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
Rot
Bonds
H don H acc LogP Smiles DOI
CHEMBL1627325 207058 0 None 1 8 Human 10.5 pEC50 = 10.5 Functional
Antagonist activity at human recombinant bradykinin 2 receptor expressed in CHO cells assessed as inhibition of bradykinin-induced intracellular calcium mobilizationAntagonist activity at human recombinant bradykinin 2 receptor expressed in CHO cells assessed as inhibition of bradykinin-induced intracellular calcium mobilization
ChEMBL None None None CSCC[C@H](NC(=O)CNC(=O)[C@@H](NC(=O)CNC(=O)[C@@H](NC(=O)[C@H](NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](N)CO)C(C)(C)C)C(C)C)[C@@H](C)O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCCCN)C(=O)N[C@H](C(=O)N[C@@H](CO)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CO)C(=O)O)[C@@H](C)O 10.1021/jm900604g
3812 708 37 None -1 3 Human 10.3 pEC50 = 10.3 Functional
Antagonist activity at human recombinant bradykinin 2 receptor expressed in CHO cells assessed as inhibition of bradykinin-induced intracellular calcium mobilizationAntagonist activity at human recombinant bradykinin 2 receptor expressed in CHO cells assessed as inhibition of bradykinin-induced intracellular calcium mobilization
ChEMBL None None None None 10.1021/jm900604g
439201 708 37 None -1 3 Human 10.3 pEC50 = 10.3 Functional
Antagonist activity at human recombinant bradykinin 2 receptor expressed in CHO cells assessed as inhibition of bradykinin-induced intracellular calcium mobilizationAntagonist activity at human recombinant bradykinin 2 receptor expressed in CHO cells assessed as inhibition of bradykinin-induced intracellular calcium mobilization
ChEMBL None None None None 10.1021/jm900604g
649 708 37 None -1 3 Human 10.3 pEC50 = 10.3 Functional
Antagonist activity at human recombinant bradykinin 2 receptor expressed in CHO cells assessed as inhibition of bradykinin-induced intracellular calcium mobilizationAntagonist activity at human recombinant bradykinin 2 receptor expressed in CHO cells assessed as inhibition of bradykinin-induced intracellular calcium mobilization
ChEMBL None None None None 10.1021/jm900604g
CHEMBL406291 708 37 None -1 3 Human 10.3 pEC50 = 10.3 Functional
Antagonist activity at human recombinant bradykinin 2 receptor expressed in CHO cells assessed as inhibition of bradykinin-induced intracellular calcium mobilizationAntagonist activity at human recombinant bradykinin 2 receptor expressed in CHO cells assessed as inhibition of bradykinin-induced intracellular calcium mobilization
ChEMBL None None None None 10.1021/jm900604g
DB12126 708 37 None -1 3 Human 10.3 pEC50 = 10.3 Functional
Antagonist activity at human recombinant bradykinin 2 receptor expressed in CHO cells assessed as inhibition of bradykinin-induced intracellular calcium mobilizationAntagonist activity at human recombinant bradykinin 2 receptor expressed in CHO cells assessed as inhibition of bradykinin-induced intracellular calcium mobilization
ChEMBL None None None None 10.1021/jm900604g
9851817 9574 0 None - 1 Guinea pig 7.0 pEC50 = 7 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 607 8 1 5 7.3 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(F)(F)F)cc4)c3Cl)cccc2s1 10.1016/s0960-894x(98)00736-7
CHEMBL112991 9574 0 None - 1 Guinea pig 7.0 pEC50 = 7 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 607 8 1 5 7.3 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(F)(F)F)cc4)c3Cl)cccc2s1 10.1016/s0960-894x(98)00736-7
44340964 9600 0 None - 1 Guinea pig 6.0 pEC50 = 6.0 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 609 10 1 6 6.7 COc1c(N(C)C(=O)CNC(=O)/C=C/c2ccc(C(F)(F)F)cc2)ccc(SC)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
