0 Human 9.1 pIC50 = 9.1 Binding
Binding affinity against AT1 receptor in human adrenal tissueBinding affinity against AT1 receptor in human adrenal tissue
ChEMBL 604 8 0 9 5.5 Cn1nnnc1-c1ccccc1-c1ccc(Cn2cnc3ccc(N(Cc4cccnc4)C(=O)c4ccccc4)cc3c2=O)cc1 10.1016/0960-894X(95)00224-H
44277871 99226 0 None - 0 Rabbit 9.1 pIC50 = 9.1 Binding
Binding affinity against AT1 receptor in rabbit aortaBinding affinity against AT1 receptor in rabbit aorta
ChEMBL 599 10 1 9 5.8 CCCCCN(C(=O)c1ccc(O)cc1)c1ccc2ncn(Cc3ccc(-c4ccccc4-c4nnnn4C)cc3)c(=O)c2c1 10.1016/0960-894X(95)00224-H
CHEMBL28464 99226 0 None - 0 Rabbit 9.1 pIC50 = 9.1 Binding
Binding affinity against AT1 receptor in rabbit aortaBinding affinity against AT1 receptor in rabbit aorta
ChEMBL 599 10 1 9 5.8 CCCCCN(C(=O)c1ccc(O)cc1)c1ccc2ncn(Cc3ccc(-c4ccccc4-c4nnnn4C)cc3)c(=O)c2c1 10.1016/0960-894X(95)00224-H
192626 15468 13 None - 0 Rabbit 9.1 pIC50 = 9.1 Binding
Displacement of [1251][Sar1,IIe8]AII from rabbit aorta Angiotensin II receptor, type 1Displacement of [1251][Sar1,IIe8]AII from rabbit aorta Angiotensin II receptor, type 1
ChEMBL 499 11 1 5 6.8 CCCc1cc(Cn2c(CC)nc3c(C)cc(C)nc32)cc(CCC)c1OC(C(=O)O)c1ccccc1 10.1021/jm00075a033
CHEMBL122212 15468 13 None - 0 Rabbit 9.1 pIC50 = 9.1 Binding
Displacement of [1251][Sar1,IIe8]AII from rabbit aorta Angiotensin II receptor, type 1Displacement of [1251][Sar1,IIe8]AII from rabbit aorta Angiotensin II receptor, type 1
ChEMBL 499 11 1 5 6.8 CCCc1cc(Cn2c(CC)nc3c(C)cc(C)nc32)cc(CCC)c1OC(C(=O)O)c1ccccc1 10.1021/jm00075a033
1481 2027 109 None - 3 Rat 9.1 pIC50 = 9.1 Binding
Displacement of [125I]- Ang II from type 1 Angiotensin II receptorDisplacement of [125I]- Ang II from type 1 Angiotensin II receptor
ChEMBL 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 10.1016/S0960-894X(01)80526-6
3749 2027 109 None - 3 Rat 9.1 pIC50 = 9.1 Binding
Displacement of [125I]- Ang II from type 1 Angiotensin II receptorDisplacement of [125I]- Ang II from type 1 Angiotensin II receptor
ChEMBL 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 10.1016/S0960-894X(01)80526-6
589 2027 109 None - 3 Rat 9.1 pIC50 = 9.1 Binding
Displacement of [125I]- Ang II from type 1 Angiotensin II receptorDisplacement of [125I]- Ang II from type 1 Angiotensin II receptor
ChEMBL 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 10.1016/S0960-894X(01)80526-6
6908 2027 109 None - 3 Rat 9.1 pIC50 = 9.1 Binding
Displacement of [125I]- Ang II from type 1 Angiotensin II receptorDisplacement of [125I]- Ang II from type 1 Angiotensin II receptor
ChEMBL 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 10.1016/S0960-894X(01)80526-6
CHEMBL1513 2027 109 None - 3 Rat 9.1 pIC50 = 9.1 Binding
Displacement of [125I]- Ang II from type 1 Angiotensin II receptorDisplacement of [125I]- Ang II from type 1 Angiotensin II receptor
ChEMBL 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 10.1016/S0960-894X(01)80526-6
DB01029 2027 109 None - 3 Rat 9.1 pIC50 = 9.1 Binding
Displacement of [125I]- Ang II from type 1 Angiotensin II receptorDisplacement of [125I]- Ang II from type 1 Angiotensin II receptor
ChEMBL 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 10.1016/S0960-894X(01)80526-6
44285267 147904 27 None - 0 Rat 9.1 pIC50 = 9.1 Binding
Displacement of [125I]- Ang II from type 1 Angiotensin II receptorDisplacement of [125I]- Ang II from type 1 Angiotensin II receptor
ChEMBL 414 6 1 5 4.4 CCCC1=NC2(CCCC2)C(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80526-6
CHEMBL39379 147904 27 None - 0 Rat 9.1 pIC50 = 9.1 Binding
Displacement of [125I]- Ang II from type 1 Angiotensin II receptorDisplacement of [125I]- Ang II from type 1 Angiotensin II receptor
ChEMBL 414 6 1 5 4.4 CCCC1=NC2(CCCC2)C(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80526-6
44274731 99592 0 None - 0 Rabbit 9.1 pIC50 = 9.1 Binding
Displacement of [125I]Sar1-Ile8-AII (without BSA) from type 1 Angiotensin II receptor of rabbit aortaDisplacement of [125I]Sar1-Ile8-AII (without BSA) from type 1 Angiotensin II receptor of rabbit aorta
ChEMBL 498 8 1 7 4.4 CCCCc1nc2ccc([S+](C)[O-])cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80335-2
CHEMBL287184 99592 0 None - 0 Rabbit 9.1 pIC50 = 9.1 Binding
Displacement of [125I]Sar1-Ile8-AII (without BSA) from type 1 Angiotensin II receptor of rabbit aortaDisplacement of [125I]Sar1-Ile8-AII (without BSA) from type 1 Angiotensin II receptor of rabbit aorta
ChEMBL 498 8 1 7 4.4 CCCCc1nc2ccc([S+](C)[O-])cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80335-2
70682146 75963 0 None - 1 Human 9.1 pIC50 = 9.1 Binding
Displacement of [125I]Sar1Ile8-Ang2 from angiotensin AT1 receptor after 180 mins by gamma countingDisplacement of [125I]Sar1Ile8-Ang2 from angiotensin AT1 receptor after 180 mins by gamma counting
ChEMBL 569 10 2 6 6.7 CCCc1nc2c(C)cc(C(=O)NCC(C)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmc.2012.05.056
CHEMBL2058860 75963 0 None - 1 Human 9.1 pIC50 = 9.1 Binding
Displacement of [125I]Sar1Ile8-Ang2 from angiotensin AT1 receptor after 180 mins by gamma countingDisplacement of [125I]Sar1Ile8-Ang2 from angiotensin AT1 receptor after 180 mins by gamma counting
ChEMBL 569 10 2 6 6.7 CCCc1nc2c(C)cc(C(=O)NCC(C)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmc.2012.05.056
10078800 108691 0 None - 0 Rabbit 9.1 pIC50 = 9.1 Binding
In vitro ability to inhibit the binding of radioligand 125I[Sar1,IIe8]AII to AT1 receptor from rabbit aortaIn vitro ability to inhibit the binding of radioligand 125I[Sar1,IIe8]AII to AT1 receptor from rabbit aorta
ChEMBL 751 13 2 8 7.6 CCCCc1nn(-c2cc(NC(C)=O)ccc2Cl)c(=O)n1Cc1ccc(-c2cc(CCC)ccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1F 10.1016/S0960-894X(01)80595-3
CHEMBL321531 108691 0 None - 0 Rabbit 9.1 pIC50 = 9.1 Binding
In vitro ability to inhibit the binding of radioligand 125I[Sar1,IIe8]AII to AT1 receptor from rabbit aortaIn vitro ability to inhibit the binding of radioligand 125I[Sar1,IIe8]AII to AT1 receptor from rabbit aorta
ChEMBL 751 13 2 8 7.6 CCCCc1nn(-c2cc(NC(C)=O)ccc2Cl)c(=O)n1Cc1ccc(-c2cc(CCC)ccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1F 10.1016/S0960-894X(01)80595-3
44311635 101741 0 None - 0 Human 9.1 pIC50 = 9.1 Binding
In vitro binding affinity of compound against Angiotensin II receptor, type 1In vitro binding affinity of compound against Angiotensin II receptor, type 1
ChEMBL 581 10 2 9 4.3 CCCc1nc(CN2CCN(c3ccccn3)CC2)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1F 10.1016/S0960-894X(00)80076-1
CHEMBL302959 101741 0 None - 0 Human 9.1 pIC50 = 9.1 Binding
In vitro binding affinity of compound against Angiotensin II receptor, type 1In vitro binding affinity of compound against Angiotensin II receptor, type 1
ChEMBL 581 10 2 9 4.3 CCCc1nc(CN2CCN(c3ccccn3)CC2)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1F 10.1016/S0960-894X(00)80076-1
10032988 116404 0 None - 0 Human 9.1 pIC50 = 9.1 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 747 13 2 9 7.6 CCCCC(=O)Nc1ccc(C(F)(F)F)c(-n2nc(CCCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1021/jm00019a004
CHEMBL338434 116404 0 None - 0 Human 9.1 pIC50 = 9.1 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 747 13 2 9 7.6 CCCCC(=O)Nc1ccc(C(F)(F)F)c(-n2nc(CCCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1021/jm00019a004
44385182 60733 0 None - 0 Rabbit 9.1 pIC50 = 9.1 Binding
Inhibition of [125I]-Sar1-Ile8-Ang II binding to Angiotensin II receptor type 1 from rabbit aortaInhibition of [125I]-Sar1-Ile8-Ang II binding to Angiotensin II receptor type 1 from rabbit aorta
ChEMBL 637 10 3 7 5.7 CCCc1nc2ccc(NC(=O)NC(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/0960-894X(96)00116-3
CHEMBL176473 60733 0 None - 0 Rabbit 9.1 pIC50 = 9.1 Binding
Inhibition of [125I]-Sar1-Ile8-Ang II binding to Angiotensin II receptor type 1 from rabbit aortaInhibition of [125I]-Sar1-Ile8-Ang II binding to Angiotensin II receptor type 1 from rabbit aorta
ChEMBL 637 10 3 7 5.7 CCCc1nc2ccc(NC(=O)NC(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/0960-894X(96)00116-3
10484866 31554 0 None - 0 Rabbit 9.1 pIC50 = 9.1 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 699 14 2 8 7.0 CCCCC(=O)Nc1cccc(-n2nc(CCCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)c4ccccc4Cl)cc3)c2=O)c1 10.1021/jm00052a006
CHEMBL140619 31554 0 None - 0 Rabbit 9.1 pIC50 = 9.1 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 699 14 2 8 7.0 CCCCC(=O)Nc1cccc(-n2nc(CCCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)c4ccccc4Cl)cc3)c2=O)c1 10.1021/jm00052a006
10372550 163953 0 None - 0 Rabbit 9.0 pIC50 = 9.0 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 698 13 1 9 7.5 CCCCC(=O)c1ccc(Cl)c(-n2nc(CCCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1007/s00044-011-9815-x
CHEMBL421478 163953 0 None - 0 Rabbit 9.0 pIC50 = 9.0 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 698 13 1 9 7.5 CCCCC(=O)c1ccc(Cl)c(-n2nc(CCCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1007/s00044-011-9815-x
10372550 163953 0 None - 0 Rabbit 9.0 pIC50 = 9.0 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 698 13 1 9 7.5 CCCCC(=O)c1ccc(Cl)c(-n2nc(CCCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1021/jm00019a004
CHEMBL421478 163953 0 None - 0 Rabbit 9.0 pIC50 = 9.0 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 698 13 1 9 7.5 CCCCC(=O)c1ccc(Cl)c(-n2nc(CCCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1021/jm00019a004
10372550 163953 0 None - 0 Rabbit 9.0 pIC50 = 9.0 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 698 13 1 9 7.5 CCCCC(=O)c1ccc(Cl)c(-n2nc(CCCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1007/s00044-011-9815-x
CHEMBL421478 163953 0 None - 0 Rabbit 9.0 pIC50 = 9.0 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 698 13 1 9 7.5 CCCCC(=O)c1ccc(Cl)c(-n2nc(CCCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1007/s00044-011-9815-x
145946921 167028 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
Displacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysisDisplacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysis
ChEMBL 592 11 1 7 5.5 CCCCc1c[n+](Cc2ccc(-c3ccccc3-c3nn[n-]n3)cc2)cn1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.ejmech.2012.12.044
CHEMBL2337687 167028 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
Displacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysisDisplacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysis
ChEMBL 592 11 1 7 5.5 CCCCc1c[n+](Cc2ccc(-c3ccccc3-c3nn[n-]n3)cc2)cn1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.ejmech.2012.12.044
CHEMBL2337688 167028 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
Displacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysisDisplacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysis
ChEMBL 592 11 1 7 5.5 CCCCc1c[n+](Cc2ccc(-c3ccccc3-c3nn[n-]n3)cc2)cn1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.ejmech.2012.12.044
CHEMBL4300967 167028 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
Displacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysisDisplacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysis
ChEMBL 592 11 1 7 5.5 CCCCc1c[n+](Cc2ccc(-c3ccccc3-c3nn[n-]n3)cc2)cn1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.ejmech.2012.12.044
44314780 102591 0 None - 0 Rabbit 9.0 pIC50 = 9.0 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membrane
ChEMBL 649 11 3 8 5.6 CCc1nc2ccc(NC(=O)NC(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC2CC2)cc1F 10.1016/0960-894X(94)85036-4
CHEMBL307430 102591 0 None - 0 Rabbit 9.0 pIC50 = 9.0 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membrane
ChEMBL 649 11 3 8 5.6 CCc1nc2ccc(NC(=O)NC(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC2CC2)cc1F 10.1016/0960-894X(94)85036-4
14956772 105454 0 None - 0 Rabbit 9.0 pIC50 = 9.0 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 510 10 1 9 4.6 CCCCCc1nn(-c2ccccc2[N+](=O)[O-])c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
CHEMBL312913 105454 0 None - 0 Rabbit 9.0 pIC50 = 9.0 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 510 10 1 9 4.6 CCCCCc1nn(-c2ccccc2[N+](=O)[O-])c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
9830839 106435 0 None - 2 Rabbit 9.0 pIC50 = 9.0 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 640 10 1 8 6.3 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2cccs2)cc1 10.1021/jm00043a020
CHEMBL314812 106435 0 None - 2 Rabbit 9.0 pIC50 = 9.0 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 640 10 1 8 6.3 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2cccs2)cc1 10.1021/jm00043a020
10078780 116403 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 749 13 2 10 6.4 CCCCc1nn(-c2cc(NC(=O)COCC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1021/jm00019a004
CHEMBL338433 116403 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 749 13 2 10 6.4 CCCCc1nn(-c2cc(NC(=O)COCC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1021/jm00019a004
10373120 117085 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 791 12 2 8 8.0 CCCCc1nn(-c2cc(NC(=O)CC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2cc(Cl)ccc2Cl)cc1F 10.1021/jm00019a004
CHEMBL340078 117085 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 791 12 2 8 8.0 CCCCc1nn(-c2cc(NC(=O)CC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2cc(Cl)ccc2Cl)cc1F 10.1021/jm00019a004
44381739 58462 0 None - 0 Rabbit 9.0 pIC50 = 9 Binding
Tested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membraneTested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membrane
ChEMBL 656 10 2 7 6.4 CCCc1nc2ccc(NC(=O)c3ccccc3)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/S0960-894X(01)81126-4
CHEMBL168771 58462 0 None - 0 Rabbit 9.0 pIC50 = 9 Binding
Tested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membraneTested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membrane
ChEMBL 656 10 2 7 6.4 CCCc1nc2ccc(NC(=O)c3ccccc3)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/S0960-894X(01)81126-4
44274854 93868 0 None - 0 Rabbit 9.0 pIC50 = 9 Binding
Ability to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitroAbility to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitro
ChEMBL 537 9 2 8 5.1 CCCCc1nc2ccc(OC(=O)NC(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80335-2
CHEMBL25056 93868 0 None - 0 Rabbit 9.0 pIC50 = 9 Binding
Ability to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitroAbility to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitro
ChEMBL 537 9 2 8 5.1 CCCCc1nc2ccc(OC(=O)NC(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80335-2
44274731 99592 0 None - 0 Rabbit 9.0 pIC50 = 9 Binding
Ability to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitroAbility to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitro
ChEMBL 498 8 1 7 4.4 CCCCc1nc2ccc([S+](C)[O-])cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80335-2
CHEMBL287184 99592 0 None - 0 Rabbit 9.0 pIC50 = 9 Binding
Ability to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitroAbility to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitro
ChEMBL 498 8 1 7 4.4 CCCCc1nc2ccc([S+](C)[O-])cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80335-2
10055448 30532 0 None - 0 Rabbit 9.0 pIC50 = 9 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 691 13 2 8 7.3 CCCCc1nn(-c2cc(NCCC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1007/s00044-013-0831-x
CHEMBL139582 30532 0 None - 0 Rabbit 9.0 pIC50 = 9 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 691 13 2 8 7.3 CCCCc1nn(-c2cc(NCCC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1007/s00044-013-0831-x
136052335 123954 0 None - 0 Human 9.0 pIC50 = 9 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 622 8 1 8 5.8 O=c1nc(-c2ccccc2-c2ccc(Cn3c(=O)n(CCc4cccc(F)c4)c(=O)c4cc(CC(F)(F)F)sc43)cc2)[nH]o1 nan
CHEMBL3640125 123954 0 None - 0 Human 9.0 pIC50 = 9 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 622 8 1 8 5.8 O=c1nc(-c2ccccc2-c2ccc(Cn3c(=O)n(CCc4cccc(F)c4)c(=O)c4cc(CC(F)(F)F)sc43)cc2)[nH]o1 nan
136052364 123957 0 None - 0 Human 9.0 pIC50 = 9 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 608 9 1 10 5.0 CCc1cc2c(=O)n(CC(=O)c3ccc(OC)cc3C)c(=O)n(Cc3ccc(-c4ccccc4-c4nc(=O)o[nH]4)cc3)c2s1 nan
CHEMBL3640128 123957 0 None - 0 Human 9.0 pIC50 = 9 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 608 9 1 10 5.0 CCc1cc2c(=O)n(CC(=O)c3ccc(OC)cc3C)c(=O)n(Cc3ccc(-c4ccccc4-c4nc(=O)o[nH]4)cc3)c2s1 nan
135876075 123960 0 None - 0 Human 9.0 pIC50 = 9 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 624 9 1 11 5.6 COc1ccc(C(=O)Cn2c(=O)c3cc(C4CC4)sc3n(Cc3ccc(-c4ccccc4-c4noc(O)n4)cc3F)c2=O)cc1 nan
CHEMBL3640131 123960 0 None - 0 Human 9.0 pIC50 = 9 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 624 9 1 11 5.6 COc1ccc(C(=O)Cn2c(=O)c3cc(C4CC4)sc3n(Cc3ccc(-c4ccccc4-c4noc(O)n4)cc3F)c2=O)cc1 nan
11755602 167871 0 None - 0 Rat 9.0 pIC50 = 9 Binding
Binding affinity against AT1 receptor in the presence of 0.01% BSABinding affinity against AT1 receptor in the presence of 0.01% BSA
ChEMBL 497 9 1 9 3.6 CCCCc1nc2ccn(CC(=O)OC)c(=O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00037a014
CHEMBL43500 167871 0 None - 0 Rat 9.0 pIC50 = 9 Binding
Binding affinity against AT1 receptor in the presence of 0.01% BSABinding affinity against AT1 receptor in the presence of 0.01% BSA
ChEMBL 497 9 1 9 3.6 CCCCc1nc2ccn(CC(=O)OC)c(=O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00037a014
44311754 102510 0 None - 0 Human 9.0 pIC50 = 9 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 757 16 1 9 9.2 CCCc1nc(CC)c(C(=O)OCc2ccccc2Sc2ccccc2)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/S0960-894X(00)80077-3
CHEMBL306761 102510 0 None - 0 Human 9.0 pIC50 = 9 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 757 16 1 9 9.2 CCCc1nc(CC)c(C(=O)OCc2ccccc2Sc2ccccc2)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/S0960-894X(00)80077-3
44311071 102927 0 None - 0 Human 9.0 pIC50 = 9 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 707 18 1 9 8.0 CCCCCCCOC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCC)nc(CC)c2C(=O)OCc2ccccc2OC)c(F)c1 10.1016/S0960-894X(00)80077-3
CHEMBL308482 102927 0 None - 0 Human 9.0 pIC50 = 9 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 707 18 1 9 8.0 CCCCCCCOC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCC)nc(CC)c2C(=O)OCc2ccccc2OC)c(F)c1 10.1016/S0960-894X(00)80077-3
3036053 100850 10 None - 0 Rat 9.0 pIC50 = 9 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 409 6 1 6 4.6 CCCc1nc2c(C)ccnc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm031100t
CHEMBL296725 100850 10 None - 0 Rat 9.0 pIC50 = 9 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 409 6 1 6 4.6 CCCc1nc2c(C)ccnc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm031100t
10322211 168894 0 None - 0 Rabbit 9.0 pIC50 = 9 Binding
Binding affinity to angiotensin AT1 receptor in rabbit aortic ringsBinding affinity to angiotensin AT1 receptor in rabbit aortic rings
ChEMBL 464 6 1 7 4.3 CCc1nc2c(C)cc(C)nc2n1Cc1ccc2c(c1)CCN2C(c1ccccc1)c1nnn[nH]1 10.1016/j.bmc.2010.10.043
CHEMBL442963 168894 0 None - 0 Rabbit 9.0 pIC50 = 9 Binding
Binding affinity to angiotensin AT1 receptor in rabbit aortic ringsBinding affinity to angiotensin AT1 receptor in rabbit aortic rings
ChEMBL 464 6 1 7 4.3 CCc1nc2c(C)cc(C)nc2n1Cc1ccc2c(c1)CCN2C(c1ccccc1)c1nnn[nH]1 10.1016/j.bmc.2010.10.043
15818748 99438 0 None - 0 Rat 9.0 pIC50 = 9 Binding
Displacement of [125I]- Ang II from type 1 Angiotensin II receptorDisplacement of [125I]- Ang II from type 1 Angiotensin II receptor
ChEMBL 543 9 1 5 5.7 CCCCC1=NC2(CCCC2)C(=O)N1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/S0960-894X(01)80526-6
CHEMBL286134 99438 0 None - 0 Rat 9.0 pIC50 = 9 Binding
Displacement of [125I]- Ang II from type 1 Angiotensin II receptorDisplacement of [125I]- Ang II from type 1 Angiotensin II receptor
ChEMBL 543 9 1 5 5.7 CCCCC1=NC2(CCCC2)C(=O)N1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/S0960-894X(01)80526-6
9850811 154190 0 None - 0 Rat 9.0 pIC50 = 9 Binding
Displacement of [125I]- Ang II from type 1 Angiotensin II receptorDisplacement of [125I]- Ang II from type 1 Angiotensin II receptor
ChEMBL 561 8 1 6 5.3 CCCC1=NC2(CCSCC2)C(=O)N1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/S0960-894X(01)80526-6
CHEMBL39996 154190 0 None - 0 Rat 9.0 pIC50 = 9 Binding
Displacement of [125I]- Ang II from type 1 Angiotensin II receptorDisplacement of [125I]- Ang II from type 1 Angiotensin II receptor
ChEMBL 561 8 1 6 5.3 CCCC1=NC2(CCSCC2)C(=O)N1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/S0960-894X(01)80526-6
2583 3705 115 None - 1 Human 9.0 pIC50 = 9 Binding
Displacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysisDisplacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysis
ChEMBL 514 7 1 5 7.3 CCCc1nc2c(n1Cc1ccc(cc1)c1ccccc1C(=O)O)cc(cc2C)c1nc2c(n1C)cccc2 10.1016/j.ejmech.2013.08.014
592 3705 115 None - 1 Human 9.0 pIC50 = 9 Binding
Displacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysisDisplacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysis
ChEMBL 514 7 1 5 7.3 CCCc1nc2c(n1Cc1ccc(cc1)c1ccccc1C(=O)O)cc(cc2C)c1nc2c(n1C)cccc2 10.1016/j.ejmech.2013.08.014
65999 3705 115 None - 1 Human 9.0 pIC50 = 9 Binding
Displacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysisDisplacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysis
ChEMBL 514 7 1 5 7.3 CCCc1nc2c(n1Cc1ccc(cc1)c1ccccc1C(=O)O)cc(cc2C)c1nc2c(n1C)cccc2 10.1016/j.ejmech.2013.08.014
CHEMBL1017 3705 115 None - 1 Human 9.0 pIC50 = 9 Binding
Displacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysisDisplacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysis
ChEMBL 514 7 1 5 7.3 CCCc1nc2c(n1Cc1ccc(cc1)c1ccccc1C(=O)O)cc(cc2C)c1nc2c(n1C)cccc2 10.1016/j.ejmech.2013.08.014
DB00966 3705 115 None - 1 Human 9.0 pIC50 = 9 Binding
Displacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysisDisplacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysis
ChEMBL 514 7 1 5 7.3 CCCc1nc2c(n1Cc1ccc(cc1)c1ccccc1C(=O)O)cc(cc2C)c1nc2c(n1C)cccc2 10.1016/j.ejmech.2013.08.014
2583 3705 115 None - 1 Human 9.0 pIC50 = 9 Binding
Displacement of [125I]Sar1 Ile8-Ang 2 from angiotensin 2 AT1 receptor after 180 mins by gamma countingDisplacement of [125I]Sar1 Ile8-Ang 2 from angiotensin 2 AT1 receptor after 180 mins by gamma counting
ChEMBL 514 7 1 5 7.3 CCCc1nc2c(n1Cc1ccc(cc1)c1ccccc1C(=O)O)cc(cc2C)c1nc2c(n1C)cccc2 10.1016/j.ejmech.2012.01.009
592 3705 115 None - 1 Human 9.0 pIC50 = 9 Binding
Displacement of [125I]Sar1 Ile8-Ang 2 from angiotensin 2 AT1 receptor after 180 mins by gamma countingDisplacement of [125I]Sar1 Ile8-Ang 2 from angiotensin 2 AT1 receptor after 180 mins by gamma counting
ChEMBL 514 7 1 5 7.3 CCCc1nc2c(n1Cc1ccc(cc1)c1ccccc1C(=O)O)cc(cc2C)c1nc2c(n1C)cccc2 10.1016/j.ejmech.2012.01.009
65999 3705 115 None - 1 Human 9.0 pIC50 = 9 Binding
Displacement of [125I]Sar1 Ile8-Ang 2 from angiotensin 2 AT1 receptor after 180 mins by gamma countingDisplacement of [125I]Sar1 Ile8-Ang 2 from angiotensin 2 AT1 receptor after 180 mins by gamma counting
ChEMBL 514 7 1 5 7.3 CCCc1nc2c(n1Cc1ccc(cc1)c1ccccc1C(=O)O)cc(cc2C)c1nc2c(n1C)cccc2 10.1016/j.ejmech.2012.01.009
CHEMBL1017 3705 115 None - 1 Human 9.0 pIC50 = 9 Binding
Displacement of [125I]Sar1 Ile8-Ang 2 from angiotensin 2 AT1 receptor after 180 mins by gamma countingDisplacement of [125I]Sar1 Ile8-Ang 2 from angiotensin 2 AT1 receptor after 180 mins by gamma counting
ChEMBL 514 7 1 5 7.3 CCCc1nc2c(n1Cc1ccc(cc1)c1ccccc1C(=O)O)cc(cc2C)c1nc2c(n1C)cccc2 10.1016/j.ejmech.2012.01.009
DB00966 3705 115 None - 1 Human 9.0 pIC50 = 9 Binding
Displacement of [125I]Sar1 Ile8-Ang 2 from angiotensin 2 AT1 receptor after 180 mins by gamma countingDisplacement of [125I]Sar1 Ile8-Ang 2 from angiotensin 2 AT1 receptor after 180 mins by gamma counting
ChEMBL 514 7 1 5 7.3 CCCc1nc2c(n1Cc1ccc(cc1)c1ccccc1C(=O)O)cc(cc2C)c1nc2c(n1C)cccc2 10.1016/j.ejmech.2012.01.009
2583 3705 115 None - 1 Human 9.0 pIC50 = 9 Binding
Displacement of [125I]Sar1Ile8-Ang2 from angiotensin AT1 receptor after 180 mins by gamma countingDisplacement of [125I]Sar1Ile8-Ang2 from angiotensin AT1 receptor after 180 mins by gamma counting
ChEMBL 514 7 1 5 7.3 CCCc1nc2c(n1Cc1ccc(cc1)c1ccccc1C(=O)O)cc(cc2C)c1nc2c(n1C)cccc2 10.1016/j.bmc.2012.05.056
592 3705 115 None - 1 Human 9.0 pIC50 = 9 Binding
Displacement of [125I]Sar1Ile8-Ang2 from angiotensin AT1 receptor after 180 mins by gamma countingDisplacement of [125I]Sar1Ile8-Ang2 from angiotensin AT1 receptor after 180 mins by gamma counting
ChEMBL 514 7 1 5 7.3 CCCc1nc2c(n1Cc1ccc(cc1)c1ccccc1C(=O)O)cc(cc2C)c1nc2c(n1C)cccc2 10.1016/j.bmc.2012.05.056
65999 3705 115 None - 1 Human 9.0 pIC50 = 9 Binding
Displacement of [125I]Sar1Ile8-Ang2 from angiotensin AT1 receptor after 180 mins by gamma countingDisplacement of [125I]Sar1Ile8-Ang2 from angiotensin AT1 receptor after 180 mins by gamma counting
ChEMBL 514 7 1 5 7.3 CCCc1nc2c(n1Cc1ccc(cc1)c1ccccc1C(=O)O)cc(cc2C)c1nc2c(n1C)cccc2 10.1016/j.bmc.2012.05.056
CHEMBL1017 3705 115 None - 1 Human 9.0 pIC50 = 9 Binding
Displacement of [125I]Sar1Ile8-Ang2 from angiotensin AT1 receptor after 180 mins by gamma countingDisplacement of [125I]Sar1Ile8-Ang2 from angiotensin AT1 receptor after 180 mins by gamma counting
ChEMBL 514 7 1 5 7.3 CCCc1nc2c(n1Cc1ccc(cc1)c1ccccc1C(=O)O)cc(cc2C)c1nc2c(n1C)cccc2 10.1016/j.bmc.2012.05.056
DB00966 3705 115 None - 1 Human 9.0 pIC50 = 9 Binding
Displacement of [125I]Sar1Ile8-Ang2 from angiotensin AT1 receptor after 180 mins by gamma countingDisplacement of [125I]Sar1Ile8-Ang2 from angiotensin AT1 receptor after 180 mins by gamma counting
ChEMBL 514 7 1 5 7.3 CCCc1nc2c(n1Cc1ccc(cc1)c1ccccc1C(=O)O)cc(cc2C)c1nc2c(n1C)cccc2 10.1016/j.bmc.2012.05.056
19939454 205813 0 None - 0 Rabbit 9.0 pIC50 = 9 Binding
In vitro ability to inhibit the binding of radioligand 125I[Sar1,IIe8]AII to AT1 receptor from rabbit aortaIn vitro ability to inhibit the binding of radioligand 125I[Sar1,IIe8]AII to AT1 receptor from rabbit aorta
ChEMBL 761 15 2 8 8.2 CCCCC(=O)Nc1ccc(Cl)c(-n2nc(CCCC)n(Cc3ccc(-c4cc(CC)ccc4S(=O)(=O)NC(=O)c4ccccc4Cl)cc3)c2=O)c1 10.1016/S0960-894X(01)80595-3
CHEMBL94793 205813 0 None - 0 Rabbit 9.0 pIC50 = 9 Binding
In vitro ability to inhibit the binding of radioligand 125I[Sar1,IIe8]AII to AT1 receptor from rabbit aortaIn vitro ability to inhibit the binding of radioligand 125I[Sar1,IIe8]AII to AT1 receptor from rabbit aorta
ChEMBL 761 15 2 8 8.2 CCCCC(=O)Nc1ccc(Cl)c(-n2nc(CCCC)n(Cc3ccc(-c4cc(CC)ccc4S(=O)(=O)NC(=O)c4ccccc4Cl)cc3)c2=O)c1 10.1016/S0960-894X(01)80595-3
3036053 100850 10 None - 0 Rabbit 9.0 pIC50 = 9 Binding
In vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranesIn vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranes
ChEMBL 409 6 1 6 4.6 CCCc1nc2c(C)ccnc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81115-X
CHEMBL296725 100850 10 None - 0 Rabbit 9.0 pIC50 = 9 Binding
In vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranesIn vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranes
ChEMBL 409 6 1 6 4.6 CCCc1nc2c(C)ccnc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81115-X
9851889 101591 0 None - 0 Rabbit 9.0 pIC50 = 9 Binding
In vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranesIn vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranes
ChEMBL 611 12 1 7 7.1 CCCCCN(C(=O)c1ccccc1)c1ccc2nc(CCC)n(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c(=O)c2c1 10.1016/S0960-894X(01)81115-X
CHEMBL302102 101591 0 None - 0 Rabbit 9.0 pIC50 = 9 Binding
In vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranesIn vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranes
ChEMBL 611 12 1 7 7.1 CCCCCN(C(=O)c1ccccc1)c1ccc2nc(CCC)n(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c(=O)c2c1 10.1016/S0960-894X(01)81115-X
3036053 100850 10 None - 0 Rabbit 9.0 pIC50 = 9 Binding
In vitro binding affinity towards Angiotensin II type 1-AT1 receptor determined as its ability to displace 125I-Sarl,Ile8-AII from the receptor expressed in rabbit aorta membrane.In vitro binding affinity towards Angiotensin II type 1-AT1 receptor determined as its ability to displace 125I-Sarl,Ile8-AII from the receptor expressed in rabbit aorta membrane.
ChEMBL 409 6 1 6 4.6 CCCc1nc2c(C)ccnc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80044-X
CHEMBL296725 100850 10 None - 0 Rabbit 9.0 pIC50 = 9 Binding
In vitro binding affinity towards Angiotensin II type 1-AT1 receptor determined as its ability to displace 125I-Sarl,Ile8-AII from the receptor expressed in rabbit aorta membrane.In vitro binding affinity towards Angiotensin II type 1-AT1 receptor determined as its ability to displace 125I-Sarl,Ile8-AII from the receptor expressed in rabbit aorta membrane.
ChEMBL 409 6 1 6 4.6 CCCc1nc2c(C)ccnc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80044-X
44289008 164301 0 None - 0 Rat 9.0 pIC50 = 9 Binding
In vitro inhibition of specific binding of [125I]AII to Angiotensin II receptor, type 1 from rat liver membraneIn vitro inhibition of specific binding of [125I]AII to Angiotensin II receptor, type 1 from rat liver membrane
ChEMBL 442 7 1 5 5.2 CCCCC1=NC2(CCCC2)CC(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81139-2
CHEMBL42200 164301 0 None - 0 Rat 9.0 pIC50 = 9 Binding
In vitro inhibition of specific binding of [125I]AII to Angiotensin II receptor, type 1 from rat liver membraneIn vitro inhibition of specific binding of [125I]AII to Angiotensin II receptor, type 1 from rat liver membrane
ChEMBL 442 7 1 5 5.2 CCCCC1=NC2(CCCC2)CC(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81139-2
10417031 106889 0 None - 0 Rabbit 9.0 pIC50 = 9 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 669 10 1 8 6.3 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2cccnc2Cl)cc1 10.1021/jm00043a020
CHEMBL317864 106889 0 None - 0 Rabbit 9.0 pIC50 = 9 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 669 10 1 8 6.3 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2cccnc2Cl)cc1 10.1021/jm00043a020
10439253 111816 0 None - 0 Rabbit 9.0 pIC50 = 9 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 652 10 1 8 6.4 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2cc(C)oc2C)cc1 10.1021/jm00043a020
CHEMBL329255 111816 0 None - 0 Rabbit 9.0 pIC50 = 9 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 652 10 1 8 6.4 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2cc(C)oc2C)cc1 10.1021/jm00043a020
10439837 16162 0 None - 0 Human 9.0 pIC50 = 9 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 717 12 2 8 6.8 CCCCc1nn(-c2cc(NC(=O)CC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)CC(C)(C)C)cc1F 10.1021/jm00019a004
CHEMBL122917 16162 0 None - 0 Human 9.0 pIC50 = 9 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 717 12 2 8 6.8 CCCCc1nn(-c2cc(NC(=O)CC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)CC(C)(C)C)cc1F 10.1021/jm00019a004
44348523 112667 0 None - 0 Human 9.0 pIC50 = 9 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 723 12 2 8 6.1 CCCNC(=O)c1ccc(C(F)(F)F)c(-n2nc(CCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)c4ccccc4)cc3F)c2=O)c1 10.1021/jm00019a004
CHEMBL331450 112667 0 None - 0 Human 9.0 pIC50 = 9 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 723 12 2 8 6.1 CCCNC(=O)c1ccc(C(F)(F)F)c(-n2nc(CCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)c4ccccc4)cc3F)c2=O)c1 10.1021/jm00019a004
10462683 112770 0 None - 0 Human 9.0 pIC50 = 9 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 735 12 2 10 6.0 CCCc1nn(-c2cc(NC(=O)COCC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1021/jm00019a004
CHEMBL331507 112770 0 None - 0 Human 9.0 pIC50 = 9 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 735 12 2 10 6.0 CCCc1nn(-c2cc(NC(=O)COCC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1021/jm00019a004
9851082 100538 0 None - 0 Human 9.0 pIC50 = 9 Binding
Inhibition of Angiotensin II receptor, type 1Inhibition of Angiotensin II receptor, type 1
ChEMBL 573 12 1 8 5.5 CCCc1nc(CC)c(C(=O)OC)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1021/jm9504722
CHEMBL294512 100538 0 None - 0 Human 9.0 pIC50 = 9 Binding
Inhibition of Angiotensin II receptor, type 1Inhibition of Angiotensin II receptor, type 1
ChEMBL 573 12 1 8 5.5 CCCc1nc(CC)c(C(=O)OC)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1021/jm9504722
44381739 58462 0 None - 0 Rabbit 9.0 pIC50 = 9 Binding
Inhibition of [125I]-Sar1-Ile8-Ang II binding to Angiotensin II receptor type 1 from rabbit aortaInhibition of [125I]-Sar1-Ile8-Ang II binding to Angiotensin II receptor type 1 from rabbit aorta
ChEMBL 656 10 2 7 6.4 CCCc1nc2ccc(NC(=O)c3ccccc3)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/0960-894X(96)00116-3
CHEMBL168771 58462 0 None - 0 Rabbit 9.0 pIC50 = 9 Binding
Inhibition of [125I]-Sar1-Ile8-Ang II binding to Angiotensin II receptor type 1 from rabbit aortaInhibition of [125I]-Sar1-Ile8-Ang II binding to Angiotensin II receptor type 1 from rabbit aorta
ChEMBL 656 10 2 7 6.4 CCCc1nc2ccc(NC(=O)c3ccccc3)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/0960-894X(96)00116-3
CHEMBL938 214120 24 None 1 2 Human 9.0 pIC50 = 9 Binding
Inhibition of human AT1 receptorInhibition of human AT1 receptor
ChEMBL None None None CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O)C(C)C)C(C)C 10.1021/jm701575k
10055448 30532 0 None - 0 Rabbit 9.0 pIC50 = 9 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 691 13 2 8 7.3 CCCCc1nn(-c2cc(NCCC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1021/jm00052a006
CHEMBL139582 30532 0 None - 0 Rabbit 9.0 pIC50 = 9 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 691 13 2 8 7.3 CCCCc1nn(-c2cc(NCCC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1021/jm00052a006
1037 1542 65 None - 1 Rat 9.0 pIC50 = 9 Binding
Tested for inhibition of [125I]- AII specific binding to rat mesenteric arteries, expressed as IC50Tested for inhibition of [125I]- AII specific binding to rat mesenteric arteries, expressed as IC50
ChEMBL 424 10 2 5 4.7 CCCCc1ncc(n1Cc1ccc(cc1)C(=O)O)/C=C(/C(=O)O)\Cc1cccs1 10.1016/S0960-894X(01)81116-1
3940 1542 65 None - 1 Rat 9.0 pIC50 = 9 Binding
Tested for inhibition of [125I]- AII specific binding to rat mesenteric arteries, expressed as IC50Tested for inhibition of [125I]- AII specific binding to rat mesenteric arteries, expressed as IC50
ChEMBL 424 10 2 5 4.7 CCCCc1ncc(n1Cc1ccc(cc1)C(=O)O)/C=C(/C(=O)O)\Cc1cccs1 10.1016/S0960-894X(01)81116-1
5281037 1542 65 None - 1 Rat 9.0 pIC50 = 9 Binding
Tested for inhibition of [125I]- AII specific binding to rat mesenteric arteries, expressed as IC50Tested for inhibition of [125I]- AII specific binding to rat mesenteric arteries, expressed as IC50
ChEMBL 424 10 2 5 4.7 CCCCc1ncc(n1Cc1ccc(cc1)C(=O)O)/C=C(/C(=O)O)\Cc1cccs1 10.1016/S0960-894X(01)81116-1
588 1542 65 None - 1 Rat 9.0 pIC50 = 9 Binding
Tested for inhibition of [125I]- AII specific binding to rat mesenteric arteries, expressed as IC50Tested for inhibition of [125I]- AII specific binding to rat mesenteric arteries, expressed as IC50
ChEMBL 424 10 2 5 4.7 CCCCc1ncc(n1Cc1ccc(cc1)C(=O)O)/C=C(/C(=O)O)\Cc1cccs1 10.1016/S0960-894X(01)81116-1
CHEMBL813 1542 65 None - 1 Rat 9.0 pIC50 = 9 Binding
Tested for inhibition of [125I]- AII specific binding to rat mesenteric arteries, expressed as IC50Tested for inhibition of [125I]- AII specific binding to rat mesenteric arteries, expressed as IC50
ChEMBL 424 10 2 5 4.7 CCCCc1ncc(n1Cc1ccc(cc1)C(=O)O)/C=C(/C(=O)O)\Cc1cccs1 10.1016/S0960-894X(01)81116-1
DB00876 1542 65 None - 1 Rat 9.0 pIC50 = 9 Binding
Tested for inhibition of [125I]- AII specific binding to rat mesenteric arteries, expressed as IC50Tested for inhibition of [125I]- AII specific binding to rat mesenteric arteries, expressed as IC50
ChEMBL 424 10 2 5 4.7 CCCCc1ncc(n1Cc1ccc(cc1)C(=O)O)/C=C(/C(=O)O)\Cc1cccs1 10.1016/S0960-894X(01)81116-1
14952924 196243 0 None - 0 Rat 9.0 pIC50 = 9.0 Binding
Tested for inhibition of [125I]- AII specific binding to rat mesenteric arteries, expressed as IC50Tested for inhibition of [125I]- AII specific binding to rat mesenteric arteries, expressed as IC50
ChEMBL 458 10 2 5 5.4 CCCCc1ncc(/C=C(\Cc2cccs2)C(=O)O)n1Cc1ccc(C(=O)O)c(Cl)c1 10.1016/S0960-894X(01)81116-1
CHEMBL57309 196243 0 None - 0 Rat 9.0 pIC50 = 9.0 Binding
Tested for inhibition of [125I]- AII specific binding to rat mesenteric arteries, expressed as IC50Tested for inhibition of [125I]- AII specific binding to rat mesenteric arteries, expressed as IC50
ChEMBL 458 10 2 5 5.4 CCCCc1ncc(/C=C(\Cc2cccs2)C(=O)O)n1Cc1ccc(C(=O)O)c(Cl)c1 10.1016/S0960-894X(01)81116-1
136052282 123955 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 594 8 1 9 5.2 O=C(Cn1c(=O)c2cc(C3CC3)sc2n(Cc2ccc(-c3ccccc3-c3nc(=O)o[nH]3)cc2)c1=O)c1ccc(F)cc1 nan
CHEMBL3640126 123955 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 594 8 1 9 5.2 O=C(Cn1c(=O)c2cc(C3CC3)sc2n(Cc2ccc(-c3ccccc3-c3nc(=O)o[nH]3)cc2)c1=O)c1ccc(F)cc1 nan
136052259 123961 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 606 9 1 11 5.5 COc1cccc(C(=O)Cn2c(=O)c3cc(C4CC4)sc3n(Cc3ccc(-c4ccccc4-c4noc(O)n4)cc3)c2=O)c1 nan
CHEMBL3640132 123961 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 606 9 1 11 5.5 COc1cccc(C(=O)Cn2c(=O)c3cc(C4CC4)sc3n(Cc3ccc(-c4ccccc4-c4noc(O)n4)cc3)c2=O)c1 nan
44277676 98848 0 None - 0 Rabbit 9.0 pIC50 = 9.0 Binding
Binding affinity against AT1 receptor in rabbit aortaBinding affinity against AT1 receptor in rabbit aorta
ChEMBL 613 11 0 9 6.1 CCCCCN(C(=O)c1ccccc1OC)c1ccc2ncn(Cc3ccc(-c4ccccc4-c4nnnn4C)cc3)c(=O)c2c1 10.1016/0960-894X(95)00224-H
CHEMBL282167 98848 0 None - 0 Rabbit 9.0 pIC50 = 9.0 Binding
Binding affinity against AT1 receptor in rabbit aortaBinding affinity against AT1 receptor in rabbit aorta
ChEMBL 613 11 0 9 6.1 CCCCCN(C(=O)c1ccccc1OC)c1ccc2ncn(Cc3ccc(-c4ccccc4-c4nnnn4C)cc3)c(=O)c2c1 10.1016/0960-894X(95)00224-H
10028209 100934 0 None - 0 Rat 9.0 pIC50 = 9.0 Binding
Binding affinity against AT1 receptor in the presence of 0.01% BSABinding affinity against AT1 receptor in the presence of 0.01% BSA
ChEMBL 482 9 2 8 2.9 CCCCc1nc2ccn(CC(N)=O)c(=O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00037a014
CHEMBL297358 100934 0 None - 0 Rat 9.0 pIC50 = 9.0 Binding
Binding affinity against AT1 receptor in the presence of 0.01% BSABinding affinity against AT1 receptor in the presence of 0.01% BSA
ChEMBL 482 9 2 8 2.9 CCCCc1nc2ccn(CC(N)=O)c(=O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00037a014
3936 2171 28 None 1 4 Human 9.0 pIC50 = 9.0 Binding
Displacement of [125-I]-[Sar1, Ile8]-angiotensin II from AT1R (unknown origin) by radioligand binding assayDisplacement of [125-I]-[Sar1, Ile8]-angiotensin II from AT1R (unknown origin) by radioligand binding assay
ChEMBL 582 11 1 8 6.8 CCCCOC(=O)NS(=O)(=O)c1sc(cc1c1ccc(cc1)Cn1c(CC)nc2c1nc(C)cc2C)CC(C)C 10.1016/j.bmc.2022.116804
6603900 2171 28 None 1 4 Human 9.0 pIC50 = 9.0 Binding
Displacement of [125-I]-[Sar1, Ile8]-angiotensin II from AT1R (unknown origin) by radioligand binding assayDisplacement of [125-I]-[Sar1, Ile8]-angiotensin II from AT1R (unknown origin) by radioligand binding assay
ChEMBL 582 11 1 8 6.8 CCCCOC(=O)NS(=O)(=O)c1sc(cc1c1ccc(cc1)Cn1c(CC)nc2c1nc(C)cc2C)CC(C)C 10.1016/j.bmc.2022.116804
CHEMBL288174 2171 28 None 1 4 Human 9.0 pIC50 = 9.0 Binding
Displacement of [125-I]-[Sar1, Ile8]-angiotensin II from AT1R (unknown origin) by radioligand binding assayDisplacement of [125-I]-[Sar1, Ile8]-angiotensin II from AT1R (unknown origin) by radioligand binding assay
ChEMBL 582 11 1 8 6.8 CCCCOC(=O)NS(=O)(=O)c1sc(cc1c1ccc(cc1)Cn1c(CC)nc2c1nc(C)cc2C)CC(C)C 10.1016/j.bmc.2022.116804
44274692 95986 0 None - 0 Rabbit 9.0 pIC50 = 9.0 Binding
Displacement of [125I]Sar1-Ile8-AII (without BSA) from type 1 Angiotensin II receptor of rabbit aortaDisplacement of [125I]Sar1-Ile8-AII (without BSA) from type 1 Angiotensin II receptor of rabbit aorta
ChEMBL 541 10 2 7 6.2 CCCCc1nc2ccc(NCc3ccccc3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80335-2
CHEMBL26217 95986 0 None - 0 Rabbit 9.0 pIC50 = 9.0 Binding
Displacement of [125I]Sar1-Ile8-AII (without BSA) from type 1 Angiotensin II receptor of rabbit aortaDisplacement of [125I]Sar1-Ile8-AII (without BSA) from type 1 Angiotensin II receptor of rabbit aorta
ChEMBL 541 10 2 7 6.2 CCCCc1nc2ccc(NCc3ccccc3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80335-2
9955424 164561 0 None - 0 Rabbit 9.0 pIC50 = 9.0 Binding
Displacement of [125I]Sar1-Ile8-AII (without BSA) from type 1 Angiotensin II receptor of rabbit aortaDisplacement of [125I]Sar1-Ile8-AII (without BSA) from type 1 Angiotensin II receptor of rabbit aorta
ChEMBL 450 7 1 6 4.9 CCCCc1nc2ccc(C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80335-2
CHEMBL422756 164561 0 None - 0 Rabbit 9.0 pIC50 = 9.0 Binding
Displacement of [125I]Sar1-Ile8-AII (without BSA) from type 1 Angiotensin II receptor of rabbit aortaDisplacement of [125I]Sar1-Ile8-AII (without BSA) from type 1 Angiotensin II receptor of rabbit aorta
ChEMBL 450 7 1 6 4.9 CCCCc1nc2ccc(C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80335-2
127034873 135913 0 None - 1 Human 9.0 pIC50 = 9.0 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 569 10 2 6 6.7 CCCc1nc2c(C)cc(C(=O)NC[C@H](C)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.ejmech.2015.09.010
CHEMBL3735744 135913 0 None - 1 Human 9.0 pIC50 = 9.0 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 569 10 2 6 6.7 CCCc1nc2c(C)cc(C(=O)NC[C@H](C)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.ejmech.2015.09.010
44379183 120289 0 None - 0 Rabbit 9.0 pIC50 = 9.0 Binding
In vitro displacement of 125I-[Sar1, Ile8] from AT1 receptors in rabbit aorta membraneIn vitro displacement of 125I-[Sar1, Ile8] from AT1 receptors in rabbit aorta membrane
ChEMBL 571 10 1 6 6.2 CCCCc1nc2ccc(C(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)C2(C)CC2)cc1 10.1016/S0960-894X(01)81125-2
CHEMBL355708 120289 0 None - 0 Rabbit 9.0 pIC50 = 9.0 Binding
In vitro displacement of 125I-[Sar1, Ile8] from AT1 receptors in rabbit aorta membraneIn vitro displacement of 125I-[Sar1, Ile8] from AT1 receptors in rabbit aorta membrane
ChEMBL 571 10 1 6 6.2 CCCCc1nc2ccc(C(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)C2(C)CC2)cc1 10.1016/S0960-894X(01)81125-2
10461785 11803 0 None - 0 Rabbit 9.0 pIC50 = 9.0 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 639 10 1 9 5.5 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ocnc2C)cc1 10.1021/jm00043a020
CHEMBL1182712 11803 0 None - 0 Rabbit 9.0 pIC50 = 9.0 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 639 10 1 9 5.5 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ocnc2C)cc1 10.1021/jm00043a020
CHEMBL262296 11803 0 None - 0 Rabbit 9.0 pIC50 = 9.0 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 639 10 1 9 5.5 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ocnc2C)cc1 10.1021/jm00043a020
10348847 112080 0 None - 0 Rabbit 9.0 pIC50 = 9.0 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 615 10 2 7 5.5 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)NC(C)C)cc1 10.1021/jm00043a020
CHEMBL330170 112080 0 None - 0 Rabbit 9.0 pIC50 = 9.0 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 615 10 2 7 5.5 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)NC(C)C)cc1 10.1021/jm00043a020
10484119 167534 0 None - 0 Rabbit 9.0 pIC50 = 9.0 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 628 10 1 7 6.4 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)CC(C)(C)C)cc1 10.1021/jm00043a020
CHEMBL432822 167534 0 None - 0 Rabbit 9.0 pIC50 = 9.0 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 628 10 1 7 6.4 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)CC(C)(C)C)cc1 10.1021/jm00043a020
10054188 205778 0 None - 0 Rabbit 9.0 pIC50 = 9.0 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 592 9 1 7 5.1 CCCCc1nn(-c2ccccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)C(F)(F)F)cc1 10.1021/jm00043a020
CHEMBL94582 205778 0 None - 0 Rabbit 9.0 pIC50 = 9.0 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 592 9 1 7 5.1 CCCCc1nn(-c2ccccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)C(F)(F)F)cc1 10.1021/jm00043a020
10462933 16687 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 777 11 2 9 7.5 CCCCc1nn(-c2cc(NC(=O)c3ccccc3)ccc2Br)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1021/jm00019a004
CHEMBL125008 16687 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 777 11 2 9 7.5 CCCCc1nn(-c2cc(NC(=O)c3ccccc3)ccc2Br)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1021/jm00019a004
3936 2171 28 None 1 4 Human 9.0 pIC50 = 9.0 Binding
Inhibition of Angiotensin II receptor, type 1Inhibition of Angiotensin II receptor, type 1
ChEMBL 582 11 1 8 6.8 CCCCOC(=O)NS(=O)(=O)c1sc(cc1c1ccc(cc1)Cn1c(CC)nc2c1nc(C)cc2C)CC(C)C 10.1021/jm9504722
6603900 2171 28 None 1 4 Human 9.0 pIC50 = 9.0 Binding
Inhibition of Angiotensin II receptor, type 1Inhibition of Angiotensin II receptor, type 1
ChEMBL 582 11 1 8 6.8 CCCCOC(=O)NS(=O)(=O)c1sc(cc1c1ccc(cc1)Cn1c(CC)nc2c1nc(C)cc2C)CC(C)C 10.1021/jm9504722
CHEMBL288174 2171 28 None 1 4 Human 9.0 pIC50 = 9.0 Binding
Inhibition of Angiotensin II receptor, type 1Inhibition of Angiotensin II receptor, type 1
ChEMBL 582 11 1 8 6.8 CCCCOC(=O)NS(=O)(=O)c1sc(cc1c1ccc(cc1)Cn1c(CC)nc2c1nc(C)cc2C)CC(C)C 10.1021/jm9504722
44381670 119965 0 None - 0 Rabbit 9.0 pIC50 = 9.0 Binding
Tested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membraneTested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membrane
ChEMBL 657 11 3 9 6.0 CCCCc1nc2ccc(NC(=O)NCC)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)Oc2occc2C)cc1 10.1016/S0960-894X(01)81126-4
CHEMBL354298 119965 0 None - 0 Rabbit 9.0 pIC50 = 9.0 Binding
Tested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membraneTested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membrane
ChEMBL 657 11 3 9 6.0 CCCCc1nc2ccc(NC(=O)NCC)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)Oc2occc2C)cc1 10.1016/S0960-894X(01)81126-4
10392378 16326 0 None - 0 Human 8.9 pIC50 = 8.9 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 535 12 1 7 5.3 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2Cc2csc(C)n2)n1Cc1ccc(C(=O)O)cc1 10.1007/s00044-009-9205-9
CHEMBL123671 16326 0 None - 0 Human 8.9 pIC50 = 8.9 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 535 12 1 7 5.3 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2Cc2csc(C)n2)n1Cc1ccc(C(=O)O)cc1 10.1007/s00044-009-9205-9
10325267 16669 0 None - 0 Human 8.9 pIC50 = 8.9 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 550 12 1 9 4.7 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2Cc2csc(N)n2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
CHEMBL124913 16669 0 None - 0 Human 8.9 pIC50 = 8.9 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 550 12 1 9 4.7 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2Cc2csc(N)n2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
14956757 67236 0 None - 1 Rabbit 8.9 pIC50 = 8.9 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 519 8 1 7 5.3 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
CHEMBL19018 67236 0 None - 1 Rabbit 8.9 pIC50 = 8.9 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 519 8 1 7 5.3 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
136052261 123953 0 None - 0 Human 8.9 pIC50 = 8.9 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 618 8 1 8 5.9 Cc1ccc(CCn2c(=O)c3cc(CC(F)(F)F)sc3n(Cc3ccc(-c4ccccc4-c4nc(=O)o[nH]4)cc3)c2=O)cc1 nan
CHEMBL3640124 123953 0 None - 0 Human 8.9 pIC50 = 8.9 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 618 8 1 8 5.9 Cc1ccc(CCn2c(=O)c3cc(CC(F)(F)F)sc3n(Cc3ccc(-c4ccccc4-c4nc(=O)o[nH]4)cc3)c2=O)cc1 nan
136052281 123959 0 None - 0 Human 8.9 pIC50 = 8.9 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 606 9 1 11 5.5 COc1ccccc1C(=O)Cn1c(=O)c2cc(C3CC3)sc2n(Cc2ccc(-c3ccccc3-c3noc(O)n3)cc2)c1=O nan
CHEMBL3640130 123959 0 None - 0 Human 8.9 pIC50 = 8.9 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 606 9 1 11 5.5 COc1ccccc1C(=O)Cn1c(=O)c2cc(C3CC3)sc2n(Cc2ccc(-c3ccccc3-c3noc(O)n3)cc2)c1=O nan
136052251 123970 0 None - 0 Human 8.9 pIC50 = 8.9 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 544 7 1 9 4.5 CCc1cc2c(=O)n(CC(=O)C(C)(C)C)c(=O)n(Cc3ccc(-c4ccccc4-c4nc(=O)o[nH]4)cc3)c2s1 nan
CHEMBL3640140 123970 0 None - 0 Human 8.9 pIC50 = 8.9 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 544 7 1 9 4.5 CCc1cc2c(=O)n(CC(=O)C(C)(C)C)c(=O)n(Cc3ccc(-c4ccccc4-c4nc(=O)o[nH]4)cc3)c2s1 nan
136052396 123988 0 None - 0 Human 8.9 pIC50 = 8.9 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 610 6 1 9 5.7 CCc1cc2c(=O)n(-c3ccc4c(c3)CC(C)(C)O4)c(=O)n(Cc3ccc(-c4ccccc4-c4nc(=O)o[nH]4)cc3F)c2s1 nan
CHEMBL3640158 123988 0 None - 0 Human 8.9 pIC50 = 8.9 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 610 6 1 9 5.7 CCc1cc2c(=O)n(-c3ccc4c(c3)CC(C)(C)O4)c(=O)n(Cc3ccc(-c4ccccc4-c4nc(=O)o[nH]4)cc3F)c2s1 nan
136052283 123989 0 None - 0 Human 8.9 pIC50 = 8.9 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 556 7 1 9 4.8 CC(C)(C)C(=O)Cn1c(=O)c2cc(C3CC3)sc2n(Cc2ccc(-c3ccccc3-c3nc(=O)o[nH]3)cc2)c1=O nan
CHEMBL3640159 123989 0 None - 0 Human 8.9 pIC50 = 8.9 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 556 7 1 9 4.8 CC(C)(C)C(=O)Cn1c(=O)c2cc(C3CC3)sc2n(Cc2ccc(-c3ccccc3-c3nc(=O)o[nH]3)cc2)c1=O nan
44277677 98849 0 None - 0 Rabbit 8.9 pIC50 = 8.9 Binding
Binding affinity against AT1 receptor in rabbit aortaBinding affinity against AT1 receptor in rabbit aorta
ChEMBL 585 9 1 9 5.5 CCCCN(C(=O)c1ccc(O)cc1)c1ccc2ncn(Cc3ccc(-c4ccccc4-c4nnnn4C)cc3)c(=O)c2c1 10.1016/0960-894X(95)00224-H
CHEMBL282168 98849 0 None - 0 Rabbit 8.9 pIC50 = 8.9 Binding
Binding affinity against AT1 receptor in rabbit aortaBinding affinity against AT1 receptor in rabbit aorta
ChEMBL 585 9 1 9 5.5 CCCCN(C(=O)c1ccc(O)cc1)c1ccc2ncn(Cc3ccc(-c4ccccc4-c4nnnn4C)cc3)c(=O)c2c1 10.1016/0960-894X(95)00224-H
18950598 15352 0 None - 0 Rabbit 8.9 pIC50 = 8.9 Binding
Displacement of [1251][Sar1,IIe8]AII from rabbit aorta Angiotensin II receptor, type 1Displacement of [1251][Sar1,IIe8]AII from rabbit aorta Angiotensin II receptor, type 1
ChEMBL 513 11 1 5 7.1 CCCc1cc(Cn2c(CC)nc3c(C)cc(C)nc32)cc(CCC)c1OC(C(=O)O)c1ccccc1C 10.1021/jm00075a033
CHEMBL121891 15352 0 None - 0 Rabbit 8.9 pIC50 = 8.9 Binding
Displacement of [1251][Sar1,IIe8]AII from rabbit aorta Angiotensin II receptor, type 1Displacement of [1251][Sar1,IIe8]AII from rabbit aorta Angiotensin II receptor, type 1
ChEMBL 513 11 1 5 7.1 CCCc1cc(Cn2c(CC)nc3c(C)cc(C)nc32)cc(CCC)c1OC(C(=O)O)c1ccccc1C 10.1021/jm00075a033
73355475 92179 0 None - 0 Human 8.9 pIC50 = 8.9 Binding
Displacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysisDisplacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysis
ChEMBL 517 9 2 4 6.9 CCCc1nc2c(C)cc(NC(=O)Cc3ccccc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2013.08.014
CHEMBL2435827 92179 0 None - 0 Human 8.9 pIC50 = 8.9 Binding
Displacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysisDisplacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysis
ChEMBL 517 9 2 4 6.9 CCCc1nc2c(C)cc(NC(=O)Cc3ccccc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2013.08.014
14956757 67236 0 None - 1 Rabbit 8.9 pIC50 = 8.9 Binding
Displacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin AT1 receptor in rabbit aortic membranesDisplacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin AT1 receptor in rabbit aortic membranes
ChEMBL 519 8 1 7 5.3 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.bmc.2010.10.043
CHEMBL19018 67236 0 None - 1 Rabbit 8.9 pIC50 = 8.9 Binding
Displacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin AT1 receptor in rabbit aortic membranesDisplacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin AT1 receptor in rabbit aortic membranes
ChEMBL 519 8 1 7 5.3 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.bmc.2010.10.043
14956779 68306 0 None - 0 Rabbit 8.9 pIC50 = 8.9 Binding
Displacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin AT1 receptor in rabbit aortic membranesDisplacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin AT1 receptor in rabbit aortic membranes
ChEMBL 445 8 1 7 4.3 CCCCc1nn(CC(C)(C)C)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.bmc.2010.10.043
CHEMBL19202 68306 0 None - 0 Rabbit 8.9 pIC50 = 8.9 Binding
Displacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin AT1 receptor in rabbit aortic membranesDisplacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin AT1 receptor in rabbit aortic membranes
ChEMBL 445 8 1 7 4.3 CCCCc1nn(CC(C)(C)C)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.bmc.2010.10.043
10078048 106384 0 None - 0 Rabbit 8.9 pIC50 = 8.9 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 654 12 1 7 6.9 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)CCC2CCCC2)cc1 10.1021/jm00043a020
CHEMBL314514 106384 0 None - 0 Rabbit 8.9 pIC50 = 8.9 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 654 12 1 7 6.9 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)CCC2CCCC2)cc1 10.1021/jm00043a020
9986951 206022 0 None - 0 Rabbit 8.9 pIC50 = 8.9 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 668 10 1 7 6.9 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccc(Cl)cc2)cc1 10.1021/jm00043a020
CHEMBL95955 206022 0 None - 0 Rabbit 8.9 pIC50 = 8.9 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 668 10 1 7 6.9 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccc(Cl)cc2)cc1 10.1021/jm00043a020
44314822 102463 0 None - 0 Human 8.9 pIC50 = 8.9 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membrane
ChEMBL 691 13 2 8 6.7 CCCCc1nc2ccc(NC(=O)N(C)C(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC2CC2)cc1F 10.1016/0960-894X(94)85036-4
CHEMBL306362 102463 0 None - 0 Human 8.9 pIC50 = 8.9 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membrane
ChEMBL 691 13 2 8 6.7 CCCCc1nc2ccc(NC(=O)N(C)C(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC2CC2)cc1F 10.1016/0960-894X(94)85036-4
44315058 70095 0 None - 0 Rabbit 8.9 pIC50 = 8.9 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membrane
ChEMBL 637 10 3 8 5.6 Cc1nc2ccc(NC(=O)NC(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/0960-894X(94)85036-4
CHEMBL194608 70095 0 None - 0 Rabbit 8.9 pIC50 = 8.9 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membrane
ChEMBL 637 10 3 8 5.6 Cc1nc2ccc(NC(=O)NC(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/0960-894X(94)85036-4
9869504 206297 3 None - 0 Human 8.9 pIC50 = 8.9 Binding
Tested for Angiotensin II receptor, type 1 affinity in the absence of BSATested for Angiotensin II receptor, type 1 affinity in the absence of BSA
ChEMBL 474 10 2 5 5.9 CCCCc1ncc(/C=C(\Cc2cccs2)C(=O)O)n1Cc1ccc(C(=O)O)c2ccccc12 10.1016/S0960-894X(01)81116-1
CHEMBL97533 206297 3 None - 0 Human 8.9 pIC50 = 8.9 Binding
Tested for Angiotensin II receptor, type 1 affinity in the absence of BSATested for Angiotensin II receptor, type 1 affinity in the absence of BSA
ChEMBL 474 10 2 5 5.9 CCCCc1ncc(/C=C(\Cc2cccs2)C(=O)O)n1Cc1ccc(C(=O)O)c2ccccc12 10.1016/S0960-894X(01)81116-1
44274673 93294 0 None - 0 Rabbit 8.9 pIC50 = 8.9 Binding
Ability to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitroAbility to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitro
ChEMBL 451 7 2 7 4.2 CCCCc1nc2ccc(N)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80335-2
CHEMBL24724 93294 0 None - 0 Rabbit 8.9 pIC50 = 8.9 Binding
Ability to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitroAbility to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitro
ChEMBL 451 7 2 7 4.2 CCCCc1nc2ccc(N)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80335-2
10254585 112392 0 None - 0 Human 8.9 pIC50 = 8.9 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 480 13 1 5 5.2 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2CCCC)n1Cc1ccc(C(=O)O)cc1 10.1007/s00044-009-9205-9
CHEMBL331042 112392 0 None - 0 Human 8.9 pIC50 = 8.9 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 480 13 1 5 5.2 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2CCCC)n1Cc1ccc(C(=O)O)cc1 10.1007/s00044-009-9205-9
136052277 123983 0 None - 0 Human 8.9 pIC50 = 8.9 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 656 10 1 11 5.3 CCc1cc2c(=O)n(CC(OC(C)=O)c3ccc(OC)cc3)c(=O)n(Cc3ccc(-c4ccccc4-c4nc(=O)o[nH]4)cc3F)c2s1 nan
CHEMBL3640153 123983 0 None - 0 Human 8.9 pIC50 = 8.9 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 656 10 1 11 5.3 CCc1cc2c(=O)n(CC(OC(C)=O)c3ccc(OC)cc3)c(=O)n(Cc3ccc(-c4ccccc4-c4nc(=O)o[nH]4)cc3F)c2s1 nan
137662335 160276 0 None - 0 Human 8.9 pIC50 = 8.9 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 593 9 1 10 4.9 CCc1cc2c(=O)n(C/C(=N\OC)c3ccccc3)c(=O)n(Cc3ccc(-c4ccccc4-c4nc(=O)o[nH]4)cc3)c2s1 nan
CHEMBL4114708 160276 0 None - 0 Human 8.9 pIC50 = 8.9 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 593 9 1 10 4.9 CCc1cc2c(=O)n(C/C(=N\OC)c3ccccc3)c(=O)n(Cc3ccc(-c4ccccc4-c4nc(=O)o[nH]4)cc3)c2s1 nan
44277902 99320 0 None - 0 Rabbit 8.9 pIC50 = 8.9 Binding
Binding affinity against AT1 receptor in rabbit aortaBinding affinity against AT1 receptor in rabbit aorta
ChEMBL 627 11 0 10 5.3 CC(=O)OCCCCN(C(=O)c1ccccc1)c1ccc2ncn(Cc3ccc(-c4ccccc4-c4nnnn4C)cc3)c(=O)c2c1 10.1016/0960-894X(95)00224-H
CHEMBL28532 99320 0 None - 0 Rabbit 8.9 pIC50 = 8.9 Binding
Binding affinity against AT1 receptor in rabbit aortaBinding affinity against AT1 receptor in rabbit aorta
ChEMBL 627 11 0 10 5.3 CC(=O)OCCCCN(C(=O)c1ccccc1)c1ccc2ncn(Cc3ccc(-c4ccccc4-c4nnnn4C)cc3)c(=O)c2c1 10.1016/0960-894X(95)00224-H
44274673 93294 0 None - 0 Rabbit 8.9 pIC50 = 8.9 Binding
Binding affinity against Angiotensin II type 1 Receptor in rabbit aortic tissueBinding affinity against Angiotensin II type 1 Receptor in rabbit aortic tissue
ChEMBL 451 7 2 7 4.2 CCCCc1nc2ccc(N)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80334-0
CHEMBL24724 93294 0 None - 0 Rabbit 8.9 pIC50 = 8.9 Binding
Binding affinity against Angiotensin II type 1 Receptor in rabbit aortic tissueBinding affinity against Angiotensin II type 1 Receptor in rabbit aortic tissue
ChEMBL 451 7 2 7 4.2 CCCCc1nc2ccc(N)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80334-0
1481 2027 109 None -1 3 Rat 8.9 pIC50 = 8.9 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 10.1021/jm00074a018
3749 2027 109 None -1 3 Rat 8.9 pIC50 = 8.9 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 10.1021/jm00074a018
589 2027 109 None -1 3 Rat 8.9 pIC50 = 8.9 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 10.1021/jm00074a018
6908 2027 109 None -1 3 Rat 8.9 pIC50 = 8.9 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 10.1021/jm00074a018
CHEMBL1513 2027 109 None -1 3 Rat 8.9 pIC50 = 8.9 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 10.1021/jm00074a018
DB01029 2027 109 None -1 3 Rat 8.9 pIC50 = 8.9 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 10.1021/jm00074a018
22574723 15747 0 None - 1 Human 8.9 pIC50 = 8.9 Binding
Displacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysisDisplacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysis
ChEMBL 549 11 2 7 5.2 CCCc1nc(CC)c(C(N)=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)c(CC)c1 10.1039/C4MD00499J
CHEMBL12233 15747 0 None - 1 Human 8.9 pIC50 = 8.9 Binding
Displacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysisDisplacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysis
ChEMBL 549 11 2 7 5.2 CCCc1nc(CC)c(C(N)=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)c(CC)c1 10.1039/C4MD00499J
57380647 69996 0 None - 1 Human 8.9 pIC50 = 8.9 Binding
Displacement of [125I]Sar1 Ile8-Ang 2 from angiotensin 2 AT1 receptor after 180 mins by gamma countingDisplacement of [125I]Sar1 Ile8-Ang 2 from angiotensin 2 AT1 receptor after 180 mins by gamma counting
ChEMBL 591 12 2 6 6.7 CCCc1nc2c(C)cc(C(=O)NCCc3cc(OC)ccc3OC)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2012.01.009
CHEMBL1945010 69996 0 None - 1 Human 8.9 pIC50 = 8.9 Binding
Displacement of [125I]Sar1 Ile8-Ang 2 from angiotensin 2 AT1 receptor after 180 mins by gamma countingDisplacement of [125I]Sar1 Ile8-Ang 2 from angiotensin 2 AT1 receptor after 180 mins by gamma counting
ChEMBL 591 12 2 6 6.7 CCCc1nc2c(C)cc(C(=O)NCCc3cc(OC)ccc3OC)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2012.01.009
70686410 75962 0 None - 1 Human 8.9 pIC50 = 8.9 Binding
Displacement of [125I]Sar1Ile8-Ang2 from angiotensin AT1 receptor after 180 mins by gamma countingDisplacement of [125I]Sar1Ile8-Ang2 from angiotensin AT1 receptor after 180 mins by gamma counting
ChEMBL 555 10 2 6 6.2 CCCc1nc2c(C)cc(C(=O)NCCc3ccccc3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmc.2012.05.056
CHEMBL2058859 75962 0 None - 1 Human 8.9 pIC50 = 8.9 Binding
Displacement of [125I]Sar1Ile8-Ang2 from angiotensin AT1 receptor after 180 mins by gamma countingDisplacement of [125I]Sar1Ile8-Ang2 from angiotensin AT1 receptor after 180 mins by gamma counting
ChEMBL 555 10 2 6 6.2 CCCc1nc2c(C)cc(C(=O)NCCc3ccccc3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmc.2012.05.056
19939409 106663 0 None - 0 Rabbit 8.9 pIC50 = 8.9 Binding
In vitro ability to inhibit the binding of radioligand 125I[Sar1,IIe8]AII to AT1 receptor from rabbit aortaIn vitro ability to inhibit the binding of radioligand 125I[Sar1,IIe8]AII to AT1 receptor from rabbit aorta
ChEMBL 710 12 1 7 7.8 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2cc(CCC)ccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1016/S0960-894X(01)80595-3
CHEMBL316299 106663 0 None - 0 Rabbit 8.9 pIC50 = 8.9 Binding
In vitro ability to inhibit the binding of radioligand 125I[Sar1,IIe8]AII to AT1 receptor from rabbit aortaIn vitro ability to inhibit the binding of radioligand 125I[Sar1,IIe8]AII to AT1 receptor from rabbit aorta
ChEMBL 710 12 1 7 7.8 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2cc(CCC)ccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1016/S0960-894X(01)80595-3
1481 2027 109 None -1 3 Rat 8.9 pIC50 = 8.9 Binding
In vitro inhibition of specific binding of [125I]AII to Angiotensin II receptor, type 1 from rat liver membraneIn vitro inhibition of specific binding of [125I]AII to Angiotensin II receptor, type 1 from rat liver membrane
ChEMBL 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 10.1016/S0960-894X(01)81139-2
3749 2027 109 None -1 3 Rat 8.9 pIC50 = 8.9 Binding
In vitro inhibition of specific binding of [125I]AII to Angiotensin II receptor, type 1 from rat liver membraneIn vitro inhibition of specific binding of [125I]AII to Angiotensin II receptor, type 1 from rat liver membrane
ChEMBL 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 10.1016/S0960-894X(01)81139-2
589 2027 109 None -1 3 Rat 8.9 pIC50 = 8.9 Binding
In vitro inhibition of specific binding of [125I]AII to Angiotensin II receptor, type 1 from rat liver membraneIn vitro inhibition of specific binding of [125I]AII to Angiotensin II receptor, type 1 from rat liver membrane
ChEMBL 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 10.1016/S0960-894X(01)81139-2
6908 2027 109 None -1 3 Rat 8.9 pIC50 = 8.9 Binding
In vitro inhibition of specific binding of [125I]AII to Angiotensin II receptor, type 1 from rat liver membraneIn vitro inhibition of specific binding of [125I]AII to Angiotensin II receptor, type 1 from rat liver membrane
ChEMBL 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 10.1016/S0960-894X(01)81139-2
CHEMBL1513 2027 109 None -1 3 Rat 8.9 pIC50 = 8.9 Binding
In vitro inhibition of specific binding of [125I]AII to Angiotensin II receptor, type 1 from rat liver membraneIn vitro inhibition of specific binding of [125I]AII to Angiotensin II receptor, type 1 from rat liver membrane
ChEMBL 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 10.1016/S0960-894X(01)81139-2
DB01029 2027 109 None -1 3 Rat 8.9 pIC50 = 8.9 Binding
In vitro inhibition of specific binding of [125I]AII to Angiotensin II receptor, type 1 from rat liver membraneIn vitro inhibition of specific binding of [125I]AII to Angiotensin II receptor, type 1 from rat liver membrane
ChEMBL 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 10.1016/S0960-894X(01)81139-2
10372341 167624 0 None - 0 Rabbit 8.9 pIC50 = 8.9 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 674 10 1 8 6.9 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccc(Cl)s2)cc1 10.1021/jm00043a020
CHEMBL433375 167624 0 None - 0 Rabbit 8.9 pIC50 = 8.9 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 674 10 1 8 6.9 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccc(Cl)s2)cc1 10.1021/jm00043a020
10077929 205604 0 None - 0 Rabbit 8.9 pIC50 = 8.9 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 643 14 2 8 5.4 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)CCCCCN)cc1 10.1021/jm00043a020
CHEMBL93606 205604 0 None - 0 Rabbit 8.9 pIC50 = 8.9 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 643 14 2 8 5.4 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)CCCCCN)cc1 10.1021/jm00043a020
10326460 206357 0 None - 0 Rabbit 8.9 pIC50 = 8.9 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 614 9 1 7 6.0 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)C(C)(C)C)cc1 10.1021/jm00043a020
CHEMBL97897 206357 0 None - 0 Rabbit 8.9 pIC50 = 8.9 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 614 9 1 7 6.0 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)C(C)(C)C)cc1 10.1021/jm00043a020
10009735 157648 0 None - 0 Rabbit 8.9 pIC50 = 8.9 Binding
Inhibition of [125I]-Sar1-Ile8-Ang II binding to Angiotensin II receptor type 1 from rabbit aortaInhibition of [125I]-Sar1-Ile8-Ang II binding to Angiotensin II receptor type 1 from rabbit aorta
ChEMBL 676 3 1 7 6.9 CCCc1nc2ccc3cc2c(=O)n1Cc1ccc(cc1)-c1ccccc1S(=O)(=O)NC(=O)CCCCCCCN3C(=O)c1ccccc1 10.1016/0960-894X(96)00116-3
CHEMBL408798 157648 0 None - 0 Rabbit 8.9 pIC50 = 8.9 Binding
Inhibition of [125I]-Sar1-Ile8-Ang II binding to Angiotensin II receptor type 1 from rabbit aortaInhibition of [125I]-Sar1-Ile8-Ang II binding to Angiotensin II receptor type 1 from rabbit aorta
ChEMBL 676 3 1 7 6.9 CCCc1nc2ccc3cc2c(=O)n1Cc1ccc(cc1)-c1ccccc1S(=O)(=O)NC(=O)CCCCCCCN3C(=O)c1ccccc1 10.1016/0960-894X(96)00116-3
76311803 84532 0 None - 0 Rabbit 8.9 pIC50 = 8.9 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 592 12 3 11 4.6 CCCCc1nnc(SCc2ccccc2-c2nnn[nH]2)n1Cc1ccc(NC(=O)c2ccccc2-c2nnn[nH]2)cc1 10.1007/s00044-011-9756-4
CHEMBL2237602 84532 0 None - 0 Rabbit 8.9 pIC50 = 8.9 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 592 12 3 11 4.6 CCCCc1nnc(SCc2ccccc2-c2nnn[nH]2)n1Cc1ccc(NC(=O)c2ccccc2-c2nnn[nH]2)cc1 10.1007/s00044-011-9756-4
9987311 116244 0 None - 0 Rabbit 8.9 pIC50 = 8.9 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 706 12 1 9 6.7 CCCCc1nn(-c2ccc(C(=O)OCC)cc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1007/s00044-013-0831-x
CHEMBL337588 116244 0 None - 0 Rabbit 8.9 pIC50 = 8.9 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 706 12 1 9 6.7 CCCCc1nn(-c2ccc(C(=O)OCC)cc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1007/s00044-013-0831-x
10414470 16933 0 None - 0 Human 8.9 pIC50 = 8.9 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 524 11 2 7 4.8 CCCCc1ncc(/C=C2/C(=O)NC(=O)N2CCCC)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9205-9
CHEMBL125542 16933 0 None - 0 Human 8.9 pIC50 = 8.9 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 524 11 2 7 4.8 CCCCc1ncc(/C=C2/C(=O)NC(=O)N2CCCC)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9205-9
44320012 167349 0 None - 1 Rabbit 8.9 pIC50 = 8.9 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 493 9 1 7 5.4 CCCCc1nn(-c2ccccc2C(C)C)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
CHEMBL431411 167349 0 None - 1 Rabbit 8.9 pIC50 = 8.9 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 493 9 1 7 5.4 CCCCc1nn(-c2ccccc2C(C)C)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
136052301 123962 0 None - 0 Human 8.9 pIC50 = 8.9 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 594 9 1 11 5.2 CCc1cc2c(=O)n(CC(=O)c3ccccc3OC)c(=O)n(Cc3ccc(-c4ccccc4-c4noc(O)n4)cc3)c2s1 nan
CHEMBL3640133 123962 0 None - 0 Human 8.9 pIC50 = 8.9 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 594 9 1 11 5.2 CCc1cc2c(=O)n(CC(=O)c3ccccc3OC)c(=O)n(Cc3ccc(-c4ccccc4-c4noc(O)n4)cc3)c2s1 nan
136052255 123966 0 None - 0 Human 8.9 pIC50 = 8.9 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 684 9 1 10 5.6 COc1ccccc1C(=O)Cn1c(=O)c2cc(CC(F)(F)F)sc2n(Cc2c(F)cc(-c3ccccc3-c3nc(=O)o[nH]3)cc2F)c1=O nan
CHEMBL3640137 123966 0 None - 0 Human 8.9 pIC50 = 8.9 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 684 9 1 10 5.6 COc1ccccc1C(=O)Cn1c(=O)c2cc(CC(F)(F)F)sc2n(Cc2c(F)cc(-c3ccccc3-c3nc(=O)o[nH]3)cc2F)c1=O nan
136052247 123976 0 None - 0 Human 8.9 pIC50 = 8.9 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 558 7 2 9 4.6 CC(C)(C)C(O)Cn1c(=O)c2cc(C3CC3)sc2n(Cc2ccc(-c3ccccc3-c3nc(=O)o[nH]3)cc2)c1=O nan
CHEMBL3640146 123976 0 None - 0 Human 8.9 pIC50 = 8.9 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 558 7 2 9 4.6 CC(C)(C)C(O)Cn1c(=O)c2cc(C3CC3)sc2n(Cc2ccc(-c3ccccc3-c3nc(=O)o[nH]3)cc2)c1=O nan
136052300 123985 0 None - 0 Human 8.9 pIC50 = 8.9 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 630 9 1 10 5.0 CCc1cc2c(=O)n(CC(=O)c3ccc(OC)c(F)c3)c(=O)n(Cc3ccc(-c4ccccc4-c4noc(=O)[nH]4)cc3F)c2s1 nan
CHEMBL3640155 123985 0 None - 0 Human 8.9 pIC50 = 8.9 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 630 9 1 10 5.0 CCc1cc2c(=O)n(CC(=O)c3ccc(OC)c(F)c3)c(=O)n(Cc3ccc(-c4ccccc4-c4noc(=O)[nH]4)cc3F)c2s1 nan
136052332 123993 0 None - 0 Human 8.9 pIC50 = 8.9 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 630 9 1 10 5.0 CCc1cc2c(=O)n(CC(=O)c3ccc(OC)cc3)c(=O)n(Cc3c(F)cc(-c4ccccc4-c4nc(=O)o[nH]4)cc3F)c2s1 nan
CHEMBL3640162 123993 0 None - 0 Human 8.9 pIC50 = 8.9 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 630 9 1 10 5.0 CCc1cc2c(=O)n(CC(=O)c3ccc(OC)cc3)c(=O)n(Cc3c(F)cc(-c4ccccc4-c4nc(=O)o[nH]4)cc3F)c2s1 nan
136052372 123997 0 None - 0 Human 8.9 pIC50 = 8.9 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 564 8 1 9 4.7 CCc1cc2c(=O)n(CC(=O)c3ccccc3)c(=O)n(Cc3ccc(-c4ccccc4-c4nc(=O)o[nH]4)cc3)c2s1 nan
CHEMBL3640166 123997 0 None - 0 Human 8.9 pIC50 = 8.9 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 564 8 1 9 4.7 CCc1cc2c(=O)n(CC(=O)c3ccccc3)c(=O)n(Cc3ccc(-c4ccccc4-c4nc(=O)o[nH]4)cc3)c2s1 nan
136052324 123999 0 None - 0 Human 8.9 pIC50 = 8.9 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 570 8 1 10 4.8 CCc1cc2c(=O)n(CC(=O)c3cccs3)c(=O)n(Cc3ccc(-c4ccccc4-c4nc(=O)o[nH]4)cc3)c2s1 nan
CHEMBL3640171 123999 0 None - 0 Human 8.9 pIC50 = 8.9 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 570 8 1 10 4.8 CCc1cc2c(=O)n(CC(=O)c3cccs3)c(=O)n(Cc3ccc(-c4ccccc4-c4nc(=O)o[nH]4)cc3)c2s1 nan
10481968 50407 0 None - 0 Human 8.9 pIC50 = 8.9 Binding
Binding affinity to angiotensin AT1 receptorBinding affinity to angiotensin AT1 receptor
ChEMBL 525 11 2 8 5.5 CCCCc1nnc(SCc2ccccc2C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.bmc.2010.10.043
CHEMBL157577 50407 0 None - 0 Human 8.9 pIC50 = 8.9 Binding
Binding affinity to angiotensin AT1 receptorBinding affinity to angiotensin AT1 receptor
ChEMBL 525 11 2 8 5.5 CCCCc1nnc(SCc2ccccc2C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.bmc.2010.10.043
15236320 172027 0 None - 0 Rabbit 8.9 pIC50 = 8.9 Binding
Compound was evaluated for inhibition of 125I[Sar1,Ile8] all binding to rabbit aorta Angiotensin II receptor, type 1Compound was evaluated for inhibition of 125I[Sar1,Ile8] all binding to rabbit aorta Angiotensin II receptor, type 1
ChEMBL 548 10 1 7 6.1 CCCCOC(=O)NS(=O)(=O)c1ccc(CC)cc1-c1ccc(Cn2c(CC)nc3c(C)cc(C)nc32)cc1 10.1016/0960-894X(96)00017-0
CHEMBL449095 172027 0 None - 0 Rabbit 8.9 pIC50 = 8.9 Binding
Compound was evaluated for inhibition of 125I[Sar1,Ile8] all binding to rabbit aorta Angiotensin II receptor, type 1Compound was evaluated for inhibition of 125I[Sar1,Ile8] all binding to rabbit aorta Angiotensin II receptor, type 1
ChEMBL 548 10 1 7 6.1 CCCCOC(=O)NS(=O)(=O)c1ccc(CC)cc1-c1ccc(Cn2c(CC)nc3c(C)cc(C)nc32)cc1 10.1016/0960-894X(96)00017-0
10054324 97888 0 None - 0 Rabbit 8.9 pIC50 = 8.9 Binding
Displacement of 125I[Sar,Ile] from rabbit aorta membrane Angiotensin II receptor type 1Displacement of 125I[Sar,Ile] from rabbit aorta membrane Angiotensin II receptor type 1
ChEMBL 600 10 1 7 5.9 CCCCc1nn(-c2ccccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/S0960-894X(01)81132-X
CHEMBL275160 97888 0 None - 0 Rabbit 8.9 pIC50 = 8.9 Binding
Displacement of 125I[Sar,Ile] from rabbit aorta membrane Angiotensin II receptor type 1Displacement of 125I[Sar,Ile] from rabbit aorta membrane Angiotensin II receptor type 1
ChEMBL 600 10 1 7 5.9 CCCCc1nn(-c2ccccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/S0960-894X(01)81132-X
10099040 119723 0 None - 0 Rabbit 8.9 pIC50 = 8.9 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 549 11 2 10 5.0 CCCCc1nnc(SCc2ccccc2-c2nn[nH]n2)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
CHEMBL352236 119723 0 None - 0 Rabbit 8.9 pIC50 = 8.9 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 549 11 2 10 5.0 CCCCc1nnc(SCc2ccccc2-c2nn[nH]n2)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
9852384 99937 3 None - 0 Rat 8.9 pIC50 = 8.9 Binding
Displacement of [125I]Ang II from AT1 receptor in rat liver membranesDisplacement of [125I]Ang II from AT1 receptor in rat liver membranes
ChEMBL 640 12 1 8 7.1 CCCCOC(=O)NS(=O)(=O)c1ccc(Cc2cccc(OC)c2)cc1-c1ccc(Cn2c(CC)nc3c(C)cc(C)nc32)cc1 10.1021/acs.jmedchem.9b01780
CHEMBL290214 99937 3 None - 0 Rat 8.9 pIC50 = 8.9 Binding
Displacement of [125I]Ang II from AT1 receptor in rat liver membranesDisplacement of [125I]Ang II from AT1 receptor in rat liver membranes
ChEMBL 640 12 1 8 7.1 CCCCOC(=O)NS(=O)(=O)c1ccc(Cc2cccc(OC)c2)cc1-c1ccc(Cn2c(CC)nc3c(C)cc(C)nc32)cc1 10.1021/acs.jmedchem.9b01780
127035265 136000 0 None - 0 Human 8.9 pIC50 = 8.9 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 601 11 2 7 7.3 CCCSc1nc2c(C)cc(C(=O)NC[C@H](C)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.ejmech.2015.09.010
CHEMBL3736514 136000 0 None - 0 Human 8.9 pIC50 = 8.9 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 601 11 2 7 7.3 CCCSc1nc2c(C)cc(C(=O)NC[C@H](C)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.ejmech.2015.09.010
10417195 108579 0 None - 0 Rabbit 8.9 pIC50 = 8.9 Binding
In vitro ability to inhibit the binding of radioligand 125I[Sar1,IIe8]AII to AT1 receptor from rabbit aortaIn vitro ability to inhibit the binding of radioligand 125I[Sar1,IIe8]AII to AT1 receptor from rabbit aorta
ChEMBL 685 13 2 9 6.2 CCCCc1nn(-c2cc(NC(C)=O)ccc2Cl)c(=O)n1Cc1ccc(-c2cc(CCC)ccc2S(=O)(=O)NC(=O)OCC)cc1F 10.1016/S0960-894X(01)80595-3
CHEMBL321313 108579 0 None - 0 Rabbit 8.9 pIC50 = 8.9 Binding
In vitro ability to inhibit the binding of radioligand 125I[Sar1,IIe8]AII to AT1 receptor from rabbit aortaIn vitro ability to inhibit the binding of radioligand 125I[Sar1,IIe8]AII to AT1 receptor from rabbit aorta
ChEMBL 685 13 2 9 6.2 CCCCc1nn(-c2cc(NC(C)=O)ccc2Cl)c(=O)n1Cc1ccc(-c2cc(CCC)ccc2S(=O)(=O)NC(=O)OCC)cc1F 10.1016/S0960-894X(01)80595-3
10054324 97888 0 None - 0 Rabbit 8.9 pIC50 = 8.9 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 600 10 1 7 5.9 CCCCc1nn(-c2ccccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1021/jm00043a020
CHEMBL275160 97888 0 None - 0 Rabbit 8.9 pIC50 = 8.9 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 600 10 1 7 5.9 CCCCc1nn(-c2ccccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1021/jm00043a020
10101690 116348 0 None - 0 Human 8.9 pIC50 = 8.9 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 767 11 2 9 7.7 CCCCc1nn(-c2cc(NC(=O)c3ccccc3)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1021/jm00019a004
CHEMBL338137 116348 0 None - 0 Human 8.9 pIC50 = 8.9 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 767 11 2 9 7.7 CCCCc1nn(-c2cc(NC(=O)c3ccccc3)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1021/jm00019a004
9852384 99937 3 None - 0 Human 8.9 pIC50 = 8.9 Binding
Inhibition of Angiotensin II receptor, type 1Inhibition of Angiotensin II receptor, type 1
ChEMBL 640 12 1 8 7.1 CCCCOC(=O)NS(=O)(=O)c1ccc(Cc2cccc(OC)c2)cc1-c1ccc(Cn2c(CC)nc3c(C)cc(C)nc32)cc1 10.1021/jm9504722
CHEMBL290214 99937 3 None - 0 Human 8.9 pIC50 = 8.9 Binding
Inhibition of Angiotensin II receptor, type 1Inhibition of Angiotensin II receptor, type 1
ChEMBL 640 12 1 8 7.1 CCCCOC(=O)NS(=O)(=O)c1ccc(Cc2cccc(OC)c2)cc1-c1ccc(Cn2c(CC)nc3c(C)cc(C)nc32)cc1 10.1021/jm9504722
44305410 161797 0 None - 0 Rat 8.9 pIC50 = 8.9 Binding
Tested for binding affinity against angiotensin II receptor in rat adrenal cortexTested for binding affinity against angiotensin II receptor in rat adrenal cortex
ChEMBL 556 10 3 8 3.5 CCCc1cc(=O)n(CCNC(=O)NC2CCCCC2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/0960-894X(95)00370-9
CHEMBL416507 161797 0 None - 0 Rat 8.9 pIC50 = 8.9 Binding
Tested for binding affinity against angiotensin II receptor in rat adrenal cortexTested for binding affinity against angiotensin II receptor in rat adrenal cortex
ChEMBL 556 10 3 8 3.5 CCCc1cc(=O)n(CCNC(=O)NC2CCCCC2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/0960-894X(95)00370-9
9987311 116244 0 None - 0 Rabbit 8.9 pIC50 = 8.9 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 706 12 1 9 6.7 CCCCc1nn(-c2ccc(C(=O)OCC)cc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1021/jm00052a006
CHEMBL337588 116244 0 None - 0 Rabbit 8.9 pIC50 = 8.9 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 706 12 1 9 6.7 CCCCc1nn(-c2ccc(C(=O)OCC)cc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1021/jm00052a006
10321941 137606 0 None - 0 Rat 8.8 pIC50 = 8.8 Binding
Tested for inhibition of [125I]- AII specific binding to rat mesenteric arteries, expressed as IC50Tested for inhibition of [125I]- AII specific binding to rat mesenteric arteries, expressed as IC50
ChEMBL 458 10 2 5 5.4 CCCCc1ncc(/C=C(\Cc2cccs2)C(=O)O)n1Cc1ccc(C(=O)O)cc1Cl 10.1016/S0960-894X(01)81116-1
CHEMBL37679 137606 0 None - 0 Rat 8.8 pIC50 = 8.8 Binding
Tested for inhibition of [125I]- AII specific binding to rat mesenteric arteries, expressed as IC50Tested for inhibition of [125I]- AII specific binding to rat mesenteric arteries, expressed as IC50
ChEMBL 458 10 2 5 5.4 CCCCc1ncc(/C=C(\Cc2cccs2)C(=O)O)n1Cc1ccc(C(=O)O)cc1Cl 10.1016/S0960-894X(01)81116-1
19010048 84530 0 None - 0 Rabbit 8.8 pIC50 = 8.8 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 568 12 3 9 5.1 CCCCc1nnc(SCc2ccccc2C(=O)O)n1Cc1ccc(NC(=O)c2ccccc2-c2nnn[nH]2)cc1 10.1007/s00044-011-9756-4
CHEMBL2237600 84530 0 None - 0 Rabbit 8.8 pIC50 = 8.8 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 568 12 3 9 5.1 CCCCc1nnc(SCc2ccccc2C(=O)O)n1Cc1ccc(NC(=O)c2ccccc2-c2nnn[nH]2)cc1 10.1007/s00044-011-9756-4
10327728 97658 0 None - 0 Rabbit 8.8 pIC50 = 8.8 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 749 9 2 9 6.7 CCc1nn(-c2cc(NC(=O)c3ccccc3)ccc2Br)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1007/s00044-011-9815-x
CHEMBL273542 97658 0 None - 0 Rabbit 8.8 pIC50 = 8.8 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 749 9 2 9 6.7 CCc1nn(-c2cc(NC(=O)c3ccccc3)ccc2Br)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1007/s00044-011-9815-x
10369867 16185 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 534 12 1 6 5.9 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2Cc2cc(C)cs2)n1Cc1ccc(C(=O)O)cc1 10.1007/s00044-009-9205-9
CHEMBL122966 16185 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 534 12 1 6 5.9 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2Cc2cc(C)cs2)n1Cc1ccc(C(=O)O)cc1 10.1007/s00044-009-9205-9
135876074 123956 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 612 9 1 10 4.9 CCc1cc2c(=O)n(CC(=O)c3ccc(OC)cc3F)c(=O)n(Cc3ccc(-c4ccccc4-c4nc(=O)o[nH]4)cc3)c2s1 nan
CHEMBL3640127 123956 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 612 9 1 10 4.9 CCc1cc2c(=O)n(CC(=O)c3ccc(OC)cc3F)c(=O)n(Cc3ccc(-c4ccccc4-c4nc(=O)o[nH]4)cc3)c2s1 nan
136052291 123972 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 642 9 1 10 5.3 COc1ccc(C(=O)Cn2c(=O)c3cc(C4CC4)sc3n(Cc3c(F)cc(-c4ccccc4-c4nc(=O)o[nH]4)cc3F)c2=O)cc1 nan
CHEMBL3640142 123972 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 642 9 1 10 5.3 COc1ccc(C(=O)Cn2c(=O)c3cc(C4CC4)sc3n(Cc3c(F)cc(-c4ccccc4-c4nc(=O)o[nH]4)cc3F)c2=O)cc1 nan
136052286 123973 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 624 8 1 9 5.5 O=C(Cn1c(=O)c2cc(CC(F)(F)F)sc2n(Cc2ccc(-c3ccccc3-c3nc(=O)o[nH]3)cc2)c1=O)C1CCCCC1 nan
CHEMBL3640143 123973 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 624 8 1 9 5.5 O=C(Cn1c(=O)c2cc(CC(F)(F)F)sc2n(Cc2ccc(-c3ccccc3-c3nc(=O)o[nH]3)cc2)c1=O)C1CCCCC1 nan
136052352 123975 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 573 8 1 10 4.9 CCc1cc2c(=O)n(C/C(=N/OC)C(C)(C)C)c(=O)n(Cc3ccc(-c4ccccc4-c4nc(=O)o[nH]4)cc3)c2s1 nan
CHEMBL3640145 123975 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 573 8 1 10 4.9 CCc1cc2c(=O)n(C/C(=N/OC)C(C)(C)C)c(=O)n(Cc3ccc(-c4ccccc4-c4nc(=O)o[nH]4)cc3)c2s1 nan
136052270 123979 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 602 10 1 11 4.0 CCc1cc2c(=O)n(CC(=O)C(C)(C)COC(C)=O)c(=O)n(Cc3ccc(-c4ccccc4-c4nc(=O)o[nH]4)cc3)c2s1 nan
CHEMBL3640149 123979 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 602 10 1 11 4.0 CCc1cc2c(=O)n(CC(=O)C(C)(C)COC(C)=O)c(=O)n(Cc3ccc(-c4ccccc4-c4nc(=O)o[nH]4)cc3)c2s1 nan
136052397 123981 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 604 8 1 10 5.4 CCc1cc2c(=O)n(CC(=O)c3ccc(Cl)s3)c(=O)n(Cc3ccc(-c4ccccc4-c4nc(=O)o[nH]4)cc3)c2s1 nan
CHEMBL3640151 123981 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 604 8 1 10 5.4 CCc1cc2c(=O)n(CC(=O)c3ccc(Cl)s3)c(=O)n(Cc3ccc(-c4ccccc4-c4nc(=O)o[nH]4)cc3)c2s1 nan
136052320 123982 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 614 9 2 10 4.7 CCc1cc2c(=O)n(CC(O)c3ccc(OC)cc3)c(=O)n(Cc3ccc(-c4ccccc4-c4nc(=O)o[nH]4)cc3F)c2s1 nan
CHEMBL3640152 123982 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 614 9 2 10 4.7 CCc1cc2c(=O)n(CC(O)c3ccc(OC)cc3)c(=O)n(Cc3ccc(-c4ccccc4-c4nc(=O)o[nH]4)cc3F)c2s1 nan
136052319 123994 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 612 9 1 10 4.9 CCc1cc2c(=O)n(CC(=O)c3ccc(OC)cc3)c(=O)n(Cc3ccc(-c4ccc(F)cc4-c4nc(=O)o[nH]4)cc3)c2s1 nan
CHEMBL3640163 123994 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 612 9 1 10 4.9 CCc1cc2c(=O)n(CC(=O)c3ccc(OC)cc3)c(=O)n(Cc3ccc(-c4ccc(F)cc4-c4nc(=O)o[nH]4)cc3)c2s1 nan
136052299 123996 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 570 8 1 9 5.0 CCc1cc2c(=O)n(CC(=O)C3CCCCC3)c(=O)n(Cc3ccc(-c4ccccc4-c4nc(=O)o[nH]4)cc3)c2s1 nan
CHEMBL3640165 123996 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 570 8 1 9 5.0 CCc1cc2c(=O)n(CC(=O)C3CCCCC3)c(=O)n(Cc3ccc(-c4ccccc4-c4nc(=O)o[nH]4)cc3)c2s1 nan
1610 2305 89 None -1 4 Rat 8.8 pIC50 = 8.8 Binding
Binding affinity against AT1 receptor in the presence of 0.01% BSABinding affinity against AT1 receptor in the presence of 0.01% BSA
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00037a014
3941 2305 89 None -1 4 Rat 8.8 pIC50 = 8.8 Binding
Binding affinity against AT1 receptor in the presence of 0.01% BSABinding affinity against AT1 receptor in the presence of 0.01% BSA
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00037a014
3961 2305 89 None -1 4 Rat 8.8 pIC50 = 8.8 Binding
Binding affinity against AT1 receptor in the presence of 0.01% BSABinding affinity against AT1 receptor in the presence of 0.01% BSA
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00037a014
590 2305 89 None -1 4 Rat 8.8 pIC50 = 8.8 Binding
Binding affinity against AT1 receptor in the presence of 0.01% BSABinding affinity against AT1 receptor in the presence of 0.01% BSA
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00037a014
CHEMBL191 2305 89 None -1 4 Rat 8.8 pIC50 = 8.8 Binding
Binding affinity against AT1 receptor in the presence of 0.01% BSABinding affinity against AT1 receptor in the presence of 0.01% BSA
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00037a014
DB00678 2305 89 None -1 4 Rat 8.8 pIC50 = 8.8 Binding
Binding affinity against AT1 receptor in the presence of 0.01% BSABinding affinity against AT1 receptor in the presence of 0.01% BSA
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00037a014
10481968 50407 0 None - 0 Rabbit 8.8 pIC50 = 8.8 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 525 11 2 8 5.5 CCCCc1nnc(SCc2ccccc2C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
CHEMBL157577 50407 0 None - 0 Rabbit 8.8 pIC50 = 8.8 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 525 11 2 8 5.5 CCCCc1nnc(SCc2ccccc2C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
9850834 154112 13 None - 1 Human 8.8 pIC50 = 8.8 Binding
Displacement of [125I]-[Sar1,Leu8]angiotensin II from human AT1 receptor expressed in african green monkey COS7 cellsDisplacement of [125I]-[Sar1,Leu8]angiotensin II from human AT1 receptor expressed in african green monkey COS7 cells
ChEMBL 562 11 1 7 6.5 CCCCOC(=O)NS(=O)(=O)c1ccc(CCC)cc1-c1ccc(Cn2c(CC)nc3c(C)cc(C)nc32)cc1 10.1021/ml500427r
CHEMBL39959 154112 13 None - 1 Human 8.8 pIC50 = 8.8 Binding
Displacement of [125I]-[Sar1,Leu8]angiotensin II from human AT1 receptor expressed in african green monkey COS7 cellsDisplacement of [125I]-[Sar1,Leu8]angiotensin II from human AT1 receptor expressed in african green monkey COS7 cells
ChEMBL 562 11 1 7 6.5 CCCCOC(=O)NS(=O)(=O)c1ccc(CCC)cc1-c1ccc(Cn2c(CC)nc3c(C)cc(C)nc32)cc1 10.1021/ml500427r
44379292 119815 0 None - 0 Rabbit 8.8 pIC50 = 8.8 Binding
In vitro displacement of 125I-[Sar1, Ile8] from AT1 receptors in rabbit aorta membraneIn vitro displacement of 125I-[Sar1, Ile8] from AT1 receptors in rabbit aorta membrane
ChEMBL 613 12 1 6 7.4 CCCCc1nc2ccc(C(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)CCC2CCCC2)cc1 10.1016/S0960-894X(01)81125-2
CHEMBL352934 119815 0 None - 0 Rabbit 8.8 pIC50 = 8.8 Binding
In vitro displacement of 125I-[Sar1, Ile8] from AT1 receptors in rabbit aorta membraneIn vitro displacement of 125I-[Sar1, Ile8] from AT1 receptors in rabbit aorta membrane
ChEMBL 613 12 1 6 7.4 CCCCc1nc2ccc(C(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)CCC2CCCC2)cc1 10.1016/S0960-894X(01)81125-2
10327728 97658 0 None - 0 Rabbit 8.8 pIC50 = 8.8 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 749 9 2 9 6.7 CCc1nn(-c2cc(NC(=O)c3ccccc3)ccc2Br)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1021/jm00019a004
CHEMBL273542 97658 0 None - 0 Rabbit 8.8 pIC50 = 8.8 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 749 9 2 9 6.7 CCc1nn(-c2cc(NC(=O)c3ccccc3)ccc2Br)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1021/jm00019a004
10438523 206393 0 None - 0 Rabbit 8.8 pIC50 = 8.8 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 598 10 1 7 5.3 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)C2CC2)cc1 10.1021/jm00043a020
CHEMBL98126 206393 0 None - 0 Rabbit 8.8 pIC50 = 8.8 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 598 10 1 7 5.3 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)C2CC2)cc1 10.1021/jm00043a020
11765454 117552 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 723 11 2 10 6.9 CCCCc1nn(-c2cc(NC(=O)c3ccco3)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1021/jm00019a004
CHEMBL340473 117552 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 723 11 2 10 6.9 CCCCc1nn(-c2cc(NC(=O)c3ccco3)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1021/jm00019a004
44315144 96131 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membrane
ChEMBL 665 13 3 8 5.2 CCCc1nc2ccc(NC(=O)NC(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)COCC(C)C)cc1F 10.1016/0960-894X(94)85036-4
CHEMBL263191 96131 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membrane
ChEMBL 665 13 3 8 5.2 CCCc1nc2ccc(NC(=O)NC(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)COCC(C)C)cc1F 10.1016/0960-894X(94)85036-4
9851889 101591 0 None - 0 Rabbit 8.8 pIC50 = 8.8 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membrane
ChEMBL 611 12 1 7 7.1 CCCCCN(C(=O)c1ccccc1)c1ccc2nc(CCC)n(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c(=O)c2c1 10.1016/0960-894X(94)85036-4
CHEMBL302102 101591 0 None - 0 Rabbit 8.8 pIC50 = 8.8 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membrane
ChEMBL 611 12 1 7 7.1 CCCCCN(C(=O)c1ccccc1)c1ccc2nc(CCC)n(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c(=O)c2c1 10.1016/0960-894X(94)85036-4
44300838 196983 0 None - 0 Rabbit 8.8 pIC50 = 8.8 Binding
Inhibition of Angiotensin II receptor type 1 in rabbit aorta binding assayInhibition of Angiotensin II receptor type 1 in rabbit aorta binding assay
ChEMBL 530 7 1 7 5.5 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccsc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/S0960-894X(01)81145-8
CHEMBL57976 196983 0 None - 0 Rabbit 8.8 pIC50 = 8.8 Binding
Inhibition of Angiotensin II receptor type 1 in rabbit aorta binding assayInhibition of Angiotensin II receptor type 1 in rabbit aorta binding assay
ChEMBL 530 7 1 7 5.5 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccsc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/S0960-894X(01)81145-8
9850834 154112 13 None - 1 Human 8.8 pIC50 = 8.8 Binding
Inhibition of Angiotensin II receptor, type 1Inhibition of Angiotensin II receptor, type 1
ChEMBL 562 11 1 7 6.5 CCCCOC(=O)NS(=O)(=O)c1ccc(CCC)cc1-c1ccc(Cn2c(CC)nc3c(C)cc(C)nc32)cc1 10.1021/jm9504722
CHEMBL39959 154112 13 None - 1 Human 8.8 pIC50 = 8.8 Binding
Inhibition of Angiotensin II receptor, type 1Inhibition of Angiotensin II receptor, type 1
ChEMBL 562 11 1 7 6.5 CCCCOC(=O)NS(=O)(=O)c1ccc(CCC)cc1-c1ccc(Cn2c(CC)nc3c(C)cc(C)nc32)cc1 10.1021/jm9504722
9851889 101591 0 None - 0 Rabbit 8.8 pIC50 = 8.8 Binding
Inhibition of [125I]-Sar1-Ile8-Ang II binding to Angiotensin II receptor type 1 from rabbit aortaInhibition of [125I]-Sar1-Ile8-Ang II binding to Angiotensin II receptor type 1 from rabbit aorta
ChEMBL 611 12 1 7 7.1 CCCCCN(C(=O)c1ccccc1)c1ccc2nc(CCC)n(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c(=O)c2c1 10.1016/0960-894X(96)00116-3
CHEMBL302102 101591 0 None - 0 Rabbit 8.8 pIC50 = 8.8 Binding
Inhibition of [125I]-Sar1-Ile8-Ang II binding to Angiotensin II receptor type 1 from rabbit aortaInhibition of [125I]-Sar1-Ile8-Ang II binding to Angiotensin II receptor type 1 from rabbit aorta
ChEMBL 611 12 1 7 7.1 CCCCCN(C(=O)c1ccccc1)c1ccc2nc(CCC)n(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c(=O)c2c1 10.1016/0960-894X(96)00116-3
44211672 157649 0 None - 0 Rabbit 8.8 pIC50 = 8.8 Binding
Inhibition of [125I]-Sar1-Ile8-Ang II binding to Angiotensin II receptor type 1 from rabbit aortaInhibition of [125I]-Sar1-Ile8-Ang II binding to Angiotensin II receptor type 1 from rabbit aorta
ChEMBL 706 4 1 8 7.4 CCCc1nc2ccc3cc2c(=O)n1Cc1ccc(cc1)-c1ccccc1S(=O)(=O)NC(=O)CCCCCCCN3C(=O)OCc1ccccc1 10.1016/0960-894X(96)00116-3
CHEMBL408799 157649 0 None - 0 Rabbit 8.8 pIC50 = 8.8 Binding
Inhibition of [125I]-Sar1-Ile8-Ang II binding to Angiotensin II receptor type 1 from rabbit aortaInhibition of [125I]-Sar1-Ile8-Ang II binding to Angiotensin II receptor type 1 from rabbit aorta
ChEMBL 706 4 1 8 7.4 CCCc1nc2ccc3cc2c(=O)n1Cc1ccc(cc1)-c1ccccc1S(=O)(=O)NC(=O)CCCCCCCN3C(=O)OCc1ccccc1 10.1016/0960-894X(96)00116-3
10327728 97658 0 None - 0 Rabbit 8.8 pIC50 = 8.8 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 749 9 2 9 6.7 CCc1nn(-c2cc(NC(=O)c3ccccc3)ccc2Br)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1007/s00044-011-9815-x
CHEMBL273542 97658 0 None - 0 Rabbit 8.8 pIC50 = 8.8 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 749 9 2 9 6.7 CCc1nn(-c2cc(NC(=O)c3ccccc3)ccc2Br)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1007/s00044-011-9815-x
10484986 118179 0 None - 0 Rabbit 8.8 pIC50 = 8.8 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 713 11 1 9 6.8 CCCCc1nn(-c2ccc([N+](=O)[O-])cc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1007/s00044-013-0831-x
CHEMBL341715 118179 0 None - 0 Rabbit 8.8 pIC50 = 8.8 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 713 11 1 9 6.8 CCCCc1nn(-c2ccc([N+](=O)[O-])cc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1007/s00044-013-0831-x
136052375 123952 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 638 8 1 8 6.3 O=c1nc(-c2ccccc2-c2ccc(Cn3c(=O)n(CCc4ccc(Cl)cc4)c(=O)c4cc(CC(F)(F)F)sc43)cc2)[nH]o1 nan
CHEMBL3640123 123952 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 638 8 1 8 6.3 O=c1nc(-c2ccccc2-c2ccc(Cn3c(=O)n(CCc4ccc(Cl)cc4)c(=O)c4cc(CC(F)(F)F)sc43)cc2)[nH]o1 nan
136052302 123967 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 642 9 1 10 5.3 COc1cc(F)ccc1C(=O)Cn1c(=O)c2cc(C3CC3)sc2n(Cc2ccc(-c3ccccc3-c3nc(=O)o[nH]3)cc2F)c1=O nan
CHEMBL3640138 123967 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 642 9 1 10 5.3 COc1cc(F)ccc1C(=O)Cn1c(=O)c2cc(C3CC3)sc2n(Cc2ccc(-c3ccccc3-c3nc(=O)o[nH]3)cc2F)c1=O nan
136052246 123968 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 624 9 1 10 5.2 COc1cc(F)ccc1C(=O)Cn1c(=O)c2cc(C3CC3)sc2n(Cc2ccc(-c3ccccc3-c3nc(=O)o[nH]3)cc2)c1=O nan
CHEMBL3640139 123968 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 624 9 1 10 5.2 COc1cc(F)ccc1C(=O)Cn1c(=O)c2cc(C3CC3)sc2n(Cc2ccc(-c3ccccc3-c3nc(=O)o[nH]3)cc2)c1=O nan
136052258 123987 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 598 8 1 9 5.8 CCc1cc2c(=O)n(-c3ccc(OC(C)C)cc3)c(=O)n(Cc3ccc(-c4ccccc4-c4nc(=O)o[nH]4)cc3F)c2s1 nan
CHEMBL3640157 123987 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 598 8 1 9 5.8 CCc1cc2c(=O)n(-c3ccc(OC(C)C)cc3)c(=O)n(Cc3ccc(-c4ccccc4-c4nc(=O)o[nH]4)cc3F)c2s1 nan
136052298 123998 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 637 11 1 11 5.3 CCO/N=C(/Cn1c(=O)c2cc(CC)sc2n(Cc2ccc(-c3ccccc3-c3nc(=O)o[nH]3)cc2)c1=O)c1ccc(OC)cc1 nan
CHEMBL3640167 123998 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 637 11 1 11 5.3 CCO/N=C(/Cn1c(=O)c2cc(CC)sc2n(Cc2ccc(-c3ccccc3-c3nc(=O)o[nH]3)cc2)c1=O)c1ccc(OC)cc1 nan
136052297 124001 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 578 8 1 8 5.8 CCc1cc2c(=O)n(CC(C)(C)c3ccccc3)c(=O)n(Cc3ccc(-c4ccccc4-c4noc(=O)[nH]4)cc3)c2s1 nan
CHEMBL3640173 124001 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 578 8 1 8 5.8 CCc1cc2c(=O)n(CC(C)(C)c3ccccc3)c(=O)n(Cc3ccc(-c4ccccc4-c4noc(=O)[nH]4)cc3)c2s1 nan
44277903 98648 0 None - 0 Rabbit 8.8 pIC50 = 8.8 Binding
Binding affinity against AT1 receptor in rabbit aortaBinding affinity against AT1 receptor in rabbit aorta
ChEMBL 585 10 0 9 5.0 CCOCCN(C(=O)c1ccccc1)c1ccc2ncn(Cc3ccc(-c4ccccc4-c4nnnn4C)cc3)c(=O)c2c1 10.1016/0960-894X(95)00224-H
CHEMBL280908 98648 0 None - 0 Rabbit 8.8 pIC50 = 8.8 Binding
Binding affinity against AT1 receptor in rabbit aortaBinding affinity against AT1 receptor in rabbit aorta
ChEMBL 585 10 0 9 5.0 CCOCCN(C(=O)c1ccccc1)c1ccc2ncn(Cc3ccc(-c4ccccc4-c4nnnn4C)cc3)c(=O)c2c1 10.1016/0960-894X(95)00224-H
11764826 97819 0 None - 0 Rabbit 8.8 pIC50 = 8.8 Binding
Displacement of 125I[Sar,Ile] from rabbit aorta membrane Angiotensin II receptor type 1Displacement of 125I[Sar,Ile] from rabbit aorta membrane Angiotensin II receptor type 1
ChEMBL 648 11 1 7 6.2 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)Cc2ccccc2)cc1 10.1016/S0960-894X(01)81132-X
CHEMBL274710 97819 0 None - 0 Rabbit 8.8 pIC50 = 8.8 Binding
Displacement of 125I[Sar,Ile] from rabbit aorta membrane Angiotensin II receptor type 1Displacement of 125I[Sar,Ile] from rabbit aorta membrane Angiotensin II receptor type 1
ChEMBL 648 11 1 7 6.2 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)Cc2ccccc2)cc1 10.1016/S0960-894X(01)81132-X
15231091 93541 0 None - 0 Rabbit 8.8 pIC50 = 8.8 Binding
Displacement of [125I]Sar1-Ile8-AII (without BSA) from type 1 Angiotensin II receptor of rabbit aortaDisplacement of [125I]Sar1-Ile8-AII (without BSA) from type 1 Angiotensin II receptor of rabbit aorta
ChEMBL 565 10 1 8 5.9 CCCCc1nc2ccc(N(C)C(=O)OCC(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80335-2
CHEMBL24861 93541 0 None - 0 Rabbit 8.8 pIC50 = 8.8 Binding
Displacement of [125I]Sar1-Ile8-AII (without BSA) from type 1 Angiotensin II receptor of rabbit aortaDisplacement of [125I]Sar1-Ile8-AII (without BSA) from type 1 Angiotensin II receptor of rabbit aorta
ChEMBL 565 10 1 8 5.9 CCCCc1nc2ccc(N(C)C(=O)OCC(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80335-2
44274823 98605 0 None - 0 Rabbit 8.8 pIC50 = 8.8 Binding
Displacement of [125I]Sar1-Ile8-AII (without BSA) from type 1 Angiotensin II receptor of rabbit aortaDisplacement of [125I]Sar1-Ile8-AII (without BSA) from type 1 Angiotensin II receptor of rabbit aorta
ChEMBL 551 10 2 8 5.8 CCCCc1nc2ccc(NC(=O)OCC(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80335-2
CHEMBL280526 98605 0 None - 0 Rabbit 8.8 pIC50 = 8.8 Binding
Displacement of [125I]Sar1-Ile8-AII (without BSA) from type 1 Angiotensin II receptor of rabbit aortaDisplacement of [125I]Sar1-Ile8-AII (without BSA) from type 1 Angiotensin II receptor of rabbit aorta
ChEMBL 551 10 2 8 5.8 CCCCc1nc2ccc(NC(=O)OCC(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80335-2
45102750 63432 3 None - 1 Human 8.8 pIC50 = 8.8 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor afterDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after
ChEMBL 477 6 1 6 5.9 CCc1nc2c(C)cc(CC(C)C)nc2n1[C@H]1CCc2cc(-c3ccccc3-c3nnn[nH]3)ccc21 10.1016/j.bmcl.2012.11.088
CHEMBL1801740 63432 3 None - 1 Human 8.8 pIC50 = 8.8 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor afterDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after
ChEMBL 477 6 1 6 5.9 CCc1nc2c(C)cc(CC(C)C)nc2n1[C@H]1CCc2cc(-c3ccccc3-c3nnn[nH]3)ccc21 10.1016/j.bmcl.2012.11.088
45102750 63432 3 None - 1 Human 8.8 pIC50 = 8.8 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation countingDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation counting
ChEMBL 477 6 1 6 5.9 CCc1nc2c(C)cc(CC(C)C)nc2n1[C@H]1CCc2cc(-c3ccccc3-c3nnn[nH]3)ccc21 10.1021/jm200409s
CHEMBL1801740 63432 3 None - 1 Human 8.8 pIC50 = 8.8 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation countingDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation counting
ChEMBL 477 6 1 6 5.9 CCc1nc2c(C)cc(CC(C)C)nc2n1[C@H]1CCc2cc(-c3ccccc3-c3nnn[nH]3)ccc21 10.1021/jm200409s
19754050 202173 0 None - 0 Rabbit 8.8 pIC50 = 8.8 Binding
In vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranesIn vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranes
ChEMBL 603 15 2 7 6.6 CCCCC(=O)Nc1cnc2c(c1)nc(CCCC)n2Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)CCCC)cc1 10.1016/S0960-894X(01)81115-X
CHEMBL68786 202173 0 None - 0 Rabbit 8.8 pIC50 = 8.8 Binding
In vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranesIn vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranes
ChEMBL 603 15 2 7 6.6 CCCCC(=O)Nc1cnc2c(c1)nc(CCCC)n2Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)CCCC)cc1 10.1016/S0960-894X(01)81115-X
11764826 97819 0 None - 0 Rabbit 8.8 pIC50 = 8.8 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 648 11 1 7 6.2 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)Cc2ccccc2)cc1 10.1021/jm00043a020
CHEMBL274710 97819 0 None - 0 Rabbit 8.8 pIC50 = 8.8 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 648 11 1 7 6.2 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)Cc2ccccc2)cc1 10.1021/jm00043a020
10233056 106662 0 None - 0 Rabbit 8.8 pIC50 = 8.8 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 637 10 1 8 5.6 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2cccn2C)cc1 10.1021/jm00043a020
CHEMBL316297 106662 0 None - 0 Rabbit 8.8 pIC50 = 8.8 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 637 10 1 8 5.6 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2cccn2C)cc1 10.1021/jm00043a020
10259525 15428 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 753 10 2 9 7.3 CCCc1nn(-c2cc(NC(=O)c3ccccc3)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1021/jm00019a004
CHEMBL122158 15428 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 753 10 2 9 7.3 CCCc1nn(-c2cc(NC(=O)c3ccccc3)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1021/jm00019a004
10259841 15967 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 815 13 2 8 7.6 CCCCNC(=O)c1ccc(Br)c(-n2nc(CCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)c4cc(Cl)ccc4Cl)cc3F)c2=O)c1 10.1021/jm00019a004
CHEMBL122401 15967 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 815 13 2 8 7.6 CCCCNC(=O)c1ccc(Br)c(-n2nc(CCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)c4cc(Cl)ccc4Cl)cc3F)c2=O)c1 10.1021/jm00019a004
44315351 104393 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membrane
ChEMBL 687 10 3 7 6.2 CCc1ccc(C(=O)NS(=O)(=O)c2ccccc2-c2ccc(Cn3c(CC)nc4ccc(NC(=O)NC(C)C)cc4c3=O)c(F)c2)c(F)c1 10.1016/0960-894X(94)85036-4
CHEMBL311160 104393 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membrane
ChEMBL 687 10 3 7 6.2 CCc1ccc(C(=O)NS(=O)(=O)c2ccccc2-c2ccc(Cn3c(CC)nc4ccc(NC(=O)NC(C)C)cc4c3=O)c(F)c2)c(F)c1 10.1016/0960-894X(94)85036-4
10484986 118179 0 None - 0 Rabbit 8.8 pIC50 = 8.8 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 713 11 1 9 6.8 CCCCc1nn(-c2ccc([N+](=O)[O-])cc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1021/jm00052a006
CHEMBL341715 118179 0 None - 0 Rabbit 8.8 pIC50 = 8.8 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 713 11 1 9 6.8 CCCCc1nn(-c2ccc([N+](=O)[O-])cc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1021/jm00052a006
10030086 16781 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 535 12 1 7 5.3 CCCCc1ncc(/C=C2\C(=O)N(CCCC)C(=O)N2Cc2csc(C)n2)n1Cc1ccc(C(=O)O)cc1 10.1007/s00044-009-9205-9
CHEMBL125383 16781 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 535 12 1 7 5.3 CCCCc1ncc(/C=C2\C(=O)N(CCCC)C(=O)N2Cc2csc(C)n2)n1Cc1ccc(C(=O)O)cc1 10.1007/s00044-009-9205-9
136052394 123965 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 598 8 1 9 5.4 CCc1cc2c(=O)n(CC(=O)c3ccc(Cl)cc3)c(=O)n(Cc3ccc(-c4ccccc4-c4nc(=O)o[nH]4)cc3)c2s1 nan
CHEMBL3640136 123965 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 598 8 1 9 5.4 CCc1cc2c(=O)n(CC(=O)c3ccc(Cl)cc3)c(=O)n(Cc3ccc(-c4ccccc4-c4nc(=O)o[nH]4)cc3)c2s1 nan
136052399 123971 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 622 8 1 9 5.6 CCc1cc2c(=O)n(CC(=O)C34CC5CC(CC(C5)C3)C4)c(=O)n(Cc3ccc(-c4ccccc4-c4nc(=O)o[nH]4)cc3)c2s1 nan
CHEMBL3640141 123971 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 622 8 1 9 5.6 CCc1cc2c(=O)n(CC(=O)C34CC5CC(CC(C5)C3)C4)c(=O)n(Cc3ccc(-c4ccccc4-c4nc(=O)o[nH]4)cc3)c2s1 nan
136052347 123974 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 618 8 1 11 4.6 CCc1cc2c(=O)n(CC(=O)c3nc4ccccc4n3C)c(=O)n(Cc3ccc(-c4ccccc4-c4nc(=O)o[nH]4)cc3)c2s1 nan
CHEMBL3640144 123974 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 618 8 1 11 4.6 CCc1cc2c(=O)n(CC(=O)c3nc4ccccc4n3C)c(=O)n(Cc3ccc(-c4ccccc4-c4nc(=O)o[nH]4)cc3)c2s1 nan
136052345 123977 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 530 7 1 9 3.9 CCc1cc2c(=O)n(CC3(C)COC3)c(=O)n(Cc3ccc(-c4ccccc4-c4nc(=O)o[nH]4)cc3)c2s1 nan
CHEMBL3640147 123977 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 530 7 1 9 3.9 CCc1cc2c(=O)n(CC3(C)COC3)c(=O)n(Cc3ccc(-c4ccccc4-c4nc(=O)o[nH]4)cc3)c2s1 nan
136052268 123978 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 560 7 2 10 3.4 CCc1cc2c(=O)n(CC3(O)CCOCC3)c(=O)n(Cc3ccc(-c4ccccc4-c4nc(=O)o[nH]4)cc3)c2s1 nan
CHEMBL3640148 123978 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 560 7 2 10 3.4 CCc1cc2c(=O)n(CC3(O)CCOCC3)c(=O)n(Cc3ccc(-c4ccccc4-c4nc(=O)o[nH]4)cc3)c2s1 nan
136052310 123986 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 626 10 1 10 5.3 CCCc1cc2c(=O)n(CC(=O)c3ccc(OC)cc3)c(=O)n(Cc3ccc(-c4ccccc4-c4nc(=O)o[nH]4)cc3F)c2s1 nan
CHEMBL3640156 123986 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 626 10 1 10 5.3 CCCc1cc2c(=O)n(CC(=O)c3ccc(OC)cc3)c(=O)n(Cc3ccc(-c4ccccc4-c4nc(=O)o[nH]4)cc3F)c2s1 nan
136052379 123992 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 672 9 1 11 5.9 CCc1cc2c(=O)n(CC(=O)c3ccc(OC)cc3)c(=O)n(Cc3ccc(-c4ccccc4-c4noc(O)n4)cc3Br)c2s1 nan
CHEMBL3640161 123992 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 672 9 1 11 5.9 CCc1cc2c(=O)n(CC(=O)c3ccc(OC)cc3)c(=O)n(Cc3ccc(-c4ccccc4-c4noc(O)n4)cc3Br)c2s1 nan
9851889 101591 0 None - 0 Rabbit 8.8 pIC50 = 8.8 Binding
Binding affinity against AT-1 receptor from rabbit aorta using [125I]-Sar1-Ile8-Ang II without BSABinding affinity against AT-1 receptor from rabbit aorta using [125I]-Sar1-Ile8-Ang II without BSA
ChEMBL 611 12 1 7 7.1 CCCCCN(C(=O)c1ccccc1)c1ccc2nc(CCC)n(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c(=O)c2c1 10.1021/jm00073a024
CHEMBL302102 101591 0 None - 0 Rabbit 8.8 pIC50 = 8.8 Binding
Binding affinity against AT-1 receptor from rabbit aorta using [125I]-Sar1-Ile8-Ang II without BSABinding affinity against AT-1 receptor from rabbit aorta using [125I]-Sar1-Ile8-Ang II without BSA
ChEMBL 611 12 1 7 7.1 CCCCCN(C(=O)c1ccccc1)c1ccc2nc(CCC)n(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c(=O)c2c1 10.1021/jm00073a024
44277573 99067 0 None - 0 Rabbit 8.8 pIC50 = 8.8 Binding
Binding affinity against AT1 receptor in rabbit aortaBinding affinity against AT1 receptor in rabbit aorta
ChEMBL 604 8 0 9 5.5 Cn1nnnc1-c1ccccc1-c1ccc(Cn2cnc3ccc(N(Cc4cccnc4)C(=O)c4ccccc4)cc3c2=O)cc1 10.1016/0960-894X(95)00224-H
CHEMBL283495 99067 0 None - 0 Rabbit 8.8 pIC50 = 8.8 Binding
Binding affinity against AT1 receptor in rabbit aortaBinding affinity against AT1 receptor in rabbit aorta
ChEMBL 604 8 0 9 5.5 Cn1nnnc1-c1ccccc1-c1ccc(Cn2cnc3ccc(N(Cc4cccnc4)C(=O)c4ccccc4)cc3c2=O)cc1 10.1016/0960-894X(95)00224-H
44277442 99820 0 None - 0 Rabbit 8.8 pIC50 = 8.8 Binding
Binding affinity against AT1 receptor in rabbit aortaBinding affinity against AT1 receptor in rabbit aorta
ChEMBL 583 10 0 8 6.1 CCCCCN(C(=O)c1ccccc1)c1ccc2ncn(Cc3ccc(-c4ccccc4-c4nnnn4C)cc3)c(=O)c2c1 10.1016/0960-894X(95)00224-H
CHEMBL28917 99820 0 None - 0 Rabbit 8.8 pIC50 = 8.8 Binding
Binding affinity against AT1 receptor in rabbit aortaBinding affinity against AT1 receptor in rabbit aorta
ChEMBL 583 10 0 8 6.1 CCCCCN(C(=O)c1ccccc1)c1ccc2ncn(Cc3ccc(-c4ccccc4-c4nnnn4C)cc3)c(=O)c2c1 10.1016/0960-894X(95)00224-H
44277451 100426 0 None - 0 Rabbit 8.8 pIC50 = 8.8 Binding
Binding affinity against AT1 receptor in rabbit aortaBinding affinity against AT1 receptor in rabbit aorta
ChEMBL 601 10 0 8 6.3 CCCCCN(C(=O)c1ccc(F)cc1)c1ccc2ncn(Cc3ccc(-c4ccccc4-c4nnnn4C)cc3)c(=O)c2c1 10.1016/0960-894X(95)00224-H
CHEMBL29386 100426 0 None - 0 Rabbit 8.8 pIC50 = 8.8 Binding
Binding affinity against AT1 receptor in rabbit aortaBinding affinity against AT1 receptor in rabbit aorta
ChEMBL 601 10 0 8 6.3 CCCCCN(C(=O)c1ccc(F)cc1)c1ccc2ncn(Cc3ccc(-c4ccccc4-c4nnnn4C)cc3)c(=O)c2c1 10.1016/0960-894X(95)00224-H
44283174 99599 0 None - 0 Rabbit 8.8 pIC50 = 8.8 Binding
Displacement of [125 I]Sar1Ile8-AII from type 1 Angiotensin II receptor of rabbit aorta membraneDisplacement of [125 I]Sar1Ile8-AII from type 1 Angiotensin II receptor of rabbit aorta membrane
ChEMBL 617 9 1 7 7.2 CCCc1nc2ccc(N(C(=O)c3ccccc3)c3ccccc3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80517-5
CHEMBL287250 99599 0 None - 0 Rabbit 8.8 pIC50 = 8.8 Binding
Displacement of [125 I]Sar1Ile8-AII from type 1 Angiotensin II receptor of rabbit aorta membraneDisplacement of [125 I]Sar1Ile8-AII from type 1 Angiotensin II receptor of rabbit aorta membrane
ChEMBL 617 9 1 7 7.2 CCCc1nc2ccc(N(C(=O)c3ccccc3)c3ccccc3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80517-5
9851889 101591 0 None - 0 Rabbit 8.8 pIC50 = 8.8 Binding
In vitro ability to inhibit the binding of radioligand 125I[Sar1,IIe8]AII to AT1 receptor from rabbit aortaIn vitro ability to inhibit the binding of radioligand 125I[Sar1,IIe8]AII to AT1 receptor from rabbit aorta
ChEMBL 611 12 1 7 7.1 CCCCCN(C(=O)c1ccccc1)c1ccc2nc(CCC)n(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c(=O)c2c1 10.1016/S0960-894X(01)80595-3
CHEMBL302102 101591 0 None - 0 Rabbit 8.8 pIC50 = 8.8 Binding
In vitro ability to inhibit the binding of radioligand 125I[Sar1,IIe8]AII to AT1 receptor from rabbit aortaIn vitro ability to inhibit the binding of radioligand 125I[Sar1,IIe8]AII to AT1 receptor from rabbit aorta
ChEMBL 611 12 1 7 7.1 CCCCCN(C(=O)c1ccccc1)c1ccc2nc(CCC)n(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c(=O)c2c1 10.1016/S0960-894X(01)80595-3
44310589 167524 0 None - 0 Rabbit 8.8 pIC50 = 8.8 Binding
In vitro binding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membraneIn vitro binding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane
ChEMBL 488 6 1 5 5.4 CCc1nc2c(C)cc(C)nn2c1Cc1ccc(-c2ccccc2NS(=O)(=O)C(F)(F)F)cc1 10.1016/S0960-894X(01)81150-1
CHEMBL432734 167524 0 None - 0 Rabbit 8.8 pIC50 = 8.8 Binding
In vitro binding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membraneIn vitro binding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane
ChEMBL 488 6 1 5 5.4 CCc1nc2c(C)cc(C)nn2c1Cc1ccc(-c2ccccc2NS(=O)(=O)C(F)(F)F)cc1 10.1016/S0960-894X(01)81150-1
9851889 101591 0 None - 0 Rabbit 8.8 pIC50 = 8.8 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 611 12 1 7 7.1 CCCCCN(C(=O)c1ccccc1)c1ccc2nc(CCC)n(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c(=O)c2c1 10.1021/jm00019a004
CHEMBL302102 101591 0 None - 0 Rabbit 8.8 pIC50 = 8.8 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 611 12 1 7 7.1 CCCCCN(C(=O)c1ccccc1)c1ccc2nc(CCC)n(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c(=O)c2c1 10.1021/jm00019a004
44377199 57103 0 None - 0 Rabbit 8.8 pIC50 = 8.8 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aortaIn vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aorta
ChEMBL 531 10 2 6 4.9 CCCc1nc(CC)c(C(=O)O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/S0960-894X(01)81124-0
CHEMBL165349 57103 0 None - 0 Rabbit 8.8 pIC50 = 8.8 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aortaIn vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aorta
ChEMBL 531 10 2 6 4.9 CCCc1nc(CC)c(C(=O)O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/S0960-894X(01)81124-0
9851889 101591 0 None - 0 Rabbit 8.8 pIC50 = 8.8 Binding
Inhibition of Angiotensin II receptor, type 1Inhibition of Angiotensin II receptor, type 1
ChEMBL 611 12 1 7 7.1 CCCCCN(C(=O)c1ccccc1)c1ccc2nc(CCC)n(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c(=O)c2c1 10.1021/jm9504722
CHEMBL302102 101591 0 None - 0 Rabbit 8.8 pIC50 = 8.8 Binding
Inhibition of Angiotensin II receptor, type 1Inhibition of Angiotensin II receptor, type 1
ChEMBL 611 12 1 7 7.1 CCCCCN(C(=O)c1ccccc1)c1ccc2nc(CCC)n(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c(=O)c2c1 10.1021/jm9504722
9801006 119211 0 None - 1 Rabbit 8.8 pIC50 = 8.8 Binding
Inhibitory activity was evaluated against angiotensin II type 1 rabbit aortaInhibitory activity was evaluated against angiotensin II type 1 rabbit aorta
ChEMBL 398 6 1 7 3.6 CCc1nc2c(CC)cn(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)n2n1 10.1021/jm9504722
CHEMBL347610 119211 0 None - 1 Rabbit 8.8 pIC50 = 8.8 Binding
Inhibitory activity was evaluated against angiotensin II type 1 rabbit aortaInhibitory activity was evaluated against angiotensin II type 1 rabbit aorta
ChEMBL 398 6 1 7 3.6 CCc1nc2c(CC)cn(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)n2n1 10.1021/jm9504722
9851889 101591 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Inhibitory concentration against angiotensin II receptor, type 1Inhibitory concentration against angiotensin II receptor, type 1
ChEMBL 611 12 1 7 7.1 CCCCCN(C(=O)c1ccccc1)c1ccc2nc(CCC)n(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c(=O)c2c1 10.1021/jm058225d
CHEMBL302102 101591 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Inhibitory concentration against angiotensin II receptor, type 1Inhibitory concentration against angiotensin II receptor, type 1
ChEMBL 611 12 1 7 7.1 CCCCCN(C(=O)c1ccccc1)c1ccc2nc(CCC)n(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c(=O)c2c1 10.1021/jm058225d
9851889 101591 0 None - 0 Rabbit 8.8 pIC50 = 8.8 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 611 12 1 7 7.1 CCCCCN(C(=O)c1ccccc1)c1ccc2nc(CCC)n(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c(=O)c2c1 10.1021/jm00052a006
CHEMBL302102 101591 0 None - 0 Rabbit 8.8 pIC50 = 8.8 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 611 12 1 7 7.1 CCCCCN(C(=O)c1ccccc1)c1ccc2nc(CCC)n(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c(=O)c2c1 10.1021/jm00052a006
10258916 29483 0 None - 0 Rabbit 8.7 pIC50 = 8.7 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 668 11 1 10 6.1 CCCCc1nn(-c2ccc(C(=O)OCC)cc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1 10.1007/s00044-013-0831-x
CHEMBL138654 29483 0 None - 0 Rabbit 8.7 pIC50 = 8.7 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 668 11 1 10 6.1 CCCCc1nn(-c2ccc(C(=O)OCC)cc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1 10.1007/s00044-013-0831-x
10010164 116881 0 None - 0 Rabbit 8.7 pIC50 = 8.7 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 729 11 2 9 6.0 CCCCNC(=O)c1ccc(Br)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1007/s00044-011-9815-x
CHEMBL339806 116881 0 None - 0 Rabbit 8.7 pIC50 = 8.7 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 729 11 2 9 6.0 CCCCNC(=O)c1ccc(Br)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1007/s00044-011-9815-x
9845644 204697 0 None - 0 Rabbit 8.7 pIC50 = 8.7 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 431 9 1 7 4.3 CCCCc1nn(C(C)CC)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
CHEMBL87964 204697 0 None - 0 Rabbit 8.7 pIC50 = 8.7 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 431 9 1 7 4.3 CCCCc1nn(C(C)CC)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
136052351 123963 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 608 9 1 11 5.5 CCc1cc2c(=O)n(CC(=O)c3ccc(OC)cc3)c(=O)n(Cc3ccc(-c4ccccc4-c4noc(O)n4)cc3C)c2s1 nan
CHEMBL3640134 123963 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 608 9 1 11 5.5 CCc1cc2c(=O)n(CC(=O)c3ccc(OC)cc3)c(=O)n(Cc3ccc(-c4ccccc4-c4noc(O)n4)cc3C)c2s1 nan
136052241 123964 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 577 8 1 10 3.3 CCc1cc2c(=O)n(CCN3CCOCC3)c(=O)n(Cc3ccc(-c4ccccc4-c4nc(=O)o[nH]4)cc3F)c2s1 nan
CHEMBL3640135 123964 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 577 8 1 10 3.3 CCc1cc2c(=O)n(CCN3CCOCC3)c(=O)n(Cc3ccc(-c4ccccc4-c4nc(=O)o[nH]4)cc3F)c2s1 nan
136052269 123980 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 546 7 2 9 4.3 CCc1cc2c(=O)n(CC(O)C(C)(C)C)c(=O)n(Cc3ccc(-c4ccccc4-c4nc(=O)o[nH]4)cc3)c2s1 nan
CHEMBL3640150 123980 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 546 7 2 9 4.3 CCc1cc2c(=O)n(CC(O)C(C)(C)C)c(=O)n(Cc3ccc(-c4ccccc4-c4nc(=O)o[nH]4)cc3)c2s1 nan
136052400 123995 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 612 9 1 10 4.9 CCc1cc2c(=O)n(CC(=O)c3ccc(OC)cc3)c(=O)n(Cc3ccc(-c4cc(F)ccc4-c4nc(=O)o[nH]4)cc3)c2s1 nan
CHEMBL3640164 123995 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 612 9 1 10 4.9 CCc1cc2c(=O)n(CC(=O)c3ccc(OC)cc3)c(=O)n(Cc3ccc(-c4cc(F)ccc4-c4nc(=O)o[nH]4)cc3)c2s1 nan
136401533 160282 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 649 12 1 11 5.5 C=CCO/N=C(\Cn1c(=O)c2cc(CC)sc2n(Cc2ccc(-c3ccccc3-c3nc(=O)o[nH]3)cc2)c1=O)c1ccc(OC)cc1 nan
CHEMBL4114807 160282 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 649 12 1 11 5.5 C=CCO/N=C(\Cn1c(=O)c2cc(CC)sc2n(Cc2ccc(-c3ccccc3-c3nc(=O)o[nH]3)cc2)c1=O)c1ccc(OC)cc1 nan
108185 1578 71 None - 1 Rat 8.7 pIC50 = 8.7 Binding
Binding affinity against AT1 receptor in the presence of 0.01% BSABinding affinity against AT1 receptor in the presence of 0.01% BSA
ChEMBL 436 8 2 6 4.5 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)C(=O)O)Cl 10.1021/jm00037a014
586 1578 71 None - 1 Rat 8.7 pIC50 = 8.7 Binding
Binding affinity against AT1 receptor in the presence of 0.01% BSABinding affinity against AT1 receptor in the presence of 0.01% BSA
ChEMBL 436 8 2 6 4.5 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)C(=O)O)Cl 10.1021/jm00037a014
CHEMBL907 1578 71 None - 1 Rat 8.7 pIC50 = 8.7 Binding
Binding affinity against AT1 receptor in the presence of 0.01% BSABinding affinity against AT1 receptor in the presence of 0.01% BSA
ChEMBL 436 8 2 6 4.5 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)C(=O)O)Cl 10.1021/jm00037a014
10010164 116881 0 None - 0 Rabbit 8.7 pIC50 = 8.7 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 729 11 2 9 6.0 CCCCNC(=O)c1ccc(Br)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1021/jm00019a004
CHEMBL339806 116881 0 None - 0 Rabbit 8.7 pIC50 = 8.7 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 729 11 2 9 6.0 CCCCNC(=O)c1ccc(Br)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1021/jm00019a004
10100074 112055 0 None - 0 Rabbit 8.7 pIC50 = 8.7 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 598 9 1 6 6.4 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2NS(=O)(=O)C(F)(F)F)cc1 10.1021/jm00043a020
CHEMBL330007 112055 0 None - 0 Rabbit 8.7 pIC50 = 8.7 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 598 9 1 6 6.4 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2NS(=O)(=O)C(F)(F)F)cc1 10.1021/jm00043a020
9810305 98107 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 701 11 2 9 6.7 CCCCc1nn(-c2cc(NC(=O)CC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1 10.1021/jm00019a004
CHEMBL276674 98107 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 701 11 2 9 6.7 CCCCc1nn(-c2cc(NC(=O)CC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1 10.1021/jm00019a004
10258916 29483 0 None - 0 Rabbit 8.7 pIC50 = 8.7 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 668 11 1 10 6.1 CCCCc1nn(-c2ccc(C(=O)OCC)cc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1 10.1021/jm00052a006
CHEMBL138654 29483 0 None - 0 Rabbit 8.7 pIC50 = 8.7 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 668 11 1 10 6.1 CCCCc1nn(-c2ccc(C(=O)OCC)cc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1 10.1021/jm00052a006
10010164 116881 0 None - 0 Rabbit 8.7 pIC50 = 8.7 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 729 11 2 9 6.0 CCCCNC(=O)c1ccc(Br)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1007/s00044-011-9815-x
CHEMBL339806 116881 0 None - 0 Rabbit 8.7 pIC50 = 8.7 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 729 11 2 9 6.0 CCCCNC(=O)c1ccc(Br)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1007/s00044-011-9815-x
10394859 17232 0 None - 0 Rabbit 8.7 pIC50 = 8.7 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 687 11 2 10 5.3 CCOCC(=O)Nc1ccc(Cl)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1007/s00044-011-9815-x
CHEMBL125760 17232 0 None - 0 Rabbit 8.7 pIC50 = 8.7 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 687 11 2 10 5.3 CCOCC(=O)Nc1ccc(Cl)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1007/s00044-011-9815-x
9960721 16120 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 549 12 0 8 5.4 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2Cc2csc(C)n2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
CHEMBL122638 16120 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 549 12 0 8 5.4 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2Cc2csc(C)n2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
59351471 123984 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 417 5 1 6 3.9 CCc1cc2c(=O)[nH]c(=O)n(Cc3ccc(-c4ccccc4C#N)cc3OC)c2s1 nan
CHEMBL3640154 123984 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 417 5 1 6 3.9 CCc1cc2c(=O)[nH]c(=O)n(Cc3ccc(-c4ccccc4C#N)cc3OC)c2s1 nan
136052367 124000 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 648 8 1 10 5.6 CCc1cc2c(=O)n(CC(=O)c3sccc3Br)c(=O)n(Cc3ccc(-c4ccccc4-c4nc(=O)o[nH]4)cc3)c2s1 nan
CHEMBL3640172 124000 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 648 8 1 10 5.6 CCc1cc2c(=O)n(CC(=O)c3sccc3Br)c(=O)n(Cc3ccc(-c4ccccc4-c4nc(=O)o[nH]4)cc3)c2s1 nan
44277652 99350 0 None - 0 Rabbit 8.7 pIC50 = 8.7 Binding
Binding affinity against AT1 receptor in rabbit aortaBinding affinity against AT1 receptor in rabbit aorta
ChEMBL 573 8 0 8 5.5 CCCN(C(=O)c1ccc(F)cc1)c1ccc2ncn(Cc3ccc(-c4ccccc4-c4nnnn4C)cc3)c(=O)c2c1 10.1016/0960-894X(95)00224-H
CHEMBL28555 99350 0 None - 0 Rabbit 8.7 pIC50 = 8.7 Binding
Binding affinity against AT1 receptor in rabbit aortaBinding affinity against AT1 receptor in rabbit aorta
ChEMBL 573 8 0 8 5.5 CCCN(C(=O)c1ccc(F)cc1)c1ccc2ncn(Cc3ccc(-c4ccccc4-c4nnnn4C)cc3)c(=O)c2c1 10.1016/0960-894X(95)00224-H
2806 3894 109 None - 1 Rat 8.7 pIC50 = 8.7 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 435 10 2 5 4.2 CCCCC(=O)N([C@H](C(=O)O)C(C)C)Cc1ccc(cc1)c1ccccc1c1nnn[nH]1 10.1021/jm031100t
3937 3894 109 None - 1 Rat 8.7 pIC50 = 8.7 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 435 10 2 5 4.2 CCCCC(=O)N([C@H](C(=O)O)C(C)C)Cc1ccc(cc1)c1ccccc1c1nnn[nH]1 10.1021/jm031100t
593 3894 109 None - 1 Rat 8.7 pIC50 = 8.7 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 435 10 2 5 4.2 CCCCC(=O)N([C@H](C(=O)O)C(C)C)Cc1ccc(cc1)c1ccccc1c1nnn[nH]1 10.1021/jm031100t
60846 3894 109 None - 1 Rat 8.7 pIC50 = 8.7 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 435 10 2 5 4.2 CCCCC(=O)N([C@H](C(=O)O)C(C)C)Cc1ccc(cc1)c1ccccc1c1nnn[nH]1 10.1021/jm031100t
CHEMBL1069 3894 109 None - 1 Rat 8.7 pIC50 = 8.7 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 435 10 2 5 4.2 CCCCC(=O)N([C@H](C(=O)O)C(C)C)Cc1ccc(cc1)c1ccccc1c1nnn[nH]1 10.1021/jm031100t
DB00177 3894 109 None - 1 Rat 8.7 pIC50 = 8.7 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 435 10 2 5 4.2 CCCCC(=O)N([C@H](C(=O)O)C(C)C)Cc1ccc(cc1)c1ccccc1c1nnn[nH]1 10.1021/jm031100t
10394859 17232 0 None - 0 Rabbit 8.7 pIC50 = 8.7 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 687 11 2 10 5.3 CCOCC(=O)Nc1ccc(Cl)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1021/jm00019a004
CHEMBL125760 17232 0 None - 0 Rabbit 8.7 pIC50 = 8.7 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 687 11 2 10 5.3 CCOCC(=O)Nc1ccc(Cl)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1021/jm00019a004
44376746 119341 0 None - 0 Rabbit 8.7 pIC50 = 8.7 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aortaIn vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aorta
ChEMBL 568 16 2 7 5.9 CCCCCCCC(=O)NS(=O)(=O)Nc1ccccc1-c1ccc(Cn2c(C(=O)OC)cnc2CCCC)cc1 10.1016/S0960-894X(01)81124-0
CHEMBL348758 119341 0 None - 0 Rabbit 8.7 pIC50 = 8.7 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aortaIn vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aorta
ChEMBL 568 16 2 7 5.9 CCCCCCCC(=O)NS(=O)(=O)Nc1ccccc1-c1ccc(Cn2c(C(=O)OC)cnc2CCCC)cc1 10.1016/S0960-894X(01)81124-0
10033136 15882 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 769 12 2 8 6.7 CCCCC(=O)Nc1ccc(Br)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)c4cc(F)ccc4F)cc3F)c2=O)c1 10.1021/jm00019a004
CHEMBL122380 15882 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 769 12 2 8 6.7 CCCCC(=O)Nc1ccc(Br)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)c4cc(F)ccc4F)cc3F)c2=O)c1 10.1021/jm00019a004
44315078 203038 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membrane
ChEMBL 693 13 2 8 6.9 CCCCc1nc2ccc(NC(=O)N(C)C(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/0960-894X(94)85036-4
CHEMBL74556 203038 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membrane
ChEMBL 693 13 2 8 6.9 CCCCc1nc2ccc(NC(=O)N(C)C(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/0960-894X(94)85036-4
44303230 198953 0 None - 0 Rabbit 8.7 pIC50 = 8.7 Binding
Inhibition of Angiotensin II receptor, type 1Inhibition of Angiotensin II receptor, type 1
ChEMBL 515 10 1 6 5.0 CCCc1nc(CC)c(C=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1021/jm9504722
CHEMBL59957 198953 0 None - 0 Rabbit 8.7 pIC50 = 8.7 Binding
Inhibition of Angiotensin II receptor, type 1Inhibition of Angiotensin II receptor, type 1
ChEMBL 515 10 1 6 5.0 CCCc1nc(CC)c(C=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1021/jm9504722
10394859 17232 0 None - 0 Rabbit 8.7 pIC50 = 8.7 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 687 11 2 10 5.3 CCOCC(=O)Nc1ccc(Cl)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1007/s00044-011-9815-x
CHEMBL125760 17232 0 None - 0 Rabbit 8.7 pIC50 = 8.7 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 687 11 2 10 5.3 CCOCC(=O)Nc1ccc(Cl)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1007/s00044-011-9815-x
76308179 84537 0 None - 0 Rabbit 8.0 pIC50 = 8 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 584 12 3 9 4.1 CCCCc1nnc([S+]([O-])Cc2ccccc2C(=O)O)n1Cc1ccc(NC(=O)c2ccccc2-c2nnn[nH]2)cc1 10.1007/s00044-011-9756-4
CHEMBL2237607 84537 0 None - 0 Rabbit 8.0 pIC50 = 8 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 584 12 3 9 4.1 CCCCc1nnc([S+]([O-])Cc2ccccc2C(=O)O)n1Cc1ccc(NC(=O)c2ccccc2-c2nnn[nH]2)cc1 10.1007/s00044-011-9756-4
10222835 204415 0 None - 0 Rabbit 8.0 pIC50 = 8 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 403 8 1 7 3.3 CCCCc1nn(CC)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
CHEMBL86084 204415 0 None - 0 Rabbit 8.0 pIC50 = 8 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 403 8 1 7 3.3 CCCCc1nn(CC)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
44459556 98265 0 None - 0 Rabbit 8.0 pIC50 = 8 Binding
Binding affinity against Angiotensin II type 1 Receptor in rabbit aortic tissueBinding affinity against Angiotensin II type 1 Receptor in rabbit aortic tissue
ChEMBL 436 6 1 6 4.6 CCCc1nc2ccc(C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80334-0
CHEMBL277902 98265 0 None - 0 Rabbit 8.0 pIC50 = 8 Binding
Binding affinity against Angiotensin II type 1 Receptor in rabbit aortic tissueBinding affinity against Angiotensin II type 1 Receptor in rabbit aortic tissue
ChEMBL 436 6 1 6 4.6 CCCc1nc2ccc(C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80334-0
19087866 98466 0 None - 0 Rabbit 8.0 pIC50 = 8 Binding
Binding affinity against Angiotensin II type 1 Receptor in rabbit aortic tissueBinding affinity against Angiotensin II type 1 Receptor in rabbit aortic tissue
ChEMBL 436 7 1 6 4.6 CCCCc1nc2ccccc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80334-0
CHEMBL279515 98466 0 None - 0 Rabbit 8.0 pIC50 = 8 Binding
Binding affinity against Angiotensin II type 1 Receptor in rabbit aortic tissueBinding affinity against Angiotensin II type 1 Receptor in rabbit aortic tissue
ChEMBL 436 7 1 6 4.6 CCCCc1nc2ccccc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80334-0
44459544 98897 0 None - 0 Rabbit 8.0 pIC50 = 8 Binding
Binding affinity against Angiotensin II type 1 Receptor in rabbit aortic tissueBinding affinity against Angiotensin II type 1 Receptor in rabbit aortic tissue
ChEMBL 454 7 1 6 4.8 CCCCc1nc2cccc(F)c2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80334-0
CHEMBL282526 98897 0 None - 0 Rabbit 8.0 pIC50 = 8 Binding
Binding affinity against Angiotensin II type 1 Receptor in rabbit aortic tissueBinding affinity against Angiotensin II type 1 Receptor in rabbit aortic tissue
ChEMBL 454 7 1 6 4.8 CCCCc1nc2cccc(F)c2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80334-0
44311428 102483 0 None - 0 Human 8.0 pIC50 = 8 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 647 17 1 8 7.1 CCCCN(Cc1ccccc1)C(=O)CCCOC(=O)c1c(CC)nc(CCC)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80077-3
CHEMBL306473 102483 0 None - 0 Human 8.0 pIC50 = 8 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 647 17 1 8 7.1 CCCCN(Cc1ccccc1)C(=O)CCCOC(=O)c1c(CC)nc(CCC)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80077-3
44311543 103651 0 None - 0 Human 8.0 pIC50 = 8 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 643 14 1 8 6.3 CCCCN(Cc1ccccc1)C(=O)C#CCOC(=O)c1c(CC)nc(CCC)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80077-3
CHEMBL309455 103651 0 None - 0 Human 8.0 pIC50 = 8 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 643 14 1 8 6.3 CCCCN(Cc1ccccc1)C(=O)C#CCOC(=O)c1c(CC)nc(CCC)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80077-3
10069786 168524 0 None - 0 Rat 8.0 pIC50 = 8 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 404 7 1 3 5.3 CCCCC1=NC2(CCCC2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00074a018
CHEMBL439968 168524 0 None - 0 Rat 8.0 pIC50 = 8 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 404 7 1 3 5.3 CCCCC1=NC2(CCCC2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00074a018
19008869 204678 0 None - 0 Rat 8.0 pIC50 = 8 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 385 5 1 4 5.0 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm031100t
CHEMBL87842 204678 0 None - 0 Rat 8.0 pIC50 = 8 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 385 5 1 4 5.0 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm031100t
10325037 119269 0 None - 0 Rabbit 8.0 pIC50 = 8 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 541 11 2 8 4.5 CCCCc1nnc([S+]([O-])Cc2ccccc2C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
CHEMBL348143 119269 0 None - 0 Rabbit 8.0 pIC50 = 8 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 541 11 2 8 4.5 CCCCc1nnc([S+]([O-])Cc2ccccc2C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
73353933 92173 0 None - 0 Human 8.0 pIC50 = 8 Binding
Displacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysisDisplacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysis
ChEMBL 554 11 2 6 5.2 CCCc1nc2c(C)cc(C(=O)NCCCN3CCOCC3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2013.08.014
CHEMBL2435821 92173 0 None - 0 Human 8.0 pIC50 = 8 Binding
Displacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysisDisplacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysis
ChEMBL 554 11 2 6 5.2 CCCc1nc2c(C)cc(C(=O)NCCCN3CCOCC3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2013.08.014
70696780 75852 0 None - 0 Bovine 8.0 pIC50 = 8 Binding
Displacement of [125I]AngII from type 1 angiotensin 2 receptor in bovine adrenal cortexDisplacement of [125I]AngII from type 1 angiotensin 2 receptor in bovine adrenal cortex
ChEMBL 592 9 1 6 7.3 CCCCc1nc2ccc(Br)cc2n1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)cc1 10.1016/j.bmc.2012.06.011
CHEMBL2058374 75852 0 None - 0 Bovine 8.0 pIC50 = 8 Binding
Displacement of [125I]AngII from type 1 angiotensin 2 receptor in bovine adrenal cortexDisplacement of [125I]AngII from type 1 angiotensin 2 receptor in bovine adrenal cortex
ChEMBL 592 9 1 6 7.3 CCCCc1nc2ccc(Br)cc2n1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)cc1 10.1016/j.bmc.2012.06.011
19102815 206132 0 None - 0 Rabbit 8.0 pIC50 = 8 Binding
In vitro ability to inhibit the binding of radioligand 125I[Sar1,IIe8]AII to AT1 receptor from rabbit aortaIn vitro ability to inhibit the binding of radioligand 125I[Sar1,IIe8]AII to AT1 receptor from rabbit aorta
ChEMBL 672 11 1 8 7.3 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2cc(CCC)ccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1 10.1016/S0960-894X(01)80595-3
CHEMBL96554 206132 0 None - 0 Rabbit 8.0 pIC50 = 8 Binding
In vitro ability to inhibit the binding of radioligand 125I[Sar1,IIe8]AII to AT1 receptor from rabbit aortaIn vitro ability to inhibit the binding of radioligand 125I[Sar1,IIe8]AII to AT1 receptor from rabbit aorta
ChEMBL 672 11 1 8 7.3 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2cc(CCC)ccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1 10.1016/S0960-894X(01)80595-3
44311342 101698 0 None - 0 Human 8.0 pIC50 = 8 Binding
In vitro binding affinity of compound against Angiotensin II receptor, type 1In vitro binding affinity of compound against Angiotensin II receptor, type 1
ChEMBL 611 12 3 7 5.9 CCCc1nc(CNC(=O)C(c2ccccc2)c2ccccc2)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80076-1
CHEMBL302760 101698 0 None - 0 Human 8.0 pIC50 = 8 Binding
In vitro binding affinity of compound against Angiotensin II receptor, type 1In vitro binding affinity of compound against Angiotensin II receptor, type 1
ChEMBL 611 12 3 7 5.9 CCCc1nc(CNC(=O)C(c2ccccc2)c2ccccc2)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80076-1
44311450 103611 0 None - 0 Human 8.0 pIC50 = 8 Binding
In vitro binding affinity of compound against Angiotensin II receptor, type 1In vitro binding affinity of compound against Angiotensin II receptor, type 1
ChEMBL 652 12 2 8 6.4 CCCc1nc(CN2CCN(c3ccccc3)C[C@H]2Cc2ccccc2)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80076-1
CHEMBL309365 103611 0 None - 0 Human 8.0 pIC50 = 8 Binding
In vitro binding affinity of compound against Angiotensin II receptor, type 1In vitro binding affinity of compound against Angiotensin II receptor, type 1
ChEMBL 652 12 2 8 6.4 CCCc1nc(CN2CCN(c3ccccc3)C[C@H]2Cc2ccccc2)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80076-1
44311688 103706 0 None - 0 Human 8.0 pIC50 = 8 Binding
In vitro binding affinity of compound against Angiotensin II receptor, type 1In vitro binding affinity of compound against Angiotensin II receptor, type 1
ChEMBL 554 10 2 8 3.5 CCCc1nc(CN2CCN(C(=O)C3CC3)CC2)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80076-1
CHEMBL309820 103706 0 None - 0 Human 8.0 pIC50 = 8 Binding
In vitro binding affinity of compound against Angiotensin II receptor, type 1In vitro binding affinity of compound against Angiotensin II receptor, type 1
ChEMBL 554 10 2 8 3.5 CCCc1nc(CN2CCN(C(=O)C3CC3)CC2)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80076-1
15222101 158004 0 None - 0 Human 8.0 pIC50 = 8 Binding
In vitro binding affinity of compound against Angiotensin II receptor, type 1In vitro binding affinity of compound against Angiotensin II receptor, type 1
ChEMBL 642 12 2 9 4.2 CCCc1nc(CN2CCN(c3ccccn3)CC2)c(C(=O)O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)C2CC2)cc1 10.1016/S0960-894X(00)80076-1
CHEMBL409170 158004 0 None - 0 Human 8.0 pIC50 = 8 Binding
In vitro binding affinity of compound against Angiotensin II receptor, type 1In vitro binding affinity of compound against Angiotensin II receptor, type 1
ChEMBL 642 12 2 9 4.2 CCCc1nc(CN2CCN(c3ccccn3)CC2)c(C(=O)O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)C2CC2)cc1 10.1016/S0960-894X(00)80076-1
44311664 202453 0 None - 0 Human 8.0 pIC50 = 8 Binding
In vitro binding affinity of compound against Angiotensin II receptor, type 1In vitro binding affinity of compound against Angiotensin II receptor, type 1
ChEMBL 680 12 2 8 5.9 CCCc1nc(CN2CCN(C(=O)C(c3ccccc3)c3ccccc3)CC2)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80076-1
CHEMBL70638 202453 0 None - 0 Human 8.0 pIC50 = 8 Binding
In vitro binding affinity of compound against Angiotensin II receptor, type 1In vitro binding affinity of compound against Angiotensin II receptor, type 1
ChEMBL 680 12 2 8 5.9 CCCc1nc(CN2CCN(C(=O)C(c3ccccc3)c3ccccc3)CC2)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80076-1
44311449 202765 0 None - 0 Human 8.0 pIC50 = 8 Binding
In vitro binding affinity of compound against Angiotensin II receptor, type 1In vitro binding affinity of compound against Angiotensin II receptor, type 1
ChEMBL 549 10 2 9 3.9 CCCc1nc(CN2CCN(c3ccccn3)CC2)c(CO)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80076-1
CHEMBL72409 202765 0 None - 0 Human 8.0 pIC50 = 8 Binding
In vitro binding affinity of compound against Angiotensin II receptor, type 1In vitro binding affinity of compound against Angiotensin II receptor, type 1
ChEMBL 549 10 2 9 3.9 CCCc1nc(CN2CCN(c3ccccn3)CC2)c(CO)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80076-1
15292111 203027 0 None - 0 Human 8.0 pIC50 = 8 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membrane
ChEMBL 665 11 2 8 6.1 CCc1nc2ccc(NC(=O)N(C)C(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/0960-894X(94)85036-4
CHEMBL74442 203027 0 None - 0 Human 8.0 pIC50 = 8 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membrane
ChEMBL 665 11 2 8 6.1 CCc1nc2ccc(NC(=O)N(C)C(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/0960-894X(94)85036-4
10100413 196903 0 None - 0 Rabbit 8.0 pIC50 = 8 Binding
Inhibition of Angiotensin II receptor type 1 in rabbit aorta binding assayInhibition of Angiotensin II receptor type 1 in rabbit aorta binding assay
ChEMBL 620 9 1 7 7.1 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2cc(Cc3ccccc3)sc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/S0960-894X(01)81145-8
CHEMBL57853 196903 0 None - 0 Rabbit 8.0 pIC50 = 8 Binding
Inhibition of Angiotensin II receptor type 1 in rabbit aorta binding assayInhibition of Angiotensin II receptor type 1 in rabbit aorta binding assay
ChEMBL 620 9 1 7 7.1 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2cc(Cc3ccccc3)sc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/S0960-894X(01)81145-8
44300798 197267 0 None - 0 Rabbit 8.0 pIC50 = 8 Binding
Inhibition of Angiotensin II receptor type 1 in rabbit aorta binding assayInhibition of Angiotensin II receptor type 1 in rabbit aorta binding assay
ChEMBL 558 8 1 7 6.1 CCc1cc(-c2ccc(Cn3c(CC)nc4c(C)cc(C)nc43)cc2)c(S(=O)(=O)NC(=O)c2ccccc2)s1 10.1016/S0960-894X(01)81145-8
CHEMBL58499 197267 0 None - 0 Rabbit 8.0 pIC50 = 8 Binding
Inhibition of Angiotensin II receptor type 1 in rabbit aorta binding assayInhibition of Angiotensin II receptor type 1 in rabbit aorta binding assay
ChEMBL 558 8 1 7 6.1 CCc1cc(-c2ccc(Cn3c(CC)nc4c(C)cc(C)nc43)cc2)c(S(=O)(=O)NC(=O)c2ccccc2)s1 10.1016/S0960-894X(01)81145-8
9845644 204697 0 None - 0 Rat 8.0 pIC50 = 8 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 431 9 1 7 4.3 CCCCc1nn(C(C)CC)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a015
CHEMBL87964 204697 0 None - 0 Rat 8.0 pIC50 = 8 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 431 9 1 7 4.3 CCCCc1nn(C(C)CC)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a015
9985329 21921 0 None - 0 Rat 8.0 pIC50 = 8 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 562 9 2 6 6.8 CCCCc1nc2ccc(N(C)C(=O)NC3CCCCC3)cc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00077a007
CHEMBL132226 21921 0 None - 0 Rat 8.0 pIC50 = 8 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 562 9 2 6 6.8 CCCCc1nc2ccc(N(C)C(=O)NC3CCCCC3)cc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00077a007
15287894 54647 0 None - 0 Rabbit 8.0 pIC50 = 8 Binding
Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)
ChEMBL 449 7 1 5 5.5 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(OC(C(=O)O)c2ccccc2Cl)cc1 10.1016/0960-894X(95)00185-V
CHEMBL16148 54647 0 None - 0 Rabbit 8.0 pIC50 = 8 Binding
Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)
ChEMBL 449 7 1 5 5.5 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(OC(C(=O)O)c2ccccc2Cl)cc1 10.1016/0960-894X(95)00185-V
10324361 16730 0 None - 0 Human 8.0 pIC50 = 8 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 519 12 0 8 4.7 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2Cc2ccno2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
CHEMBL125273 16730 0 None - 0 Human 8.0 pIC50 = 8 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 519 12 0 8 4.7 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2Cc2ccno2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
16133225 415 47 None -2 6 Human 8.0 pIC50 = 8.0 Binding
Displacement of [125-I]-[Sar1, Ile8] from recombinant human AT1R transfected in human HEK293 cells incubated for 2 hrs by liquid scintillation counter analysisDisplacement of [125-I]-[Sar1, Ile8] from recombinant human AT1R transfected in human HEK293 cells incubated for 2 hrs by liquid scintillation counter analysis
ChEMBL None None None None 10.1016/j.bmcl.2021.128086
172198 415 47 None -2 6 Human 8.0 pIC50 = 8.0 Binding
Displacement of [125-I]-[Sar1, Ile8] from recombinant human AT1R transfected in human HEK293 cells incubated for 2 hrs by liquid scintillation counter analysisDisplacement of [125-I]-[Sar1, Ile8] from recombinant human AT1R transfected in human HEK293 cells incubated for 2 hrs by liquid scintillation counter analysis
ChEMBL None None None None 10.1016/j.bmcl.2021.128086
2504 415 47 None -2 6 Human 8.0 pIC50 = 8.0 Binding
Displacement of [125-I]-[Sar1, Ile8] from recombinant human AT1R transfected in human HEK293 cells incubated for 2 hrs by liquid scintillation counter analysisDisplacement of [125-I]-[Sar1, Ile8] from recombinant human AT1R transfected in human HEK293 cells incubated for 2 hrs by liquid scintillation counter analysis
ChEMBL None None None None 10.1016/j.bmcl.2021.128086
45266664 415 47 None -2 6 Human 8.0 pIC50 = 8.0 Binding
Displacement of [125-I]-[Sar1, Ile8] from recombinant human AT1R transfected in human HEK293 cells incubated for 2 hrs by liquid scintillation counter analysisDisplacement of [125-I]-[Sar1, Ile8] from recombinant human AT1R transfected in human HEK293 cells incubated for 2 hrs by liquid scintillation counter analysis
ChEMBL None None None None 10.1016/j.bmcl.2021.128086
5272 415 47 None -2 6 Human 8.0 pIC50 = 8.0 Binding
Displacement of [125-I]-[Sar1, Ile8] from recombinant human AT1R transfected in human HEK293 cells incubated for 2 hrs by liquid scintillation counter analysisDisplacement of [125-I]-[Sar1, Ile8] from recombinant human AT1R transfected in human HEK293 cells incubated for 2 hrs by liquid scintillation counter analysis
ChEMBL None None None None 10.1016/j.bmcl.2021.128086
CHEMBL408403 415 47 None -2 6 Human 8.0 pIC50 = 8.0 Binding
Displacement of [125-I]-[Sar1, Ile8] from recombinant human AT1R transfected in human HEK293 cells incubated for 2 hrs by liquid scintillation counter analysisDisplacement of [125-I]-[Sar1, Ile8] from recombinant human AT1R transfected in human HEK293 cells incubated for 2 hrs by liquid scintillation counter analysis
ChEMBL None None None None 10.1016/j.bmcl.2021.128086
DB11842 415 47 None -2 6 Human 8.0 pIC50 = 8.0 Binding
Displacement of [125-I]-[Sar1, Ile8] from recombinant human AT1R transfected in human HEK293 cells incubated for 2 hrs by liquid scintillation counter analysisDisplacement of [125-I]-[Sar1, Ile8] from recombinant human AT1R transfected in human HEK293 cells incubated for 2 hrs by liquid scintillation counter analysis
ChEMBL None None None None 10.1016/j.bmcl.2021.128086
53309130 63426 0 None - 0 Human 8.0 pIC50 = 8.0 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation countingDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation counting
ChEMBL 449 4 1 6 5.6 Cc1cc(C)c2nc(C(C)C)n([C@H]3CCc4cc(-c5ccccc5-c5nnn[nH]5)ccc43)c2n1 10.1021/jm200409s
CHEMBL1801734 63426 0 None - 0 Human 8.0 pIC50 = 8.0 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation countingDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation counting
ChEMBL 449 4 1 6 5.6 Cc1cc(C)c2nc(C(C)C)n([C@H]3CCc4cc(-c5ccccc5-c5nnn[nH]5)ccc43)c2n1 10.1021/jm200409s
70690542 75853 0 None - 0 Bovine 8.0 pIC50 = 8.0 Binding
Displacement of [125I]AngII from type 1 angiotensin 2 receptor in bovine adrenal cortexDisplacement of [125I]AngII from type 1 angiotensin 2 receptor in bovine adrenal cortex
ChEMBL 532 9 1 6 6.6 CCCCc1nc2ccc(F)cc2n1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)cc1 10.1016/j.bmc.2012.06.011
CHEMBL2058375 75853 0 None - 0 Bovine 8.0 pIC50 = 8.0 Binding
Displacement of [125I]AngII from type 1 angiotensin 2 receptor in bovine adrenal cortexDisplacement of [125I]AngII from type 1 angiotensin 2 receptor in bovine adrenal cortex
ChEMBL 532 9 1 6 6.6 CCCCc1nc2ccc(F)cc2n1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)cc1 10.1016/j.bmc.2012.06.011
53309128 63436 0 None - 0 Human 8.0 pIC50 = 8.0 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation countingDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation counting
ChEMBL 453 6 1 4 6.4 CCc1nc2c(C)cc(CC(C)C)nc2n1[C@H]1CCc2cc(-c3ccccc3C(=O)O)ccc21 10.1021/jm200409s
CHEMBL1801744 63436 0 None - 0 Human 8.0 pIC50 = 8.0 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation countingDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation counting
ChEMBL 453 6 1 4 6.4 CCc1nc2c(C)cc(CC(C)C)nc2n1[C@H]1CCc2cc(-c3ccccc3C(=O)O)ccc21 10.1021/jm200409s
44277549 98658 0 None - 0 Human 8.0 pIC50 = 8.0 Binding
Binding affinity against AT1 receptor in human adrenal tissueBinding affinity against AT1 receptor in human adrenal tissue
ChEMBL 594 8 0 10 5.1 Cn1nnnc1-c1ccccc1-c1ccc(Cn2cnc3ccc(N(Cc4ccccn4)C(=O)c4ccco4)cc3c2=O)cc1 10.1016/0960-894X(95)00224-H
CHEMBL280988 98658 0 None - 0 Human 8.0 pIC50 = 8.0 Binding
Binding affinity against AT1 receptor in human adrenal tissueBinding affinity against AT1 receptor in human adrenal tissue
ChEMBL 594 8 0 10 5.1 Cn1nnnc1-c1ccccc1-c1ccc(Cn2cnc3ccc(N(Cc4ccccn4)C(=O)c4ccco4)cc3c2=O)cc1 10.1016/0960-894X(95)00224-H
2541 772 113 None -1 6 Human 8.0 pIC50 = 8.0 Binding
Displacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation countingDisplacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation counting
ChEMBL 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10.1021/acs.jmedchem.5b01495
587 772 113 None -1 6 Human 8.0 pIC50 = 8.0 Binding
Displacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation countingDisplacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation counting
ChEMBL 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10.1021/acs.jmedchem.5b01495
6907 772 113 None -1 6 Human 8.0 pIC50 = 8.0 Binding
Displacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation countingDisplacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation counting
ChEMBL 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10.1021/acs.jmedchem.5b01495
CHEMBL1016 772 113 None -1 6 Human 8.0 pIC50 = 8.0 Binding
Displacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation countingDisplacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation counting
ChEMBL 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10.1021/acs.jmedchem.5b01495
DB00796 772 113 None -1 6 Human 8.0 pIC50 = 8.0 Binding
Displacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation countingDisplacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation counting
ChEMBL 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10.1021/acs.jmedchem.5b01495
DB13919 772 113 None -1 6 Human 8.0 pIC50 = 8.0 Binding
Displacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation countingDisplacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation counting
ChEMBL 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10.1021/acs.jmedchem.5b01495
76315368 84517 0 None - 0 Rabbit 7.0 pIC50 = 7 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 510 10 2 8 5.3 CCCCc1nnc(Sc2ccccc2)n1Cc1ccc(NC(=O)c2ccccc2-c2nnn[nH]2)cc1 10.1007/s00044-011-9756-4
CHEMBL2237587 84517 0 None - 0 Rabbit 7.0 pIC50 = 7 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 510 10 2 8 5.3 CCCCc1nnc(Sc2ccccc2)n1Cc1ccc(NC(=O)c2ccccc2-c2nnn[nH]2)cc1 10.1007/s00044-011-9756-4
14956760 164937 0 None - 0 Rabbit 7.0 pIC50 = 7 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 466 8 2 8 3.9 CCCCc1nn(-c2ccccc2N)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
CHEMBL424053 164937 0 None - 0 Rabbit 7.0 pIC50 = 7 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 466 8 2 8 3.9 CCCCc1nn(-c2ccccc2N)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
44348352 16336 0 None - 1 Bovine 7.0 pIC50 = 7 Binding
Concentration that gives 50% inhibition for binding of 125-I-[Sar1, IIe8] angiotensin to Angiotensin II receptor, type 1 in bovine adrenal cortex membrane.Concentration that gives 50% inhibition for binding of 125-I-[Sar1, IIe8] angiotensin to Angiotensin II receptor, type 1 in bovine adrenal cortex membrane.
ChEMBL 459 8 1 6 4.5 CCOC(=O)/C=C1\N(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)C(=O)CC1(CC)CC 10.1016/S0960-894X(01)80914-8
CHEMBL123713 16336 0 None - 1 Bovine 7.0 pIC50 = 7 Binding
Concentration that gives 50% inhibition for binding of 125-I-[Sar1, IIe8] angiotensin to Angiotensin II receptor, type 1 in bovine adrenal cortex membrane.Concentration that gives 50% inhibition for binding of 125-I-[Sar1, IIe8] angiotensin to Angiotensin II receptor, type 1 in bovine adrenal cortex membrane.
ChEMBL 459 8 1 6 4.5 CCOC(=O)/C=C1\N(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)C(=O)CC1(CC)CC 10.1016/S0960-894X(01)80914-8
44285157 154155 0 None - 0 Rat 7.0 pIC50 = 7 Binding
Displacement of [125I]- Ang II from type 1 Angiotensin II receptorDisplacement of [125I]- Ang II from type 1 Angiotensin II receptor
ChEMBL 484 6 1 5 5.2 CC1=NC(c2ccccc2)(c2ccccc2)C(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80526-6
CHEMBL39978 154155 0 None - 0 Rat 7.0 pIC50 = 7 Binding
Displacement of [125I]- Ang II from type 1 Angiotensin II receptorDisplacement of [125I]- Ang II from type 1 Angiotensin II receptor
ChEMBL 484 6 1 5 5.2 CC1=NC(c2ccccc2)(c2ccccc2)C(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80526-6
10412300 47869 0 None - 0 Rabbit 7.0 pIC50 = 7 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 467 9 1 7 5.7 CCCCc1nnc(Sc2ccccc2)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
CHEMBL155154 47869 0 None - 0 Rabbit 7.0 pIC50 = 7 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 467 9 1 7 5.7 CCCCc1nnc(Sc2ccccc2)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
44311472 103303 0 None - 0 Human 7.0 pIC50 = 7 Binding
In vitro binding affinity of compound against Angiotensin II receptor, type 1In vitro binding affinity of compound against Angiotensin II receptor, type 1
ChEMBL 669 14 3 8 5.7 CCCc1nc(CN(CC(=O)O)C(=O)C(c2ccccc2)c2ccccc2)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80076-1
CHEMBL308943 103303 0 None - 0 Human 7.0 pIC50 = 7 Binding
In vitro binding affinity of compound against Angiotensin II receptor, type 1In vitro binding affinity of compound against Angiotensin II receptor, type 1
ChEMBL 669 14 3 8 5.7 CCCc1nc(CN(CC(=O)O)C(=O)C(c2ccccc2)c2ccccc2)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80076-1
10500716 10117 0 None - 0 Bovine 7.0 pIC50 = 7 Binding
In vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortexIn vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortex
ChEMBL 392 8 2 4 4.5 CCCc1nc(CC)c(C(=O)O)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm950450f
CHEMBL116054 10117 0 None - 0 Bovine 7.0 pIC50 = 7 Binding
In vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortexIn vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortex
ChEMBL 392 8 2 4 4.5 CCCc1nc(CC)c(C(=O)O)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm950450f
9867446 168740 0 None - 0 Bovine 7.0 pIC50 = 7 Binding
In vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortexIn vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortex
ChEMBL 432 8 3 7 3.1 CCCc1nc(C(=O)O)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm950450f
CHEMBL441649 168740 0 None - 0 Bovine 7.0 pIC50 = 7 Binding
In vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortexIn vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortex
ChEMBL 432 8 3 7 3.1 CCCc1nc(C(=O)O)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm950450f
44305424 102007 0 None - 0 Bovine 7.0 pIC50 = 7 Binding
Tested for binding affinity against angiotensin II receptor in bovine adrenal cortexTested for binding affinity against angiotensin II receptor in bovine adrenal cortex
ChEMBL 388 6 2 6 2.4 CCCc1cc(=O)[nH]c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/0960-894X(95)00370-9
CHEMBL304032 102007 0 None - 0 Bovine 7.0 pIC50 = 7 Binding
Tested for binding affinity against angiotensin II receptor in bovine adrenal cortexTested for binding affinity against angiotensin II receptor in bovine adrenal cortex
ChEMBL 388 6 2 6 2.4 CCCc1cc(=O)[nH]c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/0960-894X(95)00370-9
10434949 119124 0 None - 0 Rabbit 6.0 pIC50 = 6 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 472 9 2 6 5.0 CCSc1nnc(Cc2ccccc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
CHEMBL346745 119124 0 None - 0 Rabbit 6.0 pIC50 = 6 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 472 9 2 6 5.0 CCSc1nnc(Cc2ccccc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
10456123 164754 0 None - 0 Rabbit 6.0 pIC50 = 6 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 444 9 2 6 4.9 CCCCc1nnc(-c2ccco2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
CHEMBL423418 164754 0 None - 0 Rabbit 6.0 pIC50 = 6 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 444 9 2 6 4.9 CCCCc1nnc(-c2ccco2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
76310609 104756 0 None - 0 Human 6.0 pIC50 = 6 Binding
Antagonist activity at human AT1 receptor expressed in CHO cells measured after overnight incubation by luciferase reporter gene assayAntagonist activity at human AT1 receptor expressed in CHO cells measured after overnight incubation by luciferase reporter gene assay
ChEMBL 531 10 2 4 7.3 CCCn1nc2ccc(C(=O)NC(CC)c3ccccc3)cc2c1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.bmcl.2014.01.004
CHEMBL3115244 104756 0 None - 0 Human 6.0 pIC50 = 6 Binding
Antagonist activity at human AT1 receptor expressed in CHO cells measured after overnight incubation by luciferase reporter gene assayAntagonist activity at human AT1 receptor expressed in CHO cells measured after overnight incubation by luciferase reporter gene assay
ChEMBL 531 10 2 4 7.3 CCCn1nc2ccc(C(=O)NC(CC)c3ccccc3)cc2c1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.bmcl.2014.01.004
44298831 193303 0 None - 0 Bovine 6.0 pIC50 = 6 Binding
Binding affinity for angiotensin II receptor of bovine adrenal cortexBinding affinity for angiotensin II receptor of bovine adrenal cortex
ChEMBL 496 8 2 8 4.2 CC(C)COc1nc2ccc(C(C)O)cn2c(=O)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81144-6
CHEMBL54699 193303 0 None - 0 Bovine 6.0 pIC50 = 6 Binding
Binding affinity for angiotensin II receptor of bovine adrenal cortexBinding affinity for angiotensin II receptor of bovine adrenal cortex
ChEMBL 496 8 2 8 4.2 CC(C)COc1nc2ccc(C(C)O)cn2c(=O)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81144-6
10434949 119124 0 None - 0 Rabbit 6.0 pIC50 = 6 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 472 9 2 6 5.0 CCSc1nnc(Cc2ccccc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
CHEMBL346745 119124 0 None - 0 Rabbit 6.0 pIC50 = 6 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 472 9 2 6 5.0 CCSc1nnc(Cc2ccccc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
10456123 164754 0 None - 0 Rabbit 6.0 pIC50 = 6 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 444 9 2 6 4.9 CCCCc1nnc(-c2ccco2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
CHEMBL423418 164754 0 None - 0 Rabbit 6.0 pIC50 = 6 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 444 9 2 6 4.9 CCCCc1nnc(-c2ccco2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
15654731 101710 0 None - 0 Bovine 6.0 pIC50 = 6 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 482 9 1 8 4.9 CCCOc1nc2cccc(C(=O)OCC)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a016
CHEMBL302815 101710 0 None - 0 Bovine 6.0 pIC50 = 6 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 482 9 1 8 4.9 CCCOc1nc2cccc(C(=O)OCC)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a016
44305441 100465 0 None - 0 Bovine 6.0 pIC50 = 6 Binding
Tested for binding affinity against angiotensin II receptor in bovine adrenal cortexTested for binding affinity against angiotensin II receptor in bovine adrenal cortex
ChEMBL 388 5 1 7 2.0 CCc1cc(=O)n(C)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/0960-894X(95)00370-9
CHEMBL294075 100465 0 None - 0 Bovine 6.0 pIC50 = 6 Binding
Tested for binding affinity against angiotensin II receptor in bovine adrenal cortexTested for binding affinity against angiotensin II receptor in bovine adrenal cortex
ChEMBL 388 5 1 7 2.0 CCc1cc(=O)n(C)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/0960-894X(95)00370-9
44341795 9836 0 None - 0 Rat 5.0 pIC50 = 5 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 516 6 1 3 5.9 O=C(O)c1ccccc1-c1ccc(CN2C(=O)C3(CCCC3)N=C2C(F)(F)C(F)(F)C(F)(F)F)cc1 10.1021/jm00074a018
CHEMBL114625 9836 0 None - 0 Rat 5.0 pIC50 = 5 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 516 6 1 3 5.9 O=C(O)c1ccccc1-c1ccc(CN2C(=O)C3(CCCC3)N=C2C(F)(F)C(F)(F)C(F)(F)F)cc1 10.1021/jm00074a018
15144937 18629 0 None - 0 Rat 5.0 pIC50 = 5 Binding
Compound was evaluated for the inhibition of [125I]AII specific binding to rat mesenteric arteriesCompound was evaluated for the inhibition of [125I]AII specific binding to rat mesenteric arteries
ChEMBL 500 11 1 4 7.4 CCCCc1ncc(/C=C(\Cc2cccc(Oc3ccccc3)c2)C(=O)O)n1Cc1ccccc1Cl 10.1021/jm00099a013
CHEMBL128032 18629 0 None - 0 Rat 5.0 pIC50 = 5 Binding
Compound was evaluated for the inhibition of [125I]AII specific binding to rat mesenteric arteriesCompound was evaluated for the inhibition of [125I]AII specific binding to rat mesenteric arteries
ChEMBL 500 11 1 4 7.4 CCCCc1ncc(/C=C(\Cc2cccc(Oc3ccccc3)c2)C(=O)O)n1Cc1ccccc1Cl 10.1021/jm00099a013
44303886 100400 0 None - 0 Rabbit 5.0 pIC50 = 5 Binding
Inhibition of angiotensin Angiotensin II receptor, type 1 in rabbit aorta using [125I-Sar1,Ile8] angiotensin II binding assayInhibition of angiotensin Angiotensin II receptor, type 1 in rabbit aorta using [125I-Sar1,Ile8] angiotensin II binding assay
ChEMBL 522 11 1 3 6.1 CCCCCN(CCCCC)C(=O)N1CCN(C(=O)N(c2ccccc2)c2cccc(C)c2)[C@H](C(=O)O)C1 10.1016/S0960-894X(01)81007-6
CHEMBL293660 100400 0 None - 0 Rabbit 5.0 pIC50 = 5 Binding
Inhibition of angiotensin Angiotensin II receptor, type 1 in rabbit aorta using [125I-Sar1,Ile8] angiotensin II binding assayInhibition of angiotensin Angiotensin II receptor, type 1 in rabbit aorta using [125I-Sar1,Ile8] angiotensin II binding assay
ChEMBL 522 11 1 3 6.1 CCCCCN(CCCCC)C(=O)N1CCN(C(=O)N(c2ccccc2)c2cccc(C)c2)[C@H](C(=O)O)C1 10.1016/S0960-894X(01)81007-6
44303852 101866 0 None - 0 Rabbit 5.0 pIC50 = 5 Binding
Inhibition of angiotensin Angiotensin II receptor, type 1 in rabbit aorta using [125I-Sar1,Ile8] angiotensin II binding assayInhibition of angiotensin Angiotensin II receptor, type 1 in rabbit aorta using [125I-Sar1,Ile8] angiotensin II binding assay
ChEMBL 524 11 2 4 5.5 CCCCCN(CCCCC)C(=O)N1CCN(C(=O)N(c2ccccc2)c2ccc(O)cc2)[C@H](C(=O)O)C1 10.1016/S0960-894X(01)81007-6
CHEMBL303755 101866 0 None - 0 Rabbit 5.0 pIC50 = 5 Binding
Inhibition of angiotensin Angiotensin II receptor, type 1 in rabbit aorta using [125I-Sar1,Ile8] angiotensin II binding assayInhibition of angiotensin Angiotensin II receptor, type 1 in rabbit aorta using [125I-Sar1,Ile8] angiotensin II binding assay
ChEMBL 524 11 2 4 5.5 CCCCCN(CCCCC)C(=O)N1CCN(C(=O)N(c2ccccc2)c2ccc(O)cc2)[C@H](C(=O)O)C1 10.1016/S0960-894X(01)81007-6
73346387 92184 0 None - 0 Human 6.0 pIC50 = 6 Binding
Displacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysisDisplacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysis
ChEMBL 497 7 1 5 5.2 CCCc1nc2c(C)cc(C(=O)N3CCOCC3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2013.08.014
CHEMBL2435832 92184 0 None - 0 Human 6.0 pIC50 = 6 Binding
Displacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysisDisplacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysis
ChEMBL 497 7 1 5 5.2 CCCc1nc2c(C)cc(C(=O)N3CCOCC3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2013.08.014
9866104 202188 0 None - 0 Rat 7.0 pIC50 = 7 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 407 10 1 5 4.6 CCCCc1nn(CCCC)c(=O)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00067a015
CHEMBL68919 202188 0 None - 0 Rat 7.0 pIC50 = 7 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 407 10 1 5 4.6 CCCCc1nn(CCCC)c(=O)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00067a015
9850385 101209 0 None - 0 Bovine 7.0 pIC50 = 7.0 Binding
In vitro binding affinity to angiotensin II receptor in bovine adrenal cortexIn vitro binding affinity to angiotensin II receptor in bovine adrenal cortex
ChEMBL 544 8 1 8 5.2 CCCCc1nc2ccc(C3=NN4CCCC4C3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80377-2
CHEMBL299391 101209 0 None - 0 Bovine 7.0 pIC50 = 7.0 Binding
In vitro binding affinity to angiotensin II receptor in bovine adrenal cortexIn vitro binding affinity to angiotensin II receptor in bovine adrenal cortex
ChEMBL 544 8 1 8 5.2 CCCCc1nc2ccc(C3=NN4CCCC4C3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80377-2
11757908 116818 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 578 12 0 6 6.8 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2Cc2ccc3ccccc3c2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
CHEMBL339709 116818 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 578 12 0 6 6.8 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2Cc2ccc3ccccc3c2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
127034874 135869 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 547 10 3 5 6.2 CCCc1nc2c(C)cc(C(=O)NC[C@@H](O)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2015.09.010
CHEMBL3735333 135869 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 547 10 3 5 6.2 CCCc1nc2c(C)cc(C(=O)NC[C@@H](O)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2015.09.010
44212049 100981 0 None - 0 Bovine 7.0 pIC50 = 7.0 Binding
In vitro binding affinity to angiotensin II receptor in bovine adrenal cortexIn vitro binding affinity to angiotensin II receptor in bovine adrenal cortex
ChEMBL 560 8 1 7 6.7 CCCCc1nc2ccc(C3CCC4CCCC4O3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80377-2
CHEMBL297714 100981 0 None - 0 Bovine 7.0 pIC50 = 7.0 Binding
In vitro binding affinity to angiotensin II receptor in bovine adrenal cortexIn vitro binding affinity to angiotensin II receptor in bovine adrenal cortex
ChEMBL 560 8 1 7 6.7 CCCCc1nc2ccc(C3CCC4CCCC4O3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80377-2
44297113 101091 0 None - 0 Bovine 7.0 pIC50 = 7.0 Binding
In vitro binding affinity to angiotensin II receptor in bovine adrenal cortexIn vitro binding affinity to angiotensin II receptor in bovine adrenal cortex
ChEMBL 637 9 1 9 6.8 CCCCc1nc2ccc([C@@H]3C[C@H]4C(c5ccc(C)cc5)=NO[C@H]4O3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80377-2
CHEMBL298560 101091 0 None - 0 Bovine 7.0 pIC50 = 7.0 Binding
In vitro binding affinity to angiotensin II receptor in bovine adrenal cortexIn vitro binding affinity to angiotensin II receptor in bovine adrenal cortex
ChEMBL 637 9 1 9 6.8 CCCCc1nc2ccc([C@@H]3C[C@H]4C(c5ccc(C)cc5)=NO[C@H]4O3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80377-2
11388072 204107 0 None - 0 Rat 7.0 pIC50 = 7.0 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 634 9 1 9 6.3 CCCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2c(C(=O)NS(=O)(=O)c3ccc([N+](=O)[O-])cc3)cnc3ccccc23)cc1 10.1021/jm031100t
CHEMBL83414 204107 0 None - 0 Rat 7.0 pIC50 = 7.0 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 634 9 1 9 6.3 CCCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2c(C(=O)NS(=O)(=O)c3ccc([N+](=O)[O-])cc3)cnc3ccccc23)cc1 10.1021/jm031100t
57380648 70016 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Displacement of [125I]Sar1 Ile8-Ang 2 from angiotensin 2 AT1 receptor after 180 mins by gamma countingDisplacement of [125I]Sar1 Ile8-Ang 2 from angiotensin 2 AT1 receptor after 180 mins by gamma counting
ChEMBL 549 10 2 4 6.8 CCCc1nc2c(C)cc(C(=O)NCCc3ccccc3F)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2012.01.009
CHEMBL1945148 70016 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Displacement of [125I]Sar1 Ile8-Ang 2 from angiotensin 2 AT1 receptor after 180 mins by gamma countingDisplacement of [125I]Sar1 Ile8-Ang 2 from angiotensin 2 AT1 receptor after 180 mins by gamma counting
ChEMBL 549 10 2 4 6.8 CCCc1nc2c(C)cc(C(=O)NCCc3ccccc3F)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2012.01.009
127034876 135890 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 571 10 3 7 5.7 CCCc1nc2c(C)cc(C(=O)NC[C@@H](O)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.ejmech.2015.09.010
CHEMBL3735487 135890 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 571 10 3 7 5.7 CCCc1nc2c(C)cc(C(=O)NC[C@@H](O)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.ejmech.2015.09.010
10453551 18891 0 None - 0 Rat 6.0 pIC50 = 6.0 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 399 7 2 4 5.4 CCCCc1nc2cccc(N)c2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00077a007
CHEMBL128913 18891 0 None - 0 Rat 6.0 pIC50 = 6.0 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 399 7 2 4 5.4 CCCCc1nc2cccc(N)c2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00077a007
24827768 158536 0 None - 0 Rat 7.0 pIC50 = 7.0 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
ChEMBL 411 6 1 7 3.5 CCCn1c(=O)c2cccnc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm7011563
CHEMBL409744 158536 0 None - 0 Rat 7.0 pIC50 = 7.0 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
ChEMBL 411 6 1 7 3.5 CCCn1c(=O)c2cccnc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm7011563
15356438 186267 0 None - 0 Rat 5.0 pIC50 = 5.0 Binding
Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.
ChEMBL 425 9 2 5 4.2 CCCCc1nc(Cl)c(CO)n1Cc1ccc(NC(=O)C(=O)c2ccccc2)cc1 10.1021/jm00064a007
CHEMBL48955 186267 0 None - 0 Rat 5.0 pIC50 = 5.0 Binding
Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.
ChEMBL 425 9 2 5 4.2 CCCCc1nc(Cl)c(CO)n1Cc1ccc(NC(=O)C(=O)c2ccccc2)cc1 10.1021/jm00064a007
10483230 46552 0 None - 0 Rabbit 8.0 pIC50 = 8.0 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 574 11 2 8 5.1 CCCCc1nnc([S+]([O-])Cc2ccc(Cl)cc2)n1Cc1ccc(NC(=O)c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-011-9756-4
CHEMBL154027 46552 0 None - 0 Rabbit 8.0 pIC50 = 8.0 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 574 11 2 8 5.1 CCCCc1nnc([S+]([O-])Cc2ccc(Cl)cc2)n1Cc1ccc(NC(=O)c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-011-9756-4
19939367 105457 0 None - 0 Rabbit 8.0 pIC50 = 8.0 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 523 10 1 9 4.1 CCCCc1nn(Cc2ccccc2C(=O)OC)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
CHEMBL312921 105457 0 None - 0 Rabbit 8.0 pIC50 = 8.0 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 523 10 1 9 4.1 CCCCc1nn(Cc2ccccc2C(=O)OC)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
14956792 106270 0 None - 0 Rabbit 8.0 pIC50 = 8.0 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 479 9 1 7 4.6 CCCCc1nn(Cc2ccccc2C)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
CHEMBL314447 106270 0 None - 0 Rabbit 8.0 pIC50 = 8.0 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 479 9 1 7 4.6 CCCCc1nn(Cc2ccccc2C)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
14956754 156831 0 None - 0 Rabbit 8.0 pIC50 = 8.0 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 541 10 1 7 5.9 CCCCc1nn(-c2ccccc2Cc2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
CHEMBL407827 156831 0 None - 0 Rabbit 8.0 pIC50 = 8.0 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 541 10 1 7 5.9 CCCCc1nn(-c2ccccc2Cc2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
44277440 98492 0 None - 0 Rabbit 8.0 pIC50 = 8.0 Binding
Binding affinity against AT1 receptor in rabbit aortaBinding affinity against AT1 receptor in rabbit aorta
ChEMBL 604 8 0 9 5.5 Cn1nnnc1-c1ccccc1-c1ccc(Cn2cnc3ccc(N(Cc4ccccc4)C(=O)c4cccnc4)cc3c2=O)cc1 10.1016/0960-894X(95)00224-H
CHEMBL279756 98492 0 None - 0 Rabbit 8.0 pIC50 = 8.0 Binding
Binding affinity against AT1 receptor in rabbit aortaBinding affinity against AT1 receptor in rabbit aorta
ChEMBL 604 8 0 9 5.5 Cn1nnnc1-c1ccccc1-c1ccc(Cn2cnc3ccc(N(Cc4ccccc4)C(=O)c4cccnc4)cc3c2=O)cc1 10.1016/0960-894X(95)00224-H
44307171 100442 0 None - 0 Rabbit 8.0 pIC50 = 8.0 Binding
Binding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membraneBinding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane
ChEMBL 481 5 2 5 4.7 CCCc1nc2c(C)cc(C(=O)O)nc2n1Cc1cc(Br)c(O)c(Br)c1 10.1016/S0960-894X(01)81148-3
CHEMBL293926 100442 0 None - 0 Rabbit 8.0 pIC50 = 8.0 Binding
Binding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membraneBinding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane
ChEMBL 481 5 2 5 4.7 CCCc1nc2c(C)cc(C(=O)O)nc2n1Cc1cc(Br)c(O)c(Br)c1 10.1016/S0960-894X(01)81148-3
11374350 204668 0 None - 0 Rat 8.0 pIC50 = 8.0 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 450 6 1 5 6.0 CCCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2c(C(=O)O)cnc3ccccc23)cc1 10.1021/jm031100t
CHEMBL87779 204668 0 None - 0 Rat 8.0 pIC50 = 8.0 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 450 6 1 5 6.0 CCCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2c(C(=O)O)cnc3ccccc23)cc1 10.1021/jm031100t
44373246 167693 0 None - 1 Bovine 8.0 pIC50 = 8.0 Binding
Binding affinity to angiotensin AT1 receptor in bovine adrenal cortex membranesBinding affinity to angiotensin AT1 receptor in bovine adrenal cortex membranes
ChEMBL 435 5 1 6 4.5 CCc1nc2c(C)cc(C)nc2n1Cc1ccc2c(c1)C(Cc1nnn[nH]1)c1ccccc1-2 10.1016/j.bmc.2010.10.043
CHEMBL433895 167693 0 None - 1 Bovine 8.0 pIC50 = 8.0 Binding
Binding affinity to angiotensin AT1 receptor in bovine adrenal cortex membranesBinding affinity to angiotensin AT1 receptor in bovine adrenal cortex membranes
ChEMBL 435 5 1 6 4.5 CCc1nc2c(C)cc(C)nc2n1Cc1ccc2c(c1)C(Cc1nnn[nH]1)c1ccccc1-2 10.1016/j.bmc.2010.10.043
9824568 202698 0 None - 0 Human 8.0 pIC50 = 8.0 Binding
Compound was tested for inhibition against Angiotensin II receptor, type 1Compound was tested for inhibition against Angiotensin II receptor, type 1
ChEMBL 441 5 2 7 2.8 Cc1nc(C(=O)O)nc2c1CCC(=O)N2Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm0204237
CHEMBL72053 202698 0 None - 0 Human 8.0 pIC50 = 8.0 Binding
Compound was tested for inhibition against Angiotensin II receptor, type 1Compound was tested for inhibition against Angiotensin II receptor, type 1
ChEMBL 441 5 2 7 2.8 Cc1nc(C(=O)O)nc2c1CCC(=O)N2Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm0204237
108185 1578 71 None - 1 Rat 8.0 pIC50 = 8.0 Binding
Concentration required to inhibit binding of radioligand [125I]AII to Angiotensin II receptor, type 1 in rat adrenal glomerulosa tissueConcentration required to inhibit binding of radioligand [125I]AII to Angiotensin II receptor, type 1 in rat adrenal glomerulosa tissue
ChEMBL 436 8 2 6 4.5 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)C(=O)O)Cl 10.1021/jm00092a017
586 1578 71 None - 1 Rat 8.0 pIC50 = 8.0 Binding
Concentration required to inhibit binding of radioligand [125I]AII to Angiotensin II receptor, type 1 in rat adrenal glomerulosa tissueConcentration required to inhibit binding of radioligand [125I]AII to Angiotensin II receptor, type 1 in rat adrenal glomerulosa tissue
ChEMBL 436 8 2 6 4.5 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)C(=O)O)Cl 10.1021/jm00092a017
CHEMBL907 1578 71 None - 1 Rat 8.0 pIC50 = 8.0 Binding
Concentration required to inhibit binding of radioligand [125I]AII to Angiotensin II receptor, type 1 in rat adrenal glomerulosa tissueConcentration required to inhibit binding of radioligand [125I]AII to Angiotensin II receptor, type 1 in rat adrenal glomerulosa tissue
ChEMBL 436 8 2 6 4.5 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)C(=O)O)Cl 10.1021/jm00092a017
10052777 48239 0 None - 0 Rabbit 8.0 pIC50 = 8.0 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 531 10 1 7 5.5 CCCCc1nnc([S+]([O-])Cc2ccc(Cl)cc2)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
CHEMBL155638 48239 0 None - 0 Rabbit 8.0 pIC50 = 8.0 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 531 10 1 7 5.5 CCCCc1nnc([S+]([O-])Cc2ccc(Cl)cc2)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
73355474 92171 0 None - 0 Human 8.0 pIC50 = 8.0 Binding
Displacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysisDisplacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysis
ChEMBL 540 10 2 6 4.8 CCCc1nc2c(C)cc(C(=O)NCCN3CCOCC3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2013.08.014
CHEMBL2435819 92171 0 None - 0 Human 8.0 pIC50 = 8.0 Binding
Displacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysisDisplacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysis
ChEMBL 540 10 2 6 4.8 CCCc1nc2c(C)cc(C(=O)NCCN3CCOCC3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2013.08.014
70696781 75854 0 None - 0 Bovine 8.0 pIC50 = 8.0 Binding
Displacement of [125I]AngII from type 1 angiotensin 2 receptor in bovine adrenal cortexDisplacement of [125I]AngII from type 1 angiotensin 2 receptor in bovine adrenal cortex
ChEMBL 582 9 1 6 7.5 CCCCc1nc2ccc(C(F)(F)F)cc2n1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)cc1 10.1016/j.bmc.2012.06.011
CHEMBL2058376 75854 0 None - 0 Bovine 8.0 pIC50 = 8.0 Binding
Displacement of [125I]AngII from type 1 angiotensin 2 receptor in bovine adrenal cortexDisplacement of [125I]AngII from type 1 angiotensin 2 receptor in bovine adrenal cortex
ChEMBL 582 9 1 6 7.5 CCCCc1nc2ccc(C(F)(F)F)cc2n1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)cc1 10.1016/j.bmc.2012.06.011
15236329 168757 0 None - 0 Rabbit 8.0 pIC50 = 8.0 Binding
Displacement of the specific binding ligand [125I]Sar1,Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane.Displacement of the specific binding ligand [125I]Sar1,Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane.
ChEMBL 598 6 1 7 6.4 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2C2=NN(c3ccccc3Br)[S+]([O-])N2)cc1 10.1016/S0960-894X(01)81119-7
CHEMBL441837 168757 0 None - 0 Rabbit 8.0 pIC50 = 8.0 Binding
Displacement of the specific binding ligand [125I]Sar1,Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane.Displacement of the specific binding ligand [125I]Sar1,Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane.
ChEMBL 598 6 1 7 6.4 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2C2=NN(c3ccccc3Br)[S+]([O-])N2)cc1 10.1016/S0960-894X(01)81119-7
10501285 162871 0 None - 0 Bovine 8.0 pIC50 = 8.0 Binding
In vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortexIn vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortex
ChEMBL 402 7 2 6 3.7 CCCc1nc(C)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm950450f
CHEMBL419762 162871 0 None - 0 Bovine 8.0 pIC50 = 8.0 Binding
In vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortexIn vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortex
ChEMBL 402 7 2 6 3.7 CCCc1nc(C)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm950450f
44320817 106496 0 None - 0 Rat 8.0 pIC50 = 8.0 Binding
Inhibition of [125-I]-labeled angiotensin II binding to AT1 receptor in rat uterine membranesInhibition of [125-I]-labeled angiotensin II binding to AT1 receptor in rat uterine membranes
ChEMBL 529 7 1 7 5.3 CCCCc1nc(Cl)c2n1[C@H](c1ccc(-c3ccccc3-c3nn[nH]n3)cc1)CC[C@@H]2N1C(=O)CCC1=O 10.1016/S0960-894X(01)80290-0
CHEMBL315219 106496 0 None - 0 Rat 8.0 pIC50 = 8.0 Binding
Inhibition of [125-I]-labeled angiotensin II binding to AT1 receptor in rat uterine membranesInhibition of [125-I]-labeled angiotensin II binding to AT1 receptor in rat uterine membranes
ChEMBL 529 7 1 7 5.3 CCCCc1nc(Cl)c2n1[C@H](c1ccc(-c3ccccc3-c3nn[nH]n3)cc1)CC[C@@H]2N1C(=O)CCC1=O 10.1016/S0960-894X(01)80290-0
44384871 128785 0 None - 0 Rabbit 8.0 pIC50 = 8.0 Binding
Inhibition of [125I]-Sar1-Ile8-Ang II binding to Angiotensin II receptor type 1 from rabbit aortaInhibition of [125I]-Sar1-Ile8-Ang II binding to Angiotensin II receptor type 1 from rabbit aorta
ChEMBL 726 14 1 7 8.0 CCCCCN(C(=O)c1ccccc1)c1ccc2nc(CCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)c4ccccc4)cc3)c(=O)c2c1 10.1016/0960-894X(96)00116-3
CHEMBL367095 128785 0 None - 0 Rabbit 8.0 pIC50 = 8.0 Binding
Inhibition of [125I]-Sar1-Ile8-Ang II binding to Angiotensin II receptor type 1 from rabbit aortaInhibition of [125I]-Sar1-Ile8-Ang II binding to Angiotensin II receptor type 1 from rabbit aorta
ChEMBL 726 14 1 7 8.0 CCCCCN(C(=O)c1ccccc1)c1ccc2nc(CCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)c4ccccc4)cc3)c(=O)c2c1 10.1016/0960-894X(96)00116-3
11754522 21986 0 None - 0 Rat 8.0 pIC50 = 8.0 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 471 7 1 6 5.9 CCCc1nc2ccc(-c3ccccn3)cc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00077a007
CHEMBL132282 21986 0 None - 0 Rat 8.0 pIC50 = 8.0 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 471 7 1 6 5.9 CCCc1nc2ccc(-c3ccccn3)cc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00077a007
10095637 49682 0 None - 0 Rabbit 8.0 pIC50 = 8.0 Binding
Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)
ChEMBL 457 9 1 5 5.8 CCCc1cc(Cn2c(CC)nc3c(C)cc(C)nc32)ccc1OC(C(=O)O)c1ccccc1 10.1016/0960-894X(95)00185-V
CHEMBL15689 49682 0 None - 0 Rabbit 8.0 pIC50 = 8.0 Binding
Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)
ChEMBL 457 9 1 5 5.8 CCCc1cc(Cn2c(CC)nc3c(C)cc(C)nc32)ccc1OC(C(=O)O)c1ccccc1 10.1016/0960-894X(95)00185-V
19385665 50773 0 None - 0 Rabbit 8.0 pIC50 = 8.0 Binding
Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)
ChEMBL 471 9 1 5 6.1 CCCc1cc(Cn2c(CC)nc3c(C)cc(C)nc32)ccc1OC(C(=O)O)c1ccccc1C 10.1016/0960-894X(95)00185-V
CHEMBL15788 50773 0 None - 0 Rabbit 8.0 pIC50 = 8.0 Binding
Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)
ChEMBL 471 9 1 5 6.1 CCCc1cc(Cn2c(CC)nc3c(C)cc(C)nc32)ccc1OC(C(=O)O)c1ccccc1C 10.1016/0960-894X(95)00185-V
10053367 116730 0 None - 0 Human 8.0 pIC50 = 8.0 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 553 12 0 7 5.5 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2Cc2ccc(C#N)cc2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
CHEMBL339480 116730 0 None - 0 Human 8.0 pIC50 = 8.0 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 553 12 0 7 5.5 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2Cc2ccc(C#N)cc2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
10029695 157966 0 None - 0 Human 8.0 pIC50 = 8.0 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 521 10 0 8 4.7 CCCCc1ncc(/C=C2/C(=O)N(CC)C(=O)N2Cc2csc(C)n2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
CHEMBL409136 157966 0 None - 0 Human 8.0 pIC50 = 8.0 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 521 10 0 8 4.7 CCCCc1ncc(/C=C2/C(=O)N(CC)C(=O)N2Cc2csc(C)n2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
9983135 168029 0 None - 0 Human 8.0 pIC50 = 8.0 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 492 11 0 6 5.4 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2C=C(C)C)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
CHEMBL435994 168029 0 None - 0 Human 8.0 pIC50 = 8.0 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 492 11 0 6 5.4 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2C=C(C)C)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
44309702 202036 0 None - 0 Rabbit 7.9 pIC50 = 7.9 Binding
In vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranesIn vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranes
ChEMBL 591 13 2 8 6.1 CCCCOC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CC)nc3cc(NC(=O)CCCC)cnc32)cc1 10.1016/S0960-894X(01)81115-X
CHEMBL67805 202036 0 None - 0 Rabbit 7.9 pIC50 = 7.9 Binding
In vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranesIn vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranes
ChEMBL 591 13 2 8 6.1 CCCCOC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CC)nc3cc(NC(=O)CCCC)cnc32)cc1 10.1016/S0960-894X(01)81115-X
9869504 206297 3 None - 0 Rat 7.9 pIC50 = 7.9 Binding
Tested for inhibition of [125I]- AII specific binding to rat mesenteric arteries, expressed as IC50Tested for inhibition of [125I]- AII specific binding to rat mesenteric arteries, expressed as IC50
ChEMBL 474 10 2 5 5.9 CCCCc1ncc(/C=C(\Cc2cccs2)C(=O)O)n1Cc1ccc(C(=O)O)c2ccccc12 10.1016/S0960-894X(01)81116-1
CHEMBL97533 206297 3 None - 0 Rat 7.9 pIC50 = 7.9 Binding
Tested for inhibition of [125I]- AII specific binding to rat mesenteric arteries, expressed as IC50Tested for inhibition of [125I]- AII specific binding to rat mesenteric arteries, expressed as IC50
ChEMBL 474 10 2 5 5.9 CCCCc1ncc(/C=C(\Cc2cccs2)C(=O)O)n1Cc1ccc(C(=O)O)c2ccccc12 10.1016/S0960-894X(01)81116-1
76322689 84521 0 None - 0 Rabbit 7.0 pIC50 = 7.0 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 558 11 2 8 6.0 CCCCc1nnc(SCc2ccccc2Cl)n1Cc1ccc(NC(=O)c2ccccc2-c2nnn[nH]2)cc1 10.1007/s00044-011-9756-4
CHEMBL2237591 84521 0 None - 0 Rabbit 7.0 pIC50 = 7.0 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 558 11 2 8 6.0 CCCCc1nnc(SCc2ccccc2Cl)n1Cc1ccc(NC(=O)c2ccccc2-c2nnn[nH]2)cc1 10.1007/s00044-011-9756-4
14956796 204075 0 None - 0 Rabbit 7.0 pIC50 = 7.0 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 523 10 1 9 4.1 CCCCc1nn(Cc2cccc(C(=O)OC)c2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
CHEMBL83182 204075 0 None - 0 Rabbit 7.0 pIC50 = 7.0 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 523 10 1 9 4.1 CCCCc1nn(Cc2cccc(C(=O)OC)c2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
44342013 9449 0 None - 0 Rat 7.0 pIC50 = 7.0 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 509 9 1 4 6.0 CCCCC1=NC2(CCN(Cc3ccccc3)CC2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00074a018
CHEMBL112343 9449 0 None - 0 Rat 7.0 pIC50 = 7.0 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 509 9 1 4 6.0 CCCCC1=NC2(CCN(Cc3ccccc3)CC2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00074a018
19976676 204714 0 None - 0 Rat 7.0 pIC50 = 7.0 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 416 10 1 7 4.3 CCCCc1nc(CCCC)n(Cc2ccc(-c3cccnc3-c3nn[nH]n3)cc2)n1 10.1021/jm031100t
CHEMBL88067 204714 0 None - 0 Rat 7.0 pIC50 = 7.0 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 416 10 1 7 4.3 CCCCc1nc(CCCC)n(Cc2ccc(-c3cccnc3-c3nn[nH]n3)cc2)n1 10.1021/jm031100t
2541 772 113 None -1 6 Human 7.0 pIC50 = 7.0 Binding
Binding affinity to angiotensin AT1 receptorBinding affinity to angiotensin AT1 receptor
ChEMBL 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10.1016/j.bmc.2010.10.043
587 772 113 None -1 6 Human 7.0 pIC50 = 7.0 Binding
Binding affinity to angiotensin AT1 receptorBinding affinity to angiotensin AT1 receptor
ChEMBL 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10.1016/j.bmc.2010.10.043
6907 772 113 None -1 6 Human 7.0 pIC50 = 7.0 Binding
Binding affinity to angiotensin AT1 receptorBinding affinity to angiotensin AT1 receptor
ChEMBL 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10.1016/j.bmc.2010.10.043
CHEMBL1016 772 113 None -1 6 Human 7.0 pIC50 = 7.0 Binding
Binding affinity to angiotensin AT1 receptorBinding affinity to angiotensin AT1 receptor
ChEMBL 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10.1016/j.bmc.2010.10.043
DB00796 772 113 None -1 6 Human 7.0 pIC50 = 7.0 Binding
Binding affinity to angiotensin AT1 receptorBinding affinity to angiotensin AT1 receptor
ChEMBL 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10.1016/j.bmc.2010.10.043
DB13919 772 113 None -1 6 Human 7.0 pIC50 = 7.0 Binding
Binding affinity to angiotensin AT1 receptorBinding affinity to angiotensin AT1 receptor
ChEMBL 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10.1016/j.bmc.2010.10.043
2541 772 113 None - 6 Bovine 7.0 pIC50 = 7.0 Binding
Concentration required to inhibit [125I]AII binding to Angiotensin II receptor from membrane fractions of bovine adrenal cortexConcentration required to inhibit [125I]AII binding to Angiotensin II receptor from membrane fractions of bovine adrenal cortex
ChEMBL 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10.1016/S0960-894X(01)81118-5
587 772 113 None - 6 Bovine 7.0 pIC50 = 7.0 Binding
Concentration required to inhibit [125I]AII binding to Angiotensin II receptor from membrane fractions of bovine adrenal cortexConcentration required to inhibit [125I]AII binding to Angiotensin II receptor from membrane fractions of bovine adrenal cortex
ChEMBL 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10.1016/S0960-894X(01)81118-5
6907 772 113 None - 6 Bovine 7.0 pIC50 = 7.0 Binding
Concentration required to inhibit [125I]AII binding to Angiotensin II receptor from membrane fractions of bovine adrenal cortexConcentration required to inhibit [125I]AII binding to Angiotensin II receptor from membrane fractions of bovine adrenal cortex
ChEMBL 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10.1016/S0960-894X(01)81118-5
CHEMBL1016 772 113 None - 6 Bovine 7.0 pIC50 = 7.0 Binding
Concentration required to inhibit [125I]AII binding to Angiotensin II receptor from membrane fractions of bovine adrenal cortexConcentration required to inhibit [125I]AII binding to Angiotensin II receptor from membrane fractions of bovine adrenal cortex
ChEMBL 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10.1016/S0960-894X(01)81118-5
DB00796 772 113 None - 6 Bovine 7.0 pIC50 = 7.0 Binding
Concentration required to inhibit [125I]AII binding to Angiotensin II receptor from membrane fractions of bovine adrenal cortexConcentration required to inhibit [125I]AII binding to Angiotensin II receptor from membrane fractions of bovine adrenal cortex
ChEMBL 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10.1016/S0960-894X(01)81118-5
DB13919 772 113 None - 6 Bovine 7.0 pIC50 = 7.0 Binding
Concentration required to inhibit [125I]AII binding to Angiotensin II receptor from membrane fractions of bovine adrenal cortexConcentration required to inhibit [125I]AII binding to Angiotensin II receptor from membrane fractions of bovine adrenal cortex
ChEMBL 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10.1016/S0960-894X(01)81118-5
2541 772 113 None - 6 Bovine 7.0 pIC50 = 7.0 Binding
Displacement of [125 I]-AII (0.2 nM) from bovine adrenal cortical membrane angiotensin II (AII) receptor at 10e-7 MDisplacement of [125 I]-AII (0.2 nM) from bovine adrenal cortical membrane angiotensin II (AII) receptor at 10e-7 M
ChEMBL 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10.1016/0960-894X(95)00319-O
587 772 113 None - 6 Bovine 7.0 pIC50 = 7.0 Binding
Displacement of [125 I]-AII (0.2 nM) from bovine adrenal cortical membrane angiotensin II (AII) receptor at 10e-7 MDisplacement of [125 I]-AII (0.2 nM) from bovine adrenal cortical membrane angiotensin II (AII) receptor at 10e-7 M
ChEMBL 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10.1016/0960-894X(95)00319-O
6907 772 113 None - 6 Bovine 7.0 pIC50 = 7.0 Binding
Displacement of [125 I]-AII (0.2 nM) from bovine adrenal cortical membrane angiotensin II (AII) receptor at 10e-7 MDisplacement of [125 I]-AII (0.2 nM) from bovine adrenal cortical membrane angiotensin II (AII) receptor at 10e-7 M
ChEMBL 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10.1016/0960-894X(95)00319-O
CHEMBL1016 772 113 None - 6 Bovine 7.0 pIC50 = 7.0 Binding
Displacement of [125 I]-AII (0.2 nM) from bovine adrenal cortical membrane angiotensin II (AII) receptor at 10e-7 MDisplacement of [125 I]-AII (0.2 nM) from bovine adrenal cortical membrane angiotensin II (AII) receptor at 10e-7 M
ChEMBL 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10.1016/0960-894X(95)00319-O
DB00796 772 113 None - 6 Bovine 7.0 pIC50 = 7.0 Binding
Displacement of [125 I]-AII (0.2 nM) from bovine adrenal cortical membrane angiotensin II (AII) receptor at 10e-7 MDisplacement of [125 I]-AII (0.2 nM) from bovine adrenal cortical membrane angiotensin II (AII) receptor at 10e-7 M
ChEMBL 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10.1016/0960-894X(95)00319-O
DB13919 772 113 None - 6 Bovine 7.0 pIC50 = 7.0 Binding
Displacement of [125 I]-AII (0.2 nM) from bovine adrenal cortical membrane angiotensin II (AII) receptor at 10e-7 MDisplacement of [125 I]-AII (0.2 nM) from bovine adrenal cortical membrane angiotensin II (AII) receptor at 10e-7 M
ChEMBL 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10.1016/0960-894X(95)00319-O
10006742 47643 0 None - 0 Rabbit 7.0 pIC50 = 7.0 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 515 10 1 7 6.5 CCCCc1nnc(SCc2ccccc2Cl)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
CHEMBL154949 47643 0 None - 0 Rabbit 7.0 pIC50 = 7.0 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 515 10 1 7 6.5 CCCCc1nnc(SCc2ccccc2Cl)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
9847539 181447 0 None - 0 Rat 7.0 pIC50 = 7.0 Binding
In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.
ChEMBL 470 8 1 5 5.8 CCCCC1=NC(C)(C2CCCCC2)C(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81140-9
CHEMBL47810 181447 0 None - 0 Rat 7.0 pIC50 = 7.0 Binding
In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.
ChEMBL 470 8 1 5 5.8 CCCCC1=NC(C)(C2CCCCC2)C(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81140-9
44297172 161657 0 None - 0 Bovine 7.0 pIC50 = 7.0 Binding
In vitro binding affinity to angiotensin II receptor in bovine adrenal cortexIn vitro binding affinity to angiotensin II receptor in bovine adrenal cortex
ChEMBL 587 8 2 10 2.9 CCCCc1nc2ccc(C3=NN[C@H]4C(=O)N(C)C(=O)[C@@H]34)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80377-2
CHEMBL416296 161657 0 None - 0 Bovine 7.0 pIC50 = 7.0 Binding
In vitro binding affinity to angiotensin II receptor in bovine adrenal cortexIn vitro binding affinity to angiotensin II receptor in bovine adrenal cortex
ChEMBL 587 8 2 10 2.9 CCCCc1nc2ccc(C3=NN[C@H]4C(=O)N(C)C(=O)[C@@H]34)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80377-2
10671263 9867 0 None - 0 Bovine 7.0 pIC50 = 7.0 Binding
In vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortexIn vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortex
ChEMBL 450 10 3 5 5.0 CCCc1nc(C(O)(CC)CC)c(C(=O)O)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm950450f
CHEMBL114788 9867 0 None - 0 Bovine 7.0 pIC50 = 7.0 Binding
In vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortexIn vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortex
ChEMBL 450 10 3 5 5.0 CCCc1nc(C(O)(CC)CC)c(C(=O)O)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm950450f
10571686 9971 0 None - 0 Bovine 7.0 pIC50 = 7.0 Binding
In vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortexIn vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortex
ChEMBL 378 7 2 4 4.3 CCCc1nc(C)c(C(=O)O)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm950450f
CHEMBL115392 9971 0 None - 0 Bovine 7.0 pIC50 = 7.0 Binding
In vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortexIn vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortex
ChEMBL 378 7 2 4 4.3 CCCc1nc(C)c(C(=O)O)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm950450f
19939495 206080 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
In vitro inhibitory concentration against AT1 receptor from human adrenal tissues.In vitro inhibitory concentration against AT1 receptor from human adrenal tissues.