CHEMBL113176 9600 0 None - 1 Guinea pig 6.0 pEC50 = 6.0 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 609 10 1 6 6.7 COc1c(N(C)C(=O)CNC(=O)/C=C/c2ccc(C(F)(F)F)cc2)ccc(SC)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
44341039 9405 0 None - 1 Guinea pig 6.9 pEC50 = 6.9 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 597 9 1 5 6.6 COc1ccc(N(C)C(=O)CNC(=O)/C=C/c2ccc(C(F)(F)F)cc2)c(Cl)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
CHEMBL112140 9405 0 None - 1 Guinea pig 6.9 pEC50 = 6.9 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 597 9 1 5 6.6 COc1ccc(N(C)C(=O)CNC(=O)/C=C/c2ccc(C(F)(F)F)cc2)c(Cl)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
44340818 110107 0 None - 1 Guinea pig 5.9 pEC50 = 5.9 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 539 8 1 5 6.3 Cc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4scnc34)c2Cl)cc1 10.1016/s0960-894x(98)00736-7
CHEMBL325624 110107 0 None - 1 Guinea pig 5.9 pEC50 = 5.9 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 539 8 1 5 6.3 Cc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4scnc34)c2Cl)cc1 10.1016/s0960-894x(98)00736-7
18941161 9622 0 None - 1 Guinea pig 4.7 pEC50 = 4.7 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 615 9 1 5 8.0 Cc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4sc(-c5ccccc5)nc34)c2Cl)cc1 10.1016/s0960-894x(98)00736-7
CHEMBL113320 9622 0 None - 1 Guinea pig 4.7 pEC50 = 4.7 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 615 9 1 5 8.0 Cc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4sc(-c5ccccc5)nc34)c2Cl)cc1 10.1016/s0960-894x(98)00736-7
44341214 109928 0 None - 1 Guinea pig 6.7 pEC50 = 6.7 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 621 12 1 6 6.7 CCCOc1c(N(C)C(=O)CNC(=O)/C=C/c2ccc(C(F)(F)F)cc2)ccc(OC)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
CHEMBL324575 109928 0 None - 1 Guinea pig 6.7 pEC50 = 6.7 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 621 12 1 6 6.7 CCCOc1c(N(C)C(=O)CNC(=O)/C=C/c2ccc(C(F)(F)F)cc2)ccc(OC)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
18941160 9807 0 None - 1 Guinea pig 7.6 pEC50 = 7.6 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 553 8 1 5 6.6 Cc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4sc(C)nc34)c2Cl)cc1 10.1016/s0960-894x(98)00736-7
CHEMBL114401 9807 0 None - 1 Guinea pig 7.6 pEC50 = 7.6 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 553 8 1 5 6.6 Cc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4sc(C)nc34)c2Cl)cc1 10.1016/s0960-894x(98)00736-7
44214279 9609 0 None - 1 Guinea pig 6.6 pEC50 = 6.6 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 489 8 1 5 5.3 C=C/C=C/C(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccc3sc(C)nc23)c1Cl 10.1016/s0960-894x(98)00736-7
CHEMBL113222 9609 0 None - 1 Guinea pig 6.6 pEC50 = 6.6 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 489 8 1 5 5.3 C=C/C=C/C(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccc3sc(C)nc23)c1Cl 10.1016/s0960-894x(98)00736-7
10895913 9761 0 None - 1 Guinea pig 6.5 pEC50 = 6.5 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 465 7 2 5 3.9 CCNC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccc3ccc(C)nc23)c1C#N 10.1016/s0960-894x(98)00736-7
CHEMBL114180 9761 0 None - 1 Guinea pig 6.5 pEC50 = 6.5 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 465 7 2 5 3.9 CCNC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccc3ccc(C)nc23)c1C#N 10.1016/s0960-894x(98)00736-7
9831859 9599 0 None - 1 Guinea pig 6.5 pEC50 = 6.5 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 508 10 3 6 3.6 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)NCCCCN)c3C#N)c2n1 10.1016/s0960-894x(98)00736-7
CHEMBL113169 9599 0 None - 1 Guinea pig 6.5 pEC50 = 6.5 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 508 10 3 6 3.6 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)NCCCCN)c3C#N)c2n1 10.1016/s0960-894x(98)00736-7
10257108 9723 0 None - 1 Guinea pig 8.4 pEC50 = 8.4 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 554 9 1 6 5.4 COc1cccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2C#N)c1 10.1016/s0960-894x(98)00736-7
CHEMBL113963 9723 0 None - 1 Guinea pig 8.4 pEC50 = 8.4 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 554 9 1 6 5.4 COc1cccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2C#N)c1 10.1016/s0960-894x(98)00736-7
44340760 110006 0 None - 1 Guinea pig 6.4 pEC50 = 6.4 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 523 10 3 6 3.8 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)NCCCC(=O)O)c3C#N)c2n1 10.1016/s0960-894x(98)00736-7
CHEMBL324950 110006 0 None - 1 Guinea pig 6.4 pEC50 = 6.4 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 523 10 3 6 3.8 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)NCCCC(=O)O)c3C#N)c2n1 10.1016/s0960-894x(98)00736-7
22008916 9655 0 None - 1 Guinea pig 6.4 pEC50 = 6.4 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 461 8 2 6 3.3 CCNC(=O)NCC(=O)N(C)c1ccc(OC)c(COc2cccc3ccc(C)nc23)c1C#N 10.1016/s0960-894x(98)00736-7
CHEMBL113502 9655 0 None - 1 Guinea pig 6.4 pEC50 = 6.4 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 461 8 2 6 3.3 CCNC(=O)NCC(=O)N(C)c1ccc(OC)c(COc2cccc3ccc(C)nc23)c1C#N 10.1016/s0960-894x(98)00736-7
44214619 110103 0 None - 1 Guinea pig 6.3 pEC50 = 6.3 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 553 13 1 8 4.7 COC(=O)CCCCC(=O)NCC(=O)N(C)c1ccc(OC)c(COc2cccc3ccc(C)nc23)c1SC 10.1016/s0960-894x(98)00736-7
CHEMBL325601 110103 0 None - 1 Guinea pig 6.3 pEC50 = 6.3 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 553 13 1 8 4.7 COC(=O)CCCCC(=O)NCC(=O)N(C)c1ccc(OC)c(COc2cccc3ccc(C)nc23)c1SC 10.1016/s0960-894x(98)00736-7
18941145 9854 0 None - 1 Guinea pig 7.3 pEC50 = 7.3 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 569 9 1 6 6.3 COc1cccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4sc(C)nc34)c2Cl)c1 10.1016/s0960-894x(98)00736-7
CHEMBL114732 9854 0 None - 1 Guinea pig 7.3 pEC50 = 7.3 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 569 9 1 6 6.3 COc1cccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4sc(C)nc34)c2Cl)c1 10.1016/s0960-894x(98)00736-7
22008929 9643 0 None - 1 Guinea pig 7.3 pEC50 = 7.3 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 597 9 1 5 6.6 COc1c(N(C)C(=O)CNC(=O)/C=C/c2ccc(C(F)(F)F)cc2)ccc(Cl)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
CHEMBL113465 9643 0 None - 1 Guinea pig 7.3 pEC50 = 7.3 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 597 9 1 5 6.6 COc1c(N(C)C(=O)CNC(=O)/C=C/c2ccc(C(F)(F)F)cc2)ccc(Cl)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
22008895 110056 0 None - 1 Guinea pig 7.3 pEC50 = 7.3 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 592 8 1 5 6.5 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(F)(F)F)cc4)c3C#N)c2n1 10.1016/s0960-894x(98)00736-7
CHEMBL325255 110056 0 None - 1 Guinea pig 7.3 pEC50 = 7.3 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 592 8 1 5 6.5 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(F)(F)F)cc4)c3C#N)c2n1 10.1016/s0960-894x(98)00736-7