ChEMBL 728 12 1 7 8.0 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2cc(CCC)ccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1F 10.1016/S0960-894X(01)80595-3
CHEMBL96314 206080 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
In vitro inhibitory concentration against AT1 receptor from human adrenal tissues.In vitro inhibitory concentration against AT1 receptor from human adrenal tissues.
ChEMBL 728 12 1 7 8.0 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2cc(CCC)ccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1F 10.1016/S0960-894X(01)80595-3
2541 772 113 None - 6 Bovine 7.0 pIC50 = 7.0 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10.1021/jm00067a016
587 772 113 None - 6 Bovine 7.0 pIC50 = 7.0 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10.1021/jm00067a016
6907 772 113 None - 6 Bovine 7.0 pIC50 = 7.0 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10.1021/jm00067a016
CHEMBL1016 772 113 None - 6 Bovine 7.0 pIC50 = 7.0 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10.1021/jm00067a016
DB00796 772 113 None - 6 Bovine 7.0 pIC50 = 7.0 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10.1021/jm00067a016
DB13919 772 113 None - 6 Bovine 7.0 pIC50 = 7.0 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10.1021/jm00067a016
4110026 203217 1 None - 1 Bovine 7.0 pIC50 = 7.0 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 384 7 1 3 5.8 CCCCc1nc2ccccc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1007/s00044-009-9182-z
CHEMBL7632 203217 1 None - 1 Bovine 7.0 pIC50 = 7.0 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 384 7 1 3 5.8 CCCCc1nc2ccccc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1007/s00044-009-9182-z
9886554 96646 0 None - 0 Rat 6.0 pIC50 = 6.0 Binding
Activity against high affinity Angiotensin II receptor, type 1 was measured from the ability to inhibit [125I]angiotensin II binding to rat uterine membrane.Activity against high affinity Angiotensin II receptor, type 1 was measured from the ability to inhibit [125I]angiotensin II binding to rat uterine membrane.
ChEMBL 387 8 2 5 3.9 CCCCc1nc(CO)c(Cl)n1Cc1ccc(-n2cccc2C(=O)O)cc1 10.1021/jm00053a013
CHEMBL267547 96646 0 None - 0 Rat 6.0 pIC50 = 6.0 Binding
Activity against high affinity Angiotensin II receptor, type 1 was measured from the ability to inhibit [125I]angiotensin II binding to rat uterine membrane.Activity against high affinity Angiotensin II receptor, type 1 was measured from the ability to inhibit [125I]angiotensin II binding to rat uterine membrane.
ChEMBL 387 8 2 5 3.9 CCCCc1nc(CO)c(Cl)n1Cc1ccc(-n2cccc2C(=O)O)cc1 10.1021/jm00053a013
15699062 4843 0 None - 0 Rat 6.0 pIC50 = 6.0 Binding
Binding affinity against angiotensin II receptor in rat smooth muscle cell preparationsBinding affinity against angiotensin II receptor in rat smooth muscle cell preparations
ChEMBL 376 7 2 4 3.6 CCCCc1nc(CO)c(Cl)n1Cc1ccc2c(c1)CCC(C(=O)O)C2 10.1021/jm00114a021
CHEMBL104684 4843 0 None - 0 Rat 6.0 pIC50 = 6.0 Binding
Binding affinity against angiotensin II receptor in rat smooth muscle cell preparationsBinding affinity against angiotensin II receptor in rat smooth muscle cell preparations
ChEMBL 376 7 2 4 3.6 CCCCc1nc(CO)c(Cl)n1Cc1ccc2c(c1)CCC(C(=O)O)C2 10.1021/jm00114a021
15699051 5681 0 None - 0 Rat 6.0 pIC50 = 6.0 Binding
Binding affinity against angiotensin II receptor in rat smooth muscle cell preparationsBinding affinity against angiotensin II receptor in rat smooth muscle cell preparations
ChEMBL 396 7 2 6 3.8 CCCCc1nc(Cl)c(CO)n1Cc1cccc2c(-c3nn[nH]n3)cccc12 10.1021/jm00114a021
CHEMBL107862 5681 0 None - 0 Rat 6.0 pIC50 = 6.0 Binding
Binding affinity against angiotensin II receptor in rat smooth muscle cell preparationsBinding affinity against angiotensin II receptor in rat smooth muscle cell preparations
ChEMBL 396 7 2 6 3.8 CCCCc1nc(Cl)c(CO)n1Cc1cccc2c(-c3nn[nH]n3)cccc12 10.1021/jm00114a021
44293476 101478 0 None - 0 Rat 6.0 pIC50 = 6.0 Binding
Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.
ChEMBL 500 12 3 6 4.7 CCCCc1ncc(CO)n1Cc1ccc(NC(=O)[C@H](Cc2ccccc2)n2cccc2C(=O)O)cc1 10.1021/jm00064a007
CHEMBL301328 101478 0 None - 0 Rat 6.0 pIC50 = 6.0 Binding
Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.
ChEMBL 500 12 3 6 4.7 CCCCc1ncc(CO)n1Cc1ccc(NC(=O)[C@H](Cc2ccccc2)n2cccc2C(=O)O)cc1 10.1021/jm00064a007
44307088 101720 0 None - 0 Rabbit 6.0 pIC50 = 6.0 Binding
Binding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membraneBinding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane
ChEMBL 465 4 1 6 3.8 CCc1nc2c(C)cc(C)nc2n1Cc1cc(I)c(O)c(C(=O)OC)c1 10.1016/S0960-894X(01)81148-3
CHEMBL302869 101720 0 None - 0 Rabbit 6.0 pIC50 = 6.0 Binding
Binding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membraneBinding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane
ChEMBL 465 4 1 6 3.8 CCc1nc2c(C)cc(C)nc2n1Cc1cc(I)c(O)c(C(=O)OC)c1 10.1016/S0960-894X(01)81148-3
44295557 101293 0 None - 0 Bovine 6.0 pIC50 = 6.0 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 438 8 1 6 5.3 CCCCc1nc2ccc(OC)cc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
CHEMBL299980 101293 0 None - 0 Bovine 6.0 pIC50 = 6.0 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 438 8 1 6 5.3 CCCCc1nc2ccc(OC)cc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
19792135 188903 0 None - 0 Bovine 6.0 pIC50 = 6.0 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 424 7 2 6 5.0 CCCCc1nc2cccc(O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
CHEMBL51399 188903 0 None - 0 Bovine 6.0 pIC50 = 6.0 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 424 7 2 6 5.0 CCCCc1nc2cccc(O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
15355267 192591 0 None - 0 Bovine 6.0 pIC50 = 6.0 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 486 8 2 6 5.6 CCCCc1nc2cc(Cl)cc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
CHEMBL52343 192591 0 None - 0 Bovine 6.0 pIC50 = 6.0 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 486 8 2 6 5.6 CCCCc1nc2cc(Cl)cc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
4110026 203217 1 None - 1 Bovine 6.0 pIC50 = 6.0 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 384 7 1 3 5.8 CCCCc1nc2ccccc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1007/s00044-009-9182-z
CHEMBL7632 203217 1 None - 1 Bovine 6.0 pIC50 = 6.0 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 384 7 1 3 5.8 CCCCc1nc2ccccc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1007/s00044-009-9182-z
53837978 169871 0 None - 0 Human 6.0 pIC50 = 6.0 Binding
Inhibition of human AT1 receptorInhibition of human AT1 receptor
ChEMBL 507 8 1 4 5.4 COc1ccc2c(c1OCc1ccccc1)C[C@H](C(=O)O)N(C(=O)C(c1ccccc1)c1ccccc1)C2 10.1021/acs.jmedchem.9b01780
CHEMBL4448705 169871 0 None - 0 Human 6.0 pIC50 = 6.0 Binding
Inhibition of human AT1 receptorInhibition of human AT1 receptor
ChEMBL 507 8 1 4 5.4 COc1ccc2c(c1OCc1ccccc1)C[C@H](C(=O)O)N(C(=O)C(c1ccccc1)c1ccccc1)C2 10.1021/acs.jmedchem.9b01780
44306628 201776 0 None - 0 Rabbit 5.0 pIC50 = 5.0 Binding
Binding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membraneBinding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane
ChEMBL 421 3 0 3 5.2 CCc1nc2c(C)cc(C)nc2n1Cc1cc(Br)cc(Br)c1 10.1016/S0960-894X(01)81148-3
CHEMBL66056 201776 0 None - 0 Rabbit 5.0 pIC50 = 5.0 Binding
Binding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membraneBinding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane
ChEMBL 421 3 0 3 5.2 CCc1nc2c(C)cc(C)nc2n1Cc1cc(Br)cc(Br)c1 10.1016/S0960-894X(01)81148-3
44295557 101293 0 None - 0 Bovine 6.0 pIC50 = 6.0 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 438 8 1 6 5.3 CCCCc1nc2ccc(OC)cc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
CHEMBL299980 101293 0 None - 0 Bovine 6.0 pIC50 = 6.0 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 438 8 1 6 5.3 CCCCc1nc2ccc(OC)cc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
19792135 188903 0 None - 0 Bovine 6.0 pIC50 = 6.0 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 424 7 2 6 5.0 CCCCc1nc2cccc(O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
CHEMBL51399 188903 0 None - 0 Bovine 6.0 pIC50 = 6.0 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 424 7 2 6 5.0 CCCCc1nc2cccc(O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
15355267 192591 0 None - 0 Bovine 6.0 pIC50 = 6.0 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 486 8 2 6 5.6 CCCCc1nc2cc(Cl)cc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
CHEMBL52343 192591 0 None - 0 Bovine 6.0 pIC50 = 6.0 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 486 8 2 6 5.6 CCCCc1nc2cc(Cl)cc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
127034905 135823 0 None - 0 Human 6.0 pIC50 = 6.0 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 561 10 2 4 7.8 CCCc1nc2c(C)cc(C(=S)NC[C@H](C)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2015.09.010
CHEMBL3734859 135823 0 None - 0 Human 6.0 pIC50 = 6.0 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 561 10 2 4 7.8 CCCc1nc2c(C)cc(C(=S)NC[C@H](C)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2015.09.010
44293652 100945 0 None - 0 Rat 6.0 pIC50 = 6.0 Binding
Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.
ChEMBL 534 11 2 7 5.2 CCCCc1nc(Cl)c(CO)n1Cc1ccc(NC(=O)[C@H](c2ccccc2)n2cccc2C(=O)OC)cc1 10.1021/jm00064a007
CHEMBL297465 100945 0 None - 0 Rat 6.0 pIC50 = 6.0 Binding
Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.
ChEMBL 534 11 2 7 5.2 CCCCc1nc(Cl)c(CO)n1Cc1ccc(NC(=O)[C@H](c2ccccc2)n2cccc2C(=O)OC)cc1 10.1021/jm00064a007
24828714 95703 0 None - 0 Rat 6.9 pIC50 = 6.9 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
ChEMBL 453 8 1 8 4.0 CCCCn1nc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2cccnc2c1=O 10.1021/jm7011563
CHEMBL260578 95703 0 None - 0 Rat 6.9 pIC50 = 6.9 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
ChEMBL 453 8 1 8 4.0 CCCCn1nc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2cccnc2c1=O 10.1021/jm7011563
14956759 204372 0 None - 0 Rabbit 6.9 pIC50 = 6.9 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 495 9 2 8 4.0 CCCCc1nn(-c2ccccc2C(=O)O)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
CHEMBL85704 204372 0 None - 0 Rabbit 6.9 pIC50 = 6.9 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 495 9 2 8 4.0 CCCCc1nn(-c2ccccc2C(=O)O)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
73350990 92172 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysisDisplacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysis
ChEMBL 545 11 2 4 7.1 CCCc1nc2c(C)cc(C(=O)NCCCc3ccccc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2013.08.014
CHEMBL2435820 92172 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysisDisplacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysis
ChEMBL 545 11 2 4 7.1 CCCc1nc2c(C)cc(C(=O)NCCCc3ccccc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2013.08.014
19889359 159628 0 None - 0 Rat 6.9 pIC50 = 6.9 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 410 6 1 7 4.0 CCCc1nc2c(C)ccnc2n1Cc1ccc(-c2ncccc2-c2nn[nH]n2)cc1 10.1021/jm031100t
CHEMBL410939 159628 0 None - 0 Rat 6.9 pIC50 = 6.9 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 410 6 1 7 4.0 CCCc1nc2c(C)ccnc2n1Cc1ccc(-c2ncccc2-c2nn[nH]n2)cc1 10.1021/jm031100t
19889359 159628 0 None - 0 Rabbit 6.9 pIC50 = 6.9 Binding
In vitro binding affinity towards Angiotensin II type 1-AT1 receptor determined as its ability to displace 125I-Sarl,Ile8-AII from the receptor expressed in rabbit aorta membrane.In vitro binding affinity towards Angiotensin II type 1-AT1 receptor determined as its ability to displace 125I-Sarl,Ile8-AII from the receptor expressed in rabbit aorta membrane.
ChEMBL 410 6 1 7 4.0 CCCc1nc2c(C)ccnc2n1Cc1ccc(-c2ncccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80044-X
CHEMBL410939 159628 0 None - 0 Rabbit 6.9 pIC50 = 6.9 Binding
In vitro binding affinity towards Angiotensin II type 1-AT1 receptor determined as its ability to displace 125I-Sarl,Ile8-AII from the receptor expressed in rabbit aorta membrane.In vitro binding affinity towards Angiotensin II type 1-AT1 receptor determined as its ability to displace 125I-Sarl,Ile8-AII from the receptor expressed in rabbit aorta membrane.
ChEMBL 410 6 1 7 4.0 CCCc1nc2c(C)ccnc2n1Cc1ccc(-c2ncccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80044-X
10257293 16723 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 562 12 0 6 6.3 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2Cc2cccc(Cl)c2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
CHEMBL125233 16723 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 562 12 0 6 6.3 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2Cc2cccc(Cl)c2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
70690743 76267 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of 125[I-Sar1-Ile8]ANG II from human AT1 receptor expressed in HEK293 membranes after 1 hr by gamma countingDisplacement of 125[I-Sar1-Ile8]ANG II from human AT1 receptor expressed in HEK293 membranes after 1 hr by gamma counting
ChEMBL 466 8 2 6 4.4 CCCCc1c(Br)nc(CO)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.ejmech.2012.07.040
CHEMBL2063981 76267 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of 125[I-Sar1-Ile8]ANG II from human AT1 receptor expressed in HEK293 membranes after 1 hr by gamma countingDisplacement of 125[I-Sar1-Ile8]ANG II from human AT1 receptor expressed in HEK293 membranes after 1 hr by gamma counting
ChEMBL 466 8 2 6 4.4 CCCCc1c(Br)nc(CO)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.ejmech.2012.07.040
70690743 76267 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of 125[I-Sar1-Ile8]ANG II from human AT1 receptor expressed in HEK293 membranes after 1 hr by gamma countingDisplacement of 125[I-Sar1-Ile8]ANG II from human AT1 receptor expressed in HEK293 membranes after 1 hr by gamma counting
ChEMBL 466 8 2 6 4.4 CCCCc1c(Br)nc(CO)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.ejmech.2012.07.040
CHEMBL2063981 76267 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of 125[I-Sar1-Ile8]ANG II from human AT1 receptor expressed in HEK293 membranes after 1 hr by gamma countingDisplacement of 125[I-Sar1-Ile8]ANG II from human AT1 receptor expressed in HEK293 membranes after 1 hr by gamma counting
ChEMBL 466 8 2 6 4.4 CCCCc1c(Br)nc(CO)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.ejmech.2012.07.040
14950487 94156 0 None - 0 Guinea pig 5.9 pIC50 = 5.9 Binding
Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1
ChEMBL 401 6 2 6 3.8 Cc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c(C(=O)O)c(C)n1 10.1021/jm00061a016
CHEMBL25220 94156 0 None - 0 Guinea pig 5.9 pIC50 = 5.9 Binding
Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1
ChEMBL 401 6 2 6 3.8 Cc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c(C(=O)O)c(C)n1 10.1021/jm00061a016
70688502 75960 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of [125I]Sar1Ile8-Ang2 from angiotensin AT1 receptor after 180 mins by gamma countingDisplacement of [125I]Sar1Ile8-Ang2 from angiotensin AT1 receptor after 180 mins by gamma counting
ChEMBL 571 10 2 7 6.1 CCCc1nc2c(C)cc(C(=O)NCc3ccc(OC)cc3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmc.2012.05.056
CHEMBL2058857 75960 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of [125I]Sar1Ile8-Ang2 from angiotensin AT1 receptor after 180 mins by gamma countingDisplacement of [125I]Sar1Ile8-Ang2 from angiotensin AT1 receptor after 180 mins by gamma counting
ChEMBL 571 10 2 7 6.1 CCCc1nc2c(C)cc(C(=O)NCc3ccc(OC)cc3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmc.2012.05.056
44459867 93439 0 None - 0 Rabbit 7.9 pIC50 = 7.9 Binding
Ability to displace [125I]Sar1-Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitroAbility to displace [125I]Sar1-Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitro
ChEMBL 504 7 1 6 5.7 CCCCc1nc2ccc(C(F)(F)F)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80334-0
CHEMBL24802 93439 0 None - 0 Rabbit 7.9 pIC50 = 7.9 Binding
Ability to displace [125I]Sar1-Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitroAbility to displace [125I]Sar1-Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitro
ChEMBL 504 7 1 6 5.7 CCCCc1nc2ccc(C(F)(F)F)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80334-0
44274710 99461 0 None - 0 Rabbit 7.9 pIC50 = 7.9 Binding
Ability to displace [125I]Sar1-Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitroAbility to displace [125I]Sar1-Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitro
ChEMBL 562 7 1 6 5.2 CCCCc1nc2ccc(I)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80334-0
CHEMBL286260 99461 0 None - 0 Rabbit 7.9 pIC50 = 7.9 Binding
Ability to displace [125I]Sar1-Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitroAbility to displace [125I]Sar1-Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitro
ChEMBL 562 7 1 6 5.2 CCCCc1nc2ccc(I)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80334-0
14956793 204575 0 None - 0 Rabbit 7.9 pIC50 = 7.9 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 479 9 1 7 4.6 CCCCc1nn(Cc2cccc(C)c2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
CHEMBL87129 204575 0 None - 0 Rabbit 7.9 pIC50 = 7.9 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 479 9 1 7 4.6 CCCCc1nn(Cc2cccc(C)c2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
14956798 204673 0 None - 0 Rabbit 7.9 pIC50 = 7.9 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 523 10 1 9 4.0 CCCCc1nn(C(C(=O)OC)c2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
CHEMBL87798 204673 0 None - 0 Rabbit 7.9 pIC50 = 7.9 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 523 10 1 9 4.0 CCCCc1nn(C(C(=O)OC)c2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
11397357 106518 0 None - 0 Rat 7.9 pIC50 = 7.9 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 474 6 1 7 5.4 CCCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2c(-c3nn[nH]n3)cnc3ccccc23)cc1 10.1021/jm031100t
CHEMBL315387 106518 0 None - 0 Rat 7.9 pIC50 = 7.9 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 474 6 1 7 5.4 CCCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2c(-c3nn[nH]n3)cnc3ccccc23)cc1 10.1021/jm031100t
9954408 206218 0 None - 1 Human 7.9 pIC50 = 7.9 Binding
Binding affinity to angiotensin AT1 receptorBinding affinity to angiotensin AT1 receptor
ChEMBL 430 10 1 6 4.7 CCCCc1cn(CCCC)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.bmc.2010.10.043
CHEMBL9714 206218 0 None - 1 Human 7.9 pIC50 = 7.9 Binding
Binding affinity to angiotensin AT1 receptorBinding affinity to angiotensin AT1 receptor
ChEMBL 430 10 1 6 4.7 CCCCc1cn(CCCC)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.bmc.2010.10.043
70684240 75855 0 None - 0 Bovine 7.9 pIC50 = 7.9 Binding
Displacement of [125I]AngII from type 1 angiotensin 2 receptor in bovine adrenal cortexDisplacement of [125I]AngII from type 1 angiotensin 2 receptor in bovine adrenal cortex
ChEMBL 559 10 1 8 6.4 CCCCc1nc2ccc([N+](=O)[O-])cc2n1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)cc1 10.1016/j.bmc.2012.06.011
CHEMBL2058377 75855 0 None - 0 Bovine 7.9 pIC50 = 7.9 Binding
Displacement of [125I]AngII from type 1 angiotensin 2 receptor in bovine adrenal cortexDisplacement of [125I]AngII from type 1 angiotensin 2 receptor in bovine adrenal cortex
ChEMBL 559 10 1 8 6.4 CCCCc1nc2ccc([N+](=O)[O-])cc2n1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)cc1 10.1016/j.bmc.2012.06.011
44274710 99461 0 None - 0 Rabbit 7.9 pIC50 = 7.9 Binding
Displacement of [125I]Sar1-Ile8-AII (without BSA) from type 1 Angiotensin II receptor of rabbit aortaDisplacement of [125I]Sar1-Ile8-AII (without BSA) from type 1 Angiotensin II receptor of rabbit aorta
ChEMBL 562 7 1 6 5.2 CCCCc1nc2ccc(I)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80335-2
CHEMBL286260 99461 0 None - 0 Rabbit 7.9 pIC50 = 7.9 Binding
Displacement of [125I]Sar1-Ile8-AII (without BSA) from type 1 Angiotensin II receptor of rabbit aortaDisplacement of [125I]Sar1-Ile8-AII (without BSA) from type 1 Angiotensin II receptor of rabbit aorta
ChEMBL 562 7 1 6 5.2 CCCCc1nc2ccc(I)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80335-2
19422649 100813 0 None - 0 Rat 7.9 pIC50 = 7.9 Binding
In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.
ChEMBL 446 8 1 3 6.3 CCCCC1=NC(C)(C2CCCCC2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/S0960-894X(01)81140-9
CHEMBL296492 100813 0 None - 0 Rat 7.9 pIC50 = 7.9 Binding
In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.
ChEMBL 446 8 1 3 6.3 CCCCC1=NC(C)(C2CCCCC2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/S0960-894X(01)81140-9
44379347 119968 0 None - 0 Rabbit 7.9 pIC50 = 7.9 Binding
In vitro displacement of 125I-[Sar1, Ile8] from AT1 receptors in rabbit aorta membraneIn vitro displacement of 125I-[Sar1, Ile8] from AT1 receptors in rabbit aorta membrane
ChEMBL 544 9 1 7 4.3 CCCc1nc2ccc(N(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)C2CC2)cc1 10.1016/S0960-894X(01)81125-2
CHEMBL354338 119968 0 None - 0 Rabbit 7.9 pIC50 = 7.9 Binding
In vitro displacement of 125I-[Sar1, Ile8] from AT1 receptors in rabbit aorta membraneIn vitro displacement of 125I-[Sar1, Ile8] from AT1 receptors in rabbit aorta membrane
ChEMBL 544 9 1 7 4.3 CCCc1nc2ccc(N(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)C2CC2)cc1 10.1016/S0960-894X(01)81125-2
44379291 119994 0 None - 0 Rabbit 7.9 pIC50 = 7.9 Binding
In vitro displacement of 125I-[Sar1, Ile8] from AT1 receptors in rabbit aorta membraneIn vitro displacement of 125I-[Sar1, Ile8] from AT1 receptors in rabbit aorta membrane
ChEMBL 702 15 2 8 7.5 CCCCc1nc2ccc(C(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)CCCCCNC(=O)OC(C)(C)C)cc1 10.1016/S0960-894X(01)81125-2
CHEMBL354535 119994 0 None - 0 Rabbit 7.9 pIC50 = 7.9 Binding
In vitro displacement of 125I-[Sar1, Ile8] from AT1 receptors in rabbit aorta membraneIn vitro displacement of 125I-[Sar1, Ile8] from AT1 receptors in rabbit aorta membrane
ChEMBL 702 15 2 8 7.5 CCCCc1nc2ccc(C(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)CCCCCNC(=O)OC(C)(C)C)cc1 10.1016/S0960-894X(01)81125-2
3081289 9914 10 None - 0 Bovine 7.9 pIC50 = 7.9 Binding
In vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortexIn vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortex
ChEMBL 416 8 2 6 4.0 CCCc1nc(CC)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm950450f
CHEMBL115021 9914 10 None - 0 Bovine 7.9 pIC50 = 7.9 Binding
In vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortexIn vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortex
ChEMBL 416 8 2 6 4.0 CCCc1nc(CC)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm950450f
44377075 119459 0 None - 0 Rabbit 7.9 pIC50 = 7.9 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aortaIn vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aorta
ChEMBL 479 10 1 6 4.1 CCCc1nc(CC)c(C=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)C2CC2)cc1 10.1016/S0960-894X(01)81124-0
CHEMBL349869 119459 0 None - 0 Rabbit 7.9 pIC50 = 7.9 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aortaIn vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aorta
ChEMBL 479 10 1 6 4.1 CCCc1nc(CC)c(C=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)C2CC2)cc1 10.1016/S0960-894X(01)81124-0
44315180 102410 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membrane
ChEMBL 621 9 2 8 4.9 Cc1nc2ccc(NC(=O)N(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC2CC2)cc1F 10.1016/0960-894X(94)85036-4
CHEMBL305956 102410 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membrane
ChEMBL 621 9 2 8 4.9 Cc1nc2ccc(NC(=O)N(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC2CC2)cc1F 10.1016/0960-894X(94)85036-4
15292112 102462 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membrane
ChEMBL 635 11 3 8 5.2 CCNC(=O)Nc1ccc2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OCCC4CC4)cc3F)c(=O)c2c1 10.1016/0960-894X(94)85036-4
CHEMBL306361 102462 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membrane
ChEMBL 635 11 3 8 5.2 CCNC(=O)Nc1ccc2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OCCC4CC4)cc3F)c(=O)c2c1 10.1016/0960-894X(94)85036-4
14951068 101622 0 None - 0 Rat 7.9 pIC50 = 7.9 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 475 12 2 8 3.5 CCCCc1nn(CCCCC(=O)O)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a015
CHEMBL302261 101622 0 None - 0 Rat 7.9 pIC50 = 7.9 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 475 12 2 8 3.5 CCCCc1nn(CCCCC(=O)O)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a015
14951083 102120 0 None - 0 Rat 7.9 pIC50 = 7.9 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 509 11 1 8 4.7 CCCCc1nn(CC(OC)c2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a015
CHEMBL304134 102120 0 None - 0 Rat 7.9 pIC50 = 7.9 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 509 11 1 8 4.7 CCCCc1nn(CC(OC)c2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a015
44270330 51454 0 None - 0 Rabbit 7.9 pIC50 = 7.9 Binding
Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)
ChEMBL 471 10 1 5 6.2 CCCCc1cc(Cn2c(CC)nc3c(C)cc(C)nc32)ccc1OC(C(=O)O)c1ccccc1 10.1016/0960-894X(95)00185-V
CHEMBL15847 51454 0 None - 0 Rabbit 7.9 pIC50 = 7.9 Binding
Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)
ChEMBL 471 10 1 5 6.2 CCCCc1cc(Cn2c(CC)nc3c(C)cc(C)nc32)ccc1OC(C(=O)O)c1ccccc1 10.1016/0960-894X(95)00185-V
44270278 98395 0 None - 0 Rabbit 7.9 pIC50 = 7.9 Binding
Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)
ChEMBL 443 8 1 5 5.4 CCc1cc(Cn2c(CC)nc3c(C)cc(C)nc32)ccc1OC(C(=O)O)c1ccccc1 10.1016/0960-894X(95)00185-V
CHEMBL278983 98395 0 None - 0 Rabbit 7.9 pIC50 = 7.9 Binding
Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)
ChEMBL 443 8 1 5 5.4 CCc1cc(Cn2c(CC)nc3c(C)cc(C)nc32)ccc1OC(C(=O)O)c1ccccc1 10.1016/0960-894X(95)00185-V
10324657 113205 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 528 12 0 6 5.7 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2Cc2ccccc2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
CHEMBL332323 113205 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 528 12 0 6 5.7 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2Cc2ccccc2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
46184983 86378 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor afterDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after
ChEMBL 513 6 1 7 5.2 CCc1nc2ccn(Cc3ccccc3)c(=O)c2n1[C@H]1CCc2cc(-c3ccccc3-c3nnn[nH]3)ccc21 10.1016/j.bmcl.2012.11.088
CHEMBL2322437 86378 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor afterDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after
ChEMBL 513 6 1 7 5.2 CCc1nc2ccn(Cc3ccccc3)c(=O)c2n1[C@H]1CCc2cc(-c3ccccc3-c3nnn[nH]3)ccc21 10.1016/j.bmcl.2012.11.088
44295057 100851 0 None - 1 Bovine 6.9 pIC50 = 6.9 Binding
Ability to displace [125I]- labelled [Sar1,Ileu8] from angiotensin II receptor of bovine adrenal cortex membranesAbility to displace [125I]- labelled [Sar1,Ileu8] from angiotensin II receptor of bovine adrenal cortex membranes
ChEMBL 473 7 1 6 4.8 CCOC(=O)/C=C1\CC(C)(C(C)C)CC(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80474-6
CHEMBL296731 100851 0 None - 1 Bovine 6.9 pIC50 = 6.9 Binding
Ability to displace [125I]- labelled [Sar1,Ileu8] from angiotensin II receptor of bovine adrenal cortex membranesAbility to displace [125I]- labelled [Sar1,Ileu8] from angiotensin II receptor of bovine adrenal cortex membranes
ChEMBL 473 7 1 6 4.8 CCOC(=O)/C=C1\CC(C)(C(C)C)CC(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80474-6
44295068 188423 0 None - 0 Bovine 6.9 pIC50 = 6.9 Binding
Ability to displace [125I]- labelled [Sar1,Ileu8] from angiotensin II receptor of bovine adrenal cortex membranesAbility to displace [125I]- labelled [Sar1,Ileu8] from angiotensin II receptor of bovine adrenal cortex membranes
ChEMBL 473 8 1 6 4.9 CCCC1(C)CC(=O)N(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/C(=C/C(=O)OCC)C1 10.1016/S0960-894X(00)80474-6
CHEMBL50906 188423 0 None - 0 Bovine 6.9 pIC50 = 6.9 Binding
Ability to displace [125I]- labelled [Sar1,Ileu8] from angiotensin II receptor of bovine adrenal cortex membranesAbility to displace [125I]- labelled [Sar1,Ileu8] from angiotensin II receptor of bovine adrenal cortex membranes
ChEMBL 473 8 1 6 4.9 CCCC1(C)CC(=O)N(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/C(=C/C(=O)OCC)C1 10.1016/S0960-894X(00)80474-6
44274691 95110 0 None - 0 Rabbit 6.9 pIC50 = 6.9 Binding
Ability to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitroAbility to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitro
ChEMBL 583 9 2 8 4.9 CCCCc1nc2ccc(NS(=O)(=O)C(F)(F)F)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80335-2
CHEMBL25767 95110 0 None - 0 Rabbit 6.9 pIC50 = 6.9 Binding
Ability to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitroAbility to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitro
ChEMBL 583 9 2 8 4.9 CCCCc1nc2ccc(NS(=O)(=O)C(F)(F)F)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80335-2
19010044 84527 0 None - 0 Rabbit 6.9 pIC50 = 6.9 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 582 12 2 10 5.2 CCCCc1nnc(SCc2ccc(C(=O)OC)cc2)n1Cc1ccc(NC(=O)c2ccccc2-c2nnn[nH]2)cc1 10.1007/s00044-011-9756-4
CHEMBL2237597 84527 0 None - 0 Rabbit 6.9 pIC50 = 6.9 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 582 12 2 10 5.2 CCCCc1nnc(SCc2ccc(C(=O)OC)cc2)n1Cc1ccc(NC(=O)c2ccccc2-c2nnn[nH]2)cc1 10.1007/s00044-011-9756-4
14956742 204595 0 None - 0 Rabbit 6.9 pIC50 = 6.9 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 485 8 1 7 4.9 CCCCc1nn(-c2cccc(Cl)c2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
CHEMBL87275 204595 0 None - 0 Rabbit 6.9 pIC50 = 6.9 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 485 8 1 7 4.9 CCCCc1nn(-c2cccc(Cl)c2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
9984755 47673 0 None - 0 Rabbit 6.9 pIC50 = 6.9 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 539 11 1 9 5.6 CCCCc1nnc(SCc2ccc(C(=O)OC)cc2)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
CHEMBL154975 47673 0 None - 0 Rabbit 6.9 pIC50 = 6.9 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 539 11 1 9 5.6 CCCCc1nnc(SCc2ccc(C(=O)OC)cc2)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
10074143 48717 0 None - 0 Rabbit 6.9 pIC50 = 6.9 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 486 10 2 6 5.5 CCCc1nnc(SCc2ccccc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
CHEMBL156070 48717 0 None - 0 Rabbit 6.9 pIC50 = 6.9 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 486 10 2 6 5.5 CCCc1nnc(SCc2ccccc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
1610 2305 89 None - 4 Bovine 6.9 pIC50 = 6.9 Binding
Displacement of [125I]angiotensin-2 from bovine adrenal cortex AT1 receptorDisplacement of [125I]angiotensin-2 from bovine adrenal cortex AT1 receptor
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmcl.2007.02.042
3941 2305 89 None - 4 Bovine 6.9 pIC50 = 6.9 Binding
Displacement of [125I]angiotensin-2 from bovine adrenal cortex AT1 receptorDisplacement of [125I]angiotensin-2 from bovine adrenal cortex AT1 receptor
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmcl.2007.02.042
3961 2305 89 None - 4 Bovine 6.9 pIC50 = 6.9 Binding
Displacement of [125I]angiotensin-2 from bovine adrenal cortex AT1 receptorDisplacement of [125I]angiotensin-2 from bovine adrenal cortex AT1 receptor
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmcl.2007.02.042
590 2305 89 None - 4 Bovine 6.9 pIC50 = 6.9 Binding
Displacement of [125I]angiotensin-2 from bovine adrenal cortex AT1 receptorDisplacement of [125I]angiotensin-2 from bovine adrenal cortex AT1 receptor
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmcl.2007.02.042
CHEMBL191 2305 89 None - 4 Bovine 6.9 pIC50 = 6.9 Binding
Displacement of [125I]angiotensin-2 from bovine adrenal cortex AT1 receptorDisplacement of [125I]angiotensin-2 from bovine adrenal cortex AT1 receptor
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmcl.2007.02.042
DB00678 2305 89 None - 4 Bovine 6.9 pIC50 = 6.9 Binding
Displacement of [125I]angiotensin-2 from bovine adrenal cortex AT1 receptorDisplacement of [125I]angiotensin-2 from bovine adrenal cortex AT1 receptor
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmcl.2007.02.042
44358304 116278 0 None - 0 Rabbit 6.9 pIC50 = 6.9 Binding
Displacement of the specific binding ligand [125I]Sar1,Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane.Displacement of the specific binding ligand [125I]Sar1,Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane.
ChEMBL 521 5 1 6 5.9 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2C2=NS(=O)(=O)c3ccccc3N2)cc1 10.1016/S0960-894X(01)81119-7
CHEMBL337787 116278 0 None - 0 Rabbit 6.9 pIC50 = 6.9 Binding
Displacement of the specific binding ligand [125I]Sar1,Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane.Displacement of the specific binding ligand [125I]Sar1,Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane.
ChEMBL 521 5 1 6 5.9 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2C2=NS(=O)(=O)c3ccccc3N2)cc1 10.1016/S0960-894X(01)81119-7
1610 2305 89 None - 4 Bovine 6.9 pIC50 = 6.9 Binding
In vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortexIn vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortex
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm950450f
3941 2305 89 None - 4 Bovine 6.9 pIC50 = 6.9 Binding
In vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortexIn vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortex
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm950450f
3961 2305 89 None - 4 Bovine 6.9 pIC50 = 6.9 Binding
In vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortexIn vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortex
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm950450f
590 2305 89 None - 4 Bovine 6.9 pIC50 = 6.9 Binding
In vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortexIn vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortex
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm950450f
CHEMBL191 2305 89 None - 4 Bovine 6.9 pIC50 = 6.9 Binding
In vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortexIn vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortex
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm950450f
DB00678 2305 89 None - 4 Bovine 6.9 pIC50 = 6.9 Binding
In vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortexIn vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortex
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm950450f
11754802 116006 0 None - 0 Guinea pig 6.9 pIC50 = 6.9 Binding
In vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparationIn vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparation
ChEMBL 441 6 1 5 5.9 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2c(Cl)cccc2n1 10.1021/jm00100a007
CHEMBL336167 116006 0 None - 0 Guinea pig 6.9 pIC50 = 6.9 Binding
In vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparationIn vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparation
ChEMBL 441 6 1 5 5.9 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2c(Cl)cccc2n1 10.1021/jm00100a007
15231808 105508 0 None - 0 Rat 6.9 pIC50 = 6.9 Binding
Inhibition of [125-I]-labeled angiotensin II binding to AT1 receptor in rat uterine membranesInhibition of [125-I]-labeled angiotensin II binding to AT1 receptor in rat uterine membranes
ChEMBL 396 6 1 5 5.1 CCCCc1ncc2n1C(c1ccc(-c3ccccc3-c3nn[nH]n3)cc1)CC=C2 10.1016/S0960-894X(01)80290-0
CHEMBL313239 105508 0 None - 0 Rat 6.9 pIC50 = 6.9 Binding
Inhibition of [125-I]-labeled angiotensin II binding to AT1 receptor in rat uterine membranesInhibition of [125-I]-labeled angiotensin II binding to AT1 receptor in rat uterine membranes
ChEMBL 396 6 1 5 5.1 CCCCc1ncc2n1C(c1ccc(-c3ccccc3-c3nn[nH]n3)cc1)CC=C2 10.1016/S0960-894X(01)80290-0
14950499 99044 0 None - 0 Guinea pig 6.9 pIC50 = 6.9 Binding
Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1
ChEMBL 387 6 2 6 3.6 Cc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c(CO)c(C)n1 10.1021/jm00061a016
CHEMBL283372 99044 0 None - 0 Guinea pig 6.9 pIC50 = 6.9 Binding
Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1
ChEMBL 387 6 2 6 3.6 Cc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c(CO)c(C)n1 10.1021/jm00061a016
1610 2305 89 None - 4 Bovine 6.9 pIC50 = 6.9 Binding
Inhibition of [125l]-All binding to bovine adrenal cortexInhibition of [125l]-All binding to bovine adrenal cortex
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(01)81143-4
3941 2305 89 None - 4 Bovine 6.9 pIC50 = 6.9 Binding
Inhibition of [125l]-All binding to bovine adrenal cortexInhibition of [125l]-All binding to bovine adrenal cortex
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(01)81143-4
3961 2305 89 None - 4 Bovine 6.9 pIC50 = 6.9 Binding
Inhibition of [125l]-All binding to bovine adrenal cortexInhibition of [125l]-All binding to bovine adrenal cortex
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(01)81143-4
590 2305 89 None - 4 Bovine 6.9 pIC50 = 6.9 Binding
Inhibition of [125l]-All binding to bovine adrenal cortexInhibition of [125l]-All binding to bovine adrenal cortex
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(01)81143-4
CHEMBL191 2305 89 None - 4 Bovine 6.9 pIC50 = 6.9 Binding
Inhibition of [125l]-All binding to bovine adrenal cortexInhibition of [125l]-All binding to bovine adrenal cortex
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(01)81143-4
DB00678 2305 89 None - 4 Bovine 6.9 pIC50 = 6.9 Binding
Inhibition of [125l]-All binding to bovine adrenal cortexInhibition of [125l]-All binding to bovine adrenal cortex
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(01)81143-4
15654764 102219 0 None - 0 Bovine 6.9 pIC50 = 6.9 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 470 8 2 7 5.1 CCCSc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a016
CHEMBL304772 102219 0 None - 0 Bovine 6.9 pIC50 = 6.9 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 470 8 2 7 5.1 CCCSc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a016
10181864 202585 0 None - 0 Bovine 6.9 pIC50 = 6.9 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 442 6 2 7 4.4 CSc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a016
CHEMBL71384 202585 0 None - 0 Bovine 6.9 pIC50 = 6.9 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 442 6 2 7 4.4 CSc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a016
19385644 98283 0 None - 0 Rabbit 6.9 pIC50 = 6.9 Binding
Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)
ChEMBL 519 9 1 6 6.1 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(OC(C(=O)O)c2ccccc2)c(C(=O)c2ccccc2)c1 10.1016/0960-894X(95)00185-V
CHEMBL278061 98283 0 None - 0 Rabbit 6.9 pIC50 = 6.9 Binding
Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)
ChEMBL 519 9 1 6 6.1 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(OC(C(=O)O)c2ccccc2)c(C(=O)c2ccccc2)c1 10.1016/0960-894X(95)00185-V
10481742 119558 0 None - 0 Rabbit 5.9 pIC50 = 5.9 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 518 11 2 7 6.1 CCCSc1nnc(CSc2ccccc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
CHEMBL350697 119558 0 None - 0 Rabbit 5.9 pIC50 = 5.9 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 518 11 2 7 6.1 CCCSc1nnc(CSc2ccccc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
44352156 168055 0 None - 0 Bovine 5.9 pIC50 = 5.9 Binding
Concentration required to inhibit [125I]AII binding to Angiotensin II receptor from membrane fractions of bovine adrenal cortexConcentration required to inhibit [125I]AII binding to Angiotensin II receptor from membrane fractions of bovine adrenal cortex
ChEMBL 432 6 1 7 5.4 CCSc1nc2c(C)scc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81118-5
CHEMBL436192 168055 0 None - 0 Bovine 5.9 pIC50 = 5.9 Binding
Concentration required to inhibit [125I]AII binding to Angiotensin II receptor from membrane fractions of bovine adrenal cortexConcentration required to inhibit [125I]AII binding to Angiotensin II receptor from membrane fractions of bovine adrenal cortex
ChEMBL 432 6 1 7 5.4 CCSc1nc2c(C)scc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81118-5
15780090 99976 0 None - 0 Rabbit 5.9 pIC50 = 5.9 Binding
Displacement of [125 I]Sar1Ile8-AII from type 1 Angiotensin II receptor of rabbit aorta membraneDisplacement of [125 I]Sar1Ile8-AII from type 1 Angiotensin II receptor of rabbit aorta membrane
ChEMBL 631 9 1 7 7.3 CC(C)c1nc2ccc(N(Cc3ccccc3)C(=O)c3ccccc3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80517-5
CHEMBL290669 99976 0 None - 0 Rabbit 5.9 pIC50 = 5.9 Binding
Displacement of [125 I]Sar1Ile8-AII from type 1 Angiotensin II receptor of rabbit aorta membraneDisplacement of [125 I]Sar1Ile8-AII from type 1 Angiotensin II receptor of rabbit aorta membrane
ChEMBL 631 9 1 7 7.3 CC(C)c1nc2ccc(N(Cc3ccccc3)C(=O)c3ccccc3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80517-5
10481742 119558 0 None - 0 Rabbit 5.9 pIC50 = 5.9 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 518 11 2 7 6.1 CCCSc1nnc(CSc2ccccc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
CHEMBL350697 119558 0 None - 0 Rabbit 5.9 pIC50 = 5.9 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 518 11 2 7 6.1 CCCSc1nnc(CSc2ccccc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
19792113 187627 0 None - 0 Bovine 5.9 pIC50 = 5.9 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 508 11 1 7 6.2 CCCCOC(=O)c1cccc2nc(CCCC)n(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c12 10.1007/s00044-009-9182-z
CHEMBL49930 187627 0 None - 0 Bovine 5.9 pIC50 = 5.9 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 508 11 1 7 6.2 CCCCOC(=O)c1cccc2nc(CCCC)n(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c12 10.1007/s00044-009-9182-z
10322185 19721 0 None - 0 Guinea pig 5.9 pIC50 = 5.9 Binding
In vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparationIn vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparation
ChEMBL 427 5 1 5 5.6 Cc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2cc(Cl)ccc2n1 10.1021/jm00100a007
CHEMBL130275 19721 0 None - 0 Guinea pig 5.9 pIC50 = 5.9 Binding
In vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparationIn vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparation
ChEMBL 427 5 1 5 5.6 Cc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2cc(Cl)ccc2n1 10.1021/jm00100a007
10000936 20035 0 None - 0 Rat 5.9 pIC50 = 5.9 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 398 7 1 3 6.1 CCCCc1nc2c(C)cccc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00077a007
CHEMBL130539 20035 0 None - 0 Rat 5.9 pIC50 = 5.9 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 398 7 1 3 6.1 CCCCc1nc2c(C)cccc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00077a007
10250277 21378 0 None - 0 Rat 5.9 pIC50 = 5.9 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 398 7 1 3 6.1 CCCCc1nc2cc(C)ccc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00077a007
CHEMBL131722 21378 0 None - 0 Rat 5.9 pIC50 = 5.9 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 398 7 1 3 6.1 CCCCc1nc2cc(C)ccc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00077a007
15696755 147479 1 None - 0 Rat 4.9 pIC50 = 4.9 Binding
Compound was evaluated for the inhibition of Angiotensin II receptor induced vasoconstriction of the rabbit aortaCompound was evaluated for the inhibition of Angiotensin II receptor induced vasoconstriction of the rabbit aorta
ChEMBL 306 7 1 3 3.6 CCCCc1ncc(CC(=O)O)n1Cc1ccccc1Cl 10.1021/jm00099a013
CHEMBL39345 147479 1 None - 0 Rat 4.9 pIC50 = 4.9 Binding
Compound was evaluated for the inhibition of Angiotensin II receptor induced vasoconstriction of the rabbit aortaCompound was evaluated for the inhibition of Angiotensin II receptor induced vasoconstriction of the rabbit aorta
ChEMBL 306 7 1 3 3.6 CCCCc1ncc(CC(=O)O)n1Cc1ccccc1Cl 10.1021/jm00099a013
24827771 95923 0 None - 0 Rat 6.9 pIC50 = 6.9 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
ChEMBL 439 7 1 7 4.1 CC(C)CCn1c(=O)c2cccnc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm7011563
CHEMBL261765 95923 0 None - 0 Rat 6.9 pIC50 = 6.9 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
ChEMBL 439 7 1 7 4.1 CC(C)CCn1c(=O)c2cccnc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm7011563
24828035 96460 0 None - 0 Rat 6.9 pIC50 = 6.9 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
ChEMBL 454 8 2 8 3.9 CCCCn1c(=O)c2ccc(NC)nc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm7011563
CHEMBL265958 96460 0 None - 0 Rat 6.9 pIC50 = 6.9 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
ChEMBL 454 8 2 8 3.9 CCCCn1c(=O)c2ccc(NC)nc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm7011563
689043 36550 109 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of [125-I]-[Sar1, AngII from AT1R (unknown origin) expressed in Escherichia coli BL 21 (DE3) incubated for 2 hrs by radioimmunoassayDisplacement of [125-I]-[Sar1, AngII from AT1R (unknown origin) expressed in Escherichia coli BL 21 (DE3) incubated for 2 hrs by radioimmunoassay
ChEMBL 180 2 3 3 1.2 O=C(O)/C=C/c1ccc(O)c(O)c1 10.1021/acs.jmedchem.1c00123
CHEMBL145 36550 109 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of [125-I]-[Sar1, AngII from AT1R (unknown origin) expressed in Escherichia coli BL 21 (DE3) incubated for 2 hrs by radioimmunoassayDisplacement of [125-I]-[Sar1, AngII from AT1R (unknown origin) expressed in Escherichia coli BL 21 (DE3) incubated for 2 hrs by radioimmunoassay
ChEMBL 180 2 3 3 1.2 O=C(O)/C=C/c1ccc(O)c(O)c1 10.1021/acs.jmedchem.1c00123
18655106 198775 0 None - 0 Rabbit 4.9 pIC50 = 4.9 Binding
Inhibition of angiotensin Angiotensin II receptor, type 1 in rabbit aorta using [125I-Sar1,Ile8] angiotensin II binding assayInhibition of angiotensin Angiotensin II receptor, type 1 in rabbit aorta using [125I-Sar1,Ile8] angiotensin II binding assay
ChEMBL 464 10 0 2 6.4 CCCCCN(CCCCC)C(=O)N1CCN(C(=O)N(c2ccccc2)c2ccccc2)CC1 10.1016/S0960-894X(01)81007-6
CHEMBL59854 198775 0 None - 0 Rabbit 4.9 pIC50 = 4.9 Binding
Inhibition of angiotensin Angiotensin II receptor, type 1 in rabbit aorta using [125I-Sar1,Ile8] angiotensin II binding assayInhibition of angiotensin Angiotensin II receptor, type 1 in rabbit aorta using [125I-Sar1,Ile8] angiotensin II binding assay
ChEMBL 464 10 0 2 6.4 CCCCCN(CCCCC)C(=O)N1CCN(C(=O)N(c2ccccc2)c2ccccc2)CC1 10.1016/S0960-894X(01)81007-6
76310606 104752 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Antagonist activity at human AT1 receptor expressed in CHO cells measured after overnight incubation by luciferase reporter gene assayAntagonist activity at human AT1 receptor expressed in CHO cells measured after overnight incubation by luciferase reporter gene assay
ChEMBL 531 10 2 4 7.3 CCCc1nc2cc(C(=O)NC(CC)c3ccccc3)ccc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.bmcl.2014.01.004
CHEMBL3115236 104752 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Antagonist activity at human AT1 receptor expressed in CHO cells measured after overnight incubation by luciferase reporter gene assayAntagonist activity at human AT1 receptor expressed in CHO cells measured after overnight incubation by luciferase reporter gene assay
ChEMBL 531 10 2 4 7.3 CCCc1nc2cc(C(=O)NC(CC)c3ccccc3)ccc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.bmcl.2014.01.004
127036106 135832 0 None - 1 Human 6.9 pIC50 = 6.9 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 571 10 3 7 5.7 CCCc1nc2c(C)cc(C(=O)N[C@H](CO)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.ejmech.2015.09.010
CHEMBL3734949 135832 0 None - 1 Human 6.9 pIC50 = 6.9 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 571 10 3 7 5.7 CCCc1nc2c(C)cc(C(=O)N[C@H](CO)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.ejmech.2015.09.010
44294022 186033 0 None - 0 Rat 5.9 pIC50 = 5.9 Binding
Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.
ChEMBL 543 12 2 6 5.7 CCCCc1nc(Cl)c(CC(=O)O)n1Cc1ccc(NC(=O)[C@H](Cc2ccccc2)n2ccc(C#N)c2)cc1 10.1021/jm00064a007
CHEMBL48798 186033 0 None - 0 Rat 5.9 pIC50 = 5.9 Binding
Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.
ChEMBL 543 12 2 6 5.7 CCCCc1nc(Cl)c(CC(=O)O)n1Cc1ccc(NC(=O)[C@H](Cc2ccccc2)n2ccc(C#N)c2)cc1 10.1021/jm00064a007
44275144 93216 0 None - 0 Rabbit 7.9 pIC50 = 7.9 Binding
Ability to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitroAbility to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitro
ChEMBL 496 9 1 8 4.7 CCCCc1nc2cc(OC)c(OC)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80335-2
CHEMBL24688 93216 0 None - 0 Rabbit 7.9 pIC50 = 7.9 Binding
Ability to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitroAbility to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitro
ChEMBL 496 9 1 8 4.7 CCCCc1nc2cc(OC)c(OC)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80335-2
44275144 93216 0 None - 0 Rabbit 7.9 pIC50 = 7.9 Binding
Binding affinity against Angiotensin II type 1 Receptor in rabbit aortic tissueBinding affinity against Angiotensin II type 1 Receptor in rabbit aortic tissue
ChEMBL 496 9 1 8 4.7 CCCCc1nc2cc(OC)c(OC)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80334-0
CHEMBL24688 93216 0 None - 0 Rabbit 7.9 pIC50 = 7.9 Binding
Binding affinity against Angiotensin II type 1 Receptor in rabbit aortic tissueBinding affinity against Angiotensin II type 1 Receptor in rabbit aortic tissue
ChEMBL 496 9 1 8 4.7 CCCCc1nc2cc(OC)c(OC)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80334-0
11340575 106487 0 None - 0 Rat 7.9 pIC50 = 7.9 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 479 7 2 6 5.9 CCCCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2c(C(=O)O)c(N)nc3ccccc23)cc1 10.1021/jm031100t
CHEMBL315165 106487 0 None - 0 Rat 7.9 pIC50 = 7.9 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 479 7 2 6 5.9 CCCCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2c(C(=O)O)c(N)nc3ccccc23)cc1 10.1021/jm031100t
11476484 204332 0 None - 0 Rat 7.9 pIC50 = 7.9 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 451 5 2 6 5.2 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2c(C(=O)O)c(N)nc3ccccc23)cc1 10.1021/jm031100t
CHEMBL85405 204332 0 None - 0 Rat 7.9 pIC50 = 7.9 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 451 5 2 6 5.2 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2c(C(=O)O)c(N)nc3ccccc23)cc1 10.1021/jm031100t
11351776 204478 0 None - 0 Rat 7.9 pIC50 = 7.9 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 465 6 2 6 5.6 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2c(C(=O)O)c(NC)nc3ccccc23)cc1 10.1021/jm031100t
CHEMBL86562 204478 0 None - 0 Rat 7.9 pIC50 = 7.9 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 465 6 2 6 5.6 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2c(C(=O)O)c(NC)nc3ccccc23)cc1 10.1021/jm031100t
9896251 98305 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Compound was evaluated for inhibitory activity against human Angiotensin II receptor, type 1Compound was evaluated for inhibitory activity against human Angiotensin II receptor, type 1
ChEMBL 682 12 1 9 7.1 CCCc1cc(Cn2c(CC)nc3c(C)cc(C)nc32)ccc1OC(C(=O)NS(=O)(=O)c1ccc(C(C)C)cc1)c1ccc2c(c1)OCO2 10.1021/jm020138n
CHEMBL278176 98305 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Compound was evaluated for inhibitory activity against human Angiotensin II receptor, type 1Compound was evaluated for inhibitory activity against human Angiotensin II receptor, type 1
ChEMBL 682 12 1 9 7.1 CCCc1cc(Cn2c(CC)nc3c(C)cc(C)nc32)ccc1OC(C(=O)NS(=O)(=O)c1ccc(C(C)C)cc1)c1ccc2c(c1)OCO2 10.1021/jm020138n
127034758 135834 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Displacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysisDisplacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysis
ChEMBL 681 12 1 8 7.7 CCCc1cc(Cn2c(CC)nc3c(C)cc(C)cc32)ccc1OC(C(=O)NS(=O)(=O)c1ccc(C(C)C)cc1)c1ccc2c(c1)OCO2 10.1039/C4MD00499J
CHEMBL3734968 135834 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Displacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysisDisplacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysis
ChEMBL 681 12 1 8 7.7 CCCc1cc(Cn2c(CC)nc3c(C)cc(C)cc32)ccc1OC(C(=O)NS(=O)(=O)c1ccc(C(C)C)cc1)c1ccc2c(c1)OCO2 10.1039/C4MD00499J
9913391 50874 0 None - 0 Rabbit 7.9 pIC50 = 7.9 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 488 8 1 7 5.7 CCCCc1nn2c(C)c(-c3ccccc3)nc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
CHEMBL157980 50874 0 None - 0 Rabbit 7.9 pIC50 = 7.9 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 488 8 1 7 5.7 CCCCc1nn2c(C)c(-c3ccccc3)nc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
73357017 92183 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Displacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysisDisplacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysis
ChEMBL 483 10 2 4 6.2 CCCCNC(=O)c1cc(C)c2nc(CCC)n(Cc3ccc(-c4ccccc4C(=O)O)cc3)c2c1 10.1016/j.ejmech.2013.08.014
CHEMBL2435831 92183 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Displacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysisDisplacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysis
ChEMBL 483 10 2 4 6.2 CCCCNC(=O)c1cc(C)c2nc(CCC)n(Cc3ccc(-c4ccccc4C(=O)O)cc3)c2c1 10.1016/j.ejmech.2013.08.014
10027148 116140 0 None - 0 Guinea pig 7.9 pIC50 = 7.9 Binding
In vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparationIn vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparation
ChEMBL 421 6 1 5 5.5 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2c(C)cccc2n1 10.1021/jm00100a007
CHEMBL337017 116140 0 None - 0 Guinea pig 7.9 pIC50 = 7.9 Binding
In vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparationIn vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparation
ChEMBL 421 6 1 5 5.5 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2c(C)cccc2n1 10.1021/jm00100a007
44377262 56839 0 None - 0 Rabbit 7.9 pIC50 = 7.9 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aortaIn vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aorta
ChEMBL 450 8 0 8 4.4 CCCCc1nc(Cl)c(C(=O)OC)n1Cc1ccc(-c2ccccc2-n2cnnn2)cc1 10.1016/S0960-894X(01)81124-0
CHEMBL164617 56839 0 None - 0 Rabbit 7.9 pIC50 = 7.9 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aortaIn vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aorta
ChEMBL 450 8 0 8 4.4 CCCCc1nc(Cl)c(C(=O)OC)n1Cc1ccc(-c2ccccc2-n2cnnn2)cc1 10.1016/S0960-894X(01)81124-0
10437270 106916 0 None - 0 Rabbit 7.9 pIC50 = 7.9 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 538 9 1 7 4.6 CCCCc1nn(-c2ccccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(C)=O)cc1 10.1021/jm00043a020
CHEMBL318042 106916 0 None - 0 Rabbit 7.9 pIC50 = 7.9 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 538 9 1 7 4.6 CCCCc1nn(-c2ccccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(C)=O)cc1 10.1021/jm00043a020
10416422 206250 0 None - 0 Rabbit 7.9 pIC50 = 7.9 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 620 9 1 7 5.8 CCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1021/jm00043a020
CHEMBL97295 206250 0 None - 0 Rabbit 7.9 pIC50 = 7.9 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 620 9 1 7 5.8 CCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1021/jm00043a020
10437261 116508 0 None - 0 Rat 7.9 pIC50 = 7.9 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 538 7 1 7 6.7 CCCc1nc2c(C)cc(-c3nc4ccccc4n3C)cc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00077a007
CHEMBL338954 116508 0 None - 0 Rat 7.9 pIC50 = 7.9 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 538 7 1 7 6.7 CCCc1nc2c(C)cc(-c3nc4ccccc4n3C)cc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00077a007
44404967 134882 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Inhibitory concentration against angiotensin II receptor, type 1Inhibitory concentration against angiotensin II receptor, type 1
ChEMBL 680 12 1 8 7.3 CCCc1cc(Cn2c(CC)nc3c(C)cc(C)nc32)ccc1OC(C(=O)NS(=O)(=O)c1ccc(C(C)C)cc1)c1ccc2c(c1)OCC2 10.1021/jm058225d
CHEMBL372814 134882 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Inhibitory concentration against angiotensin II receptor, type 1Inhibitory concentration against angiotensin II receptor, type 1
ChEMBL 680 12 1 8 7.3 CCCc1cc(Cn2c(CC)nc3c(C)cc(C)nc32)ccc1OC(C(=O)NS(=O)(=O)c1ccc(C(C)C)cc1)c1ccc2c(c1)OCC2 10.1021/jm058225d
53309129 63425 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation countingDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation counting
ChEMBL 449 5 1 6 5.4 CCCc1nc2c(C)cc(C)nc2n1[C@H]1CCc2cc(-c3ccccc3-c3nnn[nH]3)ccc21 10.1021/jm200409s
CHEMBL1801714 63425 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation countingDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation counting
ChEMBL 449 5 1 6 5.4 CCCc1nc2c(C)cc(C)nc2n1[C@H]1CCc2cc(-c3ccccc3-c3nnn[nH]3)ccc21 10.1021/jm200409s
71521416 86386 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor afterDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after
ChEMBL 538 6 1 8 5.1 CCc1nc2ccn(Cc3ccccc3C#N)c(=O)c2n1[C@H]1CCc2cc(-c3ccccc3-c3nnn[nH]3)ccc21 10.1016/j.bmcl.2012.11.088
CHEMBL2322445 86386 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor afterDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after
ChEMBL 538 6 1 8 5.1 CCc1nc2ccn(Cc3ccccc3C#N)c(=O)c2n1[C@H]1CCc2cc(-c3ccccc3-c3nnn[nH]3)ccc21 10.1016/j.bmcl.2012.11.088
76322690 84524 0 None - 0 Rabbit 6.9 pIC50 = 6.9 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 569 12 2 10 5.3 CCCCc1nnc(SCc2ccccc2[N+](=O)[O-])n1Cc1ccc(NC(=O)c2ccccc2-c2nnn[nH]2)cc1 10.1007/s00044-011-9756-4
CHEMBL2237594 84524 0 None - 0 Rabbit 6.9 pIC50 = 6.9 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 569 12 2 10 5.3 CCCCc1nnc(SCc2ccccc2[N+](=O)[O-])n1Cc1ccc(NC(=O)c2ccccc2-c2nnn[nH]2)cc1 10.1007/s00044-011-9756-4
10055421 51118 0 None - 0 Rabbit 6.9 pIC50 = 6.9 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 526 11 1 9 5.7 CCCCc1nnc(SCc2ccccc2[N+](=O)[O-])n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
CHEMBL158188 51118 0 None - 0 Rabbit 6.9 pIC50 = 6.9 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 526 11 1 9 5.7 CCCCc1nnc(SCc2ccccc2[N+](=O)[O-])n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
15698058 186530 0 None - 0 Bovine 6.9 pIC50 = 6.9 Binding
In vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortexIn vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortex
ChEMBL 412 8 2 4 5.0 CCCCc1nc(Cl)c(C(=O)O)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm950450f
CHEMBL49170 186530 0 None - 0 Bovine 6.9 pIC50 = 6.9 Binding
In vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortexIn vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortex
ChEMBL 412 8 2 4 5.0 CCCCc1nc(Cl)c(C(=O)O)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm950450f
14950501 84571 0 None - 0 Guinea pig 6.9 pIC50 = 6.9 Binding
Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1
ChEMBL 371 5 1 5 4.4 Cc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c(C)c(C)n1 10.1021/jm00061a016
CHEMBL22387 84571 0 None - 0 Guinea pig 6.9 pIC50 = 6.9 Binding
Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1
ChEMBL 371 5 1 5 4.4 Cc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c(C)c(C)n1 10.1021/jm00061a016
15698058 186530 0 None - 0 Bovine 6.9 pIC50 = 6.9 Binding
Inhibition of [125l]-All binding to bovine adrenal cortexInhibition of [125l]-All binding to bovine adrenal cortex
ChEMBL 412 8 2 4 5.0 CCCCc1nc(Cl)c(C(=O)O)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/S0960-894X(01)81143-4
CHEMBL49170 186530 0 None - 0 Bovine 6.9 pIC50 = 6.9 Binding
Inhibition of [125l]-All binding to bovine adrenal cortexInhibition of [125l]-All binding to bovine adrenal cortex
ChEMBL 412 8 2 4 5.0 CCCCc1nc(Cl)c(C(=O)O)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/S0960-894X(01)81143-4
15355266 192978 0 None - 0 Bovine 5.9 pIC50 = 5.9 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 466 8 2 6 5.3 CCCCc1nc2cc(C)cc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
CHEMBL53074 192978 0 None - 0 Bovine 5.9 pIC50 = 5.9 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 466 8 2 6 5.3 CCCCc1nc2cc(C)cc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
44358503 27321 0 None - 0 Rabbit 5.9 pIC50 = 5.9 Binding
Displacement of the specific binding ligand [125I]Sar1,Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane.Displacement of the specific binding ligand [125I]Sar1,Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane.
ChEMBL 523 5 2 6 5.7 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2C2Nc3ccccc3S(=O)(=O)N2)cc1 10.1016/S0960-894X(01)81119-7
CHEMBL136911 27321 0 None - 0 Rabbit 5.9 pIC50 = 5.9 Binding
Displacement of the specific binding ligand [125I]Sar1,Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane.Displacement of the specific binding ligand [125I]Sar1,Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane.
ChEMBL 523 5 2 6 5.7 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2C2Nc3ccccc3S(=O)(=O)N2)cc1 10.1016/S0960-894X(01)81119-7
44288370 100638 0 None - 0 Rat 5.9 pIC50 = 5.9 Binding
In vitro inhibition of specific binding of [125I]AII to Angiotensin II receptor, type 1 from rat liver membraneIn vitro inhibition of specific binding of [125I]AII to Angiotensin II receptor, type 1 from rat liver membrane
ChEMBL 418 7 1 3 5.5 CCCCC1=NC(=O)C2(CCCC2)CN1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/S0960-894X(01)81139-2
CHEMBL295181 100638 0 None - 0 Rat 5.9 pIC50 = 5.9 Binding
In vitro inhibition of specific binding of [125I]AII to Angiotensin II receptor, type 1 from rat liver membraneIn vitro inhibition of specific binding of [125I]AII to Angiotensin II receptor, type 1 from rat liver membrane
ChEMBL 418 7 1 3 5.5 CCCCC1=NC(=O)C2(CCCC2)CN1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/S0960-894X(01)81139-2
10455118 115924 0 None - 0 Guinea pig 5.9 pIC50 = 5.9 Binding
In vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparationIn vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparation
ChEMBL 389 4 1 4 5.6 Cc1cc(/C=C/c2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2ccccc2n1 10.1021/jm00100a007
CHEMBL336056 115924 0 None - 0 Guinea pig 5.9 pIC50 = 5.9 Binding
In vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparationIn vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparation
ChEMBL 389 4 1 4 5.6 Cc1cc(/C=C/c2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2ccccc2n1 10.1021/jm00100a007
11757357 206243 0 None - 0 Rabbit 5.9 pIC50 = 5.9 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 552 9 1 6 5.8 CCCCc1nn(-c2ccccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(C)(C)C)cc1 10.1021/jm00043a020
CHEMBL97273 206243 0 None - 0 Rabbit 5.9 pIC50 = 5.9 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 552 9 1 6 5.8 CCCCc1nn(-c2ccccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(C)(C)C)cc1 10.1021/jm00043a020
19792113 187627 0 None - 0 Bovine 5.9 pIC50 = 5.9 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 508 11 1 7 6.2 CCCCOC(=O)c1cccc2nc(CCCC)n(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c12 10.1007/s00044-009-9182-z
CHEMBL49930 187627 0 None - 0 Bovine 5.9 pIC50 = 5.9 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 508 11 1 7 6.2 CCCCOC(=O)c1cccc2nc(CCCC)n(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c12 10.1007/s00044-009-9182-z
15355266 192978 0 None - 0 Bovine 5.9 pIC50 = 5.9 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 466 8 2 6 5.3 CCCCc1nc2cc(C)cc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
CHEMBL53074 192978 0 None - 0 Bovine 5.9 pIC50 = 5.9 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 466 8 2 6 5.3 CCCCc1nc2cc(C)cc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
19792097 101145 0 None - 0 Bovine 4.9 pIC50 = 4.9 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 451 8 2 6 4.4 CCCCc1nc2c(C(N)=O)cccc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
CHEMBL298950 101145 0 None - 0 Bovine 4.9 pIC50 = 4.9 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 451 8 2 6 4.4 CCCCc1nc2c(C(N)=O)cccc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
15654717 102158 0 None - 0 Bovine 4.9 pIC50 = 4.9 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 440 7 2 7 4.0 CCOc1nc2cc(C(=O)O)ccc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a016
CHEMBL304360 102158 0 None - 0 Bovine 4.9 pIC50 = 4.9 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 440 7 2 7 4.0 CCOc1nc2cc(C(=O)O)ccc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a016
19792097 101145 0 None - 0 Bovine 4.9 pIC50 = 4.9 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 451 8 2 6 4.4 CCCCc1nc2c(C(N)=O)cccc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
CHEMBL298950 101145 0 None - 0 Bovine 4.9 pIC50 = 4.9 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 451 8 2 6 4.4 CCCCc1nc2c(C(N)=O)cccc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
9894381 101557 0 None - 0 Bovine 6.9 pIC50 = 6.9 Binding
In vitro binding affinity to angiotensin II receptor in bovine adrenal cortexIn vitro binding affinity to angiotensin II receptor in bovine adrenal cortex
ChEMBL 574 8 1 7 7.0 CCCCc1nc2ccc(C3CCC4CCCCC4O3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80377-2
CHEMBL301827 101557 0 None - 0 Bovine 6.9 pIC50 = 6.9 Binding
In vitro binding affinity to angiotensin II receptor in bovine adrenal cortexIn vitro binding affinity to angiotensin II receptor in bovine adrenal cortex
ChEMBL 574 8 1 7 7.0 CCCCc1nc2ccc(C3CCC4CCCCC4O3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80377-2
164625885 185674 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of [125-I]-[Sar1, Ile8] from recombinant human AT1R transfected in human HEK293 cells incubated for 2 hrs by liquid scintillation counter analysisDisplacement of [125-I]-[Sar1, Ile8] from recombinant human AT1R transfected in human HEK293 cells incubated for 2 hrs by liquid scintillation counter analysis
ChEMBL 969 22 11 11 1.1 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@@H](N)CCCNC(=N)N)C(C)C)C(=O)N1Cc2cc(O)ccc2C[C@H]1C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O 10.1016/j.bmcl.2021.128086
CHEMBL4873899 185674 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of [125-I]-[Sar1, Ile8] from recombinant human AT1R transfected in human HEK293 cells incubated for 2 hrs by liquid scintillation counter analysisDisplacement of [125-I]-[Sar1, Ile8] from recombinant human AT1R transfected in human HEK293 cells incubated for 2 hrs by liquid scintillation counter analysis
ChEMBL 969 22 11 11 1.1 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@@H](N)CCCNC(=N)N)C(C)C)C(=O)N1Cc2cc(O)ccc2C[C@H]1C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O 10.1016/j.bmcl.2021.128086
73352461 92182 0 None - 0 Human 5.9 pIC50 = 5.9 Binding
Displacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysisDisplacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysis
ChEMBL 469 9 2 4 5.9 CCCNC(=O)c1cc(C)c2nc(CCC)n(Cc3ccc(-c4ccccc4C(=O)O)cc3)c2c1 10.1016/j.ejmech.2013.08.014
CHEMBL2435830 92182 0 None - 0 Human 5.9 pIC50 = 5.9 Binding
Displacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysisDisplacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysis
ChEMBL 469 9 2 4 5.9 CCCNC(=O)c1cc(C)c2nc(CCC)n(Cc3ccc(-c4ccccc4C(=O)O)cc3)c2c1 10.1016/j.ejmech.2013.08.014
127035247 135983 0 None - 0 Human 5.9 pIC50 = 5.9 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 549 9 2 5 7.0 CSc1nc2c(C)cc(C(=O)NC[C@@H](C)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2015.09.010
CHEMBL3736338 135983 0 None - 0 Human 5.9 pIC50 = 5.9 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 549 9 2 5 7.0 CSc1nc2c(C)cc(C(=O)NC[C@@H](C)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2015.09.010
19792093 101449 0 None - 0 Bovine 5.9 pIC50 = 5.9 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 480 9 1 7 5.5 CCCCc1nc2cccc(C(=O)OCC)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
CHEMBL301072 101449 0 None - 0 Bovine 5.9 pIC50 = 5.9 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 480 9 1 7 5.5 CCCCc1nc2cccc(C(=O)OCC)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
10030665 48596 0 None - 0 Rabbit 7.9 pIC50 = 7.9 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 558 12 2 8 5.7 CCCCc1nnc(SCc2ccccc2C(=O)OC)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
CHEMBL155948 48596 0 None - 0 Rabbit 7.9 pIC50 = 7.9 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 558 12 2 8 5.7 CCCCc1nnc(SCc2ccccc2C(=O)OC)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
10369225 48730 0 None - 0 Rabbit 7.9 pIC50 = 7.9 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 514 11 2 6 6.2 CCCCc1nnc(SCc2ccccc2C)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
CHEMBL156084 48730 0 None - 0 Rabbit 7.9 pIC50 = 7.9 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 514 11 2 6 6.2 CCCCc1nnc(SCc2ccccc2C)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
14956766 106483 0 None - 0 Rabbit 7.9 pIC50 = 7.9 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 471 7 1 7 4.5 CCCc1nn(-c2ccccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
CHEMBL315128 106483 0 None - 0 Rabbit 7.9 pIC50 = 7.9 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 471 7 1 7 4.5 CCCc1nn(-c2ccccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
1610 2305 89 None -1 4 Rat 7.9 pIC50 = 7.9 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00074a018
3941 2305 89 None -1 4 Rat 7.9 pIC50 = 7.9 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00074a018
3961 2305 89 None -1 4 Rat 7.9 pIC50 = 7.9 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00074a018
590 2305 89 None -1 4 Rat 7.9 pIC50 = 7.9 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00074a018
CHEMBL191 2305 89 None -1 4 Rat 7.9 pIC50 = 7.9 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00074a018
DB00678 2305 89 None -1 4 Rat 7.9 pIC50 = 7.9 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00074a018
10030665 48596 0 None - 0 Rabbit 7.9 pIC50 = 7.9 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 558 12 2 8 5.7 CCCCc1nnc(SCc2ccccc2C(=O)OC)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
CHEMBL155948 48596 0 None - 0 Rabbit 7.9 pIC50 = 7.9 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 558 12 2 8 5.7 CCCCc1nnc(SCc2ccccc2C(=O)OC)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
10369225 48730 0 None - 0 Rabbit 7.9 pIC50 = 7.9 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 514 11 2 6 6.2 CCCCc1nnc(SCc2ccccc2C)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
CHEMBL156084 48730 0 None - 0 Rabbit 7.9 pIC50 = 7.9 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 514 11 2 6 6.2 CCCCc1nnc(SCc2ccccc2C)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
10259265 109541 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
In vitro inhibitory concentration against AT1 receptor from human adrenal tissues.In vitro inhibitory concentration against AT1 receptor from human adrenal tissues.
ChEMBL 713 12 2 9 7.0 CCCCc1nn(-c2cc(NC(C)=O)ccc2Cl)c(=O)n1Cc1ccc(-c2cc(CCC)ccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1016/S0960-894X(01)80595-3
CHEMBL323506 109541 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
In vitro inhibitory concentration against AT1 receptor from human adrenal tissues.In vitro inhibitory concentration against AT1 receptor from human adrenal tissues.
ChEMBL 713 12 2 9 7.0 CCCCc1nn(-c2cc(NC(C)=O)ccc2Cl)c(=O)n1Cc1ccc(-c2cc(CCC)ccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1016/S0960-894X(01)80595-3
15171393 85502 0 None - 0 Guinea pig 7.9 pIC50 = 7.9 Binding
Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1
ChEMBL 447 7 1 5 5.7 Cc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c(Cc2ccccc2)c(C)n1 10.1021/jm00061a016
CHEMBL23006 85502 0 None - 0 Guinea pig 7.9 pIC50 = 7.9 Binding
Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1
ChEMBL 447 7 1 5 5.7 Cc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c(Cc2ccccc2)c(C)n1 10.1021/jm00061a016
14950512 99353 0 None - 0 Guinea pig 7.9 pIC50 = 7.9 Binding
Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1
ChEMBL 511 7 1 5 5.2 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c(I)c(CC)n1 10.1021/jm00061a016
CHEMBL285560 99353 0 None - 0 Guinea pig 7.9 pIC50 = 7.9 Binding
Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1
ChEMBL 511 7 1 5 5.2 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c(I)c(CC)n1 10.1021/jm00061a016
44305409 201113 0 None - 0 Bovine 7.9 pIC50 = 7.9 Binding
Tested for binding affinity against angiotensin II receptor in rat adrenal cortexTested for binding affinity against angiotensin II receptor in rat adrenal cortex
ChEMBL 625 12 2 8 4.8 CCCc1cc(=O)n(CCNC(=O)C(c2ccccc2)c2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/0960-894X(95)00370-9
CHEMBL62314 201113 0 None - 0 Bovine 7.9 pIC50 = 7.9 Binding
Tested for binding affinity against angiotensin II receptor in rat adrenal cortexTested for binding affinity against angiotensin II receptor in rat adrenal cortex
ChEMBL 625 12 2 8 4.8 CCCc1cc(=O)n(CCNC(=O)C(c2ccccc2)c2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/0960-894X(95)00370-9
19385623 50149 0 None - 0 Rabbit 7.9 pIC50 = 7.9 Binding
Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)
ChEMBL 429 7 1 5 5.2 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(OC(C(=O)O)c2ccccc2)c(C)c1 10.1016/0960-894X(95)00185-V
CHEMBL15730 50149 0 None - 0 Rabbit 7.9 pIC50 = 7.9 Binding
Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)
ChEMBL 429 7 1 5 5.2 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(OC(C(=O)O)c2ccccc2)c(C)c1 10.1016/0960-894X(95)00185-V
10371118 15326 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 586 13 0 8 5.5 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2Cc2ccc(C(=O)OC)cc2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
CHEMBL121733 15326 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 586 13 0 8 5.5 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2Cc2ccc(C(=O)OC)cc2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
10415119 117568 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 548 13 0 7 5.8 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2CCc2cccs2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
CHEMBL340605 117568 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 548 13 0 7 5.8 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2CCc2cccs2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
10030426 16428 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 548 13 0 7 5.8 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2CCc2ccsc2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
CHEMBL124144 16428 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 548 13 0 7 5.8 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2CCc2ccsc2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
44315304 203291 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membrane
ChEMBL 663 10 2 8 6.1 CCc1nc2ccc(NC(=O)N(C)C(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCC=C(C)C)cc1F 10.1016/0960-894X(94)85036-4
CHEMBL76821 203291 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membrane
ChEMBL 663 10 2 8 6.1 CCc1nc2ccc(NC(=O)N(C)C(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCC=C(C)C)cc1F 10.1016/0960-894X(94)85036-4
76319035 84541 0 None - 0 Rabbit 6.9 pIC50 = 6.9 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 541 11 3 8 5.4 CCCCc1nnc(NCc2ccc(Cl)cc2)n1Cc1ccc(NC(=O)c2ccccc2-c2nnn[nH]2)cc1 10.1007/s00044-011-9756-4
CHEMBL2237611 84541 0 None - 0 Rabbit 6.9 pIC50 = 6.9 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 541 11 3 8 5.4 CCCCc1nnc(NCc2ccc(Cl)cc2)n1Cc1ccc(NC(=O)c2ccccc2-c2nnn[nH]2)cc1 10.1007/s00044-011-9756-4
11511750 96094 1 None - 0 Rat 6.9 pIC50 = 6.9 Binding
Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.
ChEMBL 483 10 2 6 4.6 CCCCc1nc(Cl)c(CC(=O)OC)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00064a007
CHEMBL262958 96094 1 None - 0 Rat 6.9 pIC50 = 6.9 Binding
Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.
ChEMBL 483 10 2 6 4.6 CCCCc1nc(Cl)c(CC(=O)OC)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00064a007
44294051 174377 0 None - 0 Rat 6.9 pIC50 = 6.9 Binding
Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.
ChEMBL 604 14 2 7 6.3 CCCCc1nc(Cl)c(CC(=O)O)n1Cc1ccc(NC(=O)[C@H](Cc2ccccc2)n2ccc(C(=O)OCC)c2C)cc1 10.1021/jm00064a007
CHEMBL45659 174377 0 None - 0 Rat 6.9 pIC50 = 6.9 Binding
Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.
ChEMBL 604 14 2 7 6.3 CCCCc1nc(Cl)c(CC(=O)O)n1Cc1ccc(NC(=O)[C@H](Cc2ccccc2)n2ccc(C(=O)OCC)c2C)cc1 10.1021/jm00064a007
44294031 183372 0 None - 0 Rat 6.9 pIC50 = 6.9 Binding
Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.
ChEMBL 532 12 2 5 6.1 CCCCc1nc(Cl)c(CC(=O)O)n1Cc1ccc(NC(=O)[C@H](Cc2ccccc2)n2cccc2C)cc1 10.1021/jm00064a007
CHEMBL48168 183372 0 None - 0 Rat 6.9 pIC50 = 6.9 Binding
Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.
ChEMBL 532 12 2 5 6.1 CCCCc1nc(Cl)c(CC(=O)O)n1Cc1ccc(NC(=O)[C@H](Cc2ccccc2)n2cccc2C)cc1 10.1021/jm00064a007
44341713 9624 0 None - 0 Rat 6.9 pIC50 = 6.9 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 515 7 1 4 4.9 CCCCC1=NC2(CCN(C(=O)C(F)(F)F)CC2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00074a018
CHEMBL113330 9624 0 None - 0 Rat 6.9 pIC50 = 6.9 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 515 7 1 4 4.9 CCCCC1=NC2(CCN(C(=O)C(F)(F)F)CC2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00074a018
15171409 204558 0 None - 0 Guinea pig 6.9 pIC50 = 6.9 Binding
Compound was tested for in vitro inhibition of specific binding of [I-125]AII to Angiotensin II receptor, type 1 in guinea pig adrenal membrane preparationCompound was tested for in vitro inhibition of specific binding of [I-125]AII to Angiotensin II receptor, type 1 in guinea pig adrenal membrane preparation
ChEMBL 441 7 1 6 5.0 CCc1cc(OCc2ccc(-c3ccc(OC)cc3-c3nn[nH]n3)cc2)c2c(n1)CCCC2 10.1016/S0960-894X(01)80295-X
CHEMBL87034 204558 0 None - 0 Guinea pig 6.9 pIC50 = 6.9 Binding
Compound was tested for in vitro inhibition of specific binding of [I-125]AII to Angiotensin II receptor, type 1 in guinea pig adrenal membrane preparationCompound was tested for in vitro inhibition of specific binding of [I-125]AII to Angiotensin II receptor, type 1 in guinea pig adrenal membrane preparation
ChEMBL 441 7 1 6 5.0 CCc1cc(OCc2ccc(-c3ccc(OC)cc3-c3nn[nH]n3)cc2)c2c(n1)CCCC2 10.1016/S0960-894X(01)80295-X
44348042 16581 0 None - 0 Bovine 6.9 pIC50 = 6.9 Binding
Concentration that gives 50% inhibition for binding of 125-I-[Sar1, IIe8] angiotensin to Angiotensin II receptor, type 1 in bovine adrenal cortex membrane.Concentration that gives 50% inhibition for binding of 125-I-[Sar1, IIe8] angiotensin to Angiotensin II receptor, type 1 in bovine adrenal cortex membrane.
ChEMBL 471 6 1 6 4.7 CCOC(=O)/C=C1\N(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)C(=O)CC12CCCCC2 10.1016/S0960-894X(01)80914-8
CHEMBL124449 16581 0 None - 0 Bovine 6.9 pIC50 = 6.9 Binding
Concentration that gives 50% inhibition for binding of 125-I-[Sar1, IIe8] angiotensin to Angiotensin II receptor, type 1 in bovine adrenal cortex membrane.Concentration that gives 50% inhibition for binding of 125-I-[Sar1, IIe8] angiotensin to Angiotensin II receptor, type 1 in bovine adrenal cortex membrane.
ChEMBL 471 6 1 6 4.7 CCOC(=O)/C=C1\N(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)C(=O)CC12CCCCC2 10.1016/S0960-894X(01)80914-8
127028595 136829 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptorDisplacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptor
ChEMBL 616 11 3 7 5.9 CCCc1nc2c(C)cc(C(=O)NCCc3ccc(F)cc3)cc2n1Cc1ccc(-c2ccccc2C(=O)Nc2nnn[nH]2)cc1 10.1039/C5MD00169B
CHEMBL3753047 136829 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptorDisplacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptor
ChEMBL 616 11 3 7 5.9 CCCc1nc2c(C)cc(C(=O)NCCc3ccc(F)cc3)cc2n1Cc1ccc(-c2ccccc2C(=O)Nc2nnn[nH]2)cc1 10.1039/C5MD00169B
9986861 119165 0 None - 0 Rabbit 6.9 pIC50 = 6.9 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 498 10 2 7 5.8 CCCCc1nnc(NCc2ccc(Cl)cc2)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
CHEMBL347236 119165 0 None - 0 Rabbit 6.9 pIC50 = 6.9 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 498 10 2 7 5.8 CCCCc1nnc(NCc2ccc(Cl)cc2)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
44438868 91558 0 None - 1 Bovine 6.9 pIC50 = 6.9 Binding
Displacement of [125I]angiotensin-2 from bovine adrenal cortex AT1 receptorDisplacement of [125I]angiotensin-2 from bovine adrenal cortex AT1 receptor
ChEMBL 427 6 1 8 3.4 CCc1nc2cccc(C(=O)OC)c2n1Cc1ccc(-n2cccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2007.02.042
CHEMBL241684 91558 0 None - 1 Bovine 6.9 pIC50 = 6.9 Binding
Displacement of [125I]angiotensin-2 from bovine adrenal cortex AT1 receptorDisplacement of [125I]angiotensin-2 from bovine adrenal cortex AT1 receptor
ChEMBL 427 6 1 8 3.4 CCc1nc2cccc(C(=O)OC)c2n1Cc1ccc(-n2cccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2007.02.042
10412769 20036 0 None - 0 Guinea pig 6.9 pIC50 = 6.9 Binding
In vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparationIn vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparation
ChEMBL 441 6 1 5 5.9 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2cccc(Cl)c2n1 10.1021/jm00100a007
CHEMBL130540 20036 0 None - 0 Guinea pig 6.9 pIC50 = 6.9 Binding
In vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparationIn vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparation
ChEMBL 441 6 1 5 5.9 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2cccc(Cl)c2n1 10.1021/jm00100a007
10049787 22251 0 None - 0 Guinea pig 6.9 pIC50 = 6.9 Binding
In vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparationIn vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparation
ChEMBL 421 6 1 5 5.5 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2ccc(C)cc2n1 10.1021/jm00100a007
CHEMBL132509 22251 0 None - 0 Guinea pig 6.9 pIC50 = 6.9 Binding
In vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparationIn vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparation
ChEMBL 421 6 1 5 5.5 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2ccc(C)cc2n1 10.1021/jm00100a007
168288304 190767 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Inhibition of human AT1R expressed in HEK293 cells by non-linear regression analysisInhibition of human AT1R expressed in HEK293 cells by non-linear regression analysis
ChEMBL 806 14 5 15 6.8 CCCCc1nc(Cl)c(COC(=O)CCC(=O)Oc2cc(-c3oc4cc(O)cc(O)c4c(=O)c3O)ccc2O)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.ejmech.2021.114068
CHEMBL5192190 190767 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Inhibition of human AT1R expressed in HEK293 cells by non-linear regression analysisInhibition of human AT1R expressed in HEK293 cells by non-linear regression analysis
ChEMBL 806 14 5 15 6.8 CCCCc1nc(Cl)c(COC(=O)CCC(=O)Oc2cc(-c3oc4cc(O)cc(O)c4c(=O)c3O)ccc2O)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.ejmech.2021.114068
168293707 191557 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Inhibition of human AT1R expressed in HEK293 cells by non-linear regression analysisInhibition of human AT1R expressed in HEK293 cells by non-linear regression analysis
ChEMBL 806 14 5 15 6.8 CCCCc1nc(Cl)c(COC(=O)CCC(=O)Oc2ccc(-c3oc4cc(O)cc(O)c4c(=O)c3O)cc2O)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.ejmech.2021.114068
CHEMBL5203983 191557 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Inhibition of human AT1R expressed in HEK293 cells by non-linear regression analysisInhibition of human AT1R expressed in HEK293 cells by non-linear regression analysis
ChEMBL 806 14 5 15 6.8 CCCCc1nc(Cl)c(COC(=O)CCC(=O)Oc2ccc(-c3oc4cc(O)cc(O)c4c(=O)c3O)cc2O)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.ejmech.2021.114068
19385652 47239 0 None - 0 Rabbit 6.9 pIC50 = 6.9 Binding
Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)
ChEMBL 459 9 1 6 5.3 CCOc1cc(Cn2c(CC)nc3c(C)cc(C)nc32)ccc1OC(C(=O)O)c1ccccc1 10.1016/0960-894X(95)00185-V
CHEMBL15458 47239 0 None - 0 Rabbit 6.9 pIC50 = 6.9 Binding
Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)
ChEMBL 459 9 1 6 5.3 CCOc1cc(Cn2c(CC)nc3c(C)cc(C)nc32)ccc1OC(C(=O)O)c1ccccc1 10.1016/0960-894X(95)00185-V
10456700 119150 0 None - 0 Rabbit 5.9 pIC50 = 5.9 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 455 9 2 6 4.7 CCCCc1nnc(-c2ccncc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
CHEMBL347050 119150 0 None - 0 Rabbit 5.9 pIC50 = 5.9 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 455 9 2 6 4.7 CCCCc1nnc(-c2ccncc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
44459583 92829 0 None - 0 Rabbit 5.9 pIC50 = 5.9 Binding
Binding affinity against Angiotensin II type 1 Receptor in rabbit aortic tissueBinding affinity against Angiotensin II type 1 Receptor in rabbit aortic tissue
ChEMBL 426 7 1 4 5.5 CCCCc1nc2c(C)cccc2c(=O)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/S0960-894X(00)80334-0
CHEMBL24499 92829 0 None - 0 Rabbit 5.9 pIC50 = 5.9 Binding
Binding affinity against Angiotensin II type 1 Receptor in rabbit aortic tissueBinding affinity against Angiotensin II type 1 Receptor in rabbit aortic tissue
ChEMBL 426 7 1 4 5.5 CCCCc1nc2c(C)cccc2c(=O)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/S0960-894X(00)80334-0
15699069 5006 0 None - 0 Rat 5.9 pIC50 = 5.9 Binding
Binding affinity against angiotensin II receptor in rat smooth muscle cell preparationsBinding affinity against angiotensin II receptor in rat smooth muscle cell preparations
ChEMBL 400 7 2 6 3.2 CCCCc1nc(CO)c(Cl)n1Cc1ccc2c(c1)CCC(c1nnn[nH]1)C2 10.1021/jm00114a021
CHEMBL105525 5006 0 None - 0 Rat 5.9 pIC50 = 5.9 Binding
Binding affinity against angiotensin II receptor in rat smooth muscle cell preparationsBinding affinity against angiotensin II receptor in rat smooth muscle cell preparations
ChEMBL 400 7 2 6 3.2 CCCCc1nc(CO)c(Cl)n1Cc1ccc2c(c1)CCC(c1nnn[nH]1)C2 10.1021/jm00114a021
44285212 149916 0 None - 0 Rat 5.9 pIC50 = 5.9 Binding
Displacement of [125I]- Ang II from type 1 Angiotensin II receptorDisplacement of [125I]- Ang II from type 1 Angiotensin II receptor
ChEMBL 546 7 1 5 6.3 O=C1N(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)C(c2ccccc2)=NC1(c1ccccc1)c1ccccc1 10.1016/S0960-894X(01)80526-6
CHEMBL39542 149916 0 None - 0 Rat 5.9 pIC50 = 5.9 Binding
Displacement of [125I]- Ang II from type 1 Angiotensin II receptorDisplacement of [125I]- Ang II from type 1 Angiotensin II receptor
ChEMBL 546 7 1 5 6.3 O=C1N(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)C(c2ccccc2)=NC1(c1ccccc1)c1ccccc1 10.1016/S0960-894X(01)80526-6
10456700 119150 0 None - 0 Rabbit 5.9 pIC50 = 5.9 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 455 9 2 6 4.7 CCCCc1nnc(-c2ccncc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
CHEMBL347050 119150 0 None - 0 Rabbit 5.9 pIC50 = 5.9 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 455 9 2 6 4.7 CCCCc1nnc(-c2ccncc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
44563174 173838 0 None - 0 Bovine 5.9 pIC50 = 5.9 Binding
Displacement of [125I]Ang2 from AT1 receptor in bovine adrenal cortexDisplacement of [125I]Ang2 from AT1 receptor in bovine adrenal cortex
ChEMBL 536 7 1 5 8.0 CCCc1nc2c(C)cc(-c3nc4ccccc4n3C)cc2n1Cc1ccc(-c2ccccc2-c2ncc[nH]2)cc1 10.1016/j.bmc.2008.10.040
CHEMBL455286 173838 0 None - 0 Bovine 5.9 pIC50 = 5.9 Binding
Displacement of [125I]Ang2 from AT1 receptor in bovine adrenal cortexDisplacement of [125I]Ang2 from AT1 receptor in bovine adrenal cortex
ChEMBL 536 7 1 5 8.0 CCCc1nc2c(C)cc(-c3nc4ccccc4n3C)cc2n1Cc1ccc(-c2ccccc2-c2ncc[nH]2)cc1 10.1016/j.bmc.2008.10.040
19792093 101449 0 None - 0 Bovine 5.9 pIC50 = 5.9 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 480 9 1 7 5.5 CCCCc1nc2cccc(C(=O)OCC)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
CHEMBL301072 101449 0 None - 0 Bovine 5.9 pIC50 = 5.9 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 480 9 1 7 5.5 CCCCc1nc2cccc(C(=O)OCC)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
44303888 201579 0 None - 0 Rabbit 5.9 pIC50 = 5.9 Binding
Inhibition of angiotensin Angiotensin II receptor, type 1 in rabbit aorta using [125I-Sar1,Ile8] angiotensin II binding assayInhibition of angiotensin Angiotensin II receptor, type 1 in rabbit aorta using [125I-Sar1,Ile8] angiotensin II binding assay
ChEMBL 552 12 2 4 5.5 CCCCCN(CCCCC)C(=O)N1CCN(C(=O)N(c2ccccc2)c2ccc(C(=O)O)cc2)[C@H](C(=O)O)C1 10.1016/S0960-894X(01)81007-6
CHEMBL64674 201579 0 None - 0 Rabbit 5.9 pIC50 = 5.9 Binding
Inhibition of angiotensin Angiotensin II receptor, type 1 in rabbit aorta using [125I-Sar1,Ile8] angiotensin II binding assayInhibition of angiotensin Angiotensin II receptor, type 1 in rabbit aorta using [125I-Sar1,Ile8] angiotensin II binding assay
ChEMBL 552 12 2 4 5.5 CCCCCN(CCCCC)C(=O)N1CCN(C(=O)N(c2ccccc2)c2ccc(C(=O)O)cc2)[C@H](C(=O)O)C1 10.1016/S0960-894X(01)81007-6
44298775 195961 0 None - 0 Bovine 4.9 pIC50 = 4.9 Binding
Binding affinity for angiotensin II receptor of bovine adrenal cortexBinding affinity for angiotensin II receptor of bovine adrenal cortex
ChEMBL 410 5 1 7 3.1 COc1nc2ccccn2c(=O)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81144-6
CHEMBL57090 195961 0 None - 0 Bovine 4.9 pIC50 = 4.9 Binding
Binding affinity for angiotensin II receptor of bovine adrenal cortexBinding affinity for angiotensin II receptor of bovine adrenal cortex
ChEMBL 410 5 1 7 3.1 COc1nc2ccccn2c(=O)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81144-6
10620305 9998 0 None - 0 Bovine 4.9 pIC50 = 4.9 Binding
In vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortexIn vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortex
ChEMBL 388 7 2 6 3.4 CCCc1nc(C(=O)O)cn1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm950450f
CHEMBL115560 9998 0 None - 0 Bovine 4.9 pIC50 = 4.9 Binding
In vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortexIn vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortex
ChEMBL 388 7 2 6 3.4 CCCc1nc(C(=O)O)cn1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm950450f
73349423 92174 0 None - 0 Human 5.8 pIC50 = 5.8 Binding
Displacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysisDisplacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysis
ChEMBL 441 7 2 4 5.7 CCCc1nc2c(C)cc(NC(C)=O)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2013.08.014
CHEMBL2435822 92174 0 None - 0 Human 5.8 pIC50 = 5.8 Binding
Displacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysisDisplacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysis
ChEMBL 441 7 2 4 5.7 CCCc1nc2c(C)cc(NC(C)=O)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2013.08.014
24828294 95370 0 None - 0 Rat 6.8 pIC50 = 6.8 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
ChEMBL 411 7 1 7 4.3 CCCn1nc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2cccnc21 10.1021/jm7011563
CHEMBL258891 95370 0 None - 0 Rat 6.8 pIC50 = 6.8 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
ChEMBL 411 7 1 7 4.3 CCCn1nc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2cccnc21 10.1021/jm7011563
44294052 100918 0 None - 0 Rat 5.8 pIC50 = 5.8 Binding
Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.
ChEMBL 618 14 1 8 6.4 CCCCc1nc(Cl)c(CC(=O)OC)n1Cc1ccc(NC(=O)[C@H](Cc2ccccc2)n2ccc(C(=O)OCC)c2C)cc1 10.1021/jm00064a007
CHEMBL297265 100918 0 None - 0 Rat 5.8 pIC50 = 5.8 Binding
Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.
ChEMBL 618 14 1 8 6.4 CCCCc1nc(Cl)c(CC(=O)OC)n1Cc1ccc(NC(=O)[C@H](Cc2ccccc2)n2ccc(C(=O)OCC)c2C)cc1 10.1021/jm00064a007
10347373 48257 0 None - 0 Rabbit 7.8 pIC50 = 7.8 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 544 12 3 7 5.6 CCCCc1nnc(SCc2cccc(C(=O)O)c2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
CHEMBL155661 48257 0 None - 0 Rabbit 7.8 pIC50 = 7.8 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 544 12 3 7 5.6 CCCCc1nnc(SCc2cccc(C(=O)O)c2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
11755714 119722 0 None - 0 Rabbit 7.8 pIC50 = 7.8 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 500 11 2 6 5.9 CCCCc1nnc(SCc2ccccc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
CHEMBL352235 119722 0 None - 0 Rabbit 7.8 pIC50 = 7.8 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 500 11 2 6 5.9 CCCCc1nnc(SCc2ccccc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
14956744 204433 0 None - 0 Rabbit 7.8 pIC50 = 7.8 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 481 9 1 8 4.3 CCCCc1nn(-c2cccc(OC)c2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
CHEMBL86255 204433 0 None - 0 Rabbit 7.8 pIC50 = 7.8 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 481 9 1 8 4.3 CCCCc1nn(-c2cccc(OC)c2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
44459896 95817 0 None - 0 Rabbit 7.8 pIC50 = 7.8 Binding
Binding affinity against Angiotensin II type 1 Receptor in rabbit aortic tissueBinding affinity against Angiotensin II type 1 Receptor in rabbit aortic tissue
ChEMBL 470 7 1 6 5.3 CCCCc1nc2cc(Cl)ccc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80334-0
CHEMBL26113 95817 0 None - 0 Rabbit 7.8 pIC50 = 7.8 Binding
Binding affinity against Angiotensin II type 1 Receptor in rabbit aortic tissueBinding affinity against Angiotensin II type 1 Receptor in rabbit aortic tissue
ChEMBL 470 7 1 6 5.3 CCCCc1nc2cc(Cl)ccc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80334-0
10347373 48257 0 None - 0 Rabbit 7.8 pIC50 = 7.8 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 544 12 3 7 5.6 CCCCc1nnc(SCc2cccc(C(=O)O)c2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
CHEMBL155661 48257 0 None - 0 Rabbit 7.8 pIC50 = 7.8 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 544 12 3 7 5.6 CCCCc1nnc(SCc2cccc(C(=O)O)c2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
11755714 119722 0 None - 0 Rabbit 7.8 pIC50 = 7.8 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 500 11 2 6 5.9 CCCCc1nnc(SCc2ccccc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
CHEMBL352235 119722 0 None - 0 Rabbit 7.8 pIC50 = 7.8 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 500 11 2 6 5.9 CCCCc1nnc(SCc2ccccc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
44377263 164335 0 None - 0 Rabbit 7.8 pIC50 = 7.8 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aortaIn vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aorta
ChEMBL 416 8 0 8 3.7 CCCCc1ncc(C(=O)OC)n1Cc1ccc(-c2ccccc2-n2cnnn2)cc1 10.1016/S0960-894X(01)81124-0
CHEMBL422200 164335 0 None - 0 Rabbit 7.8 pIC50 = 7.8 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aortaIn vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aorta
ChEMBL 416 8 0 8 3.7 CCCCc1ncc(C(=O)OC)n1Cc1ccc(-c2ccccc2-n2cnnn2)cc1 10.1016/S0960-894X(01)81124-0
10417195 108579 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
In vitro inhibitory concentration against AT1 receptor from human adrenal tissues.In vitro inhibitory concentration against AT1 receptor from human adrenal tissues.
ChEMBL 685 13 2 9 6.2 CCCCc1nn(-c2cc(NC(C)=O)ccc2Cl)c(=O)n1Cc1ccc(-c2cc(CCC)ccc2S(=O)(=O)NC(=O)OCC)cc1F 10.1016/S0960-894X(01)80595-3
CHEMBL321313 108579 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
In vitro inhibitory concentration against AT1 receptor from human adrenal tissues.In vitro inhibitory concentration against AT1 receptor from human adrenal tissues.
ChEMBL 685 13 2 9 6.2 CCCCc1nn(-c2cc(NC(C)=O)ccc2Cl)c(=O)n1Cc1ccc(-c2cc(CCC)ccc2S(=O)(=O)NC(=O)OCC)cc1F 10.1016/S0960-894X(01)80595-3
44315058 70095 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membrane
ChEMBL 637 10 3 8 5.6 Cc1nc2ccc(NC(=O)NC(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/0960-894X(94)85036-4
CHEMBL194608 70095 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membrane
ChEMBL 637 10 3 8 5.6 Cc1nc2ccc(NC(=O)NC(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/0960-894X(94)85036-4
44372814 119272 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
Inhibition of Angiotensin II receptor, type 1Inhibition of Angiotensin II receptor, type 1
ChEMBL 672 11 2 6 6.7 CCCCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)C(=O)N1CCN(C(=O)N(c2ccccc2)c2ccccc2)[C@H](C(=O)O)C1 10.1021/jm9504722
CHEMBL348157 119272 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
Inhibition of Angiotensin II receptor, type 1Inhibition of Angiotensin II receptor, type 1
ChEMBL 672 11 2 6 6.7 CCCCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)C(=O)N1CCN(C(=O)N(c2ccccc2)c2ccccc2)[C@H](C(=O)O)C1 10.1021/jm9504722
44320519 106676 0 None - 0 Rat 7.8 pIC50 = 7.8 Binding
Inhibition of [125-I]-labeled angiotensin II binding to AT1 receptor in rat uterine membranesInhibition of [125-I]-labeled angiotensin II binding to AT1 receptor in rat uterine membranes
ChEMBL 495 7 1 7 4.6 CCCCc1ncc2n1[C@H](c1ccc(-c3ccccc3-c3nn[nH]n3)cc1)CC[C@@H]2N1C(=O)CCC1=O 10.1016/S0960-894X(01)80290-0
CHEMBL316392 106676 0 None - 0 Rat 7.8 pIC50 = 7.8 Binding
Inhibition of [125-I]-labeled angiotensin II binding to AT1 receptor in rat uterine membranesInhibition of [125-I]-labeled angiotensin II binding to AT1 receptor in rat uterine membranes
ChEMBL 495 7 1 7 4.6 CCCCc1ncc2n1[C@H](c1ccc(-c3ccccc3-c3nn[nH]n3)cc1)CC[C@@H]2N1C(=O)CCC1=O 10.1016/S0960-894X(01)80290-0
44309299 101855 0 None - 0 Rat 7.8 pIC50 = 7.8 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 537 12 0 9 5.1 CCCCc1nn(CC(OCC)c2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nnn(C)n2)cc1 10.1021/jm00067a015
CHEMBL303683 101855 0 None - 0 Rat 7.8 pIC50 = 7.8 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 537 12 0 9 5.1 CCCCc1nn(CC(OCC)c2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nnn(C)n2)cc1 10.1021/jm00067a015
10223724 204033 0 None - 0 Rat 7.8 pIC50 = 7.8 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 417 9 1 7 3.7 CCCCc1nn(CCC)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a015
CHEMBL82797 204033 0 None - 0 Rat 7.8 pIC50 = 7.8 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 417 9 1 7 3.7 CCCCc1nn(CCC)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a015
14951062 204656 0 None - 0 Rat 7.8 pIC50 = 7.8 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 429 9 1 7 3.7 CCCCc1nn(CC2CC2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a015
CHEMBL87669 204656 0 None - 0 Rat 7.8 pIC50 = 7.8 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 429 9 1 7 3.7 CCCCc1nn(CC2CC2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a015
10411441 51498 0 None - 0 Rabbit 7.8 pIC50 = 7.8 Binding
Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)
ChEMBL 449 7 1 5 5.5 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(OC(C(=O)O)c2ccccc2)c(Cl)c1 10.1016/0960-894X(95)00185-V
CHEMBL15850 51498 0 None - 0 Rabbit 7.8 pIC50 = 7.8 Binding
Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)
ChEMBL 449 7 1 5 5.5 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(OC(C(=O)O)c2ccccc2)c(Cl)c1 10.1016/0960-894X(95)00185-V
44381431 58178 0 None - 0 Rabbit 7.8 pIC50 = 7.8 Binding
Tested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membraneTested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membrane
ChEMBL 578 11 1 9 5.2 CCCCOC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCC)nc3ccc([N+](=O)[O-])cc3c2=O)cc1 10.1016/S0960-894X(01)81126-4
CHEMBL168346 58178 0 None - 0 Rabbit 7.8 pIC50 = 7.8 Binding
Tested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membraneTested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membrane
ChEMBL 578 11 1 9 5.2 CCCCOC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCC)nc3ccc([N+](=O)[O-])cc3c2=O)cc1 10.1016/S0960-894X(01)81126-4
53309273 63429 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation countingDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation counting
ChEMBL 463 5 1 6 5.6 CCc1c(C)nc2c(nc(CC)n2[C@H]2CCc3cc(-c4ccccc4-c4nnn[nH]4)ccc32)c1C 10.1021/jm200409s
CHEMBL1801737 63429 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation countingDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation counting
ChEMBL 463 5 1 6 5.6 CCc1c(C)nc2c(nc(CC)n2[C@H]2CCc3cc(-c4ccccc4-c4nnn[nH]4)ccc32)c1C 10.1021/jm200409s
10324179 113864 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 514 11 1 6 5.4 CCCCc1ncc(/C=C2/C(=O)NC(=O)N2CCCC)n1Cc1ccc(-c2ccccc2C(=O)OC)cc1 10.1007/s00044-009-9205-9
CHEMBL333126 113864 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 514 11 1 6 5.4 CCCCc1ncc(/C=C2/C(=O)NC(=O)N2CCCC)n1Cc1ccc(-c2ccccc2C(=O)OC)cc1 10.1007/s00044-009-9205-9
44342089 9935 0 None - 0 Rat 6.8 pIC50 = 6.8 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 442 7 0 6 4.8 CCCCC1=NC2(CCCC2)C(=O)N1Cc1ccc(-c2ccccc2-c2nnnn2C)cc1 10.1021/jm00074a018
CHEMBL115193 9935 0 None - 0 Rat 6.8 pIC50 = 6.8 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 442 7 0 6 4.8 CCCCC1=NC2(CCCC2)C(=O)N1Cc1ccc(-c2ccccc2-c2nnnn2C)cc1 10.1021/jm00074a018
44341702 9988 0 None - 0 Rat 6.8 pIC50 = 6.8 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 434 11 1 3 6.3 CCCCC1=NC(CCC)(CCC)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00074a018
CHEMBL115492 9988 0 None - 0 Rat 6.8 pIC50 = 6.8 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 434 11 1 3 6.3 CCCCC1=NC(CCC)(CCC)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00074a018
19976810 204621 0 None - 0 Rat 6.8 pIC50 = 6.8 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 416 10 1 7 4.3 CCCCc1nc(CCCC)n(Cc2ccc(-c3cnccc3-c3nn[nH]n3)cc2)n1 10.1021/jm031100t
CHEMBL87411 204621 0 None - 0 Rat 6.8 pIC50 = 6.8 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 416 10 1 7 4.3 CCCCc1nc(CCCC)n(Cc2ccc(-c3cnccc3-c3nn[nH]n3)cc2)n1 10.1021/jm031100t
1610 2305 89 None - 4 Bovine 6.8 pIC50 = 6.8 Binding
Displacement of [125 I]-AII (0.2 nM) from bovine adrenal cortical membrane angiotensin II (AII) receptor at 10e-7 MDisplacement of [125 I]-AII (0.2 nM) from bovine adrenal cortical membrane angiotensin II (AII) receptor at 10e-7 M
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/0960-894X(95)00319-O
3941 2305 89 None - 4 Bovine 6.8 pIC50 = 6.8 Binding
Displacement of [125 I]-AII (0.2 nM) from bovine adrenal cortical membrane angiotensin II (AII) receptor at 10e-7 MDisplacement of [125 I]-AII (0.2 nM) from bovine adrenal cortical membrane angiotensin II (AII) receptor at 10e-7 M
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/0960-894X(95)00319-O
3961 2305 89 None - 4 Bovine 6.8 pIC50 = 6.8 Binding
Displacement of [125 I]-AII (0.2 nM) from bovine adrenal cortical membrane angiotensin II (AII) receptor at 10e-7 MDisplacement of [125 I]-AII (0.2 nM) from bovine adrenal cortical membrane angiotensin II (AII) receptor at 10e-7 M
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/0960-894X(95)00319-O
590 2305 89 None - 4 Bovine 6.8 pIC50 = 6.8 Binding
Displacement of [125 I]-AII (0.2 nM) from bovine adrenal cortical membrane angiotensin II (AII) receptor at 10e-7 MDisplacement of [125 I]-AII (0.2 nM) from bovine adrenal cortical membrane angiotensin II (AII) receptor at 10e-7 M
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/0960-894X(95)00319-O
CHEMBL191 2305 89 None - 4 Bovine 6.8 pIC50 = 6.8 Binding
Displacement of [125 I]-AII (0.2 nM) from bovine adrenal cortical membrane angiotensin II (AII) receptor at 10e-7 MDisplacement of [125 I]-AII (0.2 nM) from bovine adrenal cortical membrane angiotensin II (AII) receptor at 10e-7 M
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/0960-894X(95)00319-O
DB00678 2305 89 None - 4 Bovine 6.8 pIC50 = 6.8 Binding
Displacement of [125 I]-AII (0.2 nM) from bovine adrenal cortical membrane angiotensin II (AII) receptor at 10e-7 MDisplacement of [125 I]-AII (0.2 nM) from bovine adrenal cortical membrane angiotensin II (AII) receptor at 10e-7 M
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/0960-894X(95)00319-O
19422654 100915 0 None - 0 Rat 6.8 pIC50 = 6.8 Binding
In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.
ChEMBL 460 9 1 3 6.7 CCCCC1=NC(C)(CC2CCCCC2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/S0960-894X(01)81140-9
CHEMBL297250 100915 0 None - 0 Rat 6.8 pIC50 = 6.8 Binding
In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.
ChEMBL 460 9 1 3 6.7 CCCCC1=NC(C)(CC2CCCCC2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/S0960-894X(01)81140-9
44297010 101143 0 None - 0 Bovine 6.8 pIC50 = 6.8 Binding
In vitro binding affinity to angiotensin II receptor in bovine adrenal cortexIn vitro binding affinity to angiotensin II receptor in bovine adrenal cortex
ChEMBL 577 8 1 10 4.1 CCCCc1nc2ccc([C@@H]3[C@@H]4C(=O)OC[C@@H]4ON3C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80377-2
CHEMBL298943 101143 0 None - 0 Bovine 6.8 pIC50 = 6.8 Binding
In vitro binding affinity to angiotensin II receptor in bovine adrenal cortexIn vitro binding affinity to angiotensin II receptor in bovine adrenal cortex
ChEMBL 577 8 1 10 4.1 CCCCc1nc2ccc([C@@H]3[C@@H]4C(=O)OC[C@@H]4ON3C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80377-2
19102815 206132 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
In vitro inhibitory concentration against AT1 receptor from human adrenal tissues.In vitro inhibitory concentration against AT1 receptor from human adrenal tissues.
ChEMBL 672 11 1 8 7.3 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2cc(CCC)ccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1 10.1016/S0960-894X(01)80595-3
CHEMBL96554 206132 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
In vitro inhibitory concentration against AT1 receptor from human adrenal tissues.In vitro inhibitory concentration against AT1 receptor from human adrenal tissues.
ChEMBL 672 11 1 8 7.3 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2cc(CCC)ccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1 10.1016/S0960-894X(01)80595-3
44296547 187745 0 None - 0 Bovine 6.8 pIC50 = 6.8 Binding
Inhibition of [125l]-All binding to bovine adrenal cortexInhibition of [125l]-All binding to bovine adrenal cortex
ChEMBL 380 7 3 5 3.1 CCc1nc(CO)c(C(=O)O)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/S0960-894X(01)81143-4
CHEMBL50092 187745 0 None - 0 Bovine 6.8 pIC50 = 6.8 Binding
Inhibition of [125l]-All binding to bovine adrenal cortexInhibition of [125l]-All binding to bovine adrenal cortex
ChEMBL 380 7 3 5 3.1 CCc1nc(CO)c(C(=O)O)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/S0960-894X(01)81143-4
2583 3705 115 None - 1 Human 6.8 pIC50 = 6.8 Binding
Inhibition of angiotensin AT1 receptorInhibition of angiotensin AT1 receptor
ChEMBL 514 7 1 5 7.3 CCCc1nc2c(n1Cc1ccc(cc1)c1ccccc1C(=O)O)cc(cc2C)c1nc2c(n1C)cccc2 10.1016/j.bmc.2012.05.056
592 3705 115 None - 1 Human 6.8 pIC50 = 6.8 Binding
Inhibition of angiotensin AT1 receptorInhibition of angiotensin AT1 receptor
ChEMBL 514 7 1 5 7.3 CCCc1nc2c(n1Cc1ccc(cc1)c1ccccc1C(=O)O)cc(cc2C)c1nc2c(n1C)cccc2 10.1016/j.bmc.2012.05.056
65999 3705 115 None - 1 Human 6.8 pIC50 = 6.8 Binding
Inhibition of angiotensin AT1 receptorInhibition of angiotensin AT1 receptor
ChEMBL 514 7 1 5 7.3 CCCc1nc2c(n1Cc1ccc(cc1)c1ccccc1C(=O)O)cc(cc2C)c1nc2c(n1C)cccc2 10.1016/j.bmc.2012.05.056
CHEMBL1017 3705 115 None - 1 Human 6.8 pIC50 = 6.8 Binding
Inhibition of angiotensin AT1 receptorInhibition of angiotensin AT1 receptor
ChEMBL 514 7 1 5 7.3 CCCc1nc2c(n1Cc1ccc(cc1)c1ccccc1C(=O)O)cc(cc2C)c1nc2c(n1C)cccc2 10.1016/j.bmc.2012.05.056
DB00966 3705 115 None - 1 Human 6.8 pIC50 = 6.8 Binding
Inhibition of angiotensin AT1 receptorInhibition of angiotensin AT1 receptor
ChEMBL 514 7 1 5 7.3 CCCc1nc2c(n1Cc1ccc(cc1)c1ccccc1C(=O)O)cc(cc2C)c1nc2c(n1C)cccc2 10.1016/j.bmc.2012.05.056
1610 2305 89 None - 4 Bovine 6.8 pIC50 = 6.8 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00067a016
3941 2305 89 None - 4 Bovine 6.8 pIC50 = 6.8 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00067a016
3961 2305 89 None - 4 Bovine 6.8 pIC50 = 6.8 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00067a016
590 2305 89 None - 4 Bovine 6.8 pIC50 = 6.8 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00067a016
CHEMBL191 2305 89 None - 4 Bovine 6.8 pIC50 = 6.8 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00067a016
DB00678 2305 89 None - 4 Bovine 6.8 pIC50 = 6.8 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00067a016
15654750 103108 0 None - 0 Bovine 6.8 pIC50 = 6.8 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 456 7 2 7 4.5 CSCc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a016
CHEMBL308651 103108 0 None - 0 Bovine 6.8 pIC50 = 6.8 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 456 7 2 7 4.5 CSCc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a016
44563176 170868 0 None - 0 Bovine 5.8 pIC50 = 5.8 Binding
Displacement of [125I]Ang2 from AT1 receptor in bovine adrenal cortexDisplacement of [125I]Ang2 from AT1 receptor in bovine adrenal cortex
ChEMBL 537 7 1 6 7.4 CCCc1nc2c(C)cc(-c3nc4ccccc4n3C)cc2n1Cc1ccc(-c2ccccc2-c2ncn[nH]2)cc1 10.1016/j.bmc.2008.10.040
CHEMBL446314 170868 0 None - 0 Bovine 5.8 pIC50 = 5.8 Binding
Displacement of [125I]Ang2 from AT1 receptor in bovine adrenal cortexDisplacement of [125I]Ang2 from AT1 receptor in bovine adrenal cortex
ChEMBL 537 7 1 6 7.4 CCCc1nc2c(C)cc(-c3nc4ccccc4n3C)cc2n1Cc1ccc(-c2ccccc2-c2ncn[nH]2)cc1 10.1016/j.bmc.2008.10.040
19792183 101296 0 None - 0 Bovine 5.8 pIC50 = 5.8 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 442 7 1 5 5.9 CCCCc1nc2cc(Cl)ccc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
CHEMBL299994 101296 0 None - 0 Bovine 5.8 pIC50 = 5.8 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 442 7 1 5 5.9 CCCCc1nc2cc(Cl)ccc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
44210317 102723 0 None - 0 Bovine 5.8 pIC50 = 5.8 Binding
Inhibition of [125I][Ile5]-AII binding to bovine adrenal cortex membrane Angiotensin II receptor type 1Inhibition of [125I][Ile5]-AII binding to bovine adrenal cortex membrane Angiotensin II receptor type 1
ChEMBL 532 5 1 3 5.3 CCCCc1nc2ccccc2n1Cc1cc(I)c(O)c(I)c1 10.1016/S0960-894X(01)81149-5
CHEMBL308424 102723 0 None - 0 Bovine 5.8 pIC50 = 5.8 Binding
Inhibition of [125I][Ile5]-AII binding to bovine adrenal cortex membrane Angiotensin II receptor type 1Inhibition of [125I][Ile5]-AII binding to bovine adrenal cortex membrane Angiotensin II receptor type 1
ChEMBL 532 5 1 3 5.3 CCCCc1nc2ccccc2n1Cc1cc(I)c(O)c(I)c1 10.1016/S0960-894X(01)81149-5
14951055 202619 0 None - 0 Rat 5.8 pIC50 = 5.8 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 351 7 2 5 3.7 CCCCc1nnc(O)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00067a015
CHEMBL71518 202619 0 None - 0 Rat 5.8 pIC50 = 5.8 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 351 7 2 5 3.7 CCCCc1nnc(O)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00067a015
19792183 101296 0 None - 0 Bovine 5.8 pIC50 = 5.8 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 442 7 1 5 5.9 CCCCc1nc2cc(Cl)ccc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
CHEMBL299994 101296 0 None - 0 Bovine 5.8 pIC50 = 5.8 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 442 7 1 5 5.9 CCCCc1nc2cc(Cl)ccc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
127034757 135859 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Displacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysisDisplacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysis
ChEMBL 679 12 2 7 7.5 CCCc1nc2c(C)cc(C(=O)NCCc3ccc(F)cc3)cc2n1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)cc1 10.1039/C4MD00499J
CHEMBL3735265 135859 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Displacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysisDisplacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysis
ChEMBL 679 12 2 7 7.5 CCCc1nc2c(C)cc(C(=O)NCCc3ccc(F)cc3)cc2n1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)cc1 10.1039/C4MD00499J
127036104 135934 0 None - 0 Human 5.8 pIC50 = 5.8 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 555 9 2 6 6.7 CCCc1nc2c(C)cc(C(=O)N[C@@H](C)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.ejmech.2015.09.010
CHEMBL3735910 135934 0 None - 0 Human 5.8 pIC50 = 5.8 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 555 9 2 6 6.7 CCCc1nc2c(C)cc(C(=O)N[C@@H](C)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.ejmech.2015.09.010
127036294 135815 0 None - 0 Human 5.8 pIC50 = 5.8 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 555 9 2 6 6.7 CCCc1nc2c(C)cc(C(=O)N[C@H](C)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.ejmech.2015.09.010
CHEMBL3734815 135815 0 None - 0 Human 5.8 pIC50 = 5.8 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 555 9 2 6 6.7 CCCc1nc2c(C)cc(C(=O)N[C@H](C)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.ejmech.2015.09.010
24828567 95842 0 None - 0 Rat 6.8 pIC50 = 6.8 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
ChEMBL 410 6 1 5 4.4 CCCC1c2ncccc2C(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm7011563
CHEMBL261248 95842 0 None - 0 Rat 6.8 pIC50 = 6.8 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
ChEMBL 410 6 1 5 4.4 CCCC1c2ncccc2C(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm7011563
44296953 193085 0 None - 0 Bovine 6.8 pIC50 = 6.8 Binding
In vitro binding affinity to angiotensin II receptor in bovine adrenal cortexIn vitro binding affinity to angiotensin II receptor in bovine adrenal cortex
ChEMBL 561 8 1 8 5.7 CCCCc1nc2ccc([C@H]3C4CCCC4ON3C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80377-2
CHEMBL53803 193085 0 None - 0 Bovine 6.8 pIC50 = 6.8 Binding
In vitro binding affinity to angiotensin II receptor in bovine adrenal cortexIn vitro binding affinity to angiotensin II receptor in bovine adrenal cortex
ChEMBL 561 8 1 8 5.7 CCCCc1nc2ccc([C@H]3C4CCCC4ON3C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80377-2
127035514 135887 0 None - 1 Human 6.8 pIC50 = 6.8 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 585 11 2 7 6.3 CCCc1nc2c(C)cc(C(=O)N[C@H](COC)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.ejmech.2015.09.010
CHEMBL3735446 135887 0 None - 1 Human 6.8 pIC50 = 6.8 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 585 11 2 7 6.3 CCCc1nc2c(C)cc(C(=O)N[C@H](COC)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.ejmech.2015.09.010
10094859 19775 0 None - 0 Rat 6.8 pIC50 = 6.8 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 441 8 1 4 5.8 CCCc1nc2c(C)cc(CN(C)C)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00077a007
CHEMBL130322 19775 0 None - 0 Rat 6.8 pIC50 = 6.8 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 441 8 1 4 5.8 CCCc1nc2c(C)cc(CN(C)C)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00077a007
10371295 113013 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 596 12 0 6 6.7 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2Cc2ccc(C(F)(F)F)cc2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
CHEMBL332152 113013 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 596 12 0 6 6.7 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2Cc2ccc(C(F)(F)F)cc2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
14956745 204536 0 None - 0 Rabbit 7.8 pIC50 = 7.8 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 465 8 1 7 4.6 CCCCc1nn(-c2ccc(C)cc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
CHEMBL86906 204536 0 None - 0 Rabbit 7.8 pIC50 = 7.8 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 465 8 1 7 4.6 CCCCc1nn(-c2ccc(C)cc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
44307122 201298 0 None - 0 Rabbit 7.8 pIC50 = 7.8 Binding
Binding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membraneBinding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane
ChEMBL 349 3 1 4 4.7 CCc1nc2c(C)cc(C)nc2n1Cc1cc(Cl)c(O)c(Cl)c1 10.1016/S0960-894X(01)81148-3
CHEMBL63144 201298 0 None - 0 Rabbit 7.8 pIC50 = 7.8 Binding
Binding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membraneBinding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane
ChEMBL 349 3 1 4 4.7 CCc1nc2c(C)cc(C)nc2n1Cc1cc(Cl)c(O)c(Cl)c1 10.1016/S0960-894X(01)81148-3
9823146 19150 0 None - 1 Human 7.8 pIC50 = 7.8 Binding
Binding affinity to angiotensin AT1 receptorBinding affinity to angiotensin AT1 receptor
ChEMBL 415 10 1 6 4.9 CCCCc1nc(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)n(CCCC)n1 10.1016/j.bmc.2010.10.043
CHEMBL12909 19150 0 None - 1 Human 7.8 pIC50 = 7.8 Binding
Binding affinity to angiotensin AT1 receptorBinding affinity to angiotensin AT1 receptor
ChEMBL 415 10 1 6 4.9 CCCCc1nc(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)n(CCCC)n1 10.1016/j.bmc.2010.10.043
127035410 135849 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
Displacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysisDisplacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysis
ChEMBL 557 8 1 8 5.7 CCCc1nc2c(n1Cc1ccc(-c3ccccc3S(=O)(=O)Nc3onc(C)c3C)c(C#N)c1)C(=O)CCCC2 10.1039/C4MD00499J
CHEMBL3735155 135849 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
Displacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysisDisplacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysis
ChEMBL 557 8 1 8 5.7 CCCc1nc2c(n1Cc1ccc(-c3ccccc3S(=O)(=O)Nc3onc(C)c3C)c(C#N)c1)C(=O)CCCC2 10.1039/C4MD00499J
70692693 75847 0 None - 0 Bovine 7.8 pIC50 = 7.8 Binding
Displacement of [125I]AngII from type 1 angiotensin 2 receptor in bovine adrenal cortexDisplacement of [125I]AngII from type 1 angiotensin 2 receptor in bovine adrenal cortex
ChEMBL 500 8 1 6 6.1 CCCc1nc2ccccc2n1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)cc1 10.1016/j.bmc.2012.06.011
CHEMBL2058369 75847 0 None - 0 Bovine 7.8 pIC50 = 7.8 Binding
Displacement of [125I]AngII from type 1 angiotensin 2 receptor in bovine adrenal cortexDisplacement of [125I]AngII from type 1 angiotensin 2 receptor in bovine adrenal cortex
ChEMBL 500 8 1 6 6.1 CCCc1nc2ccccc2n1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)cc1 10.1016/j.bmc.2012.06.011
44438880 91540 0 None - 1 Bovine 7.8 pIC50 = 7.8 Binding
Displacement of [125I]angiotensin-2 from bovine adrenal cortex AT1 receptorDisplacement of [125I]angiotensin-2 from bovine adrenal cortex AT1 receptor
ChEMBL 427 7 2 7 3.7 CCCc1nc2cccc(C(=O)O)c2n1Cc1ccc(-n2cccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2007.02.042
CHEMBL241523 91540 0 None - 1 Bovine 7.8 pIC50 = 7.8 Binding
Displacement of [125I]angiotensin-2 from bovine adrenal cortex AT1 receptorDisplacement of [125I]angiotensin-2 from bovine adrenal cortex AT1 receptor
ChEMBL 427 7 2 7 3.7 CCCc1nc2cccc(C(=O)O)c2n1Cc1ccc(-n2cccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2007.02.042
44297143 100768 0 None - 0 Bovine 7.8 pIC50 = 7.8 Binding
In vitro binding affinity to angiotensin II receptor in bovine adrenal cortexIn vitro binding affinity to angiotensin II receptor in bovine adrenal cortex
ChEMBL 547 8 1 8 5.3 CCCCc1nc2ccc([C@@H]3[C@H]4CCCN3OC4)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80377-2
CHEMBL296173 100768 0 None - 0 Bovine 7.8 pIC50 = 7.8 Binding
In vitro binding affinity to angiotensin II receptor in bovine adrenal cortexIn vitro binding affinity to angiotensin II receptor in bovine adrenal cortex
ChEMBL 547 8 1 8 5.3 CCCCc1nc2ccc([C@@H]3[C@H]4CCCN3OC4)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80377-2
9886863 33682 0 None - 0 Guinea pig 7.8 pIC50 = 7.8 Binding
In vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparationIn vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparation
ChEMBL 393 5 1 5 5.0 Cc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2ccccc2n1 10.1021/jm00100a007
CHEMBL142380 33682 0 None - 0 Guinea pig 7.8 pIC50 = 7.8 Binding
In vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparationIn vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparation
ChEMBL 393 5 1 5 5.0 Cc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2ccccc2n1 10.1021/jm00100a007
10078800 108691 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
In vitro inhibitory concentration against AT1 receptor from human adrenal tissues.In vitro inhibitory concentration against AT1 receptor from human adrenal tissues.
ChEMBL 751 13 2 8 7.6 CCCCc1nn(-c2cc(NC(C)=O)ccc2Cl)c(=O)n1Cc1ccc(-c2cc(CCC)ccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1F 10.1016/S0960-894X(01)80595-3
CHEMBL321531 108691 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
In vitro inhibitory concentration against AT1 receptor from human adrenal tissues.In vitro inhibitory concentration against AT1 receptor from human adrenal tissues.
ChEMBL 751 13 2 8 7.6 CCCCc1nn(-c2cc(NC(C)=O)ccc2Cl)c(=O)n1Cc1ccc(-c2cc(CCC)ccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1F 10.1016/S0960-894X(01)80595-3
9886863 33682 0 None - 0 Guinea pig 7.8 pIC50 = 7.8 Binding
Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1
ChEMBL 393 5 1 5 5.0 Cc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2ccccc2n1 10.1021/jm00061a016
CHEMBL142380 33682 0 None - 0 Guinea pig 7.8 pIC50 = 7.8 Binding
Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1
ChEMBL 393 5 1 5 5.0 Cc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2ccccc2n1 10.1021/jm00061a016
14951066 102572 0 None - 0 Rat 7.8 pIC50 = 7.8 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 489 9 1 9 3.6 CCCCc1nn(CC(=O)OC(C)(C)C)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a015
CHEMBL307310 102572 0 None - 0 Rat 7.8 pIC50 = 7.8 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 489 9 1 9 3.6 CCCCc1nn(CC(=O)OC(C)(C)C)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a015
10183373 164447 0 None - 0 Rat 7.8 pIC50 = 7.8 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 465 9 1 7 4.3 CCCCc1nn(Cc2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a015
CHEMBL422593 164447 0 None - 0 Rat 7.8 pIC50 = 7.8 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 465 9 1 7 4.3 CCCCc1nn(Cc2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a015
19811543 201671 0 None - 0 Bovine 7.8 pIC50 = 7.8 Binding
Tested for binding affinity against angiotensin II receptor in bovine adrenal cortexTested for binding affinity against angiotensin II receptor in bovine adrenal cortex
ChEMBL 444 9 1 7 3.7 CCCCn1c(=O)cc(CCC)n(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c1=O 10.1016/0960-894X(95)00370-9
CHEMBL65224 201671 0 None - 0 Bovine 7.8 pIC50 = 7.8 Binding
Tested for binding affinity against angiotensin II receptor in bovine adrenal cortexTested for binding affinity against angiotensin II receptor in bovine adrenal cortex
ChEMBL 444 9 1 7 3.7 CCCCn1c(=O)cc(CCC)n(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c1=O 10.1016/0960-894X(95)00370-9
19385586 49443 0 None - 0 Rabbit 7.8 pIC50 = 7.8 Binding
Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)
ChEMBL 479 8 1 6 5.5 CCc1nc2c(C)cc(C)nc2n1Cc1cc(Cl)c(OC(C(=O)O)c2ccccc2)c(OC)c1 10.1016/0960-894X(95)00185-V
CHEMBL15669 49443 0 None - 0 Rabbit 7.8 pIC50 = 7.8 Binding
Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)
ChEMBL 479 8 1 6 5.5 CCc1nc2c(C)cc(C)nc2n1Cc1cc(Cl)c(OC(C(=O)O)c2ccccc2)c(OC)c1 10.1016/0960-894X(95)00185-V
10049400 154889 0 None - 0 Rabbit 7.8 pIC50 = 7.8 Binding
Tested in vitro for Angiotensin II receptor, type 1 binding affinity using rabbit aorta binding assayTested in vitro for Angiotensin II receptor, type 1 binding affinity using rabbit aorta binding assay
ChEMBL 449 8 1 5 5.6 CCCc1nc2c(C)ccnc2n1Cc1ccc(OC(C(=O)O)c2ccccc2Cl)cc1 10.1016/0960-894X(94)00476-V
CHEMBL40381 154889 0 None - 0 Rabbit 7.8 pIC50 = 7.8 Binding
Tested in vitro for Angiotensin II receptor, type 1 binding affinity using rabbit aorta binding assayTested in vitro for Angiotensin II receptor, type 1 binding affinity using rabbit aorta binding assay
ChEMBL 449 8 1 5 5.6 CCCc1nc2c(C)ccnc2n1Cc1ccc(OC(C(=O)O)c2ccccc2Cl)cc1 10.1016/0960-894X(94)00476-V
44381603 58789 0 None - 0 Rabbit 7.8 pIC50 = 7.8 Binding
Tested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membraneTested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membrane
ChEMBL 532 8 2 7 3.8 CCCc1nc2ccc(NC(C)=O)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(C)=O)cc1 10.1016/S0960-894X(01)81126-4
CHEMBL169798 58789 0 None - 0 Rabbit 7.8 pIC50 = 7.8 Binding
Tested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membraneTested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membrane
ChEMBL 532 8 2 7 3.8 CCCc1nc2ccc(NC(C)=O)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(C)=O)cc1 10.1016/S0960-894X(01)81126-4
1610 2305 89 None 1 4 Human 7.8 pIC50 = 7.8 Binding
Displacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptorDisplacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptor
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1039/C5MD00169B
3941 2305 89 None 1 4 Human 7.8 pIC50 = 7.8 Binding
Displacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptorDisplacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptor
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1039/C5MD00169B
3961 2305 89 None 1 4 Human 7.8 pIC50 = 7.8 Binding
Displacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptorDisplacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptor
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1039/C5MD00169B
590 2305 89 None 1 4 Human 7.8 pIC50 = 7.8 Binding
Displacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptorDisplacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptor
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1039/C5MD00169B
CHEMBL191 2305 89 None 1 4 Human 7.8 pIC50 = 7.8 Binding
Displacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptorDisplacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptor
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1039/C5MD00169B
DB00678 2305 89 None 1 4 Human 7.8 pIC50 = 7.8 Binding
Displacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptorDisplacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptor
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1039/C5MD00169B
1610 2305 89 None 1 4 Human 7.8 pIC50 = 7.8 Binding
Displacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysisDisplacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysis
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.ejmech.2013.08.014
3941 2305 89 None 1 4 Human 7.8 pIC50 = 7.8 Binding
Displacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysisDisplacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysis
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.ejmech.2013.08.014
3961 2305 89 None 1 4 Human 7.8 pIC50 = 7.8 Binding
Displacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysisDisplacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysis
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.ejmech.2013.08.014
590 2305 89 None 1 4 Human 7.8 pIC50 = 7.8 Binding
Displacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysisDisplacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysis
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.ejmech.2013.08.014
CHEMBL191 2305 89 None 1 4 Human 7.8 pIC50 = 7.8 Binding
Displacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysisDisplacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysis
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.ejmech.2013.08.014
DB00678 2305 89 None 1 4 Human 7.8 pIC50 = 7.8 Binding
Displacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysisDisplacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysis
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.ejmech.2013.08.014
1610 2305 89 None 1 4 Human 7.8 pIC50 = 7.8 Binding
Displacement of [125I]Sar1 Ile8-Ang 2 from angiotensin 2 AT1 receptor after 180 mins by gamma countingDisplacement of [125I]Sar1 Ile8-Ang 2 from angiotensin 2 AT1 receptor after 180 mins by gamma counting
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.ejmech.2012.01.009
3941 2305 89 None 1 4 Human 7.8 pIC50 = 7.8 Binding
Displacement of [125I]Sar1 Ile8-Ang 2 from angiotensin 2 AT1 receptor after 180 mins by gamma countingDisplacement of [125I]Sar1 Ile8-Ang 2 from angiotensin 2 AT1 receptor after 180 mins by gamma counting
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.ejmech.2012.01.009
3961 2305 89 None 1 4 Human 7.8 pIC50 = 7.8 Binding
Displacement of [125I]Sar1 Ile8-Ang 2 from angiotensin 2 AT1 receptor after 180 mins by gamma countingDisplacement of [125I]Sar1 Ile8-Ang 2 from angiotensin 2 AT1 receptor after 180 mins by gamma counting
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.ejmech.2012.01.009
590 2305 89 None 1 4 Human 7.8 pIC50 = 7.8 Binding
Displacement of [125I]Sar1 Ile8-Ang 2 from angiotensin 2 AT1 receptor after 180 mins by gamma countingDisplacement of [125I]Sar1 Ile8-Ang 2 from angiotensin 2 AT1 receptor after 180 mins by gamma counting
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.ejmech.2012.01.009
CHEMBL191 2305 89 None 1 4 Human 7.8 pIC50 = 7.8 Binding
Displacement of [125I]Sar1 Ile8-Ang 2 from angiotensin 2 AT1 receptor after 180 mins by gamma countingDisplacement of [125I]Sar1 Ile8-Ang 2 from angiotensin 2 AT1 receptor after 180 mins by gamma counting
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.ejmech.2012.01.009
DB00678 2305 89 None 1 4 Human 7.8 pIC50 = 7.8 Binding
Displacement of [125I]Sar1 Ile8-Ang 2 from angiotensin 2 AT1 receptor after 180 mins by gamma countingDisplacement of [125I]Sar1 Ile8-Ang 2 from angiotensin 2 AT1 receptor after 180 mins by gamma counting
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.ejmech.2012.01.009
1610 2305 89 None 1 4 Human 7.8 pIC50 = 7.8 Binding
Displacement of [125I]Sar1Ile8-Ang2 from angiotensin AT1 receptor after 180 mins by gamma countingDisplacement of [125I]Sar1Ile8-Ang2 from angiotensin AT1 receptor after 180 mins by gamma counting
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmc.2012.05.056
3941 2305 89 None 1 4 Human 7.8 pIC50 = 7.8 Binding
Displacement of [125I]Sar1Ile8-Ang2 from angiotensin AT1 receptor after 180 mins by gamma countingDisplacement of [125I]Sar1Ile8-Ang2 from angiotensin AT1 receptor after 180 mins by gamma counting
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmc.2012.05.056
3961 2305 89 None 1 4 Human 7.8 pIC50 = 7.8 Binding
Displacement of [125I]Sar1Ile8-Ang2 from angiotensin AT1 receptor after 180 mins by gamma countingDisplacement of [125I]Sar1Ile8-Ang2 from angiotensin AT1 receptor after 180 mins by gamma counting
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmc.2012.05.056
590 2305 89 None 1 4 Human 7.8 pIC50 = 7.8 Binding
Displacement of [125I]Sar1Ile8-Ang2 from angiotensin AT1 receptor after 180 mins by gamma countingDisplacement of [125I]Sar1Ile8-Ang2 from angiotensin AT1 receptor after 180 mins by gamma counting
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmc.2012.05.056
CHEMBL191 2305 89 None 1 4 Human 7.8 pIC50 = 7.8 Binding
Displacement of [125I]Sar1Ile8-Ang2 from angiotensin AT1 receptor after 180 mins by gamma countingDisplacement of [125I]Sar1Ile8-Ang2 from angiotensin AT1 receptor after 180 mins by gamma counting
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmc.2012.05.056
DB00678 2305 89 None 1 4 Human 7.8 pIC50 = 7.8 Binding
Displacement of [125I]Sar1Ile8-Ang2 from angiotensin AT1 receptor after 180 mins by gamma countingDisplacement of [125I]Sar1Ile8-Ang2 from angiotensin AT1 receptor after 180 mins by gamma counting
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmc.2012.05.056
10323969 16216 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 507 9 0 8 4.3 CCCCc1ncc(/C=C2/C(=O)N(C)C(=O)N2Cc2csc(C)n2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
CHEMBL123091 16216 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 507 9 0 8 4.3 CCCCc1ncc(/C=C2/C(=O)N(C)C(=O)N2Cc2csc(C)n2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
70682146 75963 0 None - 1 Human 7.8 pIC50 = 7.8 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 569 10 2 6 6.7 CCCc1nc2c(C)cc(C(=O)NCC(C)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.ejmech.2015.09.010
CHEMBL2058860 75963 0 None - 1 Human 7.8 pIC50 = 7.8 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 569 10 2 6 6.7 CCCc1nc2c(C)cc(C(=O)NCC(C)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.ejmech.2015.09.010
10325767 112562 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 573 13 0 8 5.6 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2Cc2ccc([N+](=O)[O-])cc2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
CHEMBL331219 112562 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 573 13 0 8 5.6 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2Cc2ccc([N+](=O)[O-])cc2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
53309275 63431 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation countingDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation counting
ChEMBL 463 5 1 6 5.8 CCc1cc(C)c2nc(C(C)C)n([C@H]3CCc4cc(-c5ccccc5-c5nnn[nH]5)ccc43)c2n1 10.1021/jm200409s
CHEMBL1801739 63431 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation countingDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation counting
ChEMBL 463 5 1 6 5.8 CCc1cc(C)c2nc(C(C)C)n([C@H]3CCc4cc(-c5ccccc5-c5nnn[nH]5)ccc43)c2n1 10.1021/jm200409s
44306647 100424 0 None - 0 Rabbit 6.8 pIC50 = 6.8 Binding
Binding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membraneBinding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane
ChEMBL 425 6 1 7 4.6 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(Oc2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81148-3
CHEMBL293846 100424 0 None - 0 Rabbit 6.8 pIC50 = 6.8 Binding
Binding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membraneBinding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane
ChEMBL 425 6 1 7 4.6 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(Oc2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81148-3
127034756 135817 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Displacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysisDisplacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysis
ChEMBL 679 12 2 7 7.5 CCCc1nc2c(C)cc(C(=O)NCCc3ccccc3F)cc2n1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)cc1 10.1039/C4MD00499J
CHEMBL3734829 135817 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Displacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysisDisplacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysis
ChEMBL 679 12 2 7 7.5 CCCc1nc2c(C)cc(C(=O)NCCc3ccccc3F)cc2n1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)cc1 10.1039/C4MD00499J
15780064 99149 0 None - 0 Rabbit 6.8 pIC50 = 6.8 Binding
Displacement of [125 I]Sar1Ile8-AII from type 1 Angiotensin II receptor of rabbit aorta membraneDisplacement of [125 I]Sar1Ile8-AII from type 1 Angiotensin II receptor of rabbit aorta membrane
ChEMBL 613 10 1 8 6.7 CCc1nc2ccc(N(Cc3ccccc3)C(=O)OCC(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80517-5
CHEMBL284123 99149 0 None - 0 Rabbit 6.8 pIC50 = 6.8 Binding
Displacement of [125 I]Sar1Ile8-AII from type 1 Angiotensin II receptor of rabbit aorta membraneDisplacement of [125 I]Sar1Ile8-AII from type 1 Angiotensin II receptor of rabbit aorta membrane
ChEMBL 613 10 1 8 6.7 CCc1nc2ccc(N(Cc3ccccc3)C(=O)OCC(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80517-5
1610 2305 89 None - 4 Bovine 6.8 pIC50 = 6.8 Binding
Displacement of [125I]Ang2 from AT1 receptor in bovine adrenal cortexDisplacement of [125I]Ang2 from AT1 receptor in bovine adrenal cortex
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmc.2008.10.040
3941 2305 89 None - 4 Bovine 6.8 pIC50 = 6.8 Binding
Displacement of [125I]Ang2 from AT1 receptor in bovine adrenal cortexDisplacement of [125I]Ang2 from AT1 receptor in bovine adrenal cortex
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmc.2008.10.040
3961 2305 89 None - 4 Bovine 6.8 pIC50 = 6.8 Binding
Displacement of [125I]Ang2 from AT1 receptor in bovine adrenal cortexDisplacement of [125I]Ang2 from AT1 receptor in bovine adrenal cortex
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmc.2008.10.040
590 2305 89 None - 4 Bovine 6.8 pIC50 = 6.8 Binding
Displacement of [125I]Ang2 from AT1 receptor in bovine adrenal cortexDisplacement of [125I]Ang2 from AT1 receptor in bovine adrenal cortex
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmc.2008.10.040
CHEMBL191 2305 89 None - 4 Bovine 6.8 pIC50 = 6.8 Binding
Displacement of [125I]Ang2 from AT1 receptor in bovine adrenal cortexDisplacement of [125I]Ang2 from AT1 receptor in bovine adrenal cortex
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmc.2008.10.040
DB00678 2305 89 None - 4 Bovine 6.8 pIC50 = 6.8 Binding
Displacement of [125I]Ang2 from AT1 receptor in bovine adrenal cortexDisplacement of [125I]Ang2 from AT1 receptor in bovine adrenal cortex
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmc.2008.10.040
44438901 91541 0 None - 1 Bovine 6.8 pIC50 = 6.8 Binding
Displacement of [125I]angiotensin-2 from bovine adrenal cortex AT1 receptorDisplacement of [125I]angiotensin-2 from bovine adrenal cortex AT1 receptor
ChEMBL 389 6 2 5 3.8 CCc1nc2cccc(C(=O)O)c2n1Cc1ccc(-n2cccc2C(=O)O)cc1 10.1016/j.bmcl.2007.02.042
CHEMBL241529 91541 0 None - 1 Bovine 6.8 pIC50 = 6.8 Binding
Displacement of [125I]angiotensin-2 from bovine adrenal cortex AT1 receptorDisplacement of [125I]angiotensin-2 from bovine adrenal cortex AT1 receptor
ChEMBL 389 6 2 5 3.8 CCc1nc2cccc(C(=O)O)c2n1Cc1ccc(-n2cccc2C(=O)O)cc1 10.1016/j.bmcl.2007.02.042
10390316 21801 0 None - 0 Guinea pig 6.8 pIC50 = 6.8 Binding
In vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparationIn vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparation
ChEMBL 441 6 1 5 5.9 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2ccc(Cl)cc2n1 10.1021/jm00100a007
CHEMBL132115 21801 0 None - 0 Guinea pig 6.8 pIC50 = 6.8 Binding
In vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparationIn vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparation
ChEMBL 441 6 1 5 5.9 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2ccc(Cl)cc2n1 10.1021/jm00100a007
9984310 20865 0 None - 0 Rat 6.8 pIC50 = 6.8 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 524 9 3 4 7.2 CCCCc1nc2cccc(NC(=O)NC3CCCCC3)c2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00077a007
CHEMBL131209 20865 0 None - 0 Rat 6.8 pIC50 = 6.8 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 524 9 3 4 7.2 CCCCc1nc2cccc(NC(=O)NC3CCCCC3)c2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00077a007
10367325 167835 0 None - 0 Rat 6.8 pIC50 = 6.8 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 467 8 1 4 6.8 CCCCc1nc2ccc(N3CCCCC3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00077a007
CHEMBL434815 167835 0 None - 0 Rat 6.8 pIC50 = 6.8 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 467 8 1 4 6.8 CCCCc1nc2ccc(N3CCCCC3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00077a007
1610 2305 89 None - 4 Bovine 6.8 pIC50 = 6.8 Binding
Tested for binding affinity against angiotensin II receptor in bovine adrenal cortexTested for binding affinity against angiotensin II receptor in bovine adrenal cortex
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/0960-894X(95)00370-9
3941 2305 89 None - 4 Bovine 6.8 pIC50 = 6.8 Binding
Tested for binding affinity against angiotensin II receptor in bovine adrenal cortexTested for binding affinity against angiotensin II receptor in bovine adrenal cortex
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/0960-894X(95)00370-9
3961 2305 89 None - 4 Bovine 6.8 pIC50 = 6.8 Binding
Tested for binding affinity against angiotensin II receptor in bovine adrenal cortexTested for binding affinity against angiotensin II receptor in bovine adrenal cortex
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/0960-894X(95)00370-9
590 2305 89 None - 4 Bovine 6.8 pIC50 = 6.8 Binding
Tested for binding affinity against angiotensin II receptor in bovine adrenal cortexTested for binding affinity against angiotensin II receptor in bovine adrenal cortex
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/0960-894X(95)00370-9
CHEMBL191 2305 89 None - 4 Bovine 6.8 pIC50 = 6.8 Binding
Tested for binding affinity against angiotensin II receptor in bovine adrenal cortexTested for binding affinity against angiotensin II receptor in bovine adrenal cortex
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/0960-894X(95)00370-9
DB00678 2305 89 None - 4 Bovine 6.8 pIC50 = 6.8 Binding
Tested for binding affinity against angiotensin II receptor in bovine adrenal cortexTested for binding affinity against angiotensin II receptor in bovine adrenal cortex
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/0960-894X(95)00370-9
10096347 49135 0 None - 0 Rabbit 5.8 pIC50 = 5.8 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 472 9 2 6 5.4 CCCSc1nnc(-c2ccccc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
CHEMBL156449 49135 0 None - 0 Rabbit 5.8 pIC50 = 5.8 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 472 9 2 6 5.4 CCCSc1nnc(-c2ccccc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
44298758 192904 0 None - 0 Bovine 5.8 pIC50 = 5.8 Binding
Binding affinity for angiotensin II receptor of bovine adrenal cortexBinding affinity for angiotensin II receptor of bovine adrenal cortex
ChEMBL 452 7 1 7 4.2 CCCOc1nc2ccc(C)cn2c(=O)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81144-6
CHEMBL52824 192904 0 None - 0 Bovine 5.8 pIC50 = 5.8 Binding
Binding affinity for angiotensin II receptor of bovine adrenal cortexBinding affinity for angiotensin II receptor of bovine adrenal cortex
ChEMBL 452 7 1 7 4.2 CCCOc1nc2ccc(C)cn2c(=O)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81144-6
44321129 110966 0 None - 0 Rat 5.8 pIC50 = 5.8 Binding
Displacement of [125-I]-labeled angiotensin II from Angiotensin II receptor, type 1 of rat uterine membranesDisplacement of [125-I]-labeled angiotensin II from Angiotensin II receptor, type 1 of rat uterine membranes
ChEMBL 457 8 1 7 5.0 CCCCn1nc2n(c1=O)C(c1ccc(-c3ccccc3-c3nn[nH]n3)cc1)CCC2CCC 10.1016/S0960-894X(01)80290-0
CHEMBL327614 110966 0 None - 0 Rat 5.8 pIC50 = 5.8 Binding
Displacement of [125-I]-labeled angiotensin II from Angiotensin II receptor, type 1 of rat uterine membranesDisplacement of [125-I]-labeled angiotensin II from Angiotensin II receptor, type 1 of rat uterine membranes
ChEMBL 457 8 1 7 5.0 CCCCn1nc2n(c1=O)C(c1ccc(-c3ccccc3-c3nn[nH]n3)cc1)CCC2CCC 10.1016/S0960-894X(01)80290-0
10096347 49135 0 None - 0 Rabbit 5.8 pIC50 = 5.8 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 472 9 2 6 5.4 CCCSc1nnc(-c2ccccc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
CHEMBL156449 49135 0 None - 0 Rabbit 5.8 pIC50 = 5.8 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 472 9 2 6 5.4 CCCSc1nnc(-c2ccccc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
54768660 64771 0 None - 0 Human 5.8 pIC50 = 5.8 Binding
Displacement of [125I][Sar1,Ile8]-AT-II from human recombinant AT1 receptor expressed in HEK293 cells after 120 mins by liquid scintillation countingDisplacement of [125I][Sar1,Ile8]-AT-II from human recombinant AT1 receptor expressed in HEK293 cells after 120 mins by liquid scintillation counting
ChEMBL 521 8 1 8 4.9 CCOC(=O)c1cn(Cc2ccc(-c3ccccc3-c3nnn[nH]3)cc2)nc1N(C(C)=O)c1cccc(C)c1 10.1016/j.ejmech.2011.05.056
CHEMBL1824000 64771 0 None - 0 Human 5.8 pIC50 = 5.8 Binding
Displacement of [125I][Sar1,Ile8]-AT-II from human recombinant AT1 receptor expressed in HEK293 cells after 120 mins by liquid scintillation countingDisplacement of [125I][Sar1,Ile8]-AT-II from human recombinant AT1 receptor expressed in HEK293 cells after 120 mins by liquid scintillation counting
ChEMBL 521 8 1 8 4.9 CCOC(=O)c1cn(Cc2ccc(-c3ccccc3-c3nnn[nH]3)cc2)nc1N(C(C)=O)c1cccc(C)c1 10.1016/j.ejmech.2011.05.056
44309040 102501 0 None - 0 Bovine 5.8 pIC50 = 5.8 Binding
Inhibition of [125I][Ile5]-AII binding to bovine adrenal cortex membrane Angiotensin II receptor type 1Inhibition of [125I][Ile5]-AII binding to bovine adrenal cortex membrane Angiotensin II receptor type 1
ChEMBL 370 7 1 7 3.9 CCCCc1nc2ccccc2n1Cc1cc([N+](=O)[O-])c(O)c([N+](=O)[O-])c1 10.1016/S0960-894X(01)81149-5
CHEMBL306670 102501 0 None - 0 Bovine 5.8 pIC50 = 5.8 Binding
Inhibition of [125I][Ile5]-AII binding to bovine adrenal cortex membrane Angiotensin II receptor type 1Inhibition of [125I][Ile5]-AII binding to bovine adrenal cortex membrane Angiotensin II receptor type 1
ChEMBL 370 7 1 7 3.9 CCCCc1nc2ccccc2n1Cc1cc([N+](=O)[O-])c(O)c([N+](=O)[O-])c1 10.1016/S0960-894X(01)81149-5
44459707 92912 0 None - 0 Bovine 6.8 pIC50 = 6.8 Binding
Concentration required for 50% inhibition of binding against Angiotensin II receptor, type 1 in bovine adrenal cortexConcentration required for 50% inhibition of binding against Angiotensin II receptor, type 1 in bovine adrenal cortex
ChEMBL 518 8 2 7 5.1 CCCCc1nc2cc(C3=NNC(=O)CC3C)ccc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80348-6
CHEMBL24550 92912 0 None - 0 Bovine 6.8 pIC50 = 6.8 Binding
Concentration required for 50% inhibition of binding against Angiotensin II receptor, type 1 in bovine adrenal cortexConcentration required for 50% inhibition of binding against Angiotensin II receptor, type 1 in bovine adrenal cortex
ChEMBL 518 8 2 7 5.1 CCCCc1nc2cc(C3=NNC(=O)CC3C)ccc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80348-6
127028618 136740 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Displacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptorDisplacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptor
ChEMBL 536 9 3 7 4.9 CCCc1nc2c(C)cc(C(=O)NC(C)C)cc2n1Cc1ccc(-c2ccccc2C(=O)Nc2nnn[nH]2)cc1 10.1039/C5MD00169B
CHEMBL3752198 136740 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Displacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptorDisplacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptor
ChEMBL 536 9 3 7 4.9 CCCc1nc2c(C)cc(C(=O)NC(C)C)cc2n1Cc1ccc(-c2ccccc2C(=O)Nc2nnn[nH]2)cc1 10.1039/C5MD00169B
127034903 135902 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 571 10 3 7 5.7 CCCc1nc2c(C)cc(C(=O)NC[C@H](O)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.ejmech.2015.09.010
CHEMBL3735641 135902 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 571 10 3 7 5.7 CCCc1nc2c(C)cc(C(=O)NC[C@H](O)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.ejmech.2015.09.010
24827902 157179 0 None - 0 Rat 6.8 pIC50 = 6.8 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
ChEMBL 459 7 1 7 4.5 CCCCn1c(=O)c2ccc(Cl)nc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm7011563
CHEMBL408227 157179 0 None - 0 Rat 6.8 pIC50 = 6.8 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
ChEMBL 459 7 1 7 4.5 CCCCn1c(=O)c2ccc(Cl)nc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm7011563
76325126 104753 0 None - 0 Human 5.8 pIC50 = 5.8 Binding
Antagonist activity at human AT1 receptor expressed in CHO cells measured after overnight incubation by luciferase reporter gene assayAntagonist activity at human AT1 receptor expressed in CHO cells measured after overnight incubation by luciferase reporter gene assay
ChEMBL 531 10 2 4 7.1 CCCc1nn2ccc(C(=O)NC(CC)c3ccccc3)cc2c1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.bmcl.2014.01.004
CHEMBL3115241 104753 0 None - 0 Human 5.8 pIC50 = 5.8 Binding
Antagonist activity at human AT1 receptor expressed in CHO cells measured after overnight incubation by luciferase reporter gene assayAntagonist activity at human AT1 receptor expressed in CHO cells measured after overnight incubation by luciferase reporter gene assay
ChEMBL 531 10 2 4 7.1 CCCc1nn2ccc(C(=O)NC(CC)c3ccccc3)cc2c1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.bmcl.2014.01.004
71653152 88708 0 None - 0 Human 5.8 pIC50 = 5.8 Binding
Displacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysisDisplacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysis
ChEMBL 593 11 2 7 5.9 CCCCc1n(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)cc[n+]1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.ejmech.2012.12.044
CHEMBL2337682 88708 0 None - 0 Human 5.8 pIC50 = 5.8 Binding
Displacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysisDisplacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysis
ChEMBL 593 11 2 7 5.9 CCCCc1n(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)cc[n+]1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.ejmech.2012.12.044
CHEMBL2365924 88708 0 None - 0 Human 5.8 pIC50 = 5.8 Binding
Displacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysisDisplacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysis
ChEMBL 593 11 2 7 5.9 CCCCc1n(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)cc[n+]1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.ejmech.2012.12.044
76311800 84520 0 None - 0 Rabbit 7.8 pIC50 = 7.8 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 538 11 2 8 5.7 CCCCc1nnc(SCc2ccccc2C)n1Cc1ccc(NC(=O)c2ccccc2-c2nnn[nH]2)cc1 10.1007/s00044-011-9756-4
CHEMBL2237590 84520 0 None - 0 Rabbit 7.8 pIC50 = 7.8 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 538 11 2 8 5.7 CCCCc1nnc(SCc2ccccc2C)n1Cc1ccc(NC(=O)c2ccccc2-c2nnn[nH]2)cc1 10.1007/s00044-011-9756-4
14956784 106062 0 None - 0 Rabbit 7.8 pIC50 = 7.8 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 447 9 1 9 2.5 CCCCc1nn(CC(=O)OC)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
CHEMBL314179 106062 0 None - 0 Rabbit 7.8 pIC50 = 7.8 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 447 9 1 9 2.5 CCCCc1nn(CC(=O)OC)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
14956764 204347 0 None - 0 Rabbit 7.8 pIC50 = 7.8 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 541 8 1 7 5.0 CCCCc1nn(-c2c(F)c(F)c(F)c(F)c2F)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
CHEMBL85541 204347 0 None - 0 Rabbit 7.8 pIC50 = 7.8 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 541 8 1 7 5.0 CCCCc1nn(-c2c(F)c(F)c(F)c(F)c2F)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
11316515 204461 0 None - 0 Rat 7.8 pIC50 = 7.8 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 436 5 1 5 5.6 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2c(C(=O)O)cnc3ccccc23)cc1 10.1021/jm031100t
CHEMBL86437 204461 0 None - 0 Rat 7.8 pIC50 = 7.8 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 436 5 1 5 5.6 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2c(C(=O)O)cnc3ccccc23)cc1 10.1021/jm031100t
9889557 96593 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
Binding affinity to angiotensin AT1 receptorBinding affinity to angiotensin AT1 receptor
ChEMBL 442 7 3 7 2.7 CCCCc1nc2c(=O)[nH][nH]c(=O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.bmc.2010.10.043
CHEMBL267056 96593 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
Binding affinity to angiotensin AT1 receptorBinding affinity to angiotensin AT1 receptor
ChEMBL 442 7 3 7 2.7 CCCCc1nc2c(=O)[nH][nH]c(=O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.bmc.2010.10.043
10028751 164353 0 None - 0 Rabbit 7.8 pIC50 = 7.8 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 495 10 1 7 6.1 CCCCc1nnc(SCc2ccccc2C)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
CHEMBL422333 164353 0 None - 0 Rabbit 7.8 pIC50 = 7.8 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 495 10 1 7 6.1 CCCCc1nnc(SCc2ccccc2C)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
10010164 116881 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 729 11 2 9 6.0 CCCCNC(=O)c1ccc(Br)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1021/jm00019a004
CHEMBL339806 116881 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 729 11 2 9 6.0 CCCCNC(=O)c1ccc(Br)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1021/jm00019a004
14951070 202162 0 None - 0 Rat 7.8 pIC50 = 7.8 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 489 13 2 8 3.9 CCCCc1nn(CCCCCC(=O)O)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a015
CHEMBL68731 202162 0 None - 0 Rat 7.8 pIC50 = 7.8 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 489 13 2 8 3.9 CCCCc1nn(CCCCCC(=O)O)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a015
9930953 102316 0 None - 0 Rat 7.8 pIC50 = 7.8 Binding
Tested for binding affinity against angiotensin II receptor in rat adrenal cortexTested for binding affinity against angiotensin II receptor in rat adrenal cortex
ChEMBL 402 6 1 7 2.4 CCCc1cc(=O)n(C)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/0960-894X(95)00370-9
CHEMBL305350 102316 0 None - 0 Rat 7.8 pIC50 = 7.8 Binding
Tested for binding affinity against angiotensin II receptor in rat adrenal cortexTested for binding affinity against angiotensin II receptor in rat adrenal cortex
ChEMBL 402 6 1 7 2.4 CCCc1cc(=O)n(C)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/0960-894X(95)00370-9
10393086 16325 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 562 12 0 6 6.3 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2Cc2ccc(Cl)cc2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
CHEMBL123670 16325 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 562 12 0 6 6.3 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2Cc2ccc(Cl)cc2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
11758470 112499 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 612 12 0 7 6.5 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2Cc2ccc(Br)s2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
CHEMBL331121 112499 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 612 12 0 7 6.5 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2Cc2ccc(Br)s2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
15780091 120470 0 None - 0 Rabbit 6.8 pIC50 = 6.8 Binding
Displacement of [125 I]Sar1Ile8-AII from type 1 Angiotensin II receptor of rabbit aorta membraneDisplacement of [125 I]Sar1Ile8-AII from type 1 Angiotensin II receptor of rabbit aorta membrane
ChEMBL 618 9 1 8 6.1 CCc1nc2ccc(N(Cc3ccccc3)C(=O)c3ccncc3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80517-5
CHEMBL35638 120470 0 None - 0 Rabbit 6.8 pIC50 = 6.8 Binding
Displacement of [125 I]Sar1Ile8-AII from type 1 Angiotensin II receptor of rabbit aorta membraneDisplacement of [125 I]Sar1Ile8-AII from type 1 Angiotensin II receptor of rabbit aorta membrane
ChEMBL 618 9 1 8 6.1 CCc1nc2ccc(N(Cc3ccccc3)C(=O)c3ccncc3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80517-5
9982960 119329 0 None - 0 Rabbit 6.8 pIC50 = 6.8 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 488 8 1 7 5.7 CCCCc1nn2c(-c3ccccc3)c(C)nc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
CHEMBL348616 119329 0 None - 0 Rabbit 6.8 pIC50 = 6.8 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 488 8 1 7 5.7 CCCCc1nn2c(-c3ccccc3)c(C)nc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
10475047 116929 0 None - 0 Guinea pig 6.8 pIC50 = 6.8 Binding
In vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparationIn vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparation
ChEMBL 383 6 1 3 5.7 CCc1cc(OCc2ccc(-c3ccccc3C(=O)O)cc2)c2ccccc2n1 10.1021/jm00100a007
CHEMBL339846 116929 0 None - 0 Guinea pig 6.8 pIC50 = 6.8 Binding
In vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparationIn vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparation
ChEMBL 383 6 1 3 5.7 CCc1cc(OCc2ccc(-c3ccccc3C(=O)O)cc2)c2ccccc2n1 10.1021/jm00100a007
10141058 202087 0 None - 0 Rat 6.8 pIC50 = 6.8 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 487 14 1 7 5.6 CCCCCCCCn1nc(CCCC)n(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c1=O 10.1021/jm00067a015
CHEMBL68275 202087 0 None - 0 Rat 6.8 pIC50 = 6.8 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 487 14 1 7 5.6 CCCCCCCCn1nc(CCCC)n(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c1=O 10.1021/jm00067a015
10161446 102287 0 None - 0 Bovine 6.8 pIC50 = 6.8 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 456 7 2 7 4.7 CCSc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a016
CHEMBL305190 102287 0 None - 0 Bovine 6.8 pIC50 = 6.8 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 456 7 2 7 4.7 CCSc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a016
15654758 202141 0 None - 0 Bovine 6.8 pIC50 = 6.8 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 425 6 3 7 3.7 CNc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a016
CHEMBL68597 202141 0 None - 0 Bovine 6.8 pIC50 = 6.8 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 425 6 3 7 3.7 CNc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a016
15654742 202362 0 None - 0 Bovine 6.8 pIC50 = 6.8 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 438 7 2 6 4.6 CCCc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a016
CHEMBL70074 202362 0 None - 0 Bovine 6.8 pIC50 = 6.8 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 438 7 2 6 4.6 CCCc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a016
19385675 51084 0 None - 0 Rabbit 6.8 pIC50 = 6.8 Binding
Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)
ChEMBL 445 8 1 6 4.9 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(OC(C(=O)O)c2ccccc2)c(OC)c1 10.1016/0960-894X(95)00185-V
CHEMBL15816 51084 0 None - 0 Rabbit 6.8 pIC50 = 6.8 Binding
Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)
ChEMBL 445 8 1 6 4.9 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(OC(C(=O)O)c2ccccc2)c(OC)c1 10.1016/0960-894X(95)00185-V
10004159 119032 0 None - 0 Rabbit 5.8 pIC50 = 5.8 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 455 9 2 6 4.7 CCCCc1nnc(-c2cccnc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
CHEMBL345894 119032 0 None - 0 Rabbit 5.8 pIC50 = 5.8 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 455 9 2 6 4.7 CCCCc1nnc(-c2cccnc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
44291830 178085 0 None - 0 Rat 5.8 pIC50 = 5.8 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 462 13 1 3 7.1 CCCCC1=NC(CCCC)(CCCC)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00074a018
CHEMBL46782 178085 0 None - 0 Rat 5.8 pIC50 = 5.8 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 462 13 1 3 7.1 CCCCC1=NC(CCCC)(CCCC)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00074a018
10004159 119032 0 None - 0 Rabbit 5.8 pIC50 = 5.8 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 455 9 2 6 4.7 CCCCc1nnc(-c2cccnc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
CHEMBL345894 119032 0 None - 0 Rabbit 5.8 pIC50 = 5.8 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 455 9 2 6 4.7 CCCCc1nnc(-c2cccnc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
44291830 178085 0 None - 0 Rat 5.8 pIC50 = 5.8 Binding
In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.
ChEMBL 462 13 1 3 7.1 CCCCC1=NC(CCCC)(CCCC)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/S0960-894X(01)81140-9
CHEMBL46782 178085 0 None - 0 Rat 5.8 pIC50 = 5.8 Binding
In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.
ChEMBL 462 13 1 3 7.1 CCCCC1=NC(CCCC)(CCCC)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/S0960-894X(01)81140-9
11741660 116630 0 None - 0 Rat 5.8 pIC50 = 5.8 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 399 7 2 4 5.4 CCCCc1nc2c(N)cccc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00077a007
CHEMBL339360 116630 0 None - 0 Rat 5.8 pIC50 = 5.8 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 399 7 2 4 5.4 CCCCc1nc2c(N)cccc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00077a007
4823 93116 86 None - 0 Bovine 4.8 pIC50 = 4.8 Binding
Concentration required for 50% inhibition of binding against Angiotensin II receptor, type 1 in bovine adrenal cortexConcentration required for 50% inhibition of binding against Angiotensin II receptor, type 1 in bovine adrenal cortex
ChEMBL 334 3 2 4 3.1 COc1ccc(-c2nc3cc(C4=NNC(=O)CC4C)ccc3[nH]2)cc1 10.1016/S0960-894X(01)80348-6
CHEMBL24646 93116 86 None - 0 Bovine 4.8 pIC50 = 4.8 Binding
Concentration required for 50% inhibition of binding against Angiotensin II receptor, type 1 in bovine adrenal cortexConcentration required for 50% inhibition of binding against Angiotensin II receptor, type 1 in bovine adrenal cortex
ChEMBL 334 3 2 4 3.1 COc1ccc(-c2nc3cc(C4=NNC(=O)CC4C)ccc3[nH]2)cc1 10.1016/S0960-894X(01)80348-6
164620345 185621 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Displacement of [125-I]-[Sar1, Ile8] from recombinant human AT1R transfected in human HEK293 cells incubated for 2 hrs by liquid scintillation counter analysisDisplacement of [125-I]-[Sar1, Ile8] from recombinant human AT1R transfected in human HEK293 cells incubated for 2 hrs by liquid scintillation counter analysis
ChEMBL 1084 26 13 13 0.1 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H](N)CC(=O)O)C(C)C)C(=O)N1Cc2ccc(O)cc2C[C@H]1C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O 10.1016/j.bmcl.2021.128086
CHEMBL4873167 185621 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Displacement of [125-I]-[Sar1, Ile8] from recombinant human AT1R transfected in human HEK293 cells incubated for 2 hrs by liquid scintillation counter analysisDisplacement of [125-I]-[Sar1, Ile8] from recombinant human AT1R transfected in human HEK293 cells incubated for 2 hrs by liquid scintillation counter analysis
ChEMBL 1084 26 13 13 0.1 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H](N)CC(=O)O)C(C)C)C(=O)N1Cc2ccc(O)cc2C[C@H]1C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O 10.1016/j.bmcl.2021.128086
44296955 192999 0 None - 0 Bovine 6.8 pIC50 = 6.8 Binding
In vitro binding affinity to angiotensin II receptor in bovine adrenal cortexIn vitro binding affinity to angiotensin II receptor in bovine adrenal cortex
ChEMBL 653 10 1 10 5.7 CCCCc1nc2ccc([C@H]3[C@@H]4C(=O)OC[C@@H]4ON3Cc3ccccc3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80377-2
CHEMBL53226 192999 0 None - 0 Bovine 6.8 pIC50 = 6.8 Binding
In vitro binding affinity to angiotensin II receptor in bovine adrenal cortexIn vitro binding affinity to angiotensin II receptor in bovine adrenal cortex
ChEMBL 653 10 1 10 5.7 CCCCc1nc2ccc([C@H]3[C@@H]4C(=O)OC[C@@H]4ON3Cc3ccccc3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80377-2
14956741 106558 0 None - 0 Rabbit 7.8 pIC50 = 7.8 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 465 8 1 7 4.6 CCCCc1nn(-c2cccc(C)c2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
CHEMBL315615 106558 0 None - 0 Rabbit 7.8 pIC50 = 7.8 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 465 8 1 7 4.6 CCCCc1nn(-c2cccc(C)c2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
44341731 10088 0 None - 0 Rat 7.8 pIC50 = 7.8 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 461 7 1 4 4.4 CCCCC1=NC2(CCN(C(C)=O)CC2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00074a018
CHEMBL115984 10088 0 None - 0 Rat 7.8 pIC50 = 7.8 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 461 7 1 4 4.4 CCCCC1=NC2(CCN(C(C)=O)CC2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00074a018
19889373 204447 0 None - 0 Rat 7.8 pIC50 = 7.8 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 410 5 1 7 3.9 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ncccc2-c2nn[nH]n2)cc1 10.1021/jm031100t
CHEMBL86346 204447 0 None - 0 Rat 7.8 pIC50 = 7.8 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 410 5 1 7 3.9 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ncccc2-c2nn[nH]n2)cc1 10.1021/jm031100t
1610 2305 89 None - 4 Guinea pig 7.8 pIC50 = 7.8 Binding
Compound was tested for in vitro inhibition of specific binding of [I-125]AII to Angiotensin II receptor, type 1 in guinea pig adrenal membrane preparationCompound was tested for in vitro inhibition of specific binding of [I-125]AII to Angiotensin II receptor, type 1 in guinea pig adrenal membrane preparation
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(01)80295-X
3941 2305 89 None - 4 Guinea pig 7.8 pIC50 = 7.8 Binding
Compound was tested for in vitro inhibition of specific binding of [I-125]AII to Angiotensin II receptor, type 1 in guinea pig adrenal membrane preparationCompound was tested for in vitro inhibition of specific binding of [I-125]AII to Angiotensin II receptor, type 1 in guinea pig adrenal membrane preparation
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(01)80295-X
3961 2305 89 None - 4 Guinea pig 7.8 pIC50 = 7.8 Binding
Compound was tested for in vitro inhibition of specific binding of [I-125]AII to Angiotensin II receptor, type 1 in guinea pig adrenal membrane preparationCompound was tested for in vitro inhibition of specific binding of [I-125]AII to Angiotensin II receptor, type 1 in guinea pig adrenal membrane preparation
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(01)80295-X
590 2305 89 None - 4 Guinea pig 7.8 pIC50 = 7.8 Binding
Compound was tested for in vitro inhibition of specific binding of [I-125]AII to Angiotensin II receptor, type 1 in guinea pig adrenal membrane preparationCompound was tested for in vitro inhibition of specific binding of [I-125]AII to Angiotensin II receptor, type 1 in guinea pig adrenal membrane preparation
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(01)80295-X
CHEMBL191 2305 89 None - 4 Guinea pig 7.8 pIC50 = 7.8 Binding
Compound was tested for in vitro inhibition of specific binding of [I-125]AII to Angiotensin II receptor, type 1 in guinea pig adrenal membrane preparationCompound was tested for in vitro inhibition of specific binding of [I-125]AII to Angiotensin II receptor, type 1 in guinea pig adrenal membrane preparation
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(01)80295-X
DB00678 2305 89 None - 4 Guinea pig 7.8 pIC50 = 7.8 Binding
Compound was tested for in vitro inhibition of specific binding of [I-125]AII to Angiotensin II receptor, type 1 in guinea pig adrenal membrane preparationCompound was tested for in vitro inhibition of specific binding of [I-125]AII to Angiotensin II receptor, type 1 in guinea pig adrenal membrane preparation
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(01)80295-X
24827770 95423 0 None - 1 Rat 7.8 pIC50 = 7.8 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
ChEMBL 425 7 1 7 3.9 CCCCn1c(=O)c2cccnc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm7011563
CHEMBL259114 95423 0 None - 1 Rat 7.8 pIC50 = 7.8 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
ChEMBL 425 7 1 7 3.9 CCCCn1c(=O)c2cccnc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm7011563
19422638 173634 0 None - 0 Rat 7.8 pIC50 = 7.8 Binding
In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.
ChEMBL 404 8 1 3 5.2 CCCCC1=NC(C)(C2CC2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/S0960-894X(01)81140-9
CHEMBL45485 173634 0 None - 0 Rat 7.8 pIC50 = 7.8 Binding
In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.
ChEMBL 404 8 1 3 5.2 CCCCC1=NC(C)(C2CC2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/S0960-894X(01)81140-9
1610 2305 89 None - 4 Guinea pig 7.8 pIC50 = 7.8 Binding
In vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparationIn vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparation
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00100a007
3941 2305 89 None - 4 Guinea pig 7.8 pIC50 = 7.8 Binding
In vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparationIn vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparation
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00100a007
3961 2305 89 None - 4 Guinea pig 7.8 pIC50 = 7.8 Binding
In vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparationIn vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparation
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00100a007
590 2305 89 None - 4 Guinea pig 7.8 pIC50 = 7.8 Binding
In vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparationIn vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparation
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00100a007
CHEMBL191 2305 89 None - 4 Guinea pig 7.8 pIC50 = 7.8 Binding
In vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparationIn vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparation
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00100a007
DB00678 2305 89 None - 4 Guinea pig 7.8 pIC50 = 7.8 Binding
In vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparationIn vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparation
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00100a007
10099830 107992 0 None - 0 Rabbit 7.8 pIC50 = 7.8 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 584 9 1 7 4.9 CCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)C2CC2)cc1 10.1021/jm00043a020
CHEMBL319955 107992 0 None - 0 Rabbit 7.8 pIC50 = 7.8 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 584 9 1 7 4.9 CCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)C2CC2)cc1 10.1021/jm00043a020
44315349 60056 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membrane
ChEMBL 679 10 2 9 5.1 CCc1nc2ccc(NC(=O)N3CCOCC3)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/0960-894X(94)85036-4
CHEMBL17487 60056 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membrane
ChEMBL 679 10 2 9 5.1 CCc1nc2ccc(NC(=O)N3CCOCC3)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/0960-894X(94)85036-4
1610 2305 89 None - 4 Guinea pig 7.8 pIC50 = 7.8 Binding
Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00061a016
3941 2305 89 None - 4 Guinea pig 7.8 pIC50 = 7.8 Binding
Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00061a016
3961 2305 89 None - 4 Guinea pig 7.8 pIC50 = 7.8 Binding
Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00061a016
590 2305 89 None - 4 Guinea pig 7.8 pIC50 = 7.8 Binding
Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00061a016
CHEMBL191 2305 89 None - 4 Guinea pig 7.8 pIC50 = 7.8 Binding
Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00061a016
DB00678 2305 89 None - 4 Guinea pig 7.8 pIC50 = 7.8 Binding
Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00061a016
10140958 102522 0 None - 0 Rat 7.8 pIC50 = 7.8 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 485 10 1 7 5.3 CCCCc1nn(CCC2CCCCC2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a015
CHEMBL306882 102522 0 None - 0 Rat 7.8 pIC50 = 7.8 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 485 10 1 7 5.3 CCCCc1nn(CCC2CCCCC2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a015
14956804 105506 0 None - 0 Rat 7.8 pIC50 = 7.8 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 493 11 1 7 4.9 CCCCc1nn(CCCc2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a015
CHEMBL313222 105506 0 None - 0 Rat 7.8 pIC50 = 7.8 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 493 11 1 7 4.9 CCCCc1nn(CCCc2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a015
15287891 123161 0 None - 0 Rabbit 7.8 pIC50 = 7.8 Binding
Tested in vitro for Angiotensin II receptor, type 1 binding affinity using rabbit aorta binding assayTested in vitro for Angiotensin II receptor, type 1 binding affinity using rabbit aorta binding assay
ChEMBL 459 10 1 6 5.3 CCCc1nc2c(C)ccnc2n1Cc1ccc(OC(C(=O)O)c2ccccc2OCC)cc1 10.1016/0960-894X(94)00476-V
CHEMBL36218 123161 0 None - 0 Rabbit 7.8 pIC50 = 7.8 Binding
Tested in vitro for Angiotensin II receptor, type 1 binding affinity using rabbit aorta binding assayTested in vitro for Angiotensin II receptor, type 1 binding affinity using rabbit aorta binding assay
ChEMBL 459 10 1 6 5.3 CCCc1nc2c(C)ccnc2n1Cc1ccc(OC(C(=O)O)c2ccccc2OCC)cc1 10.1016/0960-894X(94)00476-V
10007528 16102 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 542 12 0 6 6.0 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2Cc2cccc(C)c2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
CHEMBL122490 16102 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 542 12 0 6 6.0 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2Cc2cccc(C)c2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
44277595 6232 0 None - 0 Rabbit 7.7 pIC50 = 7.7 Binding
Binding affinity against AT1 receptor in rabbit aortaBinding affinity against AT1 receptor in rabbit aorta
ChEMBL 621 9 0 10 5.4 Cn1nnnc1-c1ccccc1-c1ccc(Cn2cnc3ccc(N(CC(=O)c4ccco4)C(=O)c4ccccc4)cc3c2=O)cc1 10.1016/0960-894X(95)00224-H
CHEMBL108190 6232 0 None - 0 Rabbit 7.7 pIC50 = 7.7 Binding
Binding affinity against AT1 receptor in rabbit aortaBinding affinity against AT1 receptor in rabbit aorta
ChEMBL 621 9 0 10 5.4 Cn1nnnc1-c1ccccc1-c1ccc(Cn2cnc3ccc(N(CC(=O)c4ccco4)C(=O)c4ccccc4)cc3c2=O)cc1 10.1016/0960-894X(95)00224-H
44294996 189191 0 None - 1 Bovine 6.8 pIC50 = 6.8 Binding
Ability to displace [125I]- labelled [Sar1,Ileu8] from angiotensin II receptor of bovine adrenal cortex membranesAbility to displace [125I]- labelled [Sar1,Ileu8] from angiotensin II receptor of bovine adrenal cortex membranes
ChEMBL 501 10 1 6 5.7 CCCCC1(CC)CC(=O)N(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/C(=C/C(=O)OCC)C1 10.1016/S0960-894X(00)80474-6
CHEMBL51622 189191 0 None - 1 Bovine 6.8 pIC50 = 6.8 Binding
Ability to displace [125I]- labelled [Sar1,Ileu8] from angiotensin II receptor of bovine adrenal cortex membranesAbility to displace [125I]- labelled [Sar1,Ileu8] from angiotensin II receptor of bovine adrenal cortex membranes
ChEMBL 501 10 1 6 5.7 CCCCC1(CC)CC(=O)N(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/C(=C/C(=O)OCC)C1 10.1016/S0960-894X(00)80474-6
44293657 175074 0 None - 0 Rat 6.8 pIC50 = 6.8 Binding
Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.
ChEMBL 534 12 3 6 5.3 CCCCc1nc(Cl)c(CO)n1Cc1ccc(NC(=O)[C@H](Cc2ccccc2)n2cccc2C(=O)O)cc1 10.1021/jm00064a007
CHEMBL45814 175074 0 None - 0 Rat 6.8 pIC50 = 6.8 Binding
Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.
ChEMBL 534 12 3 6 5.3 CCCCc1nc(Cl)c(CO)n1Cc1ccc(NC(=O)[C@H](Cc2ccccc2)n2cccc2C(=O)O)cc1 10.1021/jm00064a007
44293954 187106 0 None - 0 Rat 6.8 pIC50 = 6.8 Binding
Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.
ChEMBL 554 12 3 7 5.6 CCCCc1nc(Cl)c(C(=O)O)n1Cc1ccc(NC(=O)[C@H](Cc2cccs2)n2cccc2C(=O)O)cc1 10.1021/jm00064a007
CHEMBL49526 187106 0 None - 0 Rat 6.8 pIC50 = 6.8 Binding
Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.
ChEMBL 554 12 3 7 5.6 CCCCc1nc(Cl)c(C(=O)O)n1Cc1ccc(NC(=O)[C@H](Cc2cccs2)n2cccc2C(=O)O)cc1 10.1021/jm00064a007
44296985 192920 0 None - 0 Bovine 6.8 pIC50 = 6.8 Binding
In vitro binding affinity to angiotensin II receptor in bovine adrenal cortexIn vitro binding affinity to angiotensin II receptor in bovine adrenal cortex
ChEMBL 603 8 1 8 6.9 CCCCc1nc2ccc([C@H]3C4CCCCCCC4ON3C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80377-2
CHEMBL52880 192920 0 None - 0 Bovine 6.8 pIC50 = 6.8 Binding
In vitro binding affinity to angiotensin II receptor in bovine adrenal cortexIn vitro binding affinity to angiotensin II receptor in bovine adrenal cortex
ChEMBL 603 8 1 8 6.9 CCCCc1nc2ccc([C@H]3C4CCCCCCC4ON3C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80377-2
10453972 21972 0 None - 0 Guinea pig 6.8 pIC50 = 6.8 Binding
In vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparationIn vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparation
ChEMBL 369 5 1 3 5.5 Cc1cc(OCc2ccc(-c3ccccc3C(=O)O)cc2)c2ccccc2n1 10.1021/jm00100a007
CHEMBL132269 21972 0 None - 0 Guinea pig 6.8 pIC50 = 6.8 Binding
In vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparationIn vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparation
ChEMBL 369 5 1 3 5.5 Cc1cc(OCc2ccc(-c3ccccc3C(=O)O)cc2)c2ccccc2n1 10.1021/jm00100a007
14951081 201988 0 None - 0 Rat 6.8 pIC50 = 6.8 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 581 14 1 10 4.6 CCCCc1nn(CC(OCC(=O)OCC)c2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a015
CHEMBL67515 201988 0 None - 0 Rat 6.8 pIC50 = 6.8 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 581 14 1 10 4.6 CCCCc1nn(CC(OCC(=O)OCC)c2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a015
10366029 114699 0 None - 0 Rat 6.8 pIC50 = 6.8 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 441 8 2 4 5.8 CCCCc1nc2ccc(NC(C)=O)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00077a007
CHEMBL334515 114699 0 None - 0 Rat 6.8 pIC50 = 6.8 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 441 8 2 4 5.8 CCCCc1nc2ccc(NC(C)=O)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00077a007
44381714 58794 0 None - 0 Rabbit 6.8 pIC50 = 6.8 Binding
Tested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membraneTested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membrane
ChEMBL 732 11 1 7 7.6 CCc1nc2ccc(N(Cc3ccccc3)C(=O)c3ccccc3)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/S0960-894X(01)81126-4
CHEMBL169827 58794 0 None - 0 Rabbit 6.8 pIC50 = 6.8 Binding
Tested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membraneTested in vitro for binding affinity against Angiotensin II receptor, type 1 in rabbit aortic membrane
ChEMBL 732 11 1 7 7.6 CCc1nc2ccc(N(Cc3ccccc3)C(=O)c3ccccc3)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/S0960-894X(01)81126-4
44341801 9694 0 None - 0 Rat 5.8 pIC50 = 5.8 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 404 7 1 3 5.3 CCCCC1=NC(=O)C2(CCCC2)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00074a018
CHEMBL113701 9694 0 None - 0 Rat 5.8 pIC50 = 5.8 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 404 7 1 3 5.3 CCCCC1=NC(=O)C2(CCCC2)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00074a018
44341772 110090 0 None - 0 Rat 5.8 pIC50 = 5.8 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 418 7 0 4 5.4 CCCCC1=NC2(CCCC2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)OC)cc1 10.1021/jm00074a018
CHEMBL325502 110090 0 None - 0 Rat 5.8 pIC50 = 5.8 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 418 7 0 4 5.4 CCCCC1=NC2(CCCC2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)OC)cc1 10.1021/jm00074a018
44321129 110966 0 None - 0 Rat 5.8 pIC50 = 5.8 Binding
Displacement of [125-I]-labeled angiotensin II from Angiotensin II receptor, type 1 of rat uterine membranesDisplacement of [125-I]-labeled angiotensin II from Angiotensin II receptor, type 1 of rat uterine membranes
ChEMBL 457 8 1 7 5.0 CCCCn1nc2n(c1=O)C(c1ccc(-c3ccccc3-c3nn[nH]n3)cc1)CCC2CCC 10.1016/S0960-894X(01)80290-0
CHEMBL327614 110966 0 None - 0 Rat 5.8 pIC50 = 5.8 Binding
Displacement of [125-I]-labeled angiotensin II from Angiotensin II receptor, type 1 of rat uterine membranesDisplacement of [125-I]-labeled angiotensin II from Angiotensin II receptor, type 1 of rat uterine membranes
ChEMBL 457 8 1 7 5.0 CCCCn1nc2n(c1=O)C(c1ccc(-c3ccccc3-c3nn[nH]n3)cc1)CCC2CCC 10.1016/S0960-894X(01)80290-0
10026315 115591 0 None - 0 Rat 5.8 pIC50 = 5.8 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 441 8 2 4 5.8 CCCCc1nc2cccc(NC(C)=O)c2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00077a007
CHEMBL335734 115591 0 None - 0 Rat 5.8 pIC50 = 5.8 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 441 8 2 4 5.8 CCCCc1nc2cccc(NC(C)=O)c2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00077a007
24827899 96428 0 None - 0 Rat 5.7 pIC50 = 5.7 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
ChEMBL 411 5 1 7 3.4 CCn1c(=O)c2ccc(C)nc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm7011563
CHEMBL265697 96428 0 None - 0 Rat 5.7 pIC50 = 5.7 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
ChEMBL 411 5 1 7 3.4 CCn1c(=O)c2ccc(C)nc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm7011563
1610 2305 89 None -1 4 Rat 7.7 pIC50 = 7.7 Binding
Concentration required to inhibit binding of radioligand [125I]AII to angiotensin II receptor, type 1 in rat adrenal glomerulosa tissueConcentration required to inhibit binding of radioligand [125I]AII to angiotensin II receptor, type 1 in rat adrenal glomerulosa tissue
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00092a017
3941 2305 89 None -1 4 Rat 7.7 pIC50 = 7.7 Binding
Concentration required to inhibit binding of radioligand [125I]AII to angiotensin II receptor, type 1 in rat adrenal glomerulosa tissueConcentration required to inhibit binding of radioligand [125I]AII to angiotensin II receptor, type 1 in rat adrenal glomerulosa tissue
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00092a017
3961 2305 89 None -1 4 Rat 7.7 pIC50 = 7.7 Binding
Concentration required to inhibit binding of radioligand [125I]AII to angiotensin II receptor, type 1 in rat adrenal glomerulosa tissueConcentration required to inhibit binding of radioligand [125I]AII to angiotensin II receptor, type 1 in rat adrenal glomerulosa tissue
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00092a017
590 2305 89 None -1 4 Rat 7.7 pIC50 = 7.7 Binding
Concentration required to inhibit binding of radioligand [125I]AII to angiotensin II receptor, type 1 in rat adrenal glomerulosa tissueConcentration required to inhibit binding of radioligand [125I]AII to angiotensin II receptor, type 1 in rat adrenal glomerulosa tissue
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00092a017
CHEMBL191 2305 89 None -1 4 Rat 7.7 pIC50 = 7.7 Binding
Concentration required to inhibit binding of radioligand [125I]AII to angiotensin II receptor, type 1 in rat adrenal glomerulosa tissueConcentration required to inhibit binding of radioligand [125I]AII to angiotensin II receptor, type 1 in rat adrenal glomerulosa tissue
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00092a017
DB00678 2305 89 None -1 4 Rat 7.7 pIC50 = 7.7 Binding
Concentration required to inhibit binding of radioligand [125I]AII to angiotensin II receptor, type 1 in rat adrenal glomerulosa tissueConcentration required to inhibit binding of radioligand [125I]AII to angiotensin II receptor, type 1 in rat adrenal glomerulosa tissue
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00092a017
44348302 16299 0 None - 0 Rabbit 7.7 pIC50 = 7.7 Binding
Displacement of [1251][Sar1,IIe8]AII from rabbit aorta Angiotensin II receptor, type 1Displacement of [1251][Sar1,IIe8]AII from rabbit aorta Angiotensin II receptor, type 1
ChEMBL 527 12 1 5 7.3 CCCc1cc(Cn2c(CC)nc3c(C)cc(C)nc32)cc(CCC)c1OC(C(=O)O)c1ccc(CC)cc1 10.1021/jm00075a033
CHEMBL123562 16299 0 None - 0 Rabbit 7.7 pIC50 = 7.7 Binding
Displacement of [1251][Sar1,IIe8]AII from rabbit aorta Angiotensin II receptor, type 1Displacement of [1251][Sar1,IIe8]AII from rabbit aorta Angiotensin II receptor, type 1
ChEMBL 527 12 1 5 7.3 CCCc1cc(Cn2c(CC)nc3c(C)cc(C)nc32)cc(CCC)c1OC(C(=O)O)c1ccc(CC)cc1 10.1021/jm00075a033
44438870 91559 0 None - 1 Bovine 7.7 pIC50 = 7.7 Binding
Displacement of [125I]angiotensin-2 from bovine adrenal cortex AT1 receptorDisplacement of [125I]angiotensin-2 from bovine adrenal cortex AT1 receptor
ChEMBL 469 9 1 8 4.6 CCCCc1nc2cccc(C(=O)OCC)c2n1Cc1ccc(-n2cccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2007.02.042
CHEMBL241685 91559 0 None - 1 Bovine 7.7 pIC50 = 7.7 Binding
Displacement of [125I]angiotensin-2 from bovine adrenal cortex AT1 receptorDisplacement of [125I]angiotensin-2 from bovine adrenal cortex AT1 receptor
ChEMBL 469 9 1 8 4.6 CCCCc1nc2cccc(C(=O)OCC)c2n1Cc1ccc(-n2cccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2007.02.042
44291438 183239 0 None - 0 Rat 7.7 pIC50 = 7.7 Binding
In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.
ChEMBL 440 8 1 3 5.9 CCCCC1=NC(C)(c2ccccc2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/S0960-894X(01)81140-9
CHEMBL48062 183239 0 None - 0 Rat 7.7 pIC50 = 7.7 Binding
In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.
ChEMBL 440 8 1 3 5.9 CCCCC1=NC(C)(c2ccccc2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/S0960-894X(01)81140-9
44348302 16299 0 None - 0 Rabbit 7.7 pIC50 = 7.7 Binding
Inhibition of Angiotensin II receptor, type 1Inhibition of Angiotensin II receptor, type 1
ChEMBL 527 12 1 5 7.3 CCCc1cc(Cn2c(CC)nc3c(C)cc(C)nc32)cc(CCC)c1OC(C(=O)O)c1ccc(CC)cc1 10.1021/jm9504722
CHEMBL123562 16299 0 None - 0 Rabbit 7.7 pIC50 = 7.7 Binding
Inhibition of Angiotensin II receptor, type 1Inhibition of Angiotensin II receptor, type 1
ChEMBL 527 12 1 5 7.3 CCCc1cc(Cn2c(CC)nc3c(C)cc(C)nc32)cc(CCC)c1OC(C(=O)O)c1ccc(CC)cc1 10.1021/jm9504722
1610 2305 89 None -1 4 Rat 7.7 pIC50 = 7.7 Binding
Displacement of [125I]-Ang II from Angiotensin 2 type-1A receptor in rat vascular smooth muscle cells after 150 mins by gamma counting methodDisplacement of [125I]-Ang II from Angiotensin 2 type-1A receptor in rat vascular smooth muscle cells after 150 mins by gamma counting method
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmc.2016.03.028
3941 2305 89 None -1 4 Rat 7.7 pIC50 = 7.7 Binding
Displacement of [125I]-Ang II from Angiotensin 2 type-1A receptor in rat vascular smooth muscle cells after 150 mins by gamma counting methodDisplacement of [125I]-Ang II from Angiotensin 2 type-1A receptor in rat vascular smooth muscle cells after 150 mins by gamma counting method
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmc.2016.03.028
3961 2305 89 None -1 4 Rat 7.7 pIC50 = 7.7 Binding
Displacement of [125I]-Ang II from Angiotensin 2 type-1A receptor in rat vascular smooth muscle cells after 150 mins by gamma counting methodDisplacement of [125I]-Ang II from Angiotensin 2 type-1A receptor in rat vascular smooth muscle cells after 150 mins by gamma counting method
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmc.2016.03.028
590 2305 89 None -1 4 Rat 7.7 pIC50 = 7.7 Binding
Displacement of [125I]-Ang II from Angiotensin 2 type-1A receptor in rat vascular smooth muscle cells after 150 mins by gamma counting methodDisplacement of [125I]-Ang II from Angiotensin 2 type-1A receptor in rat vascular smooth muscle cells after 150 mins by gamma counting method
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmc.2016.03.028
CHEMBL191 2305 89 None -1 4 Rat 7.7 pIC50 = 7.7 Binding
Displacement of [125I]-Ang II from Angiotensin 2 type-1A receptor in rat vascular smooth muscle cells after 150 mins by gamma counting methodDisplacement of [125I]-Ang II from Angiotensin 2 type-1A receptor in rat vascular smooth muscle cells after 150 mins by gamma counting method
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmc.2016.03.028
DB00678 2305 89 None -1 4 Rat 7.7 pIC50 = 7.7 Binding
Displacement of [125I]-Ang II from Angiotensin 2 type-1A receptor in rat vascular smooth muscle cells after 150 mins by gamma counting methodDisplacement of [125I]-Ang II from Angiotensin 2 type-1A receptor in rat vascular smooth muscle cells after 150 mins by gamma counting method
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmc.2016.03.028
71521299 86382 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor afterDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after
ChEMBL 479 6 1 7 4.8 CCc1nc2ccn(CC(C)C)c(=O)c2n1[C@H]1CCc2cc(-c3ccccc3-c3nnn[nH]3)ccc21 10.1016/j.bmcl.2012.11.088
CHEMBL2322441 86382 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor afterDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after
ChEMBL 479 6 1 7 4.8 CCc1nc2ccn(CC(C)C)c(=O)c2n1[C@H]1CCc2cc(-c3ccccc3-c3nnn[nH]3)ccc21 10.1016/j.bmcl.2012.11.088
127036102 135978 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 531 9 2 4 7.2 CCCc1nc2c(C)cc(C(=O)N[C@@H](C)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2015.09.010
CHEMBL3736295 135978 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 531 9 2 4 7.2 CCCc1nc2c(C)cc(C(=O)N[C@@H](C)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2015.09.010
CHEMBL5075338 212587 0 None - 1 Human 7.7 pIC50 = 7.7 Binding
Displacement of [125-I]-[Sar1, AngII from AT1R (unknown origin) expressed in Escherichia coli BL 21 (DE3) incubated for 2 hrs by radioimmunoassayDisplacement of [125-I]-[Sar1, AngII from AT1R (unknown origin) expressed in Escherichia coli BL 21 (DE3) incubated for 2 hrs by radioimmunoassay
ChEMBL None None None CCOC(=O)[C@@H](Cc1ccc(F)cc1)NC(=O)[C@@H](CC1CCCCC1)NC(=O)[C@@H](C)NC(=O)/C=C/c1ccc(O)c(O)c1 10.1021/acs.jmedchem.1c00123
70686409 75958 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Displacement of [125I]Sar1Ile8-Ang2 from angiotensin AT1 receptor after 180 mins by gamma countingDisplacement of [125I]Sar1Ile8-Ang2 from angiotensin AT1 receptor after 180 mins by gamma counting
ChEMBL 571 10 2 7 6.1 CCCc1nc2c(C)cc(C(=O)NCc3ccccc3OC)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmc.2012.05.056
CHEMBL2058855 75958 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Displacement of [125I]Sar1Ile8-Ang2 from angiotensin AT1 receptor after 180 mins by gamma countingDisplacement of [125I]Sar1Ile8-Ang2 from angiotensin AT1 receptor after 180 mins by gamma counting
ChEMBL 571 10 2 7 6.1 CCCc1nc2c(C)cc(C(=O)NCc3ccccc3OC)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmc.2012.05.056
71521196 86380 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor afterDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after
ChEMBL 571 8 1 9 4.9 CCc1nc2ccn(CC(=O)OCc3ccccc3)c(=O)c2n1[C@H]1CCc2cc(-c3ccccc3-c3nnn[nH]3)ccc21 10.1016/j.bmcl.2012.11.088
CHEMBL2322439 86380 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor afterDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after
ChEMBL 571 8 1 9 4.9 CCc1nc2ccn(CC(=O)OCc3ccccc3)c(=O)c2n1[C@H]1CCc2cc(-c3ccccc3-c3nnn[nH]3)ccc21 10.1016/j.bmcl.2012.11.088
10098452 51150 0 None - 0 Rabbit 6.7 pIC50 = 6.7 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 528 12 2 7 5.6 CCCCc1nnc(SCC(=O)c2ccccc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
CHEMBL158209 51150 0 None - 0 Rabbit 6.7 pIC50 = 6.7 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 528 12 2 7 5.6 CCCCc1nnc(SCC(=O)c2ccccc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
44341651 109981 0 None - 0 Rat 6.7 pIC50 = 6.7 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 406 7 2 3 4.8 CCCCC1NC2(CCCC2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00074a018
CHEMBL324785 109981 0 None - 0 Rat 6.7 pIC50 = 6.7 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 406 7 2 3 4.8 CCCCC1NC2(CCCC2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00074a018
10098452 51150 0 None - 0 Rabbit 6.7 pIC50 = 6.7 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 528 12 2 7 5.6 CCCCc1nnc(SCC(=O)c2ccccc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
CHEMBL158209 51150 0 None - 0 Rabbit 6.7 pIC50 = 6.7 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 528 12 2 7 5.6 CCCCc1nnc(SCC(=O)c2ccccc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
15231798 204706 0 None - 0 Rat 6.7 pIC50 = 6.7 Binding
Inhibition of [125-I]-labeled angiotensin II binding to AT1 receptor in rat uterine membranesInhibition of [125-I]-labeled angiotensin II binding to AT1 receptor in rat uterine membranes
ChEMBL 452 9 1 5 6.4 CCCCc1nc(CCCC)n2c1C=CCC2c1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80290-0
CHEMBL88014 204706 0 None - 0 Rat 6.7 pIC50 = 6.7 Binding
Inhibition of [125-I]-labeled angiotensin II binding to AT1 receptor in rat uterine membranesInhibition of [125-I]-labeled angiotensin II binding to AT1 receptor in rat uterine membranes
ChEMBL 452 9 1 5 6.4 CCCCc1nc(CCCC)n2c1C=CCC2c1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80290-0
14950502 85194 0 None - 0 Guinea pig 6.7 pIC50 = 6.7 Binding
Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1
ChEMBL 385 6 1 6 3.9 Cc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c(C=O)c(C)n1 10.1021/jm00061a016
CHEMBL22837 85194 0 None - 0 Guinea pig 6.7 pIC50 = 6.7 Binding
Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1
ChEMBL 385 6 1 6 3.9 Cc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c(C=O)c(C)n1 10.1021/jm00061a016
15654756 101914 0 None - 0 Bovine 6.7 pIC50 = 6.7 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 454 8 2 7 4.4 CCCOc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a016
CHEMBL303955 101914 0 None - 0 Bovine 6.7 pIC50 = 6.7 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 454 8 2 7 4.4 CCCOc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a016
15654741 202277 0 None - 0 Bovine 6.7 pIC50 = 6.7 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 410 5 2 6 3.9 Cc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a016
CHEMBL69522 202277 0 None - 0 Bovine 6.7 pIC50 = 6.7 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 410 5 2 6 3.9 Cc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a016
22596780 202685 1 None - 0 Bovine 6.7 pIC50 = 6.7 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 416 7 2 5 4.5 CCOc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00067a016
CHEMBL71954 202685 1 None - 0 Bovine 6.7 pIC50 = 6.7 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 416 7 2 5 4.5 CCOc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00067a016
10321914 119530 0 None - 0 Rabbit 5.7 pIC50 = 5.7 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 458 8 2 6 5.1 CCSc1nnc(-c2ccccc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
CHEMBL350446 119530 0 None - 0 Rabbit 5.7 pIC50 = 5.7 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 458 8 2 6 5.1 CCSc1nnc(-c2ccccc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
10321914 119530 0 None - 0 Rabbit 5.7 pIC50 = 5.7 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 458 8 2 6 5.1 CCSc1nnc(-c2ccccc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
CHEMBL350446 119530 0 None - 0 Rabbit 5.7 pIC50 = 5.7 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 458 8 2 6 5.1 CCSc1nnc(-c2ccccc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
54768661 64772 0 None - 0 Human 5.7 pIC50 = 5.7 Binding
Displacement of [125I][Sar1,Ile8]-AT-II from human recombinant AT1 receptor expressed in HEK293 cells after 120 mins by liquid scintillation countingDisplacement of [125I][Sar1,Ile8]-AT-II from human recombinant AT1 receptor expressed in HEK293 cells after 120 mins by liquid scintillation counting
ChEMBL 535 8 1 8 5.3 CCOC(=O)c1cn(Cc2ccc(-c3ccccc3-c3nnn[nH]3)cc2)nc1N(C(C)=O)c1cc(C)cc(C)c1 10.1016/j.ejmech.2011.05.056
CHEMBL1824001 64772 0 None - 0 Human 5.7 pIC50 = 5.7 Binding
Displacement of [125I][Sar1,Ile8]-AT-II from human recombinant AT1 receptor expressed in HEK293 cells after 120 mins by liquid scintillation countingDisplacement of [125I][Sar1,Ile8]-AT-II from human recombinant AT1 receptor expressed in HEK293 cells after 120 mins by liquid scintillation counting
ChEMBL 535 8 1 8 5.3 CCOC(=O)c1cn(Cc2ccc(-c3ccccc3-c3nnn[nH]3)cc2)nc1N(C(C)=O)c1cc(C)cc(C)c1 10.1016/j.ejmech.2011.05.056
44293991 101197 0 None - 0 Rat 5.7 pIC50 = 5.7 Binding
Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.
ChEMBL 532 12 1 6 5.9 CCCCc1nc(Cl)c(CC(=O)OC)n1Cc1ccc(NC(=O)[C@H](Cc2ccccc2)n2cccc2)cc1 10.1021/jm00064a007
CHEMBL299324 101197 0 None - 0 Rat 5.7 pIC50 = 5.7 Binding
Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.
ChEMBL 532 12 1 6 5.9 CCCCc1nc(Cl)c(CC(=O)OC)n1Cc1ccc(NC(=O)[C@H](Cc2ccccc2)n2cccc2)cc1 10.1021/jm00064a007
11757216 16427 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 547 12 0 8 5.3 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2Cc2c(C)noc2C)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
CHEMBL124141 16427 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 547 12 0 8 5.3 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2Cc2c(C)noc2C)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
57380649 70017 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Displacement of [125I]Sar1 Ile8-Ang 2 from angiotensin 2 AT1 receptor after 180 mins by gamma countingDisplacement of [125I]Sar1 Ile8-Ang 2 from angiotensin 2 AT1 receptor after 180 mins by gamma counting
ChEMBL 549 10 2 4 6.8 CCCc1nc2c(C)cc(C(=O)NCCc3ccc(F)cc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2012.01.009
CHEMBL1945149 70017 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Displacement of [125I]Sar1 Ile8-Ang 2 from angiotensin 2 AT1 receptor after 180 mins by gamma countingDisplacement of [125I]Sar1 Ile8-Ang 2 from angiotensin 2 AT1 receptor after 180 mins by gamma counting
ChEMBL 549 10 2 4 6.8 CCCc1nc2c(C)cc(C(=O)NCCc3ccc(F)cc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2012.01.009
2121583 23158 9 None - 0 Human 6.7 pIC50 = 6.7 Binding
Displacement of [125I-Sar1-Ile8]Ang2 from human AT1 receptor expressed in HEK293 cell membrane incubated for 1 hr by gamma counting methodDisplacement of [125I-Sar1-Ile8]Ang2 from human AT1 receptor expressed in HEK293 cell membrane incubated for 1 hr by gamma counting method
ChEMBL 397 7 1 4 4.0 CN(Cc1cn(-c2ccccc2)nc1-c1ccc(Cl)cc1)C(=O)CCC(=O)O 10.1016/j.bmc.2016.07.047
CHEMBL1332729 23158 9 None - 0 Human 6.7 pIC50 = 6.7 Binding
Displacement of [125I-Sar1-Ile8]Ang2 from human AT1 receptor expressed in HEK293 cell membrane incubated for 1 hr by gamma counting methodDisplacement of [125I-Sar1-Ile8]Ang2 from human AT1 receptor expressed in HEK293 cell membrane incubated for 1 hr by gamma counting method
ChEMBL 397 7 1 4 4.0 CN(Cc1cn(-c2ccccc2)nc1-c1ccc(Cl)cc1)C(=O)CCC(=O)O 10.1016/j.bmc.2016.07.047
2121583 23158 9 None - 0 Human 6.7 pIC50 = 6.7 Binding
Displacement of [125I-Sar1-Ile8]Ang2 from human AT1 receptor expressed in HEK293 cell membrane incubated for 1 hr by gamma counting methodDisplacement of [125I-Sar1-Ile8]Ang2 from human AT1 receptor expressed in HEK293 cell membrane incubated for 1 hr by gamma counting method
ChEMBL 397 7 1 4 4.0 CN(Cc1cn(-c2ccccc2)nc1-c1ccc(Cl)cc1)C(=O)CCC(=O)O 10.1016/j.bmc.2016.07.047
CHEMBL1332729 23158 9 None - 0 Human 6.7 pIC50 = 6.7 Binding
Displacement of [125I-Sar1-Ile8]Ang2 from human AT1 receptor expressed in HEK293 cell membrane incubated for 1 hr by gamma counting methodDisplacement of [125I-Sar1-Ile8]Ang2 from human AT1 receptor expressed in HEK293 cell membrane incubated for 1 hr by gamma counting method
ChEMBL 397 7 1 4 4.0 CN(Cc1cn(-c2ccccc2)nc1-c1ccc(Cl)cc1)C(=O)CCC(=O)O 10.1016/j.bmc.2016.07.047
44274672 91109 0 None - 0 Rabbit 8.7 pIC50 = 8.7 Binding
Ability to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitroAbility to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitro
ChEMBL 465 8 2 7 4.7 CCCCc1nc2ccc(NC)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80335-2
CHEMBL24053 91109 0 None - 0 Rabbit 8.7 pIC50 = 8.7 Binding
Ability to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitroAbility to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitro
ChEMBL 465 8 2 7 4.7 CCCCc1nc2ccc(NC)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80335-2
44274824 98793 0 None - 0 Rabbit 8.7 pIC50 = 8.7 Binding
Ability to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitroAbility to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitro
ChEMBL 535 11 2 7 5.8 CCCCC(=O)Nc1ccc2nc(CCCC)n(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c(=O)c2c1 10.1016/S0960-894X(00)80335-2
CHEMBL281846 98793 0 None - 0 Rabbit 8.7 pIC50 = 8.7 Binding
Ability to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitroAbility to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitro
ChEMBL 535 11 2 7 5.8 CCCCC(=O)Nc1ccc2nc(CCCC)n(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c(=O)c2c1 10.1016/S0960-894X(00)80335-2
14956756 204637 0 None - 0 Rabbit 8.7 pIC50 = 8.7 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 529 8 1 7 5.0 CCCCc1nn(-c2ccccc2Br)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
CHEMBL87513 204637 0 None - 0 Rabbit 8.7 pIC50 = 8.7 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 529 8 1 7 5.0 CCCCc1nn(-c2ccccc2Br)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
2583 3705 115 None - 1 Human 8.7 pIC50 = 8.7 Binding
Antagonist activity at human AT1 receptor expressed in CHO cells measured after overnight incubation by luciferase reporter gene assayAntagonist activity at human AT1 receptor expressed in CHO cells measured after overnight incubation by luciferase reporter gene assay
ChEMBL 514 7 1 5 7.3 CCCc1nc2c(n1Cc1ccc(cc1)c1ccccc1C(=O)O)cc(cc2C)c1nc2c(n1C)cccc2 10.1016/j.bmcl.2014.01.004
592 3705 115 None - 1 Human 8.7 pIC50 = 8.7 Binding
Antagonist activity at human AT1 receptor expressed in CHO cells measured after overnight incubation by luciferase reporter gene assayAntagonist activity at human AT1 receptor expressed in CHO cells measured after overnight incubation by luciferase reporter gene assay
ChEMBL 514 7 1 5 7.3 CCCc1nc2c(n1Cc1ccc(cc1)c1ccccc1C(=O)O)cc(cc2C)c1nc2c(n1C)cccc2 10.1016/j.bmcl.2014.01.004
65999 3705 115 None - 1 Human 8.7 pIC50 = 8.7 Binding
Antagonist activity at human AT1 receptor expressed in CHO cells measured after overnight incubation by luciferase reporter gene assayAntagonist activity at human AT1 receptor expressed in CHO cells measured after overnight incubation by luciferase reporter gene assay
ChEMBL 514 7 1 5 7.3 CCCc1nc2c(n1Cc1ccc(cc1)c1ccccc1C(=O)O)cc(cc2C)c1nc2c(n1C)cccc2 10.1016/j.bmcl.2014.01.004
CHEMBL1017 3705 115 None - 1 Human 8.7 pIC50 = 8.7 Binding
Antagonist activity at human AT1 receptor expressed in CHO cells measured after overnight incubation by luciferase reporter gene assayAntagonist activity at human AT1 receptor expressed in CHO cells measured after overnight incubation by luciferase reporter gene assay
ChEMBL 514 7 1 5 7.3 CCCc1nc2c(n1Cc1ccc(cc1)c1ccccc1C(=O)O)cc(cc2C)c1nc2c(n1C)cccc2 10.1016/j.bmcl.2014.01.004
DB00966 3705 115 None - 1 Human 8.7 pIC50 = 8.7 Binding
Antagonist activity at human AT1 receptor expressed in CHO cells measured after overnight incubation by luciferase reporter gene assayAntagonist activity at human AT1 receptor expressed in CHO cells measured after overnight incubation by luciferase reporter gene assay
ChEMBL 514 7 1 5 7.3 CCCc1nc2c(n1Cc1ccc(cc1)c1ccccc1C(=O)O)cc(cc2C)c1nc2c(n1C)cccc2 10.1016/j.bmcl.2014.01.004
136401481 160279 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 651 11 1 11 5.7 CCc1cc2c(=O)n(C/C(=N\OC(C)C)c3ccc(OC)cc3)c(=O)n(Cc3ccc(-c4ccccc4-c4nc(=O)o[nH]4)cc3)c2s1 nan
CHEMBL4114737 160279 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 651 11 1 11 5.7 CCc1cc2c(=O)n(C/C(=N\OC(C)C)c3ccc(OC)cc3)c(=O)n(Cc3ccc(-c4ccccc4-c4nc(=O)o[nH]4)cc3)c2s1 nan
44274824 98793 0 None - 0 Rabbit 8.7 pIC50 = 8.7 Binding
Binding affinity against Angiotensin II type 1 Receptor in rabbit aortic tissueBinding affinity against Angiotensin II type 1 Receptor in rabbit aortic tissue
ChEMBL 535 11 2 7 5.8 CCCCC(=O)Nc1ccc2nc(CCCC)n(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c(=O)c2c1 10.1016/S0960-894X(00)80334-0
CHEMBL281846 98793 0 None - 0 Rabbit 8.7 pIC50 = 8.7 Binding
Binding affinity against Angiotensin II type 1 Receptor in rabbit aortic tissueBinding affinity against Angiotensin II type 1 Receptor in rabbit aortic tissue
ChEMBL 535 11 2 7 5.8 CCCCC(=O)Nc1ccc2nc(CCCC)n(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c(=O)c2c1 10.1016/S0960-894X(00)80334-0
44311583 202411 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 610 12 1 8 6.9 CCCc1nc(CC)c(C(=O)OCc2ccccc2C(=O)c2ccccc2)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80077-3
CHEMBL70353 202411 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 610 12 1 8 6.9 CCCc1nc(CC)c(C(=O)OCc2ccccc2C(=O)c2ccccc2)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80077-3
10209324 14321 0 None - 1 Human 8.7 pIC50 = 8.7 Binding
Displacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysisDisplacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysis
ChEMBL 546 8 1 7 6.2 CCCc1nc2c(n1Cc1ccc(-c3ccccc3S(=O)(=O)Nc3onc(C)c3C)c(C)c1)C(=O)CCCC2 10.1039/C4MD00499J
CHEMBL12013 14321 0 None - 1 Human 8.7 pIC50 = 8.7 Binding
Displacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysisDisplacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysis
ChEMBL 546 8 1 7 6.2 CCCc1nc2c(n1Cc1ccc(-c3ccccc3S(=O)(=O)Nc3onc(C)c3C)c(C)c1)C(=O)CCCC2 10.1039/C4MD00499J
9871837 15019 0 None - 1 Human 8.7 pIC50 = 8.7 Binding
Displacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysisDisplacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysis
ChEMBL 535 10 2 7 4.9 CCCc1nc(CC)c(C(N)=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)c(C)c1 10.1039/C4MD00499J
CHEMBL12106 15019 0 None - 1 Human 8.7 pIC50 = 8.7 Binding
Displacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysisDisplacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysis
ChEMBL 535 10 2 7 4.9 CCCc1nc(CC)c(C(N)=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)c(C)c1 10.1039/C4MD00499J
15222070 101814 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
In vitro binding affinity of compound against Angiotensin II receptor, type 1In vitro binding affinity of compound against Angiotensin II receptor, type 1
ChEMBL 577 9 2 9 3.8 CCCc1nc(C(=O)N2CCN(c3ccccn3)CC2)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80076-1
CHEMBL303426 101814 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
In vitro binding affinity of compound against Angiotensin II receptor, type 1In vitro binding affinity of compound against Angiotensin II receptor, type 1
ChEMBL 577 9 2 9 3.8 CCCc1nc(C(=O)N2CCN(c3ccccn3)CC2)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80076-1
44311662 102195 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
In vitro binding affinity of compound against Angiotensin II receptor, type 1In vitro binding affinity of compound against Angiotensin II receptor, type 1
ChEMBL 624 17 2 7 5.8 CCCCN(Cc1nc(CCC)n(Cc2ccc(-c3ccccc3S(=O)(=O)NC(=O)CCC)cc2)c1C(=O)O)C(=O)CCC 10.1016/S0960-894X(00)80076-1
CHEMBL304620 102195 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
In vitro binding affinity of compound against Angiotensin II receptor, type 1In vitro binding affinity of compound against Angiotensin II receptor, type 1
ChEMBL 624 17 2 7 5.8 CCCCN(Cc1nc(CCC)n(Cc2ccc(-c3ccccc3S(=O)(=O)NC(=O)CCC)cc2)c1C(=O)O)C(=O)CCC 10.1016/S0960-894X(00)80076-1
15222094 102488 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
In vitro binding affinity of compound against Angiotensin II receptor, type 1In vitro binding affinity of compound against Angiotensin II receptor, type 1
ChEMBL 596 10 2 8 5.4 CCCc1nc(CN2CCN(c3ccccc3Cl)CC2)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80076-1
CHEMBL306489 102488 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
In vitro binding affinity of compound against Angiotensin II receptor, type 1In vitro binding affinity of compound against Angiotensin II receptor, type 1
ChEMBL 596 10 2 8 5.4 CCCc1nc(CN2CCN(c3ccccc3Cl)CC2)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80076-1
44311681 102536 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
In vitro binding affinity of compound against Angiotensin II receptor, type 1In vitro binding affinity of compound against Angiotensin II receptor, type 1
ChEMBL 592 11 2 9 4.8 CCCc1nc(CN2CCN(c3ccccc3OC)CC2)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80076-1
CHEMBL306961 102536 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
In vitro binding affinity of compound against Angiotensin II receptor, type 1In vitro binding affinity of compound against Angiotensin II receptor, type 1
ChEMBL 592 11 2 9 4.8 CCCc1nc(CN2CCN(c3ccccc3OC)CC2)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80076-1
15222092 103334 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
In vitro binding affinity of compound against Angiotensin II receptor, type 1In vitro binding affinity of compound against Angiotensin II receptor, type 1
ChEMBL 564 10 2 10 3.5 CCCc1nc(CN2CCN(c3ncccn3)CC2)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80076-1
CHEMBL309165 103334 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
In vitro binding affinity of compound against Angiotensin II receptor, type 1In vitro binding affinity of compound against Angiotensin II receptor, type 1
ChEMBL 564 10 2 10 3.5 CCCc1nc(CN2CCN(c3ncccn3)CC2)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80076-1
44311451 103612 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
In vitro binding affinity of compound against Angiotensin II receptor, type 1In vitro binding affinity of compound against Angiotensin II receptor, type 1
ChEMBL 576 10 2 8 5.1 CCCc1nc(CN2CCN(c3ccccc3)C[C@H]2C)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80076-1
CHEMBL309367 103612 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
In vitro binding affinity of compound against Angiotensin II receptor, type 1In vitro binding affinity of compound against Angiotensin II receptor, type 1
ChEMBL 576 10 2 8 5.1 CCCc1nc(CN2CCN(c3ccccc3)C[C@H]2C)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80076-1
44311497 167283 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
In vitro binding affinity of compound against Angiotensin II receptor, type 1In vitro binding affinity of compound against Angiotensin II receptor, type 1
ChEMBL 547 10 1 9 4.3 CCCc1nc(CN2CCN(c3ccccn3)CC2)c(C=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80076-1
CHEMBL430997 167283 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
In vitro binding affinity of compound against Angiotensin II receptor, type 1In vitro binding affinity of compound against Angiotensin II receptor, type 1
ChEMBL 547 10 1 9 4.3 CCCc1nc(CN2CCN(c3ccccn3)CC2)c(C=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80076-1
44311663 202479 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
In vitro binding affinity of compound against Angiotensin II receptor, type 1In vitro binding affinity of compound against Angiotensin II receptor, type 1
ChEMBL 561 10 2 7 5.8 CCCc1nc(CN2CCC(c3ccccc3)CC2)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80076-1
CHEMBL70796 202479 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
In vitro binding affinity of compound against Angiotensin II receptor, type 1In vitro binding affinity of compound against Angiotensin II receptor, type 1
ChEMBL 561 10 2 7 5.8 CCCc1nc(CN2CCC(c3ccccc3)CC2)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80076-1
44311499 202684 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
In vitro binding affinity of compound against Angiotensin II receptor, type 1In vitro binding affinity of compound against Angiotensin II receptor, type 1
ChEMBL 557 17 2 7 6.6 CCCCCN(CCCCC)Cc1nc(CCC)n(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c1C(=O)O 10.1016/S0960-894X(00)80076-1
CHEMBL71953 202684 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
In vitro binding affinity of compound against Angiotensin II receptor, type 1In vitro binding affinity of compound against Angiotensin II receptor, type 1
ChEMBL 557 17 2 7 6.6 CCCCCN(CCCCC)Cc1nc(CCC)n(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c1C(=O)O 10.1016/S0960-894X(00)80076-1
44311648 202812 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
In vitro binding affinity of compound against Angiotensin II receptor, type 1In vitro binding affinity of compound against Angiotensin II receptor, type 1
ChEMBL 577 11 2 9 4.5 CCCCc1nc(CN2CCN(c3ccccn3)CC2)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80076-1
CHEMBL72721 202812 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
In vitro binding affinity of compound against Angiotensin II receptor, type 1In vitro binding affinity of compound against Angiotensin II receptor, type 1
ChEMBL 577 11 2 9 4.5 CCCCc1nc(CN2CCN(c3ccccn3)CC2)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80076-1
44311758 202955 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
In vitro binding affinity of compound against Angiotensin II receptor, type 1In vitro binding affinity of compound against Angiotensin II receptor, type 1
ChEMBL 626 12 3 7 6.7 CCCc1nc(CN(Cc2ccccc2)C(=O)Nc2ccccc2)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80076-1
CHEMBL73780 202955 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
In vitro binding affinity of compound against Angiotensin II receptor, type 1In vitro binding affinity of compound against Angiotensin II receptor, type 1
ChEMBL 626 12 3 7 6.7 CCCc1nc(CN(Cc2ccccc2)C(=O)Nc2ccccc2)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80076-1
19742811 57105 0 None - 0 Rabbit 8.7 pIC50 = 8.7 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aortaIn vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aorta
ChEMBL 551 10 2 6 5.4 CCCCc1nc(Cl)c(C(=O)O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/S0960-894X(01)81124-0
CHEMBL165354 57105 0 None - 0 Rabbit 8.7 pIC50 = 8.7 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aortaIn vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aorta
ChEMBL 551 10 2 6 5.4 CCCCc1nc(Cl)c(C(=O)O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/S0960-894X(01)81124-0
10077555 205667 0 None - 0 Rabbit 8.7 pIC50 = 8.7 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 616 12 1 8 5.0 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)CCOC)cc1 10.1021/jm00043a020
CHEMBL93956 205667 0 None - 0 Rabbit 8.7 pIC50 = 8.7 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 616 12 1 8 5.0 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)CCOC)cc1 10.1021/jm00043a020
10440144 116381 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 763 10 2 9 7.1 CCCc1nn(-c2cc(NC(=O)c3ccccc3)ccc2Br)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1021/jm00019a004
CHEMBL338342 116381 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 763 10 2 9 7.1 CCCc1nn(-c2cc(NC(=O)c3ccccc3)ccc2Br)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1021/jm00019a004
44315349 60056 0 None - 0 Rabbit 8.7 pIC50 = 8.7 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membrane
ChEMBL 679 10 2 9 5.1 CCc1nc2ccc(NC(=O)N3CCOCC3)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/0960-894X(94)85036-4
CHEMBL17487 60056 0 None - 0 Rabbit 8.7 pIC50 = 8.7 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membrane
ChEMBL 679 10 2 9 5.1 CCc1nc2ccc(NC(=O)N3CCOCC3)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/0960-894X(94)85036-4
2583 3705 115 None - 1 Human 8.7 pIC50 = 8.7 Binding
Inhibition of AT1 receptor (unknown origin)Inhibition of AT1 receptor (unknown origin)
ChEMBL 514 7 1 5 7.3 CCCc1nc2c(n1Cc1ccc(cc1)c1ccccc1C(=O)O)cc(cc2C)c1nc2c(n1C)cccc2 10.1016/j.ejmech.2019.04.030
592 3705 115 None - 1 Human 8.7 pIC50 = 8.7 Binding
Inhibition of AT1 receptor (unknown origin)Inhibition of AT1 receptor (unknown origin)
ChEMBL 514 7 1 5 7.3 CCCc1nc2c(n1Cc1ccc(cc1)c1ccccc1C(=O)O)cc(cc2C)c1nc2c(n1C)cccc2 10.1016/j.ejmech.2019.04.030
65999 3705 115 None - 1 Human 8.7 pIC50 = 8.7 Binding
Inhibition of AT1 receptor (unknown origin)Inhibition of AT1 receptor (unknown origin)
ChEMBL 514 7 1 5 7.3 CCCc1nc2c(n1Cc1ccc(cc1)c1ccccc1C(=O)O)cc(cc2C)c1nc2c(n1C)cccc2 10.1016/j.ejmech.2019.04.030
CHEMBL1017 3705 115 None - 1 Human 8.7 pIC50 = 8.7 Binding
Inhibition of AT1 receptor (unknown origin)Inhibition of AT1 receptor (unknown origin)
ChEMBL 514 7 1 5 7.3 CCCc1nc2c(n1Cc1ccc(cc1)c1ccccc1C(=O)O)cc(cc2C)c1nc2c(n1C)cccc2 10.1016/j.ejmech.2019.04.030
DB00966 3705 115 None - 1 Human 8.7 pIC50 = 8.7 Binding
Inhibition of AT1 receptor (unknown origin)Inhibition of AT1 receptor (unknown origin)
ChEMBL 514 7 1 5 7.3 CCCc1nc2c(n1Cc1ccc(cc1)c1ccccc1C(=O)O)cc(cc2C)c1nc2c(n1C)cccc2 10.1016/j.ejmech.2019.04.030
108185 1578 71 None - 1 Human 8.7 pIC50 = 8.7 Binding
Inhibition of ATR1 (unknown origin)Inhibition of ATR1 (unknown origin)
ChEMBL 436 8 2 6 4.5 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)C(=O)O)Cl 10.1021/acs.jmedchem.9b00179
586 1578 71 None - 1 Human 8.7 pIC50 = 8.7 Binding
Inhibition of ATR1 (unknown origin)Inhibition of ATR1 (unknown origin)
ChEMBL 436 8 2 6 4.5 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)C(=O)O)Cl 10.1021/acs.jmedchem.9b00179
CHEMBL907 1578 71 None - 1 Human 8.7 pIC50 = 8.7 Binding
Inhibition of ATR1 (unknown origin)Inhibition of ATR1 (unknown origin)
ChEMBL 436 8 2 6 4.5 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)C(=O)O)Cl 10.1021/acs.jmedchem.9b00179
1037 1542 65 None - 1 Human 8.7 pIC50 = 8.7 Binding
Tested for Angiotensin II receptor, type 1 affinity in the absence of bovine serum albumin (BSA)Tested for Angiotensin II receptor, type 1 affinity in the absence of bovine serum albumin (BSA)
ChEMBL 424 10 2 5 4.7 CCCCc1ncc(n1Cc1ccc(cc1)C(=O)O)/C=C(/C(=O)O)\Cc1cccs1 10.1016/S0960-894X(01)81116-1
3940 1542 65 None - 1 Human 8.7 pIC50 = 8.7 Binding
Tested for Angiotensin II receptor, type 1 affinity in the absence of bovine serum albumin (BSA)Tested for Angiotensin II receptor, type 1 affinity in the absence of bovine serum albumin (BSA)
ChEMBL 424 10 2 5 4.7 CCCCc1ncc(n1Cc1ccc(cc1)C(=O)O)/C=C(/C(=O)O)\Cc1cccs1 10.1016/S0960-894X(01)81116-1
5281037 1542 65 None - 1 Human 8.7 pIC50 = 8.7 Binding
Tested for Angiotensin II receptor, type 1 affinity in the absence of bovine serum albumin (BSA)Tested for Angiotensin II receptor, type 1 affinity in the absence of bovine serum albumin (BSA)
ChEMBL 424 10 2 5 4.7 CCCCc1ncc(n1Cc1ccc(cc1)C(=O)O)/C=C(/C(=O)O)\Cc1cccs1 10.1016/S0960-894X(01)81116-1
588 1542 65 None - 1 Human 8.7 pIC50 = 8.7 Binding
Tested for Angiotensin II receptor, type 1 affinity in the absence of bovine serum albumin (BSA)Tested for Angiotensin II receptor, type 1 affinity in the absence of bovine serum albumin (BSA)
ChEMBL 424 10 2 5 4.7 CCCCc1ncc(n1Cc1ccc(cc1)C(=O)O)/C=C(/C(=O)O)\Cc1cccs1 10.1016/S0960-894X(01)81116-1
CHEMBL813 1542 65 None - 1 Human 8.7 pIC50 = 8.7 Binding
Tested for Angiotensin II receptor, type 1 affinity in the absence of bovine serum albumin (BSA)Tested for Angiotensin II receptor, type 1 affinity in the absence of bovine serum albumin (BSA)
ChEMBL 424 10 2 5 4.7 CCCCc1ncc(n1Cc1ccc(cc1)C(=O)O)/C=C(/C(=O)O)\Cc1cccs1 10.1016/S0960-894X(01)81116-1
DB00876 1542 65 None - 1 Human 8.7 pIC50 = 8.7 Binding
Tested for Angiotensin II receptor, type 1 affinity in the absence of bovine serum albumin (BSA)Tested for Angiotensin II receptor, type 1 affinity in the absence of bovine serum albumin (BSA)
ChEMBL 424 10 2 5 4.7 CCCCc1ncc(n1Cc1ccc(cc1)C(=O)O)/C=C(/C(=O)O)\Cc1cccs1 10.1016/S0960-894X(01)81116-1
44285372 99814 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
The compound was tested for the ability to displace 50% of totally specifically bound [125I]- Ang II from Angiotensin II receptor, type 1 siteThe compound was tested for the ability to displace 50% of totally specifically bound [125I]- Ang II from Angiotensin II receptor, type 1 site
ChEMBL 446 6 1 6 4.3 CCCC1=NC2(CCSCC2)C(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80526-6
CHEMBL289105 99814 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
The compound was tested for the ability to displace 50% of totally specifically bound [125I]- Ang II from Angiotensin II receptor, type 1 siteThe compound was tested for the ability to displace 50% of totally specifically bound [125I]- Ang II from Angiotensin II receptor, type 1 site
ChEMBL 446 6 1 6 4.3 CCCC1=NC2(CCSCC2)C(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80526-6
44338666 110456 0 None - 0 Rabbit 8.7 pIC50 = 8.7 Binding
Binding affinity against AT-1 receptor from rabbit aorta using [125I]-Sar1-Ile8-Ang II without BSABinding affinity against AT-1 receptor from rabbit aorta using [125I]-Sar1-Ile8-Ang II without BSA
ChEMBL 551 9 1 8 5.5 CCCc1nc2ccc(N(C)C(=O)OCC(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00073a024
CHEMBL326217 110456 0 None - 0 Rabbit 8.7 pIC50 = 8.7 Binding
Binding affinity against AT-1 receptor from rabbit aorta using [125I]-Sar1-Ile8-Ang II without BSABinding affinity against AT-1 receptor from rabbit aorta using [125I]-Sar1-Ile8-Ang II without BSA
ChEMBL 551 9 1 8 5.5 CCCc1nc2ccc(N(C)C(=O)OCC(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00073a024
9850834 154112 13 None - 1 Rabbit 8.7 pIC50 = 8.7 Binding
Compound was evaluated for inhibition of 125I[Sar1,Ile8] all binding to rabbit aorta Angiotensin II receptor, type 1Compound was evaluated for inhibition of 125I[Sar1,Ile8] all binding to rabbit aorta Angiotensin II receptor, type 1
ChEMBL 562 11 1 7 6.5 CCCCOC(=O)NS(=O)(=O)c1ccc(CCC)cc1-c1ccc(Cn2c(CC)nc3c(C)cc(C)nc32)cc1 10.1016/0960-894X(96)00017-0
CHEMBL39959 154112 13 None - 1 Rabbit 8.7 pIC50 = 8.7 Binding
Compound was evaluated for inhibition of 125I[Sar1,Ile8] all binding to rabbit aorta Angiotensin II receptor, type 1Compound was evaluated for inhibition of 125I[Sar1,Ile8] all binding to rabbit aorta Angiotensin II receptor, type 1
ChEMBL 562 11 1 7 6.5 CCCCOC(=O)NS(=O)(=O)c1ccc(CCC)cc1-c1ccc(Cn2c(CC)nc3c(C)cc(C)nc32)cc1 10.1016/0960-894X(96)00017-0
14956779 68306 0 None - 0 Rabbit 8.7 pIC50 = 8.7 Binding
Displacement of 125I[Sar,Ile] from rabbit aorta membrane Angiotensin II receptor type 1Displacement of 125I[Sar,Ile] from rabbit aorta membrane Angiotensin II receptor type 1
ChEMBL 445 8 1 7 4.3 CCCCc1nn(CC(C)(C)C)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81132-X
CHEMBL19202 68306 0 None - 0 Rabbit 8.7 pIC50 = 8.7 Binding
Displacement of 125I[Sar,Ile] from rabbit aorta membrane Angiotensin II receptor type 1Displacement of 125I[Sar,Ile] from rabbit aorta membrane Angiotensin II receptor type 1
ChEMBL 445 8 1 7 4.3 CCCCc1nn(CC(C)(C)C)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81132-X
10031067 99875 3 None - 3 Human 8.7 pIC50 = 8.7 Binding
Displacement of [125I]-[Sar1,Leu8]angiotensin II from human AT1 receptor expressed in african green monkey COS7 cellsDisplacement of [125I]-[Sar1,Leu8]angiotensin II from human AT1 receptor expressed in african green monkey COS7 cells
ChEMBL 576 11 1 7 6.7 CCCCOC(=O)NS(=O)(=O)c1ccc(CC(C)C)cc1-c1ccc(Cn2c(CC)nc3c(C)cc(C)nc32)cc1 10.1021/ml500427r
CHEMBL289614 99875 3 None - 3 Human 8.7 pIC50 = 8.7 Binding
Displacement of [125I]-[Sar1,Leu8]angiotensin II from human AT1 receptor expressed in african green monkey COS7 cellsDisplacement of [125I]-[Sar1,Leu8]angiotensin II from human AT1 receptor expressed in african green monkey COS7 cells
ChEMBL 576 11 1 7 6.7 CCCCOC(=O)NS(=O)(=O)c1ccc(CC(C)C)cc1-c1ccc(Cn2c(CC)nc3c(C)cc(C)nc32)cc1 10.1021/ml500427r
127030943 138652 0 None - 1 Human 8.7 pIC50 = 8.7 Binding
Displacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation countingDisplacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation counting
ChEMBL 1216 35 15 14 -0.7 CCC(=O)NCCCCNC(=O)/N=C(\N)NCCC[C@H](NC(=O)[C@@H](N)CC(=O)O)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O)[C@@H](C)CC)C(C)C 10.1021/acs.jmedchem.5b01495
CHEMBL3787243 138652 0 None - 1 Human 8.7 pIC50 = 8.7 Binding
Displacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation countingDisplacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation counting
ChEMBL 1216 35 15 14 -0.7 CCC(=O)NCCCCNC(=O)/N=C(\N)NCCC[C@H](NC(=O)[C@@H](N)CC(=O)O)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O)[C@@H](C)CC)C(C)C 10.1021/acs.jmedchem.5b01495
CHEMBL3787375 138652 0 None - 1 Human 8.7 pIC50 = 8.7 Binding
Displacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation countingDisplacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation counting
ChEMBL 1216 35 15 14 -0.7 CCC(=O)NCCCCNC(=O)/N=C(\N)NCCC[C@H](NC(=O)[C@@H](N)CC(=O)O)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O)[C@@H](C)CC)C(C)C 10.1021/acs.jmedchem.5b01495
CHEMBL3787700 138652 0 None - 1 Human 8.7 pIC50 = 8.7 Binding
Displacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation countingDisplacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation counting
ChEMBL 1216 35 15 14 -0.7 CCC(=O)NCCCCNC(=O)/N=C(\N)NCCC[C@H](NC(=O)[C@@H](N)CC(=O)O)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O)[C@@H](C)CC)C(C)C 10.1021/acs.jmedchem.5b01495
44277462 14588 0 None - 0 Rabbit 8.7 pIC50 = 8.7 Binding
Binding affinity against AT1 receptor in rabbit aortaBinding affinity against AT1 receptor in rabbit aorta
ChEMBL 665 11 2 10 5.2 CCCCN(C(=O)c1ccc(OP(=O)(O)O)cc1)c1ccc2ncn(Cc3ccc(-c4ccccc4-c4nnnn4C)cc3)c(=O)c2c1 10.1016/0960-894X(95)00224-H
CHEMBL1206522 14588 0 None - 0 Rabbit 8.7 pIC50 = 8.7 Binding
Binding affinity against AT1 receptor in rabbit aortaBinding affinity against AT1 receptor in rabbit aorta
ChEMBL 665 11 2 10 5.2 CCCCN(C(=O)c1ccc(OP(=O)(O)O)cc1)c1ccc2ncn(Cc3ccc(-c4ccccc4-c4nnnn4C)cc3)c(=O)c2c1 10.1016/0960-894X(95)00224-H
CHEMBL281890 14588 0 None - 0 Rabbit 8.7 pIC50 = 8.7 Binding
Binding affinity against AT1 receptor in rabbit aortaBinding affinity against AT1 receptor in rabbit aorta
ChEMBL 665 11 2 10 5.2 CCCCN(C(=O)c1ccc(OP(=O)(O)O)cc1)c1ccc2ncn(Cc3ccc(-c4ccccc4-c4nnnn4C)cc3)c(=O)c2c1 10.1016/0960-894X(95)00224-H
44277548 98938 0 None - 0 Rabbit 8.7 pIC50 = 8.7 Binding
Binding affinity against AT1 receptor in rabbit aortaBinding affinity against AT1 receptor in rabbit aorta
ChEMBL 615 12 0 10 4.6 COCCOCCN(C(=O)c1ccccc1)c1ccc2ncn(Cc3ccc(-c4ccccc4-c4nnnn4C)cc3)c(=O)c2c1 10.1016/0960-894X(95)00224-H
CHEMBL282777 98938 0 None - 0 Rabbit 8.7 pIC50 = 8.7 Binding
Binding affinity against AT1 receptor in rabbit aortaBinding affinity against AT1 receptor in rabbit aorta
ChEMBL 615 12 0 10 4.6 COCCOCCN(C(=O)c1ccccc1)c1ccc2ncn(Cc3ccc(-c4ccccc4-c4nnnn4C)cc3)c(=O)c2c1 10.1016/0960-894X(95)00224-H
10479475 114714 0 None - 0 Rabbit 8.7 pIC50 = 8.7 Binding
In vitro binding affinity for angiotensin II AT1 receptor in rabbit aortaIn vitro binding affinity for angiotensin II AT1 receptor in rabbit aorta
ChEMBL 462 6 1 6 4.2 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(C)=O)cc1 10.1021/jm00050a002
CHEMBL334670 114714 0 None - 0 Rabbit 8.7 pIC50 = 8.7 Binding
In vitro binding affinity for angiotensin II AT1 receptor in rabbit aortaIn vitro binding affinity for angiotensin II AT1 receptor in rabbit aorta
ChEMBL 462 6 1 6 4.2 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(C)=O)cc1 10.1021/jm00050a002
44288322 154650 0 None - 0 Rat 8.7 pIC50 = 8.7 Binding
In vitro inhibition of specific binding of [125I]AII to Angiotensin II receptor, type 1 from rat liver membraneIn vitro inhibition of specific binding of [125I]AII to Angiotensin II receptor, type 1 from rat liver membrane
ChEMBL 470 7 1 5 5.8 CCCCC1=NC2(CCCC2)C(C)(C)C(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81139-2
CHEMBL40251 154650 0 None - 0 Rat 8.7 pIC50 = 8.7 Binding
In vitro inhibition of specific binding of [125I]AII to Angiotensin II receptor, type 1 from rat liver membraneIn vitro inhibition of specific binding of [125I]AII to Angiotensin II receptor, type 1 from rat liver membrane
ChEMBL 470 7 1 5 5.8 CCCCC1=NC2(CCCC2)C(C)(C)C(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81139-2
10393837 167370 0 None - 0 Rabbit 8.7 pIC50 = 8.7 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 602 10 1 8 5.5 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCC)cc1 10.1021/jm00043a020
CHEMBL431619 167370 0 None - 0 Rabbit 8.7 pIC50 = 8.7 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 602 10 1 8 5.5 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCC)cc1 10.1021/jm00043a020
10462573 116495 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 719 11 2 9 6.8 CCCCC(=O)Nc1ccc(C(F)(F)F)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1021/jm00019a004
CHEMBL338889 116495 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 719 11 2 9 6.8 CCCCC(=O)Nc1ccc(C(F)(F)F)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1021/jm00019a004
10372550 163953 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 698 13 1 9 7.5 CCCCC(=O)c1ccc(Cl)c(-n2nc(CCCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1021/jm00019a004
CHEMBL421478 163953 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 698 13 1 9 7.5 CCCCC(=O)c1ccc(Cl)c(-n2nc(CCCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1021/jm00019a004
44315344 104589 0 None - 0 Rabbit 8.7 pIC50 = 8.7 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membrane
ChEMBL 665 12 2 8 5.2 CCc1nc2ccc(NC(=O)N(C)C(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)COCC(C)C)cc1F 10.1016/0960-894X(94)85036-4
CHEMBL311386 104589 0 None - 0 Rabbit 8.7 pIC50 = 8.7 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membrane
ChEMBL 665 12 2 8 5.2 CCc1nc2ccc(NC(=O)N(C)C(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)COCC(C)C)cc1F 10.1016/0960-894X(94)85036-4
18950607 50132 0 None - 0 Rabbit 8.7 pIC50 = 8.7 Binding
Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)
ChEMBL 489 9 1 5 6.2 C=CCc1cc(Cn2c(CC)nc3c(C)cc(C)nc32)cc(Cl)c1OC(C(=O)O)c1ccccc1 10.1016/0960-894X(95)00185-V
CHEMBL15729 50132 0 None - 0 Rabbit 8.7 pIC50 = 8.7 Binding
Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)
ChEMBL 489 9 1 5 6.2 C=CCc1cc(Cn2c(CC)nc3c(C)cc(C)nc32)cc(Cl)c1OC(C(=O)O)c1ccccc1 10.1016/0960-894X(95)00185-V
10004646 17756 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 464 9 2 6 4.1 CCCCc1ncc(/C=C2/C(=O)NC(=O)N2Cc2cccs2)n1Cc1ccc(C(=O)O)cc1 10.1007/s00044-009-9205-9
CHEMBL126037 17756 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 464 9 2 6 4.1 CCCCc1ncc(/C=C2/C(=O)NC(=O)N2Cc2cccs2)n1Cc1ccc(C(=O)O)cc1 10.1007/s00044-009-9205-9
136052253 123991 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 624 10 1 11 4.7 CCc1cc2c(=O)n(CC(=O)c3ccc(OC)cc3)c(=O)n(Cc3ccc(-c4ccccc4-c4nc(=O)o[nH]4)cc3OC)c2s1 nan
CHEMBL3640160 123991 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Binding Assay: Binding assay using human AT1.Binding Assay: Binding assay using human AT1.