44340859 9933 0 None - 1 Guinea pig 7.2 pEC50 = 7.2 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 599 11 2 8 5.0 COc1ccc(N(C)C(=O)CNC(=O)/C=C/c2ccc(NC(C)=O)nc2)c(SC)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
CHEMBL115163 9933 0 None - 1 Guinea pig 7.2 pEC50 = 7.2 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 599 11 2 8 5.0 COc1ccc(N(C)C(=O)CNC(=O)/C=C/c2ccc(NC(C)=O)nc2)c(SC)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
44340951 9892 0 None - 1 Guinea pig 6.2 pEC50 = 6.2 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 587 11 1 7 6.4 COc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(SC)c(COc3cccc4ccc(C)nc34)c2SC)cc1 10.1016/s0960-894x(98)00736-7
CHEMBL114915 9892 0 None - 1 Guinea pig 6.2 pEC50 = 6.2 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 587 11 1 7 6.4 COc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(SC)c(COc3cccc4ccc(C)nc34)c2SC)cc1 10.1016/s0960-894x(98)00736-7
3812 708 37 None -1 3 Human 8.8 pED50 = 8.8 Functional
In vitro 50 % Maximal response in jugular vein expressing B2 receptorIn vitro 50 % Maximal response in jugular vein expressing B2 receptor
ChEMBL None None None None 10.1021/jm00144a008
439201 708 37 None -1 3 Human 8.8 pED50 = 8.8 Functional
In vitro 50 % Maximal response in jugular vein expressing B2 receptorIn vitro 50 % Maximal response in jugular vein expressing B2 receptor
ChEMBL None None None None 10.1021/jm00144a008
649 708 37 None -1 3 Human 8.8 pED50 = 8.8 Functional
In vitro 50 % Maximal response in jugular vein expressing B2 receptorIn vitro 50 % Maximal response in jugular vein expressing B2 receptor
ChEMBL None None None None 10.1021/jm00144a008
CHEMBL406291 708 37 None -1 3 Human 8.8 pED50 = 8.8 Functional
In vitro 50 % Maximal response in jugular vein expressing B2 receptorIn vitro 50 % Maximal response in jugular vein expressing B2 receptor
ChEMBL None None None None 10.1021/jm00144a008
DB12126 708 37 None -1 3 Human 8.8 pED50 = 8.8 Functional
In vitro 50 % Maximal response in jugular vein expressing B2 receptorIn vitro 50 % Maximal response in jugular vein expressing B2 receptor
ChEMBL None None None None 10.1021/jm00144a008
CHEMBL2372138 208434 0 None - 1 Human 8.0 pED50 = 8 Functional
In vitro 50 % Maximal response in jugular vein expressing B2 receptorIn vitro 50 % Maximal response in jugular vein expressing B2 receptor
ChEMBL None None None [N-]=[N+]=Nc1ccc(C[C@H](NC(=O)CNC(=O)[C@@H]2CCCN2C(=O)[C@@H]2CCCN2C(=O)[C@@H](N)CCCNC(=N)N)C(=O)N[C@@H](CO)C(=O)N2CCC[C@H]2C(=O)N[C@@H](Cc2ccccc2)C(=O)N[C@@H](CCCNC(=N)N)C(=O)O)cc1 10.1021/jm00144a008
CHEMBL2372165 208438 0 None - 1 Human 7.7 pED50 = 7.7 Functional
In vitro 50 % Maximal response in jugular vein expressing B2 receptorIn vitro 50 % Maximal response in jugular vein expressing B2 receptor
ChEMBL None None None NC(N)=NCCC[C@H](NC(=O)[C@H](Cc1ccc(N)cc1)NC(=O)[C@@H]1CCCN1C(=O)[C@H](CO)NC(=O)[C@H](Cc1ccccc1)NC(=O)CNC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)[C@@H](N)CCCN=C(N)N)C(=O)O 10.1021/jm00144a008
CHEMBL2372173 208441 0 None - 1 Human 7.6 pED50 = 7.6 Functional
In vitro 50 % Maximal response in jugular vein expressing B2 receptorIn vitro 50 % Maximal response in jugular vein expressing B2 receptor
ChEMBL None None None NC(N)=NCCC[C@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H]1CCCN1C(=O)[C@H](CO)NC(=O)[C@H](Cc1ccc([N+](=O)[O-])cc1)NC(=O)CNC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)[C@@H](N)CCCN=C(N)N)C(=O)O 10.1021/jm00144a008
CHEMBL2372157 208436 0 None - 1 Human 7.6 pED50 = 7.6 Functional
In vitro 50 % Maximal response in jugular vein expressing B2 receptorIn vitro 50 % Maximal response in jugular vein expressing B2 receptor
ChEMBL None None None N#[N+]c1ccc(C[C@H](NC(=O)CNC(=O)[C@@H]2CCCN2C(=O)[C@@H]2CCCN2C(=O)[C@@H](N)CCCN=C(N)N)C(=O)N[C@@H](CO)C(=O)N2CCC[C@H]2C(=O)N[C@@H](Cc2ccccc2)C(=O)N[C@@H](CCCN=C(N)N)C(=O)O)cc1 10.1021/jm00144a008
CHEMBL2372164 208437 0 None - 1 Human 7.6 pED50 = 7.6 Functional
In vitro 50 % Maximal response in jugular vein expressing B2 receptorIn vitro 50 % Maximal response in jugular vein expressing B2 receptor
ChEMBL None None None N#[N+]c1ccc(C[C@H](NC(=O)[C@@H]2CCCN2C(=O)[C@H](CO)NC(=O)[C@H](Cc2ccccc2)NC(=O)CNC(=O)[C@@H]2CCCN2C(=O)[C@@H]2CCCN2C(=O)[C@@H](N)CCCN=C(N)N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)O)cc1 10.1021/jm00144a008
CHEMBL2372172 208440 0 None - 1 Human 7.2 pED50 = 7.2 Functional
In vitro 50 % Maximal response in jugular vein expressing B2 receptorIn vitro 50 % Maximal response in jugular vein expressing B2 receptor
ChEMBL None None None NC(N)=NCCC[C@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H]1CCCN1C(=O)[C@H](CO)NC(=O)[C@H](Cc1ccc(N)cc1)NC(=O)CNC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)[C@@H](N)CCCN=C(N)N)C(=O)O 10.1021/jm00144a008
CHEMBL2372156 208435 0 None - 1 Human 8.2 pED50 = 8.2 Functional
In vitro 50 % Maximal response in jugular vein expressing B2 receptorIn vitro 50 % Maximal response in jugular vein expressing B2 receptor
ChEMBL None None None NC(N)=NCCC[C@H](NC(=O)[C@H](Cc1ccc([N+](=O)[O-])cc1)NC(=O)[C@@H]1CCCN1C(=O)[C@H](CO)NC(=O)[C@H](Cc1ccccc1)NC(=O)CNC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)[C@@H](N)CCCN=C(N)N)C(=O)O 10.1021/jm00144a008
CHEMBL2372168 208439 0 None - 1 Human 8.2 pED50 = 8.2 Functional
In vitro 50 % Maximal response in jugular vein expressing B2 receptorIn vitro 50 % Maximal response in jugular vein expressing B2 receptor
ChEMBL None None None [N-]=[N+]=Nc1ccc(C[C@H](NC(=O)[C@@H]2CCCN2C(=O)[C@H](CO)NC(=O)[C@H](Cc2ccccc2)NC(=O)CNC(=O)[C@@H]2CCCN2C(=O)[C@@H]2CCCN2C(=O)[C@@H](N)CCCN=C(N)N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)O)cc1 10.1021/jm00144a008
44191040 194300 0 None - 1 Human 9.3 pIC50 = 9.3 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 519 6 0 7 5.5 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(C)ccnc3Cn3cccc(C(F)(F)F)c3=O)c2n1 10.1021/jm9002445
CHEMBL559825 194300 0 None - 1 Human 9.3 pIC50 = 9.3 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 519 6 0 7 5.5 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(C)ccnc3Cn3cccc(C(F)(F)F)c3=O)c2n1 10.1021/jm9002445
667 1934 32 None 2 2 Guinea pig 9.0 pIC50 = 9.0 Functional
In vitro antagonistic activity for Bradykinin receptor B2 by guinea pig ileal membrane receptor assay.In vitro antagonistic activity for Bradykinin receptor B2 by guinea pig ileal membrane receptor assay.
ChEMBL None None None None 10.1021/jm00015a001
71364 1934 32 None 2 2 Guinea pig 9.0 pIC50 = 9.0 Functional
In vitro antagonistic activity for Bradykinin receptor B2 by guinea pig ileal membrane receptor assay.In vitro antagonistic activity for Bradykinin receptor B2 by guinea pig ileal membrane receptor assay.
ChEMBL None None None None 10.1021/jm00015a001
CHEMBL2028850 1934 32 None 2 2 Guinea pig 9.0 pIC50 = 9.0 Functional
In vitro antagonistic activity for Bradykinin receptor B2 by guinea pig ileal membrane receptor assay.In vitro antagonistic activity for Bradykinin receptor B2 by guinea pig ileal membrane receptor assay.
ChEMBL None None None None 10.1021/jm00015a001
DB06196 1934 32 None 2 2 Guinea pig 9.0 pIC50 = 9.0 Functional
In vitro antagonistic activity for Bradykinin receptor B2 by guinea pig ileal membrane receptor assay.In vitro antagonistic activity for Bradykinin receptor B2 by guinea pig ileal membrane receptor assay.