ChEMBL 624 10 1 11 4.7 CCc1cc2c(=O)n(CC(=O)c3ccc(OC)cc3)c(=O)n(Cc3ccc(-c4ccccc4-c4nc(=O)o[nH]4)cc3OC)c2s1 nan
44278118 96525 0 None - 0 Rabbit 8.6 pIC50 = 8.6 Binding
Binding affinity against AT1 receptor in rabbit aortaBinding affinity against AT1 receptor in rabbit aorta
ChEMBL 587 9 0 8 5.9 CCCCN(C(=O)c1ccc(F)cc1)c1ccc2ncn(Cc3ccc(-c4ccccc4-c4nnnn4C)cc3)c(=O)c2c1 10.1016/0960-894X(95)00224-H
CHEMBL266480 96525 0 None - 0 Rabbit 8.6 pIC50 = 8.6 Binding
Binding affinity against AT1 receptor in rabbit aortaBinding affinity against AT1 receptor in rabbit aorta
ChEMBL 587 9 0 8 5.9 CCCCN(C(=O)c1ccc(F)cc1)c1ccc2ncn(Cc3ccc(-c4ccccc4-c4nnnn4C)cc3)c(=O)c2c1 10.1016/0960-894X(95)00224-H
44277737 100142 0 None - 0 Rabbit 8.6 pIC50 = 8.6 Binding
Binding affinity against AT1 receptor in rabbit aortaBinding affinity against AT1 receptor in rabbit aorta
ChEMBL 627 11 0 10 5.3 CCOC(=O)CCCN(C(=O)c1ccccc1)c1ccc2ncn(Cc3ccc(-c4ccccc4-c4nnnn4C)cc3)c(=O)c2c1 10.1016/0960-894X(95)00224-H
CHEMBL29192 100142 0 None - 0 Rabbit 8.6 pIC50 = 8.6 Binding
Binding affinity against AT1 receptor in rabbit aortaBinding affinity against AT1 receptor in rabbit aorta
ChEMBL 627 11 0 10 5.3 CCOC(=O)CCCN(C(=O)c1ccccc1)c1ccc2ncn(Cc3ccc(-c4ccccc4-c4nnnn4C)cc3)c(=O)c2c1 10.1016/0960-894X(95)00224-H
44315180 102410 0 None - 0 Rabbit 8.6 pIC50 = 8.6 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membrane
ChEMBL 621 9 2 8 4.9 Cc1nc2ccc(NC(=O)N(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC2CC2)cc1F 10.1016/0960-894X(94)85036-4
CHEMBL305956 102410 0 None - 0 Rabbit 8.6 pIC50 = 8.6 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membrane
ChEMBL 621 9 2 8 4.9 Cc1nc2ccc(NC(=O)N(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC2CC2)cc1F 10.1016/0960-894X(94)85036-4
44315059 202996 0 None - 0 Rabbit 8.6 pIC50 = 8.6 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membrane
ChEMBL 671 11 2 9 5.9 CCc1nc2ccc(NC(=O)c3ccccn3)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/0960-894X(94)85036-4
CHEMBL74144 202996 0 None - 0 Rabbit 8.6 pIC50 = 8.6 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membrane
ChEMBL 671 11 2 9 5.9 CCc1nc2ccc(NC(=O)c3ccccn3)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/0960-894X(94)85036-4
44315057 203111 0 None - 0 Rabbit 8.6 pIC50 = 8.6 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membrane
ChEMBL 651 10 2 8 5.9 Cc1nc2ccc(NC(=O)N(C)C(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/0960-894X(94)85036-4
CHEMBL75401 203111 0 None - 0 Rabbit 8.6 pIC50 = 8.6 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membrane
ChEMBL 651 10 2 8 5.9 Cc1nc2ccc(NC(=O)N(C)C(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/0960-894X(94)85036-4
19802473 197018 0 None - 0 Rabbit 8.6 pIC50 = 8.6 Binding
Inhibition of Angiotensin II receptor type 1 in rabbit aorta binding assayInhibition of Angiotensin II receptor type 1 in rabbit aorta binding assay
ChEMBL 415 5 1 7 4.6 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccsc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81145-8
CHEMBL58156 197018 0 None - 0 Rabbit 8.6 pIC50 = 8.6 Binding
Inhibition of Angiotensin II receptor type 1 in rabbit aorta binding assayInhibition of Angiotensin II receptor type 1 in rabbit aorta binding assay
ChEMBL 415 5 1 7 4.6 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccsc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81145-8
44305267 201701 0 None - 0 Rat 8.6 pIC50 = 8.6 Binding
Tested for binding affinity against angiotensin II receptor in rat adrenal cortexTested for binding affinity against angiotensin II receptor in rat adrenal cortex
ChEMBL 536 9 1 9 3.7 CCCc1cc(=O)n(Cc2ccccc2C(=O)OC)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/0960-894X(95)00370-9
CHEMBL65503 201701 0 None - 0 Rat 8.6 pIC50 = 8.6 Binding
Tested for binding affinity against angiotensin II receptor in rat adrenal cortexTested for binding affinity against angiotensin II receptor in rat adrenal cortex
ChEMBL 536 9 1 9 3.7 CCCc1cc(=O)n(Cc2ccccc2C(=O)OC)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/0960-894X(95)00370-9
10101582 118858 0 None - 0 Rabbit 8.6 pIC50 = 8.6 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 747 15 2 8 7.4 CCCCCNC(=O)c1ccc(-n2nc(CCCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)c4ccccc4Cl)cc3)c2=O)c(Cl)c1 10.1007/s00044-013-0831-x
CHEMBL344466 118858 0 None - 0 Rabbit 8.6 pIC50 = 8.6 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 747 15 2 8 7.4 CCCCCNC(=O)c1ccc(-n2nc(CCCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)c4ccccc4Cl)cc3)c2=O)c(Cl)c1 10.1007/s00044-013-0831-x
9979771 17249 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 424 10 2 5 3.7 CCCCc1ncc(/C=C2\C(=O)NC(=O)N2CCCC)n1Cc1ccc(C(=O)O)cc1 10.1007/s00044-009-9205-9
CHEMBL125766 17249 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 424 10 2 5 3.7 CCCCc1ncc(/C=C2\C(=O)NC(=O)N2CCCC)n1Cc1ccc(C(=O)O)cc1 10.1007/s00044-009-9205-9
9935106 64936 0 None - 0 Rabbit 8.6 pIC50 = 8.6 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 485 8 1 7 4.9 CCCCc1nn(-c2ccccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
CHEMBL18287 64936 0 None - 0 Rabbit 8.6 pIC50 = 8.6 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 485 8 1 7 4.9 CCCCc1nn(-c2ccccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
44338708 109942 0 None - 0 Rabbit 8.6 pIC50 = 8.6 Binding
Binding affinity against AT-1 receptor from rabbit aorta using [125I]-Sar1-Ile8-Ang II without BSABinding affinity against AT-1 receptor from rabbit aorta using [125I]-Sar1-Ile8-Ang II without BSA
ChEMBL 611 12 1 7 7.0 CCCCC(=O)N(Cc1ccccc1)c1ccc2nc(CCC)n(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c(=O)c2c1 10.1021/jm00073a024
CHEMBL324629 109942 0 None - 0 Rabbit 8.6 pIC50 = 8.6 Binding
Binding affinity against AT-1 receptor from rabbit aorta using [125I]-Sar1-Ile8-Ang II without BSABinding affinity against AT-1 receptor from rabbit aorta using [125I]-Sar1-Ile8-Ang II without BSA
ChEMBL 611 12 1 7 7.0 CCCCC(=O)N(Cc1ccccc1)c1ccc2nc(CCC)n(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c(=O)c2c1 10.1021/jm00073a024
44277443 99821 0 None - 0 Rabbit 8.6 pIC50 = 8.6 Binding
Binding affinity against AT1 receptor in rabbit aortaBinding affinity against AT1 receptor in rabbit aorta
ChEMBL 583 10 0 8 6.0 CCCCC(=O)N(Cc1ccccc1)c1ccc2ncn(Cc3ccc(-c4ccccc4-c4nnnn4C)cc3)c(=O)c2c1 10.1016/0960-894X(95)00224-H
CHEMBL28918 99821 0 None - 0 Rabbit 8.6 pIC50 = 8.6 Binding
Binding affinity against AT1 receptor in rabbit aortaBinding affinity against AT1 receptor in rabbit aorta
ChEMBL 583 10 0 8 6.0 CCCCC(=O)N(Cc1ccccc1)c1ccc2ncn(Cc3ccc(-c4ccccc4-c4nnnn4C)cc3)c(=O)c2c1 10.1016/0960-894X(95)00224-H
CHEMBL938 214120 24 None - 2 Rat 8.6 pIC50 = 8.6 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL None None None CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O)C(C)C)C(C)C 10.1021/jm00074a018
9935106 64936 0 None - 0 Rabbit 8.6 pIC50 = 8.6 Binding
Displacement of 125I[Sar,Ile] from rabbit aorta membrane Angiotensin II receptor type 1Displacement of 125I[Sar,Ile] from rabbit aorta membrane Angiotensin II receptor type 1
ChEMBL 485 8 1 7 4.9 CCCCc1nn(-c2ccccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81132-X
CHEMBL18287 64936 0 None - 0 Rabbit 8.6 pIC50 = 8.6 Binding
Displacement of 125I[Sar,Ile] from rabbit aorta membrane Angiotensin II receptor type 1Displacement of 125I[Sar,Ile] from rabbit aorta membrane Angiotensin II receptor type 1
ChEMBL 485 8 1 7 4.9 CCCCc1nn(-c2ccccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81132-X
57380412 70169 0 None - 1 Human 8.6 pIC50 = 8.6 Binding
Displacement of [125I]Sar1 Ile8-Ang 2 from angiotensin 2 AT1 receptor after 180 mins by gamma countingDisplacement of [125I]Sar1 Ile8-Ang 2 from angiotensin 2 AT1 receptor after 180 mins by gamma counting
ChEMBL 547 10 2 5 6.6 CCCc1nc2c(C)cc(C(=O)NCc3ccccc3OC)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2012.01.009
CHEMBL1947129 70169 0 None - 1 Human 8.6 pIC50 = 8.6 Binding
Displacement of [125I]Sar1 Ile8-Ang 2 from angiotensin 2 AT1 receptor after 180 mins by gamma countingDisplacement of [125I]Sar1 Ile8-Ang 2 from angiotensin 2 AT1 receptor after 180 mins by gamma counting
ChEMBL 547 10 2 5 6.6 CCCc1nc2c(C)cc(C(=O)NCc3ccccc3OC)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2012.01.009
44303230 198953 0 None - 0 Rabbit 8.6 pIC50 = 8.6 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aortaIn vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aorta
ChEMBL 515 10 1 6 5.0 CCCc1nc(CC)c(C=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/S0960-894X(01)81124-0
CHEMBL59957 198953 0 None - 0 Rabbit 8.6 pIC50 = 8.6 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aortaIn vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aorta
ChEMBL 515 10 1 6 5.0 CCCc1nc(CC)c(C=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/S0960-894X(01)81124-0
10349506 206309 0 None - 0 Rabbit 8.6 pIC50 = 8.6 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 668 10 1 7 6.9 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2cccc(Cl)c2)cc1 10.1021/jm00043a020
CHEMBL97615 206309 0 None - 0 Rabbit 8.6 pIC50 = 8.6 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 668 10 1 7 6.9 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2cccc(Cl)c2)cc1 10.1021/jm00043a020
44305681 102141 0 None - 0 Rat 8.6 pIC50 = 8.6 Binding
Tested for binding affinity against angiotensin II receptor in rat adrenal cortexTested for binding affinity against angiotensin II receptor in rat adrenal cortex
ChEMBL 550 10 1 9 4.1 CCCCc1cc(=O)n(Cc2ccccc2C(=O)OC)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/0960-894X(95)00370-9
CHEMBL304251 102141 0 None - 0 Rat 8.6 pIC50 = 8.6 Binding
Tested for binding affinity against angiotensin II receptor in rat adrenal cortexTested for binding affinity against angiotensin II receptor in rat adrenal cortex
ChEMBL 550 10 1 9 4.1 CCCCc1cc(=O)n(Cc2ccccc2C(=O)OC)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/0960-894X(95)00370-9
10101582 118858 0 None - 0 Rabbit 8.6 pIC50 = 8.6 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 747 15 2 8 7.4 CCCCCNC(=O)c1ccc(-n2nc(CCCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)c4ccccc4Cl)cc3)c2=O)c(Cl)c1 10.1021/jm00052a006
CHEMBL344466 118858 0 None - 0 Rabbit 8.6 pIC50 = 8.6 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 747 15 2 8 7.4 CCCCCNC(=O)c1ccc(-n2nc(CCCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)c4ccccc4Cl)cc3)c2=O)c(Cl)c1 10.1021/jm00052a006
76333687 84821 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 506 11 1 6 5.0 CCCCc1ncc(/C=C2\C(=O)NC(=O)N2CCCC)n1Cc1ccc(C2(C(=O)OC)CCCC2)cc1 10.1007/s00044-009-9205-9
CHEMBL2259779 84821 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 506 11 1 6 5.0 CCCCc1ncc(/C=C2\C(=O)NC(=O)N2CCCC)n1Cc1ccc(C2(C(=O)OC)CCCC2)cc1 10.1007/s00044-009-9205-9
15231091 93541 0 None - 0 Rabbit 8.6 pIC50 = 8.6 Binding
Binding affinity against AT-1 receptor from rabbit aorta using [125I]-Sar1-Ile8-Ang II without BSABinding affinity against AT-1 receptor from rabbit aorta using [125I]-Sar1-Ile8-Ang II without BSA
ChEMBL 565 10 1 8 5.9 CCCCc1nc2ccc(N(C)C(=O)OCC(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00073a024
CHEMBL24861 93541 0 None - 0 Rabbit 8.6 pIC50 = 8.6 Binding
Binding affinity against AT-1 receptor from rabbit aorta using [125I]-Sar1-Ile8-Ang II without BSABinding affinity against AT-1 receptor from rabbit aorta using [125I]-Sar1-Ile8-Ang II without BSA
ChEMBL 565 10 1 8 5.9 CCCCc1nc2ccc(N(C)C(=O)OCC(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00073a024
44338697 109158 0 None - 0 Rabbit 8.6 pIC50 = 8.6 Binding
Binding affinity against AT-1 receptor from rabbit aorta using [125I]-Sar1-Ile8-Ang II without BSABinding affinity against AT-1 receptor from rabbit aorta using [125I]-Sar1-Ile8-Ang II without BSA
ChEMBL 613 11 1 8 6.8 CCCOC(=O)N(Cc1ccccc1)c1ccc2nc(CCC)n(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c(=O)c2c1 10.1021/jm00073a024
CHEMBL322471 109158 0 None - 0 Rabbit 8.6 pIC50 = 8.6 Binding
Binding affinity against AT-1 receptor from rabbit aorta using [125I]-Sar1-Ile8-Ang II without BSABinding affinity against AT-1 receptor from rabbit aorta using [125I]-Sar1-Ile8-Ang II without BSA
ChEMBL 613 11 1 8 6.8 CCCOC(=O)N(Cc1ccccc1)c1ccc2nc(CCC)n(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c(=O)c2c1 10.1021/jm00073a024
44277738 99710 0 None - 0 Rabbit 8.6 pIC50 = 8.6 Binding
Binding affinity against AT1 receptor in rabbit aortaBinding affinity against AT1 receptor in rabbit aorta
ChEMBL 589 7 0 8 6.3 Cn1nnnc1-c1ccccc1-c1ccc(Cn2cnc3ccc(N(C(=O)c4ccccc4)c4ccccc4)cc3c2=O)cc1 10.1016/0960-894X(95)00224-H
CHEMBL28816 99710 0 None - 0 Rabbit 8.6 pIC50 = 8.6 Binding
Binding affinity against AT1 receptor in rabbit aortaBinding affinity against AT1 receptor in rabbit aorta
ChEMBL 589 7 0 8 6.3 Cn1nnnc1-c1ccccc1-c1ccc(Cn2cnc3ccc(N(C(=O)c4ccccc4)c4ccccc4)cc3c2=O)cc1 10.1016/0960-894X(95)00224-H
76324571 103491 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Binding affinity to AT1 receptor (unknown origin)Binding affinity to AT1 receptor (unknown origin)
ChEMBL 378 7 1 8 1.9 CCCCc1nn(C)c(=O)n1Cc1ccc(-n2cccc2-c2nnn[nH]2)cc1 10.1016/j.bmc.2013.10.017
CHEMBL3092993 103491 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Binding affinity to AT1 receptor (unknown origin)Binding affinity to AT1 receptor (unknown origin)
ChEMBL 378 7 1 8 1.9 CCCCc1nn(C)c(=O)n1Cc1ccc(-n2cccc2-c2nnn[nH]2)cc1 10.1016/j.bmc.2013.10.017
9939191 98476 1 None - 1 Human 8.6 pIC50 = 8.6 Binding
In vitro binding affinity towards Angiotensin II receptor, type 1 to displace 125I[Sar,Ile] from human adrenal tissue preparationIn vitro binding affinity towards Angiotensin II receptor, type 1 to displace 125I[Sar,Ile] from human adrenal tissue preparation
ChEMBL 634 10 1 7 6.2 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/S0960-894X(01)81132-X
CHEMBL279629 98476 1 None - 1 Human 8.6 pIC50 = 8.6 Binding
In vitro binding affinity towards Angiotensin II receptor, type 1 to displace 125I[Sar,Ile] from human adrenal tissue preparationIn vitro binding affinity towards Angiotensin II receptor, type 1 to displace 125I[Sar,Ile] from human adrenal tissue preparation
ChEMBL 634 10 1 7 6.2 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/S0960-894X(01)81132-X
CHEMBL97539 98476 1 None - 1 Human 8.6 pIC50 = 8.6 Binding
In vitro binding affinity towards Angiotensin II receptor, type 1 to displace 125I[Sar,Ile] from human adrenal tissue preparationIn vitro binding affinity towards Angiotensin II receptor, type 1 to displace 125I[Sar,Ile] from human adrenal tissue preparation
ChEMBL 634 10 1 7 6.2 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/S0960-894X(01)81132-X
15231091 93541 0 None - 0 Rabbit 8.6 pIC50 = 8.6 Binding
Inhibition of Angiotensin II receptor, type 1Inhibition of Angiotensin II receptor, type 1
ChEMBL 565 10 1 8 5.9 CCCCc1nc2ccc(N(C)C(=O)OCC(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm9504722
CHEMBL24861 93541 0 None - 0 Rabbit 8.6 pIC50 = 8.6 Binding
Inhibition of Angiotensin II receptor, type 1Inhibition of Angiotensin II receptor, type 1
ChEMBL 565 10 1 8 5.9 CCCCc1nc2ccc(N(C)C(=O)OCC(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm9504722
10095986 16301 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 464 9 2 6 4.1 CCCCc1ncc(/C=C2\C(=O)NC(=O)N2Cc2cccs2)n1Cc1ccc(C(=O)O)cc1 10.1007/s00044-009-9205-9
CHEMBL123568 16301 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 464 9 2 6 4.1 CCCCc1ncc(/C=C2\C(=O)NC(=O)N2Cc2cccs2)n1Cc1ccc(C(=O)O)cc1 10.1007/s00044-009-9205-9
44277901 100909 0 None - 0 Rabbit 8.6 pIC50 = 8.6 Binding
Binding affinity against AT1 receptor in rabbit aortaBinding affinity against AT1 receptor in rabbit aorta
ChEMBL 585 10 1 9 4.7 Cn1nnnc1-c1ccccc1-c1ccc(Cn2cnc3ccc(N(CCCCO)C(=O)c4ccccc4)cc3c2=O)cc1 10.1016/0960-894X(95)00224-H
CHEMBL29722 100909 0 None - 0 Rabbit 8.6 pIC50 = 8.6 Binding
Binding affinity against AT1 receptor in rabbit aortaBinding affinity against AT1 receptor in rabbit aorta
ChEMBL 585 10 1 9 4.7 Cn1nnnc1-c1ccccc1-c1ccc(Cn2cnc3ccc(N(CCCCO)C(=O)c4ccccc4)cc3c2=O)cc1 10.1016/0960-894X(95)00224-H
11764669 66471 0 None - 0 Rabbit 8.6 pIC50 = 8.6 Binding
Displacement of 125I[Sar,Ile] from rabbit aorta membrane Angiotensin II receptor type 1Displacement of 125I[Sar,Ile] from rabbit aorta membrane Angiotensin II receptor type 1
ChEMBL 634 10 1 7 6.5 CCCCc1nn(-c2c(Cl)cccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/S0960-894X(01)81132-X
CHEMBL18606 66471 0 None - 0 Rabbit 8.6 pIC50 = 8.6 Binding
Displacement of 125I[Sar,Ile] from rabbit aorta membrane Angiotensin II receptor type 1Displacement of 125I[Sar,Ile] from rabbit aorta membrane Angiotensin II receptor type 1
ChEMBL 634 10 1 7 6.5 CCCCc1nn(-c2c(Cl)cccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/S0960-894X(01)81132-X
46910495 75964 0 None - 1 Human 8.6 pIC50 = 8.6 Binding
Displacement of [125I]Sar1Ile8-Ang2 from angiotensin AT1 receptor after 180 mins by gamma countingDisplacement of [125I]Sar1Ile8-Ang2 from angiotensin AT1 receptor after 180 mins by gamma counting
ChEMBL 585 11 2 7 6.2 CCCc1nc2c(C)cc(C(=O)NCCc3cccc(OC)c3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmc.2012.05.056
CHEMBL2058861 75964 0 None - 1 Human 8.6 pIC50 = 8.6 Binding
Displacement of [125I]Sar1Ile8-Ang2 from angiotensin AT1 receptor after 180 mins by gamma countingDisplacement of [125I]Sar1Ile8-Ang2 from angiotensin AT1 receptor after 180 mins by gamma counting
ChEMBL 585 11 2 7 6.2 CCCc1nc2c(C)cc(C(=O)NCCc3cccc(OC)c3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmc.2012.05.056
54578725 64781 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Displacement of [125I][Sar1,Ile8]-AT-II from human recombinant AT1 receptor expressed in HEK293 cells after 120 mins by liquid scintillation countingDisplacement of [125I][Sar1,Ile8]-AT-II from human recombinant AT1 receptor expressed in HEK293 cells after 120 mins by liquid scintillation counting
ChEMBL 403 8 3 7 4.0 CCCCn1ncc(C(=O)O)c1Nc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.ejmech.2011.05.056
CHEMBL1824184 64781 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Displacement of [125I][Sar1,Ile8]-AT-II from human recombinant AT1 receptor expressed in HEK293 cells after 120 mins by liquid scintillation countingDisplacement of [125I][Sar1,Ile8]-AT-II from human recombinant AT1 receptor expressed in HEK293 cells after 120 mins by liquid scintillation counting
ChEMBL 403 8 3 7 4.0 CCCCn1ncc(C(=O)O)c1Nc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.ejmech.2011.05.056
44211506 57222 0 None - 0 Rabbit 8.6 pIC50 = 8.6 Binding
In vitro displacement of 125I-[Sar1, Ile8] from AT1 receptors in rabbit aorta membraneIn vitro displacement of 125I-[Sar1, Ile8] from AT1 receptors in rabbit aorta membrane
ChEMBL 557 10 1 6 5.8 CCCCc1nc2ccc(C(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)C2CC2)cc1 10.1016/S0960-894X(01)81125-2
CHEMBL166338 57222 0 None - 0 Rabbit 8.6 pIC50 = 8.6 Binding
In vitro displacement of 125I-[Sar1, Ile8] from AT1 receptors in rabbit aorta membraneIn vitro displacement of 125I-[Sar1, Ile8] from AT1 receptors in rabbit aorta membrane
ChEMBL 557 10 1 6 5.8 CCCCc1nc2ccc(C(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)C2CC2)cc1 10.1016/S0960-894X(01)81125-2
44376780 56195 0 None - 0 Rabbit 8.6 pIC50 = 8.6 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aortaIn vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aorta
ChEMBL 509 10 1 7 4.1 CCCc1nc(CC)c(C(=O)OC)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)C2CC2)cc1 10.1016/S0960-894X(01)81124-0
CHEMBL163486 56195 0 None - 0 Rabbit 8.6 pIC50 = 8.6 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aortaIn vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aorta
ChEMBL 509 10 1 7 4.1 CCCc1nc(CC)c(C(=O)OC)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)C2CC2)cc1 10.1016/S0960-894X(01)81124-0
10349845 11242 0 None - 0 Rabbit 8.6 pIC50 = 8.6 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 708 10 1 8 7.6 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2cc(Cl)sc2Cl)cc1 10.1021/jm00043a020
CHEMBL1179731 11242 0 None - 0 Rabbit 8.6 pIC50 = 8.6 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 708 10 1 8 7.6 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2cc(Cl)sc2Cl)cc1 10.1021/jm00043a020
CHEMBL97271 11242 0 None - 0 Rabbit 8.6 pIC50 = 8.6 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 708 10 1 8 7.6 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2cc(Cl)sc2Cl)cc1 10.1021/jm00043a020
11764669 66471 0 None - 0 Rabbit 8.6 pIC50 = 8.6 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 634 10 1 7 6.5 CCCCc1nn(-c2c(Cl)cccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1021/jm00043a020
CHEMBL18606 66471 0 None - 0 Rabbit 8.6 pIC50 = 8.6 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 634 10 1 7 6.5 CCCCc1nn(-c2c(Cl)cccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1021/jm00043a020
10054753 206395 0 None - 0 Rabbit 8.6 pIC50 = 8.6 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 629 9 2 7 5.9 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)NC(C)(C)C)cc1 10.1021/jm00043a020
CHEMBL98140 206395 0 None - 0 Rabbit 8.6 pIC50 = 8.6 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 629 9 2 7 5.9 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)NC(C)(C)C)cc1 10.1021/jm00043a020
135723840 138599 0 None - 1 Rat 8.6 pIC50 = 8.6 Binding
Displacement of [125I]-Ang II from Angiotensin 2 type-1A receptor in rat vascular smooth muscle cells after 150 mins by gamma counting methodDisplacement of [125I]-Ang II from Angiotensin 2 type-1A receptor in rat vascular smooth muscle cells after 150 mins by gamma counting method
ChEMBL 452 8 2 6 4.6 CCCCc1nc(Cl)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2noc(=O)[nH]2)cc1 10.1016/j.bmc.2016.03.028
CHEMBL3787059 138599 0 None - 1 Rat 8.6 pIC50 = 8.6 Binding
Displacement of [125I]-Ang II from Angiotensin 2 type-1A receptor in rat vascular smooth muscle cells after 150 mins by gamma counting methodDisplacement of [125I]-Ang II from Angiotensin 2 type-1A receptor in rat vascular smooth muscle cells after 150 mins by gamma counting method
ChEMBL 452 8 2 6 4.6 CCCCc1nc(Cl)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2noc(=O)[nH]2)cc1 10.1016/j.bmc.2016.03.028
9984303 17400 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 524 11 2 7 4.8 CCCCc1ncc(/C=C2\C(=O)NC(=O)N2CCCC)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9205-9
CHEMBL125818 17400 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 524 11 2 7 4.8 CCCCc1ncc(/C=C2\C(=O)NC(=O)N2CCCC)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9205-9
127035264 135970 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 601 11 2 7 7.3 CCCSc1nc2c(C)cc(C(=O)NC[C@@H](C)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.ejmech.2015.09.010
CHEMBL3736244 135970 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 601 11 2 7 7.3 CCCSc1nc2c(C)cc(C(=O)NC[C@@H](C)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.ejmech.2015.09.010
183134 203126 13 None - 1 Human 8.6 pIC50 = 8.6 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation countingDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation counting
ChEMBL 409 5 1 6 4.5 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm200409s
CHEMBL7550 203126 13 None - 1 Human 8.6 pIC50 = 8.6 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation countingDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation counting
ChEMBL 409 5 1 6 4.5 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm200409s
2806 3894 109 None - 1 Human 8.6 pIC50 = 8.6 Binding
Tested for inhibition of Angiotensin II receptor, type 1 in the absence of bovine serum albumin (BSA)Tested for inhibition of Angiotensin II receptor, type 1 in the absence of bovine serum albumin (BSA)
ChEMBL 435 10 2 5 4.2 CCCCC(=O)N([C@H](C(=O)O)C(C)C)Cc1ccc(cc1)c1ccccc1c1nnn[nH]1 10.1016/S0960-894X(01)81117-3
3937 3894 109 None - 1 Human 8.6 pIC50 = 8.6 Binding
Tested for inhibition of Angiotensin II receptor, type 1 in the absence of bovine serum albumin (BSA)Tested for inhibition of Angiotensin II receptor, type 1 in the absence of bovine serum albumin (BSA)
ChEMBL 435 10 2 5 4.2 CCCCC(=O)N([C@H](C(=O)O)C(C)C)Cc1ccc(cc1)c1ccccc1c1nnn[nH]1 10.1016/S0960-894X(01)81117-3
593 3894 109 None - 1 Human 8.6 pIC50 = 8.6 Binding
Tested for inhibition of Angiotensin II receptor, type 1 in the absence of bovine serum albumin (BSA)Tested for inhibition of Angiotensin II receptor, type 1 in the absence of bovine serum albumin (BSA)
ChEMBL 435 10 2 5 4.2 CCCCC(=O)N([C@H](C(=O)O)C(C)C)Cc1ccc(cc1)c1ccccc1c1nnn[nH]1 10.1016/S0960-894X(01)81117-3
60846 3894 109 None - 1 Human 8.6 pIC50 = 8.6 Binding
Tested for inhibition of Angiotensin II receptor, type 1 in the absence of bovine serum albumin (BSA)Tested for inhibition of Angiotensin II receptor, type 1 in the absence of bovine serum albumin (BSA)
ChEMBL 435 10 2 5 4.2 CCCCC(=O)N([C@H](C(=O)O)C(C)C)Cc1ccc(cc1)c1ccccc1c1nnn[nH]1 10.1016/S0960-894X(01)81117-3
CHEMBL1069 3894 109 None - 1 Human 8.6 pIC50 = 8.6 Binding
Tested for inhibition of Angiotensin II receptor, type 1 in the absence of bovine serum albumin (BSA)Tested for inhibition of Angiotensin II receptor, type 1 in the absence of bovine serum albumin (BSA)
ChEMBL 435 10 2 5 4.2 CCCCC(=O)N([C@H](C(=O)O)C(C)C)Cc1ccc(cc1)c1ccccc1c1nnn[nH]1 10.1016/S0960-894X(01)81117-3
DB00177 3894 109 None - 1 Human 8.6 pIC50 = 8.6 Binding
Tested for inhibition of Angiotensin II receptor, type 1 in the absence of bovine serum albumin (BSA)Tested for inhibition of Angiotensin II receptor, type 1 in the absence of bovine serum albumin (BSA)
ChEMBL 435 10 2 5 4.2 CCCCC(=O)N([C@H](C(=O)O)C(C)C)Cc1ccc(cc1)c1ccccc1c1nnn[nH]1 10.1016/S0960-894X(01)81117-3
10342301 17741 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 424 10 2 5 3.7 CCCCc1ncc(/C=C2/C(=O)NC(=O)N2CCCC)n1Cc1ccc(C(=O)O)cc1 10.1007/s00044-009-9205-9
CHEMBL125937 17741 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 424 10 2 5 3.7 CCCCc1ncc(/C=C2/C(=O)NC(=O)N2CCCC)n1Cc1ccc(C(=O)O)cc1 10.1007/s00044-009-9205-9
44277547 98733 0 None - 0 Rabbit 8.6 pIC50 = 8.6 Binding
Binding affinity against AT1 receptor in rabbit aortaBinding affinity against AT1 receptor in rabbit aorta
ChEMBL 589 10 0 9 6.2 CCCCCN(C(=O)c1cccs1)c1ccc2ncn(Cc3ccc(-c4ccccc4-c4nnnn4C)cc3)c(=O)c2c1 10.1016/0960-894X(95)00224-H
CHEMBL281453 98733 0 None - 0 Rabbit 8.6 pIC50 = 8.6 Binding
Binding affinity against AT1 receptor in rabbit aortaBinding affinity against AT1 receptor in rabbit aorta
ChEMBL 589 10 0 9 6.2 CCCCCN(C(=O)c1cccs1)c1ccc2ncn(Cc3ccc(-c4ccccc4-c4nnnn4C)cc3)c(=O)c2c1 10.1016/0960-894X(95)00224-H
44277463 100823 0 None - 0 Rabbit 8.6 pIC50 = 8.6 Binding
Binding affinity against AT1 receptor in rabbit aortaBinding affinity against AT1 receptor in rabbit aorta
ChEMBL 584 10 0 9 5.5 CCCCCN(C(=O)c1ccncc1)c1ccc2ncn(Cc3ccc(-c4ccccc4-c4nnnn4C)cc3)c(=O)c2c1 10.1016/0960-894X(95)00224-H
CHEMBL29654 100823 0 None - 0 Rabbit 8.6 pIC50 = 8.6 Binding
Binding affinity against AT1 receptor in rabbit aortaBinding affinity against AT1 receptor in rabbit aorta
ChEMBL 584 10 0 9 5.5 CCCCCN(C(=O)c1ccncc1)c1ccc2ncn(Cc3ccc(-c4ccccc4-c4nnnn4C)cc3)c(=O)c2c1 10.1016/0960-894X(95)00224-H
44348408 113061 0 None - 0 Rabbit 8.6 pIC50 = 8.6 Binding
Displacement of [1251][Sar1,IIe8]AII from rabbit aorta Angiotensin II receptor, type 1Displacement of [1251][Sar1,IIe8]AII from rabbit aorta Angiotensin II receptor, type 1
ChEMBL 533 11 1 5 7.4 CCCc1cc(Cn2c(CC)nc3c(C)cc(C)nc32)cc(CCC)c1OC(C(=O)O)c1ccc(Cl)cc1 10.1021/jm00075a033
CHEMBL332239 113061 0 None - 0 Rabbit 8.6 pIC50 = 8.6 Binding
Displacement of [1251][Sar1,IIe8]AII from rabbit aorta Angiotensin II receptor, type 1Displacement of [1251][Sar1,IIe8]AII from rabbit aorta Angiotensin II receptor, type 1
ChEMBL 533 11 1 5 7.4 CCCc1cc(Cn2c(CC)nc3c(C)cc(C)nc32)cc(CCC)c1OC(C(=O)O)c1ccc(Cl)cc1 10.1021/jm00075a033
44379086 56269 0 None - 0 Rabbit 8.6 pIC50 = 8.6 Binding
In vitro displacement of 125I-[Sar1, Ile8] from AT1 receptors in rabbit aorta membraneIn vitro displacement of 125I-[Sar1, Ile8] from AT1 receptors in rabbit aorta membrane
ChEMBL 543 9 1 6 5.4 CCCc1nc2ccc(C(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)C2CC2)cc1 10.1016/S0960-894X(01)81125-2
CHEMBL164174 56269 0 None - 0 Rabbit 8.6 pIC50 = 8.6 Binding
In vitro displacement of 125I-[Sar1, Ile8] from AT1 receptors in rabbit aorta membraneIn vitro displacement of 125I-[Sar1, Ile8] from AT1 receptors in rabbit aorta membrane
ChEMBL 543 9 1 6 5.4 CCCc1nc2ccc(C(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)C2CC2)cc1 10.1016/S0960-894X(01)81125-2
108185 1578 71 None - 1 Rabbit 8.6 pIC50 = 8.6 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 436 8 2 6 4.5 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)C(=O)O)Cl 10.1021/jm00043a020
586 1578 71 None - 1 Rabbit 8.6 pIC50 = 8.6 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 436 8 2 6 4.5 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)C(=O)O)Cl 10.1021/jm00043a020
CHEMBL907 1578 71 None - 1 Rabbit 8.6 pIC50 = 8.6 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 436 8 2 6 4.5 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)C(=O)O)Cl 10.1021/jm00043a020
10372723 106821 0 None - 0 Rabbit 8.6 pIC50 = 8.6 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 724 12 1 7 7.7 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)C(c2ccccc2)c2ccccc2)cc1 10.1021/jm00043a020
CHEMBL317368 106821 0 None - 0 Rabbit 8.6 pIC50 = 8.6 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 724 12 1 7 7.7 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)C(c2ccccc2)c2ccccc2)cc1 10.1021/jm00043a020
10349029 206346 0 None - 0 Rabbit 8.6 pIC50 = 8.6 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 628 10 1 8 5.0 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)C2CCOC2)cc1 10.1021/jm00043a020
CHEMBL97812 206346 0 None - 0 Rabbit 8.6 pIC50 = 8.6 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 628 10 1 8 5.0 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)C2CCOC2)cc1 10.1021/jm00043a020
145946921 167028 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Displacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysisDisplacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysis
ChEMBL 592 11 1 7 5.5 CCCCc1c[n+](Cc2ccc(-c3ccccc3-c3nn[n-]n3)cc2)cn1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.ejmech.2012.12.044
CHEMBL2337687 167028 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Displacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysisDisplacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysis
ChEMBL 592 11 1 7 5.5 CCCCc1c[n+](Cc2ccc(-c3ccccc3-c3nn[n-]n3)cc2)cn1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.ejmech.2012.12.044
CHEMBL2337688 167028 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Displacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysisDisplacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysis
ChEMBL 592 11 1 7 5.5 CCCCc1c[n+](Cc2ccc(-c3ccccc3-c3nn[n-]n3)cc2)cn1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.ejmech.2012.12.044
CHEMBL4300967 167028 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Displacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysisDisplacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysis
ChEMBL 592 11 1 7 5.5 CCCCc1c[n+](Cc2ccc(-c3ccccc3-c3nn[n-]n3)cc2)cn1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.ejmech.2012.12.044
10298977 204590 0 None - 0 Rabbit 8.5 pIC50 = 8.5 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 471 9 1 7 4.9 CCCCc1nn(CC2CCCCC2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
CHEMBL87239 204590 0 None - 0 Rabbit 8.5 pIC50 = 8.5 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 471 9 1 7 4.9 CCCCc1nn(CC2CCCCC2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
131654 204667 10 None - 1 Rabbit 8.5 pIC50 = 8.5 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 431 10 1 7 4.1 CCCCc1nn(CCCC)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
CHEMBL87778 204667 10 None - 1 Rabbit 8.5 pIC50 = 8.5 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 431 10 1 7 4.1 CCCCc1nn(CCCC)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
10055096 97820 0 None - 0 Rabbit 8.5 pIC50 = 8.5 Binding
Displacement of 125I[Sar,Ile] from rabbit aorta membrane Angiotensin II receptor type 1Displacement of 125I[Sar,Ile] from rabbit aorta membrane Angiotensin II receptor type 1
ChEMBL 656 15 1 7 7.3 CCCCCCCC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCCC)nn(-c3ccccc3C(F)(F)F)c2=O)cc1 10.1016/S0960-894X(01)81132-X
CHEMBL274712 97820 0 None - 0 Rabbit 8.5 pIC50 = 8.5 Binding
Displacement of 125I[Sar,Ile] from rabbit aorta membrane Angiotensin II receptor type 1Displacement of 125I[Sar,Ile] from rabbit aorta membrane Angiotensin II receptor type 1
ChEMBL 656 15 1 7 7.3 CCCCCCCC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCCC)nn(-c3ccccc3C(F)(F)F)c2=O)cc1 10.1016/S0960-894X(01)81132-X
25147556 173281 0 None - 0 Bovine 8.5 pIC50 = 8.5 Binding
Displacement of radiolabeled angiotensin 2 from angiotensin AT1 receptor in bovine adrenal cortex membranesDisplacement of radiolabeled angiotensin 2 from angiotensin AT1 receptor in bovine adrenal cortex membranes
ChEMBL 538 7 1 6 6.9 CCCc1nc2c(C)cc(-c3nc4ccccc4n3C)cc2n1Cc1ccc(-c2ccccc2C2=NCCN2)cc1 10.1016/j.bmc.2010.10.043
CHEMBL453934 173281 0 None - 0 Bovine 8.5 pIC50 = 8.5 Binding
Displacement of radiolabeled angiotensin 2 from angiotensin AT1 receptor in bovine adrenal cortex membranesDisplacement of radiolabeled angiotensin 2 from angiotensin AT1 receptor in bovine adrenal cortex membranes
ChEMBL 538 7 1 6 6.9 CCCc1nc2c(C)cc(-c3nc4ccccc4n3C)cc2n1Cc1ccc(-c2ccccc2C2=NCCN2)cc1 10.1016/j.bmc.2010.10.043
44377261 119400 0 None - 0 Rabbit 8.5 pIC50 = 8.5 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aortaIn vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aorta
ChEMBL 402 8 1 7 3.6 CCCCc1ncc(C(=O)O)n1Cc1ccc(-c2ccccc2-n2cnnn2)cc1 10.1016/S0960-894X(01)81124-0
CHEMBL349389 119400 0 None - 0 Rabbit 8.5 pIC50 = 8.5 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aortaIn vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aorta
ChEMBL 402 8 1 7 3.6 CCCCc1ncc(C(=O)O)n1Cc1ccc(-c2ccccc2-n2cnnn2)cc1 10.1016/S0960-894X(01)81124-0
10055096 97820 0 None - 0 Rabbit 8.5 pIC50 = 8.5 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 656 15 1 7 7.3 CCCCCCCC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCCC)nn(-c3ccccc3C(F)(F)F)c2=O)cc1 10.1021/jm00043a020
CHEMBL274712 97820 0 None - 0 Rabbit 8.5 pIC50 = 8.5 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 656 15 1 7 7.3 CCCCCCCC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCCC)nn(-c3ccccc3C(F)(F)F)c2=O)cc1 10.1021/jm00043a020
44316916 203575 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Tested for inhibition of Angiotensin II specific binding to Angiotensin II receptor, type 1 in the recombinant human AT-1 receptor expressed in LhAT-1D6 cellsTested for inhibition of Angiotensin II specific binding to Angiotensin II receptor, type 1 in the recombinant human AT-1 receptor expressed in LhAT-1D6 cells
ChEMBL 474 12 4 5 4.2 CCCCc1ncc(CN[C@H](Cc2c[nH]c3ccccc23)C(=O)O)n1Cc1ccc(C(=O)O)cc1 10.1016/0960-894X(94)00456-P
CHEMBL79242 203575 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Tested for inhibition of Angiotensin II specific binding to Angiotensin II receptor, type 1 in the recombinant human AT-1 receptor expressed in LhAT-1D6 cellsTested for inhibition of Angiotensin II specific binding to Angiotensin II receptor, type 1 in the recombinant human AT-1 receptor expressed in LhAT-1D6 cells
ChEMBL 474 12 4 5 4.2 CCCCc1ncc(CN[C@H](Cc2c[nH]c3ccccc23)C(=O)O)n1Cc1ccc(C(=O)O)cc1 10.1016/0960-894X(94)00456-P
44295009 186578 0 None - 1 Bovine 7.7 pIC50 = 7.7 Binding
Ability to displace [125I]- labelled [Sar1,Ileu8] from angiotensin II receptor of bovine adrenal cortex membranesAbility to displace [125I]- labelled [Sar1,Ileu8] from angiotensin II receptor of bovine adrenal cortex membranes
ChEMBL 473 8 1 6 4.9 CCOC(=O)/C=C1\CC(CC)(CC)CC(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80474-6
CHEMBL49207 186578 0 None - 1 Bovine 7.7 pIC50 = 7.7 Binding
Ability to displace [125I]- labelled [Sar1,Ileu8] from angiotensin II receptor of bovine adrenal cortex membranesAbility to displace [125I]- labelled [Sar1,Ileu8] from angiotensin II receptor of bovine adrenal cortex membranes
ChEMBL 473 8 1 6 4.9 CCOC(=O)/C=C1\CC(CC)(CC)CC(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80474-6
44275060 99241 0 None - 0 Rabbit 7.7 pIC50 = 7.7 Binding
Ability to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitroAbility to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitro
ChEMBL 576 7 2 7 6.3 O=C(O)c1ccccc1-c1ccc(-c2nc3ccccc3c(=O)n2Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)cc1 10.1016/S0960-894X(00)80335-2
CHEMBL284764 99241 0 None - 0 Rabbit 7.7 pIC50 = 7.7 Binding
Ability to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitroAbility to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitro
ChEMBL 576 7 2 7 6.3 O=C(O)c1ccccc1-c1ccc(-c2nc3ccccc3c(=O)n2Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)cc1 10.1016/S0960-894X(00)80335-2
10370172 50541 0 None - 0 Rabbit 7.7 pIC50 = 7.7 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 544 12 3 7 5.5 CCCCc1nnc(SC(C(=O)O)c2ccccc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
CHEMBL157690 50541 0 None - 0 Rabbit 7.7 pIC50 = 7.7 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 544 12 3 7 5.5 CCCCc1nnc(SC(C(=O)O)c2ccccc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
44277444 100457 0 None - 0 Rabbit 7.7 pIC50 = 7.7 Binding
Binding affinity against AT1 receptor in rabbit aortaBinding affinity against AT1 receptor in rabbit aorta
ChEMBL 569 11 0 8 6.5 CCCCCN(Cc1ccccc1)c1ccc2ncn(Cc3ccc(-c4ccccc4-c4nnnn4C)cc3)c(=O)c2c1 10.1016/0960-894X(95)00224-H
CHEMBL29402 100457 0 None - 0 Rabbit 7.7 pIC50 = 7.7 Binding
Binding affinity against AT1 receptor in rabbit aortaBinding affinity against AT1 receptor in rabbit aorta
ChEMBL 569 11 0 8 6.5 CCCCCN(Cc1ccccc1)c1ccc2ncn(Cc3ccc(-c4ccccc4-c4nnnn4C)cc3)c(=O)c2c1 10.1016/0960-894X(95)00224-H
15356436 101531 0 None - 0 Rat 7.7 pIC50 = 7.7 Binding
Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.
ChEMBL 514 12 3 6 4.9 CCCCc1ncc(C(=O)O)n1Cc1ccc(NC(=O)[C@H](Cc2ccccc2)n2cccc2C(=O)O)cc1 10.1021/jm00064a007
CHEMBL301705 101531 0 None - 0 Rat 7.7 pIC50 = 7.7 Binding
Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.
ChEMBL 514 12 3 6 4.9 CCCCc1ncc(C(=O)O)n1Cc1ccc(NC(=O)[C@H](Cc2ccccc2)n2cccc2C(=O)O)cc1 10.1021/jm00064a007
44311406 103317 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 701 13 1 8 8.6 CCCc1nc(CC)c(C(=O)OCc2ccc(C(=O)N(c3ccccc3)c3ccccc3)cc2)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80077-3
CHEMBL309081 103317 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 701 13 1 8 8.6 CCCc1nc(CC)c(C(=O)OCc2ccc(C(=O)N(c3ccccc3)c3ccccc3)cc2)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80077-3
44341670 9847 0 None - 0 Rat 7.7 pIC50 = 7.7 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 434 9 1 3 6.0 CCCCC1=NC(C(C)C)(C(C)C)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00074a018
CHEMBL114687 9847 0 None - 0 Rat 7.7 pIC50 = 7.7 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 434 9 1 3 6.0 CCCCC1=NC(C(C)C)(C(C)C)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00074a018
44322315 204525 0 None - 0 Guinea pig 7.7 pIC50 = 7.7 Binding
Compound was tested for in vitro inhibition of specific binding of [I-125]AII to AT1 receptor in guinea pig adrenal membrane preparationCompound was tested for in vitro inhibition of specific binding of [I-125]AII to AT1 receptor in guinea pig adrenal membrane preparation
ChEMBL 469 7 1 7 4.7 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)c(C(=O)OC)c2)c2c(n1)CCCC2 10.1016/S0960-894X(01)80295-X
CHEMBL86858 204525 0 None - 0 Guinea pig 7.7 pIC50 = 7.7 Binding
Compound was tested for in vitro inhibition of specific binding of [I-125]AII to AT1 receptor in guinea pig adrenal membrane preparationCompound was tested for in vitro inhibition of specific binding of [I-125]AII to AT1 receptor in guinea pig adrenal membrane preparation
ChEMBL 469 7 1 7 4.7 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)c(C(=O)OC)c2)c2c(n1)CCCC2 10.1016/S0960-894X(01)80295-X
44285177 138114 0 None - 0 Rat 7.7 pIC50 = 7.7 Binding
Displacement of [125I]- Ang II from type 1 Angiotensin II receptorDisplacement of [125I]- Ang II from type 1 Angiotensin II receptor
ChEMBL 496 6 1 5 4.9 CCCC1=NC(C(F)(F)F)(C(F)(F)F)C(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80526-6
CHEMBL37768 138114 0 None - 0 Rat 7.7 pIC50 = 7.7 Binding
Displacement of [125I]- Ang II from type 1 Angiotensin II receptorDisplacement of [125I]- Ang II from type 1 Angiotensin II receptor
ChEMBL 496 6 1 5 4.9 CCCC1=NC(C(F)(F)F)(C(F)(F)F)C(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80526-6
10370172 50541 0 None - 0 Rabbit 7.7 pIC50 = 7.7 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 544 12 3 7 5.5 CCCCc1nnc(SC(C(=O)O)c2ccccc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
CHEMBL157690 50541 0 None - 0 Rabbit 7.7 pIC50 = 7.7 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 544 12 3 7 5.5 CCCCc1nnc(SC(C(=O)O)c2ccccc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
73349424 92185 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Displacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysisDisplacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysis
ChEMBL 495 7 1 4 6.3 CCCc1nc2c(C)cc(C(=O)N3CCCCC3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2013.08.014
CHEMBL2435833 92185 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Displacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysisDisplacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysis
ChEMBL 495 7 1 4 6.3 CCCc1nc2c(C)cc(C(=O)N3CCCCC3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2013.08.014
44311568 97719 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
In vitro binding affinity of compound against Angiotensin II receptor, type 1In vitro binding affinity of compound against Angiotensin II receptor, type 1
ChEMBL 607 13 2 8 6.2 CCCc1nc(CN(Cc2ccccc2)C(=O)OCC(C)C)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80076-1
CHEMBL273992 97719 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
In vitro binding affinity of compound against Angiotensin II receptor, type 1In vitro binding affinity of compound against Angiotensin II receptor, type 1
ChEMBL 607 13 2 8 6.2 CCCc1nc(CN(Cc2ccccc2)C(=O)OCC(C)C)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80076-1
44311636 202420 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
In vitro binding affinity of compound against Angiotensin II receptor, type 1In vitro binding affinity of compound against Angiotensin II receptor, type 1
ChEMBL 549 9 2 9 3.8 CCc1nc(CN2CCN(c3ccccn3)CC2)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80076-1
CHEMBL70389 202420 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
In vitro binding affinity of compound against Angiotensin II receptor, type 1In vitro binding affinity of compound against Angiotensin II receptor, type 1
ChEMBL 549 9 2 9 3.8 CCc1nc(CN2CCN(c3ccccn3)CC2)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80076-1
44311569 202988 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
In vitro binding affinity of compound against Angiotensin II receptor, type 1In vitro binding affinity of compound against Angiotensin II receptor, type 1
ChEMBL 625 13 2 7 6.2 CCCc1nc(CN(Cc2ccccc2)C(=O)Cc2ccccc2)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80076-1
CHEMBL74113 202988 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
In vitro binding affinity of compound against Angiotensin II receptor, type 1In vitro binding affinity of compound against Angiotensin II receptor, type 1
ChEMBL 625 13 2 7 6.2 CCCc1nc(CN(Cc2ccccc2)C(=O)Cc2ccccc2)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80076-1
44377086 119433 0 None - 0 Rabbit 7.7 pIC50 = 7.7 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aortaIn vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aorta
ChEMBL 546 11 2 7 4.8 CCCCc1ncc(C(=O)OC)n1Cc1ccc(-c2ccccc2NS(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/S0960-894X(01)81124-0
CHEMBL349652 119433 0 None - 0 Rabbit 7.7 pIC50 = 7.7 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aortaIn vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aorta
ChEMBL 546 11 2 7 4.8 CCCCc1ncc(C(=O)OC)n1Cc1ccc(-c2ccccc2NS(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/S0960-894X(01)81124-0
10202093 204699 0 None - 0 Rat 7.7 pIC50 = 7.7 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 417 8 1 7 3.9 CCCCc1nn(C(C)C)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a015
CHEMBL87985 204699 0 None - 0 Rat 7.7 pIC50 = 7.7 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 417 8 1 7 3.9 CCCCc1nn(C(C)C)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a015
44305267 201701 0 None - 0 Bovine 7.7 pIC50 = 7.7 Binding
Tested for binding affinity against angiotensin II receptor in bovine adrenal cortexTested for binding affinity against angiotensin II receptor in bovine adrenal cortex
ChEMBL 536 9 1 9 3.7 CCCc1cc(=O)n(Cc2ccccc2C(=O)OC)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/0960-894X(95)00370-9
CHEMBL65503 201701 0 None - 0 Bovine 7.7 pIC50 = 7.7 Binding
Tested for binding affinity against angiotensin II receptor in bovine adrenal cortexTested for binding affinity against angiotensin II receptor in bovine adrenal cortex
ChEMBL 536 9 1 9 3.7 CCCc1cc(=O)n(Cc2ccccc2C(=O)OC)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/0960-894X(95)00370-9
19385603 98311 0 None - 0 Rabbit 7.7 pIC50 = 7.7 Binding
Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)
ChEMBL 455 9 1 5 5.6 C=CCc1cc(Cn2c(CC)nc3c(C)cc(C)nc32)ccc1OC(C(=O)O)c1ccccc1 10.1016/0960-894X(95)00185-V
CHEMBL278234 98311 0 None - 0 Rabbit 7.7 pIC50 = 7.7 Binding
Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)
ChEMBL 455 9 1 5 5.6 C=CCc1cc(Cn2c(CC)nc3c(C)cc(C)nc32)ccc1OC(C(=O)O)c1ccccc1 10.1016/0960-894X(95)00185-V
1481 2027 109 None 1 3 Human 7.7 pIC50 = 7.7 Binding
Binding affinity to angiotensin AT1 receptorBinding affinity to angiotensin AT1 receptor
ChEMBL 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 10.1016/j.bmc.2010.10.043
3749 2027 109 None 1 3 Human 7.7 pIC50 = 7.7 Binding
Binding affinity to angiotensin AT1 receptorBinding affinity to angiotensin AT1 receptor
ChEMBL 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 10.1016/j.bmc.2010.10.043
589 2027 109 None 1 3 Human 7.7 pIC50 = 7.7 Binding
Binding affinity to angiotensin AT1 receptorBinding affinity to angiotensin AT1 receptor
ChEMBL 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 10.1016/j.bmc.2010.10.043
6908 2027 109 None 1 3 Human 7.7 pIC50 = 7.7 Binding
Binding affinity to angiotensin AT1 receptorBinding affinity to angiotensin AT1 receptor
ChEMBL 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 10.1016/j.bmc.2010.10.043
CHEMBL1513 2027 109 None 1 3 Human 7.7 pIC50 = 7.7 Binding
Binding affinity to angiotensin AT1 receptorBinding affinity to angiotensin AT1 receptor
ChEMBL 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 10.1016/j.bmc.2010.10.043
DB01029 2027 109 None 1 3 Human 7.7 pIC50 = 7.7 Binding
Binding affinity to angiotensin AT1 receptorBinding affinity to angiotensin AT1 receptor
ChEMBL 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 10.1016/j.bmc.2010.10.043
44294976 161106 0 None - 0 Bovine 6.7 pIC50 = 6.7 Binding
Ability to displace [125I]- labelled [Sar1,Ileu8] from angiotensin II receptor of bovine adrenal cortex membranesAbility to displace [125I]- labelled [Sar1,Ileu8] from angiotensin II receptor of bovine adrenal cortex membranes
ChEMBL 431 6 1 6 3.7 CCOC(=O)/C=C1\CC(C)CC(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80474-6
CHEMBL413098 161106 0 None - 0 Bovine 6.7 pIC50 = 6.7 Binding
Ability to displace [125I]- labelled [Sar1,Ileu8] from angiotensin II receptor of bovine adrenal cortex membranesAbility to displace [125I]- labelled [Sar1,Ileu8] from angiotensin II receptor of bovine adrenal cortex membranes
ChEMBL 431 6 1 6 3.7 CCOC(=O)/C=C1\CC(C)CC(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80474-6
15699056 109179 0 None - 0 Rat 6.7 pIC50 = 6.7 Binding
Binding affinity against Angiotensin II receptor in rat smooth muscle cell preparationsBinding affinity against Angiotensin II receptor in rat smooth muscle cell preparations
ChEMBL 396 7 2 6 3.8 CCCCc1nc(CO)c(Cl)n1Cc1ccc2cc(-c3nn[nH]n3)ccc2c1 10.1021/jm00114a021
CHEMBL322683 109179 0 None - 0 Rat 6.7 pIC50 = 6.7 Binding
Binding affinity against Angiotensin II receptor in rat smooth muscle cell preparationsBinding affinity against Angiotensin II receptor in rat smooth muscle cell preparations
ChEMBL 396 7 2 6 3.8 CCCCc1nc(CO)c(Cl)n1Cc1ccc2cc(-c3nn[nH]n3)ccc2c1 10.1021/jm00114a021
44459821 95924 0 None - 0 Rabbit 6.7 pIC50 = 6.7 Binding
Binding affinity against Angiotensin II type 1 Receptor in rabbit aortic tissueBinding affinity against Angiotensin II type 1 Receptor in rabbit aortic tissue
ChEMBL 412 7 1 4 5.2 CCCCc1nc2ccccc2c(=O)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/S0960-894X(00)80334-0
CHEMBL26179 95924 0 None - 0 Rabbit 6.7 pIC50 = 6.7 Binding
Binding affinity against Angiotensin II type 1 Receptor in rabbit aortic tissueBinding affinity against Angiotensin II type 1 Receptor in rabbit aortic tissue
ChEMBL 412 7 1 4 5.2 CCCCc1nc2ccccc2c(=O)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/S0960-894X(00)80334-0
11930 1002 0 None - 2 Rabbit 6.7 pIC50 = 6.7 Binding
Displacement of [125 I]Sar1Ile8-AII from type 1 Angiotensin II receptor of rabbit aorta membraneDisplacement of [125 I]Sar1Ile8-AII from type 1 Angiotensin II receptor of rabbit aorta membrane
ChEMBL 623 9 1 8 6.8 CCc1nc2c(cc(cc2)N(Cc2ccccc2)C(=O)c2cccs2)c(=O)n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1 10.1016/S0960-894X(01)80517-5
15780052 1002 0 None - 2 Rabbit 6.7 pIC50 = 6.7 Binding
Displacement of [125 I]Sar1Ile8-AII from type 1 Angiotensin II receptor of rabbit aorta membraneDisplacement of [125 I]Sar1Ile8-AII from type 1 Angiotensin II receptor of rabbit aorta membrane
ChEMBL 623 9 1 8 6.8 CCc1nc2c(cc(cc2)N(Cc2ccccc2)C(=O)c2cccs2)c(=O)n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1 10.1016/S0960-894X(01)80517-5
CHEMBL289472 1002 0 None - 2 Rabbit 6.7 pIC50 = 6.7 Binding
Displacement of [125 I]Sar1Ile8-AII from type 1 Angiotensin II receptor of rabbit aorta membraneDisplacement of [125 I]Sar1Ile8-AII from type 1 Angiotensin II receptor of rabbit aorta membrane
ChEMBL 623 9 1 8 6.8 CCc1nc2c(cc(cc2)N(Cc2ccccc2)C(=O)c2cccs2)c(=O)n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1 10.1016/S0960-894X(01)80517-5
44438869 145790 0 None - 1 Bovine 6.7 pIC50 = 6.7 Binding
Displacement of [125I]angiotensin-2 from bovine adrenal cortex AT1 receptorDisplacement of [125I]angiotensin-2 from bovine adrenal cortex AT1 receptor
ChEMBL 413 5 1 8 3.2 COC(=O)c1cccc2nc(C)n(Cc3ccc(-n4cccc4-c4nnn[nH]4)cc3)c12 10.1016/j.bmcl.2007.02.042
CHEMBL392118 145790 0 None - 1 Bovine 6.7 pIC50 = 6.7 Binding
Displacement of [125I]angiotensin-2 from bovine adrenal cortex AT1 receptorDisplacement of [125I]angiotensin-2 from bovine adrenal cortex AT1 receptor
ChEMBL 413 5 1 8 3.2 COC(=O)c1cccc2nc(C)n(Cc3ccc(-n4cccc4-c4nnn[nH]4)cc3)c12 10.1016/j.bmcl.2007.02.042
10600595 110647 18 None - 0 Bovine 6.7 pIC50 = 6.7 Binding
In vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortexIn vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortex
ChEMBL 474 9 2 8 4.1 CCCc1nc(C(C)(C)O)c(C(=O)OCC)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm950450f
CHEMBL326400 110647 18 None - 0 Bovine 6.7 pIC50 = 6.7 Binding
In vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortexIn vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortex
ChEMBL 474 9 2 8 4.1 CCCc1nc(C(C)(C)O)c(C(=O)OCC)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm950450f
44342142 9839 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Tested for inhibition of Angiotensin II receptor, type 1 in the absence of bovine serum albumin (BSA)Tested for inhibition of Angiotensin II receptor, type 1 in the absence of bovine serum albumin (BSA)
ChEMBL 407 9 2 5 3.5 CCCCC(=O)N(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)[C@H](C)C(=O)O 10.1016/S0960-894X(01)81117-3
CHEMBL114653 9839 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Tested for inhibition of Angiotensin II receptor, type 1 in the absence of bovine serum albumin (BSA)Tested for inhibition of Angiotensin II receptor, type 1 in the absence of bovine serum albumin (BSA)
ChEMBL 407 9 2 5 3.5 CCCCC(=O)N(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)[C@H](C)C(=O)O 10.1016/S0960-894X(01)81117-3
10363869 20251 0 None - 0 Rat 5.7 pIC50 = 5.7 Binding
Activity against high affinity Angiotensin II receptor, type 1 was measured from the ability to inhibit [125I]angiotensin II binding to rat uterine membrane.Activity against high affinity Angiotensin II receptor, type 1 was measured from the ability to inhibit [125I]angiotensin II binding to rat uterine membrane.
ChEMBL 404 10 1 7 4.0 CCCCc1nc(CCCC)n(Cc2ccc(-n3ccc(-c4nn[nH]n4)c3)cc2)n1 10.1021/jm00053a013
CHEMBL13071 20251 0 None - 0 Rat 5.7 pIC50 = 5.7 Binding
Activity against high affinity Angiotensin II receptor, type 1 was measured from the ability to inhibit [125I]angiotensin II binding to rat uterine membrane.Activity against high affinity Angiotensin II receptor, type 1 was measured from the ability to inhibit [125I]angiotensin II binding to rat uterine membrane.
ChEMBL 404 10 1 7 4.0 CCCCc1nc(CCCC)n(Cc2ccc(-n3ccc(-c4nn[nH]n4)c3)cc2)n1 10.1021/jm00053a013
54768659 64770 0 None - 0 Human 5.7 pIC50 = 5.7 Binding
Displacement of [125I][Sar1,Ile8]-AT-II from human recombinant AT1 receptor expressed in HEK293 cells after 120 mins by liquid scintillation countingDisplacement of [125I][Sar1,Ile8]-AT-II from human recombinant AT1 receptor expressed in HEK293 cells after 120 mins by liquid scintillation counting
ChEMBL 507 8 1 8 4.6 CCOC(=O)c1cn(Cc2ccc(-c3ccccc3-c3nnn[nH]3)cc2)nc1N(C(C)=O)c1ccccc1 10.1016/j.ejmech.2011.05.056
CHEMBL1823999 64770 0 None - 0 Human 5.7 pIC50 = 5.7 Binding
Displacement of [125I][Sar1,Ile8]-AT-II from human recombinant AT1 receptor expressed in HEK293 cells after 120 mins by liquid scintillation countingDisplacement of [125I][Sar1,Ile8]-AT-II from human recombinant AT1 receptor expressed in HEK293 cells after 120 mins by liquid scintillation counting
ChEMBL 507 8 1 8 4.6 CCOC(=O)c1cn(Cc2ccc(-c3ccccc3-c3nnn[nH]3)cc2)nc1N(C(C)=O)c1ccccc1 10.1016/j.ejmech.2011.05.056
10096495 19166 0 None - 0 Guinea pig 5.7 pIC50 = 5.7 Binding
In vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparationIn vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparation
ChEMBL 475 6 1 5 6.2 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2cccc(C(F)(F)F)c2n1 10.1021/jm00100a007
CHEMBL129194 19166 0 None - 0 Guinea pig 5.7 pIC50 = 5.7 Binding
In vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparationIn vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparation
ChEMBL 475 6 1 5 6.2 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2cccc(C(F)(F)F)c2n1 10.1021/jm00100a007
15699055 5047 0 None - 0 Rat 4.7 pIC50 = 4.7 Binding
Binding affinity against Angiotensin II receptor in rat smooth muscle cell preparationsBinding affinity against Angiotensin II receptor in rat smooth muscle cell preparations
ChEMBL 396 7 2 6 3.8 CCCCc1nc(Cl)c(CO)n1Cc1ccc2ccc(-c3nn[nH]n3)cc2c1 10.1021/jm00114a021
CHEMBL105724 5047 0 None - 0 Rat 4.7 pIC50 = 4.7 Binding
Binding affinity against Angiotensin II receptor in rat smooth muscle cell preparationsBinding affinity against Angiotensin II receptor in rat smooth muscle cell preparations
ChEMBL 396 7 2 6 3.8 CCCCc1nc(Cl)c(CO)n1Cc1ccc2ccc(-c3nn[nH]n3)cc2c1 10.1021/jm00114a021
10810628 193013 0 None - 0 Bovine 4.7 pIC50 = 4.7 Binding
In vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortexIn vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortex
ChEMBL 394 8 3 5 3.4 CCCc1nc(C(=O)O)c(CO)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm950450f
CHEMBL53322 193013 0 None - 0 Bovine 4.7 pIC50 = 4.7 Binding
In vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortexIn vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortex
ChEMBL 394 8 3 5 3.4 CCCc1nc(C(=O)O)c(CO)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm950450f
44309366 202392 0 None - 0 Bovine 4.7 pIC50 = 4.7 Binding
Inhibition of [125I][Ile5]-AII binding to bovine adrenal cortex membrane Angiotensin II receptor type 1Inhibition of [125I][Ile5]-AII binding to bovine adrenal cortex membrane Angiotensin II receptor type 1
ChEMBL 294 5 1 3 4.4 CCCCc1nc2ccccc2n1Cc1ccc(O)c(C)c1 10.1016/S0960-894X(01)81149-5
CHEMBL70239 202392 0 None - 0 Bovine 4.7 pIC50 = 4.7 Binding
Inhibition of [125I][Ile5]-AII binding to bovine adrenal cortex membrane Angiotensin II receptor type 1Inhibition of [125I][Ile5]-AII binding to bovine adrenal cortex membrane Angiotensin II receptor type 1
ChEMBL 294 5 1 3 4.4 CCCCc1nc2ccccc2n1Cc1ccc(O)c(C)c1 10.1016/S0960-894X(01)81149-5
10810628 193013 0 None - 0 Bovine 4.7 pIC50 = 4.7 Binding
Inhibition of [125l]-All binding to bovine adrenal cortexInhibition of [125l]-All binding to bovine adrenal cortex
ChEMBL 394 8 3 5 3.4 CCCc1nc(C(=O)O)c(CO)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/S0960-894X(01)81143-4
CHEMBL53322 193013 0 None - 0 Bovine 4.7 pIC50 = 4.7 Binding
Inhibition of [125l]-All binding to bovine adrenal cortexInhibition of [125l]-All binding to bovine adrenal cortex
ChEMBL 394 8 3 5 3.4 CCCc1nc(C(=O)O)c(CO)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/S0960-894X(01)81143-4
127035068 135837 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Displacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysisDisplacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysis
ChEMBL 633 10 2 7 7.7 CCCc1nc2c(C)cc(C(=O)Nc3ccccc3)cc2n1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)cc1 10.1039/C4MD00499J
CHEMBL3735036 135837 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Displacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysisDisplacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysis
ChEMBL 633 10 2 7 7.7 CCCc1nc2c(C)cc(C(=O)Nc3ccccc3)cc2n1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)cc1 10.1039/C4MD00499J
164611280 184406 0 None - 0 Human 5.7 pIC50 = 5.7 Binding
Displacement of [125-I]-[Sar1, Ile8] from recombinant human AT1R transfected in human HEK293 cells incubated for 2 hrs by liquid scintillation counter analysisDisplacement of [125-I]-[Sar1, Ile8] from recombinant human AT1R transfected in human HEK293 cells incubated for 2 hrs by liquid scintillation counter analysis
ChEMBL 969 22 11 11 1.1 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@@H](N)CCCNC(=N)N)C(C)C)C(=O)N1Cc2ccc(O)cc2C[C@H]1C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O 10.1016/j.bmcl.2021.128086
CHEMBL4854474 184406 0 None - 0 Human 5.7 pIC50 = 5.7 Binding
Displacement of [125-I]-[Sar1, Ile8] from recombinant human AT1R transfected in human HEK293 cells incubated for 2 hrs by liquid scintillation counter analysisDisplacement of [125-I]-[Sar1, Ile8] from recombinant human AT1R transfected in human HEK293 cells incubated for 2 hrs by liquid scintillation counter analysis
ChEMBL 969 22 11 11 1.1 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@@H](N)CCCNC(=N)N)C(C)C)C(=O)N1Cc2ccc(O)cc2C[C@H]1C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O 10.1016/j.bmcl.2021.128086
53309272 63428 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation countingDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation counting
ChEMBL 449 4 1 6 5.3 CCc1nc2c(C)c(C)c(C)nc2n1[C@H]1CCc2cc(-c3ccccc3-c3nnn[nH]3)ccc21 10.1021/jm200409s
CHEMBL1801736 63428 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation countingDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation counting
ChEMBL 449 4 1 6 5.3 CCc1nc2c(C)c(C)c(C)nc2n1[C@H]1CCc2cc(-c3ccccc3-c3nnn[nH]3)ccc21 10.1021/jm200409s
1315061 28018 9 None - 0 Human 5.7 pIC50 = 5.7 Binding
Displacement of [125I-Sar1-Ile8]Ang2 from human AT1 receptor expressed in HEK293 cell membrane incubated for 1 hr by gamma counting methodDisplacement of [125I-Sar1-Ile8]Ang2 from human AT1 receptor expressed in HEK293 cell membrane incubated for 1 hr by gamma counting method
ChEMBL 409 7 1 4 3.3 Cc1ccc(CN(c2ccc(C(=O)NCc3ccccn3)cc2)S(C)(=O)=O)cc1 10.1016/j.bmc.2016.07.047
CHEMBL1374011 28018 9 None - 0 Human 5.7 pIC50 = 5.7 Binding
Displacement of [125I-Sar1-Ile8]Ang2 from human AT1 receptor expressed in HEK293 cell membrane incubated for 1 hr by gamma counting methodDisplacement of [125I-Sar1-Ile8]Ang2 from human AT1 receptor expressed in HEK293 cell membrane incubated for 1 hr by gamma counting method
ChEMBL 409 7 1 4 3.3 Cc1ccc(CN(c2ccc(C(=O)NCc3ccccn3)cc2)S(C)(=O)=O)cc1 10.1016/j.bmc.2016.07.047
70682147 75969 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Displacement of [125I]Sar1Ile8-Ang2 from angiotensin AT1 receptor after 180 mins by gamma countingDisplacement of [125I]Sar1Ile8-Ang2 from angiotensin AT1 receptor after 180 mins by gamma counting
ChEMBL 573 10 2 6 6.3 CCCc1nc2c(C)cc(C(=O)NCCc3ccc(F)cc3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmc.2012.05.056
CHEMBL2058866 75969 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Displacement of [125I]Sar1Ile8-Ang2 from angiotensin AT1 receptor after 180 mins by gamma countingDisplacement of [125I]Sar1Ile8-Ang2 from angiotensin AT1 receptor after 180 mins by gamma counting
ChEMBL 573 10 2 6 6.3 CCCc1nc2c(C)cc(C(=O)NCCc3ccc(F)cc3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmc.2012.05.056
10029950 50354 0 None - 0 Rabbit 7.7 pIC50 = 7.7 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 530 12 2 7 5.9 CCCCc1nnc(SCc2cccc(OC)c2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
CHEMBL157524 50354 0 None - 0 Rabbit 7.7 pIC50 = 7.7 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 530 12 2 7 5.9 CCCCc1nnc(SCc2cccc(OC)c2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
14956750 204355 0 None - 0 Rabbit 7.7 pIC50 = 7.7 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 469 8 1 7 4.4 CCCCc1nn(-c2ccc(F)cc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
CHEMBL85596 204355 0 None - 0 Rabbit 7.7 pIC50 = 7.7 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 469 8 1 7 4.4 CCCCc1nn(-c2ccc(F)cc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
44277653 100925 0 None - 0 Rabbit 7.7 pIC50 = 7.7 Binding
Binding affinity against AT1 receptor in rabbit aortaBinding affinity against AT1 receptor in rabbit aorta
ChEMBL 645 11 0 9 5.9 CCCCCN(C(=O)c1ccc([S+](C)[O-])cc1)c1ccc2ncn(Cc3ccc(-c4ccccc4-c4nnnn4C)cc3)c(=O)c2c1 10.1016/0960-894X(95)00224-H
CHEMBL29730 100925 0 None - 0 Rabbit 7.7 pIC50 = 7.7 Binding
Binding affinity against AT1 receptor in rabbit aortaBinding affinity against AT1 receptor in rabbit aorta
ChEMBL 645 11 0 9 5.9 CCCCCN(C(=O)c1ccc([S+](C)[O-])cc1)c1ccc2ncn(Cc3ccc(-c4ccccc4-c4nnnn4C)cc3)c(=O)c2c1 10.1016/0960-894X(95)00224-H
18004820 16261 0 None - 1 Human 7.7 pIC50 = 7.7 Binding
Displacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysisDisplacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysis
ChEMBL 527 9 2 7 4.7 CCCc1nc(Cl)c(C(N)=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)cc1 10.1039/C4MD00499J
CHEMBL12333 16261 0 None - 1 Human 7.7 pIC50 = 7.7 Binding
Displacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysisDisplacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysis
ChEMBL 527 9 2 7 4.7 CCCc1nc(Cl)c(C(N)=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)cc1 10.1039/C4MD00499J
10029950 50354 0 None - 0 Rabbit 7.7 pIC50 = 7.7 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 530 12 2 7 5.9 CCCCc1nnc(SCc2cccc(OC)c2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
CHEMBL157524 50354 0 None - 0 Rabbit 7.7 pIC50 = 7.7 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 530 12 2 7 5.9 CCCCc1nnc(SCc2cccc(OC)c2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
44377198 56212 0 None - 0 Rabbit 7.7 pIC50 = 7.7 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aortaIn vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aorta
ChEMBL 531 10 1 7 4.8 CCCCc1ncc(C(=O)OC)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/S0960-894X(01)81124-0
CHEMBL163628 56212 0 None - 0 Rabbit 7.7 pIC50 = 7.7 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aortaIn vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aorta
ChEMBL 531 10 1 7 4.8 CCCCc1ncc(C(=O)OC)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/S0960-894X(01)81124-0
10259334 206288 0 None - 0 Rabbit 7.7 pIC50 = 7.7 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 724 13 1 10 6.3 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2cc(OC)c(OC)c(OC)c2)cc1 10.1021/jm00043a020
CHEMBL97500 206288 0 None - 0 Rabbit 7.7 pIC50 = 7.7 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 724 13 1 10 6.3 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2cc(OC)c(OC)c(OC)c2)cc1 10.1021/jm00043a020
23590371 160846 0 None - 0 Rat 7.7 pIC50 = 7.7 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 553 12 1 10 4.2 CCCCc1nn(CC(=O)c2cc(OC)ccc2OC)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a015
CHEMBL412664 160846 0 None - 0 Rat 7.7 pIC50 = 7.7 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 553 12 1 10 4.2 CCCCc1nn(CC(=O)c2cc(OC)ccc2OC)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a015
10076199 116142 0 None - 0 Rat 7.7 pIC50 = 7.7 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 548 9 3 6 6.7 CCCCc1nc2ccc(NC(=O)NC3CCCCC3)cc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00077a007
CHEMBL337025 116142 0 None - 0 Rat 7.7 pIC50 = 7.7 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 548 9 3 6 6.7 CCCCc1nc2ccc(NC(=O)NC3CCCCC3)cc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00077a007
9805344 98570 0 None - 0 Rabbit 7.7 pIC50 = 7.7 Binding
Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)
ChEMBL 483 7 1 5 6.2 CCc1nc2c(C)cc(C)nc2n1Cc1cc(Cl)c(OC(C(=O)O)c2ccccc2)c(Cl)c1 10.1016/0960-894X(95)00185-V
CHEMBL280290 98570 0 None - 0 Rabbit 7.7 pIC50 = 7.7 Binding
Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)
ChEMBL 483 7 1 5 6.2 CCc1nc2c(C)cc(C)nc2n1Cc1cc(Cl)c(OC(C(=O)O)c2ccccc2)c(Cl)c1 10.1016/0960-894X(95)00185-V
15287886 137072 0 None - 0 Rabbit 7.7 pIC50 = 7.7 Binding
Tested in vitro for Angiotensin II receptor, type 1 binding affinity using rabbit aorta binding assayTested in vitro for Angiotensin II receptor, type 1 binding affinity using rabbit aorta binding assay
ChEMBL 483 8 1 5 6.3 CCCc1nc2c(C)ccnc2n1Cc1ccc(OC(C(=O)O)c2c(Cl)cccc2Cl)cc1 10.1016/0960-894X(94)00476-V
CHEMBL37566 137072 0 None - 0 Rabbit 7.7 pIC50 = 7.7 Binding
Tested in vitro for Angiotensin II receptor, type 1 binding affinity using rabbit aorta binding assayTested in vitro for Angiotensin II receptor, type 1 binding affinity using rabbit aorta binding assay
ChEMBL 483 8 1 5 6.3 CCCc1nc2c(C)ccnc2n1Cc1ccc(OC(C(=O)O)c2c(Cl)cccc2Cl)cc1 10.1016/0960-894X(94)00476-V
44286911 161228 0 None - 0 Rabbit 7.7 pIC50 = 7.7 Binding
Tested in vitro for Angiotensin II receptor, type 1 binding affinity using rabbit aorta binding assayTested in vitro for Angiotensin II receptor, type 1 binding affinity using rabbit aorta binding assay
ChEMBL 378 5 1 2 6.2 O=C(O)C(Oc1ccc(Cl)cc1C1CCCCC1)c1ccc(Cl)cc1 10.1016/0960-894X(94)00476-V
CHEMBL41416 161228 0 None - 0 Rabbit 7.7 pIC50 = 7.7 Binding
Tested in vitro for Angiotensin II receptor, type 1 binding affinity using rabbit aorta binding assayTested in vitro for Angiotensin II receptor, type 1 binding affinity using rabbit aorta binding assay
ChEMBL 378 5 1 2 6.2 O=C(O)C(Oc1ccc(Cl)cc1C1CCCCC1)c1ccc(Cl)cc1 10.1016/0960-894X(94)00476-V
44277462 14588 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Binding affinity against AT1 receptor in human adrenal tissueBinding affinity against AT1 receptor in human adrenal tissue
ChEMBL 665 11 2 10 5.2 CCCCN(C(=O)c1ccc(OP(=O)(O)O)cc1)c1ccc2ncn(Cc3ccc(-c4ccccc4-c4nnnn4C)cc3)c(=O)c2c1 10.1016/0960-894X(95)00224-H
CHEMBL1206522 14588 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Binding affinity against AT1 receptor in human adrenal tissueBinding affinity against AT1 receptor in human adrenal tissue
ChEMBL 665 11 2 10 5.2 CCCCN(C(=O)c1ccc(OP(=O)(O)O)cc1)c1ccc2ncn(Cc3ccc(-c4ccccc4-c4nnnn4C)cc3)c(=O)c2c1 10.1016/0960-894X(95)00224-H
CHEMBL281890 14588 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Binding affinity against AT1 receptor in human adrenal tissueBinding affinity against AT1 receptor in human adrenal tissue
ChEMBL 665 11 2 10 5.2 CCCCN(C(=O)c1ccc(OP(=O)(O)O)cc1)c1ccc2ncn(Cc3ccc(-c4ccccc4-c4nnnn4C)cc3)c(=O)c2c1 10.1016/0960-894X(95)00224-H
10077513 17077 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 612 12 0 7 6.5 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2Cc2cc(Br)cs2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
CHEMBL125697 17077 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 612 12 0 7 6.5 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2Cc2cc(Br)cs2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
44294989 162643 0 None - 0 Bovine 6.7 pIC50 = 6.7 Binding
Ability to displace [125I]- labelled [Sar1,Ileu8] from angiotensin II receptor of bovine adrenal cortex membranesAbility to displace [125I]- labelled [Sar1,Ileu8] from angiotensin II receptor of bovine adrenal cortex membranes
ChEMBL 459 7 1 6 4.5 CCC1(CC)CC(=O)N(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/C(=C/C(=O)OC)C1 10.1016/S0960-894X(00)80474-6
CHEMBL418269 162643 0 None - 0 Bovine 6.7 pIC50 = 6.7 Binding
Ability to displace [125I]- labelled [Sar1,Ileu8] from angiotensin II receptor of bovine adrenal cortex membranesAbility to displace [125I]- labelled [Sar1,Ileu8] from angiotensin II receptor of bovine adrenal cortex membranes
ChEMBL 459 7 1 6 4.5 CCC1(CC)CC(=O)N(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/C(=C/C(=O)OC)C1 10.1016/S0960-894X(00)80474-6
44293466 100658 0 None - 0 Rat 6.7 pIC50 = 6.7 Binding
Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.
ChEMBL 604 14 1 8 6.0 CCCCc1nc(Cl)c(CCC(=O)OC)n1Cc1ccc(NC(=O)[C@H](Cc2ccccc2)n2cccc2C(=O)OC)cc1 10.1021/jm00064a007
CHEMBL295311 100658 0 None - 0 Rat 6.7 pIC50 = 6.7 Binding
Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.
ChEMBL 604 14 1 8 6.0 CCCCc1nc(Cl)c(CCC(=O)OC)n1Cc1ccc(NC(=O)[C@H](Cc2ccccc2)n2cccc2C(=O)OC)cc1 10.1021/jm00064a007
44293962 100905 0 None - 0 Rat 6.7 pIC50 = 6.7 Binding
Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.
ChEMBL 518 12 2 5 5.8 CCCCc1nc(Cl)c(CC(=O)O)n1Cc1ccc(NC(=O)[C@H](Cc2ccccc2)n2cccc2)cc1 10.1021/jm00064a007
CHEMBL297202 100905 0 None - 0 Rat 6.7 pIC50 = 6.7 Binding
Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.
ChEMBL 518 12 2 5 5.8 CCCCc1nc(Cl)c(CC(=O)O)n1Cc1ccc(NC(=O)[C@H](Cc2ccccc2)n2cccc2)cc1 10.1021/jm00064a007
44293990 186734 0 None - 0 Rat 6.7 pIC50 = 6.7 Binding
Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.
ChEMBL 548 12 2 7 5.4 CCCCc1nc(Cl)c(CO)n1Cc1ccc(NC(=O)[C@H](Cc2ccccc2)n2cccc2C(=O)OC)cc1 10.1021/jm00064a007
CHEMBL49306 186734 0 None - 0 Rat 6.7 pIC50 = 6.7 Binding
Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.
ChEMBL 548 12 2 7 5.4 CCCCc1nc(Cl)c(CO)n1Cc1ccc(NC(=O)[C@H](Cc2ccccc2)n2cccc2C(=O)OC)cc1 10.1021/jm00064a007
10073122 119270 0 None - 0 Rabbit 5.7 pIC50 = 5.7 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 464 8 2 6 4.8 CCCSc1nnc(C(F)(F)F)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
CHEMBL348149 119270 0 None - 0 Rabbit 5.7 pIC50 = 5.7 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 464 8 2 6 4.8 CCCSc1nnc(C(F)(F)F)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
44291654 173685 0 None - 0 Rat 5.7 pIC50 = 5.7 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 462 11 1 3 6.8 CCCCC1=NC(CC(C)C)(CC(C)C)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00074a018
CHEMBL45493 173685 0 None - 0 Rat 5.7 pIC50 = 5.7 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 462 11 1 3 6.8 CCCCC1=NC(CC(C)C)(CC(C)C)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00074a018
10073122 119270 0 None - 0 Rabbit 5.7 pIC50 = 5.7 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 464 8 2 6 4.8 CCCSc1nnc(C(F)(F)F)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
CHEMBL348149 119270 0 None - 0 Rabbit 5.7 pIC50 = 5.7 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 464 8 2 6 4.8 CCCSc1nnc(C(F)(F)F)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
44291654 173685 0 None - 0 Rat 5.7 pIC50 = 5.7 Binding
In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.
ChEMBL 462 11 1 3 6.8 CCCCC1=NC(CC(C)C)(CC(C)C)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/S0960-894X(01)81140-9
CHEMBL45493 173685 0 None - 0 Rat 5.7 pIC50 = 5.7 Binding
In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.
ChEMBL 462 11 1 3 6.8 CCCCC1=NC(CC(C)C)(CC(C)C)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/S0960-894X(01)81140-9
44296533 193064 0 None - 0 Bovine 5.7 pIC50 = 5.7 Binding
Inhibition of [125l]-All binding to bovine adrenal cortexInhibition of [125l]-All binding to bovine adrenal cortex
ChEMBL 393 8 3 4 4.0 CCCc1cc(C(=O)O)c(CO)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/S0960-894X(01)81143-4
CHEMBL53631 193064 0 None - 0 Bovine 5.7 pIC50 = 5.7 Binding
Inhibition of [125l]-All binding to bovine adrenal cortexInhibition of [125l]-All binding to bovine adrenal cortex
ChEMBL 393 8 3 4 4.0 CCCc1cc(C(=O)O)c(CO)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/S0960-894X(01)81143-4
44304147 100296 0 None - 0 Rabbit 4.7 pIC50 = 4.7 Binding
Inhibition of Angiotensin II receptor, type 1 in rabbit aorta using [125I-Sar1,Ile8] angiotensin II binding assayInhibition of Angiotensin II receptor, type 1 in rabbit aorta using [125I-Sar1,Ile8] angiotensin II binding assay
ChEMBL 522 11 0 4 5.9 CCCCCN(CCCCC)C(=O)N1CCN(C(=O)N(c2ccccc2)c2ccccc2)[C@H](C(=O)OC)C1 10.1016/S0960-894X(01)81007-6
CHEMBL292939 100296 0 None - 0 Rabbit 4.7 pIC50 = 4.7 Binding
Inhibition of Angiotensin II receptor, type 1 in rabbit aorta using [125I-Sar1,Ile8] angiotensin II binding assayInhibition of Angiotensin II receptor, type 1 in rabbit aorta using [125I-Sar1,Ile8] angiotensin II binding assay
ChEMBL 522 11 0 4 5.9 CCCCCN(CCCCC)C(=O)N1CCN(C(=O)N(c2ccccc2)c2ccccc2)[C@H](C(=O)OC)C1 10.1016/S0960-894X(01)81007-6
46910583 69994 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Displacement of [125I]Sar1 Ile8-Ang 2 from angiotensin 2 AT1 receptor after 180 mins by gamma countingDisplacement of [125I]Sar1 Ile8-Ang 2 from angiotensin 2 AT1 receptor after 180 mins by gamma counting
ChEMBL 561 11 2 5 6.7 CCCc1nc2c(C)cc(C(=O)NCCc3ccc(OC)cc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2012.01.009
CHEMBL1945008 69994 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Displacement of [125I]Sar1 Ile8-Ang 2 from angiotensin 2 AT1 receptor after 180 mins by gamma countingDisplacement of [125I]Sar1 Ile8-Ang 2 from angiotensin 2 AT1 receptor after 180 mins by gamma counting
ChEMBL 561 11 2 5 6.7 CCCc1nc2c(C)cc(C(=O)NCCc3ccc(OC)cc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2012.01.009
127036297 135891 0 None - 1 Human 6.7 pIC50 = 6.7 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 547 10 3 5 6.2 CCCc1nc2c(C)cc(C(=O)N[C@H](CO)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2015.09.010
CHEMBL3735492 135891 0 None - 1 Human 6.7 pIC50 = 6.7 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 547 10 3 5 6.2 CCCc1nc2c(C)cc(C(=O)N[C@H](CO)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2015.09.010
11190917 168231 0 None - 0 Rat 6.7 pIC50 = 6.7 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 484 6 1 5 6.2 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2c(CC(=O)O)c(Cl)nc3ccccc23)cc1 10.1021/jm031100t
CHEMBL437659 168231 0 None - 0 Rat 6.7 pIC50 = 6.7 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 484 6 1 5 6.2 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2c(CC(=O)O)c(Cl)nc3ccccc23)cc1 10.1021/jm031100t
127035219 135822 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Displacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysisDisplacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysis
ChEMBL 677 12 2 8 7.4 CCCc1nc2c(C)cc(C(=O)NCc3ccccc3OC)cc2n1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)cc1 10.1039/C4MD00499J
CHEMBL3734849 135822 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Displacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysisDisplacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysis
ChEMBL 677 12 2 8 7.4 CCCc1nc2c(C)cc(C(=O)NCc3ccccc3OC)cc2n1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)cc1 10.1039/C4MD00499J
4803452 39381 7 None - 0 Human 5.7 pIC50 = 5.7 Binding
Displacement of [125I-Sar1-Ile8]Ang2 from human AT1 receptor expressed in HEK293 cell membrane incubated for 1 hr by gamma counting methodDisplacement of [125I-Sar1-Ile8]Ang2 from human AT1 receptor expressed in HEK293 cell membrane incubated for 1 hr by gamma counting method
ChEMBL 457 6 1 4 3.6 Cc1ccc(C)c(NC(=O)CN(C)C(=O)c2ccc(S(=O)(=O)N3CCCCCC3)cc2)c1 10.1016/j.bmc.2016.07.047
CHEMBL1474431 39381 7 None - 0 Human 5.7 pIC50 = 5.7 Binding
Displacement of [125I-Sar1-Ile8]Ang2 from human AT1 receptor expressed in HEK293 cell membrane incubated for 1 hr by gamma counting methodDisplacement of [125I-Sar1-Ile8]Ang2 from human AT1 receptor expressed in HEK293 cell membrane incubated for 1 hr by gamma counting method
ChEMBL 457 6 1 4 3.6 Cc1ccc(C)c(NC(=O)CN(C)C(=O)c2ccc(S(=O)(=O)N3CCCCCC3)cc2)c1 10.1016/j.bmc.2016.07.047
10275744 204388 0 None - 0 Rabbit 7.7 pIC50 = 7.7 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 451 8 1 7 4.3 CCCCc1nn(-c2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
CHEMBL85876 204388 0 None - 0 Rabbit 7.7 pIC50 = 7.7 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 451 8 1 7 4.3 CCCCc1nn(-c2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
15356432 186077 0 None - 0 Rat 7.7 pIC50 = 7.7 Binding
Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.
ChEMBL 576 14 3 6 5.9 CCCCc1nc(Cl)c(CCC(=O)O)n1Cc1ccc(NC(=O)[C@H](Cc2ccccc2)n2cccc2C(=O)O)cc1 10.1021/jm00064a007
CHEMBL48824 186077 0 None - 0 Rat 7.7 pIC50 = 7.7 Binding
Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.
ChEMBL 576 14 3 6 5.9 CCCCc1nc(Cl)c(CCC(=O)O)n1Cc1ccc(NC(=O)[C@H](Cc2ccccc2)n2cccc2C(=O)O)cc1 10.1021/jm00064a007
44307195 101775 0 None - 0 Rabbit 7.7 pIC50 = 7.7 Binding
Binding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membraneBinding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane
ChEMBL 452 4 1 6 3.9 CCc1nc2c(C)cc(C)nc2n1Cc1cc(I)c(O)c([N+](=O)[O-])c1 10.1016/S0960-894X(01)81148-3
CHEMBL303186 101775 0 None - 0 Rabbit 7.7 pIC50 = 7.7 Binding
Binding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membraneBinding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane
ChEMBL 452 4 1 6 3.9 CCc1nc2c(C)cc(C)nc2n1Cc1cc(I)c(O)c([N+](=O)[O-])c1 10.1016/S0960-894X(01)81148-3
44264673 202976 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Binding affinity to angiotensin AT1 receptorBinding affinity to angiotensin AT1 receptor
ChEMBL 402 7 2 6 4.3 CCCCc1nc2cnnc(O)c2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.bmc.2010.10.043
CHEMBL7396 202976 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Binding affinity to angiotensin AT1 receptorBinding affinity to angiotensin AT1 receptor
ChEMBL 402 7 2 6 4.3 CCCCc1nc2cnnc(O)c2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.bmc.2010.10.043
44459662 95585 0 None - 0 Bovine 7.7 pIC50 = 7.7 Binding
Concentration required for 50% inhibition of binding against Angiotensin II receptor, type 1 in bovine adrenal cortexConcentration required for 50% inhibition of binding against Angiotensin II receptor, type 1 in bovine adrenal cortex
ChEMBL 518 8 2 7 5.1 CCCCc1nc2ccc(C3=NNC(=O)CC3C)cc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80348-6
CHEMBL25989 95585 0 None - 0 Bovine 7.7 pIC50 = 7.7 Binding
Concentration required for 50% inhibition of binding against Angiotensin II receptor, type 1 in bovine adrenal cortexConcentration required for 50% inhibition of binding against Angiotensin II receptor, type 1 in bovine adrenal cortex
ChEMBL 518 8 2 7 5.1 CCCCc1nc2ccc(C3=NNC(=O)CC3C)cc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80348-6
108185 1578 71 None - 1 Bovine 7.7 pIC50 = 7.7 Binding
In vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortexIn vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortex
ChEMBL 436 8 2 6 4.5 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)C(=O)O)Cl 10.1021/jm950450f
586 1578 71 None - 1 Bovine 7.7 pIC50 = 7.7 Binding
In vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortexIn vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortex
ChEMBL 436 8 2 6 4.5 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)C(=O)O)Cl 10.1021/jm950450f
CHEMBL907 1578 71 None - 1 Bovine 7.7 pIC50 = 7.7 Binding
In vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortexIn vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortex
ChEMBL 436 8 2 6 4.5 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)C(=O)O)Cl 10.1021/jm950450f
10027836 18745 0 None - 0 Guinea pig 7.7 pIC50 = 7.7 Binding
In vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparationIn vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparation
ChEMBL 437 7 1 6 5.2 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2cc(OC)ccc2n1 10.1021/jm00100a007
CHEMBL128644 18745 0 None - 0 Guinea pig 7.7 pIC50 = 7.7 Binding
In vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparationIn vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparation
ChEMBL 437 7 1 6 5.2 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2cc(OC)ccc2n1 10.1021/jm00100a007
44309264 102191 0 None - 0 Rat 7.7 pIC50 = 7.7 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 555 12 2 10 4.0 CCCCc1nn(CC(O)c2cc(OC)ccc2OC)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a015
CHEMBL304600 102191 0 None - 0 Rat 7.7 pIC50 = 7.7 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 555 12 2 10 4.0 CCCCc1nn(CC(O)c2cc(OC)ccc2OC)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a015
10222835 204415 0 None - 0 Rat 7.7 pIC50 = 7.7 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 403 8 1 7 3.3 CCCCc1nn(CC)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a015
CHEMBL86084 204415 0 None - 0 Rat 7.7 pIC50 = 7.7 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 403 8 1 7 3.3 CCCCc1nn(CC)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a015
108185 1578 71 None - 1 Bovine 7.7 pIC50 = 7.7 Binding
Inhibition of [125l]-All binding to bovine adrenal cortexInhibition of [125l]-All binding to bovine adrenal cortex
ChEMBL 436 8 2 6 4.5 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)C(=O)O)Cl 10.1016/S0960-894X(01)81143-4
586 1578 71 None - 1 Bovine 7.7 pIC50 = 7.7 Binding
Inhibition of [125l]-All binding to bovine adrenal cortexInhibition of [125l]-All binding to bovine adrenal cortex
ChEMBL 436 8 2 6 4.5 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)C(=O)O)Cl 10.1016/S0960-894X(01)81143-4
CHEMBL907 1578 71 None - 1 Bovine 7.7 pIC50 = 7.7 Binding
Inhibition of [125l]-All binding to bovine adrenal cortexInhibition of [125l]-All binding to bovine adrenal cortex
ChEMBL 436 8 2 6 4.5 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)C(=O)O)Cl 10.1016/S0960-894X(01)81143-4
46910494 75965 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Displacement of [125I]Sar1Ile8-Ang2 from angiotensin AT1 receptor after 180 mins by gamma countingDisplacement of [125I]Sar1Ile8-Ang2 from angiotensin AT1 receptor after 180 mins by gamma counting
ChEMBL 585 11 2 7 6.2 CCCc1nc2c(C)cc(C(=O)NCCc3ccc(OC)cc3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmc.2012.05.056
CHEMBL2058862 75965 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Displacement of [125I]Sar1Ile8-Ang2 from angiotensin AT1 receptor after 180 mins by gamma countingDisplacement of [125I]Sar1Ile8-Ang2 from angiotensin AT1 receptor after 180 mins by gamma counting
ChEMBL 585 11 2 7 6.2 CCCc1nc2c(C)cc(C(=O)NCCc3ccc(OC)cc3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmc.2012.05.056
44341489 9195 0 None - 0 Rat 6.7 pIC50 = 6.7 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 575 12 4 6 2.7 CCCCC1=NC2(CCN(C(=O)C(N)CCCN=C(N)N)CC2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00074a018
CHEMBL110974 9195 0 None - 0 Rat 6.7 pIC50 = 6.7 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 575 12 4 6 2.7 CCCCC1=NC2(CCN(C(=O)C(N)CCCN=C(N)N)CC2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00074a018
10096463 48603 0 None - 0 Rabbit 6.7 pIC50 = 6.7 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 474 8 1 7 5.4 CCCCc1nn2c(-c3ccccc3)cnc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
CHEMBL155954 48603 0 None - 0 Rabbit 6.7 pIC50 = 6.7 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 474 8 1 7 5.4 CCCCc1nn2c(-c3ccccc3)cnc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
10435012 116496 0 None - 0 Guinea pig 6.7 pIC50 = 6.7 Binding
In vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparationIn vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparation
ChEMBL 437 7 1 6 5.2 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2ccc(OC)cc2n1 10.1021/jm00100a007
CHEMBL338900 116496 0 None - 0 Guinea pig 6.7 pIC50 = 6.7 Binding
In vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparationIn vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparation
ChEMBL 437 7 1 6 5.2 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2ccc(OC)cc2n1 10.1021/jm00100a007
44309242 201763 0 None - 0 Bovine 5.7 pIC50 = 5.7 Binding
Inhibition of [125I][Ile5]-AII binding to bovine adrenal cortex membrane Angiotensin II receptor type 1Inhibition of [125I][Ile5]-AII binding to bovine adrenal cortex membrane Angiotensin II receptor type 1
ChEMBL 339 6 1 5 4.3 CCCCc1nc2ccccc2n1Cc1cc(C)c(O)c([N+](=O)[O-])c1 10.1016/S0960-894X(01)81149-5
CHEMBL65955 201763 0 None - 0 Bovine 5.7 pIC50 = 5.7 Binding
Inhibition of [125I][Ile5]-AII binding to bovine adrenal cortex membrane Angiotensin II receptor type 1Inhibition of [125I][Ile5]-AII binding to bovine adrenal cortex membrane Angiotensin II receptor type 1
ChEMBL 339 6 1 5 4.3 CCCCc1nc2ccccc2n1Cc1cc(C)c(O)c([N+](=O)[O-])c1 10.1016/S0960-894X(01)81149-5
44308785 202370 0 None - 0 Bovine 5.7 pIC50 = 5.7 Binding
Inhibition of [125I][Ile5]-AII binding to bovine adrenal cortex membrane Angiotensin II receptor type 1Inhibition of [125I][Ile5]-AII binding to bovine adrenal cortex membrane Angiotensin II receptor type 1
ChEMBL 420 5 1 3 5.0 CCCCc1nc2ccccc2n1Cc1cc(C)c(O)c(I)c1 10.1016/S0960-894X(01)81149-5
CHEMBL70134 202370 0 None - 0 Bovine 5.7 pIC50 = 5.7 Binding
Inhibition of [125I][Ile5]-AII binding to bovine adrenal cortex membrane Angiotensin II receptor type 1Inhibition of [125I][Ile5]-AII binding to bovine adrenal cortex membrane Angiotensin II receptor type 1
ChEMBL 420 5 1 3 5.0 CCCCc1nc2ccccc2n1Cc1cc(C)c(O)c(I)c1 10.1016/S0960-894X(01)81149-5
14956797 204683 0 None - 0 Rabbit 7.6 pIC50 = 7.6 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 523 10 1 9 4.1 CCCCc1nn(Cc2ccc(C(=O)OC)cc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
CHEMBL87885 204683 0 None - 0 Rabbit 7.6 pIC50 = 7.6 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 523 10 1 9 4.1 CCCCc1nn(Cc2ccc(C(=O)OC)cc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
76321525 104755 0 None - 0 Human 7.6 pIC50 = 7.6 Binding
Antagonist activity at human AT1 receptor expressed in CHO cells measured after overnight incubation by luciferase reporter gene assayAntagonist activity at human AT1 receptor expressed in CHO cells measured after overnight incubation by luciferase reporter gene assay
ChEMBL 552 9 1 7 7.2 CCCc1nn2ccc(-c3nc4ccccc4n3CCC)cc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.bmcl.2014.01.004
CHEMBL3115243 104755 0 None - 0 Human 7.6 pIC50 = 7.6 Binding
Antagonist activity at human AT1 receptor expressed in CHO cells measured after overnight incubation by luciferase reporter gene assayAntagonist activity at human AT1 receptor expressed in CHO cells measured after overnight incubation by luciferase reporter gene assay
ChEMBL 552 9 1 7 7.2 CCCc1nn2ccc(-c3nc4ccccc4n3CCC)cc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.bmcl.2014.01.004
44278151 98643 0 None - 0 Rabbit 7.6 pIC50 = 7.6 Binding
Binding affinity against AT1 receptor in rabbit aortaBinding affinity against AT1 receptor in rabbit aorta
ChEMBL 619 11 0 9 5.4 CCCCS(=O)(=O)N(Cc1ccccc1)c1ccc2ncn(Cc3ccc(-c4ccccc4-c4nnnn4C)cc3)c(=O)c2c1 10.1016/0960-894X(95)00224-H
CHEMBL280875 98643 0 None - 0 Rabbit 7.6 pIC50 = 7.6 Binding
Binding affinity against AT1 receptor in rabbit aortaBinding affinity against AT1 receptor in rabbit aorta
ChEMBL 619 11 0 9 5.4 CCCCS(=O)(=O)N(Cc1ccccc1)c1ccc2ncn(Cc3ccc(-c4ccccc4-c4nnnn4C)cc3)c(=O)c2c1 10.1016/0960-894X(95)00224-H
9824568 202698 0 None - 0 Human 7.6 pIC50 = 7.6 Binding
Compound was tested in vitro for inhibitory activity against human Angiotensin II receptor in cultured preadipocytesCompound was tested in vitro for inhibitory activity against human Angiotensin II receptor in cultured preadipocytes
ChEMBL 441 5 2 7 2.8 Cc1nc(C(=O)O)nc2c1CCC(=O)N2Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/s0960-894x(02)00303-7
CHEMBL72053 202698 0 None - 0 Human 7.6 pIC50 = 7.6 Binding
Compound was tested in vitro for inhibitory activity against human Angiotensin II receptor in cultured preadipocytesCompound was tested in vitro for inhibitory activity against human Angiotensin II receptor in cultured preadipocytes
ChEMBL 441 5 2 7 2.8 Cc1nc(C(=O)O)nc2c1CCC(=O)N2Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/s0960-894x(02)00303-7
127035716 135898 0 None - 1 Human 7.6 pIC50 = 7.6 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 545 10 2 4 7.2 CCCc1nc2c(C)cc(C(=O)NC[C@H](C)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2015.09.010
CHEMBL3735588 135898 0 None - 1 Human 7.6 pIC50 = 7.6 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 545 10 2 4 7.2 CCCc1nc2c(C)cc(C(=O)NC[C@H](C)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2015.09.010
44211673 59393 0 None - 0 Rabbit 7.6 pIC50 = 7.6 Binding
Inhibition of [125I]-Sar1-Ile8-Ang II binding to Angiotensin II receptor type 1 from rabbit aortaInhibition of [125I]-Sar1-Ile8-Ang II binding to Angiotensin II receptor type 1 from rabbit aorta
ChEMBL 678 4 1 8 6.6 CCCc1nc2ccc3cc2c(=O)n1Cc1ccc(cc1)-c1ccccc1S(=O)(=O)NC(=O)CCCCCN3C(=O)OCc1ccccc1 10.1016/0960-894X(96)00116-3
CHEMBL172376 59393 0 None - 0 Rabbit 7.6 pIC50 = 7.6 Binding
Inhibition of [125I]-Sar1-Ile8-Ang II binding to Angiotensin II receptor type 1 from rabbit aortaInhibition of [125I]-Sar1-Ile8-Ang II binding to Angiotensin II receptor type 1 from rabbit aorta
ChEMBL 678 4 1 8 6.6 CCCc1nc2ccc3cc2c(=O)n1Cc1ccc(cc1)-c1ccccc1S(=O)(=O)NC(=O)CCCCCN3C(=O)OCc1ccccc1 10.1016/0960-894X(96)00116-3
14950503 99078 0 None - 0 Guinea pig 7.6 pIC50 = 7.6 Binding
Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1
ChEMBL 429 7 1 7 4.2 CCc1nc(C)cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c1C(=O)OC 10.1021/jm00061a016
CHEMBL283579 99078 0 None - 0 Guinea pig 7.6 pIC50 = 7.6 Binding
Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1
ChEMBL 429 7 1 7 4.2 CCc1nc(C)cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c1C(=O)OC 10.1021/jm00061a016
44305410 161797 0 None - 0 Bovine 7.6 pIC50 = 7.6 Binding
Tested for binding affinity against angiotensin II receptor in bovine adrenal cortexTested for binding affinity against angiotensin II receptor in bovine adrenal cortex
ChEMBL 556 10 3 8 3.5 CCCc1cc(=O)n(CCNC(=O)NC2CCCCC2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/0960-894X(95)00370-9
CHEMBL416507 161797 0 None - 0 Bovine 7.6 pIC50 = 7.6 Binding
Tested for binding affinity against angiotensin II receptor in bovine adrenal cortexTested for binding affinity against angiotensin II receptor in bovine adrenal cortex
ChEMBL 556 10 3 8 3.5 CCCc1cc(=O)n(CCNC(=O)NC2CCCCC2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/0960-894X(95)00370-9
73346386 92170 0 None - 1 Human 7.6 pIC50 = 7.6 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 531 10 2 4 6.7 CCCc1nc2c(C)cc(C(=O)NCCc3ccccc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2015.09.010
CHEMBL2435818 92170 0 None - 1 Human 7.6 pIC50 = 7.6 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 531 10 2 4 6.7 CCCc1nc2c(C)cc(C(=O)NCCc3ccccc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2015.09.010
10460186 116346 0 None - 0 Human 7.6 pIC50 = 7.6 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 548 12 0 7 6.0 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2Cc2sccc2C)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
CHEMBL338123 116346 0 None - 0 Human 7.6 pIC50 = 7.6 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 548 12 0 7 6.0 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2Cc2sccc2C)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
70694919 76269 0 None - 0 Human 7.6 pIC50 = 7.6 Binding
Displacement of 125[I-Sar1-Ile8]ANG II from human AT1 receptor expressed in HEK293 membranes after 1 hr by gamma countingDisplacement of 125[I-Sar1-Ile8]ANG II from human AT1 receptor expressed in HEK293 membranes after 1 hr by gamma counting
ChEMBL 386 8 1 6 3.9 CCCCc1cnc(C=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.ejmech.2012.07.040
CHEMBL2063983 76269 0 None - 0 Human 7.6 pIC50 = 7.6 Binding
Displacement of 125[I-Sar1-Ile8]ANG II from human AT1 receptor expressed in HEK293 membranes after 1 hr by gamma countingDisplacement of 125[I-Sar1-Ile8]ANG II from human AT1 receptor expressed in HEK293 membranes after 1 hr by gamma counting
ChEMBL 386 8 1 6 3.9 CCCCc1cnc(C=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.ejmech.2012.07.040
130762 97782 9 None - 0 Rabbit 6.6 pIC50 = 6.6 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 398 8 2 4 4.8 CCCCc1nc(Cl)c(CO)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
CHEMBL274447 97782 9 None - 0 Rabbit 6.6 pIC50 = 6.6 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 398 8 2 4 4.8 CCCCc1nc(Cl)c(CO)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
44291524 183684 0 None - 0 Rat 6.6 pIC50 = 6.6 Binding
In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.
ChEMBL 462 11 1 3 6.8 CCCCC1=NC(C)(CC(C)CC(C)C)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/S0960-894X(01)81140-9
CHEMBL48392 183684 0 None - 0 Rat 6.6 pIC50 = 6.6 Binding
In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.
ChEMBL 462 11 1 3 6.8 CCCCC1=NC(C)(CC(C)CC(C)C)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/S0960-894X(01)81140-9
24827769 95424 0 None - 0 Rat 5.6 pIC50 = 5.6 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
ChEMBL 425 6 1 7 3.7 CC(C)Cn1c(=O)c2cccnc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm7011563
CHEMBL259116 95424 0 None - 0 Rat 5.6 pIC50 = 5.6 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
ChEMBL 425 6 1 7 3.7 CC(C)Cn1c(=O)c2cccnc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm7011563
54771778 64775 0 None - 0 Human 5.6 pIC50 = 5.6 Binding
Displacement of [125I][Sar1,Ile8]-AT-II from human recombinant AT1 receptor expressed in HEK293 cells after 120 mins by liquid scintillation countingDisplacement of [125I][Sar1,Ile8]-AT-II from human recombinant AT1 receptor expressed in HEK293 cells after 120 mins by liquid scintillation counting
ChEMBL 479 8 2 8 5.0 CCOC(=O)c1cn(Cc2ccc(-c3ccccc3-c3nnn[nH]3)cc2)nc1Nc1cccc(C)c1 10.1016/j.ejmech.2011.05.056
CHEMBL1824004 64775 0 None - 0 Human 5.6 pIC50 = 5.6 Binding
Displacement of [125I][Sar1,Ile8]-AT-II from human recombinant AT1 receptor expressed in HEK293 cells after 120 mins by liquid scintillation countingDisplacement of [125I][Sar1,Ile8]-AT-II from human recombinant AT1 receptor expressed in HEK293 cells after 120 mins by liquid scintillation counting
ChEMBL 479 8 2 8 5.0 CCOC(=O)c1cn(Cc2ccc(-c3ccccc3-c3nnn[nH]3)cc2)nc1Nc1cccc(C)c1 10.1016/j.ejmech.2011.05.056
14956757 67236 0 None - 1 Rabbit 4.6 pIC50 = 4.6 Binding
Inhibitory activity against Angiotensin II receptor, type 1 bindingInhibitory activity against Angiotensin II receptor, type 1 binding
ChEMBL 519 8 1 7 5.3 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm990504b
CHEMBL19018 67236 0 None - 1 Rabbit 4.6 pIC50 = 4.6 Binding
Inhibitory activity against Angiotensin II receptor, type 1 bindingInhibitory activity against Angiotensin II receptor, type 1 binding
ChEMBL 519 8 1 7 5.3 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm990504b
15287889 99958 0 None - 0 Rabbit 6.6 pIC50 = 6.6 Binding
Tested in vitro for Angiotensin II receptor, type 1 binding affinity using rabbit aorta binding assayTested in vitro for Angiotensin II receptor, type 1 binding affinity using rabbit aorta binding assay
ChEMBL 459 9 2 6 4.6 CCCc1nc2c(C)ccnc2n1Cc1ccc(OC(C(=O)O)c2ccccc2C(=O)O)cc1 10.1016/0960-894X(94)00476-V
CHEMBL290465 99958 0 None - 0 Rabbit 6.6 pIC50 = 6.6 Binding
Tested in vitro for Angiotensin II receptor, type 1 binding affinity using rabbit aorta binding assayTested in vitro for Angiotensin II receptor, type 1 binding affinity using rabbit aorta binding assay
ChEMBL 459 9 2 6 4.6 CCCc1nc2c(C)ccnc2n1Cc1ccc(OC(C(=O)O)c2ccccc2C(=O)O)cc1 10.1016/0960-894X(94)00476-V
19008935 161296 0 None - 0 Human 6.6 pIC50 = 6.6 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation countingDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation counting
ChEMBL 463 6 1 6 5.8 CCCCc1nc2c(C)cc(C)nc2n1C1CCc2cc(-c3ccccc3-c3nn[nH]n3)ccc21 10.1021/jm200409s
CHEMBL414836 161296 0 None - 0 Human 6.6 pIC50 = 6.6 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation countingDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation counting
ChEMBL 463 6 1 6 5.8 CCCCc1nc2c(C)cc(C)nc2n1C1CCc2cc(-c3ccccc3-c3nn[nH]n3)ccc21 10.1021/jm200409s
19010059 84528 0 None - 0 Rabbit 7.6 pIC50 = 7.6 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 568 12 3 9 5.1 CCCCc1nnc(SCc2ccc(C(=O)O)cc2)n1Cc1ccc(NC(=O)c2ccccc2-c2nnn[nH]2)cc1 10.1007/s00044-011-9756-4
CHEMBL2237598 84528 0 None - 0 Rabbit 7.6 pIC50 = 7.6 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 568 12 3 9 5.1 CCCCc1nnc(SCc2ccc(C(=O)O)cc2)n1Cc1ccc(NC(=O)c2ccccc2-c2nnn[nH]2)cc1 10.1007/s00044-011-9756-4
73349223 91744 0 None - 0 Rabbit 7.6 pIC50 = 7.6 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 713 14 2 8 7.3 CCCCC(=O)Nc1ccc(C)c(-n2nc(CCCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)c4ccccc4Cl)cc3)c2=O)c1 10.1007/s00044-013-0831-x
CHEMBL2425138 91744 0 None - 0 Rabbit 7.6 pIC50 = 7.6 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 713 14 2 8 7.3 CCCCC(=O)Nc1ccc(C)c(-n2nc(CCCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)c4ccccc4Cl)cc3)c2=O)c1 10.1007/s00044-013-0831-x
44293696 101168 0 None - 0 Rat 7.6 pIC50 = 7.6 Binding
Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.
ChEMBL 568 13 3 7 5.5 CCCCc1nc(Cl)c(CC(=O)O)n1Cc1ccc(NC(=O)[C@H](Cc2cccs2)n2cccc2C(=O)O)cc1 10.1021/jm00064a007
CHEMBL299130 101168 0 None - 0 Rat 7.6 pIC50 = 7.6 Binding
Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.
ChEMBL 568 13 3 7 5.5 CCCCc1nc(Cl)c(CC(=O)O)n1Cc1ccc(NC(=O)[C@H](Cc2cccs2)n2cccc2C(=O)O)cc1 10.1021/jm00064a007
44341794 9776 0 None - 0 Rat 7.6 pIC50 = 7.6 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 418 8 1 3 5.7 CCCCCC1=NC2(CCCC2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00074a018
CHEMBL114267 9776 0 None - 0 Rat 7.6 pIC50 = 7.6 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 418 8 1 3 5.7 CCCCCC1=NC2(CCCC2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00074a018
53320976 57289 0 None - 0 Guinea pig 7.6 pIC50 = 7.6 Binding
Binding affinity to angiotensin AT1 receptor in guinea pig adrenal cortex membranesBinding affinity to angiotensin AT1 receptor in guinea pig adrenal cortex membranes
ChEMBL 394 5 1 6 4.8 CCc1cc(Oc2ccc(-c3ccccc3-c3nnn[nH]3)cc2)c2ncccc2n1 10.1016/j.bmc.2010.10.043
CHEMBL1668124 57289 0 None - 0 Guinea pig 7.6 pIC50 = 7.6 Binding
Binding affinity to angiotensin AT1 receptor in guinea pig adrenal cortex membranesBinding affinity to angiotensin AT1 receptor in guinea pig adrenal cortex membranes
ChEMBL 394 5 1 6 4.8 CCc1cc(Oc2ccc(-c3ccccc3-c3nnn[nH]3)cc2)c2ncccc2n1 10.1016/j.bmc.2010.10.043
10280531 162369 0 None - 1 Human 7.6 pIC50 = 7.6 Binding
Displacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysisDisplacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysis
ChEMBL 541 10 2 7 5.1 CCCCc1nc(Cl)c(C(N)=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)cc1 10.1039/C4MD00499J
CHEMBL417429 162369 0 None - 1 Human 7.6 pIC50 = 7.6 Binding
Displacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysisDisplacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysis
ChEMBL 541 10 2 7 5.1 CCCCc1nc(Cl)c(C(N)=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)cc1 10.1039/C4MD00499J
70694919 76269 0 None - 0 Human 7.6 pIC50 = 7.6 Binding
Displacement of 125[I-Sar1-Ile8]ANG II from human AT1 receptor expressed in HEK293 membranes after 1 hr by gamma countingDisplacement of 125[I-Sar1-Ile8]ANG II from human AT1 receptor expressed in HEK293 membranes after 1 hr by gamma counting
ChEMBL 386 8 1 6 3.9 CCCCc1cnc(C=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.ejmech.2012.07.040
CHEMBL2063983 76269 0 None - 0 Human 7.6 pIC50 = 7.6 Binding
Displacement of 125[I-Sar1-Ile8]ANG II from human AT1 receptor expressed in HEK293 membranes after 1 hr by gamma countingDisplacement of 125[I-Sar1-Ile8]ANG II from human AT1 receptor expressed in HEK293 membranes after 1 hr by gamma counting
ChEMBL 386 8 1 6 3.9 CCCCc1cnc(C=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.ejmech.2012.07.040
10436877 47716 0 None - 0 Rabbit 7.6 pIC50 = 7.6 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 525 11 2 8 5.5 CCCCc1nnc(SCc2ccc(C(=O)O)cc2)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
CHEMBL155008 47716 0 None - 0 Rabbit 7.6 pIC50 = 7.6 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 525 11 2 8 5.5 CCCCc1nnc(SCc2ccc(C(=O)O)cc2)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
9914502 119187 0 None - 0 Rabbit 7.6 pIC50 = 7.6 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 515 10 1 7 6.5 CCCCc1nnc(SCc2ccc(Cl)cc2)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
CHEMBL347392 119187 0 None - 0 Rabbit 7.6 pIC50 = 7.6 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 515 10 1 7 6.5 CCCCc1nnc(SCc2ccc(Cl)cc2)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
10327728 97658 0 None - 0 Human 7.6 pIC50 = 7.6 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 749 9 2 9 6.7 CCc1nn(-c2cc(NC(=O)c3ccccc3)ccc2Br)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1021/jm00019a004
CHEMBL273542 97658 0 None - 0 Human 7.6 pIC50 = 7.6 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 749 9 2 9 6.7 CCc1nn(-c2cc(NC(=O)c3ccccc3)ccc2Br)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1021/jm00019a004
44300734 101323 0 None - 0 Rabbit 7.6 pIC50 = 7.6 Binding
Inhibition of Angiotensin II receptor type 1 in rabbit aorta binding assayInhibition of Angiotensin II receptor type 1 in rabbit aorta binding assay
ChEMBL 586 9 1 7 6.7 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2cc(CC(C)C)sc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/S0960-894X(01)81145-8
CHEMBL300154 101323 0 None - 0 Rabbit 7.6 pIC50 = 7.6 Binding
Inhibition of Angiotensin II receptor type 1 in rabbit aorta binding assayInhibition of Angiotensin II receptor type 1 in rabbit aorta binding assay
ChEMBL 586 9 1 7 6.7 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2cc(CC(C)C)sc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/S0960-894X(01)81145-8
9982171 20290 0 None - 0 Rat 7.6 pIC50 = 7.6 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 470 8 2 4 5.9 CCCCc1nc2ccc(NC(=O)N(C)C)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00077a007
CHEMBL130741 20290 0 None - 0 Rat 7.6 pIC50 = 7.6 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 470 8 2 4 5.9 CCCCc1nc2ccc(NC(=O)N(C)C)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00077a007
11765394 118259 0 None - 0 Rabbit 7.6 pIC50 = 7.6 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 713 14 2 8 7.3 CCCCC(=O)Nc1cccc(-n2nc(CCCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)c4ccccc4Cl)cc3)c2=O)c1C 10.1021/jm00052a006
CHEMBL341986 118259 0 None - 0 Rabbit 7.6 pIC50 = 7.6 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 713 14 2 8 7.3 CCCCC(=O)Nc1cccc(-n2nc(CCCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)c4ccccc4Cl)cc3)c2=O)c1C 10.1021/jm00052a006
44341946 9487 12 None - 0 Human 7.6 pIC50 = 7.6 Binding
Tested for inhibition of Angiotensin II receptor, type 1 in the absence of bovine serum albumin (BSA)Tested for inhibition of Angiotensin II receptor, type 1 in the absence of bovine serum albumin (BSA)
ChEMBL 407 9 2 5 3.5 CCCCC(=O)N(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)[C@@H](C)C(=O)O 10.1016/S0960-894X(01)81117-3
CHEMBL112523 9487 12 None - 0 Human 7.6 pIC50 = 7.6 Binding
Tested for inhibition of Angiotensin II receptor, type 1 in the absence of bovine serum albumin (BSA)Tested for inhibition of Angiotensin II receptor, type 1 in the absence of bovine serum albumin (BSA)
ChEMBL 407 9 2 5 3.5 CCCCC(=O)N(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)[C@@H](C)C(=O)O 10.1016/S0960-894X(01)81117-3
71521195 86379 0 None - 0 Human 7.6 pIC50 = 7.6 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor afterDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after
ChEMBL 508 6 1 8 3.2 CCc1nc2ccn(CC(=O)N(C)C)c(=O)c2n1[C@H]1CCc2cc(-c3ccccc3-c3nnn[nH]3)ccc21 10.1016/j.bmcl.2012.11.088
CHEMBL2322438 86379 0 None - 0 Human 7.6 pIC50 = 7.6 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor afterDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after
ChEMBL 508 6 1 8 3.2 CCc1nc2ccn(CC(=O)N(C)C)c(=O)c2n1[C@H]1CCc2cc(-c3ccccc3-c3nnn[nH]3)ccc21 10.1016/j.bmcl.2012.11.088
44293939 100716 0 None - 0 Rat 6.6 pIC50 = 6.6 Binding
Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.
ChEMBL 590 14 2 7 6.0 CCCCc1nc(Cl)c(CC(=O)O)n1Cc1ccc(NC(=O)[C@H](Cc2ccccc2)n2ccc(C(=O)OCC)c2)cc1 10.1021/jm00064a007
CHEMBL295737 100716 0 None - 0 Rat 6.6 pIC50 = 6.6 Binding
Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.
ChEMBL 590 14 2 7 6.0 CCCCc1nc(Cl)c(CC(=O)O)n1Cc1ccc(NC(=O)[C@H](Cc2ccccc2)n2ccc(C(=O)OCC)c2)cc1 10.1021/jm00064a007
10414026 156957 0 None - 0 Rat 6.6 pIC50 = 6.6 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 511 7 1 7 6.7 CCCc1nc2ccc(-c3nc4ccccc4o3)cc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00077a007
CHEMBL407978 156957 0 None - 0 Rat 6.6 pIC50 = 6.6 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 511 7 1 7 6.7 CCCc1nc2ccc(-c3nc4ccccc4o3)cc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00077a007
44298772 193891 0 None - 0 Bovine 5.6 pIC50 = 5.6 Binding
Binding affinity for angiotensin II receptor of bovine adrenal cortexBinding affinity for angiotensin II receptor of bovine adrenal cortex
ChEMBL 452 8 1 7 4.3 CCCCOc1nc2ccccn2c(=O)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81144-6
CHEMBL55507 193891 0 None - 0 Bovine 5.6 pIC50 = 5.6 Binding
Binding affinity for angiotensin II receptor of bovine adrenal cortexBinding affinity for angiotensin II receptor of bovine adrenal cortex
ChEMBL 452 8 1 7 4.3 CCCCOc1nc2ccccn2c(=O)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81144-6
44295568 101116 0 None - 0 Bovine 5.6 pIC50 = 5.6 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 465 9 1 6 5.3 CCCCc1nc2cccc(CN(C)C)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
CHEMBL298741 101116 0 None - 0 Bovine 5.6 pIC50 = 5.6 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 465 9 1 6 5.3 CCCCc1nc2cccc(CN(C)C)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
10255042 116304 0 None - 0 Rat 5.6 pIC50 = 5.6 Binding
Inhibition of [125I]angiotensin II receptor specific binding to rat mesenteric arteriesInhibition of [125I]angiotensin II receptor specific binding to rat mesenteric arteries
ChEMBL 490 10 1 4 7.3 CCCCc1ncc(/C=C(/C(=O)O)C(c2ccccc2)c2cccs2)n1Cc1ccccc1Cl 10.1021/jm00099a013
CHEMBL337928 116304 0 None - 0 Rat 5.6 pIC50 = 5.6 Binding
Inhibition of [125I]angiotensin II receptor specific binding to rat mesenteric arteriesInhibition of [125I]angiotensin II receptor specific binding to rat mesenteric arteries
ChEMBL 490 10 1 4 7.3 CCCCc1ncc(/C=C(/C(=O)O)C(c2ccccc2)c2cccs2)n1Cc1ccccc1Cl 10.1021/jm00099a013
44305823 162355 0 None - 0 Bovine 5.6 pIC50 = 5.6 Binding
Tested for binding affinity against angiotensin II receptor in bovine adrenal cortexTested for binding affinity against angiotensin II receptor in bovine adrenal cortex
ChEMBL 400 5 1 7 2.3 Cn1c(=O)cc(C2CC2)n(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c1=O 10.1016/0960-894X(95)00370-9
CHEMBL417410 162355 0 None - 0 Bovine 5.6 pIC50 = 5.6 Binding
Tested for binding affinity against angiotensin II receptor in bovine adrenal cortexTested for binding affinity against angiotensin II receptor in bovine adrenal cortex
ChEMBL 400 5 1 7 2.3 Cn1c(=O)cc(C2CC2)n(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c1=O 10.1016/0960-894X(95)00370-9
44295568 101116 0 None - 0 Bovine 5.6 pIC50 = 5.6 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 465 9 1 6 5.3 CCCCc1nc2cccc(CN(C)C)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
CHEMBL298741 101116 0 None - 0 Bovine 5.6 pIC50 = 5.6 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 465 9 1 6 5.3 CCCCc1nc2cccc(CN(C)C)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
10459724 17778 0 None - 0 Human 6.6 pIC50 = 6.6 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 532 12 1 7 4.7 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2Cc2c[nH]c(C)n2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
CHEMBL126170 17778 0 None - 0 Human 6.6 pIC50 = 6.6 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 532 12 1 7 4.7 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2Cc2c[nH]c(C)n2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
70688681 76271 0 None - 0 Human 6.6 pIC50 = 6.6 Binding
Displacement of 125[I-Sar1-Ile8]ANG II from human AT1 receptor expressed in HEK293 membranes after 1 hr by gamma countingDisplacement of 125[I-Sar1-Ile8]ANG II from human AT1 receptor expressed in HEK293 membranes after 1 hr by gamma counting
ChEMBL 364 8 2 4 4.1 CCCCc1cnc(CO)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2012.07.040
CHEMBL2063985 76271 0 None - 0 Human 6.6 pIC50 = 6.6 Binding
Displacement of 125[I-Sar1-Ile8]ANG II from human AT1 receptor expressed in HEK293 membranes after 1 hr by gamma countingDisplacement of 125[I-Sar1-Ile8]ANG II from human AT1 receptor expressed in HEK293 membranes after 1 hr by gamma counting
ChEMBL 364 8 2 4 4.1 CCCCc1cnc(CO)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2012.07.040
70688681 76271 0 None - 0 Human 6.6 pIC50 = 6.6 Binding
Displacement of 125[I-Sar1-Ile8]ANG II from human AT1 receptor expressed in HEK293 membranes after 1 hr by gamma countingDisplacement of 125[I-Sar1-Ile8]ANG II from human AT1 receptor expressed in HEK293 membranes after 1 hr by gamma counting
ChEMBL 364 8 2 4 4.1 CCCCc1cnc(CO)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2012.07.040
CHEMBL2063985 76271 0 None - 0 Human 6.6 pIC50 = 6.6 Binding
Displacement of 125[I-Sar1-Ile8]ANG II from human AT1 receptor expressed in HEK293 membranes after 1 hr by gamma countingDisplacement of 125[I-Sar1-Ile8]ANG II from human AT1 receptor expressed in HEK293 membranes after 1 hr by gamma counting
ChEMBL 364 8 2 4 4.1 CCCCc1cnc(CO)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2012.07.040
44306706 201391 0 None - 0 Rabbit 7.6 pIC50 = 7.6 Binding
Binding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membraneBinding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane
ChEMBL 654 10 1 6 7.6 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(Oc2ccccc2NS(=O)(=O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F)cc1 10.1016/S0960-894X(01)81148-3
CHEMBL63879 201391 0 None - 0 Rabbit 7.6 pIC50 = 7.6 Binding
Binding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membraneBinding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane
ChEMBL 654 10 1 6 7.6 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(Oc2ccccc2NS(=O)(=O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F)cc1 10.1016/S0960-894X(01)81148-3
44379185 57235 0 None - 0 Rabbit 7.6 pIC50 = 7.6 Binding
In vitro displacement of 125I-[Sar1, Ile8] from AT1 receptors in rabbit aorta membraneIn vitro displacement of 125I-[Sar1, Ile8] from AT1 receptors in rabbit aorta membrane
ChEMBL 603 13 2 7 5.6 CCCc1nc2ccc(C(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)CCCCC(=O)O)cc1 10.1016/S0960-894X(01)81125-2
CHEMBL166428 57235 0 None - 0 Rabbit 7.6 pIC50 = 7.6 Binding
In vitro displacement of 125I-[Sar1, Ile8] from AT1 receptors in rabbit aorta membraneIn vitro displacement of 125I-[Sar1, Ile8] from AT1 receptors in rabbit aorta membrane
ChEMBL 603 13 2 7 5.6 CCCc1nc2ccc(C(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)CCCCC(=O)O)cc1 10.1016/S0960-894X(01)81125-2
14950506 85353 0 None - 0 Guinea pig 7.6 pIC50 = 7.6 Binding
Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1
ChEMBL 434 6 1 6 5.2 Cc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c(-c2ccncc2)c(C)n1 10.1021/jm00061a016
CHEMBL22945 85353 0 None - 0 Guinea pig 7.6 pIC50 = 7.6 Binding
Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1
ChEMBL 434 6 1 6 5.2 Cc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c(-c2ccncc2)c(C)n1 10.1021/jm00061a016
15171385 166385 0 None - 0 Guinea pig 7.6 pIC50 = 7.6 Binding
Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1
ChEMBL 425 6 1 5 5.3 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2c(n1)CCCCC2 10.1021/jm00061a016
CHEMBL428711 166385 0 None - 0 Guinea pig 7.6 pIC50 = 7.6 Binding
Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1
ChEMBL 425 6 1 5 5.3 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2c(n1)CCCCC2 10.1021/jm00061a016
14951063 101656 0 None - 0 Rat 7.6 pIC50 = 7.6 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 551 10 1 8 5.1 CCCCc1nn(CC(=O)C23C[C@H]4C[C@@H](C2)C[C@@H](C3)C4)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a015
CHEMBL302478 101656 0 None - 0 Rat 7.6 pIC50 = 7.6 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 551 10 1 8 5.1 CCCCc1nn(CC(=O)C23C[C@H]4C[C@@H](C2)C[C@@H](C3)C4)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a015
44305400 201248 0 None - 0 Bovine 7.6 pIC50 = 7.6 Binding
Tested for binding affinity against angiotensin II receptor in bovine adrenal cortexTested for binding affinity against angiotensin II receptor in bovine adrenal cortex
ChEMBL 478 8 1 7 3.9 CCCc1cc(=O)n(Cc2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/0960-894X(95)00370-9
CHEMBL62936 201248 0 None - 0 Bovine 7.6 pIC50 = 7.6 Binding
Tested for binding affinity against angiotensin II receptor in bovine adrenal cortexTested for binding affinity against angiotensin II receptor in bovine adrenal cortex
ChEMBL 478 8 1 7 3.9 CCCc1cc(=O)n(Cc2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/0960-894X(95)00370-9
76315849 84972 0 None - 0 Human 7.6 pIC50 = 7.6 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 626 13 0 7 6.5 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2CCc2csc(Br)c2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
CHEMBL2263542 84972 0 None - 0 Human 7.6 pIC50 = 7.6 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 626 13 0 7 6.5 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2CCc2csc(Br)c2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
9912059 184764 0 None - 1 Bovine 6.6 pIC50 = 6.6 Binding
Ability to displace [125I]- labelled [Sar1,Ileu8] from angiotensin II receptor of bovine adrenal cortex membranesAbility to displace [125I]- labelled [Sar1,Ileu8] from angiotensin II receptor of bovine adrenal cortex membranes
ChEMBL 459 7 1 6 4.5 CCOC(=O)/C=C1\CC(C)(CC)CC(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80474-6
CHEMBL48602 184764 0 None - 1 Bovine 6.6 pIC50 = 6.6 Binding
Ability to displace [125I]- labelled [Sar1,Ileu8] from angiotensin II receptor of bovine adrenal cortex membranesAbility to displace [125I]- labelled [Sar1,Ileu8] from angiotensin II receptor of bovine adrenal cortex membranes
ChEMBL 459 7 1 6 4.5 CCOC(=O)/C=C1\CC(C)(CC)CC(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80474-6
44306709 102203 0 None - 0 Rabbit 6.6 pIC50 = 6.6 Binding
Binding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membraneBinding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane
ChEMBL 547 6 1 5 5.7 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1cc(Br)c(O)c(Br)c1 10.1016/S0960-894X(01)81148-3
CHEMBL304655 102203 0 None - 0 Rabbit 6.6 pIC50 = 6.6 Binding
Binding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membraneBinding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane
ChEMBL 547 6 1 5 5.7 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1cc(Br)c(O)c(Br)c1 10.1016/S0960-894X(01)81148-3
44341585 9799 0 None - 0 Rat 6.6 pIC50 = 6.6 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 522 9 3 6 3.6 CCCCC1=NC2(CCN(C(=O)C(N)CS)CC2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00074a018
CHEMBL114368 9799 0 None - 0 Rat 6.6 pIC50 = 6.6 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 522 9 3 6 3.6 CCCCC1=NC2(CCN(C(=O)C(N)CS)CC2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00074a018
44298759 189270 0 None - 0 Bovine 6.6 pIC50 = 6.6 Binding
Binding affinity for angiotensin II receptor of bovine adrenal cortexBinding affinity for angiotensin II receptor of bovine adrenal cortex
ChEMBL 438 7 1 7 3.9 CCCOc1nc2ccccn2c(=O)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81144-6
CHEMBL51689 189270 0 None - 0 Bovine 6.6 pIC50 = 6.6 Binding
Binding affinity for angiotensin II receptor of bovine adrenal cortexBinding affinity for angiotensin II receptor of bovine adrenal cortex
ChEMBL 438 7 1 7 3.9 CCCOc1nc2ccccn2c(=O)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81144-6
19976317 204654 0 None - 0 Rat 6.6 pIC50 = 6.6 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 416 10 1 7 4.3 CCCCc1nc(CCCC)n(Cc2ccc(-c3ccncc3-c3nn[nH]n3)cc2)n1 10.1021/jm031100t
CHEMBL87655 204654 0 None - 0 Rat 6.6 pIC50 = 6.6 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 416 10 1 7 4.3 CCCCc1nc(CCCC)n(Cc2ccc(-c3ccncc3-c3nn[nH]n3)cc2)n1 10.1021/jm031100t
9912059 184764 0 None - 1 Bovine 6.6 pIC50 = 6.6 Binding
Binding affinity to angiotensin AT1 receptor in bovine adrenal cortex membranesBinding affinity to angiotensin AT1 receptor in bovine adrenal cortex membranes
ChEMBL 459 7 1 6 4.5 CCOC(=O)/C=C1\CC(C)(CC)CC(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.bmc.2010.10.043
CHEMBL48602 184764 0 None - 1 Bovine 6.6 pIC50 = 6.6 Binding
Binding affinity to angiotensin AT1 receptor in bovine adrenal cortex membranesBinding affinity to angiotensin AT1 receptor in bovine adrenal cortex membranes
ChEMBL 459 7 1 6 4.5 CCOC(=O)/C=C1\CC(C)(CC)CC(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.bmc.2010.10.043
44348378 163650 0 None - 0 Bovine 6.6 pIC50 = 6.6 Binding
Concentration that gives 50% inhibition for binding of 125-I-[Sar1, IIe8] angiotensin to Angiotensin II receptor, type 1 in bovine adrenal cortex membrane.Concentration that gives 50% inhibition for binding of 125-I-[Sar1, IIe8] angiotensin to Angiotensin II receptor, type 1 in bovine adrenal cortex membrane.
ChEMBL 457 6 1 6 4.3 CCOC(=O)/C=C1\N(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)C(=O)CC12CCCC2 10.1016/S0960-894X(01)80914-8
CHEMBL421094 163650 0 None - 0 Bovine 6.6 pIC50 = 6.6 Binding
Concentration that gives 50% inhibition for binding of 125-I-[Sar1, IIe8] angiotensin to Angiotensin II receptor, type 1 in bovine adrenal cortex membrane.Concentration that gives 50% inhibition for binding of 125-I-[Sar1, IIe8] angiotensin to Angiotensin II receptor, type 1 in bovine adrenal cortex membrane.
ChEMBL 457 6 1 6 4.3 CCOC(=O)/C=C1\N(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)C(=O)CC12CCCC2 10.1016/S0960-894X(01)80914-8
71521507 86366 0 None - 0 Human 6.6 pIC50 = 6.6 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor afterDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after
ChEMBL 514 6 1 8 4.6 CCc1nc2ccn(Cc3ccncc3)c(=O)c2n1[C@H]1CCc2cc(-c3ccccc3-c3nnn[nH]3)ccc21 10.1016/j.bmcl.2012.11.088
CHEMBL2322173 86366 0 None - 0 Human 6.6 pIC50 = 6.6 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor afterDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after
ChEMBL 514 6 1 8 4.6 CCc1nc2ccn(Cc3ccncc3)c(=O)c2n1[C@H]1CCc2cc(-c3ccccc3-c3nnn[nH]3)ccc21 10.1016/j.bmcl.2012.11.088
19889599 101359 0 None - 0 Bovine 6.6 pIC50 = 6.6 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 494 10 1 7 5.4 CCCCc1nc2cccc(CC(=O)OCC)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
CHEMBL300451 101359 0 None - 0 Bovine 6.6 pIC50 = 6.6 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 494 10 1 7 5.4 CCCCc1nc2cccc(CC(=O)OCC)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
44438902 168819 0 None - 1 Bovine 6.6 pIC50 = 6.6 Binding
Displacement of [125I]angiotensin-2 from bovine adrenal cortex AT1 receptorDisplacement of [125I]angiotensin-2 from bovine adrenal cortex AT1 receptor
ChEMBL 375 5 2 5 3.6 Cc1nc2cccc(C(=O)O)c2n1Cc1ccc(-n2cccc2C(=O)O)cc1 10.1016/j.bmcl.2007.02.042
CHEMBL442251 168819 0 None - 1 Bovine 6.6 pIC50 = 6.6 Binding
Displacement of [125I]angiotensin-2 from bovine adrenal cortex AT1 receptorDisplacement of [125I]angiotensin-2 from bovine adrenal cortex AT1 receptor
ChEMBL 375 5 2 5 3.6 Cc1nc2cccc(C(=O)O)c2n1Cc1ccc(-n2cccc2C(=O)O)cc1 10.1016/j.bmcl.2007.02.042
15654748 202219 0 None - 0 Bovine 6.6 pIC50 = 6.6 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 440 7 2 7 3.8 COCc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a016
CHEMBL69144 202219 0 None - 0 Bovine 6.6 pIC50 = 6.6 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 440 7 2 7 3.8 COCc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a016
9912059 184764 0 None - 1 Bovine 6.6 pIC50 = 6.6 Binding
Inhibitory activity was evaluated against Angiotensin II receptor, type 1 in bovine adrenal membraneInhibitory activity was evaluated against Angiotensin II receptor, type 1 in bovine adrenal membrane
ChEMBL 459 7 1 6 4.5 CCOC(=O)/C=C1\CC(C)(CC)CC(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm9504722
CHEMBL48602 184764 0 None - 1 Bovine 6.6 pIC50 = 6.6 Binding
Inhibitory activity was evaluated against Angiotensin II receptor, type 1 in bovine adrenal membraneInhibitory activity was evaluated against Angiotensin II receptor, type 1 in bovine adrenal membrane
ChEMBL 459 7 1 6 4.5 CCOC(=O)/C=C1\CC(C)(CC)CC(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm9504722
19889599 101359 0 None - 0 Bovine 6.6 pIC50 = 6.6 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 494 10 1 7 5.4 CCCCc1nc2cccc(CC(=O)OCC)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
CHEMBL300451 101359 0 None - 0 Bovine 6.6 pIC50 = 6.6 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 494 10 1 7 5.4 CCCCc1nc2cccc(CC(=O)OCC)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
44294181 186643 0 None - 0 Rat 5.6 pIC50 = 5.6 Binding
Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.
ChEMBL 607 14 2 8 6.2 CCCCc1nc(-n2cccc2)c(C(=O)OCC)n1Cc1ccc(NC(=O)[C@H](Cc2ccccc2)n2cccc2C(=O)O)cc1 10.1021/jm00064a007
CHEMBL49257 186643 0 None - 0 Rat 5.6 pIC50 = 5.6 Binding
Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.
ChEMBL 607 14 2 8 6.2 CCCCc1nc(-n2cccc2)c(C(=O)OCC)n1Cc1ccc(NC(=O)[C@H](Cc2ccccc2)n2cccc2C(=O)O)cc1 10.1021/jm00064a007
44341785 10037 0 None - 0 Rat 5.6 pIC50 = 5.6 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 438 6 1 3 5.3 O=C(O)c1ccccc1-c1ccc(CN2C(=O)C3(CCCC3)N=C2Cc2ccccc2)cc1 10.1021/jm00074a018
CHEMBL115771 10037 0 None - 0 Rat 5.6 pIC50 = 5.6 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 438 6 1 3 5.3 O=C(O)c1ccccc1-c1ccc(CN2C(=O)C3(CCCC3)N=C2Cc2ccccc2)cc1 10.1021/jm00074a018
44309021 202271 0 None - 0 Bovine 5.6 pIC50 = 5.6 Binding
Inhibition of [125I][Ile5]-AII binding to bovine adrenal cortex membrane Angiotensin II receptor type 1Inhibition of [125I][Ile5]-AII binding to bovine adrenal cortex membrane Angiotensin II receptor type 1
ChEMBL 436 5 1 3 5.7 CCCCc1nc2ccccc2n1Cc1cc(Br)c(O)c(Br)c1 10.1016/S0960-894X(01)81149-5
CHEMBL69475 202271 0 None - 0 Bovine 5.6 pIC50 = 5.6 Binding
Inhibition of [125I][Ile5]-AII binding to bovine adrenal cortex membrane Angiotensin II receptor type 1Inhibition of [125I][Ile5]-AII binding to bovine adrenal cortex membrane Angiotensin II receptor type 1
ChEMBL 436 5 1 3 5.7 CCCCc1nc2ccccc2n1Cc1cc(Br)c(O)c(Br)c1 10.1016/S0960-894X(01)81149-5
44303857 100330 0 None - 0 Rabbit 4.6 pIC50 = 4.6 Binding
Inhibition of Angiotensin II receptor, type 1 in rabbit aorta using [125I-Sar1,Ile8] angiotensin II binding assayInhibition of Angiotensin II receptor, type 1 in rabbit aorta using [125I-Sar1,Ile8] angiotensin II binding assay
ChEMBL 508 11 1 3 5.8 CCCCCN(CCCCC)C(=O)N1CCN(C(=O)N(c2ccccc2)c2ccccc2)C[C@H]1C(=O)O 10.1016/S0960-894X(01)81007-6
CHEMBL293195 100330 0 None - 0 Rabbit 4.6 pIC50 = 4.6 Binding
Inhibition of Angiotensin II receptor, type 1 in rabbit aorta using [125I-Sar1,Ile8] angiotensin II binding assayInhibition of Angiotensin II receptor, type 1 in rabbit aorta using [125I-Sar1,Ile8] angiotensin II binding assay
ChEMBL 508 11 1 3 5.8 CCCCCN(CCCCC)C(=O)N1CCN(C(=O)N(c2ccccc2)c2ccccc2)C[C@H]1C(=O)O 10.1016/S0960-894X(01)81007-6
24829094 158514 0 None - 0 Rat 6.6 pIC50 = 6.6 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
ChEMBL 425 8 1 7 4.7 CCCCn1nc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2cccnc21 10.1021/jm7011563
CHEMBL409722 158514 0 None - 0 Rat 6.6 pIC50 = 6.6 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
ChEMBL 425 8 1 7 4.7 CCCCn1nc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2cccnc21 10.1021/jm7011563
15144943 17848 0 None - 0 Rat 4.6 pIC50 = 4.6 Binding
Inhibition of [125I]angiotensin II receptor specific binding to rat mesenteric arteriesInhibition of [125I]angiotensin II receptor specific binding to rat mesenteric arteries
ChEMBL 476 9 1 3 6.9 CCCCc1ncc(/C=C(\Cc2ccc(Cl)c(Cl)c2)C(=O)O)n1Cc1ccccc1Cl 10.1021/jm00099a013
CHEMBL126521 17848 0 None - 0 Rat 4.6 pIC50 = 4.6 Binding
Inhibition of [125I]angiotensin II receptor specific binding to rat mesenteric arteriesInhibition of [125I]angiotensin II receptor specific binding to rat mesenteric arteries
ChEMBL 476 9 1 3 6.9 CCCCc1ncc(/C=C(\Cc2ccc(Cl)c(Cl)c2)C(=O)O)n1Cc1ccccc1Cl 10.1021/jm00099a013
2121575 59214 7 None - 0 Human 5.6 pIC50 = 5.6 Binding
Displacement of [125I-Sar1-Ile8]Ang2 from human AT1 receptor expressed in HEK293 cell membrane incubated for 1 hr by gamma counting methodDisplacement of [125I-Sar1-Ile8]Ang2 from human AT1 receptor expressed in HEK293 cell membrane incubated for 1 hr by gamma counting method
ChEMBL 381 7 1 4 3.5 CN(Cc1cn(-c2ccccc2)nc1-c1ccc(F)cc1)C(=O)CCC(=O)O 10.1016/j.bmc.2016.07.047
CHEMBL1716544 59214 7 None - 0 Human 5.6 pIC50 = 5.6 Binding
Displacement of [125I-Sar1-Ile8]Ang2 from human AT1 receptor expressed in HEK293 cell membrane incubated for 1 hr by gamma counting methodDisplacement of [125I-Sar1-Ile8]Ang2 from human AT1 receptor expressed in HEK293 cell membrane incubated for 1 hr by gamma counting method
ChEMBL 381 7 1 4 3.5 CN(Cc1cn(-c2ccccc2)nc1-c1ccc(F)cc1)C(=O)CCC(=O)O 10.1016/j.bmc.2016.07.047
24828706 157927 0 None - 0 Rat 6.6 pIC50 = 6.6 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
ChEMBL 455 8 1 8 3.9 CCCCn1c(=O)c2ccc(OC)nc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm7011563
CHEMBL409095 157927 0 None - 0 Rat 6.6 pIC50 = 6.6 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
ChEMBL 455 8 1 8 3.9 CCCCn1c(=O)c2ccc(OC)nc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm7011563
44274707 93915 0 None - 0 Rabbit 7.6 pIC50 = 7.6 Binding
Ability to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitroAbility to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitro
ChEMBL 454 7 1 6 4.8 CCCCc1nc2ccc(F)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80335-2
CHEMBL25075 93915 0 None - 0 Rabbit 7.6 pIC50 = 7.6 Binding
Ability to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitroAbility to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitro
ChEMBL 454 7 1 6 4.8 CCCCc1nc2ccc(F)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80335-2
10482257 50451 0 None - 0 Rabbit 7.6 pIC50 = 7.6 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 534 11 2 6 6.6 CCCCc1nnc(SCc2cccc(Cl)c2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
CHEMBL157620 50451 0 None - 0 Rabbit 7.6 pIC50 = 7.6 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 534 11 2 6 6.6 CCCCc1nnc(SCc2cccc(Cl)c2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
44274707 93915 0 None - 0 Rabbit 7.6 pIC50 = 7.6 Binding
Binding affinity against Angiotensin II type 1 Receptor in rabbit aortic tissueBinding affinity against Angiotensin II type 1 Receptor in rabbit aortic tissue
ChEMBL 454 7 1 6 4.8 CCCCc1nc2ccc(F)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80334-0
CHEMBL25075 93915 0 None - 0 Rabbit 7.6 pIC50 = 7.6 Binding
Binding affinity against Angiotensin II type 1 Receptor in rabbit aortic tissueBinding affinity against Angiotensin II type 1 Receptor in rabbit aortic tissue
ChEMBL 454 7 1 6 4.8 CCCCc1nc2ccc(F)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80334-0
1610 2305 89 None -1 4 Rat 7.6 pIC50 = 7.6 Binding
Binding affinity against angiotensin II receptor in rat smooth muscle cell preparationsBinding affinity against angiotensin II receptor in rat smooth muscle cell preparations
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00114a021
3941 2305 89 None -1 4 Rat 7.6 pIC50 = 7.6 Binding
Binding affinity against angiotensin II receptor in rat smooth muscle cell preparationsBinding affinity against angiotensin II receptor in rat smooth muscle cell preparations
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00114a021
3961 2305 89 None -1 4 Rat 7.6 pIC50 = 7.6 Binding
Binding affinity against angiotensin II receptor in rat smooth muscle cell preparationsBinding affinity against angiotensin II receptor in rat smooth muscle cell preparations
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00114a021
590 2305 89 None -1 4 Rat 7.6 pIC50 = 7.6 Binding
Binding affinity against angiotensin II receptor in rat smooth muscle cell preparationsBinding affinity against angiotensin II receptor in rat smooth muscle cell preparations
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00114a021
CHEMBL191 2305 89 None -1 4 Rat 7.6 pIC50 = 7.6 Binding
Binding affinity against angiotensin II receptor in rat smooth muscle cell preparationsBinding affinity against angiotensin II receptor in rat smooth muscle cell preparations
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00114a021
DB00678 2305 89 None -1 4 Rat 7.6 pIC50 = 7.6 Binding
Binding affinity against angiotensin II receptor in rat smooth muscle cell preparationsBinding affinity against angiotensin II receptor in rat smooth muscle cell preparations
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00114a021
11527144 178516 0 None - 1 Bovine 7.6 pIC50 = 7.6 Binding
Binding affinity expressed as inhibitory concentration towards bovine adrenal cortex angiotensin II receptor was measuredBinding affinity expressed as inhibitory concentration towards bovine adrenal cortex angiotensin II receptor was measured
ChEMBL 561 8 1 8 5.6 CCCCc1nc2ccc([C@]3(C)C[C@H]4CCCN4O3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80366-2
CHEMBL297425 178516 0 None - 1 Bovine 7.6 pIC50 = 7.6 Binding
Binding affinity expressed as inhibitory concentration towards bovine adrenal cortex angiotensin II receptor was measuredBinding affinity expressed as inhibitory concentration towards bovine adrenal cortex angiotensin II receptor was measured
ChEMBL 561 8 1 8 5.6 CCCCc1nc2ccc([C@]3(C)C[C@H]4CCCN4O3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80366-2
CHEMBL47177 178516 0 None - 1 Bovine 7.6 pIC50 = 7.6 Binding
Binding affinity expressed as inhibitory concentration towards bovine adrenal cortex angiotensin II receptor was measuredBinding affinity expressed as inhibitory concentration towards bovine adrenal cortex angiotensin II receptor was measured
ChEMBL 561 8 1 8 5.6 CCCCc1nc2ccc([C@]3(C)C[C@H]4CCCN4O3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80366-2
10482257 50451 0 None - 0 Rabbit 7.6 pIC50 = 7.6 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 534 11 2 6 6.6 CCCCc1nnc(SCc2cccc(Cl)c2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
CHEMBL157620 50451 0 None - 0 Rabbit 7.6 pIC50 = 7.6 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 534 11 2 6 6.6 CCCCc1nnc(SCc2cccc(Cl)c2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
10028993 116314 0 None - 0 Guinea pig 7.6 pIC50 = 7.6 Binding
In vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparationIn vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparation
ChEMBL 465 8 1 6 6.0 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2cc(OC(C)C)ccc2n1 10.1021/jm00100a007
CHEMBL337955 116314 0 None - 0 Guinea pig 7.6 pIC50 = 7.6 Binding
In vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparationIn vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparation
ChEMBL 465 8 1 6 6.0 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2cc(OC(C)C)ccc2n1 10.1021/jm00100a007
9984807 117940 0 None - 0 Guinea pig 7.6 pIC50 = 7.6 Binding
In vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparationIn vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparation
ChEMBL 505 8 1 6 6.2 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2cc(OCC(F)(F)F)ccc2n1 10.1021/jm00100a007
CHEMBL341210 117940 0 None - 0 Guinea pig 7.6 pIC50 = 7.6 Binding
In vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparationIn vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparation
ChEMBL 505 8 1 6 6.2 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2cc(OCC(F)(F)F)ccc2n1 10.1021/jm00100a007
131590 20488 37 None - 3 Rat 7.6 pIC50 = 7.6 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 524 9 3 4 7.2 CCCCc1nc2ccc(NC(=O)NC3CCCCC3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00077a007
CHEMBL130896 20488 37 None - 3 Rat 7.6 pIC50 = 7.6 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 524 9 3 4 7.2 CCCCc1nc2ccc(NC(=O)NC3CCCCC3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00077a007
9984731 21161 0 None - 0 Rat 7.6 pIC50 = 7.6 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 538 9 2 4 7.3 CCCCc1nc2ccc(N(C)C(=O)NC3CCCCC3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00077a007
CHEMBL131433 21161 0 None - 0 Rat 7.6 pIC50 = 7.6 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 538 9 2 4 7.3 CCCCc1nc2ccc(N(C)C(=O)NC3CCCCC3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00077a007
127029203 136889 0 None - 0 Human 7.6 pIC50 = 7.6 Binding
Displacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptorDisplacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptor
ChEMBL 628 12 3 8 5.8 CCCc1nc2c(C)cc(C(=O)NCCc3ccccc3OC)cc2n1Cc1ccc(-c2ccccc2C(=O)Nc2nnn[nH]2)cc1 10.1039/C5MD00169B
CHEMBL3753458 136889 0 None - 0 Human 7.6 pIC50 = 7.6 Binding
Displacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptorDisplacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptor
ChEMBL 628 12 3 8 5.8 CCCc1nc2c(C)cc(C(=O)NCCc3ccccc3OC)cc2n1Cc1ccc(-c2ccccc2C(=O)Nc2nnn[nH]2)cc1 10.1039/C5MD00169B
44315057 203111 0 None - 0 Human 7.6 pIC50 = 7.6 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membrane
ChEMBL 651 10 2 8 5.9 Cc1nc2ccc(NC(=O)N(C)C(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/0960-894X(94)85036-4
CHEMBL75401 203111 0 None - 0 Human 7.6 pIC50 = 7.6 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membrane
ChEMBL 651 10 2 8 5.9 Cc1nc2ccc(NC(=O)N(C)C(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/0960-894X(94)85036-4
10076109 112344 0 None - 0 Human 6.6 pIC50 = 6.6 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 545 12 0 7 4.3 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2Cc2cccc[n+]2[O-])n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
CHEMBL330942 112344 0 None - 0 Human 6.6 pIC50 = 6.6 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 545 12 0 7 4.3 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2Cc2cccc[n+]2[O-])n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
44341453 9577 0 None - 0 Rat 6.6 pIC50 = 6.6 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 494 8 1 3 7.1 CCCCC1=NC2(CCC(c3ccccc3)CC2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00074a018
CHEMBL113039 9577 0 None - 0 Rat 6.6 pIC50 = 6.6 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 494 8 1 3 7.1 CCCCC1=NC2(CCC(c3ccccc3)CC2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00074a018
44342048 110120 0 None - 0 Rat 6.6 pIC50 = 6.6 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 376 7 1 3 4.5 CCCCC1=NC2(CC2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00074a018
CHEMBL325684 110120 0 None - 0 Rat 6.6 pIC50 = 6.6 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 376 7 1 3 4.5 CCCCC1=NC2(CC2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00074a018
135987615 100110 0 None - 0 Bovine 6.6 pIC50 = 6.6 Binding
Displacement of [125 I]-AII (0.2 nM) from bovine adrenal cortical membrane angiotensin II (AII) receptor at 10e-7 MDisplacement of [125 I]-AII (0.2 nM) from bovine adrenal cortical membrane angiotensin II (AII) receptor at 10e-7 M
ChEMBL 441 6 3 8 4.2 CNc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2noc(O)n2)cc1 10.1016/0960-894X(95)00319-O
CHEMBL291689 100110 0 None - 0 Bovine 6.6 pIC50 = 6.6 Binding
Displacement of [125 I]-AII (0.2 nM) from bovine adrenal cortical membrane angiotensin II (AII) receptor at 10e-7 MDisplacement of [125 I]-AII (0.2 nM) from bovine adrenal cortical membrane angiotensin II (AII) receptor at 10e-7 M
ChEMBL 441 6 3 8 4.2 CNc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2noc(O)n2)cc1 10.1016/0960-894X(95)00319-O
9933755 54746 0 None - 0 Rabbit 6.6 pIC50 = 6.6 Binding
Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)
ChEMBL 456 9 1 5 5.3 CCCCc1nc2ccc(C)cc2c(=O)n1Cc1ccc(OC(C(=O)O)c2ccccc2)cc1 10.1016/0960-894X(95)00185-V
CHEMBL16165 54746 0 None - 0 Rabbit 6.6 pIC50 = 6.6 Binding
Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)
ChEMBL 456 9 1 5 5.3 CCCCc1nc2ccc(C)cc2c(=O)n1Cc1ccc(OC(C(=O)O)c2ccccc2)cc1 10.1016/0960-894X(95)00185-V
44293439 101166 0 None - 0 Rat 5.6 pIC50 = 5.6 Binding
Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.
ChEMBL 493 11 2 8 3.8 CCCCc1nc(Cl)c(CO)n1Cc1ccc(NC(=O)C(Cc2ccccc2)n2cnnn2)cc1 10.1021/jm00064a007
CHEMBL299105 101166 0 None - 0 Rat 5.6 pIC50 = 5.6 Binding
Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.
ChEMBL 493 11 2 8 3.8 CCCCc1nc(Cl)c(CO)n1Cc1ccc(NC(=O)C(Cc2ccccc2)n2cnnn2)cc1 10.1021/jm00064a007
15356440 162106 0 None - 0 Rat 5.6 pIC50 = 5.6 Binding
Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.
ChEMBL 450 10 2 5 4.7 CCCCc1nc(Cl)c(CO)n1Cc1ccc(NC(=O)C(C#N)Cc2ccccc2)cc1 10.1021/jm00064a007
CHEMBL417009 162106 0 None - 0 Rat 5.6 pIC50 = 5.6 Binding
Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.
ChEMBL 450 10 2 5 4.7 CCCCc1nc(Cl)c(CO)n1Cc1ccc(NC(=O)C(C#N)Cc2ccccc2)cc1 10.1021/jm00064a007
19792151 101332 0 None - 0 Bovine 5.6 pIC50 = 5.6 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 466 9 2 6 4.9 CCCCc1nc2cccc(CC(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
CHEMBL300239 101332 0 None - 0 Bovine 5.6 pIC50 = 5.6 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 466 9 2 6 4.9 CCCCc1nc2cccc(CC(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
9978845 130177 0 None - 0 Rat 5.6 pIC50 = 5.6 Binding
Inhibition of [125I]angiotensin II receptor specific binding to rat mesenteric arteriesInhibition of [125I]angiotensin II receptor specific binding to rat mesenteric arteries
ChEMBL 408 9 1 3 5.6 CCCCc1ncc(/C=C(\Cc2ccccc2)C(=O)O)n1Cc1ccccc1Cl 10.1021/jm00099a013
CHEMBL36846 130177 0 None - 0 Rat 5.6 pIC50 = 5.6 Binding
Inhibition of [125I]angiotensin II receptor specific binding to rat mesenteric arteriesInhibition of [125I]angiotensin II receptor specific binding to rat mesenteric arteries
ChEMBL 408 9 1 3 5.6 CCCCc1ncc(/C=C(\Cc2ccccc2)C(=O)O)n1Cc1ccccc1Cl 10.1021/jm00099a013
11167226 106433 0 None - 0 Rat 6.6 pIC50 = 6.6 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 466 6 2 6 5.7 CCCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2c(C(=O)O)c(O)nc3ccccc23)cc1 10.1021/jm031100t
CHEMBL314807 106433 0 None - 0 Rat 6.6 pIC50 = 6.6 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 466 6 2 6 5.7 CCCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2c(C(=O)O)c(O)nc3ccccc23)cc1 10.1021/jm031100t
3846 96364 4 None - 0 Rabbit 7.6 pIC50 = 7.6 Binding
Ability to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitroAbility to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitro
ChEMBL 452 7 2 7 4.3 CCCCc1nc2ccc(O)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/S0960-894X(00)80335-2
CHEMBL26514 96364 4 None - 0 Rabbit 7.6 pIC50 = 7.6 Binding
Ability to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitroAbility to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitro
ChEMBL 452 7 2 7 4.3 CCCCc1nc2ccc(O)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/S0960-894X(00)80335-2
14956749 204486 0 None - 0 Rabbit 7.6 pIC50 = 7.6 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 479 9 1 7 4.8 CCCCc1nn(-c2ccc(CC)cc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
CHEMBL86613 204486 0 None - 0 Rabbit 7.6 pIC50 = 7.6 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 479 9 1 7 4.8 CCCCc1nn(-c2ccc(CC)cc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
15356431 100969 0 None - 0 Rat 7.6 pIC50 = 7.6 Binding
Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.
ChEMBL 562 13 3 6 5.5 CCCCc1nc(Cl)c(CC(=O)O)n1Cc1ccc(NC(=O)[C@H](Cc2ccccc2)n2cccc2C(=O)O)cc1 10.1021/jm00064a007
CHEMBL297653 100969 0 None - 0 Rat 7.6 pIC50 = 7.6 Binding
Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.
ChEMBL 562 13 3 6 5.5 CCCCc1nc(Cl)c(CC(=O)O)n1Cc1ccc(NC(=O)[C@H](Cc2ccccc2)n2cccc2C(=O)O)cc1 10.1021/jm00064a007
44341796 162848 0 None - 0 Rat 7.6 pIC50 = 7.6 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 390 6 1 3 4.9 CCCC1=NC2(CCCC2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00074a018
CHEMBL419583 162848 0 None - 0 Rat 7.6 pIC50 = 7.6 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 390 6 1 3 4.9 CCCC1=NC2(CCCC2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00074a018
44322239 204984 0 None - 0 Guinea pig 7.6 pIC50 = 7.6 Binding
Compound was tested for in vitro inhibition of specific binding of [I-125]AII to AT1 receptor in guinea pig adrenal membrane preparationCompound was tested for in vitro inhibition of specific binding of [I-125]AII to AT1 receptor in guinea pig adrenal membrane preparation
ChEMBL 455 7 2 6 4.6 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)c(C(=O)O)c2)c2c(n1)CCCC2 10.1016/S0960-894X(01)80295-X
CHEMBL89846 204984 0 None - 0 Guinea pig 7.6 pIC50 = 7.6 Binding
Compound was tested for in vitro inhibition of specific binding of [I-125]AII to AT1 receptor in guinea pig adrenal membrane preparationCompound was tested for in vitro inhibition of specific binding of [I-125]AII to AT1 receptor in guinea pig adrenal membrane preparation
ChEMBL 455 7 2 6 4.6 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)c(C(=O)O)c2)c2c(n1)CCCC2 10.1016/S0960-894X(01)80295-X
11527144 178516 0 None - 1 Bovine 7.6 pIC50 = 7.6 Binding
In vitro binding affinity to angiotensin II receptor in bovine adrenal cortexIn vitro binding affinity to angiotensin II receptor in bovine adrenal cortex
ChEMBL 561 8 1 8 5.6 CCCCc1nc2ccc([C@]3(C)C[C@H]4CCCN4O3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80377-2
CHEMBL297425 178516 0 None - 1 Bovine 7.6 pIC50 = 7.6 Binding
In vitro binding affinity to angiotensin II receptor in bovine adrenal cortexIn vitro binding affinity to angiotensin II receptor in bovine adrenal cortex
ChEMBL 561 8 1 8 5.6 CCCCc1nc2ccc([C@]3(C)C[C@H]4CCCN4O3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80377-2
CHEMBL47177 178516 0 None - 1 Bovine 7.6 pIC50 = 7.6 Binding
In vitro binding affinity to angiotensin II receptor in bovine adrenal cortexIn vitro binding affinity to angiotensin II receptor in bovine adrenal cortex
ChEMBL 561 8 1 8 5.6 CCCCc1nc2ccc([C@]3(C)C[C@H]4CCCN4O3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80377-2
44305681 102141 0 None - 0 Bovine 7.6 pIC50 = 7.6 Binding
Tested for binding affinity against angiotensin II receptor in bovine adrenal cortexTested for binding affinity against angiotensin II receptor in bovine adrenal cortex
ChEMBL 550 10 1 9 4.1 CCCCc1cc(=O)n(Cc2ccccc2C(=O)OC)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/0960-894X(95)00370-9
CHEMBL304251 102141 0 None - 0 Bovine 7.6 pIC50 = 7.6 Binding
Tested for binding affinity against angiotensin II receptor in bovine adrenal cortexTested for binding affinity against angiotensin II receptor in bovine adrenal cortex
ChEMBL 550 10 1 9 4.1 CCCCc1cc(=O)n(Cc2ccccc2C(=O)OC)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/0960-894X(95)00370-9
9800025 18310 0 None - 0 Rat 6.6 pIC50 = 6.6 Binding
Activity against high affinity Angiotensin II receptor, type 1 was measured from the ability to inhibit [125I]angiotensin II binding to rat uterine membrane.Activity against high affinity Angiotensin II receptor, type 1 was measured from the ability to inhibit [125I]angiotensin II binding to rat uterine membrane.
ChEMBL 380 10 1 5 4.5 CCCCc1nc(CCCC)n(Cc2ccc(-n3cccc3C(=O)O)cc2)n1 10.1021/jm00053a013
CHEMBL12737 18310 0 None - 0 Rat 6.6 pIC50 = 6.6 Binding
Activity against high affinity Angiotensin II receptor, type 1 was measured from the ability to inhibit [125I]angiotensin II binding to rat uterine membrane.Activity against high affinity Angiotensin II receptor, type 1 was measured from the ability to inhibit [125I]angiotensin II binding to rat uterine membrane.
ChEMBL 380 10 1 5 4.5 CCCCc1nc(CCCC)n(Cc2ccc(-n3cccc3C(=O)O)cc2)n1 10.1021/jm00053a013
10739982 9972 0 None - 0 Bovine 6.6 pIC50 = 6.6 Binding
In vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortexIn vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortex
ChEMBL 404 8 2 4 5.0 C=C(C)c1nc(CCC)n(Cc2ccc(-c3ccccc3C(=O)O)cc2)c1C(=O)O 10.1021/jm950450f
CHEMBL115393 9972 0 None - 0 Bovine 6.6 pIC50 = 6.6 Binding
In vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortexIn vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortex
ChEMBL 404 8 2 4 5.0 C=C(C)c1nc(CCC)n(Cc2ccc(-c3ccccc3C(=O)O)cc2)c1C(=O)O 10.1021/jm950450f
10410297 164749 0 None - 0 Guinea pig 6.6 pIC50 = 6.6 Binding
In vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparationIn vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparation
ChEMBL 391 5 1 4 5.2 Cc1cc(CCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2ccccc2n1 10.1021/jm00100a007
CHEMBL423370 164749 0 None - 0 Guinea pig 6.6 pIC50 = 6.6 Binding
In vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparationIn vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparation
ChEMBL 391 5 1 4 5.2 Cc1cc(CCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2ccccc2n1 10.1021/jm00100a007
44341923 109823 0 None - 0 Human 6.6 pIC50 = 6.6 Binding
Tested for inhibition of Angiotensin II receptor, type 1 in the absence of bovine serum albumin (BSA)Tested for inhibition of Angiotensin II receptor, type 1 in the absence of bovine serum albumin (BSA)
ChEMBL 421 10 2 5 4.1 CCCCC(=O)N(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)[C@H](CO)C(C)C 10.1016/S0960-894X(01)81117-3
CHEMBL323911 109823 0 None - 0 Human 6.6 pIC50 = 6.6 Binding
Tested for inhibition of Angiotensin II receptor, type 1 in the absence of bovine serum albumin (BSA)Tested for inhibition of Angiotensin II receptor, type 1 in the absence of bovine serum albumin (BSA)
ChEMBL 421 10 2 5 4.1 CCCCC(=O)N(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)[C@H](CO)C(C)C 10.1016/S0960-894X(01)81117-3
10523819 192806 0 None - 0 Bovine 5.6 pIC50 = 5.6 Binding
In vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortexIn vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortex
ChEMBL 380 8 3 5 3.2 CCCc1nc(CO)c(CO)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm950450f
CHEMBL52601 192806 0 None - 0 Bovine 5.6 pIC50 = 5.6 Binding
In vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortexIn vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortex
ChEMBL 380 8 3 5 3.2 CCCc1nc(CO)c(CO)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm950450f
10523819 192806 0 None - 0 Bovine 5.6 pIC50 = 5.6 Binding
Inhibition of [125l]-All binding to bovine adrenal cortexInhibition of [125l]-All binding to bovine adrenal cortex
ChEMBL 380 8 3 5 3.2 CCCc1nc(CO)c(CO)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/S0960-894X(01)81143-4
CHEMBL52601 192806 0 None - 0 Bovine 5.6 pIC50 = 5.6 Binding
Inhibition of [125l]-All binding to bovine adrenal cortexInhibition of [125l]-All binding to bovine adrenal cortex
ChEMBL 380 8 3 5 3.2 CCCc1nc(CO)c(CO)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/S0960-894X(01)81143-4
44274741 92812 0 None - 0 Rabbit 7.6 pIC50 = 7.6 Binding
Ability to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitroAbility to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitro
ChEMBL 481 8 1 8 4.5 CCCCc1nc2ccc([N+](=O)[O-])cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80335-2
CHEMBL24488 92812 0 None - 0 Rabbit 7.6 pIC50 = 7.6 Binding
Ability to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitroAbility to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitro
ChEMBL 481 8 1 8 4.5 CCCCc1nc2ccc([N+](=O)[O-])cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80335-2
76311804 84540 0 None - 0 Rabbit 7.6 pIC50 = 7.6 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 507 11 3 8 4.7 CCCCc1nnc(NCc2ccccc2)n1Cc1ccc(NC(=O)c2ccccc2-c2nnn[nH]2)cc1 10.1007/s00044-011-9756-4
CHEMBL2237610 84540 0 None - 0 Rabbit 7.6 pIC50 = 7.6 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 507 11 3 8 4.7 CCCCc1nnc(NCc2ccccc2)n1Cc1ccc(NC(=O)c2ccccc2-c2nnn[nH]2)cc1 10.1007/s00044-011-9756-4
44274741 92812 0 None - 0 Rabbit 7.6 pIC50 = 7.6 Binding
Binding affinity against Angiotensin II type 1 Receptor in rabbit aortic tissueBinding affinity against Angiotensin II type 1 Receptor in rabbit aortic tissue
ChEMBL 481 8 1 8 4.5 CCCCc1nc2ccc([N+](=O)[O-])cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80334-0
CHEMBL24488 92812 0 None - 0 Rabbit 7.6 pIC50 = 7.6 Binding
Binding affinity against Angiotensin II type 1 Receptor in rabbit aortic tissueBinding affinity against Angiotensin II type 1 Receptor in rabbit aortic tissue
ChEMBL 481 8 1 8 4.5 CCCCc1nc2ccc([N+](=O)[O-])cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80334-0
127035070 135936 0 None - 0 Human 7.6 pIC50 = 7.6 Binding
Displacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysisDisplacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysis
ChEMBL 647 11 2 7 7.3 CCCc1nc2c(C)cc(C(=O)NCc3ccccc3)cc2n1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)cc1 10.1039/C4MD00499J
CHEMBL3735931 135936 0 None - 0 Human 7.6 pIC50 = 7.6 Binding
Displacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysisDisplacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysis
ChEMBL 647 11 2 7 7.3 CCCc1nc2c(C)cc(C(=O)NCc3ccccc3)cc2n1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)cc1 10.1039/C4MD00499J
10370801 48150 0 None - 0 Rabbit 7.6 pIC50 = 7.6 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 570 12 2 9 4.4 CCCCc1nnc([S+]([O-])Cc2ccc(OC)cc2)n1Cc1ccc(NC(=O)c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
CHEMBL155554 48150 0 None - 0 Rabbit 7.6 pIC50 = 7.6 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 570 12 2 9 4.4 CCCCc1nnc([S+]([O-])Cc2ccc(OC)cc2)n1Cc1ccc(NC(=O)c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
10077702 50640 0 None - 0 Rabbit 7.6 pIC50 = 7.6 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 464 10 2 7 5.1 CCCCc1nnc(NCc2ccccc2)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
CHEMBL157779 50640 0 None - 0 Rabbit 7.6 pIC50 = 7.6 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 464 10 2 7 5.1 CCCCc1nnc(NCc2ccccc2)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
70686381 75846 0 None - 0 Bovine 7.6 pIC50 = 7.6 Binding
Displacement of [125I]AngII from type 1 angiotensin 2 receptor in bovine adrenal cortexDisplacement of [125I]AngII from type 1 angiotensin 2 receptor in bovine adrenal cortex
ChEMBL 486 7 1 6 5.7 CCc1nc2ccccc2n1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)cc1 10.1016/j.bmc.2012.06.011
CHEMBL2058368 75846 0 None - 0 Bovine 7.6 pIC50 = 7.6 Binding
Displacement of [125I]AngII from type 1 angiotensin 2 receptor in bovine adrenal cortexDisplacement of [125I]AngII from type 1 angiotensin 2 receptor in bovine adrenal cortex
ChEMBL 486 7 1 6 5.7 CCc1nc2ccccc2n1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)cc1 10.1016/j.bmc.2012.06.011
10573495 9696 0 None - 0 Bovine 7.6 pIC50 = 7.6 Binding
In vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortexIn vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortex
ChEMBL 408 8 3 5 4.0 CCCc1nc(C(C)O)c(C(=O)O)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm950450f
CHEMBL113714 9696 0 None - 0 Bovine 7.6 pIC50 = 7.6 Binding
In vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortexIn vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortex
ChEMBL 408 8 3 5 4.0 CCCc1nc(C(C)O)c(C(=O)O)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm950450f
10764699 113907 0 None - 0 Bovine 7.6 pIC50 = 7.6 Binding
In vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortexIn vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortex
ChEMBL 422 8 3 5 4.2 CCCc1nc(C(C)(C)O)c(C(=O)O)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm950450f
CHEMBL333155 113907 0 None - 0 Bovine 7.6 pIC50 = 7.6 Binding
In vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortexIn vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortex
ChEMBL 422 8 3 5 4.2 CCCc1nc(C(C)(C)O)c(C(=O)O)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm950450f
10078475 112818 0 None - 0 Human 7.6 pIC50 = 7.6 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 705 9 2 9 6.6 CCc1nn(-c2cc(NC(=O)c3ccccc3)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1021/jm00019a004
CHEMBL331632 112818 0 None - 0 Human 7.6 pIC50 = 7.6 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 705 9 2 9 6.6 CCc1nn(-c2cc(NC(=O)c3ccccc3)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1021/jm00019a004
1610 2305 89 None 1 4 Human 7.6 pIC50 = 7.6 Binding
Inhibition against human angiotensin II receptor, type 1 (AG2-R)Inhibition against human angiotensin II receptor, type 1 (AG2-R)
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm0309452
3941 2305 89 None 1 4 Human 7.6 pIC50 = 7.6 Binding
Inhibition against human angiotensin II receptor, type 1 (AG2-R)Inhibition against human angiotensin II receptor, type 1 (AG2-R)
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm0309452
3961 2305 89 None 1 4 Human 7.6 pIC50 = 7.6 Binding
Inhibition against human angiotensin II receptor, type 1 (AG2-R)Inhibition against human angiotensin II receptor, type 1 (AG2-R)
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm0309452
590 2305 89 None 1 4 Human 7.6 pIC50 = 7.6 Binding
Inhibition against human angiotensin II receptor, type 1 (AG2-R)Inhibition against human angiotensin II receptor, type 1 (AG2-R)
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm0309452
CHEMBL191 2305 89 None 1 4 Human 7.6 pIC50 = 7.6 Binding
Inhibition against human angiotensin II receptor, type 1 (AG2-R)Inhibition against human angiotensin II receptor, type 1 (AG2-R)
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm0309452
DB00678 2305 89 None 1 4 Human 7.6 pIC50 = 7.6 Binding
Inhibition against human angiotensin II receptor, type 1 (AG2-R)Inhibition against human angiotensin II receptor, type 1 (AG2-R)
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm0309452
2541 772 113 None 1 6 Rabbit 7.6 pIC50 = 7.6 Binding
Inhibitory activity against Angiotensin II receptor, type 1 in rabbit aortaInhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta
ChEMBL 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10.1021/jm9504722
587 772 113 None 1 6 Rabbit 7.6 pIC50 = 7.6 Binding
Inhibitory activity against Angiotensin II receptor, type 1 in rabbit aortaInhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta
ChEMBL 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10.1021/jm9504722
6907 772 113 None 1 6 Rabbit 7.6 pIC50 = 7.6 Binding
Inhibitory activity against Angiotensin II receptor, type 1 in rabbit aortaInhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta
ChEMBL 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10.1021/jm9504722
CHEMBL1016 772 113 None 1 6 Rabbit 7.6 pIC50 = 7.6 Binding
Inhibitory activity against Angiotensin II receptor, type 1 in rabbit aortaInhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta
ChEMBL 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10.1021/jm9504722
DB00796 772 113 None 1 6 Rabbit 7.6 pIC50 = 7.6 Binding
Inhibitory activity against Angiotensin II receptor, type 1 in rabbit aortaInhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta
ChEMBL 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10.1021/jm9504722
DB13919 772 113 None 1 6 Rabbit 7.6 pIC50 = 7.6 Binding
Inhibitory activity against Angiotensin II receptor, type 1 in rabbit aortaInhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta
ChEMBL 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10.1021/jm9504722
127034038 138654 0 None - 1 Human 7.6 pIC50 = 7.6 Binding
Displacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation countingDisplacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation counting
ChEMBL 1656 46 15 20 2.5 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCN/C(N)=N/C(=O)NCCCCNC(=O)CCCCC[n+]1cc(S(=O)(=O)[O-])ccc1/C=C/c1cc2ccc(N(CC)CC)cc2oc1=O)NC(=O)[C@@H](N)CC(=O)O)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O 10.1021/acs.jmedchem.5b01495
CHEMBL3785563 138654 0 None - 1 Human 7.6 pIC50 = 7.6 Binding
Displacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation countingDisplacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation counting
ChEMBL 1656 46 15 20 2.5 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCN/C(N)=N/C(=O)NCCCCNC(=O)CCCCC[n+]1cc(S(=O)(=O)[O-])ccc1/C=C/c1cc2ccc(N(CC)CC)cc2oc1=O)NC(=O)[C@@H](N)CC(=O)O)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O 10.1021/acs.jmedchem.5b01495
CHEMBL3787702 138654 0 None - 1 Human 7.6 pIC50 = 7.6 Binding
Displacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation countingDisplacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation counting
ChEMBL 1656 46 15 20 2.5 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCN/C(N)=N/C(=O)NCCCCNC(=O)CCCCC[n+]1cc(S(=O)(=O)[O-])ccc1/C=C/c1cc2ccc(N(CC)CC)cc2oc1=O)NC(=O)[C@@H](N)CC(=O)O)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O 10.1021/acs.jmedchem.5b01495
1610 2305 89 None 1 4 Human 7.5 pIC50 = 7.5 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.ejmech.2015.09.010
3941 2305 89 None 1 4 Human 7.5 pIC50 = 7.5 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.ejmech.2015.09.010
3961 2305 89 None 1 4 Human 7.5 pIC50 = 7.5 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.ejmech.2015.09.010
590 2305 89 None 1 4 Human 7.5 pIC50 = 7.5 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.ejmech.2015.09.010
CHEMBL191 2305 89 None 1 4 Human 7.5 pIC50 = 7.5 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.ejmech.2015.09.010
DB00678 2305 89 None 1 4 Human 7.5 pIC50 = 7.5 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.ejmech.2015.09.010
14951086 168899 0 None - 0 Rat 6.6 pIC50 = 6.6 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 585 13 1 8 6.2 CCCCc1nn(CC(OCc2ccccc2)c2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a015
CHEMBL443005 168899 0 None - 0 Rat 6.6 pIC50 = 6.6 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 585 13 1 8 6.2 CCCCc1nn(CC(OCc2ccccc2)c2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a015
14956803 204552 0 None - 0 Rat 6.6 pIC50 = 6.6 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 515 9 1 7 5.5 CCCCc1nn(Cc2ccc3ccccc3c2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a015
CHEMBL86986 204552 0 None - 0 Rat 6.6 pIC50 = 6.6 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 515 9 1 7 5.5 CCCCc1nn(Cc2ccc3ccccc3c2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a015
15699076 4997 0 None - 0 Rat 5.6 pIC50 = 5.6 Binding
Binding affinity against angiotensin II receptor in rat smooth muscle cell preparationsBinding affinity against angiotensin II receptor in rat smooth muscle cell preparations
ChEMBL 390 7 2 4 4.0 CCCCc1nc(CO)c(Cl)n1Cc1ccc2c(c1)CCC(C)(C(=O)O)C2 10.1021/jm00114a021
CHEMBL105486 4997 0 None - 0 Rat 5.6 pIC50 = 5.6 Binding
Binding affinity against angiotensin II receptor in rat smooth muscle cell preparationsBinding affinity against angiotensin II receptor in rat smooth muscle cell preparations
ChEMBL 390 7 2 4 4.0 CCCCc1nc(CO)c(Cl)n1Cc1ccc2c(c1)CCC(C)(C(=O)O)C2 10.1021/jm00114a021
44323112 111140 0 None - 0 Rat 5.6 pIC50 = 5.6 Binding
Concentration required to inhibit binding of radioligand [125I]AII to angiotensin II receptor, type 1 in rat adrenal glomerulosa tissueConcentration required to inhibit binding of radioligand [125I]AII to angiotensin II receptor, type 1 in rat adrenal glomerulosa tissue
ChEMBL 440 8 2 6 4.8 CCCCc1nc(Cl)c(CO)n1Cc1ccc(C2=C(c3nn[nH]n3)CCCCC2)cc1 10.1021/jm00092a017
CHEMBL328552 111140 0 None - 0 Rat 5.6 pIC50 = 5.6 Binding
Concentration required to inhibit binding of radioligand [125I]AII to angiotensin II receptor, type 1 in rat adrenal glomerulosa tissueConcentration required to inhibit binding of radioligand [125I]AII to angiotensin II receptor, type 1 in rat adrenal glomerulosa tissue
ChEMBL 440 8 2 6 4.8 CCCCc1nc(Cl)c(CO)n1Cc1ccc(C2=C(c3nn[nH]n3)CCCCC2)cc1 10.1021/jm00092a017
19792154 189205 0 None - 0 Bovine 5.6 pIC50 = 5.6 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 438 8 1 6 5.3 CCCCc1nc2cccc(OC)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
CHEMBL51634 189205 0 None - 0 Bovine 5.6 pIC50 = 5.6 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 438 8 1 6 5.3 CCCCc1nc2cccc(OC)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
19792154 189205 0 None - 0 Bovine 5.6 pIC50 = 5.6 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 438 8 1 6 5.3 CCCCc1nc2cccc(OC)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
CHEMBL51634 189205 0 None - 0 Bovine 5.6 pIC50 = 5.6 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 438 8 1 6 5.3 CCCCc1nc2cccc(OC)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
19792151 101332 0 None - 0 Bovine 5.6 pIC50 = 5.6 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 466 9 2 6 4.9 CCCCc1nc2cccc(CC(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
CHEMBL300239 101332 0 None - 0 Bovine 5.6 pIC50 = 5.6 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 466 9 2 6 4.9 CCCCc1nc2cccc(CC(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
46232959 199232 0 None - 0 Human 6.5 pIC50 = 6.5 Binding
Antagonist activity at human AT1 receptor expressed in CHO cells measured after overnight incubation by luciferase reporter gene assayAntagonist activity at human AT1 receptor expressed in CHO cells measured after overnight incubation by luciferase reporter gene assay
ChEMBL 531 10 2 4 7.3 CCCc1nc2ccc(C(=O)NC(CC)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.bmcl.2014.01.004
CHEMBL601678 199232 0 None - 0 Human 6.5 pIC50 = 6.5 Binding
Antagonist activity at human AT1 receptor expressed in CHO cells measured after overnight incubation by luciferase reporter gene assayAntagonist activity at human AT1 receptor expressed in CHO cells measured after overnight incubation by luciferase reporter gene assay
ChEMBL 531 10 2 4 7.3 CCCc1nc2ccc(C(=O)NC(CC)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.bmcl.2014.01.004
44274700 164679 0 None - 0 Rabbit 7.5 pIC50 = 7.5 Binding
Ability to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitroAbility to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitro
ChEMBL 470 7 1 6 5.3 CCCCc1nc2ccc(Cl)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80335-2
CHEMBL422932 164679 0 None - 0 Rabbit 7.5 pIC50 = 7.5 Binding
Ability to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitroAbility to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitro
ChEMBL 470 7 1 6 5.3 CCCCc1nc2ccc(Cl)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80335-2
44274700 164679 0 None - 0 Rabbit 7.5 pIC50 = 7.5 Binding
Binding affinity against Angiotensin II type 1 Receptor in rabbit aortic tissueBinding affinity against Angiotensin II type 1 Receptor in rabbit aortic tissue
ChEMBL 470 7 1 6 5.3 CCCCc1nc2ccc(Cl)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80334-0
CHEMBL422932 164679 0 None - 0 Rabbit 7.5 pIC50 = 7.5 Binding
Binding affinity against Angiotensin II type 1 Receptor in rabbit aortic tissueBinding affinity against Angiotensin II type 1 Receptor in rabbit aortic tissue
ChEMBL 470 7 1 6 5.3 CCCCc1nc2ccc(Cl)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80334-0
11442998 204460 0 None - 0 Rat 7.5 pIC50 = 7.5 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 479 6 1 6 5.6 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2c(C(=O)O)c(N(C)C)nc3ccccc23)cc1 10.1021/jm031100t
CHEMBL86436 204460 0 None - 0 Rat 7.5 pIC50 = 7.5 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 479 6 1 6 5.6 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2c(C(=O)O)c(N(C)C)nc3ccccc23)cc1 10.1021/jm031100t
15171421 204484 0 None - 0 Guinea pig 7.5 pIC50 = 7.5 Binding
Compound was tested for in vitro inhibition of specific binding of [I-125]AII to Angiotensin II receptor, type 1 in guinea pig adrenal membrane preparationCompound was tested for in vitro inhibition of specific binding of [I-125]AII to Angiotensin II receptor, type 1 in guinea pig adrenal membrane preparation
ChEMBL 425 6 1 5 5.3 CCc1cc(OCc2ccc(-c3c(C)cccc3-c3nn[nH]n3)cc2)c2c(n1)CCCC2 10.1016/S0960-894X(01)80295-X
CHEMBL86604 204484 0 None - 0 Guinea pig 7.5 pIC50 = 7.5 Binding
Compound was tested for in vitro inhibition of specific binding of [I-125]AII to Angiotensin II receptor, type 1 in guinea pig adrenal membrane preparationCompound was tested for in vitro inhibition of specific binding of [I-125]AII to Angiotensin II receptor, type 1 in guinea pig adrenal membrane preparation
ChEMBL 425 6 1 5 5.3 CCc1cc(OCc2ccc(-c3c(C)cccc3-c3nn[nH]n3)cc2)c2c(n1)CCCC2 10.1016/S0960-894X(01)80295-X
22407453 49474 0 None - 0 Rabbit 7.5 pIC50 = 7.5 Binding
Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)
ChEMBL 415 7 1 5 4.9 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(OC(C(=O)O)c2ccccc2)cc1 10.1016/0960-894X(95)00185-V
CHEMBL15671 49474 0 None - 0 Rabbit 7.5 pIC50 = 7.5 Binding
Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)
ChEMBL 415 7 1 5 4.9 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(OC(C(=O)O)c2ccccc2)cc1 10.1016/0960-894X(95)00185-V
71521418 86388 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor afterDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after
ChEMBL 597 7 1 8 6.1 CCc1nc2ccn(Cc3ccccc3OC(F)(F)F)c(=O)c2n1[C@H]1CCc2cc(-c3ccccc3-c3nnn[nH]3)ccc21 10.1016/j.bmcl.2012.11.088
CHEMBL2322447 86388 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor afterDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after
ChEMBL 597 7 1 8 6.1 CCc1nc2ccn(Cc3ccccc3OC(F)(F)F)c(=O)c2n1[C@H]1CCc2cc(-c3ccccc3-c3nnn[nH]3)ccc21 10.1016/j.bmcl.2012.11.088
76333686 84819 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 583 14 1 6 5.3 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2CCCC)n1Cc1ccc(S(=O)(=O)NC(F)(F)F)cc1 10.1007/s00044-009-9205-9
CHEMBL2259777 84819 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 583 14 1 6 5.3 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2CCCC)n1Cc1ccc(S(=O)(=O)NC(F)(F)F)cc1 10.1007/s00044-009-9205-9
9980304 98071 0 None - 0 Rat 6.5 pIC50 = 6.5 Binding
Activity against high affinity Angiotensin II receptor, type 1 was measured from the ability to inhibit [125I]angiotensin II binding to rat uterine membrane.Activity against high affinity Angiotensin II receptor, type 1 was measured from the ability to inhibit [125I]angiotensin II binding to rat uterine membrane.
ChEMBL 433 9 3 8 1.4 CCCCc1nc(C(N)=O)c(C(N)=O)n1Cc1ccc(-n2cccc2-c2nn[nH]n2)cc1 10.1021/jm00053a013
CHEMBL276381 98071 0 None - 0 Rat 6.5 pIC50 = 6.5 Binding
Activity against high affinity Angiotensin II receptor, type 1 was measured from the ability to inhibit [125I]angiotensin II binding to rat uterine membrane.Activity against high affinity Angiotensin II receptor, type 1 was measured from the ability to inhibit [125I]angiotensin II binding to rat uterine membrane.