ChEMBL None None None None 10.1021/jm00015a001
25019714 194898 1 None - 1 Human 9.0 pIC50 = 9.0 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 519 6 1 6 5.8 Cc1cc(-c2[nH]ncc2C)c2cccc(OCc3c(C)ccnc3Cn3cccc(C(F)(F)F)c3=O)c2n1 10.1021/jm9002445
CHEMBL563956 194898 1 None - 1 Human 9.0 pIC50 = 9.0 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 519 6 1 6 5.8 Cc1cc(-c2[nH]ncc2C)c2cccc(OCc3c(C)ccnc3Cn3cccc(C(F)(F)F)c3=O)c2n1 10.1021/jm9002445
45272156 193379 0 None - 1 Human 8.9 pIC50 = 8.9 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 556 6 0 7 6.8 Cc1cc(-c2ncsc2Cl)c2cccc(OCc3c(C)ccnc3Cn3cccc(C(F)(F)F)c3=O)c2n1 10.1021/jm9002445
CHEMBL549534 193379 0 None - 1 Human 8.9 pIC50 = 8.9 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 556 6 0 7 6.8 Cc1cc(-c2ncsc2Cl)c2cccc(OCc3c(C)ccnc3Cn3cccc(C(F)(F)F)c3=O)c2n1 10.1021/jm9002445
44190944 194249 0 None - 1 Human 8.9 pIC50 = 8.9 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 539 6 0 7 5.8 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3Cn3cccc(C(F)(F)F)c3=O)c2n1 10.1021/jm9002445
CHEMBL559436 194249 0 None - 1 Human 8.9 pIC50 = 8.9 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 539 6 0 7 5.8 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3Cn3cccc(C(F)(F)F)c3=O)c2n1 10.1021/jm9002445
44190263 194270 0 None - 1 Human 8.7 pIC50 = 8.7 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 483 7 1 6 5.4 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(C)ccnc3CNC(=O)C3CCCCC3)c2n1 10.1021/jm9002445
CHEMBL559565 194270 0 None - 1 Human 8.7 pIC50 = 8.7 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 483 7 1 6 5.4 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(C)ccnc3CNC(=O)C3CCCCC3)c2n1 10.1021/jm9002445
10327403 78160 0 None 1 2 Rat 8.7 pIC50 = 8.7 Functional
Inhibition of Bradykinin receptor B2-mediated contractions of rat uterus smooth muscleInhibition of Bradykinin receptor B2-mediated contractions of rat uterus smooth muscle
ChEMBL 702 14 4 10 3.8 CN(C)CCCN(C)CCNC(=O)c1cccn1S(=O)(=O)c1ccc(NNC(=O)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL2112220 78160 0 None 1 2 Rat 8.7 pIC50 = 8.7 Functional
Inhibition of Bradykinin receptor B2-mediated contractions of rat uterus smooth muscleInhibition of Bradykinin receptor B2-mediated contractions of rat uterus smooth muscle
ChEMBL 702 14 4 10 3.8 CN(C)CCCN(C)CCNC(=O)c1cccn1S(=O)(=O)c1ccc(NNC(=O)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
9987299 78176 0 None 2 2 Rat 7.0 pIC50 = 7.0 Functional
Inhibition of increase in [Ca2+] efflux from NG108-15 cells caused by activation of rat Bradykinin receptor B2Inhibition of increase in [Ca2+] efflux from NG108-15 cells caused by activation of rat Bradykinin receptor B2
ChEMBL 706 14 4 9 3.3 CN(C)CCCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(NNC(=O)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL2112283 78176 0 None 2 2 Rat 7.0 pIC50 = 7.0 Functional
Inhibition of increase in [Ca2+] efflux from NG108-15 cells caused by activation of rat Bradykinin receptor B2Inhibition of increase in [Ca2+] efflux from NG108-15 cells caused by activation of rat Bradykinin receptor B2
ChEMBL 706 14 4 9 3.3 CN(C)CCCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(NNC(=O)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
44190941 193750 0 None - 1 Human 7.0 pIC50 = 7.0 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 471 7 1 7 3.6 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3CNS(C)(=O)=O)c2n1 10.1021/jm9002445
CHEMBL552296 193750 0 None - 1 Human 7.0 pIC50 = 7.0 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 471 7 1 7 3.6 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3CNS(C)(=O)=O)c2n1 10.1021/jm9002445
10327403 78160 0 None -1 2 Human 7.9 pIC50 = 7.9 Functional
Antagonism of the [Ca2+] efflux actions of the human Bradykinin receptor B2 (SK-N-SH neuroblastoma)Antagonism of the [Ca2+] efflux actions of the human Bradykinin receptor B2 (SK-N-SH neuroblastoma)
ChEMBL 702 14 4 10 3.8 CN(C)CCCN(C)CCNC(=O)c1cccn1S(=O)(=O)c1ccc(NNC(=O)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL2112220 78160 0 None -1 2 Human 7.9 pIC50 = 7.9 Functional
Antagonism of the [Ca2+] efflux actions of the human Bradykinin receptor B2 (SK-N-SH neuroblastoma)Antagonism of the [Ca2+] efflux actions of the human Bradykinin receptor B2 (SK-N-SH neuroblastoma)
ChEMBL 702 14 4 10 3.8 CN(C)CCCN(C)CCNC(=O)c1cccn1S(=O)(=O)c1ccc(NNC(=O)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
44190852 193725 0 None - 1 Human 7.9 pIC50 = 7.9 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 465 6 0 7 4.8 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3COC(=O)N(C)C)c2n1 10.1021/jm9002445
CHEMBL552090 193725 0 None - 1 Human 7.9 pIC50 = 7.9 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 465 6 0 7 4.8 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3COC(=O)N(C)C)c2n1 10.1021/jm9002445
44191220 193350 0 None - 1 Human 5.9 pIC50 = 5.9 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 398 4 0 5 5.3 Cc1cc(-n2ccnc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL549337 193350 0 None - 1 Human 5.9 pIC50 = 5.9 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 398 4 0 5 5.3 Cc1cc(-n2ccnc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL2370243 208057 0 None - 1 Guinea pig 7.9 pIC50 = 7.9 Functional
In vitro antagonistic activity for Bradykinin receptor B2 by guinea pig pulmonary artery assay.In vitro antagonistic activity for Bradykinin receptor B2 by guinea pig pulmonary artery assay.
ChEMBL None None None N=C(N)NCCC[C@H](NC(=O)[C@@H]1C2CCCCC2CN1C(=O)[C@H]1Cc2ccccc2CN1C(=O)[C@H](CO)NC(=O)[C@H](NC(=O)CNC(=O)[C@@H]1C[C@@H](O)CN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H](CCCNC(=N)N)NC(=O)c1ccc(CN2CCCNCCNCCCNCC2)cc1)c1cccs1)C(=O)O 10.1021/jm00015a001
10327403 78160 0 None 1 2 Rat 6.9 pIC50 = 6.9 Functional
Inhibition of increase in [Ca2+] efflux from NG108-15 cells caused by activation of rat Bradykinin receptor B2Inhibition of increase in [Ca2+] efflux from NG108-15 cells caused by activation of rat Bradykinin receptor B2
ChEMBL 702 14 4 10 3.8 CN(C)CCCN(C)CCNC(=O)c1cccn1S(=O)(=O)c1ccc(NNC(=O)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL2112220 78160 0 None 1 2 Rat 6.9 pIC50 = 6.9 Functional
Inhibition of increase in [Ca2+] efflux from NG108-15 cells caused by activation of rat Bradykinin receptor B2Inhibition of increase in [Ca2+] efflux from NG108-15 cells caused by activation of rat Bradykinin receptor B2
ChEMBL 702 14 4 10 3.8 CN(C)CCCN(C)CCNC(=O)c1cccn1S(=O)(=O)c1ccc(NNC(=O)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
44190672 193664 0 None - 1 Human 5.8 pIC50 = 5.8 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 364 4 0 5 4.6 Cc1cc(-c2ccnn2C)c2cccc(OCc3ccncc3Cl)c2n1 10.1021/jm9002445
CHEMBL551757 193664 0 None - 1 Human 5.8 pIC50 = 5.8 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 364 4 0 5 4.6 Cc1cc(-c2ccnn2C)c2cccc(OCc3ccncc3Cl)c2n1 10.1021/jm9002445
9987299 78176 0 None -2 2 Human 7.8 pIC50 = 7.8 Functional
Antagonism of the [Ca2+] efflux actions of human Bradykinin receptor B2 (WI38 fibroblasts)Antagonism of the [Ca2+] efflux actions of human Bradykinin receptor B2 (WI38 fibroblasts)
ChEMBL 706 14 4 9 3.3 CN(C)CCCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(NNC(=O)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL2112283 78176 0 None -2 2 Human 7.8 pIC50 = 7.8 Functional