ChEMBL 433 9 3 8 1.4 CCCCc1nc(C(N)=O)c(C(N)=O)n1Cc1ccc(-n2cccc2-c2nn[nH]n2)cc1 10.1021/jm00053a013
25147556 173281 0 None - 0 Bovine 6.5 pIC50 = 6.5 Binding
Displacement of [125I]Ang2 from AT1 receptor in bovine adrenal cortexDisplacement of [125I]Ang2 from AT1 receptor in bovine adrenal cortex
ChEMBL 538 7 1 6 6.9 CCCc1nc2c(C)cc(-c3nc4ccccc4n3C)cc2n1Cc1ccc(-c2ccccc2C2=NCCN2)cc1 10.1016/j.bmc.2008.10.040
CHEMBL453934 173281 0 None - 0 Bovine 6.5 pIC50 = 6.5 Binding
Displacement of [125I]Ang2 from AT1 receptor in bovine adrenal cortexDisplacement of [125I]Ang2 from AT1 receptor in bovine adrenal cortex
ChEMBL 538 7 1 6 6.9 CCCc1nc2c(C)cc(-c3nc4ccccc4n3C)cc2n1Cc1ccc(-c2ccccc2C2=NCCN2)cc1 10.1016/j.bmc.2008.10.040
23590374 201756 0 None - 0 Rat 6.5 pIC50 = 6.5 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 491 10 1 7 5.0 CCCCc1nn(C/C=C/c2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a015
CHEMBL65905 201756 0 None - 0 Rat 6.5 pIC50 = 6.5 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 491 10 1 7 5.0 CCCCc1nn(C/C=C/c2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a015
24827900 96404 0 None - 0 Rat 6.5 pIC50 = 6.5 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
ChEMBL 425 6 1 7 3.8 CCCn1c(=O)c2ccc(C)nc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm7011563
CHEMBL265452 96404 0 None - 0 Rat 6.5 pIC50 = 6.5 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
ChEMBL 425 6 1 7 3.8 CCCn1c(=O)c2ccc(C)nc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm7011563
71623945 135928 0 None - 1 Human 6.5 pIC50 = 6.5 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 571 10 3 7 5.7 CCCc1nc2c(C)cc(C(=O)N[C@@H](CO)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.ejmech.2015.09.010
CHEMBL3735839 135928 0 None - 1 Human 6.5 pIC50 = 6.5 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 571 10 3 7 5.7 CCCc1nc2c(C)cc(C(=O)N[C@@H](CO)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.ejmech.2015.09.010
10052533 116189 0 None - 0 Rat 4.5 pIC50 = 4.5 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 524 9 3 4 7.2 CCCCc1nc2c(NC(=O)NC3CCCCC3)cccc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00077a007
CHEMBL337269 116189 0 None - 0 Rat 4.5 pIC50 = 4.5 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 524 9 3 4 7.2 CCCCc1nc2c(NC(=O)NC3CCCCC3)cccc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00077a007
44316861 203464 0 None - 0 Human 6.5 pIC50 = 6.5 Binding
Tested for inhibition of Angiotensin II specific binding to Angiotensin II receptor, type 1 in the recombinant human AT-1 receptor expressed in LhAT-1D6 cellsTested for inhibition of Angiotensin II specific binding to Angiotensin II receptor, type 1 in the recombinant human AT-1 receptor expressed in LhAT-1D6 cells
ChEMBL 345 10 3 5 2.1 CCCCc1ncc(CNCC(=O)O)n1Cc1ccc(C(=O)O)cc1 10.1016/0960-894X(94)00456-P
CHEMBL78345 203464 0 None - 0 Human 6.5 pIC50 = 6.5 Binding
Tested for inhibition of Angiotensin II specific binding to Angiotensin II receptor, type 1 in the recombinant human AT-1 receptor expressed in LhAT-1D6 cellsTested for inhibition of Angiotensin II specific binding to Angiotensin II receptor, type 1 in the recombinant human AT-1 receptor expressed in LhAT-1D6 cells
ChEMBL 345 10 3 5 2.1 CCCCc1ncc(CNCC(=O)O)n1Cc1ccc(C(=O)O)cc1 10.1016/0960-894X(94)00456-P
44274716 96407 0 None - 0 Rabbit 8.5 pIC50 = 8.5 Binding
Ability to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitroAbility to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitro
ChEMBL 514 8 1 8 4.0 CCCCc1nc2ccc(S(C)(=O)=O)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80335-2
CHEMBL26548 96407 0 None - 0 Rabbit 8.5 pIC50 = 8.5 Binding
Ability to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitroAbility to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitro
ChEMBL 514 8 1 8 4.0 CCCCc1nc2ccc(S(C)(=O)=O)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80335-2
11756787 118981 0 None - 0 Rabbit 8.5 pIC50 = 8.5 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 530 12 2 7 5.9 CCCCc1nnc(SCc2ccc(OC)cc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
CHEMBL345459 118981 0 None - 0 Rabbit 8.5 pIC50 = 8.5 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 530 12 2 7 5.9 CCCCc1nnc(SCc2ccc(OC)cc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
10053110 84822 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 543 12 1 7 5.2 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2Cc2ccc(N)cc2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
CHEMBL2259780 84822 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 543 12 1 7 5.2 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2Cc2ccc(N)cc2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
10005890 113945 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 492 9 2 5 4.7 CCCCc1ncc(/C=C2/C(=O)NC(=O)N2Cc2ccc(Cl)cc2)n1Cc1ccc(C(=O)O)cc1 10.1007/s00044-009-9205-9
CHEMBL333411 113945 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 492 9 2 5 4.7 CCCCc1ncc(/C=C2/C(=O)NC(=O)N2Cc2ccc(Cl)cc2)n1Cc1ccc(C(=O)O)cc1 10.1007/s00044-009-9205-9
10460419 99856 0 None - 0 Rat 8.5 pIC50 = 8.5 Binding
Binding affinity against AT1 receptor in the presence of 0.01% BSABinding affinity against AT1 receptor in the presence of 0.01% BSA
ChEMBL 559 10 2 8 5.2 CCCCc1nc2ccn(Cc3ccccc3C(=O)O)c(=O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00037a014
CHEMBL289448 99856 0 None - 0 Rat 8.5 pIC50 = 8.5 Binding
Binding affinity against AT1 receptor in the presence of 0.01% BSABinding affinity against AT1 receptor in the presence of 0.01% BSA
ChEMBL 559 10 2 8 5.2 CCCCc1nc2ccn(Cc3ccccc3C(=O)O)c(=O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00037a014
10005512 165601 0 None - 0 Rat 8.5 pIC50 = 8.5 Binding
Binding affinity against AT1 receptor in the presence of 0.01% BSABinding affinity against AT1 receptor in the presence of 0.01% BSA
ChEMBL 483 9 2 8 3.5 CCCCc1nc2ccn(CC(=O)O)c(=O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00037a014
CHEMBL42631 165601 0 None - 0 Rat 8.5 pIC50 = 8.5 Binding
Binding affinity against AT1 receptor in the presence of 0.01% BSABinding affinity against AT1 receptor in the presence of 0.01% BSA
ChEMBL 483 9 2 8 3.5 CCCCc1nc2ccn(CC(=O)O)c(=O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00037a014
44311775 102527 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 582 11 1 7 7.3 CCCc1nc(CC)c(C(=O)OCc2ccc(-c3ccccc3)cc2)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80077-3
CHEMBL306923 102527 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 582 11 1 7 7.3 CCCc1nc(CC)c(C(=O)OCc2ccc(-c3ccccc3)cc2)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80077-3
44311776 102528 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 582 11 1 7 7.3 CCCc1nc(CC)c(C(=O)OCc2ccccc2-c2ccccc2)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80077-3
CHEMBL306924 102528 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 582 11 1 7 7.3 CCCc1nc(CC)c(C(=O)OCc2ccccc2-c2ccccc2)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80077-3
44311755 102646 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 735 18 1 9 8.5 CCCc1nc(CC)c(C(=O)OCc2ccccc2OCCC(C)C)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/S0960-894X(00)80077-3
CHEMBL307866 102646 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 735 18 1 9 8.5 CCCc1nc(CC)c(C(=O)OCc2ccccc2OCCC(C)C)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/S0960-894X(00)80077-3
44311436 202478 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 725 15 1 8 8.7 CCCc1nc(CC)c(C(=O)OCc2ccccc2-c2ccccc2)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/S0960-894X(00)80077-3
CHEMBL70793 202478 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 725 15 1 8 8.7 CCCc1nc(CC)c(C(=O)OCc2ccccc2-c2ccccc2)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/S0960-894X(00)80077-3
10408794 76270 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Displacement of 125[I-Sar1-Ile8]ANG II from human AT1 receptor expressed in HEK293 membranes after 1 hr by gamma countingDisplacement of 125[I-Sar1-Ile8]ANG II from human AT1 receptor expressed in HEK293 membranes after 1 hr by gamma counting
ChEMBL 402 8 2 6 3.8 CCCCc1cnc(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.ejmech.2012.07.040
CHEMBL2063984 76270 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Displacement of 125[I-Sar1-Ile8]ANG II from human AT1 receptor expressed in HEK293 membranes after 1 hr by gamma countingDisplacement of 125[I-Sar1-Ile8]ANG II from human AT1 receptor expressed in HEK293 membranes after 1 hr by gamma counting
ChEMBL 402 8 2 6 3.8 CCCCc1cnc(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.ejmech.2012.07.040
44285178 99932 0 None - 0 Rat 8.5 pIC50 = 8.5 Binding
Displacement of [125I]- Ang II from type 1 Angiotensin II receptorDisplacement of [125I]- Ang II from type 1 Angiotensin II receptor
ChEMBL 386 6 1 5 3.6 CCCC1=NC2(CC2)C(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80526-6
CHEMBL290180 99932 0 None - 0 Rat 8.5 pIC50 = 8.5 Binding
Displacement of [125I]- Ang II from type 1 Angiotensin II receptorDisplacement of [125I]- Ang II from type 1 Angiotensin II receptor
ChEMBL 386 6 1 5 3.6 CCCC1=NC2(CC2)C(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80526-6
11502835 99971 0 None - 0 Rat 8.5 pIC50 = 8.5 Binding
Displacement of [125I]- Ang II from type 1 Angiotensin II receptorDisplacement of [125I]- Ang II from type 1 Angiotensin II receptor
ChEMBL 428 6 1 5 4.8 CCCC1=NC2(CCCCC2)C(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80526-6
CHEMBL290614 99971 0 None - 0 Rat 8.5 pIC50 = 8.5 Binding
Displacement of [125I]- Ang II from type 1 Angiotensin II receptorDisplacement of [125I]- Ang II from type 1 Angiotensin II receptor
ChEMBL 428 6 1 5 4.8 CCCC1=NC2(CCCCC2)C(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80526-6
44210864 147561 0 None - 0 Rat 8.5 pIC50 = 8.5 Binding
Displacement of [125I]- Ang II from type 1 Angiotensin II receptorDisplacement of [125I]- Ang II from type 1 Angiotensin II receptor
ChEMBL 503 8 1 5 4.8 CCCC1=NC(C)(C)C(=O)N1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/S0960-894X(01)80526-6
CHEMBL39352 147561 0 None - 0 Rat 8.5 pIC50 = 8.5 Binding
Displacement of [125I]- Ang II from type 1 Angiotensin II receptorDisplacement of [125I]- Ang II from type 1 Angiotensin II receptor
ChEMBL 503 8 1 5 4.8 CCCC1=NC(C)(C)C(=O)N1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/S0960-894X(01)80526-6
11756787 118981 0 None - 0 Rabbit 8.5 pIC50 = 8.5 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 530 12 2 7 5.9 CCCCc1nnc(SCc2ccc(OC)cc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
CHEMBL345459 118981 0 None - 0 Rabbit 8.5 pIC50 = 8.5 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 530 12 2 7 5.9 CCCCc1nnc(SCc2ccc(OC)cc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
73346386 92170 0 None - 1 Human 8.5 pIC50 = 8.5 Binding
Displacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysisDisplacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysis
ChEMBL 531 10 2 4 6.7 CCCc1nc2c(C)cc(C(=O)NCCc3ccccc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2013.08.014
CHEMBL2435818 92170 0 None - 1 Human 8.5 pIC50 = 8.5 Binding
Displacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysisDisplacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysis
ChEMBL 531 10 2 4 6.7 CCCc1nc2c(C)cc(C(=O)NCCc3ccccc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2013.08.014
44311739 102121 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
In vitro binding affinity of compound against Angiotensin II receptor, type 1In vitro binding affinity of compound against Angiotensin II receptor, type 1
ChEMBL 563 14 2 7 6.2 CCCCN(Cc1ccccc1)Cc1nc(CCC)n(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c1C(=O)O 10.1016/S0960-894X(00)80076-1
CHEMBL304137 102121 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
In vitro binding affinity of compound against Angiotensin II receptor, type 1In vitro binding affinity of compound against Angiotensin II receptor, type 1
ChEMBL 563 14 2 7 6.2 CCCCN(Cc1ccccc1)Cc1nc(CCC)n(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c1C(=O)O 10.1016/S0960-894X(00)80076-1
44311498 102444 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
In vitro binding affinity of compound against Angiotensin II receptor, type 1In vitro binding affinity of compound against Angiotensin II receptor, type 1
ChEMBL 580 10 2 8 4.9 CCCc1nc(CN2CCN(c3ccc(F)cc3)CC2)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80076-1
CHEMBL306216 102444 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
In vitro binding affinity of compound against Angiotensin II receptor, type 1In vitro binding affinity of compound against Angiotensin II receptor, type 1
ChEMBL 580 10 2 8 4.9 CCCc1nc(CN2CCN(c3ccc(F)cc3)CC2)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80076-1
44379182 57799 0 None - 0 Rabbit 8.5 pIC50 = 8.5 Binding
In vitro displacement of 125I-[Sar1, Ile8] from AT1 receptors in rabbit aorta membraneIn vitro displacement of 125I-[Sar1, Ile8] from AT1 receptors in rabbit aorta membrane
ChEMBL 593 10 1 6 6.7 CCCCc1nc2ccc(C(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/S0960-894X(01)81125-2
CHEMBL167662 57799 0 None - 0 Rabbit 8.5 pIC50 = 8.5 Binding
In vitro displacement of 125I-[Sar1, Ile8] from AT1 receptors in rabbit aorta membraneIn vitro displacement of 125I-[Sar1, Ile8] from AT1 receptors in rabbit aorta membrane
ChEMBL 593 10 1 6 6.7 CCCCc1nc2ccc(C(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/S0960-894X(01)81125-2
10233073 205889 0 None - 0 Rabbit 8.5 pIC50 = 8.5 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 638 10 1 8 6.1 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccoc2C)cc1 10.1021/jm00043a020
CHEMBL95198 205889 0 None - 0 Rabbit 8.5 pIC50 = 8.5 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 638 10 1 8 6.1 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccoc2C)cc1 10.1021/jm00043a020
2583 3705 115 None - 1 Human 8.5 pIC50 = 8.5 Binding
Inhibition of AT1 receptorInhibition of AT1 receptor
ChEMBL 514 7 1 5 7.3 CCCc1nc2c(n1Cc1ccc(cc1)c1ccccc1C(=O)O)cc(cc2C)c1nc2c(n1C)cccc2 10.1016/j.bmcl.2009.12.107
592 3705 115 None - 1 Human 8.5 pIC50 = 8.5 Binding
Inhibition of AT1 receptorInhibition of AT1 receptor
ChEMBL 514 7 1 5 7.3 CCCc1nc2c(n1Cc1ccc(cc1)c1ccccc1C(=O)O)cc(cc2C)c1nc2c(n1C)cccc2 10.1016/j.bmcl.2009.12.107
65999 3705 115 None - 1 Human 8.5 pIC50 = 8.5 Binding
Inhibition of AT1 receptorInhibition of AT1 receptor
ChEMBL 514 7 1 5 7.3 CCCc1nc2c(n1Cc1ccc(cc1)c1ccccc1C(=O)O)cc(cc2C)c1nc2c(n1C)cccc2 10.1016/j.bmcl.2009.12.107
CHEMBL1017 3705 115 None - 1 Human 8.5 pIC50 = 8.5 Binding
Inhibition of AT1 receptorInhibition of AT1 receptor
ChEMBL 514 7 1 5 7.3 CCCc1nc2c(n1Cc1ccc(cc1)c1ccccc1C(=O)O)cc(cc2C)c1nc2c(n1C)cccc2 10.1016/j.bmcl.2009.12.107
DB00966 3705 115 None - 1 Human 8.5 pIC50 = 8.5 Binding
Inhibition of AT1 receptorInhibition of AT1 receptor
ChEMBL 514 7 1 5 7.3 CCCc1nc2c(n1Cc1ccc(cc1)c1ccccc1C(=O)O)cc(cc2C)c1nc2c(n1C)cccc2 10.1016/j.bmcl.2009.12.107
2583 3705 115 None - 1 Rat 8.5 pIC50 = 8.5 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 514 7 1 5 7.3 CCCc1nc2c(n1Cc1ccc(cc1)c1ccccc1C(=O)O)cc(cc2C)c1nc2c(n1C)cccc2 10.1021/jm00077a007
592 3705 115 None - 1 Rat 8.5 pIC50 = 8.5 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 514 7 1 5 7.3 CCCc1nc2c(n1Cc1ccc(cc1)c1ccccc1C(=O)O)cc(cc2C)c1nc2c(n1C)cccc2 10.1021/jm00077a007
65999 3705 115 None - 1 Rat 8.5 pIC50 = 8.5 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 514 7 1 5 7.3 CCCc1nc2c(n1Cc1ccc(cc1)c1ccccc1C(=O)O)cc(cc2C)c1nc2c(n1C)cccc2 10.1021/jm00077a007
CHEMBL1017 3705 115 None - 1 Rat 8.5 pIC50 = 8.5 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 514 7 1 5 7.3 CCCc1nc2c(n1Cc1ccc(cc1)c1ccccc1C(=O)O)cc(cc2C)c1nc2c(n1C)cccc2 10.1021/jm00077a007
DB00966 3705 115 None - 1 Rat 8.5 pIC50 = 8.5 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 514 7 1 5 7.3 CCCc1nc2c(n1Cc1ccc(cc1)c1ccccc1C(=O)O)cc(cc2C)c1nc2c(n1C)cccc2 10.1021/jm00077a007
10370090 19492 0 None - 0 Rat 8.5 pIC50 = 8.5 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 541 8 1 7 5.2 CCCCc1nc2ccc(N3CCCCS3(=O)=O)cc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00077a007
CHEMBL130095 19492 0 None - 0 Rat 8.5 pIC50 = 8.5 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 541 8 1 7 5.2 CCCCc1nc2ccc(N3CCCCS3(=O)=O)cc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00077a007
10051708 20505 0 None - 0 Rat 8.5 pIC50 = 8.5 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 500 7 1 5 7.0 CCCc1nc2ccc(-c3nc4ccccc4n3C)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00077a007
CHEMBL130910 20505 0 None - 0 Rat 8.5 pIC50 = 8.5 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 500 7 1 5 7.0 CCCc1nc2ccc(-c3nc4ccccc4n3C)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00077a007
10052528 165172 0 None - 0 Rat 8.5 pIC50 = 8.5 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 524 7 1 7 6.5 CCCc1nc2c(C)cc(-c3cn4ccccc4n3)cc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00077a007
CHEMBL424629 165172 0 None - 0 Rat 8.5 pIC50 = 8.5 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 524 7 1 7 6.5 CCCc1nc2c(C)cc(-c3cn4ccccc4n3)cc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00077a007
10140613 105603 0 None - 0 Rat 8.5 pIC50 = 8.5 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 479 10 1 7 4.5 CCCCc1nn(CCc2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a015
CHEMBL313371 105603 0 None - 0 Rat 8.5 pIC50 = 8.5 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 479 10 1 7 4.5 CCCCc1nn(CCc2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a015
14956761 105478 0 None - 0 Rabbit 8.5 pIC50 = 8.5 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 494 9 1 8 4.3 CCCCc1nn(-c2ccccc2N(C)C)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
CHEMBL313025 105478 0 None - 0 Rabbit 8.5 pIC50 = 8.5 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 494 9 1 8 4.3 CCCCc1nn(-c2ccccc2N(C)C)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
14956778 204560 0 None - 0 Rabbit 8.5 pIC50 = 8.5 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 431 9 1 7 3.9 CCCCc1nn(CC(C)C)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
CHEMBL87057 204560 0 None - 0 Rabbit 8.5 pIC50 = 8.5 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 431 9 1 7 3.9 CCCCc1nn(CC(C)C)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
44277936 100826 0 None - 0 Rabbit 8.5 pIC50 = 8.5 Binding
Binding affinity against AT1 receptor in rabbit aortaBinding affinity against AT1 receptor in rabbit aorta
ChEMBL 573 10 0 9 5.7 CCCCCN(C(=O)c1ccco1)c1ccc2ncn(Cc3ccc(-c4ccccc4-c4nnnn4C)cc3)c(=O)c2c1 10.1016/0960-894X(95)00224-H
CHEMBL29658 100826 0 None - 0 Rabbit 8.5 pIC50 = 8.5 Binding
Binding affinity against AT1 receptor in rabbit aortaBinding affinity against AT1 receptor in rabbit aorta
ChEMBL 573 10 0 9 5.7 CCCCCN(C(=O)c1ccco1)c1ccc2ncn(Cc3ccc(-c4ccccc4-c4nnnn4C)cc3)c(=O)c2c1 10.1016/0960-894X(95)00224-H
9806554 164905 0 None - 0 Rat 8.5 pIC50 = 8.5 Binding
Binding affinity against AT1 receptor in the presence of 0.01% BSABinding affinity against AT1 receptor in the presence of 0.01% BSA
ChEMBL 515 9 1 7 5.5 CCCCc1nc2ccn(Cc3ccccc3)c(=O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00037a014
CHEMBL42397 164905 0 None - 0 Rat 8.5 pIC50 = 8.5 Binding
Binding affinity against AT1 receptor in the presence of 0.01% BSABinding affinity against AT1 receptor in the presence of 0.01% BSA
ChEMBL 515 9 1 7 5.5 CCCCc1nc2ccn(Cc3ccccc3)c(=O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00037a014
1610 2305 89 None 1 4 Human 8.5 pIC50 = 8.5 Binding
Displacement of [125I-Sar1-Ile8]Ang2 from human AT1 receptor expressed in HEK293 cell membrane incubated for 1 hr by gamma counting methodDisplacement of [125I-Sar1-Ile8]Ang2 from human AT1 receptor expressed in HEK293 cell membrane incubated for 1 hr by gamma counting method
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmc.2016.07.047
3941 2305 89 None 1 4 Human 8.5 pIC50 = 8.5 Binding
Displacement of [125I-Sar1-Ile8]Ang2 from human AT1 receptor expressed in HEK293 cell membrane incubated for 1 hr by gamma counting methodDisplacement of [125I-Sar1-Ile8]Ang2 from human AT1 receptor expressed in HEK293 cell membrane incubated for 1 hr by gamma counting method
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmc.2016.07.047
3961 2305 89 None 1 4 Human 8.5 pIC50 = 8.5 Binding
Displacement of [125I-Sar1-Ile8]Ang2 from human AT1 receptor expressed in HEK293 cell membrane incubated for 1 hr by gamma counting methodDisplacement of [125I-Sar1-Ile8]Ang2 from human AT1 receptor expressed in HEK293 cell membrane incubated for 1 hr by gamma counting method
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmc.2016.07.047
590 2305 89 None 1 4 Human 8.5 pIC50 = 8.5 Binding
Displacement of [125I-Sar1-Ile8]Ang2 from human AT1 receptor expressed in HEK293 cell membrane incubated for 1 hr by gamma counting methodDisplacement of [125I-Sar1-Ile8]Ang2 from human AT1 receptor expressed in HEK293 cell membrane incubated for 1 hr by gamma counting method
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmc.2016.07.047
CHEMBL191 2305 89 None 1 4 Human 8.5 pIC50 = 8.5 Binding
Displacement of [125I-Sar1-Ile8]Ang2 from human AT1 receptor expressed in HEK293 cell membrane incubated for 1 hr by gamma counting methodDisplacement of [125I-Sar1-Ile8]Ang2 from human AT1 receptor expressed in HEK293 cell membrane incubated for 1 hr by gamma counting method
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmc.2016.07.047
DB00678 2305 89 None 1 4 Human 8.5 pIC50 = 8.5 Binding
Displacement of [125I-Sar1-Ile8]Ang2 from human AT1 receptor expressed in HEK293 cell membrane incubated for 1 hr by gamma counting methodDisplacement of [125I-Sar1-Ile8]Ang2 from human AT1 receptor expressed in HEK293 cell membrane incubated for 1 hr by gamma counting method
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmc.2016.07.047
10053126 118994 0 None - 0 Rabbit 8.5 pIC50 = 8.5 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 544 12 3 7 5.6 CCCCc1nnc(SCc2ccccc2C(=O)O)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
CHEMBL345570 118994 0 None - 0 Rabbit 8.5 pIC50 = 8.5 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 544 12 3 7 5.6 CCCCc1nnc(SCc2ccccc2C(=O)O)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
76330043 84820 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 527 11 2 6 3.8 CCCCc1ncc(/C=C2/C(=O)NC(=O)N2CCCC)n1Cc1ccc(S(=O)(=O)NC(F)(F)F)cc1 10.1007/s00044-009-9205-9
CHEMBL2259778 84820 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 527 11 2 6 3.8 CCCCc1ncc(/C=C2/C(=O)NC(=O)N2CCCC)n1Cc1ccc(S(=O)(=O)NC(F)(F)F)cc1 10.1007/s00044-009-9205-9
10007312 112773 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 534 12 0 6 6.0 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2CC2CCCCC2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
CHEMBL331519 112773 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 534 12 0 6 6.0 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2CC2CCCCC2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
10482937 166573 0 None - 0 Rabbit 8.5 pIC50 = 8.5 Binding
Displacement of 125I[Sar,Ile] from rabbit aorta membrane Angiotensin II receptor type 1Displacement of 125I[Sar,Ile] from rabbit aorta membrane Angiotensin II receptor type 1
ChEMBL 560 10 1 7 5.3 CCCCc1nn(CC(C)(C)C)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/S0960-894X(01)81132-X
CHEMBL321086 166573 0 None - 0 Rabbit 8.5 pIC50 = 8.5 Binding
Displacement of 125I[Sar,Ile] from rabbit aorta membrane Angiotensin II receptor type 1Displacement of 125I[Sar,Ile] from rabbit aorta membrane Angiotensin II receptor type 1
ChEMBL 560 10 1 7 5.3 CCCCc1nn(CC(C)(C)C)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/S0960-894X(01)81132-X
CHEMBL429058 166573 0 None - 0 Rabbit 8.5 pIC50 = 8.5 Binding
Displacement of 125I[Sar,Ile] from rabbit aorta membrane Angiotensin II receptor type 1Displacement of 125I[Sar,Ile] from rabbit aorta membrane Angiotensin II receptor type 1
ChEMBL 560 10 1 7 5.3 CCCCc1nn(CC(C)(C)C)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/S0960-894X(01)81132-X
10053126 118994 0 None - 0 Rabbit 8.5 pIC50 = 8.5 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 544 12 3 7 5.6 CCCCc1nnc(SCc2ccccc2C(=O)O)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
CHEMBL345570 118994 0 None - 0 Rabbit 8.5 pIC50 = 8.5 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 544 12 3 7 5.6 CCCCc1nnc(SCc2ccccc2C(=O)O)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
19422633 179032 0 None - 0 Rat 8.5 pIC50 = 8.5 Binding
In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.
ChEMBL 432 8 1 3 5.9 CCCCC1=NC(C)(C2CCCC2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/S0960-894X(01)81140-9
CHEMBL47428 179032 0 None - 0 Rat 8.5 pIC50 = 8.5 Binding
In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.
ChEMBL 432 8 1 3 5.9 CCCCC1=NC(C)(C2CCCC2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/S0960-894X(01)81140-9
44309700 102697 0 None - 0 Rabbit 8.5 pIC50 = 8.5 Binding
In vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranesIn vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranes
ChEMBL 651 13 2 7 7.2 CCCC(=O)Nc1cnc2c(nc(CCC)n2Cc2ccc(-c3ccccc3S(=O)(=O)NC(=O)c3ccc(CCC)cc3)cc2)c1C 10.1016/S0960-894X(01)81115-X
CHEMBL308237 102697 0 None - 0 Rabbit 8.5 pIC50 = 8.5 Binding
In vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranesIn vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranes
ChEMBL 651 13 2 7 7.2 CCCC(=O)Nc1cnc2c(nc(CCC)n2Cc2ccc(-c3ccccc3S(=O)(=O)NC(=O)c3ccc(CCC)cc3)cc2)c1C 10.1016/S0960-894X(01)81115-X
10078452 106781 0 None - 0 Rabbit 8.5 pIC50 = 8.5 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 702 10 1 7 7.2 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2cccc(C(F)(F)F)c2)cc1 10.1021/jm00043a020
CHEMBL317061 106781 0 None - 0 Rabbit 8.5 pIC50 = 8.5 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 702 10 1 7 7.2 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2cccc(C(F)(F)F)c2)cc1 10.1021/jm00043a020
10482937 166573 0 None - 0 Rabbit 8.5 pIC50 = 8.5 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 560 10 1 7 5.3 CCCCc1nn(CC(C)(C)C)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1021/jm00043a020
CHEMBL321086 166573 0 None - 0 Rabbit 8.5 pIC50 = 8.5 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 560 10 1 7 5.3 CCCCc1nn(CC(C)(C)C)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1021/jm00043a020
CHEMBL429058 166573 0 None - 0 Rabbit 8.5 pIC50 = 8.5 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 560 10 1 7 5.3 CCCCc1nn(CC(C)(C)C)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1021/jm00043a020
10439275 167486 0 None - 0 Rabbit 8.5 pIC50 = 8.5 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 654 10 1 7 6.6 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)C2C(C)(C)C2(C)C)cc1 10.1021/jm00043a020
CHEMBL432392 167486 0 None - 0 Rabbit 8.5 pIC50 = 8.5 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 654 10 1 7 6.6 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)C2C(C)(C)C2(C)C)cc1 10.1021/jm00043a020
11765177 116494 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 685 11 2 9 6.4 CCCCC(=O)Nc1ccc(Cl)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1021/jm00019a004
CHEMBL338888 116494 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 685 11 2 9 6.4 CCCCC(=O)Nc1ccc(Cl)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1021/jm00019a004
44305634 101892 0 None - 0 Rat 8.5 pIC50 = 8.5 Binding
Tested for binding affinity against angiotensin II receptor in rat adrenal cortexTested for binding affinity against angiotensin II receptor in rat adrenal cortex
ChEMBL 428 8 1 7 3.0 C=CCn1c(=O)cc(CCC)n(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c1=O 10.1016/0960-894X(95)00370-9
CHEMBL303822 101892 0 None - 0 Rat 8.5 pIC50 = 8.5 Binding
Tested for binding affinity against angiotensin II receptor in rat adrenal cortexTested for binding affinity against angiotensin II receptor in rat adrenal cortex
ChEMBL 428 8 1 7 3.0 C=CCn1c(=O)cc(CCC)n(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c1=O 10.1016/0960-894X(95)00370-9
15231091 93541 0 None - 0 Rabbit 8.5 pIC50 = 8.5 Binding
Ability to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitroAbility to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitro
ChEMBL 565 10 1 8 5.9 CCCCc1nc2ccc(N(C)C(=O)OCC(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80335-2
CHEMBL24861 93541 0 None - 0 Rabbit 8.5 pIC50 = 8.5 Binding
Ability to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitroAbility to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitro
ChEMBL 565 10 1 8 5.9 CCCCc1nc2ccc(N(C)C(=O)OCC(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80335-2
10027175 15348 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 458 9 2 5 4.1 CCCCc1ncc(/C=C2\C(=O)NC(=O)N2Cc2ccccc2)n1Cc1ccc(C(=O)O)cc1 10.1007/s00044-009-9205-9
CHEMBL121874 15348 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 458 9 2 5 4.1 CCCCc1ncc(/C=C2\C(=O)NC(=O)N2Cc2ccccc2)n1Cc1ccc(C(=O)O)cc1 10.1007/s00044-009-9205-9
10075811 112771 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 534 12 0 7 5.7 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2Cc2cccs2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
CHEMBL331511 112771 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 534 12 0 7 5.7 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2Cc2cccs2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
44277439 99973 0 None - 0 Rabbit 8.5 pIC50 = 8.5 Binding
Binding affinity against AT1 receptor in rabbit aortaBinding affinity against AT1 receptor in rabbit aorta
ChEMBL 604 8 0 9 5.5 Cn1nnnc1-c1ccccc1-c1ccc(Cn2cnc3ccc(N(Cc4ccccc4)C(=O)c4ccncc4)cc3c2=O)cc1 10.1016/0960-894X(95)00224-H
CHEMBL29063 99973 0 None - 0 Rabbit 8.5 pIC50 = 8.5 Binding
Binding affinity against AT1 receptor in rabbit aortaBinding affinity against AT1 receptor in rabbit aorta
ChEMBL 604 8 0 9 5.5 Cn1nnnc1-c1ccccc1-c1ccc(Cn2cnc3ccc(N(Cc4ccccc4)C(=O)c4ccncc4)cc3c2=O)cc1 10.1016/0960-894X(95)00224-H
2806 3894 109 None - 1 Rat 8.5 pIC50 = 8.5 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
ChEMBL 435 10 2 5 4.2 CCCCC(=O)N([C@H](C(=O)O)C(C)C)Cc1ccc(cc1)c1ccccc1c1nnn[nH]1 10.1021/jm7011563
3937 3894 109 None - 1 Rat 8.5 pIC50 = 8.5 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
ChEMBL 435 10 2 5 4.2 CCCCC(=O)N([C@H](C(=O)O)C(C)C)Cc1ccc(cc1)c1ccccc1c1nnn[nH]1 10.1021/jm7011563
593 3894 109 None - 1 Rat 8.5 pIC50 = 8.5 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
ChEMBL 435 10 2 5 4.2 CCCCC(=O)N([C@H](C(=O)O)C(C)C)Cc1ccc(cc1)c1ccccc1c1nnn[nH]1 10.1021/jm7011563
60846 3894 109 None - 1 Rat 8.5 pIC50 = 8.5 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
ChEMBL 435 10 2 5 4.2 CCCCC(=O)N([C@H](C(=O)O)C(C)C)Cc1ccc(cc1)c1ccccc1c1nnn[nH]1 10.1021/jm7011563
CHEMBL1069 3894 109 None - 1 Rat 8.5 pIC50 = 8.5 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
ChEMBL 435 10 2 5 4.2 CCCCC(=O)N([C@H](C(=O)O)C(C)C)Cc1ccc(cc1)c1ccccc1c1nnn[nH]1 10.1021/jm7011563
DB00177 3894 109 None - 1 Rat 8.5 pIC50 = 8.5 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
ChEMBL 435 10 2 5 4.2 CCCCC(=O)N([C@H](C(=O)O)C(C)C)Cc1ccc(cc1)c1ccccc1c1nnn[nH]1 10.1021/jm7011563
10417321 15427 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 701 9 2 9 5.8 CCC(=O)Nc1ccc(Br)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1021/jm00019a004
CHEMBL122157 15427 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 701 9 2 9 5.8 CCC(=O)Nc1ccc(Br)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1021/jm00019a004
44305446 100270 0 None - 0 Rat 8.5 pIC50 = 8.5 Binding
Tested for binding affinity against angiotensin II receptor in rat adrenal cortexTested for binding affinity against angiotensin II receptor in rat adrenal cortex
ChEMBL 473 9 2 8 2.0 CCCc1cc(=O)n(CCNC(C)=O)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/0960-894X(95)00370-9
CHEMBL292781 100270 0 None - 0 Rat 8.5 pIC50 = 8.5 Binding
Tested for binding affinity against angiotensin II receptor in rat adrenal cortexTested for binding affinity against angiotensin II receptor in rat adrenal cortex
ChEMBL 473 9 2 8 2.0 CCCc1cc(=O)n(CCNC(C)=O)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/0960-894X(95)00370-9
15229605 47875 0 None - 0 Rabbit 8.5 pIC50 = 8.5 Binding
Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)
ChEMBL 463 7 1 5 5.8 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(OC(C(=O)O)c2ccccc2C)c(Cl)c1 10.1016/0960-894X(95)00185-V
CHEMBL15517 47875 0 None - 0 Rabbit 8.5 pIC50 = 8.5 Binding
Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)
ChEMBL 463 7 1 5 5.8 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(OC(C(=O)O)c2ccccc2C)c(Cl)c1 10.1016/0960-894X(95)00185-V
10408794 76270 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Displacement of 125[I-Sar1-Ile8]ANG II from human AT1 receptor expressed in HEK293 membranes after 1 hr by gamma countingDisplacement of 125[I-Sar1-Ile8]ANG II from human AT1 receptor expressed in HEK293 membranes after 1 hr by gamma counting
ChEMBL 402 8 2 6 3.8 CCCCc1cnc(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.ejmech.2012.07.040
CHEMBL2063984 76270 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Displacement of 125[I-Sar1-Ile8]ANG II from human AT1 receptor expressed in HEK293 membranes after 1 hr by gamma countingDisplacement of 125[I-Sar1-Ile8]ANG II from human AT1 receptor expressed in HEK293 membranes after 1 hr by gamma counting
ChEMBL 402 8 2 6 3.8 CCCCc1cnc(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.ejmech.2012.07.040
10343090 15344 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 438 10 1 6 3.8 CCCCc1ncc(/C=C2/C(=O)NC(=O)N2CCCC)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
CHEMBL121854 15344 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 438 10 1 6 3.8 CCCCc1ncc(/C=C2/C(=O)NC(=O)N2CCCC)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
127035246 135860 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 571 10 2 7 6.2 CCOc1nc2c(C)cc(C(=O)NC[C@H](C)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.ejmech.2015.09.010
CHEMBL3735290 135860 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 571 10 2 7 6.2 CCOc1nc2c(C)cc(C(=O)NC[C@H](C)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.ejmech.2015.09.010
53309404 63433 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation countingDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation counting
ChEMBL 491 6 1 6 6.4 Cc1cc(CC(C)C)nc2c1nc(C(C)C)n2[C@H]1CCc2cc(-c3ccccc3-c3nnn[nH]3)ccc21 10.1021/jm200409s
CHEMBL1801741 63433 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation countingDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation counting
ChEMBL 491 6 1 6 6.4 Cc1cc(CC(C)C)nc2c1nc(C(C)C)n2[C@H]1CCc2cc(-c3ccccc3-c3nnn[nH]3)ccc21 10.1021/jm200409s
9853391 116326 1 None - 0 Human 8.5 pIC50 = 8.5 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 729 11 2 9 6.6 CCCCC(=O)Nc1ccc(Br)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1021/jm00019a004
CHEMBL338027 116326 1 None - 0 Human 8.5 pIC50 = 8.5 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 729 11 2 9 6.6 CCCCC(=O)Nc1ccc(Br)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1021/jm00019a004
14956753 106574 0 None - 0 Rabbit 8.4 pIC50 = 8.4 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 527 9 1 7 5.9 CCCCc1nn(-c2ccccc2-c2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
CHEMBL315776 106574 0 None - 0 Rabbit 8.4 pIC50 = 8.4 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 527 9 1 7 5.9 CCCCc1nn(-c2ccccc2-c2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
10141821 99583 0 None - 1 Rat 8.4 pIC50 = 8.4 Binding
In vitro ability to displace the specific binding of [125I]-A II from receptors in rat liver membrane(type 1 receptor)In vitro ability to displace the specific binding of [125I]-A II from receptors in rat liver membrane(type 1 receptor)
ChEMBL 501 6 1 7 4.8 CCc1nn(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/c(=N/C(=O)c2ccccc2Cl)s1 10.1016/S0960-894X(96)00250-8
CHEMBL287116 99583 0 None - 1 Rat 8.4 pIC50 = 8.4 Binding
In vitro ability to displace the specific binding of [125I]-A II from receptors in rat liver membrane(type 1 receptor)In vitro ability to displace the specific binding of [125I]-A II from receptors in rat liver membrane(type 1 receptor)
ChEMBL 501 6 1 7 4.8 CCc1nn(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/c(=N/C(=O)c2ccccc2Cl)s1 10.1016/S0960-894X(96)00250-8
44379270 56547 0 None - 0 Rabbit 8.4 pIC50 = 8.4 Binding
In vitro displacement of 125I-[Sar1, Ile8] from AT1 receptors in rabbit aorta membraneIn vitro displacement of 125I-[Sar1, Ile8] from AT1 receptors in rabbit aorta membrane
ChEMBL 580 9 1 7 5.2 CCCc1nc2ccc(N(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/S0960-894X(01)81125-2
CHEMBL164395 56547 0 None - 0 Rabbit 8.4 pIC50 = 8.4 Binding
In vitro displacement of 125I-[Sar1, Ile8] from AT1 receptors in rabbit aorta membraneIn vitro displacement of 125I-[Sar1, Ile8] from AT1 receptors in rabbit aorta membrane
ChEMBL 580 9 1 7 5.2 CCCc1nc2ccc(N(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/S0960-894X(01)81125-2
23590373 102151 0 None - 0 Rat 8.4 pIC50 = 8.4 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 495 10 2 8 4.0 CCCCc1nn(CC(O)c2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a015
CHEMBL304329 102151 0 None - 0 Rat 8.4 pIC50 = 8.4 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 495 10 2 8 4.0 CCCCc1nn(CC(O)c2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a015
10078475 112818 0 None - 0 Rabbit 8.4 pIC50 = 8.4 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 705 9 2 9 6.6 CCc1nn(-c2cc(NC(=O)c3ccccc3)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1007/s00044-011-9815-x
CHEMBL331632 112818 0 None - 0 Rabbit 8.4 pIC50 = 8.4 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 705 9 2 9 6.6 CCc1nn(-c2cc(NC(=O)c3ccccc3)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1007/s00044-011-9815-x
46910493 75967 0 None - 1 Human 8.4 pIC50 = 8.4 Binding
Displacement of [125I]Sar1Ile8-Ang2 from angiotensin AT1 receptor after 180 mins by gamma countingDisplacement of [125I]Sar1Ile8-Ang2 from angiotensin AT1 receptor after 180 mins by gamma counting
ChEMBL 615 12 2 8 6.2 CCCc1nc2c(C)cc(C(=O)NCCc3ccc(OC)c(OC)c3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmc.2012.05.056
CHEMBL2058864 75967 0 None - 1 Human 8.4 pIC50 = 8.4 Binding
Displacement of [125I]Sar1Ile8-Ang2 from angiotensin AT1 receptor after 180 mins by gamma countingDisplacement of [125I]Sar1Ile8-Ang2 from angiotensin AT1 receptor after 180 mins by gamma counting
ChEMBL 615 12 2 8 6.2 CCCc1nc2c(C)cc(C(=O)NCCc3ccc(OC)c(OC)c3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmc.2012.05.056
10078475 112818 0 None - 0 Rabbit 8.4 pIC50 = 8.4 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 705 9 2 9 6.6 CCc1nn(-c2cc(NC(=O)c3ccccc3)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1021/jm00019a004
CHEMBL331632 112818 0 None - 0 Rabbit 8.4 pIC50 = 8.4 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 705 9 2 9 6.6 CCc1nn(-c2cc(NC(=O)c3ccccc3)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1021/jm00019a004
10078475 112818 0 None - 0 Rabbit 8.4 pIC50 = 8.4 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 705 9 2 9 6.6 CCc1nn(-c2cc(NC(=O)c3ccccc3)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1007/s00044-011-9815-x
CHEMBL331632 112818 0 None - 0 Rabbit 8.4 pIC50 = 8.4 Binding
Antagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptorAntagonist activity at Oryctolagus cuniculus (rabbit) aortic AT1 receptor
ChEMBL 705 9 2 9 6.6 CCc1nn(-c2cc(NC(=O)c3ccccc3)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OC(C)(C)C)cc1F 10.1007/s00044-011-9815-x
4673492 4061 5 None - 1 Guinea pig 8.4 pIC50 = 8.4 Binding
Binding affinity to angiotensin AT1 receptor in guinea pig adrenal cortex membranesBinding affinity to angiotensin AT1 receptor in guinea pig adrenal cortex membranes
ChEMBL 438 6 1 5 4.5 CCc1nc(CC)c2c(c1)N(Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)C(=O)CC2 10.1016/j.bmc.2010.10.043
8324 4061 5 None - 1 Guinea pig 8.4 pIC50 = 8.4 Binding
Binding affinity to angiotensin AT1 receptor in guinea pig adrenal cortex membranesBinding affinity to angiotensin AT1 receptor in guinea pig adrenal cortex membranes
ChEMBL 438 6 1 5 4.5 CCc1nc(CC)c2c(c1)N(Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)C(=O)CC2 10.1016/j.bmc.2010.10.043
CHEMBL159096 4061 5 None - 1 Guinea pig 8.4 pIC50 = 8.4 Binding
Binding affinity to angiotensin AT1 receptor in guinea pig adrenal cortex membranesBinding affinity to angiotensin AT1 receptor in guinea pig adrenal cortex membranes
ChEMBL 438 6 1 5 4.5 CCc1nc(CC)c2c(c1)N(Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)C(=O)CC2 10.1016/j.bmc.2010.10.043
19008869 204678 0 None - 0 Rabbit 8.4 pIC50 = 8.4 Binding
Displacement of the specific binding ligand [125I]Sar1,Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane.Displacement of the specific binding ligand [125I]Sar1,Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane.
ChEMBL 385 5 1 4 5.0 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/S0960-894X(01)81119-7
CHEMBL87842 204678 0 None - 0 Rabbit 8.4 pIC50 = 8.4 Binding
Displacement of the specific binding ligand [125I]Sar1,Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane.Displacement of the specific binding ligand [125I]Sar1,Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane.
ChEMBL 385 5 1 4 5.0 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/S0960-894X(01)81119-7
10349791 111078 0 None - 0 Rabbit 8.4 pIC50 = 8.4 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 702 10 1 7 7.2 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccc(C(F)(F)F)cc2)cc1 10.1021/jm00043a020
CHEMBL328176 111078 0 None - 0 Rabbit 8.4 pIC50 = 8.4 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 702 10 1 7 7.2 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccc(C(F)(F)F)cc2)cc1 10.1021/jm00043a020
44315060 102570 0 None - 0 Rabbit 8.4 pIC50 = 8.4 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membrane
ChEMBL 665 10 2 9 4.9 CCCCOC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CC)nc3ccc(NC(=O)N4CCOCC4)cc3c2=O)c(F)c1 10.1016/0960-894X(94)85036-4
CHEMBL307290 102570 0 None - 0 Rabbit 8.4 pIC50 = 8.4 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membrane
ChEMBL 665 10 2 9 4.9 CCCCOC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CC)nc3ccc(NC(=O)N4CCOCC4)cc3c2=O)c(F)c1 10.1016/0960-894X(94)85036-4
44338833 9074 0 None - 0 Rabbit 8.4 pIC50 = 8.4 Binding
Binding affinity against AT-1 receptor from rabbit aorta using [125I]-Sar1-Ile8-Ang II without BSABinding affinity against AT-1 receptor from rabbit aorta using [125I]-Sar1-Ile8-Ang II without BSA
ChEMBL 537 9 2 8 5.4 CCCc1nc2ccc(NC(=O)OCC(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00073a024
CHEMBL110265 9074 0 None - 0 Rabbit 8.4 pIC50 = 8.4 Binding
Binding affinity against AT-1 receptor from rabbit aorta using [125I]-Sar1-Ile8-Ang II without BSABinding affinity against AT-1 receptor from rabbit aorta using [125I]-Sar1-Ile8-Ang II without BSA
ChEMBL 537 9 2 8 5.4 CCCc1nc2ccc(NC(=O)OCC(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00073a024
44277593 98939 0 None - 0 Rabbit 8.4 pIC50 = 8.4 Binding
Binding affinity against AT1 receptor in rabbit aortaBinding affinity against AT1 receptor in rabbit aorta
ChEMBL 661 9 0 10 5.9 COC(=O)c1ccc(CN(C(=O)c2ccccc2)c2ccc3ncn(Cc4ccc(-c5ccccc5-c5nnnn5C)cc4)c(=O)c3c2)cc1 10.1016/0960-894X(95)00224-H
CHEMBL282778 98939 0 None - 0 Rabbit 8.4 pIC50 = 8.4 Binding
Binding affinity against AT1 receptor in rabbit aortaBinding affinity against AT1 receptor in rabbit aorta
ChEMBL 661 9 0 10 5.9 COC(=O)c1ccc(CN(C(=O)c2ccccc2)c2ccc3ncn(Cc4ccc(-c5ccccc5-c5nnnn5C)cc4)c(=O)c3c2)cc1 10.1016/0960-894X(95)00224-H
127029202 136791 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Displacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptorDisplacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptor
ChEMBL 598 11 3 7 5.8 CCCc1nc2c(C)cc(C(=O)NCCc3ccccc3)cc2n1Cc1ccc(-c2ccccc2C(=O)Nc2nnn[nH]2)cc1 10.1039/C5MD00169B
CHEMBL3752680 136791 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Displacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptorDisplacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptor
ChEMBL 598 11 3 7 5.8 CCCc1nc2c(C)cc(C(=O)NCCc3ccccc3)cc2n1Cc1ccc(-c2ccccc2C(=O)Nc2nnn[nH]2)cc1 10.1039/C5MD00169B
73357016 92177 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Displacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysisDisplacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysis
ChEMBL 503 8 2 4 7.0 CCCc1nc2c(C)cc(NC(=O)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2013.08.014
CHEMBL2435825 92177 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Displacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysisDisplacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysis
ChEMBL 503 8 2 4 7.0 CCCc1nc2c(C)cc(NC(=O)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2013.08.014
19939495 206080 0 None - 0 Rabbit 8.4 pIC50 = 8.4 Binding
In vitro ability to inhibit the binding of radioligand 125I[Sar1,IIe8]AII to AT1 receptor from rabbit aortaIn vitro ability to inhibit the binding of radioligand 125I[Sar1,IIe8]AII to AT1 receptor from rabbit aorta
ChEMBL 728 12 1 7 8.0 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2cc(CCC)ccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1F 10.1016/S0960-894X(01)80595-3
CHEMBL96314 206080 0 None - 0 Rabbit 8.4 pIC50 = 8.4 Binding
In vitro ability to inhibit the binding of radioligand 125I[Sar1,IIe8]AII to AT1 receptor from rabbit aortaIn vitro ability to inhibit the binding of radioligand 125I[Sar1,IIe8]AII to AT1 receptor from rabbit aorta
ChEMBL 728 12 1 7 8.0 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2cc(CCC)ccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1F 10.1016/S0960-894X(01)80595-3
10461595 206370 0 None - 0 Rabbit 8.4 pIC50 = 8.4 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 624 10 1 8 5.8 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccoc2)cc1 10.1021/jm00043a020
CHEMBL97964 206370 0 None - 0 Rabbit 8.4 pIC50 = 8.4 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 624 10 1 8 5.8 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccoc2)cc1 10.1021/jm00043a020
44211677 130079 0 None - 0 Rabbit 8.4 pIC50 = 8.4 Binding
Inhibition of [125I]-Sar1-Ile8-Ang II binding to Angiotensin II receptor type 1 from rabbit aortaInhibition of [125I]-Sar1-Ile8-Ang II binding to Angiotensin II receptor type 1 from rabbit aorta
ChEMBL 614 4 2 7 6.6 CCCc1ccc2c(c1)-c1ccc(cc1)Cn1c(CCC)nc3ccc(cc3c1=O)NCCCCCCCC(=O)NS2(=O)=O 10.1016/0960-894X(96)00116-3
CHEMBL368149 130079 0 None - 0 Rabbit 8.4 pIC50 = 8.4 Binding
Inhibition of [125I]-Sar1-Ile8-Ang II binding to Angiotensin II receptor type 1 from rabbit aortaInhibition of [125I]-Sar1-Ile8-Ang II binding to Angiotensin II receptor type 1 from rabbit aorta
ChEMBL 614 4 2 7 6.6 CCCc1ccc2c(c1)-c1ccc(cc1)Cn1c(CCC)nc3ccc(cc3c1=O)NCCCCCCCC(=O)NS2(=O)=O 10.1016/0960-894X(96)00116-3
11757471 50769 0 None - 0 Rabbit 7.5 pIC50 = 7.5 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 558 12 2 8 5.7 CCCCc1nnc(SCc2cccc(C(=O)OC)c2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
CHEMBL157878 50769 0 None - 0 Rabbit 7.5 pIC50 = 7.5 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 558 12 2 8 5.7 CCCCc1nnc(SCc2cccc(C(=O)OC)c2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
10414778 164721 0 None - 0 Rabbit 7.5 pIC50 = 7.5 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 534 11 2 6 6.6 CCCCc1nnc(SCc2ccccc2Cl)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
CHEMBL423233 164721 0 None - 0 Rabbit 7.5 pIC50 = 7.5 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 534 11 2 6 6.6 CCCCc1nnc(SCc2ccccc2Cl)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
44311609 102322 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 701 13 1 8 8.6 CCCc1nc(CC)c(C(=O)OCc2cccc(C(=O)N(c3ccccc3)c3ccccc3)c2)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80077-3
CHEMBL305369 102322 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 701 13 1 8 8.6 CCCc1nc(CC)c(C(=O)OCc2cccc(C(=O)N(c3ccccc3)c3ccccc3)c2)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80077-3
44311638 102439 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 613 18 1 8 6.7 CCCCN(CCCC)C(=O)CCCOC(=O)c1c(CC)nc(CCC)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80077-3
CHEMBL306186 102439 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 613 18 1 8 6.7 CCCCN(CCCC)C(=O)CCCOC(=O)c1c(CC)nc(CCC)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80077-3
132562 99209 3 None - 1 Guinea pig 7.5 pIC50 = 7.5 Binding
Binding affinity to angiotensin AT1 receptor in guinea pig adrenal cortex membranesBinding affinity to angiotensin AT1 receptor in guinea pig adrenal cortex membranes
ChEMBL 407 6 1 5 5.2 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2ccccc2n1 10.1016/j.bmc.2010.10.043
CHEMBL284536 99209 3 None - 1 Guinea pig 7.5 pIC50 = 7.5 Binding
Binding affinity to angiotensin AT1 receptor in guinea pig adrenal cortex membranesBinding affinity to angiotensin AT1 receptor in guinea pig adrenal cortex membranes
ChEMBL 407 6 1 5 5.2 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2ccccc2n1 10.1016/j.bmc.2010.10.043
10166561 9954 0 None - 1 Human 7.5 pIC50 = 7.5 Binding
Displacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysisDisplacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysis
ChEMBL 562 9 2 8 5.4 CCCc1nc2c(n1Cc1ccc(-c3ccccc3S(=O)(=O)Nc3onc(C)c3C)c(CO)c1)C(=O)CCCC2 10.1039/C4MD00499J
CHEMBL11528 9954 0 None - 1 Human 7.5 pIC50 = 7.5 Binding
Displacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysisDisplacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysis
ChEMBL 562 9 2 8 5.4 CCCc1nc2c(n1Cc1ccc(-c3ccccc3S(=O)(=O)Nc3onc(C)c3C)c(CO)c1)C(=O)CCCC2 10.1039/C4MD00499J
10475382 76265 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Displacement of 125[I-Sar1-Ile8]ANG II from human AT1 receptor expressed in HEK293 membranes after 1 hr by gamma countingDisplacement of 125[I-Sar1-Ile8]ANG II from human AT1 receptor expressed in HEK293 membranes after 1 hr by gamma counting
ChEMBL 388 8 2 6 3.6 CCCCc1cnc(CO)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.ejmech.2012.07.040
CHEMBL2063979 76265 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Displacement of 125[I-Sar1-Ile8]ANG II from human AT1 receptor expressed in HEK293 membranes after 1 hr by gamma countingDisplacement of 125[I-Sar1-Ile8]ANG II from human AT1 receptor expressed in HEK293 membranes after 1 hr by gamma counting
ChEMBL 388 8 2 6 3.6 CCCCc1cnc(CO)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.ejmech.2012.07.040
11757471 50769 0 None - 0 Rabbit 7.5 pIC50 = 7.5 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 558 12 2 8 5.7 CCCCc1nnc(SCc2cccc(C(=O)OC)c2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
CHEMBL157878 50769 0 None - 0 Rabbit 7.5 pIC50 = 7.5 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 558 12 2 8 5.7 CCCCc1nnc(SCc2cccc(C(=O)OC)c2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
10100625 51206 0 None - 0 Rabbit 7.5 pIC50 = 7.5 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 474 8 1 7 5.4 CCCCc1nn2cc(-c3ccccc3)nc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
CHEMBL158257 51206 0 None - 0 Rabbit 7.5 pIC50 = 7.5 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 474 8 1 7 5.4 CCCCc1nn2cc(-c3ccccc3)nc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
10414778 164721 0 None - 0 Rabbit 7.5 pIC50 = 7.5 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 534 11 2 6 6.6 CCCCc1nnc(SCc2ccccc2Cl)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
CHEMBL423233 164721 0 None - 0 Rabbit 7.5 pIC50 = 7.5 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 534 11 2 6 6.6 CCCCc1nnc(SCc2ccccc2Cl)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
44275076 93369 0 None - 0 Rabbit 7.5 pIC50 = 7.5 Binding
Displacement of [125I]Sar1-Ile8-AII (without BSA) from type 1 Angiotensin II receptor of rabbit aortaDisplacement of [125I]Sar1-Ile8-AII (without BSA) from type 1 Angiotensin II receptor of rabbit aorta
ChEMBL 546 8 1 6 7.0 CCCCc1nc2ccc(-c3ccc(Cl)cc3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80335-2
CHEMBL24764 93369 0 None - 0 Rabbit 7.5 pIC50 = 7.5 Binding
Displacement of [125I]Sar1-Ile8-AII (without BSA) from type 1 Angiotensin II receptor of rabbit aortaDisplacement of [125I]Sar1-Ile8-AII (without BSA) from type 1 Angiotensin II receptor of rabbit aorta
ChEMBL 546 8 1 6 7.0 CCCCc1nc2ccc(-c3ccc(Cl)cc3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80335-2
10765381 9467 0 None - 0 Bovine 7.5 pIC50 = 7.5 Binding
In vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortexIn vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortex
ChEMBL 436 9 3 5 4.6 CCCCc1nc(C(C)(C)O)c(C(=O)O)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm950450f
CHEMBL112414 9467 0 None - 0 Bovine 7.5 pIC50 = 7.5 Binding
In vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortexIn vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortex
ChEMBL 436 9 3 5 4.6 CCCCc1nc(C(C)(C)O)c(C(=O)O)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm950450f
1610 2305 89 None -1 4 Rabbit 7.5 pIC50 = 7.5 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00019a004
3941 2305 89 None -1 4 Rabbit 7.5 pIC50 = 7.5 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00019a004
3961 2305 89 None -1 4 Rabbit 7.5 pIC50 = 7.5 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00019a004
590 2305 89 None -1 4 Rabbit 7.5 pIC50 = 7.5 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00019a004
CHEMBL191 2305 89 None -1 4 Rabbit 7.5 pIC50 = 7.5 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00019a004
DB00678 2305 89 None -1 4 Rabbit 7.5 pIC50 = 7.5 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.In vitro inhibitory activity against Angiotensin II receptor, type 1 in rabbit aorta membrane preparations.
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00019a004
9896877 59901 0 None - 0 Rabbit 7.5 pIC50 = 7.5 Binding
Inhibition of [125I]-Sar1-Ile8-Ang II binding to Angiotensin II receptor type 1 from rabbit aortaInhibition of [125I]-Sar1-Ile8-Ang II binding to Angiotensin II receptor type 1 from rabbit aorta
ChEMBL 748 6 1 8 8.3 CCCc1ccc2c(c1)-c1ccc(cc1)Cn1c(CCC)nc3ccc(cc3c1=O)N(C(=O)OCc1ccccc1)CCCCCCCC(=O)NS2(=O)=O 10.1016/0960-894X(96)00116-3
CHEMBL174080 59901 0 None - 0 Rabbit 7.5 pIC50 = 7.5 Binding
Inhibition of [125I]-Sar1-Ile8-Ang II binding to Angiotensin II receptor type 1 from rabbit aortaInhibition of [125I]-Sar1-Ile8-Ang II binding to Angiotensin II receptor type 1 from rabbit aorta
ChEMBL 748 6 1 8 8.3 CCCc1ccc2c(c1)-c1ccc(cc1)Cn1c(CCC)nc3ccc(cc3c1=O)N(C(=O)OCc1ccccc1)CCCCCCCC(=O)NS2(=O)=O 10.1016/0960-894X(96)00116-3
14950497 85306 0 None - 0 Guinea pig 7.5 pIC50 = 7.5 Binding
Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1
ChEMBL 399 6 1 6 4.3 CC(=O)c1c(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)cc(C)nc1C 10.1021/jm00061a016
CHEMBL22908 85306 0 None - 0 Guinea pig 7.5 pIC50 = 7.5 Binding
Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1
ChEMBL 399 6 1 6 4.3 CC(=O)c1c(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)cc(C)nc1C 10.1021/jm00061a016
44308901 102627 0 None - 0 Rat 7.5 pIC50 = 7.5 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 555 13 4 10 3.2 CCCCc1nn(CC(OCC(=O)O)c2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2C2=NNNN2)cc1 10.1021/jm00067a015
CHEMBL307752 102627 0 None - 0 Rat 7.5 pIC50 = 7.5 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 555 13 4 10 3.2 CCCCc1nn(CC(OCC(=O)O)c2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2C2=NNNN2)cc1 10.1021/jm00067a015
21840324 10039 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Tested for inhibition of Angiotensin II receptor, type 1 in the absence of bovine serum albumin (BSA)Tested for inhibition of Angiotensin II receptor, type 1 in the absence of bovine serum albumin (BSA)
ChEMBL 501 11 2 5 4.9 CCCCC(=O)N(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)C(Cc1ccc(F)cc1)C(=O)O 10.1016/S0960-894X(01)81117-3
CHEMBL115783 10039 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Tested for inhibition of Angiotensin II receptor, type 1 in the absence of bovine serum albumin (BSA)Tested for inhibition of Angiotensin II receptor, type 1 in the absence of bovine serum albumin (BSA)
ChEMBL 501 11 2 5 4.9 CCCCC(=O)N(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)C(Cc1ccc(F)cc1)C(=O)O 10.1016/S0960-894X(01)81117-3
44270306 51883 0 None - 0 Rabbit 7.5 pIC50 = 7.5 Binding
Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)
ChEMBL 457 8 1 5 6.0 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(OC(C(=O)O)c2ccccc2)c(C(C)C)c1 10.1016/0960-894X(95)00185-V
CHEMBL15882 51883 0 None - 0 Rabbit 7.5 pIC50 = 7.5 Binding
Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)
ChEMBL 457 8 1 5 6.0 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(OC(C(=O)O)c2ccccc2)c(C(C)C)c1 10.1016/0960-894X(95)00185-V
10475382 76265 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Displacement of 125[I-Sar1-Ile8]ANG II from human AT1 receptor expressed in HEK293 membranes after 1 hr by gamma countingDisplacement of 125[I-Sar1-Ile8]ANG II from human AT1 receptor expressed in HEK293 membranes after 1 hr by gamma counting
ChEMBL 388 8 2 6 3.6 CCCCc1cnc(CO)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.ejmech.2012.07.040
CHEMBL2063979 76265 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Displacement of 125[I-Sar1-Ile8]ANG II from human AT1 receptor expressed in HEK293 membranes after 1 hr by gamma countingDisplacement of 125[I-Sar1-Ile8]ANG II from human AT1 receptor expressed in HEK293 membranes after 1 hr by gamma counting
ChEMBL 388 8 2 6 3.6 CCCCc1cnc(CO)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.ejmech.2012.07.040
57380415 69992 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Displacement of [125I]Sar1 Ile8-Ang 2 from angiotensin 2 AT1 receptor after 180 mins by gamma countingDisplacement of [125I]Sar1 Ile8-Ang 2 from angiotensin 2 AT1 receptor after 180 mins by gamma counting
ChEMBL 577 11 2 6 6.7 CCCc1nc2c(C)cc(C(=O)NCc3ccc(OC)c(OC)c3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2012.01.009
CHEMBL1945006 69992 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Displacement of [125I]Sar1 Ile8-Ang 2 from angiotensin 2 AT1 receptor after 180 mins by gamma countingDisplacement of [125I]Sar1 Ile8-Ang 2 from angiotensin 2 AT1 receptor after 180 mins by gamma counting
ChEMBL 577 11 2 6 6.7 CCCc1nc2c(C)cc(C(=O)NCc3ccc(OC)c(OC)c3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2012.01.009
127026336 136737 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Displacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptorDisplacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptor
ChEMBL 658 13 3 9 5.8 CCCc1nc2c(C)cc(C(=O)NCCc3cc(OC)ccc3OC)cc2n1Cc1ccc(-c2ccccc2C(=O)Nc2nnn[nH]2)cc1 10.1039/C5MD00169B
CHEMBL3752160 136737 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Displacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptorDisplacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptor
ChEMBL 658 13 3 9 5.8 CCCc1nc2c(C)cc(C(=O)NCCc3cc(OC)ccc3OC)cc2n1Cc1ccc(-c2ccccc2C(=O)Nc2nnn[nH]2)cc1 10.1039/C5MD00169B
57380416 69993 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Displacement of [125I]Sar1 Ile8-Ang 2 from angiotensin 2 AT1 receptor after 180 mins by gamma countingDisplacement of [125I]Sar1 Ile8-Ang 2 from angiotensin 2 AT1 receptor after 180 mins by gamma counting
ChEMBL 561 11 2 5 6.7 CCCc1nc2c(C)cc(C(=O)NCCc3cccc(OC)c3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2012.01.009
CHEMBL1945007 69993 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Displacement of [125I]Sar1 Ile8-Ang 2 from angiotensin 2 AT1 receptor after 180 mins by gamma countingDisplacement of [125I]Sar1 Ile8-Ang 2 from angiotensin 2 AT1 receptor after 180 mins by gamma counting
ChEMBL 561 11 2 5 6.7 CCCc1nc2c(C)cc(C(=O)NCCc3cccc(OC)c3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2012.01.009
10029332 46615 0 None - 0 Rabbit 6.5 pIC50 = 6.5 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 510 12 2 8 4.7 CCCCc1nnc(SC(CC)C(=O)OC)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
CHEMBL154083 46615 0 None - 0 Rabbit 6.5 pIC50 = 6.5 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 510 12 2 8 4.7 CCCCc1nnc(SC(CC)C(=O)OC)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
130762 97782 9 None - 0 Rat 6.5 pIC50 = 6.5 Binding
Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.
ChEMBL 398 8 2 4 4.8 CCCCc1nc(Cl)c(CO)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00064a007
CHEMBL274447 97782 9 None - 0 Rat 6.5 pIC50 = 6.5 Binding
Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.
ChEMBL 398 8 2 4 4.8 CCCCc1nc(Cl)c(CO)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00064a007
1610 2305 89 None - 4 Bovine 6.5 pIC50 = 6.5 Binding
Binding affinity for angiotensin II receptor of bovine adrenal cortexBinding affinity for angiotensin II receptor of bovine adrenal cortex
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(01)81144-6
3941 2305 89 None - 4 Bovine 6.5 pIC50 = 6.5 Binding
Binding affinity for angiotensin II receptor of bovine adrenal cortexBinding affinity for angiotensin II receptor of bovine adrenal cortex
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(01)81144-6
3961 2305 89 None - 4 Bovine 6.5 pIC50 = 6.5 Binding
Binding affinity for angiotensin II receptor of bovine adrenal cortexBinding affinity for angiotensin II receptor of bovine adrenal cortex
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(01)81144-6
590 2305 89 None - 4 Bovine 6.5 pIC50 = 6.5 Binding
Binding affinity for angiotensin II receptor of bovine adrenal cortexBinding affinity for angiotensin II receptor of bovine adrenal cortex
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(01)81144-6
CHEMBL191 2305 89 None - 4 Bovine 6.5 pIC50 = 6.5 Binding
Binding affinity for angiotensin II receptor of bovine adrenal cortexBinding affinity for angiotensin II receptor of bovine adrenal cortex
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(01)81144-6
DB00678 2305 89 None - 4 Bovine 6.5 pIC50 = 6.5 Binding
Binding affinity for angiotensin II receptor of bovine adrenal cortexBinding affinity for angiotensin II receptor of bovine adrenal cortex
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(01)81144-6
44285371 140153 0 None - 0 Rat 6.5 pIC50 = 6.5 Binding
Displacement of [125I]- Ang II from type 1 Angiotensin II receptorDisplacement of [125I]- Ang II from type 1 Angiotensin II receptor
ChEMBL 512 8 1 5 6.0 CCCC1=NC(c2ccccc2)(c2ccccc2)C(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80526-6
CHEMBL38161 140153 0 None - 0 Rat 6.5 pIC50 = 6.5 Binding
Displacement of [125I]- Ang II from type 1 Angiotensin II receptorDisplacement of [125I]- Ang II from type 1 Angiotensin II receptor
ChEMBL 512 8 1 5 6.0 CCCC1=NC(c2ccccc2)(c2ccccc2)C(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80526-6
10029332 46615 0 None - 0 Rabbit 6.5 pIC50 = 6.5 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 510 12 2 8 4.7 CCCCc1nnc(SC(CC)C(=O)OC)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
CHEMBL154083 46615 0 None - 0 Rabbit 6.5 pIC50 = 6.5 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 510 12 2 8 4.7 CCCCc1nnc(SC(CC)C(=O)OC)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
10343457 17934 0 None - 0 Rat 6.5 pIC50 = 6.5 Binding
Inhibition of [125I]angiotensin II receptor specific binding to rat mesenteric arteriesInhibition of [125I]angiotensin II receptor specific binding to rat mesenteric arteries
ChEMBL 444 10 1 5 5.7 CCCCc1ncc(/C=C(\Cc2cc(OC)cs2)C(=O)O)n1Cc1ccccc1Cl 10.1021/jm00099a013
CHEMBL126921 17934 0 None - 0 Rat 6.5 pIC50 = 6.5 Binding
Inhibition of [125I]angiotensin II receptor specific binding to rat mesenteric arteriesInhibition of [125I]angiotensin II receptor specific binding to rat mesenteric arteries
ChEMBL 444 10 1 5 5.7 CCCCc1ncc(/C=C(\Cc2cc(OC)cs2)C(=O)O)n1Cc1ccccc1Cl 10.1021/jm00099a013
14950495 98823 0 None - 0 Guinea pig 6.5 pIC50 = 6.5 Binding
Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1
ChEMBL 357 5 1 5 4.1 Cc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)cc(C)n1 10.1021/jm00061a016
CHEMBL281999 98823 0 None - 0 Guinea pig 6.5 pIC50 = 6.5 Binding
Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1
ChEMBL 357 5 1 5 4.1 Cc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)cc(C)n1 10.1021/jm00061a016
15654751 202228 0 None - 0 Bovine 6.5 pIC50 = 6.5 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 470 8 2 7 4.9 CCSCc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a016
CHEMBL69236 202228 0 None - 0 Bovine 6.5 pIC50 = 6.5 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 470 8 2 7 4.9 CCSCc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a016
5284633 10006 57 None - 0 Human 6.5 pIC50 = 6.5 Binding
Tested for inhibition of Angiotensin II receptor, type 1 in the absence of bovine serum albumin (BSA)Tested for inhibition of Angiotensin II receptor, type 1 in the absence of bovine serum albumin (BSA)
ChEMBL 435 10 2 5 4.2 CCCCC(=O)N(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)[C@@H](C(=O)O)C(C)C 10.1016/S0960-894X(01)81117-3
CHEMBL115622 10006 57 None - 0 Human 6.5 pIC50 = 6.5 Binding
Tested for inhibition of Angiotensin II receptor, type 1 in the absence of bovine serum albumin (BSA)Tested for inhibition of Angiotensin II receptor, type 1 in the absence of bovine serum albumin (BSA)
ChEMBL 435 10 2 5 4.2 CCCCC(=O)N(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)[C@@H](C(=O)O)C(C)C 10.1016/S0960-894X(01)81117-3
19422652 109992 0 None - 0 Rat 5.5 pIC50 = 5.5 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 502 9 1 3 6.9 CCCCC1=NC(c2ccccc2)(c2ccccc2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00074a018
CHEMBL324888 109992 0 None - 0 Rat 5.5 pIC50 = 5.5 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 502 9 1 3 6.9 CCCCC1=NC(c2ccccc2)(c2ccccc2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00074a018
15144944 167458 0 None - 0 Rat 5.5 pIC50 = 5.5 Binding
Inhibition of [125I]angiotensin II receptor specific binding to rat mesenteric arteriesInhibition of [125I]angiotensin II receptor specific binding to rat mesenteric arteries
ChEMBL 423 9 2 4 5.2 CCCCc1ncc(/C=C(\Cc2ccc(N)cc2)C(=O)O)n1Cc1ccccc1Cl 10.1021/jm00099a013
CHEMBL432222 167458 0 None - 0 Rat 5.5 pIC50 = 5.5 Binding
Inhibition of [125I]angiotensin II receptor specific binding to rat mesenteric arteriesInhibition of [125I]angiotensin II receptor specific binding to rat mesenteric arteries
ChEMBL 423 9 2 4 5.2 CCCCc1ncc(/C=C(\Cc2ccc(N)cc2)C(=O)O)n1Cc1ccccc1Cl 10.1021/jm00099a013
11764788 100378 0 None - 1 Rabbit 7.5 pIC50 = 7.5 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 645 11 1 9 5.8 CCCCc1nn(-c2cccc([N+](=O)[O-])c2)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1007/s00044-013-0831-x
CHEMBL293501 100378 0 None - 1 Rabbit 7.5 pIC50 = 7.5 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 645 11 1 9 5.8 CCCCc1nn(-c2cccc([N+](=O)[O-])c2)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1007/s00044-013-0831-x
10459992 113754 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 542 13 0 6 5.7 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2CCc2ccccc2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
CHEMBL333058 113754 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 542 13 0 6 5.7 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2CCc2ccccc2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
127034901 135942 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Displacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysisDisplacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysis
ChEMBL 670 12 2 9 5.5 CCCc1nc2c(C)cc(C(=O)NCCN3CCOCC3)cc2n1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)cc1 10.1039/C4MD00499J
CHEMBL3736037 135942 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Displacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysisDisplacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysis
ChEMBL 670 12 2 9 5.5 CCCc1nc2c(C)cc(C(=O)NCCN3CCOCC3)cc2n1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)cc1 10.1039/C4MD00499J
10029368 119327 0 None - 0 Rabbit 7.5 pIC50 = 7.5 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 511 11 1 8 5.8 CCCCc1nnc(SCc2ccc(OC)cc2)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
CHEMBL348606 119327 0 None - 0 Rabbit 7.5 pIC50 = 7.5 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 511 11 1 8 5.8 CCCCc1nnc(SCc2ccc(OC)cc2)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
6918269 98005 8 None - 2 Bovine 7.5 pIC50 = 7.5 Binding
In vitro binding affinity to angiotensin II receptor in bovine adrenal cortexIn vitro binding affinity to angiotensin II receptor in bovine adrenal cortex
ChEMBL 508 9 1 7 5.5 CCCCc1nc2ccc(C(C)(C)OC)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80377-2
CHEMBL275875 98005 8 None - 2 Bovine 7.5 pIC50 = 7.5 Binding
In vitro binding affinity to angiotensin II receptor in bovine adrenal cortexIn vitro binding affinity to angiotensin II receptor in bovine adrenal cortex
ChEMBL 508 9 1 7 5.5 CCCCc1nc2ccc(C(C)(C)OC)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80377-2
CHEMBL295959 98005 8 None - 2 Bovine 7.5 pIC50 = 7.5 Binding
In vitro binding affinity to angiotensin II receptor in bovine adrenal cortexIn vitro binding affinity to angiotensin II receptor in bovine adrenal cortex
ChEMBL 508 9 1 7 5.5 CCCCc1nc2ccc(C(C)(C)OC)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80377-2
132562 99209 3 None - 1 Guinea pig 7.5 pIC50 = 7.5 Binding
In vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparationIn vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparation
ChEMBL 407 6 1 5 5.2 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2ccccc2n1 10.1021/jm00100a007
CHEMBL284536 99209 3 None - 1 Guinea pig 7.5 pIC50 = 7.5 Binding
In vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparationIn vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparation
ChEMBL 407 6 1 5 5.2 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2ccccc2n1 10.1021/jm00100a007
132562 99209 3 None - 1 Guinea pig 7.5 pIC50 = 7.5 Binding
Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1
ChEMBL 407 6 1 5 5.2 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2ccccc2n1 10.1021/jm00061a016
CHEMBL284536 99209 3 None - 1 Guinea pig 7.5 pIC50 = 7.5 Binding
Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1
ChEMBL 407 6 1 5 5.2 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2ccccc2n1 10.1021/jm00061a016
9869504 206297 3 None - 0 Human 7.5 pIC50 = 7.5 Binding
Tested for Angiotensin II receptor, type 1 affinity in the presence of 0.25% BSATested for Angiotensin II receptor, type 1 affinity in the presence of 0.25% BSA
ChEMBL 474 10 2 5 5.9 CCCCc1ncc(/C=C(\Cc2cccs2)C(=O)O)n1Cc1ccc(C(=O)O)c2ccccc12 10.1016/S0960-894X(01)81116-1
CHEMBL97533 206297 3 None - 0 Human 7.5 pIC50 = 7.5 Binding
Tested for Angiotensin II receptor, type 1 affinity in the presence of 0.25% BSATested for Angiotensin II receptor, type 1 affinity in the presence of 0.25% BSA
ChEMBL 474 10 2 5 5.9 CCCCc1ncc(/C=C(\Cc2cccs2)C(=O)O)n1Cc1ccc(C(=O)O)c2ccccc12 10.1016/S0960-894X(01)81116-1
11764788 100378 0 None - 1 Rabbit 7.5 pIC50 = 7.5 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 645 11 1 9 5.8 CCCCc1nn(-c2cccc([N+](=O)[O-])c2)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1021/jm00052a006
CHEMBL293501 100378 0 None - 1 Rabbit 7.5 pIC50 = 7.5 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 645 11 1 9 5.8 CCCCc1nn(-c2cccc([N+](=O)[O-])c2)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1021/jm00052a006
76329880 84514 0 None - 0 Rabbit 6.5 pIC50 = 6.5 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 448 9 2 8 3.8 CCCCc1nnc(SC)n1Cc1ccc(NC(=O)c2ccccc2-c2nnn[nH]2)cc1 10.1007/s00044-011-9756-4
CHEMBL2237584 84514 0 None - 0 Rabbit 6.5 pIC50 = 6.5 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 448 9 2 8 3.8 CCCCc1nnc(SC)n1Cc1ccc(NC(=O)c2ccccc2-c2nnn[nH]2)cc1 10.1007/s00044-011-9756-4
44323091 204901 0 None - 0 Rat 6.5 pIC50 = 6.5 Binding
Concentration required to inhibit binding of radioligand [125I]AII to angiotensin II receptor, type 1 in rat adrenal glomerulosa tissueConcentration required to inhibit binding of radioligand [125I]AII to angiotensin II receptor, type 1 in rat adrenal glomerulosa tissue
ChEMBL 426 8 2 6 4.2 CCCCc1nc(Cl)c(C(=O)O)n1Cc1ccc(C2=C(c3nn[nH]n3)CCC2)cc1 10.1021/jm00092a017
CHEMBL89216 204901 0 None - 0 Rat 6.5 pIC50 = 6.5 Binding
Concentration required to inhibit binding of radioligand [125I]AII to angiotensin II receptor, type 1 in rat adrenal glomerulosa tissueConcentration required to inhibit binding of radioligand [125I]AII to angiotensin II receptor, type 1 in rat adrenal glomerulosa tissue
ChEMBL 426 8 2 6 4.2 CCCCc1nc(Cl)c(C(=O)O)n1Cc1ccc(C2=C(c3nn[nH]n3)CCC2)cc1 10.1021/jm00092a017
135464357 100079 0 None - 0 Bovine 6.5 pIC50 = 6.5 Binding
Displacement of [125 I]-AII (0.2 nM) from bovine adrenal cortical membrane angiotensin II (AII) receptor at 10e-7 MDisplacement of [125 I]-AII (0.2 nM) from bovine adrenal cortical membrane angiotensin II (AII) receptor at 10e-7 M
ChEMBL 440 6 2 7 4.8 CCc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2noc(O)n2)cc1 10.1016/0960-894X(95)00319-O
CHEMBL291502 100079 0 None - 0 Bovine 6.5 pIC50 = 6.5 Binding
Displacement of [125 I]-AII (0.2 nM) from bovine adrenal cortical membrane angiotensin II (AII) receptor at 10e-7 MDisplacement of [125 I]-AII (0.2 nM) from bovine adrenal cortical membrane angiotensin II (AII) receptor at 10e-7 M
ChEMBL 440 6 2 7 4.8 CCc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2noc(O)n2)cc1 10.1016/0960-894X(95)00319-O
10076683 50031 0 None - 0 Rabbit 6.5 pIC50 = 6.5 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 405 8 1 7 4.2 CCCCc1nnc(SC)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
CHEMBL157203 50031 0 None - 0 Rabbit 6.5 pIC50 = 6.5 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 405 8 1 7 4.2 CCCCc1nnc(SC)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
9980879 116221 0 None - 0 Guinea pig 6.5 pIC50 = 6.5 Binding
In vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparationIn vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparation
ChEMBL 407 5 1 5 5.3 Cc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2cccc(C)c2n1 10.1021/jm00100a007
CHEMBL337446 116221 0 None - 0 Guinea pig 6.5 pIC50 = 6.5 Binding
In vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparationIn vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparation
ChEMBL 407 5 1 5 5.3 Cc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2cccc(C)c2n1 10.1021/jm00100a007
44294703 191597 0 None - 0 Bovine 5.5 pIC50 = 5.5 Binding
Ability to displace [125I]- labelled [Sar1,Ileu8] from angiotensin II receptor of bovine adrenal cortex membranesAbility to displace [125I]- labelled [Sar1,Ileu8] from angiotensin II receptor of bovine adrenal cortex membranes
ChEMBL 443 7 1 5 4.9 CCC1(CC)CC(=O)N(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/C(=C/C(C)=O)C1 10.1016/S0960-894X(00)80474-6
CHEMBL52046 191597 0 None - 0 Bovine 5.5 pIC50 = 5.5 Binding
Ability to displace [125I]- labelled [Sar1,Ileu8] from angiotensin II receptor of bovine adrenal cortex membranesAbility to displace [125I]- labelled [Sar1,Ileu8] from angiotensin II receptor of bovine adrenal cortex membranes
ChEMBL 443 7 1 5 4.9 CCC1(CC)CC(=O)N(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/C(=C/C(C)=O)C1 10.1016/S0960-894X(00)80474-6
44348345 112333 0 None - 0 Bovine 5.5 pIC50 = 5.5 Binding
Concentration that gives 50% inhibition for binding of 125-I-[Sar1, IIe8] angiotensin to Angiotensin II receptor, type 1 in bovine adrenal cortex membrane.Concentration that gives 50% inhibition for binding of 125-I-[Sar1, IIe8] angiotensin to Angiotensin II receptor, type 1 in bovine adrenal cortex membrane.
ChEMBL 417 6 1 6 3.3 CCOC(=O)/C=C1/C(C)CC(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80914-8
CHEMBL330866 112333 0 None - 0 Bovine 5.5 pIC50 = 5.5 Binding
Concentration that gives 50% inhibition for binding of 125-I-[Sar1, IIe8] angiotensin to Angiotensin II receptor, type 1 in bovine adrenal cortex membrane.Concentration that gives 50% inhibition for binding of 125-I-[Sar1, IIe8] angiotensin to Angiotensin II receptor, type 1 in bovine adrenal cortex membrane.
ChEMBL 417 6 1 6 3.3 CCOC(=O)/C=C1/C(C)CC(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80914-8
19889589 185342 0 None - 0 Bovine 5.5 pIC50 = 5.5 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 442 7 1 5 5.9 CCCCc1nc2ccc(Cl)cc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
CHEMBL48692 185342 0 None - 0 Bovine 5.5 pIC50 = 5.5 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 442 7 1 5 5.9 CCCCc1nc2ccc(Cl)cc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
10364310 18687 0 None - 0 Guinea pig 5.5 pIC50 = 5.5 Binding
In vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparationIn vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparation
ChEMBL 411 8 1 3 6.5 CCCCc1cc(OCc2ccc(-c3ccccc3C(=O)O)cc2)c2ccccc2n1 10.1021/jm00100a007
CHEMBL128332 18687 0 None - 0 Guinea pig 5.5 pIC50 = 5.5 Binding
In vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparationIn vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparation
ChEMBL 411 8 1 3 6.5 CCCCc1cc(OCc2ccc(-c3ccccc3C(=O)O)cc2)c2ccccc2n1 10.1021/jm00100a007
19889589 185342 0 None - 0 Bovine 5.5 pIC50 = 5.5 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 442 7 1 5 5.9 CCCCc1nc2ccc(Cl)cc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
CHEMBL48692 185342 0 None - 0 Bovine 5.5 pIC50 = 5.5 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 442 7 1 5 5.9 CCCCc1nc2ccc(Cl)cc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
14962909 101248 0 None - 0 Bovine 6.5 pIC50 = 6.5 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 466 8 1 7 5.1 CCCCc1nc2cccc(C(=O)OC)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
CHEMBL299597 101248 0 None - 0 Bovine 6.5 pIC50 = 6.5 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 466 8 1 7 5.1 CCCCc1nc2cccc(C(=O)OC)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
10346400 48631 0 None - 0 Rabbit 7.5 pIC50 = 7.5 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 514 11 2 6 6.2 CCCCc1nnc(SCc2cccc(C)c2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
CHEMBL155984 48631 0 None - 0 Rabbit 7.5 pIC50 = 7.5 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 514 11 2 6 6.2 CCCCc1nnc(SCc2cccc(C)c2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
44306613 202006 0 None - 0 Rabbit 7.5 pIC50 = 7.5 Binding
Binding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membraneBinding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane
ChEMBL 485 10 1 5 7.1 CCCc1cc(Cn2c(CC)nc3c(C)cc(C)nc32)cc(CCC)c1Oc1ccccc1C(=O)O 10.1016/S0960-894X(01)81148-3
CHEMBL67616 202006 0 None - 0 Rabbit 7.5 pIC50 = 7.5 Binding
Binding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membraneBinding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane
ChEMBL 485 10 1 5 7.1 CCCc1cc(Cn2c(CC)nc3c(C)cc(C)nc32)cc(CCC)c1Oc1ccccc1C(=O)O 10.1016/S0960-894X(01)81148-3
3839 3688 78 None - 0 Human 7.5 pIC50 = 7.5 Binding
Compound was tested for inhibition against Angiotensin II receptor, type 1Compound was tested for inhibition against Angiotensin II receptor, type 1
ChEMBL 411 4 1 6 3.4 Cc1nc(C)c2c(n1)N(Cc1ccc(cc1)c1ccccc1c1nn[nH]n1)C(=O)CC2 10.1021/jm0204237
60919 3688 78 None - 0 Human 7.5 pIC50 = 7.5 Binding
Compound was tested for inhibition against Angiotensin II receptor, type 1Compound was tested for inhibition against Angiotensin II receptor, type 1
ChEMBL 411 4 1 6 3.4 Cc1nc(C)c2c(n1)N(Cc1ccc(cc1)c1ccccc1c1nn[nH]n1)C(=O)CC2 10.1021/jm0204237
6898 3688 78 None - 0 Human 7.5 pIC50 = 7.5 Binding
Compound was tested for inhibition against Angiotensin II receptor, type 1Compound was tested for inhibition against Angiotensin II receptor, type 1
ChEMBL 411 4 1 6 3.4 Cc1nc(C)c2c(n1)N(Cc1ccc(cc1)c1ccccc1c1nn[nH]n1)C(=O)CC2 10.1021/jm0204237
CHEMBL432162 3688 78 None - 0 Human 7.5 pIC50 = 7.5 Binding
Compound was tested for inhibition against Angiotensin II receptor, type 1Compound was tested for inhibition against Angiotensin II receptor, type 1
ChEMBL 411 4 1 6 3.4 Cc1nc(C)c2c(n1)N(Cc1ccc(cc1)c1ccccc1c1nn[nH]n1)C(=O)CC2 10.1021/jm0204237
DB01349 3688 78 None - 0 Human 7.5 pIC50 = 7.5 Binding
Compound was tested for inhibition against Angiotensin II receptor, type 1Compound was tested for inhibition against Angiotensin II receptor, type 1
ChEMBL 411 4 1 6 3.4 Cc1nc(C)c2c(n1)N(Cc1ccc(cc1)c1ccccc1c1nn[nH]n1)C(=O)CC2 10.1021/jm0204237
10346400 48631 0 None - 0 Rabbit 7.5 pIC50 = 7.5 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 514 11 2 6 6.2 CCCCc1nnc(SCc2cccc(C)c2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
CHEMBL155984 48631 0 None - 0 Rabbit 7.5 pIC50 = 7.5 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 514 11 2 6 6.2 CCCCc1nnc(SCc2cccc(C)c2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
44438865 92930 0 None - 1 Bovine 7.5 pIC50 = 7.5 Binding
Displacement of [125I]angiotensin-2 from bovine adrenal cortex AT1 receptorDisplacement of [125I]angiotensin-2 from bovine adrenal cortex AT1 receptor
ChEMBL 441 7 1 8 3.8 CCCc1nc2cccc(C(=O)OC)c2n1Cc1ccc(-n2cccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2007.02.042
CHEMBL245644 92930 0 None - 1 Bovine 7.5 pIC50 = 7.5 Binding
Displacement of [125I]angiotensin-2 from bovine adrenal cortex AT1 receptorDisplacement of [125I]angiotensin-2 from bovine adrenal cortex AT1 receptor
ChEMBL 441 7 1 8 3.8 CCCc1nc2cccc(C(=O)OC)c2n1Cc1ccc(-n2cccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2007.02.042
44297201 101509 0 None - 0 Bovine 7.5 pIC50 = 7.5 Binding
In vitro binding affinity to angiotensin II receptor in bovine adrenal cortexIn vitro binding affinity to angiotensin II receptor in bovine adrenal cortex
ChEMBL 617 8 1 9 6.2 CCCCc1nc2ccc([C@@H]3C[C@H]4C5CCC(C)(C)N5O[C@H]4O3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80377-2
CHEMBL301547 101509 0 None - 0 Bovine 7.5 pIC50 = 7.5 Binding
In vitro binding affinity to angiotensin II receptor in bovine adrenal cortexIn vitro binding affinity to angiotensin II receptor in bovine adrenal cortex
ChEMBL 617 8 1 9 6.2 CCCCc1nc2ccc([C@@H]3C[C@H]4C5CCC(C)(C)N5O[C@H]4O3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80377-2
44376747 119571 0 None - 0 Rabbit 7.5 pIC50 = 7.5 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aortaIn vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aorta
ChEMBL 510 11 2 7 3.9 CCCCc1ncc(C(=O)OC)n1Cc1ccc(-c2ccccc2NS(=O)(=O)NC(=O)C2CC2)cc1 10.1016/S0960-894X(01)81124-0
CHEMBL350851 119571 0 None - 0 Rabbit 7.5 pIC50 = 7.5 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aortaIn vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aorta
ChEMBL 510 11 2 7 3.9 CCCCc1ncc(C(=O)OC)n1Cc1ccc(-c2ccccc2NS(=O)(=O)NC(=O)C2CC2)cc1 10.1016/S0960-894X(01)81124-0
15654755 103318 0 None - 0 Bovine 7.5 pIC50 = 7.5 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 426 6 2 7 3.6 COc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a016
CHEMBL309084 103318 0 None - 0 Bovine 7.5 pIC50 = 7.5 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 426 6 2 7 3.6 COc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a016
127029201 136721 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Displacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptorDisplacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptor
ChEMBL 644 12 3 9 5.7 CCCc1nc2c(C)cc(C(=O)NCc3ccc(OC)c(OC)c3)cc2n1Cc1ccc(-c2ccccc2C(=O)Nc2nnn[nH]2)cc1 10.1039/C5MD00169B
CHEMBL3751994 136721 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Displacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptorDisplacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptor
ChEMBL 644 12 3 9 5.7 CCCc1nc2c(C)cc(C(=O)NCc3ccc(OC)c(OC)c3)cc2n1Cc1ccc(-c2ccccc2C(=O)Nc2nnn[nH]2)cc1 10.1039/C5MD00169B
44294649 188490 0 None - 0 Bovine 6.5 pIC50 = 6.5 Binding
Ability to displace [125I]- labelled [Sar1,Ileu8] from angiotensin II receptor of bovine adrenal cortex membranesAbility to displace [125I]- labelled [Sar1,Ileu8] from angiotensin II receptor of bovine adrenal cortex membranes
ChEMBL 445 6 1 6 4.1 CCC1(C)CC(=O)N(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/C(=C/C(=O)OC)C1 10.1016/S0960-894X(00)80474-6
CHEMBL51001 188490 0 None - 0 Bovine 6.5 pIC50 = 6.5 Binding
Ability to displace [125I]- labelled [Sar1,Ileu8] from angiotensin II receptor of bovine adrenal cortex membranesAbility to displace [125I]- labelled [Sar1,Ileu8] from angiotensin II receptor of bovine adrenal cortex membranes
ChEMBL 445 6 1 6 4.1 CCC1(C)CC(=O)N(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/C(=C/C(=O)OC)C1 10.1016/S0960-894X(00)80474-6
11755164 119200 0 None - 0 Rabbit 6.5 pIC50 = 6.5 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 486 10 2 6 5.4 CCCSc1nnc(Cc2ccccc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
CHEMBL347513 119200 0 None - 0 Rabbit 6.5 pIC50 = 6.5 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 486 10 2 6 5.4 CCCSc1nnc(Cc2ccccc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
11756222 49088 0 None - 0 Rabbit 6.5 pIC50 = 6.5 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 514 12 2 6 6.0 CCCSc1nnc(CCCc2ccccc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
CHEMBL156396 49088 0 None - 0 Rabbit 6.5 pIC50 = 6.5 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 514 12 2 6 6.0 CCCSc1nnc(CCCc2ccccc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
14962909 101248 0 None - 0 Bovine 6.5 pIC50 = 6.5 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 466 8 1 7 5.1 CCCCc1nc2cccc(C(=O)OC)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
CHEMBL299597 101248 0 None - 0 Bovine 6.5 pIC50 = 6.5 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 466 8 1 7 5.1 CCCCc1nc2cccc(C(=O)OC)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
10525501 101326 0 None - 0 Bovine 6.5 pIC50 = 6.5 Binding
In vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortexIn vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortex
ChEMBL 408 8 3 5 3.6 CCCc1nc(C(=O)O)c(C(=O)O)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm950450f
CHEMBL300186 101326 0 None - 0 Bovine 6.5 pIC50 = 6.5 Binding
In vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortexIn vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortex
ChEMBL 408 8 3 5 3.6 CCCc1nc(C(=O)O)c(C(=O)O)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm950450f
10525501 101326 0 None - 0 Bovine 6.5 pIC50 = 6.5 Binding
Inhibition of [125l]-All binding to bovine adrenal cortexInhibition of [125l]-All binding to bovine adrenal cortex
ChEMBL 408 8 3 5 3.6 CCCc1nc(C(=O)O)c(C(=O)O)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/S0960-894X(01)81143-4
CHEMBL300186 101326 0 None - 0 Bovine 6.5 pIC50 = 6.5 Binding
Inhibition of [125l]-All binding to bovine adrenal cortexInhibition of [125l]-All binding to bovine adrenal cortex
ChEMBL 408 8 3 5 3.6 CCCc1nc(C(=O)O)c(C(=O)O)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/S0960-894X(01)81143-4
15745369 10048 0 None - 0 Rat 5.5 pIC50 = 5.5 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 460 7 0 4 6.6 CCCCC1=NC2(CCCC2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)OC(C)(C)C)cc1 10.1021/jm00074a018
CHEMBL115835 10048 0 None - 0 Rat 5.5 pIC50 = 5.5 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 460 7 0 4 6.6 CCCCC1=NC2(CCCC2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)OC(C)(C)C)cc1 10.1021/jm00074a018
44322953 106056 0 None - 0 Rat 5.5 pIC50 = 5.5 Binding
Concentration required to inhibit binding of radioligand [125I]AII to angiotensin II receptor, type 1 in rat adrenal glomerulosa tissueConcentration required to inhibit binding of radioligand [125I]AII to angiotensin II receptor, type 1 in rat adrenal glomerulosa tissue
ChEMBL 426 8 2 6 4.4 CCCCc1nc(Cl)c(CO)n1Cc1ccc(C2=C(c3nn[nH]n3)CCCC2)cc1 10.1021/jm00092a017
CHEMBL314149 106056 0 None - 0 Rat 5.5 pIC50 = 5.5 Binding
Concentration required to inhibit binding of radioligand [125I]AII to angiotensin II receptor, type 1 in rat adrenal glomerulosa tissueConcentration required to inhibit binding of radioligand [125I]AII to angiotensin II receptor, type 1 in rat adrenal glomerulosa tissue
ChEMBL 426 8 2 6 4.4 CCCCc1nc(Cl)c(CO)n1Cc1ccc(C2=C(c3nn[nH]n3)CCCC2)cc1 10.1021/jm00092a017
44308996 102487 0 None - 0 Bovine 5.5 pIC50 = 5.5 Binding
Inhibition of [125I][Ile5]-AII binding to bovine adrenal cortex membrane Angiotensin II receptor type 1Inhibition of [125I][Ile5]-AII binding to bovine adrenal cortex membrane Angiotensin II receptor type 1
ChEMBL 348 5 1 3 5.4 CCCCc1nc2ccccc2n1Cc1cc(Cl)c(O)c(Cl)c1 10.1016/S0960-894X(01)81149-5
CHEMBL306486 102487 0 None - 0 Bovine 5.5 pIC50 = 5.5 Binding
Inhibition of [125I][Ile5]-AII binding to bovine adrenal cortex membrane Angiotensin II receptor type 1Inhibition of [125I][Ile5]-AII binding to bovine adrenal cortex membrane Angiotensin II receptor type 1
ChEMBL 348 5 1 3 5.4 CCCCc1nc2ccccc2n1Cc1cc(Cl)c(O)c(Cl)c1 10.1016/S0960-894X(01)81149-5
15654746 202009 0 None - 0 Bovine 5.5 pIC50 = 5.5 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 452 7 2 6 4.8 CC(C)Cc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a016
CHEMBL67636 202009 0 None - 0 Bovine 5.5 pIC50 = 5.5 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 452 7 2 6 4.8 CC(C)Cc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a016
15287888 99762 0 None - 0 Rabbit 6.5 pIC50 = 6.5 Binding
Tested in vitro for Angiotensin II receptor, type 1 binding affinity using rabbit aorta binding assayTested in vitro for Angiotensin II receptor, type 1 binding affinity using rabbit aorta binding assay
ChEMBL 421 8 1 5 5.2 CCCc1nc2c(C)ccnc2n1Cc1ccc(OC(C(=O)O)C2CCCCC2)cc1 10.1016/0960-894X(94)00476-V
CHEMBL288618 99762 0 None - 0 Rabbit 6.5 pIC50 = 6.5 Binding
Tested in vitro for Angiotensin II receptor, type 1 binding affinity using rabbit aorta binding assayTested in vitro for Angiotensin II receptor, type 1 binding affinity using rabbit aorta binding assay
ChEMBL 421 8 1 5 5.2 CCCc1nc2c(C)ccnc2n1Cc1ccc(OC(C(=O)O)C2CCCCC2)cc1 10.1016/0960-894X(94)00476-V
44294207 101070 0 None - 0 Rat 5.5 pIC50 = 5.5 Binding
Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.
ChEMBL 440 9 3 6 4.2 CCCCc1nc(Cl)c(CO)n1Cc1ccc(NC(=O)/C(=N\O)c2ccccc2)cc1 10.1021/jm00064a007
CHEMBL298364 101070 0 None - 0 Rat 5.5 pIC50 = 5.5 Binding
Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.
ChEMBL 440 9 3 6 4.2 CCCCc1nc(Cl)c(CO)n1Cc1ccc(NC(=O)/C(=N\O)c2ccccc2)cc1 10.1021/jm00064a007
44320536 204658 0 None - 0 Rat 6.5 pIC50 = 6.5 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 468 5 1 5 4.1 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(C2=C3C=CC=CC3N(C)C(=O)C2C(=O)O)cc1 10.1021/jm031100t
CHEMBL87694 204658 0 None - 0 Rat 6.5 pIC50 = 6.5 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 468 5 1 5 4.1 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(C2=C3C=CC=CC3N(C)C(=O)C2C(=O)O)cc1 10.1021/jm031100t
57380413 70170 0 None - 0 Human 6.5 pIC50 = 6.5 Binding
Displacement of [125I]Sar1 Ile8-Ang 2 from angiotensin 2 AT1 receptor after 180 mins by gamma countingDisplacement of [125I]Sar1 Ile8-Ang 2 from angiotensin 2 AT1 receptor after 180 mins by gamma counting
ChEMBL 547 10 2 5 6.6 CCCc1nc2c(C)cc(C(=O)NCc3cccc(OC)c3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2012.01.009
CHEMBL1947130 70170 0 None - 0 Human 6.5 pIC50 = 6.5 Binding
Displacement of [125I]Sar1 Ile8-Ang 2 from angiotensin 2 AT1 receptor after 180 mins by gamma countingDisplacement of [125I]Sar1 Ile8-Ang 2 from angiotensin 2 AT1 receptor after 180 mins by gamma counting
ChEMBL 547 10 2 5 6.6 CCCc1nc2c(C)cc(C(=O)NCc3cccc(OC)c3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2012.01.009
15355268 101199 0 None - 0 Bovine 6.5 pIC50 = 6.5 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 466 8 2 6 5.3 CCCCc1nc2ccc(C)c(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
CHEMBL299340 101199 0 None - 0 Bovine 6.5 pIC50 = 6.5 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 466 8 2 6 5.3 CCCCc1nc2ccc(C)c(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
44274746 99196 0 None - 0 Rabbit 7.5 pIC50 = 7.5 Binding
Ability to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitroAbility to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitro
ChEMBL 591 7 3 8 5.9 Nc1ccc2nc(-c3ccc(-c4ccccc4C(=O)O)cc3)n(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c(=O)c2c1 10.1016/S0960-894X(00)80335-2
CHEMBL284455 99196 0 None - 0 Rabbit 7.5 pIC50 = 7.5 Binding
Ability to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitroAbility to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitro
ChEMBL 591 7 3 8 5.9 Nc1ccc2nc(-c3ccc(-c4ccccc4C(=O)O)cc3)n(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c(=O)c2c1 10.1016/S0960-894X(00)80335-2
10408951 18642 0 None - 0 Rat 7.5 pIC50 = 7.5 Binding
Activity against high affinity Angiotensin II receptor, type 1 was measured from the ability to inhibit [125I]angiotensin II binding to rat uterine membrane.Activity against high affinity Angiotensin II receptor, type 1 was measured from the ability to inhibit [125I]angiotensin II binding to rat uterine membrane.
ChEMBL 404 10 1 7 4.0 CCCCc1nc(CCCC)n(Cc2ccc(-n3cccc3-c3nn[nH]n3)cc2)n1 10.1021/jm00053a013
CHEMBL12810 18642 0 None - 0 Rat 7.5 pIC50 = 7.5 Binding
Activity against high affinity Angiotensin II receptor, type 1 was measured from the ability to inhibit [125I]angiotensin II binding to rat uterine membrane.Activity against high affinity Angiotensin II receptor, type 1 was measured from the ability to inhibit [125I]angiotensin II binding to rat uterine membrane.
ChEMBL 404 10 1 7 4.0 CCCCc1nc(CCCC)n(Cc2ccc(-n3cccc3-c3nn[nH]n3)cc2)n1 10.1021/jm00053a013
14956751 204568 0 None - 0 Rabbit 7.5 pIC50 = 7.5 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 509 9 1 9 4.1 CCCCc1nn(-c2ccc(C(=O)OC)cc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
CHEMBL87073 204568 0 None - 0 Rabbit 7.5 pIC50 = 7.5 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 509 9 1 9 4.1 CCCCc1nn(-c2ccc(C(=O)OC)cc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
9824290 193231 0 None - 0 Rat 7.5 pIC50 = 7.5 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 435 5 1 4 6.2 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2c(C(=O)O)ccc3ccccc23)cc1 10.1021/jm031100t
CHEMBL541212 193231 0 None - 0 Rat 7.5 pIC50 = 7.5 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 435 5 1 4 6.2 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2c(C(=O)O)ccc3ccccc23)cc1 10.1021/jm031100t
10483230 46552 0 None - 0 Rabbit 7.5 pIC50 = 7.5 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 574 11 2 8 5.1 CCCCc1nnc([S+]([O-])Cc2ccc(Cl)cc2)n1Cc1ccc(NC(=O)c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
CHEMBL154027 46552 0 None - 0 Rabbit 7.5 pIC50 = 7.5 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 574 11 2 8 5.1 CCCCc1nnc([S+]([O-])Cc2ccc(Cl)cc2)n1Cc1ccc(NC(=O)c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
44438885 90509 0 None - 1 Bovine 7.5 pIC50 = 7.5 Binding
Displacement of [125I]angiotensin-2 from bovine adrenal cortex AT1 receptorDisplacement of [125I]angiotensin-2 from bovine adrenal cortex AT1 receptor
ChEMBL 417 8 2 5 4.6 CCCCc1nc2cccc(C(=O)O)c2n1Cc1ccc(-n2cccc2C(=O)O)cc1 10.1016/j.bmcl.2007.02.042
CHEMBL239378 90509 0 None - 1 Bovine 7.5 pIC50 = 7.5 Binding
Displacement of [125I]angiotensin-2 from bovine adrenal cortex AT1 receptorDisplacement of [125I]angiotensin-2 from bovine adrenal cortex AT1 receptor
ChEMBL 417 8 2 5 4.6 CCCCc1nc2cccc(C(=O)O)c2n1Cc1ccc(-n2cccc2C(=O)O)cc1 10.1016/j.bmcl.2007.02.042
44315060 102570 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membrane
ChEMBL 665 10 2 9 4.9 CCCCOC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CC)nc3ccc(NC(=O)N4CCOCC4)cc3c2=O)c(F)c1 10.1016/0960-894X(94)85036-4
CHEMBL307290 102570 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membrane
ChEMBL 665 10 2 9 4.9 CCCCOC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CC)nc3ccc(NC(=O)N4CCOCC4)cc3c2=O)c(F)c1 10.1016/0960-894X(94)85036-4
10414301 21985 0 None - 0 Rat 7.5 pIC50 = 7.5 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 519 11 1 5 6.0 CCCCc1nc2ccc(N(C)S(=O)(=O)CCC)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00077a007
CHEMBL132280 21985 0 None - 0 Rat 7.5 pIC50 = 7.5 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 519 11 1 5 6.0 CCCCc1nc2ccc(N(C)S(=O)(=O)CCC)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00077a007
44295069 100662 0 None - 0 Bovine 6.5 pIC50 = 6.5 Binding
Ability to displace [125I]- labelled [Sar1,Ileu8] from angiotensin II receptor of bovine adrenal cortex membranesAbility to displace [125I]- labelled [Sar1,Ileu8] from angiotensin II receptor of bovine adrenal cortex membranes
ChEMBL 501 10 1 6 5.7 CCCC1(CCC)CC(=O)N(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/C(=C/C(=O)OCC)C1 10.1016/S0960-894X(00)80474-6
CHEMBL295369 100662 0 None - 0 Bovine 6.5 pIC50 = 6.5 Binding
Ability to displace [125I]- labelled [Sar1,Ileu8] from angiotensin II receptor of bovine adrenal cortex membranesAbility to displace [125I]- labelled [Sar1,Ileu8] from angiotensin II receptor of bovine adrenal cortex membranes
ChEMBL 501 10 1 6 5.7 CCCC1(CCC)CC(=O)N(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/C(=C/C(=O)OCC)C1 10.1016/S0960-894X(00)80474-6
10028212 48639 0 None - 0 Rabbit 6.5 pIC50 = 6.5 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 482 11 2 8 3.9 CCCCc1nnc(SCC(=O)OC)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
CHEMBL155992 48639 0 None - 0 Rabbit 6.5 pIC50 = 6.5 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 482 11 2 8 3.9 CCCCc1nnc(SCC(=O)OC)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
44293816 185021 0 None - 0 Rat 6.5 pIC50 = 6.5 Binding
Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.
ChEMBL 563 11 1 7 6.5 CCCCc1nc2c(C)cc(C)nc2n1Cc1ccc(NC(=O)[C@H](Cc2ccccc2)n2cccc2C(=O)OC)cc1 10.1021/jm00064a007
CHEMBL48640 185021 0 None - 0 Rat 6.5 pIC50 = 6.5 Binding
Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.
ChEMBL 563 11 1 7 6.5 CCCCc1nc2c(C)cc(C)nc2n1Cc1ccc(NC(=O)[C@H](Cc2ccccc2)n2cccc2C(=O)OC)cc1 10.1021/jm00064a007
44307174 100262 0 None - 0 Rabbit 6.5 pIC50 = 6.5 Binding
Binding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membraneBinding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane
ChEMBL 366 6 1 6 4.0 C=CCc1cc(Cn2c(CC)nc3c(C)cc(C)nc32)cc([N+](=O)[O-])c1O 10.1016/S0960-894X(01)81148-3
CHEMBL292739 100262 0 None - 0 Rabbit 6.5 pIC50 = 6.5 Binding
Binding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membraneBinding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane
ChEMBL 366 6 1 6 4.0 C=CCc1cc(Cn2c(CC)nc3c(C)cc(C)nc32)cc([N+](=O)[O-])c1O 10.1016/S0960-894X(01)81148-3
1610 2305 89 None - 4 Bovine 6.5 pIC50 = 6.5 Binding
Binding affinity expressed as inhibitory concentration towards bovine adrenal cortex angiotensin II receptor was measuredBinding affinity expressed as inhibitory concentration towards bovine adrenal cortex angiotensin II receptor was measured
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(00)80366-2
3941 2305 89 None - 4 Bovine 6.5 pIC50 = 6.5 Binding
Binding affinity expressed as inhibitory concentration towards bovine adrenal cortex angiotensin II receptor was measuredBinding affinity expressed as inhibitory concentration towards bovine adrenal cortex angiotensin II receptor was measured
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(00)80366-2
3961 2305 89 None - 4 Bovine 6.5 pIC50 = 6.5 Binding
Binding affinity expressed as inhibitory concentration towards bovine adrenal cortex angiotensin II receptor was measuredBinding affinity expressed as inhibitory concentration towards bovine adrenal cortex angiotensin II receptor was measured
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(00)80366-2
590 2305 89 None - 4 Bovine 6.5 pIC50 = 6.5 Binding
Binding affinity expressed as inhibitory concentration towards bovine adrenal cortex angiotensin II receptor was measuredBinding affinity expressed as inhibitory concentration towards bovine adrenal cortex angiotensin II receptor was measured
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(00)80366-2
CHEMBL191 2305 89 None - 4 Bovine 6.5 pIC50 = 6.5 Binding
Binding affinity expressed as inhibitory concentration towards bovine adrenal cortex angiotensin II receptor was measuredBinding affinity expressed as inhibitory concentration towards bovine adrenal cortex angiotensin II receptor was measured
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(00)80366-2
DB00678 2305 89 None - 4 Bovine 6.5 pIC50 = 6.5 Binding
Binding affinity expressed as inhibitory concentration towards bovine adrenal cortex angiotensin II receptor was measuredBinding affinity expressed as inhibitory concentration towards bovine adrenal cortex angiotensin II receptor was measured
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(00)80366-2
10028212 48639 0 None - 0 Rabbit 6.5 pIC50 = 6.5 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 482 11 2 8 3.9 CCCCc1nnc(SCC(=O)OC)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
CHEMBL155992 48639 0 None - 0 Rabbit 6.5 pIC50 = 6.5 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 482 11 2 8 3.9 CCCCc1nnc(SCC(=O)OC)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
19792124 187666 0 None - 0 Bovine 6.5 pIC50 = 6.5 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 422 7 1 5 5.6 CCCCc1nc2cccc(C)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
CHEMBL49980 187666 0 None - 0 Bovine 6.5 pIC50 = 6.5 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 422 7 1 5 5.6 CCCCc1nc2cccc(C)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
1610 2305 89 None - 4 Bovine 6.5 pIC50 = 6.5 Binding
In vitro binding affinity to angiotensin II receptor in bovine adrenal cortexIn vitro binding affinity to angiotensin II receptor in bovine adrenal cortex
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(01)80377-2
3941 2305 89 None - 4 Bovine 6.5 pIC50 = 6.5 Binding
In vitro binding affinity to angiotensin II receptor in bovine adrenal cortexIn vitro binding affinity to angiotensin II receptor in bovine adrenal cortex
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(01)80377-2
3961 2305 89 None - 4 Bovine 6.5 pIC50 = 6.5 Binding
In vitro binding affinity to angiotensin II receptor in bovine adrenal cortexIn vitro binding affinity to angiotensin II receptor in bovine adrenal cortex
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(01)80377-2
590 2305 89 None - 4 Bovine 6.5 pIC50 = 6.5 Binding
In vitro binding affinity to angiotensin II receptor in bovine adrenal cortexIn vitro binding affinity to angiotensin II receptor in bovine adrenal cortex
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(01)80377-2
CHEMBL191 2305 89 None - 4 Bovine 6.5 pIC50 = 6.5 Binding
In vitro binding affinity to angiotensin II receptor in bovine adrenal cortexIn vitro binding affinity to angiotensin II receptor in bovine adrenal cortex
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(01)80377-2
DB00678 2305 89 None - 4 Bovine 6.5 pIC50 = 6.5 Binding
In vitro binding affinity to angiotensin II receptor in bovine adrenal cortexIn vitro binding affinity to angiotensin II receptor in bovine adrenal cortex
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(01)80377-2
10341766 116563 0 None - 0 Rat 6.5 pIC50 = 6.5 Binding
Inhibition of [125I]angiotensin II receptor specific binding to rat mesenteric arteriesInhibition of [125I]angiotensin II receptor specific binding to rat mesenteric arteries
ChEMBL 414 9 1 4 5.7 CCCCc1ncc(/C=C(\Cc2ccsc2)C(=O)O)n1Cc1ccccc1Cl 10.1021/jm00099a013
CHEMBL339233 116563 0 None - 0 Rat 6.5 pIC50 = 6.5 Binding
Inhibition of [125I]angiotensin II receptor specific binding to rat mesenteric arteriesInhibition of [125I]angiotensin II receptor specific binding to rat mesenteric arteries
ChEMBL 414 9 1 4 5.7 CCCCc1ncc(/C=C(\Cc2ccsc2)C(=O)O)n1Cc1ccccc1Cl 10.1021/jm00099a013
19792124 187666 0 None - 0 Bovine 6.5 pIC50 = 6.5 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 422 7 1 5 5.6 CCCCc1nc2cccc(C)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
CHEMBL49980 187666 0 None - 0 Bovine 6.5 pIC50 = 6.5 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 422 7 1 5 5.6 CCCCc1nc2cccc(C)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
44341650 169309 0 None - 0 Rat 5.5 pIC50 = 5.5 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 406 7 2 3 4.8 CCCCC1NC(=O)C2(CCCC2)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00074a018
CHEMBL444060 169309 0 None - 0 Rat 5.5 pIC50 = 5.5 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 406 7 2 3 4.8 CCCCC1NC(=O)C2(CCCC2)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00074a018
44352233 18731 0 None - 0 Bovine 5.5 pIC50 = 5.5 Binding
Concentration required to inhibit [125I]AII binding to Angiotensin II receptor from membrane fractions of bovine adrenal cortexConcentration required to inhibit [125I]AII binding to Angiotensin II receptor from membrane fractions of bovine adrenal cortex
ChEMBL 383 6 1 6 4.0 CCCc1cn2nccc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81118-5
CHEMBL128590 18731 0 None - 0 Bovine 5.5 pIC50 = 5.5 Binding
Concentration required to inhibit [125I]AII binding to Angiotensin II receptor from membrane fractions of bovine adrenal cortexConcentration required to inhibit [125I]AII binding to Angiotensin II receptor from membrane fractions of bovine adrenal cortex
ChEMBL 383 6 1 6 4.0 CCCc1cn2nccc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81118-5
44308795 202204 0 None - 0 Bovine 4.5 pIC50 = 4.5 Binding
Inhibition of [125I][Ile5]-AII binding to bovine adrenal cortex membrane Angiotensin II receptor type 1Inhibition of [125I][Ile5]-AII binding to bovine adrenal cortex membrane Angiotensin II receptor type 1
ChEMBL 532 5 1 3 5.3 CCCCc1nc2ccccc2n1Cc1ccc(I)c(O)c1I 10.1016/S0960-894X(01)81149-5
CHEMBL69025 202204 0 None - 0 Bovine 4.5 pIC50 = 4.5 Binding
Inhibition of [125I][Ile5]-AII binding to bovine adrenal cortex membrane Angiotensin II receptor type 1Inhibition of [125I][Ile5]-AII binding to bovine adrenal cortex membrane Angiotensin II receptor type 1
ChEMBL 532 5 1 3 5.3 CCCCc1nc2ccccc2n1Cc1ccc(I)c(O)c1I 10.1016/S0960-894X(01)81149-5
71652856 88700 0 None - 0 Human 6.5 pIC50 = 6.5 Binding
Displacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysisDisplacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysis
ChEMBL 545 11 2 3 6.9 CCCCc1c[n+](Cc2ccc(-c3ccccc3C(=O)O)cc2)cn1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2012.12.044
CHEMBL2337684 88700 0 None - 0 Human 6.5 pIC50 = 6.5 Binding
Displacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysisDisplacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysis
ChEMBL 545 11 2 3 6.9 CCCCc1c[n+](Cc2ccc(-c3ccccc3C(=O)O)cc2)cn1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2012.12.044
CHEMBL2365829 88700 0 None - 0 Human 6.5 pIC50 = 6.5 Binding
Displacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysisDisplacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysis
ChEMBL 545 11 2 3 6.9 CCCCc1c[n+](Cc2ccc(-c3ccccc3C(=O)O)cc2)cn1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2012.12.044
44210830 57166 0 None - 0 Rabbit 7.5 pIC50 = 7.5 Binding
Binding affinity to Angiotensin II receptor, type 1 in rabbit aorta binding assayBinding affinity to Angiotensin II receptor, type 1 in rabbit aorta binding assay
ChEMBL 461 6 1 6 5.9 CCCc1nc2c(C)ccnc2n1Cc1ccc2c(c1)SC(C(=O)O)(c1ccccc1)S2 10.1016/S0960-894X(01)80193-1
CHEMBL165850 57166 0 None - 0 Rabbit 7.5 pIC50 = 7.5 Binding
Binding affinity to Angiotensin II receptor, type 1 in rabbit aorta binding assayBinding affinity to Angiotensin II receptor, type 1 in rabbit aorta binding assay
ChEMBL 461 6 1 6 5.9 CCCc1nc2c(C)ccnc2n1Cc1ccc2c(c1)SC(C(=O)O)(c1ccccc1)S2 10.1016/S0960-894X(01)80193-1
14950496 84580 0 None - 0 Guinea pig 7.5 pIC50 = 7.5 Binding
Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1
ChEMBL 483 5 1 5 4.7 Cc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c(I)c(C)n1 10.1021/jm00061a016
CHEMBL22391 84580 0 None - 0 Guinea pig 7.5 pIC50 = 7.5 Binding
Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1
ChEMBL 483 5 1 5 4.7 Cc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c(I)c(C)n1 10.1021/jm00061a016
10436618 21467 0 None - 0 Rat 7.5 pIC50 = 7.5 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 517 8 1 5 5.7 CCCCc1nc2ccc(N3CCCCS3(=O)=O)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00077a007
CHEMBL131839 21467 0 None - 0 Rat 7.5 pIC50 = 7.5 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 517 8 1 5 5.7 CCCCc1nc2ccc(N3CCCCS3(=O)=O)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00077a007
44305634 101892 0 None - 0 Bovine 7.5 pIC50 = 7.5 Binding
Tested for binding affinity against angiotensin II receptor in bovine adrenal cortexTested for binding affinity against angiotensin II receptor in bovine adrenal cortex
ChEMBL 428 8 1 7 3.0 C=CCn1c(=O)cc(CCC)n(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c1=O 10.1016/0960-894X(95)00370-9
CHEMBL303822 101892 0 None - 0 Bovine 7.5 pIC50 = 7.5 Binding
Tested for binding affinity against angiotensin II receptor in bovine adrenal cortexTested for binding affinity against angiotensin II receptor in bovine adrenal cortex
ChEMBL 428 8 1 7 3.0 C=CCn1c(=O)cc(CCC)n(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c1=O 10.1016/0960-894X(95)00370-9
11757112 112457 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 542 12 0 6 6.0 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2Cc2ccc(C)cc2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
CHEMBL331081 112457 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 542 12 0 6 6.0 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2Cc2ccc(C)cc2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
44293818 101366 0 None - 0 Rat 6.5 pIC50 = 6.5 Binding
Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.
ChEMBL 579 13 3 7 5.7 CCCCc1nc(-n2cccc2)c(C(=O)O)n1Cc1ccc(NC(=O)[C@H](Cc2ccccc2)n2cccc2C(=O)O)cc1 10.1021/jm00064a007
CHEMBL300487 101366 0 None - 0 Rat 6.5 pIC50 = 6.5 Binding
Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.
ChEMBL 579 13 3 7 5.7 CCCCc1nc(-n2cccc2)c(C(=O)O)n1Cc1ccc(NC(=O)[C@H](Cc2ccccc2)n2cccc2C(=O)O)cc1 10.1021/jm00064a007
15355268 101199 0 None - 0 Bovine 6.5 pIC50 = 6.5 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 466 8 2 6 5.3 CCCCc1nc2ccc(C)c(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
CHEMBL299340 101199 0 None - 0 Bovine 6.5 pIC50 = 6.5 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 466 8 2 6 5.3 CCCCc1nc2ccc(C)c(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
14962904 192489 0 None - 0 Bovine 5.5 pIC50 = 5.5 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 466 8 1 7 5.0 CCCCc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nnnn2C)cc1 10.1007/s00044-009-9182-z
CHEMBL52265 192489 0 None - 0 Bovine 5.5 pIC50 = 5.5 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 466 8 1 7 5.0 CCCCc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nnnn2C)cc1 10.1007/s00044-009-9182-z
14962904 192489 0 None - 0 Bovine 5.5 pIC50 = 5.5 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 466 8 1 7 5.0 CCCCc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nnnn2C)cc1 10.1007/s00044-009-9182-z
CHEMBL52265 192489 0 None - 0 Bovine 5.5 pIC50 = 5.5 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 466 8 1 7 5.0 CCCCc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nnnn2C)cc1 10.1007/s00044-009-9182-z
127034919 135979 0 None - 0 Human 6.5 pIC50 = 6.5 Binding
Displacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysisDisplacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysis
ChEMBL 599 10 2 7 6.6 CCCc1nc2c(C)cc(C(=O)NC(C)C)cc2n1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)cc1 10.1039/C4MD00499J
CHEMBL3736310 135979 0 None - 0 Human 6.5 pIC50 = 6.5 Binding
Displacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysisDisplacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysis
ChEMBL 599 10 2 7 6.6 CCCc1nc2c(C)cc(C(=O)NC(C)C)cc2n1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)cc1 10.1039/C4MD00499J
127034739 135836 0 None - 0 Human 6.5 pIC50 = 6.5 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 585 10 2 6 7.3 CCCc1nc2c(C)cc(C(=S)NC[C@@H](C)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.ejmech.2015.09.010
CHEMBL3734989 135836 0 None - 0 Human 6.5 pIC50 = 6.5 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 585 10 2 6 7.3 CCCc1nc2c(C)cc(C(=S)NC[C@@H](C)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.ejmech.2015.09.010
127026058 136709 0 None - 0 Human 6.5 pIC50 = 6.5 Binding
Displacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptorDisplacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptor
ChEMBL 600 10 3 8 6.0 CCCc1nc2c(C)cc(C(=O)Nc3ccccc3OC)cc2n1Cc1ccc(-c2ccccc2C(=O)Nc2nnn[nH]2)cc1 10.1039/C5MD00169B
CHEMBL3751899 136709 0 None - 0 Human 6.5 pIC50 = 6.5 Binding
Displacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptorDisplacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptor
ChEMBL 600 10 3 8 6.0 CCCc1nc2c(C)cc(C(=O)Nc3ccccc3OC)cc2n1Cc1ccc(-c2ccccc2C(=O)Nc2nnn[nH]2)cc1 10.1039/C5MD00169B
71521298 86381 0 None - 0 Human 6.5 pIC50 = 6.5 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor afterDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after
ChEMBL 481 6 2 8 3.2 CCc1nc2ccn(CC(=O)O)c(=O)c2n1[C@H]1CCc2cc(-c3ccccc3-c3nnn[nH]3)ccc21 10.1016/j.bmcl.2012.11.088
CHEMBL2322440 86381 0 None - 0 Human 6.5 pIC50 = 6.5 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor afterDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after
ChEMBL 481 6 2 8 3.2 CCc1nc2ccn(CC(=O)O)c(=O)c2n1[C@H]1CCc2cc(-c3ccccc3-c3nnn[nH]3)ccc21 10.1016/j.bmcl.2012.11.088
76329882 84519 0 None - 0 Rabbit 7.5 pIC50 = 7.5 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 538 12 2 8 5.4 CCCCc1nnc(SCCc2ccccc2)n1Cc1ccc(NC(=O)c2ccccc2-c2nnn[nH]2)cc1 10.1007/s00044-011-9756-4
CHEMBL2237589 84519 0 None - 0 Rabbit 7.5 pIC50 = 7.5 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 538 12 2 8 5.4 CCCCc1nnc(SCCc2ccccc2)n1Cc1ccc(NC(=O)c2ccccc2-c2nnn[nH]2)cc1 10.1007/s00044-011-9756-4
19422640 100012 0 None - 0 Rat 7.5 pIC50 = 7.5 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 378 7 1 3 4.8 CCCCC1=NC(C)(C)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00074a018
CHEMBL290988 100012 0 None - 0 Rat 7.5 pIC50 = 7.5 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 378 7 1 3 4.8 CCCCC1=NC(C)(C)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00074a018
44377171 119693 0 None - 0 Rabbit 7.5 pIC50 = 7.5 Binding
Binding affinity to Angiotensin II receptor, type 1 in rabbit aorta binding assayBinding affinity to Angiotensin II receptor, type 1 in rabbit aorta binding assay
ChEMBL 485 6 1 8 5.4 CCCc1nc2c(C)ccnc2n1Cc1ccc2c(c1)SC(c1ccccc1)(c1nn[nH]n1)S2 10.1016/S0960-894X(01)80193-1
CHEMBL352042 119693 0 None - 0 Rabbit 7.5 pIC50 = 7.5 Binding
Binding affinity to Angiotensin II receptor, type 1 in rabbit aorta binding assayBinding affinity to Angiotensin II receptor, type 1 in rabbit aorta binding assay
ChEMBL 485 6 1 8 5.4 CCCc1nc2c(C)ccnc2n1Cc1ccc2c(c1)SC(c1ccccc1)(c1nn[nH]n1)S2 10.1016/S0960-894X(01)80193-1
10323527 47747 0 None - 0 Rabbit 7.5 pIC50 = 7.5 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 495 11 1 7 5.9 CCCCc1nnc(SCCc2ccccc2)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
CHEMBL155035 47747 0 None - 0 Rabbit 7.5 pIC50 = 7.5 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 495 11 1 7 5.9 CCCCc1nnc(SCCc2ccccc2)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
19422640 100012 0 None - 0 Rat 7.5 pIC50 = 7.5 Binding
In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.
ChEMBL 378 7 1 3 4.8 CCCCC1=NC(C)(C)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/S0960-894X(01)81140-9
CHEMBL290988 100012 0 None - 0 Rat 7.5 pIC50 = 7.5 Binding
In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.
ChEMBL 378 7 1 3 4.8 CCCCC1=NC(C)(C)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/S0960-894X(01)81140-9
14951061 202633 0 None - 0 Rat 7.5 pIC50 = 7.5 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 501 11 1 7 5.7 CCCCc1nn(CCC(C)CC(C)(C)C)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a015
CHEMBL71613 202633 0 None - 0 Rat 7.5 pIC50 = 7.5 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 501 11 1 7 5.7 CCCCc1nn(CCC(C)CC(C)(C)C)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a015
1610 2305 89 None -1 4 Rat 7.5 pIC50 = 7.5 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00077a007
3941 2305 89 None -1 4 Rat 7.5 pIC50 = 7.5 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00077a007
3961 2305 89 None -1 4 Rat 7.5 pIC50 = 7.5 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00077a007
590 2305 89 None -1 4 Rat 7.5 pIC50 = 7.5 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00077a007
CHEMBL191 2305 89 None -1 4 Rat 7.5 pIC50 = 7.5 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00077a007
DB00678 2305 89 None -1 4 Rat 7.5 pIC50 = 7.5 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00077a007
14952925 195137 0 None - 0 Rat 7.5 pIC50 = 7.5 Binding
Tested for inhibition of [125I]- AII specific binding to rat mesenteric arteries, expressed as IC50Tested for inhibition of [125I]- AII specific binding to rat mesenteric arteries, expressed as IC50
ChEMBL 492 10 2 5 6.1 CCCCc1ncc(/C=C(\Cc2cccs2)C(=O)O)n1Cc1cc(Cl)c(C(=O)O)cc1Cl 10.1016/S0960-894X(01)81116-1
CHEMBL56574 195137 0 None - 0 Rat 7.5 pIC50 = 7.5 Binding
Tested for inhibition of [125I]- AII specific binding to rat mesenteric arteries, expressed as IC50Tested for inhibition of [125I]- AII specific binding to rat mesenteric arteries, expressed as IC50
ChEMBL 492 10 2 5 6.1 CCCCc1ncc(/C=C(\Cc2cccs2)C(=O)O)n1Cc1cc(Cl)c(C(=O)O)cc1Cl 10.1016/S0960-894X(01)81116-1
10098291 15368 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 523 10 1 9 3.6 CCCCc1ncc(/C=C2/C(=O)N(CO)C(=O)N2Cc2csc(C)n2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
CHEMBL121990 15368 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 523 10 1 9 3.6 CCCCc1ncc(/C=C2/C(=O)N(CO)C(=O)N2Cc2csc(C)n2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
76322687 84512 0 None - 0 Rabbit 6.5 pIC50 = 6.5 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 535 10 2 8 4.4 CCCCc1nnc(C(=O)N(C)c2ccccc2)n1Cc1ccc(NC(=O)c2ccccc2-c2nnn[nH]2)cc1 10.1007/s00044-011-9756-4
CHEMBL2237582 84512 0 None - 0 Rabbit 6.5 pIC50 = 6.5 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 535 10 2 8 4.4 CCCCc1nnc(C(=O)N(C)c2ccccc2)n1Cc1ccc(NC(=O)c2ccccc2-c2nnn[nH]2)cc1 10.1007/s00044-011-9756-4
44342045 109874 0 None - 0 Rat 6.5 pIC50 = 6.5 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 488 7 1 3 7.6 CCCCC1=NC2(CCCCCCCCCC2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00074a018
CHEMBL324245 109874 0 None - 0 Rat 6.5 pIC50 = 6.5 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 488 7 1 3 7.6 CCCCC1=NC2(CCCCCCCCCC2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00074a018
10323388 49028 0 None - 0 Rabbit 6.5 pIC50 = 6.5 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 492 9 1 7 4.8 CCCCc1nnc(C(=O)N(C)c2ccccc2)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
CHEMBL156352 49028 0 None - 0 Rabbit 6.5 pIC50 = 6.5 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 492 9 1 7 4.8 CCCCc1nnc(C(=O)N(C)c2ccccc2)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
1610 2305 89 None 1 4 Human 6.5 pIC50 = 6.5 Binding
Inhibition of ATR1 (unknown origin)Inhibition of ATR1 (unknown origin)
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/acs.jmedchem.9b00179
3941 2305 89 None 1 4 Human 6.5 pIC50 = 6.5 Binding
Inhibition of ATR1 (unknown origin)Inhibition of ATR1 (unknown origin)
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/acs.jmedchem.9b00179
3961 2305 89 None 1 4 Human 6.5 pIC50 = 6.5 Binding
Inhibition of ATR1 (unknown origin)Inhibition of ATR1 (unknown origin)
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/acs.jmedchem.9b00179
590 2305 89 None 1 4 Human 6.5 pIC50 = 6.5 Binding
Inhibition of ATR1 (unknown origin)Inhibition of ATR1 (unknown origin)
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/acs.jmedchem.9b00179
CHEMBL191 2305 89 None 1 4 Human 6.5 pIC50 = 6.5 Binding
Inhibition of ATR1 (unknown origin)Inhibition of ATR1 (unknown origin)
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/acs.jmedchem.9b00179
DB00678 2305 89 None 1 4 Human 6.5 pIC50 = 6.5 Binding
Inhibition of ATR1 (unknown origin)Inhibition of ATR1 (unknown origin)
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/acs.jmedchem.9b00179
130762 97782 9 None - 0 Rat 6.5 pIC50 = 6.5 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 398 8 2 4 4.8 CCCCc1nc(Cl)c(CO)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00077a007
CHEMBL274447 97782 9 None - 0 Rat 6.5 pIC50 = 6.5 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 398 8 2 4 4.8 CCCCc1nc(Cl)c(CO)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00077a007
44323113 204930 0 None - 0 Rat 5.5 pIC50 = 5.5 Binding
Concentration required to inhibit binding of radioligand [125I]AII to angiotensin II receptor, type 1 in rat adrenal glomerulosa tissueConcentration required to inhibit binding of radioligand [125I]AII to angiotensin II receptor, type 1 in rat adrenal glomerulosa tissue
ChEMBL 412 8 2 6 4.0 CCCCc1nc(Cl)c(CO)n1Cc1ccc(C2=C(c3nn[nH]n3)CCC2)cc1 10.1021/jm00092a017
CHEMBL89403 204930 0 None - 0 Rat 5.5 pIC50 = 5.5 Binding
Concentration required to inhibit binding of radioligand [125I]AII to angiotensin II receptor, type 1 in rat adrenal glomerulosa tissueConcentration required to inhibit binding of radioligand [125I]AII to angiotensin II receptor, type 1 in rat adrenal glomerulosa tissue
ChEMBL 412 8 2 6 4.0 CCCCc1nc(Cl)c(CO)n1Cc1ccc(C2=C(c3nn[nH]n3)CCC2)cc1 10.1021/jm00092a017
76322688 84516 0 None - 0 Rabbit 7.4 pIC50 = 7.4 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 530 11 2 8 5.8 CCCCc1nnc(SCC2CCCCC2)n1Cc1ccc(NC(=O)c2ccccc2-c2nnn[nH]2)cc1 10.1007/s00044-011-9756-4
CHEMBL2237586 84516 0 None - 0 Rabbit 7.4 pIC50 = 7.4 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 530 11 2 8 5.8 CCCCc1nnc(SCC2CCCCC2)n1Cc1ccc(NC(=O)c2ccccc2-c2nnn[nH]2)cc1 10.1007/s00044-011-9756-4
19010047 84531 0 None - 0 Rabbit 7.4 pIC50 = 7.4 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 554 12 3 9 4.9 CCCCc1nnc(SCc2ccccc2CO)n1Cc1ccc(NC(=O)c2ccccc2-c2nnn[nH]2)cc1 10.1007/s00044-011-9756-4
CHEMBL2237601 84531 0 None - 0 Rabbit 7.4 pIC50 = 7.4 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 554 12 3 9 4.9 CCCCc1nnc(SCc2ccccc2CO)n1Cc1ccc(NC(=O)c2ccccc2-c2nnn[nH]2)cc1 10.1007/s00044-011-9756-4
15224461 19212 0 None - 0 Bovine 7.4 pIC50 = 7.4 Binding
Concentration required to inhibit [125I]AII binding to Angiotensin II receptor from membrane fractions of bovine adrenal cortexConcentration required to inhibit [125I]AII binding to Angiotensin II receptor from membrane fractions of bovine adrenal cortex
ChEMBL 467 8 2 7 4.7 CCCCc1nc2c(C)cnc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81118-5
CHEMBL129447 19212 0 None - 0 Bovine 7.4 pIC50 = 7.4 Binding
Concentration required to inhibit [125I]AII binding to Angiotensin II receptor from membrane fractions of bovine adrenal cortexConcentration required to inhibit [125I]AII binding to Angiotensin II receptor from membrane fractions of bovine adrenal cortex
ChEMBL 467 8 2 7 4.7 CCCCc1nc2c(C)cnc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81118-5
9986992 51216 0 None - 0 Rabbit 7.4 pIC50 = 7.4 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 511 11 2 8 5.3 CCCCc1nnc(SCc2ccccc2CO)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
CHEMBL158267 51216 0 None - 0 Rabbit 7.4 pIC50 = 7.4 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 511 11 2 8 5.3 CCCCc1nnc(SCc2ccccc2CO)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
10032191 119056 0 None - 0 Rabbit 7.4 pIC50 = 7.4 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 487 10 1 7 6.2 CCCCc1nnc(SCC2CCCCC2)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
CHEMBL346145 119056 0 None - 0 Rabbit 7.4 pIC50 = 7.4 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 487 10 1 7 6.2 CCCCc1nnc(SCC2CCCCC2)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
1610 2305 89 None -1 4 Rat 7.4 pIC50 = 7.4 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00067a015
3941 2305 89 None -1 4 Rat 7.4 pIC50 = 7.4 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00067a015
3961 2305 89 None -1 4 Rat 7.4 pIC50 = 7.4 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00067a015
590 2305 89 None -1 4 Rat 7.4 pIC50 = 7.4 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00067a015
CHEMBL191 2305 89 None -1 4 Rat 7.4 pIC50 = 7.4 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00067a015
DB00678 2305 89 None -1 4 Rat 7.4 pIC50 = 7.4 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00067a015
14951090 102722 0 None - 0 Rat 7.4 pIC50 = 7.4 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 579 13 1 10 4.7 CCCCc1nn(C(CC(=O)OCC)C(=O)c2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a015
CHEMBL308416 102722 0 None - 0 Rat 7.4 pIC50 = 7.4 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 579 13 1 10 4.7 CCCCc1nn(C(CC(=O)OCC)C(=O)c2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a015
44287123 99715 0 None - 0 Rabbit 7.4 pIC50 = 7.4 Binding
Tested in vitro for Angiotensin II receptor, type 1 binding affinity using rabbit aorta binding assayTested in vitro for Angiotensin II receptor, type 1 binding affinity using rabbit aorta binding assay
ChEMBL 465 8 1 5 6.1 CCCc1nc2c(C)ccnc2n1Cc1ccc(OC(C(=O)O)c2cccc3ccccc23)cc1 10.1016/0960-894X(94)00476-V
CHEMBL288222 99715 0 None - 0 Rabbit 7.4 pIC50 = 7.4 Binding
Tested in vitro for Angiotensin II receptor, type 1 binding affinity using rabbit aorta binding assayTested in vitro for Angiotensin II receptor, type 1 binding affinity using rabbit aorta binding assay
ChEMBL 465 8 1 5 6.1 CCCc1nc2c(C)ccnc2n1Cc1ccc(OC(C(=O)O)c2cccc3ccccc23)cc1 10.1016/0960-894X(94)00476-V
127029204 136776 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Displacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptorDisplacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptor
ChEMBL 628 12 3 8 5.8 CCCc1nc2c(C)cc(C(=O)NCCc3cccc(OC)c3)cc2n1Cc1ccc(-c2ccccc2C(=O)Nc2nnn[nH]2)cc1 10.1039/C5MD00169B
CHEMBL3752530 136776 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Displacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptorDisplacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptor
ChEMBL 628 12 3 8 5.8 CCCc1nc2c(C)cc(C(=O)NCCc3cccc(OC)c3)cc2n1Cc1ccc(-c2ccccc2C(=O)Nc2nnn[nH]2)cc1 10.1039/C5MD00169B
71521503 86390 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor afterDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after
ChEMBL 527 6 1 7 5.5 CCc1nc2ccn(Cc3cccc(C)c3)c(=O)c2n1[C@H]1CCc2cc(-c3ccccc3-c3nnn[nH]3)ccc21 10.1016/j.bmcl.2012.11.088
CHEMBL2322449 86390 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor afterDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after
ChEMBL 527 6 1 7 5.5 CCc1nc2ccn(Cc3cccc(C)c3)c(=O)c2n1[C@H]1CCc2cc(-c3ccccc3-c3nnn[nH]3)ccc21 10.1016/j.bmcl.2012.11.088
135723833 196824 0 None - 0 Bovine 6.4 pIC50 = 6.4 Binding
Displacement of [125 I]-AII (0.2 nM) from bovine adrenal cortical membrane angiotensin II (AII) receptor at 10e-7 MDisplacement of [125 I]-AII (0.2 nM) from bovine adrenal cortical membrane angiotensin II (AII) receptor at 10e-7 M
ChEMBL 442 6 2 8 4.2 COc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2noc(O)n2)cc1 10.1016/0960-894X(95)00319-O
CHEMBL57783 196824 0 None - 0 Bovine 6.4 pIC50 = 6.4 Binding
Displacement of [125 I]-AII (0.2 nM) from bovine adrenal cortical membrane angiotensin II (AII) receptor at 10e-7 MDisplacement of [125 I]-AII (0.2 nM) from bovine adrenal cortical membrane angiotensin II (AII) receptor at 10e-7 M
ChEMBL 442 6 2 8 4.2 COc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2noc(O)n2)cc1 10.1016/0960-894X(95)00319-O
10811315 109774 0 None - 0 Bovine 6.4 pIC50 = 6.4 Binding
In vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortexIn vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortex
ChEMBL 406 8 2 4 5.1 CCCc1nc(C(C)C)c(C(=O)O)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm950450f
CHEMBL323819 109774 0 None - 0 Bovine 6.4 pIC50 = 6.4 Binding
In vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortexIn vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortex
ChEMBL 406 8 2 4 5.1 CCCc1nc(C(C)C)c(C(=O)O)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm950450f
10412363 20660 0 None - 0 Guinea pig 6.4 pIC50 = 6.4 Binding
In vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparationIn vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparation
ChEMBL 432 6 1 6 5.1 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2cc(C#N)ccc2n1 10.1021/jm00100a007
CHEMBL131050 20660 0 None - 0 Guinea pig 6.4 pIC50 = 6.4 Binding
In vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparationIn vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparation
ChEMBL 432 6 1 6 5.1 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2cc(C#N)ccc2n1 10.1021/jm00100a007
121879 2195 19 None - 1 Human 5.4 pIC50 = 5.4 Binding
Inhibition against human angiotensin II receptor, type 1 (AG2-R)Inhibition against human angiotensin II receptor, type 1 (AG2-R)
ChEMBL 509 7 3 6 3.6 O=C(CC(N)(C)C)N[C@@H]1CCc2c(N(C1=O)Cc1ccc(cc1)c1ccccc1c1nnn[nH]1)cccc2 10.1021/jm0309452
5868 2195 19 None - 1 Human 5.4 pIC50 = 5.4 Binding
Inhibition against human angiotensin II receptor, type 1 (AG2-R)Inhibition against human angiotensin II receptor, type 1 (AG2-R)
ChEMBL 509 7 3 6 3.6 O=C(CC(N)(C)C)N[C@@H]1CCc2c(N(C1=O)Cc1ccc(cc1)c1ccccc1c1nnn[nH]1)cccc2 10.1021/jm0309452
CHEMBL308716 2195 19 None - 1 Human 5.4 pIC50 = 5.4 Binding
Inhibition against human angiotensin II receptor, type 1 (AG2-R)Inhibition against human angiotensin II receptor, type 1 (AG2-R)
ChEMBL 509 7 3 6 3.6 O=C(CC(N)(C)C)N[C@@H]1CCc2c(N(C1=O)Cc1ccc(cc1)c1ccccc1c1nnn[nH]1)cccc2 10.1021/jm0309452
1610 2305 89 None -1 4 Rat 4.4 pIC50 = 4.4 Binding
Activity against high affinity Angiotensin II receptor, type 1 was measured from the ability to inhibit [125I]angiotensin II binding to rat uterine membrane.Activity against high affinity Angiotensin II receptor, type 1 was measured from the ability to inhibit [125I]angiotensin II binding to rat uterine membrane.
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00053a013
3941 2305 89 None -1 4 Rat 4.4 pIC50 = 4.4 Binding
Activity against high affinity Angiotensin II receptor, type 1 was measured from the ability to inhibit [125I]angiotensin II binding to rat uterine membrane.Activity against high affinity Angiotensin II receptor, type 1 was measured from the ability to inhibit [125I]angiotensin II binding to rat uterine membrane.
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00053a013
3961 2305 89 None -1 4 Rat 4.4 pIC50 = 4.4 Binding
Activity against high affinity Angiotensin II receptor, type 1 was measured from the ability to inhibit [125I]angiotensin II binding to rat uterine membrane.Activity against high affinity Angiotensin II receptor, type 1 was measured from the ability to inhibit [125I]angiotensin II binding to rat uterine membrane.
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00053a013
590 2305 89 None -1 4 Rat 4.4 pIC50 = 4.4 Binding
Activity against high affinity Angiotensin II receptor, type 1 was measured from the ability to inhibit [125I]angiotensin II binding to rat uterine membrane.Activity against high affinity Angiotensin II receptor, type 1 was measured from the ability to inhibit [125I]angiotensin II binding to rat uterine membrane.
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00053a013
CHEMBL191 2305 89 None -1 4 Rat 4.4 pIC50 = 4.4 Binding
Activity against high affinity Angiotensin II receptor, type 1 was measured from the ability to inhibit [125I]angiotensin II binding to rat uterine membrane.Activity against high affinity Angiotensin II receptor, type 1 was measured from the ability to inhibit [125I]angiotensin II binding to rat uterine membrane.
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00053a013
DB00678 2305 89 None -1 4 Rat 4.4 pIC50 = 4.4 Binding
Activity against high affinity Angiotensin II receptor, type 1 was measured from the ability to inhibit [125I]angiotensin II binding to rat uterine membrane.Activity against high affinity Angiotensin II receptor, type 1 was measured from the ability to inhibit [125I]angiotensin II binding to rat uterine membrane.
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00053a013
127028617 137030 0 None - 0 Human 6.4 pIC50 = 6.4 Binding
Displacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptorDisplacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptor
ChEMBL 536 10 3 7 4.9 CCCNC(=O)c1cc(C)c2nc(CCC)n(Cc3ccc(-c4ccccc4C(=O)Nc4nnn[nH]4)cc3)c2c1 10.1039/C5MD00169B
CHEMBL3754661 137030 0 None - 0 Human 6.4 pIC50 = 6.4 Binding
Displacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptorDisplacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptor
ChEMBL 536 10 3 7 4.9 CCCNC(=O)c1cc(C)c2nc(CCC)n(Cc3ccc(-c4ccccc4C(=O)Nc4nnn[nH]4)cc3)c2c1 10.1039/C5MD00169B
127034740 135955 0 None - 0 Human 6.4 pIC50 = 6.4 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 585 10 2 6 7.3 CCCc1nc2c(C)cc(C(=S)NC[C@H](C)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.ejmech.2015.09.010
CHEMBL3736166 135955 0 None - 0 Human 6.4 pIC50 = 6.4 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 585 10 2 6 7.3 CCCc1nc2c(C)cc(C(=S)NC[C@H](C)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.ejmech.2015.09.010
127035544 135824 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Displacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysisDisplacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysis
ChEMBL 721 14 2 9 7.4 CCCc1nc2c(C)cc(C(=O)NCCc3cc(OC)ccc3OC)cc2n1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)cc1 10.1039/C4MD00499J
CHEMBL3734870 135824 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Displacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysisDisplacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysis
ChEMBL 721 14 2 9 7.4 CCCc1nc2c(C)cc(C(=O)NCCc3cc(OC)ccc3OC)cc2n1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)cc1 10.1039/C4MD00499J
19029576 99498 0 None - 1 Rat 7.4 pIC50 = 7.4 Binding
In vitro ability to displace the specific binding of [125I]-A II from receptors in rat liver membrane(type 1 receptor)In vitro ability to displace the specific binding of [125I]-A II from receptors in rat liver membrane(type 1 receptor)
ChEMBL 467 6 1 7 4.1 CCc1nn(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/c(=N/C(=O)c2ccccc2)s1 10.1016/S0960-894X(96)00250-8
CHEMBL286537 99498 0 None - 1 Rat 7.4 pIC50 = 7.4 Binding
In vitro ability to displace the specific binding of [125I]-A II from receptors in rat liver membrane(type 1 receptor)In vitro ability to displace the specific binding of [125I]-A II from receptors in rat liver membrane(type 1 receptor)
ChEMBL 467 6 1 7 4.1 CCc1nn(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/c(=N/C(=O)c2ccccc2)s1 10.1016/S0960-894X(96)00250-8
10692816 9824 0 None - 0 Bovine 7.4 pIC50 = 7.4 Binding
In vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortexIn vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortex
ChEMBL 408 7 3 5 3.8 CCc1nc(C(C)(C)O)c(C(=O)O)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm950450f
CHEMBL114527 9824 0 None - 0 Bovine 7.4 pIC50 = 7.4 Binding
In vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortexIn vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortex
ChEMBL 408 7 3 5 3.8 CCc1nc(C(C)(C)O)c(C(=O)O)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm950450f
70688504 75968 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]Sar1Ile8-Ang2 from angiotensin AT1 receptor after 180 mins by gamma countingDisplacement of [125I]Sar1Ile8-Ang2 from angiotensin AT1 receptor after 180 mins by gamma counting
ChEMBL 573 10 2 6 6.3 CCCc1nc2c(C)cc(C(=O)NCCc3ccccc3F)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmc.2012.05.056
CHEMBL2058865 75968 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]Sar1Ile8-Ang2 from angiotensin AT1 receptor after 180 mins by gamma countingDisplacement of [125I]Sar1Ile8-Ang2 from angiotensin AT1 receptor after 180 mins by gamma counting
ChEMBL 573 10 2 6 6.3 CCCc1nc2c(C)cc(C(=O)NCCc3ccccc3F)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmc.2012.05.056
71521301 86384 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor afterDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after
ChEMBL 531 6 1 7 5.3 CCc1nc2ccn(Cc3ccccc3F)c(=O)c2n1[C@H]1CCc2cc(-c3ccccc3-c3nnn[nH]3)ccc21 10.1016/j.bmcl.2012.11.088
CHEMBL2322443 86384 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor afterDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after
ChEMBL 531 6 1 7 5.3 CCc1nc2ccn(Cc3ccccc3F)c(=O)c2n1[C@H]1CCc2cc(-c3ccccc3-c3nnn[nH]3)ccc21 10.1016/j.bmcl.2012.11.088
76308180 84538 0 None - 0 Rabbit 6.4 pIC50 = 6.4 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 508 11 2 8 4.7 CCCCc1nnc(OCc2ccccc2)n1Cc1ccc(NC(=O)c2ccccc2-c2nnn[nH]2)cc1 10.1007/s00044-011-9756-4
CHEMBL2237608 84538 0 None - 0 Rabbit 6.4 pIC50 = 6.4 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 508 11 2 8 4.7 CCCCc1nnc(OCc2ccccc2)n1Cc1ccc(NC(=O)c2ccccc2-c2nnn[nH]2)cc1 10.1007/s00044-011-9756-4
44459780 91716 0 None - 0 Rabbit 6.4 pIC50 = 6.4 Binding
Binding affinity against Angiotensin II type 1 Receptor in rabbit aortic tissueBinding affinity against Angiotensin II type 1 Receptor in rabbit aortic tissue
ChEMBL 426 7 1 4 5.5 CCCCc1nc2cc(C)ccc2c(=O)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/S0960-894X(00)80334-0
CHEMBL24218 91716 0 None - 0 Rabbit 6.4 pIC50 = 6.4 Binding
Binding affinity against Angiotensin II type 1 Receptor in rabbit aortic tissueBinding affinity against Angiotensin II type 1 Receptor in rabbit aortic tissue
ChEMBL 426 7 1 4 5.5 CCCCc1nc2cc(C)ccc2c(=O)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/S0960-894X(00)80334-0
44459634 95681 0 None - 0 Rabbit 6.4 pIC50 = 6.4 Binding
Binding affinity against Angiotensin II type 1 Receptor in rabbit aortic tissueBinding affinity against Angiotensin II type 1 Receptor in rabbit aortic tissue
ChEMBL 426 7 1 4 5.5 CCCCc1nc2cccc(C)c2c(=O)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/S0960-894X(00)80334-0
CHEMBL26048 95681 0 None - 0 Rabbit 6.4 pIC50 = 6.4 Binding
Binding affinity against Angiotensin II type 1 Receptor in rabbit aortic tissueBinding affinity against Angiotensin II type 1 Receptor in rabbit aortic tissue
ChEMBL 426 7 1 4 5.5 CCCCc1nc2cccc(C)c2c(=O)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/S0960-894X(00)80334-0
44294023 183985 0 None - 0 Rat 6.4 pIC50 = 6.4 Binding
Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.
ChEMBL 546 12 2 5 6.4 CCCCc1nc(Cl)c(CC(=O)O)n1Cc1ccc(NC(=O)[C@H](Cc2ccccc2)n2c(C)ccc2C)cc1 10.1021/jm00064a007
CHEMBL48486 183985 0 None - 0 Rat 6.4 pIC50 = 6.4 Binding
Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.
ChEMBL 546 12 2 5 6.4 CCCCc1nc(Cl)c(CC(=O)O)n1Cc1ccc(NC(=O)[C@H](Cc2ccccc2)n2c(C)ccc2C)cc1 10.1021/jm00064a007
10069271 34240 0 None - 0 Guinea pig 6.4 pIC50 = 6.4 Binding
Binding affinity to angiotensin AT1 receptor in guinea pig adrenal cortex membranesBinding affinity to angiotensin AT1 receptor in guinea pig adrenal cortex membranes
ChEMBL 395 4 1 5 5.5 Cc1cc(Sc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2ccccc2n1 10.1016/j.bmc.2010.10.043
CHEMBL142860 34240 0 None - 0 Guinea pig 6.4 pIC50 = 6.4 Binding
Binding affinity to angiotensin AT1 receptor in guinea pig adrenal cortex membranesBinding affinity to angiotensin AT1 receptor in guinea pig adrenal cortex membranes
ChEMBL 395 4 1 5 5.5 Cc1cc(Sc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2ccccc2n1 10.1016/j.bmc.2010.10.043
10389770 119125 0 None - 0 Rabbit 6.4 pIC50 = 6.4 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 465 10 1 7 5.1 CCCCc1nnc(OCc2ccccc2)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
CHEMBL346773 119125 0 None - 0 Rabbit 6.4 pIC50 = 6.4 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 465 10 1 7 5.1 CCCCc1nnc(OCc2ccccc2)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
10252966 32587 0 None - 0 Guinea pig 6.4 pIC50 = 6.4 Binding
In vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparationIn vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparation
ChEMBL 409 5 1 5 5.7 Cc1cc(SCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2ccccc2n1 10.1021/jm00100a007
CHEMBL141447 32587 0 None - 0 Guinea pig 6.4 pIC50 = 6.4 Binding
In vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparationIn vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparation
ChEMBL 409 5 1 5 5.7 Cc1cc(SCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2ccccc2n1 10.1021/jm00100a007
127034918 135922 0 None - 0 Human 6.4 pIC50 = 6.4 Binding
Displacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysisDisplacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysis
ChEMBL 599 11 2 7 6.6 CCCNC(=O)c1cc(C)c2nc(CCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)Nc4onc(C)c4C)cc3)c2c1 10.1039/C4MD00499J
CHEMBL3735797 135922 0 None - 0 Human 6.4 pIC50 = 6.4 Binding
Displacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysisDisplacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysis
ChEMBL 599 11 2 7 6.6 CCCNC(=O)c1cc(C)c2nc(CCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)Nc4onc(C)c4C)cc3)c2c1 10.1039/C4MD00499J
11527144 178516 0 None - 1 Bovine 7.4 pIC50 = 7.4 Binding
Binding affinity expressed as inhibitory concentration towards bovine adrenal cortex angiotensin II receptor was measuredBinding affinity expressed as inhibitory concentration towards bovine adrenal cortex angiotensin II receptor was measured
ChEMBL 561 8 1 8 5.6 CCCCc1nc2ccc([C@]3(C)C[C@H]4CCCN4O3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80366-2
CHEMBL297425 178516 0 None - 1 Bovine 7.4 pIC50 = 7.4 Binding
Binding affinity expressed as inhibitory concentration towards bovine adrenal cortex angiotensin II receptor was measuredBinding affinity expressed as inhibitory concentration towards bovine adrenal cortex angiotensin II receptor was measured
ChEMBL 561 8 1 8 5.6 CCCCc1nc2ccc([C@]3(C)C[C@H]4CCCN4O3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80366-2
CHEMBL47177 178516 0 None - 1 Bovine 7.4 pIC50 = 7.4 Binding
Binding affinity expressed as inhibitory concentration towards bovine adrenal cortex angiotensin II receptor was measuredBinding affinity expressed as inhibitory concentration towards bovine adrenal cortex angiotensin II receptor was measured
ChEMBL 561 8 1 8 5.6 CCCCc1nc2ccc([C@]3(C)C[C@H]4CCCN4O3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80366-2
44342047 9686 0 None - 0 Rat 7.4 pIC50 = 7.4 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 390 7 1 3 4.9 CCCCC1=NC2(CCC2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00074a018
CHEMBL113674 9686 0 None - 0 Rat 7.4 pIC50 = 7.4 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 390 7 1 3 4.9 CCCCC1=NC2(CCC2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00074a018
3839 3688 78 None - 0 Human 7.4 pIC50 = 7.4 Binding
Compound was tested in vitro for inhibitory activity against human Angiotensin II receptor in cultured preadipocytesCompound was tested in vitro for inhibitory activity against human Angiotensin II receptor in cultured preadipocytes
ChEMBL 411 4 1 6 3.4 Cc1nc(C)c2c(n1)N(Cc1ccc(cc1)c1ccccc1c1nn[nH]n1)C(=O)CC2 10.1016/s0960-894x(02)00303-7
60919 3688 78 None - 0 Human 7.4 pIC50 = 7.4 Binding
Compound was tested in vitro for inhibitory activity against human Angiotensin II receptor in cultured preadipocytesCompound was tested in vitro for inhibitory activity against human Angiotensin II receptor in cultured preadipocytes
ChEMBL 411 4 1 6 3.4 Cc1nc(C)c2c(n1)N(Cc1ccc(cc1)c1ccccc1c1nn[nH]n1)C(=O)CC2 10.1016/s0960-894x(02)00303-7
6898 3688 78 None - 0 Human 7.4 pIC50 = 7.4 Binding
Compound was tested in vitro for inhibitory activity against human Angiotensin II receptor in cultured preadipocytesCompound was tested in vitro for inhibitory activity against human Angiotensin II receptor in cultured preadipocytes
ChEMBL 411 4 1 6 3.4 Cc1nc(C)c2c(n1)N(Cc1ccc(cc1)c1ccccc1c1nn[nH]n1)C(=O)CC2 10.1016/s0960-894x(02)00303-7
CHEMBL432162 3688 78 None - 0 Human 7.4 pIC50 = 7.4 Binding
Compound was tested in vitro for inhibitory activity against human Angiotensin II receptor in cultured preadipocytesCompound was tested in vitro for inhibitory activity against human Angiotensin II receptor in cultured preadipocytes
ChEMBL 411 4 1 6 3.4 Cc1nc(C)c2c(n1)N(Cc1ccc(cc1)c1ccccc1c1nn[nH]n1)C(=O)CC2 10.1016/s0960-894x(02)00303-7
DB01349 3688 78 None - 0 Human 7.4 pIC50 = 7.4 Binding
Compound was tested in vitro for inhibitory activity against human Angiotensin II receptor in cultured preadipocytesCompound was tested in vitro for inhibitory activity against human Angiotensin II receptor in cultured preadipocytes
ChEMBL 411 4 1 6 3.4 Cc1nc(C)c2c(n1)N(Cc1ccc(cc1)c1ccccc1c1nn[nH]n1)C(=O)CC2 10.1016/s0960-894x(02)00303-7
9830481 193002 0 None - 0 Bovine 7.4 pIC50 = 7.4 Binding
In vitro binding affinity to angiotensin II receptor in bovine adrenal cortexIn vitro binding affinity to angiotensin II receptor in bovine adrenal cortex
ChEMBL 617 8 1 9 5.9 CCCCc1nc2ccc([C@H]3OC[C@@H]4ON5[C@@H](CCC5(C)C)[C@H]34)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80377-2
CHEMBL53244 193002 0 None - 0 Bovine 7.4 pIC50 = 7.4 Binding
In vitro binding affinity to angiotensin II receptor in bovine adrenal cortexIn vitro binding affinity to angiotensin II receptor in bovine adrenal cortex
ChEMBL 617 8 1 9 5.9 CCCCc1nc2ccc([C@H]3OC[C@@H]4ON5[C@@H](CCC5(C)C)[C@H]34)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80377-2
15287892 99881 0 None - 0 Rabbit 7.4 pIC50 = 7.4 Binding
Tested in vitro for Angiotensin II receptor, type 1 binding affinity using rabbit aorta binding assayTested in vitro for Angiotensin II receptor, type 1 binding affinity using rabbit aorta binding assay
ChEMBL 445 9 1 6 5.0 CCCc1nc2c(C)ccnc2n1Cc1ccc(OC(C(=O)O)c2ccccc2OC)cc1 10.1016/0960-894X(94)00476-V
CHEMBL289640 99881 0 None - 0 Rabbit 7.4 pIC50 = 7.4 Binding
Tested in vitro for Angiotensin II receptor, type 1 binding affinity using rabbit aorta binding assayTested in vitro for Angiotensin II receptor, type 1 binding affinity using rabbit aorta binding assay
ChEMBL 445 9 1 6 5.0 CCCc1nc2c(C)ccnc2n1Cc1ccc(OC(C(=O)O)c2ccccc2OC)cc1 10.1016/0960-894X(94)00476-V
127035515 135919 0 None - 1 Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 585 11 2 7 6.3 CCCc1nc2c(C)cc(C(=O)N[C@@H](COC)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.ejmech.2015.09.010
CHEMBL3735769 135919 0 None - 1 Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 585 11 2 7 6.3 CCCc1nc2c(C)cc(C(=O)N[C@@H](COC)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.ejmech.2015.09.010
44459856 96063 0 None - 0 Rabbit 6.4 pIC50 = 6.4 Binding
Binding affinity against Angiotensin II type 1 Receptor in rabbit aortic tissueBinding affinity against Angiotensin II type 1 Receptor in rabbit aortic tissue
ChEMBL 462 7 1 4 6.3 CCCCc1nc2cc3ccccc3cc2c(=O)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/S0960-894X(00)80334-0
CHEMBL26277 96063 0 None - 0 Rabbit 6.4 pIC50 = 6.4 Binding
Binding affinity against Angiotensin II type 1 Receptor in rabbit aortic tissueBinding affinity against Angiotensin II type 1 Receptor in rabbit aortic tissue
ChEMBL 462 7 1 4 6.3 CCCCc1nc2cc3ccccc3cc2c(=O)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/S0960-894X(00)80334-0
11755164 119200 0 None - 0 Rabbit 6.4 pIC50 = 6.4 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 486 10 2 6 5.4 CCCSc1nnc(Cc2ccccc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
CHEMBL347513 119200 0 None - 0 Rabbit 6.4 pIC50 = 6.4 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 486 10 2 6 5.4 CCCSc1nnc(Cc2ccccc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
127037497 135965 0 None - 0 Human 6.4 pIC50 = 6.4 Binding
Displacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysisDisplacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysis
ChEMBL 613 9 2 7 6.9 CCCc1nc2c(C)cc(C(=O)NC(C)(C)C)cc2n1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)cc1 10.1039/C4MD00499J
CHEMBL3736225 135965 0 None - 0 Human 6.4 pIC50 = 6.4 Binding
Displacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysisDisplacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysis
ChEMBL 613 9 2 7 6.9 CCCc1nc2c(C)cc(C(=O)NC(C)(C)C)cc2n1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)cc1 10.1039/C4MD00499J
73357018 92186 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysisDisplacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysis
ChEMBL 517 8 2 4 7.3 CCCc1nc2c(C)cc(C(=O)Nc3ccc(C)cc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2013.08.014
CHEMBL2435834 92186 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysisDisplacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysis
ChEMBL 517 8 2 4 7.3 CCCc1nc2c(C)cc(C(=O)Nc3ccc(C)cc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2013.08.014
24828707 95478 0 None - 1 Rat 7.4 pIC50 = 7.4 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
ChEMBL 425 7 1 7 3.9 CCCCn1c2ncccc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm7011563
CHEMBL259353 95478 0 None - 1 Rat 7.4 pIC50 = 7.4 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
ChEMBL 425 7 1 7 3.9 CCCCn1c2ncccc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm7011563
44377111 119366 0 None - 0 Rabbit 7.4 pIC50 = 7.4 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aortaIn vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aorta
ChEMBL 495 10 1 7 3.9 CCCCc1ncc(C(=O)OC)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)C2CC2)cc1 10.1016/S0960-894X(01)81124-0
CHEMBL349020 119366 0 None - 0 Rabbit 7.4 pIC50 = 7.4 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aortaIn vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aorta
ChEMBL 495 10 1 7 3.9 CCCCc1ncc(C(=O)OC)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)C2CC2)cc1 10.1016/S0960-894X(01)81124-0
8374 2866 36 None - 1 Human 7.4 pIC50 = 7.4 Binding
Inhibition of human AT1 receptorInhibition of human AT1 receptor
ChEMBL 507 8 1 4 5.4 COc1ccc2c(c1OCc1ccccc1)C[C@H](N(C2)C(=O)C(c1ccccc1)c1ccccc1)C(=O)O 10.1021/acs.jmedchem.9b01780
9937291 2866 36 None - 1 Human 7.4 pIC50 = 7.4 Binding
Inhibition of human AT1 receptorInhibition of human AT1 receptor
ChEMBL 507 8 1 4 5.4 COc1ccc2c(c1OCc1ccccc1)C[C@H](N(C2)C(=O)C(c1ccccc1)c1ccccc1)C(=O)O 10.1021/acs.jmedchem.9b01780
CHEMBL34124 2866 36 None - 1 Human 7.4 pIC50 = 7.4 Binding
Inhibition of human AT1 receptorInhibition of human AT1 receptor
ChEMBL 507 8 1 4 5.4 COc1ccc2c(c1OCc1ccccc1)C[C@H](N(C2)C(=O)C(c1ccccc1)c1ccccc1)C(=O)O 10.1021/acs.jmedchem.9b01780
DB16266 2866 36 None - 1 Human 7.4 pIC50 = 7.4 Binding
Inhibition of human AT1 receptorInhibition of human AT1 receptor
ChEMBL 507 8 1 4 5.4 COc1ccc2c(c1OCc1ccccc1)C[C@H](N(C2)C(=O)C(c1ccccc1)c1ccccc1)C(=O)O 10.1021/acs.jmedchem.9b01780
15654759 202393 0 None - 0 Bovine 7.4 pIC50 = 7.4 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 453 8 3 7 4.5 CCCNc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a016
CHEMBL70242 202393 0 None - 0 Bovine 7.4 pIC50 = 7.4 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 453 8 3 7 4.5 CCCNc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a016
197647 117570 6 None - 0 Bovine 6.4 pIC50 = 6.4 Binding
Concentration required to inhibit [125I]AII binding to Angiotensin II receptor from membrane fractions of bovine adrenal cortexConcentration required to inhibit [125I]AII binding to Angiotensin II receptor from membrane fractions of bovine adrenal cortex
ChEMBL 396 6 1 6 4.3 CCOc1nc2ccccc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81118-5
CHEMBL340612 117570 6 None - 0 Bovine 6.4 pIC50 = 6.4 Binding
Concentration required to inhibit [125I]AII binding to Angiotensin II receptor from membrane fractions of bovine adrenal cortexConcentration required to inhibit [125I]AII binding to Angiotensin II receptor from membrane fractions of bovine adrenal cortex
ChEMBL 396 6 1 6 4.3 CCOc1nc2ccccc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81118-5
44323090 106074 0 None - 0 Rat 6.4 pIC50 = 6.4 Binding
Concentration required to inhibit binding of radioligand [125I]AII to angiotensin II receptor, type 1 in rat adrenal glomerulosa tissueConcentration required to inhibit binding of radioligand [125I]AII to angiotensin II receptor, type 1 in rat adrenal glomerulosa tissue
ChEMBL 454 8 2 6 5.0 CCCCc1nc(Cl)c(C(=O)O)n1Cc1ccc(C2=C(c3nn[nH]n3)CCCCC2)cc1 10.1021/jm00092a017
CHEMBL314220 106074 0 None - 0 Rat 6.4 pIC50 = 6.4 Binding
Concentration required to inhibit binding of radioligand [125I]AII to angiotensin II receptor, type 1 in rat adrenal glomerulosa tissueConcentration required to inhibit binding of radioligand [125I]AII to angiotensin II receptor, type 1 in rat adrenal glomerulosa tissue
ChEMBL 454 8 2 6 5.0 CCCCc1nc(Cl)c(C(=O)O)n1Cc1ccc(C2=C(c3nn[nH]n3)CCCCC2)cc1 10.1021/jm00092a017
127028620 136983 0 None - 0 Human 6.4 pIC50 = 6.4 Binding
Displacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptorDisplacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptor
ChEMBL 550 8 3 7 5.3 CCCc1nc2c(C)cc(C(=O)NC(C)(C)C)cc2n1Cc1ccc(-c2ccccc2C(=O)Nc2nnn[nH]2)cc1 10.1039/C5MD00169B
CHEMBL3754198 136983 0 None - 0 Human 6.4 pIC50 = 6.4 Binding
Displacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptorDisplacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptor
ChEMBL 550 8 3 7 5.3 CCCc1nc2c(C)cc(C(=O)NC(C)(C)C)cc2n1Cc1ccc(-c2ccccc2C(=O)Nc2nnn[nH]2)cc1 10.1039/C5MD00169B
135723837 101186 0 None - 0 Bovine 6.4 pIC50 = 6.4 Binding
Displacement of [125 I]-AII (0.2 nM) from bovine adrenal cortical membrane angiotensin II (AII) receptor at 10e-7 MDisplacement of [125 I]-AII (0.2 nM) from bovine adrenal cortical membrane angiotensin II (AII) receptor at 10e-7 M
ChEMBL 458 6 2 8 4.9 CSc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2noc(O)n2)cc1 10.1016/0960-894X(95)00319-O
CHEMBL299269 101186 0 None - 0 Bovine 6.4 pIC50 = 6.4 Binding
Displacement of [125 I]-AII (0.2 nM) from bovine adrenal cortical membrane angiotensin II (AII) receptor at 10e-7 MDisplacement of [125 I]-AII (0.2 nM) from bovine adrenal cortical membrane angiotensin II (AII) receptor at 10e-7 M
ChEMBL 458 6 2 8 4.9 CSc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2noc(O)n2)cc1 10.1016/0960-894X(95)00319-O
10027681 18688 0 None - 0 Rat 6.4 pIC50 = 6.4 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 469 12 2 4 7.4 CCCCCNc1ccc2nc(CCCC)n(Cc3ccc(-c4ccccc4C(=O)O)cc3)c2c1 10.1021/jm00077a007
CHEMBL128340 18688 0 None - 0 Rat 6.4 pIC50 = 6.4 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 469 12 2 4 7.4 CCCCCNc1ccc2nc(CCCC)n(Cc3ccc(-c4ccccc4C(=O)O)cc3)c2c1 10.1021/jm00077a007
54768876 64773 0 None - 0 Human 5.4 pIC50 = 5.4 Binding
Displacement of [125I][Sar1,Ile8]-AT-II from human recombinant AT1 receptor expressed in HEK293 cells after 120 mins by liquid scintillation countingDisplacement of [125I][Sar1,Ile8]-AT-II from human recombinant AT1 receptor expressed in HEK293 cells after 120 mins by liquid scintillation counting
ChEMBL 521 8 1 8 4.9 CCOC(=O)c1cn(Cc2ccc(-c3ccccc3-c3nnn[nH]3)cc2)nc1N(C(C)=O)c1ccc(C)cc1 10.1016/j.ejmech.2011.05.056
CHEMBL1824002 64773 0 None - 0 Human 5.4 pIC50 = 5.4 Binding
Displacement of [125I][Sar1,Ile8]-AT-II from human recombinant AT1 receptor expressed in HEK293 cells after 120 mins by liquid scintillation countingDisplacement of [125I][Sar1,Ile8]-AT-II from human recombinant AT1 receptor expressed in HEK293 cells after 120 mins by liquid scintillation counting
ChEMBL 521 8 1 8 4.9 CCOC(=O)c1cn(Cc2ccc(-c3ccccc3-c3nnn[nH]3)cc2)nc1N(C(C)=O)c1ccc(C)cc1 10.1016/j.ejmech.2011.05.056
15654745 202214 0 None - 0 Bovine 5.4 pIC50 = 5.4 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 452 7 2 6 5.1 CCC(C)c1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a016
CHEMBL69124 202214 0 None - 0 Bovine 5.4 pIC50 = 5.4 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 452 7 2 6 5.1 CCC(C)c1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a016
22850669 201288 0 None - 0 Rabbit 4.4 pIC50 = 4.4 Binding
Inhibition of angiotensin Angiotensin II receptor, type 1 in rabbit aorta using [125I-Sar1,Ile8] angiotensin II binding assayInhibition of angiotensin Angiotensin II receptor, type 1 in rabbit aorta using [125I-Sar1,Ile8] angiotensin II binding assay
ChEMBL 508 11 1 3 5.8 CCCCCN(CCCCC)C(=O)N1CCN(C(=O)N(c2ccccc2)c2ccccc2)[C@H](C(=O)O)C1 10.1016/S0960-894X(01)81007-6
CHEMBL63109 201288 0 None - 0 Rabbit 4.4 pIC50 = 4.4 Binding
Inhibition of angiotensin Angiotensin II receptor, type 1 in rabbit aorta using [125I-Sar1,Ile8] angiotensin II binding assayInhibition of angiotensin Angiotensin II receptor, type 1 in rabbit aorta using [125I-Sar1,Ile8] angiotensin II binding assay
ChEMBL 508 11 1 3 5.8 CCCCCN(CCCCC)C(=O)N1CCN(C(=O)N(c2ccccc2)c2ccccc2)[C@H](C(=O)O)C1 10.1016/S0960-894X(01)81007-6
44274734 90760 0 None - 0 Rabbit 8.4 pIC50 = 8.4 Binding
Ability to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitroAbility to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitro
ChEMBL 464 8 1 6 5.2 CCCCc1nc2ccc(CC)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80335-2
CHEMBL23994 90760 0 None - 0 Rabbit 8.4 pIC50 = 8.4 Binding
Ability to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitroAbility to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitro
ChEMBL 464 8 1 6 5.2 CCCCc1nc2ccc(CC)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80335-2
9955424 164561 0 None - 0 Rabbit 8.4 pIC50 = 8.4 Binding
Ability to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitroAbility to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitro
ChEMBL 450 7 1 6 4.9 CCCCc1nc2ccc(C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80335-2
CHEMBL422756 164561 0 None - 0 Rabbit 8.4 pIC50 = 8.4 Binding
Ability to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitroAbility to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitro
ChEMBL 450 7 1 6 4.9 CCCCc1nc2ccc(C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80335-2
10049809 112887 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 458 9 2 5 4.1 CCCCc1ncc(/C=C2/C(=O)NC(=O)N2Cc2ccccc2)n1Cc1ccc(C(=O)O)cc1 10.1007/s00044-009-9205-9
CHEMBL331859 112887 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 458 9 2 5 4.1 CCCCc1ncc(/C=C2/C(=O)NC(=O)N2Cc2ccccc2)n1Cc1ccc(C(=O)O)cc1 10.1007/s00044-009-9205-9
44274823 98605 0 None - 0 Rabbit 8.4 pIC50 = 8.4 Binding
Binding affinity against AT-1 receptor from rabbit aorta using [125I]-Sar1-Ile8-Ang II without BSABinding affinity against AT-1 receptor from rabbit aorta using [125I]-Sar1-Ile8-Ang II without BSA
ChEMBL 551 10 2 8 5.8 CCCCc1nc2ccc(NC(=O)OCC(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00073a024
CHEMBL280526 98605 0 None - 0 Rabbit 8.4 pIC50 = 8.4 Binding
Binding affinity against AT-1 receptor from rabbit aorta using [125I]-Sar1-Ile8-Ang II without BSABinding affinity against AT-1 receptor from rabbit aorta using [125I]-Sar1-Ile8-Ang II without BSA
ChEMBL 551 10 2 8 5.8 CCCCc1nc2ccc(NC(=O)OCC(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00073a024
44277677 98849 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Binding affinity against AT1 receptor in human adrenal tissueBinding affinity against AT1 receptor in human adrenal tissue
ChEMBL 585 9 1 9 5.5 CCCCN(C(=O)c1ccc(O)cc1)c1ccc2ncn(Cc3ccc(-c4ccccc4-c4nnnn4C)cc3)c(=O)c2c1 10.1016/0960-894X(95)00224-H
CHEMBL282168 98849 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Binding affinity against AT1 receptor in human adrenal tissueBinding affinity against AT1 receptor in human adrenal tissue
ChEMBL 585 9 1 9 5.5 CCCCN(C(=O)c1ccc(O)cc1)c1ccc2ncn(Cc3ccc(-c4ccccc4-c4nnnn4C)cc3)c(=O)c2c1 10.1016/0960-894X(95)00224-H
9955424 164561 0 None - 0 Rabbit 8.4 pIC50 = 8.4 Binding
Binding affinity against Angiotensin II type 1 Receptor in rabbit aortic tissueBinding affinity against Angiotensin II type 1 Receptor in rabbit aortic tissue
ChEMBL 450 7 1 6 4.9 CCCCc1nc2ccc(C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80334-0
CHEMBL422756 164561 0 None - 0 Rabbit 8.4 pIC50 = 8.4 Binding
Binding affinity against Angiotensin II type 1 Receptor in rabbit aortic tissueBinding affinity against Angiotensin II type 1 Receptor in rabbit aortic tissue
ChEMBL 450 7 1 6 4.9 CCCCc1nc2ccc(C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80334-0
19889336 178780 0 None - 0 Rat 8.4 pIC50 = 8.4 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 410 6 1 7 4.0 CCCc1nc2c(C)ccnc2n1Cc1ccc(-c2ccncc2-c2nn[nH]n2)cc1 10.1021/jm031100t
CHEMBL47382 178780 0 None - 0 Rat 8.4 pIC50 = 8.4 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 410 6 1 7 4.0 CCCc1nc2c(C)ccnc2n1Cc1ccc(-c2ccncc2-c2nn[nH]n2)cc1 10.1021/jm031100t
18950592 16596 0 None - 0 Rabbit 8.4 pIC50 = 8.4 Binding
Displacement of [1251][Sar1,IIe8]AII from rabbit aorta Angiotensin II receptor, type 1Displacement of [1251][Sar1,IIe8]AII from rabbit aorta Angiotensin II receptor, type 1
ChEMBL 513 11 1 5 7.1 CCCc1cc(Cn2c(CC)nc3c(C)cc(C)nc32)cc(CCC)c1OC(C(=O)O)c1ccc(C)cc1 10.1021/jm00075a033
CHEMBL124541 16596 0 None - 0 Rabbit 8.4 pIC50 = 8.4 Binding
Displacement of [1251][Sar1,IIe8]AII from rabbit aorta Angiotensin II receptor, type 1Displacement of [1251][Sar1,IIe8]AII from rabbit aorta Angiotensin II receptor, type 1
ChEMBL 513 11 1 5 7.1 CCCc1cc(Cn2c(CC)nc3c(C)cc(C)nc32)cc(CCC)c1OC(C(=O)O)c1ccc(C)cc1 10.1021/jm00075a033
44285370 138702 0 None - 0 Rat 8.4 pIC50 = 8.4 Binding
Displacement of [125I]- Ang II from type 1 Angiotensin II receptorDisplacement of [125I]- Ang II from type 1 Angiotensin II receptor
ChEMBL 388 6 1 5 3.9 CCCC1=NC(C)(C)C(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80526-6
CHEMBL37892 138702 0 None - 0 Rat 8.4 pIC50 = 8.4 Binding
Displacement of [125I]- Ang II from type 1 Angiotensin II receptorDisplacement of [125I]- Ang II from type 1 Angiotensin II receptor
ChEMBL 388 6 1 5 3.9 CCCC1=NC(C)(C)C(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80526-6
44209671 93156 0 None - 0 Rabbit 8.4 pIC50 = 8.4 Binding
Displacement of [125I]Sar1-Ile8-AII (without BSA) from type 1 Angiotensin II receptor of rabbit aortaDisplacement of [125I]Sar1-Ile8-AII (without BSA) from type 1 Angiotensin II receptor of rabbit aorta
ChEMBL 478 8 1 6 5.8 CCCCc1nc2ccc(C(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80335-2
CHEMBL24661 93156 0 None - 0 Rabbit 8.4 pIC50 = 8.4 Binding
Displacement of [125I]Sar1-Ile8-AII (without BSA) from type 1 Angiotensin II receptor of rabbit aortaDisplacement of [125I]Sar1-Ile8-AII (without BSA) from type 1 Angiotensin II receptor of rabbit aorta
ChEMBL 478 8 1 6 5.8 CCCCc1nc2ccc(C(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80335-2
19889336 178780 0 None - 0 Rabbit 8.4 pIC50 = 8.4 Binding
In vitro binding affinity towards Angiotensin II type 1-AT1 receptor determined as its ability to displace 125I-Sarl,Ile8-AII from the receptor expressed in rabbit aorta membrane.In vitro binding affinity towards Angiotensin II type 1-AT1 receptor determined as its ability to displace 125I-Sarl,Ile8-AII from the receptor expressed in rabbit aorta membrane.
ChEMBL 410 6 1 7 4.0 CCCc1nc2c(C)ccnc2n1Cc1ccc(-c2ccncc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80044-X
CHEMBL47382 178780 0 None - 0 Rabbit 8.4 pIC50 = 8.4 Binding
In vitro binding affinity towards Angiotensin II type 1-AT1 receptor determined as its ability to displace 125I-Sarl,Ile8-AII from the receptor expressed in rabbit aorta membrane.In vitro binding affinity towards Angiotensin II type 1-AT1 receptor determined as its ability to displace 125I-Sarl,Ile8-AII from the receptor expressed in rabbit aorta membrane.
ChEMBL 410 6 1 7 4.0 CCCc1nc2c(C)ccnc2n1Cc1ccc(-c2ccncc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80044-X
44379293 119771 0 None - 0 Rabbit 8.4 pIC50 = 8.4 Binding
In vitro displacement of 125I-[Sar1, Ile8] from AT1 receptors in rabbit aorta membraneIn vitro displacement of 125I-[Sar1, Ile8] from AT1 receptors in rabbit aorta membrane
ChEMBL 611 10 1 6 6.8 CCCCc1nc2ccc(C(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccc(F)cc2)cc1 10.1016/S0960-894X(01)81125-2
CHEMBL352639 119771 0 None - 0 Rabbit 8.4 pIC50 = 8.4 Binding
In vitro displacement of 125I-[Sar1, Ile8] from AT1 receptors in rabbit aorta membraneIn vitro displacement of 125I-[Sar1, Ile8] from AT1 receptors in rabbit aorta membrane
ChEMBL 611 10 1 6 6.8 CCCCc1nc2ccc(C(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccc(F)cc2)cc1 10.1016/S0960-894X(01)81125-2
44315350 104726 0 None - 0 Rabbit 8.4 pIC50 = 8.4 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membrane
ChEMBL 645 9 3 7 5.2 CCNC(=O)Nc1ccc2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)c4ccccc4F)cc3F)c(=O)c2c1 10.1016/0960-894X(94)85036-4
CHEMBL311484 104726 0 None - 0 Rabbit 8.4 pIC50 = 8.4 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of rabbit aorta membrane
ChEMBL 645 9 3 7 5.2 CCNC(=O)Nc1ccc2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)c4ccccc4F)cc3F)c(=O)c2c1 10.1016/0960-894X(94)85036-4
9895984 203031 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of rat adrenal membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of rat adrenal membrane
ChEMBL 661 13 2 8 6.5 CCCCOC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCCC)nc3ccc(NC(=O)N(C)C(C)C)cc3c2=O)cc1 10.1016/0960-894X(94)85036-4
CHEMBL74476 203031 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of rat adrenal membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of rat adrenal membrane
ChEMBL 661 13 2 8 6.5 CCCCOC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCCC)nc3ccc(NC(=O)N(C)C(C)C)cc3c2=O)cc1 10.1016/0960-894X(94)85036-4
44372686 96194 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Inhibition of Angiotensin II receptor, type 1Inhibition of Angiotensin II receptor, type 1
ChEMBL 600 4 2 7 6.2 CCCc1ccc2c(c1)-c1ccc(cc1)Cn1c(CCC)nc3ccc(cc3c1=O)NCCCCCCC(=O)NS2(=O)=O 10.1021/jm9504722
CHEMBL263714 96194 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Inhibition of Angiotensin II receptor, type 1Inhibition of Angiotensin II receptor, type 1
ChEMBL 600 4 2 7 6.2 CCCc1ccc2c(c1)-c1ccc(cc1)Cn1c(CCC)nc3ccc(cc3c1=O)NCCCCCCC(=O)NS2(=O)=O 10.1021/jm9504722
14950511 167830 0 None - 0 Guinea pig 8.4 pIC50 = 8.4 Binding
Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1
ChEMBL 475 8 1 6 5.6 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c(C(=O)c2ccccc2)c(C)n1 10.1021/jm00061a016
CHEMBL434768 167830 0 None - 0 Guinea pig 8.4 pIC50 = 8.4 Binding
Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1
ChEMBL 475 8 1 6 5.6 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c(C(=O)c2ccccc2)c(C)n1 10.1021/jm00061a016
10074895 18903 0 None - 0 Rat 8.4 pIC50 = 8.4 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 505 8 1 6 5.8 CCCCc1nc2ccc(N3CCCCC3=O)cc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00077a007
CHEMBL128922 18903 0 None - 0 Rat 8.4 pIC50 = 8.4 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 505 8 1 6 5.8 CCCCc1nc2ccc(N3CCCCC3=O)cc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00077a007
10074709 19313 0 None - 0 Rat 8.4 pIC50 = 8.4 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 500 7 1 5 7.0 CCCc1nc2c(C)cc(-c3cn4ccccc4n3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00077a007
CHEMBL129950 19313 0 None - 0 Rat 8.4 pIC50 = 8.4 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 500 7 1 5 7.0 CCCc1nc2c(C)cc(-c3cn4ccccc4n3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00077a007
10053393 49734 0 None - 0 Rabbit 8.4 pIC50 = 8.4 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 554 12 2 9 5.4 CCCCc1nnc(SCc2ccc(OC)cc2)n1Cc1ccc(NC(=O)c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-011-9756-4
CHEMBL156934 49734 0 None - 0 Rabbit 8.4 pIC50 = 8.4 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 554 12 2 9 5.4 CCCCc1nnc(SCc2ccc(OC)cc2)n1Cc1ccc(NC(=O)c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-011-9756-4
14956738 204074 0 None - 0 Rabbit 8.4 pIC50 = 8.4 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 465 8 1 7 4.6 CCCCc1nn(-c2ccccc2C)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
CHEMBL83180 204074 0 None - 0 Rabbit 8.4 pIC50 = 8.4 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 465 8 1 7 4.6 CCCCc1nn(-c2ccccc2C)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
10053393 49734 0 None - 0 Rabbit 8.4 pIC50 = 8.4 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 554 12 2 9 5.4 CCCCc1nnc(SCc2ccc(OC)cc2)n1Cc1ccc(NC(=O)c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
CHEMBL156934 49734 0 None - 0 Rabbit 8.4 pIC50 = 8.4 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 554 12 2 9 5.4 CCCCc1nnc(SCc2ccc(OC)cc2)n1Cc1ccc(NC(=O)c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
10026681 17742 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 448 10 2 7 3.1 CCCCc1ncc(/C=C2\C(=O)NC(=O)N2CCCC)n1Cc1ccc(-c2nn[nH]n2)cc1 10.1007/s00044-009-9205-9
CHEMBL125940 17742 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 448 10 2 7 3.1 CCCCc1ncc(/C=C2\C(=O)NC(=O)N2CCCC)n1Cc1ccc(-c2nn[nH]n2)cc1 10.1007/s00044-009-9205-9
10483597 162825 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 592 13 0 9 5.5 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2Cc2ccc(C(=O)OC)s2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
CHEMBL419421 162825 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 592 13 0 9 5.5 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2Cc2ccc(C(=O)OC)s2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
44320509 204605 0 None - 0 Rat 8.4 pIC50 = 8.4 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 465 6 2 6 5.5 CCCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2c(C(=O)O)c(N)nc3ccccc23)cc1 10.1021/jm031100t
CHEMBL87327 204605 0 None - 0 Rat 8.4 pIC50 = 8.4 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 465 6 2 6 5.5 CCCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2c(C(=O)O)c(N)nc3ccccc23)cc1 10.1021/jm031100t
9915892 103130 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
In vitro binding affinity of compound against Angiotensin II receptor, type 1In vitro binding affinity of compound against Angiotensin II receptor, type 1
ChEMBL 563 10 2 9 4.1 CCCc1nc(CN2CCN(c3ccccn3)CC2)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80076-1
CHEMBL308703 103130 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
In vitro binding affinity of compound against Angiotensin II receptor, type 1In vitro binding affinity of compound against Angiotensin II receptor, type 1
ChEMBL 563 10 2 9 4.1 CCCc1nc(CN2CCN(c3ccccn3)CC2)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80076-1
9915892 103130 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Inhibition of Angiotensin II receptor, type 1Inhibition of Angiotensin II receptor, type 1
ChEMBL 563 10 2 9 4.1 CCCc1nc(CN2CCN(c3ccccn3)CC2)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm9504722
CHEMBL308703 103130 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Inhibition of Angiotensin II receptor, type 1Inhibition of Angiotensin II receptor, type 1
ChEMBL 563 10 2 9 4.1 CCCc1nc(CN2CCN(c3ccccn3)CC2)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm9504722
71652858 88710 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Displacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysisDisplacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysis
ChEMBL 623 12 3 8 5.4 CCCCc1c[n+](Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c(CO)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.ejmech.2012.12.044
CHEMBL2337677 88710 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Displacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysisDisplacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysis
ChEMBL 623 12 3 8 5.4 CCCCc1c[n+](Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c(CO)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.ejmech.2012.12.044
CHEMBL2365958 88710 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Displacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysisDisplacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysis
ChEMBL 623 12 3 8 5.4 CCCCc1c[n+](Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c(CO)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.ejmech.2012.12.044
44275097 98861 0 None - 0 Rabbit 8.4 pIC50 = 8.4 Binding
Ability to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitroAbility to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitro
ChEMBL 585 10 2 8 6.4 CCCCc1nc2ccc(NC(=O)OCc3ccccc3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80335-2
CHEMBL282236 98861 0 None - 0 Rabbit 8.4 pIC50 = 8.4 Binding
Ability to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitroAbility to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitro
ChEMBL 585 10 2 8 6.4 CCCCc1nc2ccc(NC(=O)OCc3ccccc3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80335-2
57380414 70171 0 None - 1 Human 8.4 pIC50 = 8.4 Binding
Displacement of [125I]Sar1 Ile8-Ang 2 from angiotensin 2 AT1 receptor after 180 mins by gamma countingDisplacement of [125I]Sar1 Ile8-Ang 2 from angiotensin 2 AT1 receptor after 180 mins by gamma counting
ChEMBL 547 10 2 5 6.6 CCCc1nc2c(C)cc(C(=O)NCc3ccc(OC)cc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2012.01.009
CHEMBL1947131 70171 0 None - 1 Human 8.4 pIC50 = 8.4 Binding
Displacement of [125I]Sar1 Ile8-Ang 2 from angiotensin 2 AT1 receptor after 180 mins by gamma countingDisplacement of [125I]Sar1 Ile8-Ang 2 from angiotensin 2 AT1 receptor after 180 mins by gamma counting
ChEMBL 547 10 2 5 6.6 CCCc1nc2c(C)cc(C(=O)NCc3ccc(OC)cc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2012.01.009
19754062 102499 0 None - 0 Rabbit 8.4 pIC50 = 8.4 Binding
In vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranesIn vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranes
ChEMBL 604 13 3 7 5.9 CCCCNC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCC)nc3c(C)c(NC(=O)CCC)cnc32)cc1 10.1016/S0960-894X(01)81115-X
CHEMBL306641 102499 0 None - 0 Rabbit 8.4 pIC50 = 8.4 Binding
In vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranesIn vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranes
ChEMBL 604 13 3 7 5.9 CCCCNC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCC)nc3c(C)c(NC(=O)CCC)cnc32)cc1 10.1016/S0960-894X(01)81115-X
44377067 56254 0 None - 0 Rabbit 8.4 pIC50 = 8.4 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aortaIn vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aorta
ChEMBL 495 10 2 6 4.0 CCCc1nc(CC)c(C(=O)O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)C2CC2)cc1 10.1016/S0960-894X(01)81124-0
CHEMBL164059 56254 0 None - 0 Rabbit 8.4 pIC50 = 8.4 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aortaIn vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aorta
ChEMBL 495 10 2 6 4.0 CCCc1nc(CC)c(C(=O)O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)C2CC2)cc1 10.1016/S0960-894X(01)81124-0
10031920 107488 0 None - 0 Rabbit 8.4 pIC50 = 8.4 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 628 10 1 8 5.1 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)C2CCCO2)cc1 10.1021/jm00043a020
CHEMBL319404 107488 0 None - 0 Rabbit 8.4 pIC50 = 8.4 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 628 10 1 8 5.1 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)C2CCCO2)cc1 10.1021/jm00043a020
10078554 116454 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 715 12 2 9 6.2 CCCCC(=O)Nc1ccc(Br)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)C)cc3F)c2=O)c1 10.1021/jm00019a004
CHEMBL338687 116454 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 715 12 2 9 6.2 CCCCC(=O)Nc1ccc(Br)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)C)cc3F)c2=O)c1 10.1021/jm00019a004
44305424 102007 0 None - 0 Rat 8.4 pIC50 = 8.4 Binding
Tested for binding affinity against angiotensin II receptor in rat adrenal cortexTested for binding affinity against angiotensin II receptor in rat adrenal cortex
ChEMBL 388 6 2 6 2.4 CCCc1cc(=O)[nH]c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/0960-894X(95)00370-9
CHEMBL304032 102007 0 None - 0 Rat 8.4 pIC50 = 8.4 Binding
Tested for binding affinity against angiotensin II receptor in rat adrenal cortexTested for binding affinity against angiotensin II receptor in rat adrenal cortex
ChEMBL 388 6 2 6 2.4 CCCc1cc(=O)[nH]c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/0960-894X(95)00370-9
136093942 138551 0 None - 1 Rat 8.4 pIC50 = 8.4 Binding
Displacement of [125I]-Ang II from Angiotensin 2 type-1A receptor in rat vascular smooth muscle cells after 150 mins by gamma counting methodDisplacement of [125I]-Ang II from Angiotensin 2 type-1A receptor in rat vascular smooth muscle cells after 150 mins by gamma counting method
ChEMBL 436 8 1 6 4.8 CCCCc1nc(Cl)c(C=O)n1Cc1ccc(-c2ccccc2-c2noc(=O)[nH]2)cc1 10.1016/j.bmc.2016.03.028
CHEMBL3786570 138551 0 None - 1 Rat 8.4 pIC50 = 8.4 Binding
Displacement of [125I]-Ang II from Angiotensin 2 type-1A receptor in rat vascular smooth muscle cells after 150 mins by gamma counting methodDisplacement of [125I]-Ang II from Angiotensin 2 type-1A receptor in rat vascular smooth muscle cells after 150 mins by gamma counting method
ChEMBL 436 8 1 6 4.8 CCCCc1nc(Cl)c(C=O)n1Cc1ccc(-c2ccccc2-c2noc(=O)[nH]2)cc1 10.1016/j.bmc.2016.03.028
44277567 100914 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Binding affinity against AT1 receptor in human adrenal tissueBinding affinity against AT1 receptor in human adrenal tissue
ChEMBL 605 8 0 10 4.9 Cn1nnnc1-c1ccccc1-c1ccc(Cn2cnc3ccc(N(Cc4ccccn4)C(=O)c4ccncc4)cc3c2=O)cc1 10.1016/0960-894X(95)00224-H
CHEMBL29725 100914 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Binding affinity against AT1 receptor in human adrenal tissueBinding affinity against AT1 receptor in human adrenal tissue
ChEMBL 605 8 0 10 4.9 Cn1nnnc1-c1ccccc1-c1ccc(Cn2cnc3ccc(N(Cc4ccccn4)C(=O)c4ccncc4)cc3c2=O)cc1 10.1016/0960-894X(95)00224-H
44379184 57133 0 None - 0 Rabbit 8.4 pIC50 = 8.4 Binding
In vitro displacement of 125I-[Sar1, Ile8] from AT1 receptors in rabbit aorta membraneIn vitro displacement of 125I-[Sar1, Ile8] from AT1 receptors in rabbit aorta membrane
ChEMBL 602 14 2 7 5.9 CCCCc1nc2ccc(C(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)CCCCCN)cc1 10.1016/S0960-894X(01)81125-2
CHEMBL165541 57133 0 None - 0 Rabbit 8.4 pIC50 = 8.4 Binding
In vitro displacement of 125I-[Sar1, Ile8] from AT1 receptors in rabbit aorta membraneIn vitro displacement of 125I-[Sar1, Ile8] from AT1 receptors in rabbit aorta membrane
ChEMBL 602 14 2 7 5.9 CCCCc1nc2ccc(C(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)CCCCCN)cc1 10.1016/S0960-894X(01)81125-2
14951067 201792 0 None - 0 Rat 8.4 pIC50 = 8.4 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 489 12 1 9 3.6 CCCCc1nn(CCCCC(=O)OC)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a015
CHEMBL66173 201792 0 None - 0 Rat 8.4 pIC50 = 8.4 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 489 12 1 9 3.6 CCCCc1nn(CCCCC(=O)OC)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a015
44305680 102262 0 None - 0 Bovine 8.4 pIC50 = 8.4 Binding
Tested for binding affinity against angiotensin II receptor in rat adrenal cortexTested for binding affinity against angiotensin II receptor in rat adrenal cortex
ChEMBL 561 9 1 9 3.2 CCCc1cc(=O)n(CCN2C(=O)c3ccccc3C2=O)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/0960-894X(95)00370-9
CHEMBL305032 102262 0 None - 0 Bovine 8.4 pIC50 = 8.4 Binding
Tested for binding affinity against angiotensin II receptor in rat adrenal cortexTested for binding affinity against angiotensin II receptor in rat adrenal cortex
ChEMBL 561 9 1 9 3.2 CCCc1cc(=O)n(CCN2C(=O)c3ccccc3C2=O)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/0960-894X(95)00370-9
44277937 100931 0 None - 0 Rabbit 8.4 pIC50 = 8.4 Binding
Binding affinity against AT1 receptor in rabbit aortaBinding affinity against AT1 receptor in rabbit aorta
ChEMBL 584 10 0 9 5.5 CCCCCN(C(=O)c1cccnc1)c1ccc2ncn(Cc3ccc(-c4ccccc4-c4nnnn4C)cc3)c(=O)c2c1 10.1016/0960-894X(95)00224-H
CHEMBL29734 100931 0 None - 0 Rabbit 8.4 pIC50 = 8.4 Binding
Binding affinity against AT1 receptor in rabbit aortaBinding affinity against AT1 receptor in rabbit aorta
ChEMBL 584 10 0 9 5.5 CCCCCN(C(=O)c1cccnc1)c1ccc2ncn(Cc3ccc(-c4ccccc4-c4nnnn4C)cc3)c(=O)c2c1 10.1016/0960-894X(95)00224-H
44211708 100200 0 None - 0 Rat 8.4 pIC50 = 8.4 Binding
Tested for binding affinity against angiotensin II receptor in rat adrenal cortexTested for binding affinity against angiotensin II receptor in rat adrenal cortex
ChEMBL 416 7 1 7 2.8 CCCCc1cc(=O)n(C)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/0960-894X(95)00370-9
CHEMBL292316 100200 0 None - 0 Rat 8.4 pIC50 = 8.4 Binding
Tested for binding affinity against angiotensin II receptor in rat adrenal cortexTested for binding affinity against angiotensin II receptor in rat adrenal cortex
ChEMBL 416 7 1 7 2.8 CCCCc1cc(=O)n(C)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/0960-894X(95)00370-9
10183373 164447 0 None - 0 Rabbit 8.3 pIC50 = 8.3 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 465 9 1 7 4.3 CCCCc1nn(Cc2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
CHEMBL422593 164447 0 None - 0 Rabbit 8.3 pIC50 = 8.3 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 465 9 1 7 4.3 CCCCc1nn(Cc2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
44277420 100628 0 None - 0 Rabbit 8.3 pIC50 = 8.3 Binding
Binding affinity against AT1 receptor in rabbit aortaBinding affinity against AT1 receptor in rabbit aorta
ChEMBL 603 8 0 8 6.1 Cn1nnnc1-c1ccccc1-c1ccc(Cn2cnc3ccc(N(Cc4ccccc4)C(=O)c4ccccc4)cc3c2=O)cc1 10.1016/0960-894X(95)00224-H
CHEMBL29512 100628 0 None - 0 Rabbit 8.3 pIC50 = 8.3 Binding
Binding affinity against AT1 receptor in rabbit aortaBinding affinity against AT1 receptor in rabbit aorta
ChEMBL 603 8 0 8 6.1 Cn1nnnc1-c1ccccc1-c1ccc(Cn2cnc3ccc(N(Cc4ccccc4)C(=O)c4ccccc4)cc3c2=O)cc1 10.1016/0960-894X(95)00224-H
9847539 181447 0 None - 0 Rat 8.3 pIC50 = 8.3 Binding
In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.
ChEMBL 470 8 1 5 5.8 CCCCC1=NC(C)(C2CCCCC2)C(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81140-9
CHEMBL47810 181447 0 None - 0 Rat 8.3 pIC50 = 8.3 Binding
In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.
ChEMBL 470 8 1 5 5.8 CCCCC1=NC(C)(C2CCCCC2)C(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81140-9
44309701 102698 0 None - 0 Rabbit 8.3 pIC50 = 8.3 Binding
In vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranesIn vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranes
ChEMBL 609 11 2 7 6.3 CCCC(=O)Nc1cnc2c(nc(CCC)n2Cc2ccc(-c3ccccc3S(=O)(=O)NC(=O)c3ccccc3)cc2)c1C 10.1016/S0960-894X(01)81115-X
CHEMBL308238 102698 0 None - 0 Rabbit 8.3 pIC50 = 8.3 Binding
In vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranesIn vitro binding affinity determined by its ability to displace the specific binding ligand [125I]-Sar1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membranes
ChEMBL 609 11 2 7 6.3 CCCC(=O)Nc1cnc2c(nc(CCC)n2Cc2ccc(-c3ccccc3S(=O)(=O)NC(=O)c3ccccc3)cc2)c1C 10.1016/S0960-894X(01)81115-X
10349897 113916 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 715 10 2 9 6.3 CCCCC(=O)Nc1ccc(Br)c(-n2nc(C)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1021/jm00019a004
CHEMBL333224 113916 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 715 10 2 9 6.3 CCCCC(=O)Nc1ccc(Br)c(-n2nc(C)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1021/jm00019a004
10350123 57283 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Binding affinity to angiotensin AT1 receptorBinding affinity to angiotensin AT1 receptor
ChEMBL 713 12 1 9 6.0 CCCCc1nc2ccn(CC(=O)N3CCCCC3)c(=O)c2n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCc2ccccc2)cc1F 10.1016/j.bmc.2010.10.043
CHEMBL1668007 57283 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Binding affinity to angiotensin AT1 receptorBinding affinity to angiotensin AT1 receptor
ChEMBL 713 12 1 9 6.0 CCCCc1nc2ccn(CC(=O)N3CCCCC3)c(=O)c2n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCc2ccccc2)cc1F 10.1016/j.bmc.2010.10.043
10460346 205745 0 None - 0 Rabbit 8.3 pIC50 = 8.3 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 555 9 1 7 4.9 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC#N)cc1 10.1021/jm00043a020
CHEMBL94407 205745 0 None - 0 Rabbit 8.3 pIC50 = 8.3 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 555 9 1 7 4.9 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC#N)cc1 10.1021/jm00043a020
10007306 116669 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 534 12 0 7 5.7 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2Cc2ccsc2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
CHEMBL339404 116669 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 534 12 0 7 5.7 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2Cc2ccsc2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
10325483 16188 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 560 12 2 8 5.1 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2Cc2ccc(O)c(O)c2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
CHEMBL122982 16188 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 560 12 2 8 5.1 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2Cc2ccc(O)c(O)c2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
10478294 113598 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 438 10 2 5 3.9 CCCCc1ncc(/C=C2\C(=O)NC(=O)N2CCC(C)C)n1Cc1ccc(C(=O)O)cc1 10.1007/s00044-009-9205-9
CHEMBL332766 113598 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 438 10 2 5 3.9 CCCCc1ncc(/C=C2\C(=O)NC(=O)N2CCC(C)C)n1Cc1ccc(C(=O)O)cc1 10.1007/s00044-009-9205-9
14956794 204348 0 None - 0 Rabbit 8.3 pIC50 = 8.3 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 479 9 1 7 4.9 CCCCc1nn(C(C)c2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
CHEMBL85545 204348 0 None - 0 Rabbit 8.3 pIC50 = 8.3 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 479 9 1 7 4.9 CCCCc1nn(C(C)c2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
44338834 7761 0 None - 0 Rabbit 8.3 pIC50 = 8.3 Binding
Binding affinity against AT-1 receptor from rabbit aorta using [125I]-Sar1-Ile8-Ang II without BSABinding affinity against AT-1 receptor from rabbit aorta using [125I]-Sar1-Ile8-Ang II without BSA
ChEMBL 627 11 1 8 7.0 CCCc1nc2ccc(N(Cc3ccccc3)C(=O)OCC(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00073a024
CHEMBL108981 7761 0 None - 0 Rabbit 8.3 pIC50 = 8.3 Binding
Binding affinity against AT-1 receptor from rabbit aorta using [125I]-Sar1-Ile8-Ang II without BSABinding affinity against AT-1 receptor from rabbit aorta using [125I]-Sar1-Ile8-Ang II without BSA
ChEMBL 627 11 1 8 7.0 CCCc1nc2ccc(N(Cc3ccccc3)C(=O)OCC(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00073a024
44277871 99226 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Binding affinity against AT1 receptor in human adrenal tissueBinding affinity against AT1 receptor in human adrenal tissue
ChEMBL 599 10 1 9 5.8 CCCCCN(C(=O)c1ccc(O)cc1)c1ccc2ncn(Cc3ccc(-c4ccccc4-c4nnnn4C)cc3)c(=O)c2c1 10.1016/0960-894X(95)00224-H
CHEMBL28464 99226 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Binding affinity against AT1 receptor in human adrenal tissueBinding affinity against AT1 receptor in human adrenal tissue
ChEMBL 599 10 1 9 5.8 CCCCCN(C(=O)c1ccc(O)cc1)c1ccc2ncn(Cc3ccc(-c4ccccc4-c4nnnn4C)cc3)c(=O)c2c1 10.1016/0960-894X(95)00224-H
44277594 101320 0 None - 0 Rabbit 8.3 pIC50 = 8.3 Binding
Binding affinity against AT1 receptor in rabbit aortaBinding affinity against AT1 receptor in rabbit aorta
ChEMBL 619 8 1 9 5.9 Cn1nnnc1-c1ccccc1-c1ccc(Cn2cnc3ccc(N(Cc4ccc(O)cc4)C(=O)c4ccccc4)cc3c2=O)cc1 10.1016/0960-894X(95)00224-H
CHEMBL30015 101320 0 None - 0 Rabbit 8.3 pIC50 = 8.3 Binding
Binding affinity against AT1 receptor in rabbit aortaBinding affinity against AT1 receptor in rabbit aorta
ChEMBL 619 8 1 9 5.9 Cn1nnnc1-c1ccccc1-c1ccc(Cn2cnc3ccc(N(Cc4ccc(O)cc4)C(=O)c4ccccc4)cc3c2=O)cc1 10.1016/0960-894X(95)00224-H
9935096 206026 0 None - 1 Human 8.3 pIC50 = 8.3 Binding
Binding affinity to angiotensin AT1 receptorBinding affinity to angiotensin AT1 receptor
ChEMBL 485 8 1 7 5.3 CCCCc1cn([C@@H]2[C@@H](C)CCC[C@H]2C)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)nc1 10.1016/j.bmc.2010.10.043
CHEMBL9599 206026 0 None - 1 Human 8.3 pIC50 = 8.3 Binding
Binding affinity to angiotensin AT1 receptorBinding affinity to angiotensin AT1 receptor
ChEMBL 485 8 1 7 5.3 CCCCc1cn([C@@H]2[C@@H](C)CCC[C@H]2C)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)nc1 10.1016/j.bmc.2010.10.043
44338834 7761 0 None - 0 Rabbit 8.3 pIC50 = 8.3 Binding
Displacement of [125 I]Sar1Ile8-AII from type 1 Angiotensin II receptor of rabbit aorta membraneDisplacement of [125 I]Sar1Ile8-AII from type 1 Angiotensin II receptor of rabbit aorta membrane
ChEMBL 627 11 1 8 7.0 CCCc1nc2ccc(N(Cc3ccccc3)C(=O)OCC(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80517-5
CHEMBL108981 7761 0 None - 0 Rabbit 8.3 pIC50 = 8.3 Binding
Displacement of [125 I]Sar1Ile8-AII from type 1 Angiotensin II receptor of rabbit aorta membraneDisplacement of [125 I]Sar1Ile8-AII from type 1 Angiotensin II receptor of rabbit aorta membrane
ChEMBL 627 11 1 8 7.0 CCCc1nc2ccc(N(Cc3ccccc3)C(=O)OCC(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80517-5
73350991 92178 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Displacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysisDisplacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysis
ChEMBL 517 8 2 4 7.3 CCCc1nc2c(C)cc(NC(=O)c3ccc(C)cc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2013.08.014
CHEMBL2435826 92178 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Displacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysisDisplacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysis
ChEMBL 517 8 2 4 7.3 CCCc1nc2c(C)cc(NC(=O)c3ccc(C)cc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2013.08.014
10670376 171471 0 None - 0 Bovine 8.3 pIC50 = 8.3 Binding
In vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortexIn vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortex
ChEMBL 432 8 3 7 3.5 CCCc1nc(C(C)O)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm950450f
CHEMBL447182 171471 0 None - 0 Bovine 8.3 pIC50 = 8.3 Binding
In vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortexIn vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortex
ChEMBL 432 8 3 7 3.5 CCCc1nc(C(C)O)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm950450f
44294905 188550 0 None - 1 Bovine 7.4 pIC50 = 7.4 Binding
Ability to displace [125I]- labelled [Sar1,Ileu8] from angiotensin II receptor of bovine adrenal cortex membranesAbility to displace [125I]- labelled [Sar1,Ileu8] from angiotensin II receptor of bovine adrenal cortex membranes
ChEMBL 485 6 1 6 5.1 CCOC(=O)/C=C1\CC2(CCCCC2)CC(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80474-6
CHEMBL51084 188550 0 None - 1 Bovine 7.4 pIC50 = 7.4 Binding
Ability to displace [125I]- labelled [Sar1,Ileu8] from angiotensin II receptor of bovine adrenal cortex membranesAbility to displace [125I]- labelled [Sar1,Ileu8] from angiotensin II receptor of bovine adrenal cortex membranes
ChEMBL 485 6 1 6 5.1 CCOC(=O)/C=C1\CC2(CCCCC2)CC(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80474-6
76326259 84536 0 None - 0 Rabbit 7.4 pIC50 = 7.4 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 598 12 2 10 4.2 CCCCc1nnc([S+]([O-])Cc2ccccc2C(=O)OC)n1Cc1ccc(NC(=O)c2ccccc2-c2nnn[nH]2)cc1 10.1007/s00044-011-9756-4
CHEMBL2237606 84536 0 None - 0 Rabbit 7.4 pIC50 = 7.4 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 598 12 2 10 4.2 CCCCc1nnc([S+]([O-])Cc2ccccc2C(=O)OC)n1Cc1ccc(NC(=O)c2ccccc2-c2nnn[nH]2)cc1 10.1007/s00044-011-9756-4
44311429 202900 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 649 11 1 8 6.8 CCCc1nc(CC)c(C(=O)OCC#CC(=O)N(c2ccccc2)c2ccccc2)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80077-3
CHEMBL73369 202900 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 649 11 1 8 6.8 CCCc1nc(CC)c(C(=O)OCC#CC(=O)N(c2ccccc2)c2ccccc2)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80077-3
10053412 51033 0 None - 0 Rabbit 7.4 pIC50 = 7.4 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 555 11 1 9 4.6 CCCCc1nnc([S+]([O-])Cc2ccccc2C(=O)OC)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
CHEMBL158115 51033 0 None - 0 Rabbit 7.4 pIC50 = 7.4 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 555 11 1 9 4.6 CCCCc1nnc([S+]([O-])Cc2ccccc2C(=O)OC)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
1610 2305 89 None -1 4 Rabbit 7.4 pIC50 = 7.4 Binding
Displacement of [125I]Sar1,I1e8-AII from AT1 receptor in rabbit aorta membraneDisplacement of [125I]Sar1,I1e8-AII from AT1 receptor in rabbit aorta membrane
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1039/d2md00206j
3941 2305 89 None -1 4 Rabbit 7.4 pIC50 = 7.4 Binding
Displacement of [125I]Sar1,I1e8-AII from AT1 receptor in rabbit aorta membraneDisplacement of [125I]Sar1,I1e8-AII from AT1 receptor in rabbit aorta membrane
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1039/d2md00206j
3961 2305 89 None -1 4 Rabbit 7.4 pIC50 = 7.4 Binding
Displacement of [125I]Sar1,I1e8-AII from AT1 receptor in rabbit aorta membraneDisplacement of [125I]Sar1,I1e8-AII from AT1 receptor in rabbit aorta membrane
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1039/d2md00206j
590 2305 89 None -1 4 Rabbit 7.4 pIC50 = 7.4 Binding
Displacement of [125I]Sar1,I1e8-AII from AT1 receptor in rabbit aorta membraneDisplacement of [125I]Sar1,I1e8-AII from AT1 receptor in rabbit aorta membrane
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1039/d2md00206j
CHEMBL191 2305 89 None -1 4 Rabbit 7.4 pIC50 = 7.4 Binding
Displacement of [125I]Sar1,I1e8-AII from AT1 receptor in rabbit aorta membraneDisplacement of [125I]Sar1,I1e8-AII from AT1 receptor in rabbit aorta membrane
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1039/d2md00206j
DB00678 2305 89 None -1 4 Rabbit 7.4 pIC50 = 7.4 Binding
Displacement of [125I]Sar1,I1e8-AII from AT1 receptor in rabbit aorta membraneDisplacement of [125I]Sar1,I1e8-AII from AT1 receptor in rabbit aorta membrane
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1039/d2md00206j
9909335 117941 0 None - 0 Guinea pig 7.4 pIC50 = 7.4 Binding
In vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparationIn vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparation
ChEMBL 407 5 1 5 5.5 Cc1cc(OC(C)c2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2ccccc2n1 10.1021/jm00100a007
CHEMBL341223 117941 0 None - 0 Guinea pig 7.4 pIC50 = 7.4 Binding
In vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparationIn vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparation
ChEMBL 407 5 1 5 5.5 Cc1cc(OC(C)c2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2ccccc2n1 10.1021/jm00100a007
1610 2305 89 None -1 4 Rabbit 7.4 pIC50 = 7.4 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00043a020
3941 2305 89 None -1 4 Rabbit 7.4 pIC50 = 7.4 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00043a020
3961 2305 89 None -1 4 Rabbit 7.4 pIC50 = 7.4 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00043a020
590 2305 89 None -1 4 Rabbit 7.4 pIC50 = 7.4 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00043a020
CHEMBL191 2305 89 None -1 4 Rabbit 7.4 pIC50 = 7.4 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00043a020
DB00678 2305 89 None -1 4 Rabbit 7.4 pIC50 = 7.4 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00043a020
44305446 100270 0 None - 0 Bovine 7.4 pIC50 = 7.4 Binding
Tested for binding affinity against angiotensin II receptor in bovine adrenal cortexTested for binding affinity against angiotensin II receptor in bovine adrenal cortex
ChEMBL 473 9 2 8 2.0 CCCc1cc(=O)n(CCNC(C)=O)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/0960-894X(95)00370-9
CHEMBL292781 100270 0 None - 0 Bovine 7.4 pIC50 = 7.4 Binding
Tested for binding affinity against angiotensin II receptor in bovine adrenal cortexTested for binding affinity against angiotensin II receptor in bovine adrenal cortex
ChEMBL 473 9 2 8 2.0 CCCc1cc(=O)n(CCNC(C)=O)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/0960-894X(95)00370-9
10369479 117976 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 522 15 0 6 6.0 CCCCCCN1C(=O)N(CCCC)C(=O)/C1=C/c1cnc(CCCC)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
CHEMBL341456 117976 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 522 15 0 6 6.0 CCCCCCN1C(=O)N(CCCC)C(=O)/C1=C/c1cnc(CCCC)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
127035715 135904 0 None - 1 Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 545 10 2 4 7.2 CCCc1nc2c(C)cc(C(=O)NC[C@@H](C)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2015.09.010
CHEMBL3735652 135904 0 None - 1 Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 545 10 2 4 7.2 CCCc1nc2c(C)cc(C(=O)NC[C@@H](C)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2015.09.010
76326258 84533 0 None - 0 Rabbit 6.4 pIC50 = 6.4 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 480 9 2 9 2.5 CCCCc1nnc(S(C)(=O)=O)n1Cc1ccc(NC(=O)c2ccccc2-c2nnn[nH]2)cc1 10.1007/s00044-011-9756-4
CHEMBL2237603 84533 0 None - 0 Rabbit 6.4 pIC50 = 6.4 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 480 9 2 9 2.5 CCCCc1nnc(S(C)(=O)=O)n1Cc1ccc(NC(=O)c2ccccc2-c2nnn[nH]2)cc1 10.1007/s00044-011-9756-4
44323084 204767 0 None - 0 Rat 6.4 pIC50 = 6.4 Binding
Concentration required to inhibit binding of radioligand [125I]AII to angiotensin II receptor, type 1 in rat adrenal glomerulosa tissueConcentration required to inhibit binding of radioligand [125I]AII to angiotensin II receptor, type 1 in rat adrenal glomerulosa tissue
ChEMBL 440 8 2 6 4.6 CCCCc1nc(Cl)c(C(=O)O)n1Cc1ccc(C2=C(c3nn[nH]n3)CCCC2)cc1 10.1021/jm00092a017
CHEMBL88350 204767 0 None - 0 Rat 6.4 pIC50 = 6.4 Binding
Concentration required to inhibit binding of radioligand [125I]AII to angiotensin II receptor, type 1 in rat adrenal glomerulosa tissueConcentration required to inhibit binding of radioligand [125I]AII to angiotensin II receptor, type 1 in rat adrenal glomerulosa tissue
ChEMBL 440 8 2 6 4.6 CCCCc1nc(Cl)c(C(=O)O)n1Cc1ccc(C2=C(c3nn[nH]n3)CCCC2)cc1 10.1021/jm00092a017
10094614 48982 0 None - 0 Rabbit 6.4 pIC50 = 6.4 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 437 8 1 8 2.9 CCCCc1nnc(S(C)(=O)=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
CHEMBL156307 48982 0 None - 0 Rabbit 6.4 pIC50 = 6.4 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 437 8 1 8 2.9 CCCCc1nnc(S(C)(=O)=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
15144940 117636 0 None - 0 Rat 6.4 pIC50 = 6.4 Binding
Inhibition of [125I]angiotensin II receptor specific binding to rat mesenteric arteriesInhibition of [125I]angiotensin II receptor specific binding to rat mesenteric arteries
ChEMBL 453 10 1 5 5.5 CCCCc1ncc(/C=C(\Cc2ccc([N+](=O)[O-])cc2)C(=O)O)n1Cc1ccccc1Cl 10.1021/jm00099a013
CHEMBL340825 117636 0 None - 0 Rat 6.4 pIC50 = 6.4 Binding
Inhibition of [125I]angiotensin II receptor specific binding to rat mesenteric arteriesInhibition of [125I]angiotensin II receptor specific binding to rat mesenteric arteries
ChEMBL 453 10 1 5 5.5 CCCCc1ncc(/C=C(\Cc2ccc([N+](=O)[O-])cc2)C(=O)O)n1Cc1ccccc1Cl 10.1021/jm00099a013
4110026 203217 1 None - 1 Rat 6.4 pIC50 = 6.4 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 384 7 1 3 5.8 CCCCc1nc2ccccc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00077a007
CHEMBL7632 203217 1 None - 1 Rat 6.4 pIC50 = 6.4 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 384 7 1 3 5.8 CCCCc1nc2ccccc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00077a007
44298869 101126 0 None - 0 Bovine 5.4 pIC50 = 5.4 Binding
Binding affinity for angiotensin II receptor of bovine adrenal cortexBinding affinity for angiotensin II receptor of bovine adrenal cortex
ChEMBL 452 7 1 7 4.2 CCCOc1nc2cc(C)ccn2c(=O)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81144-6
CHEMBL298836 101126 0 None - 0 Bovine 5.4 pIC50 = 5.4 Binding
Binding affinity for angiotensin II receptor of bovine adrenal cortexBinding affinity for angiotensin II receptor of bovine adrenal cortex
ChEMBL 452 7 1 7 4.2 CCCOc1nc2cc(C)ccn2c(=O)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81144-6
44298545 194245 0 None - 0 Bovine 5.4 pIC50 = 5.4 Binding
Binding affinity for angiotensin II receptor of bovine adrenal cortexBinding affinity for angiotensin II receptor of bovine adrenal cortex
ChEMBL 466 7 1 7 4.5 Cc1ccc2nc(OCC(C)C)c(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c(=O)n2c1 10.1016/S0960-894X(01)81144-6
CHEMBL55939 194245 0 None - 0 Bovine 5.4 pIC50 = 5.4 Binding
Binding affinity for angiotensin II receptor of bovine adrenal cortexBinding affinity for angiotensin II receptor of bovine adrenal cortex
ChEMBL 466 7 1 7 4.5 Cc1ccc2nc(OCC(C)C)c(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c(=O)n2c1 10.1016/S0960-894X(01)81144-6
11167180 164860 0 None - 0 Rat 7.4 pIC50 = 7.4 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 464 7 1 5 6.4 CCCCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2c(C(=O)O)cnc3ccccc23)cc1 10.1021/jm031100t
CHEMBL423861 164860 0 None - 0 Rat 7.4 pIC50 = 7.4 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 464 7 1 5 6.4 CCCCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2c(C(=O)O)cnc3ccccc23)cc1 10.1021/jm031100t
71521300 86383 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor afterDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after
ChEMBL 519 6 1 7 5.7 CCc1nc2ccn(CC3CCCCC3)c(=O)c2n1[C@H]1CCc2cc(-c3ccccc3-c3nnn[nH]3)ccc21 10.1016/j.bmcl.2012.11.088
CHEMBL2322442 86383 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor afterDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after
ChEMBL 519 6 1 7 5.7 CCc1nc2ccn(CC3CCCCC3)c(=O)c2n1[C@H]1CCc2cc(-c3ccccc3-c3nnn[nH]3)ccc21 10.1016/j.bmcl.2012.11.088
44438872 168529 0 None - 1 Bovine 7.4 pIC50 = 7.4 Binding
Displacement of [125I]angiotensin-2 from bovine adrenal cortex AT1 receptorDisplacement of [125I]angiotensin-2 from bovine adrenal cortex AT1 receptor
ChEMBL 455 8 1 8 4.2 CCCc1nc2cccc(C(=O)OCC)c2n1Cc1ccc(-n2cccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2007.02.042
CHEMBL440051 168529 0 None - 1 Bovine 7.4 pIC50 = 7.4 Binding
Displacement of [125I]angiotensin-2 from bovine adrenal cortex AT1 receptorDisplacement of [125I]angiotensin-2 from bovine adrenal cortex AT1 receptor
ChEMBL 455 8 1 8 4.2 CCCc1nc2cccc(C(=O)OCC)c2n1Cc1ccc(-n2cccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2007.02.042
10391950 114601 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 520 12 1 9 3.2 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2Cc2nn[nH]n2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
CHEMBL334326 114601 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 520 12 1 9 3.2 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2Cc2nn[nH]n2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
44307258 201950 0 None - 0 Rabbit 6.4 pIC50 = 6.4 Binding
Binding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membraneBinding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane
ChEMBL 478 5 1 4 5.3 CCCCc1nc2ccc(C)cc2c(=O)n1Cc1cc(Br)c(O)c(Br)c1 10.1016/S0960-894X(01)81148-3
CHEMBL67309 201950 0 None - 0 Rabbit 6.4 pIC50 = 6.4 Binding
Binding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membraneBinding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane
ChEMBL 478 5 1 4 5.3 CCCCc1nc2ccc(C)cc2c(=O)n1Cc1cc(Br)c(O)c(Br)c1 10.1016/S0960-894X(01)81148-3
44341787 109281 0 None - 0 Rat 6.4 pIC50 = 6.4 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 416 5 1 3 5.3 O=C(O)c1ccccc1-c1ccc(CN2C(=O)C3(CCCC3)N=C2C2CCCC2)cc1 10.1021/jm00074a018
CHEMBL323244 109281 0 None - 0 Rat 6.4 pIC50 = 6.4 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 416 5 1 3 5.3 O=C(O)c1ccccc1-c1ccc(CN2C(=O)C3(CCCC3)N=C2C2CCCC2)cc1 10.1021/jm00074a018
15780094 99336 0 None - 0 Rabbit 6.4 pIC50 = 6.4 Binding
Displacement of [125 I]Sar1Ile8-AII from type 1 Angiotensin II receptor of rabbit aorta membraneDisplacement of [125 I]Sar1Ile8-AII from type 1 Angiotensin II receptor of rabbit aorta membrane
ChEMBL 651 9 1 7 7.4 CCc1nc2ccc(N(Cc3ccccc3Cl)C(=O)c3ccccc3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80517-5
CHEMBL285433 99336 0 None - 0 Rabbit 6.4 pIC50 = 6.4 Binding
Displacement of [125 I]Sar1Ile8-AII from type 1 Angiotensin II receptor of rabbit aorta membraneDisplacement of [125 I]Sar1Ile8-AII from type 1 Angiotensin II receptor of rabbit aorta membrane
ChEMBL 651 9 1 7 7.4 CCc1nc2ccc(N(Cc3ccccc3Cl)C(=O)c3ccccc3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80517-5
70684248 75910 0 None - 0 Human 6.4 pIC50 = 6.4 Binding
Displacement of [125I]Sar1Ile8-Ang2 from angiotensin AT1 receptor after 180 mins by gamma countingDisplacement of [125I]Sar1Ile8-Ang2 from angiotensin AT1 receptor after 180 mins by gamma counting
ChEMBL 541 9 2 6 6.1 CCCc1nc2c(C)cc(C(=O)NCc3ccccc3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmc.2012.05.056
CHEMBL2058588 75910 0 None - 0 Human 6.4 pIC50 = 6.4 Binding
Displacement of [125I]Sar1Ile8-Ang2 from angiotensin AT1 receptor after 180 mins by gamma countingDisplacement of [125I]Sar1Ile8-Ang2 from angiotensin AT1 receptor after 180 mins by gamma counting
ChEMBL 541 9 2 6 6.1 CCCc1nc2c(C)cc(C(=O)NCc3ccccc3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmc.2012.05.056
15699053 108306 0 None - 0 Rat 5.4 pIC50 = 5.4 Binding
Binding affinity against angiotensin II receptor in rat smooth muscle cell preparationsBinding affinity against angiotensin II receptor in rat smooth muscle cell preparations
ChEMBL 396 7 2 6 3.8 CCCCc1nc(Cl)c(CO)n1Cc1cccc2cc(-c3nn[nH]n3)ccc12 10.1021/jm00114a021
CHEMBL320951 108306 0 None - 0 Rat 5.4 pIC50 = 5.4 Binding
Binding affinity against angiotensin II receptor in rat smooth muscle cell preparationsBinding affinity against angiotensin II receptor in rat smooth muscle cell preparations
ChEMBL 396 7 2 6 3.8 CCCCc1nc(Cl)c(CO)n1Cc1cccc2cc(-c3nn[nH]n3)ccc12 10.1021/jm00114a021
71717082 88705 0 None - 0 Human 6.4 pIC50 = 6.4 Binding
Displacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysisDisplacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysis
ChEMBL 623 12 3 8 5.4 CCCCc1n(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c(CO)c[n+]1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.ejmech.2012.12.044
CHEMBL2337683 88705 0 None - 0 Human 6.4 pIC50 = 6.4 Binding
Displacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysisDisplacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysis
ChEMBL 623 12 3 8 5.4 CCCCc1n(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c(CO)c[n+]1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.ejmech.2012.12.044
CHEMBL2365904 88705 0 None - 0 Human 6.4 pIC50 = 6.4 Binding
Displacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysisDisplacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysis
ChEMBL 623 12 3 8 5.4 CCCCc1n(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c(CO)c[n+]1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.ejmech.2012.12.044
127035069 135863 0 None - 0 Human 6.4 pIC50 = 6.4 Binding
Displacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysisDisplacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysis
ChEMBL 663 11 2 8 7.7 CCCc1nc2c(C)cc(C(=O)Nc3ccccc3OC)cc2n1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)cc1 10.1039/C4MD00499J
CHEMBL3735300 135863 0 None - 0 Human 6.4 pIC50 = 6.4 Binding
Displacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysisDisplacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysis
ChEMBL 663 11 2 8 7.7 CCCc1nc2c(C)cc(C(=O)Nc3ccccc3OC)cc2n1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)cc1 10.1039/C4MD00499J
9985434 50013 0 None - 0 Rabbit 7.4 pIC50 = 7.4 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 568 11 2 6 6.9 CCCCc1nnc(SCc2ccc(C(F)(F)F)cc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
CHEMBL157185 50013 0 None - 0 Rabbit 7.4 pIC50 = 7.4 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 568 11 2 6 6.9 CCCCc1nnc(SCc2ccc(C(F)(F)F)cc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
127035379 135971 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Displacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysisDisplacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysis
ChEMBL 691 13 2 8 7.4 CCCc1nc2c(C)cc(C(=O)NCCc3cccc(OC)c3)cc2n1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)cc1 10.1039/C4MD00499J
CHEMBL3736248 135971 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Displacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysisDisplacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysis
ChEMBL 691 13 2 8 7.4 CCCc1nc2c(C)cc(C(=O)NCCc3cccc(OC)c3)cc2n1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)cc1 10.1039/C4MD00499J
135987614 100220 0 None - 0 Bovine 7.4 pIC50 = 7.4 Binding
Displacement of [125 I]-AII (0.2 nM) from bovine adrenal cortical membrane angiotensin II (AII) receptor at 10e-7 MDisplacement of [125 I]-AII (0.2 nM) from bovine adrenal cortical membrane angiotensin II (AII) receptor at 10e-7 M
ChEMBL 455 7 3 8 4.6 CCNc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2noc(O)n2)cc1 10.1016/0960-894X(95)00319-O
CHEMBL292430 100220 0 None - 0 Bovine 7.4 pIC50 = 7.4 Binding
Displacement of [125 I]-AII (0.2 nM) from bovine adrenal cortical membrane angiotensin II (AII) receptor at 10e-7 MDisplacement of [125 I]-AII (0.2 nM) from bovine adrenal cortical membrane angiotensin II (AII) receptor at 10e-7 M
ChEMBL 455 7 3 8 4.6 CCNc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2noc(O)n2)cc1 10.1016/0960-894X(95)00319-O
44283480 99989 0 None - 0 Rabbit 7.4 pIC50 = 7.4 Binding
Displacement of [125 I]Sar1Ile8-AII from type 1 Angiotensin II receptor of rabbit aorta membraneDisplacement of [125 I]Sar1Ile8-AII from type 1 Angiotensin II receptor of rabbit aorta membrane
ChEMBL 637 9 1 8 7.3 CC(C)c1nc2ccc(N(Cc3ccccc3)C(=O)c3cccs3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80517-5
CHEMBL290768 99989 0 None - 0 Rabbit 7.4 pIC50 = 7.4 Binding
Displacement of [125 I]Sar1Ile8-AII from type 1 Angiotensin II receptor of rabbit aorta membraneDisplacement of [125 I]Sar1Ile8-AII from type 1 Angiotensin II receptor of rabbit aorta membrane
ChEMBL 637 9 1 8 7.3 CC(C)c1nc2ccc(N(Cc3ccccc3)C(=O)c3cccs3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80517-5
9985434 50013 0 None - 0 Rabbit 7.4 pIC50 = 7.4 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 568 11 2 6 6.9 CCCCc1nnc(SCc2ccc(C(F)(F)F)cc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
CHEMBL157185 50013 0 None - 0 Rabbit 7.4 pIC50 = 7.4 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 568 11 2 6 6.9 CCCCc1nnc(SCc2ccc(C(F)(F)F)cc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
44297114 101318 0 None - 0 Bovine 7.4 pIC50 = 7.4 Binding
In vitro binding affinity to angiotensin II receptor in bovine adrenal cortexIn vitro binding affinity to angiotensin II receptor in bovine adrenal cortex
ChEMBL 561 8 1 8 5.9 CCCCc1nc2ccc([C@@H]3C[C@H]4CCCCN3O4)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80377-2
CHEMBL300105 101318 0 None - 0 Bovine 7.4 pIC50 = 7.4 Binding
In vitro binding affinity to angiotensin II receptor in bovine adrenal cortexIn vitro binding affinity to angiotensin II receptor in bovine adrenal cortex
ChEMBL 561 8 1 8 5.9 CCCCc1nc2ccc([C@@H]3C[C@H]4CCCCN3O4)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80377-2
44297216 186229 0 None - 0 Bovine 7.4 pIC50 = 7.4 Binding
In vitro binding affinity to angiotensin II receptor in bovine adrenal cortexIn vitro binding affinity to angiotensin II receptor in bovine adrenal cortex
ChEMBL 575 8 1 9 4.9 CCCCc1nc2ccc([C@@H]3[C@@H]4C(=O)CC[C@@H]4ON3C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80377-2
CHEMBL48934 186229 0 None - 0 Bovine 7.4 pIC50 = 7.4 Binding
In vitro binding affinity to angiotensin II receptor in bovine adrenal cortexIn vitro binding affinity to angiotensin II receptor in bovine adrenal cortex
ChEMBL 575 8 1 9 4.9 CCCCc1nc2ccc([C@@H]3[C@@H]4C(=O)CC[C@@H]4ON3C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80377-2
14956775 202274 0 None - 0 Rat 7.4 pIC50 = 7.4 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 375 7 2 7 3.2 CCCCc1nnc(O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a015
CHEMBL69508 202274 0 None - 0 Rat 7.4 pIC50 = 7.4 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 375 7 2 7 3.2 CCCCc1nnc(O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a015
15287883 97745 0 None - 0 Rabbit 7.4 pIC50 = 7.4 Binding
Tested in vitro for Angiotensin II receptor, type 1 binding affinity using rabbit aorta binding assayTested in vitro for Angiotensin II receptor, type 1 binding affinity using rabbit aorta binding assay
ChEMBL 415 8 1 5 4.9 CCCc1nc2c(C)ccnc2n1Cc1ccc(OC(C(=O)O)c2ccccc2)cc1 10.1016/0960-894X(94)00476-V
CHEMBL274260 97745 0 None - 0 Rabbit 7.4 pIC50 = 7.4 Binding
Tested in vitro for Angiotensin II receptor, type 1 binding affinity using rabbit aorta binding assayTested in vitro for Angiotensin II receptor, type 1 binding affinity using rabbit aorta binding assay
ChEMBL 415 8 1 5 4.9 CCCc1nc2c(C)ccnc2n1Cc1ccc(OC(C(=O)O)c2ccccc2)cc1 10.1016/0960-894X(94)00476-V
71654382 88701 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysisDisplacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysis
ChEMBL 701 12 3 8 6.2 CCCCc1c(Br)[n+](Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c(CO)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.ejmech.2012.12.044
CHEMBL2337681 88701 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysisDisplacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysis
ChEMBL 701 12 3 8 6.2 CCCCc1c(Br)[n+](Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c(CO)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.ejmech.2012.12.044
CHEMBL2365830 88701 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysisDisplacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysis
ChEMBL 701 12 3 8 6.2 CCCCc1c(Br)[n+](Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c(CO)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.ejmech.2012.12.044
1610 2305 89 None - 4 Bovine 6.4 pIC50 = 6.4 Binding
Ability to displace [125I]- labelled [Sar1,Ileu8] from angiotensin II receptor of bovine adrenal cortex membranesAbility to displace [125I]- labelled [Sar1,Ileu8] from angiotensin II receptor of bovine adrenal cortex membranes
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(00)80474-6
3941 2305 89 None - 4 Bovine 6.4 pIC50 = 6.4 Binding
Ability to displace [125I]- labelled [Sar1,Ileu8] from angiotensin II receptor of bovine adrenal cortex membranesAbility to displace [125I]- labelled [Sar1,Ileu8] from angiotensin II receptor of bovine adrenal cortex membranes
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(00)80474-6
3961 2305 89 None - 4 Bovine 6.4 pIC50 = 6.4 Binding
Ability to displace [125I]- labelled [Sar1,Ileu8] from angiotensin II receptor of bovine adrenal cortex membranesAbility to displace [125I]- labelled [Sar1,Ileu8] from angiotensin II receptor of bovine adrenal cortex membranes
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(00)80474-6
590 2305 89 None - 4 Bovine 6.4 pIC50 = 6.4 Binding
Ability to displace [125I]- labelled [Sar1,Ileu8] from angiotensin II receptor of bovine adrenal cortex membranesAbility to displace [125I]- labelled [Sar1,Ileu8] from angiotensin II receptor of bovine adrenal cortex membranes
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(00)80474-6
CHEMBL191 2305 89 None - 4 Bovine 6.4 pIC50 = 6.4 Binding
Ability to displace [125I]- labelled [Sar1,Ileu8] from angiotensin II receptor of bovine adrenal cortex membranesAbility to displace [125I]- labelled [Sar1,Ileu8] from angiotensin II receptor of bovine adrenal cortex membranes
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(00)80474-6
DB00678 2305 89 None - 4 Bovine 6.4 pIC50 = 6.4 Binding
Ability to displace [125I]- labelled [Sar1,Ileu8] from angiotensin II receptor of bovine adrenal cortex membranesAbility to displace [125I]- labelled [Sar1,Ileu8] from angiotensin II receptor of bovine adrenal cortex membranes
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(00)80474-6
135415867 554 89 None - 0 Bovine 6.4 pIC50 = 6.4 Binding
Displacement of [125 I]-AII (0.2 nM) from bovine adrenal cortical membrane angiotensin II (AII) receptor at 10e-7 MDisplacement of [125 I]-AII (0.2 nM) from bovine adrenal cortical membrane angiotensin II (AII) receptor at 10e-7 M
ChEMBL 456 7 2 7 4.2 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1[nH]oc(=O)n1)c(ccc2)C(=O)O 10.1016/0960-894X(95)00319-O
6901 554 89 None - 0 Bovine 6.4 pIC50 = 6.4 Binding
Displacement of [125 I]-AII (0.2 nM) from bovine adrenal cortical membrane angiotensin II (AII) receptor at 10e-7 MDisplacement of [125 I]-AII (0.2 nM) from bovine adrenal cortical membrane angiotensin II (AII) receptor at 10e-7 M
ChEMBL 456 7 2 7 4.2 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1[nH]oc(=O)n1)c(ccc2)C(=O)O 10.1016/0960-894X(95)00319-O
CHEMBL57242 554 89 None - 0 Bovine 6.4 pIC50 = 6.4 Binding
Displacement of [125 I]-AII (0.2 nM) from bovine adrenal cortical membrane angiotensin II (AII) receptor at 10e-7 MDisplacement of [125 I]-AII (0.2 nM) from bovine adrenal cortical membrane angiotensin II (AII) receptor at 10e-7 M
ChEMBL 456 7 2 7 4.2 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1[nH]oc(=O)n1)c(ccc2)C(=O)O 10.1016/0960-894X(95)00319-O
135487973 197459 0 None - 0 Bovine 6.4 pIC50 = 6.4 Binding
Displacement of [125 I]-AII (0.2 nM) from bovine adrenal cortical membrane angiotensin II (AII) receptor at 10e-7 MDisplacement of [125 I]-AII (0.2 nM) from bovine adrenal cortical membrane angiotensin II (AII) receptor at 10e-7 M
ChEMBL 454 7 2 7 5.2 CCCc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2noc(O)n2)cc1 10.1016/0960-894X(95)00319-O
CHEMBL58938 197459 0 None - 0 Bovine 6.4 pIC50 = 6.4 Binding
Displacement of [125 I]-AII (0.2 nM) from bovine adrenal cortical membrane angiotensin II (AII) receptor at 10e-7 MDisplacement of [125 I]-AII (0.2 nM) from bovine adrenal cortical membrane angiotensin II (AII) receptor at 10e-7 M
ChEMBL 454 7 2 7 5.2 CCCc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2noc(O)n2)cc1 10.1016/0960-894X(95)00319-O
11511750 96094 1 None - 0 Rabbit 6.4 pIC50 = 6.4 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 483 10 2 6 4.6 CCCCc1nc(Cl)c(CC(=O)OC)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
CHEMBL262958 96094 1 None - 0 Rabbit 6.4 pIC50 = 6.4 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 483 10 2 6 4.6 CCCCc1nc(Cl)c(CC(=O)OC)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
15698116 167164 0 None - 0 Rat 5.4 pIC50 = 5.4 Binding
Activity against high affinity Angiotensin II receptor, type 1 was measured from the ability to inhibit [125I]angiotensin II binding to rat uterine membrane.Activity against high affinity Angiotensin II receptor, type 1 was measured from the ability to inhibit [125I]angiotensin II binding to rat uterine membrane.
ChEMBL 388 8 2 5 4.4 CCCCc1nc(Cl)c(CO)n1Cc1ccc(-c2occc2C(=O)O)cc1 10.1021/jm00053a013
CHEMBL430279 167164 0 None - 0 Rat 5.4 pIC50 = 5.4 Binding
Activity against high affinity Angiotensin II receptor, type 1 was measured from the ability to inhibit [125I]angiotensin II binding to rat uterine membrane.Activity against high affinity Angiotensin II receptor, type 1 was measured from the ability to inhibit [125I]angiotensin II binding to rat uterine membrane.
ChEMBL 388 8 2 5 4.4 CCCCc1nc(Cl)c(CO)n1Cc1ccc(-c2occc2C(=O)O)cc1 10.1021/jm00053a013
1610 2305 89 None - 4 Bovine 6.4 pIC50 = 6.4 Binding
Concentration that gives 50% inhibition for binding of 125-I-[Sar1, IIe8] angiotensin to Angiotensin II receptor, type 1 in bovine adrenal cortex membrane.Concentration that gives 50% inhibition for binding of 125-I-[Sar1, IIe8] angiotensin to Angiotensin II receptor, type 1 in bovine adrenal cortex membrane.
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(01)80914-8
3941 2305 89 None - 4 Bovine 6.4 pIC50 = 6.4 Binding
Concentration that gives 50% inhibition for binding of 125-I-[Sar1, IIe8] angiotensin to Angiotensin II receptor, type 1 in bovine adrenal cortex membrane.Concentration that gives 50% inhibition for binding of 125-I-[Sar1, IIe8] angiotensin to Angiotensin II receptor, type 1 in bovine adrenal cortex membrane.
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(01)80914-8
3961 2305 89 None - 4 Bovine 6.4 pIC50 = 6.4 Binding
Concentration that gives 50% inhibition for binding of 125-I-[Sar1, IIe8] angiotensin to Angiotensin II receptor, type 1 in bovine adrenal cortex membrane.Concentration that gives 50% inhibition for binding of 125-I-[Sar1, IIe8] angiotensin to Angiotensin II receptor, type 1 in bovine adrenal cortex membrane.
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(01)80914-8
590 2305 89 None - 4 Bovine 6.4 pIC50 = 6.4 Binding
Concentration that gives 50% inhibition for binding of 125-I-[Sar1, IIe8] angiotensin to Angiotensin II receptor, type 1 in bovine adrenal cortex membrane.Concentration that gives 50% inhibition for binding of 125-I-[Sar1, IIe8] angiotensin to Angiotensin II receptor, type 1 in bovine adrenal cortex membrane.
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(01)80914-8
CHEMBL191 2305 89 None - 4 Bovine 6.4 pIC50 = 6.4 Binding
Concentration that gives 50% inhibition for binding of 125-I-[Sar1, IIe8] angiotensin to Angiotensin II receptor, type 1 in bovine adrenal cortex membrane.Concentration that gives 50% inhibition for binding of 125-I-[Sar1, IIe8] angiotensin to Angiotensin II receptor, type 1 in bovine adrenal cortex membrane.
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(01)80914-8
DB00678 2305 89 None - 4 Bovine 6.4 pIC50 = 6.4 Binding
Concentration that gives 50% inhibition for binding of 125-I-[Sar1, IIe8] angiotensin to Angiotensin II receptor, type 1 in bovine adrenal cortex membrane.Concentration that gives 50% inhibition for binding of 125-I-[Sar1, IIe8] angiotensin to Angiotensin II receptor, type 1 in bovine adrenal cortex membrane.
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(01)80914-8
24827903 95526 0 None - 0 Rat 6.4 pIC50 = 6.4 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
ChEMBL 477 7 1 7 4.7 CCCCn1c(=O)c2cc(F)c(Cl)nc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm7011563
CHEMBL259575 95526 0 None - 0 Rat 6.4 pIC50 = 6.4 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
ChEMBL 477 7 1 7 4.7 CCCCn1c(=O)c2cc(F)c(Cl)nc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm7011563
14956743 163542 0 None - 0 Rabbit 7.4 pIC50 = 7.4 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 496 9 1 9 4.2 CCCCc1nn(-c2cccc([N+](=O)[O-])c2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
CHEMBL420970 163542 0 None - 0 Rabbit 7.4 pIC50 = 7.4 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 496 9 1 9 4.2 CCCCc1nn(-c2cccc([N+](=O)[O-])c2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
44297046 167614 0 None - 0 Bovine 7.4 pIC50 = 7.4 Binding
In vitro binding affinity to angiotensin II receptor in bovine adrenal cortexIn vitro binding affinity to angiotensin II receptor in bovine adrenal cortex
ChEMBL 551 9 2 9 4.3 CCCCc1nc2ccc([C@H]3C[C@H](CO)ON3C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80377-2
CHEMBL433278 167614 0 None - 0 Bovine 7.4 pIC50 = 7.4 Binding
In vitro binding affinity to angiotensin II receptor in bovine adrenal cortexIn vitro binding affinity to angiotensin II receptor in bovine adrenal cortex
ChEMBL 551 9 2 9 4.3 CCCCc1nc2ccc([C@H]3C[C@H](CO)ON3C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80377-2
14951088 202239 0 None - 0 Rat 7.4 pIC50 = 7.4 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 521 10 1 8 4.9 CCCCc1nn(C(C)(C)C(=O)c2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a015
CHEMBL69296 202239 0 None - 0 Rat 7.4 pIC50 = 7.4 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 521 10 1 8 4.9 CCCCc1nn(C(C)(C)C(=O)c2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a015
130762 97782 9 None - 0 Guinea pig 6.4 pIC50 = 6.4 Binding
In vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparationIn vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparation
ChEMBL 398 8 2 4 4.8 CCCCc1nc(Cl)c(CO)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00100a007
CHEMBL274447 97782 9 None - 0 Guinea pig 6.4 pIC50 = 6.4 Binding
In vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparationIn vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparation
ChEMBL 398 8 2 4 4.8 CCCCc1nc(Cl)c(CO)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00100a007
3082918 94613 1 None - 0 Rat 4.4 pIC50 = 4.4 Binding
Inhibition of [125I]angiotensin II receptor specific binding to rat mesenteric arteriesInhibition of [125I]angiotensin II receptor specific binding to rat mesenteric arteries
ChEMBL 340 7 1 3 4.2 CCCCc1nc(Cl)c(CC(=O)O)n1Cc1ccccc1Cl 10.1021/jm00099a013
CHEMBL25528 94613 1 None - 0 Rat 4.4 pIC50 = 4.4 Binding
Inhibition of [125I]angiotensin II receptor specific binding to rat mesenteric arteriesInhibition of [125I]angiotensin II receptor specific binding to rat mesenteric arteries
ChEMBL 340 7 1 3 4.2 CCCCc1nc(Cl)c(CC(=O)O)n1Cc1ccccc1Cl 10.1021/jm00099a013
127028619 136957 0 None - 0 Human 6.4 pIC50 = 6.4 Binding
Displacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptorDisplacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptor
ChEMBL 550 11 3 7 5.3 CCCCNC(=O)c1cc(C)c2nc(CCC)n(Cc3ccc(-c4ccccc4C(=O)Nc4nnn[nH]4)cc3)c2c1 10.1039/C5MD00169B
CHEMBL3754010 136957 0 None - 0 Human 6.4 pIC50 = 6.4 Binding
Displacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptorDisplacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptor
ChEMBL 550 11 3 7 5.3 CCCCNC(=O)c1cc(C)c2nc(CCC)n(Cc3ccc(-c4ccccc4C(=O)Nc4nnn[nH]4)cc3)c2c1 10.1039/C5MD00169B
10478476 102559 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Compound was tested for inhibition against Angiotensin II receptor, type 1Compound was tested for inhibition against Angiotensin II receptor, type 1
ChEMBL 441 6 3 9 1.7 O=c1ccc2c(CO)nc(CO)nc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm0204237
CHEMBL307191 102559 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Compound was tested for inhibition against Angiotensin II receptor, type 1Compound was tested for inhibition against Angiotensin II receptor, type 1
ChEMBL 441 6 3 9 1.7 O=c1ccc2c(CO)nc(CO)nc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm0204237
44312700 203019 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Compound was tested for inhibition against Angiotensin II receptor, type 1Compound was tested for inhibition against Angiotensin II receptor, type 1
ChEMBL 457 6 3 8 2.0 O=C(O)c1nc(CO)nc2c1CCC(=O)N2Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm0204237
CHEMBL74347 203019 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Compound was tested for inhibition against Angiotensin II receptor, type 1Compound was tested for inhibition against Angiotensin II receptor, type 1
ChEMBL 457 6 3 8 2.0 O=C(O)c1nc(CO)nc2c1CCC(=O)N2Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm0204237
44301981 100147 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Compound was tested in vitro for inhibitory activity against human Angiotensin II receptor in cultured preadipocytesCompound was tested in vitro for inhibitory activity against human Angiotensin II receptor in cultured preadipocytes
ChEMBL 441 5 2 7 2.8 Cc1nc(C(=O)O)c2c(n1)N(Cc1ccc(-c3ccccc3-c3nn[nH]n3)cc1)C(=O)CC2 10.1016/s0960-894x(02)00303-7
CHEMBL291944 100147 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Compound was tested in vitro for inhibitory activity against human Angiotensin II receptor in cultured preadipocytesCompound was tested in vitro for inhibitory activity against human Angiotensin II receptor in cultured preadipocytes
ChEMBL 441 5 2 7 2.8 Cc1nc(C(=O)O)c2c(n1)N(Cc1ccc(-c3ccccc3-c3nn[nH]n3)cc1)C(=O)CC2 10.1016/s0960-894x(02)00303-7
10478476 102559 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Compound was tested in vitro for inhibitory activity against human Angiotensin II receptor in cultured preadipocytesCompound was tested in vitro for inhibitory activity against human Angiotensin II receptor in cultured preadipocytes
ChEMBL 441 6 3 9 1.7 O=c1ccc2c(CO)nc(CO)nc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/s0960-894x(02)00303-7
CHEMBL307191 102559 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Compound was tested in vitro for inhibitory activity against human Angiotensin II receptor in cultured preadipocytesCompound was tested in vitro for inhibitory activity against human Angiotensin II receptor in cultured preadipocytes
ChEMBL 441 6 3 9 1.7 O=c1ccc2c(CO)nc(CO)nc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/s0960-894x(02)00303-7
127026043 136815 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Displacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptorDisplacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptor
ChEMBL 607 11 3 9 3.8 CCCc1nc2c(C)cc(C(=O)NCCN3CCOCC3)cc2n1Cc1ccc(-c2ccccc2C(=O)Nc2nnn[nH]2)cc1 10.1039/C5MD00169B
CHEMBL3752947 136815 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Displacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptorDisplacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptor
ChEMBL 607 11 3 9 3.8 CCCc1nc2c(C)cc(C(=O)NCCN3CCOCC3)cc2n1Cc1ccc(-c2ccccc2C(=O)Nc2nnn[nH]2)cc1 10.1039/C5MD00169B
44300827 101284 0 None - 0 Rabbit 7.4 pIC50 = 7.4 Binding
Inhibition of Angiotensin II receptor type 1 in rabbit aorta binding assayInhibition of Angiotensin II receptor type 1 in rabbit aorta binding assay
ChEMBL 602 8 1 7 6.1 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2cc([Si](C)(C)C)sc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/S0960-894X(01)81145-8
CHEMBL299897 101284 0 None - 0 Rabbit 7.4 pIC50 = 7.4 Binding
Inhibition of Angiotensin II receptor type 1 in rabbit aorta binding assayInhibition of Angiotensin II receptor type 1 in rabbit aorta binding assay
ChEMBL 602 8 1 7 6.1 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2cc([Si](C)(C)C)sc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/S0960-894X(01)81145-8
44211708 100200 0 None - 0 Bovine 7.4 pIC50 = 7.4 Binding
Tested for binding affinity against angiotensin II receptor in bovine adrenal cortexTested for binding affinity against angiotensin II receptor in bovine adrenal cortex
ChEMBL 416 7 1 7 2.8 CCCCc1cc(=O)n(C)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/0960-894X(95)00370-9
CHEMBL292316 100200 0 None - 0 Bovine 7.4 pIC50 = 7.4 Binding
Tested for binding affinity against angiotensin II receptor in bovine adrenal cortexTested for binding affinity against angiotensin II receptor in bovine adrenal cortex
ChEMBL 416 7 1 7 2.8 CCCCc1cc(=O)n(C)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/0960-894X(95)00370-9
44307087 202070 0 None - 0 Rabbit 6.4 pIC50 = 6.4 Binding
Binding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membraneBinding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane
ChEMBL 401 6 1 5 5.1 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(Oc2ccccc2C(=O)O)cc1 10.1016/S0960-894X(01)81148-3
CHEMBL68111 202070 0 None - 0 Rabbit 6.4 pIC50 = 6.4 Binding
Binding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membraneBinding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane
ChEMBL 401 6 1 5 5.1 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(Oc2ccccc2C(=O)O)cc1 10.1016/S0960-894X(01)81148-3
9843116 112991 78 None - 0 Rat 6.4 pIC50 = 6.4 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 385 6 0 3 5.5 CCCCC1=NC2(CCCC2)C(=O)N1Cc1ccc(-c2ccccc2C#N)cc1 10.1021/jm00074a018
CHEMBL332051 112991 78 None - 0 Rat 6.4 pIC50 = 6.4 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 385 6 0 3 5.5 CCCCC1=NC2(CCCC2)C(=O)N1Cc1ccc(-c2ccccc2C#N)cc1 10.1021/jm00074a018
19792146 101419 0 None - 0 Bovine 6.4 pIC50 = 6.4 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 500 8 1 7 5.7 CCCCc1nc2cc(Cl)cc(C(=O)OC)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
CHEMBL300861 101419 0 None - 0 Bovine 6.4 pIC50 = 6.4 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 500 8 1 7 5.7 CCCCc1nc2cc(Cl)cc(C(=O)OC)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
15069407 189041 0 None - 0 Bovine 6.4 pIC50 = 6.4 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 466 8 1 7 5.1 CCCCc1nc2ccc(C(=O)OC)cc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
CHEMBL51508 189041 0 None - 0 Bovine 6.4 pIC50 = 6.4 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 466 8 1 7 5.1 CCCCc1nc2ccc(C(=O)OC)cc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
10047444 99870 0 None - 0 Rat 6.4 pIC50 = 6.4 Binding
Inhibition of [125I]angiotensin II receptor specific binding to rat mesenteric arteriesInhibition of [125I]angiotensin II receptor specific binding to rat mesenteric arteries
ChEMBL 414 9 1 4 5.7 CCCCc1ncc(/C=C(\Cc2cccs2)C(=O)O)n1Cc1ccccc1Cl 10.1021/jm00099a013
CHEMBL289543 99870 0 None - 0 Rat 6.4 pIC50 = 6.4 Binding
Inhibition of [125I]angiotensin II receptor specific binding to rat mesenteric arteriesInhibition of [125I]angiotensin II receptor specific binding to rat mesenteric arteries
ChEMBL 414 9 1 4 5.7 CCCCc1ncc(/C=C(\Cc2cccs2)C(=O)O)n1Cc1ccccc1Cl 10.1021/jm00099a013
15654700 163193 0 None - 0 Bovine 6.4 pIC50 = 6.4 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 470 7 1 8 4.8 CCSc1nc2cccc(C(=O)OC)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a016
CHEMBL420551 163193 0 None - 0 Bovine 6.4 pIC50 = 6.4 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 470 7 1 8 4.8 CCSc1nc2cccc(C(=O)OC)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a016
15654749 202124 0 None - 0 Bovine 6.4 pIC50 = 6.4 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 454 8 2 7 4.2 CCOCc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a016
CHEMBL68494 202124 0 None - 0 Bovine 6.4 pIC50 = 6.4 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 454 8 2 7 4.2 CCOCc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a016
14952903 193892 0 None - 0 Human 6.4 pIC50 = 6.4 Binding
Tested for binding affinity to Angiotensin II receptor, type 1Tested for binding affinity to Angiotensin II receptor, type 1
ChEMBL 380 9 1 4 5.0 CCCCc1ncc(/C=C(\Cc2cccs2)C(=O)O)n1Cc1ccccc1 10.1016/S0960-894X(01)81116-1
CHEMBL55508 193892 0 None - 0 Human 6.4 pIC50 = 6.4 Binding
Tested for binding affinity to Angiotensin II receptor, type 1Tested for binding affinity to Angiotensin II receptor, type 1
ChEMBL 380 9 1 4 5.0 CCCCc1ncc(/C=C(\Cc2cccs2)C(=O)O)n1Cc1ccccc1 10.1016/S0960-894X(01)81116-1
15069407 189041 0 None - 0 Bovine 6.4 pIC50 = 6.4 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 466 8 1 7 5.1 CCCCc1nc2ccc(C(=O)OC)cc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
CHEMBL51508 189041 0 None - 0 Bovine 6.4 pIC50 = 6.4 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 466 8 1 7 5.1 CCCCc1nc2ccc(C(=O)OC)cc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
19792146 101419 0 None - 0 Bovine 6.4 pIC50 = 6.4 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 500 8 1 7 5.7 CCCCc1nc2cc(Cl)cc(C(=O)OC)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
CHEMBL300861 101419 0 None - 0 Bovine 6.4 pIC50 = 6.4 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 500 8 1 7 5.7 CCCCc1nc2cc(Cl)cc(C(=O)OC)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
44298808 101499 0 None - 0 Bovine 5.4 pIC50 = 5.4 Binding
Binding affinity for angiotensin II receptor of bovine adrenal cortexBinding affinity for angiotensin II receptor of bovine adrenal cortex
ChEMBL 424 6 1 7 3.5 CCOc1nc2ccccn2c(=O)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81144-6
CHEMBL301479 101499 0 None - 0 Bovine 5.4 pIC50 = 5.4 Binding
Binding affinity for angiotensin II receptor of bovine adrenal cortexBinding affinity for angiotensin II receptor of bovine adrenal cortex
ChEMBL 424 6 1 7 3.5 CCOc1nc2ccccn2c(=O)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81144-6
10255888 76268 0 None - 0 Human 6.4 pIC50 = 6.4 Binding
Displacement of 125[I-Sar1-Ile8]ANG II from human AT1 receptor expressed in HEK293 membranes after 1 hr by gamma countingDisplacement of 125[I-Sar1-Ile8]ANG II from human AT1 receptor expressed in HEK293 membranes after 1 hr by gamma counting
ChEMBL 514 8 2 6 4.2 CCCCc1c(I)nc(CO)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.ejmech.2012.07.040
CHEMBL2063982 76268 0 None - 0 Human 6.4 pIC50 = 6.4 Binding
Displacement of 125[I-Sar1-Ile8]ANG II from human AT1 receptor expressed in HEK293 membranes after 1 hr by gamma countingDisplacement of 125[I-Sar1-Ile8]ANG II from human AT1 receptor expressed in HEK293 membranes after 1 hr by gamma counting
ChEMBL 514 8 2 6 4.2 CCCCc1c(I)nc(CO)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.ejmech.2012.07.040
10255888 76268 0 None - 0 Human 6.4 pIC50 = 6.4 Binding
Displacement of 125[I-Sar1-Ile8]ANG II from human AT1 receptor expressed in HEK293 membranes after 1 hr by gamma countingDisplacement of 125[I-Sar1-Ile8]ANG II from human AT1 receptor expressed in HEK293 membranes after 1 hr by gamma counting
ChEMBL 514 8 2 6 4.2 CCCCc1c(I)nc(CO)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.ejmech.2012.07.040
CHEMBL2063982 76268 0 None - 0 Human 6.4 pIC50 = 6.4 Binding
Displacement of 125[I-Sar1-Ile8]ANG II from human AT1 receptor expressed in HEK293 membranes after 1 hr by gamma countingDisplacement of 125[I-Sar1-Ile8]ANG II from human AT1 receptor expressed in HEK293 membranes after 1 hr by gamma counting
ChEMBL 514 8 2 6 4.2 CCCCc1c(I)nc(CO)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.ejmech.2012.07.040
44210836 56200 0 None - 0 Rabbit 7.4 pIC50 = 7.4 Binding
Binding affinity to Angiotensin II receptor, type 1 in rabbit aorta binding assayBinding affinity to Angiotensin II receptor, type 1 in rabbit aorta binding assay
ChEMBL 453 6 1 8 3.9 CCCc1nc2c(C)ccnc2n1Cc1ccc2c(c1)OC(c1ccccc1)(c1nn[nH]n1)O2 10.1016/S0960-894X(01)80193-1
CHEMBL163523 56200 0 None - 0 Rabbit 7.4 pIC50 = 7.4 Binding
Binding affinity to Angiotensin II receptor, type 1 in rabbit aorta binding assayBinding affinity to Angiotensin II receptor, type 1 in rabbit aorta binding assay
ChEMBL 453 6 1 8 3.9 CCCc1nc2c(C)ccnc2n1Cc1ccc2c(c1)OC(c1ccccc1)(c1nn[nH]n1)O2 10.1016/S0960-894X(01)80193-1
70694736 75845 0 None - 0 Bovine 7.4 pIC50 = 7.4 Binding
Displacement of [125I]AngII from type 1 angiotensin 2 receptor in bovine adrenal cortexDisplacement of [125I]AngII from type 1 angiotensin 2 receptor in bovine adrenal cortex
ChEMBL 472 6 1 6 5.5 Cc1noc(NS(=O)(=O)c2ccccc2-c2ccc(Cn3c(C)nc4ccccc43)cc2)c1C 10.1016/j.bmc.2012.06.011
CHEMBL2058367 75845 0 None - 0 Bovine 7.4 pIC50 = 7.4 Binding
Displacement of [125I]AngII from type 1 angiotensin 2 receptor in bovine adrenal cortexDisplacement of [125I]AngII from type 1 angiotensin 2 receptor in bovine adrenal cortex
ChEMBL 472 6 1 6 5.5 Cc1noc(NS(=O)(=O)c2ccccc2-c2ccc(Cn3c(C)nc4ccccc43)cc2)c1C 10.1016/j.bmc.2012.06.011
14951085 102699 0 None - 0 Rat 7.4 pIC50 = 7.4 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 537 13 1 8 5.5 CCCCc1nn(CC(OCCC)c2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a015
CHEMBL308239 102699 0 None - 0 Rat 7.4 pIC50 = 7.4 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 537 13 1 8 5.5 CCCCc1nn(CC(OCCC)c2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a015
71521506 86365 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor afterDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after
ChEMBL 514 6 1 8 4.6 CCc1nc2ccn(Cc3cccnc3)c(=O)c2n1[C@H]1CCc2cc(-c3ccccc3-c3nnn[nH]3)ccc21 10.1016/j.bmcl.2012.11.088
CHEMBL2322172 86365 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor afterDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after
ChEMBL 514 6 1 8 4.6 CCc1nc2ccn(Cc3cccnc3)c(=O)c2n1[C@H]1CCc2cc(-c3ccccc3-c3nnn[nH]3)ccc21 10.1016/j.bmcl.2012.11.088
19792159 192667 0 None - 0 Bovine 6.4 pIC50 = 6.4 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 438 8 2 6 4.8 CCCCc1nc2cccc(CO)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
CHEMBL52398 192667 0 None - 0 Bovine 6.4 pIC50 = 6.4 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 438 8 2 6 4.8 CCCCc1nc2cccc(CO)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
19792159 192667 0 None - 0 Bovine 6.4 pIC50 = 6.4 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 438 8 2 6 4.8 CCCCc1nc2cccc(CO)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
CHEMBL52398 192667 0 None - 0 Bovine 6.4 pIC50 = 6.4 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 438 8 2 6 4.8 CCCCc1nc2cccc(CO)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
44296550 188204 0 None - 0 Bovine 5.4 pIC50 = 5.4 Binding
Inhibition of [125l]-All binding to bovine adrenal cortexInhibition of [125l]-All binding to bovine adrenal cortex
ChEMBL 407 9 2 4 4.7 CCCc1cc(COC)c(C(=O)O)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/S0960-894X(01)81143-4
CHEMBL50592 188204 0 None - 0 Bovine 5.4 pIC50 = 5.4 Binding
Inhibition of [125l]-All binding to bovine adrenal cortexInhibition of [125l]-All binding to bovine adrenal cortex
ChEMBL 407 9 2 4 4.7 CCCc1cc(COC)c(C(=O)O)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/S0960-894X(01)81143-4
CHEMBL86558 204477 0 None - 0 Rat 4.4 pIC50 = 4.4 Binding
Displacement of [125-I]-labeled angiotensin II from Angiotensin II receptor, type 1 of rat uterine membranesDisplacement of [125-I]-labeled angiotensin II from Angiotensin II receptor, type 1 of rat uterine membranes
ChEMBL 414 8 1 5 4.7 CCCCN1N=C(CCC)/C(=C/c2ccc(-c3ccccc3-c3nn[nH]n3)cc2)C1=O 10.1016/S0960-894X(01)80290-0
10642524 9513 0 None - 0 Bovine 4.4 pIC50 = 4.4 Binding
In vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortexIn vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortex
ChEMBL 364 7 2 4 3.9 CCCc1nc(C(=O)O)cn1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm950450f
CHEMBL112637 9513 0 None - 0 Bovine 4.4 pIC50 = 4.4 Binding
In vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortexIn vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortex
ChEMBL 364 7 2 4 3.9 CCCc1nc(C(=O)O)cn1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm950450f
44303859 199296 0 None - 0 Rabbit 4.4 pIC50 = 4.4 Binding
Inhibition of Angiotensin II receptor, type 1 in rabbit aorta using [125I-Sar1,Ile8] angiotensin II binding assayInhibition of Angiotensin II receptor, type 1 in rabbit aorta using [125I-Sar1,Ile8] angiotensin II binding assay
ChEMBL 514 8 1 3 5.8 CCCCCN(C(=O)N1CCN(C(=O)N(c2ccccc2)c2ccccc2)C[C@H]1C(=O)O)c1ccccc1 10.1016/S0960-894X(01)81007-6
CHEMBL60209 199296 0 None - 0 Rabbit 4.4 pIC50 = 4.4 Binding
Inhibition of Angiotensin II receptor, type 1 in rabbit aorta using [125I-Sar1,Ile8] angiotensin II binding assayInhibition of Angiotensin II receptor, type 1 in rabbit aorta using [125I-Sar1,Ile8] angiotensin II binding assay
ChEMBL 514 8 1 3 5.8 CCCCCN(C(=O)N1CCN(C(=O)N(c2ccccc2)c2ccccc2)C[C@H]1C(=O)O)c1ccccc1 10.1016/S0960-894X(01)81007-6
15654716 103296 0 None - 0 Bovine 4.4 pIC50 = 4.4 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 440 7 2 7 4.0 CCOc1nc2c(C(=O)O)cccc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a016
CHEMBL308911 103296 0 None - 0 Bovine 4.4 pIC50 = 4.4 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 440 7 2 7 4.0 CCOc1nc2c(C(=O)O)cccc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a016
10047444 99870 0 None - 0 Human 5.3 pIC50 = 5.3 Binding
Tested for binding affinity to Angiotensin II receptor, type 1Tested for binding affinity to Angiotensin II receptor, type 1
ChEMBL 414 9 1 4 5.7 CCCCc1ncc(/C=C(\Cc2cccs2)C(=O)O)n1Cc1ccccc1Cl 10.1016/S0960-894X(01)81116-1
CHEMBL289543 99870 0 None - 0 Human 5.3 pIC50 = 5.3 Binding
Tested for binding affinity to Angiotensin II receptor, type 1Tested for binding affinity to Angiotensin II receptor, type 1
ChEMBL 414 9 1 4 5.7 CCCCc1ncc(/C=C(\Cc2cccs2)C(=O)O)n1Cc1ccccc1Cl 10.1016/S0960-894X(01)81116-1
9910561 9937 0 None - 0 Bovine 7.3 pIC50 = 7.3 Binding
In vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortexIn vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortex
ChEMBL 430 8 2 6 4.6 CCCc1nc(C(C)C)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm950450f
CHEMBL115206 9937 0 None - 0 Bovine 7.3 pIC50 = 7.3 Binding
In vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortexIn vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortex
ChEMBL 430 8 2 6 4.6 CCCc1nc(C(C)C)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm950450f
9867026 202221 0 None - 0 Bovine 7.3 pIC50 = 7.3 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 424 6 2 6 4.2 CCc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a016
CHEMBL69154 202221 0 None - 0 Bovine 7.3 pIC50 = 7.3 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 424 6 2 6 4.2 CCc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a016
10004855 116212 0 None - 0 Guinea pig 6.3 pIC50 = 6.3 Binding
In vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparationIn vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparation
ChEMBL 432 6 1 6 5.1 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2ccc(C#N)cc2n1 10.1021/jm00100a007
CHEMBL337380 116212 0 None - 0 Guinea pig 6.3 pIC50 = 6.3 Binding
In vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparationIn vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparation
ChEMBL 432 6 1 6 5.1 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2ccc(C#N)cc2n1 10.1021/jm00100a007
10094851 21082 0 None - 1 Rat 6.3 pIC50 = 6.3 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 441 8 2 4 5.8 CCCCc1nc2cc(NC(C)=O)ccc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00077a007
CHEMBL131365 21082 0 None - 1 Rat 6.3 pIC50 = 6.3 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 441 8 2 4 5.8 CCCCc1nc2cc(NC(C)=O)ccc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00077a007
15699075 5335 0 None - 0 Rat 5.3 pIC50 = 5.3 Binding
Binding affinity against angiotensin II receptor in rat smooth muscle cell preparationsBinding affinity against angiotensin II receptor in rat smooth muscle cell preparations
ChEMBL 390 7 2 4 4.0 CCCCc1nc(Cl)c(CO)n1Cc1ccc2c(c1)CCC(C)(C(=O)O)C2 10.1021/jm00114a021
CHEMBL107271 5335 0 None - 0 Rat 5.3 pIC50 = 5.3 Binding
Binding affinity against angiotensin II receptor in rat smooth muscle cell preparationsBinding affinity against angiotensin II receptor in rat smooth muscle cell preparations
ChEMBL 390 7 2 4 4.0 CCCCc1nc(Cl)c(CO)n1Cc1ccc2c(c1)CCC(C)(C(=O)O)C2 10.1021/jm00114a021
10621927 110360 0 None - 0 Bovine 5.3 pIC50 = 5.3 Binding
In vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortexIn vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortex
ChEMBL 418 8 3 7 2.9 CCCc1nc(C(=O)O)c(CO)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm950450f
CHEMBL326086 110360 0 None - 0 Bovine 5.3 pIC50 = 5.3 Binding
In vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortexIn vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortex
ChEMBL 418 8 3 7 2.9 CCCc1nc(C(=O)O)c(CO)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm950450f
10094965 18720 0 None - 0 Guinea pig 5.3 pIC50 = 5.3 Binding
In vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparationIn vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparation
ChEMBL 407 5 1 5 5.3 Cc1nc2ccccc2c(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c1C 10.1021/jm00100a007
CHEMBL128536 18720 0 None - 0 Guinea pig 5.3 pIC50 = 5.3 Binding
In vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparationIn vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparation
ChEMBL 407 5 1 5 5.3 Cc1nc2ccccc2c(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c1C 10.1021/jm00100a007
24828708 159182 0 None - 0 Rat 6.3 pIC50 = 6.3 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
ChEMBL 459 7 1 7 4.5 CCCCn1c2nc(Cl)ccc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm7011563
CHEMBL410487 159182 0 None - 0 Rat 6.3 pIC50 = 6.3 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
ChEMBL 459 7 1 7 4.5 CCCCn1c2nc(Cl)ccc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm7011563
127037496 135867 0 None - 0 Human 6.3 pIC50 = 6.3 Binding
Displacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysisDisplacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysis
ChEMBL 613 12 2 7 6.9 CCCCNC(=O)c1cc(C)c2nc(CCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)Nc4onc(C)c4C)cc3)c2c1 10.1039/C4MD00499J
CHEMBL3735311 135867 0 None - 0 Human 6.3 pIC50 = 6.3 Binding
Displacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysisDisplacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysis
ChEMBL 613 12 2 7 6.9 CCCCNC(=O)c1cc(C)c2nc(CCC)n(Cc3ccc(-c4ccccc4S(=O)(=O)Nc4onc(C)c4C)cc3)c2c1 10.1039/C4MD00499J
44341792 110083 0 None - 0 Rat 7.3 pIC50 = 7.3 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 420 7 1 4 4.5 CCCCC1=NC2(CCOCC2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00074a018
CHEMBL325445 110083 0 None - 0 Rat 7.3 pIC50 = 7.3 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 420 7 1 4 4.5 CCCCC1=NC2(CCOCC2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00074a018
127035067 135856 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysisDisplacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysis
ChEMBL 683 12 2 9 5.4 CCCc1nc2c(C)cc(C(=O)NCCN3CCN(C)CC3)cc2n1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)cc1 10.1039/C4MD00499J
CHEMBL3735236 135856 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysisDisplacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysis
ChEMBL 683 12 2 9 5.4 CCCc1nc2c(C)cc(C(=O)NCCN3CCN(C)CC3)cc2n1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)cc1 10.1039/C4MD00499J
10482340 17448 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 537 11 0 9 4.2 CCCCc1ncc(/C=C2/C(=O)N(COC)C(=O)N2Cc2csc(C)n2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
CHEMBL125835 17448 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 537 11 0 9 4.2 CCCCc1ncc(/C=C2/C(=O)N(COC)C(=O)N2Cc2csc(C)n2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
10325295 117662 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 551 12 1 9 4.0 CCCCc1ncc(/C=C2/C(=O)N(CCCO)C(=O)N2Cc2csc(C)n2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
CHEMBL340882 117662 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 551 12 1 9 4.0 CCCCc1ncc(/C=C2/C(=O)N(CCCO)C(=O)N2Cc2csc(C)n2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
44295090 101171 0 None - 1 Bovine 6.3 pIC50 = 6.3 Binding
Ability to displace [125I]- labelled [Sar1,Ileu8] from angiotensin II receptor of bovine adrenal cortex membranesAbility to displace [125I]- labelled [Sar1,Ileu8] from angiotensin II receptor of bovine adrenal cortex membranes
ChEMBL 487 9 1 6 5.3 CCCCC1(C)CC(=O)N(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/C(=C/C(=O)OCC)C1 10.1016/S0960-894X(00)80474-6
CHEMBL299151 101171 0 None - 1 Bovine 6.3 pIC50 = 6.3 Binding
Ability to displace [125I]- labelled [Sar1,Ileu8] from angiotensin II receptor of bovine adrenal cortex membranesAbility to displace [125I]- labelled [Sar1,Ileu8] from angiotensin II receptor of bovine adrenal cortex membranes
ChEMBL 487 9 1 6 5.3 CCCCC1(C)CC(=O)N(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/C(=C/C(=O)OCC)C1 10.1016/S0960-894X(00)80474-6
10343392 19939 0 None - 0 Guinea pig 6.3 pIC50 = 6.3 Binding
In vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparationIn vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparation
ChEMBL 407 5 1 5 5.3 Cc1ccc2nc(C)cc(OCc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c2c1 10.1021/jm00100a007
CHEMBL130455 19939 0 None - 0 Guinea pig 6.3 pIC50 = 6.3 Binding
In vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparationIn vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparation
ChEMBL 407 5 1 5 5.3 Cc1ccc2nc(C)cc(OCc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c2c1 10.1021/jm00100a007
44309268 202158 0 None - 0 Bovine 5.3 pIC50 = 5.3 Binding
Inhibition of [125I][Ile5]-AII binding to bovine adrenal cortex membrane Angiotensin II receptor type 1Inhibition of [125I][Ile5]-AII binding to bovine adrenal cortex membrane Angiotensin II receptor type 1
ChEMBL 308 5 1 3 4.8 CCCCc1nc2ccccc2n1Cc1cc(C)c(O)c(C)c1 10.1016/S0960-894X(01)81149-5
CHEMBL68713 202158 0 None - 0 Bovine 5.3 pIC50 = 5.3 Binding
Inhibition of [125I][Ile5]-AII binding to bovine adrenal cortex membrane Angiotensin II receptor type 1Inhibition of [125I][Ile5]-AII binding to bovine adrenal cortex membrane Angiotensin II receptor type 1
ChEMBL 308 5 1 3 4.8 CCCCc1nc2ccccc2n1Cc1cc(C)c(O)c(C)c1 10.1016/S0960-894X(01)81149-5
76329884 84534 0 None - 0 Rabbit 7.3 pIC50 = 7.3 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 590 11 2 9 4.7 CCCCc1nnc(S(=O)(=O)Cc2ccc(Cl)cc2)n1Cc1ccc(NC(=O)c2ccccc2-c2nnn[nH]2)cc1 10.1007/s00044-011-9756-4
CHEMBL2237604 84534 0 None - 0 Rabbit 7.3 pIC50 = 7.3 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 590 11 2 9 4.7 CCCCc1nnc(S(=O)(=O)Cc2ccc(Cl)cc2)n1Cc1ccc(NC(=O)c2ccccc2-c2nnn[nH]2)cc1 10.1007/s00044-011-9756-4
44210646 18899 0 None - 0 Bovine 7.3 pIC50 = 7.3 Binding
Concentration required to inhibit [125I]AII binding to Angiotensin II receptor from membrane fractions of bovine adrenal cortexConcentration required to inhibit [125I]AII binding to Angiotensin II receptor from membrane fractions of bovine adrenal cortex
ChEMBL 427 7 2 7 3.7 CCCc1cn2ncc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81118-5
CHEMBL128920 18899 0 None - 0 Bovine 7.3 pIC50 = 7.3 Binding
Concentration required to inhibit [125I]AII binding to Angiotensin II receptor from membrane fractions of bovine adrenal cortexConcentration required to inhibit [125I]AII binding to Angiotensin II receptor from membrane fractions of bovine adrenal cortex
ChEMBL 427 7 2 7 3.7 CCCc1cn2ncc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81118-5
10395045 119216 0 None - 0 Rabbit 7.3 pIC50 = 7.3 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 547 10 1 8 5.1 CCCCc1nnc(S(=O)(=O)Cc2ccc(Cl)cc2)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
CHEMBL347630 119216 0 None - 0 Rabbit 7.3 pIC50 = 7.3 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 547 10 1 8 5.1 CCCCc1nnc(S(=O)(=O)Cc2ccc(Cl)cc2)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
44317214 104267 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Tested for inhibition of Angiotensin II specific binding to Angiotensin II receptor, type 1 in the recombinant human AT-1 receptor expressed in LhAT-1D6 cellsTested for inhibition of Angiotensin II specific binding to Angiotensin II receptor, type 1 in the recombinant human AT-1 receptor expressed in LhAT-1D6 cells
ChEMBL 474 12 4 5 4.2 CCCCc1ncc(CN[C@@H](Cc2c[nH]c3ccccc23)C(=O)O)n1Cc1ccc(C(=O)O)cc1 10.1016/0960-894X(94)00456-P
CHEMBL310752 104267 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Tested for inhibition of Angiotensin II specific binding to Angiotensin II receptor, type 1 in the recombinant human AT-1 receptor expressed in LhAT-1D6 cellsTested for inhibition of Angiotensin II specific binding to Angiotensin II receptor, type 1 in the recombinant human AT-1 receptor expressed in LhAT-1D6 cells
ChEMBL 474 12 4 5 4.2 CCCCc1ncc(CN[C@@H](Cc2c[nH]c3ccccc23)C(=O)O)n1Cc1ccc(C(=O)O)cc1 10.1016/0960-894X(94)00456-P
10072403 16882 0 None - 0 Rat 6.3 pIC50 = 6.3 Binding
Activity against high affinity Angiotensin II receptor, type 1 was measured from the ability to inhibit [125I]angiotensin II binding to rat uterine membrane.Activity against high affinity Angiotensin II receptor, type 1 was measured from the ability to inhibit [125I]angiotensin II binding to rat uterine membrane.
ChEMBL 449 11 1 9 3.9 CCCCc1nc(CCCC)n(Cc2ccc(-n3cc([N+](=O)[O-])cc3-c3nn[nH]n3)cc2)n1 10.1021/jm00053a013
CHEMBL12548 16882 0 None - 0 Rat 6.3 pIC50 = 6.3 Binding
Activity against high affinity Angiotensin II receptor, type 1 was measured from the ability to inhibit [125I]angiotensin II binding to rat uterine membrane.Activity against high affinity Angiotensin II receptor, type 1 was measured from the ability to inhibit [125I]angiotensin II binding to rat uterine membrane.
ChEMBL 449 11 1 9 3.9 CCCCc1nc(CCCC)n(Cc2ccc(-n3cc([N+](=O)[O-])cc3-c3nn[nH]n3)cc2)n1 10.1021/jm00053a013
11744700 119163 0 None - 0 Rabbit 6.3 pIC50 = 6.3 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 454 11 3 7 3.7 CCCCc1nnc(SCCO)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
CHEMBL347234 119163 0 None - 0 Rabbit 6.3 pIC50 = 6.3 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 454 11 3 7 3.7 CCCCc1nnc(SCCO)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
44341608 110159 0 None - 0 Rat 6.3 pIC50 = 6.3 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 567 9 2 5 5.4 CCCCC1=NC2(CCN(C(=O)c3ccccc3C(=O)O)CC2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00074a018
CHEMBL325905 110159 0 None - 0 Rat 6.3 pIC50 = 6.3 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 567 9 2 5 5.4 CCCCC1=NC2(CCN(C(=O)c3ccccc3C(=O)O)CC2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00074a018
135723851 100343 0 None - 0 Bovine 6.3 pIC50 = 6.3 Binding
Displacement of [125 I]-AII (0.2 nM) from bovine adrenal cortical membrane angiotensin II (AII) receptor at 10e-7 MDisplacement of [125 I]-AII (0.2 nM) from bovine adrenal cortical membrane angiotensin II (AII) receptor at 10e-7 M
ChEMBL 472 7 2 8 5.3 CCSc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2noc(O)n2)cc1 10.1016/0960-894X(95)00319-O
CHEMBL293308 100343 0 None - 0 Bovine 6.3 pIC50 = 6.3 Binding
Displacement of [125 I]-AII (0.2 nM) from bovine adrenal cortical membrane angiotensin II (AII) receptor at 10e-7 MDisplacement of [125 I]-AII (0.2 nM) from bovine adrenal cortical membrane angiotensin II (AII) receptor at 10e-7 M
ChEMBL 472 7 2 8 5.3 CCSc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2noc(O)n2)cc1 10.1016/0960-894X(95)00319-O
11744700 119163 0 None - 0 Rabbit 6.3 pIC50 = 6.3 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 454 11 3 7 3.7 CCCCc1nnc(SCCO)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
CHEMBL347234 119163 0 None - 0 Rabbit 6.3 pIC50 = 6.3 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 454 11 3 7 3.7 CCCCc1nnc(SCCO)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
10408577 21599 0 None - 0 Rat 6.3 pIC50 = 6.3 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 398 7 1 3 6.1 CCCCc1nc2cccc(C)c2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00077a007
CHEMBL131948 21599 0 None - 0 Rat 6.3 pIC50 = 6.3 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 398 7 1 3 6.1 CCCCc1nc2cccc(C)c2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00077a007
10253216 50432 0 None - 0 Rabbit 5.3 pIC50 = 5.3 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 450 7 2 6 4.4 CCSc1nnc(C(F)(F)F)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
CHEMBL157597 50432 0 None - 0 Rabbit 5.3 pIC50 = 5.3 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 450 7 2 6 4.4 CCSc1nnc(C(F)(F)F)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
10253216 50432 0 None - 0 Rabbit 5.3 pIC50 = 5.3 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 450 7 2 6 4.4 CCSc1nnc(C(F)(F)F)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
CHEMBL157597 50432 0 None - 0 Rabbit 5.3 pIC50 = 5.3 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 450 7 2 6 4.4 CCSc1nnc(C(F)(F)F)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
127035392 135963 0 None - 0 Human 6.3 pIC50 = 6.3 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 563 10 2 5 7.4 CCSc1nc2c(C)cc(C(=O)NC[C@H](C)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2015.09.010
CHEMBL3736202 135963 0 None - 0 Human 6.3 pIC50 = 6.3 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 563 10 2 5 7.4 CCSc1nc2c(C)cc(C(=O)NC[C@H](C)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2015.09.010
11757293 119321 0 None - 0 Rabbit 7.3 pIC50 = 7.3 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 550 11 2 6 7.1 CCCCc1nnc(SCc2ccc3ccccc3c2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
CHEMBL348568 119321 0 None - 0 Rabbit 7.3 pIC50 = 7.3 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 550 11 2 6 7.1 CCCCc1nnc(SCc2ccc3ccccc3c2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
44341756 9852 0 None - 0 Rat 7.3 pIC50 = 7.3 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 523 8 1 4 5.7 CCCCC1=NC2(CCN(C(=O)c3ccccc3)CC2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00074a018
CHEMBL114720 9852 0 None - 0 Rat 7.3 pIC50 = 7.3 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 523 8 1 4 5.7 CCCCC1=NC2(CCN(C(=O)c3ccccc3)CC2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00074a018
11757293 119321 0 None - 0 Rabbit 7.3 pIC50 = 7.3 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 550 11 2 6 7.1 CCCCc1nnc(SCc2ccc3ccccc3c2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
CHEMBL348568 119321 0 None - 0 Rabbit 7.3 pIC50 = 7.3 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 550 11 2 6 7.1 CCCCc1nnc(SCc2ccc3ccccc3c2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
14956799 106403 0 None - 0 Rabbit 6.3 pIC50 = 6.3 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 509 10 2 8 4.0 CCCCc1nn(Cc2ccccc2C(=O)O)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
CHEMBL314590 106403 0 None - 0 Rabbit 6.3 pIC50 = 6.3 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 509 10 2 8 4.0 CCCCc1nn(Cc2ccccc2C(=O)O)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
130762 97782 9 None - 0 Bovine 6.3 pIC50 = 6.3 Binding
In vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortexIn vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortex
ChEMBL 398 8 2 4 4.8 CCCCc1nc(Cl)c(CO)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm950450f
CHEMBL274447 97782 9 None - 0 Bovine 6.3 pIC50 = 6.3 Binding
In vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortexIn vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortex
ChEMBL 398 8 2 4 4.8 CCCCc1nc(Cl)c(CO)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm950450f
130762 97782 9 None - 0 Bovine 6.3 pIC50 = 6.3 Binding
Inhibition of [125l]-All binding to bovine adrenal cortexInhibition of [125l]-All binding to bovine adrenal cortex
ChEMBL 398 8 2 4 4.8 CCCCc1nc(Cl)c(CO)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/S0960-894X(01)81143-4
CHEMBL274447 97782 9 None - 0 Bovine 6.3 pIC50 = 6.3 Binding
Inhibition of [125l]-All binding to bovine adrenal cortexInhibition of [125l]-All binding to bovine adrenal cortex
ChEMBL 398 8 2 4 4.8 CCCCc1nc(Cl)c(CO)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/S0960-894X(01)81143-4
15654730 202529 0 None - 0 Bovine 6.3 pIC50 = 6.3 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 440 6 1 8 3.7 COC(=O)c1cccc2nc(OC)n(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c12 10.1021/jm00067a016
CHEMBL71038 202529 0 None - 0 Bovine 6.3 pIC50 = 6.3 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 440 6 1 8 3.7 COC(=O)c1cccc2nc(OC)n(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c12 10.1021/jm00067a016
44298546 100216 0 None - 0 Bovine 5.3 pIC50 = 5.3 Binding
Binding affinity for angiotensin II receptor of bovine adrenal cortexBinding affinity for angiotensin II receptor of bovine adrenal cortex
ChEMBL 510 8 1 9 4.1 CCOC(=O)c1ccc2nc(OC(C)C)c(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c(=O)n2c1 10.1016/S0960-894X(01)81144-6
CHEMBL292412 100216 0 None - 0 Bovine 5.3 pIC50 = 5.3 Binding
Binding affinity for angiotensin II receptor of bovine adrenal cortexBinding affinity for angiotensin II receptor of bovine adrenal cortex
ChEMBL 510 8 1 9 4.1 CCOC(=O)c1ccc2nc(OC(C)C)c(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c(=O)n2c1 10.1016/S0960-894X(01)81144-6
11785963 204110 0 None - 0 Rat 6.3 pIC50 = 6.3 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 535 10 1 6 7.2 CCCN(CCC)c1nc2ccccc2c(-c2ccc(Cn3c(CC)nc4c(C)cc(C)nc43)cc2)c1C(=O)O 10.1021/jm031100t
CHEMBL83452 204110 0 None - 0 Rat 6.3 pIC50 = 6.3 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 535 10 1 6 7.2 CCCN(CCC)c1nc2ccccc2c(-c2ccc(Cn3c(CC)nc4c(C)cc(C)nc43)cc2)c1C(=O)O 10.1021/jm031100t
127036105 135982 0 None - 1 Human 6.3 pIC50 = 6.3 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 547 10 3 5 6.2 CCCc1nc2c(C)cc(C(=O)N[C@@H](CO)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2015.09.010
CHEMBL3736336 135982 0 None - 1 Human 6.3 pIC50 = 6.3 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 547 10 3 5 6.2 CCCc1nc2c(C)cc(C(=O)N[C@@H](CO)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2015.09.010
44209951 91734 0 None - 0 Rabbit 8.3 pIC50 = 8.3 Binding
Ability to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitroAbility to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitro
ChEMBL 466 8 1 7 4.6 CCCCc1nc2ccc(OC)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80335-2
CHEMBL24240 91734 0 None - 0 Rabbit 8.3 pIC50 = 8.3 Binding
Ability to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitroAbility to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitro
ChEMBL 466 8 1 7 4.6 CCCCc1nc2ccc(OC)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80335-2
44209671 93156 0 None - 0 Rabbit 8.3 pIC50 = 8.3 Binding
Ability to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitroAbility to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitro
ChEMBL 478 8 1 6 5.8 CCCCc1nc2ccc(C(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80335-2
CHEMBL24661 93156 0 None - 0 Rabbit 8.3 pIC50 = 8.3 Binding
Ability to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitroAbility to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitro
ChEMBL 478 8 1 6 5.8 CCCCc1nc2ccc(C(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80335-2
44274671 93786 0 None - 0 Rabbit 8.3 pIC50 = 8.3 Binding
Ability to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitroAbility to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitro
ChEMBL 479 8 1 7 4.7 CCCCc1nc2ccc(N(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80335-2
CHEMBL25000 93786 0 None - 0 Rabbit 8.3 pIC50 = 8.3 Binding
Ability to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitroAbility to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitro
ChEMBL 479 8 1 7 4.7 CCCCc1nc2ccc(N(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80335-2
14956748 204246 0 None - 0 Rabbit 8.3 pIC50 = 8.3 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 481 9 1 8 4.3 CCCCc1nn(-c2ccc(OC)cc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
CHEMBL84627 204246 0 None - 0 Rabbit 8.3 pIC50 = 8.3 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 481 9 1 8 4.3 CCCCc1nn(-c2ccc(OC)cc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
44209951 91734 0 None - 0 Rabbit 8.3 pIC50 = 8.3 Binding
Binding affinity against Angiotensin II type 1 Receptor in rabbit aortic tissueBinding affinity against Angiotensin II type 1 Receptor in rabbit aortic tissue
ChEMBL 466 8 1 7 4.6 CCCCc1nc2ccc(OC)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80334-0
CHEMBL24240 91734 0 None - 0 Rabbit 8.3 pIC50 = 8.3 Binding
Binding affinity against Angiotensin II type 1 Receptor in rabbit aortic tissueBinding affinity against Angiotensin II type 1 Receptor in rabbit aortic tissue
ChEMBL 466 8 1 7 4.6 CCCCc1nc2ccc(OC)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80334-0
1610 2305 89 None -1 4 Rat 8.3 pIC50 = 8.3 Binding
Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00064a007
3941 2305 89 None -1 4 Rat 8.3 pIC50 = 8.3 Binding
Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00064a007
3961 2305 89 None -1 4 Rat 8.3 pIC50 = 8.3 Binding
Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00064a007
590 2305 89 None -1 4 Rat 8.3 pIC50 = 8.3 Binding
Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00064a007
CHEMBL191 2305 89 None -1 4 Rat 8.3 pIC50 = 8.3 Binding
Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00064a007
DB00678 2305 89 None -1 4 Rat 8.3 pIC50 = 8.3 Binding
Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00064a007
9870463 101766 0 None - 0 Rabbit 8.3 pIC50 = 8.3 Binding
Binding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membraneBinding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane
ChEMBL 495 5 1 6 4.8 CCCc1nc2c(C)cc(C(=O)OC)nc2n1Cc1cc(Br)c(O)c(Br)c1 10.1016/S0960-894X(01)81148-3
CHEMBL303147 101766 0 None - 0 Rabbit 8.3 pIC50 = 8.3 Binding
Binding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membraneBinding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane
ChEMBL 495 5 1 6 4.8 CCCc1nc2c(C)cc(C(=O)OC)nc2n1Cc1cc(Br)c(O)c(Br)c1 10.1016/S0960-894X(01)81148-3
9887844 162637 1 None - 1 Guinea pig 8.3 pIC50 = 8.3 Binding
Binding affinity to angiotensin AT1 receptor in guinea pig adrenal cortex membranesBinding affinity to angiotensin AT1 receptor in guinea pig adrenal cortex membranes
ChEMBL 411 6 1 5 4.9 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2c(n1)CCCC2 10.1016/j.bmc.2010.10.043
CHEMBL418226 162637 1 None - 1 Guinea pig 8.3 pIC50 = 8.3 Binding
Binding affinity to angiotensin AT1 receptor in guinea pig adrenal cortex membranesBinding affinity to angiotensin AT1 receptor in guinea pig adrenal cortex membranes
ChEMBL 411 6 1 5 4.9 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2c(n1)CCCC2 10.1016/j.bmc.2010.10.043
9870463 101766 0 None - 0 Rabbit 8.3 pIC50 = 8.3 Binding
Binding affinity to angiotensin AT1 receptor in rabbit aortic ringsBinding affinity to angiotensin AT1 receptor in rabbit aortic rings
ChEMBL 495 5 1 6 4.8 CCCc1nc2c(C)cc(C(=O)OC)nc2n1Cc1cc(Br)c(O)c(Br)c1 10.1016/j.bmc.2010.10.043
CHEMBL303147 101766 0 None - 0 Rabbit 8.3 pIC50 = 8.3 Binding
Binding affinity to angiotensin AT1 receptor in rabbit aortic ringsBinding affinity to angiotensin AT1 receptor in rabbit aortic rings
ChEMBL 495 5 1 6 4.8 CCCc1nc2c(C)cc(C(=O)OC)nc2n1Cc1cc(Br)c(O)c(Br)c1 10.1016/j.bmc.2010.10.043
9887844 162637 1 None - 1 Guinea pig 8.3 pIC50 = 8.3 Binding
Compound was tested for in vitro inhibition of specific binding of [I-125]AII to Angiotensin II receptor, type 1 in guinea pig adrenal membrane preparationCompound was tested for in vitro inhibition of specific binding of [I-125]AII to Angiotensin II receptor, type 1 in guinea pig adrenal membrane preparation
ChEMBL 411 6 1 5 4.9 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2c(n1)CCCC2 10.1016/S0960-894X(01)80295-X
CHEMBL418226 162637 1 None - 1 Guinea pig 8.3 pIC50 = 8.3 Binding
Compound was tested for in vitro inhibition of specific binding of [I-125]AII to Angiotensin II receptor, type 1 in guinea pig adrenal membrane preparationCompound was tested for in vitro inhibition of specific binding of [I-125]AII to Angiotensin II receptor, type 1 in guinea pig adrenal membrane preparation
ChEMBL 411 6 1 5 4.9 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2c(n1)CCCC2 10.1016/S0960-894X(01)80295-X
131654 204667 10 None - 1 Rat 8.3 pIC50 = 8.3 Binding
Displacement of [125-I]-labeled angiotensin II from Angiotensin II receptor, type 1 of rat uterine membranesDisplacement of [125-I]-labeled angiotensin II from Angiotensin II receptor, type 1 of rat uterine membranes
ChEMBL 431 10 1 7 4.1 CCCCc1nn(CCCC)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80290-0
CHEMBL87778 204667 10 None - 1 Rat 8.3 pIC50 = 8.3 Binding
Displacement of [125-I]-labeled angiotensin II from Angiotensin II receptor, type 1 of rat uterine membranesDisplacement of [125-I]-labeled angiotensin II from Angiotensin II receptor, type 1 of rat uterine membranes
ChEMBL 431 10 1 7 4.1 CCCCc1nn(CCCC)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80290-0
44275108 94298 0 None - 0 Rabbit 8.3 pIC50 = 8.3 Binding
Displacement of [125I]Sar1-Ile8-AII (without BSA) from type 1 Angiotensin II receptor of rabbit aortaDisplacement of [125I]Sar1-Ile8-AII (without BSA) from type 1 Angiotensin II receptor of rabbit aorta
ChEMBL 513 8 1 7 5.7 CCCCc1nc2ccc(-c3ccccn3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80335-2
CHEMBL25313 94298 0 None - 0 Rabbit 8.3 pIC50 = 8.3 Binding
Displacement of [125I]Sar1-Ile8-AII (without BSA) from type 1 Angiotensin II receptor of rabbit aortaDisplacement of [125I]Sar1-Ile8-AII (without BSA) from type 1 Angiotensin II receptor of rabbit aorta
ChEMBL 513 8 1 7 5.7 CCCCc1nc2ccc(-c3ccccn3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80335-2
127035717 135880 0 None - 1 Human 8.3 pIC50 = 8.3 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 569 10 2 6 6.7 CCCc1nc2c(C)cc(C(=O)NC[C@@H](C)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.ejmech.2015.09.010
CHEMBL3735409 135880 0 None - 1 Human 8.3 pIC50 = 8.3 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 569 10 2 6 6.7 CCCc1nc2c(C)cc(C(=O)NC[C@@H](C)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.ejmech.2015.09.010
10053595 102628 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
In vitro binding affinity of compound against Angiotensin II receptor, type 1In vitro binding affinity of compound against Angiotensin II receptor, type 1
ChEMBL 562 10 2 8 4.8 CCCc1nc(CN2CCN(c3ccccc3)CC2)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80076-1
CHEMBL307756 102628 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
In vitro binding affinity of compound against Angiotensin II receptor, type 1In vitro binding affinity of compound against Angiotensin II receptor, type 1
ChEMBL 562 10 2 8 4.8 CCCc1nc(CN2CCN(c3ccccc3)CC2)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80076-1
44311738 202481 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
In vitro binding affinity of compound against Angiotensin II receptor, type 1In vitro binding affinity of compound against Angiotensin II receptor, type 1
ChEMBL 590 10 2 8 4.4 CCCc1nc(CN2CCN(C(=O)c3ccccc3)CC2)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80076-1
CHEMBL70801 202481 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
In vitro binding affinity of compound against Angiotensin II receptor, type 1In vitro binding affinity of compound against Angiotensin II receptor, type 1
ChEMBL 590 10 2 8 4.4 CCCc1nc(CN2CCN(C(=O)c3ccccc3)CC2)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80076-1
44379334 57789 0 None - 0 Rabbit 8.3 pIC50 = 8.3 Binding
In vitro displacement of 125I-[Sar1, Ile8] from AT1 receptors in rabbit aorta membraneIn vitro displacement of 125I-[Sar1, Ile8] from AT1 receptors in rabbit aorta membrane
ChEMBL 585 10 2 9 4.2 CCCCc1nc2ccc(C(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81125-2
CHEMBL167584 57789 0 None - 0 Rabbit 8.3 pIC50 = 8.3 Binding
In vitro displacement of 125I-[Sar1, Ile8] from AT1 receptors in rabbit aorta membraneIn vitro displacement of 125I-[Sar1, Ile8] from AT1 receptors in rabbit aorta membrane
ChEMBL 585 10 2 9 4.2 CCCCc1nc2ccc(C(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81125-2
10054912 205888 0 None - 0 Rabbit 8.3 pIC50 = 8.3 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 640 10 1 8 6.3 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccsc2)cc1 10.1021/jm00043a020
CHEMBL95197 205888 0 None - 0 Rabbit 8.3 pIC50 = 8.3 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 640 10 1 8 6.3 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccsc2)cc1 10.1021/jm00043a020
44373417 52089 0 None - 0 Rabbit 8.3 pIC50 = 8.3 Binding
Inhibition of Angiotensin II receptor, type 1Inhibition of Angiotensin II receptor, type 1
ChEMBL 476 5 1 8 4.5 CCc1nc2c(C)cc(C)nc2n1Cc1ccc2c(ccn2C(=O)c2cccc(-c3nn[nH]n3)c2)c1 10.1021/jm9504722
CHEMBL159004 52089 0 None - 0 Rabbit 8.3 pIC50 = 8.3 Binding
Inhibition of Angiotensin II receptor, type 1Inhibition of Angiotensin II receptor, type 1
ChEMBL 476 5 1 8 4.5 CCc1nc2c(C)cc(C)nc2n1Cc1ccc2c(ccn2C(=O)c2cccc(-c3nn[nH]n3)c2)c1 10.1021/jm9504722
14950508 99097 0 None - 0 Guinea pig 8.3 pIC50 = 8.3 Binding
Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1
ChEMBL 429 7 1 7 4.2 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c(C(=O)OC)c(C)n1 10.1021/jm00061a016
CHEMBL283742 99097 0 None - 0 Guinea pig 8.3 pIC50 = 8.3 Binding
Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1
ChEMBL 429 7 1 7 4.2 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c(C(=O)OC)c(C)n1 10.1021/jm00061a016
15171368 167492 0 None - 0 Guinea pig 8.3 pIC50 = 8.3 Binding
Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1
ChEMBL 443 8 1 7 4.4 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c(C(=O)OC)c(CC)n1 10.1021/jm00061a016
CHEMBL432459 167492 0 None - 0 Guinea pig 8.3 pIC50 = 8.3 Binding
Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1
ChEMBL 443 8 1 7 4.4 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c(C(=O)OC)c(CC)n1 10.1021/jm00061a016
10480536 21414 0 None - 0 Rat 8.3 pIC50 = 8.3 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 485 7 1 6 6.3 CCCc1nc2c(C)cc(-c3ccccn3)cc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00077a007
CHEMBL131767 21414 0 None - 0 Rat 8.3 pIC50 = 8.3 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 485 7 1 6 6.3 CCCc1nc2c(C)cc(-c3ccccn3)cc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00077a007
10481936 116184 0 None - 0 Rat 8.3 pIC50 = 8.3 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 524 7 1 7 6.4 CCCc1nc2ccc(-c3nc4ccccc4n3C)cc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00077a007
CHEMBL337232 116184 0 None - 0 Rat 8.3 pIC50 = 8.3 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 524 7 1 7 6.4 CCCc1nc2ccc(-c3nc4ccccc4n3C)cc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00077a007
15287890 155218 0 None - 0 Rabbit 8.3 pIC50 = 8.3 Binding
Tested in vitro for Angiotensin II receptor, type 1 binding affinity using rabbit aorta binding assayTested in vitro for Angiotensin II receptor, type 1 binding affinity using rabbit aorta binding assay
ChEMBL 429 8 1 5 5.3 CCCc1nc2c(C)ccnc2n1Cc1ccc(OC(C(=O)O)c2ccccc2C)cc1 10.1016/0960-894X(94)00476-V
CHEMBL40585 155218 0 None - 0 Rabbit 8.3 pIC50 = 8.3 Binding
Tested in vitro for Angiotensin II receptor, type 1 binding affinity using rabbit aorta binding assayTested in vitro for Angiotensin II receptor, type 1 binding affinity using rabbit aorta binding assay
ChEMBL 429 8 1 5 5.3 CCCc1nc2c(C)ccnc2n1Cc1ccc(OC(C(=O)O)c2ccccc2C)cc1 10.1016/0960-894X(94)00476-V
44277574 101418 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Binding affinity against AT1 receptor in human adrenal tissueBinding affinity against AT1 receptor in human adrenal tissue
ChEMBL 604 8 0 9 5.5 Cn1nnnc1-c1ccccc1-c1ccc(Cn2cnc3ccc(N(Cc4ccccn4)C(=O)c4ccccc4)cc3c2=O)cc1 10.1016/0960-894X(95)00224-H
CHEMBL30086 101418 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Binding affinity against AT1 receptor in human adrenal tissueBinding affinity against AT1 receptor in human adrenal tissue
ChEMBL 604 8 0 9 5.5 Cn1nnnc1-c1ccccc1-c1ccc(Cn2cnc3ccc(N(Cc4ccccn4)C(=O)c4ccccc4)cc3c2=O)cc1 10.1016/0960-894X(95)00224-H
15231094 138754 0 None - 0 Rabbit 8.3 pIC50 = 8.3 Binding
Displacement of [125 I]Sar1Ile8-AII from type 1 Angiotensin II receptor of rabbit aorta membraneDisplacement of [125 I]Sar1Ile8-AII from type 1 Angiotensin II receptor of rabbit aorta membrane
ChEMBL 641 12 1 8 7.4 CCCCc1nc2ccc(N(Cc3ccccc3)C(=O)OCC(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80517-5
CHEMBL37919 138754 0 None - 0 Rabbit 8.3 pIC50 = 8.3 Binding
Displacement of [125 I]Sar1Ile8-AII from type 1 Angiotensin II receptor of rabbit aorta membraneDisplacement of [125 I]Sar1Ile8-AII from type 1 Angiotensin II receptor of rabbit aorta membrane
ChEMBL 641 12 1 8 7.4 CCCCc1nc2ccc(N(Cc3ccccc3)C(=O)OCC(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80517-5
71521302 86385 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor afterDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after
ChEMBL 527 6 1 7 5.5 CCc1nc2ccn(Cc3ccccc3C)c(=O)c2n1[C@H]1CCc2cc(-c3ccccc3-c3nnn[nH]3)ccc21 10.1016/j.bmcl.2012.11.088
CHEMBL2322444 86385 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor afterDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after
ChEMBL 527 6 1 7 5.5 CCc1nc2ccn(Cc3ccccc3C)c(=O)c2n1[C@H]1CCc2cc(-c3ccccc3-c3nnn[nH]3)ccc21 10.1016/j.bmcl.2012.11.088
131654 204667 10 None - 1 Rat 8.3 pIC50 = 8.3 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 431 10 1 7 4.1 CCCCc1nn(CCCC)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a015
CHEMBL87778 204667 10 None - 1 Rat 8.3 pIC50 = 8.3 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 431 10 1 7 4.1 CCCCc1nn(CCCC)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a015
44348355 112875 0 None - 0 Rabbit 8.3 pIC50 = 8.3 Binding
Displacement of [1251][Sar1,IIe8]AII from rabbit aorta Angiotensin II receptor, type 1Displacement of [1251][Sar1,IIe8]AII from rabbit aorta Angiotensin II receptor, type 1
ChEMBL 591 13 1 6 8.6 CCCc1cc(Cn2c(CC)nc3c(C)cc(C)nc32)cc(CCC)c1OC(C(=O)O)c1ccc(Oc2ccccc2)cc1 10.1021/jm00075a033
CHEMBL331797 112875 0 None - 0 Rabbit 8.3 pIC50 = 8.3 Binding
Displacement of [1251][Sar1,IIe8]AII from rabbit aorta Angiotensin II receptor, type 1Displacement of [1251][Sar1,IIe8]AII from rabbit aorta Angiotensin II receptor, type 1
ChEMBL 591 13 1 6 8.6 CCCc1cc(Cn2c(CC)nc3c(C)cc(C)nc32)cc(CCC)c1OC(C(=O)O)c1ccc(Oc2ccccc2)cc1 10.1021/jm00075a033
53309406 63435 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation countingDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation counting
ChEMBL 511 6 1 6 6.3 CCc1nc2c(C)cc(Cc3ccccc3)nc2n1[C@H]1CCc2cc(-c3ccccc3-c3nnn[nH]3)ccc21 10.1021/jm200409s
CHEMBL1801743 63435 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation countingDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation counting
ChEMBL 511 6 1 6 6.3 CCc1nc2c(C)cc(Cc3ccccc3)nc2n1[C@H]1CCc2cc(-c3ccccc3-c3nnn[nH]3)ccc21 10.1021/jm200409s
9847539 181447 0 None - 0 Rat 8.3 pIC50 = 8.3 Binding
In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.
ChEMBL 470 8 1 5 5.8 CCCCC1=NC(C)(C2CCCCC2)C(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81140-9
CHEMBL47810 181447 0 None - 0 Rat 8.3 pIC50 = 8.3 Binding
In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.
ChEMBL 470 8 1 5 5.8 CCCCC1=NC(C)(C2CCCCC2)C(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81140-9
10349256 110955 0 None - 0 Rabbit 8.3 pIC50 = 8.3 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 647 10 1 8 7.1 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2nc3ccccc3o2)cc1 10.1021/jm00043a020
CHEMBL327569 110955 0 None - 0 Rabbit 8.3 pIC50 = 8.3 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 647 10 1 8 7.1 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2nc3ccccc3o2)cc1 10.1021/jm00043a020
44300615 195098 0 None - 0 Rabbit 8.3 pIC50 = 8.3 Binding
Inhibition of Angiotensin II receptor type 1 in rabbit aorta binding assayInhibition of Angiotensin II receptor type 1 in rabbit aorta binding assay
ChEMBL 572 9 1 7 6.5 CCCc1cc(-c2ccc(Cn3c(CC)nc4c(C)cc(C)nc43)cc2)c(S(=O)(=O)NC(=O)c2ccccc2)s1 10.1016/S0960-894X(01)81145-8
CHEMBL56549 195098 0 None - 0 Rabbit 8.3 pIC50 = 8.3 Binding
Inhibition of Angiotensin II receptor type 1 in rabbit aorta binding assayInhibition of Angiotensin II receptor type 1 in rabbit aorta binding assay
ChEMBL 572 9 1 7 6.5 CCCc1cc(-c2ccc(Cn3c(CC)nc4c(C)cc(C)nc43)cc2)c(S(=O)(=O)NC(=O)c2ccccc2)s1 10.1016/S0960-894X(01)81145-8
10257584 16932 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 577 14 0 8 6.2 CCCCCCN1C(=O)/C(=C/c2cnc(CCCC)n2Cc2ccc(C(=O)OC)cc2)N(Cc2csc(C)n2)C1=O 10.1007/s00044-009-9205-9
CHEMBL125533 16932 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 577 14 0 8 6.2 CCCCCCN1C(=O)/C(=C/c2cnc(CCCC)n2Cc2ccc(C(=O)OC)cc2)N(Cc2csc(C)n2)C1=O 10.1007/s00044-009-9205-9
10168097 172483 0 None - 0 Rat 8.3 pIC50 = 8.3 Binding
Binding affinity against AT1 receptor in the presence of 0.01% BSABinding affinity against AT1 receptor in the presence of 0.01% BSA
ChEMBL 587 11 1 9 5.7 CCCCc1nc2ccn(Cc3ccccc3C(=O)OCC)c(=O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00037a014
CHEMBL45195 172483 0 None - 0 Rat 8.3 pIC50 = 8.3 Binding
Binding affinity against AT1 receptor in the presence of 0.01% BSABinding affinity against AT1 receptor in the presence of 0.01% BSA
ChEMBL 587 11 1 9 5.7 CCCCc1nc2ccn(Cc3ccccc3C(=O)OCC)c(=O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00037a014
10765180 10134 0 None - 0 Bovine 8.3 pIC50 = 8.3 Binding
In vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortexIn vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortex
ChEMBL 432 7 3 7 3.3 CCc1nc(C(C)(C)O)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm950450f
CHEMBL116094 10134 0 None - 0 Bovine 8.3 pIC50 = 8.3 Binding
In vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortexIn vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortex
ChEMBL 432 7 3 7 3.3 CCc1nc(C(C)(C)O)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm950450f
10004112 25311 0 None - 0 Rabbit 8.3 pIC50 = 8.3 Binding
Inhibition of Angiotensin II receptor, type 1Inhibition of Angiotensin II receptor, type 1
ChEMBL 454 9 1 5 5.5 C=CCN(c1ccc(Cn2c(CC)nc3c(C)cc(C)nc32)cc1)C(C(=O)O)c1ccccc1 10.1021/jm9504722
CHEMBL135089 25311 0 None - 0 Rabbit 8.3 pIC50 = 8.3 Binding
Inhibition of Angiotensin II receptor, type 1Inhibition of Angiotensin II receptor, type 1
ChEMBL 454 9 1 5 5.5 C=CCN(c1ccc(Cn2c(CC)nc3c(C)cc(C)nc32)cc1)C(C(=O)O)c1ccccc1 10.1021/jm9504722
44277489 99934 0 None - 0 Rabbit 8.3 pIC50 = 8.3 Binding
Binding affinity against AT1 receptor in rabbit aortaBinding affinity against AT1 receptor in rabbit aorta
ChEMBL 604 8 0 9 5.5 Cn1nnnc1-c1ccccc1-c1ccc(Cn2cnc3ccc(N(Cc4ccncc4)C(=O)c4ccccc4)cc3c2=O)cc1 10.1016/0960-894X(95)00224-H
CHEMBL29020 99934 0 None - 0 Rabbit 8.3 pIC50 = 8.3 Binding
Binding affinity against AT1 receptor in rabbit aortaBinding affinity against AT1 receptor in rabbit aorta
ChEMBL 604 8 0 9 5.5 Cn1nnnc1-c1ccccc1-c1ccc(Cn2cnc3ccc(N(Cc4ccncc4)C(=O)c4ccccc4)cc3c2=O)cc1 10.1016/0960-894X(95)00224-H
1610 2305 89 None 1 4 Human 8.3 pIC50 = 8.3 Binding
In vitro binding affinity of compound against Angiotensin II receptor, type 1In vitro binding affinity of compound against Angiotensin II receptor, type 1
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(00)80076-1
3941 2305 89 None 1 4 Human 8.3 pIC50 = 8.3 Binding
In vitro binding affinity of compound against Angiotensin II receptor, type 1In vitro binding affinity of compound against Angiotensin II receptor, type 1
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(00)80076-1
3961 2305 89 None 1 4 Human 8.3 pIC50 = 8.3 Binding
In vitro binding affinity of compound against Angiotensin II receptor, type 1In vitro binding affinity of compound against Angiotensin II receptor, type 1
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(00)80076-1
590 2305 89 None 1 4 Human 8.3 pIC50 = 8.3 Binding
In vitro binding affinity of compound against Angiotensin II receptor, type 1In vitro binding affinity of compound against Angiotensin II receptor, type 1
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(00)80076-1
CHEMBL191 2305 89 None 1 4 Human 8.3 pIC50 = 8.3 Binding
In vitro binding affinity of compound against Angiotensin II receptor, type 1In vitro binding affinity of compound against Angiotensin II receptor, type 1
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(00)80076-1
DB00678 2305 89 None 1 4 Human 8.3 pIC50 = 8.3 Binding
In vitro binding affinity of compound against Angiotensin II receptor, type 1In vitro binding affinity of compound against Angiotensin II receptor, type 1
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(00)80076-1
10439612 161294 0 None - 0 Rabbit 8.3 pIC50 = 8.3 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 688 10 1 7 6.8 O=C(NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCCC(F)(F)F)nn(-c3ccccc3C(F)(F)F)c2=O)cc1)c1ccccc1 10.1021/jm00043a020
CHEMBL414816 161294 0 None - 0 Rabbit 8.3 pIC50 = 8.3 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 688 10 1 7 6.8 O=C(NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCCC(F)(F)F)nn(-c3ccccc3C(F)(F)F)c2=O)cc1)c1ccccc1 10.1021/jm00043a020
10439172 205740 0 None - 0 Rabbit 8.3 pIC50 = 8.3 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 644 13 2 8 5.2 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)CCCC(=O)O)cc1 10.1021/jm00043a020
CHEMBL94355 205740 0 None - 0 Rabbit 8.3 pIC50 = 8.3 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 644 13 2 8 5.2 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)CCCC(=O)O)cc1 10.1021/jm00043a020
14956758 106036 0 None - 0 Rabbit 8.3 pIC50 = 8.3 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 509 9 1 9 4.1 CCCCc1nn(-c2ccccc2C(=O)OC)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
CHEMBL314042 106036 0 None - 0 Rabbit 8.3 pIC50 = 8.3 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 509 9 1 9 4.1 CCCCc1nn(-c2ccccc2C(=O)OC)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
9931685 204354 0 None - 1 Rat 8.3 pIC50 = 8.3 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 415 10 1 6 4.9 CCCCc1nc(CCCC)n(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)n1 10.1021/jm031100t
CHEMBL85595 204354 0 None - 1 Rat 8.3 pIC50 = 8.3 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 415 10 1 6 4.9 CCCCc1nc(CCCC)n(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)n1 10.1021/jm031100t
9931685 204354 0 None - 1 Human 8.3 pIC50 = 8.3 Binding
Binding affinity to angiotensin AT1 receptorBinding affinity to angiotensin AT1 receptor
ChEMBL 415 10 1 6 4.9 CCCCc1nc(CCCC)n(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)n1 10.1016/j.bmc.2010.10.043
CHEMBL85595 204354 0 None - 1 Human 8.3 pIC50 = 8.3 Binding
Binding affinity to angiotensin AT1 receptorBinding affinity to angiotensin AT1 receptor
ChEMBL 415 10 1 6 4.9 CCCCc1nc(CCCC)n(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)n1 10.1016/j.bmc.2010.10.043
44379335 119703 0 None - 0 Rabbit 8.3 pIC50 = 8.3 Binding
In vitro displacement of 125I-[Sar1, Ile8] from AT1 receptors in rabbit aorta membraneIn vitro displacement of 125I-[Sar1, Ile8] from AT1 receptors in rabbit aorta membrane
ChEMBL 574 10 2 6 6.0 CCCCc1nc2ccc(C(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)NC(C)C)cc1 10.1016/S0960-894X(01)81125-2
CHEMBL352137 119703 0 None - 0 Rabbit 8.3 pIC50 = 8.3 Binding
In vitro displacement of 125I-[Sar1, Ile8] from AT1 receptors in rabbit aorta membraneIn vitro displacement of 125I-[Sar1, Ile8] from AT1 receptors in rabbit aorta membrane
ChEMBL 574 10 2 6 6.0 CCCCc1nc2ccc(C(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)NC(C)C)cc1 10.1016/S0960-894X(01)81125-2
44379348 164358 0 None - 0 Rabbit 8.3 pIC50 = 8.3 Binding
In vitro displacement of 125I-[Sar1, Ile8] from AT1 receptors in rabbit aorta membraneIn vitro displacement of 125I-[Sar1, Ile8] from AT1 receptors in rabbit aorta membrane
ChEMBL 558 10 1 7 4.7 CCCCc1nc2ccc(N(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)C2CC2)cc1 10.1016/S0960-894X(01)81125-2
CHEMBL422374 164358 0 None - 0 Rabbit 8.3 pIC50 = 8.3 Binding
In vitro displacement of 125I-[Sar1, Ile8] from AT1 receptors in rabbit aorta membraneIn vitro displacement of 125I-[Sar1, Ile8] from AT1 receptors in rabbit aorta membrane
ChEMBL 558 10 1 7 4.7 CCCCc1nc2ccc(N(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)C2CC2)cc1 10.1016/S0960-894X(01)81125-2
10160805 202357 0 None - 0 Rat 8.3 pIC50 = 8.3 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 445 11 1 7 4.5 CCCCCn1nc(CCCC)n(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c1=O 10.1021/jm00067a015
CHEMBL70029 202357 0 None - 0 Rat 8.3 pIC50 = 8.3 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 445 11 1 7 4.5 CCCCCn1nc(CCCC)n(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c1=O 10.1021/jm00067a015
1610 2305 89 None 1 4 Human 8.3 pIC50 = 8.3 Binding
Displacement of 125[I-Sar1-Ile8]ANG II from human AT1 receptor expressed in HEK293 membranes after 1 hr by gamma countingDisplacement of 125[I-Sar1-Ile8]ANG II from human AT1 receptor expressed in HEK293 membranes after 1 hr by gamma counting
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.ejmech.2012.07.040
3941 2305 89 None 1 4 Human 8.3 pIC50 = 8.3 Binding
Displacement of 125[I-Sar1-Ile8]ANG II from human AT1 receptor expressed in HEK293 membranes after 1 hr by gamma countingDisplacement of 125[I-Sar1-Ile8]ANG II from human AT1 receptor expressed in HEK293 membranes after 1 hr by gamma counting
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.ejmech.2012.07.040
3961 2305 89 None 1 4 Human 8.3 pIC50 = 8.3 Binding
Displacement of 125[I-Sar1-Ile8]ANG II from human AT1 receptor expressed in HEK293 membranes after 1 hr by gamma countingDisplacement of 125[I-Sar1-Ile8]ANG II from human AT1 receptor expressed in HEK293 membranes after 1 hr by gamma counting
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.ejmech.2012.07.040
590 2305 89 None 1 4 Human 8.3 pIC50 = 8.3 Binding
Displacement of 125[I-Sar1-Ile8]ANG II from human AT1 receptor expressed in HEK293 membranes after 1 hr by gamma countingDisplacement of 125[I-Sar1-Ile8]ANG II from human AT1 receptor expressed in HEK293 membranes after 1 hr by gamma counting
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.ejmech.2012.07.040
CHEMBL191 2305 89 None 1 4 Human 8.3 pIC50 = 8.3 Binding
Displacement of 125[I-Sar1-Ile8]ANG II from human AT1 receptor expressed in HEK293 membranes after 1 hr by gamma countingDisplacement of 125[I-Sar1-Ile8]ANG II from human AT1 receptor expressed in HEK293 membranes after 1 hr by gamma counting
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.ejmech.2012.07.040
DB00678 2305 89 None 1 4 Human 8.3 pIC50 = 8.3 Binding
Displacement of 125[I-Sar1-Ile8]ANG II from human AT1 receptor expressed in HEK293 membranes after 1 hr by gamma countingDisplacement of 125[I-Sar1-Ile8]ANG II from human AT1 receptor expressed in HEK293 membranes after 1 hr by gamma counting
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.ejmech.2012.07.040
1610 2305 89 None 1 4 Human 8.3 pIC50 = 8.3 Binding
Displacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysisDisplacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysis
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.ejmech.2012.12.044
3941 2305 89 None 1 4 Human 8.3 pIC50 = 8.3 Binding
Displacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysisDisplacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysis
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.ejmech.2012.12.044
3961 2305 89 None 1 4 Human 8.3 pIC50 = 8.3 Binding
Displacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysisDisplacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysis
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.ejmech.2012.12.044
590 2305 89 None 1 4 Human 8.3 pIC50 = 8.3 Binding
Displacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysisDisplacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysis
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.ejmech.2012.12.044
CHEMBL191 2305 89 None 1 4 Human 8.3 pIC50 = 8.3 Binding
Displacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysisDisplacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysis
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.ejmech.2012.12.044
DB00678 2305 89 None 1 4 Human 8.3 pIC50 = 8.3 Binding
Displacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysisDisplacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysis
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.ejmech.2012.12.044
14956769 106619 0 None - 0 Rabbit 8.2 pIC50 = 8.2 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 499 9 1 7 5.3 CCCCCc1nn(-c2ccccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
CHEMBL316052 106619 0 None - 0 Rabbit 8.2 pIC50 = 8.2 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 499 9 1 7 5.3 CCCCCc1nn(-c2ccccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
44277443 99821 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
Binding affinity against AT1 receptor in human adrenal tissueBinding affinity against AT1 receptor in human adrenal tissue
ChEMBL 583 10 0 8 6.0 CCCCC(=O)N(Cc1ccccc1)c1ccc2ncn(Cc3ccc(-c4ccccc4-c4nnnn4C)cc3)c(=O)c2c1 10.1016/0960-894X(95)00224-H
CHEMBL28918 99821 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
Binding affinity against AT1 receptor in human adrenal tissueBinding affinity against AT1 receptor in human adrenal tissue
ChEMBL 583 10 0 8 6.0 CCCCC(=O)N(Cc1ccccc1)c1ccc2ncn(Cc3ccc(-c4ccccc4-c4nnnn4C)cc3)c(=O)c2c1 10.1016/0960-894X(95)00224-H
44310609 202049 0 None - 0 Rabbit 8.2 pIC50 = 8.2 Binding
In vitro binding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membraneIn vitro binding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane
ChEMBL 409 5 1 6 4.3 CCc1nc2c(C)cc(C)nn2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81150-1
CHEMBL67919 202049 0 None - 0 Rabbit 8.2 pIC50 = 8.2 Binding
In vitro binding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membraneIn vitro binding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane
ChEMBL 409 5 1 6 4.3 CCc1nc2c(C)cc(C)nn2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81150-1
10008962 118755 0 None - 0 Rabbit 8.2 pIC50 = 8.2 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 615 10 2 8 5.4 CCCCc1nn(-c2cccc(N)c2)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1007/s00044-013-0831-x
CHEMBL343719 118755 0 None - 0 Rabbit 8.2 pIC50 = 8.2 Binding
Antagonist activity at AT1 receptor in rabbit aorta membranesAntagonist activity at AT1 receptor in rabbit aorta membranes
ChEMBL 615 10 2 8 5.4 CCCCc1nn(-c2cccc(N)c2)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1007/s00044-013-0831-x
10369701 16104 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 529 12 0 7 5.1 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2Cc2ccccn2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
CHEMBL122494 16104 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 529 12 0 7 5.1 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2Cc2ccccn2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
14956762 98361 0 None - 0 Rabbit 8.2 pIC50 = 8.2 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 519 8 1 7 5.6 CCCCc1nn(-c2c(Cl)cccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
CHEMBL278741 98361 0 None - 0 Rabbit 8.2 pIC50 = 8.2 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 519 8 1 7 5.6 CCCCc1nn(-c2c(Cl)cccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
14956762 98361 0 None - 0 Rabbit 8.2 pIC50 = 8.2 Binding
Displacement of 125I[Sar,Ile] from rabbit aorta membrane Angiotensin II receptor type 1Displacement of 125I[Sar,Ile] from rabbit aorta membrane Angiotensin II receptor type 1
ChEMBL 519 8 1 7 5.6 CCCCc1nn(-c2c(Cl)cccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81132-X
CHEMBL278741 98361 0 None - 0 Rabbit 8.2 pIC50 = 8.2 Binding
Displacement of 125I[Sar,Ile] from rabbit aorta membrane Angiotensin II receptor type 1Displacement of 125I[Sar,Ile] from rabbit aorta membrane Angiotensin II receptor type 1
ChEMBL 519 8 1 7 5.6 CCCCc1nn(-c2c(Cl)cccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81132-X
44377123 119457 0 None - 0 Rabbit 8.2 pIC50 = 8.2 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aortaIn vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aorta
ChEMBL 481 10 2 6 3.9 CCCCc1ncc(C(=O)O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)C2CC2)cc1 10.1016/S0960-894X(01)81124-0
CHEMBL349856 119457 0 None - 0 Rabbit 8.2 pIC50 = 8.2 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aortaIn vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aorta
ChEMBL 481 10 2 6 3.9 CCCCc1ncc(C(=O)O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)C2CC2)cc1 10.1016/S0960-894X(01)81124-0
10100723 205705 0 None - 0 Rabbit 8.2 pIC50 = 8.2 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 646 9 1 7 6.1 CC1CC1Cc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1021/jm00043a020
CHEMBL94176 205705 0 None - 0 Rabbit 8.2 pIC50 = 8.2 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 646 9 1 7 6.1 CC1CC1Cc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1021/jm00043a020
44315282 96163 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membrane
ChEMBL 683 10 2 7 6.4 CCc1ccc(C(=O)NS(=O)(=O)c2ccccc2-c2ccc(Cn3c(CC)nc4ccc(NC(=O)N(C)C(C)C)cc4c3=O)c(F)c2)cc1 10.1016/0960-894X(94)85036-4
CHEMBL263452 96163 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membrane
ChEMBL 683 10 2 7 6.4 CCc1ccc(C(=O)NS(=O)(=O)c2ccccc2-c2ccc(Cn3c(CC)nc4ccc(NC(=O)N(C)C(C)C)cc4c3=O)c(F)c2)cc1 10.1016/0960-894X(94)85036-4
10008962 118755 0 None - 0 Rabbit 8.2 pIC50 = 8.2 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 615 10 2 8 5.4 CCCCc1nn(-c2cccc(N)c2)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1021/jm00052a006
CHEMBL343719 118755 0 None - 0 Rabbit 8.2 pIC50 = 8.2 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 615 10 2 8 5.4 CCCCc1nn(-c2cccc(N)c2)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1 10.1021/jm00052a006
44379217 57826 0 None - 0 Rabbit 8.2 pIC50 = 8.2 Binding
In vitro displacement of 125I-[Sar1, Ile8] from AT1 receptors in rabbit aorta membraneIn vitro displacement of 125I-[Sar1, Ile8] from AT1 receptors in rabbit aorta membrane
ChEMBL 608 10 2 6 7.1 CCCCc1nc2ccc(C(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)Nc2ccccc2)cc1 10.1016/S0960-894X(01)81125-2
CHEMBL167929 57826 0 None - 0 Rabbit 8.2 pIC50 = 8.2 Binding
In vitro displacement of 125I-[Sar1, Ile8] from AT1 receptors in rabbit aorta membraneIn vitro displacement of 125I-[Sar1, Ile8] from AT1 receptors in rabbit aorta membrane
ChEMBL 608 10 2 6 7.1 CCCCc1nc2ccc(C(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)Nc2ccccc2)cc1 10.1016/S0960-894X(01)81125-2
10416957 110998 0 None - 0 Rabbit 8.2 pIC50 = 8.2 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 662 10 1 7 6.8 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2c(C)cccc2C)cc1 10.1021/jm00043a020
CHEMBL327791 110998 0 None - 0 Rabbit 8.2 pIC50 = 8.2 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 662 10 1 7 6.8 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2c(C)cccc2C)cc1 10.1021/jm00043a020
10372810 105708 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
In vitro inhibitory concentration against AT1 receptor from human adrenal tissues.In vitro inhibitory concentration against AT1 receptor from human adrenal tissues.
ChEMBL 735 13 2 8 7.1 CCCCc1nn(-c2cc(NC(C)=O)ccc2Cl)c(=O)n1Cc1ccc(-c2cc(CCC)ccc2S(=O)(=O)NC(=O)c2ccccc2F)cc1F 10.1016/S0960-894X(01)80595-3
CHEMBL313868 105708 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
In vitro inhibitory concentration against AT1 receptor from human adrenal tissues.In vitro inhibitory concentration against AT1 receptor from human adrenal tissues.
ChEMBL 735 13 2 8 7.1 CCCCc1nn(-c2cc(NC(C)=O)ccc2Cl)c(=O)n1Cc1ccc(-c2cc(CCC)ccc2S(=O)(=O)NC(=O)c2ccccc2F)cc1F 10.1016/S0960-894X(01)80595-3
135723852 138597 0 None - 1 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125I]-Ang II from Angiotensin 2 type-1A receptor in rat vascular smooth muscle cells after 150 mins by gamma counting methodDisplacement of [125I]-Ang II from Angiotensin 2 type-1A receptor in rat vascular smooth muscle cells after 150 mins by gamma counting method
ChEMBL 438 8 2 6 4.4 CCCCc1nc(Cl)c(CO)n1Cc1ccc(-c2ccccc2-c2noc(=O)[nH]2)cc1 10.1016/j.bmc.2016.03.028
CHEMBL3787050 138597 0 None - 1 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125I]-Ang II from Angiotensin 2 type-1A receptor in rat vascular smooth muscle cells after 150 mins by gamma counting methodDisplacement of [125I]-Ang II from Angiotensin 2 type-1A receptor in rat vascular smooth muscle cells after 150 mins by gamma counting method
ChEMBL 438 8 2 6 4.4 CCCCc1nc(Cl)c(CO)n1Cc1ccc(-c2ccccc2-c2noc(=O)[nH]2)cc1 10.1016/j.bmc.2016.03.028
44274745 91343 0 None - 0 Rabbit 7.3 pIC50 = 7.3 Binding
Ability to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitroAbility to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitro
ChEMBL 633 8 3 8 6.3 CC(=O)Nc1ccc2nc(-c3ccc(-c4ccccc4C(=O)O)cc3)n(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c(=O)c2c1 10.1016/S0960-894X(00)80335-2
CHEMBL24111 91343 0 None - 0 Rabbit 7.3 pIC50 = 7.3 Binding
Ability to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitroAbility to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitro
ChEMBL 633 8 3 8 6.3 CC(=O)Nc1ccc2nc(-c3ccc(-c4ccccc4C(=O)O)cc3)n(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c(=O)c2c1 10.1016/S0960-894X(00)80335-2
10370801 48150 0 None - 0 Rabbit 7.3 pIC50 = 7.3 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 570 12 2 9 4.4 CCCCc1nnc([S+]([O-])Cc2ccc(OC)cc2)n1Cc1ccc(NC(=O)c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-011-9756-4
CHEMBL155554 48150 0 None - 0 Rabbit 7.3 pIC50 = 7.3 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 570 12 2 9 4.4 CCCCc1nnc([S+]([O-])Cc2ccc(OC)cc2)n1Cc1ccc(NC(=O)c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-011-9756-4
127035082 135975 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysisDisplacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysis
ChEMBL 677 12 2 8 7.4 CCCc1nc2c(C)cc(C(=O)NCc3cccc(OC)c3)cc2n1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)cc1 10.1039/C4MD00499J
CHEMBL3736262 135975 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysisDisplacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysis
ChEMBL 677 12 2 8 7.4 CCCc1nc2c(C)cc(C(=O)NCc3cccc(OC)c3)cc2n1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)cc1 10.1039/C4MD00499J
1610 2305 89 None -1 4 Rabbit 7.3 pIC50 = 7.3 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00057a009
3941 2305 89 None -1 4 Rabbit 7.3 pIC50 = 7.3 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00057a009
3961 2305 89 None -1 4 Rabbit 7.3 pIC50 = 7.3 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00057a009
590 2305 89 None -1 4 Rabbit 7.3 pIC50 = 7.3 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00057a009
CHEMBL191 2305 89 None -1 4 Rabbit 7.3 pIC50 = 7.3 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00057a009
DB00678 2305 89 None -1 4 Rabbit 7.3 pIC50 = 7.3 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00057a009
9984390 119023 0 None - 0 Rabbit 7.3 pIC50 = 7.3 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 527 11 1 8 4.8 CCCCc1nnc([S+]([O-])Cc2ccc(OC)cc2)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
CHEMBL345826 119023 0 None - 0 Rabbit 7.3 pIC50 = 7.3 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 527 11 1 8 4.8 CCCCc1nnc([S+]([O-])Cc2ccc(OC)cc2)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
1610 2305 89 None -1 4 Rabbit 7.3 pIC50 = 7.3 Binding
In vitro binding affinity for angiotensin II AT1 receptor in rabbit aortaIn vitro binding affinity for angiotensin II AT1 receptor in rabbit aorta
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00050a002
3941 2305 89 None -1 4 Rabbit 7.3 pIC50 = 7.3 Binding
In vitro binding affinity for angiotensin II AT1 receptor in rabbit aortaIn vitro binding affinity for angiotensin II AT1 receptor in rabbit aorta
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00050a002
3961 2305 89 None -1 4 Rabbit 7.3 pIC50 = 7.3 Binding
In vitro binding affinity for angiotensin II AT1 receptor in rabbit aortaIn vitro binding affinity for angiotensin II AT1 receptor in rabbit aorta
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00050a002
590 2305 89 None -1 4 Rabbit 7.3 pIC50 = 7.3 Binding
In vitro binding affinity for angiotensin II AT1 receptor in rabbit aortaIn vitro binding affinity for angiotensin II AT1 receptor in rabbit aorta
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00050a002
CHEMBL191 2305 89 None -1 4 Rabbit 7.3 pIC50 = 7.3 Binding
In vitro binding affinity for angiotensin II AT1 receptor in rabbit aortaIn vitro binding affinity for angiotensin II AT1 receptor in rabbit aorta
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00050a002
DB00678 2305 89 None -1 4 Rabbit 7.3 pIC50 = 7.3 Binding
In vitro binding affinity for angiotensin II AT1 receptor in rabbit aortaIn vitro binding affinity for angiotensin II AT1 receptor in rabbit aorta
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00050a002
9888820 9858 29 None - 0 Bovine 7.3 pIC50 = 7.3 Binding
In vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortexIn vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortex
ChEMBL 428 8 2 6 4.5 C=C(C)c1nc(CCC)n(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c1C(=O)O 10.1021/jm950450f
CHEMBL114752 9858 29 None - 0 Bovine 7.3 pIC50 = 7.3 Binding
In vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortexIn vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortex
ChEMBL 428 8 2 6 4.5 C=C(C)c1nc(CCC)n(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c1C(=O)O 10.1021/jm950450f
44376992 56810 0 None - 0 Rabbit 7.3 pIC50 = 7.3 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aortaIn vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aorta
ChEMBL 422 8 1 7 4.1 CCCCc1nc(Cl)c(CO)n1Cc1ccc(-c2ccccc2-n2cnnn2)cc1 10.1016/S0960-894X(01)81124-0
CHEMBL164552 56810 0 None - 0 Rabbit 7.3 pIC50 = 7.3 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aortaIn vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aorta
ChEMBL 422 8 1 7 4.1 CCCCc1nc(Cl)c(CO)n1Cc1ccc(-c2ccccc2-n2cnnn2)cc1 10.1016/S0960-894X(01)81124-0
9953638 84618 0 None - 0 Guinea pig 7.3 pIC50 = 7.3 Binding
Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1
ChEMBL 415 6 1 7 3.9 COC(=O)c1c(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)cc(C)nc1C 10.1021/jm00061a016
CHEMBL22426 84618 0 None - 0 Guinea pig 7.3 pIC50 = 7.3 Binding
Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1
ChEMBL 415 6 1 7 3.9 COC(=O)c1c(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)cc(C)nc1C 10.1021/jm00061a016
9887844 162637 1 None - 1 Guinea pig 7.3 pIC50 = 7.3 Binding
Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1
ChEMBL 411 6 1 5 4.9 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2c(n1)CCCC2 10.1021/jm00061a016
CHEMBL418226 162637 1 None - 1 Guinea pig 7.3 pIC50 = 7.3 Binding
Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1
ChEMBL 411 6 1 5 4.9 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2c(n1)CCCC2 10.1021/jm00061a016
14956802 204582 0 None - 0 Rat 7.3 pIC50 = 7.3 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 515 9 1 7 5.5 CCCCc1nn(Cc2cccc3ccccc23)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a015
CHEMBL87184 204582 0 None - 0 Rat 7.3 pIC50 = 7.3 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 515 9 1 7 5.5 CCCCc1nn(Cc2cccc3ccccc23)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a015
19385729 50591 0 None - 0 Rabbit 7.3 pIC50 = 7.3 Binding
Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)
ChEMBL 471 7 1 5 6.2 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(OC(C(=O)O)c2ccccc2)c(C(C)(C)C)c1 10.1016/0960-894X(95)00185-V
CHEMBL15774 50591 0 None - 0 Rabbit 7.3 pIC50 = 7.3 Binding
Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)
ChEMBL 471 7 1 5 6.2 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(OC(C(=O)O)c2ccccc2)c(C(C)(C)C)c1 10.1016/0960-894X(95)00185-V
15356434 101243 0 None - 0 Rat 6.3 pIC50 = 6.3 Binding
Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.
ChEMBL 590 13 1 8 5.7 CCCCc1nc(Cl)c(CC(=O)OC)n1Cc1ccc(NC(=O)[C@H](Cc2ccccc2)n2cccc2C(=O)OC)cc1 10.1021/jm00064a007
CHEMBL299557 101243 0 None - 0 Rat 6.3 pIC50 = 6.3 Binding
Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.
ChEMBL 590 13 1 8 5.7 CCCCc1nc(Cl)c(CC(=O)OC)n1Cc1ccc(NC(=O)[C@H](Cc2ccccc2)n2cccc2C(=O)OC)cc1 10.1021/jm00064a007
9869596 114752 0 None - 0 Bovine 6.3 pIC50 = 6.3 Binding
Concentration required to inhibit [125I]AII binding to Angiotensin II receptor from membrane fractions of bovine adrenal cortexConcentration required to inhibit [125I]AII binding to Angiotensin II receptor from membrane fractions of bovine adrenal cortex
ChEMBL 476 7 2 8 5.1 CCSc1nc2c(C)sc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81118-5
CHEMBL334838 114752 0 None - 0 Bovine 6.3 pIC50 = 6.3 Binding
Concentration required to inhibit [125I]AII binding to Angiotensin II receptor from membrane fractions of bovine adrenal cortexConcentration required to inhibit [125I]AII binding to Angiotensin II receptor from membrane fractions of bovine adrenal cortex
ChEMBL 476 7 2 8 5.1 CCSc1nc2c(C)sc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81118-5
44321050 204511 0 None - 0 Rat 6.3 pIC50 = 6.3 Binding
Displacement of [125-I]-labeled angiotensin II from Angiotensin II receptor, type 1 of rat uterine membranesDisplacement of [125-I]-labeled angiotensin II from Angiotensin II receptor, type 1 of rat uterine membranes
ChEMBL 416 9 1 5 4.5 CCCCN1N=C(CCC)C(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)C1=O 10.1016/S0960-894X(01)80290-0
CHEMBL86764 204511 0 None - 0 Rat 6.3 pIC50 = 6.3 Binding
Displacement of [125-I]-labeled angiotensin II from Angiotensin II receptor, type 1 of rat uterine membranesDisplacement of [125-I]-labeled angiotensin II from Angiotensin II receptor, type 1 of rat uterine membranes
ChEMBL 416 9 1 5 4.5 CCCCN1N=C(CCC)C(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)C1=O 10.1016/S0960-894X(01)80290-0
9939191 98476 1 None - 1 Rabbit 6.3 pIC50 = 6.3 Binding
Inhibition of Angiotensin II receptor, type 1Inhibition of Angiotensin II receptor, type 1
ChEMBL 634 10 1 7 6.2 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1021/jm9504722
CHEMBL279629 98476 1 None - 1 Rabbit 6.3 pIC50 = 6.3 Binding
Inhibition of Angiotensin II receptor, type 1Inhibition of Angiotensin II receptor, type 1
ChEMBL 634 10 1 7 6.2 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1021/jm9504722
CHEMBL97539 98476 1 None - 1 Rabbit 6.3 pIC50 = 6.3 Binding
Inhibition of Angiotensin II receptor, type 1Inhibition of Angiotensin II receptor, type 1
ChEMBL 634 10 1 7 6.2 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1021/jm9504722
15144942 116487 0 None - 0 Rat 5.3 pIC50 = 5.3 Binding
Inhibition of [125I]angiotensin II receptor specific binding to rat mesenteric arteriesInhibition of [125I]angiotensin II receptor specific binding to rat mesenteric arteries
ChEMBL 422 9 1 3 5.9 CCCCc1ncc(/C=C(\Cc2ccccc2C)C(=O)O)n1Cc1ccccc1Cl 10.1021/jm00099a013
CHEMBL338813 116487 0 None - 0 Rat 5.3 pIC50 = 5.3 Binding
Inhibition of [125I]angiotensin II receptor specific binding to rat mesenteric arteriesInhibition of [125I]angiotensin II receptor specific binding to rat mesenteric arteries
ChEMBL 422 9 1 3 5.9 CCCCc1ncc(/C=C(\Cc2ccccc2C)C(=O)O)n1Cc1ccccc1Cl 10.1021/jm00099a013
71653009 88711 0 None - 0 Human 6.3 pIC50 = 6.3 Binding
Displacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysisDisplacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysis
ChEMBL 575 12 3 4 6.4 CCCCc1c[n+](Cc2ccc(-c3ccccc3C(=O)O)cc2)c(CO)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2012.12.044
CHEMBL2337685 88711 0 None - 0 Human 6.3 pIC50 = 6.3 Binding
Displacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysisDisplacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysis
ChEMBL 575 12 3 4 6.4 CCCCc1c[n+](Cc2ccc(-c3ccccc3C(=O)O)cc2)c(CO)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2012.12.044
CHEMBL2366019 88711 0 None - 0 Human 6.3 pIC50 = 6.3 Binding
Displacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysisDisplacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysis
ChEMBL 575 12 3 4 6.4 CCCCc1c[n+](Cc2ccc(-c3ccccc3C(=O)O)cc2)c(CO)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2012.12.044
127035557 135895 0 None - 0 Human 6.3 pIC50 = 6.3 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 587 10 2 7 6.9 CCSc1nc2c(C)cc(C(=O)NC[C@H](C)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.ejmech.2015.09.010
CHEMBL3735558 135895 0 None - 0 Human 6.3 pIC50 = 6.3 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 587 10 2 7 6.9 CCSc1nc2c(C)cc(C(=O)NC[C@H](C)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.ejmech.2015.09.010
44306646 201316 0 None - 0 Rabbit 7.3 pIC50 = 7.3 Binding
Binding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membraneBinding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane
ChEMBL 504 7 1 6 5.7 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(Oc2ccccc2NS(=O)(=O)C(F)(F)F)cc1 10.1016/S0960-894X(01)81148-3
CHEMBL63280 201316 0 None - 0 Rabbit 7.3 pIC50 = 7.3 Binding
Binding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membraneBinding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane
ChEMBL 504 7 1 6 5.7 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(Oc2ccccc2NS(=O)(=O)C(F)(F)F)cc1 10.1016/S0960-894X(01)81148-3
10646584 10145 0 None - 0 Bovine 7.3 pIC50 = 7.3 Binding
In vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortexIn vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortex
ChEMBL 436 9 3 5 4.6 CCCc1nc(C(C)(O)CC)c(C(=O)O)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm950450f
CHEMBL116102 10145 0 None - 0 Bovine 7.3 pIC50 = 7.3 Binding
In vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortexIn vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortex
ChEMBL 436 9 3 5 4.6 CCCc1nc(C(C)(O)CC)c(C(=O)O)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm950450f
22850667 199106 0 None - 0 Rabbit 5.3 pIC50 = 5.3 Binding
Inhibition of angiotensin Angiotensin II receptor, type 1 in rabbit aorta using [125I-Sar1,Ile8] angiotensin II binding assayInhibition of angiotensin Angiotensin II receptor, type 1 in rabbit aorta using [125I-Sar1,Ile8] angiotensin II binding assay
ChEMBL 542 11 1 3 6.5 CCCCCN(CCCCC)C(=O)N1CCN(C(=O)N(c2ccccc2)c2cccc(Cl)c2)[C@H](C(=O)O)C1 10.1016/S0960-894X(01)81007-6
CHEMBL60071 199106 0 None - 0 Rabbit 5.3 pIC50 = 5.3 Binding
Inhibition of angiotensin Angiotensin II receptor, type 1 in rabbit aorta using [125I-Sar1,Ile8] angiotensin II binding assayInhibition of angiotensin Angiotensin II receptor, type 1 in rabbit aorta using [125I-Sar1,Ile8] angiotensin II binding assay
ChEMBL 542 11 1 3 6.5 CCCCCN(CCCCC)C(=O)N1CCN(C(=O)N(c2ccccc2)c2cccc(Cl)c2)[C@H](C(=O)O)C1 10.1016/S0960-894X(01)81007-6
10050519 98044 0 None - 0 Rat 7.3 pIC50 = 7.3 Binding
Activity against high affinity Angiotensin II receptor, type 1 was measured from the ability to inhibit [125I]angiotensin II binding to rat uterine membrane.Activity against high affinity Angiotensin II receptor, type 1 was measured from the ability to inhibit [125I]angiotensin II binding to rat uterine membrane.
ChEMBL 472 10 1 7 5.3 CCCCc1nc(CCCC)n(Cc2ccc(-n3c(Cl)cc(Cl)c3-c3nn[nH]n3)cc2)n1 10.1021/jm00053a013
CHEMBL276150 98044 0 None - 0 Rat 7.3 pIC50 = 7.3 Binding
Activity against high affinity Angiotensin II receptor, type 1 was measured from the ability to inhibit [125I]angiotensin II binding to rat uterine membrane.Activity against high affinity Angiotensin II receptor, type 1 was measured from the ability to inhibit [125I]angiotensin II binding to rat uterine membrane.
ChEMBL 472 10 1 7 5.3 CCCCc1nc(CCCC)n(Cc2ccc(-n3c(Cl)cc(Cl)c3-c3nn[nH]n3)cc2)n1 10.1021/jm00053a013
11477098 204492 0 None - 0 Rat 7.3 pIC50 = 7.3 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 477 5 1 8 4.6 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2c(C(=O)O)c3nnnn3c3ccccc23)cc1 10.1021/jm031100t
CHEMBL86655 204492 0 None - 0 Rat 7.3 pIC50 = 7.3 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 477 5 1 8 4.6 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2c(C(=O)O)c3nnnn3c3ccccc23)cc1 10.1021/jm031100t
19422629 97934 0 None - 0 Rat 7.3 pIC50 = 7.3 Binding
In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.
ChEMBL 460 9 1 3 6.7 CCCCC1=NC(CC)(C2CCCCC2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/S0960-894X(01)81140-9
CHEMBL275437 97934 0 None - 0 Rat 7.3 pIC50 = 7.3 Binding
In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.
ChEMBL 460 9 1 3 6.7 CCCCC1=NC(CC)(C2CCCCC2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/S0960-894X(01)81140-9
57380213 70168 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of [125I]Sar1 Ile8-Ang 2 from angiotensin 2 AT1 receptor after 180 mins by gamma countingDisplacement of [125I]Sar1 Ile8-Ang 2 from angiotensin 2 AT1 receptor after 180 mins by gamma counting
ChEMBL 517 9 2 4 6.6 CCCc1nc2c(C)cc(C(=O)NCc3ccccc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2012.01.009
CHEMBL1947128 70168 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of [125I]Sar1 Ile8-Ang 2 from angiotensin 2 AT1 receptor after 180 mins by gamma countingDisplacement of [125I]Sar1 Ile8-Ang 2 from angiotensin 2 AT1 receptor after 180 mins by gamma counting
ChEMBL 517 9 2 4 6.6 CCCc1nc2c(C)cc(C(=O)NCc3ccccc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2012.01.009
44305654 100302 0 None - 0 Bovine 6.3 pIC50 = 6.3 Binding
Tested for binding affinity against angiotensin II receptor in bovine adrenal cortexTested for binding affinity against angiotensin II receptor in bovine adrenal cortex
ChEMBL 502 8 1 8 4.8 CCCCc1cc(=O)n2nc(-c3ccccc3)nc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/0960-894X(95)00370-9
CHEMBL293001 100302 0 None - 0 Bovine 6.3 pIC50 = 6.3 Binding
Tested for binding affinity against angiotensin II receptor in bovine adrenal cortexTested for binding affinity against angiotensin II receptor in bovine adrenal cortex
ChEMBL 502 8 1 8 4.8 CCCCc1cc(=O)n2nc(-c3ccccc3)nc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/0960-894X(95)00370-9
10071111 119123 0 None - 0 Rabbit 5.3 pIC50 = 5.3 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 426 9 2 7 3.5 CCSc1nnc(COC)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
CHEMBL346742 119123 0 None - 0 Rabbit 5.3 pIC50 = 5.3 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 426 9 2 7 3.5 CCSc1nnc(COC)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
44341786 164739 0 None - 0 Rat 5.3 pIC50 = 5.3 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 424 5 1 3 5.2 O=C(O)c1ccccc1-c1ccc(CN2C(=O)C3(CCCC3)N=C2c2ccccc2)cc1 10.1021/jm00074a018
CHEMBL423325 164739 0 None - 0 Rat 5.3 pIC50 = 5.3 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 424 5 1 3 5.2 O=C(O)c1ccccc1-c1ccc(CN2C(=O)C3(CCCC3)N=C2c2ccccc2)cc1 10.1021/jm00074a018
10071111 119123 0 None - 0 Rabbit 5.3 pIC50 = 5.3 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 426 9 2 7 3.5 CCSc1nnc(COC)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
CHEMBL346742 119123 0 None - 0 Rabbit 5.3 pIC50 = 5.3 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 426 9 2 7 3.5 CCSc1nnc(COC)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
24827772 95331 0 None - 0 Rat 7.3 pIC50 = 7.3 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
ChEMBL 439 8 1 7 4.3 CCCCCn1c(=O)c2cccnc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm7011563
CHEMBL258685 95331 0 None - 0 Rat 7.3 pIC50 = 7.3 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
ChEMBL 439 8 1 7 4.3 CCCCCn1c(=O)c2cccnc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm7011563
44297144 167443 0 None - 0 Bovine 7.3 pIC50 = 7.3 Binding
In vitro binding affinity to angiotensin II receptor in bovine adrenal cortexIn vitro binding affinity to angiotensin II receptor in bovine adrenal cortex
ChEMBL 617 8 1 9 5.9 CCCCc1nc2ccc([C@H]3OC[C@H]4[C@@H]3ON3[C@@H]4CCC3(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80377-2
CHEMBL432128 167443 0 None - 0 Bovine 7.3 pIC50 = 7.3 Binding
In vitro binding affinity to angiotensin II receptor in bovine adrenal cortexIn vitro binding affinity to angiotensin II receptor in bovine adrenal cortex
ChEMBL 617 8 1 9 5.9 CCCCc1nc2ccc([C@H]3OC[C@H]4[C@@H]3ON3[C@@H]4CCC3(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80377-2
44288321 154648 0 None - 0 Rat 7.3 pIC50 = 7.3 Binding
In vitro inhibition of specific binding of [125I]AII to Angiotensin II receptor, type 1 from rat liver membraneIn vitro inhibition of specific binding of [125I]AII to Angiotensin II receptor, type 1 from rat liver membrane
ChEMBL 418 7 1 3 5.7 CCCCC1=NC2(CCCC2)CC(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/S0960-894X(01)81139-2
CHEMBL40250 154648 0 None - 0 Rat 7.3 pIC50 = 7.3 Binding
In vitro inhibition of specific binding of [125I]AII to Angiotensin II receptor, type 1 from rat liver membraneIn vitro inhibition of specific binding of [125I]AII to Angiotensin II receptor, type 1 from rat liver membrane
ChEMBL 418 7 1 3 5.7 CCCCC1=NC2(CCCC2)CC(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/S0960-894X(01)81139-2
127026042 136720 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptorDisplacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptor
ChEMBL 620 11 3 9 3.8 CCCc1nc2c(C)cc(C(=O)NCCN3CCN(C)CC3)cc2n1Cc1ccc(-c2ccccc2C(=O)Nc2nnn[nH]2)cc1 10.1039/C5MD00169B
CHEMBL3751986 136720 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptorDisplacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptor
ChEMBL 620 11 3 9 3.8 CCCc1nc2c(C)cc(C(=O)NCCN3CCN(C)CC3)cc2n1Cc1ccc(-c2ccccc2C(=O)Nc2nnn[nH]2)cc1 10.1039/C5MD00169B
127036867 136844 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptorDisplacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptor
ChEMBL 614 11 3 8 5.7 CCCc1nc2c(C)cc(C(=O)NCc3cccc(OC)c3)cc2n1Cc1ccc(-c2ccccc2C(=O)Nc2nnn[nH]2)cc1 10.1039/C5MD00169B
CHEMBL3753134 136844 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptorDisplacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptor
ChEMBL 614 11 3 8 5.7 CCCc1nc2c(C)cc(C(=O)NCc3cccc(OC)c3)cc2n1Cc1ccc(-c2ccccc2C(=O)Nc2nnn[nH]2)cc1 10.1039/C5MD00169B
15287884 154690 0 None - 0 Rabbit 6.3 pIC50 = 6.3 Binding
Tested in vitro for Angiotensin II receptor, type 1 binding affinity using rabbit aorta binding assayTested in vitro for Angiotensin II receptor, type 1 binding affinity using rabbit aorta binding assay
ChEMBL 449 8 1 5 5.6 CCCc1nc2c(C)ccnc2n1Cc1ccc(OC(C(=O)O)c2ccc(Cl)cc2)cc1 10.1016/0960-894X(94)00476-V
CHEMBL40273 154690 0 None - 0 Rabbit 6.3 pIC50 = 6.3 Binding
Tested in vitro for Angiotensin II receptor, type 1 binding affinity using rabbit aorta binding assayTested in vitro for Angiotensin II receptor, type 1 binding affinity using rabbit aorta binding assay
ChEMBL 449 8 1 5 5.6 CCCc1nc2c(C)ccnc2n1Cc1ccc(OC(C(=O)O)c2ccc(Cl)cc2)cc1 10.1016/0960-894X(94)00476-V
15171420 204952 0 None - 0 Guinea pig 7.3 pIC50 = 7.3 Binding
Compound was tested for in vitro inhibition of specific binding of [I-125]AII to Angiotensin II receptor, type 1 in guinea pig adrenal membrane preparationCompound was tested for in vitro inhibition of specific binding of [I-125]AII to Angiotensin II receptor, type 1 in guinea pig adrenal membrane preparation
ChEMBL 425 6 1 5 5.3 CCc1cc(OCc2ccc(-c3ccc(C)cc3-c3nn[nH]n3)cc2)c2c(n1)CCCC2 10.1016/S0960-894X(01)80295-X
CHEMBL89614 204952 0 None - 0 Guinea pig 7.3 pIC50 = 7.3 Binding
Compound was tested for in vitro inhibition of specific binding of [I-125]AII to Angiotensin II receptor, type 1 in guinea pig adrenal membrane preparationCompound was tested for in vitro inhibition of specific binding of [I-125]AII to Angiotensin II receptor, type 1 in guinea pig adrenal membrane preparation
ChEMBL 425 6 1 5 5.3 CCc1cc(OCc2ccc(-c3ccc(C)cc3-c3nn[nH]n3)cc2)c2c(n1)CCCC2 10.1016/S0960-894X(01)80295-X
44352199 21790 0 None - 0 Bovine 7.3 pIC50 = 7.3 Binding
Concentration required to inhibit [125I]AII binding to Angiotensin II receptor from membrane fractions of bovine adrenal cortexConcentration required to inhibit [125I]AII binding to Angiotensin II receptor from membrane fractions of bovine adrenal cortex
ChEMBL 423 7 1 6 5.0 CCCCc1nc2c(C)cncc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81118-5
CHEMBL132109 21790 0 None - 0 Bovine 7.3 pIC50 = 7.3 Binding
Concentration required to inhibit [125I]AII binding to Angiotensin II receptor from membrane fractions of bovine adrenal cortexConcentration required to inhibit [125I]AII binding to Angiotensin II receptor from membrane fractions of bovine adrenal cortex
ChEMBL 423 7 1 6 5.0 CCCCc1nc2c(C)cncc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81118-5
1610 2305 89 None -1 4 Rabbit 7.3 pIC50 = 7.3 Binding
Displacement of [1251][Sar1,IIe8]AII from rabbit aorta Angiotensin II receptor, type 1Displacement of [1251][Sar1,IIe8]AII from rabbit aorta Angiotensin II receptor, type 1
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00075a033
3941 2305 89 None -1 4 Rabbit 7.3 pIC50 = 7.3 Binding
Displacement of [1251][Sar1,IIe8]AII from rabbit aorta Angiotensin II receptor, type 1Displacement of [1251][Sar1,IIe8]AII from rabbit aorta Angiotensin II receptor, type 1
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00075a033
3961 2305 89 None -1 4 Rabbit 7.3 pIC50 = 7.3 Binding
Displacement of [1251][Sar1,IIe8]AII from rabbit aorta Angiotensin II receptor, type 1Displacement of [1251][Sar1,IIe8]AII from rabbit aorta Angiotensin II receptor, type 1
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00075a033
590 2305 89 None -1 4 Rabbit 7.3 pIC50 = 7.3 Binding
Displacement of [1251][Sar1,IIe8]AII from rabbit aorta Angiotensin II receptor, type 1Displacement of [1251][Sar1,IIe8]AII from rabbit aorta Angiotensin II receptor, type 1
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00075a033
CHEMBL191 2305 89 None -1 4 Rabbit 7.3 pIC50 = 7.3 Binding
Displacement of [1251][Sar1,IIe8]AII from rabbit aorta Angiotensin II receptor, type 1Displacement of [1251][Sar1,IIe8]AII from rabbit aorta Angiotensin II receptor, type 1
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00075a033
DB00678 2305 89 None -1 4 Rabbit 7.3 pIC50 = 7.3 Binding
Displacement of [1251][Sar1,IIe8]AII from rabbit aorta Angiotensin II receptor, type 1Displacement of [1251][Sar1,IIe8]AII from rabbit aorta Angiotensin II receptor, type 1
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00075a033
14950504 85051 0 None - 0 Guinea pig 7.3 pIC50 = 7.3 Binding
Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1
ChEMBL 443 8 1 7 4.6 CCCc1nc(C)cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c1C(=O)OC 10.1021/jm00061a016
CHEMBL22692 85051 0 None - 0 Guinea pig 7.3 pIC50 = 7.3 Binding
Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1
ChEMBL 443 8 1 7 4.6 CCCc1nc(C)cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c1C(=O)OC 10.1021/jm00061a016
10052319 162771 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 518 12 1 7 4.4 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2Cc2c[nH]cn2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
CHEMBL419058 162771 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 518 12 1 7 4.4 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2Cc2c[nH]cn2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
9807638 186553 0 None - 1 Bovine 6.3 pIC50 = 6.3 Binding
Ability to displace [125I]- labelled [Sar1,Ileu8] from angiotensin II receptor of bovine adrenal cortex membranesAbility to displace [125I]- labelled [Sar1,Ileu8] from angiotensin II receptor of bovine adrenal cortex membranes
ChEMBL 471 6 1 6 4.7 CCOC(=O)/C=C1\CC2(CCCC2)CC(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80474-6
CHEMBL49192 186553 0 None - 1 Bovine 6.3 pIC50 = 6.3 Binding
Ability to displace [125I]- labelled [Sar1,Ileu8] from angiotensin II receptor of bovine adrenal cortex membranesAbility to displace [125I]- labelled [Sar1,Ileu8] from angiotensin II receptor of bovine adrenal cortex membranes
ChEMBL 471 6 1 6 4.7 CCOC(=O)/C=C1\CC2(CCCC2)CC(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80474-6
11743916 118944 0 None - 0 Rabbit 6.3 pIC50 = 6.3 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 439 10 1 7 4.3 CCCCc1nnc(SCC(=O)OC)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
CHEMBL345127 118944 0 None - 0 Rabbit 6.3 pIC50 = 6.3 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 439 10 1 7 4.3 CCCCc1nnc(SCC(=O)OC)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
19792121 188839 0 None - 0 Bovine 6.3 pIC50 = 6.3 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 493 9 2 6 5.4 CCCCc1nc2cccc(C(=O)NC(C)C)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
CHEMBL51340 188839 0 None - 0 Bovine 6.3 pIC50 = 6.3 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 493 9 2 6 5.4 CCCCc1nc2cccc(C(=O)NC(C)C)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
10363552 20400 0 None - 0 Rat 6.3 pIC50 = 6.3 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 399 7 2 4 5.4 CCCCc1nc2ccc(N)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00077a007
CHEMBL130828 20400 0 None - 0 Rat 6.3 pIC50 = 6.3 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 399 7 2 4 5.4 CCCCc1nc2ccc(N)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00077a007
15699068 5277 0 None - 0 Rat 5.3 pIC50 = 5.3 Binding
Binding affinity against angiotensin II receptor in rat smooth muscle cell preparationsBinding affinity against angiotensin II receptor in rat smooth muscle cell preparations
ChEMBL 400 7 2 6 3.2 CCCCc1nc(Cl)c(CO)n1Cc1ccc2c(c1)CCC(c1nnn[nH]1)C2 10.1021/jm00114a021
CHEMBL106934 5277 0 None - 0 Rat 5.3 pIC50 = 5.3 Binding
Binding affinity against angiotensin II receptor in rat smooth muscle cell preparationsBinding affinity against angiotensin II receptor in rat smooth muscle cell preparations
ChEMBL 400 7 2 6 3.2 CCCCc1nc(Cl)c(CO)n1Cc1ccc2c(c1)CCC(c1nnn[nH]1)C2 10.1021/jm00114a021
44303884 201136 0 None - 0 Rabbit 5.3 pIC50 = 5.3 Binding
Inhibition of angiotensin Angiotensin II receptor, type 1 in rabbit aorta using [125I-Sar1,Ile8] angiotensin II binding assayInhibition of angiotensin Angiotensin II receptor, type 1 in rabbit aorta using [125I-Sar1,Ile8] angiotensin II binding assay
ChEMBL 586 11 1 3 6.6 CCCCCN(CCCCC)C(=O)N1CCN(C(=O)N(c2ccccc2)c2ccc(Br)cc2)[C@H](C(=O)O)C1 10.1016/S0960-894X(01)81007-6
CHEMBL62422 201136 0 None - 0 Rabbit 5.3 pIC50 = 5.3 Binding
Inhibition of angiotensin Angiotensin II receptor, type 1 in rabbit aorta using [125I-Sar1,Ile8] angiotensin II binding assayInhibition of angiotensin Angiotensin II receptor, type 1 in rabbit aorta using [125I-Sar1,Ile8] angiotensin II binding assay
ChEMBL 586 11 1 3 6.6 CCCCCN(CCCCC)C(=O)N1CCN(C(=O)N(c2ccccc2)c2ccc(Br)cc2)[C@H](C(=O)O)C1 10.1016/S0960-894X(01)81007-6
44459611 99616 0 None - 0 Bovine 4.3 pIC50 = 4.3 Binding
Concentration required for 50% inhibition of binding against Angiotensin II receptor, type 1 in bovine adrenal cortexConcentration required for 50% inhibition of binding against Angiotensin II receptor, type 1 in bovine adrenal cortex
ChEMBL 568 7 2 7 5.9 COc1ccc(-c2nc3cc(C4=NN(Cc5ccc(-c6ccccc6-c6nn[nH]n6)cc5)C(=O)CC4C)ccc3[nH]2)cc1 10.1016/S0960-894X(01)80348-6
CHEMBL287374 99616 0 None - 0 Bovine 4.3 pIC50 = 4.3 Binding
Concentration required for 50% inhibition of binding against Angiotensin II receptor, type 1 in bovine adrenal cortexConcentration required for 50% inhibition of binding against Angiotensin II receptor, type 1 in bovine adrenal cortex
ChEMBL 568 7 2 7 5.9 COc1ccc(-c2nc3cc(C4=NN(Cc5ccc(-c6ccccc6-c6nn[nH]n6)cc5)C(=O)CC4C)ccc3[nH]2)cc1 10.1016/S0960-894X(01)80348-6
19792121 188839 0 None - 0 Bovine 6.3 pIC50 = 6.3 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 493 9 2 6 5.4 CCCCc1nc2cccc(C(=O)NC(C)C)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
CHEMBL51340 188839 0 None - 0 Bovine 6.3 pIC50 = 6.3 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 493 9 2 6 5.4 CCCCc1nc2cccc(C(=O)NC(C)C)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
127036868 136825 0 None - 0 Human 6.3 pIC50 = 6.3 Binding
Displacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptorDisplacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptor
ChEMBL 614 11 3 8 5.7 CCCc1nc2c(C)cc(C(=O)NCc3ccc(OC)cc3)cc2n1Cc1ccc(-c2ccccc2C(=O)Nc2nnn[nH]2)cc1 10.1039/C5MD00169B
CHEMBL3753007 136825 0 None - 0 Human 6.3 pIC50 = 6.3 Binding
Displacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptorDisplacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptor
ChEMBL 614 11 3 8 5.7 CCCc1nc2c(C)cc(C(=O)NCc3ccc(OC)cc3)cc2n1Cc1ccc(-c2ccccc2C(=O)Nc2nnn[nH]2)cc1 10.1039/C5MD00169B
10001717 47977 0 None - 0 Rabbit 7.3 pIC50 = 7.3 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 412 7 1 7 4.1 CCCCc1nn2cc(C)nc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
CHEMBL155305 47977 0 None - 0 Rabbit 7.3 pIC50 = 7.3 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 412 7 1 7 4.1 CCCCc1nn2cc(C)nc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
9985840 119505 0 None - 0 Rabbit 7.3 pIC50 = 7.3 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 426 8 1 7 4.3 CCCCc1nn2cc(CC)nc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
CHEMBL350241 119505 0 None - 0 Rabbit 7.3 pIC50 = 7.3 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 426 8 1 7 4.3 CCCCc1nn2cc(CC)nc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
9930953 102316 0 None - 0 Bovine 7.3 pIC50 = 7.3 Binding
Tested for binding affinity against angiotensin II receptor in bovine adrenal cortexTested for binding affinity against angiotensin II receptor in bovine adrenal cortex
ChEMBL 402 6 1 7 2.4 CCCc1cc(=O)n(C)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/0960-894X(95)00370-9
CHEMBL305350 102316 0 None - 0 Bovine 7.3 pIC50 = 7.3 Binding
Tested for binding affinity against angiotensin II receptor in bovine adrenal cortexTested for binding affinity against angiotensin II receptor in bovine adrenal cortex
ChEMBL 402 6 1 7 2.4 CCCc1cc(=O)n(C)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/0960-894X(95)00370-9
3025727 183488 10 None - 0 Bovine 6.3 pIC50 = 6.3 Binding
Displacement of [125I]-angiotensin 2 from angiotensin AT1 receptor in bovine adrenal cortical membranesDisplacement of [125I]-angiotensin 2 from angiotensin AT1 receptor in bovine adrenal cortical membranes
ChEMBL 452 8 2 6 5.0 CCCCc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.bmc.2010.10.043
CHEMBL48242 183488 10 None - 0 Bovine 6.3 pIC50 = 6.3 Binding
Displacement of [125I]-angiotensin 2 from angiotensin AT1 receptor in bovine adrenal cortical membranesDisplacement of [125I]-angiotensin 2 from angiotensin AT1 receptor in bovine adrenal cortical membranes
ChEMBL 452 8 2 6 5.0 CCCCc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.bmc.2010.10.043
3025727 183488 10 None - 0 Bovine 6.3 pIC50 = 6.3 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 452 8 2 6 5.0 CCCCc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
CHEMBL48242 183488 10 None - 0 Bovine 6.3 pIC50 = 6.3 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 452 8 2 6 5.0 CCCCc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
44358531 118843 0 None - 0 Rabbit 6.3 pIC50 = 6.3 Binding
Displacement of the specific binding ligand [125I]Sar1,Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane.Displacement of the specific binding ligand [125I]Sar1,Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane.
ChEMBL 636 6 3 8 5.0 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2C2Nc3cc(Cl)c(S(N)(=O)=O)cc3S(=O)(=O)N2)cc1 10.1016/S0960-894X(01)81119-7
CHEMBL344388 118843 0 None - 0 Rabbit 6.3 pIC50 = 6.3 Binding
Displacement of the specific binding ligand [125I]Sar1,Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane.Displacement of the specific binding ligand [125I]Sar1,Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane.
ChEMBL 636 6 3 8 5.0 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2C2Nc3cc(Cl)c(S(N)(=O)=O)cc3S(=O)(=O)N2)cc1 10.1016/S0960-894X(01)81119-7
3025727 183488 10 None - 0 Bovine 6.3 pIC50 = 6.3 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 452 8 2 6 5.0 CCCCc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a016
CHEMBL48242 183488 10 None - 0 Bovine 6.3 pIC50 = 6.3 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 452 8 2 6 5.0 CCCCc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a016
3025727 183488 10 None - 0 Bovine 6.3 pIC50 = 6.3 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 452 8 2 6 5.0 CCCCc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
CHEMBL48242 183488 10 None - 0 Bovine 6.3 pIC50 = 6.3 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 452 8 2 6 5.0 CCCCc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
44459759 99210 0 None - 0 Bovine 5.3 pIC50 = 5.3 Binding
Concentration required for 50% inhibition of binding against Angiotensin II receptor, type 1 in bovine adrenal cortexConcentration required for 50% inhibition of binding against Angiotensin II receptor, type 1 in bovine adrenal cortex
ChEMBL 568 7 2 8 5.5 COc1ccc(-c2nc3cc(C4=NNC(=O)CC4C)ccc3n2Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)cc1 10.1016/S0960-894X(01)80348-6
CHEMBL284546 99210 0 None - 0 Bovine 5.3 pIC50 = 5.3 Binding
Concentration required for 50% inhibition of binding against Angiotensin II receptor, type 1 in bovine adrenal cortexConcentration required for 50% inhibition of binding against Angiotensin II receptor, type 1 in bovine adrenal cortex
ChEMBL 568 7 2 8 5.5 COc1ccc(-c2nc3cc(C4=NNC(=O)CC4C)ccc3n2Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)cc1 10.1016/S0960-894X(01)80348-6
15662012 188730 0 None - 0 Bovine 5.3 pIC50 = 5.3 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 452 8 2 6 5.0 CCCCc1nc2cc(C(=O)O)ccc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
CHEMBL51246 188730 0 None - 0 Bovine 5.3 pIC50 = 5.3 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 452 8 2 6 5.0 CCCCc1nc2cc(C(=O)O)ccc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
15699052 109274 0 None - 0 Rat 4.3 pIC50 = 4.3 Binding
Binding affinity against angiotensin II receptor in rat smooth muscle cell preparationsBinding affinity against angiotensin II receptor in rat smooth muscle cell preparations
ChEMBL 396 7 2 6 3.8 CCCCc1nc(Cl)c(CO)n1Cc1ccc2cccc(-c3nn[nH]n3)c2c1 10.1021/jm00114a021
CHEMBL323179 109274 0 None - 0 Rat 4.3 pIC50 = 4.3 Binding
Binding affinity against angiotensin II receptor in rat smooth muscle cell preparationsBinding affinity against angiotensin II receptor in rat smooth muscle cell preparations
ChEMBL 396 7 2 6 3.8 CCCCc1nc(Cl)c(CO)n1Cc1ccc2cccc(-c3nn[nH]n3)c2c1 10.1021/jm00114a021
44291477 100863 0 None - 0 Rat 7.3 pIC50 = 7.3 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 406 9 1 3 5.5 CCCCC1=NC(CC)(CC)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00074a018
CHEMBL296883 100863 0 None - 0 Rat 7.3 pIC50 = 7.3 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 406 9 1 3 5.5 CCCCC1=NC(CC)(CC)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00074a018
9888865 57180 0 None - 0 Rabbit 7.3 pIC50 = 7.3 Binding
Binding affinity to Angiotensin II receptor, type 1 in rabbit aorta binding assayBinding affinity to Angiotensin II receptor, type 1 in rabbit aorta binding assay
ChEMBL 429 6 1 6 4.4 CCCc1nc2c(C)ccnc2n1Cc1ccc2c(c1)OC(C(=O)O)(c1ccccc1)O2 10.1016/S0960-894X(01)80193-1
CHEMBL165974 57180 0 None - 0 Rabbit 7.3 pIC50 = 7.3 Binding
Binding affinity to Angiotensin II receptor, type 1 in rabbit aorta binding assayBinding affinity to Angiotensin II receptor, type 1 in rabbit aorta binding assay
ChEMBL 429 6 1 6 4.4 CCCc1nc2c(C)ccnc2n1Cc1ccc2c(c1)OC(C(=O)O)(c1ccccc1)O2 10.1016/S0960-894X(01)80193-1
127035084 135847 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysisDisplacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysis
ChEMBL 707 13 2 9 7.4 CCCc1nc2c(C)cc(C(=O)NCc3ccc(OC)c(OC)c3)cc2n1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)cc1 10.1039/C4MD00499J
CHEMBL3735151 135847 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysisDisplacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysis
ChEMBL 707 13 2 9 7.4 CCCc1nc2c(C)cc(C(=O)NCc3ccc(OC)c(OC)c3)cc2n1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)cc1 10.1039/C4MD00499J
44291477 100863 0 None - 0 Rat 7.3 pIC50 = 7.3 Binding
In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.
ChEMBL 406 9 1 3 5.5 CCCCC1=NC(CC)(CC)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/S0960-894X(01)81140-9
CHEMBL296883 100863 0 None - 0 Rat 7.3 pIC50 = 7.3 Binding
In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.
ChEMBL 406 9 1 3 5.5 CCCCC1=NC(CC)(CC)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/S0960-894X(01)81140-9
18942290 192865 0 None - 0 Bovine 7.3 pIC50 = 7.3 Binding
In vitro binding affinity to angiotensin II receptor in bovine adrenal cortexIn vitro binding affinity to angiotensin II receptor in bovine adrenal cortex
ChEMBL 558 8 1 8 5.6 CCCCc1nc2ccc(C3=NN4CCCCC4C3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80377-2
CHEMBL52700 192865 0 None - 0 Bovine 7.3 pIC50 = 7.3 Binding
In vitro binding affinity to angiotensin II receptor in bovine adrenal cortexIn vitro binding affinity to angiotensin II receptor in bovine adrenal cortex
ChEMBL 558 8 1 8 5.6 CCCCc1nc2ccc(C3=NN4CCCCC4C3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80377-2
15654747 202126 0 None - 0 Bovine 6.3 pIC50 = 6.3 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 466 9 2 6 5.4 CCCCCc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a016
CHEMBL68516 202126 0 None - 0 Bovine 6.3 pIC50 = 6.3 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 466 9 2 6 5.4 CCCCCc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a016
15662012 188730 0 None - 0 Bovine 5.3 pIC50 = 5.3 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 452 8 2 6 5.0 CCCCc1nc2cc(C(=O)O)ccc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
CHEMBL51246 188730 0 None - 0 Bovine 5.3 pIC50 = 5.3 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 452 8 2 6 5.0 CCCCc1nc2cc(C(=O)O)ccc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
76315365 84510 0 None - 0 Rabbit 7.2 pIC50 = 7.2 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 535 11 3 8 4.0 CCCCc1nnc(C(=O)NCc2ccccc2)n1Cc1ccc(NC(=O)c2ccccc2-c2nnn[nH]2)cc1 10.1007/s00044-011-9756-4
CHEMBL2237580 84510 0 None - 0 Rabbit 7.2 pIC50 = 7.2 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 535 11 3 8 4.0 CCCCc1nnc(C(=O)NCc2ccccc2)n1Cc1ccc(NC(=O)c2ccccc2-c2nnn[nH]2)cc1 10.1007/s00044-011-9756-4
10078057 50347 0 None - 0 Rabbit 7.2 pIC50 = 7.2 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 492 10 2 7 4.4 CCCCc1nnc(C(=O)NCc2ccccc2)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
CHEMBL157512 50347 0 None - 0 Rabbit 7.2 pIC50 = 7.2 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 492 10 2 7 4.4 CCCCc1nnc(C(=O)NCc2ccccc2)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
44358303 30645 0 None - 0 Rabbit 7.2 pIC50 = 7.2 Binding
Displacement of the specific binding ligand [125I]Sar1,Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane.Displacement of the specific binding ligand [125I]Sar1,Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane.
ChEMBL 520 6 1 7 5.7 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2N2N=C(c3ccccc3)N[S+]2[O-])cc1 10.1016/S0960-894X(01)81119-7
CHEMBL139739 30645 0 None - 0 Rabbit 7.2 pIC50 = 7.2 Binding
Displacement of the specific binding ligand [125I]Sar1,Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane.Displacement of the specific binding ligand [125I]Sar1,Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane.
ChEMBL 520 6 1 7 5.7 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2N2N=C(c3ccccc3)N[S+]2[O-])cc1 10.1016/S0960-894X(01)81119-7
15287887 144647 0 None - 0 Rabbit 7.2 pIC50 = 7.2 Binding
Tested in vitro for Angiotensin II receptor, type 1 binding affinity using rabbit aorta binding assayTested in vitro for Angiotensin II receptor, type 1 binding affinity using rabbit aorta binding assay
ChEMBL 460 9 1 7 4.9 CCCc1nc2c(C)ccnc2n1Cc1ccc(OC(C(=O)O)c2ccccc2[N+](=O)[O-])cc1 10.1016/0960-894X(94)00476-V
CHEMBL39124 144647 0 None - 0 Rabbit 7.2 pIC50 = 7.2 Binding
Tested in vitro for Angiotensin II receptor, type 1 binding affinity using rabbit aorta binding assayTested in vitro for Angiotensin II receptor, type 1 binding affinity using rabbit aorta binding assay
ChEMBL 460 9 1 7 4.9 CCCc1nc2c(C)ccnc2n1Cc1ccc(OC(C(=O)O)c2ccccc2[N+](=O)[O-])cc1 10.1016/0960-894X(94)00476-V
127034920 135995 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 547 10 2 5 6.7 CCOc1nc2c(C)cc(C(=O)NC[C@@H](C)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2015.09.010
CHEMBL3736451 135995 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 547 10 2 5 6.7 CCOc1nc2c(C)cc(C(=O)NC[C@@H](C)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2015.09.010
46910582 69995 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Displacement of [125I]Sar1 Ile8-Ang 2 from angiotensin 2 AT1 receptor after 180 mins by gamma countingDisplacement of [125I]Sar1 Ile8-Ang 2 from angiotensin 2 AT1 receptor after 180 mins by gamma counting
ChEMBL 591 12 2 6 6.7 CCCc1nc2c(C)cc(C(=O)NCCc3ccc(OC)c(OC)c3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2012.01.009
CHEMBL1945009 69995 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Displacement of [125I]Sar1 Ile8-Ang 2 from angiotensin 2 AT1 receptor after 180 mins by gamma countingDisplacement of [125I]Sar1 Ile8-Ang 2 from angiotensin 2 AT1 receptor after 180 mins by gamma counting
ChEMBL 591 12 2 6 6.7 CCCc1nc2c(C)cc(C(=O)NCCc3ccc(OC)c(OC)c3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2012.01.009
127036107 135980 0 None - 1 Human 7.2 pIC50 = 7.2 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 561 11 2 5 6.8 CCCc1nc2c(C)cc(C(=O)N[C@H](COC)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2015.09.010
CHEMBL3736319 135980 0 None - 1 Human 7.2 pIC50 = 7.2 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 561 11 2 5 6.8 CCCc1nc2c(C)cc(C(=O)N[C@H](COC)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2015.09.010
9940350 203040 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Inhibition of Angiotensin II receptor, type 1Inhibition of Angiotensin II receptor, type 1
ChEMBL 753 16 1 9 8.3 CCCc1nc(CC)c(C(=O)OCc2ccccc2C(=O)c2ccccc2)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1021/jm9504722
CHEMBL74573 203040 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Inhibition of Angiotensin II receptor, type 1Inhibition of Angiotensin II receptor, type 1
ChEMBL 753 16 1 9 8.3 CCCc1nc(CC)c(C(=O)OCc2ccccc2C(=O)c2ccccc2)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1021/jm9504722
10072002 114731 0 None - 0 Rat 5.2 pIC50 = 5.2 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 441 8 2 4 5.8 CCCCc1nc2c(NC(C)=O)cccc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00077a007
CHEMBL334741 114731 0 None - 0 Rat 5.2 pIC50 = 5.2 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 441 8 2 4 5.8 CCCCc1nc2c(NC(C)=O)cccc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00077a007
11328411 105674 0 None - 0 Rat 6.2 pIC50 = 6.2 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 450 6 1 5 5.5 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2c(CC(=O)O)cnc3ccccc23)cc1 10.1021/jm031100t
CHEMBL313718 105674 0 None - 0 Rat 6.2 pIC50 = 6.2 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 450 6 1 5 5.5 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2c(CC(=O)O)cnc3ccccc23)cc1 10.1021/jm031100t
10786794 162330 0 None - 0 Bovine 7.2 pIC50 = 7.2 Binding
In vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortexIn vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortex
ChEMBL 394 8 3 5 3.4 CCCc1nc(CO)c(C(=O)O)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm950450f
CHEMBL417366 162330 0 None - 0 Bovine 7.2 pIC50 = 7.2 Binding
In vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortexIn vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortex
ChEMBL 394 8 3 5 3.4 CCCc1nc(CO)c(C(=O)O)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm950450f
10786794 162330 0 None - 0 Bovine 7.2 pIC50 = 7.2 Binding
Inhibition of [125l]-All binding to bovine adrenal cortexInhibition of [125l]-All binding to bovine adrenal cortex
ChEMBL 394 8 3 5 3.4 CCCc1nc(CO)c(C(=O)O)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/S0960-894X(01)81143-4
CHEMBL417366 162330 0 None - 0 Bovine 7.2 pIC50 = 7.2 Binding
Inhibition of [125l]-All binding to bovine adrenal cortexInhibition of [125l]-All binding to bovine adrenal cortex
ChEMBL 394 8 3 5 3.4 CCCc1nc(CO)c(C(=O)O)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/S0960-894X(01)81143-4
15654757 101744 0 None - 0 Bovine 6.2 pIC50 = 6.2 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 494 7 2 7 4.6 O=C(O)c1cccc2nc(OCC(F)(F)F)n(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c12 10.1021/jm00067a016
CHEMBL302973 101744 0 None - 0 Bovine 6.2 pIC50 = 6.2 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 494 7 2 7 4.6 O=C(O)c1cccc2nc(OCC(F)(F)F)n(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c12 10.1021/jm00067a016
15654752 101771 0 None - 0 Bovine 6.2 pIC50 = 6.2 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 454 8 2 7 3.8 COCCc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a016
CHEMBL303170 101771 0 None - 0 Bovine 6.2 pIC50 = 6.2 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 454 8 2 7 3.8 COCCc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a016
44295010 186651 0 None - 1 Bovine 5.2 pIC50 = 5.2 Binding
Ability to displace [125I]- labelled [Sar1,Ileu8] from angiotensin II receptor of bovine adrenal cortex membranesAbility to displace [125I]- labelled [Sar1,Ileu8] from angiotensin II receptor of bovine adrenal cortex membranes
ChEMBL 445 6 1 6 4.1 CCOC(=O)/C=C1\CC(C)(C)CC(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80474-6
CHEMBL49262 186651 0 None - 1 Bovine 5.2 pIC50 = 5.2 Binding
Ability to displace [125I]- labelled [Sar1,Ileu8] from angiotensin II receptor of bovine adrenal cortex membranesAbility to displace [125I]- labelled [Sar1,Ileu8] from angiotensin II receptor of bovine adrenal cortex membranes
ChEMBL 445 6 1 6 4.1 CCOC(=O)/C=C1\CC(C)(C)CC(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80474-6
54768877 64774 0 None - 0 Human 5.2 pIC50 = 5.2 Binding
Displacement of [125I][Sar1,Ile8]-AT-II from human recombinant AT1 receptor expressed in HEK293 cells after 120 mins by liquid scintillation countingDisplacement of [125I][Sar1,Ile8]-AT-II from human recombinant AT1 receptor expressed in HEK293 cells after 120 mins by liquid scintillation counting
ChEMBL 535 9 1 8 5.2 CCOC(=O)c1cn(Cc2ccc(-c3ccccc3-c3nnn[nH]3)cc2)nc1N(C(C)=O)c1ccc(CC)cc1 10.1016/j.ejmech.2011.05.056
CHEMBL1824003 64774 0 None - 0 Human 5.2 pIC50 = 5.2 Binding
Displacement of [125I][Sar1,Ile8]-AT-II from human recombinant AT1 receptor expressed in HEK293 cells after 120 mins by liquid scintillation countingDisplacement of [125I][Sar1,Ile8]-AT-II from human recombinant AT1 receptor expressed in HEK293 cells after 120 mins by liquid scintillation counting
ChEMBL 535 9 1 8 5.2 CCOC(=O)c1cn(Cc2ccc(-c3ccccc3-c3nnn[nH]3)cc2)nc1N(C(C)=O)c1ccc(CC)cc1 10.1016/j.ejmech.2011.05.056
14951089 102457 0 None - 0 Rat 5.2 pIC50 = 5.2 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 583 12 1 8 6.0 CCCCc1nn(C(Cc2ccccc2)C(=O)c2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a015
CHEMBL306328 102457 0 None - 0 Rat 5.2 pIC50 = 5.2 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 583 12 1 8 6.0 CCCCc1nn(C(Cc2ccccc2)C(=O)c2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a015
44341597 9850 0 None - 0 Rat 7.2 pIC50 = 7.2 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 505 9 2 5 3.8 CCCCC1=NC2(CCN(C(=O)CC(=O)O)CC2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00074a018
CHEMBL114710 9850 0 None - 0 Rat 7.2 pIC50 = 7.2 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 505 9 2 5 3.8 CCCCC1=NC2(CCN(C(=O)CC(=O)O)CC2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00074a018
44315350 104726 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membrane
ChEMBL 645 9 3 7 5.2 CCNC(=O)Nc1ccc2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)c4ccccc4F)cc3F)c(=O)c2c1 10.1016/0960-894X(94)85036-4
CHEMBL311484 104726 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membrane
ChEMBL 645 9 3 7 5.2 CCNC(=O)Nc1ccc2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)c4ccccc4F)cc3F)c(=O)c2c1 10.1016/0960-894X(94)85036-4
10275744 204388 0 None - 0 Rat 7.2 pIC50 = 7.2 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 451 8 1 7 4.3 CCCCc1nn(-c2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a015
CHEMBL85876 204388 0 None - 0 Rat 7.2 pIC50 = 7.2 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 451 8 1 7 4.3 CCCCc1nn(-c2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a015
44293656 187420 0 None - 0 Rat 6.2 pIC50 = 6.2 Binding
Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.
ChEMBL 514 13 2 7 5.4 CCCCc1nc(Cl)c(CO)n1Cc1ccc(NC(=O)[C@H](CCCC)n2cccc2C(=O)OC)cc1 10.1021/jm00064a007
CHEMBL49748 187420 0 None - 0 Rat 6.2 pIC50 = 6.2 Binding
Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.
ChEMBL 514 13 2 7 5.4 CCCCc1nc(Cl)c(CO)n1Cc1ccc(NC(=O)[C@H](CCCC)n2cccc2C(=O)OC)cc1 10.1021/jm00064a007
15780089 99335 0 None - 0 Rabbit 6.2 pIC50 = 6.2 Binding
Displacement of [125 I]Sar1Ile8-AII from type 1 Angiotensin II receptor of rabbit aorta membraneDisplacement of [125 I]Sar1Ile8-AII from type 1 Angiotensin II receptor of rabbit aorta membrane
ChEMBL 603 8 1 7 6.4 Cc1nc2ccc(N(Cc3ccccc3)C(=O)c3ccccc3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80517-5
CHEMBL285432 99335 0 None - 0 Rabbit 6.2 pIC50 = 6.2 Binding
Displacement of [125 I]Sar1Ile8-AII from type 1 Angiotensin II receptor of rabbit aorta membraneDisplacement of [125 I]Sar1Ile8-AII from type 1 Angiotensin II receptor of rabbit aorta membrane
ChEMBL 603 8 1 7 6.4 Cc1nc2ccc(N(Cc3ccccc3)C(=O)c3ccccc3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80517-5
44303887 201621 0 None - 0 Rabbit 4.2 pIC50 = 4.2 Binding
Inhibition of angiotensin Angiotensin II receptor, type 1 in rabbit aorta using [125I-Sar1,Ile8] angiotensin II binding assayInhibition of angiotensin Angiotensin II receptor, type 1 in rabbit aorta using [125I-Sar1,Ile8] angiotensin II binding assay
ChEMBL 586 11 1 3 6.6 CCCCCN(CCCCC)C(=O)N1CCN(C(=O)N(c2ccccc2)c2cccc(Br)c2)[C@H](C(=O)O)C1 10.1016/S0960-894X(01)81007-6
CHEMBL64861 201621 0 None - 0 Rabbit 4.2 pIC50 = 4.2 Binding
Inhibition of angiotensin Angiotensin II receptor, type 1 in rabbit aorta using [125I-Sar1,Ile8] angiotensin II binding assayInhibition of angiotensin Angiotensin II receptor, type 1 in rabbit aorta using [125I-Sar1,Ile8] angiotensin II binding assay
ChEMBL 586 11 1 3 6.6 CCCCCN(CCCCC)C(=O)N1CCN(C(=O)N(c2ccccc2)c2cccc(Br)c2)[C@H](C(=O)O)C1 10.1016/S0960-894X(01)81007-6
71521194 86370 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor afterDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after
ChEMBL 423 4 2 6 3.7 CCc1nc2cc[nH]c(=O)c2n1[C@H]1CCc2cc(-c3ccccc3-c3nnn[nH]3)ccc21 10.1016/j.bmcl.2012.11.088
CHEMBL2322177 86370 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor afterDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after
ChEMBL 423 4 2 6 3.7 CCc1nc2cc[nH]c(=O)c2n1[C@H]1CCc2cc(-c3ccccc3-c3nnn[nH]3)ccc21 10.1016/j.bmcl.2012.11.088
24828038 158896 0 None - 0 Rat 6.2 pIC50 = 6.2 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
ChEMBL 424 7 1 6 4.5 CCCCn1c(=O)c2ccccc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm7011563
CHEMBL410125 158896 0 None - 0 Rat 6.2 pIC50 = 6.2 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
ChEMBL 424 7 1 6 4.5 CCCCn1c(=O)c2ccccc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm7011563
19087866 98466 0 None - 0 Rabbit 8.2 pIC50 = 8.2 Binding
Ability to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitroAbility to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitro
ChEMBL 436 7 1 6 4.6 CCCCc1nc2ccccc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80335-2
CHEMBL279515 98466 0 None - 0 Rabbit 8.2 pIC50 = 8.2 Binding
Ability to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitroAbility to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitro
ChEMBL 436 7 1 6 4.6 CCCCc1nc2ccccc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80335-2
14956801 204380 0 None - 0 Rabbit 8.2 pIC50 = 8.2 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 555 9 1 7 5.0 CCCCc1nn(Cc2c(F)c(F)c(F)c(F)c2F)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
CHEMBL85765 204380 0 None - 0 Rabbit 8.2 pIC50 = 8.2 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 555 9 1 7 5.0 CCCCc1nn(Cc2c(F)c(F)c(F)c(F)c2F)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
60165459 104759 3 None - 0 Human 8.2 pIC50 = 8.2 Binding
Antagonist activity at human AT1 receptor expressed in CHO cells measured after overnight incubation by luciferase reporter gene assayAntagonist activity at human AT1 receptor expressed in CHO cells measured after overnight incubation by luciferase reporter gene assay
ChEMBL 566 10 1 7 7.7 CCCCn1c(-c2ccc3nn(CCC)c(Cc4ccc(-c5ccccc5-c5nn[nH]n5)cc4)c3c2)nc2ccccc21 10.1016/j.bmcl.2014.01.004
CHEMBL3115247 104759 3 None - 0 Human 8.2 pIC50 = 8.2 Binding
Antagonist activity at human AT1 receptor expressed in CHO cells measured after overnight incubation by luciferase reporter gene assayAntagonist activity at human AT1 receptor expressed in CHO cells measured after overnight incubation by luciferase reporter gene assay
ChEMBL 566 10 1 7 7.7 CCCCn1c(-c2ccc3nn(CCC)c(Cc4ccc(-c5ccccc5-c5nn[nH]n5)cc4)c3c2)nc2ccccc21 10.1016/j.bmcl.2014.01.004
44277594 101320 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
Binding affinity against AT1 receptor in human adrenal tissueBinding affinity against AT1 receptor in human adrenal tissue
ChEMBL 619 8 1 9 5.9 Cn1nnnc1-c1ccccc1-c1ccc(Cn2cnc3ccc(N(Cc4ccc(O)cc4)C(=O)c4ccccc4)cc3c2=O)cc1 10.1016/0960-894X(95)00224-H
CHEMBL30015 101320 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
Binding affinity against AT1 receptor in human adrenal tissueBinding affinity against AT1 receptor in human adrenal tissue
ChEMBL 619 8 1 9 5.9 Cn1nnnc1-c1ccccc1-c1ccc(Cn2cnc3ccc(N(Cc4ccc(O)cc4)C(=O)c4ccccc4)cc3c2=O)cc1 10.1016/0960-894X(95)00224-H
44306651 100061 0 None - 0 Rabbit 8.2 pIC50 = 8.2 Binding
Binding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membraneBinding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane
ChEMBL 533 3 1 4 4.6 CCc1nc2c(C)cc(C)nc2n1Cc1cc(I)c(O)c(I)c1 10.1016/S0960-894X(01)81148-3
CHEMBL291358 100061 0 None - 0 Rabbit 8.2 pIC50 = 8.2 Binding
Binding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membraneBinding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane
ChEMBL 533 3 1 4 4.6 CCc1nc2c(C)cc(C)nc2n1Cc1cc(I)c(O)c(I)c1 10.1016/S0960-894X(01)81148-3
3081289 9914 10 None - 0 Human 8.2 pIC50 = 8.2 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 416 8 2 6 4.0 CCCc1nc(CC)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80077-3
CHEMBL115021 9914 10 None - 0 Human 8.2 pIC50 = 8.2 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 416 8 2 6 4.0 CCCc1nc(CC)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80077-3
6918269 98005 8 None 776 2 Human 8.2 pIC50 = 8.2 Binding
Binding affinity to angiotensin AT1 receptorBinding affinity to angiotensin AT1 receptor
ChEMBL 508 9 1 7 5.5 CCCCc1nc2ccc(C(C)(C)OC)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.bmc.2010.10.043
CHEMBL275875 98005 8 None 776 2 Human 8.2 pIC50 = 8.2 Binding
Binding affinity to angiotensin AT1 receptorBinding affinity to angiotensin AT1 receptor
ChEMBL 508 9 1 7 5.5 CCCCc1nc2ccc(C(C)(C)OC)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.bmc.2010.10.043
CHEMBL295959 98005 8 None 776 2 Human 8.2 pIC50 = 8.2 Binding
Binding affinity to angiotensin AT1 receptorBinding affinity to angiotensin AT1 receptor
ChEMBL 508 9 1 7 5.5 CCCCc1nc2ccc(C(C)(C)OC)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.bmc.2010.10.043
19771826 204889 0 None - 0 Guinea pig 8.2 pIC50 = 8.2 Binding
Compound was tested for in vitro inhibition of specific binding of [I-125]AII to AT1 receptor in guinea pig adrenal membrane preparationCompound was tested for in vitro inhibition of specific binding of [I-125]AII to AT1 receptor in guinea pig adrenal membrane preparation
ChEMBL 453 7 1 6 5.2 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)c(C(C)=O)c2)c2c(n1)CCCC2 10.1016/S0960-894X(01)80295-X
CHEMBL89143 204889 0 None - 0 Guinea pig 8.2 pIC50 = 8.2 Binding
Compound was tested for in vitro inhibition of specific binding of [I-125]AII to AT1 receptor in guinea pig adrenal membrane preparationCompound was tested for in vitro inhibition of specific binding of [I-125]AII to AT1 receptor in guinea pig adrenal membrane preparation
ChEMBL 453 7 1 6 5.2 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)c(C(C)=O)c2)c2c(n1)CCCC2 10.1016/S0960-894X(01)80295-X
9895957 10558 12 None -5 3 Human 8.2 pIC50 = 8.2 Binding
Displacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysisDisplacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysis
ChEMBL 659 11 1 7 6.8 CCCCC1=NC2(CCCC2)C(=O)N1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)c(CN2CCC(C)(C)C2=O)c1 10.1039/C4MD00499J
CHEMBL11706 10558 12 None -5 3 Human 8.2 pIC50 = 8.2 Binding
Displacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysisDisplacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysis
ChEMBL 659 11 1 7 6.8 CCCCC1=NC2(CCCC2)C(=O)N1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)c(CN2CCC(C)(C)C2=O)c1 10.1039/C4MD00499J
1610 2305 89 None 1 4 Human 8.2 pIC50 = 8.2 Binding
Displacement of 125[I-Sar1-Ile8]ANG II from human AT1 receptor expressed in HEK293 membranes after 1 hr by gamma countingDisplacement of 125[I-Sar1-Ile8]ANG II from human AT1 receptor expressed in HEK293 membranes after 1 hr by gamma counting
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.ejmech.2012.07.040
3941 2305 89 None 1 4 Human 8.2 pIC50 = 8.2 Binding
Displacement of 125[I-Sar1-Ile8]ANG II from human AT1 receptor expressed in HEK293 membranes after 1 hr by gamma countingDisplacement of 125[I-Sar1-Ile8]ANG II from human AT1 receptor expressed in HEK293 membranes after 1 hr by gamma counting
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.ejmech.2012.07.040
3961 2305 89 None 1 4 Human 8.2 pIC50 = 8.2 Binding
Displacement of 125[I-Sar1-Ile8]ANG II from human AT1 receptor expressed in HEK293 membranes after 1 hr by gamma countingDisplacement of 125[I-Sar1-Ile8]ANG II from human AT1 receptor expressed in HEK293 membranes after 1 hr by gamma counting
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.ejmech.2012.07.040
590 2305 89 None 1 4 Human 8.2 pIC50 = 8.2 Binding
Displacement of 125[I-Sar1-Ile8]ANG II from human AT1 receptor expressed in HEK293 membranes after 1 hr by gamma countingDisplacement of 125[I-Sar1-Ile8]ANG II from human AT1 receptor expressed in HEK293 membranes after 1 hr by gamma counting
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.ejmech.2012.07.040
CHEMBL191 2305 89 None 1 4 Human 8.2 pIC50 = 8.2 Binding
Displacement of 125[I-Sar1-Ile8]ANG II from human AT1 receptor expressed in HEK293 membranes after 1 hr by gamma countingDisplacement of 125[I-Sar1-Ile8]ANG II from human AT1 receptor expressed in HEK293 membranes after 1 hr by gamma counting
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.ejmech.2012.07.040
DB00678 2305 89 None 1 4 Human 8.2 pIC50 = 8.2 Binding
Displacement of 125[I-Sar1-Ile8]ANG II from human AT1 receptor expressed in HEK293 membranes after 1 hr by gamma countingDisplacement of 125[I-Sar1-Ile8]ANG II from human AT1 receptor expressed in HEK293 membranes after 1 hr by gamma counting
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.ejmech.2012.07.040
108185 1578 71 None - 1 Rabbit 8.2 pIC50 = 8.2 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 436 8 2 6 4.5 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)C(=O)O)Cl 10.1021/jm00057a009
586 1578 71 None - 1 Rabbit 8.2 pIC50 = 8.2 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 436 8 2 6 4.5 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)C(=O)O)Cl 10.1021/jm00057a009
CHEMBL907 1578 71 None - 1 Rabbit 8.2 pIC50 = 8.2 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 436 8 2 6 4.5 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)C(=O)O)Cl 10.1021/jm00057a009
15236334 165037 0 None - 0 Rabbit 8.2 pIC50 = 8.2 Binding
Displacement of the specific binding ligand [125I]Sar1,Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane.Displacement of the specific binding ligand [125I]Sar1,Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane.
ChEMBL 520 6 1 7 5.7 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2C2=NN(c3ccccc3)[S+]([O-])N2)cc1 10.1016/S0960-894X(01)81119-7
CHEMBL424289 165037 0 None - 0 Rabbit 8.2 pIC50 = 8.2 Binding
Displacement of the specific binding ligand [125I]Sar1,Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane.Displacement of the specific binding ligand [125I]Sar1,Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane.
ChEMBL 520 6 1 7 5.7 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2C2=NN(c3ccccc3)[S+]([O-])N2)cc1 10.1016/S0960-894X(01)81119-7
108185 1578 71 None - 1 Rabbit 8.2 pIC50 = 8.2 Binding
In vitro binding affinity for angiotensin II AT1 receptor in rabbit aortaIn vitro binding affinity for angiotensin II AT1 receptor in rabbit aorta
ChEMBL 436 8 2 6 4.5 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)C(=O)O)Cl 10.1021/jm00050a002
586 1578 71 None - 1 Rabbit 8.2 pIC50 = 8.2 Binding
In vitro binding affinity for angiotensin II AT1 receptor in rabbit aortaIn vitro binding affinity for angiotensin II AT1 receptor in rabbit aorta
ChEMBL 436 8 2 6 4.5 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)C(=O)O)Cl 10.1021/jm00050a002
CHEMBL907 1578 71 None - 1 Rabbit 8.2 pIC50 = 8.2 Binding
In vitro binding affinity for angiotensin II AT1 receptor in rabbit aortaIn vitro binding affinity for angiotensin II AT1 receptor in rabbit aorta
ChEMBL 436 8 2 6 4.5 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)C(=O)O)Cl 10.1021/jm00050a002
10394727 102575 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
In vitro binding affinity of compound against Angiotensin II receptor, type 1In vitro binding affinity of compound against Angiotensin II receptor, type 1
ChEMBL 672 15 2 9 5.4 CCCCCC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCC)nc(CN3CCN(c4ccccn4)CC3)c2C(=O)O)cc1 10.1016/S0960-894X(00)80076-1
CHEMBL307321 102575 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
In vitro binding affinity of compound against Angiotensin II receptor, type 1In vitro binding affinity of compound against Angiotensin II receptor, type 1
ChEMBL 672 15 2 9 5.4 CCCCCC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCC)nc(CN3CCN(c4ccccn4)CC3)c2C(=O)O)cc1 10.1016/S0960-894X(00)80076-1
44311650 102713 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
In vitro binding affinity of compound against Angiotensin II receptor, type 1In vitro binding affinity of compound against Angiotensin II receptor, type 1
ChEMBL 674 14 2 10 5.2 CCCCOC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCC)nc(CN3CCN(c4ccccn4)CC3)c2C(=O)O)cc1 10.1016/S0960-894X(00)80076-1
CHEMBL308361 102713 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
In vitro binding affinity of compound against Angiotensin II receptor, type 1In vitro binding affinity of compound against Angiotensin II receptor, type 1
ChEMBL 674 14 2 10 5.2 CCCCOC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCC)nc(CN3CCN(c4ccccn4)CC3)c2C(=O)O)cc1 10.1016/S0960-894X(00)80076-1
44311607 202473 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
In vitro binding affinity of compound against Angiotensin II receptor, type 1In vitro binding affinity of compound against Angiotensin II receptor, type 1
ChEMBL 517 9 3 8 4.5 CCCc1nc(CNC(=O)OC(C)(C)C)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80076-1
CHEMBL70770 202473 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
In vitro binding affinity of compound against Angiotensin II receptor, type 1In vitro binding affinity of compound against Angiotensin II receptor, type 1
ChEMBL 517 9 3 8 4.5 CCCc1nc(CNC(=O)OC(C)(C)C)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80076-1
15222103 202824 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
In vitro binding affinity of compound against Angiotensin II receptor, type 1In vitro binding affinity of compound against Angiotensin II receptor, type 1
ChEMBL 678 12 2 9 5.1 CCCc1nc(CN2CCN(c3ccccn3)CC2)c(C(=O)O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/S0960-894X(00)80076-1
CHEMBL72819 202824 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
In vitro binding affinity of compound against Angiotensin II receptor, type 1In vitro binding affinity of compound against Angiotensin II receptor, type 1
ChEMBL 678 12 2 9 5.1 CCCc1nc(CN2CCN(c3ccccn3)CC2)c(C(=O)O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/S0960-894X(00)80076-1
3081289 9914 10 None - 0 Rabbit 8.2 pIC50 = 8.2 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aortaIn vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aorta
ChEMBL 416 8 2 6 4.0 CCCc1nc(CC)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81124-0
CHEMBL115021 9914 10 None - 0 Rabbit 8.2 pIC50 = 8.2 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aortaIn vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aorta
ChEMBL 416 8 2 6 4.0 CCCc1nc(CC)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81124-0
44376760 164831 0 None - 0 Rabbit 8.2 pIC50 = 8.2 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aortaIn vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aorta
ChEMBL 532 11 3 6 4.7 CCCCc1ncc(C(=O)O)n1Cc1ccc(-c2ccccc2NS(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/S0960-894X(01)81124-0
CHEMBL423801 164831 0 None - 0 Rabbit 8.2 pIC50 = 8.2 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aortaIn vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aorta
ChEMBL 532 11 3 6 4.7 CCCCc1ncc(C(=O)O)n1Cc1ccc(-c2ccccc2NS(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/S0960-894X(01)81124-0
14950498 98554 0 None - 0 Guinea pig 8.2 pIC50 = 8.2 Binding
Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1
ChEMBL 461 7 1 6 5.4 Cc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c(C(=O)c2ccccc2)c(C)n1 10.1021/jm00061a016
CHEMBL280189 98554 0 None - 0 Guinea pig 8.2 pIC50 = 8.2 Binding
Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1
ChEMBL 461 7 1 6 5.4 Cc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c(C(=O)c2ccccc2)c(C)n1 10.1021/jm00061a016
14950505 98687 0 None - 0 Guinea pig 8.2 pIC50 = 8.2 Binding
Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1
ChEMBL 433 6 1 5 5.8 Cc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c(-c2ccccc2)c(C)n1 10.1021/jm00061a016
CHEMBL281192 98687 0 None - 0 Guinea pig 8.2 pIC50 = 8.2 Binding
Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1
ChEMBL 433 6 1 5 5.8 Cc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c(-c2ccccc2)c(C)n1 10.1021/jm00061a016
44341922 10304 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
Tested for inhibition of Angiotensin II receptor, type 1 in the absence of bovine serum albumin (BSA)Tested for inhibition of Angiotensin II receptor, type 1 in the absence of bovine serum albumin (BSA)
ChEMBL 434 10 2 5 3.6 CCCCC(=O)N(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)[C@H](C(N)=O)C(C)C 10.1016/S0960-894X(01)81117-3
CHEMBL116298 10304 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
Tested for inhibition of Angiotensin II receptor, type 1 in the absence of bovine serum albumin (BSA)Tested for inhibition of Angiotensin II receptor, type 1 in the absence of bovine serum albumin (BSA)
ChEMBL 434 10 2 5 3.6 CCCCC(=O)N(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)[C@H](C(N)=O)C(C)C 10.1016/S0960-894X(01)81117-3
9888876 48710 0 None - 0 Rabbit 8.2 pIC50 = 8.2 Binding
Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)
ChEMBL 429 7 1 5 5.2 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(OC(C(=O)O)c2ccccc2C)cc1 10.1016/0960-894X(95)00185-V
CHEMBL15606 48710 0 None - 0 Rabbit 8.2 pIC50 = 8.2 Binding
Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)
ChEMBL 429 7 1 5 5.2 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(OC(C(=O)O)c2ccccc2C)cc1 10.1016/0960-894X(95)00185-V
10437754 119191 0 None - 0 Rabbit 8.2 pIC50 = 8.2 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 558 12 2 8 5.6 CCCCc1nnc(SC(C(=O)OC)c2ccccc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
CHEMBL347404 119191 0 None - 0 Rabbit 8.2 pIC50 = 8.2 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 558 12 2 8 5.6 CCCCc1nnc(SC(C(=O)OC)c2ccccc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
76319527 84966 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 514 11 0 6 5.7 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2c2ccccc2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
CHEMBL2263317 84966 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 514 11 0 6 5.7 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2c2ccccc2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
10437754 119191 0 None - 0 Rabbit 8.2 pIC50 = 8.2 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 558 12 2 8 5.6 CCCCc1nnc(SC(C(=O)OC)c2ccccc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
CHEMBL347404 119191 0 None - 0 Rabbit 8.2 pIC50 = 8.2 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 558 12 2 8 5.6 CCCCc1nnc(SC(C(=O)OC)c2ccccc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
10394859 17232 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 687 11 2 10 5.3 CCOCC(=O)Nc1ccc(Cl)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1021/jm00019a004
CHEMBL125760 17232 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 687 11 2 10 5.3 CCOCC(=O)Nc1ccc(Cl)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1021/jm00019a004
127029976 138674 0 None - 1 Human 8.2 pIC50 = 8.2 Binding
Displacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation countingDisplacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation counting
ChEMBL 1160 33 15 14 -1.2 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCN/C(N)=N/C(=O)NCCCCN)NC(=O)[C@@H](N)CC(=O)O)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O 10.1021/acs.jmedchem.5b01495
CHEMBL3786145 138674 0 None - 1 Human 8.2 pIC50 = 8.2 Binding
Displacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation countingDisplacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation counting
ChEMBL 1160 33 15 14 -1.2 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCN/C(N)=N/C(=O)NCCCCN)NC(=O)[C@@H](N)CC(=O)O)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O 10.1021/acs.jmedchem.5b01495
CHEMBL3787767 138674 0 None - 1 Human 8.2 pIC50 = 8.2 Binding
Displacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation countingDisplacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation counting
ChEMBL 1160 33 15 14 -1.2 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCN/C(N)=N/C(=O)NCCCCN)NC(=O)[C@@H](N)CC(=O)O)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O 10.1021/acs.jmedchem.5b01495
44376781 55964 0 None - 0 Rabbit 8.2 pIC50 = 8.2 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aortaIn vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aorta
ChEMBL 517 10 2 6 4.8 CCCCc1ncc(C(=O)O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/S0960-894X(01)81124-0
CHEMBL162859 55964 0 None - 0 Rabbit 8.2 pIC50 = 8.2 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aortaIn vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aorta
ChEMBL 517 10 2 6 4.8 CCCCc1ncc(C(=O)O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/S0960-894X(01)81124-0
44305663 100517 0 None - 0 Rat 8.2 pIC50 = 8.2 Binding
Tested for binding affinity against angiotensin II receptor in rat adrenal cortexTested for binding affinity against angiotensin II receptor in rat adrenal cortex
ChEMBL 412 6 1 8 2.7 CCCc1cc2ncnn2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/0960-894X(95)00370-9
CHEMBL294358 100517 0 None - 0 Rat 8.2 pIC50 = 8.2 Binding
Tested for binding affinity against angiotensin II receptor in rat adrenal cortexTested for binding affinity against angiotensin II receptor in rat adrenal cortex
ChEMBL 412 6 1 8 2.7 CCCc1cc2ncnn2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/0960-894X(95)00370-9
127034922 135827 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 571 10 2 7 6.2 CCOc1nc2c(C)cc(C(=O)NC[C@@H](C)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.ejmech.2015.09.010
CHEMBL3734891 135827 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 571 10 2 7 6.2 CCOc1nc2c(C)cc(C(=O)NC[C@@H](C)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.ejmech.2015.09.010
44274823 98605 0 None - 0 Rabbit 8.2 pIC50 = 8.2 Binding
Ability to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitroAbility to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitro
ChEMBL 551 10 2 8 5.8 CCCCc1nc2ccc(NC(=O)OCC(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80335-2
CHEMBL280526 98605 0 None - 0 Rabbit 8.2 pIC50 = 8.2 Binding
Ability to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitroAbility to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitro
ChEMBL 551 10 2 8 5.8 CCCCc1nc2ccc(NC(=O)OCC(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80335-2
10076191 117934 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 548 13 0 6 5.8 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2CCCC(F)(F)F)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
CHEMBL341151 117934 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 548 13 0 6 5.8 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2CCCC(F)(F)F)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
44277874 99080 0 None - 0 Rabbit 8.2 pIC50 = 8.2 Binding
Binding affinity against AT1 receptor in rabbit aortaBinding affinity against AT1 receptor in rabbit aorta
ChEMBL 629 11 0 9 6.9 CCCCCN(C(=O)c1ccc(SC)cc1)c1ccc2ncn(Cc3ccc(-c4ccccc4-c4nnnn4C)cc3)c(=O)c2c1 10.1016/0960-894X(95)00224-H
CHEMBL28359 99080 0 None - 0 Rabbit 8.2 pIC50 = 8.2 Binding
Binding affinity against AT1 receptor in rabbit aortaBinding affinity against AT1 receptor in rabbit aorta
ChEMBL 629 11 0 9 6.9 CCCCCN(C(=O)c1ccc(SC)cc1)c1ccc2ncn(Cc3ccc(-c4ccccc4-c4nnnn4C)cc3)c(=O)c2c1 10.1016/0960-894X(95)00224-H
44459903 99029 0 None - 0 Rabbit 8.2 pIC50 = 8.2 Binding
Binding affinity against Angiotensin II type 1 Receptor in rabbit aortic tissueBinding affinity against Angiotensin II type 1 Receptor in rabbit aortic tissue
ChEMBL 464 8 1 6 5.3 CCCCCc1nc2ccc(C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80334-0
CHEMBL283292 99029 0 None - 0 Rabbit 8.2 pIC50 = 8.2 Binding
Binding affinity against Angiotensin II type 1 Receptor in rabbit aortic tissueBinding affinity against Angiotensin II type 1 Receptor in rabbit aortic tissue
ChEMBL 464 8 1 6 5.3 CCCCCc1nc2ccc(C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80334-0
9931685 204354 0 None - 1 Rat 8.2 pIC50 = 8.2 Binding
Activity against high affinity Angiotensin II receptor, type 1 was measured from the ability to inhibit [125I]angiotensin II binding to rat uterine membrane.Activity against high affinity Angiotensin II receptor, type 1 was measured from the ability to inhibit [125I]angiotensin II binding to rat uterine membrane.
ChEMBL 415 10 1 6 4.9 CCCCc1nc(CCCC)n(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)n1 10.1021/jm00053a013
CHEMBL85595 204354 0 None - 1 Rat 8.2 pIC50 = 8.2 Binding
Activity against high affinity Angiotensin II receptor, type 1 was measured from the ability to inhibit [125I]angiotensin II binding to rat uterine membrane.Activity against high affinity Angiotensin II receptor, type 1 was measured from the ability to inhibit [125I]angiotensin II binding to rat uterine membrane.
ChEMBL 415 10 1 6 4.9 CCCCc1nc(CCCC)n(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)n1 10.1021/jm00053a013
44277481 101087 0 None - 0 Rabbit 8.2 pIC50 = 8.2 Binding
Binding affinity against AT1 receptor in rabbit aortaBinding affinity against AT1 receptor in rabbit aorta
ChEMBL 647 9 1 9 5.8 Cn1nnnc1-c1ccccc1-c1ccc(Cn2cnc3ccc(N(Cc4ccc(C(=O)O)cc4)C(=O)c4ccccc4)cc3c2=O)cc1 10.1016/0960-894X(95)00224-H
CHEMBL29853 101087 0 None - 0 Rabbit 8.2 pIC50 = 8.2 Binding
Binding affinity against AT1 receptor in rabbit aortaBinding affinity against AT1 receptor in rabbit aorta
ChEMBL 647 9 1 9 5.8 Cn1nnnc1-c1ccccc1-c1ccc(Cn2cnc3ccc(N(Cc4ccc(C(=O)O)cc4)C(=O)c4ccccc4)cc3c2=O)cc1 10.1016/0960-894X(95)00224-H
9932483 206098 0 None - 1 Human 8.2 pIC50 = 8.2 Binding
Binding affinity to angiotensin AT1 receptorBinding affinity to angiotensin AT1 receptor
ChEMBL 431 10 1 7 4.1 CCCCc1cn(CCCC)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)nc1 10.1016/j.bmc.2010.10.043
CHEMBL9642 206098 0 None - 1 Human 8.2 pIC50 = 8.2 Binding
Binding affinity to angiotensin AT1 receptorBinding affinity to angiotensin AT1 receptor
ChEMBL 431 10 1 7 4.1 CCCCc1cn(CCCC)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)nc1 10.1016/j.bmc.2010.10.043
44358381 29131 0 None - 0 Rabbit 8.2 pIC50 = 8.2 Binding
Displacement of the specific binding ligand [125I]Sar1,Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane.Displacement of the specific binding ligand [125I]Sar1,Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane.
ChEMBL 634 6 2 8 5.2 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2C2=NS(=O)(=O)c3cc(S(N)(=O)=O)c(Cl)cc3N2)cc1 10.1016/S0960-894X(01)81119-7
CHEMBL138358 29131 0 None - 0 Rabbit 8.2 pIC50 = 8.2 Binding
Displacement of the specific binding ligand [125I]Sar1,Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane.Displacement of the specific binding ligand [125I]Sar1,Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane.
ChEMBL 634 6 2 8 5.2 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2C2=NS(=O)(=O)c3cc(S(N)(=O)=O)c(Cl)cc3N2)cc1 10.1016/S0960-894X(01)81119-7
19029589 118250 0 None - 0 Rat 8.2 pIC50 = 8.2 Binding
In vitro ability to displace the specific binding of [125I]-A II from receptors in rat liver membrane(type 1 receptor)In vitro ability to displace the specific binding of [125I]-A II from receptors in rat liver membrane(type 1 receptor)
ChEMBL 431 6 1 7 3.2 CCc1nn(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/c(=N/C(=O)C2CC2)s1 10.1016/S0960-894X(96)00250-8
CHEMBL34190 118250 0 None - 0 Rat 8.2 pIC50 = 8.2 Binding
In vitro ability to displace the specific binding of [125I]-A II from receptors in rat liver membrane(type 1 receptor)In vitro ability to displace the specific binding of [125I]-A II from receptors in rat liver membrane(type 1 receptor)
ChEMBL 431 6 1 7 3.2 CCc1nn(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/c(=N/C(=O)C2CC2)s1 10.1016/S0960-894X(96)00250-8
76311802 84525 0 None - 0 Rabbit 8.2 pIC50 = 8.2 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 569 12 2 10 5.3 CCCCc1nnc(SCc2ccc([N+](=O)[O-])cc2)n1Cc1ccc(NC(=O)c2ccccc2-c2nnn[nH]2)cc1 10.1007/s00044-011-9756-4
CHEMBL2237595 84525 0 None - 0 Rabbit 8.2 pIC50 = 8.2 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 569 12 2 10 5.3 CCCCc1nnc(SCc2ccc([N+](=O)[O-])cc2)n1Cc1ccc(NC(=O)c2ccccc2-c2nnn[nH]2)cc1 10.1007/s00044-011-9756-4
10048770 117877 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 438 10 2 5 3.9 CCCCc1ncc(/C=C2/C(=O)NC(=O)N2CCC(C)C)n1Cc1ccc(C(=O)O)cc1 10.1007/s00044-009-9205-9
CHEMBL341070 117877 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 438 10 2 5 3.9 CCCCc1ncc(/C=C2/C(=O)NC(=O)N2CCC(C)C)n1Cc1ccc(C(=O)O)cc1 10.1007/s00044-009-9205-9
14956740 204084 0 None - 0 Rabbit 8.2 pIC50 = 8.2 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 481 9 1 8 4.3 CCCCc1nn(-c2ccccc2OC)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
CHEMBL83248 204084 0 None - 0 Rabbit 8.2 pIC50 = 8.2 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 481 9 1 8 4.3 CCCCc1nn(-c2ccccc2OC)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
9984360 119102 0 None - 0 Rabbit 8.2 pIC50 = 8.2 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 526 11 1 9 5.7 CCCCc1nnc(SCc2ccc([N+](=O)[O-])cc2)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
CHEMBL346542 119102 0 None - 0 Rabbit 8.2 pIC50 = 8.2 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 526 11 1 9 5.7 CCCCc1nnc(SCc2ccc([N+](=O)[O-])cc2)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
44277574 101418 0 None - 0 Rabbit 8.2 pIC50 = 8.2 Binding
Binding affinity against AT1 receptor in rabbit aortaBinding affinity against AT1 receptor in rabbit aorta
ChEMBL 604 8 0 9 5.5 Cn1nnnc1-c1ccccc1-c1ccc(Cn2cnc3ccc(N(Cc4ccccn4)C(=O)c4ccccc4)cc3c2=O)cc1 10.1016/0960-894X(95)00224-H
CHEMBL30086 101418 0 None - 0 Rabbit 8.2 pIC50 = 8.2 Binding
Binding affinity against AT1 receptor in rabbit aortaBinding affinity against AT1 receptor in rabbit aorta
ChEMBL 604 8 0 9 5.5 Cn1nnnc1-c1ccccc1-c1ccc(Cn2cnc3ccc(N(Cc4ccccn4)C(=O)c4ccccc4)cc3c2=O)cc1 10.1016/0960-894X(95)00224-H
1610 2305 89 None -1 4 Rat 8.2 pIC50 = 8.2 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm031100t
3941 2305 89 None -1 4 Rat 8.2 pIC50 = 8.2 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm031100t
3961 2305 89 None -1 4 Rat 8.2 pIC50 = 8.2 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm031100t
590 2305 89 None -1 4 Rat 8.2 pIC50 = 8.2 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm031100t
CHEMBL191 2305 89 None -1 4 Rat 8.2 pIC50 = 8.2 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm031100t
DB00678 2305 89 None -1 4 Rat 8.2 pIC50 = 8.2 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm031100t
1610 2305 89 None -1 4 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm7011563
3941 2305 89 None -1 4 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm7011563
3961 2305 89 None -1 4 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm7011563
590 2305 89 None -1 4 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm7011563
CHEMBL191 2305 89 None -1 4 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm7011563
DB00678 2305 89 None -1 4 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm7011563
10053499 48512 0 None - 0 Rabbit 8.2 pIC50 = 8.2 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 558 11 2 8 6.0 CCCCc1nnc(SCc2ccc(Cl)cc2)n1Cc1ccc(NC(=O)c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-011-9756-4
CHEMBL155877 48512 0 None - 0 Rabbit 8.2 pIC50 = 8.2 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 558 11 2 8 6.0 CCCCc1nnc(SCc2ccc(Cl)cc2)n1Cc1ccc(NC(=O)c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-011-9756-4
10482258 119157 0 None - 0 Rabbit 8.2 pIC50 = 8.2 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 534 11 2 6 6.6 CCCCc1nnc(SCc2ccc(Cl)cc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
CHEMBL347135 119157 0 None - 0 Rabbit 8.2 pIC50 = 8.2 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 534 11 2 6 6.6 CCCCc1nnc(SCc2ccc(Cl)cc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
9888159 106470 0 None - 0 Rat 8.2 pIC50 = 8.2 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 416 10 1 7 4.3 CCCCc1nc(CCCC)n(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cn2)n1 10.1021/jm031100t
CHEMBL315022 106470 0 None - 0 Rat 8.2 pIC50 = 8.2 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 416 10 1 7 4.3 CCCCc1nc(CCCC)n(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cn2)n1 10.1021/jm031100t
44348259 15841 0 None - 0 Rabbit 8.2 pIC50 = 8.2 Binding
Displacement of [1251][Sar1,IIe8]AII from rabbit aorta Angiotensin II receptor, type 1Displacement of [1251][Sar1,IIe8]AII from rabbit aorta Angiotensin II receptor, type 1
ChEMBL 575 12 1 5 8.4 CCCc1cc(Cn2c(CC)nc3c(C)cc(C)nc32)cc(CCC)c1OC(C(=O)O)c1cccc(-c2ccccc2)c1 10.1021/jm00075a033
CHEMBL122367 15841 0 None - 0 Rabbit 8.2 pIC50 = 8.2 Binding
Displacement of [1251][Sar1,IIe8]AII from rabbit aorta Angiotensin II receptor, type 1Displacement of [1251][Sar1,IIe8]AII from rabbit aorta Angiotensin II receptor, type 1
ChEMBL 575 12 1 5 8.4 CCCc1cc(Cn2c(CC)nc3c(C)cc(C)nc32)cc(CCC)c1OC(C(=O)O)c1cccc(-c2ccccc2)c1 10.1021/jm00075a033
10053499 48512 0 None - 0 Rabbit 8.2 pIC50 = 8.2 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 558 11 2 8 6.0 CCCCc1nnc(SCc2ccc(Cl)cc2)n1Cc1ccc(NC(=O)c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
CHEMBL155877 48512 0 None - 0 Rabbit 8.2 pIC50 = 8.2 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 558 11 2 8 6.0 CCCCc1nnc(SCc2ccc(Cl)cc2)n1Cc1ccc(NC(=O)c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
10482258 119157 0 None - 0 Rabbit 8.2 pIC50 = 8.2 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 534 11 2 6 6.6 CCCCc1nnc(SCc2ccc(Cl)cc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
CHEMBL347135 119157 0 None - 0 Rabbit 8.2 pIC50 = 8.2 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 534 11 2 6 6.6 CCCCc1nnc(SCc2ccc(Cl)cc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
71520500 86368 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor afterDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after
ChEMBL 541 6 1 7 5.8 CCc1nc2c(C)cn(Cc3ccccc3C)c(=O)c2n1[C@H]1CCc2cc(-c3ccccc3-c3nnn[nH]3)ccc21 10.1016/j.bmcl.2012.11.088
CHEMBL2322175 86368 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor afterDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after
ChEMBL 541 6 1 7 5.8 CCc1nc2c(C)cn(Cc3ccccc3C)c(=O)c2n1[C@H]1CCc2cc(-c3ccccc3-c3nnn[nH]3)ccc21 10.1016/j.bmcl.2012.11.088
53309274 63430 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation countingDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation counting
ChEMBL 449 5 1 6 5.2 CCc1cc(C)c2nc(CC)n([C@H]3CCc4cc(-c5ccccc5-c5nnn[nH]5)ccc43)c2n1 10.1021/jm200409s
CHEMBL1801738 63430 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation countingDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation counting
ChEMBL 449 5 1 6 5.2 CCc1cc(C)c2nc(CC)n([C@H]3CCc4cc(-c5ccccc5-c5nnn[nH]5)ccc43)c2n1 10.1021/jm200409s
44277442 99820 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
Binding affinity against AT1 receptor in human adrenal tissueBinding affinity against AT1 receptor in human adrenal tissue
ChEMBL 583 10 0 8 6.1 CCCCCN(C(=O)c1ccccc1)c1ccc2ncn(Cc3ccc(-c4ccccc4-c4nnnn4C)cc3)c(=O)c2c1 10.1016/0960-894X(95)00224-H
CHEMBL28917 99820 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
Binding affinity against AT1 receptor in human adrenal tissueBinding affinity against AT1 receptor in human adrenal tissue
ChEMBL 583 10 0 8 6.1 CCCCCN(C(=O)c1ccccc1)c1ccc2ncn(Cc3ccc(-c4ccccc4-c4nnnn4C)cc3)c(=O)c2c1 10.1016/0960-894X(95)00224-H
132706 1638 19 None - 1 Rat 8.2 pIC50 = 8.2 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 416 10 1 7 4.3 CCCCc1nc(nn1Cc1ccc(nc1)c1ccccc1c1n[nH]nn1)CCCC 10.1021/jm031100t
6896 1638 19 None - 1 Rat 8.2 pIC50 = 8.2 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 416 10 1 7 4.3 CCCCc1nc(nn1Cc1ccc(nc1)c1ccccc1c1n[nH]nn1)CCCC 10.1021/jm031100t
CHEMBL315021 1638 19 None - 1 Rat 8.2 pIC50 = 8.2 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 416 10 1 7 4.3 CCCCc1nc(nn1Cc1ccc(nc1)c1ccccc1c1n[nH]nn1)CCCC 10.1021/jm031100t
DB01342 1638 19 None - 1 Rat 8.2 pIC50 = 8.2 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 416 10 1 7 4.3 CCCCc1nc(nn1Cc1ccc(nc1)c1ccccc1c1n[nH]nn1)CCCC 10.1021/jm031100t
10344235 204430 0 None - 0 Rat 8.2 pIC50 = 8.2 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 460 5 1 7 5.1 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2c(-c3nn[nH]n3)cnc3ccccc23)cc1 10.1021/jm031100t
CHEMBL86247 204430 0 None - 0 Rat 8.2 pIC50 = 8.2 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 460 5 1 7 5.1 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2c(-c3nn[nH]n3)cnc3ccccc23)cc1 10.1021/jm031100t
132706 1638 19 None - 1 Human 8.2 pIC50 = 8.2 Binding
Binding affinity to angiotensin AT1 receptorBinding affinity to angiotensin AT1 receptor
ChEMBL 416 10 1 7 4.3 CCCCc1nc(nn1Cc1ccc(nc1)c1ccccc1c1n[nH]nn1)CCCC 10.1016/j.bmc.2010.10.043
6896 1638 19 None - 1 Human 8.2 pIC50 = 8.2 Binding
Binding affinity to angiotensin AT1 receptorBinding affinity to angiotensin AT1 receptor
ChEMBL 416 10 1 7 4.3 CCCCc1nc(nn1Cc1ccc(nc1)c1ccccc1c1n[nH]nn1)CCCC 10.1016/j.bmc.2010.10.043
CHEMBL315021 1638 19 None - 1 Human 8.2 pIC50 = 8.2 Binding
Binding affinity to angiotensin AT1 receptorBinding affinity to angiotensin AT1 receptor
ChEMBL 416 10 1 7 4.3 CCCCc1nc(nn1Cc1ccc(nc1)c1ccccc1c1n[nH]nn1)CCCC 10.1016/j.bmc.2010.10.043
DB01342 1638 19 None - 1 Human 8.2 pIC50 = 8.2 Binding
Binding affinity to angiotensin AT1 receptorBinding affinity to angiotensin AT1 receptor
ChEMBL 416 10 1 7 4.3 CCCCc1nc(nn1Cc1ccc(nc1)c1ccccc1c1n[nH]nn1)CCCC 10.1016/j.bmc.2010.10.043
10344235 204430 0 None - 0 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
ChEMBL 460 5 1 7 5.1 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2c(-c3nn[nH]n3)cnc3ccccc23)cc1 10.1021/jm7011563
CHEMBL86247 204430 0 None - 0 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
ChEMBL 460 5 1 7 5.1 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2c(-c3nn[nH]n3)cnc3ccccc23)cc1 10.1021/jm7011563
15224471 154283 0 None - 1 Bovine 8.2 pIC50 = 8.2 Binding
Displacement of [125I]angiotensin-2 from bovine adrenal cortex AT1 receptorDisplacement of [125I]angiotensin-2 from bovine adrenal cortex AT1 receptor
ChEMBL 441 8 2 7 4.1 CCCCc1nc2cccc(C(=O)O)c2n1Cc1ccc(-n2cccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2007.02.042
CHEMBL400424 154283 0 None - 1 Bovine 8.2 pIC50 = 8.2 Binding
Displacement of [125I]angiotensin-2 from bovine adrenal cortex AT1 receptorDisplacement of [125I]angiotensin-2 from bovine adrenal cortex AT1 receptor
ChEMBL 441 8 2 7 4.1 CCCCc1nc2cccc(C(=O)O)c2n1Cc1ccc(-n2cccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2007.02.042
10645687 10062 0 None - 0 Bovine 8.2 pIC50 = 8.2 Binding
In vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortexIn vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortex
ChEMBL 418 8 3 7 2.9 CCCc1nc(CO)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm950450f
CHEMBL115946 10062 0 None - 0 Bovine 8.2 pIC50 = 8.2 Binding
In vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortexIn vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortex
ChEMBL 418 8 3 7 2.9 CCCc1nc(CO)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm950450f
10368143 46481 0 None - 0 Rabbit 7.2 pIC50 = 7.2 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 486 10 2 6 5.8 CCCCc1nnc(Sc2ccccc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
CHEMBL153968 46481 0 None - 0 Rabbit 7.2 pIC50 = 7.2 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 486 10 2 6 5.8 CCCCc1nnc(Sc2ccccc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
10459507 47446 0 None - 0 Rabbit 7.2 pIC50 = 7.2 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 525 11 2 7 5.8 CCCCc1nnc(SCc2ccccc2C#N)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
CHEMBL154772 47446 0 None - 0 Rabbit 7.2 pIC50 = 7.2 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 525 11 2 7 5.8 CCCCc1nnc(SCc2ccccc2C#N)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
14956775 202274 0 None - 0 Rabbit 7.2 pIC50 = 7.2 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 375 7 2 7 3.2 CCCCc1nnc(O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
CHEMBL69508 202274 0 None - 0 Rabbit 7.2 pIC50 = 7.2 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 375 7 2 7 3.2 CCCCc1nnc(O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
76310610 104758 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Antagonist activity at human AT1 receptor expressed in CHO cells measured after overnight incubation by luciferase reporter gene assayAntagonist activity at human AT1 receptor expressed in CHO cells measured after overnight incubation by luciferase reporter gene assay
ChEMBL 542 10 1 5 8.2 CCCCn1c(-c2ccc3nn(CCC)c(Cc4ccc(-c5ccccc5C(=O)O)cc4)c3c2)nc2ccccc21 10.1016/j.bmcl.2014.01.004
CHEMBL3115246 104758 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Antagonist activity at human AT1 receptor expressed in CHO cells measured after overnight incubation by luciferase reporter gene assayAntagonist activity at human AT1 receptor expressed in CHO cells measured after overnight incubation by luciferase reporter gene assay
ChEMBL 542 10 1 5 8.2 CCCCn1c(-c2ccc3nn(CCC)c(Cc4ccc(-c5ccccc5C(=O)O)cc4)c3c2)nc2ccccc21 10.1016/j.bmcl.2014.01.004
44293815 183655 0 None - 0 Rat 7.2 pIC50 = 7.2 Binding
Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.
ChEMBL 549 11 2 6 6.4 CCCCc1nc2c(C)cc(C)nc2n1Cc1ccc(NC(=O)[C@H](Cc2ccccc2)n2cccc2C(=O)O)cc1 10.1021/jm00064a007
CHEMBL48363 183655 0 None - 0 Rat 7.2 pIC50 = 7.2 Binding
Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.
ChEMBL 549 11 2 6 6.4 CCCCc1nc2c(C)cc(C)nc2n1Cc1ccc(NC(=O)[C@H](Cc2ccccc2)n2cccc2C(=O)O)cc1 10.1021/jm00064a007
44341824 9906 0 None - 0 Rat 7.2 pIC50 = 7.2 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 452 7 1 3 5.5 CCCCC1=NC2(Cc3ccccc3C2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00074a018
CHEMBL114983 9906 0 None - 0 Rat 7.2 pIC50 = 7.2 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 452 7 1 3 5.5 CCCCC1=NC2(Cc3ccccc3C2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00074a018
19889356 179307 0 None - 0 Rat 7.2 pIC50 = 7.2 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 410 6 1 7 4.0 CCCc1nc2c(C)ccnc2n1Cc1ccc(-c2cccnc2-c2nn[nH]n2)cc1 10.1021/jm031100t
CHEMBL47459 179307 0 None - 0 Rat 7.2 pIC50 = 7.2 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 410 6 1 7 4.0 CCCc1nc2c(C)ccnc2n1Cc1ccc(-c2cccnc2-c2nn[nH]n2)cc1 10.1021/jm031100t
44348332 15346 0 None - 0 Bovine 7.2 pIC50 = 7.2 Binding
Concentration that gives 50% inhibition for binding of 125-I-[Sar1, IIe8] angiotensin to Angiotensin II receptor, type 1 in bovine adrenal cortex membrane.Concentration that gives 50% inhibition for binding of 125-I-[Sar1, IIe8] angiotensin to Angiotensin II receptor, type 1 in bovine adrenal cortex membrane.
ChEMBL 485 6 1 6 5.1 CCOC(=O)/C=C1\N(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)C(=O)CC12CCCCCC2 10.1016/S0960-894X(01)80914-8
CHEMBL121871 15346 0 None - 0 Bovine 7.2 pIC50 = 7.2 Binding
Concentration that gives 50% inhibition for binding of 125-I-[Sar1, IIe8] angiotensin to Angiotensin II receptor, type 1 in bovine adrenal cortex membrane.Concentration that gives 50% inhibition for binding of 125-I-[Sar1, IIe8] angiotensin to Angiotensin II receptor, type 1 in bovine adrenal cortex membrane.
ChEMBL 485 6 1 6 5.1 CCOC(=O)/C=C1\N(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)C(=O)CC12CCCCCC2 10.1016/S0960-894X(01)80914-8
44348323 16266 0 None - 0 Bovine 7.2 pIC50 = 7.2 Binding
Concentration that gives 50% inhibition for binding of 125-I-[Sar1, IIe8] angiotensin to Angiotensin II receptor, type 1 in bovine adrenal cortex membrane.Concentration that gives 50% inhibition for binding of 125-I-[Sar1, IIe8] angiotensin to Angiotensin II receptor, type 1 in bovine adrenal cortex membrane.
ChEMBL 445 7 1 6 4.1 CCOC(=O)/C=C1\N(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)C(=O)CC1(C)CC 10.1016/S0960-894X(01)80914-8
CHEMBL123348 16266 0 None - 0 Bovine 7.2 pIC50 = 7.2 Binding
Concentration that gives 50% inhibition for binding of 125-I-[Sar1, IIe8] angiotensin to Angiotensin II receptor, type 1 in bovine adrenal cortex membrane.Concentration that gives 50% inhibition for binding of 125-I-[Sar1, IIe8] angiotensin to Angiotensin II receptor, type 1 in bovine adrenal cortex membrane.
ChEMBL 445 7 1 6 4.1 CCOC(=O)/C=C1\N(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)C(=O)CC1(C)CC 10.1016/S0960-894X(01)80914-8
10368143 46481 0 None - 0 Rabbit 7.2 pIC50 = 7.2 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 486 10 2 6 5.8 CCCCc1nnc(Sc2ccccc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
CHEMBL153968 46481 0 None - 0 Rabbit 7.2 pIC50 = 7.2 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 486 10 2 6 5.8 CCCCc1nnc(Sc2ccccc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
10459507 47446 0 None - 0 Rabbit 7.2 pIC50 = 7.2 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 525 11 2 7 5.8 CCCCc1nnc(SCc2ccccc2C#N)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
CHEMBL154772 47446 0 None - 0 Rabbit 7.2 pIC50 = 7.2 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 525 11 2 7 5.8 CCCCc1nnc(SCc2ccccc2C#N)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
19889356 179307 0 None - 0 Rabbit 7.2 pIC50 = 7.2 Binding
In vitro binding affinity towards Angiotensin II type 1-AT1 receptor determined as its ability to displace 125I-Sarl,Ile8-AII from the receptor expressed in rabbit aorta membrane.In vitro binding affinity towards Angiotensin II type 1-AT1 receptor determined as its ability to displace 125I-Sarl,Ile8-AII from the receptor expressed in rabbit aorta membrane.
ChEMBL 410 6 1 7 4.0 CCCc1nc2c(C)ccnc2n1Cc1ccc(-c2cccnc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80044-X
CHEMBL47459 179307 0 None - 0 Rabbit 7.2 pIC50 = 7.2 Binding
In vitro binding affinity towards Angiotensin II type 1-AT1 receptor determined as its ability to displace 125I-Sarl,Ile8-AII from the receptor expressed in rabbit aorta membrane.In vitro binding affinity towards Angiotensin II type 1-AT1 receptor determined as its ability to displace 125I-Sarl,Ile8-AII from the receptor expressed in rabbit aorta membrane.
ChEMBL 410 6 1 7 4.0 CCCc1nc2c(C)ccnc2n1Cc1ccc(-c2cccnc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80044-X
10642523 109964 0 None - 0 Bovine 7.2 pIC50 = 7.2 Binding
In vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortexIn vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortex
ChEMBL 364 7 2 4 3.9 CCCc1ncc(C(=O)O)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm950450f
CHEMBL324729 109964 0 None - 0 Bovine 7.2 pIC50 = 7.2 Binding
In vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortexIn vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortex
ChEMBL 364 7 2 4 3.9 CCCc1ncc(C(=O)O)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm950450f
9982103 114644 0 None - 0 Guinea pig 7.2 pIC50 = 7.2 Binding
In vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparationIn vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparation
ChEMBL 432 6 1 6 5.1 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2c(C#N)cccc2n1 10.1021/jm00100a007
CHEMBL334431 114644 0 None - 0 Guinea pig 7.2 pIC50 = 7.2 Binding
In vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparationIn vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparation
ChEMBL 432 6 1 6 5.1 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2c(C#N)cccc2n1 10.1021/jm00100a007
44341924 11205 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Tested for inhibition of Angiotensin II receptor, type 1 in the absence of bovine serum albumin (BSA)Tested for inhibition of Angiotensin II receptor, type 1 in the absence of bovine serum albumin (BSA)
ChEMBL 489 11 2 5 5.5 CCCCC(=O)N(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)[C@@H](CC1CCCCC1)C(=O)O 10.1016/S0960-894X(01)81117-3
CHEMBL117941 11205 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Tested for inhibition of Angiotensin II receptor, type 1 in the absence of bovine serum albumin (BSA)Tested for inhibition of Angiotensin II receptor, type 1 in the absence of bovine serum albumin (BSA)
ChEMBL 489 11 2 5 5.5 CCCCC(=O)N(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)[C@@H](CC1CCCCC1)C(=O)O 10.1016/S0960-894X(01)81117-3
11561462 110632 55 None - 0 Human 7.2 pIC50 = 7.2 Binding
Tested for inhibition of Angiotensin II receptor, type 1 in the absence of bovine serum albumin (BSA)Tested for inhibition of Angiotensin II receptor, type 1 in the absence of bovine serum albumin (BSA)
ChEMBL 449 10 1 6 4.3 CCCCC(=O)N(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)[C@H](C(=O)OC)C(C)C 10.1016/S0960-894X(01)81117-3
CHEMBL326349 110632 55 None - 0 Human 7.2 pIC50 = 7.2 Binding
Tested for inhibition of Angiotensin II receptor, type 1 in the absence of bovine serum albumin (BSA)Tested for inhibition of Angiotensin II receptor, type 1 in the absence of bovine serum albumin (BSA)
ChEMBL 449 10 1 6 4.3 CCCCC(=O)N(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)[C@H](C(=O)OC)C(C)C 10.1016/S0960-894X(01)81117-3
15287885 161254 0 None - 0 Rabbit 7.2 pIC50 = 7.2 Binding
Tested in vitro for Angiotensin II receptor, type 1 binding affinity using rabbit aorta binding assayTested in vitro for Angiotensin II receptor, type 1 binding affinity using rabbit aorta binding assay
ChEMBL 449 8 1 5 5.6 CCCc1nc2c(C)ccnc2n1Cc1ccc(OC(C(=O)O)c2cccc(Cl)c2)cc1 10.1016/0960-894X(94)00476-V
CHEMBL41440 161254 0 None - 0 Rabbit 7.2 pIC50 = 7.2 Binding
Tested in vitro for Angiotensin II receptor, type 1 binding affinity using rabbit aorta binding assayTested in vitro for Angiotensin II receptor, type 1 binding affinity using rabbit aorta binding assay
ChEMBL 449 8 1 5 5.6 CCCc1nc2c(C)ccnc2n1Cc1ccc(OC(C(=O)O)c2cccc(Cl)c2)cc1 10.1016/0960-894X(94)00476-V
15699054 108984 0 None - 0 Rat 6.2 pIC50 = 6.2 Binding
Binding affinity against angiotensin II receptor in rat smooth muscle cell preparationsBinding affinity against angiotensin II receptor in rat smooth muscle cell preparations
ChEMBL 396 7 2 6 3.8 CCCCc1nc(Cl)c(CO)n1Cc1ccc2cc(-c3nn[nH]n3)ccc2c1 10.1021/jm00114a021
CHEMBL322071 108984 0 None - 0 Rat 6.2 pIC50 = 6.2 Binding
Binding affinity against angiotensin II receptor in rat smooth muscle cell preparationsBinding affinity against angiotensin II receptor in rat smooth muscle cell preparations
ChEMBL 396 7 2 6 3.8 CCCCc1nc(Cl)c(CO)n1Cc1ccc2cc(-c3nn[nH]n3)ccc2c1 10.1021/jm00114a021
24828034 165866 0 None - 0 Rat 6.2 pIC50 = 6.2 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
ChEMBL 510 8 1 9 3.7 CCCCn1c(=O)c2ccc(N3CCOCC3)nc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm7011563
CHEMBL427738 165866 0 None - 0 Rat 6.2 pIC50 = 6.2 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
ChEMBL 510 8 1 9 3.7 CCCCn1c(=O)c2ccc(N3CCOCC3)nc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm7011563
19792191 97913 0 None - 0 Bovine 6.2 pIC50 = 6.2 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 452 9 1 6 5.4 CCCCc1nc2cccc(COC)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
CHEMBL275304 97913 0 None - 0 Bovine 6.2 pIC50 = 6.2 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 452 9 1 6 5.4 CCCCc1nc2cccc(COC)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
10503729 9578 0 None - 0 Bovine 6.2 pIC50 = 6.2 Binding
In vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortexIn vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortex
ChEMBL 450 9 2 6 4.7 CCCc1nc(C(C)(C)O)c(C(=O)OCC)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm950450f
CHEMBL113040 9578 0 None - 0 Bovine 6.2 pIC50 = 6.2 Binding
In vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortexIn vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortex
ChEMBL 450 9 2 6 4.7 CCCc1nc(C(C)(C)O)c(C(=O)OCC)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm950450f
11741515 116330 0 None - 0 Guinea pig 6.2 pIC50 = 6.2 Binding
In vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparationIn vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparation
ChEMBL 397 7 1 3 6.1 CCCc1cc(OCc2ccc(-c3ccccc3C(=O)O)cc2)c2ccccc2n1 10.1021/jm00100a007
CHEMBL338048 116330 0 None - 0 Guinea pig 6.2 pIC50 = 6.2 Binding
In vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparationIn vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparation
ChEMBL 397 7 1 3 6.1 CCCc1cc(OCc2ccc(-c3ccccc3C(=O)O)cc2)c2ccccc2n1 10.1021/jm00100a007
21840429 110418 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Tested for inhibition of Angiotensin II receptor, type 1 in the absence of bovine serum albumin (BSA)Tested for inhibition of Angiotensin II receptor, type 1 in the absence of bovine serum albumin (BSA)
ChEMBL 393 9 2 5 3.1 CCCCC(=O)N(CC(=O)O)Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81117-3
CHEMBL326140 110418 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Tested for inhibition of Angiotensin II receptor, type 1 in the absence of bovine serum albumin (BSA)Tested for inhibition of Angiotensin II receptor, type 1 in the absence of bovine serum albumin (BSA)
ChEMBL 393 9 2 5 3.1 CCCCC(=O)N(CC(=O)O)Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81117-3
44298570 100532 0 None - 0 Bovine 5.2 pIC50 = 5.2 Binding
Binding affinity for angiotensin II receptor of bovine adrenal cortexBinding affinity for angiotensin II receptor of bovine adrenal cortex
ChEMBL 452 7 1 7 4.2 CCCOc1nc2c(C)cccn2c(=O)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81144-6
CHEMBL294485 100532 0 None - 0 Bovine 5.2 pIC50 = 5.2 Binding
Binding affinity for angiotensin II receptor of bovine adrenal cortexBinding affinity for angiotensin II receptor of bovine adrenal cortex
ChEMBL 452 7 1 7 4.2 CCCOc1nc2c(C)cccn2c(=O)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81144-6
44298809 193831 0 None - 0 Bovine 5.2 pIC50 = 5.2 Binding
Binding affinity for angiotensin II receptor of bovine adrenal cortexBinding affinity for angiotensin II receptor of bovine adrenal cortex
ChEMBL 452 6 1 7 4.2 Cc1ccc2nc(OC(C)C)c(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c(=O)n2c1 10.1016/S0960-894X(01)81144-6
CHEMBL55366 193831 0 None - 0 Bovine 5.2 pIC50 = 5.2 Binding
Binding affinity for angiotensin II receptor of bovine adrenal cortexBinding affinity for angiotensin II receptor of bovine adrenal cortex
ChEMBL 452 6 1 7 4.2 Cc1ccc2nc(OC(C)C)c(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c(=O)n2c1 10.1016/S0960-894X(01)81144-6
19792191 97913 0 None - 0 Bovine 6.2 pIC50 = 6.2 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 452 9 1 6 5.4 CCCCc1nc2cccc(COC)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
CHEMBL275304 97913 0 None - 0 Bovine 6.2 pIC50 = 6.2 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 452 9 1 6 5.4 CCCCc1nc2cccc(COC)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
18572337 80730 9 None - 0 Human 4.2 pIC50 = 4.2 Binding
Inhibition of AT1 receptorInhibition of AT1 receptor
ChEMBL 419 6 0 9 3.5 O=C(Oc1coc(CSc2ncccn2)cc1=O)c1cc([N+](=O)[O-])ccc1Cl 10.1016/j.bmcl.2012.08.105
CHEMBL2158005 80730 9 None - 0 Human 4.2 pIC50 = 4.2 Binding
Inhibition of AT1 receptorInhibition of AT1 receptor
ChEMBL 419 6 0 9 3.5 O=C(Oc1coc(CSc2ncccn2)cc1=O)c1cc([N+](=O)[O-])ccc1Cl 10.1016/j.bmcl.2012.08.105
127035248 135905 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 549 9 2 5 7.0 CSc1nc2c(C)cc(C(=O)NC[C@H](C)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2015.09.010
CHEMBL3735653 135905 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 549 9 2 5 7.0 CSc1nc2c(C)cc(C(=O)NC[C@H](C)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2015.09.010
9937461 101340 0 None - 0 Bovine 7.2 pIC50 = 7.2 Binding
In vitro binding affinity to angiotensin II receptor in bovine adrenal cortexIn vitro binding affinity to angiotensin II receptor in bovine adrenal cortex
ChEMBL 551 9 2 9 4.3 CCCCc1nc2ccc([C@@H]3C[C@H](CO)ON3C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80377-2
CHEMBL300279 101340 0 None - 0 Bovine 7.2 pIC50 = 7.2 Binding
In vitro binding affinity to angiotensin II receptor in bovine adrenal cortexIn vitro binding affinity to angiotensin II receptor in bovine adrenal cortex
ChEMBL 551 9 2 9 4.3 CCCCc1nc2ccc([C@@H]3C[C@H](CO)ON3C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80377-2
127035263 135924 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 577 11 2 5 7.8 CCCSc1nc2c(C)cc(C(=O)NC[C@H](C)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2015.09.010
CHEMBL3735804 135924 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 577 11 2 5 7.8 CCCSc1nc2c(C)cc(C(=O)NC[C@H](C)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2015.09.010
44341836 109911 0 None - 0 Rat 7.2 pIC50 = 7.2 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 470 7 1 3 6.2 CCCCC1=NC2(C(=O)N1Cc1ccc(-c3ccccc3C(=O)O)cc1)C1CC3CC(C1)CC2C3 10.1021/jm00074a018
CHEMBL324452 109911 0 None - 0 Rat 7.2 pIC50 = 7.2 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 470 7 1 3 6.2 CCCCC1=NC2(C(=O)N1Cc1ccc(-c3ccccc3C(=O)O)cc1)C1CC3CC(C1)CC2C3 10.1021/jm00074a018
15654703 202595 0 None - 0 Bovine 7.2 pIC50 = 7.2 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 439 7 3 7 4.1 CCNc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a016
CHEMBL71410 202595 0 None - 0 Bovine 7.2 pIC50 = 7.2 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 439 7 3 7 4.1 CCNc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a016
44305663 100517 0 None - 0 Bovine 7.2 pIC50 = 7.2 Binding
Tested for binding affinity against angiotensin II receptor in bovine adrenal cortexTested for binding affinity against angiotensin II receptor in bovine adrenal cortex
ChEMBL 412 6 1 8 2.7 CCCc1cc2ncnn2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/0960-894X(95)00370-9
CHEMBL294358 100517 0 None - 0 Bovine 7.2 pIC50 = 7.2 Binding
Tested for binding affinity against angiotensin II receptor in bovine adrenal cortexTested for binding affinity against angiotensin II receptor in bovine adrenal cortex
ChEMBL 412 6 1 8 2.7 CCCc1cc2ncnn2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/0960-894X(95)00370-9
19385598 98393 0 None - 0 Rabbit 7.2 pIC50 = 7.2 Binding
Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)
ChEMBL 457 8 1 6 5.1 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(OC(C(=O)O)c2ccccc2)c(C(C)=O)c1 10.1016/0960-894X(95)00185-V
CHEMBL278955 98393 0 None - 0 Rabbit 7.2 pIC50 = 7.2 Binding
Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)
ChEMBL 457 8 1 6 5.1 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(OC(C(=O)O)c2ccccc2)c(C(C)=O)c1 10.1016/0960-894X(95)00185-V
135723843 100476 0 None - 0 Bovine 6.2 pIC50 = 6.2 Binding
Displacement of [125 I]-AII (0.2 nM) from bovine adrenal cortical membrane angiotensin II (AII) receptor at 10e-7 MDisplacement of [125 I]-AII (0.2 nM) from bovine adrenal cortical membrane angiotensin II (AII) receptor at 10e-7 M
ChEMBL 468 8 2 7 5.5 CCCCc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2noc(O)n2)cc1 10.1016/0960-894X(95)00319-O
CHEMBL294140 100476 0 None - 0 Bovine 6.2 pIC50 = 6.2 Binding
Displacement of [125 I]-AII (0.2 nM) from bovine adrenal cortical membrane angiotensin II (AII) receptor at 10e-7 MDisplacement of [125 I]-AII (0.2 nM) from bovine adrenal cortical membrane angiotensin II (AII) receptor at 10e-7 M
ChEMBL 468 8 2 7 5.5 CCCCc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2noc(O)n2)cc1 10.1016/0960-894X(95)00319-O
15654753 202517 0 None - 0 Bovine 6.2 pIC50 = 6.2 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 470 8 2 7 4.5 CSCCc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a016
CHEMBL70947 202517 0 None - 0 Bovine 6.2 pIC50 = 6.2 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 470 8 2 7 4.5 CSCCc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a016
127035393 135855 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 587 10 2 7 6.9 CCSc1nc2c(C)cc(C(=O)NC[C@@H](C)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.ejmech.2015.09.010
CHEMBL3735227 135855 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 587 10 2 7 6.9 CCSc1nc2c(C)cc(C(=O)NC[C@@H](C)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.ejmech.2015.09.010
76315369 84539 0 None - 0 Rabbit 7.2 pIC50 = 7.2 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 522 12 2 8 4.7 CCCCc1nnc(OCCc2ccccc2)n1Cc1ccc(NC(=O)c2ccccc2-c2nnn[nH]2)cc1 10.1007/s00044-011-9756-4
CHEMBL2237609 84539 0 None - 0 Rabbit 7.2 pIC50 = 7.2 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 522 12 2 8 4.7 CCCCc1nnc(OCCc2ccccc2)n1Cc1ccc(NC(=O)c2ccccc2-c2nnn[nH]2)cc1 10.1007/s00044-011-9756-4
10005344 46892 0 None - 0 Rabbit 7.2 pIC50 = 7.2 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 479 11 1 7 5.1 CCCCc1nnc(OCCc2ccccc2)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
CHEMBL154315 46892 0 None - 0 Rabbit 7.2 pIC50 = 7.2 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 479 11 1 7 5.1 CCCCc1nnc(OCCc2ccccc2)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
44320816 204541 0 None - 0 Rat 7.2 pIC50 = 7.2 Binding
Inhibition of [125-I]-labeled angiotensin II binding to AT1 receptor in rat uterine membranesInhibition of [125-I]-labeled angiotensin II binding to AT1 receptor in rat uterine membranes
ChEMBL 414 10 1 5 5.5 CCCCc1cn(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c(CCCC)n1 10.1016/S0960-894X(01)80290-0
CHEMBL86935 204541 0 None - 0 Rat 7.2 pIC50 = 7.2 Binding
Inhibition of [125-I]-labeled angiotensin II binding to AT1 receptor in rat uterine membranesInhibition of [125-I]-labeled angiotensin II binding to AT1 receptor in rat uterine membranes
ChEMBL 414 10 1 5 5.5 CCCCc1cn(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c(CCCC)n1 10.1016/S0960-894X(01)80290-0
71521585 86367 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor afterDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after
ChEMBL 532 6 1 9 4.8 CCc1nc2ccn(Cc3c(C)noc3C)c(=O)c2n1[C@H]1CCc2cc(-c3ccccc3-c3nnn[nH]3)ccc21 10.1016/j.bmcl.2012.11.088
CHEMBL2322174 86367 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor afterDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after
ChEMBL 532 6 1 9 4.8 CCc1nc2ccn(Cc3c(C)noc3C)c(=O)c2n1[C@H]1CCc2cc(-c3ccccc3-c3nnn[nH]3)ccc21 10.1016/j.bmcl.2012.11.088
71521505 86393 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor afterDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after
ChEMBL 514 6 1 8 4.6 CCc1nc2ccn(Cc3ccccn3)c(=O)c2n1[C@H]1CCc2cc(-c3ccccc3-c3nnn[nH]3)ccc21 10.1016/j.bmcl.2012.11.088
CHEMBL2322451 86393 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor afterDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after
ChEMBL 514 6 1 8 4.6 CCc1nc2ccn(Cc3ccccn3)c(=O)c2n1[C@H]1CCc2cc(-c3ccccc3-c3nnn[nH]3)ccc21 10.1016/j.bmcl.2012.11.088
70684421 76266 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Displacement of 125[I-Sar1-Ile8]ANG II from human AT1 receptor expressed in HEK293 membranes after 1 hr by gamma countingDisplacement of 125[I-Sar1-Ile8]ANG II from human AT1 receptor expressed in HEK293 membranes after 1 hr by gamma counting
ChEMBL 422 8 2 6 4.3 CCCCc1c(Cl)nc(CO)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.ejmech.2012.07.040
CHEMBL2063980 76266 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Displacement of 125[I-Sar1-Ile8]ANG II from human AT1 receptor expressed in HEK293 membranes after 1 hr by gamma countingDisplacement of 125[I-Sar1-Ile8]ANG II from human AT1 receptor expressed in HEK293 membranes after 1 hr by gamma counting
ChEMBL 422 8 2 6 4.3 CCCCc1c(Cl)nc(CO)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.ejmech.2012.07.040
9979266 116777 0 None - 0 Guinea pig 5.2 pIC50 = 5.2 Binding
In vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparationIn vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparation
ChEMBL 379 5 1 5 4.7 c1ccc(-c2nn[nH]n2)c(-c2ccc(COc3ccnc4ccccc34)cc2)c1 10.1021/jm00100a007
CHEMBL339592 116777 0 None - 0 Guinea pig 5.2 pIC50 = 5.2 Binding
In vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparationIn vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparation
ChEMBL 379 5 1 5 4.7 c1ccc(-c2nn[nH]n2)c(-c2ccc(COc3ccnc4ccccc34)cc2)c1 10.1021/jm00100a007
70684421 76266 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Displacement of 125[I-Sar1-Ile8]ANG II from human AT1 receptor expressed in HEK293 membranes after 1 hr by gamma countingDisplacement of 125[I-Sar1-Ile8]ANG II from human AT1 receptor expressed in HEK293 membranes after 1 hr by gamma counting
ChEMBL 422 8 2 6 4.3 CCCCc1c(Cl)nc(CO)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.ejmech.2012.07.040
CHEMBL2063980 76266 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Displacement of 125[I-Sar1-Ile8]ANG II from human AT1 receptor expressed in HEK293 membranes after 1 hr by gamma countingDisplacement of 125[I-Sar1-Ile8]ANG II from human AT1 receptor expressed in HEK293 membranes after 1 hr by gamma counting
ChEMBL 422 8 2 6 4.3 CCCCc1c(Cl)nc(CO)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.ejmech.2012.07.040
71654380 88713 0 None - 0 Human 5.2 pIC50 = 5.2 Binding
Displacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysisDisplacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysis
ChEMBL 657 12 3 8 6.1 CCCCc1c(Cl)[n+](Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c(CO)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.ejmech.2012.12.044
CHEMBL2337680 88713 0 None - 0 Human 5.2 pIC50 = 5.2 Binding
Displacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysisDisplacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysis
ChEMBL 657 12 3 8 6.1 CCCCc1c(Cl)[n+](Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c(CO)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.ejmech.2012.12.044
CHEMBL2366021 88713 0 None - 0 Human 5.2 pIC50 = 5.2 Binding
Displacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysisDisplacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysis
ChEMBL 657 12 3 8 6.1 CCCCc1c(Cl)[n+](Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c(CO)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.ejmech.2012.12.044
44315344 104589 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membrane
ChEMBL 665 12 2 8 5.2 CCc1nc2ccc(NC(=O)N(C)C(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)COCC(C)C)cc1F 10.1016/0960-894X(94)85036-4
CHEMBL311386 104589 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membrane
ChEMBL 665 12 2 8 5.2 CCc1nc2ccc(NC(=O)N(C)C(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)COCC(C)C)cc1F 10.1016/0960-894X(94)85036-4
19036230 101271 0 None - 0 Bovine 7.2 pIC50 = 7.2 Binding
Inhibition of [125l]-All binding to bovine adrenal cortexInhibition of [125l]-All binding to bovine adrenal cortex
ChEMBL 408 9 3 5 3.8 CCCCc1nc(CO)c(C(=O)O)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/S0960-894X(01)81143-4
CHEMBL299809 101271 0 None - 0 Bovine 7.2 pIC50 = 7.2 Binding
Inhibition of [125l]-All binding to bovine adrenal cortexInhibition of [125l]-All binding to bovine adrenal cortex
ChEMBL 408 9 3 5 3.8 CCCCc1nc(CO)c(C(=O)O)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/S0960-894X(01)81143-4
15287883 97745 0 None - 0 Rabbit 7.2 pIC50 = 7.2 Binding
Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)
ChEMBL 415 8 1 5 4.9 CCCc1nc2c(C)ccnc2n1Cc1ccc(OC(C(=O)O)c2ccccc2)cc1 10.1016/0960-894X(95)00185-V
CHEMBL274260 97745 0 None - 0 Rabbit 7.2 pIC50 = 7.2 Binding
Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)
ChEMBL 415 8 1 5 4.9 CCCc1nc2c(C)ccnc2n1Cc1ccc(OC(C(=O)O)c2ccccc2)cc1 10.1016/0960-894X(95)00185-V
15654760 101709 0 None - 0 Bovine 6.2 pIC50 = 6.2 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 467 9 3 7 4.8 CCCCNc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a016
CHEMBL302811 101709 0 None - 0 Bovine 6.2 pIC50 = 6.2 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 467 9 3 7 4.8 CCCCNc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a016
44342002 9840 0 None - 0 Rat 7.2 pIC50 = 7.2 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 432 7 1 3 5.9 CCCCC1=NC2(CCC(C)CC2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00074a018
CHEMBL114656 9840 0 None - 0 Rat 7.2 pIC50 = 7.2 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 432 7 1 3 5.9 CCCCC1=NC2(CCC(C)CC2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00074a018
11352388 105452 0 None - 0 Rat 7.2 pIC50 = 7.2 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 493 8 2 6 6.4 CCCNc1nc2ccccc2c(-c2ccc(Cn3c(CC)nc4c(C)cc(C)nc43)cc2)c1C(=O)O 10.1021/jm031100t
CHEMBL312889 105452 0 None - 0 Rat 7.2 pIC50 = 7.2 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 493 8 2 6 6.4 CCCNc1nc2ccccc2c(-c2ccc(Cn3c(CC)nc4c(C)cc(C)nc43)cc2)c1C(=O)O 10.1021/jm031100t
9983514 19266 0 None - 0 Guinea pig 7.2 pIC50 = 7.2 Binding
In vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparationIn vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparation
ChEMBL 465 7 1 7 5.0 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2cc(C(=O)OC)ccc2n1 10.1021/jm00100a007
CHEMBL129872 19266 0 None - 0 Guinea pig 7.2 pIC50 = 7.2 Binding
In vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparationIn vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparation
ChEMBL 465 7 1 7 5.0 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2cc(C(=O)OC)ccc2n1 10.1021/jm00100a007
15654696 103290 58 None - 0 Bovine 7.2 pIC50 = 7.2 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 454 7 1 8 4.1 CCOc1nc2cccc(C(=O)OC)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a016
CHEMBL308884 103290 58 None - 0 Bovine 7.2 pIC50 = 7.2 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 454 7 1 8 4.1 CCOc1nc2cccc(C(=O)OC)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a016
44341698 159377 0 None - 0 Rat 6.2 pIC50 = 6.2 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 442 7 0 6 4.8 CCCCC1=NC2(CCCC2)C(=O)N1Cc1ccc(-c2ccccc2-c2nnn(C)n2)cc1 10.1021/jm00074a018
CHEMBL410724 159377 0 None - 0 Rat 6.2 pIC50 = 6.2 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 442 7 0 6 4.8 CCCCC1=NC2(CCCC2)C(=O)N1Cc1ccc(-c2ccccc2-c2nnn(C)n2)cc1 10.1021/jm00074a018
44295673 162217 0 None - 0 Bovine 6.2 pIC50 = 6.2 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 428 8 2 4 5.5 CCCCc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1007/s00044-009-9182-z
CHEMBL417196 162217 0 None - 0 Bovine 6.2 pIC50 = 6.2 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 428 8 2 4 5.5 CCCCc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1007/s00044-009-9182-z
44295673 162217 0 None - 0 Bovine 6.2 pIC50 = 6.2 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 428 8 2 4 5.5 CCCCc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1007/s00044-009-9182-z
CHEMBL417196 162217 0 None - 0 Bovine 6.2 pIC50 = 6.2 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 428 8 2 4 5.5 CCCCc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1007/s00044-009-9182-z
44305289 201577 0 None - 0 Bovine 5.2 pIC50 = 5.2 Binding
Tested for binding affinity against angiotensin II receptor in bovine adrenal cortexTested for binding affinity against angiotensin II receptor in bovine adrenal cortex
ChEMBL 416 6 1 7 2.7 CCCc1c(C)c(=O)n(C)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/0960-894X(95)00370-9
CHEMBL64670 201577 0 None - 0 Bovine 5.2 pIC50 = 5.2 Binding
Tested for binding affinity against angiotensin II receptor in bovine adrenal cortexTested for binding affinity against angiotensin II receptor in bovine adrenal cortex
ChEMBL 416 6 1 7 2.7 CCCc1c(C)c(=O)n(C)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/0960-894X(95)00370-9
18654313 63424 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation countingDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation counting
ChEMBL 435 4 1 6 5.0 CCc1nc2c(C)cc(C)nc2n1[C@@H]1CCc2cc(-c3ccccc3-c3nnn[nH]3)ccc21 10.1021/jm200409s
CHEMBL1801713 63424 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation countingDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation counting
ChEMBL 435 4 1 6 5.0 CCc1nc2c(C)cc(C)nc2n1[C@@H]1CCc2cc(-c3ccccc3-c3nnn[nH]3)ccc21 10.1021/jm200409s
15171411 204471 0 None - 0 Guinea pig 7.2 pIC50 = 7.2 Binding
Compound was tested for in vitro inhibition of specific binding of [I-125]AII to Angiotensin II receptor, type 1 in guinea pig adrenal membrane preparationCompound was tested for in vitro inhibition of specific binding of [I-125]AII to Angiotensin II receptor, type 1 in guinea pig adrenal membrane preparation
ChEMBL 441 7 1 6 5.0 CCc1cc(OCc2ccc(-c3cc(OC)ccc3-c3nn[nH]n3)cc2)c2c(n1)CCCC2 10.1016/S0960-894X(01)80295-X
CHEMBL86495 204471 0 None - 0 Guinea pig 7.2 pIC50 = 7.2 Binding
Compound was tested for in vitro inhibition of specific binding of [I-125]AII to Angiotensin II receptor, type 1 in guinea pig adrenal membrane preparationCompound was tested for in vitro inhibition of specific binding of [I-125]AII to Angiotensin II receptor, type 1 in guinea pig adrenal membrane preparation
ChEMBL 441 7 1 6 5.0 CCc1cc(OCc2ccc(-c3cc(OC)ccc3-c3nn[nH]n3)cc2)c2c(n1)CCCC2 10.1016/S0960-894X(01)80295-X
71521419 86389 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor afterDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after
ChEMBL 531 6 1 7 5.3 CCc1nc2ccn(Cc3cccc(F)c3)c(=O)c2n1[C@H]1CCc2cc(-c3ccccc3-c3nnn[nH]3)ccc21 10.1016/j.bmcl.2012.11.088
CHEMBL2322448 86389 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor afterDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after
ChEMBL 531 6 1 7 5.3 CCc1nc2ccn(Cc3cccc(F)c3)c(=O)c2n1[C@H]1CCc2cc(-c3ccccc3-c3nnn[nH]3)ccc21 10.1016/j.bmcl.2012.11.088
127026041 136992 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Displacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptorDisplacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptor
ChEMBL 605 11 3 8 5.0 CCCc1nc2c(C)cc(C(=O)NCCN3CCCCC3)cc2n1Cc1ccc(-c2ccccc2C(=O)Nc2nnn[nH]2)cc1 10.1039/C5MD00169B
CHEMBL3754267 136992 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Displacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptorDisplacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptor
ChEMBL 605 11 3 8 5.0 CCCc1nc2c(C)cc(C(=O)NCCN3CCCCC3)cc2n1Cc1ccc(-c2ccccc2C(=O)Nc2nnn[nH]2)cc1 10.1039/C5MD00169B
44293911 187649 0 None - 0 Rat 6.2 pIC50 = 6.2 Binding
Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.
ChEMBL 510 11 2 6 5.9 CCCCc1nc(Cl)c(C(=O)O)n1Cc1ccc(NC(=O)[C@H](Cc2cccs2)n2cccc2)cc1 10.1021/jm00064a007
CHEMBL49954 187649 0 None - 0 Rat 6.2 pIC50 = 6.2 Binding
Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.
ChEMBL 510 11 2 6 5.9 CCCCc1nc(Cl)c(C(=O)O)n1Cc1ccc(NC(=O)[C@H](Cc2cccs2)n2cccc2)cc1 10.1021/jm00064a007
127035381 135937 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 573 9 2 7 6.5 CSc1nc2c(C)cc(C(=O)NC[C@H](C)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.ejmech.2015.09.010
CHEMBL3735940 135937 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 573 9 2 7 6.5 CSc1nc2c(C)cc(C(=O)NC[C@H](C)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.ejmech.2015.09.010
14956800 204420 0 None - 0 Rabbit 7.2 pIC50 = 7.2 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 509 10 2 8 4.0 CCCCc1nn(C(C(=O)O)c2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
CHEMBL86143 204420 0 None - 0 Rabbit 7.2 pIC50 = 7.2 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 509 10 2 8 4.0 CCCCc1nn(C(C(=O)O)c2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
22850890 189172 0 None - 0 Bovine 7.2 pIC50 = 7.2 Binding
In vitro binding affinity to angiotensin II receptor in bovine adrenal cortexIn vitro binding affinity to angiotensin II receptor in bovine adrenal cortex
ChEMBL 577 8 1 10 4.1 CCCCc1nc2ccc([C@H]3[C@@H]4C(=O)OC[C@@H]4ON3C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80377-2
CHEMBL51606 189172 0 None - 0 Bovine 7.2 pIC50 = 7.2 Binding
In vitro binding affinity to angiotensin II receptor in bovine adrenal cortexIn vitro binding affinity to angiotensin II receptor in bovine adrenal cortex
ChEMBL 577 8 1 10 4.1 CCCCc1nc2ccc([C@H]3[C@@H]4C(=O)OC[C@@H]4ON3C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80377-2
44294562 188547 0 None - 0 Bovine 6.2 pIC50 = 6.2 Binding
Ability to displace [125I]- labelled [Sar1,Ileu8] from angiotensin II receptor of bovine adrenal cortex membranesAbility to displace [125I]- labelled [Sar1,Ileu8] from angiotensin II receptor of bovine adrenal cortex membranes
ChEMBL 501 10 1 6 5.7 CCCCCC1(C)CC(=O)N(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/C(=C/C(=O)OCC)C1 10.1016/S0960-894X(00)80474-6
CHEMBL51078 188547 0 None - 0 Bovine 6.2 pIC50 = 6.2 Binding
Ability to displace [125I]- labelled [Sar1,Ileu8] from angiotensin II receptor of bovine adrenal cortex membranesAbility to displace [125I]- labelled [Sar1,Ileu8] from angiotensin II receptor of bovine adrenal cortex membranes
ChEMBL 501 10 1 6 5.7 CCCCCC1(C)CC(=O)N(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/C(=C/C(=O)OCC)C1 10.1016/S0960-894X(00)80474-6
44563175 188494 0 None - 0 Bovine 6.2 pIC50 = 6.2 Binding
Displacement of [125I]Ang2 from AT1 receptor in bovine adrenal cortexDisplacement of [125I]Ang2 from AT1 receptor in bovine adrenal cortex
ChEMBL 570 7 1 5 8.6 CCCc1nc2c(C)cc(-c3nc4ccccc4n3C)cc2n1Cc1ccc(-c2ccccc2-c2ncc(Cl)[nH]2)cc1 10.1016/j.bmc.2008.10.040
CHEMBL510065 188494 0 None - 0 Bovine 6.2 pIC50 = 6.2 Binding
Displacement of [125I]Ang2 from AT1 receptor in bovine adrenal cortexDisplacement of [125I]Ang2 from AT1 receptor in bovine adrenal cortex
ChEMBL 570 7 1 5 8.6 CCCc1nc2c(C)cc(-c3nc4ccccc4n3C)cc2n1Cc1ccc(-c2ccccc2-c2ncc(Cl)[nH]2)cc1 10.1016/j.bmc.2008.10.040
14956746 204463 0 None - 0 Rabbit 7.2 pIC50 = 7.2 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 485 8 1 7 4.9 CCCCc1nn(-c2ccc(Cl)cc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
CHEMBL86440 204463 0 None - 0 Rabbit 7.2 pIC50 = 7.2 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 485 8 1 7 4.9 CCCCc1nn(-c2ccc(Cl)cc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
44270285 98595 0 None - 0 Rabbit 7.2 pIC50 = 7.2 Binding
Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)
ChEMBL 415 7 1 5 4.7 CCc1nc2c(C)cc(C)nn2c1Cc1ccc(OC(C(=O)O)c2ccccc2)cc1 10.1016/0960-894X(95)00185-V
CHEMBL280456 98595 0 None - 0 Rabbit 7.2 pIC50 = 7.2 Binding
Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)
ChEMBL 415 7 1 5 4.7 CCc1nc2c(C)cc(C)nn2c1Cc1ccc(OC(C(=O)O)c2ccccc2)cc1 10.1016/0960-894X(95)00185-V
127026040 136941 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Displacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptorDisplacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptor
ChEMBL 591 11 3 8 4.6 CCCc1nc2c(C)cc(C(=O)NCCN3CCCC3)cc2n1Cc1ccc(-c2ccccc2C(=O)Nc2nnn[nH]2)cc1 10.1039/C5MD00169B
CHEMBL3753888 136941 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Displacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptorDisplacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptor
ChEMBL 591 11 3 8 4.6 CCCc1nc2c(C)cc(C(=O)NCCN3CCCC3)cc2n1Cc1ccc(-c2ccccc2C(=O)Nc2nnn[nH]2)cc1 10.1039/C5MD00169B
44298833 196822 0 None - 0 Bovine 4.2 pIC50 = 4.2 Binding
Binding affinity for angiotensin II receptor of bovine adrenal cortexBinding affinity for angiotensin II receptor of bovine adrenal cortex
ChEMBL 482 7 2 8 3.6 CC(C)Oc1nc2ccc(C(=O)O)cn2c(=O)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81144-6
CHEMBL57781 196822 0 None - 0 Bovine 4.2 pIC50 = 4.2 Binding
Binding affinity for angiotensin II receptor of bovine adrenal cortexBinding affinity for angiotensin II receptor of bovine adrenal cortex
ChEMBL 482 7 2 8 3.6 CC(C)Oc1nc2ccc(C(=O)O)cn2c(=O)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81144-6
127035249 135985 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 573 9 2 7 6.5 CSc1nc2c(C)cc(C(=O)NC[C@@H](C)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.ejmech.2015.09.010
CHEMBL3736346 135985 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 573 9 2 7 6.5 CSc1nc2c(C)cc(C(=O)NC[C@@H](C)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.ejmech.2015.09.010
44274733 98935 0 None - 0 Rabbit 8.2 pIC50 = 8.2 Binding
Ability to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitroAbility to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitro
ChEMBL 482 8 1 7 5.4 CCCCc1nc2ccc(SC)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80335-2
CHEMBL282746 98935 0 None - 0 Rabbit 8.2 pIC50 = 8.2 Binding
Ability to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitroAbility to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitro
ChEMBL 482 8 1 7 5.4 CCCCc1nc2ccc(SC)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80335-2
15171415 106442 0 None - 0 Guinea pig 8.2 pIC50 = 8.2 Binding
Compound was tested for in vitro inhibition of specific binding of [I-125]AII to AT1 receptor in guinea pig adrenal membrane preparationCompound was tested for in vitro inhibition of specific binding of [I-125]AII to AT1 receptor in guinea pig adrenal membrane preparation
ChEMBL 445 6 1 5 5.6 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)c(Cl)c2)c2c(n1)CCCC2 10.1016/S0960-894X(01)80295-X
CHEMBL314859 106442 0 None - 0 Guinea pig 8.2 pIC50 = 8.2 Binding
Compound was tested for in vitro inhibition of specific binding of [I-125]AII to AT1 receptor in guinea pig adrenal membrane preparationCompound was tested for in vitro inhibition of specific binding of [I-125]AII to AT1 receptor in guinea pig adrenal membrane preparation
ChEMBL 445 6 1 5 5.6 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)c(Cl)c2)c2c(n1)CCCC2 10.1016/S0960-894X(01)80295-X
127035757 135969 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
Displacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysisDisplacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysis
ChEMBL 591 10 1 8 6.2 CCCCc1nn(-c2ccccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)cc1 10.1039/C4MD00499J
CHEMBL3736242 135969 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
Displacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysisDisplacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysis
ChEMBL 591 10 1 8 6.2 CCCCc1nn(-c2ccccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)cc1 10.1039/C4MD00499J
71520501 86369 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor afterDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after
ChEMBL 552 6 1 8 5.4 CCc1nc2c(C)cn(Cc3ccccc3C#N)c(=O)c2n1[C@H]1CCc2cc(-c3ccccc3-c3nnn[nH]3)ccc21 10.1016/j.bmcl.2012.11.088
CHEMBL2322176 86369 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor afterDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after
ChEMBL 552 6 1 8 5.4 CCc1nc2c(C)cn(Cc3ccccc3C#N)c(=O)c2n1[C@H]1CCc2cc(-c3ccccc3-c3nnn[nH]3)ccc21 10.1016/j.bmcl.2012.11.088
44376991 119776 0 None - 0 Rabbit 8.2 pIC50 = 8.2 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aortaIn vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aorta
ChEMBL 436 8 1 7 4.3 CCCCc1nc(Cl)c(C(=O)O)n1Cc1ccc(-c2ccccc2-n2cnnn2)cc1 10.1016/S0960-894X(01)81124-0
CHEMBL352675 119776 0 None - 0 Rabbit 8.2 pIC50 = 8.2 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aortaIn vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aorta
ChEMBL 436 8 1 7 4.3 CCCCc1nc(Cl)c(C(=O)O)n1Cc1ccc(-c2ccccc2-n2cnnn2)cc1 10.1016/S0960-894X(01)81124-0
10075750 107059 0 None - 0 Rabbit 8.2 pIC50 = 8.2 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 532 10 1 7 4.8 CCCCc1nn(C(C)C)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1021/jm00043a020
CHEMBL318891 107059 0 None - 0 Rabbit 8.2 pIC50 = 8.2 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 532 10 1 7 4.8 CCCCc1nn(C(C)C)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1021/jm00043a020
9851889 101591 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of rat adrenal membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of rat adrenal membrane
ChEMBL 611 12 1 7 7.1 CCCCCN(C(=O)c1ccccc1)c1ccc2nc(CCC)n(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c(=O)c2c1 10.1016/0960-894X(94)85036-4
CHEMBL302102 101591 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of rat adrenal membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of rat adrenal membrane
ChEMBL 611 12 1 7 7.1 CCCCCN(C(=O)c1ccccc1)c1ccc2nc(CCC)n(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c(=O)c2c1 10.1016/0960-894X(94)85036-4
19010079 84518 0 None - 0 Rabbit 8.2 pIC50 = 8.2 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 524 11 2 8 5.4 CCCCc1nnc(SCc2ccccc2)n1Cc1ccc(NC(=O)c2ccccc2-c2nnn[nH]2)cc1 10.1007/s00044-011-9756-4
CHEMBL2237588 84518 0 None - 0 Rabbit 8.2 pIC50 = 8.2 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 524 11 2 8 5.4 CCCCc1nnc(SCc2ccccc2)n1Cc1ccc(NC(=O)c2ccccc2-c2nnn[nH]2)cc1 10.1007/s00044-011-9756-4
10367792 17744 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 478 9 1 7 4.2 CCCCc1ncc(/C=C2/C(=O)NC(=O)N2Cc2cccs2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
CHEMBL125958 17744 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 478 9 1 7 4.2 CCCCc1ncc(/C=C2/C(=O)NC(=O)N2Cc2cccs2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
9981102 163629 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 448 10 2 7 3.1 CCCCc1ncc(/C=C2/C(=O)NC(=O)N2CCCC)n1Cc1ccc(-c2nn[nH]n2)cc1 10.1007/s00044-009-9205-9
CHEMBL421074 163629 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 448 10 2 7 3.1 CCCCc1ncc(/C=C2/C(=O)NC(=O)N2CCCC)n1Cc1ccc(-c2nn[nH]n2)cc1 10.1007/s00044-009-9205-9
10096735 119012 0 None - 0 Rabbit 8.2 pIC50 = 8.2 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 481 10 1 7 5.8 CCCCc1nnc(SCc2ccccc2)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
CHEMBL345717 119012 0 None - 0 Rabbit 8.2 pIC50 = 8.2 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 481 10 1 7 5.8 CCCCc1nnc(SCc2ccccc2)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
44277873 98402 0 None - 0 Rabbit 8.1 pIC50 = 8.1 Binding
Binding affinity against AT1 receptor in rabbit aortaBinding affinity against AT1 receptor in rabbit aorta
ChEMBL 661 11 0 10 5.5 CCCCCN(C(=O)c1ccc(S(C)(=O)=O)cc1)c1ccc2ncn(Cc3ccc(-c4ccccc4-c4nnnn4C)cc3)c(=O)c2c1 10.1016/0960-894X(95)00224-H
CHEMBL27903 98402 0 None - 0 Rabbit 8.1 pIC50 = 8.1 Binding
Binding affinity against AT1 receptor in rabbit aortaBinding affinity against AT1 receptor in rabbit aorta
ChEMBL 661 11 0 10 5.5 CCCCCN(C(=O)c1ccc(S(C)(=O)=O)cc1)c1ccc2ncn(Cc3ccc(-c4ccccc4-c4nnnn4C)cc3)c(=O)c2c1 10.1016/0960-894X(95)00224-H
44342039 10181 0 None - 0 Rat 8.1 pIC50 = 8.1 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 418 7 1 3 5.7 CCCCC1=NC2(CCCCC2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00074a018
CHEMBL116170 10181 0 None - 0 Rat 8.1 pIC50 = 8.1 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 418 7 1 3 5.7 CCCCC1=NC2(CCCCC2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00074a018
19029573 120194 0 None - 0 Rat 8.1 pIC50 = 8.1 Binding
In vitro ability to displace the specific binding of [125I]-A II from receptors in rat liver membrane(type 1 receptor)In vitro ability to displace the specific binding of [125I]-A II from receptors in rat liver membrane(type 1 receptor)
ChEMBL 405 5 1 7 2.9 CCc1nn(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/c(=N/C(C)=O)s1 10.1016/S0960-894X(96)00250-8
CHEMBL35475 120194 0 None - 0 Rat 8.1 pIC50 = 8.1 Binding
In vitro ability to displace the specific binding of [125I]-A II from receptors in rat liver membrane(type 1 receptor)In vitro ability to displace the specific binding of [125I]-A II from receptors in rat liver membrane(type 1 receptor)
ChEMBL 405 5 1 7 2.9 CCc1nn(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/c(=N/C(C)=O)s1 10.1016/S0960-894X(96)00250-8
44314780 102591 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membrane
ChEMBL 649 11 3 8 5.6 CCc1nc2ccc(NC(=O)NC(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC2CC2)cc1F 10.1016/0960-894X(94)85036-4
CHEMBL307430 102591 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membrane
ChEMBL 649 11 3 8 5.6 CCc1nc2ccc(NC(=O)NC(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC2CC2)cc1F 10.1016/0960-894X(94)85036-4
127034921 135992 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 547 10 2 5 6.7 CCOc1nc2c(C)cc(C(=O)NC[C@H](C)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2015.09.010
CHEMBL3736440 135992 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 547 10 2 5 6.7 CCOc1nc2c(C)cc(C(=O)NC[C@H](C)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2015.09.010
44291781 180966 0 None - 0 Rat 8.1 pIC50 = 8.1 Binding
In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.
ChEMBL 406 8 1 3 5.4 CCCCC1=NC(C)(C(C)C)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/S0960-894X(01)81140-9
CHEMBL47669 180966 0 None - 0 Rat 8.1 pIC50 = 8.1 Binding
In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.
ChEMBL 406 8 1 3 5.4 CCCCC1=NC(C)(C(C)C)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/S0960-894X(01)81140-9
1037 1542 65 None - 1 Human 8.1 pIC50 = 8.1 Binding
Tested for Angiotensin II receptor, type 1 affinity in the presence of 0.25% bovine serum albumin (BSA)Tested for Angiotensin II receptor, type 1 affinity in the presence of 0.25% bovine serum albumin (BSA)
ChEMBL 424 10 2 5 4.7 CCCCc1ncc(n1Cc1ccc(cc1)C(=O)O)/C=C(/C(=O)O)\Cc1cccs1 10.1016/S0960-894X(01)81116-1
3940 1542 65 None - 1 Human 8.1 pIC50 = 8.1 Binding
Tested for Angiotensin II receptor, type 1 affinity in the presence of 0.25% bovine serum albumin (BSA)Tested for Angiotensin II receptor, type 1 affinity in the presence of 0.25% bovine serum albumin (BSA)
ChEMBL 424 10 2 5 4.7 CCCCc1ncc(n1Cc1ccc(cc1)C(=O)O)/C=C(/C(=O)O)\Cc1cccs1 10.1016/S0960-894X(01)81116-1
5281037 1542 65 None - 1 Human 8.1 pIC50 = 8.1 Binding
Tested for Angiotensin II receptor, type 1 affinity in the presence of 0.25% bovine serum albumin (BSA)Tested for Angiotensin II receptor, type 1 affinity in the presence of 0.25% bovine serum albumin (BSA)
ChEMBL 424 10 2 5 4.7 CCCCc1ncc(n1Cc1ccc(cc1)C(=O)O)/C=C(/C(=O)O)\Cc1cccs1 10.1016/S0960-894X(01)81116-1
588 1542 65 None - 1 Human 8.1 pIC50 = 8.1 Binding
Tested for Angiotensin II receptor, type 1 affinity in the presence of 0.25% bovine serum albumin (BSA)Tested for Angiotensin II receptor, type 1 affinity in the presence of 0.25% bovine serum albumin (BSA)
ChEMBL 424 10 2 5 4.7 CCCCc1ncc(n1Cc1ccc(cc1)C(=O)O)/C=C(/C(=O)O)\Cc1cccs1 10.1016/S0960-894X(01)81116-1
CHEMBL813 1542 65 None - 1 Human 8.1 pIC50 = 8.1 Binding
Tested for Angiotensin II receptor, type 1 affinity in the presence of 0.25% bovine serum albumin (BSA)Tested for Angiotensin II receptor, type 1 affinity in the presence of 0.25% bovine serum albumin (BSA)
ChEMBL 424 10 2 5 4.7 CCCCc1ncc(n1Cc1ccc(cc1)C(=O)O)/C=C(/C(=O)O)\Cc1cccs1 10.1016/S0960-894X(01)81116-1
DB00876 1542 65 None - 1 Human 8.1 pIC50 = 8.1 Binding
Tested for Angiotensin II receptor, type 1 affinity in the presence of 0.25% bovine serum albumin (BSA)Tested for Angiotensin II receptor, type 1 affinity in the presence of 0.25% bovine serum albumin (BSA)
ChEMBL 424 10 2 5 4.7 CCCCc1ncc(n1Cc1ccc(cc1)C(=O)O)/C=C(/C(=O)O)\Cc1cccs1 10.1016/S0960-894X(01)81116-1
11757193 51059 0 None - 0 Rabbit 8.1 pIC50 = 8.1 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 546 12 2 7 4.9 CCCCc1nnc([S+]([O-])Cc2ccc(OC)cc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
CHEMBL158133 51059 0 None - 0 Rabbit 8.1 pIC50 = 8.1 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 546 12 2 7 4.9 CCCCc1nnc([S+]([O-])Cc2ccc(OC)cc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
2806 3894 109 None - 1 Human 8.1 pIC50 = 8.1 Binding
Displacement of [125-I]-[Sar1, AngII from AT1R (unknown origin) expressed in Escherichia coli BL 21 (DE3) incubated for 2 hrs by radioimmunoassayDisplacement of [125-I]-[Sar1, AngII from AT1R (unknown origin) expressed in Escherichia coli BL 21 (DE3) incubated for 2 hrs by radioimmunoassay
ChEMBL 435 10 2 5 4.2 CCCCC(=O)N([C@H](C(=O)O)C(C)C)Cc1ccc(cc1)c1ccccc1c1nnn[nH]1 10.1021/acs.jmedchem.1c00123
3937 3894 109 None - 1 Human 8.1 pIC50 = 8.1 Binding
Displacement of [125-I]-[Sar1, AngII from AT1R (unknown origin) expressed in Escherichia coli BL 21 (DE3) incubated for 2 hrs by radioimmunoassayDisplacement of [125-I]-[Sar1, AngII from AT1R (unknown origin) expressed in Escherichia coli BL 21 (DE3) incubated for 2 hrs by radioimmunoassay
ChEMBL 435 10 2 5 4.2 CCCCC(=O)N([C@H](C(=O)O)C(C)C)Cc1ccc(cc1)c1ccccc1c1nnn[nH]1 10.1021/acs.jmedchem.1c00123
593 3894 109 None - 1 Human 8.1 pIC50 = 8.1 Binding
Displacement of [125-I]-[Sar1, AngII from AT1R (unknown origin) expressed in Escherichia coli BL 21 (DE3) incubated for 2 hrs by radioimmunoassayDisplacement of [125-I]-[Sar1, AngII from AT1R (unknown origin) expressed in Escherichia coli BL 21 (DE3) incubated for 2 hrs by radioimmunoassay
ChEMBL 435 10 2 5 4.2 CCCCC(=O)N([C@H](C(=O)O)C(C)C)Cc1ccc(cc1)c1ccccc1c1nnn[nH]1 10.1021/acs.jmedchem.1c00123
60846 3894 109 None - 1 Human 8.1 pIC50 = 8.1 Binding
Displacement of [125-I]-[Sar1, AngII from AT1R (unknown origin) expressed in Escherichia coli BL 21 (DE3) incubated for 2 hrs by radioimmunoassayDisplacement of [125-I]-[Sar1, AngII from AT1R (unknown origin) expressed in Escherichia coli BL 21 (DE3) incubated for 2 hrs by radioimmunoassay
ChEMBL 435 10 2 5 4.2 CCCCC(=O)N([C@H](C(=O)O)C(C)C)Cc1ccc(cc1)c1ccccc1c1nnn[nH]1 10.1021/acs.jmedchem.1c00123
CHEMBL1069 3894 109 None - 1 Human 8.1 pIC50 = 8.1 Binding
Displacement of [125-I]-[Sar1, AngII from AT1R (unknown origin) expressed in Escherichia coli BL 21 (DE3) incubated for 2 hrs by radioimmunoassayDisplacement of [125-I]-[Sar1, AngII from AT1R (unknown origin) expressed in Escherichia coli BL 21 (DE3) incubated for 2 hrs by radioimmunoassay
ChEMBL 435 10 2 5 4.2 CCCCC(=O)N([C@H](C(=O)O)C(C)C)Cc1ccc(cc1)c1ccccc1c1nnn[nH]1 10.1021/acs.jmedchem.1c00123
DB00177 3894 109 None - 1 Human 8.1 pIC50 = 8.1 Binding
Displacement of [125-I]-[Sar1, AngII from AT1R (unknown origin) expressed in Escherichia coli BL 21 (DE3) incubated for 2 hrs by radioimmunoassayDisplacement of [125-I]-[Sar1, AngII from AT1R (unknown origin) expressed in Escherichia coli BL 21 (DE3) incubated for 2 hrs by radioimmunoassay
ChEMBL 435 10 2 5 4.2 CCCCC(=O)N([C@H](C(=O)O)C(C)C)Cc1ccc(cc1)c1ccccc1c1nnn[nH]1 10.1021/acs.jmedchem.1c00123
11757193 51059 0 None - 0 Rabbit 8.1 pIC50 = 8.1 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 546 12 2 7 4.9 CCCCc1nnc([S+]([O-])Cc2ccc(OC)cc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
CHEMBL158133 51059 0 None - 0 Rabbit 8.1 pIC50 = 8.1 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 546 12 2 7 4.9 CCCCc1nnc([S+]([O-])Cc2ccc(OC)cc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
44379269 56858 0 None - 0 Rabbit 8.1 pIC50 = 8.1 Binding
In vitro displacement of 125I-[Sar1, Ile8] from AT1 receptors in rabbit aorta membraneIn vitro displacement of 125I-[Sar1, Ile8] from AT1 receptors in rabbit aorta membrane
ChEMBL 644 12 1 8 5.9 CCCCc1nc2ccc(N(C)C(=O)OCC(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)C2CC2)cc1 10.1016/S0960-894X(01)81125-2
CHEMBL164769 56858 0 None - 0 Rabbit 8.1 pIC50 = 8.1 Binding
In vitro displacement of 125I-[Sar1, Ile8] from AT1 receptors in rabbit aorta membraneIn vitro displacement of 125I-[Sar1, Ile8] from AT1 receptors in rabbit aorta membrane
ChEMBL 644 12 1 8 5.9 CCCCc1nc2ccc(N(C)C(=O)OCC(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)C2CC2)cc1 10.1016/S0960-894X(01)81125-2
44376779 56194 0 None - 0 Rabbit 8.1 pIC50 = 8.1 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aortaIn vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aorta
ChEMBL 496 11 3 6 3.8 CCCCc1ncc(C(=O)O)n1Cc1ccc(-c2ccccc2NS(=O)(=O)NC(=O)C2CC2)cc1 10.1016/S0960-894X(01)81124-0
CHEMBL163485 56194 0 None - 0 Rabbit 8.1 pIC50 = 8.1 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aortaIn vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aorta
ChEMBL 496 11 3 6 3.8 CCCCc1ncc(C(=O)O)n1Cc1ccc(-c2ccccc2NS(=O)(=O)NC(=O)C2CC2)cc1 10.1016/S0960-894X(01)81124-0
44277549 98658 0 None - 0 Rabbit 8.1 pIC50 = 8.1 Binding
Binding affinity against AT1 receptor in rabbit aortaBinding affinity against AT1 receptor in rabbit aorta
ChEMBL 594 8 0 10 5.1 Cn1nnnc1-c1ccccc1-c1ccc(Cn2cnc3ccc(N(Cc4ccccn4)C(=O)c4ccco4)cc3c2=O)cc1 10.1016/0960-894X(95)00224-H
CHEMBL280988 98658 0 None - 0 Rabbit 8.1 pIC50 = 8.1 Binding
Binding affinity against AT1 receptor in rabbit aortaBinding affinity against AT1 receptor in rabbit aorta
ChEMBL 594 8 0 10 5.1 Cn1nnnc1-c1ccccc1-c1ccc(Cn2cnc3ccc(N(Cc4ccccn4)C(=O)c4ccco4)cc3c2=O)cc1 10.1016/0960-894X(95)00224-H
44300637 100445 0 None - 0 Rabbit 8.1 pIC50 = 8.1 Binding
Inhibition of Angiotensin II receptor type 1 in rabbit aorta binding assayInhibition of Angiotensin II receptor type 1 in rabbit aorta binding assay
ChEMBL 600 11 1 7 7.2 CCCCCc1cc(-c2ccc(Cn3c(CC)nc4c(C)cc(C)nc43)cc2)c(S(=O)(=O)NC(=O)c2ccccc2)s1 10.1016/S0960-894X(01)81145-8
CHEMBL293949 100445 0 None - 0 Rabbit 8.1 pIC50 = 8.1 Binding
Inhibition of Angiotensin II receptor type 1 in rabbit aorta binding assayInhibition of Angiotensin II receptor type 1 in rabbit aorta binding assay
ChEMBL 600 11 1 7 7.2 CCCCCc1cc(-c2ccc(Cn3c(CC)nc4c(C)cc(C)nc43)cc2)c(S(=O)(=O)NC(=O)c2ccccc2)s1 10.1016/S0960-894X(01)81145-8
10436523 118945 0 None - 0 Rabbit 8.1 pIC50 = 8.1 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 514 11 2 6 6.2 CCCCc1nnc(SCc2ccc(C)cc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
CHEMBL345139 118945 0 None - 0 Rabbit 8.1 pIC50 = 8.1 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 514 11 2 6 6.2 CCCCc1nnc(SCc2ccc(C)cc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
10436523 118945 0 None - 0 Rabbit 8.1 pIC50 = 8.1 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 514 11 2 6 6.2 CCCCc1nnc(SCc2ccc(C)cc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
CHEMBL345139 118945 0 None - 0 Rabbit 8.1 pIC50 = 8.1 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 514 11 2 6 6.2 CCCCc1nnc(SCc2ccc(C)cc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
44274716 96407 0 None - 0 Rabbit 8.1 pIC50 = 8.1 Binding
Displacement of [125I]Sar1-Ile8-AII (without BSA) from type 1 Angiotensin II receptor of rabbit aortaDisplacement of [125I]Sar1-Ile8-AII (without BSA) from type 1 Angiotensin II receptor of rabbit aorta
ChEMBL 514 8 1 8 4.0 CCCCc1nc2ccc(S(C)(=O)=O)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80335-2
CHEMBL26548 96407 0 None - 0 Rabbit 8.1 pIC50 = 8.1 Binding
Displacement of [125I]Sar1-Ile8-AII (without BSA) from type 1 Angiotensin II receptor of rabbit aortaDisplacement of [125I]Sar1-Ile8-AII (without BSA) from type 1 Angiotensin II receptor of rabbit aorta
ChEMBL 514 8 1 8 4.0 CCCCc1nc2ccc(S(C)(=O)=O)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80335-2
54178446 63423 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation countingDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation counting
ChEMBL 435 4 1 6 5.0 CCc1nc2c(C)cc(C)nc2n1[C@H]1CCc2cc(-c3ccccc3-c3nnn[nH]3)ccc21 10.1021/jm200409s
CHEMBL1801712 63423 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation countingDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation counting
ChEMBL 435 4 1 6 5.0 CCc1nc2c(C)cc(C)nc2n1[C@H]1CCc2cc(-c3ccccc3-c3nnn[nH]3)ccc21 10.1021/jm200409s
44291782 182825 0 None - 0 Rat 8.1 pIC50 = 8.1 Binding
In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.
ChEMBL 456 8 1 5 5.4 CCCCC1=NC(C)(C2CCCC2)C(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81140-9
CHEMBL47985 182825 0 None - 0 Rat 8.1 pIC50 = 8.1 Binding
In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.
ChEMBL 456 8 1 5 5.4 CCCCC1=NC(C)(C2CCCC2)C(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81140-9
14956755 105656 0 None - 0 Rabbit 8.1 pIC50 = 8.1 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 469 8 1 7 4.4 CCCCc1nn(-c2ccccc2F)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
CHEMBL313579 105656 0 None - 0 Rabbit 8.1 pIC50 = 8.1 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 469 8 1 7 4.4 CCCCc1nn(-c2ccccc2F)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
10202093 204699 0 None - 0 Rabbit 8.1 pIC50 = 8.1 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 417 8 1 7 3.9 CCCCc1nn(C(C)C)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
CHEMBL87985 204699 0 None - 0 Rabbit 8.1 pIC50 = 8.1 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 417 8 1 7 3.9 CCCCc1nn(C(C)C)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
11443112 106136 0 None - 0 Rat 8.1 pIC50 = 8.1 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 484 6 1 5 6.6 CCCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2c(C(=O)O)c(Cl)nc3ccccc23)cc1 10.1021/jm031100t
CHEMBL314315 106136 0 None - 0 Rat 8.1 pIC50 = 8.1 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 484 6 1 5 6.6 CCCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2c(C(=O)O)c(Cl)nc3ccccc23)cc1 10.1021/jm031100t
158781 43900 93 None - 0 Bovine 8.1 pIC50 = 8.1 Binding
Displacement of radiolabeled angiotensin 2 from angiotensin AT1 receptor in bovine adrenal cortex membranesDisplacement of radiolabeled angiotensin 2 from angiotensin AT1 receptor in bovine adrenal cortex membranes
ChEMBL 446 8 3 7 3.7 CCCc1nc(C(C)(C)O)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmc.2010.10.043
CHEMBL1516 43900 93 None - 0 Bovine 8.1 pIC50 = 8.1 Binding
Displacement of radiolabeled angiotensin 2 from angiotensin AT1 receptor in bovine adrenal cortex membranesDisplacement of radiolabeled angiotensin 2 from angiotensin AT1 receptor in bovine adrenal cortex membranes
ChEMBL 446 8 3 7 3.7 CCCc1nc(C(C)(C)O)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmc.2010.10.043
10048120 118974 0 None - 0 Rabbit 8.1 pIC50 = 8.1 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 426 7 1 7 4.4 CCCCc1nn2c(C)c(C)nc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
CHEMBL345404 118974 0 None - 0 Rabbit 8.1 pIC50 = 8.1 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 426 7 1 7 4.4 CCCCc1nn2c(C)c(C)nc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
14951059 204693 0 None - 0 Rat 8.1 pIC50 = 8.1 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 493 10 1 8 4.2 CCCCc1nn(CC(=O)c2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a015
CHEMBL87942 204693 0 None - 0 Rat 8.1 pIC50 = 8.1 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 493 10 1 8 4.2 CCCCc1nn(CC(=O)c2ccccc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a015
10346399 47304 0 None - 0 Rabbit 7.2 pIC50 = 7.2 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 514 12 2 6 6.0 CCCCc1nnc(SCCc2ccccc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
CHEMBL154640 47304 0 None - 0 Rabbit 7.2 pIC50 = 7.2 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 514 12 2 6 6.0 CCCCc1nnc(SCCc2ccccc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
11758329 116402 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 603 12 0 8 6.0 CCCCc1ncc(/C=C2/C(=O)N(CCCC(F)(F)F)C(=O)N2Cc2csc(C)n2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
CHEMBL338431 116402 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 603 12 0 8 6.0 CCCCc1ncc(/C=C2/C(=O)N(CCCC(F)(F)F)C(=O)N2Cc2csc(C)n2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
14956776 105475 0 None - 0 Rabbit 7.2 pIC50 = 7.2 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 389 7 1 7 2.8 CCCCc1nn(C)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
CHEMBL313017 105475 0 None - 0 Rabbit 7.2 pIC50 = 7.2 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 389 7 1 7 2.8 CCCCc1nn(C)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
10346399 47304 0 None - 0 Rabbit 7.2 pIC50 = 7.2 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 514 12 2 6 6.0 CCCCc1nnc(SCCc2ccccc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
CHEMBL154640 47304 0 None - 0 Rabbit 7.2 pIC50 = 7.2 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 514 12 2 6 6.0 CCCCc1nnc(SCCc2ccccc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
24828705 157148 0 None - 0 Rat 7.2 pIC50 = 7.2 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
ChEMBL 443 7 1 7 4.0 CCCCn1c(=O)c2cc(F)cnc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm7011563
CHEMBL408188 157148 0 None - 0 Rat 7.2 pIC50 = 7.2 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
ChEMBL 443 7 1 7 4.0 CCCCn1c(=O)c2cc(F)cnc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm7011563
127036108 135842 0 None - 1 Human 7.2 pIC50 = 7.2 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 561 11 2 5 6.8 CCCc1nc2c(C)cc(C(=O)N[C@@H](COC)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2015.09.010
CHEMBL3735098 135842 0 None - 1 Human 7.2 pIC50 = 7.2 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 561 11 2 5 6.8 CCCc1nc2c(C)cc(C(=O)N[C@@H](COC)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2015.09.010
10368898 18694 0 None - 0 Guinea pig 7.2 pIC50 = 7.2 Binding
In vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparationIn vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparation
ChEMBL 469 9 1 6 5.6 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2cc(OCCF)ccc2n1 10.1021/jm00100a007
CHEMBL128389 18694 0 None - 0 Guinea pig 7.2 pIC50 = 7.2 Binding
In vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparationIn vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparation
ChEMBL 469 9 1 6 5.6 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2cc(OCCF)ccc2n1 10.1021/jm00100a007
9932352 16718 0 None - 0 Rat 6.2 pIC50 = 6.2 Binding
Inhibition of [125I]angiotensin II receptor specific binding to rat mesenteric arteriesInhibition of [125I]angiotensin II receptor specific binding to rat mesenteric arteries
ChEMBL 428 9 1 4 6.0 CCCCc1ncc(/C=C(\Cc2ccc(C)s2)C(=O)O)n1Cc1ccccc1Cl 10.1021/jm00099a013
CHEMBL125212 16718 0 None - 0 Rat 6.2 pIC50 = 6.2 Binding
Inhibition of [125I]angiotensin II receptor specific binding to rat mesenteric arteriesInhibition of [125I]angiotensin II receptor specific binding to rat mesenteric arteries
ChEMBL 428 9 1 4 6.0 CCCCc1ncc(/C=C(\Cc2ccc(C)s2)C(=O)O)n1Cc1ccccc1Cl 10.1021/jm00099a013
44341797 110137 0 None - 0 Rat 5.2 pIC50 = 5.2 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 362 4 1 3 4.1 CC1=NC2(CCCC2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00074a018
CHEMBL325751 110137 0 None - 0 Rat 5.2 pIC50 = 5.2 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 362 4 1 3 4.1 CC1=NC2(CCCC2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00074a018
44274706 96291 0 None - 0 Bovine 5.2 pIC50 = 5.2 Binding
Concentration required for 50% inhibition of binding against Angiotensin II receptor, type 1 in bovine adrenal cortexConcentration required for 50% inhibition of binding against Angiotensin II receptor, type 1 in bovine adrenal cortex
ChEMBL 518 8 2 6 5.5 CCCCc1nc2cc(C3=NN(Cc4ccc(-c5ccccc5-c5nn[nH]n5)cc4)C(=O)CC3C)ccc2[nH]1 10.1016/S0960-894X(01)80348-6
CHEMBL26449 96291 0 None - 0 Bovine 5.2 pIC50 = 5.2 Binding
Concentration required for 50% inhibition of binding against Angiotensin II receptor, type 1 in bovine adrenal cortexConcentration required for 50% inhibition of binding against Angiotensin II receptor, type 1 in bovine adrenal cortex
ChEMBL 518 8 2 6 5.5 CCCCc1nc2cc(C3=NN(Cc4ccc(-c5ccccc5-c5nn[nH]n5)cc4)C(=O)CC3C)ccc2[nH]1 10.1016/S0960-894X(01)80348-6
71653750 88707 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Displacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysisDisplacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysis
ChEMBL 671 11 2 7 6.7 CCCCc1c(Br)[n+](Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)cn1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.ejmech.2012.12.044
CHEMBL2337679 88707 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Displacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysisDisplacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysis
ChEMBL 671 11 2 7 6.7 CCCCc1c(Br)[n+](Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)cn1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.ejmech.2012.12.044
CHEMBL2365906 88707 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Displacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysisDisplacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysis
ChEMBL 671 11 2 7 6.7 CCCCc1c(Br)[n+](Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)cn1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.ejmech.2012.12.044
44289028 100700 0 None - 0 Rat 7.2 pIC50 = 7.2 Binding
In vitro inhibition of specific binding of [125I]AII to Angiotensin II receptor, type 1 from rat liver membraneIn vitro inhibition of specific binding of [125I]AII to Angiotensin II receptor, type 1 from rat liver membrane
ChEMBL 418 7 1 3 5.5 CCCCC1=NCC2(CCCC2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/S0960-894X(01)81139-2
CHEMBL295646 100700 0 None - 0 Rat 7.2 pIC50 = 7.2 Binding
In vitro inhibition of specific binding of [125I]AII to Angiotensin II receptor, type 1 from rat liver membraneIn vitro inhibition of specific binding of [125I]AII to Angiotensin II receptor, type 1 from rat liver membrane
ChEMBL 418 7 1 3 5.5 CCCCC1=NCC2(CCCC2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/S0960-894X(01)81139-2
10320063 17943 0 None - 0 Rat 7.1 pIC50 = 7.1 Binding
Activity against high affinity Angiotensin II receptor, type 1 was measured from the ability to inhibit [125I]angiotensin II binding to rat uterine membrane.Activity against high affinity Angiotensin II receptor, type 1 was measured from the ability to inhibit [125I]angiotensin II binding to rat uterine membrane.
ChEMBL 422 10 1 7 4.1 CCCCc1nc(CCCC)n(Cc2ccc(-n3c(F)ccc3-c3nn[nH]n3)cc2)n1 10.1021/jm00053a013
CHEMBL12693 17943 0 None - 0 Rat 7.1 pIC50 = 7.1 Binding
Activity against high affinity Angiotensin II receptor, type 1 was measured from the ability to inhibit [125I]angiotensin II binding to rat uterine membrane.Activity against high affinity Angiotensin II receptor, type 1 was measured from the ability to inhibit [125I]angiotensin II binding to rat uterine membrane.
ChEMBL 422 10 1 7 4.1 CCCCc1nc(CCCC)n(Cc2ccc(-n3c(F)ccc3-c3nn[nH]n3)cc2)n1 10.1021/jm00053a013
76329881 84515 0 None - 0 Rabbit 7.1 pIC50 = 7.1 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 490 11 2 8 4.9 CCCCc1nnc(SCC(C)C)n1Cc1ccc(NC(=O)c2ccccc2-c2nnn[nH]2)cc1 10.1007/s00044-011-9756-4
CHEMBL2237585 84515 0 None - 0 Rabbit 7.1 pIC50 = 7.1 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 490 11 2 8 4.9 CCCCc1nnc(SCC(C)C)n1Cc1ccc(NC(=O)c2ccccc2-c2nnn[nH]2)cc1 10.1007/s00044-011-9756-4
15780085 117634 0 None - 0 Rabbit 7.1 pIC50 = 7.1 Binding
Displacement of [125 I]Sar1Ile8-AII from type 1 Angiotensin II receptor of rabbit aorta membraneDisplacement of [125 I]Sar1Ile8-AII from type 1 Angiotensin II receptor of rabbit aorta membrane
ChEMBL 617 9 1 7 6.7 CCc1nc2ccc(N(Cc3ccccc3)C(=O)c3ccccc3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80517-5
CHEMBL34082 117634 0 None - 0 Rabbit 7.1 pIC50 = 7.1 Binding
Displacement of [125 I]Sar1Ile8-AII from type 1 Angiotensin II receptor of rabbit aorta membraneDisplacement of [125 I]Sar1Ile8-AII from type 1 Angiotensin II receptor of rabbit aorta membrane
ChEMBL 617 9 1 7 6.7 CCc1nc2ccc(N(Cc3ccccc3)C(=O)c3ccccc3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80517-5
9981071 118949 0 None - 0 Rabbit 7.1 pIC50 = 7.1 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 447 10 1 7 5.3 CCCCc1nnc(SCC(C)C)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
CHEMBL345181 118949 0 None - 0 Rabbit 7.1 pIC50 = 7.1 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 447 10 1 7 5.3 CCCCc1nnc(SCC(C)C)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
10345129 48837 0 None - 0 Rabbit 6.1 pIC50 = 6.1 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 481 11 3 7 3.5 CCCCc1nnc(SCC(=O)NC)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
CHEMBL156181 48837 0 None - 0 Rabbit 6.1 pIC50 = 6.1 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 481 11 3 7 3.5 CCCCc1nnc(SCC(=O)NC)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
10345129 48837 0 None - 0 Rabbit 6.1 pIC50 = 6.1 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 481 11 3 7 3.5 CCCCc1nnc(SCC(=O)NC)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
CHEMBL156181 48837 0 None - 0 Rabbit 6.1 pIC50 = 6.1 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 481 11 3 7 3.5 CCCCc1nnc(SCC(=O)NC)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
19792156 189392 0 None - 0 Bovine 5.1 pIC50 = 5.1 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 466 8 1 7 5.1 CCCCc1nc2c(C(=O)OC)cccc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
CHEMBL51712 189392 0 None - 0 Bovine 5.1 pIC50 = 5.1 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 466 8 1 7 5.1 CCCCc1nc2c(C(=O)OC)cccc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
19792156 189392 0 None - 0 Bovine 5.1 pIC50 = 5.1 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 466 8 1 7 5.1 CCCCc1nc2c(C(=O)OC)cccc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
CHEMBL51712 189392 0 None - 0 Bovine 5.1 pIC50 = 5.1 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 466 8 1 7 5.1 CCCCc1nc2c(C(=O)OC)cccc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
71611145 184269 0 None - 0 Human 4.1 pIC50 = 4.1 Binding
Displacement of [125-I]-[Sar1, Ile8] from recombinant human AT1R transfected in human HEK293 cells incubated for 2 hrs by liquid scintillation counter analysisDisplacement of [125-I]-[Sar1, Ile8] from recombinant human AT1R transfected in human HEK293 cells incubated for 2 hrs by liquid scintillation counter analysis
ChEMBL 1072 29 14 13 -0.1 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H](N)CC(=O)O)C(C)C)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O 10.1016/j.bmcl.2021.128086
CHEMBL4852514 184269 0 None - 0 Human 4.1 pIC50 = 4.1 Binding
Displacement of [125-I]-[Sar1, Ile8] from recombinant human AT1R transfected in human HEK293 cells incubated for 2 hrs by liquid scintillation counter analysisDisplacement of [125-I]-[Sar1, Ile8] from recombinant human AT1R transfected in human HEK293 cells incubated for 2 hrs by liquid scintillation counter analysis
ChEMBL 1072 29 14 13 -0.1 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H](N)CC(=O)O)C(C)C)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O 10.1016/j.bmcl.2021.128086
127036866 136732 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptorDisplacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptor
ChEMBL 614 11 3 8 5.7 CCCc1nc2c(C)cc(C(=O)NCc3ccccc3OC)cc2n1Cc1ccc(-c2ccccc2C(=O)Nc2nnn[nH]2)cc1 10.1039/C5MD00169B
CHEMBL3752117 136732 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptorDisplacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptor
ChEMBL 614 11 3 8 5.7 CCCc1nc2c(C)cc(C(=O)NCc3ccccc3OC)cc2n1Cc1ccc(-c2ccccc2C(=O)Nc2nnn[nH]2)cc1 10.1039/C5MD00169B
127028930 136767 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptorDisplacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptor
ChEMBL 570 9 3 7 6.0 CCCc1nc2c(C)cc(C(=O)Nc3ccccc3)cc2n1Cc1ccc(-c2ccccc2C(=O)Nc2nnn[nH]2)cc1 10.1039/C5MD00169B
CHEMBL3752444 136767 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptorDisplacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptor
ChEMBL 570 9 3 7 6.0 CCCc1nc2c(C)cc(C(=O)Nc3ccccc3)cc2n1Cc1ccc(-c2ccccc2C(=O)Nc2nnn[nH]2)cc1 10.1039/C5MD00169B
44341488 9372 0 None - 0 Rat 6.1 pIC50 = 6.1 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 532 10 2 5 4.7 CCCCC1=NC2(CCN(C(=O)C(N)C(C)CC)CC2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00074a018
CHEMBL111968 9372 0 None - 0 Rat 6.1 pIC50 = 6.1 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 532 10 2 5 4.7 CCCCC1=NC2(CCN(C(=O)C(N)C(C)CC)CC2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00074a018
10455288 16660 0 None - 0 Rat 6.1 pIC50 = 6.1 Binding
Inhibition of [125I]angiotensin II receptor specific binding to rat mesenteric arteriesInhibition of [125I]angiotensin II receptor specific binding to rat mesenteric arteries
ChEMBL 428 9 1 4 6.0 CCCCc1ncc(/C=C(\Cc2sccc2C)C(=O)O)n1Cc1ccccc1Cl 10.1021/jm00099a013
CHEMBL124859 16660 0 None - 0 Rat 6.1 pIC50 = 6.1 Binding
Inhibition of [125I]angiotensin II receptor specific binding to rat mesenteric arteriesInhibition of [125I]angiotensin II receptor specific binding to rat mesenteric arteries
ChEMBL 428 9 1 4 6.0 CCCCc1ncc(/C=C(\Cc2sccc2C)C(=O)O)n1Cc1ccccc1Cl 10.1021/jm00099a013
127034904 135927 0 None - 0 Human 6.1 pIC50 = 6.1 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 561 10 2 4 7.8 CCCc1nc2c(C)cc(C(=S)NC[C@@H](C)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2015.09.010
CHEMBL3735831 135927 0 None - 0 Human 6.1 pIC50 = 6.1 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 561 10 2 4 7.8 CCCc1nc2c(C)cc(C(=S)NC[C@@H](C)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2015.09.010
11155548 204682 0 None - 0 Rat 7.1 pIC50 = 7.1 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 466 6 1 6 5.6 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2c(C(=O)O)c(OC)nc3ccccc23)cc1 10.1021/jm031100t
CHEMBL87884 204682 0 None - 0 Rat 7.1 pIC50 = 7.1 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 466 6 1 6 5.6 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2c(C(=O)O)c(OC)nc3ccccc23)cc1 10.1021/jm031100t
15069406 101265 0 None - 0 Bovine 6.1 pIC50 = 6.1 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 466 8 1 7 5.1 CCCCc1nc2cc(C(=O)OC)ccc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
CHEMBL299753 101265 0 None - 0 Bovine 6.1 pIC50 = 6.1 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 466 8 1 7 5.1 CCCCc1nc2cc(C(=O)OC)ccc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
15069406 101265 0 None - 0 Bovine 6.1 pIC50 = 6.1 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 466 8 1 7 5.1 CCCCc1nc2cc(C(=O)OC)ccc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
CHEMBL299753 101265 0 None - 0 Bovine 6.1 pIC50 = 6.1 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 466 8 1 7 5.1 CCCCc1nc2cc(C(=O)OC)ccc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
53309405 63434 0 None - 0 Human 6.1 pIC50 = 6.1 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation countingDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation counting
ChEMBL 477 6 1 6 5.9 CCc1nc2c(CC(C)C)cc(C)nc2n1[C@H]1CCc2cc(-c3ccccc3-c3nnn[nH]3)ccc21 10.1021/jm200409s
CHEMBL1801742 63434 0 None - 0 Human 6.1 pIC50 = 6.1 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation countingDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation counting
ChEMBL 477 6 1 6 5.9 CCc1nc2c(CC(C)C)cc(C)nc2n1[C@H]1CCc2cc(-c3ccccc3-c3nnn[nH]3)ccc21 10.1021/jm200409s
10323718 119009 0 None - 0 Rabbit 7.1 pIC50 = 7.1 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 500 11 2 6 5.6 CCCSc1nnc(CCc2ccccc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
CHEMBL345696 119009 0 None - 0 Rabbit 7.1 pIC50 = 7.1 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 500 11 2 6 5.6 CCCSc1nnc(CCc2ccccc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
10323718 119009 0 None - 0 Rabbit 7.1 pIC50 = 7.1 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 500 11 2 6 5.6 CCCSc1nnc(CCc2ccccc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
CHEMBL345696 119009 0 None - 0 Rabbit 7.1 pIC50 = 7.1 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 500 11 2 6 5.6 CCCSc1nnc(CCc2ccccc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
127035380 135990 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysisDisplacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysis
ChEMBL 691 13 2 8 7.4 CCCc1nc2c(C)cc(C(=O)NCCc3ccc(OC)cc3)cc2n1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)cc1 10.1039/C4MD00499J
CHEMBL3736414 135990 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysisDisplacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysis
ChEMBL 691 13 2 8 7.4 CCCc1nc2c(C)cc(C(=O)NCCc3ccc(OC)cc3)cc2n1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)cc1 10.1039/C4MD00499J
24827904 95976 0 None - 0 Rat 7.1 pIC50 = 7.1 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
ChEMBL 459 7 1 7 4.5 CCCCn1c(=O)c2cc(Cl)cnc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm7011563
CHEMBL262098 95976 0 None - 0 Rat 7.1 pIC50 = 7.1 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
ChEMBL 459 7 1 7 4.5 CCCCn1c(=O)c2cc(Cl)cnc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm7011563
44297202 101267 0 None - 0 Bovine 7.1 pIC50 = 7.1 Binding
In vitro binding affinity to angiotensin II receptor in bovine adrenal cortexIn vitro binding affinity to angiotensin II receptor in bovine adrenal cortex
ChEMBL 623 9 1 9 6.5 CCCCc1nc2ccc([C@@H]3C[C@H]4C(c5ccccc5)=NO[C@H]4O3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80377-2
CHEMBL299770 101267 0 None - 0 Bovine 7.1 pIC50 = 7.1 Binding
In vitro binding affinity to angiotensin II receptor in bovine adrenal cortexIn vitro binding affinity to angiotensin II receptor in bovine adrenal cortex
ChEMBL 623 9 1 9 6.5 CCCCc1nc2ccc([C@@H]3C[C@H]4C(c5ccccc5)=NO[C@H]4O3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80377-2
44292497 14596 0 None - 0 Bovine 7.1 pIC50 = 7.1 Binding
Binding affinity expressed as inhibitory concentration towards bovine adrenal cortex angiotensin II receptor was measuredBinding affinity expressed as inhibitory concentration towards bovine adrenal cortex angiotensin II receptor was measured
ChEMBL 561 8 1 8 5.6 CCCCc1nc2ccc([C@@]3(C)C[C@@H]4CCCN4O3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/S0960-894X(00)80366-2
CHEMBL1206677 14596 0 None - 0 Bovine 7.1 pIC50 = 7.1 Binding
Binding affinity expressed as inhibitory concentration towards bovine adrenal cortex angiotensin II receptor was measuredBinding affinity expressed as inhibitory concentration towards bovine adrenal cortex angiotensin II receptor was measured
ChEMBL 561 8 1 8 5.6 CCCCc1nc2ccc([C@@]3(C)C[C@@H]4CCCN4O3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/S0960-894X(00)80366-2
CHEMBL295174 14596 0 None - 0 Bovine 7.1 pIC50 = 7.1 Binding
Binding affinity expressed as inhibitory concentration towards bovine adrenal cortex angiotensin II receptor was measuredBinding affinity expressed as inhibitory concentration towards bovine adrenal cortex angiotensin II receptor was measured
ChEMBL 561 8 1 8 5.6 CCCCc1nc2ccc([C@@]3(C)C[C@@H]4CCCN4O3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/S0960-894X(00)80366-2
44287133 137071 0 None - 0 Rabbit 7.1 pIC50 = 7.1 Binding
Tested in vitro for Angiotensin II receptor, type 1 binding affinity using rabbit aorta binding assayTested in vitro for Angiotensin II receptor, type 1 binding affinity using rabbit aorta binding assay
ChEMBL 439 8 1 7 4.4 CCCc1nc2c(C)ccnc2n1Cc1ccc(OC(c2ccccc2)c2nnn[nH]2)cc1 10.1016/0960-894X(94)00476-V
CHEMBL37565 137071 0 None - 0 Rabbit 7.1 pIC50 = 7.1 Binding
Tested in vitro for Angiotensin II receptor, type 1 binding affinity using rabbit aorta binding assayTested in vitro for Angiotensin II receptor, type 1 binding affinity using rabbit aorta binding assay
ChEMBL 439 8 1 7 4.4 CCCc1nc2c(C)ccnc2n1Cc1ccc(OC(c2ccccc2)c2nnn[nH]2)cc1 10.1016/0960-894X(94)00476-V
10457332 51131 0 None - 0 Rabbit 6.1 pIC50 = 6.1 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 468 11 3 7 3.8 CCCCc1nnc(SCC(=O)O)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
CHEMBL158196 51131 0 None - 0 Rabbit 6.1 pIC50 = 6.1 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 468 11 3 7 3.8 CCCCc1nnc(SCC(=O)O)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
10457332 51131 0 None - 0 Rabbit 6.1 pIC50 = 6.1 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 468 11 3 7 3.8 CCCCc1nnc(SCC(=O)O)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
CHEMBL158196 51131 0 None - 0 Rabbit 6.1 pIC50 = 6.1 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 468 11 3 7 3.8 CCCCc1nnc(SCC(=O)O)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
46910581 75966 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]Sar1Ile8-Ang2 from angiotensin AT1 receptor after 180 mins by gamma countingDisplacement of [125I]Sar1Ile8-Ang2 from angiotensin AT1 receptor after 180 mins by gamma counting
ChEMBL 615 12 2 8 6.2 CCCc1nc2c(C)cc(C(=O)NCCc3cc(OC)ccc3OC)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmc.2012.05.056
CHEMBL2058863 75966 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]Sar1Ile8-Ang2 from angiotensin AT1 receptor after 180 mins by gamma countingDisplacement of [125I]Sar1Ile8-Ang2 from angiotensin AT1 receptor after 180 mins by gamma counting
ChEMBL 615 12 2 8 6.2 CCCc1nc2c(C)cc(C(=O)NCCc3cc(OC)ccc3OC)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmc.2012.05.056
10416836 107405 0 None - 0 Rabbit 7.1 pIC50 = 7.1 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 651 11 1 8 6.8 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2ccc([N+](=O)[O-])cc2)cc1 10.1021/jm00043a020
CHEMBL319313 107405 0 None - 0 Rabbit 7.1 pIC50 = 7.1 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 651 11 1 8 6.8 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2ccc([N+](=O)[O-])cc2)cc1 10.1021/jm00043a020
70690562 75959 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]Sar1Ile8-Ang2 from angiotensin AT1 receptor after 180 mins by gamma countingDisplacement of [125I]Sar1Ile8-Ang2 from angiotensin AT1 receptor after 180 mins by gamma counting
ChEMBL 571 10 2 7 6.1 CCCc1nc2c(C)cc(C(=O)NCc3cccc(OC)c3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmc.2012.05.056
CHEMBL2058856 75959 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]Sar1Ile8-Ang2 from angiotensin AT1 receptor after 180 mins by gamma countingDisplacement of [125I]Sar1Ile8-Ang2 from angiotensin AT1 receptor after 180 mins by gamma counting
ChEMBL 571 10 2 7 6.1 CCCc1nc2c(C)cc(C(=O)NCc3cccc(OC)c3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmc.2012.05.056
76319036 84542 0 None - 0 Rabbit 6.1 pIC50 = 6.1 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 537 12 3 9 4.7 CCCCc1nnc(NCc2ccc(OC)cc2)n1Cc1ccc(NC(=O)c2ccccc2-c2nnn[nH]2)cc1 10.1007/s00044-011-9756-4
CHEMBL2237612 84542 0 None - 0 Rabbit 6.1 pIC50 = 6.1 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 537 12 3 9 4.7 CCCCc1nnc(NCc2ccc(OC)cc2)n1Cc1ccc(NC(=O)c2ccccc2-c2nnn[nH]2)cc1 10.1007/s00044-011-9756-4
44307107 98229 0 None - 0 Rabbit 6.1 pIC50 = 6.1 Binding
Binding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membraneBinding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane
ChEMBL 417 4 1 6 3.9 CCc1nc2c(C)cc(C)nc2n1Cc1cc(Br)c(O)c(C(=O)OC)c1 10.1016/S0960-894X(01)81148-3
CHEMBL277614 98229 0 None - 0 Rabbit 6.1 pIC50 = 6.1 Binding
Binding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membraneBinding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane
ChEMBL 417 4 1 6 3.9 CCc1nc2c(C)cc(C)nc2n1Cc1cc(Br)c(O)c(C(=O)OC)c1 10.1016/S0960-894X(01)81148-3
10435850 48332 0 None - 0 Rabbit 6.1 pIC50 = 6.1 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 494 11 2 8 5.1 CCCCc1nnc(NCc2ccc(OC)cc2)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
CHEMBL155724 48332 0 None - 0 Rabbit 6.1 pIC50 = 6.1 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 494 11 2 8 5.1 CCCCc1nnc(NCc2ccc(OC)cc2)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
127035391 135875 0 None - 0 Human 6.1 pIC50 = 6.1 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 563 10 2 5 7.4 CCSc1nc2c(C)cc(C(=O)NC[C@@H](C)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2015.09.010
CHEMBL3735390 135875 0 None - 0 Human 6.1 pIC50 = 6.1 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 563 10 2 5 7.4 CCSc1nc2c(C)cc(C(=O)NC[C@@H](C)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2015.09.010
14956774 204505 0 None - 0 Rabbit 7.1 pIC50 = 7.1 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 452 8 1 8 3.7 CCCCc1nn(-c2ccccn2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
CHEMBL86741 204505 0 None - 0 Rabbit 7.1 pIC50 = 7.1 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 452 8 1 8 3.7 CCCCc1nn(-c2ccccn2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
15780095 98130 0 None - 0 Rabbit 7.1 pIC50 = 7.1 Binding
Displacement of [125 I]Sar1Ile8-AII from type 1 Angiotensin II receptor of rabbit aorta membraneDisplacement of [125 I]Sar1Ile8-AII from type 1 Angiotensin II receptor of rabbit aorta membrane
ChEMBL 595 9 1 7 6.5 CCc1nc2ccc(N(CC=C(C)C)C(=O)c3ccccc3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80517-5
CHEMBL276853 98130 0 None - 0 Rabbit 7.1 pIC50 = 7.1 Binding
Displacement of [125 I]Sar1Ile8-AII from type 1 Angiotensin II receptor of rabbit aorta membraneDisplacement of [125 I]Sar1Ile8-AII from type 1 Angiotensin II receptor of rabbit aorta membrane
ChEMBL 595 9 1 7 6.5 CCc1nc2ccc(N(CC=C(C)C)C(=O)c3ccccc3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80517-5
44297217 101085 0 None - 0 Bovine 7.1 pIC50 = 7.1 Binding
In vitro binding affinity to angiotensin II receptor in bovine adrenal cortexIn vitro binding affinity to angiotensin II receptor in bovine adrenal cortex
ChEMBL 651 10 1 9 6.5 CCCCc1nc2ccc([C@H]3[C@@H]4C(=O)CC[C@@H]4ON3Cc3ccccc3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80377-2
CHEMBL298509 101085 0 None - 0 Bovine 7.1 pIC50 = 7.1 Binding
In vitro binding affinity to angiotensin II receptor in bovine adrenal cortexIn vitro binding affinity to angiotensin II receptor in bovine adrenal cortex
ChEMBL 651 10 1 9 6.5 CCCCc1nc2ccc([C@H]3[C@@H]4C(=O)CC[C@@H]4ON3Cc3ccccc3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80377-2
135723817 100289 0 None - 0 Bovine 6.1 pIC50 = 6.1 Binding
Displacement of [125 I]-AII (0.2 nM) from bovine adrenal cortical membrane angiotensin II (AII) receptor at 10e-7 MDisplacement of [125 I]-AII (0.2 nM) from bovine adrenal cortical membrane angiotensin II (AII) receptor at 10e-7 M
ChEMBL 470 8 2 8 5.0 CCCOc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2noc(O)n2)cc1 10.1016/0960-894X(95)00319-O
CHEMBL292914 100289 0 None - 0 Bovine 6.1 pIC50 = 6.1 Binding
Displacement of [125 I]-AII (0.2 nM) from bovine adrenal cortical membrane angiotensin II (AII) receptor at 10e-7 MDisplacement of [125 I]-AII (0.2 nM) from bovine adrenal cortical membrane angiotensin II (AII) receptor at 10e-7 M
ChEMBL 470 8 2 8 5.0 CCCOc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2noc(O)n2)cc1 10.1016/0960-894X(95)00319-O
44274692 95986 0 None - 0 Rabbit 8.1 pIC50 = 8.1 Binding
Ability to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitroAbility to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitro
ChEMBL 541 10 2 7 6.2 CCCCc1nc2ccc(NCc3ccccc3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80335-2
CHEMBL26217 95986 0 None - 0 Rabbit 8.1 pIC50 = 8.1 Binding
Ability to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitroAbility to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitro
ChEMBL 541 10 2 7 6.2 CCCCc1nc2ccc(NCc3ccccc3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80335-2
10324870 112801 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 535 12 0 8 5.1 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2Cc2cscn2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
CHEMBL331546 112801 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 535 12 0 8 5.1 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2Cc2cscn2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
11758341 116767 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 603 13 1 7 6.5 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2Cc2csc(C)n2)n1Cc1ccc(C2(C(=O)O)CCCC2)cc1 10.1007/s00044-009-9205-9
CHEMBL339544 116767 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 603 13 1 7 6.5 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2Cc2csc(C)n2)n1Cc1ccc(C2(C(=O)O)CCCC2)cc1 10.1007/s00044-009-9205-9
44306652 201642 0 None - 0 Rabbit 8.1 pIC50 = 8.1 Binding
Binding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membraneBinding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane
ChEMBL 437 3 1 4 4.9 CCc1nc2c(C)cc(C)nc2n1Cc1cc(Br)c(O)c(Br)c1 10.1016/S0960-894X(01)81148-3
CHEMBL64983 201642 0 None - 0 Rabbit 8.1 pIC50 = 8.1 Binding
Binding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membraneBinding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane
ChEMBL 437 3 1 4 4.9 CCc1nc2c(C)cc(C)nc2n1Cc1cc(Br)c(O)c(Br)c1 10.1016/S0960-894X(01)81148-3
44311584 102294 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 695 16 1 8 8.1 CCCCN(Cc1ccccc1)C(=O)c1ccc(COC(=O)c2c(CC)nc(CCC)n2Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)cc1 10.1016/S0960-894X(00)80077-3
CHEMBL305239 102294 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 695 16 1 8 8.1 CCCCN(Cc1ccccc1)C(=O)c1ccc(COC(=O)c2c(CC)nc(CCC)n2Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)cc1 10.1016/S0960-894X(00)80077-3
19771800 204645 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
Compound was tested for in vitro inhibition of specific binding of [I-125]AII to AT1 receptor in guinea pig adrenal membrane preparationCompound was tested for in vitro inhibition of specific binding of [I-125]AII to AT1 receptor in guinea pig adrenal membrane preparation
ChEMBL 441 7 1 6 5.0 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)c(OC)c2)c2c(n1)CCCC2 10.1016/S0960-894X(01)80295-X
CHEMBL87603 204645 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
Compound was tested for in vitro inhibition of specific binding of [I-125]AII to AT1 receptor in guinea pig adrenal membrane preparationCompound was tested for in vitro inhibition of specific binding of [I-125]AII to AT1 receptor in guinea pig adrenal membrane preparation
ChEMBL 441 7 1 6 5.0 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)c(OC)c2)c2c(n1)CCCC2 10.1016/S0960-894X(01)80295-X
20747575 97959 0 None - 1 Human 8.1 pIC50 = 8.1 Binding
Displacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysisDisplacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysis
ChEMBL 579 12 2 8 5.0 CCCc1nc(CC)c(C(=O)NC)n1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)c(COC)c1 10.1039/C4MD00499J
CHEMBL275545 97959 0 None - 1 Human 8.1 pIC50 = 8.1 Binding
Displacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysisDisplacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysis
ChEMBL 579 12 2 8 5.0 CCCc1nc(CC)c(C(=O)NC)n1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)c(COC)c1 10.1039/C4MD00499J
127035085 135896 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Displacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysisDisplacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysis
ChEMBL 661 12 2 7 7.4 CCCc1nc2c(C)cc(C(=O)NCCc3ccccc3)cc2n1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)cc1 10.1039/C4MD00499J
CHEMBL3735574 135896 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Displacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysisDisplacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysis
ChEMBL 661 12 2 7 7.4 CCCc1nc2c(C)cc(C(=O)NCCc3ccccc3)cc2n1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)cc1 10.1039/C4MD00499J
44285327 168025 0 None - 0 Rat 8.1 pIC50 = 8.1 Binding
Displacement of [125I]- Ang II from type 1 Angiotensin II receptorDisplacement of [125I]- Ang II from type 1 Angiotensin II receptor
ChEMBL 430 6 1 6 3.6 CCCC1=NC2(CCOCC2)C(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80526-6
CHEMBL435953 168025 0 None - 0 Rat 8.1 pIC50 = 8.1 Binding
Displacement of [125I]- Ang II from type 1 Angiotensin II receptorDisplacement of [125I]- Ang II from type 1 Angiotensin II receptor
ChEMBL 430 6 1 6 3.6 CCCC1=NC2(CCOCC2)C(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80526-6
44311496 202533 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
In vitro binding affinity of compound against Angiotensin II receptor, type 1In vitro binding affinity of compound against Angiotensin II receptor, type 1
ChEMBL 722 15 2 8 7.2 CCCc1nc(CN(Cc2ccccc2)C(=O)c2ccccc2)c(C(=O)O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCC(C)C)cc1 10.1016/S0960-894X(00)80076-1
CHEMBL71069 202533 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
In vitro binding affinity of compound against Angiotensin II receptor, type 1In vitro binding affinity of compound against Angiotensin II receptor, type 1
ChEMBL 722 15 2 8 7.2 CCCc1nc(CN(Cc2ccccc2)C(=O)c2ccccc2)c(C(=O)O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCC(C)C)cc1 10.1016/S0960-894X(00)80076-1
44379350 120259 0 None - 0 Rabbit 8.1 pIC50 = 8.1 Binding
In vitro displacement of 125I-[Sar1, Ile8] from AT1 receptors in rabbit aorta membraneIn vitro displacement of 125I-[Sar1, Ile8] from AT1 receptors in rabbit aorta membrane
ChEMBL 599 10 1 7 6.8 CCCCc1nc2ccc(C(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2cccs2)cc1 10.1016/S0960-894X(01)81125-2
CHEMBL355443 120259 0 None - 0 Rabbit 8.1 pIC50 = 8.1 Binding
In vitro displacement of 125I-[Sar1, Ile8] from AT1 receptors in rabbit aorta membraneIn vitro displacement of 125I-[Sar1, Ile8] from AT1 receptors in rabbit aorta membrane
ChEMBL 599 10 1 7 6.8 CCCCc1nc2ccc(C(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2cccs2)cc1 10.1016/S0960-894X(01)81125-2
9843950 100092 0 None - 0 Rabbit 8.1 pIC50 = 8.1 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aortaIn vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aorta
ChEMBL 400 8 1 6 4.1 CCCc1nc(CC)c(C=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81124-0
CHEMBL291582 100092 0 None - 0 Rabbit 8.1 pIC50 = 8.1 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aortaIn vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aorta
ChEMBL 400 8 1 6 4.1 CCCc1nc(CC)c(C=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81124-0
14950510 85254 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1
ChEMBL 413 7 1 6 4.6 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c(C(C)=O)c(C)n1 10.1021/jm00061a016
CHEMBL22879 85254 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1
ChEMBL 413 7 1 6 4.6 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c(C(C)=O)c(C)n1 10.1021/jm00061a016
15171369 98994 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1
ChEMBL 397 6 1 5 4.6 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2c(n1)CCC2 10.1021/jm00061a016
CHEMBL283110 98994 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1
ChEMBL 397 6 1 5 4.6 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2c(n1)CCC2 10.1021/jm00061a016
10345638 20297 0 None - 0 Rat 8.1 pIC50 = 8.1 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 494 8 2 6 5.4 CCCCc1nc2ccc(NC(=O)N(C)C)cc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00077a007
CHEMBL130746 20297 0 None - 0 Rat 8.1 pIC50 = 8.1 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 494 8 2 6 5.4 CCCCc1nc2ccc(NC(=O)N(C)C)cc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00077a007
1610 2305 89 None 1 4 Human 8.1 pIC50 = 8.1 Binding
Tested for inhibition of Angiotensin II receptor, type 1 in the absence of bovine serum albumin (BSA)Tested for inhibition of Angiotensin II receptor, type 1 in the absence of bovine serum albumin (BSA)
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(01)81117-3
3941 2305 89 None 1 4 Human 8.1 pIC50 = 8.1 Binding
Tested for inhibition of Angiotensin II receptor, type 1 in the absence of bovine serum albumin (BSA)Tested for inhibition of Angiotensin II receptor, type 1 in the absence of bovine serum albumin (BSA)
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(01)81117-3
3961 2305 89 None 1 4 Human 8.1 pIC50 = 8.1 Binding
Tested for inhibition of Angiotensin II receptor, type 1 in the absence of bovine serum albumin (BSA)Tested for inhibition of Angiotensin II receptor, type 1 in the absence of bovine serum albumin (BSA)
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(01)81117-3
590 2305 89 None 1 4 Human 8.1 pIC50 = 8.1 Binding
Tested for inhibition of Angiotensin II receptor, type 1 in the absence of bovine serum albumin (BSA)Tested for inhibition of Angiotensin II receptor, type 1 in the absence of bovine serum albumin (BSA)
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(01)81117-3
CHEMBL191 2305 89 None 1 4 Human 8.1 pIC50 = 8.1 Binding
Tested for inhibition of Angiotensin II receptor, type 1 in the absence of bovine serum albumin (BSA)Tested for inhibition of Angiotensin II receptor, type 1 in the absence of bovine serum albumin (BSA)
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(01)81117-3
DB00678 2305 89 None 1 4 Human 8.1 pIC50 = 8.1 Binding
Tested for inhibition of Angiotensin II receptor, type 1 in the absence of bovine serum albumin (BSA)Tested for inhibition of Angiotensin II receptor, type 1 in the absence of bovine serum albumin (BSA)
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(01)81117-3
19385601 51624 0 None - 0 Rabbit 8.1 pIC50 = 8.1 Binding
Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)
ChEMBL 491 9 1 5 6.5 CCCc1cc(Cn2c(CC)nc3c(C)cc(C)nc32)ccc1OC(C(=O)O)c1ccccc1Cl 10.1016/0960-894X(95)00185-V
CHEMBL15860 51624 0 None - 0 Rabbit 8.1 pIC50 = 8.1 Binding
Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)
ChEMBL 491 9 1 5 6.5 CCCc1cc(Cn2c(CC)nc3c(C)cc(C)nc32)ccc1OC(C(=O)O)c1ccccc1Cl 10.1016/0960-894X(95)00185-V
158781 43900 93 None - 0 Bovine 8.1 pIC50 = 8.1 Binding
Binding affinity to angiotensin AT1 receptor in bovine adrenal cortex membranesBinding affinity to angiotensin AT1 receptor in bovine adrenal cortex membranes
ChEMBL 446 8 3 7 3.7 CCCc1nc(C(C)(C)O)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmc.2010.10.043
CHEMBL1516 43900 93 None - 0 Bovine 8.1 pIC50 = 8.1 Binding
Binding affinity to angiotensin AT1 receptor in bovine adrenal cortex membranesBinding affinity to angiotensin AT1 receptor in bovine adrenal cortex membranes
ChEMBL 446 8 3 7 3.7 CCCc1nc(C(C)(C)O)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmc.2010.10.043
158781 43900 93 None - 0 Bovine 8.1 pIC50 = 8.1 Binding
In vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortexIn vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortex
ChEMBL 446 8 3 7 3.7 CCCc1nc(C(C)(C)O)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1021/jm950450f
CHEMBL1516 43900 93 None - 0 Bovine 8.1 pIC50 = 8.1 Binding
In vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortexIn vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortex
ChEMBL 446 8 3 7 3.7 CCCc1nc(C(C)(C)O)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1021/jm950450f
9874508 202964 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membrane
ChEMBL 663 11 2 8 5.9 CCc1nc2ccc(NC(=O)N(C)C(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC2CC2)cc1F 10.1016/0960-894X(94)85036-4
CHEMBL73876 202964 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membrane
ChEMBL 663 11 2 8 5.9 CCc1nc2ccc(NC(=O)N(C)C(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC2CC2)cc1F 10.1016/0960-894X(94)85036-4
10223724 204033 0 None - 0 Rabbit 8.1 pIC50 = 8.1 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 417 9 1 7 3.7 CCCCc1nn(CCC)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
CHEMBL82797 204033 0 None - 0 Rabbit 8.1 pIC50 = 8.1 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 417 9 1 7 3.7 CCCCc1nn(CCC)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
53309271 63427 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation countingDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation counting
ChEMBL 447 4 1 6 5.3 Cc1cc(C)c2nc(C3CC3)n([C@H]3CCc4cc(-c5ccccc5-c5nnn[nH]5)ccc43)c2n1 10.1021/jm200409s
CHEMBL1801735 63427 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation countingDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation counting
ChEMBL 447 4 1 6 5.3 Cc1cc(C)c2nc(C3CC3)n([C@H]3CCc4cc(-c5ccccc5-c5nnn[nH]5)ccc43)c2n1 10.1021/jm200409s
1610 2305 89 None -1 4 Rat 8.1 pIC50 = 8.1 Binding
Tested for binding affinity against angiotensin II receptor in rat adrenal cortexTested for binding affinity against angiotensin II receptor in rat adrenal cortex
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/0960-894X(95)00370-9
3941 2305 89 None -1 4 Rat 8.1 pIC50 = 8.1 Binding
Tested for binding affinity against angiotensin II receptor in rat adrenal cortexTested for binding affinity against angiotensin II receptor in rat adrenal cortex
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/0960-894X(95)00370-9
3961 2305 89 None -1 4 Rat 8.1 pIC50 = 8.1 Binding
Tested for binding affinity against angiotensin II receptor in rat adrenal cortexTested for binding affinity against angiotensin II receptor in rat adrenal cortex
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/0960-894X(95)00370-9
590 2305 89 None -1 4 Rat 8.1 pIC50 = 8.1 Binding
Tested for binding affinity against angiotensin II receptor in rat adrenal cortexTested for binding affinity against angiotensin II receptor in rat adrenal cortex
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/0960-894X(95)00370-9
CHEMBL191 2305 89 None -1 4 Rat 8.1 pIC50 = 8.1 Binding
Tested for binding affinity against angiotensin II receptor in rat adrenal cortexTested for binding affinity against angiotensin II receptor in rat adrenal cortex
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/0960-894X(95)00370-9
DB00678 2305 89 None -1 4 Rat 8.1 pIC50 = 8.1 Binding
Tested for binding affinity against angiotensin II receptor in rat adrenal cortexTested for binding affinity against angiotensin II receptor in rat adrenal cortex
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/0960-894X(95)00370-9
10414273 114036 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 518 12 0 7 5.3 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2Cc2ccoc2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
CHEMBL333722 114036 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 518 12 0 7 5.3 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2Cc2ccoc2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
44277872 96105 0 None - 0 Rabbit 8.1 pIC50 = 8.1 Binding
Binding affinity against AT1 receptor in rabbit aortaBinding affinity against AT1 receptor in rabbit aorta
ChEMBL 689 13 0 9 7.7 CCCCCN(C(=O)c1ccc(OCc2ccccc2)cc1)c1ccc2ncn(Cc3ccc(-c4ccccc4-c4nnnn4C)cc3)c(=O)c2c1 10.1016/0960-894X(95)00224-H
CHEMBL263038 96105 0 None - 0 Rabbit 8.1 pIC50 = 8.1 Binding
Binding affinity against AT1 receptor in rabbit aortaBinding affinity against AT1 receptor in rabbit aorta
ChEMBL 689 13 0 9 7.7 CCCCCN(C(=O)c1ccc(OCc2ccccc2)cc1)c1ccc2ncn(Cc3ccc(-c4ccccc4-c4nnnn4C)cc3)c(=O)c2c1 10.1016/0960-894X(95)00224-H
10256564 16075 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 533 12 0 8 5.0 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2Cc2cc(C)on2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
CHEMBL122458 16075 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 533 12 0 8 5.0 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2Cc2cc(C)on2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
10391038 116419 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 494 13 0 6 5.3 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2CCCC)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
CHEMBL338514 116419 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 494 13 0 6 5.3 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2CCCC)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
70694737 75850 0 None - 0 Bovine 8.1 pIC50 = 8.1 Binding
Displacement of [125I]AngII from type 1 angiotensin 2 receptor in bovine adrenal cortexDisplacement of [125I]AngII from type 1 angiotensin 2 receptor in bovine adrenal cortex
ChEMBL 544 10 1 7 6.5 CCCCc1nc2ccc(OC)cc2n1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)cc1 10.1016/j.bmc.2012.06.011
CHEMBL2058372 75850 0 None - 0 Bovine 8.1 pIC50 = 8.1 Binding
Displacement of [125I]AngII from type 1 angiotensin 2 receptor in bovine adrenal cortexDisplacement of [125I]AngII from type 1 angiotensin 2 receptor in bovine adrenal cortex
ChEMBL 544 10 1 7 6.5 CCCCc1nc2ccc(OC)cc2n1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)cc1 10.1016/j.bmc.2012.06.011
44342046 110046 0 None - 0 Rat 8.1 pIC50 = 8.1 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 432 7 1 3 6.1 CCCCC1=NC2(CCCCCC2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00074a018
CHEMBL325201 110046 0 None - 0 Rat 8.1 pIC50 = 8.1 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 432 7 1 3 6.1 CCCCC1=NC2(CCCCCC2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00074a018
10226439 202169 0 None - 0 Rat 8.1 pIC50 = 8.1 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 459 12 1 7 4.9 CCCCCCn1nc(CCCC)n(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c1=O 10.1021/jm00067a015
CHEMBL68760 202169 0 None - 0 Rat 8.1 pIC50 = 8.1 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 459 12 1 7 4.9 CCCCCCn1nc(CCCC)n(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c1=O 10.1021/jm00067a015
44376822 119535 0 None - 0 Rabbit 8.1 pIC50 = 8.1 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aortaIn vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aorta
ChEMBL 565 10 1 7 5.5 CCCCc1nc(Cl)c(C(=O)OC)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/S0960-894X(01)81124-0
CHEMBL350493 119535 0 None - 0 Rabbit 8.1 pIC50 = 8.1 Binding
In vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aortaIn vitro inhibitory activity against Angiotensin II receptor, type 1 to displace 125I-Sar,Ile8-AII in rabbit aorta
ChEMBL 565 10 1 7 5.5 CCCCc1nc(Cl)c(C(=O)OC)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/S0960-894X(01)81124-0
10439858 16667 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 719 11 2 9 6.2 CCCCNC(=O)c1ccc(C(F)(F)F)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1021/jm00019a004
CHEMBL124903 16667 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 719 11 2 9 6.2 CCCCNC(=O)c1ccc(C(F)(F)F)c(-n2nc(CC)n(Cc3ccc(-c4ccccc4S(=O)(=O)NC(=O)OC(C)(C)C)cc3F)c2=O)c1 10.1021/jm00019a004
44384872 59665 0 None - 0 Rabbit 8.1 pIC50 = 8.1 Binding
Inhibition of [125I]-Sar1-Ile8-Ang II binding to Angiotensin II receptor type 1 from rabbit aortaInhibition of [125I]-Sar1-Ile8-Ang II binding to Angiotensin II receptor type 1 from rabbit aorta
ChEMBL 575 9 3 7 4.4 CCCc1nc2ccc(NC(=O)NC(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(C)=O)cc1 10.1016/0960-894X(96)00116-3
CHEMBL173455 59665 0 None - 0 Rabbit 8.1 pIC50 = 8.1 Binding
Inhibition of [125I]-Sar1-Ile8-Ang II binding to Angiotensin II receptor type 1 from rabbit aortaInhibition of [125I]-Sar1-Ile8-Ang II binding to Angiotensin II receptor type 1 from rabbit aorta
ChEMBL 575 9 3 7 4.4 CCCc1nc2ccc(NC(=O)NC(C)C)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(C)=O)cc1 10.1016/0960-894X(96)00116-3
76322692 84535 0 None - 0 Rabbit 8.1 pIC50 = 8.1 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 585 12 2 10 4.3 CCCCc1nnc([S+]([O-])Cc2ccc([N+](=O)[O-])cc2)n1Cc1ccc(NC(=O)c2ccccc2-c2nnn[nH]2)cc1 10.1007/s00044-011-9756-4
CHEMBL2237605 84535 0 None - 0 Rabbit 8.1 pIC50 = 8.1 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 585 12 2 10 4.3 CCCCc1nnc([S+]([O-])Cc2ccc([N+](=O)[O-])cc2)n1Cc1ccc(NC(=O)c2ccccc2-c2nnn[nH]2)cc1 10.1007/s00044-011-9756-4
10392565 167838 0 None - 0 Rabbit 8.1 pIC50 = 8.1 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 542 11 1 9 4.7 CCCCc1nnc([S+]([O-])Cc2ccc([N+](=O)[O-])cc2)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
CHEMBL434844 167838 0 None - 0 Rabbit 8.1 pIC50 = 8.1 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 542 11 1 9 4.7 CCCCc1nnc([S+]([O-])Cc2ccc([N+](=O)[O-])cc2)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
44274824 98793 0 None - 0 Rabbit 8.1 pIC50 = 8.1 Binding
Displacement of [125I]Sar1-Ile8-AII (without BSA) from type 1 Angiotensin II receptor of rabbit aortaDisplacement of [125I]Sar1-Ile8-AII (without BSA) from type 1 Angiotensin II receptor of rabbit aorta
ChEMBL 535 11 2 7 5.8 CCCCC(=O)Nc1ccc2nc(CCCC)n(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c(=O)c2c1 10.1016/S0960-894X(00)80335-2
CHEMBL281846 98793 0 None - 0 Rabbit 8.1 pIC50 = 8.1 Binding
Displacement of [125I]Sar1-Ile8-AII (without BSA) from type 1 Angiotensin II receptor of rabbit aortaDisplacement of [125I]Sar1-Ile8-AII (without BSA) from type 1 Angiotensin II receptor of rabbit aorta
ChEMBL 535 11 2 7 5.8 CCCCC(=O)Nc1ccc2nc(CCCC)n(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c(=O)c2c1 10.1016/S0960-894X(00)80335-2
14956747 204247 0 None - 0 Rabbit 7.1 pIC50 = 7.1 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 496 9 1 9 4.2 CCCCc1nn(-c2ccc([N+](=O)[O-])cc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
CHEMBL84630 204247 0 None - 0 Rabbit 7.1 pIC50 = 7.1 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 496 9 1 9 4.2 CCCCc1nn(-c2ccc([N+](=O)[O-])cc2)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
15356433 183412 0 None - 0 Rat 7.1 pIC50 = 7.1 Binding
Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.
ChEMBL 548 12 3 6 5.5 CCCCc1nc(Cl)c(C(=O)O)n1Cc1ccc(NC(=O)[C@H](Cc2ccccc2)n2cccc2C(=O)O)cc1 10.1021/jm00064a007
CHEMBL48195 183412 0 None - 0 Rat 7.1 pIC50 = 7.1 Binding
Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.
ChEMBL 548 12 3 6 5.5 CCCCc1nc(Cl)c(C(=O)O)n1Cc1ccc(NC(=O)[C@H](Cc2ccccc2)n2cccc2C(=O)O)cc1 10.1021/jm00064a007
44341802 110865 0 None - 0 Rat 7.1 pIC50 = 7.1 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 420 7 1 3 6.1 CCCCC1=NC2(CCCC2)C(=S)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00074a018
CHEMBL327018 110865 0 None - 0 Rat 7.1 pIC50 = 7.1 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 420 7 1 3 6.1 CCCCC1=NC2(CCCC2)C(=S)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00074a018
19422646 168866 0 None - 0 Rat 7.1 pIC50 = 7.1 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 430 9 1 3 5.5 CCCCC1=NC(C2CC2)(C2CC2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00074a018
CHEMBL44268 168866 0 None - 0 Rat 7.1 pIC50 = 7.1 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 430 9 1 3 5.5 CCCCC1=NC(C2CC2)(C2CC2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00074a018
19422646 168866 0 None - 0 Rat 7.1 pIC50 = 7.1 Binding
In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.
ChEMBL 430 9 1 3 5.5 CCCCC1=NC(C2CC2)(C2CC2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/S0960-894X(01)81140-9
CHEMBL44268 168866 0 None - 0 Rat 7.1 pIC50 = 7.1 Binding
In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.
ChEMBL 430 9 1 3 5.5 CCCCC1=NC(C2CC2)(C2CC2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/S0960-894X(01)81140-9
15287893 161392 0 None - 0 Rabbit 7.1 pIC50 = 7.1 Binding
Tested in vitro for Angiotensin II receptor, type 1 binding affinity using rabbit aorta binding assayTested in vitro for Angiotensin II receptor, type 1 binding affinity using rabbit aorta binding assay
ChEMBL 515 14 1 6 6.9 CCCCCCOc1ccccc1C(Oc1ccc(Cn2c(CCC)nc3c(C)ccnc32)cc1)C(=O)O 10.1016/0960-894X(94)00476-V
CHEMBL41566 161392 0 None - 0 Rabbit 7.1 pIC50 = 7.1 Binding
Tested in vitro for Angiotensin II receptor, type 1 binding affinity using rabbit aorta binding assayTested in vitro for Angiotensin II receptor, type 1 binding affinity using rabbit aorta binding assay
ChEMBL 515 14 1 6 6.9 CCCCCCOc1ccccc1C(Oc1ccc(Cn2c(CCC)nc3c(C)ccnc32)cc1)C(=O)O 10.1016/0960-894X(94)00476-V
44293697 99774 0 None - 0 Rat 6.1 pIC50 = 6.1 Binding
Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.
ChEMBL 596 13 1 9 5.7 CCCCc1nc(Cl)c(CC(=O)OC)n1Cc1ccc(NC(=O)[C@H](Cc2cccs2)n2cccc2C(=O)OC)cc1 10.1021/jm00064a007
CHEMBL288753 99774 0 None - 0 Rat 6.1 pIC50 = 6.1 Binding
Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.
ChEMBL 596 13 1 9 5.7 CCCCc1nc(Cl)c(CC(=O)OC)n1Cc1ccc(NC(=O)[C@H](Cc2cccs2)n2cccc2C(=O)OC)cc1 10.1021/jm00064a007
44341607 9936 0 None - 0 Rat 6.1 pIC50 = 6.1 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 534 10 3 6 3.1 CCCCC1=NC2(CCN(C(=O)C(N)CC(=O)O)CC2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00074a018
CHEMBL115204 9936 0 None - 0 Rat 6.1 pIC50 = 6.1 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 534 10 3 6 3.1 CCCCC1=NC2(CCN(C(=O)C(N)CC(=O)O)CC2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00074a018
15654754 101595 0 None - 0 Bovine 6.1 pIC50 = 6.1 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 439 7 3 7 3.3 CNCc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a016
CHEMBL302127 101595 0 None - 0 Bovine 6.1 pIC50 = 6.1 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 439 7 3 7 3.3 CNCc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a016
11756569 115960 0 None - 0 Rat 6.1 pIC50 = 6.1 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 524 9 3 4 7.2 CCCCc1nc2cc(NC(=O)NC3CCCCC3)ccc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00077a007
CHEMBL336130 115960 0 None - 0 Rat 6.1 pIC50 = 6.1 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 524 9 3 4 7.2 CCCCc1nc2cc(NC(=O)NC3CCCCC3)ccc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00077a007
127035083 135820 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysisDisplacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysis
ChEMBL 677 12 2 8 7.4 CCCc1nc2c(C)cc(C(=O)NCc3ccc(OC)cc3)cc2n1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)cc1 10.1039/C4MD00499J
CHEMBL3734835 135820 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysisDisplacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysis
ChEMBL 677 12 2 8 7.4 CCCc1nc2c(C)cc(C(=O)NCc3ccc(OC)cc3)cc2n1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)cc1 10.1039/C4MD00499J
24827901 158869 0 None - 0 Rat 7.1 pIC50 = 7.1 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
ChEMBL 439 7 1 7 4.2 CCCCn1c(=O)c2ccc(C)nc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm7011563
CHEMBL410105 158869 0 None - 0 Rat 7.1 pIC50 = 7.1 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
ChEMBL 439 7 1 7 4.2 CCCCn1c(=O)c2ccc(C)nc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm7011563
11754954 167817 0 None - 0 Rat 7.1 pIC50 = 7.1 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 481 8 1 4 6.3 CCCCc1nc2ccc(N3CCCCC3=O)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00077a007
CHEMBL434640 167817 0 None - 0 Rat 7.1 pIC50 = 7.1 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 481 8 1 4 6.3 CCCCc1nc2ccc(N3CCCCC3=O)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00077a007
71521504 86392 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor afterDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after
ChEMBL 581 6 1 7 6.2 CCc1nc2ccn(Cc3cccc(C(F)(F)F)c3)c(=O)c2n1[C@H]1CCc2cc(-c3ccccc3-c3nnn[nH]3)ccc21 10.1016/j.bmcl.2012.11.088
CHEMBL2322450 86392 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor afterDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after
ChEMBL 581 6 1 7 6.2 CCc1nc2ccn(Cc3cccc(C(F)(F)F)c3)c(=O)c2n1[C@H]1CCc2cc(-c3ccccc3-c3nnn[nH]3)ccc21 10.1016/j.bmcl.2012.11.088
44309398 101782 0 None - 0 Bovine 4.1 pIC50 = 4.1 Binding
Inhibition of [125I][Ile5]-AII binding to bovine adrenal cortex membrane Angiotensin II receptor type 1Inhibition of [125I][Ile5]-AII binding to bovine adrenal cortex membrane Angiotensin II receptor type 1
ChEMBL 546 6 1 3 5.5 CCCCc1nc2ccccc2n1CCc1cc(I)c(O)c(I)c1 10.1016/S0960-894X(01)81149-5
CHEMBL303247 101782 0 None - 0 Bovine 4.1 pIC50 = 4.1 Binding
Inhibition of [125I][Ile5]-AII binding to bovine adrenal cortex membrane Angiotensin II receptor type 1Inhibition of [125I][Ile5]-AII binding to bovine adrenal cortex membrane Angiotensin II receptor type 1
ChEMBL 546 6 1 3 5.5 CCCCc1nc2ccccc2n1CCc1cc(I)c(O)c(I)c1 10.1016/S0960-894X(01)81149-5
44320733 204719 0 None - 0 Rat 6.1 pIC50 = 6.1 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 386 5 1 5 4.4 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ncccc2C(=O)O)cc1 10.1021/jm031100t
CHEMBL88081 204719 0 None - 0 Rat 6.1 pIC50 = 6.1 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 386 5 1 5 4.4 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ncccc2C(=O)O)cc1 10.1021/jm031100t
127036865 136886 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptorDisplacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptor
ChEMBL 584 10 3 7 5.7 CCCc1nc2c(C)cc(C(=O)NCc3ccccc3)cc2n1Cc1ccc(-c2ccccc2C(=O)Nc2nnn[nH]2)cc1 10.1039/C5MD00169B
CHEMBL3753406 136886 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptorDisplacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptor
ChEMBL 584 10 3 7 5.7 CCCc1nc2c(C)cc(C(=O)NCc3ccccc3)cc2n1Cc1ccc(-c2ccccc2C(=O)Nc2nnn[nH]2)cc1 10.1039/C5MD00169B
15654743 167581 0 None - 0 Bovine 7.1 pIC50 = 7.1 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 438 6 2 6 4.8 CC(C)c1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a016
CHEMBL433099 167581 0 None - 0 Bovine 7.1 pIC50 = 7.1 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 438 6 2 6 4.8 CC(C)c1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a016
44283175 119851 0 None - 0 Rabbit 6.1 pIC50 = 6.1 Binding
Displacement of [125 I]Sar1Ile8-AII from type 1 Angiotensin II receptor of rabbit aorta membraneDisplacement of [125 I]Sar1Ile8-AII from type 1 Angiotensin II receptor of rabbit aorta membrane
ChEMBL 637 8 1 7 7.1 Cc1nc2ccc(N(Cc3ccccc3Cl)C(=O)c3ccccc3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80517-5
CHEMBL35324 119851 0 None - 0 Rabbit 6.1 pIC50 = 6.1 Binding
Displacement of [125 I]Sar1Ile8-AII from type 1 Angiotensin II receptor of rabbit aorta membraneDisplacement of [125 I]Sar1Ile8-AII from type 1 Angiotensin II receptor of rabbit aorta membrane
ChEMBL 637 8 1 7 7.1 Cc1nc2ccc(N(Cc3ccccc3Cl)C(=O)c3ccccc3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80517-5
10028815 206345 0 None - 0 Rabbit 6.1 pIC50 = 6.1 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 496 8 1 6 4.4 CCCCc1nn(-c2ccccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(N)(=O)=O)cc1 10.1021/jm00043a020
CHEMBL97783 206345 0 None - 0 Rabbit 6.1 pIC50 = 6.1 Binding
In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AIIIn vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII
ChEMBL 496 8 1 6 4.4 CCCCc1nn(-c2ccccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(N)(=O)=O)cc1 10.1021/jm00043a020
10250336 18683 0 None - 1 Rat 6.1 pIC50 = 6.1 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 399 7 2 4 5.4 CCCCc1nc2cc(N)ccc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00077a007
CHEMBL128318 18683 0 None - 1 Rat 6.1 pIC50 = 6.1 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 399 7 2 4 5.4 CCCCc1nc2cc(N)ccc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00077a007
44310590 202655 0 None - 0 Rabbit 7.1 pIC50 = 7.1 Binding
In vitro binding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membraneIn vitro binding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane
ChEMBL 385 5 1 4 4.9 CCc1nc2c(C)cc(C)nn2c1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/S0960-894X(01)81150-1
CHEMBL71730 202655 0 None - 0 Rabbit 7.1 pIC50 = 7.1 Binding
In vitro binding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membraneIn vitro binding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane
ChEMBL 385 5 1 4 4.9 CCc1nc2c(C)cc(C)nn2c1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/S0960-894X(01)81150-1
44305654 100302 0 None - 0 Rat 7.1 pIC50 = 7.1 Binding
Tested for binding affinity against angiotensin II receptor in rat adrenal cortexTested for binding affinity against angiotensin II receptor in rat adrenal cortex
ChEMBL 502 8 1 8 4.8 CCCCc1cc(=O)n2nc(-c3ccccc3)nc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/0960-894X(95)00370-9
CHEMBL293001 100302 0 None - 0 Rat 7.1 pIC50 = 7.1 Binding
Tested for binding affinity against angiotensin II receptor in rat adrenal cortexTested for binding affinity against angiotensin II receptor in rat adrenal cortex
ChEMBL 502 8 1 8 4.8 CCCCc1cc(=O)n2nc(-c3ccccc3)nc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/0960-894X(95)00370-9
71653748 88706 0 None - 0 Human 6.1 pIC50 = 6.1 Binding
Displacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysisDisplacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysis
ChEMBL 627 11 2 7 6.6 CCCCc1c(Cl)[n+](Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)cn1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.ejmech.2012.12.044
CHEMBL2337678 88706 0 None - 0 Human 6.1 pIC50 = 6.1 Binding
Displacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysisDisplacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysis
ChEMBL 627 11 2 7 6.6 CCCCc1c(Cl)[n+](Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)cn1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.ejmech.2012.12.044
CHEMBL2365905 88706 0 None - 0 Human 6.1 pIC50 = 6.1 Binding
Displacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysisDisplacement of [125I-Sar1-Ile8]-ANG2 from human Angiotensin 2 type-1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysis
ChEMBL 627 11 2 7 6.6 CCCCc1c(Cl)[n+](Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)cn1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.ejmech.2012.12.044
44293406 184274 0 None - 0 Rat 5.1 pIC50 = 5.1 Binding
Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.
ChEMBL 458 10 2 7 3.6 CCCCc1nc(Cl)c(CO)n1Cc1ccc(NC(=O)Cn2cccc2C(=O)OC)cc1 10.1021/jm00064a007
CHEMBL48526 184274 0 None - 0 Rat 5.1 pIC50 = 5.1 Binding
Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.
ChEMBL 458 10 2 7 3.6 CCCCc1nc(Cl)c(CO)n1Cc1ccc(NC(=O)Cn2cccc2C(=O)OC)cc1 10.1021/jm00064a007
15654744 101664 0 None - 0 Bovine 7.1 pIC50 = 7.1 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 436 6 2 6 4.5 O=C(O)c1cccc2nc(C3CC3)n(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c12 10.1021/jm00067a016
CHEMBL302520 101664 0 None - 0 Bovine 7.1 pIC50 = 7.1 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 436 6 2 6 4.5 O=C(O)c1cccc2nc(C3CC3)n(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c12 10.1021/jm00067a016
10502342 168498 0 None - 0 Bovine 6.1 pIC50 = 6.1 Binding
In vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortexIn vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortex
ChEMBL 422 9 2 6 3.9 CCCc1nc(CO)c(C(=O)OCC)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm950450f
CHEMBL439743 168498 0 None - 0 Bovine 6.1 pIC50 = 6.1 Binding
In vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortexIn vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortex
ChEMBL 422 9 2 6 3.9 CCCc1nc(CO)c(C(=O)OCC)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm950450f
10502342 168498 0 None - 0 Bovine 6.1 pIC50 = 6.1 Binding
Inhibition of [125l]-All binding to bovine adrenal cortexInhibition of [125l]-All binding to bovine adrenal cortex
ChEMBL 422 9 2 6 3.9 CCCc1nc(CO)c(C(=O)OCC)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/S0960-894X(01)81143-4
CHEMBL439743 168498 0 None - 0 Bovine 6.1 pIC50 = 6.1 Binding
Inhibition of [125l]-All binding to bovine adrenal cortexInhibition of [125l]-All binding to bovine adrenal cortex
ChEMBL 422 9 2 6 3.9 CCCc1nc(CO)c(C(=O)OCC)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/S0960-894X(01)81143-4
44287536 161364 0 None - 0 Rabbit 6.1 pIC50 = 6.1 Binding
Tested in vitro for Angiotensin II receptor, type 1 binding affinity using rabbit aorta binding assayTested in vitro for Angiotensin II receptor, type 1 binding affinity using rabbit aorta binding assay
ChEMBL 381 9 1 5 4.4 CCCc1nc2c(C)ccnc2n1Cc1ccc(OC(CCC)C(=O)O)cc1 10.1016/0960-894X(94)00476-V
CHEMBL41534 161364 0 None - 0 Rabbit 6.1 pIC50 = 6.1 Binding
Tested in vitro for Angiotensin II receptor, type 1 binding affinity using rabbit aorta binding assayTested in vitro for Angiotensin II receptor, type 1 binding affinity using rabbit aorta binding assay
ChEMBL 381 9 1 5 4.4 CCCc1nc2c(C)ccnc2n1Cc1ccc(OC(CCC)C(=O)O)cc1 10.1016/0960-894X(94)00476-V
76328690 104754 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Antagonist activity at human AT1 receptor expressed in CHO cells measured after overnight incubation by luciferase reporter gene assayAntagonist activity at human AT1 receptor expressed in CHO cells measured after overnight incubation by luciferase reporter gene assay
ChEMBL 528 9 1 5 7.7 CCCc1nn2ccc(-c3nc4ccccc4n3CCC)cc2c1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.bmcl.2014.01.004
CHEMBL3115242 104754 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Antagonist activity at human AT1 receptor expressed in CHO cells measured after overnight incubation by luciferase reporter gene assayAntagonist activity at human AT1 receptor expressed in CHO cells measured after overnight incubation by luciferase reporter gene assay
ChEMBL 528 9 1 5 7.7 CCCc1nn2ccc(-c3nc4ccccc4n3CCC)cc2c1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.bmcl.2014.01.004
44315059 202996 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membrane
ChEMBL 671 11 2 9 5.9 CCc1nc2ccc(NC(=O)c3ccccn3)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/0960-894X(94)85036-4
CHEMBL74144 202996 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
In vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membraneIn vivo inhibitory concentration against Angiotensin II receptor, type 1 of human adrenal membrane
ChEMBL 671 11 2 9 5.9 CCc1nc2ccc(NC(=O)c3ccccn3)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)OCCC(C)C)cc1F 10.1016/0960-894X(94)85036-4
44307257 102114 0 None - 0 Rabbit 6.1 pIC50 = 6.1 Binding
Binding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membraneBinding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane
ChEMBL 326 4 1 6 3.3 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(O)c([N+](=O)[O-])c1 10.1016/S0960-894X(01)81148-3
CHEMBL304116 102114 0 None - 0 Rabbit 6.1 pIC50 = 6.1 Binding
Binding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membraneBinding affinity evaluated by its ability to displace the specific binding ligand 125I-SAR1, Ile8-AII from Angiotensin II receptor, type 1 in rabbit aorta membrane
ChEMBL 326 4 1 6 3.3 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(O)c([N+](=O)[O-])c1 10.1016/S0960-894X(01)81148-3
135723836 100558 0 None - 0 Bovine 6.1 pIC50 = 6.1 Binding
Displacement of [125 I]-AII (0.2 nM) from bovine adrenal cortical membrane angiotensin II (AII) receptor at 10e-7 MDisplacement of [125 I]-AII (0.2 nM) from bovine adrenal cortical membrane angiotensin II (AII) receptor at 10e-7 M
ChEMBL 486 8 2 8 5.7 CCCSc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2noc(O)n2)cc1 10.1016/0960-894X(95)00319-O
CHEMBL294598 100558 0 None - 0 Bovine 6.1 pIC50 = 6.1 Binding
Displacement of [125 I]-AII (0.2 nM) from bovine adrenal cortical membrane angiotensin II (AII) receptor at 10e-7 MDisplacement of [125 I]-AII (0.2 nM) from bovine adrenal cortical membrane angiotensin II (AII) receptor at 10e-7 M
ChEMBL 486 8 2 8 5.7 CCCSc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2noc(O)n2)cc1 10.1016/0960-894X(95)00319-O
15654733 202624 0 None - 0 Bovine 6.1 pIC50 = 6.1 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 466 8 1 8 4.3 C=CCOc1nc2cccc(C(=O)OC)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a016
CHEMBL71550 202624 0 None - 0 Bovine 6.1 pIC50 = 6.1 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 466 8 1 8 4.3 C=CCOc1nc2cccc(C(=O)OC)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a016
10250278 20119 0 None - 0 Rat 6.1 pIC50 = 6.1 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 398 7 1 3 6.1 CCCCc1nc2ccc(C)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00077a007
CHEMBL130600 20119 0 None - 0 Rat 6.1 pIC50 = 6.1 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 398 7 1 3 6.1 CCCCc1nc2ccc(C)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00077a007
15288898 202567 0 None - 0 Bovine 5.1 pIC50 = 5.1 Binding
Inhibition of [125I][Ile5]-AII binding to bovine adrenal cortex membrane Angiotensin II receptor type 1Inhibition of [125I][Ile5]-AII binding to bovine adrenal cortex membrane Angiotensin II receptor type 1
ChEMBL 280 5 1 3 4.1 CCCCc1nc2ccccc2n1Cc1ccc(O)cc1 10.1016/S0960-894X(01)81149-5
CHEMBL71254 202567 0 None - 0 Bovine 5.1 pIC50 = 5.1 Binding
Inhibition of [125I][Ile5]-AII binding to bovine adrenal cortex membrane Angiotensin II receptor type 1Inhibition of [125I][Ile5]-AII binding to bovine adrenal cortex membrane Angiotensin II receptor type 1
ChEMBL 280 5 1 3 4.1 CCCCc1nc2ccccc2n1Cc1ccc(O)cc1 10.1016/S0960-894X(01)81149-5
44303883 201204 0 None - 0 Rabbit 5.1 pIC50 = 5.1 Binding
Inhibition of angiotensin Angiotensin II receptor, type 1 in rabbit aorta using [125I-Sar1,Ile8] angiotensin II binding assayInhibition of angiotensin Angiotensin II receptor, type 1 in rabbit aorta using [125I-Sar1,Ile8] angiotensin II binding assay
ChEMBL 634 11 1 3 6.4 CCCCCN(CCCCC)C(=O)N1CCN(C(=O)N(c2ccccc2)c2ccc(I)cc2)[C@H](C(=O)O)C1 10.1016/S0960-894X(01)81007-6
CHEMBL62744 201204 0 None - 0 Rabbit 5.1 pIC50 = 5.1 Binding
Inhibition of angiotensin Angiotensin II receptor, type 1 in rabbit aorta using [125I-Sar1,Ile8] angiotensin II binding assayInhibition of angiotensin Angiotensin II receptor, type 1 in rabbit aorta using [125I-Sar1,Ile8] angiotensin II binding assay
ChEMBL 634 11 1 3 6.4 CCCCCN(CCCCC)C(=O)N1CCN(C(=O)N(c2ccccc2)c2ccc(I)cc2)[C@H](C(=O)O)C1 10.1016/S0960-894X(01)81007-6
14950500 99100 0 None - 0 Guinea pig 7.1 pIC50 = 7.1 Binding
Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1
ChEMBL 401 7 1 6 4.3 COCc1c(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)cc(C)nc1C 10.1021/jm00061a016
CHEMBL283770 99100 0 None - 0 Guinea pig 7.1 pIC50 = 7.1 Binding
Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1
ChEMBL 401 7 1 6 4.3 COCc1c(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)cc(C)nc1C 10.1021/jm00061a016
10457997 18632 0 None - 0 Rat 7.1 pIC50 = 7.1 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 483 11 2 4 6.9 CCCCC(=O)Nc1ccc2nc(CCCC)n(Cc3ccc(-c4ccccc4C(=O)O)cc3)c2c1 10.1021/jm00077a007
CHEMBL128049 18632 0 None - 0 Rat 7.1 pIC50 = 7.1 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
ChEMBL 483 11 2 4 6.9 CCCCC(=O)Nc1ccc2nc(CCCC)n(Cc3ccc(-c4ccccc4C(=O)O)cc3)c2c1 10.1021/jm00077a007
76308196 84556 0 None - 0 Rabbit 6.1 pIC50 = 6.1 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 410 8 3 6 3.9 CCCCc1nnc(S)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
CHEMBL2237877 84556 0 None - 0 Rabbit 6.1 pIC50 = 6.1 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 410 8 3 6 3.9 CCCCc1nnc(S)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
10021888 49102 0 None - 0 Rabbit 6.1 pIC50 = 6.1 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 367 7 2 5 4.3 CCCCc1nnc(S)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
CHEMBL156408 49102 0 None - 0 Rabbit 6.1 pIC50 = 6.1 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 367 7 2 5 4.3 CCCCc1nnc(S)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
10346301 167811 0 None - 0 Guinea pig 6.1 pIC50 = 6.1 Binding
In vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparationIn vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparation
ChEMBL 475 6 1 5 6.2 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2cc(C(F)(F)F)ccc2n1 10.1021/jm00100a007
CHEMBL434615 167811 0 None - 0 Guinea pig 6.1 pIC50 = 6.1 Binding
In vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparationIn vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparation
ChEMBL 475 6 1 5 6.2 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2cc(C(F)(F)F)ccc2n1 10.1021/jm00100a007
44373238 96627 0 None - 0 Human 5.1 pIC50 = 5.1 Binding
Inhibition of Angiotensin II receptor, type 1Inhibition of Angiotensin II receptor, type 1
ChEMBL 1051 29 11 12 1.9 CC[C@@H](C)[C@H](NC(=O)[C@@H]1CCCN1C(=O)[C@H](Cc1c[nH]cn1)NC(=O)[C@H](CCCCNC(=O)[C@H](CCCN=C(N)N)NC(=O)OCc1ccccc1)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)c1ccccc1)C(=O)O 10.1021/jm9504722
CHEMBL267354 96627 0 None - 0 Human 5.1 pIC50 = 5.1 Binding
Inhibition of Angiotensin II receptor, type 1Inhibition of Angiotensin II receptor, type 1
ChEMBL 1051 29 11 12 1.9 CC[C@@H](C)[C@H](NC(=O)[C@@H]1CCCN1C(=O)[C@H](Cc1c[nH]cn1)NC(=O)[C@H](CCCCNC(=O)[C@H](CCCN=C(N)N)NC(=O)OCc1ccccc1)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)c1ccccc1)C(=O)O 10.1021/jm9504722
44300735 100280 0 None - 0 Rabbit 7.1 pIC50 = 7.1 Binding
Inhibition of Angiotensin II receptor type 1 in rabbit aorta binding assayInhibition of Angiotensin II receptor type 1 in rabbit aorta binding assay
ChEMBL 629 9 1 9 5.3 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2cc(CN3CCOCC3)sc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/S0960-894X(01)81145-8
CHEMBL292829 100280 0 None - 0 Rabbit 7.1 pIC50 = 7.1 Binding
Inhibition of Angiotensin II receptor type 1 in rabbit aorta binding assayInhibition of Angiotensin II receptor type 1 in rabbit aorta binding assay
ChEMBL 629 9 1 9 5.3 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2cc(CN3CCOCC3)sc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/S0960-894X(01)81145-8
127035558 135811 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 577 11 2 5 7.8 CCCSc1nc2c(C)cc(C(=O)NC[C@@H](C)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2015.09.010
CHEMBL3734763 135811 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 577 11 2 5 7.8 CCCSc1nc2c(C)cc(C(=O)NC[C@@H](C)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2015.09.010
127026027 136736 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptorDisplacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptor
ChEMBL 628 12 3 8 5.8 CCCc1nc2c(C)cc(C(=O)NCCc3ccc(OC)cc3)cc2n1Cc1ccc(-c2ccccc2C(=O)Nc2nnn[nH]2)cc1 10.1039/C5MD00169B
CHEMBL3752145 136736 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptorDisplacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptor
ChEMBL 628 12 3 8 5.8 CCCc1nc2c(C)cc(C(=O)NCCc3ccc(OC)cc3)cc2n1Cc1ccc(-c2ccccc2C(=O)Nc2nnn[nH]2)cc1 10.1039/C5MD00169B
19792197 193255 0 None - 0 Bovine 6.1 pIC50 = 6.1 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 480 8 1 7 5.4 CCCCc1nc2cc(C)cc(C(=O)OC)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
CHEMBL54194 193255 0 None - 0 Bovine 6.1 pIC50 = 6.1 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 480 8 1 7 5.4 CCCCc1nc2cc(C)cc(C(=O)OC)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
19792197 193255 0 None - 0 Bovine 6.1 pIC50 = 6.1 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 480 8 1 7 5.4 CCCCc1nc2cc(C)cc(C(=O)OC)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
CHEMBL54194 193255 0 None - 0 Bovine 6.1 pIC50 = 6.1 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 480 8 1 7 5.4 CCCCc1nc2cc(C)cc(C(=O)OC)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
10457516 16593 0 None - 0 Rat 7.1 pIC50 = 7.1 Binding
Activity against high affinity Angiotensin II receptor, type 1 was measured from the ability to inhibit [125I]angiotensin II binding to rat uterine membrane.Activity against high affinity Angiotensin II receptor, type 1 was measured from the ability to inhibit [125I]angiotensin II binding to rat uterine membrane.
ChEMBL 472 10 1 7 5.0 CCCCc1nc(CCCC)n(Cc2ccc(-n3c(-c4nn[nH]n4)ccc3C(F)(F)F)cc2)n1 10.1021/jm00053a013
CHEMBL12451 16593 0 None - 0 Rat 7.1 pIC50 = 7.1 Binding
Activity against high affinity Angiotensin II receptor, type 1 was measured from the ability to inhibit [125I]angiotensin II binding to rat uterine membrane.Activity against high affinity Angiotensin II receptor, type 1 was measured from the ability to inhibit [125I]angiotensin II binding to rat uterine membrane.
ChEMBL 472 10 1 7 5.0 CCCCc1nc(CCCC)n(Cc2ccc(-n3c(-c4nn[nH]n4)ccc3C(F)(F)F)cc2)n1 10.1021/jm00053a013
1610 2305 89 None 1 4 Human 7.1 pIC50 = 7.1 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00019a004
3941 2305 89 None 1 4 Human 7.1 pIC50 = 7.1 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00019a004
3961 2305 89 None 1 4 Human 7.1 pIC50 = 7.1 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00019a004
590 2305 89 None 1 4 Human 7.1 pIC50 = 7.1 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00019a004
CHEMBL191 2305 89 None 1 4 Human 7.1 pIC50 = 7.1 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00019a004
DB00678 2305 89 None 1 4 Human 7.1 pIC50 = 7.1 Binding
In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.In vitro inhibitory activity against angiotensin II receptor type 1, in human adrenal membrane preparations.
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00019a004
19919870 84823 0 None - 0 Human 6.1 pIC50 = 6.1 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 604 13 0 6 7.3 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2Cc2ccc(-c3ccccc3)cc2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
CHEMBL2259781 84823 0 None - 0 Human 6.1 pIC50 = 6.1 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 604 13 0 6 7.3 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2Cc2ccc(-c3ccccc3)cc2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
76315366 84511 0 None - 0 Rabbit 7.1 pIC50 = 7.1 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 549 11 2 8 4.4 CCCCc1nnc(C(=O)N(C)Cc2ccccc2)n1Cc1ccc(NC(=O)c2ccccc2-c2nnn[nH]2)cc1 10.1007/s00044-011-9756-4
CHEMBL2237581 84511 0 None - 0 Rabbit 7.1 pIC50 = 7.1 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 549 11 2 8 4.4 CCCCc1nnc(C(=O)N(C)Cc2ccccc2)n1Cc1ccc(NC(=O)c2ccccc2-c2nnn[nH]2)cc1 10.1007/s00044-011-9756-4
9986953 46315 0 None - 0 Rabbit 7.1 pIC50 = 7.1 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 506 10 1 7 4.8 CCCCc1nnc(C(=O)N(C)Cc2ccccc2)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
CHEMBL153825 46315 0 None - 0 Rabbit 7.1 pIC50 = 7.1 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 506 10 1 7 4.8 CCCCc1nnc(C(=O)N(C)Cc2ccccc2)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
76315367 84513 0 None - 0 Rabbit 6.1 pIC50 = 6.1 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 466 9 2 6 5.5 CCCCc1nnc(SC(C)(C)C)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
CHEMBL2237583 84513 0 None - 0 Rabbit 6.1 pIC50 = 6.1 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 466 9 2 6 5.5 CCCCc1nnc(SC(C)(C)C)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
44341791 9863 0 None - 0 Rat 6.1 pIC50 = 6.1 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 419 7 2 4 4.1 CCCCC1=NC2(CCNCC2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00074a018
CHEMBL114771 9863 0 None - 0 Rat 6.1 pIC50 = 6.1 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 419 7 2 4 4.1 CCCCC1=NC2(CCNCC2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00074a018
10002423 48947 0 None - 0 Rabbit 6.1 pIC50 = 6.1 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 423 8 1 5 5.9 CCCCc1nnc(SC(C)(C)C)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
CHEMBL156279 48947 0 None - 0 Rabbit 6.1 pIC50 = 6.1 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 423 8 1 5 5.9 CCCCc1nnc(SC(C)(C)C)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
15699061 5221 0 None - 0 Rat 5.1 pIC50 = 5.1 Binding
Binding affinity against angiotensin II receptor in rat smooth muscle cell preparationsBinding affinity against angiotensin II receptor in rat smooth muscle cell preparations
ChEMBL 376 7 2 4 3.6 CCCCc1nc(Cl)c(CO)n1Cc1ccc2c(c1)CCC(C(=O)O)C2 10.1021/jm00114a021
CHEMBL106682 5221 0 None - 0 Rat 5.1 pIC50 = 5.1 Binding
Binding affinity against angiotensin II receptor in rat smooth muscle cell preparationsBinding affinity against angiotensin II receptor in rat smooth muscle cell preparations
ChEMBL 376 7 2 4 3.6 CCCCc1nc(Cl)c(CO)n1Cc1ccc2c(c1)CCC(C(=O)O)C2 10.1021/jm00114a021
44274772 98171 0 None - 0 Rabbit 8.1 pIC50 = 8.1 Binding
Ability to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitroAbility to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitro
ChEMBL 493 8 2 7 4.6 CCCCc1nc2ccc(NC(C)=O)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80335-2
CHEMBL277182 98171 0 None - 0 Rabbit 8.1 pIC50 = 8.1 Binding
Ability to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitroAbility to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitro
ChEMBL 493 8 2 7 4.6 CCCCc1nc2ccc(NC(C)=O)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80335-2
10369902 164074 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 535 11 0 8 5.0 CCCCc1ncc(/C=C2/C(=O)N(CCC)C(=O)N2Cc2csc(C)n2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
CHEMBL421629 164074 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 535 11 0 8 5.0 CCCCc1ncc(/C=C2/C(=O)N(CCC)C(=O)N2Cc2csc(C)n2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
44274772 98171 0 None - 0 Rabbit 8.1 pIC50 = 8.1 Binding
Binding affinity against Angiotensin II type 1 Receptor in rabbit aortic tissueBinding affinity against Angiotensin II type 1 Receptor in rabbit aortic tissue
ChEMBL 493 8 2 7 4.6 CCCCc1nc2ccc(NC(C)=O)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80334-0
CHEMBL277182 98171 0 None - 0 Rabbit 8.1 pIC50 = 8.1 Binding
Binding affinity against Angiotensin II type 1 Receptor in rabbit aortic tissueBinding affinity against Angiotensin II type 1 Receptor in rabbit aortic tissue
ChEMBL 493 8 2 7 4.6 CCCCc1nc2ccc(NC(C)=O)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80334-0
44311616 101657 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 610 12 1 8 6.9 CCCc1nc(CC)c(C(=O)OCc2ccc(C(=O)c3ccccc3)cc2)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80077-3
CHEMBL302485 101657 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 610 12 1 8 6.9 CCCc1nc(CC)c(C(=O)OCc2ccc(C(=O)c3ccccc3)cc2)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80077-3
44311571 202740 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 610 12 1 8 6.9 CCCc1nc(CC)c(C(=O)OCc2cccc(C(=O)c3ccccc3)c2)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80077-3
CHEMBL72249 202740 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Binding affinity for Angiotensin II receptor, type 1Binding affinity for Angiotensin II receptor, type 1
ChEMBL 610 12 1 8 6.9 CCCc1nc(CC)c(C(=O)OCc2cccc(C(=O)c3ccccc3)c2)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80077-3
11328757 204241 0 None - 0 Rat 8.1 pIC50 = 8.1 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 464 6 1 5 6.3 CCCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2c(C(=O)O)c(C)nc3ccccc23)cc1 10.1021/jm031100t
CHEMBL84573 204241 0 None - 0 Rat 8.1 pIC50 = 8.1 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 464 6 1 5 6.3 CCCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2c(C(=O)O)c(C)nc3ccccc23)cc1 10.1021/jm031100t
15171413 106462 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
Compound was tested for in vitro inhibition of specific binding of [I-125]AII to Angiotensin II receptor, type 1 in guinea pig adrenal membrane preparationCompound was tested for in vitro inhibition of specific binding of [I-125]AII to Angiotensin II receptor, type 1 in guinea pig adrenal membrane preparation
ChEMBL 429 6 1 5 5.1 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2F)c2c(n1)CCCC2 10.1016/S0960-894X(01)80295-X
CHEMBL314982 106462 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
Compound was tested for in vitro inhibition of specific binding of [I-125]AII to Angiotensin II receptor, type 1 in guinea pig adrenal membrane preparationCompound was tested for in vitro inhibition of specific binding of [I-125]AII to Angiotensin II receptor, type 1 in guinea pig adrenal membrane preparation
ChEMBL 429 6 1 5 5.1 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2F)c2c(n1)CCCC2 10.1016/S0960-894X(01)80295-X
15818746 123538 0 None - 0 Rat 8.1 pIC50 = 8.1 Binding
Displacement of [125I]- Ang II from type 1 Angiotensin II receptorDisplacement of [125I]- Ang II from type 1 Angiotensin II receptor
ChEMBL 529 8 1 5 5.3 CCCC1=NC2(CCCC2)C(=O)N1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/S0960-894X(01)80526-6
CHEMBL36324 123538 0 None - 0 Rat 8.1 pIC50 = 8.1 Binding
Displacement of [125I]- Ang II from type 1 Angiotensin II receptorDisplacement of [125I]- Ang II from type 1 Angiotensin II receptor
ChEMBL 529 8 1 5 5.3 CCCC1=NC2(CCCC2)C(=O)N1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/S0960-894X(01)80526-6
44311567 102526 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
In vitro binding affinity of compound against Angiotensin II receptor, type 1In vitro binding affinity of compound against Angiotensin II receptor, type 1
ChEMBL 607 11 2 8 6.4 CCCc1nc(CN(Cc2ccccc2)C(=O)OC(C)(C)C)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80076-1
CHEMBL306922 102526 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
In vitro binding affinity of compound against Angiotensin II receptor, type 1In vitro binding affinity of compound against Angiotensin II receptor, type 1
ChEMBL 607 11 2 8 6.4 CCCc1nc(CN(Cc2ccccc2)C(=O)OC(C)(C)C)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(00)80076-1
14950509 82998 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1
ChEMBL 443 8 1 7 4.6 CCCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c(C(=O)OC)c(C)n1 10.1021/jm00061a016
CHEMBL21968 82998 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1Inhibition of [125I]angiotensin binding to a guinea pig adrenal membrane preparation which corresponds to Angiotensin II receptor, type 1
ChEMBL 443 8 1 7 4.6 CCCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c(C(=O)OC)c(C)n1 10.1021/jm00061a016
14951064 202026 0 None - 0 Rat 8.1 pIC50 = 8.1 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 461 10 1 9 2.8 CCCCc1nn(CC(=O)OCC)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a015
CHEMBL67764 202026 0 None - 0 Rat 8.1 pIC50 = 8.1 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 461 10 1 9 2.8 CCCCc1nn(CC(=O)OCC)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a015
70684239 75849 0 None - 0 Bovine 8.0 pIC50 = 8.0 Binding
Displacement of [125I]AngII from type 1 angiotensin 2 receptor in bovine adrenal cortexDisplacement of [125I]AngII from type 1 angiotensin 2 receptor in bovine adrenal cortex
ChEMBL 528 9 1 6 6.8 CCCCc1nc2ccc(C)cc2n1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)cc1 10.1016/j.bmc.2012.06.011
CHEMBL2058371 75849 0 None - 0 Bovine 8.0 pIC50 = 8.0 Binding
Displacement of [125I]AngII from type 1 angiotensin 2 receptor in bovine adrenal cortexDisplacement of [125I]AngII from type 1 angiotensin 2 receptor in bovine adrenal cortex
ChEMBL 528 9 1 6 6.8 CCCCc1nc2ccc(C)cc2n1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)cc1 10.1016/j.bmc.2012.06.011
10763626 168973 0 None - 0 Human 8.0 pIC50 = 8.0 Binding
Displacement of [125I][Sar1,Ile8]-AT-II from human recombinant AT1 receptor expressed in HEK293 cells after 120 mins by liquid scintillation countingDisplacement of [125I][Sar1,Ile8]-AT-II from human recombinant AT1 receptor expressed in HEK293 cells after 120 mins by liquid scintillation counting
ChEMBL 402 8 2 6 3.8 CCCCn1ncc(C(=O)O)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.ejmech.2011.05.056
CHEMBL443559 168973 0 None - 0 Human 8.0 pIC50 = 8.0 Binding
Displacement of [125I][Sar1,Ile8]-AT-II from human recombinant AT1 receptor expressed in HEK293 cells after 120 mins by liquid scintillation countingDisplacement of [125I][Sar1,Ile8]-AT-II from human recombinant AT1 receptor expressed in HEK293 cells after 120 mins by liquid scintillation counting
ChEMBL 402 8 2 6 3.8 CCCCn1ncc(C(=O)O)c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.ejmech.2011.05.056
10834137 9952 0 None - 0 Bovine 8.0 pIC50 = 8.0 Binding
In vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortexIn vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortex
ChEMBL 388 7 2 6 3.4 CCCc1ncc(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm950450f
CHEMBL115273 9952 0 None - 0 Bovine 8.0 pIC50 = 8.0 Binding
In vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortexIn vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortex
ChEMBL 388 7 2 6 3.4 CCCc1ncc(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm950450f
44277487 98802 0 None - 0 Rabbit 8.0 pIC50 = 8.0 Binding
Binding affinity against AT1 receptor in rabbit aortaBinding affinity against AT1 receptor in rabbit aorta
ChEMBL 604 8 0 9 5.5 Cn1nnnc1-c1ccccc1-c1ccc(Cn2cnc3ccc(N(Cc4ccccc4)C(=O)c4ccccn4)cc3c2=O)cc1 10.1016/0960-894X(95)00224-H
CHEMBL281891 98802 0 None - 0 Rabbit 8.0 pIC50 = 8.0 Binding
Binding affinity against AT1 receptor in rabbit aortaBinding affinity against AT1 receptor in rabbit aorta
ChEMBL 604 8 0 9 5.5 Cn1nnnc1-c1ccccc1-c1ccc(Cn2cnc3ccc(N(Cc4ccccc4)C(=O)c4ccccn4)cc3c2=O)cc1 10.1016/0960-894X(95)00224-H
10457566 201105 0 None - 0 Bovine 8.0 pIC50 = 8.0 Binding
Tested for binding affinity against angiotensin II receptor in bovine adrenal cortexTested for binding affinity against angiotensin II receptor in bovine adrenal cortex
ChEMBL 473 8 1 8 1.9 CCCc1cc(=O)n(CC(=O)N(C)C)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/0960-894X(95)00370-9
CHEMBL62269 201105 0 None - 0 Bovine 8.0 pIC50 = 8.0 Binding
Tested for binding affinity against angiotensin II receptor in bovine adrenal cortexTested for binding affinity against angiotensin II receptor in bovine adrenal cortex
ChEMBL 473 8 1 8 1.9 CCCc1cc(=O)n(CC(=O)N(C)C)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/0960-894X(95)00370-9
14956771 204620 0 None - 0 Rabbit 8.0 pIC50 = 8.0 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 482 8 1 9 3.8 CCCc1nn(-c2ccccc2[N+](=O)[O-])c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
CHEMBL87392 204620 0 None - 0 Rabbit 8.0 pIC50 = 8.0 Binding
Antagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albuminAntagonist activity at angiotensin 2 type-1 receptor in Oryctolagus cuniculus (rabbit) aorta in presence of bovine serum albumin
ChEMBL 482 8 1 9 3.8 CCCc1nn(-c2ccccc2[N+](=O)[O-])c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9197-5
44277938 100667 0 None - 0 Rabbit 8.0 pIC50 = 8.0 Binding
Binding affinity against AT1 receptor in rabbit aortaBinding affinity against AT1 receptor in rabbit aorta
ChEMBL 599 10 1 9 4.8 Cn1nnnc1-c1ccccc1-c1ccc(Cn2cnc3ccc(N(CCCC(=O)O)C(=O)c4ccccc4)cc3c2=O)cc1 10.1016/0960-894X(95)00224-H
CHEMBL29540 100667 0 None - 0 Rabbit 8.0 pIC50 = 8.0 Binding
Binding affinity against AT1 receptor in rabbit aortaBinding affinity against AT1 receptor in rabbit aorta
ChEMBL 599 10 1 9 4.8 Cn1nnnc1-c1ccccc1-c1ccc(Cn2cnc3ccc(N(CCCC(=O)O)C(=O)c4ccccc4)cc3c2=O)cc1 10.1016/0960-894X(95)00224-H
9912098 108040 0 None - 0 Bovine 8.0 pIC50 = 8.0 Binding
In vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortexIn vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortex
ChEMBL 460 9 3 7 4.0 CCCCc1nc(C(C)(C)O)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm950450f
CHEMBL320135 108040 0 None - 0 Bovine 8.0 pIC50 = 8.0 Binding
In vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortexIn vitro for inhibition of [125I]-angiotensin II (0.1 nM) binding to angiotensin II receptor type 1 in membrane fractions of bovine adrenal cortex
ChEMBL 460 9 3 7 4.0 CCCCc1nc(C(C)(C)O)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm950450f
19385680 98411 0 None - 0 Rabbit 8.0 pIC50 = 8.0 Binding
Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)
ChEMBL 487 10 1 6 5.8 CCCc1cc(Cn2c(CC)nc3c(C)cc(C)nc32)ccc1OC(C(=O)O)c1ccccc1OC 10.1016/0960-894X(95)00185-V
CHEMBL279103 98411 0 None - 0 Rabbit 8.0 pIC50 = 8.0 Binding
Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)
ChEMBL 487 10 1 6 5.8 CCCc1cc(Cn2c(CC)nc3c(C)cc(C)nc32)ccc1OC(C(=O)O)c1ccccc1OC 10.1016/0960-894X(95)00185-V
76330395 84973 0 None - 0 Human 8.0 pIC50 = 8.0 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 567 12 0 9 5.3 CCCCc1ncc(/C=C2/C(=O)N(CSCC)C(=O)N2Cc2csc(C)n2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
CHEMBL2263543 84973 0 None - 0 Human 8.0 pIC50 = 8.0 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 567 12 0 9 5.3 CCCCc1ncc(/C=C2/C(=O)N(CSCC)C(=O)N2Cc2csc(C)n2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
44277593 98939 0 None - 0 Human 8.0 pIC50 = 8.0 Binding
Binding affinity against AT1 receptor in human adrenal tissueBinding affinity against AT1 receptor in human adrenal tissue
ChEMBL 661 9 0 10 5.9 COC(=O)c1ccc(CN(C(=O)c2ccccc2)c2ccc3ncn(Cc4ccc(-c5ccccc5-c5nnnn5C)cc4)c(=O)c3c2)cc1 10.1016/0960-894X(95)00224-H
CHEMBL282778 98939 0 None - 0 Human 8.0 pIC50 = 8.0 Binding
Binding affinity against AT1 receptor in human adrenal tissueBinding affinity against AT1 receptor in human adrenal tissue
ChEMBL 661 9 0 10 5.9 COC(=O)c1ccc(CN(C(=O)c2ccccc2)c2ccc3ncn(Cc4ccc(-c5ccccc5-c5nnnn5C)cc4)c(=O)c3c2)cc1 10.1016/0960-894X(95)00224-H
44277567 100914 0 None - 0 Rabbit 8.0 pIC50 = 8.0 Binding
Binding affinity against AT1 receptor in rabbit aortaBinding affinity against AT1 receptor in rabbit aorta
ChEMBL 605 8 0 10 4.9 Cn1nnnc1-c1ccccc1-c1ccc(Cn2cnc3ccc(N(Cc4ccccn4)C(=O)c4ccncc4)cc3c2=O)cc1 10.1016/0960-894X(95)00224-H
CHEMBL29725 100914 0 None - 0 Rabbit 8.0 pIC50 = 8.0 Binding
Binding affinity against AT1 receptor in rabbit aortaBinding affinity against AT1 receptor in rabbit aorta
ChEMBL 605 8 0 10 4.9 Cn1nnnc1-c1ccccc1-c1ccc(Cn2cnc3ccc(N(Cc4ccccn4)C(=O)c4ccncc4)cc3c2=O)cc1 10.1016/0960-894X(95)00224-H
10482886 15324 0 None - 0 Human 8.0 pIC50 = 8.0 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 558 13 0 7 5.7 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2Cc2ccc(OC)cc2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
CHEMBL121718 15324 0 None - 0 Human 8.0 pIC50 = 8.0 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 558 13 0 7 5.7 CCCCc1ncc(/C=C2/C(=O)N(CCCC)C(=O)N2Cc2ccc(OC)cc2)n1Cc1ccc(C(=O)OC)cc1 10.1007/s00044-009-9205-9
70694738 75851 0 None - 0 Bovine 8.0 pIC50 = 8.0 Binding
Displacement of [125I]AngII from type 1 angiotensin 2 receptor in bovine adrenal cortexDisplacement of [125I]AngII from type 1 angiotensin 2 receptor in bovine adrenal cortex
ChEMBL 548 9 1 6 7.2 CCCCc1nc2ccc(Cl)cc2n1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)cc1 10.1016/j.bmc.2012.06.011
CHEMBL2058373 75851 0 None - 0 Bovine 8.0 pIC50 = 8.0 Binding
Displacement of [125I]AngII from type 1 angiotensin 2 receptor in bovine adrenal cortexDisplacement of [125I]AngII from type 1 angiotensin 2 receptor in bovine adrenal cortex
ChEMBL 548 9 1 6 7.2 CCCCc1nc2ccc(Cl)cc2n1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)cc1 10.1016/j.bmc.2012.06.011
17748251 92902 0 None - 1 Bovine 8.0 pIC50 = 8.0 Binding
Displacement of [125I]angiotensin-2 from bovine adrenal cortex AT1 receptorDisplacement of [125I]angiotensin-2 from bovine adrenal cortex AT1 receptor
ChEMBL 455 8 1 8 4.2 CCCCc1nc2cccc(C(=O)OC)c2n1Cc1ccc(-n2cccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2007.02.042
CHEMBL245444 92902 0 None - 1 Bovine 8.0 pIC50 = 8.0 Binding
Displacement of [125I]angiotensin-2 from bovine adrenal cortex AT1 receptorDisplacement of [125I]angiotensin-2 from bovine adrenal cortex AT1 receptor
ChEMBL 455 8 1 8 4.2 CCCCc1nc2cccc(C(=O)OC)c2n1Cc1ccc(-n2cccc2-c2nnn[nH]2)cc1 10.1016/j.bmcl.2007.02.042
1610 2305 89 None -1 4 Rat 8.0 pIC50 = 8.0 Binding
In vitro ability to displace the specific binding of [125I]-A II from receptors in rat liver membrane(type 1 receptor)In vitro ability to displace the specific binding of [125I]-A II from receptors in rat liver membrane(type 1 receptor)
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(96)00250-8
3941 2305 89 None -1 4 Rat 8.0 pIC50 = 8.0 Binding
In vitro ability to displace the specific binding of [125I]-A II from receptors in rat liver membrane(type 1 receptor)In vitro ability to displace the specific binding of [125I]-A II from receptors in rat liver membrane(type 1 receptor)
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(96)00250-8
3961 2305 89 None -1 4 Rat 8.0 pIC50 = 8.0 Binding
In vitro ability to displace the specific binding of [125I]-A II from receptors in rat liver membrane(type 1 receptor)In vitro ability to displace the specific binding of [125I]-A II from receptors in rat liver membrane(type 1 receptor)
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(96)00250-8
590 2305 89 None -1 4 Rat 8.0 pIC50 = 8.0 Binding
In vitro ability to displace the specific binding of [125I]-A II from receptors in rat liver membrane(type 1 receptor)In vitro ability to displace the specific binding of [125I]-A II from receptors in rat liver membrane(type 1 receptor)
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(96)00250-8
CHEMBL191 2305 89 None -1 4 Rat 8.0 pIC50 = 8.0 Binding
In vitro ability to displace the specific binding of [125I]-A II from receptors in rat liver membrane(type 1 receptor)In vitro ability to displace the specific binding of [125I]-A II from receptors in rat liver membrane(type 1 receptor)
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(96)00250-8
DB00678 2305 89 None -1 4 Rat 8.0 pIC50 = 8.0 Binding
In vitro ability to displace the specific binding of [125I]-A II from receptors in rat liver membrane(type 1 receptor)In vitro ability to displace the specific binding of [125I]-A II from receptors in rat liver membrane(type 1 receptor)
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(96)00250-8
14951069 202160 0 None - 0 Rat 8.0 pIC50 = 8.0 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 517 14 1 9 4.4 CCCCc1nn(CCCCCC(=O)OCC)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a015
CHEMBL68719 202160 0 None - 0 Rat 8.0 pIC50 = 8.0 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 517 14 1 9 4.4 CCCCc1nn(CCCCCC(=O)OCC)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a015
10006693 16847 0 None - 0 Human 8.0 pIC50 = 8 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 514 11 1 6 5.4 CCCCc1ncc(/C=C2\C(=O)NC(=O)N2CCCC)n1Cc1ccc(-c2ccccc2C(=O)OC)cc1 10.1007/s00044-009-9205-9
CHEMBL125454 16847 0 None - 0 Human 8.0 pIC50 = 8 Binding
Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)Antagonist activity at angiotensin 2 type-1 receptor (unknown origin)
ChEMBL 514 11 1 6 5.4 CCCCc1ncc(/C=C2\C(=O)NC(=O)N2CCCC)n1Cc1ccc(-c2ccccc2C(=O)OC)cc1 10.1007/s00044-009-9205-9
70686382 75848 0 None - 0 Bovine 8.0 pIC50 = 8 Binding
Displacement of [125I]AngII from type 1 angiotensin 2 receptor in bovine adrenal cortexDisplacement of [125I]AngII from type 1 angiotensin 2 receptor in bovine adrenal cortex
ChEMBL 514 9 1 6 6.5 CCCCc1nc2ccccc2n1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)cc1 10.1016/j.bmc.2012.06.011
CHEMBL2058370 75848 0 None - 0 Bovine 8.0 pIC50 = 8 Binding
Displacement of [125I]AngII from type 1 angiotensin 2 receptor in bovine adrenal cortexDisplacement of [125I]AngII from type 1 angiotensin 2 receptor in bovine adrenal cortex
ChEMBL 514 9 1 6 6.5 CCCCc1nc2ccccc2n1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)cc1 10.1016/j.bmc.2012.06.011
44294551 183811 0 None - 1 Bovine 7.1 pIC50 = 7.1 Binding
Ability to displace [125I]- labelled [Sar1,Ileu8] from angiotensin II receptor of bovine adrenal cortex membranesAbility to displace [125I]- labelled [Sar1,Ileu8] from angiotensin II receptor of bovine adrenal cortex membranes
ChEMBL 487 9 1 6 5.3 CCCC1(CC)CC(=O)N(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/C(=C/C(=O)OCC)C1 10.1016/S0960-894X(00)80474-6
CHEMBL48459 183811 0 None - 1 Bovine 7.1 pIC50 = 7.1 Binding
Ability to displace [125I]- labelled [Sar1,Ileu8] from angiotensin II receptor of bovine adrenal cortex membranesAbility to displace [125I]- labelled [Sar1,Ileu8] from angiotensin II receptor of bovine adrenal cortex membranes
ChEMBL 487 9 1 6 5.3 CCCC1(CC)CC(=O)N(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/C(=C/C(=O)OCC)C1 10.1016/S0960-894X(00)80474-6
76329883 84529 0 None - 0 Rabbit 7.1 pIC50 = 7.1 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 582 12 2 10 5.2 CCCCc1nnc(SCc2ccccc2C(=O)OC)n1Cc1ccc(NC(=O)c2ccccc2-c2nnn[nH]2)cc1 10.1007/s00044-011-9756-4
CHEMBL2237599 84529 0 None - 0 Rabbit 7.1 pIC50 = 7.1 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 582 12 2 10 5.2 CCCCc1nnc(SCc2ccccc2C(=O)OC)n1Cc1ccc(NC(=O)c2ccccc2-c2nnn[nH]2)cc1 10.1007/s00044-011-9756-4
127026338 136866 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptorDisplacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptor
ChEMBL 616 11 3 7 5.9 CCCc1nc2c(C)cc(C(=O)NCCc3ccccc3F)cc2n1Cc1ccc(-c2ccccc2C(=O)Nc2nnn[nH]2)cc1 10.1039/C5MD00169B
CHEMBL3753277 136866 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptorDisplacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptor
ChEMBL 616 11 3 7 5.9 CCCc1nc2c(C)cc(C(=O)NCCc3ccccc3F)cc2n1Cc1ccc(-c2ccccc2C(=O)Nc2nnn[nH]2)cc1 10.1039/C5MD00169B
10482404 47181 0 None - 0 Rabbit 7.1 pIC50 = 7.1 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 539 11 1 9 5.6 CCCCc1nnc(SCc2ccccc2C(=O)OC)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
CHEMBL154531 47181 0 None - 0 Rabbit 7.1 pIC50 = 7.1 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 539 11 1 9 5.6 CCCCc1nnc(SCc2ccccc2C(=O)OC)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
24828427 96371 0 None - 0 Rat 7.1 pIC50 = 7.1 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
ChEMBL 439 7 1 7 4.2 CCCCn1c2nc(C)ccc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm7011563
CHEMBL265208 96371 0 None - 0 Rat 7.1 pIC50 = 7.1 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
ChEMBL 439 7 1 7 4.2 CCCCn1c2nc(C)ccc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm7011563
9933179 18246 0 None - 0 Rat 7.1 pIC50 = 7.1 Binding
Inhibition of [125I]angiotensin II receptor specific binding to rat mesenteric arteriesInhibition of [125I]angiotensin II receptor specific binding to rat mesenteric arteries
ChEMBL 444 10 1 5 5.7 CCCCc1ncc(/C=C(\Cc2ccc(OC)s2)C(=O)O)n1Cc1ccccc1Cl 10.1021/jm00099a013
CHEMBL127194 18246 0 None - 0 Rat 7.1 pIC50 = 7.1 Binding
Inhibition of [125I]angiotensin II receptor specific binding to rat mesenteric arteriesInhibition of [125I]angiotensin II receptor specific binding to rat mesenteric arteries
ChEMBL 444 10 1 5 5.7 CCCCc1ncc(/C=C(\Cc2ccc(OC)s2)C(=O)O)n1Cc1ccccc1Cl 10.1021/jm00099a013
127036103 135973 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 531 9 2 4 7.2 CCCc1nc2c(C)cc(C(=O)N[C@H](C)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2015.09.010
CHEMBL3736257 135973 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 531 9 2 4 7.2 CCCc1nc2c(C)cc(C(=O)N[C@H](C)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2015.09.010
4286584 203228 7 None - 0 Bovine 6.1 pIC50 = 6.1 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 408 7 1 5 5.3 CCCCc1nc2ccccc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
CHEMBL7641 203228 7 None - 0 Bovine 6.1 pIC50 = 6.1 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 408 7 1 5 5.3 CCCCc1nc2ccccc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
44296954 101477 0 None - 0 Bovine 6.1 pIC50 = 6.1 Binding
In vitro binding affinity to angiotensin II receptor in bovine adrenal cortexIn vitro binding affinity to angiotensin II receptor in bovine adrenal cortex
ChEMBL 589 8 1 9 5.3 CCCCc1nc2ccc([C@H]3[C@@H]4C(=O)CCC[C@@H]4ON3C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80377-2
CHEMBL301325 101477 0 None - 0 Bovine 6.1 pIC50 = 6.1 Binding
In vitro binding affinity to angiotensin II receptor in bovine adrenal cortexIn vitro binding affinity to angiotensin II receptor in bovine adrenal cortex
ChEMBL 589 8 1 9 5.3 CCCCc1nc2ccc([C@H]3[C@@H]4C(=O)CCC[C@@H]4ON3C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80377-2
15662011 192746 0 None - 0 Bovine 5.1 pIC50 = 5.1 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 452 8 2 6 5.0 CCCCc1nc2ccc(C(=O)O)cc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
CHEMBL52497 192746 0 None - 0 Bovine 5.1 pIC50 = 5.1 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 452 8 2 6 5.0 CCCCc1nc2ccc(C(=O)O)cc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
10000596 20436 0 None - 0 Guinea pig 4.1 pIC50 = 4.1 Binding
In vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparationIn vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparation
ChEMBL 392 5 1 4 5.6 Cc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2ccccc2c1 10.1021/jm00100a007
CHEMBL130858 20436 0 None - 0 Guinea pig 4.1 pIC50 = 4.1 Binding
In vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparationIn vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparation
ChEMBL 392 5 1 4 5.6 Cc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2ccccc2c1 10.1021/jm00100a007
4286584 203228 7 None - 0 Bovine 6.0 pIC50 = 6.0 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 408 7 1 5 5.3 CCCCc1nc2ccccc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
CHEMBL7641 203228 7 None - 0 Bovine 6.0 pIC50 = 6.0 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 408 7 1 5 5.3 CCCCc1nc2ccccc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
15662011 192746 0 None - 0 Bovine 5.0 pIC50 = 5.0 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 452 8 2 6 5.0 CCCCc1nc2ccc(C(=O)O)cc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
CHEMBL52497 192746 0 None - 0 Bovine 5.0 pIC50 = 5.0 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 452 8 2 6 5.0 CCCCc1nc2ccc(C(=O)O)cc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
14951065 202139 0 None - 0 Rat 7.0 pIC50 = 7.0 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 433 9 2 8 2.4 CCCCc1nn(CC(=O)O)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a015
CHEMBL68582 202139 0 None - 0 Rat 7.0 pIC50 = 7.0 Binding
Inhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranesInhibition of [125I]angiotensin-II binding to the angiotensin II receptor type 1 in rat uterine membranes
ChEMBL 433 9 2 8 2.4 CCCCc1nn(CC(=O)O)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a015
19792137 84928 0 None - 0 Bovine 6.0 pIC50 = 6.0 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 494 9 1 7 5.8 CCCCc1nc2ccc(C)c(C(=O)OCC)c2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1007/s00044-009-9182-z
CHEMBL2261752 84928 0 None - 0 Bovine 6.0 pIC50 = 6.0 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 494 9 1 7 5.8 CCCCc1nc2ccc(C)c(C(=O)OCC)c2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1007/s00044-009-9182-z
19792185 188846 0 None - 0 Bovine 6.0 pIC50 = 6.0 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 438 8 1 6 5.3 CCCCc1nc2cc(OC)ccc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
CHEMBL51349 188846 0 None - 0 Bovine 6.0 pIC50 = 6.0 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 438 8 1 6 5.3 CCCCc1nc2cc(OC)ccc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
19792137 84928 0 None - 0 Bovine 6.0 pIC50 = 6.0 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 494 9 1 7 5.8 CCCCc1nc2ccc(C)c(C(=O)OCC)c2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1007/s00044-009-9182-z
CHEMBL2261752 84928 0 None - 0 Bovine 6.0 pIC50 = 6.0 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 494 9 1 7 5.8 CCCCc1nc2ccc(C)c(C(=O)OCC)c2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1007/s00044-009-9182-z
19792185 188846 0 None - 0 Bovine 6.0 pIC50 = 6.0 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 438 8 1 6 5.3 CCCCc1nc2cc(OC)ccc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
CHEMBL51349 188846 0 None - 0 Bovine 6.0 pIC50 = 6.0 Binding
Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneDisplacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membrane
ChEMBL 438 8 1 6 5.3 CCCCc1nc2cc(OC)ccc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1007/s00044-009-9182-z
44275059 99600 0 None - 0 Rabbit 7.0 pIC50 = 7.0 Binding
Ability to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitroAbility to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitro
ChEMBL 590 7 2 7 6.6 Cc1ccc2nc(-c3ccc(-c4ccccc4C(=O)O)cc3)n(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c(=O)c2c1 10.1016/S0960-894X(00)80335-2
CHEMBL287253 99600 0 None - 0 Rabbit 7.0 pIC50 = 7.0 Binding
Ability to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitroAbility to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitro
ChEMBL 590 7 2 7 6.6 Cc1ccc2nc(-c3ccc(-c4ccccc4C(=O)O)cc3)n(Cc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c(=O)c2c1 10.1016/S0960-894X(00)80335-2
44459584 96174 0 None - 0 Rabbit 7.0 pIC50 = 7.0 Binding
Binding affinity against Angiotensin II type 1 Receptor in rabbit aortic tissueBinding affinity against Angiotensin II type 1 Receptor in rabbit aortic tissue
ChEMBL 426 7 1 4 5.5 CCCCc1nc2ccc(C)cc2c(=O)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/S0960-894X(00)80334-0
CHEMBL26352 96174 0 None - 0 Rabbit 7.0 pIC50 = 7.0 Binding
Binding affinity against Angiotensin II type 1 Receptor in rabbit aortic tissueBinding affinity against Angiotensin II type 1 Receptor in rabbit aortic tissue
ChEMBL 426 7 1 4 5.5 CCCCc1nc2ccc(C)cc2c(=O)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/S0960-894X(00)80334-0
15698058 186530 0 None - 0 Rat 7.0 pIC50 = 7.0 Binding
Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.
ChEMBL 412 8 2 4 5.0 CCCCc1nc(Cl)c(C(=O)O)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00064a007
CHEMBL49170 186530 0 None - 0 Rat 7.0 pIC50 = 7.0 Binding
Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.
ChEMBL 412 8 2 4 5.0 CCCCc1nc(Cl)c(C(=O)O)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00064a007
127035545 135833 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Displacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysisDisplacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysis
ChEMBL 721 14 2 9 7.4 CCCc1nc2c(C)cc(C(=O)NCCc3ccc(OC)c(OC)c3)cc2n1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)cc1 10.1039/C4MD00499J
CHEMBL3734955 135833 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Displacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysisDisplacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysis
ChEMBL 721 14 2 9 7.4 CCCc1nc2c(C)cc(C(=O)NCCc3ccc(OC)c(OC)c3)cc2n1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)cc1 10.1039/C4MD00499J
70686380 75844 0 None - 0 Bovine 7.0 pIC50 = 7.0 Binding
Displacement of [125I]AngII from type 1 angiotensin 2 receptor in bovine adrenal cortexDisplacement of [125I]AngII from type 1 angiotensin 2 receptor in bovine adrenal cortex
ChEMBL 458 6 1 6 5.2 Cc1noc(NS(=O)(=O)c2ccccc2-c2ccc(Cn3cnc4ccccc43)cc2)c1C 10.1016/j.bmc.2012.06.011
CHEMBL2058366 75844 0 None - 0 Bovine 7.0 pIC50 = 7.0 Binding
Displacement of [125I]AngII from type 1 angiotensin 2 receptor in bovine adrenal cortexDisplacement of [125I]AngII from type 1 angiotensin 2 receptor in bovine adrenal cortex
ChEMBL 458 6 1 6 5.2 Cc1noc(NS(=O)(=O)c2ccccc2-c2ccc(Cn3cnc4ccccc43)cc2)c1C 10.1016/j.bmc.2012.06.011
44438900 147303 0 None - 1 Bovine 7.0 pIC50 = 7.0 Binding
Displacement of [125I]angiotensin-2 from bovine adrenal cortex AT1 receptorDisplacement of [125I]angiotensin-2 from bovine adrenal cortex AT1 receptor
ChEMBL 403 7 2 5 4.2 CCCc1nc2cccc(C(=O)O)c2n1Cc1ccc(-n2cccc2C(=O)O)cc1 10.1016/j.bmcl.2007.02.042
CHEMBL393305 147303 0 None - 1 Bovine 7.0 pIC50 = 7.0 Binding
Displacement of [125I]angiotensin-2 from bovine adrenal cortex AT1 receptorDisplacement of [125I]angiotensin-2 from bovine adrenal cortex AT1 receptor
ChEMBL 403 7 2 5 4.2 CCCc1nc2cccc(C(=O)O)c2n1Cc1ccc(-n2cccc2C(=O)O)cc1 10.1016/j.bmcl.2007.02.042
15171407 204263 0 None - 0 Guinea pig 7.0 pIC50 = 7.0 Binding
Compound was tested for in vitro inhibition of specific binding of [I-125]AII to Angiotensin II receptor, type 1 in guinea pig adrenal membrane preparationCompound was tested for in vitro inhibition of specific binding of [I-125]AII to Angiotensin II receptor, type 1 in guinea pig adrenal membrane preparation
ChEMBL 445 6 1 5 5.6 CCc1cc(OCc2ccc(-c3ccc(Cl)cc3-c3nn[nH]n3)cc2)c2c(n1)CCCC2 10.1016/S0960-894X(01)80295-X
CHEMBL84792 204263 0 None - 0 Guinea pig 7.0 pIC50 = 7.0 Binding
Compound was tested for in vitro inhibition of specific binding of [I-125]AII to Angiotensin II receptor, type 1 in guinea pig adrenal membrane preparationCompound was tested for in vitro inhibition of specific binding of [I-125]AII to Angiotensin II receptor, type 1 in guinea pig adrenal membrane preparation
ChEMBL 445 6 1 5 5.6 CCc1cc(OCc2ccc(-c3ccc(Cl)cc3-c3nn[nH]n3)cc2)c2c(n1)CCCC2 10.1016/S0960-894X(01)80295-X
127026337 137006 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Displacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptorDisplacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptor
ChEMBL 658 13 3 9 5.8 CCCc1nc2c(C)cc(C(=O)NCCc3ccc(OC)c(OC)c3)cc2n1Cc1ccc(-c2ccccc2C(=O)Nc2nnn[nH]2)cc1 10.1039/C5MD00169B
CHEMBL3754394 137006 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Displacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptorDisplacement of 125I-labelled Sar1-Ile8-angiotensin-2 from human AT1 receptor
ChEMBL 658 13 3 9 5.8 CCCc1nc2c(C)cc(C(=O)NCCc3ccc(OC)c(OC)c3)cc2n1Cc1ccc(-c2ccccc2C(=O)Nc2nnn[nH]2)cc1 10.1039/C5MD00169B
15287882 49459 0 None - 0 Rabbit 7.0 pIC50 = 7.0 Binding
Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)
ChEMBL 414 9 1 4 5.6 CCCCc1nc2ccccc2n1Cc1ccc(OC(C(=O)O)c2ccccc2)cc1 10.1016/0960-894X(95)00185-V
CHEMBL15670 49459 0 None - 0 Rabbit 7.0 pIC50 = 7.0 Binding
Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)
ChEMBL 414 9 1 4 5.6 CCCCc1nc2ccccc2n1Cc1ccc(OC(C(=O)O)c2ccccc2)cc1 10.1016/0960-894X(95)00185-V
127034875 135816 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 547 10 3 5 6.2 CCCc1nc2c(C)cc(C(=O)NC[C@H](O)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2015.09.010
CHEMBL3734819 135816 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Displacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 minsDisplacement of [125I]Sar1Ile8-Ang2 from human AT1 receptor expressed in CHO-K1 cell membranes after 180 mins
ChEMBL 547 10 3 5 6.2 CCCc1nc2c(C)cc(C(=O)NC[C@H](O)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2015.09.010
10389251 47379 0 None - 0 Rabbit 6.0 pIC50 = 6.0 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 454 9 2 5 5.3 CCCCc1nnc(-c2ccccc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
CHEMBL154708 47379 0 None - 0 Rabbit 6.0 pIC50 = 6.0 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 454 9 2 5 5.3 CCCCc1nnc(-c2ccccc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1007/s00044-011-9756-4
44293817 185785 0 None - 0 Rat 6.0 pIC50 = 6.0 Binding
Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.
ChEMBL 534 11 2 5 6.7 CCCCc1nc2c(C)cccc2n1Cc1ccc(NC(=O)[C@H](Cc2ccccc2)n2cccc2C(=O)O)cc1 10.1021/jm00064a007
CHEMBL48756 185785 0 None - 0 Rat 6.0 pIC50 = 6.0 Binding
Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.Binding affinity against angiotensin II receptor type 1 (AT1) from rat liver.
ChEMBL 534 11 2 5 6.7 CCCCc1nc2c(C)cccc2n1Cc1ccc(NC(=O)[C@H](Cc2ccccc2)n2cccc2C(=O)O)cc1 10.1021/jm00064a007
10389251 47379 0 None - 0 Rabbit 6.0 pIC50 = 6.0 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 454 9 2 5 5.3 CCCCc1nnc(-c2ccccc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
CHEMBL154708 47379 0 None - 0 Rabbit 6.0 pIC50 = 6.0 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 454 9 2 5 5.3 CCCCc1nnc(-c2ccccc2)n1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm00057a009
15654718 101786 0 None - 0 Bovine 6.0 pIC50 = 6.0 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 440 7 2 7 4.0 CCOc1nc2ccc(C(=O)O)cc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a016
CHEMBL303264 101786 0 None - 0 Bovine 6.0 pIC50 = 6.0 Binding
Inhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortexInhibition of specific binding of [125 I ] Angiotensin-II (0.2 nM) to bovine adrenal cortex
ChEMBL 440 7 2 7 4.0 CCOc1nc2ccc(C(=O)O)cc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00067a016
76319034 84523 0 None - 0 Rabbit 7.0 pIC50 = 7.0 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 572 12 2 8 6.4 CCCCCc1nnc(SCc2ccc(Cl)cc2)n1Cc1ccc(NC(=O)c2ccccc2-c2nnn[nH]2)cc1 10.1007/s00044-011-9756-4
CHEMBL2237593 84523 0 None - 0 Rabbit 7.0 pIC50 = 7.0 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 572 12 2 8 6.4 CCCCCc1nnc(SCc2ccc(Cl)cc2)n1Cc1ccc(NC(=O)c2ccccc2-c2nnn[nH]2)cc1 10.1007/s00044-011-9756-4
76322691 84526 0 None - 0 Rabbit 7.0 pIC50 = 7.0 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 554 12 2 9 5.4 CCCCc1nnc(SCc2cccc(OC)c2)n1Cc1ccc(NC(=O)c2ccccc2-c2nnn[nH]2)cc1 10.1007/s00044-011-9756-4
CHEMBL2237596 84526 0 None - 0 Rabbit 7.0 pIC50 = 7.0 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 554 12 2 9 5.4 CCCCc1nnc(SCc2cccc(OC)c2)n1Cc1ccc(NC(=O)c2ccccc2-c2nnn[nH]2)cc1 10.1007/s00044-011-9756-4
127034916 135864 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Displacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysisDisplacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysis
ChEMBL 668 12 2 8 6.6 CCCc1nc2c(C)cc(C(=O)NCCN3CCCCC3)cc2n1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)cc1 10.1039/C4MD00499J
CHEMBL3735302 135864 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Displacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysisDisplacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysis
ChEMBL 668 12 2 8 6.6 CCCc1nc2c(C)cc(C(=O)NCCN3CCCCC3)cc2n1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)cc1 10.1039/C4MD00499J
10052714 48908 0 None - 0 Rabbit 7.0 pIC50 = 7.0 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 529 11 1 7 6.9 CCCCCc1nnc(SCc2ccc(Cl)cc2)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
CHEMBL156243 48908 0 None - 0 Rabbit 7.0 pIC50 = 7.0 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 529 11 1 7 6.9 CCCCCc1nnc(SCc2ccc(Cl)cc2)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
10029367 50395 0 None - 0 Rabbit 7.0 pIC50 = 7.0 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 511 11 1 8 5.8 CCCCc1nnc(SCc2cccc(OC)c2)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
CHEMBL157565 50395 0 None - 0 Rabbit 7.0 pIC50 = 7.0 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 511 11 1 8 5.8 CCCCc1nnc(SCc2cccc(OC)c2)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
44296945 101513 0 None - 0 Bovine 7.0 pIC50 = 7.0 Binding
In vitro binding affinity to angiotensin II receptor in bovine adrenal cortexIn vitro binding affinity to angiotensin II receptor in bovine adrenal cortex
ChEMBL 653 10 1 10 5.7 CCCCc1nc2ccc([C@@H]3[C@@H]4C(=O)OC[C@@H]4ON3Cc3ccccc3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80377-2
CHEMBL301569 101513 0 None - 0 Bovine 7.0 pIC50 = 7.0 Binding
In vitro binding affinity to angiotensin II receptor in bovine adrenal cortexIn vitro binding affinity to angiotensin II receptor in bovine adrenal cortex
ChEMBL 653 10 1 10 5.7 CCCCc1nc2ccc([C@@H]3[C@@H]4C(=O)OC[C@@H]4ON3Cc3ccccc3)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80377-2
71521417 86387 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor afterDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after
ChEMBL 581 6 1 7 6.2 CCc1nc2ccn(Cc3ccccc3C(F)(F)F)c(=O)c2n1[C@H]1CCc2cc(-c3ccccc3-c3nnn[nH]3)ccc21 10.1016/j.bmcl.2012.11.088
CHEMBL2322446 86387 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor afterDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after
ChEMBL 581 6 1 7 6.2 CCc1nc2ccn(Cc3ccccc3C(F)(F)F)c(=O)c2n1[C@H]1CCc2cc(-c3ccccc3-c3nnn[nH]3)ccc21 10.1016/j.bmcl.2012.11.088
44274747 99197 0 None - 0 Rabbit 6.0 pIC50 = 6.0 Binding
Ability to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitroAbility to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitro
ChEMBL 621 8 2 9 6.2 O=C(O)c1ccccc1-c1ccc(-c2nc3ccc([N+](=O)[O-])cc3c(=O)n2Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)cc1 10.1016/S0960-894X(00)80335-2
CHEMBL284469 99197 0 None - 0 Rabbit 6.0 pIC50 = 6.0 Binding
Ability to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitroAbility to displace [125I]Sar1-Ile8-AII from angiotensin II receptor, type 1 in rabbit aorta in presence of 0.2% bovine serum albumin (BSA) was determined in vitro
ChEMBL 621 8 2 9 6.2 O=C(O)c1ccccc1-c1ccc(-c2nc3ccc([N+](=O)[O-])cc3c(=O)n2Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)cc1 10.1016/S0960-894X(00)80335-2
10475572 18413 0 None - 0 Rat 7.0 pIC50 = 7.0 Binding
Activity against high affinity Angiotensin II receptor, type 1 was measured from the ability to inhibit [125I]angiotensin II binding to rat uterine membrane.Activity against high affinity Angiotensin II receptor, type 1 was measured from the ability to inhibit [125I]angiotensin II binding to rat uterine membrane.
ChEMBL 391 10 1 4 5.4 CCCCc1nc(CCCC)n(Cc2ccc(-c3ccccc3C(=O)O)cc2)n1 10.1021/jm00053a013
CHEMBL12766 18413 0 None - 0 Rat 7.0 pIC50 = 7.0 Binding
Activity against high affinity Angiotensin II receptor, type 1 was measured from the ability to inhibit [125I]angiotensin II binding to rat uterine membrane.Activity against high affinity Angiotensin II receptor, type 1 was measured from the ability to inhibit [125I]angiotensin II binding to rat uterine membrane.
ChEMBL 391 10 1 4 5.4 CCCCc1nc(CCCC)n(Cc2ccc(-c3ccccc3C(=O)O)cc2)n1 10.1021/jm00053a013
127034917 135999 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Displacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysisDisplacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysis
ChEMBL 654 12 2 8 6.2 CCCc1nc2c(C)cc(C(=O)NCCN3CCCC3)cc2n1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)cc1 10.1039/C4MD00499J
CHEMBL3736507 135999 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Displacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysisDisplacement of 125I-labeled Sar1-Ile8-angiotensin II from human AT1 receptor incubated for 2 hrs by gamma counting analysis
ChEMBL 654 12 2 8 6.2 CCCc1nc2c(C)cc(C(=O)NCCN3CCCC3)cc2n1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)cc1 10.1039/C4MD00499J
1610 2305 89 None - 4 Bovine 7.0 pIC50 = 7.0 Binding
Displacement of [125I]AngII from type 1 angiotensin 2 receptor in bovine adrenal cortexDisplacement of [125I]AngII from type 1 angiotensin 2 receptor in bovine adrenal cortex
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmc.2012.06.011
3941 2305 89 None - 4 Bovine 7.0 pIC50 = 7.0 Binding
Displacement of [125I]AngII from type 1 angiotensin 2 receptor in bovine adrenal cortexDisplacement of [125I]AngII from type 1 angiotensin 2 receptor in bovine adrenal cortex
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmc.2012.06.011
3961 2305 89 None - 4 Bovine 7.0 pIC50 = 7.0 Binding
Displacement of [125I]AngII from type 1 angiotensin 2 receptor in bovine adrenal cortexDisplacement of [125I]AngII from type 1 angiotensin 2 receptor in bovine adrenal cortex
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmc.2012.06.011
590 2305 89 None - 4 Bovine 7.0 pIC50 = 7.0 Binding
Displacement of [125I]AngII from type 1 angiotensin 2 receptor in bovine adrenal cortexDisplacement of [125I]AngII from type 1 angiotensin 2 receptor in bovine adrenal cortex
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmc.2012.06.011
CHEMBL191 2305 89 None - 4 Bovine 7.0 pIC50 = 7.0 Binding
Displacement of [125I]AngII from type 1 angiotensin 2 receptor in bovine adrenal cortexDisplacement of [125I]AngII from type 1 angiotensin 2 receptor in bovine adrenal cortex
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmc.2012.06.011
DB00678 2305 89 None - 4 Bovine 7.0 pIC50 = 7.0 Binding
Displacement of [125I]AngII from type 1 angiotensin 2 receptor in bovine adrenal cortexDisplacement of [125I]AngII from type 1 angiotensin 2 receptor in bovine adrenal cortex
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmc.2012.06.011
24828568 159046 0 None - 0 Rat 7.0 pIC50 = 7.0 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
ChEMBL 424 7 1 5 4.8 CCCCC1c2ncccc2C(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm7011563
CHEMBL410325 159046 0 None - 0 Rat 7.0 pIC50 = 7.0 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
ChEMBL 424 7 1 5 4.8 CCCCC1c2ncccc2C(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm7011563
44270367 162660 0 None - 0 Rabbit 7.0 pIC50 = 7.0 Binding
Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)
ChEMBL 505 9 1 5 6.5 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(OC(C(=O)O)c2ccccc2)c(Cc2ccccc2)c1 10.1016/0960-894X(95)00185-V
CHEMBL418354 162660 0 None - 0 Rabbit 7.0 pIC50 = 7.0 Binding
Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)
ChEMBL 505 9 1 5 6.5 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(OC(C(=O)O)c2ccccc2)c(Cc2ccccc2)c1 10.1016/0960-894X(95)00185-V
44342001 9831 0 None - 0 Rat 6.0 pIC50 = 6.0 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 477 9 2 5 3.9 CCCCC1=NC2(CCN(CC(=O)O)CC2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00074a018
CHEMBL114590 9831 0 None - 0 Rat 6.0 pIC50 = 6.0 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
ChEMBL 477 9 2 5 3.9 CCCCC1=NC2(CCN(CC(=O)O)CC2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00074a018
4286584 203228 7 None - 0 Rabbit 7.0 pIC50 = 7.0 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 408 7 1 5 5.3 CCCCc1nc2ccccc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
CHEMBL7641 203228 7 None - 0 Rabbit 7.0 pIC50 = 7.0 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 408 7 1 5 5.3 CCCCc1nc2ccccc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
19008901 62299 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation countingDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation counting
ChEMBL 435 4 1 6 5.0 CCc1nc2c(C)cc(C)nc2n1C1CCc2cc(-c3ccccc3-c3nn[nH]n3)ccc21 10.1021/jm200409s
CHEMBL178380 62299 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation countingDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation counting
ChEMBL 435 4 1 6 5.0 CCc1nc2c(C)cc(C)nc2n1C1CCc2cc(-c3ccccc3-c3nn[nH]n3)ccc21 10.1021/jm200409s
70688503 75961 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Displacement of [125I]Sar1Ile8-Ang2 from angiotensin AT1 receptor after 180 mins by gamma countingDisplacement of [125I]Sar1Ile8-Ang2 from angiotensin AT1 receptor after 180 mins by gamma counting
ChEMBL 601 11 2 8 6.1 CCCc1nc2c(C)cc(C(=O)NCc3ccc(OC)c(OC)c3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmc.2012.05.056
CHEMBL2058858 75961 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Displacement of [125I]Sar1Ile8-Ang2 from angiotensin AT1 receptor after 180 mins by gamma countingDisplacement of [125I]Sar1Ile8-Ang2 from angiotensin AT1 receptor after 180 mins by gamma counting
ChEMBL 601 11 2 8 6.1 CCCc1nc2c(C)cc(C(=O)NCc3ccc(OC)c(OC)c3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmc.2012.05.056
10005096 18695 0 None - 0 Guinea pig 6.0 pIC50 = 6.0 Binding
In vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparationIn vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparation
ChEMBL 437 7 1 6 5.2 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2cccc(OC)c2n1 10.1021/jm00100a007
CHEMBL128397 18695 0 None - 0 Guinea pig 6.0 pIC50 = 6.0 Binding
In vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparationIn vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparation
ChEMBL 437 7 1 6 5.2 CCc1cc(OCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2cccc(OC)c2n1 10.1021/jm00100a007
76317815 104757 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Antagonist activity at human AT1 receptor expressed in CHO cells measured after overnight incubation by luciferase reporter gene assayAntagonist activity at human AT1 receptor expressed in CHO cells measured after overnight incubation by luciferase reporter gene assay
ChEMBL 555 10 2 6 6.6 CCCc1nn2ccc(C(=O)NC(CC)c3ccccc3)cc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.bmcl.2014.01.004
CHEMBL3115245 104757 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Antagonist activity at human AT1 receptor expressed in CHO cells measured after overnight incubation by luciferase reporter gene assayAntagonist activity at human AT1 receptor expressed in CHO cells measured after overnight incubation by luciferase reporter gene assay
ChEMBL 555 10 2 6 6.6 CCCc1nn2ccc(C(=O)NC(CC)c3ccccc3)cc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.bmcl.2014.01.004
76311801 84522 0 None - 0 Rabbit 7.0 pIC50 = 7.0 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 544 10 2 8 5.7 CCCc1nnc(SCc2ccc(Cl)cc2)n1Cc1ccc(NC(=O)c2ccccc2-c2nnn[nH]2)cc1 10.1007/s00044-011-9756-4
CHEMBL2237592 84522 0 None - 0 Rabbit 7.0 pIC50 = 7.0 Binding
Antagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aortaAntagonist activity at AT1 receptor in Oryctolagus cuniculus (rabbit) aorta
ChEMBL 544 10 2 8 5.7 CCCc1nnc(SCc2ccc(Cl)cc2)n1Cc1ccc(NC(=O)c2ccccc2-c2nnn[nH]2)cc1 10.1007/s00044-011-9756-4
19976416 204446 0 None - 0 Rat 7.0 pIC50 = 7.0 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 416 10 1 7 4.3 CCCCc1nc(CCCC)n(Cc2ccc(-c3ncccc3-c3nn[nH]n3)cc2)n1 10.1021/jm031100t
CHEMBL86344 204446 0 None - 0 Rat 7.0 pIC50 = 7.0 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
ChEMBL 416 10 1 7 4.3 CCCCc1nc(CCCC)n(Cc2ccc(-c3ncccc3-c3nn[nH]n3)cc2)n1 10.1021/jm031100t
10032367 53689 0 None - 0 Rabbit 7.0 pIC50 = 7.0 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 501 9 1 7 6.1 CCCc1nnc(SCc2ccc(Cl)cc2)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
CHEMBL160573 53689 0 None - 0 Rabbit 7.0 pIC50 = 7.0 Binding
Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1Displacement of [125I]-Sar1-Ile8-A II at the rabbit aorta angiotensin II receptor, type 1
ChEMBL 501 9 1 7 6.1 CCCc1nnc(SCc2ccc(Cl)cc2)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00057a009
22850888 192898 0 None - 0 Bovine 7.0 pIC50 = 7.0 Binding
In vitro binding affinity to angiotensin II receptor in bovine adrenal cortexIn vitro binding affinity to angiotensin II receptor in bovine adrenal cortex
ChEMBL 561 8 1 8 5.7 CCCCc1nc2ccc([C@H]3[C@@H]4CCC[C@@H]4ON3C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80377-2
CHEMBL52791 192898 0 None - 0 Bovine 7.0 pIC50 = 7.0 Binding
In vitro binding affinity to angiotensin II receptor in bovine adrenal cortexIn vitro binding affinity to angiotensin II receptor in bovine adrenal cortex
ChEMBL 561 8 1 8 5.7 CCCCc1nc2ccc([C@H]3[C@@H]4CCC[C@@H]4ON3C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80377-2
9894404 192993 0 None - 0 Bovine 7.0 pIC50 = 7.0 Binding
In vitro binding affinity to angiotensin II receptor in bovine adrenal cortexIn vitro binding affinity to angiotensin II receptor in bovine adrenal cortex
ChEMBL 575 8 1 9 4.9 CCCCc1nc2ccc([C@H]3[C@@H]4C(=O)CC[C@@H]4ON3C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80377-2
CHEMBL53174 192993 0 None - 0 Bovine 7.0 pIC50 = 7.0 Binding
In vitro binding affinity to angiotensin II receptor in bovine adrenal cortexIn vitro binding affinity to angiotensin II receptor in bovine adrenal cortex
ChEMBL 575 8 1 9 4.9 CCCCc1nc2ccc([C@H]3[C@@H]4C(=O)CC[C@@H]4ON3C)cc2c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)80377-2
132387 161772 18 None 9 3 Rabbit 10.3 pKd = 10.3 Binding
pA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic ringspA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic rings
ChEMBL 414 8 2 6 4.0 CCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1ncccc1C(=O)O 10.1016/S0960-894X(01)81142-2
CHEMBL416477 161772 18 None 9 3 Rabbit 10.3 pKd = 10.3 Binding
pA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic ringspA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic rings
ChEMBL 414 8 2 6 4.0 CCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1ncccc1C(=O)O 10.1016/S0960-894X(01)81142-2
132387 161772 18 None 9 3 Rabbit 10.1 pKd = 10.1 Binding
Compound was evaluated for in vitro potency against angiotensin II receptor, type 1 in isolated rabbit aorta; value ranges from 10.1-10.7Compound was evaluated for in vitro potency against angiotensin II receptor, type 1 in isolated rabbit aorta; value ranges from 10.1-10.7
ChEMBL 414 8 2 6 4.0 CCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1ncccc1C(=O)O 10.1021/jm00098a018
CHEMBL416477 161772 18 None 9 3 Rabbit 10.1 pKd = 10.1 Binding
Compound was evaluated for in vitro potency against angiotensin II receptor, type 1 in isolated rabbit aorta; value ranges from 10.1-10.7Compound was evaluated for in vitro potency against angiotensin II receptor, type 1 in isolated rabbit aorta; value ranges from 10.1-10.7
ChEMBL 414 8 2 6 4.0 CCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1ncccc1C(=O)O 10.1021/jm00098a018
192314 113989 26 None 15 3 Rabbit 9.9 pKd = 9.9 Binding
Compound was evaluated for in vitro potency against angiotensin II receptor, type 1 in isolated rabbit aortaCompound was evaluated for in vitro potency against angiotensin II receptor, type 1 in isolated rabbit aorta
ChEMBL 429 9 2 7 3.8 CCCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1ncncc1C(=O)O 10.1021/jm00098a018
CHEMBL1237157 113989 26 None 15 3 Rabbit 9.9 pKd = 9.9 Binding
Compound was evaluated for in vitro potency against angiotensin II receptor, type 1 in isolated rabbit aortaCompound was evaluated for in vitro potency against angiotensin II receptor, type 1 in isolated rabbit aorta
ChEMBL 429 9 2 7 3.8 CCCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1ncncc1C(=O)O 10.1021/jm00098a018
CHEMBL333534 113989 26 None 15 3 Rabbit 9.9 pKd = 9.9 Binding
Compound was evaluated for in vitro potency against angiotensin II receptor, type 1 in isolated rabbit aortaCompound was evaluated for in vitro potency against angiotensin II receptor, type 1 in isolated rabbit aorta
ChEMBL 429 9 2 7 3.8 CCCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1ncncc1C(=O)O 10.1021/jm00098a018
15657904 186889 4 None - 1 Rabbit 9.9 pKd = 9.9 Binding
pA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic ringspA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic rings
ChEMBL 415 8 2 7 3.4 CCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1ncncc1C(=O)O 10.1016/S0960-894X(01)81142-2
CHEMBL49410 186889 4 None - 1 Rabbit 9.9 pKd = 9.9 Binding
pA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic ringspA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic rings
ChEMBL 415 8 2 7 3.4 CCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1ncncc1C(=O)O 10.1016/S0960-894X(01)81142-2
10432780 163949 0 None 10 3 Rabbit 9.6 pKd = 9.6 Binding
Compound was evaluated for in vitro potency against angiotensin II receptor, type 1 in isolated rabbit aortaCompound was evaluated for in vitro potency against angiotensin II receptor, type 1 in isolated rabbit aorta
ChEMBL 429 8 2 7 3.7 CCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1nc(C)ncc1C(=O)O 10.1021/jm00098a018
CHEMBL421473 163949 0 None 10 3 Rabbit 9.6 pKd = 9.6 Binding
Compound was evaluated for in vitro potency against angiotensin II receptor, type 1 in isolated rabbit aortaCompound was evaluated for in vitro potency against angiotensin II receptor, type 1 in isolated rabbit aorta
ChEMBL 429 8 2 7 3.7 CCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1nc(C)ncc1C(=O)O 10.1021/jm00098a018
15657949 16719 0 None - 1 Rabbit 9.5 pKd = 9.5 Binding
Compound was evaluated for in vitro potency against angiotensin II receptor, type 1 in isolated rabbit aortaCompound was evaluated for in vitro potency against angiotensin II receptor, type 1 in isolated rabbit aorta
ChEMBL 428 9 2 6 4.4 CCCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1ncccc1C(=O)O 10.1021/jm00098a018
CHEMBL125218 16719 0 None - 1 Rabbit 9.5 pKd = 9.5 Binding
Compound was evaluated for in vitro potency against angiotensin II receptor, type 1 in isolated rabbit aortaCompound was evaluated for in vitro potency against angiotensin II receptor, type 1 in isolated rabbit aorta
ChEMBL 428 9 2 6 4.4 CCCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1ncccc1C(=O)O 10.1021/jm00098a018
CHEMBL5075338 212587 0 None - 1 Human 9.3 pKd = 9.3 Binding
Binding affinity to AT1R (unknown origin) expressed in Escherichia coli strain BL 21 (DE3) incubated for 20 mins by SDS PAGE analysisBinding affinity to AT1R (unknown origin) expressed in Escherichia coli strain BL 21 (DE3) incubated for 20 mins by SDS PAGE analysis
ChEMBL None None None CCOC(=O)[C@@H](Cc1ccc(F)cc1)NC(=O)[C@@H](CC1CCCCC1)NC(=O)[C@@H](C)NC(=O)/C=C/c1ccc(O)c(O)c1 10.1021/acs.jmedchem.1c00123
CHEMBL266899 208952 0 None - 1 Human 9.3 pKd = 9.3 Binding
Binding affinity was determined against Angiotensin II receptor, type 1Binding affinity was determined against Angiotensin II receptor, type 1
ChEMBL None None None CNCC(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)N1CCC[C@@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O)C(C)C)C(C)C 10.1021/jm9507744
127030943 138652 0 None - 1 Human 9.0 pKd = 9.0 Binding
Binding affinity to human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation countingBinding affinity to human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation counting
ChEMBL 1216 35 15 14 -0.7 CCC(=O)NCCCCNC(=O)/N=C(\N)NCCC[C@H](NC(=O)[C@@H](N)CC(=O)O)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O)[C@@H](C)CC)C(C)C 10.1021/acs.jmedchem.5b01495
CHEMBL3787243 138652 0 None - 1 Human 9.0 pKd = 9.0 Binding
Binding affinity to human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation countingBinding affinity to human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation counting
ChEMBL 1216 35 15 14 -0.7 CCC(=O)NCCCCNC(=O)/N=C(\N)NCCC[C@H](NC(=O)[C@@H](N)CC(=O)O)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O)[C@@H](C)CC)C(C)C 10.1021/acs.jmedchem.5b01495
CHEMBL3787375 138652 0 None - 1 Human 9.0 pKd = 9.0 Binding
Binding affinity to human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation countingBinding affinity to human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation counting
ChEMBL 1216 35 15 14 -0.7 CCC(=O)NCCCCNC(=O)/N=C(\N)NCCC[C@H](NC(=O)[C@@H](N)CC(=O)O)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O)[C@@H](C)CC)C(C)C 10.1021/acs.jmedchem.5b01495
CHEMBL3787700 138652 0 None - 1 Human 9.0 pKd = 9.0 Binding
Binding affinity to human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation countingBinding affinity to human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation counting
ChEMBL 1216 35 15 14 -0.7 CCC(=O)NCCCCNC(=O)/N=C(\N)NCCC[C@H](NC(=O)[C@@H](N)CC(=O)O)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O)[C@@H](C)CC)C(C)C 10.1021/acs.jmedchem.5b01495
44348262 16152 0 None - 1 Rabbit 9.0 pKd = 9 Binding
In vitro binding affinity against Angiotensin II receptor in rabbit aorta ringsIn vitro binding affinity against Angiotensin II receptor in rabbit aorta rings
ChEMBL 469 6 1 6 4.0 CCOC(=O)/C=C1\C2C3CCC(C3)C2C(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81127-6
CHEMBL122891 16152 0 None - 1 Rabbit 9.0 pKd = 9 Binding
In vitro binding affinity against Angiotensin II receptor in rabbit aorta ringsIn vitro binding affinity against Angiotensin II receptor in rabbit aorta rings
ChEMBL 469 6 1 6 4.0 CCOC(=O)/C=C1\C2C3CCC(C3)C2C(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81127-6
9912059 184764 0 None - 1 Rabbit 9.0 pKd = 9 Binding
In vitro binding affinity against Angiotensin II receptor in rabbit aorta ringsIn vitro binding affinity against Angiotensin II receptor in rabbit aorta rings
ChEMBL 459 7 1 6 4.5 CCOC(=O)/C=C1\CC(C)(CC)CC(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81127-6
CHEMBL48602 184764 0 None - 1 Rabbit 9.0 pKd = 9 Binding
In vitro binding affinity against Angiotensin II receptor in rabbit aorta ringsIn vitro binding affinity against Angiotensin II receptor in rabbit aorta rings
ChEMBL 459 7 1 6 4.5 CCOC(=O)/C=C1\CC(C)(CC)CC(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81127-6
10745817 118857 0 None - 1 Rat 8.9 pKd = 8.9 Binding
The compound was evaluated for the direct binding of tritiated compound to the recombinant Angiotensin II receptor, type 1 stably expressed in CHO cells.The compound was evaluated for the direct binding of tritiated compound to the recombinant Angiotensin II receptor, type 1 stably expressed in CHO cells.
ChEMBL 580 12 3 7 5.4 CCCCc1ncc(CNc2ccccc2C(=O)O)n1Cc1ccc(C(=O)NS(=O)(=O)c2ccccc2Cl)cc1 10.1021/jm991050l
CHEMBL2111973 118857 0 None - 1 Rat 8.9 pKd = 8.9 Binding
The compound was evaluated for the direct binding of tritiated compound to the recombinant Angiotensin II receptor, type 1 stably expressed in CHO cells.The compound was evaluated for the direct binding of tritiated compound to the recombinant Angiotensin II receptor, type 1 stably expressed in CHO cells.
ChEMBL 580 12 3 7 5.4 CCCCc1ncc(CNc2ccccc2C(=O)O)n1Cc1ccc(C(=O)NS(=O)(=O)c2ccccc2Cl)cc1 10.1021/jm991050l
CHEMBL344464 118857 0 None - 1 Rat 8.9 pKd = 8.9 Binding
The compound was evaluated for the direct binding of tritiated compound to the recombinant Angiotensin II receptor, type 1 stably expressed in CHO cells.The compound was evaluated for the direct binding of tritiated compound to the recombinant Angiotensin II receptor, type 1 stably expressed in CHO cells.
ChEMBL 580 12 3 7 5.4 CCCCc1ncc(CNc2ccccc2C(=O)O)n1Cc1ccc(C(=O)NS(=O)(=O)c2ccccc2Cl)cc1 10.1021/jm991050l
CHEMBL428475 211689 0 None - 1 Bovine 8.9 pKd = 8.9 Binding
Dissociation constant for [125 I] Ang binding to type 1 Angiotensin II receptor of bovine adrenocortical membranesDissociation constant for [125 I] Ang binding to type 1 Angiotensin II receptor of bovine adrenocortical membranes
ChEMBL None None None CNCC(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)N1CCC[C@H]1C(=O)N[C@H](Cc1ccccc1)C(=O)O)C(C)C)C(C)C 10.1021/jm9608669
10094936 16642 0 None 9 3 Rabbit 8.8 pKd = 8.8 Binding
Compound was evaluated for in vitro potency against angiotensin II receptor, type 1 in isolated rabbit aortaCompound was evaluated for in vitro potency against angiotensin II receptor, type 1 in isolated rabbit aorta
ChEMBL 443 9 2 7 4.1 CCCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1nc(C)ncc1C(=O)O 10.1021/jm00098a018
CHEMBL1237156 16642 0 None 9 3 Rabbit 8.8 pKd = 8.8 Binding
Compound was evaluated for in vitro potency against angiotensin II receptor, type 1 in isolated rabbit aortaCompound was evaluated for in vitro potency against angiotensin II receptor, type 1 in isolated rabbit aorta
ChEMBL 443 9 2 7 4.1 CCCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1nc(C)ncc1C(=O)O 10.1021/jm00098a018
CHEMBL124772 16642 0 None 9 3 Rabbit 8.8 pKd = 8.8 Binding
Compound was evaluated for in vitro potency against angiotensin II receptor, type 1 in isolated rabbit aortaCompound was evaluated for in vitro potency against angiotensin II receptor, type 1 in isolated rabbit aorta
ChEMBL 443 9 2 7 4.1 CCCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1nc(C)ncc1C(=O)O 10.1021/jm00098a018
1610 2305 89 None -1 4 Rabbit 8.8 pKd = 8.8 Binding
In vitro binding affinity against Angiotensin II receptor in rabbit aorta ringsIn vitro binding affinity against Angiotensin II receptor in rabbit aorta rings
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(01)81127-6
3941 2305 89 None -1 4 Rabbit 8.8 pKd = 8.8 Binding
In vitro binding affinity against Angiotensin II receptor in rabbit aorta ringsIn vitro binding affinity against Angiotensin II receptor in rabbit aorta rings
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(01)81127-6
3961 2305 89 None -1 4 Rabbit 8.8 pKd = 8.8 Binding
In vitro binding affinity against Angiotensin II receptor in rabbit aorta ringsIn vitro binding affinity against Angiotensin II receptor in rabbit aorta rings
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(01)81127-6
590 2305 89 None -1 4 Rabbit 8.8 pKd = 8.8 Binding
In vitro binding affinity against Angiotensin II receptor in rabbit aorta ringsIn vitro binding affinity against Angiotensin II receptor in rabbit aorta rings
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(01)81127-6
CHEMBL191 2305 89 None -1 4 Rabbit 8.8 pKd = 8.8 Binding
In vitro binding affinity against Angiotensin II receptor in rabbit aorta ringsIn vitro binding affinity against Angiotensin II receptor in rabbit aorta rings
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(01)81127-6
DB00678 2305 89 None -1 4 Rabbit 8.8 pKd = 8.8 Binding
In vitro binding affinity against Angiotensin II receptor in rabbit aorta ringsIn vitro binding affinity against Angiotensin II receptor in rabbit aorta rings
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(01)81127-6
CHEMBL216830 207587 26 None - 1 Human 8.8 pKd = 8.8 Binding
Binding affinity to human AT1 receptorBinding affinity to human AT1 receptor
ChEMBL None None None None 10.1021/acs.jmedchem.8b00435
127034873 135913 0 None - 1 Rabbit 8.8 pKd = 8.8 Binding
Antagonist activity against AT1 receptor in Japanese White rabbit aortic strips assessed as reduction in angiotension-2-induced contractile response after 60 mins by Schild's plot analysisAntagonist activity against AT1 receptor in Japanese White rabbit aortic strips assessed as reduction in angiotension-2-induced contractile response after 60 mins by Schild's plot analysis
ChEMBL 569 10 2 6 6.7 CCCc1nc2c(C)cc(C(=O)NC[C@H](C)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.ejmech.2015.09.010
CHEMBL3735744 135913 0 None - 1 Rabbit 8.8 pKd = 8.8 Binding
Antagonist activity against AT1 receptor in Japanese White rabbit aortic strips assessed as reduction in angiotension-2-induced contractile response after 60 mins by Schild's plot analysisAntagonist activity against AT1 receptor in Japanese White rabbit aortic strips assessed as reduction in angiotension-2-induced contractile response after 60 mins by Schild's plot analysis
ChEMBL 569 10 2 6 6.7 CCCc1nc2c(C)cc(C(=O)NC[C@H](C)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.ejmech.2015.09.010
127035715 135904 0 None - 1 Rabbit 8.7 pKd = 8.7 Binding
Antagonist activity against AT1 receptor in Japanese White rabbit aortic strips assessed as reduction in angiotension-2-induced contractile response after 60 mins by Schild's plot analysisAntagonist activity against AT1 receptor in Japanese White rabbit aortic strips assessed as reduction in angiotension-2-induced contractile response after 60 mins by Schild's plot analysis
ChEMBL 545 10 2 4 7.2 CCCc1nc2c(C)cc(C(=O)NC[C@@H](C)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2015.09.010
CHEMBL3735652 135904 0 None - 1 Rabbit 8.7 pKd = 8.7 Binding
Antagonist activity against AT1 receptor in Japanese White rabbit aortic strips assessed as reduction in angiotension-2-induced contractile response after 60 mins by Schild's plot analysisAntagonist activity against AT1 receptor in Japanese White rabbit aortic strips assessed as reduction in angiotension-2-induced contractile response after 60 mins by Schild's plot analysis
ChEMBL 545 10 2 4 7.2 CCCc1nc2c(C)cc(C(=O)NC[C@@H](C)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2015.09.010
10408684 168595 0 None - 1 Rabbit 8.7 pKd = 8.7 Binding
Compound was evaluated for in vitro potency against angiotensin II receptor, type 1 in isolated rabbit aorta; value ranges from 8.70-8.83Compound was evaluated for in vitro potency against angiotensin II receptor, type 1 in isolated rabbit aorta; value ranges from 8.70-8.83
ChEMBL 400 7 2 6 3.7 CCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1ncccc1C(=O)O 10.1021/jm00098a018
CHEMBL440521 168595 0 None - 1 Rabbit 8.7 pKd = 8.7 Binding
Compound was evaluated for in vitro potency against angiotensin II receptor, type 1 in isolated rabbit aorta; value ranges from 8.70-8.83Compound was evaluated for in vitro potency against angiotensin II receptor, type 1 in isolated rabbit aorta; value ranges from 8.70-8.83
ChEMBL 400 7 2 6 3.7 CCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1ncccc1C(=O)O 10.1021/jm00098a018
44348285 16240 0 None - 1 Rabbit 8.0 pKd = 8 Binding
In vitro binding affinity against Angiotensin II receptor in rabbit aorta ringsIn vitro binding affinity against Angiotensin II receptor in rabbit aorta rings
ChEMBL 481 6 1 6 4.2 CCOC(=O)/C=C1\C2C3C=CC(CC3)C2C(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81127-6
CHEMBL123208 16240 0 None - 1 Rabbit 8.0 pKd = 8 Binding
In vitro binding affinity against Angiotensin II receptor in rabbit aorta ringsIn vitro binding affinity against Angiotensin II receptor in rabbit aorta rings
ChEMBL 481 6 1 6 4.2 CCOC(=O)/C=C1\C2C3C=CC(CC3)C2C(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81127-6
44294528 101555 0 None - 1 Rabbit 8.0 pKd = 8.0 Binding
pA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic ringspA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic rings
ChEMBL 440 8 1 9 3.4 CCCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1ncnc2c1nnn2C 10.1016/S0960-894X(01)81142-2
CHEMBL301819 101555 0 None - 1 Rabbit 8.0 pKd = 8.0 Binding
pA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic ringspA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic rings
ChEMBL 440 8 1 9 3.4 CCCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1ncnc2c1nnn2C 10.1016/S0960-894X(01)81142-2
44294996 189191 0 None - 1 Rabbit 7.0 pKd = 7 Binding
In vitro binding affinity against Angiotensin II receptor in rabbit aorta ringsIn vitro binding affinity against Angiotensin II receptor in rabbit aorta rings
ChEMBL 501 10 1 6 5.7 CCCCC1(CC)CC(=O)N(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/C(=C/C(=O)OCC)C1 10.1016/S0960-894X(01)81127-6
CHEMBL51622 189191 0 None - 1 Rabbit 7.0 pKd = 7 Binding
In vitro binding affinity against Angiotensin II receptor in rabbit aorta ringsIn vitro binding affinity against Angiotensin II receptor in rabbit aorta rings
ChEMBL 501 10 1 6 5.7 CCCCC1(CC)CC(=O)N(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/C(=C/C(=O)OCC)C1 10.1016/S0960-894X(01)81127-6
10629796 96423 0 None - 1 Bovine 7.0 pKd = 7.0 Binding
Dissociation constant for [125 I] Ang binding to type 1 Angiotensin II receptor of bovine adrenocortical membranesDissociation constant for [125 I] Ang binding to type 1 Angiotensin II receptor of bovine adrenocortical membranes
ChEMBL 989 27 12 12 -1.1 CC(C)[C@H](NC(=O)[C@H](CCCN=C(N)N)NC(=O)CCO)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O)C(C)C 10.1021/jm9608669
CHEMBL265681 96423 0 None - 1 Bovine 7.0 pKd = 7.0 Binding
Dissociation constant for [125 I] Ang binding to type 1 Angiotensin II receptor of bovine adrenocortical membranesDissociation constant for [125 I] Ang binding to type 1 Angiotensin II receptor of bovine adrenocortical membranes
ChEMBL 989 27 12 12 -1.1 CC(C)[C@H](NC(=O)[C@H](CCCN=C(N)N)NC(=O)CCO)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O)C(C)C 10.1021/jm9608669
9957348 186133 0 None - 1 Rabbit 7.0 pKd = 7.0 Binding
pA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic ringspA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic rings
ChEMBL 493 9 1 8 5.1 CCCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1ncnc2ccc(C(=O)OC)cc12 10.1016/S0960-894X(01)81142-2
CHEMBL48868 186133 0 None - 1 Rabbit 7.0 pKd = 7.0 Binding
pA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic ringspA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic rings
ChEMBL 493 9 1 8 5.1 CCCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1ncnc2ccc(C(=O)OC)cc12 10.1016/S0960-894X(01)81142-2
11744384 32116 0 None - 1 Rat 7.9 pKd = 7.9 Binding
The compound was evaluated for the direct binding of tritiated compound to the recombinant Angiotensin II receptor, type 1 stably expressed in CHO cells.The compound was evaluated for the direct binding of tritiated compound to the recombinant Angiotensin II receptor, type 1 stably expressed in CHO cells.
ChEMBL 448 11 3 6 5.2 CCCCc1ncc(CNc2cc(N=[N+]=[N-])ccc2C(=O)O)n1Cc1ccc(C(=O)O)cc1 10.1021/jm991050l
CHEMBL141065 32116 0 None - 1 Rat 7.9 pKd = 7.9 Binding
The compound was evaluated for the direct binding of tritiated compound to the recombinant Angiotensin II receptor, type 1 stably expressed in CHO cells.The compound was evaluated for the direct binding of tritiated compound to the recombinant Angiotensin II receptor, type 1 stably expressed in CHO cells.
ChEMBL 448 11 3 6 5.2 CCCCc1ncc(CNc2cc(N=[N+]=[N-])ccc2C(=O)O)n1Cc1ccc(C(=O)O)cc1 10.1021/jm991050l
CHEMBL2111972 32116 0 None - 1 Rat 7.9 pKd = 7.9 Binding
The compound was evaluated for the direct binding of tritiated compound to the recombinant Angiotensin II receptor, type 1 stably expressed in CHO cells.The compound was evaluated for the direct binding of tritiated compound to the recombinant Angiotensin II receptor, type 1 stably expressed in CHO cells.
ChEMBL 448 11 3 6 5.2 CCCCc1ncc(CNc2cc(N=[N+]=[N-])ccc2C(=O)O)n1Cc1ccc(C(=O)O)cc1 10.1021/jm991050l
44294791 183342 0 None - 1 Rabbit 6.9 pKd = 6.9 Binding
pA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic ringspA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic rings
ChEMBL 437 8 1 8 4.1 CCCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1ncnc2nccnc12 10.1016/S0960-894X(01)81142-2
CHEMBL48145 183342 0 None - 1 Rabbit 6.9 pKd = 6.9 Binding
pA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic ringspA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic rings
ChEMBL 437 8 1 8 4.1 CCCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1ncnc2nccnc12 10.1016/S0960-894X(01)81142-2
9909542 176897 0 None - 1 Rabbit 7.9 pKd = 7.9 Binding
pA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic ringspA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic rings
ChEMBL 411 7 2 7 3.6 CCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1[nH]cnc2ncnc1-2 10.1016/S0960-894X(01)81142-2
CHEMBL46392 176897 0 None - 1 Rabbit 7.9 pKd = 7.9 Binding
pA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic ringspA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic rings
ChEMBL 411 7 2 7 3.6 CCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1[nH]cnc2ncnc1-2 10.1016/S0960-894X(01)81142-2
10365342 112983 0 None 16 2 Rabbit 7.9 pKd = 7.9 Binding
Compound was evaluated for in vitro potency against AT1 receptor in isolated rabbit aorta; value ranges from 7.91-7.97Compound was evaluated for in vitro potency against AT1 receptor in isolated rabbit aorta; value ranges from 7.91-7.97
ChEMBL 429 9 3 7 4.0 CCCCc1ncc(C(=O)O)c(NCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)n1 10.1021/jm00098a018
CHEMBL331983 112983 0 None 16 2 Rabbit 7.9 pKd = 7.9 Binding
Compound was evaluated for in vitro potency against AT1 receptor in isolated rabbit aorta; value ranges from 7.91-7.97Compound was evaluated for in vitro potency against AT1 receptor in isolated rabbit aorta; value ranges from 7.91-7.97
ChEMBL 429 9 3 7 4.0 CCCCc1ncc(C(=O)O)c(NCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)n1 10.1021/jm00098a018
44383615 165387 0 None - 1 Rabbit 7.9 pKd = 7.9 Binding
In vitro binding affinity against Angiotensin II receptor in rabbit aorta ringsIn vitro binding affinity against Angiotensin II receptor in rabbit aorta rings
ChEMBL 471 6 1 6 4.7 CCOC(=O)/C=C1\CC2(CCCCC2)C(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81127-6
CHEMBL425139 165387 0 None - 1 Rabbit 7.9 pKd = 7.9 Binding
In vitro binding affinity against Angiotensin II receptor in rabbit aorta ringsIn vitro binding affinity against Angiotensin II receptor in rabbit aorta rings
ChEMBL 471 6 1 6 4.7 CCOC(=O)/C=C1\CC2(CCCCC2)C(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81127-6
44294551 183811 0 None - 1 Rabbit 7.9 pKd = 7.9 Binding
In vitro binding affinity against Angiotensin II receptor in rabbit aorta ringsIn vitro binding affinity against Angiotensin II receptor in rabbit aorta rings
ChEMBL 487 9 1 6 5.3 CCCC1(CC)CC(=O)N(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/C(=C/C(=O)OCC)C1 10.1016/S0960-894X(01)81127-6
CHEMBL48459 183811 0 None - 1 Rabbit 7.9 pKd = 7.9 Binding
In vitro binding affinity against Angiotensin II receptor in rabbit aorta ringsIn vitro binding affinity against Angiotensin II receptor in rabbit aorta rings
ChEMBL 487 9 1 6 5.3 CCCC1(CC)CC(=O)N(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/C(=C/C(=O)OCC)C1 10.1016/S0960-894X(01)81127-6
9807638 186553 0 None - 1 Rabbit 7.9 pKd = 7.9 Binding
In vitro binding affinity against Angiotensin II receptor in rabbit aorta ringsIn vitro binding affinity against Angiotensin II receptor in rabbit aorta rings
ChEMBL 471 6 1 6 4.7 CCOC(=O)/C=C1\CC2(CCCC2)CC(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81127-6
CHEMBL49192 186553 0 None - 1 Rabbit 7.9 pKd = 7.9 Binding
In vitro binding affinity against Angiotensin II receptor in rabbit aorta ringsIn vitro binding affinity against Angiotensin II receptor in rabbit aorta rings
ChEMBL 471 6 1 6 4.7 CCOC(=O)/C=C1\CC2(CCCC2)CC(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81127-6
44294464 187196 0 None - 1 Rabbit 6.9 pKd = 6.9 Binding
pA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic ringspA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic rings
ChEMBL 397 6 3 7 3.4 CCc1nc(NCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2c[nH]nc2n1 10.1016/S0960-894X(01)81142-2
CHEMBL49587 187196 0 None - 1 Rabbit 6.9 pKd = 6.9 Binding
pA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic ringspA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic rings
ChEMBL 397 6 3 7 3.4 CCc1nc(NCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2c[nH]nc2n1 10.1016/S0960-894X(01)81142-2
71623945 135928 0 None - 1 Rabbit 7.8 pKd = 7.8 Binding
Antagonist activity against AT1 receptor in Japanese White rabbit aortic strips assessed as reduction in angiotension-2-induced contractile response after 60 mins by Schild's plot analysisAntagonist activity against AT1 receptor in Japanese White rabbit aortic strips assessed as reduction in angiotension-2-induced contractile response after 60 mins by Schild's plot analysis
ChEMBL 571 10 3 7 5.7 CCCc1nc2c(C)cc(C(=O)N[C@@H](CO)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.ejmech.2015.09.010
CHEMBL3735839 135928 0 None - 1 Rabbit 7.8 pKd = 7.8 Binding
Antagonist activity against AT1 receptor in Japanese White rabbit aortic strips assessed as reduction in angiotension-2-induced contractile response after 60 mins by Schild's plot analysisAntagonist activity against AT1 receptor in Japanese White rabbit aortic strips assessed as reduction in angiotension-2-induced contractile response after 60 mins by Schild's plot analysis
ChEMBL 571 10 3 7 5.7 CCCc1nc2c(C)cc(C(=O)N[C@@H](CO)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.ejmech.2015.09.010
44295057 100851 0 None - 1 Rabbit 7.8 pKd = 7.8 Binding
In vitro binding affinity against Angiotensin II receptor in rabbit aorta ringsIn vitro binding affinity against Angiotensin II receptor in rabbit aorta rings
ChEMBL 473 7 1 6 4.8 CCOC(=O)/C=C1\CC(C)(C(C)C)CC(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81127-6
CHEMBL296731 100851 0 None - 1 Rabbit 7.8 pKd = 7.8 Binding
In vitro binding affinity against Angiotensin II receptor in rabbit aorta ringsIn vitro binding affinity against Angiotensin II receptor in rabbit aorta rings
ChEMBL 473 7 1 6 4.8 CCOC(=O)/C=C1\CC(C)(C(C)C)CC(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81127-6
44294699 186703 0 None - 1 Rabbit 6.8 pKd = 6.8 Binding
pA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic ringspA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic rings
ChEMBL 501 9 1 8 5.1 CCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1ncnc2c1ncn2Cc1ccccc1 10.1016/S0960-894X(01)81142-2
CHEMBL49294 186703 0 None - 1 Rabbit 6.8 pKd = 6.8 Binding
pA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic ringspA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic rings
ChEMBL 501 9 1 8 5.1 CCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1ncnc2c1ncn2Cc1ccccc1 10.1016/S0960-894X(01)81142-2
CHEMBL408098 210943 0 None - 1 Bovine 5.8 pKd = 5.8 Binding
Dissociation constant for [125 I] Ang binding to type 1 Angiotensin II receptor of bovine adrenocortical membranesDissociation constant for [125 I] Ang binding to type 1 Angiotensin II receptor of bovine adrenocortical membranes
ChEMBL None None None CCCCCCCCCCCCCCCCCCOc1ccc(C[C@H](NC(=O)[C@@H](NC(=O)[C@H](CCCN=C(N)N)NC(=O)CNC)C(C)C)C(=O)N[C@H](C(=O)N[C@@H](Cc2c[nH]cn2)C(=O)N2CCC[C@H]2C(=O)N[C@H](CC2=CCCC=C2)C(=O)O)C(C)C)cc1 10.1021/jm9608669
CHEMBL268804 209009 0 None -2 2 Bovine 7.8 pKd = 7.8 Binding
Dissociation constant for [125 I] Ang binding to type 1 Angiotensin II receptor of bovine adrenocortical membranesDissociation constant for [125 I] Ang binding to type 1 Angiotensin II receptor of bovine adrenocortical membranes
ChEMBL None None None CNCC(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)N1CCC[C@H]1C(=O)N[C@H](Cc1ccc2ccccc2c1)C(=O)O)C(C)C)C(C)C 10.1021/jm9608669
CHEMBL406519 210855 0 None - 1 Bovine 7.8 pKd = 7.8 Binding
Dissociation constant for [125 I] Ang binding to type 1 Angiotensin II receptor of bovine adrenocortical membranesDissociation constant for [125 I] Ang binding to type 1 Angiotensin II receptor of bovine adrenocortical membranes
ChEMBL None None None CC(=O)N[C@@H](CO)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O)C(C)C)C(C)C 10.1021/jm9608669
1610 2305 89 None -1 4 Rabbit 7.7 pKd = 7.7 Binding
Antagonist activity against AT1 receptor in Japanese White rabbit aortic strips assessed as reduction in angiotension-2-induced contractile response after 60 mins by Schild's plot analysisAntagonist activity against AT1 receptor in Japanese White rabbit aortic strips assessed as reduction in angiotension-2-induced contractile response after 60 mins by Schild's plot analysis
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.ejmech.2015.09.010
3941 2305 89 None -1 4 Rabbit 7.7 pKd = 7.7 Binding
Antagonist activity against AT1 receptor in Japanese White rabbit aortic strips assessed as reduction in angiotension-2-induced contractile response after 60 mins by Schild's plot analysisAntagonist activity against AT1 receptor in Japanese White rabbit aortic strips assessed as reduction in angiotension-2-induced contractile response after 60 mins by Schild's plot analysis
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.ejmech.2015.09.010
3961 2305 89 None -1 4 Rabbit 7.7 pKd = 7.7 Binding
Antagonist activity against AT1 receptor in Japanese White rabbit aortic strips assessed as reduction in angiotension-2-induced contractile response after 60 mins by Schild's plot analysisAntagonist activity against AT1 receptor in Japanese White rabbit aortic strips assessed as reduction in angiotension-2-induced contractile response after 60 mins by Schild's plot analysis
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.ejmech.2015.09.010
590 2305 89 None -1 4 Rabbit 7.7 pKd = 7.7 Binding
Antagonist activity against AT1 receptor in Japanese White rabbit aortic strips assessed as reduction in angiotension-2-induced contractile response after 60 mins by Schild's plot analysisAntagonist activity against AT1 receptor in Japanese White rabbit aortic strips assessed as reduction in angiotension-2-induced contractile response after 60 mins by Schild's plot analysis
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.ejmech.2015.09.010
CHEMBL191 2305 89 None -1 4 Rabbit 7.7 pKd = 7.7 Binding
Antagonist activity against AT1 receptor in Japanese White rabbit aortic strips assessed as reduction in angiotension-2-induced contractile response after 60 mins by Schild's plot analysisAntagonist activity against AT1 receptor in Japanese White rabbit aortic strips assessed as reduction in angiotension-2-induced contractile response after 60 mins by Schild's plot analysis
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.ejmech.2015.09.010
DB00678 2305 89 None -1 4 Rabbit 7.7 pKd = 7.7 Binding
Antagonist activity against AT1 receptor in Japanese White rabbit aortic strips assessed as reduction in angiotension-2-induced contractile response after 60 mins by Schild's plot analysisAntagonist activity against AT1 receptor in Japanese White rabbit aortic strips assessed as reduction in angiotension-2-induced contractile response after 60 mins by Schild's plot analysis
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.ejmech.2015.09.010
44348369 16145 0 None - 1 Rabbit 7.7 pKd = 7.7 Binding
In vitro binding affinity against Angiotensin II receptor in rabbit aorta ringsIn vitro binding affinity against Angiotensin II receptor in rabbit aorta rings
ChEMBL 495 6 1 6 4.5 CCOC(=O)/C=C1\C2C3C=CC(CCC3)C2C(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81127-6
CHEMBL122855 16145 0 None - 1 Rabbit 7.7 pKd = 7.7 Binding
In vitro binding affinity against Angiotensin II receptor in rabbit aorta ringsIn vitro binding affinity against Angiotensin II receptor in rabbit aorta rings
ChEMBL 495 6 1 6 4.5 CCOC(=O)/C=C1\C2C3C=CC(CCC3)C2C(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81127-6
16133225 415 47 None -2 6 Human 8.7 pKd = 8.7 Binding
Binding affinity was determined against Angiotensin II receptor, type 1Binding affinity was determined against Angiotensin II receptor, type 1
ChEMBL None None None None 10.1021/jm9507744
172198 415 47 None -2 6 Human 8.7 pKd = 8.7 Binding
Binding affinity was determined against Angiotensin II receptor, type 1Binding affinity was determined against Angiotensin II receptor, type 1
ChEMBL None None None None 10.1021/jm9507744
2504 415 47 None -2 6 Human 8.7 pKd = 8.7 Binding
Binding affinity was determined against Angiotensin II receptor, type 1Binding affinity was determined against Angiotensin II receptor, type 1
ChEMBL None None None None 10.1021/jm9507744
45266664 415 47 None -2 6 Human 8.7 pKd = 8.7 Binding
Binding affinity was determined against Angiotensin II receptor, type 1Binding affinity was determined against Angiotensin II receptor, type 1
ChEMBL None None None None 10.1021/jm9507744
5272 415 47 None -2 6 Human 8.7 pKd = 8.7 Binding
Binding affinity was determined against Angiotensin II receptor, type 1Binding affinity was determined against Angiotensin II receptor, type 1
ChEMBL None None None None 10.1021/jm9507744
CHEMBL408403 415 47 None -2 6 Human 8.7 pKd = 8.7 Binding
Binding affinity was determined against Angiotensin II receptor, type 1Binding affinity was determined against Angiotensin II receptor, type 1
ChEMBL None None None None 10.1021/jm9507744
DB11842 415 47 None -2 6 Human 8.7 pKd = 8.7 Binding
Binding affinity was determined against Angiotensin II receptor, type 1Binding affinity was determined against Angiotensin II receptor, type 1
ChEMBL None None None None 10.1021/jm9507744
9912059 184764 0 None - 1 Rabbit 8.6 pKd = 8.6 Binding
In vitro binding affinity against Angiotensin II receptor in rabbit aorta ringsIn vitro binding affinity against Angiotensin II receptor in rabbit aorta rings
ChEMBL 459 7 1 6 4.5 CCOC(=O)/C=C1\CC(C)(CC)CC(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81127-6
CHEMBL48602 184764 0 None - 1 Rabbit 8.6 pKd = 8.6 Binding
In vitro binding affinity against Angiotensin II receptor in rabbit aorta ringsIn vitro binding affinity against Angiotensin II receptor in rabbit aorta rings
ChEMBL 459 7 1 6 4.5 CCOC(=O)/C=C1\CC(C)(CC)CC(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81127-6
44294466 187316 0 None - 1 Rabbit 8.6 pKd = 8.6 Binding
pA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic ringspA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic rings
ChEMBL 451 7 3 7 4.4 CCc1nc(NCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2cc(C(=O)O)ccc2n1 10.1016/S0960-894X(01)81142-2
CHEMBL49663 187316 0 None - 1 Rabbit 8.6 pKd = 8.6 Binding
pA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic ringspA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic rings
ChEMBL 451 7 3 7 4.4 CCc1nc(NCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2cc(C(=O)O)ccc2n1 10.1016/S0960-894X(01)81142-2
44294483 101263 0 None - 1 Rabbit 8.6 pKd = 8.6 Binding
pA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic ringspA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic rings
ChEMBL 437 7 2 7 4.7 CCc1nc(NCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2cc(OC)ccc2n1 10.1016/S0960-894X(01)81142-2
CHEMBL299741 101263 0 None - 1 Rabbit 8.6 pKd = 8.6 Binding
pA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic ringspA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic rings
ChEMBL 437 7 2 7 4.7 CCc1nc(NCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2cc(OC)ccc2n1 10.1016/S0960-894X(01)81142-2
15294417 183527 0 None - 1 Rabbit 8.5 pKd = 8.5 Binding
pA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic ringspA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic rings
ChEMBL 407 6 2 6 4.7 CCc1nc(NCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2ccccc2n1 10.1016/S0960-894X(01)81142-2
CHEMBL48270 183527 0 None - 1 Rabbit 8.5 pKd = 8.5 Binding
pA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic ringspA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic rings
ChEMBL 407 6 2 6 4.7 CCc1nc(NCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2ccccc2n1 10.1016/S0960-894X(01)81142-2
CHEMBL415025 211411 0 None - 1 Human 7.7 pKd = 7.7 Binding
Binding affinity was determined against Angiotensin II receptor, type 1Binding affinity was determined against Angiotensin II receptor, type 1
ChEMBL None None None CNCC(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H]1CCSS[C@@H]2C[C@H](C(=O)N[C@@H](Cc3ccccc3)C(=O)O)N(C2)C(=O)[C@@H](Cc2c[nH]cn2)NC1=O)C(C)C 10.1021/jm9507744
CHEMBL384349 210566 0 None -2 2 Bovine 6.7 pKd = 6.7 Binding
Dissociation constant for [125 I] Ang binding to type 1 Angiotensin II receptor of bovine adrenocortical membranesDissociation constant for [125 I] Ang binding to type 1 Angiotensin II receptor of bovine adrenocortical membranes
ChEMBL None None None CCCCCCCCCCCCCCCC(=O)Oc1ccc(C[C@H](NC(=O)[C@@H](NC(=O)[C@H](CCCN=C(N)N)NC(=O)CNC)C(C)C)C(=O)N[C@H](C(=O)N[C@@H](Cc2c[nH]cn2)C(=O)N2CCC[C@H]2C(=O)N[C@H](Cc2ccc3ccccc3c2)C(=O)O)C(C)C)cc1 10.1021/jm9608669
CHEMBL402669 210772 0 None - 1 Bovine 5.7 pKd = 5.7 Binding
Dissociation constant for [125 I] Ang binding to type 1 Angiotensin II receptor of bovine adrenocortical membranesDissociation constant for [125 I] Ang binding to type 1 Angiotensin II receptor of bovine adrenocortical membranes
ChEMBL None None None CCCCCCCCCCCCCCCC(=O)OC[C@H](NC(C)=O)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)N1CCC[C@H]1C(=O)N[C@H](Cc1cccc2ccccc12)C(=O)O)C(C)C)C(C)C 10.1021/jm9608669
CHEMBL406170 210840 0 None - 1 Human 5.6 pKd = 5.6 Binding
Binding affinity was determined against Angiotensin II receptor, type 1Binding affinity was determined against Angiotensin II receptor, type 1
ChEMBL None None None CNCC(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H]1CSS[C@@H]2C[C@H](C(=O)N[C@@H](Cc3ccccc3)C(=O)O)N(C2)C(=O)[C@@H](Cc2c[nH]cn2)NC1=O)C(C)C 10.1021/jm9507744
127035717 135880 0 None - 1 Rabbit 7.6 pKd = 7.6 Binding
Antagonist activity against AT1 receptor in Japanese White rabbit aortic strips assessed as reduction in angiotension-2-induced contractile response after 60 mins by Schild's plot analysisAntagonist activity against AT1 receptor in Japanese White rabbit aortic strips assessed as reduction in angiotension-2-induced contractile response after 60 mins by Schild's plot analysis
ChEMBL 569 10 2 6 6.7 CCCc1nc2c(C)cc(C(=O)NC[C@@H](C)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.ejmech.2015.09.010
CHEMBL3735409 135880 0 None - 1 Rabbit 7.6 pKd = 7.6 Binding
Antagonist activity against AT1 receptor in Japanese White rabbit aortic strips assessed as reduction in angiotension-2-induced contractile response after 60 mins by Schild's plot analysisAntagonist activity against AT1 receptor in Japanese White rabbit aortic strips assessed as reduction in angiotension-2-induced contractile response after 60 mins by Schild's plot analysis
ChEMBL 569 10 2 6 6.7 CCCc1nc2c(C)cc(C(=O)NC[C@@H](C)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.ejmech.2015.09.010
10701559 155138 0 None - 1 Bovine 5.6 pKd = 5.6 Binding
Dissociation constant for [125 I] Ang binding to type 1 Angiotensin II receptor of bovine adrenocortical membranesDissociation constant for [125 I] Ang binding to type 1 Angiotensin II receptor of bovine adrenocortical membranes
ChEMBL 1227 42 11 13 4.9 CCCCCCCCCCCCCCCC(=O)OCCC(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O)C(C)C)C(C)C 10.1021/jm9608669
CHEMBL405031 155138 0 None - 1 Bovine 5.6 pKd = 5.6 Binding
Dissociation constant for [125 I] Ang binding to type 1 Angiotensin II receptor of bovine adrenocortical membranesDissociation constant for [125 I] Ang binding to type 1 Angiotensin II receptor of bovine adrenocortical membranes
ChEMBL 1227 42 11 13 4.9 CCCCCCCCCCCCCCCC(=O)OCCC(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O)C(C)C)C(C)C 10.1021/jm9608669
44294540 101357 0 None - 1 Rabbit 7.5 pKd = 7.5 Binding
pA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic ringspA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic rings
ChEMBL 455 8 2 9 3.7 CCCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1ncnc2c1nc(O)n2C 10.1016/S0960-894X(01)81142-2
CHEMBL300438 101357 0 None - 1 Rabbit 7.5 pKd = 7.5 Binding
pA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic ringspA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic rings
ChEMBL 455 8 2 9 3.7 CCCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1ncnc2c1nc(O)n2C 10.1016/S0960-894X(01)81142-2
9864307 16234 0 None - 1 Rabbit 5.5 pKd = 5.5 Binding
Compound was evaluated for in vitro potency against Angiotensin II receptor, type 1 in isolated rabbit aorta; value ranges from 5.53-5.69Compound was evaluated for in vitro potency against Angiotensin II receptor, type 1 in isolated rabbit aorta; value ranges from 5.53-5.69
ChEMBL 373 6 3 7 2.6 O=C(O)c1cncnc1NCc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00098a018
CHEMBL123152 16234 0 None - 1 Rabbit 5.5 pKd = 5.5 Binding
Compound was evaluated for in vitro potency against Angiotensin II receptor, type 1 in isolated rabbit aorta; value ranges from 5.53-5.69Compound was evaluated for in vitro potency against Angiotensin II receptor, type 1 in isolated rabbit aorta; value ranges from 5.53-5.69
ChEMBL 373 6 3 7 2.6 O=C(O)c1cncnc1NCc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00098a018
70682146 75963 0 None - 1 Rabbit 8.5 pKd = 8.5 Binding
Antagonist activity against AT1 receptor in Japanese White rabbit aortic strips assessed as reduction in angiotension-2-induced contractile response after 60 mins by Schild's plot analysisAntagonist activity against AT1 receptor in Japanese White rabbit aortic strips assessed as reduction in angiotension-2-induced contractile response after 60 mins by Schild's plot analysis
ChEMBL 569 10 2 6 6.7 CCCc1nc2c(C)cc(C(=O)NCC(C)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.ejmech.2015.09.010
CHEMBL2058860 75963 0 None - 1 Rabbit 8.5 pKd = 8.5 Binding
Antagonist activity against AT1 receptor in Japanese White rabbit aortic strips assessed as reduction in angiotension-2-induced contractile response after 60 mins by Schild's plot analysisAntagonist activity against AT1 receptor in Japanese White rabbit aortic strips assessed as reduction in angiotension-2-induced contractile response after 60 mins by Schild's plot analysis
ChEMBL 569 10 2 6 6.7 CCCc1nc2c(C)cc(C(=O)NCC(C)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.ejmech.2015.09.010
127036108 135842 0 None - 1 Rabbit 8.5 pKd = 8.5 Binding
Antagonist activity against AT1 receptor in Japanese White rabbit aortic strips assessed as reduction in angiotension-2-induced contractile response after 60 mins by Schild's plot analysisAntagonist activity against AT1 receptor in Japanese White rabbit aortic strips assessed as reduction in angiotension-2-induced contractile response after 60 mins by Schild's plot analysis
ChEMBL 561 11 2 5 6.8 CCCc1nc2c(C)cc(C(=O)N[C@@H](COC)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2015.09.010
CHEMBL3735098 135842 0 None - 1 Rabbit 8.5 pKd = 8.5 Binding
Antagonist activity against AT1 receptor in Japanese White rabbit aortic strips assessed as reduction in angiotension-2-induced contractile response after 60 mins by Schild's plot analysisAntagonist activity against AT1 receptor in Japanese White rabbit aortic strips assessed as reduction in angiotension-2-induced contractile response after 60 mins by Schild's plot analysis
ChEMBL 561 11 2 5 6.8 CCCc1nc2c(C)cc(C(=O)N[C@@H](COC)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2015.09.010
127035514 135887 0 None - 1 Rabbit 8.5 pKd = 8.5 Binding
Antagonist activity against AT1 receptor in Japanese White rabbit aortic strips assessed as reduction in angiotension-2-induced contractile response after 60 mins by Schild's plot analysisAntagonist activity against AT1 receptor in Japanese White rabbit aortic strips assessed as reduction in angiotension-2-induced contractile response after 60 mins by Schild's plot analysis
ChEMBL 585 11 2 7 6.3 CCCc1nc2c(C)cc(C(=O)N[C@H](COC)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.ejmech.2015.09.010
CHEMBL3735446 135887 0 None - 1 Rabbit 8.5 pKd = 8.5 Binding
Antagonist activity against AT1 receptor in Japanese White rabbit aortic strips assessed as reduction in angiotension-2-induced contractile response after 60 mins by Schild's plot analysisAntagonist activity against AT1 receptor in Japanese White rabbit aortic strips assessed as reduction in angiotension-2-induced contractile response after 60 mins by Schild's plot analysis
ChEMBL 585 11 2 7 6.3 CCCc1nc2c(C)cc(C(=O)N[C@H](COC)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.ejmech.2015.09.010
44382928 58884 0 None - 1 Rabbit 8.5 pKd = 8.5 Binding
In vitro binding affinity against Angiotensin II receptor in rabbit aorta ringsIn vitro binding affinity against Angiotensin II receptor in rabbit aorta rings
ChEMBL 457 6 1 6 4.3 CCOC(=O)/C=C1\CC2(CCCC2)C(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81127-6
CHEMBL170196 58884 0 None - 1 Rabbit 8.5 pKd = 8.5 Binding
In vitro binding affinity against Angiotensin II receptor in rabbit aorta ringsIn vitro binding affinity against Angiotensin II receptor in rabbit aorta rings
ChEMBL 457 6 1 6 4.3 CCOC(=O)/C=C1\CC2(CCCC2)C(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81127-6
9978737 118374 1 None - 1 Rat 8.5 pKd = 8.5 Binding
The compound was evaluated for the direct binding of tritiated compound to the recombinant Angiotensin II receptor, type 1 stably expressed in CHO cells.The compound was evaluated for the direct binding of tritiated compound to the recombinant Angiotensin II receptor, type 1 stably expressed in CHO cells.
ChEMBL 407 10 3 5 4.3 CCCCc1ncc(CNc2ccccc2C(=O)O)n1Cc1ccc(C(=O)O)cc1 10.1021/jm991050l
CHEMBL2111971 118374 1 None - 1 Rat 8.5 pKd = 8.5 Binding
The compound was evaluated for the direct binding of tritiated compound to the recombinant Angiotensin II receptor, type 1 stably expressed in CHO cells.The compound was evaluated for the direct binding of tritiated compound to the recombinant Angiotensin II receptor, type 1 stably expressed in CHO cells.
ChEMBL 407 10 3 5 4.3 CCCCc1ncc(CNc2ccccc2C(=O)O)n1Cc1ccc(C(=O)O)cc1 10.1021/jm991050l
CHEMBL342261 118374 1 None - 1 Rat 8.5 pKd = 8.5 Binding
The compound was evaluated for the direct binding of tritiated compound to the recombinant Angiotensin II receptor, type 1 stably expressed in CHO cells.The compound was evaluated for the direct binding of tritiated compound to the recombinant Angiotensin II receptor, type 1 stably expressed in CHO cells.
ChEMBL 407 10 3 5 4.3 CCCCc1ncc(CNc2ccccc2C(=O)O)n1Cc1ccc(C(=O)O)cc1 10.1021/jm991050l
CHEMBL415157 211416 0 None 10 2 Bovine 8.5 pKd = 8.5 Binding
Dissociation constant for [125 I] Ang binding to type 1 Angiotensin II receptor of bovine adrenocortical membranesDissociation constant for [125 I] Ang binding to type 1 Angiotensin II receptor of bovine adrenocortical membranes
ChEMBL None None None CCCCCCCCCCCCCCCC(=O)Oc1ccc(C[C@H](NC(=O)[C@@H](NC(=O)[C@H](CCCN=C(N)N)NC(=O)CNC)C(C)C)C(=O)N[C@H](C(=O)N[C@@H](Cc2c[nH]cn2)C(=O)N2CCC[C@H]2C(=O)N[C@H](Cc2ccccc2)C(=O)O)C(C)C)cc1 10.1021/jm9608669
127036107 135980 0 None - 1 Rabbit 8.4 pKd = 8.4 Binding
Antagonist activity against AT1 receptor in Japanese White rabbit aortic strips assessed as reduction in angiotension-2-induced contractile response after 60 mins by Schild's plot analysisAntagonist activity against AT1 receptor in Japanese White rabbit aortic strips assessed as reduction in angiotension-2-induced contractile response after 60 mins by Schild's plot analysis
ChEMBL 561 11 2 5 6.8 CCCc1nc2c(C)cc(C(=O)N[C@H](COC)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2015.09.010
CHEMBL3736319 135980 0 None - 1 Rabbit 8.4 pKd = 8.4 Binding
Antagonist activity against AT1 receptor in Japanese White rabbit aortic strips assessed as reduction in angiotension-2-induced contractile response after 60 mins by Schild's plot analysisAntagonist activity against AT1 receptor in Japanese White rabbit aortic strips assessed as reduction in angiotension-2-induced contractile response after 60 mins by Schild's plot analysis
ChEMBL 561 11 2 5 6.8 CCCc1nc2c(C)cc(C(=O)N[C@H](COC)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2015.09.010
1610 2305 89 None -1 4 Rabbit 8.4 pKd = 8.4 Binding
pA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic ringspA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic rings
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(01)81142-2
3941 2305 89 None -1 4 Rabbit 8.4 pKd = 8.4 Binding
pA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic ringspA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic rings
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(01)81142-2
3961 2305 89 None -1 4 Rabbit 8.4 pKd = 8.4 Binding
pA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic ringspA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic rings
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(01)81142-2
590 2305 89 None -1 4 Rabbit 8.4 pKd = 8.4 Binding
pA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic ringspA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic rings
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(01)81142-2
CHEMBL191 2305 89 None -1 4 Rabbit 8.4 pKd = 8.4 Binding
pA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic ringspA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic rings
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(01)81142-2
DB00678 2305 89 None -1 4 Rabbit 8.4 pKd = 8.4 Binding
pA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic ringspA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic rings
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/S0960-894X(01)81142-2
127036297 135891 0 None - 1 Rabbit 8.4 pKd = 8.4 Binding
Antagonist activity against AT1 receptor in Japanese White rabbit aortic strips assessed as reduction in angiotension-2-induced contractile response after 60 mins by Schild's plot analysisAntagonist activity against AT1 receptor in Japanese White rabbit aortic strips assessed as reduction in angiotension-2-induced contractile response after 60 mins by Schild's plot analysis
ChEMBL 547 10 3 5 6.2 CCCc1nc2c(C)cc(C(=O)N[C@H](CO)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2015.09.010
CHEMBL3735492 135891 0 None - 1 Rabbit 8.4 pKd = 8.4 Binding
Antagonist activity against AT1 receptor in Japanese White rabbit aortic strips assessed as reduction in angiotension-2-induced contractile response after 60 mins by Schild's plot analysisAntagonist activity against AT1 receptor in Japanese White rabbit aortic strips assessed as reduction in angiotension-2-induced contractile response after 60 mins by Schild's plot analysis
ChEMBL 547 10 3 5 6.2 CCCc1nc2c(C)cc(C(=O)N[C@H](CO)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2015.09.010
44382968 164660 0 None - 1 Rabbit 8.4 pKd = 8.4 Binding
In vitro binding affinity against Angiotensin II receptor in rabbit aorta ringsIn vitro binding affinity against Angiotensin II receptor in rabbit aorta rings
ChEMBL 485 6 1 6 5.1 CCOC(=O)/C=C1\CC2(CCCCCC2)C(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81127-6
CHEMBL422912 164660 0 None - 1 Rabbit 8.4 pKd = 8.4 Binding
In vitro binding affinity against Angiotensin II receptor in rabbit aorta ringsIn vitro binding affinity against Angiotensin II receptor in rabbit aorta rings
ChEMBL 485 6 1 6 5.1 CCOC(=O)/C=C1\CC2(CCCCCC2)C(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81127-6
44295009 186578 0 None - 1 Rabbit 8.4 pKd = 8.4 Binding
In vitro binding affinity against Angiotensin II receptor in rabbit aorta ringsIn vitro binding affinity against Angiotensin II receptor in rabbit aorta rings
ChEMBL 473 8 1 6 4.9 CCOC(=O)/C=C1\CC(CC)(CC)CC(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81127-6
CHEMBL49207 186578 0 None - 1 Rabbit 8.4 pKd = 8.4 Binding
In vitro binding affinity against Angiotensin II receptor in rabbit aorta ringsIn vitro binding affinity against Angiotensin II receptor in rabbit aorta rings
ChEMBL 473 8 1 6 4.9 CCOC(=O)/C=C1\CC(CC)(CC)CC(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81127-6
44294967 187761 0 None - 1 Rabbit 7.5 pKd = 7.5 Binding
pA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic ringspA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic rings
ChEMBL 467 9 1 8 4.6 CCCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1ncnc2c1nc(CC)n2C 10.1016/S0960-894X(01)81142-2
CHEMBL50109 187761 0 None - 1 Rabbit 7.5 pKd = 7.5 Binding
pA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic ringspA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic rings
ChEMBL 467 9 1 8 4.6 CCCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1ncnc2c1nc(CC)n2C 10.1016/S0960-894X(01)81142-2
155541125 172386 0 None - 1 Human 6.5 pKd = 6.5 Binding
Binding affinity to human AT1 receptorBinding affinity to human AT1 receptor
ChEMBL 904 27 12 11 -1.2 CC[C@H](C)[C@H](NC(=O)[C@@H]1CCCN1C(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)[C@@H](C)CC)C(C)C)C(=O)O 10.1021/acs.jmedchem.8b00435
CHEMBL4517561 172386 0 None - 1 Human 6.5 pKd = 6.5 Binding
Binding affinity to human AT1 receptorBinding affinity to human AT1 receptor
ChEMBL 904 27 12 11 -1.2 CC[C@H](C)[C@H](NC(=O)[C@@H]1CCCN1C(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)[C@@H](C)CC)C(C)C)C(=O)O 10.1021/acs.jmedchem.8b00435
44295090 101171 0 None - 1 Rabbit 7.5 pKd = 7.5 Binding
In vitro binding affinity against Angiotensin II receptor in rabbit aorta ringsIn vitro binding affinity against Angiotensin II receptor in rabbit aorta rings
ChEMBL 487 9 1 6 5.3 CCCCC1(C)CC(=O)N(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/C(=C/C(=O)OCC)C1 10.1016/S0960-894X(01)81127-6
CHEMBL299151 101171 0 None - 1 Rabbit 7.5 pKd = 7.5 Binding
In vitro binding affinity against Angiotensin II receptor in rabbit aorta ringsIn vitro binding affinity against Angiotensin II receptor in rabbit aorta rings
ChEMBL 487 9 1 6 5.3 CCCCC1(C)CC(=O)N(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/C(=C/C(=O)OCC)C1 10.1016/S0960-894X(01)81127-6
CHEMBL264230 208854 0 None -3 2 Bovine 6.5 pKd = 6.5 Binding
Dissociation constant for [125 I] Ang binding to type 1 Angiotensin II receptor of bovine adrenocortical membranesDissociation constant for [125 I] Ang binding to type 1 Angiotensin II receptor of bovine adrenocortical membranes
ChEMBL None None None CC(=O)N[C@@H](CO)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)N1CCC[C@H]1C(=O)N[C@H](Cc1cccc2ccccc12)C(=O)O)C(C)C)C(C)C 10.1021/jm9608669
44294520 183696 0 None - 1 Rabbit 6.5 pKd = 6.5 Binding
pA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic ringspA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic rings
ChEMBL 411 7 2 7 3.6 CCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1[nH]cnc2nncc1-2 10.1016/S0960-894X(01)81142-2
CHEMBL48400 183696 0 None - 1 Rabbit 6.5 pKd = 6.5 Binding
pA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic ringspA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic rings
ChEMBL 411 7 2 7 3.6 CCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1[nH]cnc2nncc1-2 10.1016/S0960-894X(01)81142-2
44294485 171990 0 None - 1 Rabbit 7.5 pKd = 7.5 Binding
pA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic ringspA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic rings
ChEMBL 479 9 2 7 5.0 CCCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1ncnc2cc(C(=O)O)ccc12 10.1016/S0960-894X(01)81142-2
CHEMBL448727 171990 0 None - 1 Rabbit 7.5 pKd = 7.5 Binding
pA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic ringspA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic rings
ChEMBL 479 9 2 7 5.0 CCCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1ncnc2cc(C(=O)O)ccc12 10.1016/S0960-894X(01)81142-2
44295010 186651 0 None - 1 Rabbit 7.4 pKd = 7.4 Binding
In vitro binding affinity against Angiotensin II receptor in rabbit aorta ringsIn vitro binding affinity against Angiotensin II receptor in rabbit aorta rings
ChEMBL 445 6 1 6 4.1 CCOC(=O)/C=C1\CC(C)(C)CC(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81127-6
CHEMBL49262 186651 0 None - 1 Rabbit 7.4 pKd = 7.4 Binding
In vitro binding affinity against Angiotensin II receptor in rabbit aorta ringsIn vitro binding affinity against Angiotensin II receptor in rabbit aorta rings
ChEMBL 445 6 1 6 4.1 CCOC(=O)/C=C1\CC(C)(C)CC(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81127-6
44294515 191215 0 None - 1 Rabbit 7.4 pKd = 7.4 Binding
pA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic ringspA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic rings
ChEMBL 501 9 1 9 3.8 CCCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1ncnc2c1nc([S+](C)[O-])n2C 10.1016/S0960-894X(01)81142-2
CHEMBL51987 191215 0 None - 1 Rabbit 7.4 pKd = 7.4 Binding
pA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic ringspA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic rings
ChEMBL 501 9 1 9 3.8 CCCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1ncnc2c1nc([S+](C)[O-])n2C 10.1016/S0960-894X(01)81142-2
44294676 187177 0 None - 1 Rabbit 7.3 pKd = 7.3 Binding
pA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic ringspA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic rings
ChEMBL 451 7 1 7 4.7 CCc1nc(N(C)Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2cc(OC)ccc2n1 10.1016/S0960-894X(01)81142-2
CHEMBL49573 187177 0 None - 1 Rabbit 7.3 pKd = 7.3 Binding
pA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic ringspA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic rings
ChEMBL 451 7 1 7 4.7 CCc1nc(N(C)Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2cc(OC)ccc2n1 10.1016/S0960-894X(01)81142-2
44294616 187647 0 None - 1 Rabbit 7.3 pKd = 7.3 Binding
pA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic ringspA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic rings
ChEMBL 465 9 1 7 5.3 CCCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1ncnc2ccc(OC)cc12 10.1016/S0960-894X(01)81142-2
CHEMBL49952 187647 0 None - 1 Rabbit 7.3 pKd = 7.3 Binding
pA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic ringspA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic rings
ChEMBL 465 9 1 7 5.3 CCCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1ncnc2ccc(OC)cc12 10.1016/S0960-894X(01)81142-2
CHEMBL406888 210868 0 None - 1 Bovine 6.3 pKd = 6.3 Binding
Dissociation constant for [125 I] Ang binding to type 1 Angiotensin II receptor of bovine adrenocortical membranesDissociation constant for [125 I] Ang binding to type 1 Angiotensin II receptor of bovine adrenocortical membranes
ChEMBL None None None CCCCCCCCCCCCCCCC(=O)OC[C@H](NC(C)=O)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O)C(C)C)C(C)C 10.1021/jm9608669
44294905 188550 0 None - 1 Rabbit 8.3 pKd = 8.3 Binding
In vitro binding affinity against Angiotensin II receptor in rabbit aorta ringsIn vitro binding affinity against Angiotensin II receptor in rabbit aorta rings
ChEMBL 485 6 1 6 5.1 CCOC(=O)/C=C1\CC2(CCCCC2)CC(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81127-6
CHEMBL51084 188550 0 None - 1 Rabbit 8.3 pKd = 8.3 Binding
In vitro binding affinity against Angiotensin II receptor in rabbit aorta ringsIn vitro binding affinity against Angiotensin II receptor in rabbit aorta rings
ChEMBL 485 6 1 6 5.1 CCOC(=O)/C=C1\CC2(CCCCC2)CC(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81127-6
44294465 187110 0 None - 1 Rabbit 8.3 pKd = 8.3 Binding
pA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic ringspA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic rings
ChEMBL 411 6 2 8 3.4 CCc1nc(NCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2ncn(C)c2n1 10.1016/S0960-894X(01)81142-2
CHEMBL49528 187110 0 None - 1 Rabbit 8.3 pKd = 8.3 Binding
pA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic ringspA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic rings
ChEMBL 411 6 2 8 3.4 CCc1nc(NCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2ncn(C)c2n1 10.1016/S0960-894X(01)81142-2
1610 2305 89 None -1 4 Rabbit 8.3 pKd = 8.3 Binding
Compound was evaluated for in vitro potency against angiotensin II receptor, type 1 in isolated rabbit aorta; value ranges from 8.27-8.70Compound was evaluated for in vitro potency against angiotensin II receptor, type 1 in isolated rabbit aorta; value ranges from 8.27-8.70
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00098a018
3941 2305 89 None -1 4 Rabbit 8.3 pKd = 8.3 Binding
Compound was evaluated for in vitro potency against angiotensin II receptor, type 1 in isolated rabbit aorta; value ranges from 8.27-8.70Compound was evaluated for in vitro potency against angiotensin II receptor, type 1 in isolated rabbit aorta; value ranges from 8.27-8.70
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00098a018
3961 2305 89 None -1 4 Rabbit 8.3 pKd = 8.3 Binding
Compound was evaluated for in vitro potency against angiotensin II receptor, type 1 in isolated rabbit aorta; value ranges from 8.27-8.70Compound was evaluated for in vitro potency against angiotensin II receptor, type 1 in isolated rabbit aorta; value ranges from 8.27-8.70
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00098a018
590 2305 89 None -1 4 Rabbit 8.3 pKd = 8.3 Binding
Compound was evaluated for in vitro potency against angiotensin II receptor, type 1 in isolated rabbit aorta; value ranges from 8.27-8.70Compound was evaluated for in vitro potency against angiotensin II receptor, type 1 in isolated rabbit aorta; value ranges from 8.27-8.70
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00098a018
CHEMBL191 2305 89 None -1 4 Rabbit 8.3 pKd = 8.3 Binding
Compound was evaluated for in vitro potency against angiotensin II receptor, type 1 in isolated rabbit aorta; value ranges from 8.27-8.70Compound was evaluated for in vitro potency against angiotensin II receptor, type 1 in isolated rabbit aorta; value ranges from 8.27-8.70
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00098a018
DB00678 2305 89 None -1 4 Rabbit 8.3 pKd = 8.3 Binding
Compound was evaluated for in vitro potency against angiotensin II receptor, type 1 in isolated rabbit aorta; value ranges from 8.27-8.70Compound was evaluated for in vitro potency against angiotensin II receptor, type 1 in isolated rabbit aorta; value ranges from 8.27-8.70
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00098a018
127035716 135898 0 None - 1 Rabbit 8.3 pKd = 8.3 Binding
Antagonist activity against AT1 receptor in Japanese White rabbit aortic strips assessed as reduction in angiotension-2-induced contractile response after 60 mins by Schild's plot analysisAntagonist activity against AT1 receptor in Japanese White rabbit aortic strips assessed as reduction in angiotension-2-induced contractile response after 60 mins by Schild's plot analysis
ChEMBL 545 10 2 4 7.2 CCCc1nc2c(C)cc(C(=O)NC[C@H](C)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2015.09.010
CHEMBL3735588 135898 0 None - 1 Rabbit 8.3 pKd = 8.3 Binding
Antagonist activity against AT1 receptor in Japanese White rabbit aortic strips assessed as reduction in angiotension-2-induced contractile response after 60 mins by Schild's plot analysisAntagonist activity against AT1 receptor in Japanese White rabbit aortic strips assessed as reduction in angiotension-2-induced contractile response after 60 mins by Schild's plot analysis
ChEMBL 545 10 2 4 7.2 CCCc1nc2c(C)cc(C(=O)NC[C@H](C)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2015.09.010
16133225 415 47 None -34 6 Bovine 8.2 pKd = 8.2 Binding
Dissociation constant for [125 I] Ang binding to type 1 Angiotensin II receptor of bovine adrenocortical membranesDissociation constant for [125 I] Ang binding to type 1 Angiotensin II receptor of bovine adrenocortical membranes
ChEMBL None None None None 10.1021/jm9608669
172198 415 47 None -34 6 Bovine 8.2 pKd = 8.2 Binding
Dissociation constant for [125 I] Ang binding to type 1 Angiotensin II receptor of bovine adrenocortical membranesDissociation constant for [125 I] Ang binding to type 1 Angiotensin II receptor of bovine adrenocortical membranes
ChEMBL None None None None 10.1021/jm9608669
2504 415 47 None -34 6 Bovine 8.2 pKd = 8.2 Binding
Dissociation constant for [125 I] Ang binding to type 1 Angiotensin II receptor of bovine adrenocortical membranesDissociation constant for [125 I] Ang binding to type 1 Angiotensin II receptor of bovine adrenocortical membranes
ChEMBL None None None None 10.1021/jm9608669
45266664 415 47 None -34 6 Bovine 8.2 pKd = 8.2 Binding
Dissociation constant for [125 I] Ang binding to type 1 Angiotensin II receptor of bovine adrenocortical membranesDissociation constant for [125 I] Ang binding to type 1 Angiotensin II receptor of bovine adrenocortical membranes
ChEMBL None None None None 10.1021/jm9608669
5272 415 47 None -34 6 Bovine 8.2 pKd = 8.2 Binding
Dissociation constant for [125 I] Ang binding to type 1 Angiotensin II receptor of bovine adrenocortical membranesDissociation constant for [125 I] Ang binding to type 1 Angiotensin II receptor of bovine adrenocortical membranes
ChEMBL None None None None 10.1021/jm9608669
CHEMBL408403 415 47 None -34 6 Bovine 8.2 pKd = 8.2 Binding
Dissociation constant for [125 I] Ang binding to type 1 Angiotensin II receptor of bovine adrenocortical membranesDissociation constant for [125 I] Ang binding to type 1 Angiotensin II receptor of bovine adrenocortical membranes
ChEMBL None None None None 10.1021/jm9608669
DB11842 415 47 None -34 6 Bovine 8.2 pKd = 8.2 Binding
Dissociation constant for [125 I] Ang binding to type 1 Angiotensin II receptor of bovine adrenocortical membranesDissociation constant for [125 I] Ang binding to type 1 Angiotensin II receptor of bovine adrenocortical membranes
ChEMBL None None None None 10.1021/jm9608669
CHEMBL414918 211403 0 None - 1 Human 7.2 pKd = 7.2 Binding
Binding affinity was determined against Angiotensin II receptor, type 1Binding affinity was determined against Angiotensin II receptor, type 1
ChEMBL None None None CNCC(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@H](C(=O)N[C@H](Cc1ccc(O)cc1)C(=O)N1CCC[C@@H]1C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)N1CCC[C@@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O)C(C)C 10.1021/jm9507744
44348285 16240 0 None - 1 Rabbit 8.2 pKd = 8.2 Binding
In vitro binding affinity against Angiotensin II receptor in rabbit aorta ringsIn vitro binding affinity against Angiotensin II receptor in rabbit aorta rings
ChEMBL 481 6 1 6 4.2 CCOC(=O)/C=C1\C2C3C=CC(CC3)C2C(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81127-6
CHEMBL123208 16240 0 None - 1 Rabbit 8.2 pKd = 8.2 Binding
In vitro binding affinity against Angiotensin II receptor in rabbit aorta ringsIn vitro binding affinity against Angiotensin II receptor in rabbit aorta rings
ChEMBL 481 6 1 6 4.2 CCOC(=O)/C=C1\C2C3C=CC(CC3)C2C(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81127-6
44211278 186038 0 None - 1 Rabbit 8.2 pKd = 8.2 Binding
pA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic ringspA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic rings
ChEMBL 480 9 2 8 4.4 CCCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1ncnc2ccc(C(=O)O)nc12 10.1016/S0960-894X(01)81142-2
CHEMBL48799 186038 0 None - 1 Rabbit 8.2 pKd = 8.2 Binding
pA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic ringspA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic rings
ChEMBL 480 9 2 8 4.4 CCCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1ncnc2ccc(C(=O)O)nc12 10.1016/S0960-894X(01)81142-2
44211265 176887 0 None - 1 Rabbit 8.2 pKd = 8.2 Binding
pA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic ringspA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic rings
ChEMBL 425 8 2 7 4.0 CCCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1[nH]cnc2ncnc1-2 10.1016/S0960-894X(01)81142-2
CHEMBL46391 176887 0 None - 1 Rabbit 8.2 pKd = 8.2 Binding
pA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic ringspA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic rings
ChEMBL 425 8 2 7 4.0 CCCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1[nH]cnc2ncnc1-2 10.1016/S0960-894X(01)81142-2
127035515 135919 0 None - 1 Rabbit 8.2 pKd = 8.2 Binding
Antagonist activity against AT1 receptor in Japanese White rabbit aortic strips assessed as reduction in angiotension-2-induced contractile response after 60 mins by Schild's plot analysisAntagonist activity against AT1 receptor in Japanese White rabbit aortic strips assessed as reduction in angiotension-2-induced contractile response after 60 mins by Schild's plot analysis
ChEMBL 585 11 2 7 6.3 CCCc1nc2c(C)cc(C(=O)N[C@@H](COC)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.ejmech.2015.09.010
CHEMBL3735769 135919 0 None - 1 Rabbit 8.2 pKd = 8.2 Binding
Antagonist activity against AT1 receptor in Japanese White rabbit aortic strips assessed as reduction in angiotension-2-induced contractile response after 60 mins by Schild's plot analysisAntagonist activity against AT1 receptor in Japanese White rabbit aortic strips assessed as reduction in angiotension-2-induced contractile response after 60 mins by Schild's plot analysis
ChEMBL 585 11 2 7 6.3 CCCc1nc2c(C)cc(C(=O)N[C@@H](COC)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.ejmech.2015.09.010
44339988 160448 0 None -1 2 Bovine 5.2 pKd = 5.2 Binding
Dissociation constant for [125 I] Ang binding to type 1 Angiotensin II receptor of bovine adrenocortical membranesDissociation constant for [125 I] Ang binding to type 1 Angiotensin II receptor of bovine adrenocortical membranes
ChEMBL 989 27 12 12 -1.1 CC(C)[C@H](NC(=O)[C@H](CCCN=C(N)N)NC(=O)CCO)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)N1CCC[C@H]1C(=O)N[C@H](Cc1ccccc1)C(=O)O)C(C)C 10.1021/jm9608669
CHEMBL411624 160448 0 None -1 2 Bovine 5.2 pKd = 5.2 Binding
Dissociation constant for [125 I] Ang binding to type 1 Angiotensin II receptor of bovine adrenocortical membranesDissociation constant for [125 I] Ang binding to type 1 Angiotensin II receptor of bovine adrenocortical membranes
ChEMBL 989 27 12 12 -1.1 CC(C)[C@H](NC(=O)[C@H](CCCN=C(N)N)NC(=O)CCO)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)N1CCC[C@H]1C(=O)N[C@H](Cc1ccccc1)C(=O)O)C(C)C 10.1021/jm9608669
44211267 177205 0 None - 1 Rabbit 8.1 pKd = 8.1 Binding
pA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic ringspA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic rings
ChEMBL 469 9 2 9 3.2 CCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1ncnc2c1ncn2CC(=O)O 10.1016/S0960-894X(01)81142-2
CHEMBL46433 177205 0 None - 1 Rabbit 8.1 pKd = 8.1 Binding
pA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic ringspA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic rings
ChEMBL 469 9 2 9 3.2 CCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1ncnc2c1ncn2CC(=O)O 10.1016/S0960-894X(01)81142-2
127036105 135982 0 None - 1 Rabbit 8.1 pKd = 8.1 Binding
Antagonist activity against AT1 receptor in Japanese White rabbit aortic strips assessed as reduction in angiotension-2-induced contractile response after 60 mins by Schild's plot analysisAntagonist activity against AT1 receptor in Japanese White rabbit aortic strips assessed as reduction in angiotension-2-induced contractile response after 60 mins by Schild's plot analysis
ChEMBL 547 10 3 5 6.2 CCCc1nc2c(C)cc(C(=O)N[C@@H](CO)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2015.09.010
CHEMBL3736336 135982 0 None - 1 Rabbit 8.1 pKd = 8.1 Binding
Antagonist activity against AT1 receptor in Japanese White rabbit aortic strips assessed as reduction in angiotension-2-induced contractile response after 60 mins by Schild's plot analysisAntagonist activity against AT1 receptor in Japanese White rabbit aortic strips assessed as reduction in angiotension-2-induced contractile response after 60 mins by Schild's plot analysis
ChEMBL 547 10 3 5 6.2 CCCc1nc2c(C)cc(C(=O)N[C@@H](CO)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2015.09.010
CHEMBL412717 211263 0 None - 1 Bovine 8.1 pKd = 8.1 Binding
Dissociation constant for [125 I] Ang binding to type 1 Angiotensin II receptor of bovine adrenocortical membranesDissociation constant for [125 I] Ang binding to type 1 Angiotensin II receptor of bovine adrenocortical membranes
ChEMBL None None None None 10.1021/jm9608669
127036106 135832 0 None - 1 Rabbit 8.1 pKd = 8.1 Binding
Antagonist activity against AT1 receptor in Japanese White rabbit aortic strips assessed as reduction in angiotension-2-induced contractile response after 60 mins by Schild's plot analysisAntagonist activity against AT1 receptor in Japanese White rabbit aortic strips assessed as reduction in angiotension-2-induced contractile response after 60 mins by Schild's plot analysis
ChEMBL 571 10 3 7 5.7 CCCc1nc2c(C)cc(C(=O)N[C@H](CO)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.ejmech.2015.09.010
CHEMBL3734949 135832 0 None - 1 Rabbit 8.1 pKd = 8.1 Binding
Antagonist activity against AT1 receptor in Japanese White rabbit aortic strips assessed as reduction in angiotension-2-induced contractile response after 60 mins by Schild's plot analysisAntagonist activity against AT1 receptor in Japanese White rabbit aortic strips assessed as reduction in angiotension-2-induced contractile response after 60 mins by Schild's plot analysis
ChEMBL 571 10 3 7 5.7 CCCc1nc2c(C)cc(C(=O)N[C@H](CO)c3ccccc3)cc2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.ejmech.2015.09.010
44211263 191524 0 None - 1 Rabbit 8.1 pKd = 8.1 Binding
pA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic ringspA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic rings
ChEMBL 439 8 2 7 4.3 CCCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1[nH]cnc2nc(C)nc1-2 10.1016/S0960-894X(01)81142-2
CHEMBL52036 191524 0 None - 1 Rabbit 8.1 pKd = 8.1 Binding
pA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic ringspA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic rings
ChEMBL 439 8 2 7 4.3 CCCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1[nH]cnc2nc(C)nc1-2 10.1016/S0960-894X(01)81142-2
44295009 186578 0 None - 1 Rabbit 8.1 pKd = 8.1 Binding
In vitro binding affinity against Angiotensin II receptor in rabbit aorta ringsIn vitro binding affinity against Angiotensin II receptor in rabbit aorta rings
ChEMBL 473 8 1 6 4.9 CCOC(=O)/C=C1\CC(CC)(CC)CC(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81127-6
CHEMBL49207 186578 0 None - 1 Rabbit 8.1 pKd = 8.1 Binding
In vitro binding affinity against Angiotensin II receptor in rabbit aorta ringsIn vitro binding affinity against Angiotensin II receptor in rabbit aorta rings
ChEMBL 473 8 1 6 4.9 CCOC(=O)/C=C1\CC(CC)(CC)CC(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81127-6
44294721 100737 0 None - 1 Rabbit 7.1 pKd = 7.1 Binding
pA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic ringspA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic rings
ChEMBL 464 8 1 9 3.9 CCCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1ncnc2c1nc(C#N)n2C 10.1016/S0960-894X(01)81142-2
CHEMBL295935 100737 0 None - 1 Rabbit 7.1 pKd = 7.1 Binding
pA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic ringspA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic rings
ChEMBL 464 8 1 9 3.9 CCCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1ncnc2c1nc(C#N)n2C 10.1016/S0960-894X(01)81142-2
10321186 15323 0 None - 1 Rabbit 7.1 pKd = 7.1 Binding
Compound was evaluated for in vitro potency against Angiotensin II receptor, type 1 in isolated rabbit aorta; value ranges from 7.13-7.17Compound was evaluated for in vitro potency against Angiotensin II receptor, type 1 in isolated rabbit aorta; value ranges from 7.13-7.17
ChEMBL 443 9 2 7 4.0 CCCCc1ncc(C(=O)O)c(N(C)Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)n1 10.1021/jm00098a018
CHEMBL121705 15323 0 None - 1 Rabbit 7.1 pKd = 7.1 Binding
Compound was evaluated for in vitro potency against Angiotensin II receptor, type 1 in isolated rabbit aorta; value ranges from 7.13-7.17Compound was evaluated for in vitro potency against Angiotensin II receptor, type 1 in isolated rabbit aorta; value ranges from 7.13-7.17
ChEMBL 443 9 2 7 4.0 CCCCc1ncc(C(=O)O)c(N(C)Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)n1 10.1021/jm00098a018
44294518 187683 0 None - 1 Rabbit 7.1 pKd = 7.1 Binding
pA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic ringspA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic rings
ChEMBL 469 9 2 9 3.2 CCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1ncnc2ncn(CC(=O)O)c12 10.1016/S0960-894X(01)81142-2
CHEMBL50007 187683 0 None - 1 Rabbit 7.1 pKd = 7.1 Binding
pA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic ringspA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic rings
ChEMBL 469 9 2 9 3.2 CCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1ncnc2ncn(CC(=O)O)c12 10.1016/S0960-894X(01)81142-2
CHEMBL216678 207582 0 None - 1 Human 6.1 pKd = 6.1 Binding
Binding affinity was determined against Angiotensin II receptor, type 1Binding affinity was determined against Angiotensin II receptor, type 1
ChEMBL None None None CNCC(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H]1CCSS[C@@H]2C[C@@H](C(=O)N[C@@H](Cc3ccccc3)C(=O)O)N(C2)C(=O)[C@@H](Cc2c[nH]cn2)NC1=O)C(C)C 10.1021/jm9507744
44294610 187552 0 None - 1 Rabbit 6.1 pKd = 6.1 Binding
pA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic ringspA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic rings
ChEMBL 436 8 1 7 4.7 CCCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1ncnc2cccnc12 10.1016/S0960-894X(01)81142-2
CHEMBL49848 187552 0 None - 1 Rabbit 6.1 pKd = 6.1 Binding
pA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic ringspA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic rings
ChEMBL 436 8 1 7 4.7 CCCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1ncnc2cccnc12 10.1016/S0960-894X(01)81142-2
73346386 92170 0 None - 1 Rabbit 8.1 pKd = 8.1 Binding
Antagonist activity against AT1 receptor in Japanese White rabbit aortic strips assessed as reduction in angiotension-2-induced contractile response after 60 mins by Schild's plot analysisAntagonist activity against AT1 receptor in Japanese White rabbit aortic strips assessed as reduction in angiotension-2-induced contractile response after 60 mins by Schild's plot analysis
ChEMBL 531 10 2 4 6.7 CCCc1nc2c(C)cc(C(=O)NCCc3ccccc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2015.09.010
CHEMBL2435818 92170 0 None - 1 Rabbit 8.1 pKd = 8.1 Binding
Antagonist activity against AT1 receptor in Japanese White rabbit aortic strips assessed as reduction in angiotension-2-induced contractile response after 60 mins by Schild's plot analysisAntagonist activity against AT1 receptor in Japanese White rabbit aortic strips assessed as reduction in angiotension-2-induced contractile response after 60 mins by Schild's plot analysis
ChEMBL 531 10 2 4 6.7 CCCc1nc2c(C)cc(C(=O)NCCc3ccccc3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1016/j.ejmech.2015.09.010
10048997 15311 0 None 14 2 Rabbit 8.1 pKd = 8.1 Binding
Compound was evaluated for in vitro potency against angiotensin II receptor, type 1 in isolated rabbit aorta; value ranges from 8.08-8.22Compound was evaluated for in vitro potency against angiotensin II receptor, type 1 in isolated rabbit aorta; value ranges from 8.08-8.22
ChEMBL 442 9 2 6 4.7 CCCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1nc(C)ccc1C(=O)O 10.1021/jm00098a018
CHEMBL121635 15311 0 None 14 2 Rabbit 8.1 pKd = 8.1 Binding
Compound was evaluated for in vitro potency against angiotensin II receptor, type 1 in isolated rabbit aorta; value ranges from 8.08-8.22Compound was evaluated for in vitro potency against angiotensin II receptor, type 1 in isolated rabbit aorta; value ranges from 8.08-8.22
ChEMBL 442 9 2 6 4.7 CCCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1nc(C)ccc1C(=O)O 10.1021/jm00098a018
44211264 101327 0 None - 1 Rabbit 8.1 pKd = 8.1 Binding
pA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic ringspA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic rings
ChEMBL 439 8 1 8 4.0 CCCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1ncnc2c1ncn2C 10.1016/S0960-894X(01)81142-2
CHEMBL300194 101327 0 None - 1 Rabbit 8.1 pKd = 8.1 Binding
pA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic ringspA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic rings
ChEMBL 439 8 1 8 4.0 CCCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1ncnc2c1ncn2C 10.1016/S0960-894X(01)81142-2
44294618 187800 0 None - 1 Rabbit 8.1 pKd = 8.1 Binding
pA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic ringspA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic rings
ChEMBL 437 7 2 7 4.7 CCc1nc(NCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2c(OC)cccc2n1 10.1016/S0960-894X(01)81142-2
CHEMBL50174 187800 0 None - 1 Rabbit 8.1 pKd = 8.1 Binding
pA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic ringspA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic rings
ChEMBL 437 7 2 7 4.7 CCc1nc(NCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2c(OC)cccc2n1 10.1016/S0960-894X(01)81142-2
44294637 162585 0 None - 1 Rabbit 7.1 pKd = 7.1 Binding
pA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic ringspA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic rings
ChEMBL 451 8 2 7 5.0 CCCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1ncnc2ccc(O)cc12 10.1016/S0960-894X(01)81142-2
CHEMBL417910 162585 0 None - 1 Rabbit 7.1 pKd = 7.1 Binding
pA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic ringspA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic rings
ChEMBL 451 8 2 7 5.0 CCCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1ncnc2ccc(O)cc12 10.1016/S0960-894X(01)81142-2
44294822 100677 0 None - 1 Rabbit 8.0 pKd = 8.0 Binding
pA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic ringspA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic rings
ChEMBL 453 8 1 8 4.3 CCCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1ncnc2c1nc(C)n2C 10.1016/S0960-894X(01)81142-2
CHEMBL295498 100677 0 None - 1 Rabbit 8.0 pKd = 8.0 Binding
pA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic ringspA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic rings
ChEMBL 453 8 1 8 4.3 CCCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1ncnc2c1nc(C)n2C 10.1016/S0960-894X(01)81142-2
44211277 187373 0 None - 1 Rabbit 8.0 pKd = 8.0 Binding
pA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic ringspA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic rings
ChEMBL 479 9 2 7 5.0 CCCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1ncnc2ccc(C(=O)O)cc12 10.1016/S0960-894X(01)81142-2
CHEMBL49715 187373 0 None - 1 Rabbit 8.0 pKd = 8.0 Binding
pA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic ringspA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic rings
ChEMBL 479 9 2 7 5.0 CCCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1ncnc2ccc(C(=O)O)cc12 10.1016/S0960-894X(01)81142-2
44294459 183516 0 None - 1 Rabbit 6.0 pKd = 6.0 Binding
pA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic ringspA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic rings
ChEMBL 425 7 1 8 3.6 CCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1ncnc2ncn(C)c12 10.1016/S0960-894X(01)81142-2
CHEMBL48259 183516 0 None - 1 Rabbit 6.0 pKd = 6.0 Binding
pA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic ringspA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic rings
ChEMBL 425 7 1 8 3.6 CCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1ncnc2ncn(C)c12 10.1016/S0960-894X(01)81142-2
44294539 164312 0 None - 1 Rabbit 7.0 pKd = 7.0 Binding
pA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic ringspA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic rings
ChEMBL 426 7 1 8 4.2 CCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1ncnc2oc(C)nc12 10.1016/S0960-894X(01)81142-2
CHEMBL422050 164312 0 None - 1 Rabbit 7.0 pKd = 7.0 Binding
pA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic ringspA2 value determined in vitro against angiotensin II receptor, type 1 using rabbit aortic rings
ChEMBL 426 7 1 8 4.2 CCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1ncnc2oc(C)nc12 10.1016/S0960-894X(01)81142-2
CHEMBL216061 207561 10 None 1 2 Rat 9.8 pKi = 9.8 Binding
Binding affinity for angiotensin II receptor, type 1 in rat liver membrane using [125I]-Ang II as radioligand, in pH 7.4 Tris-HCl buffer for 2 hr at 25 degree CBinding affinity for angiotensin II receptor, type 1 in rat liver membrane using [125I]-Ang II as radioligand, in pH 7.4 Tris-HCl buffer for 2 hr at 25 degree C
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCN=C(N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O 10.1021/jm050280z
16133225 415 47 None -2 6 Human 9.8 pKi = 9.8 Binding
Displacement of [3H]-Angiotensin 2 from human placental AT1 receptor expressed in African green monkey COS7 cell membranes after 90 mins by gamma countingDisplacement of [3H]-Angiotensin 2 from human placental AT1 receptor expressed in African green monkey COS7 cell membranes after 90 mins by gamma counting
ChEMBL None None None None 10.1021/acs.jmedchem.5b01495
172198 415 47 None -2 6 Human 9.8 pKi = 9.8 Binding
Displacement of [3H]-Angiotensin 2 from human placental AT1 receptor expressed in African green monkey COS7 cell membranes after 90 mins by gamma countingDisplacement of [3H]-Angiotensin 2 from human placental AT1 receptor expressed in African green monkey COS7 cell membranes after 90 mins by gamma counting
ChEMBL None None None None 10.1021/acs.jmedchem.5b01495
2504 415 47 None -2 6 Human 9.8 pKi = 9.8 Binding
Displacement of [3H]-Angiotensin 2 from human placental AT1 receptor expressed in African green monkey COS7 cell membranes after 90 mins by gamma countingDisplacement of [3H]-Angiotensin 2 from human placental AT1 receptor expressed in African green monkey COS7 cell membranes after 90 mins by gamma counting
ChEMBL None None None None 10.1021/acs.jmedchem.5b01495
45266664 415 47 None -2 6 Human 9.8 pKi = 9.8 Binding
Displacement of [3H]-Angiotensin 2 from human placental AT1 receptor expressed in African green monkey COS7 cell membranes after 90 mins by gamma countingDisplacement of [3H]-Angiotensin 2 from human placental AT1 receptor expressed in African green monkey COS7 cell membranes after 90 mins by gamma counting
ChEMBL None None None None 10.1021/acs.jmedchem.5b01495
5272 415 47 None -2 6 Human 9.8 pKi = 9.8 Binding
Displacement of [3H]-Angiotensin 2 from human placental AT1 receptor expressed in African green monkey COS7 cell membranes after 90 mins by gamma countingDisplacement of [3H]-Angiotensin 2 from human placental AT1 receptor expressed in African green monkey COS7 cell membranes after 90 mins by gamma counting
ChEMBL None None None None 10.1021/acs.jmedchem.5b01495
CHEMBL408403 415 47 None -2 6 Human 9.8 pKi = 9.8 Binding
Displacement of [3H]-Angiotensin 2 from human placental AT1 receptor expressed in African green monkey COS7 cell membranes after 90 mins by gamma countingDisplacement of [3H]-Angiotensin 2 from human placental AT1 receptor expressed in African green monkey COS7 cell membranes after 90 mins by gamma counting
ChEMBL None None None None 10.1021/acs.jmedchem.5b01495
DB11842 415 47 None -2 6 Human 9.8 pKi = 9.8 Binding
Displacement of [3H]-Angiotensin 2 from human placental AT1 receptor expressed in African green monkey COS7 cell membranes after 90 mins by gamma countingDisplacement of [3H]-Angiotensin 2 from human placental AT1 receptor expressed in African green monkey COS7 cell membranes after 90 mins by gamma counting
ChEMBL None None None None 10.1021/acs.jmedchem.5b01495
CHEMBL938 214120 24 None 1 2 Human 9.8 pKi = 9.8 Binding
Binding affinity to human AT1 receptor by radioligand displacement assayBinding affinity to human AT1 receptor by radioligand displacement assay
ChEMBL None None None CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O)C(C)C)C(C)C 10.1016/j.ejmech.2013.01.044
CHEMBL938 214120 24 None 1 2 Human 9.7 pKi = 9.7 Binding
Binding affinity to AT1 receptor (unknown origin)Binding affinity to AT1 receptor (unknown origin)
ChEMBL None None None CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O)C(C)C)C(C)C 10.1021/ml500278g
1056 3307 111 None - 1 Rat 9.6 pKi = 9.6 Binding
Displacement of [125I]-SI-Ang-2 from AT1 receptor in Rattus norvegicus Sprague-Dawley (rat) liver membranes after 2 hrDisplacement of [125I]-SI-Ang-2 from AT1 receptor in Rattus norvegicus Sprague-Dawley (rat) liver membranes after 2 hr
ChEMBL 357 7 1 6 2.5 O=C1NC(=O)C(S1)Cc1ccc(cc1)OCCN(c1ccccn1)C 10.1007/s00044-008-9152-x
2405 3307 111 None - 1 Rat 9.6 pKi = 9.6 Binding
Displacement of [125I]-SI-Ang-2 from AT1 receptor in Rattus norvegicus Sprague-Dawley (rat) liver membranes after 2 hrDisplacement of [125I]-SI-Ang-2 from AT1 receptor in Rattus norvegicus Sprague-Dawley (rat) liver membranes after 2 hr
ChEMBL 357 7 1 6 2.5 O=C1NC(=O)C(S1)Cc1ccc(cc1)OCCN(c1ccccn1)C 10.1007/s00044-008-9152-x
77999 3307 111 None - 1 Rat 9.6 pKi = 9.6 Binding
Displacement of [125I]-SI-Ang-2 from AT1 receptor in Rattus norvegicus Sprague-Dawley (rat) liver membranes after 2 hrDisplacement of [125I]-SI-Ang-2 from AT1 receptor in Rattus norvegicus Sprague-Dawley (rat) liver membranes after 2 hr
ChEMBL 357 7 1 6 2.5 O=C1NC(=O)C(S1)Cc1ccc(cc1)OCCN(c1ccccn1)C 10.1007/s00044-008-9152-x
CHEMBL121 3307 111 None - 1 Rat 9.6 pKi = 9.6 Binding
Displacement of [125I]-SI-Ang-2 from AT1 receptor in Rattus norvegicus Sprague-Dawley (rat) liver membranes after 2 hrDisplacement of [125I]-SI-Ang-2 from AT1 receptor in Rattus norvegicus Sprague-Dawley (rat) liver membranes after 2 hr
ChEMBL 357 7 1 6 2.5 O=C1NC(=O)C(S1)Cc1ccc(cc1)OCCN(c1ccccn1)C 10.1007/s00044-008-9152-x
DB00412 3307 111 None - 1 Rat 9.6 pKi = 9.6 Binding
Displacement of [125I]-SI-Ang-2 from AT1 receptor in Rattus norvegicus Sprague-Dawley (rat) liver membranes after 2 hrDisplacement of [125I]-SI-Ang-2 from AT1 receptor in Rattus norvegicus Sprague-Dawley (rat) liver membranes after 2 hr
ChEMBL 357 7 1 6 2.5 O=C1NC(=O)C(S1)Cc1ccc(cc1)OCCN(c1ccccn1)C 10.1007/s00044-008-9152-x
2583 3705 115 None - 1 Rat 9.6 pKi = 9.6 Binding
Displacement of [125I]-SI-Ang-2 from AT1 receptor in Rattus norvegicus Sprague-Dawley (rat) liver membranes after 2 hrDisplacement of [125I]-SI-Ang-2 from AT1 receptor in Rattus norvegicus Sprague-Dawley (rat) liver membranes after 2 hr
ChEMBL 514 7 1 5 7.3 CCCc1nc2c(n1Cc1ccc(cc1)c1ccccc1C(=O)O)cc(cc2C)c1nc2c(n1C)cccc2 10.1007/s00044-008-9153-9
592 3705 115 None - 1 Rat 9.6 pKi = 9.6 Binding
Displacement of [125I]-SI-Ang-2 from AT1 receptor in Rattus norvegicus Sprague-Dawley (rat) liver membranes after 2 hrDisplacement of [125I]-SI-Ang-2 from AT1 receptor in Rattus norvegicus Sprague-Dawley (rat) liver membranes after 2 hr
ChEMBL 514 7 1 5 7.3 CCCc1nc2c(n1Cc1ccc(cc1)c1ccccc1C(=O)O)cc(cc2C)c1nc2c(n1C)cccc2 10.1007/s00044-008-9153-9
65999 3705 115 None - 1 Rat 9.6 pKi = 9.6 Binding
Displacement of [125I]-SI-Ang-2 from AT1 receptor in Rattus norvegicus Sprague-Dawley (rat) liver membranes after 2 hrDisplacement of [125I]-SI-Ang-2 from AT1 receptor in Rattus norvegicus Sprague-Dawley (rat) liver membranes after 2 hr
ChEMBL 514 7 1 5 7.3 CCCc1nc2c(n1Cc1ccc(cc1)c1ccccc1C(=O)O)cc(cc2C)c1nc2c(n1C)cccc2 10.1007/s00044-008-9153-9
CHEMBL1017 3705 115 None - 1 Rat 9.6 pKi = 9.6 Binding
Displacement of [125I]-SI-Ang-2 from AT1 receptor in Rattus norvegicus Sprague-Dawley (rat) liver membranes after 2 hrDisplacement of [125I]-SI-Ang-2 from AT1 receptor in Rattus norvegicus Sprague-Dawley (rat) liver membranes after 2 hr
ChEMBL 514 7 1 5 7.3 CCCc1nc2c(n1Cc1ccc(cc1)c1ccccc1C(=O)O)cc(cc2C)c1nc2c(n1C)cccc2 10.1007/s00044-008-9153-9
DB00966 3705 115 None - 1 Rat 9.6 pKi = 9.6 Binding
Displacement of [125I]-SI-Ang-2 from AT1 receptor in Rattus norvegicus Sprague-Dawley (rat) liver membranes after 2 hrDisplacement of [125I]-SI-Ang-2 from AT1 receptor in Rattus norvegicus Sprague-Dawley (rat) liver membranes after 2 hr
ChEMBL 514 7 1 5 7.3 CCCc1nc2c(n1Cc1ccc(cc1)c1ccccc1C(=O)O)cc(cc2C)c1nc2c(n1C)cccc2 10.1007/s00044-008-9153-9
2583 3705 115 None - 1 Rat 9.6 pKi = 9.6 Binding
Displacement of [125I]SI-Ang2 from AT1 receptor in Sprague-Dawley rat liver membraneDisplacement of [125I]SI-Ang2 from AT1 receptor in Sprague-Dawley rat liver membrane
ChEMBL 514 7 1 5 7.3 CCCc1nc2c(n1Cc1ccc(cc1)c1ccccc1C(=O)O)cc(cc2C)c1nc2c(n1C)cccc2 10.1021/jm901272d
592 3705 115 None - 1 Rat 9.6 pKi = 9.6 Binding
Displacement of [125I]SI-Ang2 from AT1 receptor in Sprague-Dawley rat liver membraneDisplacement of [125I]SI-Ang2 from AT1 receptor in Sprague-Dawley rat liver membrane
ChEMBL 514 7 1 5 7.3 CCCc1nc2c(n1Cc1ccc(cc1)c1ccccc1C(=O)O)cc(cc2C)c1nc2c(n1C)cccc2 10.1021/jm901272d
65999 3705 115 None - 1 Rat 9.6 pKi = 9.6 Binding
Displacement of [125I]SI-Ang2 from AT1 receptor in Sprague-Dawley rat liver membraneDisplacement of [125I]SI-Ang2 from AT1 receptor in Sprague-Dawley rat liver membrane
ChEMBL 514 7 1 5 7.3 CCCc1nc2c(n1Cc1ccc(cc1)c1ccccc1C(=O)O)cc(cc2C)c1nc2c(n1C)cccc2 10.1021/jm901272d
CHEMBL1017 3705 115 None - 1 Rat 9.6 pKi = 9.6 Binding
Displacement of [125I]SI-Ang2 from AT1 receptor in Sprague-Dawley rat liver membraneDisplacement of [125I]SI-Ang2 from AT1 receptor in Sprague-Dawley rat liver membrane
ChEMBL 514 7 1 5 7.3 CCCc1nc2c(n1Cc1ccc(cc1)c1ccccc1C(=O)O)cc(cc2C)c1nc2c(n1C)cccc2 10.1021/jm901272d
DB00966 3705 115 None - 1 Rat 9.6 pKi = 9.6 Binding
Displacement of [125I]SI-Ang2 from AT1 receptor in Sprague-Dawley rat liver membraneDisplacement of [125I]SI-Ang2 from AT1 receptor in Sprague-Dawley rat liver membrane
ChEMBL 514 7 1 5 7.3 CCCc1nc2c(n1Cc1ccc(cc1)c1ccccc1C(=O)O)cc(cc2C)c1nc2c(n1C)cccc2 10.1021/jm901272d
CHEMBL411997 211211 0 None - 1 Rat 9.6 pKi = 9.6 Binding
In vitro binding affinity at rat liver Angiotensin II receptor, type 1 was determined based on displacement of [125I]-Ang IIIn vitro binding affinity at rat liver Angiotensin II receptor, type 1 was determined based on displacement of [125I]-Ang II
ChEMBL None None None NC(N)=NCCC[C@H](NC(=O)[C@@H](N)CC(=O)O)C(=O)N[C@H]1CCSSCC[C@@H](C(=O)N[C@@H](Cc2c[nH]cn2)C(=O)N2CCC[C@H]2C(=O)N[C@@H](Cc2ccccc2)C(=O)O)NC(=O)[C@H](Cc2ccc(O)cc2)NC1=O 10.1021/jm011063a
16133225 415 47 None -2 6 Human 9.6 pKi = 9.6 Binding
Displacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation countingDisplacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation counting
ChEMBL None None None None 10.1021/acs.jmedchem.5b01495
172198 415 47 None -2 6 Human 9.6 pKi = 9.6 Binding
Displacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation countingDisplacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation counting
ChEMBL None None None None 10.1021/acs.jmedchem.5b01495
2504 415 47 None -2 6 Human 9.6 pKi = 9.6 Binding
Displacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation countingDisplacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation counting
ChEMBL None None None None 10.1021/acs.jmedchem.5b01495
45266664 415 47 None -2 6 Human 9.6 pKi = 9.6 Binding
Displacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation countingDisplacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation counting
ChEMBL None None None None 10.1021/acs.jmedchem.5b01495
5272 415 47 None -2 6 Human 9.6 pKi = 9.6 Binding
Displacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation countingDisplacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation counting
ChEMBL None None None None 10.1021/acs.jmedchem.5b01495
CHEMBL408403 415 47 None -2 6 Human 9.6 pKi = 9.6 Binding
Displacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation countingDisplacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation counting
ChEMBL None None None None 10.1021/acs.jmedchem.5b01495
DB11842 415 47 None -2 6 Human 9.6 pKi = 9.6 Binding
Displacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation countingDisplacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation counting
ChEMBL None None None None 10.1021/acs.jmedchem.5b01495
10390188 205516 0 None - 1 Human 9.5 pKi = 9.5 Binding
Ability to displace [125I]AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1Ability to displace [125I]AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1
ChEMBL 475 5 1 7 4.9 CCCc1nc2c(C)cc(C)nc2n1Cc1ccc2c(-c3nnn[nH]3)cc3ccccc3c(=O)c2c1 10.1021/jm00014a024
CHEMBL92950 205516 0 None - 1 Human 9.5 pKi = 9.5 Binding
Ability to displace [125I]AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1Ability to displace [125I]AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1
ChEMBL 475 5 1 7 4.9 CCCc1nc2c(C)cc(C)nc2n1Cc1ccc2c(-c3nnn[nH]3)cc3ccccc3c(=O)c2c1 10.1021/jm00014a024
CHEMBL1076604 206727 0 None - 1 Human 9.5 pKi = 9.5 Binding
Displacement of [125I][Sar1,Ile8]Ang2 from human AT1 receptor N111G constitutively active mutant expressed in CHO cells by gamma countingDisplacement of [125I][Sar1,Ile8]Ang2 from human AT1 receptor N111G constitutively active mutant expressed in CHO cells by gamma counting
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](Cc1ccc(C2(C(F)(F)F)N=N2)cc1)NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O 10.1021/jm9015747
16133225 415 47 None -7 6 Rat 9.5 pKi = 9.5 Binding
In vitro binding affinity at rat liver Angiotensin II receptor, type 1 was determined based on displacement of [125I]-Ang IIIn vitro binding affinity at rat liver Angiotensin II receptor, type 1 was determined based on displacement of [125I]-Ang II
ChEMBL None None None None 10.1021/jm011063a
172198 415 47 None -7 6 Rat 9.5 pKi = 9.5 Binding
In vitro binding affinity at rat liver Angiotensin II receptor, type 1 was determined based on displacement of [125I]-Ang IIIn vitro binding affinity at rat liver Angiotensin II receptor, type 1 was determined based on displacement of [125I]-Ang II
ChEMBL None None None None 10.1021/jm011063a
2504 415 47 None -7 6 Rat 9.5 pKi = 9.5 Binding
In vitro binding affinity at rat liver Angiotensin II receptor, type 1 was determined based on displacement of [125I]-Ang IIIn vitro binding affinity at rat liver Angiotensin II receptor, type 1 was determined based on displacement of [125I]-Ang II
ChEMBL None None None None 10.1021/jm011063a
45266664 415 47 None -7 6 Rat 9.5 pKi = 9.5 Binding
In vitro binding affinity at rat liver Angiotensin II receptor, type 1 was determined based on displacement of [125I]-Ang IIIn vitro binding affinity at rat liver Angiotensin II receptor, type 1 was determined based on displacement of [125I]-Ang II
ChEMBL None None None None 10.1021/jm011063a
5272 415 47 None -7 6 Rat 9.5 pKi = 9.5 Binding
In vitro binding affinity at rat liver Angiotensin II receptor, type 1 was determined based on displacement of [125I]-Ang IIIn vitro binding affinity at rat liver Angiotensin II receptor, type 1 was determined based on displacement of [125I]-Ang II
ChEMBL None None None None 10.1021/jm011063a
CHEMBL408403 415 47 None -7 6 Rat 9.5 pKi = 9.5 Binding
In vitro binding affinity at rat liver Angiotensin II receptor, type 1 was determined based on displacement of [125I]-Ang IIIn vitro binding affinity at rat liver Angiotensin II receptor, type 1 was determined based on displacement of [125I]-Ang II
ChEMBL None None None None 10.1021/jm011063a
DB11842 415 47 None -7 6 Rat 9.5 pKi = 9.5 Binding
In vitro binding affinity at rat liver Angiotensin II receptor, type 1 was determined based on displacement of [125I]-Ang IIIn vitro binding affinity at rat liver Angiotensin II receptor, type 1 was determined based on displacement of [125I]-Ang II
ChEMBL None None None None 10.1021/jm011063a
CHEMBL938 214120 24 None 1 2 Human 9.5 pKi = 9.5 Binding
Displacement of radiolabeled saralasin from human AT1 receptorDisplacement of radiolabeled saralasin from human AT1 receptor
ChEMBL None None None CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O)C(C)C)C(C)C 10.1021/jm8007618
CHEMBL1076602 206725 0 None - 1 Human 9.4 pKi = 9.4 Binding
Displacement of [125I][Sar1,Ile8]Ang2 from human AT1 receptor N111G constitutively active mutant expressed in CHO cells by gamma countingDisplacement of [125I][Sar1,Ile8]Ang2 from human AT1 receptor N111G constitutively active mutant expressed in CHO cells by gamma counting
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccc(C2(C(F)(F)F)N=N2)cc1)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O 10.1021/jm9015747
CHEMBL1076603 206726 0 None - 1 Human 9.4 pKi = 9.4 Binding
Displacement of [125I][Sar1,Ile8]Ang2 from human AT1 receptor N111G constitutively active mutant expressed in CHO cells by gamma countingDisplacement of [125I][Sar1,Ile8]Ang2 from human AT1 receptor N111G constitutively active mutant expressed in CHO cells by gamma counting
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](Cc1ccc(C(=O)c2ccccc2)cc1)NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O 10.1021/jm9015747
6918 1010 29 None 3 3 Pig 9.4 pKi = 9.4 Binding
Displacement of [125]Ang2 from AT2 receptor in pig uterus membraneDisplacement of [125]Ang2 from AT2 receptor in pig uterus membrane
ChEMBL 475 10 1 7 5.1 CCCCOC(=O)NS(=O)(=O)c1sc(cc1c1ccc(cc1)Cn1cncc1)CC(C)C 10.1016/j.bmc.2008.05.066
9804984 1010 29 None 3 3 Pig 9.4 pKi = 9.4 Binding
Displacement of [125]Ang2 from AT2 receptor in pig uterus membraneDisplacement of [125]Ang2 from AT2 receptor in pig uterus membrane
ChEMBL 475 10 1 7 5.1 CCCCOC(=O)NS(=O)(=O)c1sc(cc1c1ccc(cc1)Cn1cncc1)CC(C)C 10.1016/j.bmc.2008.05.066
CHEMBL189568 1010 29 None 3 3 Pig 9.4 pKi = 9.4 Binding
Displacement of [125]Ang2 from AT2 receptor in pig uterus membraneDisplacement of [125]Ang2 from AT2 receptor in pig uterus membrane
ChEMBL 475 10 1 7 5.1 CCCCOC(=O)NS(=O)(=O)c1sc(cc1c1ccc(cc1)Cn1cncc1)CC(C)C 10.1016/j.bmc.2008.05.066
10479983 205589 0 None - 1 Human 9.4 pKi = 9.4 Binding
Ability to displace [125I]AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1Ability to displace [125I]AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1
ChEMBL 473 4 1 7 4.8 Cc1cc(C)c2nc(C3CC3)n(Cc3ccc4c(-c5nnn[nH]5)cc5ccccc5c(=O)c4c3)c2n1 10.1021/jm00014a024
CHEMBL93522 205589 0 None - 1 Human 9.4 pKi = 9.4 Binding
Ability to displace [125I]AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1Ability to displace [125I]AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1
ChEMBL 473 4 1 7 4.8 Cc1cc(C)c2nc(C3CC3)n(Cc3ccc4c(-c5nnn[nH]5)cc5ccccc5c(=O)c4c3)c2n1 10.1021/jm00014a024
183134 203126 13 None - 1 Rat 9.4 pKi = 9.4 Binding
Binding affinity against angiotensin II receptor from rat liverBinding affinity against angiotensin II receptor from rat liver
ChEMBL 409 5 1 6 4.5 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00070a012
CHEMBL7550 203126 13 None - 1 Rat 9.4 pKi = 9.4 Binding
Binding affinity against angiotensin II receptor from rat liverBinding affinity against angiotensin II receptor from rat liver
ChEMBL 409 5 1 6 4.5 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00070a012
9826888 206131 0 None - 1 Human 9.3 pKi = 9.3 Binding
Ability to displace [125I]AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1Ability to displace [125I]AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1
ChEMBL 490 6 1 8 4.6 CCc1cc(OCc2ccc3c(-c4nnn[nH]4)cc4ccccc4c(=O)c3c2)c2nc(OC)ccc2n1 10.1021/jm00014a024
CHEMBL96552 206131 0 None - 1 Human 9.3 pKi = 9.3 Binding
Ability to displace [125I]AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1Ability to displace [125I]AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1
ChEMBL 490 6 1 8 4.6 CCc1cc(OCc2ccc3c(-c4nnn[nH]4)cc4ccccc4c(=O)c3c2)c2nc(OC)ccc2n1 10.1021/jm00014a024
10004498 205538 0 None - 1 Human 9.3 pKi = 9.3 Binding
Ability to displace [125I]AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1Ability to displace [125I]AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1
ChEMBL 461 5 1 6 5.1 CCCc1nc2c(C)cc(C)nc2n1Cc1ccc2c(c1)Cc1ccccc1C=C2c1nnn[nH]1 10.1021/jm00014a024
CHEMBL93159 205538 0 None - 1 Human 9.3 pKi = 9.3 Binding
Ability to displace [125I]AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1Ability to displace [125I]AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1
ChEMBL 461 5 1 6 5.1 CCCc1nc2c(C)cc(C)nc2n1Cc1ccc2c(c1)Cc1ccccc1C=C2c1nnn[nH]1 10.1021/jm00014a024
16133225 415 47 None -2 6 Human 9.3 pKi = 9.3 Binding
Displacement of [125I][Sar1,Ile8]Ang2 from human AT1 receptor N111G constitutively active mutant expressed in CHO cells by gamma countingDisplacement of [125I][Sar1,Ile8]Ang2 from human AT1 receptor N111G constitutively active mutant expressed in CHO cells by gamma counting
ChEMBL None None None None 10.1021/jm9015747
172198 415 47 None -2 6 Human 9.3 pKi = 9.3 Binding
Displacement of [125I][Sar1,Ile8]Ang2 from human AT1 receptor N111G constitutively active mutant expressed in CHO cells by gamma countingDisplacement of [125I][Sar1,Ile8]Ang2 from human AT1 receptor N111G constitutively active mutant expressed in CHO cells by gamma counting
ChEMBL None None None None 10.1021/jm9015747
2504 415 47 None -2 6 Human 9.3 pKi = 9.3 Binding
Displacement of [125I][Sar1,Ile8]Ang2 from human AT1 receptor N111G constitutively active mutant expressed in CHO cells by gamma countingDisplacement of [125I][Sar1,Ile8]Ang2 from human AT1 receptor N111G constitutively active mutant expressed in CHO cells by gamma counting
ChEMBL None None None None 10.1021/jm9015747
45266664 415 47 None -2 6 Human 9.3 pKi = 9.3 Binding
Displacement of [125I][Sar1,Ile8]Ang2 from human AT1 receptor N111G constitutively active mutant expressed in CHO cells by gamma countingDisplacement of [125I][Sar1,Ile8]Ang2 from human AT1 receptor N111G constitutively active mutant expressed in CHO cells by gamma counting
ChEMBL None None None None 10.1021/jm9015747
5272 415 47 None -2 6 Human 9.3 pKi = 9.3 Binding
Displacement of [125I][Sar1,Ile8]Ang2 from human AT1 receptor N111G constitutively active mutant expressed in CHO cells by gamma countingDisplacement of [125I][Sar1,Ile8]Ang2 from human AT1 receptor N111G constitutively active mutant expressed in CHO cells by gamma counting
ChEMBL None None None None 10.1021/jm9015747
CHEMBL408403 415 47 None -2 6 Human 9.3 pKi = 9.3 Binding
Displacement of [125I][Sar1,Ile8]Ang2 from human AT1 receptor N111G constitutively active mutant expressed in CHO cells by gamma countingDisplacement of [125I][Sar1,Ile8]Ang2 from human AT1 receptor N111G constitutively active mutant expressed in CHO cells by gamma counting
ChEMBL None None None None 10.1021/jm9015747
DB11842 415 47 None -2 6 Human 9.3 pKi = 9.3 Binding
Displacement of [125I][Sar1,Ile8]Ang2 from human AT1 receptor N111G constitutively active mutant expressed in CHO cells by gamma countingDisplacement of [125I][Sar1,Ile8]Ang2 from human AT1 receptor N111G constitutively active mutant expressed in CHO cells by gamma counting
ChEMBL None None None None 10.1021/jm9015747
CHEMBL1076663 206736 0 None - 1 Human 9.3 pKi = 9.3 Binding
Displacement of [125I][Sar1,Ile8]Ang2 from human AT1 receptor N111G constitutively active mutant expressed in CHO cells by gamma countingDisplacement of [125I][Sar1,Ile8]Ang2 from human AT1 receptor N111G constitutively active mutant expressed in CHO cells by gamma counting
ChEMBL None None None CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1ccc(C2(C(F)(F)F)N=N2)cc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O)C(C)C 10.1021/jm9015747
4673492 4061 5 None - 1 Human 9.3 pKi = 9.3 Binding
Displacement of [tyrosyl-3,5-3H]angiotensin-2 from AT1 receptor (unknown origin) expressed in QBI-HEK293A cells after 2 hrsDisplacement of [tyrosyl-3,5-3H]angiotensin-2 from AT1 receptor (unknown origin) expressed in QBI-HEK293A cells after 2 hrs
ChEMBL 438 6 1 5 4.5 CCc1nc(CC)c2c(c1)N(Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)C(=O)CC2 10.1016/j.bmc.2013.09.004
8324 4061 5 None - 1 Human 9.3 pKi = 9.3 Binding
Displacement of [tyrosyl-3,5-3H]angiotensin-2 from AT1 receptor (unknown origin) expressed in QBI-HEK293A cells after 2 hrsDisplacement of [tyrosyl-3,5-3H]angiotensin-2 from AT1 receptor (unknown origin) expressed in QBI-HEK293A cells after 2 hrs
ChEMBL 438 6 1 5 4.5 CCc1nc(CC)c2c(c1)N(Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)C(=O)CC2 10.1016/j.bmc.2013.09.004
CHEMBL159096 4061 5 None - 1 Human 9.3 pKi = 9.3 Binding
Displacement of [tyrosyl-3,5-3H]angiotensin-2 from AT1 receptor (unknown origin) expressed in QBI-HEK293A cells after 2 hrsDisplacement of [tyrosyl-3,5-3H]angiotensin-2 from AT1 receptor (unknown origin) expressed in QBI-HEK293A cells after 2 hrs
ChEMBL 438 6 1 5 4.5 CCc1nc(CC)c2c(c1)N(Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)C(=O)CC2 10.1016/j.bmc.2013.09.004
CHEMBL1076601 206724 0 None - 1 Human 9.2 pKi = 9.2 Binding
Displacement of [125I][Sar1,Ile8]Ang2 from human AT1 receptor N111G constitutively active mutant expressed in CHO cells by gamma countingDisplacement of [125I][Sar1,Ile8]Ang2 from human AT1 receptor N111G constitutively active mutant expressed in CHO cells by gamma counting
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccc(C(=O)c2ccccc2)cc1)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O 10.1021/jm9015747
46880544 206733 0 None - 1 Human 9.2 pKi = 9.2 Binding
Displacement of [125I][Sar1,Ile8]Ang2 from human AT1 receptor N111G constitutively active mutant expressed in CHO cells by gamma countingDisplacement of [125I][Sar1,Ile8]Ang2 from human AT1 receptor N111G constitutively active mutant expressed in CHO cells by gamma counting
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccc(C(=O)c2ccccc2)cc1)C(=O)O 10.1021/jm9015747
CHEMBL1076632 206733 0 None - 1 Human 9.2 pKi = 9.2 Binding
Displacement of [125I][Sar1,Ile8]Ang2 from human AT1 receptor N111G constitutively active mutant expressed in CHO cells by gamma countingDisplacement of [125I][Sar1,Ile8]Ang2 from human AT1 receptor N111G constitutively active mutant expressed in CHO cells by gamma counting
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccc(C(=O)c2ccccc2)cc1)C(=O)O 10.1021/jm9015747
132387 161772 18 None -9 3 Rat 9.2 pKi = 9.2 Binding
Binding affinity against angiotensin II receptor from rat liverBinding affinity against angiotensin II receptor from rat liver
ChEMBL 414 8 2 6 4.0 CCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1ncccc1C(=O)O 10.1021/jm00070a012
CHEMBL416477 161772 18 None -9 3 Rat 9.2 pKi = 9.2 Binding
Binding affinity against angiotensin II receptor from rat liverBinding affinity against angiotensin II receptor from rat liver
ChEMBL 414 8 2 6 4.0 CCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1ncccc1C(=O)O 10.1021/jm00070a012
44282952 119910 0 None - 1 Rat 9.2 pKi = 9.2 Binding
Inhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranesInhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranes
ChEMBL 511 7 2 8 3.8 CCc1nn(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/c(=N/C(=O)c2ccccc2C(=O)O)s1 10.1016/S0960-894X(97)00026-7
CHEMBL35381 119910 0 None - 1 Rat 9.2 pKi = 9.2 Binding
Inhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranesInhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranes
ChEMBL 511 7 2 8 3.8 CCc1nn(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/c(=N/C(=O)c2ccccc2C(=O)O)s1 10.1016/S0960-894X(97)00026-7
2541 772 113 None 1 6 Rabbit 9.2 pKi = 9.2 Binding
Inhibitory activity against Angiotensin II receptor, type 1 in rat adrenal membraneInhibitory activity against Angiotensin II receptor, type 1 in rat adrenal membrane
ChEMBL 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10.1021/jm9504722
587 772 113 None 1 6 Rabbit 9.2 pKi = 9.2 Binding
Inhibitory activity against Angiotensin II receptor, type 1 in rat adrenal membraneInhibitory activity against Angiotensin II receptor, type 1 in rat adrenal membrane
ChEMBL 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10.1021/jm9504722
6907 772 113 None 1 6 Rabbit 9.2 pKi = 9.2 Binding
Inhibitory activity against Angiotensin II receptor, type 1 in rat adrenal membraneInhibitory activity against Angiotensin II receptor, type 1 in rat adrenal membrane
ChEMBL 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10.1021/jm9504722
CHEMBL1016 772 113 None 1 6 Rabbit 9.2 pKi = 9.2 Binding
Inhibitory activity against Angiotensin II receptor, type 1 in rat adrenal membraneInhibitory activity against Angiotensin II receptor, type 1 in rat adrenal membrane
ChEMBL 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10.1021/jm9504722
DB00796 772 113 None 1 6 Rabbit 9.2 pKi = 9.2 Binding
Inhibitory activity against Angiotensin II receptor, type 1 in rat adrenal membraneInhibitory activity against Angiotensin II receptor, type 1 in rat adrenal membrane
ChEMBL 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10.1021/jm9504722
DB13919 772 113 None 1 6 Rabbit 9.2 pKi = 9.2 Binding
Inhibitory activity against Angiotensin II receptor, type 1 in rat adrenal membraneInhibitory activity against Angiotensin II receptor, type 1 in rat adrenal membrane
ChEMBL 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10.1021/jm9504722
10344188 112138 0 None - 1 Human 9.2 pKi = 9.2 Binding
Ability to displace [125I]AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1Ability to displace [125I]AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1
ChEMBL 459 5 1 6 5.2 CCc1cc(OCc2ccc3c(-c4nnn[nH]4)cc4ccccc4c(=O)c3c2)c2ccccc2n1 10.1021/jm00014a024
CHEMBL330298 112138 0 None - 1 Human 9.2 pKi = 9.2 Binding
Ability to displace [125I]AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1Ability to displace [125I]AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1
ChEMBL 459 5 1 6 5.2 CCc1cc(OCc2ccc3c(-c4nnn[nH]4)cc4ccccc4c(=O)c3c2)c2ccccc2n1 10.1021/jm00014a024
10079601 210774 17 None -4 2 Human 9.2 pKi = 9.2 Binding
Binding affinity to AT1 receptor (unknown origin)Binding affinity to AT1 receptor (unknown origin)
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@@H]1CCCN1C(=O)[C@H](Cc1c[nH]cn1)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCN=C(N)N)NC(=O)CNC)C(C)C)[C@@H](C)CC)C(=O)O 10.1021/ml500278g
CHEMBL404594 210774 17 None -4 2 Human 9.2 pKi = 9.2 Binding
Binding affinity to AT1 receptor (unknown origin)Binding affinity to AT1 receptor (unknown origin)
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@@H]1CCCN1C(=O)[C@H](Cc1c[nH]cn1)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCN=C(N)N)NC(=O)CNC)C(C)C)[C@@H](C)CC)C(=O)O 10.1021/ml500278g
10004489 205017 0 None - 1 Human 9.2 pKi = 9.2 Binding
Ability to displace [125I]AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1Ability to displace [125I]AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1
ChEMBL 461 4 1 7 4.5 CCc1nc2c(C)cc(C)nc2n1Cc1ccc2c(-c3nnn[nH]3)cc3ccccc3c(=O)c2c1 10.1021/jm00014a024
CHEMBL90027 205017 0 None - 1 Human 9.2 pKi = 9.2 Binding
Ability to displace [125I]AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1Ability to displace [125I]AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1
ChEMBL 461 4 1 7 4.5 CCc1nc2c(C)cc(C)nc2n1Cc1ccc2c(-c3nnn[nH]3)cc3ccccc3c(=O)c2c1 10.1021/jm00014a024
45102750 63432 3 None - 1 Human 9.2 pKi = 9.2 Binding
Binding affinity to human Angiotensin receptor 1Binding affinity to human Angiotensin receptor 1
ChEMBL 477 6 1 6 5.9 CCc1nc2c(C)cc(CC(C)C)nc2n1[C@H]1CCc2cc(-c3ccccc3-c3nnn[nH]3)ccc21 10.1021/jm200409s
CHEMBL1801740 63432 3 None - 1 Human 9.2 pKi = 9.2 Binding
Binding affinity to human Angiotensin receptor 1Binding affinity to human Angiotensin receptor 1
ChEMBL 477 6 1 6 5.9 CCc1nc2c(C)cc(CC(C)C)nc2n1[C@H]1CCc2cc(-c3ccccc3-c3nnn[nH]3)ccc21 10.1021/jm200409s
11754146 159128 0 None - 1 Human 9.2 pKi = 9.2 Binding
Ability to displace [125I]AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1Ability to displace [125I]AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1
ChEMBL 463 5 1 7 5.3 CCCc1nc2c(C)cc(C)nc2n1Cc1ccc2c(c1)Oc1ccccc1C=C2c1nnn[nH]1 10.1021/jm00014a024
CHEMBL410417 159128 0 None - 1 Human 9.2 pKi = 9.2 Binding
Ability to displace [125I]AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1Ability to displace [125I]AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1
ChEMBL 463 5 1 7 5.3 CCCc1nc2c(C)cc(C)nc2n1Cc1ccc2c(c1)Oc1ccccc1C=C2c1nnn[nH]1 10.1021/jm00014a024
CHEMBL1076613 206729 0 None - 1 Human 9.2 pKi = 9.2 Binding
Displacement of [125I][Sar1,Ile8]Ang2 from human AT1 receptor N111G constitutively active mutant expressed in CHO cells by gamma countingDisplacement of [125I][Sar1,Ile8]Ang2 from human AT1 receptor N111G constitutively active mutant expressed in CHO cells by gamma counting
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H](N)Cc1ccc(C2(C(F)(F)F)N=N2)cc1)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O 10.1021/jm9015747
CHEMBL1076633 206734 0 None - 1 Human 9.2 pKi = 9.2 Binding
Displacement of [125I][Sar1,Ile8]Ang2 from human AT1 receptor N111G constitutively active mutant expressed in CHO cells by gamma countingDisplacement of [125I][Sar1,Ile8]Ang2 from human AT1 receptor N111G constitutively active mutant expressed in CHO cells by gamma counting
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccc(C2(C(F)(F)F)N=N2)cc1)C(=O)O 10.1021/jm9015747
CHEMBL1076662 206735 0 None - 1 Human 9.2 pKi = 9.2 Binding
Displacement of [125I][Sar1,Ile8]Ang2 from human AT1 receptor N111G constitutively active mutant expressed in CHO cells by gamma countingDisplacement of [125I][Sar1,Ile8]Ang2 from human AT1 receptor N111G constitutively active mutant expressed in CHO cells by gamma counting
ChEMBL None None None CNCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1ccc(C(=O)c2ccccc2)cc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O)C(C)C 10.1021/jm9015747
CHEMBL1076603 206726 0 None - 1 Human 9.2 pKi = 9.2 Binding
Displacement of [125I][Sar1,Ile8]Ang2 from wild-type human AT1 receptor expressed in CHO cells by gamma countingDisplacement of [125I][Sar1,Ile8]Ang2 from wild-type human AT1 receptor expressed in CHO cells by gamma counting
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](Cc1ccc(C(=O)c2ccccc2)cc1)NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O 10.1021/jm9015747
11994289 82051 0 None -1 2 Pig 9.2 pKi = 9.2 Binding
Displacement of [125]Ang2 from AT2 receptor in pig uterus membraneDisplacement of [125]Ang2 from AT2 receptor in pig uterus membrane
ChEMBL 469 10 1 6 5.0 CCCCOC(=O)NS(=O)(=O)c1ccc(CC(C)C)cc1-c1ccc(Cn2ccnc2)cc1 10.1016/j.bmc.2008.05.066
CHEMBL217673 82051 0 None -1 2 Pig 9.2 pKi = 9.2 Binding
Displacement of [125]Ang2 from AT2 receptor in pig uterus membraneDisplacement of [125]Ang2 from AT2 receptor in pig uterus membrane
ChEMBL 469 10 1 6 5.0 CCCCOC(=O)NS(=O)(=O)c1ccc(CC(C)C)cc1-c1ccc(Cn2ccnc2)cc1 10.1016/j.bmc.2008.05.066
10031067 99875 3 None 2 3 Pig 9.2 pKi = 9.2 Binding
Displacement of [125]Ang2 from AT2 receptor in pig uterus membraneDisplacement of [125]Ang2 from AT2 receptor in pig uterus membrane
ChEMBL 576 11 1 7 6.7 CCCCOC(=O)NS(=O)(=O)c1ccc(CC(C)C)cc1-c1ccc(Cn2c(CC)nc3c(C)cc(C)nc32)cc1 10.1016/j.bmc.2008.05.066
CHEMBL289614 99875 3 None 2 3 Pig 9.2 pKi = 9.2 Binding
Displacement of [125]Ang2 from AT2 receptor in pig uterus membraneDisplacement of [125]Ang2 from AT2 receptor in pig uterus membrane
ChEMBL 576 11 1 7 6.7 CCCCOC(=O)NS(=O)(=O)c1ccc(CC(C)C)cc1-c1ccc(Cn2c(CC)nc3c(C)cc(C)nc32)cc1 10.1016/j.bmc.2008.05.066
127030943 138652 0 None - 1 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation countingDisplacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation counting
ChEMBL 1216 35 15 14 -0.7 CCC(=O)NCCCCNC(=O)/N=C(\N)NCCC[C@H](NC(=O)[C@@H](N)CC(=O)O)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O)[C@@H](C)CC)C(C)C 10.1021/acs.jmedchem.5b01495
CHEMBL3787243 138652 0 None - 1 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation countingDisplacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation counting
ChEMBL 1216 35 15 14 -0.7 CCC(=O)NCCCCNC(=O)/N=C(\N)NCCC[C@H](NC(=O)[C@@H](N)CC(=O)O)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O)[C@@H](C)CC)C(C)C 10.1021/acs.jmedchem.5b01495
CHEMBL3787375 138652 0 None - 1 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation countingDisplacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation counting
ChEMBL 1216 35 15 14 -0.7 CCC(=O)NCCCCNC(=O)/N=C(\N)NCCC[C@H](NC(=O)[C@@H](N)CC(=O)O)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O)[C@@H](C)CC)C(C)C 10.1021/acs.jmedchem.5b01495
CHEMBL3787700 138652 0 None - 1 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation countingDisplacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation counting
ChEMBL 1216 35 15 14 -0.7 CCC(=O)NCCCCNC(=O)/N=C(\N)NCCC[C@H](NC(=O)[C@@H](N)CC(=O)O)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O)[C@@H](C)CC)C(C)C 10.1021/acs.jmedchem.5b01495
132387 161772 18 None -12 3 Rat 9.1 pKi = 9.1 Binding
Compound was evaluated for binding affinity against angiotensin II receptor, type 1 in rat liverCompound was evaluated for binding affinity against angiotensin II receptor, type 1 in rat liver
ChEMBL 414 8 2 6 4.0 CCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1ncccc1C(=O)O 10.1021/jm00098a018
CHEMBL416477 161772 18 None -12 3 Rat 9.1 pKi = 9.1 Binding
Compound was evaluated for binding affinity against angiotensin II receptor, type 1 in rat liverCompound was evaluated for binding affinity against angiotensin II receptor, type 1 in rat liver
ChEMBL 414 8 2 6 4.0 CCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1ncccc1C(=O)O 10.1021/jm00098a018
87219032 175392 0 None - 1 Human 9.1 pKi = 9.1 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 541 13 3 6 5.6 CCOc1nc(CC)c(CNC(=O)[C@@H](CS)CC(C)C)n1Cc1ccc(-c2ccccc2C(=O)O)cc1F 10.1021/acsmedchemlett.8b00462
CHEMBL4588688 175392 0 None - 1 Human 9.1 pKi = 9.1 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 541 13 3 6 5.6 CCOc1nc(CC)c(CNC(=O)[C@@H](CS)CC(C)C)n1Cc1ccc(-c2ccccc2C(=O)O)cc1F 10.1021/acsmedchemlett.8b00462
9891811 119224 1 None 8128 2 Rat 9.1 pKi = 9.1 Binding
Binding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranesBinding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranes
ChEMBL 475 8 2 7 4.8 CCCCc1nc(Cl)c(C(=O)O)n1Cc1cccc2c1ccn2-c1ccccc1-c1nn[nH]n1 10.1016/S0960-894X(01)81137-9
CHEMBL347703 119224 1 None 8128 2 Rat 9.1 pKi = 9.1 Binding
Binding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranesBinding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranes
ChEMBL 475 8 2 7 4.8 CCCCc1nc(Cl)c(C(=O)O)n1Cc1cccc2c1ccn2-c1ccccc1-c1nn[nH]n1 10.1016/S0960-894X(01)81137-9
CHEMBL4524047 119224 1 None 8128 2 Rat 9.1 pKi = 9.1 Binding
Binding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranesBinding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranes
ChEMBL 475 8 2 7 4.8 CCCCc1nc(Cl)c(C(=O)O)n1Cc1cccc2c1ccn2-c1ccccc1-c1nn[nH]n1 10.1016/S0960-894X(01)81137-9
1481 2027 109 None 1 3 Human 9.1 pKi = 9.1 Binding
Binding affinity to AT1 receptorBinding affinity to AT1 receptor
ChEMBL 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 10.1021/jm300682j
3749 2027 109 None 1 3 Human 9.1 pKi = 9.1 Binding
Binding affinity to AT1 receptorBinding affinity to AT1 receptor
ChEMBL 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 10.1021/jm300682j
589 2027 109 None 1 3 Human 9.1 pKi = 9.1 Binding
Binding affinity to AT1 receptorBinding affinity to AT1 receptor
ChEMBL 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 10.1021/jm300682j
6908 2027 109 None 1 3 Human 9.1 pKi = 9.1 Binding
Binding affinity to AT1 receptorBinding affinity to AT1 receptor
ChEMBL 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 10.1021/jm300682j
CHEMBL1513 2027 109 None 1 3 Human 9.1 pKi = 9.1 Binding
Binding affinity to AT1 receptorBinding affinity to AT1 receptor
ChEMBL 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 10.1021/jm300682j
DB01029 2027 109 None 1 3 Human 9.1 pKi = 9.1 Binding
Binding affinity to AT1 receptorBinding affinity to AT1 receptor
ChEMBL 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 10.1021/jm300682j
10257882 3576 37 None 11 2 Human 9.1 pKi = 9.1 Binding
Binding affinity to AT1 receptorBinding affinity to AT1 receptor
ChEMBL 592 12 1 7 6.5 CCCCC1=NC2(C(=O)N1Cc1ccc(c(c1)COCC)c1ccccc1S(=O)(=O)Nc1noc(c1C)C)CCCC2 10.1021/jm300682j
8448 3576 37 None 11 2 Human 9.1 pKi = 9.1 Binding
Binding affinity to AT1 receptorBinding affinity to AT1 receptor
ChEMBL 592 12 1 7 6.5 CCCCC1=NC2(C(=O)N1Cc1ccc(c(c1)COCC)c1ccccc1S(=O)(=O)Nc1noc(c1C)C)CCCC2 10.1021/jm300682j
CHEMBL539423 3576 37 None 11 2 Human 9.1 pKi = 9.1 Binding
Binding affinity to AT1 receptorBinding affinity to AT1 receptor
ChEMBL 592 12 1 7 6.5 CCCCC1=NC2(C(=O)N1Cc1ccc(c(c1)COCC)c1ccccc1S(=O)(=O)Nc1noc(c1C)C)CCCC2 10.1021/jm300682j
DB12548 3576 37 None 11 2 Human 9.1 pKi = 9.1 Binding
Binding affinity to AT1 receptorBinding affinity to AT1 receptor
ChEMBL 592 12 1 7 6.5 CCCCC1=NC2(C(=O)N1Cc1ccc(c(c1)COCC)c1ccccc1S(=O)(=O)Nc1noc(c1C)C)CCCC2 10.1021/jm300682j
1481 2027 109 None -1 3 Rat 9.1 pKi = 9.1 Binding
Compound was evaluated for its binding affinity towards rat Angiotensin II receptor, type 1Compound was evaluated for its binding affinity towards rat Angiotensin II receptor, type 1
ChEMBL 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 10.1021/jm020138n
3749 2027 109 None -1 3 Rat 9.1 pKi = 9.1 Binding
Compound was evaluated for its binding affinity towards rat Angiotensin II receptor, type 1Compound was evaluated for its binding affinity towards rat Angiotensin II receptor, type 1
ChEMBL 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 10.1021/jm020138n
589 2027 109 None -1 3 Rat 9.1 pKi = 9.1 Binding
Compound was evaluated for its binding affinity towards rat Angiotensin II receptor, type 1Compound was evaluated for its binding affinity towards rat Angiotensin II receptor, type 1
ChEMBL 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 10.1021/jm020138n
6908 2027 109 None -1 3 Rat 9.1 pKi = 9.1 Binding
Compound was evaluated for its binding affinity towards rat Angiotensin II receptor, type 1Compound was evaluated for its binding affinity towards rat Angiotensin II receptor, type 1
ChEMBL 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 10.1021/jm020138n
CHEMBL1513 2027 109 None -1 3 Rat 9.1 pKi = 9.1 Binding
Compound was evaluated for its binding affinity towards rat Angiotensin II receptor, type 1Compound was evaluated for its binding affinity towards rat Angiotensin II receptor, type 1
ChEMBL 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 10.1021/jm020138n
DB01029 2027 109 None -1 3 Rat 9.1 pKi = 9.1 Binding
Compound was evaluated for its binding affinity towards rat Angiotensin II receptor, type 1Compound was evaluated for its binding affinity towards rat Angiotensin II receptor, type 1
ChEMBL 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 10.1021/jm020138n
CHEMBL1076612 206728 0 None - 1 Human 9.1 pKi = 9.1 Binding
Displacement of [125I][Sar1,Ile8]Ang2 from human AT1 receptor N111G constitutively active mutant expressed in CHO cells by gamma countingDisplacement of [125I][Sar1,Ile8]Ang2 from human AT1 receptor N111G constitutively active mutant expressed in CHO cells by gamma counting
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H](N)Cc1ccc(C(=O)c2ccccc2)cc1)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O 10.1021/jm9015747
46880544 206733 0 None - 1 Human 9.1 pKi = 9.1 Binding
Displacement of [125I][Sar1,Ile8]Ang2 from wild-type human AT1 receptor expressed in CHO cells by gamma countingDisplacement of [125I][Sar1,Ile8]Ang2 from wild-type human AT1 receptor expressed in CHO cells by gamma counting
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccc(C(=O)c2ccccc2)cc1)C(=O)O 10.1021/jm9015747
CHEMBL1076632 206733 0 None - 1 Human 9.1 pKi = 9.1 Binding
Displacement of [125I][Sar1,Ile8]Ang2 from wild-type human AT1 receptor expressed in CHO cells by gamma countingDisplacement of [125I][Sar1,Ile8]Ang2 from wild-type human AT1 receptor expressed in CHO cells by gamma counting
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccc(C(=O)c2ccccc2)cc1)C(=O)O 10.1021/jm9015747
1481 2027 109 None 1 3 Human 9.1 pKi = 9.1 Binding
Inhibitory concentration against angiotensin II receptor, type 1Inhibitory concentration against angiotensin II receptor, type 1
ChEMBL 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 10.1021/jm058225d
3749 2027 109 None 1 3 Human 9.1 pKi = 9.1 Binding
Inhibitory concentration against angiotensin II receptor, type 1Inhibitory concentration against angiotensin II receptor, type 1
ChEMBL 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 10.1021/jm058225d
589 2027 109 None 1 3 Human 9.1 pKi = 9.1 Binding
Inhibitory concentration against angiotensin II receptor, type 1Inhibitory concentration against angiotensin II receptor, type 1
ChEMBL 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 10.1021/jm058225d
6908 2027 109 None 1 3 Human 9.1 pKi = 9.1 Binding
Inhibitory concentration against angiotensin II receptor, type 1Inhibitory concentration against angiotensin II receptor, type 1
ChEMBL 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 10.1021/jm058225d
CHEMBL1513 2027 109 None 1 3 Human 9.1 pKi = 9.1 Binding
Inhibitory concentration against angiotensin II receptor, type 1Inhibitory concentration against angiotensin II receptor, type 1
ChEMBL 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 10.1021/jm058225d
DB01029 2027 109 None 1 3 Human 9.1 pKi = 9.1 Binding
Inhibitory concentration against angiotensin II receptor, type 1Inhibitory concentration against angiotensin II receptor, type 1
ChEMBL 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 10.1021/jm058225d
10257882 3576 37 None 11 2 Human 9.1 pKi = 9.1 Binding
Inhibitory concentration against angiotensin II receptor, type 1Inhibitory concentration against angiotensin II receptor, type 1
ChEMBL 592 12 1 7 6.5 CCCCC1=NC2(C(=O)N1Cc1ccc(c(c1)COCC)c1ccccc1S(=O)(=O)Nc1noc(c1C)C)CCCC2 10.1021/jm058225d
8448 3576 37 None 11 2 Human 9.1 pKi = 9.1 Binding
Inhibitory concentration against angiotensin II receptor, type 1Inhibitory concentration against angiotensin II receptor, type 1
ChEMBL 592 12 1 7 6.5 CCCCC1=NC2(C(=O)N1Cc1ccc(c(c1)COCC)c1ccccc1S(=O)(=O)Nc1noc(c1C)C)CCCC2 10.1021/jm058225d
CHEMBL539423 3576 37 None 11 2 Human 9.1 pKi = 9.1 Binding
Inhibitory concentration against angiotensin II receptor, type 1Inhibitory concentration against angiotensin II receptor, type 1
ChEMBL 592 12 1 7 6.5 CCCCC1=NC2(C(=O)N1Cc1ccc(c(c1)COCC)c1ccccc1S(=O)(=O)Nc1noc(c1C)C)CCCC2 10.1021/jm058225d
DB12548 3576 37 None 11 2 Human 9.1 pKi = 9.1 Binding
Inhibitory concentration against angiotensin II receptor, type 1Inhibitory concentration against angiotensin II receptor, type 1
ChEMBL 592 12 1 7 6.5 CCCCC1=NC2(C(=O)N1Cc1ccc(c(c1)COCC)c1ccccc1S(=O)(=O)Nc1noc(c1C)C)CCCC2 10.1021/jm058225d
14956739 204569 0 None - 1 Rabbit 9.1 pKi = 9.1 Binding
Binding affinity to Angiotensin II receptor, type 1Binding affinity to Angiotensin II receptor, type 1
ChEMBL 496 9 1 9 4.2 CCCCc1nn(-c2ccccc2[N+](=O)[O-])c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm990504b
CHEMBL87074 204569 0 None - 1 Rabbit 9.1 pKi = 9.1 Binding
Binding affinity to Angiotensin II receptor, type 1Binding affinity to Angiotensin II receptor, type 1
ChEMBL 496 9 1 9 4.2 CCCCc1nn(-c2ccccc2[N+](=O)[O-])c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm990504b
3047757 166887 19 None - 1 Rabbit 9.1 pKi = 9.1 Binding
Binding affinity was evaluated towards Angiotensin II receptor, type 1 in rabbit aortaBinding affinity was evaluated towards Angiotensin II receptor, type 1 in rabbit aorta
ChEMBL 554 10 1 9 5.2 CCCCc1nc(C)n(Cc2sccc2C(=O)OC)c(=O)c1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1021/jm9504722
CHEMBL429847 166887 19 None - 1 Rabbit 9.1 pKi = 9.1 Binding
Binding affinity was evaluated towards Angiotensin II receptor, type 1 in rabbit aortaBinding affinity was evaluated towards Angiotensin II receptor, type 1 in rabbit aorta
ChEMBL 554 10 1 9 5.2 CCCCc1nc(C)n(Cc2sccc2C(=O)OC)c(=O)c1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1021/jm9504722
16133225 415 47 None -2 6 Human 9.1 pKi = 9.1 Binding
Displacement of [125I][Sar1,Ile8]Ang2 from wild-type human AT1 receptor expressed in CHO cells by gamma countingDisplacement of [125I][Sar1,Ile8]Ang2 from wild-type human AT1 receptor expressed in CHO cells by gamma counting
ChEMBL None None None None 10.1021/jm9015747
172198 415 47 None -2 6 Human 9.1 pKi = 9.1 Binding
Displacement of [125I][Sar1,Ile8]Ang2 from wild-type human AT1 receptor expressed in CHO cells by gamma countingDisplacement of [125I][Sar1,Ile8]Ang2 from wild-type human AT1 receptor expressed in CHO cells by gamma counting
ChEMBL None None None None 10.1021/jm9015747
2504 415 47 None -2 6 Human 9.1 pKi = 9.1 Binding
Displacement of [125I][Sar1,Ile8]Ang2 from wild-type human AT1 receptor expressed in CHO cells by gamma countingDisplacement of [125I][Sar1,Ile8]Ang2 from wild-type human AT1 receptor expressed in CHO cells by gamma counting
ChEMBL None None None None 10.1021/jm9015747
45266664 415 47 None -2 6 Human 9.1 pKi = 9.1 Binding
Displacement of [125I][Sar1,Ile8]Ang2 from wild-type human AT1 receptor expressed in CHO cells by gamma countingDisplacement of [125I][Sar1,Ile8]Ang2 from wild-type human AT1 receptor expressed in CHO cells by gamma counting
ChEMBL None None None None 10.1021/jm9015747
5272 415 47 None -2 6 Human 9.1 pKi = 9.1 Binding
Displacement of [125I][Sar1,Ile8]Ang2 from wild-type human AT1 receptor expressed in CHO cells by gamma countingDisplacement of [125I][Sar1,Ile8]Ang2 from wild-type human AT1 receptor expressed in CHO cells by gamma counting
ChEMBL None None None None 10.1021/jm9015747
CHEMBL408403 415 47 None -2 6 Human 9.1 pKi = 9.1 Binding
Displacement of [125I][Sar1,Ile8]Ang2 from wild-type human AT1 receptor expressed in CHO cells by gamma countingDisplacement of [125I][Sar1,Ile8]Ang2 from wild-type human AT1 receptor expressed in CHO cells by gamma counting
ChEMBL None None None None 10.1021/jm9015747
DB11842 415 47 None -2 6 Human 9.1 pKi = 9.1 Binding
Displacement of [125I][Sar1,Ile8]Ang2 from wild-type human AT1 receptor expressed in CHO cells by gamma countingDisplacement of [125I][Sar1,Ile8]Ang2 from wild-type human AT1 receptor expressed in CHO cells by gamma counting
ChEMBL None None None None 10.1021/jm9015747
CHEMBL1076633 206734 0 None - 1 Human 9.1 pKi = 9.1 Binding
Displacement of [125I][Sar1,Ile8]Ang2 from wild-type human AT1 receptor expressed in CHO cells by gamma countingDisplacement of [125I][Sar1,Ile8]Ang2 from wild-type human AT1 receptor expressed in CHO cells by gamma counting
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccc(C2(C(F)(F)F)N=N2)cc1)C(=O)O 10.1021/jm9015747
16133225 415 47 None -7 6 Rat 9.0 pKi = 9.0 Binding
Binding affinity for angiotensin II receptor, type 1 in rat liver membrane using [125I]-Ang II as radioligand, in pH 7.4 Tris-HCl buffer for 2 hr at 25 degree CBinding affinity for angiotensin II receptor, type 1 in rat liver membrane using [125I]-Ang II as radioligand, in pH 7.4 Tris-HCl buffer for 2 hr at 25 degree C
ChEMBL None None None None 10.1021/jm050280z
172198 415 47 None -7 6 Rat 9.0 pKi = 9.0 Binding
Binding affinity for angiotensin II receptor, type 1 in rat liver membrane using [125I]-Ang II as radioligand, in pH 7.4 Tris-HCl buffer for 2 hr at 25 degree CBinding affinity for angiotensin II receptor, type 1 in rat liver membrane using [125I]-Ang II as radioligand, in pH 7.4 Tris-HCl buffer for 2 hr at 25 degree C
ChEMBL None None None None 10.1021/jm050280z
2504 415 47 None -7 6 Rat 9.0 pKi = 9.0 Binding
Binding affinity for angiotensin II receptor, type 1 in rat liver membrane using [125I]-Ang II as radioligand, in pH 7.4 Tris-HCl buffer for 2 hr at 25 degree CBinding affinity for angiotensin II receptor, type 1 in rat liver membrane using [125I]-Ang II as radioligand, in pH 7.4 Tris-HCl buffer for 2 hr at 25 degree C
ChEMBL None None None None 10.1021/jm050280z
45266664 415 47 None -7 6 Rat 9.0 pKi = 9.0 Binding
Binding affinity for angiotensin II receptor, type 1 in rat liver membrane using [125I]-Ang II as radioligand, in pH 7.4 Tris-HCl buffer for 2 hr at 25 degree CBinding affinity for angiotensin II receptor, type 1 in rat liver membrane using [125I]-Ang II as radioligand, in pH 7.4 Tris-HCl buffer for 2 hr at 25 degree C
ChEMBL None None None None 10.1021/jm050280z
5272 415 47 None -7 6 Rat 9.0 pKi = 9.0 Binding
Binding affinity for angiotensin II receptor, type 1 in rat liver membrane using [125I]-Ang II as radioligand, in pH 7.4 Tris-HCl buffer for 2 hr at 25 degree CBinding affinity for angiotensin II receptor, type 1 in rat liver membrane using [125I]-Ang II as radioligand, in pH 7.4 Tris-HCl buffer for 2 hr at 25 degree C
ChEMBL None None None None 10.1021/jm050280z
CHEMBL408403 415 47 None -7 6 Rat 9.0 pKi = 9.0 Binding
Binding affinity for angiotensin II receptor, type 1 in rat liver membrane using [125I]-Ang II as radioligand, in pH 7.4 Tris-HCl buffer for 2 hr at 25 degree CBinding affinity for angiotensin II receptor, type 1 in rat liver membrane using [125I]-Ang II as radioligand, in pH 7.4 Tris-HCl buffer for 2 hr at 25 degree C
ChEMBL None None None None 10.1021/jm050280z
DB11842 415 47 None -7 6 Rat 9.0 pKi = 9.0 Binding
Binding affinity for angiotensin II receptor, type 1 in rat liver membrane using [125I]-Ang II as radioligand, in pH 7.4 Tris-HCl buffer for 2 hr at 25 degree CBinding affinity for angiotensin II receptor, type 1 in rat liver membrane using [125I]-Ang II as radioligand, in pH 7.4 Tris-HCl buffer for 2 hr at 25 degree C
ChEMBL None None None None 10.1021/jm050280z
10322229 120981 0 None 1 2 Human 9.0 pKi = 9 Binding
Binding affinity to angiotensin AT1 receptorBinding affinity to angiotensin AT1 receptor
ChEMBL 464 8 2 6 4.9 CCCCC1=NC(Cl)=C(C(=O)O)C(C)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.bmc.2010.10.043
CHEMBL358335 120981 0 None 1 2 Human 9.0 pKi = 9 Binding
Binding affinity to angiotensin AT1 receptorBinding affinity to angiotensin AT1 receptor
ChEMBL 464 8 2 6 4.9 CCCCC1=NC(Cl)=C(C(=O)O)C(C)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.bmc.2010.10.043
10410148 203410 0 None - 1 Rat 9.0 pKi = 9 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 425 6 2 8 3.4 CCCc1nc(C)n2nc(N)nc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00041a016
CHEMBL77959 203410 0 None - 1 Rat 9.0 pKi = 9 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 425 6 2 8 3.4 CCCc1nc(C)n2nc(N)nc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00041a016
25141239 183274 0 None - 1 Pig 9.0 pKi = 9 Binding
Displacement of [125]Ang2 from AT2 receptor in pig uterus membraneDisplacement of [125]Ang2 from AT2 receptor in pig uterus membrane
ChEMBL 528 11 2 6 5.8 CCCCOC(=O)NS(=O)(=O)c1sc(CC(C)C)cc1-c1ccc(C(=O)NCc2ccccc2)cc1 10.1016/j.bmc.2008.05.066
CHEMBL480906 183274 0 None - 1 Pig 9.0 pKi = 9 Binding
Displacement of [125]Ang2 from AT2 receptor in pig uterus membraneDisplacement of [125]Ang2 from AT2 receptor in pig uterus membrane
ChEMBL 528 11 2 6 5.8 CCCCOC(=O)NS(=O)(=O)c1sc(CC(C)C)cc1-c1ccc(C(=O)NCc2ccccc2)cc1 10.1016/j.bmc.2008.05.066
10322229 120981 0 None -1 2 Rat 9.0 pKi = 9 Binding
Inhibition of [125I]- Sar,Ile8-angiotensin II binding to rat adrenal cortical membrane angiotensin II receptorInhibition of [125I]- Sar,Ile8-angiotensin II binding to rat adrenal cortical membrane angiotensin II receptor
ChEMBL 464 8 2 6 4.9 CCCCC1=NC(Cl)=C(C(=O)O)C(C)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00103a014
CHEMBL358335 120981 0 None -1 2 Rat 9.0 pKi = 9 Binding
Inhibition of [125I]- Sar,Ile8-angiotensin II binding to rat adrenal cortical membrane angiotensin II receptorInhibition of [125I]- Sar,Ile8-angiotensin II binding to rat adrenal cortical membrane angiotensin II receptor
ChEMBL 464 8 2 6 4.9 CCCCC1=NC(Cl)=C(C(=O)O)C(C)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00103a014
10366402 205103 0 None - 1 Human 9.0 pKi = 9.0 Binding
Ability to displace [125I]AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1Ability to displace [125I]AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1
ChEMBL 448 5 2 8 3.8 CCc1cc(NCc2ccc3c(-c4nnn[nH]4)cc4ccccc4c(=O)c3c2)n2nccc2n1 10.1021/jm00014a024
CHEMBL90513 205103 0 None - 1 Human 9.0 pKi = 9.0 Binding
Ability to displace [125I]AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1Ability to displace [125I]AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1
ChEMBL 448 5 2 8 3.8 CCc1cc(NCc2ccc3c(-c4nnn[nH]4)cc4ccccc4c(=O)c3c2)n2nccc2n1 10.1021/jm00014a024
1481 2027 109 None 1 3 Human 9.0 pKi = 9.0 Binding
Compound was evaluated for its binding affinity towards human Angiotensin II receptor, type 1Compound was evaluated for its binding affinity towards human Angiotensin II receptor, type 1
ChEMBL 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 10.1021/jm020138n
3749 2027 109 None 1 3 Human 9.0 pKi = 9.0 Binding
Compound was evaluated for its binding affinity towards human Angiotensin II receptor, type 1Compound was evaluated for its binding affinity towards human Angiotensin II receptor, type 1
ChEMBL 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 10.1021/jm020138n
589 2027 109 None 1 3 Human 9.0 pKi = 9.0 Binding
Compound was evaluated for its binding affinity towards human Angiotensin II receptor, type 1Compound was evaluated for its binding affinity towards human Angiotensin II receptor, type 1
ChEMBL 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 10.1021/jm020138n
6908 2027 109 None 1 3 Human 9.0 pKi = 9.0 Binding
Compound was evaluated for its binding affinity towards human Angiotensin II receptor, type 1Compound was evaluated for its binding affinity towards human Angiotensin II receptor, type 1
ChEMBL 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 10.1021/jm020138n
CHEMBL1513 2027 109 None 1 3 Human 9.0 pKi = 9.0 Binding
Compound was evaluated for its binding affinity towards human Angiotensin II receptor, type 1Compound was evaluated for its binding affinity towards human Angiotensin II receptor, type 1
ChEMBL 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 10.1021/jm020138n
DB01029 2027 109 None 1 3 Human 9.0 pKi = 9.0 Binding
Compound was evaluated for its binding affinity towards human Angiotensin II receptor, type 1Compound was evaluated for its binding affinity towards human Angiotensin II receptor, type 1
ChEMBL 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 10.1021/jm020138n
3936 2171 28 None 1 4 Human 9.0 pKi = 9.0 Binding
Displacement of 125I-[Sar1,Ile8]ANGII form AT1 receptor (unknown origin)Displacement of 125I-[Sar1,Ile8]ANGII form AT1 receptor (unknown origin)
ChEMBL 582 11 1 8 6.8 CCCCOC(=O)NS(=O)(=O)c1sc(cc1c1ccc(cc1)Cn1c(CC)nc2c1nc(C)cc2C)CC(C)C 10.1016/j.bmc.2022.116790
6603900 2171 28 None 1 4 Human 9.0 pKi = 9.0 Binding
Displacement of 125I-[Sar1,Ile8]ANGII form AT1 receptor (unknown origin)Displacement of 125I-[Sar1,Ile8]ANGII form AT1 receptor (unknown origin)
ChEMBL 582 11 1 8 6.8 CCCCOC(=O)NS(=O)(=O)c1sc(cc1c1ccc(cc1)Cn1c(CC)nc2c1nc(C)cc2C)CC(C)C 10.1016/j.bmc.2022.116790
CHEMBL288174 2171 28 None 1 4 Human 9.0 pKi = 9.0 Binding
Displacement of 125I-[Sar1,Ile8]ANGII form AT1 receptor (unknown origin)Displacement of 125I-[Sar1,Ile8]ANGII form AT1 receptor (unknown origin)
ChEMBL 582 11 1 8 6.8 CCCCOC(=O)NS(=O)(=O)c1sc(cc1c1ccc(cc1)Cn1c(CC)nc2c1nc(C)cc2C)CC(C)C 10.1016/j.bmc.2022.116790
3936 2171 28 None -1 4 Rat 9.0 pKi = 9.0 Binding
Displacement of [125]Ang2 from AT1 receptor in rat liver membraneDisplacement of [125]Ang2 from AT1 receptor in rat liver membrane
ChEMBL 582 11 1 8 6.8 CCCCOC(=O)NS(=O)(=O)c1sc(cc1c1ccc(cc1)Cn1c(CC)nc2c1nc(C)cc2C)CC(C)C 10.1016/j.bmc.2008.05.066
6603900 2171 28 None -1 4 Rat 9.0 pKi = 9.0 Binding
Displacement of [125]Ang2 from AT1 receptor in rat liver membraneDisplacement of [125]Ang2 from AT1 receptor in rat liver membrane
ChEMBL 582 11 1 8 6.8 CCCCOC(=O)NS(=O)(=O)c1sc(cc1c1ccc(cc1)Cn1c(CC)nc2c1nc(C)cc2C)CC(C)C 10.1016/j.bmc.2008.05.066
CHEMBL288174 2171 28 None -1 4 Rat 9.0 pKi = 9.0 Binding
Displacement of [125]Ang2 from AT1 receptor in rat liver membraneDisplacement of [125]Ang2 from AT1 receptor in rat liver membrane
ChEMBL 582 11 1 8 6.8 CCCCOC(=O)NS(=O)(=O)c1sc(cc1c1ccc(cc1)Cn1c(CC)nc2c1nc(C)cc2C)CC(C)C 10.1016/j.bmc.2008.05.066
10006413 37237 0 None - 1 Rat 9.0 pKi = 9.0 Binding
Inhibition of [125I]- Sar,Ile8-angiotensin II binding to rat adrenal cortical membrane angiotensin II receptorInhibition of [125I]- Sar,Ile8-angiotensin II binding to rat adrenal cortical membrane angiotensin II receptor
ChEMBL 506 9 1 7 5.7 CCCCC1=NC(C)(C)C(C(=O)OCC)=C(Cl)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00103a014
CHEMBL145564 37237 0 None - 1 Rat 9.0 pKi = 9.0 Binding
Inhibition of [125I]- Sar,Ile8-angiotensin II binding to rat adrenal cortical membrane angiotensin II receptorInhibition of [125I]- Sar,Ile8-angiotensin II binding to rat adrenal cortical membrane angiotensin II receptor
ChEMBL 506 9 1 7 5.7 CCCCC1=NC(C)(C)C(C(=O)OCC)=C(Cl)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00103a014
14956757 67236 0 None - 1 Rabbit 8.9 pKi = 8.9 Binding
Binding affinity to Angiotensin II receptor, type 1Binding affinity to Angiotensin II receptor, type 1
ChEMBL 519 8 1 7 5.3 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm990504b
CHEMBL19018 67236 0 None - 1 Rabbit 8.9 pKi = 8.9 Binding
Binding affinity to Angiotensin II receptor, type 1Binding affinity to Angiotensin II receptor, type 1
ChEMBL 519 8 1 7 5.3 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm990504b
45102601 168993 9 None 1995 2 Human 8.9 pKi = 8.9 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 527 12 3 6 5.4 CCOc1nc(CC)c(CNC(=O)[C@@H](S)CC(C)C)n1Cc1ccc(-c2ccccc2C(=O)O)cc1F 10.1021/acsmedchemlett.8b00462
CHEMBL4435800 168993 9 None 1995 2 Human 8.9 pKi = 8.9 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 527 12 3 6 5.4 CCOc1nc(CC)c(CNC(=O)[C@@H](S)CC(C)C)n1Cc1ccc(-c2ccccc2C(=O)O)cc1F 10.1021/acsmedchemlett.8b00462
87218373 169667 0 None - 1 Human 8.9 pKi = 8.9 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 541 13 3 6 5.6 CCOc1nc(CC)c(CNC(=O)[C@@H](CS)CC(C)C)n1Cc1ccc(-c2ccccc2C(=O)O)c(F)c1 10.1021/acsmedchemlett.8b00462
CHEMBL4445778 169667 0 None - 1 Human 8.9 pKi = 8.9 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 541 13 3 6 5.6 CCOc1nc(CC)c(CNC(=O)[C@@H](CS)CC(C)C)n1Cc1ccc(-c2ccccc2C(=O)O)c(F)c1 10.1021/acsmedchemlett.8b00462
87218514 175502 0 None - 1 Human 8.9 pKi = 8.9 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 523 13 3 6 5.5 CCOc1nc(CC)c(CNC(=O)[C@@H](CS)CC(C)C)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/acsmedchemlett.8b00462
CHEMBL4591218 175502 0 None - 1 Human 8.9 pKi = 8.9 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 523 13 3 6 5.5 CCOc1nc(CC)c(CNC(=O)[C@@H](CS)CC(C)C)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/acsmedchemlett.8b00462
10050044 111027 0 None - 1 Human 8.9 pKi = 8.9 Binding
Ability to displace [125I]AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1Ability to displace [125I]AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1
ChEMBL 463 5 1 6 4.9 CCc1cc(OCc2ccc3c(-c4nnn[nH]4)cc4ccccc4c(=O)c3c2)c2c(n1)CCCC2 10.1021/jm00014a024
CHEMBL327903 111027 0 None - 1 Human 8.9 pKi = 8.9 Binding
Ability to displace [125I]AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1Ability to displace [125I]AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1
ChEMBL 463 5 1 6 4.9 CCc1cc(OCc2ccc3c(-c4nnn[nH]4)cc4ccccc4c(=O)c3c2)c2c(n1)CCCC2 10.1021/jm00014a024
CHEMBL1076604 206727 0 None - 1 Human 8.9 pKi = 8.9 Binding
Displacement of [125I][Sar1,Ile8]Ang2 from wild-type human AT1 receptor expressed in CHO cells by gamma countingDisplacement of [125I][Sar1,Ile8]Ang2 from wild-type human AT1 receptor expressed in CHO cells by gamma counting
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](Cc1ccc(C2(C(F)(F)F)N=N2)cc1)NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O 10.1021/jm9015747
145957897 161511 0 None - 1 Human 8.9 pKi = 8.9 Binding
Displacement of [125I-Sar1-Ile8]-Ang2 from human angiotensin 2 receptor type 1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysisDisplacement of [125I-Sar1-Ile8]-Ang2 from human angiotensin 2 receptor type 1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysis
ChEMBL 984 28 14 13 -1.8 CC[C@H](C)[C@H](NC(=O)[C@@H]1CCCN1C(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H](N)CO)C(C)C)[C@@H](C)CC)C(=O)O 10.1016/j.ejmech.2017.12.021
CHEMBL4160691 161511 0 None - 1 Human 8.9 pKi = 8.9 Binding
Displacement of [125I-Sar1-Ile8]-Ang2 from human angiotensin 2 receptor type 1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysisDisplacement of [125I-Sar1-Ile8]-Ang2 from human angiotensin 2 receptor type 1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysis
ChEMBL 984 28 14 13 -1.8 CC[C@H](C)[C@H](NC(=O)[C@@H]1CCCN1C(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H](N)CO)C(C)C)[C@@H](C)CC)C(=O)O 10.1016/j.ejmech.2017.12.021
44320012 167349 0 None - 1 Rabbit 8.9 pKi = 8.9 Binding
Binding affinity to Angiotensin II receptor, type 1Binding affinity to Angiotensin II receptor, type 1
ChEMBL 493 9 1 7 5.4 CCCCc1nn(-c2ccccc2C(C)C)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm990504b
CHEMBL431411 167349 0 None - 1 Rabbit 8.9 pKi = 8.9 Binding
Binding affinity to Angiotensin II receptor, type 1Binding affinity to Angiotensin II receptor, type 1
ChEMBL 493 9 1 7 5.4 CCCCc1nn(-c2ccccc2C(C)C)c(=O)n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm990504b
10603443 34573 0 None - 1 Rat 8.8 pKi = 8.8 Binding
The compound was evaluated for the inhibition of [125I]-Sar-AII binding to Angiotensin II receptor, type 1 from purified rat liver membranes.The compound was evaluated for the inhibition of [125I]-Sar-AII binding to Angiotensin II receptor, type 1 from purified rat liver membranes.
ChEMBL 587 13 3 8 5.6 CCCCc1ncc(CNc2ccccc2C(=O)O)n1Cc1ccc(C(=O)NS(=O)(=O)c2ccccc2N=[N+]=[N-])cc1 10.1021/jm991050l
CHEMBL143118 34573 0 None - 1 Rat 8.8 pKi = 8.8 Binding
The compound was evaluated for the inhibition of [125I]-Sar-AII binding to Angiotensin II receptor, type 1 from purified rat liver membranes.The compound was evaluated for the inhibition of [125I]-Sar-AII binding to Angiotensin II receptor, type 1 from purified rat liver membranes.
ChEMBL 587 13 3 8 5.6 CCCCc1ncc(CNc2ccccc2C(=O)O)n1Cc1ccc(C(=O)NS(=O)(=O)c2ccccc2N=[N+]=[N-])cc1 10.1021/jm991050l
9939191 98476 1 None - 1 Human 8.8 pKi = 8.8 Binding
Binding affinity to angiotensin AT1 receptorBinding affinity to angiotensin AT1 receptor
ChEMBL 634 10 1 7 6.2 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/j.bmc.2010.10.043
CHEMBL279629 98476 1 None - 1 Human 8.8 pKi = 8.8 Binding
Binding affinity to angiotensin AT1 receptorBinding affinity to angiotensin AT1 receptor
ChEMBL 634 10 1 7 6.2 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/j.bmc.2010.10.043
CHEMBL97539 98476 1 None - 1 Human 8.8 pKi = 8.8 Binding
Binding affinity to angiotensin AT1 receptorBinding affinity to angiotensin AT1 receptor
ChEMBL 634 10 1 7 6.2 CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1016/j.bmc.2010.10.043
10079766 96521 0 None - 1 Rat 8.8 pKi = 8.8 Binding
In vitro binding affinity at rat liver Angiotensin II receptor, type 1 was determined based on displacement of [125I]-Ang IIIn vitro binding affinity at rat liver Angiotensin II receptor, type 1 was determined based on displacement of [125I]-Ang II
ChEMBL 1045 22 13 14 -2.0 NC(N)=NCCC[C@H](NC(=O)[C@@H](N)CC(=O)O)C(=O)N[C@H]1CS/C=C/CC[C@@H](C(=O)N[C@@H](Cc2c[nH]cn2)C(=O)N2CCC[C@H]2C(=O)N[C@@H](Cc2ccccc2)C(=O)O)NC(=O)[C@H](Cc2ccc(O)cc2)NC1=O 10.1021/jm011063a
CHEMBL266450 96521 0 None - 1 Rat 8.8 pKi = 8.8 Binding
In vitro binding affinity at rat liver Angiotensin II receptor, type 1 was determined based on displacement of [125I]-Ang IIIn vitro binding affinity at rat liver Angiotensin II receptor, type 1 was determined based on displacement of [125I]-Ang II
ChEMBL 1045 22 13 14 -2.0 NC(N)=NCCC[C@H](NC(=O)[C@@H](N)CC(=O)O)C(=O)N[C@H]1CS/C=C/CC[C@@H](C(=O)N[C@@H](Cc2c[nH]cn2)C(=O)N2CCC[C@H]2C(=O)N[C@@H](Cc2ccccc2)C(=O)O)NC(=O)[C@H](Cc2ccc(O)cc2)NC1=O 10.1021/jm011063a
10011335 160709 0 None - 1 Rat 8.8 pKi = 8.8 Binding
In vitro binding affinity at rat liver Angiotensin II receptor, type 1 was determined based on displacement of [125I]-Ang IIIn vitro binding affinity at rat liver Angiotensin II receptor, type 1 was determined based on displacement of [125I]-Ang II
ChEMBL 1045 22 13 14 -2.0 NC(N)=NCCC[C@H](NC(=O)[C@@H](N)CC(=O)O)C(=O)N[C@H]1CS/C=C\CC[C@@H](C(=O)N[C@@H](Cc2c[nH]cn2)C(=O)N2CCC[C@H]2C(=O)N[C@@H](Cc2ccccc2)C(=O)O)NC(=O)[C@H](Cc2ccc(O)cc2)NC1=O 10.1021/jm011063a
CHEMBL412045 160709 0 None - 1 Rat 8.8 pKi = 8.8 Binding
In vitro binding affinity at rat liver Angiotensin II receptor, type 1 was determined based on displacement of [125I]-Ang IIIn vitro binding affinity at rat liver Angiotensin II receptor, type 1 was determined based on displacement of [125I]-Ang II
ChEMBL 1045 22 13 14 -2.0 NC(N)=NCCC[C@H](NC(=O)[C@@H](N)CC(=O)O)C(=O)N[C@H]1CS/C=C\CC[C@@H](C(=O)N[C@@H](Cc2c[nH]cn2)C(=O)N2CCC[C@H]2C(=O)N[C@@H](Cc2ccccc2)C(=O)O)NC(=O)[C@H](Cc2ccc(O)cc2)NC1=O 10.1021/jm011063a
192314 113989 26 None -15 3 Rat 8.8 pKi = 8.8 Binding
Binding affinity against angiotensin II receptor from rat liverBinding affinity against angiotensin II receptor from rat liver
ChEMBL 429 9 2 7 3.8 CCCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1ncncc1C(=O)O 10.1021/jm00070a012
CHEMBL1237157 113989 26 None -15 3 Rat 8.8 pKi = 8.8 Binding
Binding affinity against angiotensin II receptor from rat liverBinding affinity against angiotensin II receptor from rat liver
ChEMBL 429 9 2 7 3.8 CCCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1ncncc1C(=O)O 10.1021/jm00070a012
CHEMBL333534 113989 26 None -15 3 Rat 8.8 pKi = 8.8 Binding
Binding affinity against angiotensin II receptor from rat liverBinding affinity against angiotensin II receptor from rat liver
ChEMBL 429 9 2 7 3.8 CCCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1ncncc1C(=O)O 10.1021/jm00070a012
72168 102201 20 None - 1 Human 8.7 pKi = 8.7 Binding
Displacement of [3H]-angiotensin 2 from angiotensin AT1 receptorDisplacement of [3H]-angiotensin 2 from angiotensin AT1 receptor
ChEMBL 554 8 2 7 6.0 CCCCc1nc(Cl)c(C(=O)O)n1Cc1ccc2oc(-c3ccccc3-c3nnn[nH]3)c(Br)c2c1 10.1016/j.bmc.2010.10.043
CHEMBL304639 102201 20 None - 1 Human 8.7 pKi = 8.7 Binding
Displacement of [3H]-angiotensin 2 from angiotensin AT1 receptorDisplacement of [3H]-angiotensin 2 from angiotensin AT1 receptor
ChEMBL 554 8 2 7 6.0 CCCCc1nc(Cl)c(C(=O)O)n1Cc1ccc2oc(-c3ccccc3-c3nnn[nH]3)c(Br)c2c1 10.1016/j.bmc.2010.10.043
10393016 205198 0 None - 1 Human 8.0 pKi = 8 Binding
Binding affinity against AT1 in human hepatoma cell line, PLC-PRF-5Binding affinity against AT1 in human hepatoma cell line, PLC-PRF-5
ChEMBL 559 9 1 5 4.9 CCCCN1C(=O)C2(CCCC2)C(=O)N1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1021/jm9904147
CHEMBL91113 205198 0 None - 1 Human 8.0 pKi = 8 Binding
Binding affinity against AT1 in human hepatoma cell line, PLC-PRF-5Binding affinity against AT1 in human hepatoma cell line, PLC-PRF-5
ChEMBL 559 9 1 5 4.9 CCCCN1C(=O)C2(CCCC2)C(=O)N1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1021/jm9904147
9895957 10558 12 None -5 3 Human 8.0 pKi = 8 Binding
Binding affinity at type 1 angiotensin 2 receptorBinding affinity at type 1 angiotensin 2 receptor
ChEMBL 659 11 1 7 6.8 CCCCC1=NC2(CCCC2)C(=O)N1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)c(CN2CCC(C)(C)C2=O)c1 10.1016/j.bmc.2012.06.011
CHEMBL11706 10558 12 None -5 3 Human 8.0 pKi = 8 Binding
Binding affinity at type 1 angiotensin 2 receptorBinding affinity at type 1 angiotensin 2 receptor
ChEMBL 659 11 1 7 6.8 CCCCC1=NC2(CCCC2)C(=O)N1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)c(CN2CCC(C)(C)C2=O)c1 10.1016/j.bmc.2012.06.011
9895957 10558 12 None -5 3 Human 8.0 pKi = 8 Binding
Compound was evaluated for its binding affinity towards human Angiotensin II receptor, type 1Compound was evaluated for its binding affinity towards human Angiotensin II receptor, type 1
ChEMBL 659 11 1 7 6.8 CCCCC1=NC2(CCCC2)C(=O)N1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)c(CN2CCC(C)(C)C2=O)c1 10.1021/jm020138n
CHEMBL11706 10558 12 None -5 3 Human 8.0 pKi = 8 Binding
Compound was evaluated for its binding affinity towards human Angiotensin II receptor, type 1Compound was evaluated for its binding affinity towards human Angiotensin II receptor, type 1
ChEMBL 659 11 1 7 6.8 CCCCC1=NC2(CCCC2)C(=O)N1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)c(CN2CCC(C)(C)C2=O)c1 10.1021/jm020138n
155514738 169331 0 None - 1 Human 8.0 pKi = 8 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 656 15 4 8 5.3 CCCCc1nc(Cl)c(CNC(=O)CNC(=O)C(CS)Cc2ccccc2)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1021/acsmedchemlett.8b00462
CHEMBL4440944 169331 0 None - 1 Human 8.0 pKi = 8 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 656 15 4 8 5.3 CCCCc1nc(Cl)c(CNC(=O)CNC(=O)C(CS)Cc2ccccc2)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1021/acsmedchemlett.8b00462
71465043 171400 0 None - 1 Human 8.0 pKi = 8 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 565 13 3 7 6.0 CCCCc1nc(Cl)c(CNC(=O)C(CS)CC(C)C)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1021/acsmedchemlett.8b00462
CHEMBL4470834 171400 0 None - 1 Human 8.0 pKi = 8 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 565 13 3 7 6.0 CCCCc1nc(Cl)c(CNC(=O)C(CS)CC(C)C)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1021/acsmedchemlett.8b00462
10409294 104899 0 None - 1 Rat 8.0 pKi = 8 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 410 6 1 7 3.8 CCCc1nc(C)n2cnnc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00041a016
CHEMBL311657 104899 0 None - 1 Rat 8.0 pKi = 8 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 410 6 1 7 3.8 CCCc1nc(C)n2cnnc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00041a016
10410197 162776 0 None - 1 Rat 8.0 pKi = 8 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 426 6 2 8 3.5 CCCc1nc(C)n2c(O)nnc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00041a016
CHEMBL419089 162776 0 None - 1 Rat 8.0 pKi = 8 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 426 6 2 8 3.5 CCCc1nc(C)n2c(O)nnc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00041a016
9933044 167447 0 None - 1 Rat 8.0 pKi = 8 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 442 6 2 8 4.1 CCCc1nc(C)n2nc(S)nc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00041a016
CHEMBL432153 167447 0 None - 1 Rat 8.0 pKi = 8 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 442 6 2 8 4.1 CCCc1nc(C)n2nc(S)nc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00041a016
10411083 203321 0 None - 1 Rat 8.0 pKi = 8 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 442 7 3 9 2.7 CCCc1nc(CO)n2nc(O)nc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00041a016
CHEMBL77036 203321 0 None - 1 Rat 8.0 pKi = 8 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 442 7 3 9 2.7 CCCc1nc(CO)n2nc(O)nc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00041a016
53319274 57280 0 None - 1 Human 8.0 pKi = 8 Binding
Displacement of [3H]-angiotensin 2 from angiotensin AT1 receptor in human PLC-PRF5 cellsDisplacement of [3H]-angiotensin 2 from angiotensin AT1 receptor in human PLC-PRF5 cells
ChEMBL 559 9 1 7 4.2 CCCCN1CC2(CN1Cc1ccc(-c3ccccc3S(=O)(=O)NC(=O)c3ccccc3)cc1)C(=O)CCC2=O 10.1016/j.bmc.2010.10.043
CHEMBL1668000 57280 0 None - 1 Human 8.0 pKi = 8 Binding
Displacement of [3H]-angiotensin 2 from angiotensin AT1 receptor in human PLC-PRF5 cellsDisplacement of [3H]-angiotensin 2 from angiotensin AT1 receptor in human PLC-PRF5 cells
ChEMBL 559 9 1 7 4.2 CCCCN1CC2(CN1Cc1ccc(-c3ccccc3S(=O)(=O)NC(=O)c3ccccc3)cc1)C(=O)CCC2=O 10.1016/j.bmc.2010.10.043
9895957 10558 12 None -5 3 Human 8.0 pKi = 8 Binding
Inhibitory concentration against angiotensin II receptor, type 1Inhibitory concentration against angiotensin II receptor, type 1
ChEMBL 659 11 1 7 6.8 CCCCC1=NC2(CCCC2)C(=O)N1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)c(CN2CCC(C)(C)C2=O)c1 10.1021/jm058225d
CHEMBL11706 10558 12 None -5 3 Human 8.0 pKi = 8 Binding
Inhibitory concentration against angiotensin II receptor, type 1Inhibitory concentration against angiotensin II receptor, type 1
ChEMBL 659 11 1 7 6.8 CCCCC1=NC2(CCCC2)C(=O)N1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)c(CN2CCC(C)(C)C2=O)c1 10.1021/jm058225d
2541 772 113 None -1 6 Human 8.0 pKi = 8.0 Binding
Displacement of [125I-Sar1-Ile8]-Ang2 from human angiotensin 2 receptor type 1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysisDisplacement of [125I-Sar1-Ile8]-Ang2 from human angiotensin 2 receptor type 1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysis
ChEMBL 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10.1016/j.ejmech.2017.12.021
587 772 113 None -1 6 Human 8.0 pKi = 8.0 Binding
Displacement of [125I-Sar1-Ile8]-Ang2 from human angiotensin 2 receptor type 1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysisDisplacement of [125I-Sar1-Ile8]-Ang2 from human angiotensin 2 receptor type 1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysis
ChEMBL 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10.1016/j.ejmech.2017.12.021
6907 772 113 None -1 6 Human 8.0 pKi = 8.0 Binding
Displacement of [125I-Sar1-Ile8]-Ang2 from human angiotensin 2 receptor type 1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysisDisplacement of [125I-Sar1-Ile8]-Ang2 from human angiotensin 2 receptor type 1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysis
ChEMBL 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10.1016/j.ejmech.2017.12.021
CHEMBL1016 772 113 None -1 6 Human 8.0 pKi = 8.0 Binding
Displacement of [125I-Sar1-Ile8]-Ang2 from human angiotensin 2 receptor type 1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysisDisplacement of [125I-Sar1-Ile8]-Ang2 from human angiotensin 2 receptor type 1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysis
ChEMBL 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10.1016/j.ejmech.2017.12.021
DB00796 772 113 None -1 6 Human 8.0 pKi = 8.0 Binding
Displacement of [125I-Sar1-Ile8]-Ang2 from human angiotensin 2 receptor type 1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysisDisplacement of [125I-Sar1-Ile8]-Ang2 from human angiotensin 2 receptor type 1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysis
ChEMBL 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10.1016/j.ejmech.2017.12.021
DB13919 772 113 None -1 6 Human 8.0 pKi = 8.0 Binding
Displacement of [125I-Sar1-Ile8]-Ang2 from human angiotensin 2 receptor type 1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysisDisplacement of [125I-Sar1-Ile8]-Ang2 from human angiotensin 2 receptor type 1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysis
ChEMBL 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10.1016/j.ejmech.2017.12.021
44567746 190811 0 None - 1 Pig 8.0 pKi = 8.0 Binding
Displacement of [125]Ang2 from AT2 receptor in pig uterus membraneDisplacement of [125]Ang2 from AT2 receptor in pig uterus membrane
ChEMBL 478 10 2 6 4.7 CCCCOC(=O)NS(=O)(=O)c1sc(CC(C)C)cc1-c1ccc(C(=O)NC2CC2)cc1 10.1016/j.bmc.2008.05.066
CHEMBL519274 190811 0 None - 1 Pig 8.0 pKi = 8.0 Binding
Displacement of [125]Ang2 from AT2 receptor in pig uterus membraneDisplacement of [125]Ang2 from AT2 receptor in pig uterus membrane
ChEMBL 478 10 2 6 4.7 CCCCOC(=O)NS(=O)(=O)c1sc(CC(C)C)cc1-c1ccc(C(=O)NC2CC2)cc1 10.1016/j.bmc.2008.05.066
44567782 183132 0 None - 1 Pig 8.0 pKi = 8.0 Binding
Displacement of [125]Ang2 from AT2 receptor in pig uterus membraneDisplacement of [125]Ang2 from AT2 receptor in pig uterus membrane
ChEMBL 521 10 2 8 5.5 CCCCOC(=O)NS(=O)(=O)c1sc(CC(C)C)cc1-c1ccc(C(=O)Nc2nccs2)cc1 10.1016/j.bmc.2008.05.066
CHEMBL480341 183132 0 None - 1 Pig 8.0 pKi = 8.0 Binding
Displacement of [125]Ang2 from AT2 receptor in pig uterus membraneDisplacement of [125]Ang2 from AT2 receptor in pig uterus membrane
ChEMBL 521 10 2 8 5.5 CCCCOC(=O)NS(=O)(=O)c1sc(CC(C)C)cc1-c1ccc(C(=O)Nc2nccs2)cc1 10.1016/j.bmc.2008.05.066
87218444 170872 0 None - 1 Human 7.0 pKi = 7 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 541 13 3 5 6.5 CCCCc1nc(Cl)c(CNC(=O)[C@H](CS)CC(C)C)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/acsmedchemlett.8b00462
CHEMBL4463203 170872 0 None - 1 Human 7.0 pKi = 7 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 541 13 3 5 6.5 CCCCc1nc(Cl)c(CNC(=O)[C@H](CS)CC(C)C)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/acsmedchemlett.8b00462
6918 1010 29 None -25118 3 Human 5.0 pKi = 5 Binding
Binding affinity to AT1 receptor (unknown origin)Binding affinity to AT1 receptor (unknown origin)
ChEMBL 475 10 1 7 5.1 CCCCOC(=O)NS(=O)(=O)c1sc(cc1c1ccc(cc1)Cn1cncc1)CC(C)C 10.1021/acs.jmedchem.8b00294
9804984 1010 29 None -25118 3 Human 5.0 pKi = 5 Binding
Binding affinity to AT1 receptor (unknown origin)Binding affinity to AT1 receptor (unknown origin)
ChEMBL 475 10 1 7 5.1 CCCCOC(=O)NS(=O)(=O)c1sc(cc1c1ccc(cc1)Cn1cncc1)CC(C)C 10.1021/acs.jmedchem.8b00294
CHEMBL189568 1010 29 None -25118 3 Human 5.0 pKi = 5 Binding
Binding affinity to AT1 receptor (unknown origin)Binding affinity to AT1 receptor (unknown origin)
ChEMBL 475 10 1 7 5.1 CCCCOC(=O)NS(=O)(=O)c1sc(cc1c1ccc(cc1)Cn1cncc1)CC(C)C 10.1021/acs.jmedchem.8b00294
19029492 117558 0 None - 1 Rat 7.0 pKi = 7.0 Binding
Inhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranesInhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranes
ChEMBL 485 6 1 7 4.3 CCc1nn(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/c(=N/C(=O)c2ccc(F)cc2)s1 10.1016/S0960-894X(97)00026-7
CHEMBL340518 117558 0 None - 1 Rat 7.0 pKi = 7.0 Binding
Inhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranesInhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranes
ChEMBL 485 6 1 7 4.3 CCc1nn(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/c(=N/C(=O)c2ccc(F)cc2)s1 10.1016/S0960-894X(97)00026-7
44567709 190055 0 None - 1 Pig 7.0 pKi = 7.0 Binding
Displacement of [125]Ang2 from AT2 receptor in pig uterus membraneDisplacement of [125]Ang2 from AT2 receptor in pig uterus membrane
ChEMBL 438 9 2 6 3.9 CCCCOC(=O)NS(=O)(=O)c1sc(CC(C)C)cc1-c1ccc(C(N)=O)cc1 10.1016/j.bmc.2008.05.066
CHEMBL518157 190055 0 None - 1 Pig 7.0 pKi = 7.0 Binding
Displacement of [125]Ang2 from AT2 receptor in pig uterus membraneDisplacement of [125]Ang2 from AT2 receptor in pig uterus membrane
ChEMBL 438 9 2 6 3.9 CCCCOC(=O)NS(=O)(=O)c1sc(CC(C)C)cc1-c1ccc(C(N)=O)cc1 10.1016/j.bmc.2008.05.066
10027078 203483 0 None - 1 Rat 7.0 pKi = 7.0 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 456 7 2 8 4.5 CCCCc1nc(C)n2c(S)nnc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00041a016
CHEMBL78532 203483 0 None - 1 Rat 7.0 pKi = 7.0 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 456 7 2 8 4.5 CCCCc1nc(C)n2c(S)nnc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00041a016
10074277 203649 0 None - 1 Rat 8.0 pKi = 8.0 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 489 7 2 9 2.5 CCCc1nc(C)n2nc(S(N)(=O)=O)nc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00041a016
CHEMBL79879 203649 0 None - 1 Rat 8.0 pKi = 8.0 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 489 7 2 9 2.5 CCCc1nc(C)n2nc(S(N)(=O)=O)nc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00041a016
10343950 203474 0 None - 1 Rat 7.0 pKi = 7.0 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 454 8 1 8 4.0 CCCc1nc(COC)n2nc(C)nc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00041a016
CHEMBL78433 203474 0 None - 1 Rat 7.0 pKi = 7.0 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 454 8 1 8 4.0 CCCc1nc(COC)n2nc(C)nc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00041a016
11754586 106593 0 None - 1 Human 7.9 pKi = 7.9 Binding
Ability to displace [125I]AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1Ability to displace [125I]AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1
ChEMBL 472 7 1 7 4.6 CCCCc1nc(Cl)c(C=O)n1Cc1ccc2c(-c3nnn[nH]3)cc3ccccc3c(=O)c2c1 10.1021/jm00014a024
CHEMBL315881 106593 0 None - 1 Human 7.9 pKi = 7.9 Binding
Ability to displace [125I]AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1Ability to displace [125I]AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1
ChEMBL 472 7 1 7 4.6 CCCCc1nc(Cl)c(C=O)n1Cc1ccc2c(-c3nnn[nH]3)cc3ccccc3c(=O)c2c1 10.1021/jm00014a024
10001600 103616 0 None - 1 Rat 7.9 pKi = 7.9 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 410 6 1 7 3.8 CCCc1nc(C)n2ncnc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00041a016
CHEMBL309384 103616 0 None - 1 Rat 7.9 pKi = 7.9 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 410 6 1 7 3.8 CCCc1nc(C)n2ncnc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00041a016
10391688 105240 0 None - 1 Rat 7.9 pKi = 7.9 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 512 9 1 10 3.2 CCCc1nc(C)n2c(=O)n(CC(=O)OCC)nc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00041a016
CHEMBL312632 105240 0 None - 1 Rat 7.9 pKi = 7.9 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 512 9 1 10 3.2 CCCc1nc(C)n2c(=O)n(CC(=O)OCC)nc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00041a016
1610 2305 89 None 1 4 Human 7.9 pKi = 7.9 Binding
Displacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation countingDisplacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation counting
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/acs.jmedchem.5b01495
3941 2305 89 None 1 4 Human 7.9 pKi = 7.9 Binding
Displacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation countingDisplacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation counting
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/acs.jmedchem.5b01495
3961 2305 89 None 1 4 Human 7.9 pKi = 7.9 Binding
Displacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation countingDisplacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation counting
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/acs.jmedchem.5b01495
590 2305 89 None 1 4 Human 7.9 pKi = 7.9 Binding
Displacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation countingDisplacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation counting
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/acs.jmedchem.5b01495
CHEMBL191 2305 89 None 1 4 Human 7.9 pKi = 7.9 Binding
Displacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation countingDisplacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation counting
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/acs.jmedchem.5b01495
DB00678 2305 89 None 1 4 Human 7.9 pKi = 7.9 Binding
Displacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation countingDisplacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation counting
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/acs.jmedchem.5b01495
9956392 100536 0 None - 1 Rat 7.9 pKi = 7.9 Binding
Inhibition of [125I]Sar1,Ile8 angiotensin II binding to Angiotensin II receptor type 1 in rat adrenocortical membraneInhibition of [125I]Sar1,Ile8 angiotensin II binding to Angiotensin II receptor type 1 in rat adrenocortical membrane
ChEMBL 463 6 2 6 5.8 Cc1cccc2nc(C3CC3)c(Oc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c(C(=O)O)c12 10.1016/S0960-894X(01)81146-X
CHEMBL294500 100536 0 None - 1 Rat 7.9 pKi = 7.9 Binding
Inhibition of [125I]Sar1,Ile8 angiotensin II binding to Angiotensin II receptor type 1 in rat adrenocortical membraneInhibition of [125I]Sar1,Ile8 angiotensin II binding to Angiotensin II receptor type 1 in rat adrenocortical membrane
ChEMBL 463 6 2 6 5.8 Cc1cccc2nc(C3CC3)c(Oc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c(C(=O)O)c12 10.1016/S0960-894X(01)81146-X
5311345 2960 39 None -10 2 Human 7.9 pKi = 7.9 Binding
Inhibition of human AT1 receptorInhibition of human AT1 receptor
ChEMBL 508 7 1 5 4.5 OC(=O)[C@@H]1Cc2c(CN1C(=O)C(c1ccccc1)c1ccccc1)ncn2Cc1ccc(c(c1)C)N(C)C 10.1021/acs.jmedchem.9b01780
597 2960 39 None -10 2 Human 7.9 pKi = 7.9 Binding
Inhibition of human AT1 receptorInhibition of human AT1 receptor
ChEMBL 508 7 1 5 4.5 OC(=O)[C@@H]1Cc2c(CN1C(=O)C(c1ccccc1)c1ccccc1)ncn2Cc1ccc(c(c1)C)N(C)C 10.1021/acs.jmedchem.9b01780
CHEMBL321820 2960 39 None -10 2 Human 7.9 pKi = 7.9 Binding
Inhibition of human AT1 receptorInhibition of human AT1 receptor
ChEMBL 508 7 1 5 4.5 OC(=O)[C@@H]1Cc2c(CN1C(=O)C(c1ccccc1)c1ccccc1)ncn2Cc1ccc(c(c1)C)N(C)C 10.1021/acs.jmedchem.9b01780
9978737 118374 1 None - 1 Rat 7.9 pKi = 7.9 Binding
The compound was evaluated for the inhibition of [125I]-Sar-AII binding to Angiotensin II receptor, type 1 from purified rat liver membranes.The compound was evaluated for the inhibition of [125I]-Sar-AII binding to Angiotensin II receptor, type 1 from purified rat liver membranes.
ChEMBL 407 10 3 5 4.3 CCCCc1ncc(CNc2ccccc2C(=O)O)n1Cc1ccc(C(=O)O)cc1 10.1021/jm991050l
CHEMBL2111971 118374 1 None - 1 Rat 7.9 pKi = 7.9 Binding
The compound was evaluated for the inhibition of [125I]-Sar-AII binding to Angiotensin II receptor, type 1 from purified rat liver membranes.The compound was evaluated for the inhibition of [125I]-Sar-AII binding to Angiotensin II receptor, type 1 from purified rat liver membranes.
ChEMBL 407 10 3 5 4.3 CCCCc1ncc(CNc2ccccc2C(=O)O)n1Cc1ccc(C(=O)O)cc1 10.1021/jm991050l
CHEMBL342261 118374 1 None - 1 Rat 7.9 pKi = 7.9 Binding
The compound was evaluated for the inhibition of [125I]-Sar-AII binding to Angiotensin II receptor, type 1 from purified rat liver membranes.The compound was evaluated for the inhibition of [125I]-Sar-AII binding to Angiotensin II receptor, type 1 from purified rat liver membranes.
ChEMBL 407 10 3 5 4.3 CCCCc1ncc(CNc2ccccc2C(=O)O)n1Cc1ccc(C(=O)O)cc1 10.1021/jm991050l
CHEMBL1076630 206731 0 None - 1 Human 7.9 pKi = 7.9 Binding
Displacement of [125I][Sar1,Ile8]Ang2 from human AT1 receptor N111G constitutively active mutant expressed in CHO cells by gamma countingDisplacement of [125I][Sar1,Ile8]Ang2 from human AT1 receptor N111G constitutively active mutant expressed in CHO cells by gamma counting
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N[C@@H](Cc1ccc(C(=O)c2ccccc2)cc1)C(=O)N[C@@H](Cc1ccccc1)C(=O)O 10.1021/jm9015747
168289415 190710 0 None - 1 Human 6.9 pKi = 6.9 Binding
Displacement of 125I-[Sar1,Ile8]ANGII form recombinant human full length AT1 receptor expressed in HEK293 cells incubated for 120 mins by scintillation counting methodDisplacement of 125I-[Sar1,Ile8]ANGII form recombinant human full length AT1 receptor expressed in HEK293 cells incubated for 120 mins by scintillation counting method
ChEMBL 527 8 1 9 4.8 CCCc1nc(-c2ccc(Cn3c(CC)nc4c(C)cc(C)nc43)cc2)c(S(=O)(=O)NC(=O)OC)s1 10.1016/j.bmc.2022.116790
CHEMBL5191326 190710 0 None - 1 Human 6.9 pKi = 6.9 Binding
Displacement of 125I-[Sar1,Ile8]ANGII form recombinant human full length AT1 receptor expressed in HEK293 cells incubated for 120 mins by scintillation counting methodDisplacement of 125I-[Sar1,Ile8]ANGII form recombinant human full length AT1 receptor expressed in HEK293 cells incubated for 120 mins by scintillation counting method
ChEMBL 527 8 1 9 4.8 CCCc1nc(-c2ccc(Cn3c(CC)nc4c(C)cc(C)nc43)cc2)c(S(=O)(=O)NC(=O)OC)s1 10.1016/j.bmc.2022.116790
23298215 167502 0 None - 1 Rat 6.9 pKi = 6.9 Binding
Inhibition of [125I]Sar1,Ile8 angiotensin II binding to Angiotensin II receptor type 1 in rat adrenocortical membraneInhibition of [125I]Sar1,Ile8 angiotensin II binding to Angiotensin II receptor type 1 in rat adrenocortical membrane
ChEMBL 493 7 3 7 5.1 O=C(O)c1cccc2nc(C3CC3)c(Oc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c(C(=O)O)c12 10.1016/S0960-894X(01)81146-X
CHEMBL432529 167502 0 None - 1 Rat 6.9 pKi = 6.9 Binding
Inhibition of [125I]Sar1,Ile8 angiotensin II binding to Angiotensin II receptor type 1 in rat adrenocortical membraneInhibition of [125I]Sar1,Ile8 angiotensin II binding to Angiotensin II receptor type 1 in rat adrenocortical membrane
ChEMBL 493 7 3 7 5.1 O=C(O)c1cccc2nc(C3CC3)c(Oc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c(C(=O)O)c12 10.1016/S0960-894X(01)81146-X
44567849 188623 0 None - 1 Pig 6.9 pKi = 6.9 Binding
Displacement of [125]Ang2 from AT2 receptor in pig uterus membraneDisplacement of [125]Ang2 from AT2 receptor in pig uterus membrane
ChEMBL 488 11 1 5 5.2 CCCCOC(=O)NS(=O)(=O)c1cc(CC(C)C)ccc1-c1ccc(C(=O)N(CC)CC)cc1 10.1016/j.bmc.2008.05.066
CHEMBL511490 188623 0 None - 1 Pig 6.9 pKi = 6.9 Binding
Displacement of [125]Ang2 from AT2 receptor in pig uterus membraneDisplacement of [125]Ang2 from AT2 receptor in pig uterus membrane
ChEMBL 488 11 1 5 5.2 CCCCOC(=O)NS(=O)(=O)c1cc(CC(C)C)ccc1-c1ccc(C(=O)N(CC)CC)cc1 10.1016/j.bmc.2008.05.066
10048997 15311 0 None -14 2 Rat 6.9 pKi = 6.9 Binding
Compound was evaluated for binding affinity against angiotensin II receptor, type 1 in rat liverCompound was evaluated for binding affinity against angiotensin II receptor, type 1 in rat liver
ChEMBL 442 9 2 6 4.7 CCCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1nc(C)ccc1C(=O)O 10.1021/jm00098a018
CHEMBL121635 15311 0 None -14 2 Rat 6.9 pKi = 6.9 Binding
Compound was evaluated for binding affinity against angiotensin II receptor, type 1 in rat liverCompound was evaluated for binding affinity against angiotensin II receptor, type 1 in rat liver
ChEMBL 442 9 2 6 4.7 CCCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1nc(C)ccc1C(=O)O 10.1021/jm00098a018
155520317 169911 0 None - 1 Human 6.9 pKi = 6.9 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 527 12 3 5 6.3 CCCCc1nc(Cl)c(CNC(=O)[C@H](S)CC(C)C)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/acsmedchemlett.8b00462
CHEMBL4449166 169911 0 None - 1 Human 6.9 pKi = 6.9 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 527 12 3 5 6.3 CCCCc1nc(Cl)c(CNC(=O)[C@H](S)CC(C)C)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/acsmedchemlett.8b00462
155523092 170237 0 None - 1 Human 6.9 pKi = 6.9 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 527 12 3 5 6.1 CCCCc1nc(Cl)c(CNC(=O)C(CS)C(C)C)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/acsmedchemlett.8b00462
CHEMBL4453362 170237 0 None - 1 Human 6.9 pKi = 6.9 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 527 12 3 5 6.1 CCCCc1nc(Cl)c(CNC(=O)C(CS)C(C)C)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/acsmedchemlett.8b00462
87219128 172309 0 None - 1 Human 6.9 pKi = 6.9 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 541 14 3 5 6.6 CCCCc1nc(Cl)c(CNC(=O)C(CS)CCCC)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/acsmedchemlett.8b00462
CHEMBL4515703 172309 0 None - 1 Human 6.9 pKi = 6.9 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 541 14 3 5 6.6 CCCCc1nc(Cl)c(CNC(=O)C(CS)CCCC)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/acsmedchemlett.8b00462
87218933 174500 0 None - 1 Human 6.9 pKi = 6.9 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 555 14 3 5 6.9 CCCCc1nc(Cl)c(CNC(=O)C(CS)CCC(C)C)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/acsmedchemlett.8b00462
CHEMBL4568554 174500 0 None - 1 Human 6.9 pKi = 6.9 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 555 14 3 5 6.9 CCCCc1nc(Cl)c(CNC(=O)C(CS)CCC(C)C)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/acsmedchemlett.8b00462
10049001 203708 0 None - 1 Rat 6.9 pKi = 6.9 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 442 6 2 8 4.1 CCCc1nc(C)n2c(S)nnc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00041a016
CHEMBL80219 203708 0 None - 1 Rat 6.9 pKi = 6.9 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 442 6 2 8 4.1 CCCc1nc(C)n2c(S)nnc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00041a016
10697700 205164 0 None - 1 Human 7.9 pKi = 7.9 Binding
Binding affinity against AT1 in human hepatoma cell line, PLC-PRF-5Binding affinity against AT1 in human hepatoma cell line, PLC-PRF-5
ChEMBL 539 11 1 5 4.8 CCCCC(=O)NS(=O)(=O)c1ccccc1-c1ccc(CN2C(=O)C3(CCCC3)C(=O)N2CCCC)cc1 10.1021/jm9904147
CHEMBL90872 205164 0 None - 1 Human 7.9 pKi = 7.9 Binding
Binding affinity against AT1 in human hepatoma cell line, PLC-PRF-5Binding affinity against AT1 in human hepatoma cell line, PLC-PRF-5
ChEMBL 539 11 1 5 4.8 CCCCC(=O)NS(=O)(=O)c1ccccc1-c1ccc(CN2C(=O)C3(CCCC3)C(=O)N2CCCC)cc1 10.1021/jm9904147
44284308 14592 0 None - 1 Rat 7.9 pKi = 7.9 Binding
Binding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranesBinding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranes
ChEMBL 617 12 1 10 6.4 CCCCc1nc(Cl)c(C(=O)OC(OC(=O)C(C)C)C(C)C)n1Cc1cccc2c1ccn2-c1ccccc1-c1nn[nH]n1 10.1016/S0960-894X(01)81137-9
CHEMBL1206594 14592 0 None - 1 Rat 7.9 pKi = 7.9 Binding
Binding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranesBinding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranes
ChEMBL 617 12 1 10 6.4 CCCCc1nc(Cl)c(C(=O)OC(OC(=O)C(C)C)C(C)C)n1Cc1cccc2c1ccn2-c1ccccc1-c1nn[nH]n1 10.1016/S0960-894X(01)81137-9
CHEMBL2079769 14592 0 None - 1 Rat 7.9 pKi = 7.9 Binding
Binding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranesBinding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranes
ChEMBL 617 12 1 10 6.4 CCCCc1nc(Cl)c(C(=O)OC(OC(=O)C(C)C)C(C)C)n1Cc1cccc2c1ccn2-c1ccccc1-c1nn[nH]n1 10.1016/S0960-894X(01)81137-9
CHEMBL4299329 211856 0 None - 1 Human 7.9 pKi = 7.9 Binding
Displacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation countingDisplacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation counting
ChEMBL None None None CC[C@@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@@H](CCCN/C(N)=N/C(=O)NCCCCNC(=O)CCCCCN1/C(=C\C=C\C=C\C2=[N+](C)c3ccccc3C2(C)C)C(C)(C)c2ccccc21)NC(=O)[C@@H](N)CC(=O)O)C(C)C)C(=O)N[C@H](Cc1cnc[nH]1)C(=O)N1CCC[C@@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O 10.1021/acs.jmedchem.5b01495
CHEMBL4302429 211856 0 None - 1 Human 7.9 pKi = 7.9 Binding
Displacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation countingDisplacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation counting
ChEMBL None None None CC[C@@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@@H](CCCN/C(N)=N/C(=O)NCCCCNC(=O)CCCCCN1/C(=C\C=C\C=C\C2=[N+](C)c3ccccc3C2(C)C)C(C)(C)c2ccccc21)NC(=O)[C@@H](N)CC(=O)O)C(C)C)C(=O)N[C@H](Cc1cnc[nH]1)C(=O)N1CCC[C@@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O 10.1021/acs.jmedchem.5b01495
45488134 195292 0 None - 1 Rat 7.9 pKi = 7.9 Binding
Displacement of [125I]SI-Ang2 from AT1 receptor in Sprague-Dawley rat liver membraneDisplacement of [125I]SI-Ang2 from AT1 receptor in Sprague-Dawley rat liver membrane
ChEMBL 490 8 1 7 5.2 CCCc1nc2c(C)cc(-c3nc4ccccc4n3C)cc2n1Cc1ccc(CCc2nnn[nH]2)cc1 10.1021/jm901272d
CHEMBL566614 195292 0 None - 1 Rat 7.9 pKi = 7.9 Binding
Displacement of [125I]SI-Ang2 from AT1 receptor in Sprague-Dawley rat liver membraneDisplacement of [125I]SI-Ang2 from AT1 receptor in Sprague-Dawley rat liver membrane
ChEMBL 490 8 1 7 5.2 CCCc1nc2c(C)cc(-c3nc4ccccc4n3C)cc2n1Cc1ccc(CCc2nnn[nH]2)cc1 10.1021/jm901272d
1610 2305 89 None -1 4 Rat 7.9 pKi = 7.9 Binding
Displacement of [125I]-Ang II from Angiotensin 2 type-1A receptor in rat vascular smooth muscle cells after 150 mins by gamma counting methodDisplacement of [125I]-Ang II from Angiotensin 2 type-1A receptor in rat vascular smooth muscle cells after 150 mins by gamma counting method
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmc.2016.03.028
3941 2305 89 None -1 4 Rat 7.9 pKi = 7.9 Binding
Displacement of [125I]-Ang II from Angiotensin 2 type-1A receptor in rat vascular smooth muscle cells after 150 mins by gamma counting methodDisplacement of [125I]-Ang II from Angiotensin 2 type-1A receptor in rat vascular smooth muscle cells after 150 mins by gamma counting method
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmc.2016.03.028
3961 2305 89 None -1 4 Rat 7.9 pKi = 7.9 Binding
Displacement of [125I]-Ang II from Angiotensin 2 type-1A receptor in rat vascular smooth muscle cells after 150 mins by gamma counting methodDisplacement of [125I]-Ang II from Angiotensin 2 type-1A receptor in rat vascular smooth muscle cells after 150 mins by gamma counting method
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmc.2016.03.028
590 2305 89 None -1 4 Rat 7.9 pKi = 7.9 Binding
Displacement of [125I]-Ang II from Angiotensin 2 type-1A receptor in rat vascular smooth muscle cells after 150 mins by gamma counting methodDisplacement of [125I]-Ang II from Angiotensin 2 type-1A receptor in rat vascular smooth muscle cells after 150 mins by gamma counting method
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmc.2016.03.028
CHEMBL191 2305 89 None -1 4 Rat 7.9 pKi = 7.9 Binding
Displacement of [125I]-Ang II from Angiotensin 2 type-1A receptor in rat vascular smooth muscle cells after 150 mins by gamma counting methodDisplacement of [125I]-Ang II from Angiotensin 2 type-1A receptor in rat vascular smooth muscle cells after 150 mins by gamma counting method
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmc.2016.03.028
DB00678 2305 89 None -1 4 Rat 7.9 pKi = 7.9 Binding
Displacement of [125I]-Ang II from Angiotensin 2 type-1A receptor in rat vascular smooth muscle cells after 150 mins by gamma counting methodDisplacement of [125I]-Ang II from Angiotensin 2 type-1A receptor in rat vascular smooth muscle cells after 150 mins by gamma counting method
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1016/j.bmc.2016.03.028
23298206 100273 0 None - 1 Rat 5.9 pKi = 5.9 Binding
Inhibition of [125I]Sar1,Ile8 angiotensin II binding to Angiotensin II receptor type 1 in rat adrenocortical membraneInhibition of [125I]Sar1,Ile8 angiotensin II binding to Angiotensin II receptor type 1 in rat adrenocortical membrane
ChEMBL 463 6 2 6 5.8 Cc1cccc2c(C(=O)O)c(Oc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c(C3CC3)nc12 10.1016/S0960-894X(01)81146-X
CHEMBL292792 100273 0 None - 1 Rat 5.9 pKi = 5.9 Binding
Inhibition of [125I]Sar1,Ile8 angiotensin II binding to Angiotensin II receptor type 1 in rat adrenocortical membraneInhibition of [125I]Sar1,Ile8 angiotensin II binding to Angiotensin II receptor type 1 in rat adrenocortical membrane
ChEMBL 463 6 2 6 5.8 Cc1cccc2c(C(=O)O)c(Oc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c(C3CC3)nc12 10.1016/S0960-894X(01)81146-X
19029534 18361 0 None - 1 Rat 6.9 pKi = 6.9 Binding
Inhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranesInhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranes
ChEMBL 485 6 1 7 4.3 CCc1nn(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/c(=N/C(=O)c2cccc(F)c2)s1 10.1016/S0960-894X(97)00026-7
CHEMBL127605 18361 0 None - 1 Rat 6.9 pKi = 6.9 Binding
Inhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranesInhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranes
ChEMBL 485 6 1 7 4.3 CCc1nn(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/c(=N/C(=O)c2cccc(F)c2)s1 10.1016/S0960-894X(97)00026-7
10458763 203220 0 None - 1 Rat 6.9 pKi = 6.9 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 503 8 2 9 2.7 CCCc1nc(C)n2nc(S(=O)(=O)NC)nc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00041a016
CHEMBL76359 203220 0 None - 1 Rat 6.9 pKi = 6.9 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 503 8 2 9 2.7 CCCc1nc(C)n2nc(S(=O)(=O)NC)nc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00041a016
10095683 120985 0 None -1 2 Rat 7.9 pKi = 7.9 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
ChEMBL 458 7 1 5 4.4 CCCCN1C(=O)CC2(CCCC2)C(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm7011563
CHEMBL358359 120985 0 None -1 2 Rat 7.9 pKi = 7.9 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
ChEMBL 458 7 1 5 4.4 CCCCN1C(=O)CC2(CCCC2)C(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm7011563
10095683 120985 0 None 1 2 Human 7.9 pKi = 7.9 Binding
In vitro binding affinity towards Angiotensin II receptor, type 1 of human hepatoma cell line PLC-PRF-5In vitro binding affinity towards Angiotensin II receptor, type 1 of human hepatoma cell line PLC-PRF-5
ChEMBL 458 7 1 5 4.4 CCCCN1C(=O)CC2(CCCC2)C(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm010457z
CHEMBL358359 120985 0 None 1 2 Human 7.9 pKi = 7.9 Binding
In vitro binding affinity towards Angiotensin II receptor, type 1 of human hepatoma cell line PLC-PRF-5In vitro binding affinity towards Angiotensin II receptor, type 1 of human hepatoma cell line PLC-PRF-5
ChEMBL 458 7 1 5 4.4 CCCCN1C(=O)CC2(CCCC2)C(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm010457z
15480220 199040 0 None - 1 Rat 7.9 pKi = 7.9 Binding
Inhibition of [125I]Sar1,Ile8 angiotensin II binding to Angiotensin II receptor type 1 in rat adrenocortical membraneInhibition of [125I]Sar1,Ile8 angiotensin II binding to Angiotensin II receptor type 1 in rat adrenocortical membrane
ChEMBL 467 6 2 6 5.6 O=C(O)c1c(Oc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c(C2CC2)nc2ccc(F)cc12 10.1016/S0960-894X(01)81146-X
CHEMBL60010 199040 0 None - 1 Rat 7.9 pKi = 7.9 Binding
Inhibition of [125I]Sar1,Ile8 angiotensin II binding to Angiotensin II receptor type 1 in rat adrenocortical membraneInhibition of [125I]Sar1,Ile8 angiotensin II binding to Angiotensin II receptor type 1 in rat adrenocortical membrane
ChEMBL 467 6 2 6 5.6 O=C(O)c1c(Oc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c(C2CC2)nc2ccc(F)cc12 10.1016/S0960-894X(01)81146-X
1610 2305 89 None -1 4 Rat 7.8 pKi = 7.8 Binding
Binding affinity against angiotensin II receptor from rat liver; n=8Binding affinity against angiotensin II receptor from rat liver; n=8
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00070a012
3941 2305 89 None -1 4 Rat 7.8 pKi = 7.8 Binding
Binding affinity against angiotensin II receptor from rat liver; n=8Binding affinity against angiotensin II receptor from rat liver; n=8
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00070a012
3961 2305 89 None -1 4 Rat 7.8 pKi = 7.8 Binding
Binding affinity against angiotensin II receptor from rat liver; n=8Binding affinity against angiotensin II receptor from rat liver; n=8
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00070a012
590 2305 89 None -1 4 Rat 7.8 pKi = 7.8 Binding
Binding affinity against angiotensin II receptor from rat liver; n=8Binding affinity against angiotensin II receptor from rat liver; n=8
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00070a012
CHEMBL191 2305 89 None -1 4 Rat 7.8 pKi = 7.8 Binding
Binding affinity against angiotensin II receptor from rat liver; n=8Binding affinity against angiotensin II receptor from rat liver; n=8
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00070a012
DB00678 2305 89 None -1 4 Rat 7.8 pKi = 7.8 Binding
Binding affinity against angiotensin II receptor from rat liver; n=8Binding affinity against angiotensin II receptor from rat liver; n=8
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00070a012
1610 2305 89 None -1 4 Rat 7.8 pKi = 7.8 Binding
Compound was evaluated for binding affinity against angiotensin II receptor, type 1 in rat liverCompound was evaluated for binding affinity against angiotensin II receptor, type 1 in rat liver
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00098a018
3941 2305 89 None -1 4 Rat 7.8 pKi = 7.8 Binding
Compound was evaluated for binding affinity against angiotensin II receptor, type 1 in rat liverCompound was evaluated for binding affinity against angiotensin II receptor, type 1 in rat liver
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00098a018
3961 2305 89 None -1 4 Rat 7.8 pKi = 7.8 Binding
Compound was evaluated for binding affinity against angiotensin II receptor, type 1 in rat liverCompound was evaluated for binding affinity against angiotensin II receptor, type 1 in rat liver
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00098a018
590 2305 89 None -1 4 Rat 7.8 pKi = 7.8 Binding
Compound was evaluated for binding affinity against angiotensin II receptor, type 1 in rat liverCompound was evaluated for binding affinity against angiotensin II receptor, type 1 in rat liver
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00098a018
CHEMBL191 2305 89 None -1 4 Rat 7.8 pKi = 7.8 Binding
Compound was evaluated for binding affinity against angiotensin II receptor, type 1 in rat liverCompound was evaluated for binding affinity against angiotensin II receptor, type 1 in rat liver
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00098a018
DB00678 2305 89 None -1 4 Rat 7.8 pKi = 7.8 Binding
Compound was evaluated for binding affinity against angiotensin II receptor, type 1 in rat liverCompound was evaluated for binding affinity against angiotensin II receptor, type 1 in rat liver
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00098a018
44254496 5534 0 None - 1 Human 6.9 pKi = 6.9 Binding
Displacement of [3H]valsartan from human recombinant AT1 receptor expressed in CHO cells after 40 mins by liquid scintillation countingDisplacement of [3H]valsartan from human recombinant AT1 receptor expressed in CHO cells after 40 mins by liquid scintillation counting
ChEMBL 770 18 7 8 2.1 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](CN)C(C)C)C(=O)N[C@H]1Cc2ccccc2CN(CC(=O)N[C@@H](Cc2ccccc2)C(=O)O)C1=O 10.1021/jm900651p
CHEMBL1077582 5534 0 None - 1 Human 6.9 pKi = 6.9 Binding
Displacement of [3H]valsartan from human recombinant AT1 receptor expressed in CHO cells after 40 mins by liquid scintillation countingDisplacement of [3H]valsartan from human recombinant AT1 receptor expressed in CHO cells after 40 mins by liquid scintillation counting
ChEMBL 770 18 7 8 2.1 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](CN)C(C)C)C(=O)N[C@H]1Cc2ccccc2CN(CC(=O)N[C@@H](Cc2ccccc2)C(=O)O)C1=O 10.1021/jm900651p
19029594 17900 0 None - 1 Rat 6.9 pKi = 6.9 Binding
Inhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranesInhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranes
ChEMBL 512 7 1 9 4.1 CCc1nn(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/c(=N/C(=O)c2ccc([N+](=O)[O-])cc2)s1 10.1016/S0960-894X(97)00026-7
CHEMBL126801 17900 0 None - 1 Rat 6.9 pKi = 6.9 Binding
Inhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranesInhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranes
ChEMBL 512 7 1 9 4.1 CCc1nn(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/c(=N/C(=O)c2ccc([N+](=O)[O-])cc2)s1 10.1016/S0960-894X(97)00026-7
19029638 163648 0 None - 1 Rat 6.9 pKi = 6.9 Binding
Inhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranesInhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranes
ChEMBL 512 7 1 9 4.1 CCc1nn(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/c(=N/C(=O)c2cccc([N+](=O)[O-])c2)s1 10.1016/S0960-894X(97)00026-7
CHEMBL421092 163648 0 None - 1 Rat 6.9 pKi = 6.9 Binding
Inhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranesInhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranes
ChEMBL 512 7 1 9 4.1 CCc1nn(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/c(=N/C(=O)c2cccc([N+](=O)[O-])c2)s1 10.1016/S0960-894X(97)00026-7
10052744 14627 0 None - 1 Rat 5.8 pKi = 5.8 Binding
Inhibition of [125I]- Sar,Ile8-angiotensin II binding to rat adrenal cortical membrane angiotensin II receptorInhibition of [125I]- Sar,Ile8-angiotensin II binding to rat adrenal cortical membrane angiotensin II receptor
ChEMBL 530 10 1 5 7.2 CCCCC1=NC(Cl)=C(C(=O)OCC)C(c2ccccc2)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00103a014
CHEMBL1207064 14627 0 None - 1 Rat 5.8 pKi = 5.8 Binding
Inhibition of [125I]- Sar,Ile8-angiotensin II binding to rat adrenal cortical membrane angiotensin II receptorInhibition of [125I]- Sar,Ile8-angiotensin II binding to rat adrenal cortical membrane angiotensin II receptor
ChEMBL 530 10 1 5 7.2 CCCCC1=NC(Cl)=C(C(=O)OCC)C(c2ccccc2)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00103a014
CHEMBL343622 14627 0 None - 1 Rat 5.8 pKi = 5.8 Binding
Inhibition of [125I]- Sar,Ile8-angiotensin II binding to rat adrenal cortical membrane angiotensin II receptorInhibition of [125I]- Sar,Ile8-angiotensin II binding to rat adrenal cortical membrane angiotensin II receptor
ChEMBL 530 10 1 5 7.2 CCCCC1=NC(Cl)=C(C(=O)OCC)C(c2ccccc2)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00103a014
44567819 183323 0 None - 1 Pig 6.8 pKi = 6.8 Binding
Displacement of [125]Ang2 from AT2 receptor in pig uterus membraneDisplacement of [125]Ang2 from AT2 receptor in pig uterus membrane
ChEMBL 488 11 1 5 5.2 CCCCOC(=O)NS(=O)(=O)c1ccc(CC(C)C)cc1-c1ccc(C(=O)N(CC)CC)cc1 10.1016/j.bmc.2008.05.066
CHEMBL481294 183323 0 None - 1 Pig 6.8 pKi = 6.8 Binding
Displacement of [125]Ang2 from AT2 receptor in pig uterus membraneDisplacement of [125]Ang2 from AT2 receptor in pig uterus membrane
ChEMBL 488 11 1 5 5.2 CCCCOC(=O)NS(=O)(=O)c1ccc(CC(C)C)cc1-c1ccc(C(=O)N(CC)CC)cc1 10.1016/j.bmc.2008.05.066
10005278 203469 0 None - 1 Rat 6.8 pKi = 6.8 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 478 6 1 7 4.8 CCCc1nc(C)n2nc(C(F)(F)F)nc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00041a016
CHEMBL78399 203469 0 None - 1 Rat 6.8 pKi = 6.8 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 478 6 1 7 4.8 CCCc1nc(C)n2nc(C(F)(F)F)nc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00041a016
10049622 103652 0 None - 1 Rat 7.8 pKi = 7.8 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 454 8 1 8 4.0 CCCc1nc(C)n2nc(COC)nc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00041a016
CHEMBL309458 103652 0 None - 1 Rat 7.8 pKi = 7.8 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 454 8 1 8 4.0 CCCc1nc(C)n2nc(COC)nc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00041a016
19029579 18303 0 None - 1 Rat 7.8 pKi = 7.8 Binding
Inhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranesInhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranes
ChEMBL 513 6 1 7 5.1 O=C(/N=c1\sc(C2CC2)nn1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1ccccc1Cl 10.1016/S0960-894X(97)00026-7
CHEMBL127332 18303 0 None - 1 Rat 7.8 pKi = 7.8 Binding
Inhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranesInhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranes
ChEMBL 513 6 1 7 5.1 O=C(/N=c1\sc(C2CC2)nn1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1ccccc1Cl 10.1016/S0960-894X(97)00026-7
10094936 16642 0 None -9 3 Rat 7.8 pKi = 7.8 Binding
Binding affinity against angiotensin II receptor from rat liverBinding affinity against angiotensin II receptor from rat liver
ChEMBL 443 9 2 7 4.1 CCCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1nc(C)ncc1C(=O)O 10.1021/jm00070a012
CHEMBL1237156 16642 0 None -9 3 Rat 7.8 pKi = 7.8 Binding
Binding affinity against angiotensin II receptor from rat liverBinding affinity against angiotensin II receptor from rat liver
ChEMBL 443 9 2 7 4.1 CCCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1nc(C)ncc1C(=O)O 10.1021/jm00070a012
CHEMBL124772 16642 0 None -9 3 Rat 7.8 pKi = 7.8 Binding
Binding affinity against angiotensin II receptor from rat liverBinding affinity against angiotensin II receptor from rat liver
ChEMBL 443 9 2 7 4.1 CCCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1nc(C)ncc1C(=O)O 10.1021/jm00070a012
10094936 16642 0 None -9 3 Rat 7.8 pKi = 7.8 Binding
Compound was evaluated for binding affinity against angiotensin II receptor, type 1 in rat liverCompound was evaluated for binding affinity against angiotensin II receptor, type 1 in rat liver
ChEMBL 443 9 2 7 4.1 CCCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1nc(C)ncc1C(=O)O 10.1021/jm00098a018
CHEMBL1237156 16642 0 None -9 3 Rat 7.8 pKi = 7.8 Binding
Compound was evaluated for binding affinity against angiotensin II receptor, type 1 in rat liverCompound was evaluated for binding affinity against angiotensin II receptor, type 1 in rat liver
ChEMBL 443 9 2 7 4.1 CCCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1nc(C)ncc1C(=O)O 10.1021/jm00098a018
CHEMBL124772 16642 0 None -9 3 Rat 7.8 pKi = 7.8 Binding
Compound was evaluated for binding affinity against angiotensin II receptor, type 1 in rat liverCompound was evaluated for binding affinity against angiotensin II receptor, type 1 in rat liver
ChEMBL 443 9 2 7 4.1 CCCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1nc(C)ncc1C(=O)O 10.1021/jm00098a018
44475015 170948 0 None - 1 Human 7.8 pKi = 7.8 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 541 13 3 5 6.5 CCCCc1nc(Cl)c(CNC(=O)[C@@H](CS)CC(C)C)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/acsmedchemlett.8b00462
CHEMBL4464191 170948 0 None - 1 Human 7.8 pKi = 7.8 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 541 13 3 5 6.5 CCCCc1nc(Cl)c(CNC(=O)[C@@H](CS)CC(C)C)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/acsmedchemlett.8b00462
155557693 174086 0 None - 1 Human 7.8 pKi = 7.8 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 599 13 3 7 6.2 CCCCc1nc(Cl)c(CNC(=O)C(CS)Cc2ccccc2)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1021/acsmedchemlett.8b00462
CHEMBL4558883 174086 0 None - 1 Human 7.8 pKi = 7.8 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 599 13 3 7 6.2 CCCCc1nc(Cl)c(CNC(=O)C(CS)Cc2ccccc2)n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1021/acsmedchemlett.8b00462
10003793 14500 0 None - 1 Rat 6.8 pKi = 6.8 Binding
Inhibition of [125I]- Sar,Ile8-angiotensin II binding to rat adrenal cortical membrane angiotensin II receptorInhibition of [125I]- Sar,Ile8-angiotensin II binding to rat adrenal cortical membrane angiotensin II receptor
ChEMBL 448 9 1 6 4.5 CCCCc1nc(C)c(C(=O)OCC)c(=O)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00103a014
CHEMBL1205758 14500 0 None - 1 Rat 6.8 pKi = 6.8 Binding
Inhibition of [125I]- Sar,Ile8-angiotensin II binding to rat adrenal cortical membrane angiotensin II receptorInhibition of [125I]- Sar,Ile8-angiotensin II binding to rat adrenal cortical membrane angiotensin II receptor
ChEMBL 448 9 1 6 4.5 CCCCc1nc(C)c(C(=O)OCC)c(=O)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00103a014
CHEMBL145276 14500 0 None - 1 Rat 6.8 pKi = 6.8 Binding
Inhibition of [125I]- Sar,Ile8-angiotensin II binding to rat adrenal cortical membrane angiotensin II receptorInhibition of [125I]- Sar,Ile8-angiotensin II binding to rat adrenal cortical membrane angiotensin II receptor
ChEMBL 448 9 1 6 4.5 CCCCc1nc(C)c(C(=O)OCC)c(=O)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00103a014
10504330 205077 0 None - 1 Human 6.8 pKi = 6.8 Binding
Binding affinity against AT1 in human hepatoma cell line, PLC-PRF-5Binding affinity against AT1 in human hepatoma cell line, PLC-PRF-5
ChEMBL 464 5 1 5 4.4 O=C1N(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)N(c2ccccc2)C(=O)C12CCCC2 10.1021/jm9904147
CHEMBL90411 205077 0 None - 1 Human 6.8 pKi = 6.8 Binding
Binding affinity against AT1 in human hepatoma cell line, PLC-PRF-5Binding affinity against AT1 in human hepatoma cell line, PLC-PRF-5
ChEMBL 464 5 1 5 4.4 O=C1N(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)N(c2ccccc2)C(=O)C12CCCC2 10.1021/jm9904147
155535176 171454 0 None - 1 Human 6.8 pKi = 6.8 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 625 13 3 5 7.9 CCCCc1nc(Cl)c(CNC(=O)C(CS)Cc2ccc3ccccc3c2)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/acsmedchemlett.8b00462
CHEMBL4471668 171454 0 None - 1 Human 6.8 pKi = 6.8 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 625 13 3 5 7.9 CCCCc1nc(Cl)c(CNC(=O)C(CS)Cc2ccc3ccccc3c2)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/acsmedchemlett.8b00462
46935636 102086 0 None -31622 2 Human 5.8 pKi = 5.8 Binding
Displacement of [tyrosyl-3,5-3H]angiotensin-2 from AT1 receptor (unknown origin) expressed in QBI-HEK293A cells after 2 hrsDisplacement of [tyrosyl-3,5-3H]angiotensin-2 from AT1 receptor (unknown origin) expressed in QBI-HEK293A cells after 2 hrs
ChEMBL 524 7 1 6 5.9 O=C(O)c1ccccc1-c1ccc(CN2CCC(COC(=O)c3c4n(c5ccccc35)CCCO4)CC2)cc1 10.1016/j.bmc.2013.09.004
CHEMBL2440460 102086 0 None -31622 2 Human 5.8 pKi = 5.8 Binding
Displacement of [tyrosyl-3,5-3H]angiotensin-2 from AT1 receptor (unknown origin) expressed in QBI-HEK293A cells after 2 hrsDisplacement of [tyrosyl-3,5-3H]angiotensin-2 from AT1 receptor (unknown origin) expressed in QBI-HEK293A cells after 2 hrs
ChEMBL 524 7 1 6 5.9 O=C(O)c1ccccc1-c1ccc(CN2CCC(COC(=O)c3c4n(c5ccccc35)CCCO4)CC2)cc1 10.1016/j.bmc.2013.09.004
CHEMBL3040772 102086 0 None -31622 2 Human 5.8 pKi = 5.8 Binding
Displacement of [tyrosyl-3,5-3H]angiotensin-2 from AT1 receptor (unknown origin) expressed in QBI-HEK293A cells after 2 hrsDisplacement of [tyrosyl-3,5-3H]angiotensin-2 from AT1 receptor (unknown origin) expressed in QBI-HEK293A cells after 2 hrs
ChEMBL 524 7 1 6 5.9 O=C(O)c1ccccc1-c1ccc(CN2CCC(COC(=O)c3c4n(c5ccccc35)CCCO4)CC2)cc1 10.1016/j.bmc.2013.09.004
10391609 14498 0 None - 1 Rat 5.8 pKi = 5.8 Binding
Inhibition of [125I]- Sar,Ile8-angiotensin II binding to rat adrenal cortical membrane angiotensin II receptorInhibition of [125I]- Sar,Ile8-angiotensin II binding to rat adrenal cortical membrane angiotensin II receptor
ChEMBL 510 10 1 6 5.8 CCCCc1nc(-c2ccccc2)c(C(=O)OCC)c(=O)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00103a014
CHEMBL1205753 14498 0 None - 1 Rat 5.8 pKi = 5.8 Binding
Inhibition of [125I]- Sar,Ile8-angiotensin II binding to rat adrenal cortical membrane angiotensin II receptorInhibition of [125I]- Sar,Ile8-angiotensin II binding to rat adrenal cortical membrane angiotensin II receptor
ChEMBL 510 10 1 6 5.8 CCCCc1nc(-c2ccccc2)c(C(=O)OCC)c(=O)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00103a014
CHEMBL144952 14498 0 None - 1 Rat 5.8 pKi = 5.8 Binding
Inhibition of [125I]- Sar,Ile8-angiotensin II binding to rat adrenal cortical membrane angiotensin II receptorInhibition of [125I]- Sar,Ile8-angiotensin II binding to rat adrenal cortical membrane angiotensin II receptor
ChEMBL 510 10 1 6 5.8 CCCCc1nc(-c2ccccc2)c(C(=O)OCC)c(=O)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00103a014
45488167 195468 0 None - 1 Rat 5.8 pKi = 5.8 Binding
Displacement of [125I]SI-Ang2 from AT1 receptor in Sprague-Dawley rat liver membraneDisplacement of [125I]SI-Ang2 from AT1 receptor in Sprague-Dawley rat liver membrane
ChEMBL 520 10 1 8 5.2 CCCc1nc2c(C)cc(-c3nc4ccccc4n3C)cc2n1CCOc1ccc(CCc2nnn[nH]2)cc1 10.1021/jm901272d
CHEMBL567898 195468 0 None - 1 Rat 5.8 pKi = 5.8 Binding
Displacement of [125I]SI-Ang2 from AT1 receptor in Sprague-Dawley rat liver membraneDisplacement of [125I]SI-Ang2 from AT1 receptor in Sprague-Dawley rat liver membrane
ChEMBL 520 10 1 8 5.2 CCCc1nc2c(C)cc(-c3nc4ccccc4n3C)cc2n1CCOc1ccc(CCc2nnn[nH]2)cc1 10.1021/jm901272d
44567850 183371 0 None - 1 Pig 6.8 pKi = 6.8 Binding
Displacement of [125]Ang2 from AT2 receptor in pig uterus membraneDisplacement of [125]Ang2 from AT2 receptor in pig uterus membrane
ChEMBL 522 11 1 5 5.6 CCCCOC(=O)NS(=O)(=O)c1ccc(Cc2ccccc2)cc1-c1ccc(C(=O)N(CC)CC)cc1 10.1016/j.bmc.2008.05.066
CHEMBL481664 183371 0 None - 1 Pig 6.8 pKi = 6.8 Binding
Displacement of [125]Ang2 from AT2 receptor in pig uterus membraneDisplacement of [125]Ang2 from AT2 receptor in pig uterus membrane
ChEMBL 522 11 1 5 5.6 CCCCOC(=O)NS(=O)(=O)c1ccc(Cc2ccccc2)cc1-c1ccc(C(=O)N(CC)CC)cc1 10.1016/j.bmc.2008.05.066
1610 2305 89 None 1 4 Human 7.8 pKi = 7.8 Binding
Displacement of [3H]-Angiotensin 2 from AT1 receptor in human PLC/PRF/5 cells after 20 mins by liquid scintillation countingDisplacement of [3H]-Angiotensin 2 from AT1 receptor in human PLC/PRF/5 cells after 20 mins by liquid scintillation counting
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/acs.jmedchem.5b01495
3941 2305 89 None 1 4 Human 7.8 pKi = 7.8 Binding
Displacement of [3H]-Angiotensin 2 from AT1 receptor in human PLC/PRF/5 cells after 20 mins by liquid scintillation countingDisplacement of [3H]-Angiotensin 2 from AT1 receptor in human PLC/PRF/5 cells after 20 mins by liquid scintillation counting
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/acs.jmedchem.5b01495
3961 2305 89 None 1 4 Human 7.8 pKi = 7.8 Binding
Displacement of [3H]-Angiotensin 2 from AT1 receptor in human PLC/PRF/5 cells after 20 mins by liquid scintillation countingDisplacement of [3H]-Angiotensin 2 from AT1 receptor in human PLC/PRF/5 cells after 20 mins by liquid scintillation counting
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/acs.jmedchem.5b01495
590 2305 89 None 1 4 Human 7.8 pKi = 7.8 Binding
Displacement of [3H]-Angiotensin 2 from AT1 receptor in human PLC/PRF/5 cells after 20 mins by liquid scintillation countingDisplacement of [3H]-Angiotensin 2 from AT1 receptor in human PLC/PRF/5 cells after 20 mins by liquid scintillation counting
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/acs.jmedchem.5b01495
CHEMBL191 2305 89 None 1 4 Human 7.8 pKi = 7.8 Binding
Displacement of [3H]-Angiotensin 2 from AT1 receptor in human PLC/PRF/5 cells after 20 mins by liquid scintillation countingDisplacement of [3H]-Angiotensin 2 from AT1 receptor in human PLC/PRF/5 cells after 20 mins by liquid scintillation counting
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/acs.jmedchem.5b01495
DB00678 2305 89 None 1 4 Human 7.8 pKi = 7.8 Binding
Displacement of [3H]-Angiotensin 2 from AT1 receptor in human PLC/PRF/5 cells after 20 mins by liquid scintillation countingDisplacement of [3H]-Angiotensin 2 from AT1 receptor in human PLC/PRF/5 cells after 20 mins by liquid scintillation counting
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/acs.jmedchem.5b01495
19029509 17869 0 None - 1 Rat 7.8 pKi = 7.8 Binding
Inhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranesInhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranes
ChEMBL 487 5 1 7 4.5 Cc1nn(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/c(=N/C(=O)c2ccccc2Cl)s1 10.1016/S0960-894X(97)00026-7
CHEMBL126643 17869 0 None - 1 Rat 7.8 pKi = 7.8 Binding
Inhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranesInhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranes
ChEMBL 487 5 1 7 4.5 Cc1nn(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/c(=N/C(=O)c2ccccc2Cl)s1 10.1016/S0960-894X(97)00026-7
123794 878 40 None -67608 2 Rat 5.8 pKi = 5.8 Binding
Displacement of [125I]Ang II from AT1 receptor in rat SMC membranes incubated for 60 mins by gamma counting methodDisplacement of [125I]Ang II from AT1 receptor in rat SMC membranes incubated for 60 mins by gamma counting method
ChEMBL None None None None 10.1021/acs.jmedchem.9b01780
3944 878 40 None -67608 2 Rat 5.8 pKi = 5.8 Binding
Displacement of [125I]Ang II from AT1 receptor in rat SMC membranes incubated for 60 mins by gamma counting methodDisplacement of [125I]Ang II from AT1 receptor in rat SMC membranes incubated for 60 mins by gamma counting method
ChEMBL None None None None 10.1021/acs.jmedchem.9b01780
594 878 40 None -67608 2 Rat 5.8 pKi = 5.8 Binding
Displacement of [125I]Ang II from AT1 receptor in rat SMC membranes incubated for 60 mins by gamma counting methodDisplacement of [125I]Ang II from AT1 receptor in rat SMC membranes incubated for 60 mins by gamma counting method
ChEMBL None None None None 10.1021/acs.jmedchem.9b01780
CHEMBL1885579 878 40 None -67608 2 Rat 5.8 pKi = 5.8 Binding
Displacement of [125I]Ang II from AT1 receptor in rat SMC membranes incubated for 60 mins by gamma counting methodDisplacement of [125I]Ang II from AT1 receptor in rat SMC membranes incubated for 60 mins by gamma counting method
ChEMBL None None None None 10.1021/acs.jmedchem.9b01780
10004228 203296 0 None - 1 Rat 6.8 pKi = 6.8 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 456 7 1 8 4.5 CCCc1nc(C)n2nc(SC)nc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00041a016
CHEMBL76866 203296 0 None - 1 Rat 6.8 pKi = 6.8 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 456 7 1 8 4.5 CCCc1nc(C)n2nc(SC)nc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00041a016
10005644 203799 0 None - 1 Rat 6.8 pKi = 6.8 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 486 7 1 7 5.5 CCCc1nc(C)n2nc(-c3ccccc3)nc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00041a016
CHEMBL80854 203799 0 None - 1 Rat 6.8 pKi = 6.8 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 486 7 1 7 5.5 CCCc1nc(C)n2nc(-c3ccccc3)nc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00041a016
CHEMBL1076601 206724 0 None - 1 Human 7.7 pKi = 7.7 Binding
Displacement of [125I][Sar1,Ile8]Ang2 from wild-type human AT1 receptor expressed in CHO cells by gamma countingDisplacement of [125I][Sar1,Ile8]Ang2 from wild-type human AT1 receptor expressed in CHO cells by gamma counting
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccc(C(=O)c2ccccc2)cc1)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O 10.1021/jm9015747
168294859 191668 0 None -19 2 Human 6.8 pKi = 6.8 Binding
Displacement of [125-I]-[Sar1Ile8]-angiotensin II from human AT1R expressed in HEK293 cell membrane assessed as inhibition constant by radioligand binding assayDisplacement of [125-I]-[Sar1Ile8]-angiotensin II from human AT1R expressed in HEK293 cell membrane assessed as inhibition constant by radioligand binding assay
ChEMBL 561 13 1 6 7.3 CCCCOC(=O)NS(=O)(=O)c1ccc(CCC)cc1-c1ccc(Cn2c(CCCC)nc3ccccc32)cc1 10.1016/j.bmc.2022.116804
CHEMBL5205769 191668 0 None -19 2 Human 6.8 pKi = 6.8 Binding
Displacement of [125-I]-[Sar1Ile8]-angiotensin II from human AT1R expressed in HEK293 cell membrane assessed as inhibition constant by radioligand binding assayDisplacement of [125-I]-[Sar1Ile8]-angiotensin II from human AT1R expressed in HEK293 cell membrane assessed as inhibition constant by radioligand binding assay
ChEMBL 561 13 1 6 7.3 CCCCOC(=O)NS(=O)(=O)c1ccc(CCC)cc1-c1ccc(Cn2c(CCCC)nc3ccccc32)cc1 10.1016/j.bmc.2022.116804
10029566 203358 0 None - 1 Rat 6.7 pKi = 6.7 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 517 8 1 9 3.1 CCCc1nc(C)n2nc(S(=O)(=O)N(C)C)nc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00041a016
CHEMBL77384 203358 0 None - 1 Rat 6.7 pKi = 6.7 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 517 8 1 9 3.1 CCCc1nc(C)n2nc(S(=O)(=O)N(C)C)nc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00041a016
59984617 84839 0 None - 1 Rat 6.7 pKi = 6.7 Binding
Displacement of [125I]-SI-Ang-2 from AT1 receptor in Rattus norvegicus Sprague-Dawley (rat) liver membranes after 2 hrDisplacement of [125I]-SI-Ang-2 from AT1 receptor in Rattus norvegicus Sprague-Dawley (rat) liver membranes after 2 hr
ChEMBL 558 8 2 6 7.0 CCCc1nc2c(C)cc(-c3nc4ccccc4n3C)cc2n1Cc1ccc(-c2ccc(C(=O)O)cc2C(=O)O)cc1 10.1007/s00044-008-9153-9
CHEMBL2260199 84839 0 None - 1 Rat 6.7 pKi = 6.7 Binding
Displacement of [125I]-SI-Ang-2 from AT1 receptor in Rattus norvegicus Sprague-Dawley (rat) liver membranes after 2 hrDisplacement of [125I]-SI-Ang-2 from AT1 receptor in Rattus norvegicus Sprague-Dawley (rat) liver membranes after 2 hr
ChEMBL 558 8 2 6 7.0 CCCc1nc2c(C)cc(-c3nc4ccccc4n3C)cc2n1Cc1ccc(-c2ccc(C(=O)O)cc2C(=O)O)cc1 10.1007/s00044-008-9153-9
CHEMBL1076612 206728 0 None - 1 Human 7.7 pKi = 7.7 Binding
Displacement of [125I][Sar1,Ile8]Ang2 from wild-type human AT1 receptor expressed in CHO cells by gamma countingDisplacement of [125I][Sar1,Ile8]Ang2 from wild-type human AT1 receptor expressed in CHO cells by gamma counting
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H](N)Cc1ccc(C(=O)c2ccccc2)cc1)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O 10.1021/jm9015747
87218987 170430 0 None - 1 Human 7.7 pKi = 7.7 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 523 13 3 6 5.6 CCCOc1nc(CC)c(CNC(=O)[C@@H](S)CC(C)C)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/acsmedchemlett.8b00462
CHEMBL4456519 170430 0 None - 1 Human 7.7 pKi = 7.7 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 523 13 3 6 5.6 CCCOc1nc(CC)c(CNC(=O)[C@@H](S)CC(C)C)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/acsmedchemlett.8b00462
10415026 165110 0 None - 1 Rat 6.7 pKi = 6.7 Binding
Inhibition of [125I]- Sar,Ile8-angiotensin II binding to rat adrenal cortical membrane angiotensin II receptorInhibition of [125I]- Sar,Ile8-angiotensin II binding to rat adrenal cortical membrane angiotensin II receptor
ChEMBL 544 10 1 5 7.5 CCCCC1=NC(c2ccc(Cl)cc2)=C(C(=O)OCC)C(C)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00103a014
CHEMBL424483 165110 0 None - 1 Rat 6.7 pKi = 6.7 Binding
Inhibition of [125I]- Sar,Ile8-angiotensin II binding to rat adrenal cortical membrane angiotensin II receptorInhibition of [125I]- Sar,Ile8-angiotensin II binding to rat adrenal cortical membrane angiotensin II receptor
ChEMBL 544 10 1 5 7.5 CCCCC1=NC(c2ccc(Cl)cc2)=C(C(=O)OCC)C(C)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00103a014
19029491 116450 0 None - 1 Rat 6.7 pKi = 6.7 Binding
Inhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranesInhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranes
ChEMBL 501 6 1 7 4.8 CCc1nn(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/c(=N/C(=O)c2cccc(Cl)c2)s1 10.1016/S0960-894X(97)00026-7
CHEMBL338670 116450 0 None - 1 Rat 6.7 pKi = 6.7 Binding
Inhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranesInhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranes
ChEMBL 501 6 1 7 4.8 CCc1nn(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/c(=N/C(=O)c2cccc(Cl)c2)s1 10.1016/S0960-894X(97)00026-7
10365342 112983 0 None -16 2 Rat 6.7 pKi = 6.7 Binding
Compound was evaluated for binding affinity against AT1 receptor in rat liverCompound was evaluated for binding affinity against AT1 receptor in rat liver
ChEMBL 429 9 3 7 4.0 CCCCc1ncc(C(=O)O)c(NCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)n1 10.1021/jm00098a018
CHEMBL331983 112983 0 None -16 2 Rat 6.7 pKi = 6.7 Binding
Compound was evaluated for binding affinity against AT1 receptor in rat liverCompound was evaluated for binding affinity against AT1 receptor in rat liver
ChEMBL 429 9 3 7 4.0 CCCCc1ncc(C(=O)O)c(NCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)n1 10.1021/jm00098a018
155516694 169535 0 None - 1 Human 6.7 pKi = 6.7 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 507 12 3 5 5.9 CCCCc1nc(C)c(CNC(=O)[C@@H](S)CC(C)C)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/acsmedchemlett.8b00462
CHEMBL4443691 169535 0 None - 1 Human 6.7 pKi = 6.7 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 507 12 3 5 5.9 CCCCc1nc(C)c(CNC(=O)[C@@H](S)CC(C)C)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/acsmedchemlett.8b00462
19029483 18625 0 None - 1 Rat 6.7 pKi = 6.7 Binding
Inhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranesInhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranes
ChEMBL 529 8 1 7 5.6 CCCCc1nn(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/c(=N/C(=O)c2ccccc2Cl)s1 10.1016/S0960-894X(97)00026-7
CHEMBL128003 18625 0 None - 1 Rat 6.7 pKi = 6.7 Binding
Inhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranesInhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranes
ChEMBL 529 8 1 7 5.6 CCCCc1nn(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/c(=N/C(=O)c2ccccc2Cl)s1 10.1016/S0960-894X(97)00026-7
10790260 205040 0 None - 1 Human 5.7 pKi = 5.7 Binding
Binding affinity against AT1 in human hepatoma cell line, PLC-PRF-5Binding affinity against AT1 in human hepatoma cell line, PLC-PRF-5
ChEMBL 463 8 2 4 4.1 CCCCN1C(=O)C2(CCCC2)C(=O)N1Cc1ccc(C(=O)Nc2ccccc2C(=O)O)cc1 10.1021/jm9904147
CHEMBL90187 205040 0 None - 1 Human 5.7 pKi = 5.7 Binding
Binding affinity against AT1 in human hepatoma cell line, PLC-PRF-5Binding affinity against AT1 in human hepatoma cell line, PLC-PRF-5
ChEMBL 463 8 2 4 4.1 CCCCN1C(=O)C2(CCCC2)C(=O)N1Cc1ccc(C(=O)Nc2ccccc2C(=O)O)cc1 10.1021/jm9904147
1481 2027 109 None 1 3 Human 8.7 pKi = 8.7 Binding
Binding affinity against AT1 in human hepatoma cell line, PLC-PRF-5Binding affinity against AT1 in human hepatoma cell line, PLC-PRF-5
ChEMBL 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 10.1021/jm9904147
3749 2027 109 None 1 3 Human 8.7 pKi = 8.7 Binding
Binding affinity against AT1 in human hepatoma cell line, PLC-PRF-5Binding affinity against AT1 in human hepatoma cell line, PLC-PRF-5
ChEMBL 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 10.1021/jm9904147
589 2027 109 None 1 3 Human 8.7 pKi = 8.7 Binding
Binding affinity against AT1 in human hepatoma cell line, PLC-PRF-5Binding affinity against AT1 in human hepatoma cell line, PLC-PRF-5
ChEMBL 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 10.1021/jm9904147
6908 2027 109 None 1 3 Human 8.7 pKi = 8.7 Binding
Binding affinity against AT1 in human hepatoma cell line, PLC-PRF-5Binding affinity against AT1 in human hepatoma cell line, PLC-PRF-5
ChEMBL 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 10.1021/jm9904147
CHEMBL1513 2027 109 None 1 3 Human 8.7 pKi = 8.7 Binding
Binding affinity against AT1 in human hepatoma cell line, PLC-PRF-5Binding affinity against AT1 in human hepatoma cell line, PLC-PRF-5
ChEMBL 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 10.1021/jm9904147
DB01029 2027 109 None 1 3 Human 8.7 pKi = 8.7 Binding
Binding affinity against AT1 in human hepatoma cell line, PLC-PRF-5Binding affinity against AT1 in human hepatoma cell line, PLC-PRF-5
ChEMBL 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 10.1021/jm9904147
135723840 138599 0 None - 1 Rat 8.7 pKi = 8.7 Binding
Displacement of [125I]-Ang II from Angiotensin 2 type-1A receptor in rat vascular smooth muscle cells after 150 mins by gamma counting methodDisplacement of [125I]-Ang II from Angiotensin 2 type-1A receptor in rat vascular smooth muscle cells after 150 mins by gamma counting method
ChEMBL 452 8 2 6 4.6 CCCCc1nc(Cl)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2noc(=O)[nH]2)cc1 10.1016/j.bmc.2016.03.028
CHEMBL3787059 138599 0 None - 1 Rat 8.7 pKi = 8.7 Binding
Displacement of [125I]-Ang II from Angiotensin 2 type-1A receptor in rat vascular smooth muscle cells after 150 mins by gamma counting methodDisplacement of [125I]-Ang II from Angiotensin 2 type-1A receptor in rat vascular smooth muscle cells after 150 mins by gamma counting method
ChEMBL 452 8 2 6 4.6 CCCCc1nc(Cl)c(C(=O)O)n1Cc1ccc(-c2ccccc2-c2noc(=O)[nH]2)cc1 10.1016/j.bmc.2016.03.028
3936 2171 28 None -1 4 Pig 8.7 pKi = 8.7 Binding
Displacement of [125]Ang2 from AT2 receptor in pig uterus membraneDisplacement of [125]Ang2 from AT2 receptor in pig uterus membrane
ChEMBL 582 11 1 8 6.8 CCCCOC(=O)NS(=O)(=O)c1sc(cc1c1ccc(cc1)Cn1c(CC)nc2c1nc(C)cc2C)CC(C)C 10.1016/j.bmc.2008.05.066
6603900 2171 28 None -1 4 Pig 8.7 pKi = 8.7 Binding
Displacement of [125]Ang2 from AT2 receptor in pig uterus membraneDisplacement of [125]Ang2 from AT2 receptor in pig uterus membrane
ChEMBL 582 11 1 8 6.8 CCCCOC(=O)NS(=O)(=O)c1sc(cc1c1ccc(cc1)Cn1c(CC)nc2c1nc(C)cc2C)CC(C)C 10.1016/j.bmc.2008.05.066
CHEMBL288174 2171 28 None -1 4 Pig 8.7 pKi = 8.7 Binding
Displacement of [125]Ang2 from AT2 receptor in pig uterus membraneDisplacement of [125]Ang2 from AT2 receptor in pig uterus membrane
ChEMBL 582 11 1 8 6.8 CCCCOC(=O)NS(=O)(=O)c1sc(cc1c1ccc(cc1)Cn1c(CC)nc2c1nc(C)cc2C)CC(C)C 10.1016/j.bmc.2008.05.066
1481 2027 109 None 1 3 Human 8.7 pKi = 8.7 Binding
In vitro binding affinity towards Angiotensin II receptor, type 1 of human hepatoma cell line PLC-PRF-5In vitro binding affinity towards Angiotensin II receptor, type 1 of human hepatoma cell line PLC-PRF-5
ChEMBL 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 10.1021/jm010457z
3749 2027 109 None 1 3 Human 8.7 pKi = 8.7 Binding
In vitro binding affinity towards Angiotensin II receptor, type 1 of human hepatoma cell line PLC-PRF-5In vitro binding affinity towards Angiotensin II receptor, type 1 of human hepatoma cell line PLC-PRF-5
ChEMBL 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 10.1021/jm010457z
589 2027 109 None 1 3 Human 8.7 pKi = 8.7 Binding
In vitro binding affinity towards Angiotensin II receptor, type 1 of human hepatoma cell line PLC-PRF-5In vitro binding affinity towards Angiotensin II receptor, type 1 of human hepatoma cell line PLC-PRF-5
ChEMBL 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 10.1021/jm010457z
6908 2027 109 None 1 3 Human 8.7 pKi = 8.7 Binding
In vitro binding affinity towards Angiotensin II receptor, type 1 of human hepatoma cell line PLC-PRF-5In vitro binding affinity towards Angiotensin II receptor, type 1 of human hepatoma cell line PLC-PRF-5
ChEMBL 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 10.1021/jm010457z
CHEMBL1513 2027 109 None 1 3 Human 8.7 pKi = 8.7 Binding
In vitro binding affinity towards Angiotensin II receptor, type 1 of human hepatoma cell line PLC-PRF-5In vitro binding affinity towards Angiotensin II receptor, type 1 of human hepatoma cell line PLC-PRF-5
ChEMBL 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 10.1021/jm010457z
DB01029 2027 109 None 1 3 Human 8.7 pKi = 8.7 Binding
In vitro binding affinity towards Angiotensin II receptor, type 1 of human hepatoma cell line PLC-PRF-5In vitro binding affinity towards Angiotensin II receptor, type 1 of human hepatoma cell line PLC-PRF-5
ChEMBL 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 10.1021/jm010457z
44350610 117650 0 None - 1 Rat 8.7 pKi = 8.7 Binding
Inhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranesInhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranes
ChEMBL 525 8 2 8 4.2 CCCc1nn(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/c(=N/C(=O)c2ccccc2C(=O)O)s1 10.1016/S0960-894X(97)00026-7
CHEMBL340863 117650 0 None - 1 Rat 8.7 pKi = 8.7 Binding
Inhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranesInhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranes
ChEMBL 525 8 2 8 4.2 CCCc1nn(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/c(=N/C(=O)c2ccccc2C(=O)O)s1 10.1016/S0960-894X(97)00026-7
10005741 110949 0 None - 1 Human 8.7 pKi = 8.7 Binding
Ability to displace [125I]AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1Ability to displace [125I]AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1
ChEMBL 488 7 2 7 4.5 CCCCc1nc(Cl)c(C(=O)O)n1Cc1ccc2c(-c3nnn[nH]3)cc3ccccc3c(=O)c2c1 10.1021/jm00014a024
CHEMBL327535 110949 0 None - 1 Human 8.7 pKi = 8.7 Binding
Ability to displace [125I]AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1Ability to displace [125I]AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1
ChEMBL 488 7 2 7 4.5 CCCCc1nc(Cl)c(C(=O)O)n1Cc1ccc2c(-c3nnn[nH]3)cc3ccccc3c(=O)c2c1 10.1021/jm00014a024
10031067 99875 3 None -2 3 Rat 8.7 pKi = 8.7 Binding
Displacement of [125]Ang2 from AT1 receptor in rat liver membraneDisplacement of [125]Ang2 from AT1 receptor in rat liver membrane
ChEMBL 576 11 1 7 6.7 CCCCOC(=O)NS(=O)(=O)c1ccc(CC(C)C)cc1-c1ccc(Cn2c(CC)nc3c(C)cc(C)nc32)cc1 10.1016/j.bmc.2008.05.066
CHEMBL289614 99875 3 None -2 3 Rat 8.7 pKi = 8.7 Binding
Displacement of [125]Ang2 from AT1 receptor in rat liver membraneDisplacement of [125]Ang2 from AT1 receptor in rat liver membrane
ChEMBL 576 11 1 7 6.7 CCCCOC(=O)NS(=O)(=O)c1ccc(CC(C)C)cc1-c1ccc(Cn2c(CC)nc3c(C)cc(C)nc32)cc1 10.1016/j.bmc.2008.05.066
127029976 138674 0 None - 1 Human 8.7 pKi = 8.7 Binding
Displacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation countingDisplacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation counting
ChEMBL 1160 33 15 14 -1.2 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCN/C(N)=N/C(=O)NCCCCN)NC(=O)[C@@H](N)CC(=O)O)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O 10.1021/acs.jmedchem.5b01495
CHEMBL3786145 138674 0 None - 1 Human 8.7 pKi = 8.7 Binding
Displacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation countingDisplacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation counting
ChEMBL 1160 33 15 14 -1.2 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCN/C(N)=N/C(=O)NCCCCN)NC(=O)[C@@H](N)CC(=O)O)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O 10.1021/acs.jmedchem.5b01495
CHEMBL3787767 138674 0 None - 1 Human 8.7 pKi = 8.7 Binding
Displacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation countingDisplacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation counting
ChEMBL 1160 33 15 14 -1.2 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCN/C(N)=N/C(=O)NCCCCN)NC(=O)[C@@H](N)CC(=O)O)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O 10.1021/acs.jmedchem.5b01495
23298214 101529 0 None - 1 Rat 8.7 pKi = 8.7 Binding
Inhibition of [125I]Sar1,Ile8 angiotensin II binding to Angiotensin II receptor type 1 in rat adrenocortical membraneInhibition of [125I]Sar1,Ile8 angiotensin II binding to Angiotensin II receptor type 1 in rat adrenocortical membrane
ChEMBL 450 6 2 7 4.8 O=C(O)c1c(Oc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c(C2CC2)nc2cccnc12 10.1016/S0960-894X(01)81146-X
CHEMBL301689 101529 0 None - 1 Rat 8.7 pKi = 8.7 Binding
Inhibition of [125I]Sar1,Ile8 angiotensin II binding to Angiotensin II receptor type 1 in rat adrenocortical membraneInhibition of [125I]Sar1,Ile8 angiotensin II binding to Angiotensin II receptor type 1 in rat adrenocortical membrane
ChEMBL 450 6 2 7 4.8 O=C(O)c1c(Oc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c(C2CC2)nc2cccnc12 10.1016/S0960-894X(01)81146-X
19029671 117571 0 None - 1 Rat 8.6 pKi = 8.6 Binding
Inhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranesInhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranes
ChEMBL 497 7 1 8 4.2 CCc1nn(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/c(=N/C(=O)c2ccccc2OC)s1 10.1016/S0960-894X(97)00026-7
CHEMBL340618 117571 0 None - 1 Rat 8.6 pKi = 8.6 Binding
Inhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranesInhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranes
ChEMBL 497 7 1 8 4.2 CCc1nn(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/c(=N/C(=O)c2ccccc2OC)s1 10.1016/S0960-894X(97)00026-7
10745817 118857 0 None - 1 Rat 8.6 pKi = 8.6 Binding
The compound was evaluated for the inhibition of [125I]-Sar-AII binding to Angiotensin II receptor, type 1 from purified rat liver membranes.The compound was evaluated for the inhibition of [125I]-Sar-AII binding to Angiotensin II receptor, type 1 from purified rat liver membranes.
ChEMBL 580 12 3 7 5.4 CCCCc1ncc(CNc2ccccc2C(=O)O)n1Cc1ccc(C(=O)NS(=O)(=O)c2ccccc2Cl)cc1 10.1021/jm991050l
CHEMBL2111973 118857 0 None - 1 Rat 8.6 pKi = 8.6 Binding
The compound was evaluated for the inhibition of [125I]-Sar-AII binding to Angiotensin II receptor, type 1 from purified rat liver membranes.The compound was evaluated for the inhibition of [125I]-Sar-AII binding to Angiotensin II receptor, type 1 from purified rat liver membranes.
ChEMBL 580 12 3 7 5.4 CCCCc1ncc(CNc2ccccc2C(=O)O)n1Cc1ccc(C(=O)NS(=O)(=O)c2ccccc2Cl)cc1 10.1021/jm991050l
CHEMBL344464 118857 0 None - 1 Rat 8.6 pKi = 8.6 Binding
The compound was evaluated for the inhibition of [125I]-Sar-AII binding to Angiotensin II receptor, type 1 from purified rat liver membranes.The compound was evaluated for the inhibition of [125I]-Sar-AII binding to Angiotensin II receptor, type 1 from purified rat liver membranes.
ChEMBL 580 12 3 7 5.4 CCCCc1ncc(CNc2ccccc2C(=O)O)n1Cc1ccc(C(=O)NS(=O)(=O)c2ccccc2Cl)cc1 10.1021/jm991050l
87219174 169187 0 None - 1 Human 8.6 pKi = 8.6 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 537 14 3 6 5.9 CCCOc1nc(CC)c(CNC(=O)[C@@H](CS)CC(C)C)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/acsmedchemlett.8b00462
CHEMBL4438878 169187 0 None - 1 Human 8.6 pKi = 8.6 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 537 14 3 6 5.9 CCCOc1nc(CC)c(CNC(=O)[C@@H](CS)CC(C)C)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/acsmedchemlett.8b00462
44567745 183293 0 None - 1 Pig 8.6 pKi = 8.6 Binding
Displacement of [125]Ang2 from AT2 receptor in pig uterus membraneDisplacement of [125]Ang2 from AT2 receptor in pig uterus membrane
ChEMBL 480 10 2 6 5.0 CCCCOC(=O)NS(=O)(=O)c1sc(CC(C)C)cc1-c1ccc(C(=O)NC(C)C)cc1 10.1016/j.bmc.2008.05.066
CHEMBL481089 183293 0 None - 1 Pig 8.6 pKi = 8.6 Binding
Displacement of [125]Ang2 from AT2 receptor in pig uterus membraneDisplacement of [125]Ang2 from AT2 receptor in pig uterus membrane
ChEMBL 480 10 2 6 5.0 CCCCOC(=O)NS(=O)(=O)c1sc(CC(C)C)cc1-c1ccc(C(=O)NC(C)C)cc1 10.1016/j.bmc.2008.05.066
44350616 18624 0 None - 1 Rat 8.6 pKi = 8.6 Binding
Inhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranesInhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranes
ChEMBL 497 6 2 8 3.6 Cc1nn(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/c(=N/C(=O)c2ccccc2C(=O)O)s1 10.1016/S0960-894X(97)00026-7
CHEMBL127988 18624 0 None - 1 Rat 8.6 pKi = 8.6 Binding
Inhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranesInhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranes
ChEMBL 497 6 2 8 3.6 Cc1nn(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/c(=N/C(=O)c2ccccc2C(=O)O)s1 10.1016/S0960-894X(97)00026-7
10345537 111099 0 None - 1 Human 8.6 pKi = 8.6 Binding
Ability to displace [125I]AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1Ability to displace [125I]AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1
ChEMBL 492 6 2 8 4.0 CCOc1nc2cccc(C(=O)O)c2n1Cc1ccc2c(-c3nnn[nH]3)cc3ccccc3c(=O)c2c1 10.1021/jm00014a024
CHEMBL328296 111099 0 None - 1 Human 8.6 pKi = 8.6 Binding
Ability to displace [125I]AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1Ability to displace [125I]AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1
ChEMBL 492 6 2 8 4.0 CCOc1nc2cccc(C(=O)O)c2n1Cc1ccc2c(-c3nnn[nH]3)cc3ccccc3c(=O)c2c1 10.1021/jm00014a024
10481196 112236 0 None - 1 Human 8.6 pKi = 8.6 Binding
Ability to displace [125I]AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1Ability to displace [125I]AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1
ChEMBL 503 6 2 7 4.9 CCc1cc(OCc2ccc3c(-c4nnn[nH]4)cc4ccccc4c(=O)c3c2)c2cc(C(=O)O)ccc2n1 10.1021/jm00014a024
CHEMBL330508 112236 0 None - 1 Human 8.6 pKi = 8.6 Binding
Ability to displace [125I]AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1Ability to displace [125I]AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1
ChEMBL 503 6 2 7 4.9 CCc1cc(OCc2ccc3c(-c4nnn[nH]4)cc4ccccc4c(=O)c3c2)c2cc(C(=O)O)ccc2n1 10.1021/jm00014a024
10432780 163949 0 None -10 3 Rat 8.6 pKi = 8.6 Binding
Binding affinity against angiotensin II receptor from rat liverBinding affinity against angiotensin II receptor from rat liver
ChEMBL 429 8 2 7 3.7 CCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1nc(C)ncc1C(=O)O 10.1021/jm00070a012
CHEMBL421473 163949 0 None -10 3 Rat 8.6 pKi = 8.6 Binding
Binding affinity against angiotensin II receptor from rat liverBinding affinity against angiotensin II receptor from rat liver
ChEMBL 429 8 2 7 3.7 CCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1nc(C)ncc1C(=O)O 10.1021/jm00070a012
10432780 163949 0 None -10 3 Rat 8.6 pKi = 8.6 Binding
Compound was evaluated for binding affinity against angiotensin II receptor, type 1 in rat liverCompound was evaluated for binding affinity against angiotensin II receptor, type 1 in rat liver
ChEMBL 429 8 2 7 3.7 CCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1nc(C)ncc1C(=O)O 10.1021/jm00098a018
CHEMBL421473 163949 0 None -10 3 Rat 8.6 pKi = 8.6 Binding
Compound was evaluated for binding affinity against angiotensin II receptor, type 1 in rat liverCompound was evaluated for binding affinity against angiotensin II receptor, type 1 in rat liver
ChEMBL 429 8 2 7 3.7 CCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1nc(C)ncc1C(=O)O 10.1021/jm00098a018
127029977 138675 0 None - 1 Human 8.6 pKi = 8.6 Binding
Displacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation countingDisplacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation counting
ChEMBL 1220 37 15 16 -2.0 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCN/C(N)=N/C(=O)NCCOCCOCCN)NC(=O)[C@@H](N)CC(=O)O)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O 10.1021/acs.jmedchem.5b01495
CHEMBL3786986 138675 0 None - 1 Human 8.6 pKi = 8.6 Binding
Displacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation countingDisplacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation counting
ChEMBL 1220 37 15 16 -2.0 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCN/C(N)=N/C(=O)NCCOCCOCCN)NC(=O)[C@@H](N)CC(=O)O)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O 10.1021/acs.jmedchem.5b01495
CHEMBL3787768 138675 0 None - 1 Human 8.6 pKi = 8.6 Binding
Displacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation countingDisplacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation counting
ChEMBL 1220 37 15 16 -2.0 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCN/C(N)=N/C(=O)NCCOCCOCCN)NC(=O)[C@@H](N)CC(=O)O)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O 10.1021/acs.jmedchem.5b01495
44325313 205697 0 None - 1 Human 8.5 pKi = 8.5 Binding
Ability to displace [125I]AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1Ability to displace [125I]AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1
ChEMBL 480 6 2 8 4.3 CCOC(=O)c1c(NCc2ccc3c(-c4nnn[nH]4)cc4ccccc4c(=O)c3c2)cc(C)nc1C 10.1021/jm00014a024
CHEMBL94106 205697 0 None - 1 Human 8.5 pKi = 8.5 Binding
Ability to displace [125I]AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1Ability to displace [125I]AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1
ChEMBL 480 6 2 8 4.3 CCOC(=O)c1c(NCc2ccc3c(-c4nnn[nH]4)cc4ccccc4c(=O)c3c2)cc(C)nc1C 10.1021/jm00014a024
127866 102319 13 None - 1 Rat 8.5 pKi = 8.5 Binding
Inhibition of [125I]Sar1,Ile8 angiotensin II binding to Angiotensin II receptor type 1 in rat adrenocortical membraneInhibition of [125I]Sar1,Ile8 angiotensin II binding to Angiotensin II receptor type 1 in rat adrenocortical membrane
ChEMBL 449 6 2 6 5.5 O=C(O)c1c(Oc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c(C2CC2)nc2ccccc12 10.1016/S0960-894X(01)81146-X
CHEMBL305365 102319 13 None - 1 Rat 8.5 pKi = 8.5 Binding
Inhibition of [125I]Sar1,Ile8 angiotensin II binding to Angiotensin II receptor type 1 in rat adrenocortical membraneInhibition of [125I]Sar1,Ile8 angiotensin II binding to Angiotensin II receptor type 1 in rat adrenocortical membrane
ChEMBL 449 6 2 6 5.5 O=C(O)c1c(Oc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c(C2CC2)nc2ccccc12 10.1016/S0960-894X(01)81146-X
127866 102319 13 None - 1 Rat 8.5 pKi = 8.5 Binding
Receptor binding affinity determined from competitive binding assay using 1251 labelled [Sar1,Ile8] angiotensin II in rat adrenocortical membranesReceptor binding affinity determined from competitive binding assay using 1251 labelled [Sar1,Ile8] angiotensin II in rat adrenocortical membranes
ChEMBL 449 6 2 6 5.5 O=C(O)c1c(Oc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c(C2CC2)nc2ccccc12 10.1016/S0960-894X(01)81147-1
CHEMBL305365 102319 13 None - 1 Rat 8.5 pKi = 8.5 Binding
Receptor binding affinity determined from competitive binding assay using 1251 labelled [Sar1,Ile8] angiotensin II in rat adrenocortical membranesReceptor binding affinity determined from competitive binding assay using 1251 labelled [Sar1,Ile8] angiotensin II in rat adrenocortical membranes
ChEMBL 449 6 2 6 5.5 O=C(O)c1c(Oc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c(C2CC2)nc2ccccc12 10.1016/S0960-894X(01)81147-1
132404 119268 11 None 36 2 Human 7.7 pKi = 7.7 Binding
Ki value was evaluated against Angiotensin II receptor, type 1Ki value was evaluated against Angiotensin II receptor, type 1
ChEMBL 637 13 3 5 8.0 CCCCCN(C(=O)NC)c1ccc2nc(CCCC)n(Cc3ccc(NC(=O)c4c(Cl)ccc(Cl)c4C(=O)O)cc3)c2c1 10.1021/jm9504722
CHEMBL348126 119268 11 None 36 2 Human 7.7 pKi = 7.7 Binding
Ki value was evaluated against Angiotensin II receptor, type 1Ki value was evaluated against Angiotensin II receptor, type 1
ChEMBL 637 13 3 5 8.0 CCCCCN(C(=O)NC)c1ccc2nc(CCCC)n(Cc3ccc(NC(=O)c4c(Cl)ccc(Cl)c4C(=O)O)cc3)c2c1 10.1021/jm9504722
15658054 204989 0 None - 1 Rat 7.7 pKi = 7.7 Binding
Binding affinity against angiotensin II receptor from rat liverBinding affinity against angiotensin II receptor from rat liver
ChEMBL 429 8 2 8 3.7 CCOC(=O)c1cnc(CC)nc1NCc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00070a012
CHEMBL89877 204989 0 None - 1 Rat 7.7 pKi = 7.7 Binding
Binding affinity against angiotensin II receptor from rat liverBinding affinity against angiotensin II receptor from rat liver
ChEMBL 429 8 2 8 3.7 CCOC(=O)c1cnc(CC)nc1NCc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00070a012
19029687 19162 0 None - 1 Rat 7.7 pKi = 7.7 Binding
Inhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranesInhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranes
ChEMBL 515 7 1 7 5.2 CCCc1nn(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/c(=N/C(=O)c2ccccc2Cl)s1 10.1016/S0960-894X(97)00026-7
CHEMBL129181 19162 0 None - 1 Rat 7.7 pKi = 7.7 Binding
Inhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranesInhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranes
ChEMBL 515 7 1 7 5.2 CCCc1nn(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/c(=N/C(=O)c2ccccc2Cl)s1 10.1016/S0960-894X(97)00026-7
11744384 32116 0 None - 1 Rat 7.7 pKi = 7.7 Binding
The compound was evaluated for the inhibition of [125I]-Sar-AII binding to Angiotensin II receptor, type 1 from purified rat liver membranes.The compound was evaluated for the inhibition of [125I]-Sar-AII binding to Angiotensin II receptor, type 1 from purified rat liver membranes.
ChEMBL 448 11 3 6 5.2 CCCCc1ncc(CNc2cc(N=[N+]=[N-])ccc2C(=O)O)n1Cc1ccc(C(=O)O)cc1 10.1021/jm991050l
CHEMBL141065 32116 0 None - 1 Rat 7.7 pKi = 7.7 Binding
The compound was evaluated for the inhibition of [125I]-Sar-AII binding to Angiotensin II receptor, type 1 from purified rat liver membranes.The compound was evaluated for the inhibition of [125I]-Sar-AII binding to Angiotensin II receptor, type 1 from purified rat liver membranes.
ChEMBL 448 11 3 6 5.2 CCCCc1ncc(CNc2cc(N=[N+]=[N-])ccc2C(=O)O)n1Cc1ccc(C(=O)O)cc1 10.1021/jm991050l
CHEMBL2111972 32116 0 None - 1 Rat 7.7 pKi = 7.7 Binding
The compound was evaluated for the inhibition of [125I]-Sar-AII binding to Angiotensin II receptor, type 1 from purified rat liver membranes.The compound was evaluated for the inhibition of [125I]-Sar-AII binding to Angiotensin II receptor, type 1 from purified rat liver membranes.
ChEMBL 448 11 3 6 5.2 CCCCc1ncc(CNc2cc(N=[N+]=[N-])ccc2C(=O)O)n1Cc1ccc(C(=O)O)cc1 10.1021/jm991050l
45488164 196144 0 None - 1 Rat 5.7 pKi = 5.7 Binding
Displacement of [125I]SI-Ang2 from AT1 receptor in Sprague-Dawley rat liver membraneDisplacement of [125I]SI-Ang2 from AT1 receptor in Sprague-Dawley rat liver membrane
ChEMBL 602 12 1 7 7.4 CCCc1nc2c(C)cc(-c3nc4ccccc4n3C)cc2n1CCOc1ccc(CC(C)(Oc2ccccc2)C(=O)O)cc1 10.1021/jm901272d
CHEMBL572276 196144 0 None - 1 Rat 5.7 pKi = 5.7 Binding
Displacement of [125I]SI-Ang2 from AT1 receptor in Sprague-Dawley rat liver membraneDisplacement of [125I]SI-Ang2 from AT1 receptor in Sprague-Dawley rat liver membrane
ChEMBL 602 12 1 7 7.4 CCCc1nc2c(C)cc(-c3nc4ccccc4n3C)cc2n1CCOc1ccc(CC(C)(Oc2ccccc2)C(=O)O)cc1 10.1021/jm901272d
118719137 114933 0 None -4 2 Human 5.7 pKi = 5.7 Binding
Displacement of [125I]-angiotensin 2 from human angiotensin 2 type-1 receptor expressed in CHO cell membranes after 1 hr by gamma counting analysisDisplacement of [125I]-angiotensin 2 from human angiotensin 2 type-1 receptor expressed in CHO cell membranes after 1 hr by gamma counting analysis
ChEMBL 1405 38 7 16 7.6 CCN(CC)c1ccc2c(-c3ccc(S(=O)(=O)NCCCCCCCCCCCCNC(=O)NCCCC[C@H](NC(=O)Cc4csc(=N)n4C)C(=O)N[C@@H](Cc4cn(Cc5ccccc5)c[n+]4C)C(=O)NC4CCN(C)CC4)cc3S(=O)(=O)[O-])c3ccc(=[N+](CC)CC)cc-3oc2c1 10.1021/jm401789v
CHEMBL3234445 114933 0 None -4 2 Human 5.7 pKi = 5.7 Binding
Displacement of [125I]-angiotensin 2 from human angiotensin 2 type-1 receptor expressed in CHO cell membranes after 1 hr by gamma counting analysisDisplacement of [125I]-angiotensin 2 from human angiotensin 2 type-1 receptor expressed in CHO cell membranes after 1 hr by gamma counting analysis
ChEMBL 1405 38 7 16 7.6 CCN(CC)c1ccc2c(-c3ccc(S(=O)(=O)NCCCCCCCCCCCCNC(=O)NCCCC[C@H](NC(=O)Cc4csc(=N)n4C)C(=O)N[C@@H](Cc4cn(Cc5ccccc5)c[n+]4C)C(=O)NC4CCN(C)CC4)cc3S(=O)(=O)[O-])c3ccc(=[N+](CC)CC)cc-3oc2c1 10.1021/jm401789v
CHEMBL3350781 114933 0 None -4 2 Human 5.7 pKi = 5.7 Binding
Displacement of [125I]-angiotensin 2 from human angiotensin 2 type-1 receptor expressed in CHO cell membranes after 1 hr by gamma counting analysisDisplacement of [125I]-angiotensin 2 from human angiotensin 2 type-1 receptor expressed in CHO cell membranes after 1 hr by gamma counting analysis
ChEMBL 1405 38 7 16 7.6 CCN(CC)c1ccc2c(-c3ccc(S(=O)(=O)NCCCCCCCCCCCCNC(=O)NCCCC[C@H](NC(=O)Cc4csc(=N)n4C)C(=O)N[C@@H](Cc4cn(Cc5ccccc5)c[n+]4C)C(=O)NC4CCN(C)CC4)cc3S(=O)(=O)[O-])c3ccc(=[N+](CC)CC)cc-3oc2c1 10.1021/jm401789v
10252692 203463 0 None - 1 Rat 6.7 pKi = 6.7 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 440 7 2 8 3.8 CCCc1nc(CC)n2nc(O)nc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00041a016
CHEMBL78342 203463 0 None - 1 Rat 6.7 pKi = 6.7 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 440 7 2 8 3.8 CCCc1nc(CC)n2nc(O)nc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00041a016
10050933 203779 0 None - 1 Rat 7.6 pKi = 7.6 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 482 8 1 9 4.0 CCCc1nc(C)n2nc(C(=O)OCC)nc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00041a016
CHEMBL80688 203779 0 None - 1 Rat 7.6 pKi = 7.6 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 482 8 1 9 4.0 CCCc1nc(C)n2nc(C(=O)OCC)nc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00041a016
132840 104997 18 None 1 3 Human 7.6 pKi = 7.6 Binding
Binding affinity to angiotensin AT1 receptorBinding affinity to angiotensin AT1 receptor
ChEMBL 426 6 2 8 3.5 CCCc1nc(C)n2nc(O)nc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.bmc.2010.10.043
CHEMBL312104 104997 18 None 1 3 Human 7.6 pKi = 7.6 Binding
Binding affinity to angiotensin AT1 receptorBinding affinity to angiotensin AT1 receptor
ChEMBL 426 6 2 8 3.5 CCCc1nc(C)n2nc(O)nc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/j.bmc.2010.10.043
132840 104997 18 None -1 3 Rat 7.6 pKi = 7.6 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 426 6 2 8 3.5 CCCc1nc(C)n2nc(O)nc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00041a016
CHEMBL312104 104997 18 None -1 3 Rat 7.6 pKi = 7.6 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 426 6 2 8 3.5 CCCc1nc(C)n2nc(O)nc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00041a016
CHEMBL1076602 206725 0 None - 1 Human 7.6 pKi = 7.6 Binding
Displacement of [125I][Sar1,Ile8]Ang2 from wild-type human AT1 receptor expressed in CHO cells by gamma countingDisplacement of [125I][Sar1,Ile8]Ang2 from wild-type human AT1 receptor expressed in CHO cells by gamma counting
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccc(C2(C(F)(F)F)N=N2)cc1)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O 10.1021/jm9015747
145957579 161749 0 None - 1 Human 4.6 pKi = 4.6 Binding
Displacement of [125I-Sar1-Ile8]-Ang2 from human angiotensin 2 receptor type 1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysisDisplacement of [125I-Sar1-Ile8]-Ang2 from human angiotensin 2 receptor type 1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysis
ChEMBL 497 7 0 3 7.0 CCCCC1=N/C(=C\c2ccc(Br)cc2)C(=O)N1Cc1ccc(-c2ccccc2C#N)cc1 10.1016/j.ejmech.2017.12.021
CHEMBL4164514 161749 0 None - 1 Human 4.6 pKi = 4.6 Binding
Displacement of [125I-Sar1-Ile8]-Ang2 from human angiotensin 2 receptor type 1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysisDisplacement of [125I-Sar1-Ile8]-Ang2 from human angiotensin 2 receptor type 1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysis
ChEMBL 497 7 0 3 7.0 CCCCC1=N/C(=C\c2ccc(Br)cc2)C(=O)N1Cc1ccc(-c2ccccc2C#N)cc1 10.1016/j.ejmech.2017.12.021
5249743 106529 1 None 1 2 Human 7.6 pKi = 7.6 Binding
Binding affinity against AT1 in human hepatoma cell line, PLC-PRF-5Binding affinity against AT1 in human hepatoma cell line, PLC-PRF-5
ChEMBL 444 7 1 5 4.0 CCCCN1C(=O)C2(CCCC2)C(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm9904147
CHEMBL315444 106529 1 None 1 2 Human 7.6 pKi = 7.6 Binding
Binding affinity against AT1 in human hepatoma cell line, PLC-PRF-5Binding affinity against AT1 in human hepatoma cell line, PLC-PRF-5
ChEMBL 444 7 1 5 4.0 CCCCN1C(=O)C2(CCCC2)C(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm9904147
10674630 205095 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity against AT1 in human hepatoma cell line, PLC-PRF-5Binding affinity against AT1 in human hepatoma cell line, PLC-PRF-5
ChEMBL 573 10 1 5 5.3 CCCCCN1C(=O)C2(CCCC2)C(=O)N1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1021/jm9904147
CHEMBL90483 205095 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity against AT1 in human hepatoma cell line, PLC-PRF-5Binding affinity against AT1 in human hepatoma cell line, PLC-PRF-5
ChEMBL 573 10 1 5 5.3 CCCCCN1C(=O)C2(CCCC2)C(=O)N1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1021/jm9904147
11577472 14428 0 None - 1 Rat 7.6 pKi = 7.6 Binding
Binding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranesBinding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranes
ChEMBL 503 9 1 8 5.2 CCCCc1nc(Cl)c(C(=O)OCC)n1Cc1cccc2c1ccn2-c1ccccc1-c1nn[nH]n1 10.1016/S0960-894X(01)81137-9
CHEMBL1204970 14428 0 None - 1 Rat 7.6 pKi = 7.6 Binding
Binding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranesBinding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranes
ChEMBL 503 9 1 8 5.2 CCCCc1nc(Cl)c(C(=O)OCC)n1Cc1cccc2c1ccn2-c1ccccc1-c1nn[nH]n1 10.1016/S0960-894X(01)81137-9
CHEMBL2021416 14428 0 None - 1 Rat 7.6 pKi = 7.6 Binding
Binding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranesBinding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranes
ChEMBL 503 9 1 8 5.2 CCCCc1nc(Cl)c(C(=O)OCC)n1Cc1cccc2c1ccn2-c1ccccc1-c1nn[nH]n1 10.1016/S0960-894X(01)81137-9
5249743 106529 1 None -1 2 Rat 7.6 pKi = 7.6 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
ChEMBL 444 7 1 5 4.0 CCCCN1C(=O)C2(CCCC2)C(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm7011563
CHEMBL315444 106529 1 None -1 2 Rat 7.6 pKi = 7.6 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
ChEMBL 444 7 1 5 4.0 CCCCN1C(=O)C2(CCCC2)C(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm7011563
53317942 57279 0 None - 1 Human 7.6 pKi = 7.6 Binding
Displacement of [3H]-angiotensin 2 from angiotensin AT1 receptor in human PLC-PRF5 cellsDisplacement of [3H]-angiotensin 2 from angiotensin AT1 receptor in human PLC-PRF5 cells
ChEMBL 444 7 1 7 3.3 CCCCN1CC2(CN1Cc1ccc(-c3ccccc3-c3nnn[nH]3)cc1)C(=O)CCC2=O 10.1016/j.bmc.2010.10.043
CHEMBL1667999 57279 0 None - 1 Human 7.6 pKi = 7.6 Binding
Displacement of [3H]-angiotensin 2 from angiotensin AT1 receptor in human PLC-PRF5 cellsDisplacement of [3H]-angiotensin 2 from angiotensin AT1 receptor in human PLC-PRF5 cells
ChEMBL 444 7 1 7 3.3 CCCCN1CC2(CN1Cc1ccc(-c3ccccc3-c3nnn[nH]3)cc1)C(=O)CCC2=O 10.1016/j.bmc.2010.10.043
1610 2305 89 None -1 4 Rat 7.6 pKi = 7.6 Binding
In vitro binding affinity at rat liver Angiotensin II receptor, type 1 was determined based on displacement of [125I]-Ang IIIn vitro binding affinity at rat liver Angiotensin II receptor, type 1 was determined based on displacement of [125I]-Ang II
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm011063a
3941 2305 89 None -1 4 Rat 7.6 pKi = 7.6 Binding
In vitro binding affinity at rat liver Angiotensin II receptor, type 1 was determined based on displacement of [125I]-Ang IIIn vitro binding affinity at rat liver Angiotensin II receptor, type 1 was determined based on displacement of [125I]-Ang II
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm011063a
3961 2305 89 None -1 4 Rat 7.6 pKi = 7.6 Binding
In vitro binding affinity at rat liver Angiotensin II receptor, type 1 was determined based on displacement of [125I]-Ang IIIn vitro binding affinity at rat liver Angiotensin II receptor, type 1 was determined based on displacement of [125I]-Ang II
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm011063a
590 2305 89 None -1 4 Rat 7.6 pKi = 7.6 Binding
In vitro binding affinity at rat liver Angiotensin II receptor, type 1 was determined based on displacement of [125I]-Ang IIIn vitro binding affinity at rat liver Angiotensin II receptor, type 1 was determined based on displacement of [125I]-Ang II
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm011063a
CHEMBL191 2305 89 None -1 4 Rat 7.6 pKi = 7.6 Binding
In vitro binding affinity at rat liver Angiotensin II receptor, type 1 was determined based on displacement of [125I]-Ang IIIn vitro binding affinity at rat liver Angiotensin II receptor, type 1 was determined based on displacement of [125I]-Ang II
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm011063a
DB00678 2305 89 None -1 4 Rat 7.6 pKi = 7.6 Binding
In vitro binding affinity at rat liver Angiotensin II receptor, type 1 was determined based on displacement of [125I]-Ang IIIn vitro binding affinity at rat liver Angiotensin II receptor, type 1 was determined based on displacement of [125I]-Ang II
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm011063a
5249743 106529 1 None 1 2 Human 7.6 pKi = 7.6 Binding
In vitro binding affinity towards Angiotensin II receptor, type 1 of human hepatoma cell line PLC-PRF-5In vitro binding affinity towards Angiotensin II receptor, type 1 of human hepatoma cell line PLC-PRF-5
ChEMBL 444 7 1 5 4.0 CCCCN1C(=O)C2(CCCC2)C(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm010457z
CHEMBL315444 106529 1 None 1 2 Human 7.6 pKi = 7.6 Binding
In vitro binding affinity towards Angiotensin II receptor, type 1 of human hepatoma cell line PLC-PRF-5In vitro binding affinity towards Angiotensin II receptor, type 1 of human hepatoma cell line PLC-PRF-5
ChEMBL 444 7 1 5 4.0 CCCCN1C(=O)C2(CCCC2)C(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm010457z
87218826 171521 0 None - 1 Human 6.6 pKi = 6.6 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 581 13 3 5 7.4 CCCCc1nc(Cl)c(CNC(=O)C(CS)CC2CCCCC2)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/acsmedchemlett.8b00462
CHEMBL4472489 171521 0 None - 1 Human 6.6 pKi = 6.6 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 581 13 3 5 7.4 CCCCc1nc(Cl)c(CNC(=O)C(CS)CC2CCCCC2)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/acsmedchemlett.8b00462
45488163 196080 0 None - 1 Rat 5.6 pKi = 5.6 Binding
Displacement of [125I]SI-Ang2 from AT1 receptor in Sprague-Dawley rat liver membraneDisplacement of [125I]SI-Ang2 from AT1 receptor in Sprague-Dawley rat liver membrane
ChEMBL 630 13 0 8 7.9 CCCc1nc2c(C)cc(-c3nc4ccccc4n3C)cc2n1CCOc1ccc(CC(C)(Oc2ccccc2)C(=O)OCC)cc1 10.1021/jm901272d
CHEMBL571763 196080 0 None - 1 Rat 5.6 pKi = 5.6 Binding
Displacement of [125I]SI-Ang2 from AT1 receptor in Sprague-Dawley rat liver membraneDisplacement of [125I]SI-Ang2 from AT1 receptor in Sprague-Dawley rat liver membrane
ChEMBL 630 13 0 8 7.9 CCCc1nc2c(C)cc(-c3nc4ccccc4n3C)cc2n1CCOc1ccc(CC(C)(Oc2ccccc2)C(=O)OCC)cc1 10.1021/jm901272d
163409136 190298 2 None 18 2 Human 7.6 pKi = 7.6 Binding
Displacement of 125I-[Sar1,Ile8]ANGII form recombinant human full length AT1 receptor expressed in HEK293 cells incubated for 120 mins by scintillation counting methodDisplacement of 125I-[Sar1,Ile8]ANGII form recombinant human full length AT1 receptor expressed in HEK293 cells incubated for 120 mins by scintillation counting method
ChEMBL 583 11 1 9 6.2 CCCCOC(=O)NS(=O)(=O)c1sc(CC(C)C)nc1-c1ccc(Cn2c(CC)nc3c(C)cc(C)nc32)cc1 10.1016/j.bmc.2022.116790
CHEMBL5185088 190298 2 None 18 2 Human 7.6 pKi = 7.6 Binding
Displacement of 125I-[Sar1,Ile8]ANGII form recombinant human full length AT1 receptor expressed in HEK293 cells incubated for 120 mins by scintillation counting methodDisplacement of 125I-[Sar1,Ile8]ANGII form recombinant human full length AT1 receptor expressed in HEK293 cells incubated for 120 mins by scintillation counting method
ChEMBL 583 11 1 9 6.2 CCCCOC(=O)NS(=O)(=O)c1sc(CC(C)C)nc1-c1ccc(Cn2c(CC)nc3c(C)cc(C)nc32)cc1 10.1016/j.bmc.2022.116790
CHEMBL1076613 206729 0 None - 1 Human 7.6 pKi = 7.6 Binding
Displacement of [125I][Sar1,Ile8]Ang2 from wild-type human AT1 receptor expressed in CHO cells by gamma countingDisplacement of [125I][Sar1,Ile8]Ang2 from wild-type human AT1 receptor expressed in CHO cells by gamma counting
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H](N)Cc1ccc(C2(C(F)(F)F)N=N2)cc1)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O 10.1021/jm9015747
10433378 203199 0 None - 1 Rat 7.6 pKi = 7.6 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 440 7 2 8 3.3 CCCc1nc(CO)n2nc(C)nc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00041a016
CHEMBL76149 203199 0 None - 1 Rat 7.6 pKi = 7.6 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 440 7 2 8 3.3 CCCc1nc(CO)n2nc(C)nc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00041a016
10071944 203298 0 None - 1 Rat 7.6 pKi = 7.6 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 440 7 1 8 3.8 CCCc1nc(C)n2nc(OC)nc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00041a016
CHEMBL76900 203298 0 None - 1 Rat 7.6 pKi = 7.6 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 440 7 1 8 3.8 CCCc1nc(C)n2nc(OC)nc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00041a016
19029650 20025 0 None - 1 Rat 7.6 pKi = 7.6 Binding
Inhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranesInhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranes
ChEMBL 497 7 1 8 4.2 CCc1nn(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/c(=N/C(=O)c2ccc(OC)cc2)s1 10.1016/S0960-894X(97)00026-7
CHEMBL130530 20025 0 None - 1 Rat 7.6 pKi = 7.6 Binding
Inhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranesInhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranes
ChEMBL 497 7 1 8 4.2 CCc1nn(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/c(=N/C(=O)c2ccc(OC)cc2)s1 10.1016/S0960-894X(97)00026-7
168295859 191677 0 None 50 2 Human 7.6 pKi = 7.6 Binding
Displacement of 125I-[Sar1,Ile8]ANGII form recombinant human full length AT1 receptor expressed in HEK293 cells incubated for 120 mins by scintillation counting methodDisplacement of 125I-[Sar1,Ile8]ANGII form recombinant human full length AT1 receptor expressed in HEK293 cells incubated for 120 mins by scintillation counting method
ChEMBL 569 11 1 9 6.0 CCCCOC(=O)NS(=O)(=O)c1sc(CCC)nc1-c1ccc(Cn2c(CC)nc3c(C)cc(C)nc32)cc1 10.1016/j.bmc.2022.116790
CHEMBL5205969 191677 0 None 50 2 Human 7.6 pKi = 7.6 Binding
Displacement of 125I-[Sar1,Ile8]ANGII form recombinant human full length AT1 receptor expressed in HEK293 cells incubated for 120 mins by scintillation counting methodDisplacement of 125I-[Sar1,Ile8]ANGII form recombinant human full length AT1 receptor expressed in HEK293 cells incubated for 120 mins by scintillation counting method
ChEMBL 569 11 1 9 6.0 CCCCOC(=O)NS(=O)(=O)c1sc(CCC)nc1-c1ccc(Cn2c(CC)nc3c(C)cc(C)nc32)cc1 10.1016/j.bmc.2022.116790
45488125 195467 0 None - 1 Rat 5.6 pKi = 5.6 Binding
Displacement of [125I]SI-Ang2 from AT1 receptor in Sprague-Dawley rat liver membraneDisplacement of [125I]SI-Ang2 from AT1 receptor in Sprague-Dawley rat liver membrane
ChEMBL 360 7 1 5 3.6 CCCc1nc2c(C)cccc2n1Cc1ccc(CCc2nnn[nH]2)cc1 10.1021/jm901272d
CHEMBL567897 195467 0 None - 1 Rat 5.6 pKi = 5.6 Binding
Displacement of [125I]SI-Ang2 from AT1 receptor in Sprague-Dawley rat liver membraneDisplacement of [125I]SI-Ang2 from AT1 receptor in Sprague-Dawley rat liver membrane
ChEMBL 360 7 1 5 3.6 CCCc1nc2c(C)cccc2n1Cc1ccc(CCc2nnn[nH]2)cc1 10.1021/jm901272d
10742620 57282 0 None 16 2 Human 7.5 pKi = 7.5 Binding
Binding affinity to angiotensin AT1 receptorBinding affinity to angiotensin AT1 receptor
ChEMBL 460 7 2 6 5.1 CCCc1nc2ccccc2n1C(F)(F)C(O)c1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmc.2010.10.043
CHEMBL1668003 57282 0 None 16 2 Human 7.5 pKi = 7.5 Binding
Binding affinity to angiotensin AT1 receptorBinding affinity to angiotensin AT1 receptor
ChEMBL 460 7 2 6 5.1 CCCc1nc2ccccc2n1C(F)(F)C(O)c1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1016/j.bmc.2010.10.043
131590 20488 37 None 1 3 Human 7.5 pKi = 7.5 Binding
Ki value was evaluated against Angiotensin II receptor, type 1Ki value was evaluated against Angiotensin II receptor, type 1
ChEMBL 524 9 3 4 7.2 CCCCc1nc2ccc(NC(=O)NC3CCCCC3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm9504722
CHEMBL130896 20488 37 None 1 3 Human 7.5 pKi = 7.5 Binding
Ki value was evaluated against Angiotensin II receptor, type 1Ki value was evaluated against Angiotensin II receptor, type 1
ChEMBL 524 9 3 4 7.2 CCCCc1nc2ccc(NC(=O)NC3CCCCC3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm9504722
131590 20488 37 None -1 3 Rabbit 7.5 pKi = 7.5 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 524 9 3 4 7.2 CCCCc1nc2ccc(NC(=O)NC3CCCCC3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00052a006
CHEMBL130896 20488 37 None -1 3 Rabbit 7.5 pKi = 7.5 Binding
Tested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparationTested for in vitro binding affinity against angiotensin I (AT1) receptor to competitively block the specific binding of [125I]- [Sar1,Ile8] AII to a rabbit aorta AT1 receptor preparation
ChEMBL 524 9 3 4 7.2 CCCCc1nc2ccc(NC(=O)NC3CCCCC3)cc2n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00052a006
44567851 183213 0 None - 1 Pig 6.5 pKi = 6.5 Binding
Displacement of [125]Ang2 from AT2 receptor in pig uterus membraneDisplacement of [125]Ang2 from AT2 receptor in pig uterus membrane
ChEMBL 522 11 1 5 5.6 CCCCOC(=O)NS(=O)(=O)c1cc(Cc2ccccc2)ccc1-c1ccc(C(=O)N(CC)CC)cc1 10.1016/j.bmc.2008.05.066
CHEMBL480506 183213 0 None - 1 Pig 6.5 pKi = 6.5 Binding
Displacement of [125]Ang2 from AT2 receptor in pig uterus membraneDisplacement of [125]Ang2 from AT2 receptor in pig uterus membrane
ChEMBL 522 11 1 5 5.6 CCCCOC(=O)NS(=O)(=O)c1cc(Cc2ccccc2)ccc1-c1ccc(C(=O)N(CC)CC)cc1 10.1016/j.bmc.2008.05.066
19029656 117950 0 None - 1 Rat 6.5 pKi = 6.5 Binding
Inhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranesInhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranes
ChEMBL 545 6 1 7 4.9 CCc1nn(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/c(=N/C(=O)c2cccc(Br)c2)s1 10.1016/S0960-894X(97)00026-7
CHEMBL341292 117950 0 None - 1 Rat 6.5 pKi = 6.5 Binding
Inhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranesInhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranes
ChEMBL 545 6 1 7 4.9 CCc1nn(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/c(=N/C(=O)c2cccc(Br)c2)s1 10.1016/S0960-894X(97)00026-7
2806 3894 109 None - 1 Human 8.5 pKi = 8.5 Binding
Displacement of [125I-Sar1-Ile8]-Ang2 from human angiotensin 2 receptor type 1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysisDisplacement of [125I-Sar1-Ile8]-Ang2 from human angiotensin 2 receptor type 1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysis
ChEMBL 435 10 2 5 4.2 CCCCC(=O)N([C@H](C(=O)O)C(C)C)Cc1ccc(cc1)c1ccccc1c1nnn[nH]1 10.1016/j.ejmech.2017.12.021
3937 3894 109 None - 1 Human 8.5 pKi = 8.5 Binding
Displacement of [125I-Sar1-Ile8]-Ang2 from human angiotensin 2 receptor type 1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysisDisplacement of [125I-Sar1-Ile8]-Ang2 from human angiotensin 2 receptor type 1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysis
ChEMBL 435 10 2 5 4.2 CCCCC(=O)N([C@H](C(=O)O)C(C)C)Cc1ccc(cc1)c1ccccc1c1nnn[nH]1 10.1016/j.ejmech.2017.12.021
593 3894 109 None - 1 Human 8.5 pKi = 8.5 Binding
Displacement of [125I-Sar1-Ile8]-Ang2 from human angiotensin 2 receptor type 1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysisDisplacement of [125I-Sar1-Ile8]-Ang2 from human angiotensin 2 receptor type 1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysis
ChEMBL 435 10 2 5 4.2 CCCCC(=O)N([C@H](C(=O)O)C(C)C)Cc1ccc(cc1)c1ccccc1c1nnn[nH]1 10.1016/j.ejmech.2017.12.021
60846 3894 109 None - 1 Human 8.5 pKi = 8.5 Binding
Displacement of [125I-Sar1-Ile8]-Ang2 from human angiotensin 2 receptor type 1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysisDisplacement of [125I-Sar1-Ile8]-Ang2 from human angiotensin 2 receptor type 1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysis
ChEMBL 435 10 2 5 4.2 CCCCC(=O)N([C@H](C(=O)O)C(C)C)Cc1ccc(cc1)c1ccccc1c1nnn[nH]1 10.1016/j.ejmech.2017.12.021
CHEMBL1069 3894 109 None - 1 Human 8.5 pKi = 8.5 Binding
Displacement of [125I-Sar1-Ile8]-Ang2 from human angiotensin 2 receptor type 1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysisDisplacement of [125I-Sar1-Ile8]-Ang2 from human angiotensin 2 receptor type 1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysis
ChEMBL 435 10 2 5 4.2 CCCCC(=O)N([C@H](C(=O)O)C(C)C)Cc1ccc(cc1)c1ccccc1c1nnn[nH]1 10.1016/j.ejmech.2017.12.021
DB00177 3894 109 None - 1 Human 8.5 pKi = 8.5 Binding
Displacement of [125I-Sar1-Ile8]-Ang2 from human angiotensin 2 receptor type 1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysisDisplacement of [125I-Sar1-Ile8]-Ang2 from human angiotensin 2 receptor type 1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysis
ChEMBL 435 10 2 5 4.2 CCCCC(=O)N([C@H](C(=O)O)C(C)C)Cc1ccc(cc1)c1ccccc1c1nnn[nH]1 10.1016/j.ejmech.2017.12.021
25141238 191936 0 None - 1 Pig 8.5 pKi = 8.5 Binding
Displacement of [125]Ang2 from AT2 receptor in pig uterus membraneDisplacement of [125]Ang2 from AT2 receptor in pig uterus membrane
ChEMBL 494 11 1 6 5.3 CCCCOC(=O)NS(=O)(=O)c1sc(CC(C)C)cc1-c1ccc(C(=O)N(CC)CC)cc1 10.1016/j.bmc.2008.05.066
CHEMBL521093 191936 0 None - 1 Pig 8.5 pKi = 8.5 Binding
Displacement of [125]Ang2 from AT2 receptor in pig uterus membraneDisplacement of [125]Ang2 from AT2 receptor in pig uterus membrane
ChEMBL 494 11 1 6 5.3 CCCCOC(=O)NS(=O)(=O)c1sc(CC(C)C)cc1-c1ccc(C(=O)N(CC)CC)cc1 10.1016/j.bmc.2008.05.066
127031545 138653 0 None - 1 Human 8.5 pKi = 8.5 Binding
Displacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation countingDisplacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation counting
ChEMBL 1276 39 15 16 -1.4 CCC(=O)NCCOCCOCCNC(=O)/N=C(\N)NCCC[C@H](NC(=O)[C@@H](N)CC(=O)O)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O)[C@@H](C)CC)C(C)C 10.1021/acs.jmedchem.5b01495
CHEMBL3787379 138653 0 None - 1 Human 8.5 pKi = 8.5 Binding
Displacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation countingDisplacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation counting
ChEMBL 1276 39 15 16 -1.4 CCC(=O)NCCOCCOCCNC(=O)/N=C(\N)NCCC[C@H](NC(=O)[C@@H](N)CC(=O)O)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O)[C@@H](C)CC)C(C)C 10.1021/acs.jmedchem.5b01495
CHEMBL3787701 138653 0 None - 1 Human 8.5 pKi = 8.5 Binding
Displacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation countingDisplacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation counting
ChEMBL 1276 39 15 16 -1.4 CCC(=O)NCCOCCOCCNC(=O)/N=C(\N)NCCC[C@H](NC(=O)[C@@H](N)CC(=O)O)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O)[C@@H](C)CC)C(C)C 10.1021/acs.jmedchem.5b01495
192314 113989 26 None -26 3 Rat 8.5 pKi = 8.5 Binding
Compound was evaluated for binding affinity against angiotensin II receptor, type 1 in rat liverCompound was evaluated for binding affinity against angiotensin II receptor, type 1 in rat liver
ChEMBL 429 9 2 7 3.8 CCCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1ncncc1C(=O)O 10.1021/jm00098a018
CHEMBL1237157 113989 26 None -26 3 Rat 8.5 pKi = 8.5 Binding
Compound was evaluated for binding affinity against angiotensin II receptor, type 1 in rat liverCompound was evaluated for binding affinity against angiotensin II receptor, type 1 in rat liver
ChEMBL 429 9 2 7 3.8 CCCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1ncncc1C(=O)O 10.1021/jm00098a018
CHEMBL333534 113989 26 None -26 3 Rat 8.5 pKi = 8.5 Binding
Compound was evaluated for binding affinity against angiotensin II receptor, type 1 in rat liverCompound was evaluated for binding affinity against angiotensin II receptor, type 1 in rat liver
ChEMBL 429 9 2 7 3.8 CCCCN(Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1)c1ncncc1C(=O)O 10.1021/jm00098a018
136093942 138551 0 None - 1 Rat 8.5 pKi = 8.5 Binding
Displacement of [125I]-Ang II from Angiotensin 2 type-1A receptor in rat vascular smooth muscle cells after 150 mins by gamma counting methodDisplacement of [125I]-Ang II from Angiotensin 2 type-1A receptor in rat vascular smooth muscle cells after 150 mins by gamma counting method
ChEMBL 436 8 1 6 4.8 CCCCc1nc(Cl)c(C=O)n1Cc1ccc(-c2ccccc2-c2noc(=O)[nH]2)cc1 10.1016/j.bmc.2016.03.028
CHEMBL3786570 138551 0 None - 1 Rat 8.5 pKi = 8.5 Binding
Displacement of [125I]-Ang II from Angiotensin 2 type-1A receptor in rat vascular smooth muscle cells after 150 mins by gamma counting methodDisplacement of [125I]-Ang II from Angiotensin 2 type-1A receptor in rat vascular smooth muscle cells after 150 mins by gamma counting method
ChEMBL 436 8 1 6 4.8 CCCCc1nc(Cl)c(C=O)n1Cc1ccc(-c2ccccc2-c2noc(=O)[nH]2)cc1 10.1016/j.bmc.2016.03.028
44567817 182447 0 None - 1 Pig 8.5 pKi = 8.5 Binding
Displacement of [125]Ang2 from AT2 receptor in pig uterus membraneDisplacement of [125]Ang2 from AT2 receptor in pig uterus membrane
ChEMBL 506 9 1 6 5.5 CCCCOC(=O)NS(=O)(=O)c1sc(CC(C)C)cc1-c1ccc(C(=O)N2CCCCC2)cc1 10.1016/j.bmc.2008.05.066
CHEMBL479399 182447 0 None - 1 Pig 8.5 pKi = 8.5 Binding
Displacement of [125]Ang2 from AT2 receptor in pig uterus membraneDisplacement of [125]Ang2 from AT2 receptor in pig uterus membrane
ChEMBL 506 9 1 6 5.5 CCCCOC(=O)NS(=O)(=O)c1sc(CC(C)C)cc1-c1ccc(C(=O)N2CCCCC2)cc1 10.1016/j.bmc.2008.05.066
23298216 162617 0 None - 1 Rat 8.5 pKi = 8.5 Binding
Inhibition of [125I]Sar1,Ile8 angiotensin II binding to Angiotensin II receptor type 1 in rat adrenocortical membraneInhibition of [125I]Sar1,Ile8 angiotensin II binding to Angiotensin II receptor type 1 in rat adrenocortical membrane
ChEMBL 423 5 2 6 4.9 Cc1nc2ccccc2c(C(=O)O)c1Oc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81146-X
CHEMBL418122 162617 0 None - 1 Rat 8.5 pKi = 8.5 Binding
Inhibition of [125I]Sar1,Ile8 angiotensin II binding to Angiotensin II receptor type 1 in rat adrenocortical membraneInhibition of [125I]Sar1,Ile8 angiotensin II binding to Angiotensin II receptor type 1 in rat adrenocortical membrane
ChEMBL 423 5 2 6 4.9 Cc1nc2ccccc2c(C(=O)O)c1Oc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81146-X
19029654 18144 0 None - 1 Rat 8.5 pKi = 8.5 Binding
Inhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranesInhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranes
ChEMBL 512 7 1 9 4.1 CCc1nn(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/c(=N/C(=O)c2ccccc2[N+](=O)[O-])s1 10.1016/S0960-894X(97)00026-7
CHEMBL127090 18144 0 None - 1 Rat 8.5 pKi = 8.5 Binding
Inhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranesInhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranes
ChEMBL 512 7 1 9 4.1 CCc1nn(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/c(=N/C(=O)c2ccccc2[N+](=O)[O-])s1 10.1016/S0960-894X(97)00026-7
10141821 99583 0 None - 1 Rat 8.5 pKi = 8.5 Binding
Inhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranesInhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranes
ChEMBL 501 6 1 7 4.8 CCc1nn(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/c(=N/C(=O)c2ccccc2Cl)s1 10.1016/S0960-894X(97)00026-7
CHEMBL287116 99583 0 None - 1 Rat 8.5 pKi = 8.5 Binding
Inhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranesInhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranes
ChEMBL 501 6 1 7 4.8 CCc1nn(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/c(=N/C(=O)c2ccccc2Cl)s1 10.1016/S0960-894X(97)00026-7
9804423 201027 0 None - 1 Rat 8.5 pKi = 8.5 Binding
Inhibition of [125I]Sar1,Ile8 angiotensin II binding to Angiotensin II receptor type 1 in rat adrenocortical membraneInhibition of [125I]Sar1,Ile8 angiotensin II binding to Angiotensin II receptor type 1 in rat adrenocortical membrane
ChEMBL 451 7 2 6 5.5 CCCc1nc2ccccc2c(C(=O)O)c1Oc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81146-X
CHEMBL61814 201027 0 None - 1 Rat 8.5 pKi = 8.5 Binding
Inhibition of [125I]Sar1,Ile8 angiotensin II binding to Angiotensin II receptor type 1 in rat adrenocortical membraneInhibition of [125I]Sar1,Ile8 angiotensin II binding to Angiotensin II receptor type 1 in rat adrenocortical membrane
ChEMBL 451 7 2 6 5.5 CCCc1nc2ccccc2c(C(=O)O)c1Oc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81146-X
19029618 117339 0 None - 1 Rat 8.5 pKi = 8.5 Binding
Inhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranesInhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranes
ChEMBL 545 6 1 7 4.9 CCc1nn(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/c(=N/C(=O)c2ccccc2Br)s1 10.1016/S0960-894X(97)00026-7
CHEMBL340304 117339 0 None - 1 Rat 8.5 pKi = 8.5 Binding
Inhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranesInhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranes
ChEMBL 545 6 1 7 4.9 CCc1nn(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/c(=N/C(=O)c2ccccc2Br)s1 10.1016/S0960-894X(97)00026-7
2541 772 113 None -1 6 Human 8.5 pKi = 8.5 Binding
Displacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation countingDisplacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation counting
ChEMBL 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10.1021/acs.jmedchem.5b01495
587 772 113 None -1 6 Human 8.5 pKi = 8.5 Binding
Displacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation countingDisplacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation counting
ChEMBL 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10.1021/acs.jmedchem.5b01495
6907 772 113 None -1 6 Human 8.5 pKi = 8.5 Binding
Displacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation countingDisplacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation counting
ChEMBL 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10.1021/acs.jmedchem.5b01495
CHEMBL1016 772 113 None -1 6 Human 8.5 pKi = 8.5 Binding
Displacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation countingDisplacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation counting
ChEMBL 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10.1021/acs.jmedchem.5b01495
DB00796 772 113 None -1 6 Human 8.5 pKi = 8.5 Binding
Displacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation countingDisplacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation counting
ChEMBL 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10.1021/acs.jmedchem.5b01495
DB13919 772 113 None -1 6 Human 8.5 pKi = 8.5 Binding
Displacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation countingDisplacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation counting
ChEMBL 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10.1021/acs.jmedchem.5b01495
1610 2305 89 None -1 4 Rat 8.4 pKi = 8.4 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00041a016
3941 2305 89 None -1 4 Rat 8.4 pKi = 8.4 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00041a016
3961 2305 89 None -1 4 Rat 8.4 pKi = 8.4 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00041a016
590 2305 89 None -1 4 Rat 8.4 pKi = 8.4 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00041a016
CHEMBL191 2305 89 None -1 4 Rat 8.4 pKi = 8.4 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00041a016
DB00678 2305 89 None -1 4 Rat 8.4 pKi = 8.4 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/jm00041a016
CHEMBL1076631 206732 0 None - 1 Human 8.4 pKi = 8.4 Binding
Displacement of [125I][Sar1,Ile8]Ang2 from human AT1 receptor N111G constitutively active mutant expressed in CHO cells by gamma countingDisplacement of [125I][Sar1,Ile8]Ang2 from human AT1 receptor N111G constitutively active mutant expressed in CHO cells by gamma counting
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N[C@@H](Cc1ccc(C2(C(F)(F)F)N=N2)cc1)C(=O)N[C@@H](Cc1ccccc1)C(=O)O 10.1021/jm9015747
44350472 18110 0 None - 1 Rat 8.4 pKi = 8.4 Binding
Inhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranesInhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranes
ChEMBL 593 6 1 7 4.7 CCc1nn(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/c(=N/C(=O)c2ccccc2I)s1 10.1016/S0960-894X(97)00026-7
CHEMBL127068 18110 0 None - 1 Rat 8.4 pKi = 8.4 Binding
Inhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranesInhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranes
ChEMBL 593 6 1 7 4.7 CCc1nn(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/c(=N/C(=O)c2ccccc2I)s1 10.1016/S0960-894X(97)00026-7
10096683 205350 0 None - 1 Human 8.4 pKi = 8.4 Binding
Ability to displace [125I]AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1Ability to displace [125I]AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1
ChEMBL 480 6 2 8 4.4 CCOc1nc2cccc(C(=O)O)c2n1Cc1ccc2c(c1)Oc1ccccc1C=C2c1nnn[nH]1 10.1021/jm00014a024
CHEMBL91928 205350 0 None - 1 Human 8.4 pKi = 8.4 Binding
Ability to displace [125I]AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1Ability to displace [125I]AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1
ChEMBL 480 6 2 8 4.4 CCOc1nc2cccc(C(=O)O)c2n1Cc1ccc2c(c1)Oc1ccccc1C=C2c1nnn[nH]1 10.1021/jm00014a024
3936 2171 28 None -1 4 Rat 8.4 pKi = 8.4 Binding
Displacement of [125I]Ang II from AT1 receptor in rat liver membranesDisplacement of [125I]Ang II from AT1 receptor in rat liver membranes
ChEMBL 582 11 1 8 6.8 CCCCOC(=O)NS(=O)(=O)c1sc(cc1c1ccc(cc1)Cn1c(CC)nc2c1nc(C)cc2C)CC(C)C 10.1021/acs.jmedchem.9b01780
6603900 2171 28 None -1 4 Rat 8.4 pKi = 8.4 Binding
Displacement of [125I]Ang II from AT1 receptor in rat liver membranesDisplacement of [125I]Ang II from AT1 receptor in rat liver membranes
ChEMBL 582 11 1 8 6.8 CCCCOC(=O)NS(=O)(=O)c1sc(cc1c1ccc(cc1)Cn1c(CC)nc2c1nc(C)cc2C)CC(C)C 10.1021/acs.jmedchem.9b01780
CHEMBL288174 2171 28 None -1 4 Rat 8.4 pKi = 8.4 Binding
Displacement of [125I]Ang II from AT1 receptor in rat liver membranesDisplacement of [125I]Ang II from AT1 receptor in rat liver membranes
ChEMBL 582 11 1 8 6.8 CCCCOC(=O)NS(=O)(=O)c1sc(cc1c1ccc(cc1)Cn1c(CC)nc2c1nc(C)cc2C)CC(C)C 10.1021/acs.jmedchem.9b01780
3936 2171 28 None -1 4 Rat 8.4 pKi = 8.4 Binding
Displacement of [I125I]AngII form AT1 receptor in rat liver membrane incubated for 1.5 hrs by gamma counting methodDisplacement of [I125I]AngII form AT1 receptor in rat liver membrane incubated for 1.5 hrs by gamma counting method
ChEMBL 582 11 1 8 6.8 CCCCOC(=O)NS(=O)(=O)c1sc(cc1c1ccc(cc1)Cn1c(CC)nc2c1nc(C)cc2C)CC(C)C 10.1016/j.bmc.2022.116790
6603900 2171 28 None -1 4 Rat 8.4 pKi = 8.4 Binding
Displacement of [I125I]AngII form AT1 receptor in rat liver membrane incubated for 1.5 hrs by gamma counting methodDisplacement of [I125I]AngII form AT1 receptor in rat liver membrane incubated for 1.5 hrs by gamma counting method
ChEMBL 582 11 1 8 6.8 CCCCOC(=O)NS(=O)(=O)c1sc(cc1c1ccc(cc1)Cn1c(CC)nc2c1nc(C)cc2C)CC(C)C 10.1016/j.bmc.2022.116790
CHEMBL288174 2171 28 None -1 4 Rat 8.4 pKi = 8.4 Binding
Displacement of [I125I]AngII form AT1 receptor in rat liver membrane incubated for 1.5 hrs by gamma counting methodDisplacement of [I125I]AngII form AT1 receptor in rat liver membrane incubated for 1.5 hrs by gamma counting method
ChEMBL 582 11 1 8 6.8 CCCCOC(=O)NS(=O)(=O)c1sc(cc1c1ccc(cc1)Cn1c(CC)nc2c1nc(C)cc2C)CC(C)C 10.1016/j.bmc.2022.116790
44284325 14590 0 None - 1 Rat 7.5 pKi = 7.5 Binding
Binding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranesBinding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranes
ChEMBL 603 12 1 10 6.1 CCCCc1nc(Cl)c(C(=O)OC(OC(=O)CC)C(C)C)n1Cc1cccc2c1ccn2-c1ccccc1-c1nn[nH]n1 10.1016/S0960-894X(01)81137-9
CHEMBL1206585 14590 0 None - 1 Rat 7.5 pKi = 7.5 Binding
Binding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranesBinding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranes
ChEMBL 603 12 1 10 6.1 CCCCc1nc(Cl)c(C(=O)OC(OC(=O)CC)C(C)C)n1Cc1cccc2c1ccn2-c1ccccc1-c1nn[nH]n1 10.1016/S0960-894X(01)81137-9
CHEMBL2079768 14590 0 None - 1 Rat 7.5 pKi = 7.5 Binding
Binding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranesBinding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranes
ChEMBL 603 12 1 10 6.1 CCCCc1nc(Cl)c(C(=O)OC(OC(=O)CC)C(C)C)n1Cc1cccc2c1ccn2-c1ccccc1-c1nn[nH]n1 10.1016/S0960-894X(01)81137-9
10348632 203707 0 None - 1 Rat 7.5 pKi = 7.5 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 440 7 2 8 3.9 CCCCc1nc(C)n2nc(O)nc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00041a016
CHEMBL80218 203707 0 None - 1 Rat 7.5 pKi = 7.5 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 440 7 2 8 3.9 CCCCc1nc(C)n2nc(O)nc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00041a016
11672486 98046 0 None -3 2 Rat 7.5 pKi = 7.5 Binding
Binding affinity for angiotensin II receptor, type 1 in rat liver membrane using [125I]-Ang II as radioligand, in pH 7.4 Tris-HCl buffer for 2 hr at 25 degree CBinding affinity for angiotensin II receptor, type 1 in rat liver membrane using [125I]-Ang II as radioligand, in pH 7.4 Tris-HCl buffer for 2 hr at 25 degree C
ChEMBL 994 25 12 12 0.3 CC(C)[C@H](NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@@H](N)CC(=O)O)C(=O)Nc1cc(Cc2ccc(O)cc2)cc(C(=O)N[C@@H](Cc2c[nH]cn2)C(=O)N2CCC[C@H]2C(=O)N[C@@H](Cc2ccccc2)C(=O)O)c1 10.1021/jm050280z
CHEMBL276163 98046 0 None -3 2 Rat 7.5 pKi = 7.5 Binding
Binding affinity for angiotensin II receptor, type 1 in rat liver membrane using [125I]-Ang II as radioligand, in pH 7.4 Tris-HCl buffer for 2 hr at 25 degree CBinding affinity for angiotensin II receptor, type 1 in rat liver membrane using [125I]-Ang II as radioligand, in pH 7.4 Tris-HCl buffer for 2 hr at 25 degree C
ChEMBL 994 25 12 12 0.3 CC(C)[C@H](NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@@H](N)CC(=O)O)C(=O)Nc1cc(Cc2ccc(O)cc2)cc(C(=O)N[C@@H](Cc2c[nH]cn2)C(=O)N2CCC[C@H]2C(=O)N[C@@H](Cc2ccccc2)C(=O)O)c1 10.1021/jm050280z
44567781 183130 0 None - 1 Pig 7.5 pKi = 7.5 Binding
Displacement of [125]Ang2 from AT2 receptor in pig uterus membraneDisplacement of [125]Ang2 from AT2 receptor in pig uterus membrane
ChEMBL 542 11 1 6 6.1 CCCCOC(=O)NS(=O)(=O)c1sc(CC(C)C)cc1-c1ccc(C(=O)N(C)Cc2ccccc2)cc1 10.1016/j.bmc.2008.05.066
CHEMBL480340 183130 0 None - 1 Pig 7.5 pKi = 7.5 Binding
Displacement of [125]Ang2 from AT2 receptor in pig uterus membraneDisplacement of [125]Ang2 from AT2 receptor in pig uterus membrane
ChEMBL 542 11 1 6 6.1 CCCCOC(=O)NS(=O)(=O)c1sc(CC(C)C)cc1-c1ccc(C(=O)N(C)Cc2ccccc2)cc1 10.1016/j.bmc.2008.05.066
CHEMBL1076664 206737 0 None - 1 Human 7.5 pKi = 7.5 Binding
Displacement of [125I][Sar1,Ile8]Ang2 from human AT1 receptor N111G constitutively active mutant expressed in CHO cells by gamma countingDisplacement of [125I][Sar1,Ile8]Ang2 from human AT1 receptor N111G constitutively active mutant expressed in CHO cells by gamma counting
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1ccc(C(=O)c2ccccc2)cc1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O 10.1021/jm9015747
155526996 170564 0 None - 1 Human 7.5 pKi = 7.5 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 549 14 3 5 6.8 CCCCc1nc(CC(C)C)c(CNC(=O)[C@@H](S)CC(C)C)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/acsmedchemlett.8b00462
CHEMBL4458466 170564 0 None - 1 Human 7.5 pKi = 7.5 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 549 14 3 5 6.8 CCCCc1nc(CC(C)C)c(CNC(=O)[C@@H](S)CC(C)C)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/acsmedchemlett.8b00462
87218835 170608 0 None - 1 Human 7.5 pKi = 7.5 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 539 13 3 5 6.3 CCCCc1nc(Cl)c(CNC(=O)C(CS)CC2CC2)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/acsmedchemlett.8b00462
CHEMBL4459070 170608 0 None - 1 Human 7.5 pKi = 7.5 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 539 13 3 5 6.3 CCCCc1nc(Cl)c(CNC(=O)C(CS)CC2CC2)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/acsmedchemlett.8b00462
155552503 173588 0 None - 1 Human 7.5 pKi = 7.5 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 533 13 3 5 6.5 CCCCc1nc(C2CC2)c(CNC(=O)[C@@H](S)CC(C)C)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/acsmedchemlett.8b00462
CHEMBL4547120 173588 0 None - 1 Human 7.5 pKi = 7.5 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 533 13 3 5 6.5 CCCCc1nc(C2CC2)c(CNC(=O)[C@@H](S)CC(C)C)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/acsmedchemlett.8b00462
10764613 205170 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity against AT1 in human hepatoma cell line, PLC-PRF-5Binding affinity against AT1 in human hepatoma cell line, PLC-PRF-5
ChEMBL 420 7 1 3 4.5 CCCCN1C(=O)C2(CCCC2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm9904147
CHEMBL90887 205170 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity against AT1 in human hepatoma cell line, PLC-PRF-5Binding affinity against AT1 in human hepatoma cell line, PLC-PRF-5
ChEMBL 420 7 1 3 4.5 CCCCN1C(=O)C2(CCCC2)C(=O)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm9904147
145952582 162415 0 None - 1 Human 6.5 pKi = 6.5 Binding
Displacement of [125I-Sar1-Ile8]-Ang2 from human angiotensin 2 receptor type 1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysisDisplacement of [125I-Sar1-Ile8]-Ang2 from human angiotensin 2 receptor type 1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysis
ChEMBL 782 12 0 6 10.6 CCCCC1=N/C(=C\c2ccccc2Br)C(=O)N1Cc1ccc(-c2ccccc2-c2nnn(C(c3ccccc3)(c3ccccc3)c3ccccc3)n2)cc1 10.1016/j.ejmech.2017.12.021
CHEMBL4175147 162415 0 None - 1 Human 6.5 pKi = 6.5 Binding
Displacement of [125I-Sar1-Ile8]-Ang2 from human angiotensin 2 receptor type 1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysisDisplacement of [125I-Sar1-Ile8]-Ang2 from human angiotensin 2 receptor type 1 receptor expressed in HEK293 cells after 1 hr by gamma counting analysis
ChEMBL 782 12 0 6 10.6 CCCCC1=N/C(=C\c2ccccc2Br)C(=O)N1Cc1ccc(-c2ccccc2-c2nnn(C(c3ccccc3)(c3ccccc3)c3ccccc3)n2)cc1 10.1016/j.ejmech.2017.12.021
19029482 116537 0 None - 1 Rat 6.5 pKi = 6.5 Binding
Inhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranesInhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranes
ChEMBL 545 6 1 7 4.9 CCc1nn(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/c(=N/C(=O)c2ccc(Br)cc2)s1 10.1016/S0960-894X(97)00026-7
CHEMBL339120 116537 0 None - 1 Rat 6.5 pKi = 6.5 Binding
Inhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranesInhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranes
ChEMBL 545 6 1 7 4.9 CCc1nn(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/c(=N/C(=O)c2ccc(Br)cc2)s1 10.1016/S0960-894X(97)00026-7
10507383 105612 0 None - 1 Human 7.5 pKi = 7.5 Binding
Binding affinity against AT1 in human hepatoma cell line, PLC-PRF-5Binding affinity against AT1 in human hepatoma cell line, PLC-PRF-5
ChEMBL 575 12 1 5 5.6 CCCCN1C(=O)C(C)(CCCC)C(=O)N1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1021/jm9904147
CHEMBL313392 105612 0 None - 1 Human 7.5 pKi = 7.5 Binding
Binding affinity against AT1 in human hepatoma cell line, PLC-PRF-5Binding affinity against AT1 in human hepatoma cell line, PLC-PRF-5
ChEMBL 575 12 1 5 5.6 CCCCN1C(=O)C(C)(CCCC)C(=O)N1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1021/jm9904147
11801362 106590 0 None - 1 Human 7.5 pKi = 7.5 Binding
Binding affinity against AT1 in human hepatoma cell line, PLC-PRF-5Binding affinity against AT1 in human hepatoma cell line, PLC-PRF-5
ChEMBL 580 9 2 5 5.1 CCCCN1C(=O)C2(CCCC2)C(=O)N1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)NC2CCCCC2)cc1 10.1021/jm9904147
CHEMBL315873 106590 0 None - 1 Human 7.5 pKi = 7.5 Binding
Binding affinity against AT1 in human hepatoma cell line, PLC-PRF-5Binding affinity against AT1 in human hepatoma cell line, PLC-PRF-5
ChEMBL 580 9 2 5 5.1 CCCCN1C(=O)C2(CCCC2)C(=O)N1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)NC2CCCCC2)cc1 10.1021/jm9904147
10025379 203568 0 None - 1 Rat 7.5 pKi = 7.5 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 424 6 1 7 4.1 CCCc1nc(C)n2nc(C)nc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00041a016
CHEMBL79171 203568 0 None - 1 Rat 7.5 pKi = 7.5 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 424 6 1 7 4.1 CCCc1nc(C)n2nc(C)nc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00041a016
10324104 203814 0 None - 1 Rat 7.5 pKi = 7.5 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 511 10 2 10 3.8 CCCc1nc(C)n2nc(NCC(=O)OCC)nc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00041a016
CHEMBL80967 203814 0 None - 1 Rat 7.5 pKi = 7.5 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 511 10 2 10 3.8 CCCc1nc(C)n2nc(NCC(=O)OCC)nc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00041a016
9914750 201552 0 None - 1 Rat 7.5 pKi = 7.5 Binding
Inhibition of [125I]Sar1,Ile8 angiotensin II binding to Angiotensin II receptor type 1 in rat adrenocortical membraneInhibition of [125I]Sar1,Ile8 angiotensin II binding to Angiotensin II receptor type 1 in rat adrenocortical membrane
ChEMBL 483 6 2 6 6.1 O=C(O)c1c(Oc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c(C2CC2)nc2cc(Cl)ccc12 10.1016/S0960-894X(01)81146-X
CHEMBL64567 201552 0 None - 1 Rat 7.5 pKi = 7.5 Binding
Inhibition of [125I]Sar1,Ile8 angiotensin II binding to Angiotensin II receptor type 1 in rat adrenocortical membraneInhibition of [125I]Sar1,Ile8 angiotensin II binding to Angiotensin II receptor type 1 in rat adrenocortical membrane
ChEMBL 483 6 2 6 6.1 O=C(O)c1c(Oc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c(C2CC2)nc2cc(Cl)ccc12 10.1016/S0960-894X(01)81146-X
19029652 117580 0 None - 1 Rat 6.5 pKi = 6.5 Binding
Inhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranesInhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranes
ChEMBL 501 6 1 7 4.8 CCc1nn(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/c(=N/C(=O)c2ccc(Cl)cc2)s1 10.1016/S0960-894X(97)00026-7
CHEMBL340662 117580 0 None - 1 Rat 6.5 pKi = 6.5 Binding
Inhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranesInhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranes
ChEMBL 501 6 1 7 4.8 CCc1nn(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/c(=N/C(=O)c2ccc(Cl)cc2)s1 10.1016/S0960-894X(97)00026-7
23298208 201465 0 None - 1 Rat 7.5 pKi = 7.5 Binding
Inhibition of [125I]Sar1,Ile8 angiotensin II binding to Angiotensin II receptor type 1 in rat adrenocortical membraneInhibition of [125I]Sar1,Ile8 angiotensin II binding to Angiotensin II receptor type 1 in rat adrenocortical membrane
ChEMBL 479 7 2 7 5.5 COc1ccc2nc(C3CC3)c(Oc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c(C(=O)O)c2c1 10.1016/S0960-894X(01)81146-X
CHEMBL64220 201465 0 None - 1 Rat 7.5 pKi = 7.5 Binding
Inhibition of [125I]Sar1,Ile8 angiotensin II binding to Angiotensin II receptor type 1 in rat adrenocortical membraneInhibition of [125I]Sar1,Ile8 angiotensin II binding to Angiotensin II receptor type 1 in rat adrenocortical membrane
ChEMBL 479 7 2 7 5.5 COc1ccc2nc(C3CC3)c(Oc3ccc(-c4ccccc4-c4nn[nH]n4)cc3)c(C(=O)O)c2c1 10.1016/S0960-894X(01)81146-X
10765881 205169 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity against AT1 in human hepatoma cell line, PLC-PRF-5Binding affinity against AT1 in human hepatoma cell line, PLC-PRF-5
ChEMBL 448 8 1 4 4.1 CCCCN1C(=O)C2(CCCC2)C(=O)N1Cc1ccc(C(=O)c2ccccc2C(=O)O)cc1 10.1021/jm9904147
CHEMBL90885 205169 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity against AT1 in human hepatoma cell line, PLC-PRF-5Binding affinity against AT1 in human hepatoma cell line, PLC-PRF-5
ChEMBL 448 8 1 4 4.1 CCCCN1C(=O)C2(CCCC2)C(=O)N1Cc1ccc(C(=O)c2ccccc2C(=O)O)cc1 10.1021/jm9904147
44567818 183294 0 None - 1 Pig 6.5 pKi = 6.5 Binding
Displacement of [125]Ang2 from AT2 receptor in pig uterus membraneDisplacement of [125]Ang2 from AT2 receptor in pig uterus membrane
ChEMBL 508 9 1 7 4.3 CCCCOC(=O)NS(=O)(=O)c1sc(CC(C)C)cc1-c1ccc(C(=O)N2CCOCC2)cc1 10.1016/j.bmc.2008.05.066
CHEMBL481106 183294 0 None - 1 Pig 6.5 pKi = 6.5 Binding
Displacement of [125]Ang2 from AT2 receptor in pig uterus membraneDisplacement of [125]Ang2 from AT2 receptor in pig uterus membrane
ChEMBL 508 9 1 7 4.3 CCCCOC(=O)NS(=O)(=O)c1sc(CC(C)C)cc1-c1ccc(C(=O)N2CCOCC2)cc1 10.1016/j.bmc.2008.05.066
10321731 162883 0 None - 1 Rat 7.5 pKi = 7.5 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 454 7 2 8 3.5 CCCc1nc(C)n2nc(C(=O)O)nc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00041a016
CHEMBL419835 162883 0 None - 1 Rat 7.5 pKi = 7.5 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 454 7 2 8 3.5 CCCc1nc(C)n2nc(C(=O)O)nc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00041a016
10251107 203287 0 None - 1 Rat 7.5 pKi = 7.5 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 412 5 2 8 3.1 CCc1nc(C)n2nc(O)nc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00041a016
CHEMBL76787 203287 0 None - 1 Rat 7.5 pKi = 7.5 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 412 5 2 8 3.1 CCc1nc(C)n2nc(O)nc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00041a016
44350526 18008 0 None - 1 Rat 7.5 pKi = 7.5 Binding
Inhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranesInhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranes
ChEMBL 481 6 1 7 4.5 CCc1nn(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/c(=N/C(=O)c2ccccc2C)s1 10.1016/S0960-894X(97)00026-7
CHEMBL127002 18008 0 None - 1 Rat 7.5 pKi = 7.5 Binding
Inhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranesInhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranes
ChEMBL 481 6 1 7 4.5 CCc1nn(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/c(=N/C(=O)c2ccccc2C)s1 10.1016/S0960-894X(97)00026-7
19029576 99498 0 None - 1 Rat 7.4 pKi = 7.4 Binding
Inhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranesInhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranes
ChEMBL 467 6 1 7 4.1 CCc1nn(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/c(=N/C(=O)c2ccccc2)s1 10.1016/S0960-894X(97)00026-7
CHEMBL286537 99498 0 None - 1 Rat 7.4 pKi = 7.4 Binding
Inhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranesInhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranes
ChEMBL 467 6 1 7 4.1 CCc1nn(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/c(=N/C(=O)c2ccccc2)s1 10.1016/S0960-894X(97)00026-7
44567744 183292 0 None - 1 Pig 7.4 pKi = 7.4 Binding
Displacement of [125]Ang2 from AT2 receptor in pig uterus membraneDisplacement of [125]Ang2 from AT2 receptor in pig uterus membrane
ChEMBL 466 9 1 6 4.5 CCCCOC(=O)NS(=O)(=O)c1sc(CC(C)C)cc1-c1ccc(C(=O)N(C)C)cc1 10.1016/j.bmc.2008.05.066
CHEMBL481088 183292 0 None - 1 Pig 7.4 pKi = 7.4 Binding
Displacement of [125]Ang2 from AT2 receptor in pig uterus membraneDisplacement of [125]Ang2 from AT2 receptor in pig uterus membrane
ChEMBL 466 9 1 6 4.5 CCCCOC(=O)NS(=O)(=O)c1sc(CC(C)C)cc1-c1ccc(C(=O)N(C)C)cc1 10.1016/j.bmc.2008.05.066
18950393 167603 0 None - 1 Rat 5.4 pKi = 5.4 Binding
Binding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranesBinding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranes
ChEMBL 441 8 2 7 4.1 CCCCc1ncc(C(=O)O)n1Cc1cccc2c1ccn2-c1ccccc1-c1nn[nH]n1 10.1016/S0960-894X(01)81137-9
CHEMBL433230 167603 0 None - 1 Rat 5.4 pKi = 5.4 Binding
Binding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranesBinding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranes
ChEMBL 441 8 2 7 4.1 CCCCc1ncc(C(=O)O)n1Cc1cccc2c1ccn2-c1ccccc1-c1nn[nH]n1 10.1016/S0960-894X(01)81137-9
44312565 203053 0 None - 1 Human 6.4 pKi = 6.4 Binding
Inhibition constant against Angiotensin II receptor, type 1 was determinedInhibition constant against Angiotensin II receptor, type 1 was determined
ChEMBL 437 9 3 6 3.1 CC(O)CCC(=O)N(c1ccc(-c2ccccc2-c2nn[nH]n2)cc1)[C@H](C(=O)O)C(C)C 10.1021/jm0204237
CHEMBL74767 203053 0 None - 1 Human 6.4 pKi = 6.4 Binding
Inhibition constant against Angiotensin II receptor, type 1 was determinedInhibition constant against Angiotensin II receptor, type 1 was determined
ChEMBL 437 9 3 6 3.1 CC(O)CCC(=O)N(c1ccc(-c2ccccc2-c2nn[nH]n2)cc1)[C@H](C(=O)O)C(C)C 10.1021/jm0204237
9872676 77811 0 None -9332 17 Human 5.4 pKi = 5.4 Binding
Binding affinity to human AT1 receptorBinding affinity to human AT1 receptor
ChEMBL 565 11 2 10 4.8 COc1nc(NCCCN2CCOCC2)nc(OC)c1NC(=O)c1ccc(Oc2cc3c(cc2C)CCC3(C)C)o1 10.1021/jm060012g
CHEMBL210514 77811 0 None -9332 17 Human 5.4 pKi = 5.4 Binding
Binding affinity to human AT1 receptorBinding affinity to human AT1 receptor
ChEMBL 565 11 2 10 4.8 COc1nc(NCCCN2CCOCC2)nc(OC)c1NC(=O)c1ccc(Oc2cc3c(cc2C)CCC3(C)C)o1 10.1021/jm060012g
10790818 205184 0 None - 1 Human 6.4 pKi = 6.4 Binding
Binding affinity against AT1 in human hepatoma cell line, PLC-PRF-5Binding affinity against AT1 in human hepatoma cell line, PLC-PRF-5
ChEMBL 478 5 1 5 4.7 Cc1ccc(N2C(=O)C3(CCCC3)C(=O)N2Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)cc1 10.1021/jm9904147
CHEMBL90999 205184 0 None - 1 Human 6.4 pKi = 6.4 Binding
Binding affinity against AT1 in human hepatoma cell line, PLC-PRF-5Binding affinity against AT1 in human hepatoma cell line, PLC-PRF-5
ChEMBL 478 5 1 5 4.7 Cc1ccc(N2C(=O)C3(CCCC3)C(=O)N2Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)cc1 10.1021/jm9904147
44283775 14595 0 None - 1 Rat 7.4 pKi = 7.4 Binding
Binding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranesBinding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranes
ChEMBL 591 9 1 8 6.8 CCCCc1nc(Cl)c(C(=O)Oc2ccc3c(c2)CCC3)n1Cc1cccc2c1ccn2-c1ccccc1-c1nn[nH]n1 10.1016/S0960-894X(01)81137-9
CHEMBL1206631 14595 0 None - 1 Rat 7.4 pKi = 7.4 Binding
Binding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranesBinding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranes
ChEMBL 591 9 1 8 6.8 CCCCc1nc(Cl)c(C(=O)Oc2ccc3c(c2)CCC3)n1Cc1cccc2c1ccn2-c1ccccc1-c1nn[nH]n1 10.1016/S0960-894X(01)81137-9
CHEMBL2079770 14595 0 None - 1 Rat 7.4 pKi = 7.4 Binding
Binding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranesBinding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranes
ChEMBL 591 9 1 8 6.8 CCCCc1nc(Cl)c(C(=O)Oc2ccc3c(c2)CCC3)n1Cc1cccc2c1ccn2-c1ccccc1-c1nn[nH]n1 10.1016/S0960-894X(01)81137-9
87218678 169756 0 None - 1 Human 7.4 pKi = 7.4 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 521 13 3 5 6.2 CCCCc1nc(CC)c(CNC(=O)[C@@H](S)CC(C)C)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/acsmedchemlett.8b00462
CHEMBL4447138 169756 0 None - 1 Human 7.4 pKi = 7.4 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 521 13 3 5 6.2 CCCCc1nc(CC)c(CNC(=O)[C@@H](S)CC(C)C)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/acsmedchemlett.8b00462
75031588 173126 0 None - 1 Human 7.4 pKi = 7.4 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 541 13 3 5 6.5 CCCCc1nc(Cl)c(CNC(=O)C(CS)CC(C)C)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/acsmedchemlett.8b00462
CHEMBL4535903 173126 0 None - 1 Human 7.4 pKi = 7.4 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 541 13 3 5 6.5 CCCCc1nc(Cl)c(CNC(=O)C(CS)CC(C)C)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/acsmedchemlett.8b00462
168274602 189772 0 None -97 2 Human 6.4 pKi = 6.4 Binding
Displacement of [125-I]-[Sar1Ile8]-angiotensin II from human AT1R expressed in HEK293 cell membrane assessed as inhibition constant by radioligand binding assayDisplacement of [125-I]-[Sar1Ile8]-angiotensin II from human AT1R expressed in HEK293 cell membrane assessed as inhibition constant by radioligand binding assay
ChEMBL 547 11 1 6 7.0 CCCCOC(=O)NS(=O)(=O)c1ccc(CCC)cc1-c1ccc(Cn2c(C(C)C)nc3ccccc32)cc1 10.1016/j.bmc.2022.116804
CHEMBL5177359 189772 0 None -97 2 Human 6.4 pKi = 6.4 Binding
Displacement of [125-I]-[Sar1Ile8]-angiotensin II from human AT1R expressed in HEK293 cell membrane assessed as inhibition constant by radioligand binding assayDisplacement of [125-I]-[Sar1Ile8]-angiotensin II from human AT1R expressed in HEK293 cell membrane assessed as inhibition constant by radioligand binding assay
ChEMBL 547 11 1 6 7.0 CCCCOC(=O)NS(=O)(=O)c1ccc(CCC)cc1-c1ccc(Cn2c(C(C)C)nc3ccccc32)cc1 10.1016/j.bmc.2022.116804
10695405 204784 0 None - 1 Human 6.4 pKi = 6.4 Binding
Binding affinity against AT1 in human hepatoma cell line, PLC-PRF-5Binding affinity against AT1 in human hepatoma cell line, PLC-PRF-5
ChEMBL 463 8 2 4 4.1 CCCCN1C(=O)C2(CCCC2)C(=O)N1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm9904147
CHEMBL88471 204784 0 None - 1 Human 6.4 pKi = 6.4 Binding
Binding affinity against AT1 in human hepatoma cell line, PLC-PRF-5Binding affinity against AT1 in human hepatoma cell line, PLC-PRF-5
ChEMBL 463 8 2 4 4.1 CCCCN1C(=O)C2(CCCC2)C(=O)N1Cc1ccc(NC(=O)c2ccccc2C(=O)O)cc1 10.1021/jm9904147
155522135 170078 0 None - 1 Human 6.4 pKi = 6.4 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 651 14 3 5 8.4 CCCCc1nc(Cl)c(CNC(=O)C(CS)Cc2ccc(-c3ccccc3)cc2)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/acsmedchemlett.8b00462
CHEMBL4451425 170078 0 None - 1 Human 6.4 pKi = 6.4 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 651 14 3 5 8.4 CCCCc1nc(Cl)c(CNC(=O)C(CS)Cc2ccc(-c3ccccc3)cc2)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/acsmedchemlett.8b00462
87218371 173089 0 None - 1 Human 6.4 pKi = 6.4 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 625 13 3 5 7.9 CCCCc1nc(Cl)c(CNC(=O)C(CS)Cc2cccc3ccccc23)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/acsmedchemlett.8b00462
CHEMBL4534876 173089 0 None - 1 Human 6.4 pKi = 6.4 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 625 13 3 5 7.9 CCCCc1nc(Cl)c(CNC(=O)C(CS)Cc2cccc3ccccc23)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/acsmedchemlett.8b00462
10095241 110969 0 None - 1 Human 8.4 pKi = 8.4 Binding
Ability to displace [125I]AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1Ability to displace [125I]AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1
ChEMBL 449 4 1 6 4.7 Cc1cc(OCc2ccc3c(-c4nnn[nH]4)cc4ccccc4c(=O)c3c2)c2c(n1)CCCC2 10.1021/jm00014a024
CHEMBL327633 110969 0 None - 1 Human 8.4 pKi = 8.4 Binding
Ability to displace [125I]AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1Ability to displace [125I]AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1
ChEMBL 449 4 1 6 4.7 Cc1cc(OCc2ccc3c(-c4nnn[nH]4)cc4ccccc4c(=O)c3c2)c2c(n1)CCCC2 10.1021/jm00014a024
10028164 112071 0 None - 1 Human 8.4 pKi = 8.4 Binding
Ability to displace [125I]AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1Ability to displace [125I]AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1
ChEMBL 481 6 1 8 4.3 CCOC(=O)c1c(OCc2ccc3c(-c4nnn[nH]4)cc4ccccc4c(=O)c3c2)cc(C)nc1C 10.1021/jm00014a024
CHEMBL330109 112071 0 None - 1 Human 8.4 pKi = 8.4 Binding
Ability to displace [125I]AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1Ability to displace [125I]AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1
ChEMBL 481 6 1 8 4.3 CCOC(=O)c1c(OCc2ccc3c(-c4nnn[nH]4)cc4ccccc4c(=O)c3c2)cc(C)nc1C 10.1021/jm00014a024
135723852 138597 0 None - 1 Rat 8.4 pKi = 8.4 Binding
Displacement of [125I]-Ang II from Angiotensin 2 type-1A receptor in rat vascular smooth muscle cells after 150 mins by gamma counting methodDisplacement of [125I]-Ang II from Angiotensin 2 type-1A receptor in rat vascular smooth muscle cells after 150 mins by gamma counting method
ChEMBL 438 8 2 6 4.4 CCCCc1nc(Cl)c(CO)n1Cc1ccc(-c2ccccc2-c2noc(=O)[nH]2)cc1 10.1016/j.bmc.2016.03.028
CHEMBL3787050 138597 0 None - 1 Rat 8.4 pKi = 8.4 Binding
Displacement of [125I]-Ang II from Angiotensin 2 type-1A receptor in rat vascular smooth muscle cells after 150 mins by gamma counting methodDisplacement of [125I]-Ang II from Angiotensin 2 type-1A receptor in rat vascular smooth muscle cells after 150 mins by gamma counting method
ChEMBL 438 8 2 6 4.4 CCCCc1nc(Cl)c(CO)n1Cc1ccc(-c2ccccc2-c2noc(=O)[nH]2)cc1 10.1016/j.bmc.2016.03.028
44284107 14427 0 None - 1 Rat 8.4 pKi = 8.4 Binding
Binding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranesBinding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranes
ChEMBL 561 10 1 10 5.1 CCCCc1nc(Cl)c(C(=O)OC(C)OC(C)=O)n1Cc1cccc2c1ccn2-c1ccccc1-c1nn[nH]n1 10.1016/S0960-894X(01)81137-9
CHEMBL1204966 14427 0 None - 1 Rat 8.4 pKi = 8.4 Binding
Binding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranesBinding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranes
ChEMBL 561 10 1 10 5.1 CCCCc1nc(Cl)c(C(=O)OC(C)OC(C)=O)n1Cc1cccc2c1ccn2-c1ccccc1-c1nn[nH]n1 10.1016/S0960-894X(01)81137-9
CHEMBL2079784 14427 0 None - 1 Rat 8.4 pKi = 8.4 Binding
Binding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranesBinding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranes
ChEMBL 561 10 1 10 5.1 CCCCc1nc(Cl)c(C(=O)OC(C)OC(C)=O)n1Cc1cccc2c1ccn2-c1ccccc1-c1nn[nH]n1 10.1016/S0960-894X(01)81137-9
23298211 162647 0 None - 1 Rat 8.3 pKi = 8.3 Binding
Inhibition of [125I]Sar1,Ile8 angiotensin II binding to Angiotensin II receptor type 1 in rat adrenocortical membraneInhibition of [125I]Sar1,Ile8 angiotensin II binding to Angiotensin II receptor type 1 in rat adrenocortical membrane
ChEMBL 450 6 2 7 4.8 O=C(O)c1c(Oc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c(C2CC2)nc2ncccc12 10.1016/S0960-894X(01)81146-X
CHEMBL418306 162647 0 None - 1 Rat 8.3 pKi = 8.3 Binding
Inhibition of [125I]Sar1,Ile8 angiotensin II binding to Angiotensin II receptor type 1 in rat adrenocortical membraneInhibition of [125I]Sar1,Ile8 angiotensin II binding to Angiotensin II receptor type 1 in rat adrenocortical membrane
ChEMBL 450 6 2 7 4.8 O=C(O)c1c(Oc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c(C2CC2)nc2ncccc12 10.1016/S0960-894X(01)81146-X
11813485 17890 0 None 8 2 Rat 8.3 pKi = 8.3 Binding
Compound was evaluated for its binding affinity towards rat Angiotensin II receptor, type 1Compound was evaluated for its binding affinity towards rat Angiotensin II receptor, type 1
ChEMBL 534 9 1 6 6.0 CCCCC1=NC2(CCCC2)C(=O)N1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)cc1 10.1021/jm020138n
CHEMBL126755 17890 0 None 8 2 Rat 8.3 pKi = 8.3 Binding
Compound was evaluated for its binding affinity towards rat Angiotensin II receptor, type 1Compound was evaluated for its binding affinity towards rat Angiotensin II receptor, type 1
ChEMBL 534 9 1 6 6.0 CCCCC1=NC2(CCCC2)C(=O)N1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)cc1 10.1021/jm020138n
10697829 205399 0 None - 1 Human 7.4 pKi = 7.4 Binding
Binding affinity against AT1 in human hepatoma cell line, PLC-PRF-5Binding affinity against AT1 in human hepatoma cell line, PLC-PRF-5
ChEMBL 545 8 1 5 4.5 CCCN1C(=O)C2(CCCC2)C(=O)N1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1021/jm9904147
CHEMBL92225 205399 0 None - 1 Human 7.4 pKi = 7.4 Binding
Binding affinity against AT1 in human hepatoma cell line, PLC-PRF-5Binding affinity against AT1 in human hepatoma cell line, PLC-PRF-5
ChEMBL 545 8 1 5 4.5 CCCN1C(=O)C2(CCCC2)C(=O)N1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1021/jm9904147
168290795 191340 0 None -33 2 Human 6.4 pKi = 6.4 Binding
Displacement of [125-I]-[Sar1Ile8]-angiotensin II from human AT1R expressed in HEK293 cell membrane assessed as inhibition constant by radioligand binding assayDisplacement of [125-I]-[Sar1Ile8]-angiotensin II from human AT1R expressed in HEK293 cell membrane assessed as inhibition constant by radioligand binding assay
ChEMBL 559 11 1 6 7.2 CCCCOC(=O)NS(=O)(=O)c1ccc(CCC)cc1-c1ccc(Cn2c(C3CCC3)nc3ccccc32)cc1 10.1016/j.bmc.2022.116804
CHEMBL5200734 191340 0 None -33 2 Human 6.4 pKi = 6.4 Binding
Displacement of [125-I]-[Sar1Ile8]-angiotensin II from human AT1R expressed in HEK293 cell membrane assessed as inhibition constant by radioligand binding assayDisplacement of [125-I]-[Sar1Ile8]-angiotensin II from human AT1R expressed in HEK293 cell membrane assessed as inhibition constant by radioligand binding assay
ChEMBL 559 11 1 6 7.2 CCCCOC(=O)NS(=O)(=O)c1ccc(CCC)cc1-c1ccc(Cn2c(C3CCC3)nc3ccccc32)cc1 10.1016/j.bmc.2022.116804
10790819 110961 0 None - 1 Human 6.4 pKi = 6.4 Binding
Binding affinity against AT1 in human hepatoma cell line, PLC-PRF-5Binding affinity against AT1 in human hepatoma cell line, PLC-PRF-5
ChEMBL 478 6 1 5 4.4 O=C1N(Cc2ccccc2)N(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)C(=O)C12CCCC2 10.1021/jm9904147
CHEMBL327594 110961 0 None - 1 Human 6.4 pKi = 6.4 Binding
Binding affinity against AT1 in human hepatoma cell line, PLC-PRF-5Binding affinity against AT1 in human hepatoma cell line, PLC-PRF-5
ChEMBL 478 6 1 5 4.4 O=C1N(Cc2ccccc2)N(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)C(=O)C12CCCC2 10.1021/jm9904147
44567852 183214 0 None - 1 Pig 6.4 pKi = 6.4 Binding
Displacement of [125]Ang2 from AT2 receptor in pig uterus membraneDisplacement of [125]Ang2 from AT2 receptor in pig uterus membrane
ChEMBL 432 9 1 5 4.1 CCCCOC(=O)NS(=O)(=O)c1ccccc1-c1ccc(C(=O)N(CC)CC)cc1 10.1016/j.bmc.2008.05.066
CHEMBL480507 183214 0 None - 1 Pig 6.4 pKi = 6.4 Binding
Displacement of [125]Ang2 from AT2 receptor in pig uterus membraneDisplacement of [125]Ang2 from AT2 receptor in pig uterus membrane
ChEMBL 432 9 1 5 4.1 CCCCOC(=O)NS(=O)(=O)c1ccccc1-c1ccc(C(=O)N(CC)CC)cc1 10.1016/j.bmc.2008.05.066
123814 417 26 None - 1 Human 6.4 pKi = 6.4 Binding
Displacement of [3H]valsartan from human AT1 receptor expressed in CHO cellsDisplacement of [3H]valsartan from human AT1 receptor expressed in CHO cells
ChEMBL None None None None 10.1021/jm701490g
5368 417 26 None - 1 Human 6.4 pKi = 6.4 Binding
Displacement of [3H]valsartan from human AT1 receptor expressed in CHO cellsDisplacement of [3H]valsartan from human AT1 receptor expressed in CHO cells
ChEMBL None None None None 10.1021/jm701490g
CHEMBL261120 417 26 None - 1 Human 6.4 pKi = 6.4 Binding
Displacement of [3H]valsartan from human AT1 receptor expressed in CHO cellsDisplacement of [3H]valsartan from human AT1 receptor expressed in CHO cells
ChEMBL None None None None 10.1021/jm701490g
123814 417 26 None - 1 Human 6.4 pKi = 6.4 Binding
Displacement of [3H]valsartan from human recombinant AT1 receptor expressed in CHO cells after 40 mins by liquid scintillation countingDisplacement of [3H]valsartan from human recombinant AT1 receptor expressed in CHO cells after 40 mins by liquid scintillation counting
ChEMBL None None None None 10.1021/jm900651p
5368 417 26 None - 1 Human 6.4 pKi = 6.4 Binding
Displacement of [3H]valsartan from human recombinant AT1 receptor expressed in CHO cells after 40 mins by liquid scintillation countingDisplacement of [3H]valsartan from human recombinant AT1 receptor expressed in CHO cells after 40 mins by liquid scintillation counting
ChEMBL None None None None 10.1021/jm900651p
CHEMBL261120 417 26 None - 1 Human 6.4 pKi = 6.4 Binding
Displacement of [3H]valsartan from human recombinant AT1 receptor expressed in CHO cells after 40 mins by liquid scintillation countingDisplacement of [3H]valsartan from human recombinant AT1 receptor expressed in CHO cells after 40 mins by liquid scintillation counting
ChEMBL None None None None 10.1021/jm900651p
10480349 203697 0 None - 1 Rat 7.4 pKi = 7.4 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 481 7 3 8 3.2 CCCc1nc(C)n2c(O)nnc2c1Cc1ccc(NC(=O)c2ccccc2S(=O)(=O)O)cc1 10.1021/jm00041a016
CHEMBL80167 203697 0 None - 1 Rat 7.4 pKi = 7.4 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 481 7 3 8 3.2 CCCc1nc(C)n2c(O)nnc2c1Cc1ccc(NC(=O)c2ccccc2S(=O)(=O)O)cc1 10.1021/jm00041a016
10050326 118685 0 None - 1 Rat 7.4 pKi = 7.4 Binding
Inhibition of [125I]- Sar,Ile8-angiotensin II binding to rat adrenal cortical membrane angiotensin II receptorInhibition of [125I]- Sar,Ile8-angiotensin II binding to rat adrenal cortical membrane angiotensin II receptor
ChEMBL 468 9 1 5 5.9 CCCCC1=NC(Cl)=C(C(=O)OCC)C(C)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00103a014
CHEMBL343251 118685 0 None - 1 Rat 7.4 pKi = 7.4 Binding
Inhibition of [125I]- Sar,Ile8-angiotensin II binding to rat adrenal cortical membrane angiotensin II receptorInhibition of [125I]- Sar,Ile8-angiotensin II binding to rat adrenal cortical membrane angiotensin II receptor
ChEMBL 468 9 1 5 5.9 CCCCC1=NC(Cl)=C(C(=O)OCC)C(C)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00103a014
168279676 190525 0 None -11 2 Human 6.4 pKi = 6.4 Binding
Displacement of [125-I]-[Sar1Ile8]-angiotensin II from human AT1R expressed in HEK293 cell membrane assessed as inhibition constant by radioligand binding assayDisplacement of [125-I]-[Sar1Ile8]-angiotensin II from human AT1R expressed in HEK293 cell membrane assessed as inhibition constant by radioligand binding assay
ChEMBL 573 11 1 6 7.6 CCCCOC(=O)NS(=O)(=O)c1ccc(CCC)cc1-c1ccc(Cn2c(C3CCCC3)nc3ccccc32)cc1 10.1016/j.bmc.2022.116804
CHEMBL5188126 190525 0 None -11 2 Human 6.4 pKi = 6.4 Binding
Displacement of [125-I]-[Sar1Ile8]-angiotensin II from human AT1R expressed in HEK293 cell membrane assessed as inhibition constant by radioligand binding assayDisplacement of [125-I]-[Sar1Ile8]-angiotensin II from human AT1R expressed in HEK293 cell membrane assessed as inhibition constant by radioligand binding assay
ChEMBL 573 11 1 6 7.6 CCCCOC(=O)NS(=O)(=O)c1ccc(CCC)cc1-c1ccc(Cn2c(C3CCCC3)nc3ccccc32)cc1 10.1016/j.bmc.2022.116804
10744859 204855 0 None - 1 Human 7.4 pKi = 7.4 Binding
Binding affinity against AT1 in human hepatoma cell line, PLC-PRF-5Binding affinity against AT1 in human hepatoma cell line, PLC-PRF-5
ChEMBL 533 9 1 5 4.4 CCCCN1C(=O)C(C)(C)C(=O)N1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1021/jm9904147
CHEMBL88924 204855 0 None - 1 Human 7.4 pKi = 7.4 Binding
Binding affinity against AT1 in human hepatoma cell line, PLC-PRF-5Binding affinity against AT1 in human hepatoma cell line, PLC-PRF-5
ChEMBL 533 9 1 5 4.4 CCCCN1C(=O)C(C)(C)C(=O)N1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2)cc1 10.1021/jm9904147
44350541 117928 0 None - 1 Rat 6.4 pKi = 6.4 Binding
Inhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranesInhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranes
ChEMBL 535 6 1 7 5.2 CCc1nn(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/c(=N/C(=O)c2cccc(C(F)(F)F)c2)s1 10.1016/S0960-894X(97)00026-7
CHEMBL341109 117928 0 None - 1 Rat 6.4 pKi = 6.4 Binding
Inhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranesInhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranes
ChEMBL 535 6 1 7 5.2 CCc1nn(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/c(=N/C(=O)c2cccc(C(F)(F)F)c2)s1 10.1016/S0960-894X(97)00026-7
10053872 162913 0 None - 1 Rat 7.3 pKi = 7.3 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 412 6 2 8 3.2 CCCc1ncn2nc(O)nc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00041a016
CHEMBL420028 162913 0 None - 1 Rat 7.3 pKi = 7.3 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 412 6 2 8 3.2 CCCc1ncn2nc(O)nc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00041a016
168287840 190702 0 None -32 2 Human 6.3 pKi = 6.3 Binding
Displacement of [125-I]-[Sar1Ile8]-angiotensin II from human AT1R expressed in HEK293 cell membrane assessed as inhibition constant by radioligand binding assayDisplacement of [125-I]-[Sar1Ile8]-angiotensin II from human AT1R expressed in HEK293 cell membrane assessed as inhibition constant by radioligand binding assay
ChEMBL 547 12 1 6 6.9 CCCCOC(=O)NS(=O)(=O)c1ccc(CCC)cc1-c1ccc(Cn2c(CCC)nc3ccccc32)cc1 10.1016/j.bmc.2022.116804
CHEMBL5191241 190702 0 None -32 2 Human 6.3 pKi = 6.3 Binding
Displacement of [125-I]-[Sar1Ile8]-angiotensin II from human AT1R expressed in HEK293 cell membrane assessed as inhibition constant by radioligand binding assayDisplacement of [125-I]-[Sar1Ile8]-angiotensin II from human AT1R expressed in HEK293 cell membrane assessed as inhibition constant by radioligand binding assay
ChEMBL 547 12 1 6 6.9 CCCCOC(=O)NS(=O)(=O)c1ccc(CCC)cc1-c1ccc(Cn2c(CCC)nc3ccccc32)cc1 10.1016/j.bmc.2022.116804
19029545 17816 0 None - 1 Rat 7.3 pKi = 7.3 Binding
Inhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranesInhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranes
ChEMBL 481 6 1 7 4.5 CCc1nn(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/c(=N/C(=O)c2ccc(C)cc2)s1 10.1016/S0960-894X(97)00026-7
CHEMBL126351 17816 0 None - 1 Rat 7.3 pKi = 7.3 Binding
Inhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranesInhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranes
ChEMBL 481 6 1 7 4.5 CCc1nn(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/c(=N/C(=O)c2ccc(C)cc2)s1 10.1016/S0960-894X(97)00026-7
2806 3894 109 None - 1 Human 5.3 pKi = 5.3 Binding
Inhibition constant against Angiotensin II receptor, type 1 was determinedInhibition constant against Angiotensin II receptor, type 1 was determined
ChEMBL 435 10 2 5 4.2 CCCCC(=O)N([C@H](C(=O)O)C(C)C)Cc1ccc(cc1)c1ccccc1c1nnn[nH]1 10.1021/jm0204237
3937 3894 109 None - 1 Human 5.3 pKi = 5.3 Binding
Inhibition constant against Angiotensin II receptor, type 1 was determinedInhibition constant against Angiotensin II receptor, type 1 was determined
ChEMBL 435 10 2 5 4.2 CCCCC(=O)N([C@H](C(=O)O)C(C)C)Cc1ccc(cc1)c1ccccc1c1nnn[nH]1 10.1021/jm0204237
593 3894 109 None - 1 Human 5.3 pKi = 5.3 Binding
Inhibition constant against Angiotensin II receptor, type 1 was determinedInhibition constant against Angiotensin II receptor, type 1 was determined
ChEMBL 435 10 2 5 4.2 CCCCC(=O)N([C@H](C(=O)O)C(C)C)Cc1ccc(cc1)c1ccccc1c1nnn[nH]1 10.1021/jm0204237
60846 3894 109 None - 1 Human 5.3 pKi = 5.3 Binding
Inhibition constant against Angiotensin II receptor, type 1 was determinedInhibition constant against Angiotensin II receptor, type 1 was determined
ChEMBL 435 10 2 5 4.2 CCCCC(=O)N([C@H](C(=O)O)C(C)C)Cc1ccc(cc1)c1ccccc1c1nnn[nH]1 10.1021/jm0204237
CHEMBL1069 3894 109 None - 1 Human 5.3 pKi = 5.3 Binding
Inhibition constant against Angiotensin II receptor, type 1 was determinedInhibition constant against Angiotensin II receptor, type 1 was determined
ChEMBL 435 10 2 5 4.2 CCCCC(=O)N([C@H](C(=O)O)C(C)C)Cc1ccc(cc1)c1ccccc1c1nnn[nH]1 10.1021/jm0204237
DB00177 3894 109 None - 1 Human 5.3 pKi = 5.3 Binding
Inhibition constant against Angiotensin II receptor, type 1 was determinedInhibition constant against Angiotensin II receptor, type 1 was determined
ChEMBL 435 10 2 5 4.2 CCCCC(=O)N([C@H](C(=O)O)C(C)C)Cc1ccc(cc1)c1ccccc1c1nnn[nH]1 10.1021/jm0204237
44350499 193259 0 None - 1 Rat 7.3 pKi = 7.3 Binding
Inhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranesInhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranes
ChEMBL 497 7 1 8 4.2 CCc1nn(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/c(=N/C(=O)c2cccc(OC)c2)s1 10.1016/S0960-894X(97)00026-7
CHEMBL541992 193259 0 None - 1 Rat 7.3 pKi = 7.3 Binding
Inhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranesInhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranes
ChEMBL 497 7 1 8 4.2 CCc1nn(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/c(=N/C(=O)c2cccc(OC)c2)s1 10.1016/S0960-894X(97)00026-7
10388491 203396 0 None - 1 Rat 8.3 pKi = 8.3 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 439 7 2 8 3.9 CCCc1nc(C)n2nc(NC)nc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00041a016
CHEMBL77783 203396 0 None - 1 Rat 8.3 pKi = 8.3 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 439 7 2 8 3.9 CCCc1nc(C)n2nc(NC)nc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00041a016
10388529 203787 0 None - 1 Rat 8.3 pKi = 8.3 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 440 7 2 8 3.3 CCCc1nc(C)n2nc(CO)nc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00041a016
CHEMBL80773 203787 0 None - 1 Rat 8.3 pKi = 8.3 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 440 7 2 8 3.3 CCCc1nc(C)n2nc(CO)nc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00041a016
1610 2305 89 None 1 4 Human 8.3 pKi = 8.3 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/acsmedchemlett.8b00462
3941 2305 89 None 1 4 Human 8.3 pKi = 8.3 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/acsmedchemlett.8b00462
3961 2305 89 None 1 4 Human 8.3 pKi = 8.3 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/acsmedchemlett.8b00462
590 2305 89 None 1 4 Human 8.3 pKi = 8.3 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/acsmedchemlett.8b00462
CHEMBL191 2305 89 None 1 4 Human 8.3 pKi = 8.3 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/acsmedchemlett.8b00462
DB00678 2305 89 None 1 4 Human 8.3 pKi = 8.3 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 10.1021/acsmedchemlett.8b00462
87218492 170328 0 None - 1 Human 8.3 pKi = 8.3 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 535 14 3 5 6.4 CCCCc1nc(CC)c(CNC(=O)[C@@H](CS)CC(C)C)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/acsmedchemlett.8b00462
CHEMBL4454778 170328 0 None - 1 Human 8.3 pKi = 8.3 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 535 14 3 5 6.4 CCCCc1nc(CC)c(CNC(=O)[C@@H](CS)CC(C)C)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/acsmedchemlett.8b00462
87218698 171713 0 None - 1 Human 8.3 pKi = 8.3 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 527 12 3 6 5.4 CCOc1nc(CC)c(CNC(=O)[C@@H](S)CC(C)C)n1Cc1ccc(-c2ccccc2C(=O)O)c(F)c1 10.1021/acsmedchemlett.8b00462
CHEMBL4474870 171713 0 None - 1 Human 8.3 pKi = 8.3 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 527 12 3 6 5.4 CCOc1nc(CC)c(CNC(=O)[C@@H](S)CC(C)C)n1Cc1ccc(-c2ccccc2C(=O)O)c(F)c1 10.1021/acsmedchemlett.8b00462
25190005 173455 0 None - 1 Human 8.3 pKi = 8.3 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 545 12 3 6 5.5 CCOc1nc(CC)c(CNC(=O)[C@@H](S)CC(C)C)n1Cc1cc(F)c(-c2ccccc2C(=O)O)cc1F 10.1021/acsmedchemlett.8b00462
CHEMBL4543532 173455 0 None - 1 Human 8.3 pKi = 8.3 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 545 12 3 6 5.5 CCOc1nc(CC)c(CNC(=O)[C@@H](S)CC(C)C)n1Cc1cc(F)c(-c2ccccc2C(=O)O)cc1F 10.1021/acsmedchemlett.8b00462
9846347 196950 0 None - 1 Rat 8.2 pKi = 8.2 Binding
Inhibition of [125I]Sar1,Ile8 angiotensin II binding to Angiotensin II receptor type 1 in rat adrenocortical membraneInhibition of [125I]Sar1,Ile8 angiotensin II binding to Angiotensin II receptor type 1 in rat adrenocortical membrane
ChEMBL 437 6 2 6 5.1 CCc1nc2ccccc2c(C(=O)O)c1Oc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81146-X
CHEMBL57907 196950 0 None - 1 Rat 8.2 pKi = 8.2 Binding
Inhibition of [125I]Sar1,Ile8 angiotensin II binding to Angiotensin II receptor type 1 in rat adrenocortical membraneInhibition of [125I]Sar1,Ile8 angiotensin II binding to Angiotensin II receptor type 1 in rat adrenocortical membrane
ChEMBL 437 6 2 6 5.1 CCc1nc2ccccc2c(C(=O)O)c1Oc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1016/S0960-894X(01)81146-X
44350543 96231 0 None - 1 Rat 8.2 pKi = 8.2 Binding
Inhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranesInhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranes
ChEMBL 535 6 1 7 5.2 CCc1nn(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/c(=N/C(=O)c2ccccc2C(F)(F)F)s1 10.1016/S0960-894X(97)00026-7
CHEMBL264003 96231 0 None - 1 Rat 8.2 pKi = 8.2 Binding
Inhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranesInhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranes
ChEMBL 535 6 1 7 5.2 CCc1nn(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/c(=N/C(=O)c2ccccc2C(F)(F)F)s1 10.1016/S0960-894X(97)00026-7
10340697 104254 0 None - 1 Rat 7.3 pKi = 7.3 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 396 6 1 7 3.5 CCCc1ncn2ncnc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00041a016
CHEMBL310678 104254 0 None - 1 Rat 7.3 pKi = 7.3 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 396 6 1 7 3.5 CCCc1ncn2ncnc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00041a016
155529942 170900 0 None - 1 Human 7.3 pKi = 7.3 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 569 15 3 5 7.3 CCCCc1nc(Cl)c(CNC(=O)C(CS)CC(CC)CC)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/acsmedchemlett.8b00462
CHEMBL4463575 170900 0 None - 1 Human 7.3 pKi = 7.3 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 569 15 3 5 7.3 CCCCc1nc(Cl)c(CNC(=O)C(CS)CC(CC)CC)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/acsmedchemlett.8b00462
155547799 173106 0 None - 1 Human 7.3 pKi = 7.3 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 521 13 3 5 6.2 CCCCc1nc(C)c(CNC(=O)[C@@H](CS)CC(C)C)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/acsmedchemlett.8b00462
CHEMBL4535256 173106 0 None - 1 Human 7.3 pKi = 7.3 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 521 13 3 5 6.2 CCCCc1nc(C)c(CNC(=O)[C@@H](CS)CC(C)C)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/acsmedchemlett.8b00462
87218352 173840 0 None - 1 Human 7.3 pKi = 7.3 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 567 13 3 5 7.0 CCCCc1nc(Cl)c(CNC(=O)C(CS)CC2CCCC2)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/acsmedchemlett.8b00462
CHEMBL4552884 173840 0 None - 1 Human 7.3 pKi = 7.3 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 567 13 3 5 7.0 CCCCc1nc(Cl)c(CNC(=O)C(CS)CC2CCCC2)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/acsmedchemlett.8b00462
45488150 195335 0 None - 1 Rat 5.3 pKi = 5.3 Binding
Displacement of [125I]SI-Ang2 from AT1 receptor in Sprague-Dawley rat liver membraneDisplacement of [125I]SI-Ang2 from AT1 receptor in Sprague-Dawley rat liver membrane
ChEMBL 362 7 1 6 3.4 CCCc1nc2c(C)cccc2n1Cc1ccc(OCc2nnn[nH]2)cc1 10.1021/jm901272d
CHEMBL567054 195335 0 None - 1 Rat 5.3 pKi = 5.3 Binding
Displacement of [125I]SI-Ang2 from AT1 receptor in Sprague-Dawley rat liver membraneDisplacement of [125I]SI-Ang2 from AT1 receptor in Sprague-Dawley rat liver membrane
ChEMBL 362 7 1 6 3.4 CCCc1nc2c(C)cccc2n1Cc1ccc(OCc2nnn[nH]2)cc1 10.1021/jm901272d
25141240 183001 0 None - 1 Pig 7.3 pKi = 7.3 Binding
Displacement of [125]Ang2 from AT2 receptor in pig uterus membraneDisplacement of [125]Ang2 from AT2 receptor in pig uterus membrane
ChEMBL 508 10 1 5 5.7 CCCCOC(=O)NS(=O)(=O)c1ccc(-c2ccccc2)cc1-c1ccc(C(=O)N(CC)CC)cc1 10.1016/j.bmc.2008.05.066
CHEMBL480122 183001 0 None - 1 Pig 7.3 pKi = 7.3 Binding
Displacement of [125]Ang2 from AT2 receptor in pig uterus membraneDisplacement of [125]Ang2 from AT2 receptor in pig uterus membrane
ChEMBL 508 10 1 5 5.7 CCCCOC(=O)NS(=O)(=O)c1ccc(-c2ccccc2)cc1-c1ccc(C(=O)N(CC)CC)cc1 10.1016/j.bmc.2008.05.066
10410991 203233 0 None - 1 Rat 7.3 pKi = 7.3 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 440 6 1 8 3.1 CCCc1nc(C)n2c(=O)n(C)nc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00041a016
CHEMBL76421 203233 0 None - 1 Rat 7.3 pKi = 7.3 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 440 6 1 8 3.1 CCCc1nc(C)n2c(=O)n(C)nc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00041a016
24828743 95708 0 None - 1 Human 6.3 pKi = 6.3 Binding
Displacement of [3H]valsartan from human AT1 receptor expressed in CHO cellsDisplacement of [3H]valsartan from human AT1 receptor expressed in CHO cells
ChEMBL 788 20 8 9 1.4 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](CN)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O 10.1021/jm701490g
CHEMBL260622 95708 0 None - 1 Human 6.3 pKi = 6.3 Binding
Displacement of [3H]valsartan from human AT1 receptor expressed in CHO cellsDisplacement of [3H]valsartan from human AT1 receptor expressed in CHO cells
ChEMBL 788 20 8 9 1.4 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](CN)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O 10.1021/jm701490g
19029649 17746 0 None - 1 Rat 6.3 pKi = 6.3 Binding
Inhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranesInhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranes
ChEMBL 535 6 1 7 5.2 CCc1nn(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/c(=N/C(=O)c2ccc(C(F)(F)F)cc2)s1 10.1016/S0960-894X(97)00026-7
CHEMBL125964 17746 0 None - 1 Rat 6.3 pKi = 6.3 Binding
Inhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranesInhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranes
ChEMBL 535 6 1 7 5.2 CCc1nn(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/c(=N/C(=O)c2ccc(C(F)(F)F)cc2)s1 10.1016/S0960-894X(97)00026-7
10457973 14499 0 None - 1 Rat 7.2 pKi = 7.2 Binding
Inhibition of [125I]- Sar,Ile8-angiotensin II binding to rat adrenal cortical membrane angiotensin II receptorInhibition of [125I]- Sar,Ile8-angiotensin II binding to rat adrenal cortical membrane angiotensin II receptor
ChEMBL 482 9 1 5 6.2 CCCCC1=NC(C)(C)C(C(=O)OCC)=C(Cl)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00103a014
CHEMBL1205756 14499 0 None - 1 Rat 7.2 pKi = 7.2 Binding
Inhibition of [125I]- Sar,Ile8-angiotensin II binding to rat adrenal cortical membrane angiotensin II receptorInhibition of [125I]- Sar,Ile8-angiotensin II binding to rat adrenal cortical membrane angiotensin II receptor
ChEMBL 482 9 1 5 6.2 CCCCC1=NC(C)(C)C(C(=O)OCC)=C(Cl)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00103a014
CHEMBL145036 14499 0 None - 1 Rat 7.2 pKi = 7.2 Binding
Inhibition of [125I]- Sar,Ile8-angiotensin II binding to rat adrenal cortical membrane angiotensin II receptorInhibition of [125I]- Sar,Ile8-angiotensin II binding to rat adrenal cortical membrane angiotensin II receptor
ChEMBL 482 9 1 5 6.2 CCCCC1=NC(C)(C)C(C(=O)OCC)=C(Cl)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00103a014
CHEMBL1076629 206730 0 None - 1 Human 7.2 pKi = 7.2 Binding
Displacement of [125I][Sar1,Ile8]Ang2 from human AT1 receptor N111G constitutively active mutant expressed in CHO cells by gamma countingDisplacement of [125I][Sar1,Ile8]Ang2 from human AT1 receptor N111G constitutively active mutant expressed in CHO cells by gamma counting
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1ccc(C2(C(F)(F)F)N=N2)cc1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O 10.1021/jm9015747
9895957 10558 12 None -3 3 Rat 8.2 pKi = 8.2 Binding
Compound was evaluated for its binding affinity towards rat Angiotensin II receptor, type 1Compound was evaluated for its binding affinity towards rat Angiotensin II receptor, type 1
ChEMBL 659 11 1 7 6.8 CCCCC1=NC2(CCCC2)C(=O)N1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)c(CN2CCC(C)(C)C2=O)c1 10.1021/jm020138n
CHEMBL11706 10558 12 None -3 3 Rat 8.2 pKi = 8.2 Binding
Compound was evaluated for its binding affinity towards rat Angiotensin II receptor, type 1Compound was evaluated for its binding affinity towards rat Angiotensin II receptor, type 1
ChEMBL 659 11 1 7 6.8 CCCCC1=NC2(CCCC2)C(=O)N1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2onc(C)c2C)c(CN2CCC(C)(C)C2=O)c1 10.1021/jm020138n
9982165 203742 0 None - 1 Rat 8.2 pKi = 8.2 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 470 8 2 9 2.6 CCCc1nc(C)n2c(=O)n(CCO)nc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00041a016
CHEMBL80446 203742 0 None - 1 Rat 8.2 pKi = 8.2 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 470 8 2 9 2.6 CCCc1nc(C)n2c(=O)n(CCO)nc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00041a016
18950387 14384 0 None - 1 Rat 8.2 pKi = 8.2 Binding
Binding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranesBinding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranes
ChEMBL 461 8 2 7 4.5 CCCCc1nc(Cl)c(CO)n1Cc1cccc2c1ccn2-c1ccccc1-c1nn[nH]n1 10.1016/S0960-894X(01)81137-9
CHEMBL1204443 14384 0 None - 1 Rat 8.2 pKi = 8.2 Binding
Binding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranesBinding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranes
ChEMBL 461 8 2 7 4.5 CCCCc1nc(Cl)c(CO)n1Cc1cccc2c1ccn2-c1ccccc1-c1nn[nH]n1 10.1016/S0960-894X(01)81137-9
CHEMBL1790055 14384 0 None - 1 Rat 8.2 pKi = 8.2 Binding
Binding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranesBinding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranes
ChEMBL 461 8 2 7 4.5 CCCCc1nc(Cl)c(CO)n1Cc1cccc2c1ccn2-c1ccccc1-c1nn[nH]n1 10.1016/S0960-894X(01)81137-9
44283773 14430 0 None - 1 Rat 8.2 pKi = 8.2 Binding
Binding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranesBinding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranes
ChEMBL 588 12 1 9 5.1 CCCCc1nc(Cl)c(C(=O)OCC(=O)N(CC)CC)n1Cc1cccc2c1ccn2-c1ccccc1-c1nn[nH]n1 10.1016/S0960-894X(01)81137-9
CHEMBL1204974 14430 0 None - 1 Rat 8.2 pKi = 8.2 Binding
Binding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranesBinding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranes
ChEMBL 588 12 1 9 5.1 CCCCc1nc(Cl)c(C(=O)OCC(=O)N(CC)CC)n1Cc1cccc2c1ccn2-c1ccccc1-c1nn[nH]n1 10.1016/S0960-894X(01)81137-9
CHEMBL2021415 14430 0 None - 1 Rat 8.2 pKi = 8.2 Binding
Binding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranesBinding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranes
ChEMBL 588 12 1 9 5.1 CCCCc1nc(Cl)c(C(=O)OCC(=O)N(CC)CC)n1Cc1cccc2c1ccn2-c1ccccc1-c1nn[nH]n1 10.1016/S0960-894X(01)81137-9
87218658 170433 0 None - 1 Human 8.2 pKi = 8.2 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 547 14 3 5 6.7 CCCCc1nc(C2CC2)c(CNC(=O)[C@@H](CS)CC(C)C)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/acsmedchemlett.8b00462
CHEMBL4456544 170433 0 None - 1 Human 8.2 pKi = 8.2 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 547 14 3 5 6.7 CCCCc1nc(C2CC2)c(CNC(=O)[C@@H](CS)CC(C)C)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/acsmedchemlett.8b00462
87219028 171025 0 None - 1 Human 8.2 pKi = 8.2 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 509 12 3 6 5.2 CCOc1nc(CC)c(CNC(=O)[C@@H](S)CC(C)C)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/acsmedchemlett.8b00462
CHEMBL4465325 171025 0 None - 1 Human 8.2 pKi = 8.2 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 509 12 3 6 5.2 CCOc1nc(CC)c(CNC(=O)[C@@H](S)CC(C)C)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/acsmedchemlett.8b00462
44567816 189741 0 None - 1 Pig 8.2 pKi = 8.2 Binding
Displacement of [125]Ang2 from AT2 receptor in pig uterus membraneDisplacement of [125]Ang2 from AT2 receptor in pig uterus membrane
ChEMBL 492 9 1 6 5.1 CCCCOC(=O)NS(=O)(=O)c1sc(CC(C)C)cc1-c1ccc(C(=O)N2CCCC2)cc1 10.1016/j.bmc.2008.05.066
CHEMBL517685 189741 0 None - 1 Pig 8.2 pKi = 8.2 Binding
Displacement of [125]Ang2 from AT2 receptor in pig uterus membraneDisplacement of [125]Ang2 from AT2 receptor in pig uterus membrane
ChEMBL 492 9 1 6 5.1 CCCCOC(=O)NS(=O)(=O)c1sc(CC(C)C)cc1-c1ccc(C(=O)N2CCCC2)cc1 10.1016/j.bmc.2008.05.066
44567780 191576 0 None - 1 Pig 8.2 pKi = 8.2 Binding
Displacement of [125]Ang2 from AT2 receptor in pig uterus membraneDisplacement of [125]Ang2 from AT2 receptor in pig uterus membrane
ChEMBL 520 10 2 6 5.9 CCCCOC(=O)NS(=O)(=O)c1sc(CC(C)C)cc1-c1ccc(C(=O)NC2CCCCC2)cc1 10.1016/j.bmc.2008.05.066
CHEMBL520421 191576 0 None - 1 Pig 8.2 pKi = 8.2 Binding
Displacement of [125]Ang2 from AT2 receptor in pig uterus membraneDisplacement of [125]Ang2 from AT2 receptor in pig uterus membrane
ChEMBL 520 10 2 6 5.9 CCCCOC(=O)NS(=O)(=O)c1sc(CC(C)C)cc1-c1ccc(C(=O)NC2CCCCC2)cc1 10.1016/j.bmc.2008.05.066
9910978 14425 0 None - 1 Rat 5.2 pKi = 5.2 Binding
Binding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranesBinding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranes
ChEMBL 437 8 1 6 5.2 CCCCc1nc(Cl)c(C=O)n1Cc1ccc2nc(-c3ccccc3C(=O)O)oc2c1 10.1016/S0960-894X(01)81137-9
CHEMBL1204954 14425 0 None - 1 Rat 5.2 pKi = 5.2 Binding
Binding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranesBinding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranes
ChEMBL 437 8 1 6 5.2 CCCCc1nc(Cl)c(C=O)n1Cc1ccc2nc(-c3ccccc3C(=O)O)oc2c1 10.1016/S0960-894X(01)81137-9
CHEMBL36259 14425 0 None - 1 Rat 5.2 pKi = 5.2 Binding
Binding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranesBinding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranes
ChEMBL 437 8 1 6 5.2 CCCCc1nc(Cl)c(C=O)n1Cc1ccc2nc(-c3ccccc3C(=O)O)oc2c1 10.1016/S0960-894X(01)81137-9
168275495 189867 0 None -66 2 Human 6.2 pKi = 6.2 Binding
Displacement of [125-I]-[Sar1Ile8]-angiotensin II from human AT1R expressed in HEK293 cell membrane assessed as inhibition constant by radioligand binding assayDisplacement of [125-I]-[Sar1Ile8]-angiotensin II from human AT1R expressed in HEK293 cell membrane assessed as inhibition constant by radioligand binding assay
ChEMBL 519 10 1 6 6.2 CCCCOC(=O)NS(=O)(=O)c1ccc(CCC)cc1-c1ccc(Cn2c(C)nc3ccccc32)cc1 10.1016/j.bmc.2022.116804
CHEMBL5178838 189867 0 None -66 2 Human 6.2 pKi = 6.2 Binding
Displacement of [125-I]-[Sar1Ile8]-angiotensin II from human AT1R expressed in HEK293 cell membrane assessed as inhibition constant by radioligand binding assayDisplacement of [125-I]-[Sar1Ile8]-angiotensin II from human AT1R expressed in HEK293 cell membrane assessed as inhibition constant by radioligand binding assay
ChEMBL 519 10 1 6 6.2 CCCCOC(=O)NS(=O)(=O)c1ccc(CCC)cc1-c1ccc(Cn2c(C)nc3ccccc32)cc1 10.1016/j.bmc.2022.116804
10251334 203283 0 None - 1 Rat 6.2 pKi = 6.2 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 416 7 2 6 4.4 CCCCc1nc(C)n2nc(O)nc2c1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00041a016
CHEMBL76775 203283 0 None - 1 Rat 6.2 pKi = 6.2 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 416 7 2 6 4.4 CCCCc1nc(C)n2nc(O)nc2c1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00041a016
155533580 171300 0 None - 1 Human 7.2 pKi = 7.2 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 527 12 3 5 6.3 CCCCc1nc(Cl)c(CNC(=O)[C@@H](S)CC(C)C)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/acsmedchemlett.8b00462
CHEMBL4469350 171300 0 None - 1 Human 7.2 pKi = 7.2 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 527 12 3 5 6.3 CCCCc1nc(Cl)c(CNC(=O)[C@@H](S)CC(C)C)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/acsmedchemlett.8b00462
87218397 170577 0 None - 1 Human 6.2 pKi = 6.2 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 541 13 3 5 6.5 CCCCc1nc(Cl)c(CNC(=O)C(CS)C(C)CC)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/acsmedchemlett.8b00462
CHEMBL4458683 170577 0 None - 1 Human 6.2 pKi = 6.2 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 541 13 3 5 6.5 CCCCc1nc(Cl)c(CNC(=O)C(CS)C(C)CC)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/acsmedchemlett.8b00462
10077050 84838 0 None - 1 Rat 6.2 pKi = 6.2 Binding
Displacement of [125I]-SI-Ang-2 from AT1 receptor in Rattus norvegicus Sprague-Dawley (rat) liver membranes after 2 hrDisplacement of [125I]-SI-Ang-2 from AT1 receptor in Rattus norvegicus Sprague-Dawley (rat) liver membranes after 2 hr
ChEMBL 586 8 0 8 7.1 CCCc1nc2c(C)cc(-c3nc4ccccc4n3C)cc2n1Cc1ccc(-c2ccc(C(=O)OC)cc2C(=O)OC)cc1 10.1007/s00044-008-9153-9
CHEMBL2260198 84838 0 None - 1 Rat 6.2 pKi = 6.2 Binding
Displacement of [125I]-SI-Ang-2 from AT1 receptor in Rattus norvegicus Sprague-Dawley (rat) liver membranes after 2 hrDisplacement of [125I]-SI-Ang-2 from AT1 receptor in Rattus norvegicus Sprague-Dawley (rat) liver membranes after 2 hr
ChEMBL 586 8 0 8 7.1 CCCc1nc2c(C)cc(-c3nc4ccccc4n3C)cc2n1Cc1ccc(-c2ccc(C(=O)OC)cc2C(=O)OC)cc1 10.1007/s00044-008-9153-9
10100370 102686 0 None - 1 Rat 6.2 pKi = 6.2 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 454 8 2 8 4.2 CCCc1nc(CCC)n2nc(O)nc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00041a016
CHEMBL308138 102686 0 None - 1 Rat 6.2 pKi = 6.2 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 454 8 2 8 4.2 CCCc1nc(CCC)n2nc(O)nc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00041a016
15657894 205354 0 None - 1 Rat 7.2 pKi = 7.2 Binding
Binding affinity against angiotensin II receptor from rat liverBinding affinity against angiotensin II receptor from rat liver
ChEMBL 401 7 3 7 3.2 CCc1ncc(C(=O)O)c(NCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)n1 10.1021/jm00070a012
CHEMBL1202852 205354 0 None - 1 Rat 7.2 pKi = 7.2 Binding
Binding affinity against angiotensin II receptor from rat liverBinding affinity against angiotensin II receptor from rat liver
ChEMBL 401 7 3 7 3.2 CCc1ncc(C(=O)O)c(NCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)n1 10.1021/jm00070a012
CHEMBL91953 205354 0 None - 1 Rat 7.2 pKi = 7.2 Binding
Binding affinity against angiotensin II receptor from rat liverBinding affinity against angiotensin II receptor from rat liver
ChEMBL 401 7 3 7 3.2 CCc1ncc(C(=O)O)c(NCc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)n1 10.1021/jm00070a012
9805192 90510 0 None - 1 Pig 8.2 pKi = 8.2 Binding
Displacement of [125]Ang2 from AT2 receptor in pig uterus membraneDisplacement of [125]Ang2 from AT2 receptor in pig uterus membrane
ChEMBL 480 10 1 6 4.5 CCCCOC(=O)NS(=O)(=O)c1sc(CC(C)C)cc1-c1ccc(CC(=O)N(C)C)cc1 10.1016/j.bmc.2008.05.066
CHEMBL239393 90510 0 None - 1 Pig 8.2 pKi = 8.2 Binding
Displacement of [125]Ang2 from AT2 receptor in pig uterus membraneDisplacement of [125]Ang2 from AT2 receptor in pig uterus membrane
ChEMBL 480 10 1 6 4.5 CCCCOC(=O)NS(=O)(=O)c1sc(CC(C)C)cc1-c1ccc(CC(=O)N(C)C)cc1 10.1016/j.bmc.2008.05.066
19029619 18305 0 None - 1 Rat 8.1 pKi = 8.1 Binding
Inhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranesInhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranes
ChEMBL 485 6 1 7 4.3 CCc1nn(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/c(=N/C(=O)c2ccccc2F)s1 10.1016/S0960-894X(97)00026-7
CHEMBL127343 18305 0 None - 1 Rat 8.1 pKi = 8.1 Binding
Inhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranesInhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranes
ChEMBL 485 6 1 7 4.3 CCc1nn(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/c(=N/C(=O)c2ccccc2F)s1 10.1016/S0960-894X(97)00026-7
44284094 14429 0 None - 1 Rat 8.1 pKi = 8.1 Binding
Binding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranesBinding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranes
ChEMBL 531 11 1 8 6.0 CCCCOC(=O)c1c(Cl)nc(CCCC)n1Cc1cccc2c1ccn2-c1ccccc1-c1nn[nH]n1 10.1016/S0960-894X(01)81137-9
CHEMBL1204972 14429 0 None - 1 Rat 8.1 pKi = 8.1 Binding
Binding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranesBinding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranes
ChEMBL 531 11 1 8 6.0 CCCCOC(=O)c1c(Cl)nc(CCCC)n1Cc1cccc2c1ccn2-c1ccccc1-c1nn[nH]n1 10.1016/S0960-894X(01)81137-9
CHEMBL2079782 14429 0 None - 1 Rat 8.1 pKi = 8.1 Binding
Binding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranesBinding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranes
ChEMBL 531 11 1 8 6.0 CCCCOC(=O)c1c(Cl)nc(CCCC)n1Cc1cccc2c1ccn2-c1ccccc1-c1nn[nH]n1 10.1016/S0960-894X(01)81137-9
155512629 169075 0 None - 1 Human 8.1 pKi = 8.1 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 563 15 3 5 7.0 CCCCc1nc(CC(C)C)c(CNC(=O)[C@@H](CS)CC(C)C)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/acsmedchemlett.8b00462
CHEMBL4437331 169075 0 None - 1 Human 8.1 pKi = 8.1 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 563 15 3 5 7.0 CCCCc1nc(CC(C)C)c(CNC(=O)[C@@H](CS)CC(C)C)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/acsmedchemlett.8b00462
168270996 189456 0 None -64 2 Human 6.2 pKi = 6.2 Binding
Displacement of [125-I]-[Sar1Ile8]-angiotensin II from human AT1R expressed in HEK293 cell membrane assessed as inhibition constant by radioligand binding assayDisplacement of [125-I]-[Sar1Ile8]-angiotensin II from human AT1R expressed in HEK293 cell membrane assessed as inhibition constant by radioligand binding assay
ChEMBL 533 11 1 6 6.5 CCCCOC(=O)NS(=O)(=O)c1ccc(CCC)cc1-c1ccc(Cn2c(CC)nc3ccccc32)cc1 10.1016/j.bmc.2022.116804
CHEMBL5172324 189456 0 None -64 2 Human 6.2 pKi = 6.2 Binding
Displacement of [125-I]-[Sar1Ile8]-angiotensin II from human AT1R expressed in HEK293 cell membrane assessed as inhibition constant by radioligand binding assayDisplacement of [125-I]-[Sar1Ile8]-angiotensin II from human AT1R expressed in HEK293 cell membrane assessed as inhibition constant by radioligand binding assay
ChEMBL 533 11 1 6 6.5 CCCCOC(=O)NS(=O)(=O)c1ccc(CCC)cc1-c1ccc(Cn2c(CC)nc3ccccc32)cc1 10.1016/j.bmc.2022.116804
168287782 191218 0 None -22 2 Human 6.2 pKi = 6.2 Binding
Displacement of [125-I]-[Sar1Ile8]-angiotensin II from human AT1R expressed in HEK293 cell membrane assessed as inhibition constant by radioligand binding assayDisplacement of [125-I]-[Sar1Ile8]-angiotensin II from human AT1R expressed in HEK293 cell membrane assessed as inhibition constant by radioligand binding assay
ChEMBL 545 11 1 6 6.8 CCCCOC(=O)NS(=O)(=O)c1ccc(CCC)cc1-c1ccc(Cn2c(C3CC3)nc3ccccc32)cc1 10.1016/j.bmc.2022.116804
CHEMBL5198739 191218 0 None -22 2 Human 6.2 pKi = 6.2 Binding
Displacement of [125-I]-[Sar1Ile8]-angiotensin II from human AT1R expressed in HEK293 cell membrane assessed as inhibition constant by radioligand binding assayDisplacement of [125-I]-[Sar1Ile8]-angiotensin II from human AT1R expressed in HEK293 cell membrane assessed as inhibition constant by radioligand binding assay
ChEMBL 545 11 1 6 6.8 CCCCOC(=O)NS(=O)(=O)c1ccc(CCC)cc1-c1ccc(Cn2c(C3CC3)nc3ccccc32)cc1 10.1016/j.bmc.2022.116804
18950379 14394 0 None - 1 Rat 6.1 pKi = 6.1 Binding
Binding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranesBinding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranes
ChEMBL 403 8 2 5 4.4 CCCCc1ncc(CO)n1Cc1ccc2c(ccn2-c2ccccc2C(=O)O)c1 10.1016/S0960-894X(01)81137-9
CHEMBL1204547 14394 0 None - 1 Rat 6.1 pKi = 6.1 Binding
Binding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranesBinding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranes
ChEMBL 403 8 2 5 4.4 CCCCc1ncc(CO)n1Cc1ccc2c(ccn2-c2ccccc2C(=O)O)c1 10.1016/S0960-894X(01)81137-9
CHEMBL287065 14394 0 None - 1 Rat 6.1 pKi = 6.1 Binding
Binding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranesBinding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranes
ChEMBL 403 8 2 5 4.4 CCCCc1ncc(CO)n1Cc1ccc2c(ccn2-c2ccccc2C(=O)O)c1 10.1016/S0960-894X(01)81137-9
18950381 14395 0 None - 1 Rat 7.1 pKi = 7.1 Binding
Binding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranesBinding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranes
ChEMBL 403 8 2 5 4.4 CCCCc1ncc(CO)n1Cc1cccc2c1ccn2-c1ccccc1C(=O)O 10.1016/S0960-894X(01)81137-9
CHEMBL1204548 14395 0 None - 1 Rat 7.1 pKi = 7.1 Binding
Binding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranesBinding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranes
ChEMBL 403 8 2 5 4.4 CCCCc1ncc(CO)n1Cc1cccc2c1ccn2-c1ccccc1C(=O)O 10.1016/S0960-894X(01)81137-9
CHEMBL288691 14395 0 None - 1 Rat 7.1 pKi = 7.1 Binding
Binding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranesBinding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranes
ChEMBL 403 8 2 5 4.4 CCCCc1ncc(CO)n1Cc1cccc2c1ccn2-c1ccccc1C(=O)O 10.1016/S0960-894X(01)81137-9
9806325 14424 0 None - 1 Rat 7.1 pKi = 7.1 Binding
Binding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranesBinding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranes
ChEMBL 509 8 2 7 5.1 CCCCc1nc(C(F)(F)F)c(C(=O)O)n1Cc1cccc2c1ccn2-c1ccccc1-c1nn[nH]n1 10.1016/S0960-894X(01)81137-9
CHEMBL1204952 14424 0 None - 1 Rat 7.1 pKi = 7.1 Binding
Binding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranesBinding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranes
ChEMBL 509 8 2 7 5.1 CCCCc1nc(C(F)(F)F)c(C(=O)O)n1Cc1cccc2c1ccn2-c1ccccc1-c1nn[nH]n1 10.1016/S0960-894X(01)81137-9
CHEMBL4524049 14424 0 None - 1 Rat 7.1 pKi = 7.1 Binding
Binding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranesBinding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranes
ChEMBL 509 8 2 7 5.1 CCCCc1nc(C(F)(F)F)c(C(=O)O)n1Cc1cccc2c1ccn2-c1ccccc1-c1nn[nH]n1 10.1016/S0960-894X(01)81137-9
155513439 169152 0 None - 1 Human 7.1 pKi = 7.1 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 589 13 3 5 7.3 CCCCc1nc(Cl)c(CNC(=O)C(CS)C(C)c2ccccc2)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/acsmedchemlett.8b00462
CHEMBL4438435 169152 0 None - 1 Human 7.1 pKi = 7.1 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 589 13 3 5 7.3 CCCCc1nc(Cl)c(CNC(=O)C(CS)C(C)c2ccccc2)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/acsmedchemlett.8b00462
155565351 174994 0 None - 1 Human 7.1 pKi = 7.1 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 575 13 3 5 6.7 CCCCc1nc(Cl)c(CNC(=O)C(CS)Cc2ccccc2)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/acsmedchemlett.8b00462
CHEMBL4579452 174994 0 None - 1 Human 7.1 pKi = 7.1 Binding
Displacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIADisplacement of Europium-labeled angiotensin-2 from human AT1 receptor expressed in CHOK1 cell membranes after 120 mins by DELFIA
ChEMBL 575 13 3 5 6.7 CCCCc1nc(Cl)c(CNC(=O)C(CS)Cc2ccccc2)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/acsmedchemlett.8b00462
19029624 17841 0 None - 1 Rat 7.1 pKi = 7.1 Binding
Inhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranesInhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranes
ChEMBL 481 6 1 7 4.5 CCc1nn(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/c(=N/C(=O)c2cccc(C)c2)s1 10.1016/S0960-894X(97)00026-7
CHEMBL126490 17841 0 None - 1 Rat 7.1 pKi = 7.1 Binding
Inhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranesInhibition of binding of [125I]All at the angiotensin II type 1 receptor (AT1 receptor) in rat liver membranes
ChEMBL 481 6 1 7 4.5 CCc1nn(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)/c(=N/C(=O)c2cccc(C)c2)s1 10.1016/S0960-894X(97)00026-7
10252591 203416 0 None - 1 Rat 8.1 pKi = 8.1 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 438 7 1 7 4.4 CCCc1nc(C)n2nc(CC)nc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00041a016
CHEMBL78021 203416 0 None - 1 Rat 8.1 pKi = 8.1 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 438 7 1 7 4.4 CCCc1nc(C)n2nc(CC)nc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00041a016
9935424 14497 0 None - 1 Rat 8.1 pKi = 8.1 Binding
Inhibition of [125I]- Sar,Ile8-angiotensin II binding to rat adrenal cortical membrane angiotensin II receptorInhibition of [125I]- Sar,Ile8-angiotensin II binding to rat adrenal cortical membrane angiotensin II receptor
ChEMBL 492 9 1 7 5.3 CCCCC1=NC(Cl)=C(C(=O)OCC)C(C)N1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1021/jm00103a014
CHEMBL1205739 14497 0 None - 1 Rat 8.1 pKi = 8.1 Binding
Inhibition of [125I]- Sar,Ile8-angiotensin II binding to rat adrenal cortical membrane angiotensin II receptorInhibition of [125I]- Sar,Ile8-angiotensin II binding to rat adrenal cortical membrane angiotensin II receptor
ChEMBL 492 9 1 7 5.3 CCCCC1=NC(Cl)=C(C(=O)OCC)C(C)N1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1021/jm00103a014
CHEMBL141659 14497 0 None - 1 Rat 8.1 pKi = 8.1 Binding
Inhibition of [125I]- Sar,Ile8-angiotensin II binding to rat adrenal cortical membrane angiotensin II receptorInhibition of [125I]- Sar,Ile8-angiotensin II binding to rat adrenal cortical membrane angiotensin II receptor
ChEMBL 492 9 1 7 5.3 CCCCC1=NC(Cl)=C(C(=O)OCC)C(C)N1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1 10.1021/jm00103a014
163409135 189580 2 None 37 2 Human 8.1 pKi = 8.1 Binding
Displacement of 125I-[Sar1,Ile8]ANGII form recombinant human full length AT1 receptor expressed in HEK293 cells incubated for 120 mins by scintillation counting methodDisplacement of 125I-[Sar1,Ile8]ANGII form recombinant human full length AT1 receptor expressed in HEK293 cells incubated for 120 mins by scintillation counting method
ChEMBL 623 11 1 9 6.5 CCCc1nc(-c2ccc(Cn3c(CC)nc4c(C)cc(C)nc43)cc2)c(S(=O)(=O)NC(=O)OCCCC(F)(F)F)s1 10.1016/j.bmc.2022.116790
CHEMBL5174180 189580 2 None 37 2 Human 8.1 pKi = 8.1 Binding
Displacement of 125I-[Sar1,Ile8]ANGII form recombinant human full length AT1 receptor expressed in HEK293 cells incubated for 120 mins by scintillation counting methodDisplacement of 125I-[Sar1,Ile8]ANGII form recombinant human full length AT1 receptor expressed in HEK293 cells incubated for 120 mins by scintillation counting method
ChEMBL 623 11 1 9 6.5 CCCc1nc(-c2ccc(Cn3c(CC)nc4c(C)cc(C)nc43)cc2)c(S(=O)(=O)NC(=O)OCCCC(F)(F)F)s1 10.1016/j.bmc.2022.116790
10254899 205158 0 None - 1 Human 8.1 pKi = 8.1 Binding
Ability to displace [125I]AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1Ability to displace [125I]AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1
ChEMBL 487 9 2 6 4.2 CCCCC(=O)N(Cc1ccc2c(-c3nnn[nH]3)cc3ccccc3c(=O)c2c1)[C@H](C(=O)O)C(C)C 10.1021/jm00014a024
CHEMBL90834 205158 0 None - 1 Human 8.1 pKi = 8.1 Binding
Ability to displace [125I]AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1Ability to displace [125I]AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1
ChEMBL 487 9 2 6 4.2 CCCCC(=O)N(Cc1ccc2c(-c3nnn[nH]3)cc3ccccc3c(=O)c2c1)[C@H](C(=O)O)C(C)C 10.1021/jm00014a024
11488492 93055 0 None - 1 Pig 8.1 pKi = 8.1 Binding
Displacement of [125]Ang2 from AT2 receptor in pig uterus membraneDisplacement of [125]Ang2 from AT2 receptor in pig uterus membrane
ChEMBL 480 10 1 6 4.8 CCCCOC(=O)NS(=O)(=O)c1sc(CC(C)C)cc1-c1ccc(CN(C)C(C)=O)cc1 10.1016/j.bmc.2008.05.066
CHEMBL246255 93055 0 None - 1 Pig 8.1 pKi = 8.1 Binding
Displacement of [125]Ang2 from AT2 receptor in pig uterus membraneDisplacement of [125]Ang2 from AT2 receptor in pig uterus membrane
ChEMBL 480 10 1 6 4.8 CCCCOC(=O)NS(=O)(=O)c1sc(CC(C)C)cc1-c1ccc(CN(C)C(C)=O)cc1 10.1016/j.bmc.2008.05.066
44284306 14591 0 None - 1 Rat 8.1 pKi = 8.1 Binding
Binding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranesBinding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranes
ChEMBL 631 11 1 10 6.8 CCCCc1nc(Cl)c(C(=O)OC(OC(=O)C(C)(C)C)C(C)C)n1Cc1cccc2c1ccn2-c1ccccc1-c1nn[nH]n1 10.1016/S0960-894X(01)81137-9
CHEMBL1206588 14591 0 None - 1 Rat 8.1 pKi = 8.1 Binding
Binding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranesBinding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranes
ChEMBL 631 11 1 10 6.8 CCCCc1nc(Cl)c(C(=O)OC(OC(=O)C(C)(C)C)C(C)C)n1Cc1cccc2c1ccn2-c1ccccc1-c1nn[nH]n1 10.1016/S0960-894X(01)81137-9
CHEMBL2079781 14591 0 None - 1 Rat 8.1 pKi = 8.1 Binding
Binding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranesBinding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranes
ChEMBL 631 11 1 10 6.8 CCCCc1nc(Cl)c(C(=O)OC(OC(=O)C(C)(C)C)C(C)C)n1Cc1cccc2c1ccn2-c1ccccc1-c1nn[nH]n1 10.1016/S0960-894X(01)81137-9
10884983 38058 0 None -1 2 Rat 7.1 pKi = 7.1 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
ChEMBL 458 7 1 5 4.4 CCCCN1C(=O)C2(CCCC2)CC(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm7011563
CHEMBL146275 38058 0 None -1 2 Rat 7.1 pKi = 7.1 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
ChEMBL 458 7 1 5 4.4 CCCCN1C(=O)C2(CCCC2)CC(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm7011563
10884983 38058 0 None 1 2 Human 7.1 pKi = 7.1 Binding
In vitro binding affinity towards Angiotensin II receptor, type 1 of human hepatoma cell line PLC-PRF-5In vitro binding affinity towards Angiotensin II receptor, type 1 of human hepatoma cell line PLC-PRF-5
ChEMBL 458 7 1 5 4.4 CCCCN1C(=O)C2(CCCC2)CC(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm010457z
CHEMBL146275 38058 0 None 1 2 Human 7.1 pKi = 7.1 Binding
In vitro binding affinity towards Angiotensin II receptor, type 1 of human hepatoma cell line PLC-PRF-5In vitro binding affinity towards Angiotensin II receptor, type 1 of human hepatoma cell line PLC-PRF-5
ChEMBL 458 7 1 5 4.4 CCCCN1C(=O)C2(CCCC2)CC(=O)N1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm010457z
10093827 203189 0 None - 1 Rat 7.1 pKi = 7.1 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 424 5 2 8 3.5 Cc1nc(C2CC2)c(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2nc(O)nn12 10.1021/jm00041a016
CHEMBL76079 203189 0 None - 1 Rat 7.1 pKi = 7.1 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 424 5 2 8 3.5 Cc1nc(C2CC2)c(Cc2ccc(-c3ccccc3-c3nn[nH]n3)cc2)c2nc(O)nn12 10.1021/jm00041a016
9980359 14625 0 None - 1 Rat 7.1 pKi = 7.1 Binding
Inhibition of [125I]- Sar,Ile8-angiotensin II binding to rat adrenal cortical membrane angiotensin II receptorInhibition of [125I]- Sar,Ile8-angiotensin II binding to rat adrenal cortical membrane angiotensin II receptor
ChEMBL 434 9 1 6 4.2 CCCCc1ncc(C(=O)OCC)c(=O)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00103a014
CHEMBL1207054 14625 0 None - 1 Rat 7.1 pKi = 7.1 Binding
Inhibition of [125I]- Sar,Ile8-angiotensin II binding to rat adrenal cortical membrane angiotensin II receptorInhibition of [125I]- Sar,Ile8-angiotensin II binding to rat adrenal cortical membrane angiotensin II receptor
ChEMBL 434 9 1 6 4.2 CCCCc1ncc(C(=O)OCC)c(=O)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00103a014
CHEMBL342287 14625 0 None - 1 Rat 7.1 pKi = 7.1 Binding
Inhibition of [125I]- Sar,Ile8-angiotensin II binding to rat adrenal cortical membrane angiotensin II receptorInhibition of [125I]- Sar,Ile8-angiotensin II binding to rat adrenal cortical membrane angiotensin II receptor
ChEMBL 434 9 1 6 4.2 CCCCc1ncc(C(=O)OCC)c(=O)n1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00103a014
18950396 14385 0 None - 1 Rat 6.1 pKi = 6.1 Binding
Binding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranesBinding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranes
ChEMBL 631 8 2 7 6.3 CCCCc1nc(Cl)c(C(=O)O)n1Cc1cccc2c1c(Br)c(Br)n2-c1ccccc1-c1nn[nH]n1 10.1016/S0960-894X(01)81137-9
CHEMBL1204444 14385 0 None - 1 Rat 6.1 pKi = 6.1 Binding
Binding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranesBinding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranes
ChEMBL 631 8 2 7 6.3 CCCCc1nc(Cl)c(C(=O)O)n1Cc1cccc2c1c(Br)c(Br)n2-c1ccccc1-c1nn[nH]n1 10.1016/S0960-894X(01)81137-9
CHEMBL4524048 14385 0 None - 1 Rat 6.1 pKi = 6.1 Binding
Binding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranesBinding affinity for Angiotensin II receptor, type 1 determined using [125I]- labeled [Sar1,Ile8] angiotensin II in rat adrenocortical membranes
ChEMBL 631 8 2 7 6.3 CCCCc1nc(Cl)c(C(=O)O)n1Cc1cccc2c1c(Br)c(Br)n2-c1ccccc1-c1nn[nH]n1 10.1016/S0960-894X(01)81137-9
10459016 36571 0 None - 1 Rat 6.1 pKi = 6.1 Binding
Inhibition of [125I]- Sar,Ile8-angiotensin II binding to rat adrenal cortical membrane angiotensin II receptorInhibition of [125I]- Sar,Ile8-angiotensin II binding to rat adrenal cortical membrane angiotensin II receptor
ChEMBL 510 10 1 5 6.8 CCCCC1=NC(c2ccccc2)=C(C(=O)OCC)C(C)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00103a014
CHEMBL145017 36571 0 None - 1 Rat 6.1 pKi = 6.1 Binding
Inhibition of [125I]- Sar,Ile8-angiotensin II binding to rat adrenal cortical membrane angiotensin II receptorInhibition of [125I]- Sar,Ile8-angiotensin II binding to rat adrenal cortical membrane angiotensin II receptor
ChEMBL 510 10 1 5 6.8 CCCCC1=NC(c2ccccc2)=C(C(=O)OCC)C(C)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00103a014
10368569 203733 0 None - 1 Rat 8.1 pKi = 8.1 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 496 9 1 9 3.9 CCCc1nc(C)n2nc(CC(=O)OCC)nc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00041a016
CHEMBL80380 203733 0 None - 1 Rat 8.1 pKi = 8.1 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 496 9 1 9 3.9 CCCc1nc(C)n2nc(CC(=O)OCC)nc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00041a016
127034038 138654 0 None - 1 Human 8.1 pKi = 8.1 Binding
Displacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation countingDisplacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation counting
ChEMBL 1656 46 15 20 2.5 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCN/C(N)=N/C(=O)NCCCCNC(=O)CCCCC[n+]1cc(S(=O)(=O)[O-])ccc1/C=C/c1cc2ccc(N(CC)CC)cc2oc1=O)NC(=O)[C@@H](N)CC(=O)O)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O 10.1021/acs.jmedchem.5b01495
CHEMBL3785563 138654 0 None - 1 Human 8.1 pKi = 8.1 Binding
Displacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation countingDisplacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation counting
ChEMBL 1656 46 15 20 2.5 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCN/C(N)=N/C(=O)NCCCCNC(=O)CCCCC[n+]1cc(S(=O)(=O)[O-])ccc1/C=C/c1cc2ccc(N(CC)CC)cc2oc1=O)NC(=O)[C@@H](N)CC(=O)O)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O 10.1021/acs.jmedchem.5b01495
CHEMBL3787702 138654 0 None - 1 Human 8.1 pKi = 8.1 Binding
Displacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation countingDisplacement of [3H]-Asp-{Nomega-[N-(4-propanoylaminobutyl)aminocarbonyl]}Arg-ValTyr-Ile-His-Pro-Phe-OH Tris(hydrotrifluoroacetate) from human AT1 receptor transfected in CHO cells co-expressing Galpha16-mtAEQ after 2 hrs by liquid scintillation counting
ChEMBL 1656 46 15 20 2.5 CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCN/C(N)=N/C(=O)NCCCCNC(=O)CCCCC[n+]1cc(S(=O)(=O)[O-])ccc1/C=C/c1cc2ccc(N(CC)CC)cc2oc1=O)NC(=O)[C@@H](N)CC(=O)O)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O 10.1021/acs.jmedchem.5b01495
10480064 111267 0 None - 1 Human 8.0 pKi = 8.0 Binding
Ability to displace [125I]AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1Ability to displace [125I]AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1
ChEMBL 475 9 2 6 4.5 CCCCC(=O)N(Cc1ccc2c(c1)Oc1ccccc1C=C2c1nnn[nH]1)[C@H](C(=O)O)C(C)C 10.1021/jm00014a024
CHEMBL328738 111267 0 None - 1 Human 8.0 pKi = 8.0 Binding
Ability to displace [125I]AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1Ability to displace [125I]AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1
ChEMBL 475 9 2 6 4.5 CCCCC(=O)N(Cc1ccc2c(c1)Oc1ccccc1C=C2c1nnn[nH]1)[C@H](C(=O)O)C(C)C 10.1021/jm00014a024
10027183 163689 0 None - 1 Rat 5.1 pKi = 5.1 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 458 7 2 9 3.9 CCCc1nc(SC)n2c(O)nnc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00041a016
CHEMBL421141 163689 0 None - 1 Rat 5.1 pKi = 5.1 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 458 7 2 9 3.9 CCCc1nc(SC)n2c(O)nnc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00041a016
168270075 189450 0 None - 1 Human 7.0 pKi = 7.0 Binding
Displacement of 125I-[Sar1,Ile8]ANGII form recombinant human full length AT1 receptor expressed in HEK293 cells incubated for 120 mins by scintillation counting methodDisplacement of 125I-[Sar1,Ile8]ANGII form recombinant human full length AT1 receptor expressed in HEK293 cells incubated for 120 mins by scintillation counting method
ChEMBL 541 8 1 9 5.0 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2nc(CC(C)C)sc2S(=O)(=O)NC(=O)OC)cc1 10.1016/j.bmc.2022.116790
CHEMBL5172242 189450 0 None - 1 Human 7.0 pKi = 7.0 Binding
Displacement of 125I-[Sar1,Ile8]ANGII form recombinant human full length AT1 receptor expressed in HEK293 cells incubated for 120 mins by scintillation counting methodDisplacement of 125I-[Sar1,Ile8]ANGII form recombinant human full length AT1 receptor expressed in HEK293 cells incubated for 120 mins by scintillation counting method
ChEMBL 541 8 1 9 5.0 CCc1nc2c(C)cc(C)nc2n1Cc1ccc(-c2nc(CC(C)C)sc2S(=O)(=O)NC(=O)OC)cc1 10.1016/j.bmc.2022.116790
44567884 182417 0 None - 1 Pig 7.0 pKi = 7.0 Binding
Displacement of [125]Ang2 from AT2 receptor in pig uterus membraneDisplacement of [125]Ang2 from AT2 receptor in pig uterus membrane
ChEMBL 524 11 1 6 5.8 CCCCOC(=O)NS(=O)(=O)c1ccc(Oc2ccccc2)cc1-c1ccc(C(=O)N(CC)CC)cc1 10.1016/j.bmc.2008.05.066
CHEMBL479367 182417 0 None - 1 Pig 7.0 pKi = 7.0 Binding
Displacement of [125]Ang2 from AT2 receptor in pig uterus membraneDisplacement of [125]Ang2 from AT2 receptor in pig uterus membrane
ChEMBL 524 11 1 6 5.8 CCCCOC(=O)NS(=O)(=O)c1ccc(Oc2ccccc2)cc1-c1ccc(C(=O)N(CC)CC)cc1 10.1016/j.bmc.2008.05.066
10348903 104919 0 None - 1 Rat 7.0 pKi = 7.0 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 456 8 2 9 3.4 CCCc1nc(COC)n2nc(O)nc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00041a016
CHEMBL311825 104919 0 None - 1 Rat 7.0 pKi = 7.0 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 456 8 2 9 3.4 CCCc1nc(COC)n2nc(O)nc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00041a016
145946191 166960 0 None -1096 2 Human 4.0 pKi = 4.0 Binding
Displacement of [125I]-angiotensin 2 from human angiotensin 2 type-1 receptor expressed in CHO cell membranes after 1 hr by gamma counting analysisDisplacement of [125I]-angiotensin 2 from human angiotensin 2 type-1 receptor expressed in CHO cell membranes after 1 hr by gamma counting analysis
ChEMBL 1165 26 5 14 4.5 CCN(CC)c1ccc(C(=C2C=CC(=[N+](CC)CC)C=C2)c2ccc(S(=O)(=O)NCCCC[C@H](NC(=O)Cc3csc(=N)n3C)C(=O)N[C@@H](Cc3cn(Cc4ccccc4)c[n+]3C)C(=O)NC3CCN(C)CC3)cc2S(=O)(=O)[O-])cc1 10.1021/jm401789v
CHEMBL3234454 166960 0 None -1096 2 Human 4.0 pKi = 4.0 Binding
Displacement of [125I]-angiotensin 2 from human angiotensin 2 type-1 receptor expressed in CHO cell membranes after 1 hr by gamma counting analysisDisplacement of [125I]-angiotensin 2 from human angiotensin 2 type-1 receptor expressed in CHO cell membranes after 1 hr by gamma counting analysis
ChEMBL 1165 26 5 14 4.5 CCN(CC)c1ccc(C(=C2C=CC(=[N+](CC)CC)C=C2)c2ccc(S(=O)(=O)NCCCC[C@H](NC(=O)Cc3csc(=N)n3C)C(=O)N[C@@H](Cc3cn(Cc4ccccc4)c[n+]3C)C(=O)NC3CCN(C)CC3)cc2S(=O)(=O)[O-])cc1 10.1021/jm401789v
CHEMBL4300168 166960 0 None -1096 2 Human 4.0 pKi = 4.0 Binding
Displacement of [125I]-angiotensin 2 from human angiotensin 2 type-1 receptor expressed in CHO cell membranes after 1 hr by gamma counting analysisDisplacement of [125I]-angiotensin 2 from human angiotensin 2 type-1 receptor expressed in CHO cell membranes after 1 hr by gamma counting analysis
ChEMBL 1165 26 5 14 4.5 CCN(CC)c1ccc(C(=C2C=CC(=[N+](CC)CC)C=C2)c2ccc(S(=O)(=O)NCCCC[C@H](NC(=O)Cc3csc(=N)n3C)C(=O)N[C@@H](Cc3cn(Cc4ccccc4)c[n+]3C)C(=O)NC3CCN(C)CC3)cc2S(=O)(=O)[O-])cc1 10.1021/jm401789v
10369660 203695 0 None - 1 Rat 7.0 pKi = 7 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 528 10 1 10 4.5 CCCc1nc(C)n2nc(SCC(=O)OCC)nc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00041a016
CHEMBL80161 203695 0 None - 1 Rat 7.0 pKi = 7 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
ChEMBL 528 10 1 10 4.5 CCCc1nc(C)n2nc(SCC(=O)OCC)nc2c1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 10.1021/jm00041a016
10456328 34530 0 None - 1 Rat 6.0 pKi = 6 Binding
Inhibition of [125I]- Sar,Ile8-angiotensin II binding to rat adrenal cortical membrane angiotensin II receptorInhibition of [125I]- Sar,Ile8-angiotensin II binding to rat adrenal cortical membrane angiotensin II receptor
ChEMBL 448 9 1 5 5.7 CCCCC1=NC(C)=C(C(=O)OCC)C(C)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00103a014
CHEMBL143083 34530 0 None - 1 Rat 6.0 pKi = 6 Binding
Inhibition of [125I]- Sar,Ile8-angiotensin II binding to rat adrenal cortical membrane angiotensin II receptorInhibition of [125I]- Sar,Ile8-angiotensin II binding to rat adrenal cortical membrane angiotensin II receptor
ChEMBL 448 9 1 5 5.7 CCCCC1=NC(C)=C(C(=O)OCC)C(C)N1Cc1ccc(-c2ccccc2C(=O)O)cc1 10.1021/jm00103a014
4823 93116 86 None - 0 Bovine 8.3 pIC50 = 8.3 Binding
Concentration required for 50% inhibition of binding against Angiotensin II receptor, type 1 in bovine adrenal cortexConcentration required for 50% inhibition of binding against Angiotensin II receptor, type 1 in bovine adrenal cortex
Drug Central 334 3 2 4 3.1 COc1ccc(-c2nc3cc(C4=NNC(=O)CC4C)ccc3[nH]2)cc1 None
CHEMBL24646 93116 86 None - 0 Bovine 8.3 pIC50 = 8.3 Binding
Concentration required for 50% inhibition of binding against Angiotensin II receptor, type 1 in bovine adrenal cortexConcentration required for 50% inhibition of binding against Angiotensin II receptor, type 1 in bovine adrenal cortex
Drug Central 334 3 2 4 3.1 COc1ccc(-c2nc3cc(C4=NNC(=O)CC4C)ccc3[nH]2)cc1 None
1610 2305 89 None - 4 Bovine 8.2 pIC50 = 8.2 Binding
Displacement of [125I]AngII from type 1 angiotensin 2 receptor in bovine adrenal cortexDisplacement of [125I]AngII from type 1 angiotensin 2 receptor in bovine adrenal cortex
Drug Central 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl None
3941 2305 89 None - 4 Bovine 8.2 pIC50 = 8.2 Binding
Displacement of [125I]AngII from type 1 angiotensin 2 receptor in bovine adrenal cortexDisplacement of [125I]AngII from type 1 angiotensin 2 receptor in bovine adrenal cortex
Drug Central 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl None
3961 2305 89 None - 4 Bovine 8.2 pIC50 = 8.2 Binding
Displacement of [125I]AngII from type 1 angiotensin 2 receptor in bovine adrenal cortexDisplacement of [125I]AngII from type 1 angiotensin 2 receptor in bovine adrenal cortex
Drug Central 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl None
590 2305 89 None - 4 Bovine 8.2 pIC50 = 8.2 Binding
Displacement of [125I]AngII from type 1 angiotensin 2 receptor in bovine adrenal cortexDisplacement of [125I]AngII from type 1 angiotensin 2 receptor in bovine adrenal cortex
Drug Central 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl None
CHEMBL191 2305 89 None - 4 Bovine 8.2 pIC50 = 8.2 Binding
Displacement of [125I]AngII from type 1 angiotensin 2 receptor in bovine adrenal cortexDisplacement of [125I]AngII from type 1 angiotensin 2 receptor in bovine adrenal cortex
Drug Central 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl None
DB00678 2305 89 None - 4 Bovine 8.2 pIC50 = 8.2 Binding
Displacement of [125I]AngII from type 1 angiotensin 2 receptor in bovine adrenal cortexDisplacement of [125I]AngII from type 1 angiotensin 2 receptor in bovine adrenal cortex
Drug Central 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl None
1610 2305 89 None - 4 Guinea pig 8.1 pIC50 = 8.1 Binding
In vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparationIn vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparation
Drug Central 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl None
3941 2305 89 None - 4 Guinea pig 8.1 pIC50 = 8.1 Binding
In vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparationIn vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparation
Drug Central 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl None
3961 2305 89 None - 4 Guinea pig 8.1 pIC50 = 8.1 Binding
In vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparationIn vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparation
Drug Central 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl None
590 2305 89 None - 4 Guinea pig 8.1 pIC50 = 8.1 Binding
In vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparationIn vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparation
Drug Central 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl None
CHEMBL191 2305 89 None - 4 Guinea pig 8.1 pIC50 = 8.1 Binding
In vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparationIn vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparation
Drug Central 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl None
DB00678 2305 89 None - 4 Guinea pig 8.1 pIC50 = 8.1 Binding
In vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparationIn vitro inhibition of the specific binding of [125I]angiotensin II to a guinea pig adrenal membrane preparation
Drug Central 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl None
2806 3894 109 None - 1 Rat 8.1 pIC50 = 8.1 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
Drug Central 435 10 2 5 4.2 CCCCC(=O)N([C@H](C(=O)O)C(C)C)Cc1ccc(cc1)c1ccccc1c1nnn[nH]1 None
3937 3894 109 None - 1 Rat 8.1 pIC50 = 8.1 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
Drug Central 435 10 2 5 4.2 CCCCC(=O)N([C@H](C(=O)O)C(C)C)Cc1ccc(cc1)c1ccccc1c1nnn[nH]1 None
593 3894 109 None - 1 Rat 8.1 pIC50 = 8.1 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
Drug Central 435 10 2 5 4.2 CCCCC(=O)N([C@H](C(=O)O)C(C)C)Cc1ccc(cc1)c1ccccc1c1nnn[nH]1 None
60846 3894 109 None - 1 Rat 8.1 pIC50 = 8.1 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
Drug Central 435 10 2 5 4.2 CCCCC(=O)N([C@H](C(=O)O)C(C)C)Cc1ccc(cc1)c1ccccc1c1nnn[nH]1 None
CHEMBL1069 3894 109 None - 1 Rat 8.1 pIC50 = 8.1 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
Drug Central 435 10 2 5 4.2 CCCCC(=O)N([C@H](C(=O)O)C(C)C)Cc1ccc(cc1)c1ccccc1c1nnn[nH]1 None
DB00177 3894 109 None - 1 Rat 8.1 pIC50 = 8.1 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
Drug Central 435 10 2 5 4.2 CCCCC(=O)N([C@H](C(=O)O)C(C)C)Cc1ccc(cc1)c1ccccc1c1nnn[nH]1 None
2583 3705 115 None - 1 Rat 8.1 pIC50 = 8.1 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
Drug Central 514 7 1 5 7.3 CCCc1nc2c(n1Cc1ccc(cc1)c1ccccc1C(=O)O)cc(cc2C)c1nc2c(n1C)cccc2 None
592 3705 115 None - 1 Rat 8.1 pIC50 = 8.1 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
Drug Central 514 7 1 5 7.3 CCCc1nc2c(n1Cc1ccc(cc1)c1ccccc1C(=O)O)cc(cc2C)c1nc2c(n1C)cccc2 None
65999 3705 115 None - 1 Rat 8.1 pIC50 = 8.1 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
Drug Central 514 7 1 5 7.3 CCCc1nc2c(n1Cc1ccc(cc1)c1ccccc1C(=O)O)cc(cc2C)c1nc2c(n1C)cccc2 None
CHEMBL1017 3705 115 None - 1 Rat 8.1 pIC50 = 8.1 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
Drug Central 514 7 1 5 7.3 CCCc1nc2c(n1Cc1ccc(cc1)c1ccccc1C(=O)O)cc(cc2C)c1nc2c(n1C)cccc2 None
DB00966 3705 115 None - 1 Rat 8.1 pIC50 = 8.1 Binding
Inhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparationInhibition of specific binding of [125I]angiotensin-II to angiotensin 1 receptor in rat lung membrane preparation
Drug Central 514 7 1 5 7.3 CCCc1nc2c(n1Cc1ccc(cc1)c1ccccc1C(=O)O)cc(cc2C)c1nc2c(n1C)cccc2 None
36736 3405 0 None - 3 Rat 8.1 pIC50 = 8.1 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
Drug Central None None None None None
598 3405 0 None - 3 Rat 8.1 pIC50 = 8.1 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
Drug Central None None None None None
6324663 3405 0 None - 3 Rat 8.1 pIC50 = 8.1 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
Drug Central None None None None None
CHEMBL356431 3405 0 None - 3 Rat 8.1 pIC50 = 8.1 Binding
Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membraneBinding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membrane
Drug Central None None None None None
1037 1542 65 None - 1 Human 8.1 pIC50 = 8.1 Binding
Tested for Angiotensin II receptor, type 1 affinity in the absence of bovine serum albumin (BSA)Tested for Angiotensin II receptor, type 1 affinity in the absence of bovine serum albumin (BSA)
Drug Central 424 10 2 5 4.7 CCCCc1ncc(n1Cc1ccc(cc1)C(=O)O)/C=C(/C(=O)O)\Cc1cccs1 None
3940 1542 65 None - 1 Human 8.1 pIC50 = 8.1 Binding
Tested for Angiotensin II receptor, type 1 affinity in the absence of bovine serum albumin (BSA)Tested for Angiotensin II receptor, type 1 affinity in the absence of bovine serum albumin (BSA)
Drug Central 424 10 2 5 4.7 CCCCc1ncc(n1Cc1ccc(cc1)C(=O)O)/C=C(/C(=O)O)\Cc1cccs1 None
5281037 1542 65 None - 1 Human 8.1 pIC50 = 8.1 Binding
Tested for Angiotensin II receptor, type 1 affinity in the absence of bovine serum albumin (BSA)Tested for Angiotensin II receptor, type 1 affinity in the absence of bovine serum albumin (BSA)
Drug Central 424 10 2 5 4.7 CCCCc1ncc(n1Cc1ccc(cc1)C(=O)O)/C=C(/C(=O)O)\Cc1cccs1 None
588 1542 65 None - 1 Human 8.1 pIC50 = 8.1 Binding
Tested for Angiotensin II receptor, type 1 affinity in the absence of bovine serum albumin (BSA)Tested for Angiotensin II receptor, type 1 affinity in the absence of bovine serum albumin (BSA)
Drug Central 424 10 2 5 4.7 CCCCc1ncc(n1Cc1ccc(cc1)C(=O)O)/C=C(/C(=O)O)\Cc1cccs1 None
CHEMBL813 1542 65 None - 1 Human 8.1 pIC50 = 8.1 Binding
Tested for Angiotensin II receptor, type 1 affinity in the absence of bovine serum albumin (BSA)Tested for Angiotensin II receptor, type 1 affinity in the absence of bovine serum albumin (BSA)
Drug Central 424 10 2 5 4.7 CCCCc1ncc(n1Cc1ccc(cc1)C(=O)O)/C=C(/C(=O)O)\Cc1cccs1 None
DB00876 1542 65 None - 1 Human 8.1 pIC50 = 8.1 Binding
Tested for Angiotensin II receptor, type 1 affinity in the absence of bovine serum albumin (BSA)Tested for Angiotensin II receptor, type 1 affinity in the absence of bovine serum albumin (BSA)
Drug Central 424 10 2 5 4.7 CCCCc1ncc(n1Cc1ccc(cc1)C(=O)O)/C=C(/C(=O)O)\Cc1cccs1 None
2806 3894 109 None - 1 Rat 8.1 pIC50 = 8.1 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
Drug Central 435 10 2 5 4.2 CCCCC(=O)N([C@H](C(=O)O)C(C)C)Cc1ccc(cc1)c1ccccc1c1nnn[nH]1 None
3937 3894 109 None - 1 Rat 8.1 pIC50 = 8.1 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
Drug Central 435 10 2 5 4.2 CCCCC(=O)N([C@H](C(=O)O)C(C)C)Cc1ccc(cc1)c1ccccc1c1nnn[nH]1 None
593 3894 109 None - 1 Rat 8.1 pIC50 = 8.1 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
Drug Central 435 10 2 5 4.2 CCCCC(=O)N([C@H](C(=O)O)C(C)C)Cc1ccc(cc1)c1ccccc1c1nnn[nH]1 None
60846 3894 109 None - 1 Rat 8.1 pIC50 = 8.1 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
Drug Central 435 10 2 5 4.2 CCCCC(=O)N([C@H](C(=O)O)C(C)C)Cc1ccc(cc1)c1ccccc1c1nnn[nH]1 None
CHEMBL1069 3894 109 None - 1 Rat 8.1 pIC50 = 8.1 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
Drug Central 435 10 2 5 4.2 CCCCC(=O)N([C@H](C(=O)O)C(C)C)Cc1ccc(cc1)c1ccccc1c1nnn[nH]1 None
DB00177 3894 109 None - 1 Rat 8.1 pIC50 = 8.1 Binding
Binding affinity for rat angiotensin II receptor, type 1Binding affinity for rat angiotensin II receptor, type 1
Drug Central 435 10 2 5 4.2 CCCCC(=O)N([C@H](C(=O)O)C(C)C)Cc1ccc(cc1)c1ccccc1c1nnn[nH]1 None
1037 1542 65 None - 1 Rat 8.1 pIC50 = 8.1 Binding
Tested for inhibition of [125I]- AII specific binding to rat mesenteric arteries, expressed as IC50Tested for inhibition of [125I]- AII specific binding to rat mesenteric arteries, expressed as IC50
Drug Central 424 10 2 5 4.7 CCCCc1ncc(n1Cc1ccc(cc1)C(=O)O)/C=C(/C(=O)O)\Cc1cccs1 None
3940 1542 65 None - 1 Rat 8.1 pIC50 = 8.1 Binding
Tested for inhibition of [125I]- AII specific binding to rat mesenteric arteries, expressed as IC50Tested for inhibition of [125I]- AII specific binding to rat mesenteric arteries, expressed as IC50
Drug Central 424 10 2 5 4.7 CCCCc1ncc(n1Cc1ccc(cc1)C(=O)O)/C=C(/C(=O)O)\Cc1cccs1 None
5281037 1542 65 None - 1 Rat 8.1 pIC50 = 8.1 Binding
Tested for inhibition of [125I]- AII specific binding to rat mesenteric arteries, expressed as IC50Tested for inhibition of [125I]- AII specific binding to rat mesenteric arteries, expressed as IC50
Drug Central 424 10 2 5 4.7 CCCCc1ncc(n1Cc1ccc(cc1)C(=O)O)/C=C(/C(=O)O)\Cc1cccs1 None
588 1542 65 None - 1 Rat 8.1 pIC50 = 8.1 Binding
Tested for inhibition of [125I]- AII specific binding to rat mesenteric arteries, expressed as IC50Tested for inhibition of [125I]- AII specific binding to rat mesenteric arteries, expressed as IC50
Drug Central 424 10 2 5 4.7 CCCCc1ncc(n1Cc1ccc(cc1)C(=O)O)/C=C(/C(=O)O)\Cc1cccs1 None
CHEMBL813 1542 65 None - 1 Rat 8.1 pIC50 = 8.1 Binding
Tested for inhibition of [125I]- AII specific binding to rat mesenteric arteries, expressed as IC50Tested for inhibition of [125I]- AII specific binding to rat mesenteric arteries, expressed as IC50
Drug Central 424 10 2 5 4.7 CCCCc1ncc(n1Cc1ccc(cc1)C(=O)O)/C=C(/C(=O)O)\Cc1cccs1 None
DB00876 1542 65 None - 1 Rat 8.1 pIC50 = 8.1 Binding
Tested for inhibition of [125I]- AII specific binding to rat mesenteric arteries, expressed as IC50Tested for inhibition of [125I]- AII specific binding to rat mesenteric arteries, expressed as IC50
Drug Central 424 10 2 5 4.7 CCCCc1ncc(n1Cc1ccc(cc1)C(=O)O)/C=C(/C(=O)O)\Cc1cccs1 None
2540 4320 102 None - 4 Human 8.0 pIC50 = 8.0 Binding
Displacement of [3H]-Angiotensin 2 from human AT1 receptor transfected in CHOK1 cells preincubated for 30 mins with bovine serum albumin followed by radioligand addition by liquid scintillation countingDisplacement of [3H]-Angiotensin 2 from human AT1 receptor transfected in CHOK1 cells preincubated for 30 mins with bovine serum albumin followed by radioligand addition by liquid scintillation counting
Drug Central 610 10 1 11 6.3 CCOc1nc2cccc(C(=O)OC(C)OC(=O)OC3CCCCC3)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 None
CHEMBL1014 4320 102 None - 4 Human 8.0 pIC50 = 8.0 Binding
Displacement of [3H]-Angiotensin 2 from human AT1 receptor transfected in CHOK1 cells preincubated for 30 mins with bovine serum albumin followed by radioligand addition by liquid scintillation countingDisplacement of [3H]-Angiotensin 2 from human AT1 receptor transfected in CHOK1 cells preincubated for 30 mins with bovine serum albumin followed by radioligand addition by liquid scintillation counting
Drug Central 610 10 1 11 6.3 CCOc1nc2cccc(C(=O)OC(C)OC(=O)OC3CCCCC3)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 None
2583 3705 115 None - 1 Human 8.0 pIC50 = 8.0 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation countingDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation counting
Drug Central 514 7 1 5 7.3 CCCc1nc2c(n1Cc1ccc(cc1)c1ccccc1C(=O)O)cc(cc2C)c1nc2c(n1C)cccc2 None
592 3705 115 None - 1 Human 8.0 pIC50 = 8.0 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation countingDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation counting
Drug Central 514 7 1 5 7.3 CCCc1nc2c(n1Cc1ccc(cc1)c1ccccc1C(=O)O)cc(cc2C)c1nc2c(n1C)cccc2 None
65999 3705 115 None - 1 Human 8.0 pIC50 = 8.0 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation countingDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation counting
Drug Central 514 7 1 5 7.3 CCCc1nc2c(n1Cc1ccc(cc1)c1ccccc1C(=O)O)cc(cc2C)c1nc2c(n1C)cccc2 None
CHEMBL1017 3705 115 None - 1 Human 8.0 pIC50 = 8.0 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation countingDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation counting
Drug Central 514 7 1 5 7.3 CCCc1nc2c(n1Cc1ccc(cc1)c1ccccc1C(=O)O)cc(cc2C)c1nc2c(n1C)cccc2 None
DB00966 3705 115 None - 1 Human 8.0 pIC50 = 8.0 Binding
Displacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation countingDisplacement of [125I]Tyr4-Sar1,Ile8-Angiotensin II from human Angiotensin 1 receptor after 60 mins by scintillation counting
Drug Central 514 7 1 5 7.3 CCCc1nc2c(n1Cc1ccc(cc1)c1ccccc1C(=O)O)cc(cc2C)c1nc2c(n1C)cccc2 None
16133225 415 47 None -4 6 Rat 8.0 pIC50 = 8.0 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
Drug Central None None None None None
172198 415 47 None -4 6 Rat 8.0 pIC50 = 8.0 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
Drug Central None None None None None
2504 415 47 None -4 6 Rat 8.0 pIC50 = 8.0 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
Drug Central None None None None None
45266664 415 47 None -4 6 Rat 8.0 pIC50 = 8.0 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
Drug Central None None None None None
5272 415 47 None -4 6 Rat 8.0 pIC50 = 8.0 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
Drug Central None None None None None
CHEMBL408403 415 47 None -4 6 Rat 8.0 pIC50 = 8.0 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
Drug Central None None None None None
DB11842 415 47 None -4 6 Rat 8.0 pIC50 = 8.0 Binding
Displacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membraneDisplacement of [125I]Sar1,Ile8-Ang2 from AT1 receptor in Wistar rat hepatic membrane
Drug Central None None None None None
16133225 415 47 None -34 6 Bovine 8.1 pKd = 8.1 Binding
Dissociation constant for [125 I] Ang binding to type 1 Angiotensin II receptor of bovine adrenocortical membranesDissociation constant for [125 I] Ang binding to type 1 Angiotensin II receptor of bovine adrenocortical membranes
Drug Central None None None None None
172198 415 47 None -34 6 Bovine 8.1 pKd = 8.1 Binding
Dissociation constant for [125 I] Ang binding to type 1 Angiotensin II receptor of bovine adrenocortical membranesDissociation constant for [125 I] Ang binding to type 1 Angiotensin II receptor of bovine adrenocortical membranes
Drug Central None None None None None
2504 415 47 None -34 6 Bovine 8.1 pKd = 8.1 Binding
Dissociation constant for [125 I] Ang binding to type 1 Angiotensin II receptor of bovine adrenocortical membranesDissociation constant for [125 I] Ang binding to type 1 Angiotensin II receptor of bovine adrenocortical membranes
Drug Central None None None None None
45266664 415 47 None -34 6 Bovine 8.1 pKd = 8.1 Binding
Dissociation constant for [125 I] Ang binding to type 1 Angiotensin II receptor of bovine adrenocortical membranesDissociation constant for [125 I] Ang binding to type 1 Angiotensin II receptor of bovine adrenocortical membranes
Drug Central None None None None None
5272 415 47 None -34 6 Bovine 8.1 pKd = 8.1 Binding
Dissociation constant for [125 I] Ang binding to type 1 Angiotensin II receptor of bovine adrenocortical membranesDissociation constant for [125 I] Ang binding to type 1 Angiotensin II receptor of bovine adrenocortical membranes
Drug Central None None None None None
CHEMBL408403 415 47 None -34 6 Bovine 8.1 pKd = 8.1 Binding
Dissociation constant for [125 I] Ang binding to type 1 Angiotensin II receptor of bovine adrenocortical membranesDissociation constant for [125 I] Ang binding to type 1 Angiotensin II receptor of bovine adrenocortical membranes
Drug Central None None None None None
DB11842 415 47 None -34 6 Bovine 8.1 pKd = 8.1 Binding
Dissociation constant for [125 I] Ang binding to type 1 Angiotensin II receptor of bovine adrenocortical membranesDissociation constant for [125 I] Ang binding to type 1 Angiotensin II receptor of bovine adrenocortical membranes
Drug Central None None None None None
1610 2305 89 None -1 4 Rabbit 8.1 pKd = 8.1 Binding
In vitro binding affinity against Angiotensin II receptor in rabbit aorta ringsIn vitro binding affinity against Angiotensin II receptor in rabbit aorta rings
Drug Central 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl None
3941 2305 89 None -1 4 Rabbit 8.1 pKd = 8.1 Binding
In vitro binding affinity against Angiotensin II receptor in rabbit aorta ringsIn vitro binding affinity against Angiotensin II receptor in rabbit aorta rings
Drug Central 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl None
3961 2305 89 None -1 4 Rabbit 8.1 pKd = 8.1 Binding
In vitro binding affinity against Angiotensin II receptor in rabbit aorta ringsIn vitro binding affinity against Angiotensin II receptor in rabbit aorta rings
Drug Central 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl None
590 2305 89 None -1 4 Rabbit 8.1 pKd = 8.1 Binding
In vitro binding affinity against Angiotensin II receptor in rabbit aorta ringsIn vitro binding affinity against Angiotensin II receptor in rabbit aorta rings
Drug Central 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl None
CHEMBL191 2305 89 None -1 4 Rabbit 8.1 pKd = 8.1 Binding
In vitro binding affinity against Angiotensin II receptor in rabbit aorta ringsIn vitro binding affinity against Angiotensin II receptor in rabbit aorta rings
Drug Central 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl None
DB00678 2305 89 None -1 4 Rabbit 8.1 pKd = 8.1 Binding
In vitro binding affinity against Angiotensin II receptor in rabbit aorta ringsIn vitro binding affinity against Angiotensin II receptor in rabbit aorta rings
Drug Central 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl None
2541 772 113 None -1 6 Human 10.3 pKd = 10.3 Binding
UnclassifiedUnclassified
Guide to Pharmacology 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10079018
587 772 113 None -1 6 Human 10.3 pKd = 10.3 Binding
UnclassifiedUnclassified
Guide to Pharmacology 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10079018
6907 772 113 None -1 6 Human 10.3 pKd = 10.3 Binding
UnclassifiedUnclassified
Guide to Pharmacology 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10079018
CHEMBL1016 772 113 None -1 6 Human 10.3 pKd = 10.3 Binding
UnclassifiedUnclassified
Guide to Pharmacology 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10079018
DB00796 772 113 None -1 6 Human 10.3 pKd = 10.3 Binding
UnclassifiedUnclassified
Guide to Pharmacology 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10079018
DB13919 772 113 None -1 6 Human 10.3 pKd = 10.3 Binding
UnclassifiedUnclassified
Guide to Pharmacology 440 7 2 7 4.0 CCOc1nc2c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)c(ccc2)C(=O)O 10079018
6916 3414 0 None - 1 Human 6.5 pKd = 6.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 11901215
6914 3415 0 None - 1 Human 6.5 pKd = 6.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 12949261
6903 3411 0 None - 1 Rat 7.1 pKd = 7.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 10066768
6903 3411 0 None - 1 Rat 7.1 pKd = 7.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 11901215
3082475 3804 9 None - 1 Human 7.7 pKd = 7.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 20801892
6902 3804 9 None - 1 Human 7.7 pKd = 7.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 20801892
CHEMBL4297447 3804 9 None - 1 Human 7.7 pKd = 7.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 20801892
DB12199 3804 9 None - 1 Human 7.7 pKd = 7.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 20801892
1610 2305 89 None -1 4 Rat 8.2 pKd = 8.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 8282008
3941 2305 89 None -1 4 Rat 8.2 pKd = 8.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 8282008
3961 2305 89 None -1 4 Rat 8.2 pKd = 8.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 8282008
590 2305 89 None -1 4 Rat 8.2 pKd = 8.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 8282008
CHEMBL191 2305 89 None -1 4 Rat 8.2 pKd = 8.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 8282008
DB00678 2305 89 None -1 4 Rat 8.2 pKd = 8.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl 8282008
1481 2027 109 None 1 3 Human 8.7 pKd = 8.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 11967808
3749 2027 109 None 1 3 Human 8.7 pKd = 8.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 11967808
589 2027 109 None 1 3 Human 8.7 pKd = 8.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 11967808
6908 2027 109 None 1 3 Human 8.7 pKd = 8.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 11967808
CHEMBL1513 2027 109 None 1 3 Human 8.7 pKd = 8.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 11967808
DB01029 2027 109 None 1 3 Human 8.7 pKd = 8.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 11967808
6915 3410 0 None - 1 Human 9.1 pKd = 9.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 11901215
1037 1542 65 None - 1 Rat 9.1 pKd = 9.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology 424 10 2 5 4.7 CCCCc1ncc(n1Cc1ccc(cc1)C(=O)O)/C=C(/C(=O)O)\Cc1cccs1 8463997
3940 1542 65 None - 1 Rat 9.1 pKd = 9.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology 424 10 2 5 4.7 CCCCc1ncc(n1Cc1ccc(cc1)C(=O)O)/C=C(/C(=O)O)\Cc1cccs1 8463997
5281037 1542 65 None - 1 Rat 9.1 pKd = 9.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology 424 10 2 5 4.7 CCCCc1ncc(n1Cc1ccc(cc1)C(=O)O)/C=C(/C(=O)O)\Cc1cccs1 8463997
588 1542 65 None - 1 Rat 9.1 pKd = 9.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology 424 10 2 5 4.7 CCCCc1ncc(n1Cc1ccc(cc1)C(=O)O)/C=C(/C(=O)O)\Cc1cccs1 8463997
CHEMBL813 1542 65 None - 1 Rat 9.1 pKd = 9.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology 424 10 2 5 4.7 CCCCc1ncc(n1Cc1ccc(cc1)C(=O)O)/C=C(/C(=O)O)\Cc1cccs1 8463997
DB00876 1542 65 None - 1 Rat 9.1 pKd = 9.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology 424 10 2 5 4.7 CCCCc1ncc(n1Cc1ccc(cc1)C(=O)O)/C=C(/C(=O)O)\Cc1cccs1 8463997
6904 3412 0 None - 1 Rat 9.3 pKd = 9.3 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 10066768
6904 3412 0 None - 1 Rat 9.3 pKd = 9.3 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 11901215
6905 3416 0 None - 1 Human 9.4 pKd = 9.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 11901215
None 214394 0 125I-Angiotensin II - 1 Rat 9.2 pKi = 9.2 Binding
NoneNone
PDSP KiDatabase 395 4 1 6 4.4 CCC1=NC2=C(N1C3=CC=C(C=C3)C4=CC=CC=C4C5=NNN=N5)N=C(C=C2C)C None
16133225 415 47 125I-Angiotensin II -4 6 Rat 9.0 pKi = 9.0 Binding
NoneNone
PDSP KiDatabase None None None None None
172198 415 47 125I-Angiotensin II -4 6 Rat 9.0 pKi = 9.0 Binding
NoneNone
PDSP KiDatabase None None None None None
2504 415 47 125I-Angiotensin II -4 6 Rat 9.0 pKi = 9.0 Binding
NoneNone
PDSP KiDatabase None None None None None
45266664 415 47 125I-Angiotensin II -4 6 Rat 9.0 pKi = 9.0 Binding
NoneNone
PDSP KiDatabase None None None None None
5272 415 47 125I-Angiotensin II -4 6 Rat 9.0 pKi = 9.0 Binding
NoneNone
PDSP KiDatabase None None None None None
CHEMBL408403 415 47 125I-Angiotensin II -4 6 Rat 9.0 pKi = 9.0 Binding
NoneNone
PDSP KiDatabase None None None None None
DB11842 415 47 125I-Angiotensin II -4 6 Rat 9.0 pKi = 9.0 Binding
NoneNone
PDSP KiDatabase None None None None None
36736 3405 0 125I-Angiotensin II 5 3 Rat 8.8 pKi = 8.8 Binding
NoneNone
PDSP KiDatabase None None None None None
598 3405 0 125I-Angiotensin II 5 3 Rat 8.8 pKi = 8.8 Binding
NoneNone
PDSP KiDatabase None None None None None
6324663 3405 0 125I-Angiotensin II 5 3 Rat 8.8 pKi = 8.8 Binding
NoneNone
PDSP KiDatabase None None None None None
CHEMBL356431 3405 0 125I-Angiotensin II 5 3 Rat 8.8 pKi = 8.8 Binding
NoneNone
PDSP KiDatabase None None None None None
179 396 107 3H-angiotensin II -4365 51 Human 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 369 7 2 6 1.3 CCN1CCCC1CNC(=O)c1cc(c(cc1OC)N)S(=O)(=O)CC None
2159 396 107 3H-angiotensin II -4365 51 Human 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 369 7 2 6 1.3 CCN1CCCC1CNC(=O)c1cc(c(cc1OC)N)S(=O)(=O)CC None
963 396 107 3H-angiotensin II -4365 51 Human 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 369 7 2 6 1.3 CCN1CCCC1CNC(=O)c1cc(c(cc1OC)N)S(=O)(=O)CC None
CHEMBL243712 396 107 3H-angiotensin II -4365 51 Human 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 369 7 2 6 1.3 CCN1CCCC1CNC(=O)c1cc(c(cc1OC)N)S(=O)(=O)CC None
DB06288 396 107 3H-angiotensin II -4365 51 Human 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 369 7 2 6 1.3 CCN1CCCC1CNC(=O)c1cc(c(cc1OC)N)S(=O)(=O)CC None
135398737 942 89 3H-angiotensin II -4168 92 Human 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 326 0 1 4 3.7 CN1CCN(CC1)C1=Nc2cc(Cl)ccc2Nc2c1cccc2 None
38 942 89 3H-angiotensin II -4168 92 Human 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 326 0 1 4 3.7 CN1CCN(CC1)C1=Nc2cc(Cl)ccc2Nc2c1cccc2 None
722 942 89 3H-angiotensin II -4168 92 Human 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 326 0 1 4 3.7 CN1CCN(CC1)C1=Nc2cc(Cl)ccc2Nc2c1cccc2 None
CHEMBL42 942 89 3H-angiotensin II -4168 92 Human 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 326 0 1 4 3.7 CN1CCN(CC1)C1=Nc2cc(Cl)ccc2Nc2c1cccc2 None
DB00363 942 89 3H-angiotensin II -4168 92 Human 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 326 0 1 4 3.7 CN1CCN(CC1)C1=Nc2cc(Cl)ccc2Nc2c1cccc2 None
1353 1872 85 3H-angiotensin II -6918 86 Human 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 375 6 1 3 4.4 Fc1ccc(cc1)C(=O)CCCN1CCC(CC1)(O)c1ccc(cc1)Cl None
3559 1872 85 3H-angiotensin II -6918 86 Human 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 375 6 1 3 4.4 Fc1ccc(cc1)C(=O)CCCN1CCC(CC1)(O)c1ccc(cc1)Cl None
86 1872 85 3H-angiotensin II -6918 86 Human 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 375 6 1 3 4.4 Fc1ccc(cc1)C(=O)CCCN1CCC(CC1)(O)c1ccc(cc1)Cl None
CHEMBL54 1872 85 3H-angiotensin II -6918 86 Human 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 375 6 1 3 4.4 Fc1ccc(cc1)C(=O)CCCN1CCC(CC1)(O)c1ccc(cc1)Cl None
DB00502 1872 85 3H-angiotensin II -6918 86 Human 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 375 6 1 3 4.4 Fc1ccc(cc1)C(=O)CCCN1CCC(CC1)(O)c1ccc(cc1)Cl None
1973 201781 12 125I-[SAR1, ILe8]-AII -3 37 Rat 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 462 3 1 7 3.9 Nc1ncnc2nc(-c3ccc(N4CCOCC4)nc3)cc(-c3cccc(Br)c3)c12 None
CHEMBL1394464 201781 12 125I-[SAR1, ILe8]-AII -3 37 Rat 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 462 3 1 7 3.9 Nc1ncnc2nc(-c3ccc(N4CCOCC4)nc3)cc(-c3cccc(Br)c3)c12 None
CHEMBL66089 201781 12 125I-[SAR1, ILe8]-AII -3 37 Rat 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 462 3 1 7 3.9 Nc1ncnc2nc(-c3ccc(N4CCOCC4)nc3)cc(-c3cccc(Br)c3)c12 None
1610 2305 89 125I-Angiotensin II -1 4 Rat 7.9 pKi = 7.9 Binding
NoneNone
PDSP KiDatabase 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl None
3941 2305 89 125I-Angiotensin II -1 4 Rat 7.9 pKi = 7.9 Binding
NoneNone
PDSP KiDatabase 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl None
3961 2305 89 125I-Angiotensin II -1 4 Rat 7.9 pKi = 7.9 Binding
NoneNone
PDSP KiDatabase 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl None
590 2305 89 125I-Angiotensin II -1 4 Rat 7.9 pKi = 7.9 Binding
NoneNone
PDSP KiDatabase 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl None
CHEMBL191 2305 89 125I-Angiotensin II -1 4 Rat 7.9 pKi = 7.9 Binding
NoneNone
PDSP KiDatabase 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl None
DB00678 2305 89 125I-Angiotensin II -1 4 Rat 7.9 pKi = 7.9 Binding
NoneNone
PDSP KiDatabase 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl None
None 214393 0 125I-Angiotensin II - 1 Rat 8.5 pKi = 8.5 Binding
NoneNone
PDSP KiDatabase 424 10 2 5 4.7 CCCCC1=NC=C(N1CC2=CC=C(C=C2)C(=O)O)C=C(CC3=CC=CS3)C(=O)O None
2806 3894 109 None - 1 Human 8.3 pKi = 8.3 Binding
Inhibition constant against Angiotensin II receptor, type 1 was determinedInhibition constant against Angiotensin II receptor, type 1 was determined
Drug Central 435 10 2 5 4.2 CCCCC(=O)N([C@H](C(=O)O)C(C)C)Cc1ccc(cc1)c1ccccc1c1nnn[nH]1 None
3937 3894 109 None - 1 Human 8.3 pKi = 8.3 Binding
Inhibition constant against Angiotensin II receptor, type 1 was determinedInhibition constant against Angiotensin II receptor, type 1 was determined
Drug Central 435 10 2 5 4.2 CCCCC(=O)N([C@H](C(=O)O)C(C)C)Cc1ccc(cc1)c1ccccc1c1nnn[nH]1 None
593 3894 109 None - 1 Human 8.3 pKi = 8.3 Binding
Inhibition constant against Angiotensin II receptor, type 1 was determinedInhibition constant against Angiotensin II receptor, type 1 was determined
Drug Central 435 10 2 5 4.2 CCCCC(=O)N([C@H](C(=O)O)C(C)C)Cc1ccc(cc1)c1ccccc1c1nnn[nH]1 None
60846 3894 109 None - 1 Human 8.3 pKi = 8.3 Binding
Inhibition constant against Angiotensin II receptor, type 1 was determinedInhibition constant against Angiotensin II receptor, type 1 was determined
Drug Central 435 10 2 5 4.2 CCCCC(=O)N([C@H](C(=O)O)C(C)C)Cc1ccc(cc1)c1ccccc1c1nnn[nH]1 None
CHEMBL1069 3894 109 None - 1 Human 8.3 pKi = 8.3 Binding
Inhibition constant against Angiotensin II receptor, type 1 was determinedInhibition constant against Angiotensin II receptor, type 1 was determined
Drug Central 435 10 2 5 4.2 CCCCC(=O)N([C@H](C(=O)O)C(C)C)Cc1ccc(cc1)c1ccccc1c1nnn[nH]1 None
DB00177 3894 109 None - 1 Human 8.3 pKi = 8.3 Binding
Inhibition constant against Angiotensin II receptor, type 1 was determinedInhibition constant against Angiotensin II receptor, type 1 was determined
Drug Central 435 10 2 5 4.2 CCCCC(=O)N([C@H](C(=O)O)C(C)C)Cc1ccc(cc1)c1ccccc1c1nnn[nH]1 None
1610 2305 89 None -1 4 Rat 8.1 pKi = 8.1 Binding
Binding affinity against angiotensin II receptor from rat liver; n=8Binding affinity against angiotensin II receptor from rat liver; n=8
Drug Central 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl None
3941 2305 89 None -1 4 Rat 8.1 pKi = 8.1 Binding
Binding affinity against angiotensin II receptor from rat liver; n=8Binding affinity against angiotensin II receptor from rat liver; n=8
Drug Central 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl None
3961 2305 89 None -1 4 Rat 8.1 pKi = 8.1 Binding
Binding affinity against angiotensin II receptor from rat liver; n=8Binding affinity against angiotensin II receptor from rat liver; n=8
Drug Central 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl None
590 2305 89 None -1 4 Rat 8.1 pKi = 8.1 Binding
Binding affinity against angiotensin II receptor from rat liver; n=8Binding affinity against angiotensin II receptor from rat liver; n=8
Drug Central 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl None
CHEMBL191 2305 89 None -1 4 Rat 8.1 pKi = 8.1 Binding
Binding affinity against angiotensin II receptor from rat liver; n=8Binding affinity against angiotensin II receptor from rat liver; n=8
Drug Central 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl None
DB00678 2305 89 None -1 4 Rat 8.1 pKi = 8.1 Binding
Binding affinity against angiotensin II receptor from rat liver; n=8Binding affinity against angiotensin II receptor from rat liver; n=8
Drug Central 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl None
1610 2305 89 None -1 4 Rat 8.1 pKi = 8.1 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
Drug Central 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl None
3941 2305 89 None -1 4 Rat 8.1 pKi = 8.1 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
Drug Central 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl None
3961 2305 89 None -1 4 Rat 8.1 pKi = 8.1 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
Drug Central 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl None
590 2305 89 None -1 4 Rat 8.1 pKi = 8.1 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
Drug Central 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl None
CHEMBL191 2305 89 None -1 4 Rat 8.1 pKi = 8.1 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
Drug Central 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl None
DB00678 2305 89 None -1 4 Rat 8.1 pKi = 8.1 Binding
Displacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptorDisplacement of [125I]-Sar1-Ile8-A II from rat adrenal Angiotensin-1 (AT-1) receptor
Drug Central 422 8 2 6 4.3 CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CO)Cl None
1481 2027 109 None -1 3 Rat 8.0 pKi = 8.0 Binding
Compound was evaluated for its binding affinity towards rat Angiotensin II receptor, type 1Compound was evaluated for its binding affinity towards rat Angiotensin II receptor, type 1
Drug Central 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 None
3749 2027 109 None -1 3 Rat 8.0 pKi = 8.0 Binding
Compound was evaluated for its binding affinity towards rat Angiotensin II receptor, type 1Compound was evaluated for its binding affinity towards rat Angiotensin II receptor, type 1
Drug Central 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 None
589 2027 109 None -1 3 Rat 8.0 pKi = 8.0 Binding
Compound was evaluated for its binding affinity towards rat Angiotensin II receptor, type 1Compound was evaluated for its binding affinity towards rat Angiotensin II receptor, type 1
Drug Central 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 None
6908 2027 109 None -1 3 Rat 8.0 pKi = 8.0 Binding
Compound was evaluated for its binding affinity towards rat Angiotensin II receptor, type 1Compound was evaluated for its binding affinity towards rat Angiotensin II receptor, type 1
Drug Central 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 None
CHEMBL1513 2027 109 None -1 3 Rat 8.0 pKi = 8.0 Binding
Compound was evaluated for its binding affinity towards rat Angiotensin II receptor, type 1Compound was evaluated for its binding affinity towards rat Angiotensin II receptor, type 1
Drug Central 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 None
DB01029 2027 109 None -1 3 Rat 8.0 pKi = 8.0 Binding
Compound was evaluated for its binding affinity towards rat Angiotensin II receptor, type 1Compound was evaluated for its binding affinity towards rat Angiotensin II receptor, type 1
Drug Central 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 None
1481 2027 109 None 1 3 Human 8.0 pKi = 8.0 Binding
Inhibitory concentration against angiotensin II receptor, type 1Inhibitory concentration against angiotensin II receptor, type 1
Drug Central 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 None
3749 2027 109 None 1 3 Human 8.0 pKi = 8.0 Binding
Inhibitory concentration against angiotensin II receptor, type 1Inhibitory concentration against angiotensin II receptor, type 1
Drug Central 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 None
589 2027 109 None 1 3 Human 8.0 pKi = 8.0 Binding
Inhibitory concentration against angiotensin II receptor, type 1Inhibitory concentration against angiotensin II receptor, type 1
Drug Central 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 None
6908 2027 109 None 1 3 Human 8.0 pKi = 8.0 Binding
Inhibitory concentration against angiotensin II receptor, type 1Inhibitory concentration against angiotensin II receptor, type 1
Drug Central 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 None
CHEMBL1513 2027 109 None 1 3 Human 8.0 pKi = 8.0 Binding
Inhibitory concentration against angiotensin II receptor, type 1Inhibitory concentration against angiotensin II receptor, type 1
Drug Central 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 None
DB01029 2027 109 None 1 3 Human 8.0 pKi = 8.0 Binding
Inhibitory concentration against angiotensin II receptor, type 1Inhibitory concentration against angiotensin II receptor, type 1
Drug Central 428 7 1 5 4.8 CCCCC1=NC2(C(=O)N1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)CCCC2 None
2540 4320 102 None -1 4 Rabbit 8.0 pKi = 8.0 Binding
NoneNone
Drug Central 610 10 1 11 6.3 CCOc1nc2cccc(C(=O)OC(C)OC(=O)OC3CCCCC3)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 None
CHEMBL1014 4320 102 None -1 4 Rabbit 8.0 pKi = 8.0 Binding
NoneNone
Drug Central 610 10 1 11 6.3 CCOc1nc2cccc(C(=O)OC(C)OC(=O)OC3CCCCC3)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1 None
16133225 415 47 None -7 6 Rat 8.0 pKi = 8.0 Binding
In vitro binding affinity at rat liver Angiotensin II receptor, type 1 was determined based on displacement of [125I]-Ang IIIn vitro binding affinity at rat liver Angiotensin II receptor, type 1 was determined based on displacement of [125I]-Ang II
Drug Central None None None None None
172198 415 47 None -7 6 Rat 8.0 pKi = 8.0 Binding
In vitro binding affinity at rat liver Angiotensin II receptor, type 1 was determined based on displacement of [125I]-Ang IIIn vitro binding affinity at rat liver Angiotensin II receptor, type 1 was determined based on displacement of [125I]-Ang II
Drug Central None None None None None
2504 415 47 None -7 6 Rat 8.0 pKi = 8.0 Binding
In vitro binding affinity at rat liver Angiotensin II receptor, type 1 was determined based on displacement of [125I]-Ang IIIn vitro binding affinity at rat liver Angiotensin II receptor, type 1 was determined based on displacement of [125I]-Ang II
Drug Central None None None None None
45266664 415 47 None -7 6 Rat 8.0 pKi = 8.0 Binding
In vitro binding affinity at rat liver Angiotensin II receptor, type 1 was determined based on displacement of [125I]-Ang IIIn vitro binding affinity at rat liver Angiotensin II receptor, type 1 was determined based on displacement of [125I]-Ang II
Drug Central None None None None None
5272 415 47 None -7 6 Rat 8.0 pKi = 8.0 Binding
In vitro binding affinity at rat liver Angiotensin II receptor, type 1 was determined based on displacement of [125I]-Ang IIIn vitro binding affinity at rat liver Angiotensin II receptor, type 1 was determined based on displacement of [125I]-Ang II
Drug Central None None None None None
CHEMBL408403 415 47 None -7 6 Rat 8.0 pKi = 8.0 Binding
In vitro binding affinity at rat liver Angiotensin II receptor, type 1 was determined based on displacement of [125I]-Ang IIIn vitro binding affinity at rat liver Angiotensin II receptor, type 1 was determined based on displacement of [125I]-Ang II
Drug Central None None None None None
DB11842 415 47 None -7 6 Rat 8.0 pKi = 8.0 Binding
In vitro binding affinity at rat liver Angiotensin II receptor, type 1 was determined based on displacement of [125I]-Ang IIIn vitro binding affinity at rat liver Angiotensin II receptor, type 1 was determined based on displacement of [125I]-Ang II
Drug Central None None None None None
1056 3307 111 None - 1 Rat 8.0 pKi = 8.0 Binding
Displacement of [125I]-SI-Ang-2 from AT1 receptor in Rattus norvegicus Sprague-Dawley (rat) liver membranes after 2 hrDisplacement of [125I]-SI-Ang-2 from AT1 receptor in Rattus norvegicus Sprague-Dawley (rat) liver membranes after 2 hr
Drug Central 357 7 1 6 2.5 O=C1NC(=O)C(S1)Cc1ccc(cc1)OCCN(c1ccccn1)C None
2405 3307 111 None - 1 Rat 8.0 pKi = 8.0 Binding
Displacement of [125I]-SI-Ang-2 from AT1 receptor in Rattus norvegicus Sprague-Dawley (rat) liver membranes after 2 hrDisplacement of [125I]-SI-Ang-2 from AT1 receptor in Rattus norvegicus Sprague-Dawley (rat) liver membranes after 2 hr
Drug Central 357 7 1 6 2.5 O=C1NC(=O)C(S1)Cc1ccc(cc1)OCCN(c1ccccn1)C None
77999 3307 111 None - 1 Rat 8.0 pKi = 8.0 Binding
Displacement of [125I]-SI-Ang-2 from AT1 receptor in Rattus norvegicus Sprague-Dawley (rat) liver membranes after 2 hrDisplacement of [125I]-SI-Ang-2 from AT1 receptor in Rattus norvegicus Sprague-Dawley (rat) liver membranes after 2 hr
Drug Central 357 7 1 6 2.5 O=C1NC(=O)C(S1)Cc1ccc(cc1)OCCN(c1ccccn1)C None
CHEMBL121 3307 111 None - 1 Rat 8.0 pKi = 8.0 Binding
Displacement of [125I]-SI-Ang-2 from AT1 receptor in Rattus norvegicus Sprague-Dawley (rat) liver membranes after 2 hrDisplacement of [125I]-SI-Ang-2 from AT1 receptor in Rattus norvegicus Sprague-Dawley (rat) liver membranes after 2 hr
Drug Central 357 7 1 6 2.5 O=C1NC(=O)C(S1)Cc1ccc(cc1)OCCN(c1ccccn1)C None
DB00412 3307 111 None - 1 Rat 8.0 pKi = 8.0 Binding
Displacement of [125I]-SI-Ang-2 from AT1 receptor in Rattus norvegicus Sprague-Dawley (rat) liver membranes after 2 hrDisplacement of [125I]-SI-Ang-2 from AT1 receptor in Rattus norvegicus Sprague-Dawley (rat) liver membranes after 2 hr
Drug Central 357 7 1 6 2.5 O=C1NC(=O)C(S1)Cc1ccc(cc1)OCCN(c1ccccn1)C None
2583 3705 115 None - 1 Rat 8.0 pKi = 8.0 Binding
Displacement of [125I]SI-Ang2 from AT1 receptor in Sprague-Dawley rat liver membraneDisplacement of [125I]SI-Ang2 from AT1 receptor in Sprague-Dawley rat liver membrane
Drug Central 514 7 1 5 7.3 CCCc1nc2c(n1Cc1ccc(cc1)c1ccccc1C(=O)O)cc(cc2C)c1nc2c(n1C)cccc2 None
592 3705 115 None - 1 Rat 8.0 pKi = 8.0 Binding
Displacement of [125I]SI-Ang2 from AT1 receptor in Sprague-Dawley rat liver membraneDisplacement of [125I]SI-Ang2 from AT1 receptor in Sprague-Dawley rat liver membrane
Drug Central 514 7 1 5 7.3 CCCc1nc2c(n1Cc1ccc(cc1)c1ccccc1C(=O)O)cc(cc2C)c1nc2c(n1C)cccc2 None
65999 3705 115 None - 1 Rat 8.0 pKi = 8.0 Binding
Displacement of [125I]SI-Ang2 from AT1 receptor in Sprague-Dawley rat liver membraneDisplacement of [125I]SI-Ang2 from AT1 receptor in Sprague-Dawley rat liver membrane
Drug Central 514 7 1 5 7.3 CCCc1nc2c(n1Cc1ccc(cc1)c1ccccc1C(=O)O)cc(cc2C)c1nc2c(n1C)cccc2 None
CHEMBL1017 3705 115 None - 1 Rat 8.0 pKi = 8.0 Binding
Displacement of [125I]SI-Ang2 from AT1 receptor in Sprague-Dawley rat liver membraneDisplacement of [125I]SI-Ang2 from AT1 receptor in Sprague-Dawley rat liver membrane
Drug Central 514 7 1 5 7.3 CCCc1nc2c(n1Cc1ccc(cc1)c1ccccc1C(=O)O)cc(cc2C)c1nc2c(n1C)cccc2 None
DB00966 3705 115 None - 1 Rat 8.0 pKi = 8.0 Binding
Displacement of [125I]SI-Ang2 from AT1 receptor in Sprague-Dawley rat liver membraneDisplacement of [125I]SI-Ang2 from AT1 receptor in Sprague-Dawley rat liver membrane
Drug Central 514 7 1 5 7.3 CCCc1nc2c(n1Cc1ccc(cc1)c1ccccc1C(=O)O)cc(cc2C)c1nc2c(n1C)cccc2 None
36736 3405 0 None -5 3 Human 8.0 pKi = 8.0 Binding
Binding affinity to human AT1 receptor by radioligand displacement assayBinding affinity to human AT1 receptor by radioligand displacement assay
Drug Central None None None None None
598 3405 0 None -5 3 Human 8.0 pKi = 8.0 Binding
Binding affinity to human AT1 receptor by radioligand displacement assayBinding affinity to human AT1 receptor by radioligand displacement assay
Drug Central None None None None None
6324663 3405 0 None -5 3 Human 8.0 pKi = 8.0 Binding
Binding affinity to human AT1 receptor by radioligand displacement assayBinding affinity to human AT1 receptor by radioligand displacement assay
Drug Central None None None None None
CHEMBL356431 3405 0 None -5 3 Human 8.0 pKi = 8.0 Binding
Binding affinity to human AT1 receptor by radioligand displacement assayBinding affinity to human AT1 receptor by radioligand displacement assay
Drug Central None None None None None
11944 3803 0 None - 1 Human 8.3 pKi = 8.3 Binding
Receptor bindingReceptor binding
Guide to Pharmacology None None None None 30639099
155552190 3803 0 None - 1 Human 8.3 pKi = 8.3 Binding
Receptor bindingReceptor binding
Guide to Pharmacology None None None None 30639099
CHEMBL4544228 3803 0 None - 1 Human 8.3 pKi = 8.3 Binding
Receptor bindingReceptor binding
Guide to Pharmacology None None None None 30639099
11943 3802 0 None - 1 Human 8.6 pKi = 8.6 Binding
Receptor bindingReceptor binding
Guide to Pharmacology None None None None 30639099
145925549 3802 0 None - 1 Human 8.6 pKi = 8.6 Binding
Receptor bindingReceptor binding
Guide to Pharmacology None None None None 30639099
CHEMBL4438122 3802 0 None - 1 Human 8.6 pKi = 8.6 Binding
Receptor bindingReceptor binding
Guide to Pharmacology None None None None 30639099
11930 1002 0 None -537 2 Human 6.7 pKi = 6.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 623 9 1 8 6.8 CCc1nc2c(cc(cc2)N(Cc2ccccc2)C(=O)c2cccs2)c(=O)n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1 28379944
15780052 1002 0 None -537 2 Human 6.7 pKi = 6.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 623 9 1 8 6.8 CCc1nc2c(cc(cc2)N(Cc2ccccc2)C(=O)c2cccs2)c(=O)n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1 28379944
CHEMBL289472 1002 0 None -537 2 Human 6.7 pKi = 6.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 623 9 1 8 6.8 CCc1nc2c(cc(cc2)N(Cc2ccccc2)C(=O)c2cccs2)c(=O)n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1 28379944
11931 1045 0 None -10 2 Human 8.4 pKi = 8.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 621 10 1 8 6.7 CCCc1nc2c(cc(cc2)N(Cc2ccco2)C(=O)c2ccccc2)c(=O)n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1 28379944
126456406 1045 0 None -10 2 Human 8.4 pKi = 8.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 621 10 1 8 6.7 CCCc1nc2c(cc(cc2)N(Cc2ccco2)C(=O)c2ccccc2)c(=O)n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1 28379944
6894 414 0 None 1 2 Human 8.8 pKi = 8.8 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 21464395
91691124 414 0 None 1 2 Human 8.8 pKi = 8.8 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 21464395
136218976 150 0 None - 1 Rat 9.0 pKi = 9.0 Binding
UnclassifiedUnclassified
Guide to Pharmacology 423 9 2 5 3.7 CCC[C@H](N(C(=O)CC)Cc1ccc(cc1)c1ccccc1c1noc(=O)[nH]1)C(=O)O 22410249
6913 150 0 None - 1 Rat 9.0 pKi = 9.0 Binding
UnclassifiedUnclassified
Guide to Pharmacology 423 9 2 5 3.7 CCC[C@H](N(C(=O)CC)Cc1ccc(cc1)c1ccccc1c1noc(=O)[nH]1)C(=O)O 22410249
60921 3400 0 None - 1 Rat 9.1 pKi = 9.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology 610 8 2 6 5.9 CCc1nc(c(n1Cc1ccc2c(c1)c(Br)c(o2)c1ccccc1NS(=O)(=O)C(F)(F)F)C(=O)N)C1CC1 7853190
6899 3400 0 None - 1 Rat 9.1 pKi = 9.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology 610 8 2 6 5.9 CCc1nc(c(n1Cc1ccc2c(c1)c(Br)c(o2)c1ccccc1NS(=O)(=O)C(F)(F)F)C(=O)N)C1CC1 7853190
CHEMBL305544 3400 0 None - 1 Rat 9.1 pKi = 9.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology 610 8 2 6 5.9 CCc1nc(c(n1Cc1ccc2c(c1)c(Br)c(o2)c1ccccc1NS(=O)(=O)C(F)(F)F)C(=O)N)C1CC1 7853190
DB01347 3400 0 None - 1 Rat 9.1 pKi = 9.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology 610 8 2 6 5.9 CCc1nc(c(n1Cc1ccc2c(c1)c(Br)c(o2)c1ccccc1NS(=O)(=O)C(F)(F)F)C(=O)N)C1CC1 7853190
10257882 3576 37 None 11 2 Human 9.1 pKi = 9.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology 592 12 1 7 6.5 CCCCC1=NC2(C(=O)N1Cc1ccc(c(c1)COCC)c1ccccc1S(=O)(=O)Nc1noc(c1C)C)CCCC2 16220969
8448 3576 37 None 11 2 Human 9.1 pKi = 9.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology 592 12 1 7 6.5 CCCCC1=NC2(C(=O)N1Cc1ccc(c(c1)COCC)c1ccccc1S(=O)(=O)Nc1noc(c1C)C)CCCC2 16220969
CHEMBL539423 3576 37 None 11 2 Human 9.1 pKi = 9.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology 592 12 1 7 6.5 CCCCC1=NC2(C(=O)N1Cc1ccc(c(c1)COCC)c1ccccc1S(=O)(=O)Nc1noc(c1C)C)CCCC2 16220969
DB12548 3576 37 None 11 2 Human 9.1 pKi = 9.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology 592 12 1 7 6.5 CCCCC1=NC2(C(=O)N1Cc1ccc(c(c1)COCC)c1ccccc1S(=O)(=O)Nc1noc(c1C)C)CCCC2 16220969