Antagonism of the [Ca2+] efflux actions of human Bradykinin receptor B2 (WI38 fibroblasts)Antagonism of the [Ca2+] efflux actions of human Bradykinin receptor B2 (WI38 fibroblasts)
ChEMBL 706 14 4 9 3.3 CN(C)CCCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(NNC(=O)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
44189787 194660 0 None - 1 Human 6.8 pIC50 = 6.8 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 398 4 0 5 5.2 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL562434 194660 0 None - 1 Human 6.8 pIC50 = 6.8 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 398 4 0 5 5.2 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
44190853 194605 4 None - 1 Human 6.7 pIC50 = 6.7 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 435 7 1 6 4.0 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3CCC(N)=O)c2n1 10.1021/jm9002445
CHEMBL562097 194605 4 None - 1 Human 6.7 pIC50 = 6.7 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 435 7 1 6 4.0 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3CCC(N)=O)c2n1 10.1021/jm9002445
44190850 193543 0 None - 1 Human 8.6 pIC50 = 8.6 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 463 7 1 6 4.8 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3CNC(=O)C(C)C)c2n1 10.1021/jm9002445
CHEMBL550827 193543 0 None - 1 Human 8.6 pIC50 = 8.6 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 463 7 1 6 4.8 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3CNC(=O)C(C)C)c2n1 10.1021/jm9002445
9987299 78176 0 None 2 2 Rat 8.6 pIC50 = 8.6 Functional
Inhibition of Bradykinin receptor B2-mediated contractions of rat uterus smooth muscleInhibition of Bradykinin receptor B2-mediated contractions of rat uterus smooth muscle
ChEMBL 706 14 4 9 3.3 CN(C)CCCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(NNC(=O)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL2112283 78176 0 None 2 2 Rat 8.6 pIC50 = 8.6 Functional
Inhibition of Bradykinin receptor B2-mediated contractions of rat uterus smooth muscleInhibition of Bradykinin receptor B2-mediated contractions of rat uterus smooth muscle
ChEMBL 706 14 4 9 3.3 CN(C)CCCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(NNC(=O)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
44190851 194885 0 None - 1 Human 8.6 pIC50 = 8.6 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 464 6 1 6 4.3 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3CNC(=O)N(C)C)c2n1 10.1021/jm9002445
CHEMBL563878 194885 0 None - 1 Human 8.6 pIC50 = 8.6 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 464 6 1 6 4.3 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3CNC(=O)N(C)C)c2n1 10.1021/jm9002445
44190854 193764 0 None - 1 Human 7.6 pIC50 = 7.6 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 435 6 1 6 4.2 CC(=O)NCc1cncc(Cl)c1COc1cccc2c(-c3ccnn3C)cc(C)nc12 10.1021/jm9002445
CHEMBL552384 193764 0 None - 1 Human 7.6 pIC50 = 7.6 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 435 6 1 6 4.2 CC(=O)NCc1cncc(Cl)c1COc1cccc2c(-c3ccnn3C)cc(C)nc12 10.1021/jm9002445
44190753 195018 0 None - 1 Human 7.6 pIC50 = 7.6 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 481 7 0 7 4.8 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3SCC(=O)N(C)C)c2n1 10.1021/jm9002445
CHEMBL564841 195018 0 None - 1 Human 7.6 pIC50 = 7.6 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 481 7 0 7 4.8 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3SCC(=O)N(C)C)c2n1 10.1021/jm9002445
44190077 194786 0 None - 1 Human 5.6 pIC50 = 5.6 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 399 4 0 6 4.6 Cc1cc(-c2ncnn2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL563254 194786 0 None - 1 Human 5.6 pIC50 = 5.6 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 399 4 0 6 4.6 Cc1cc(-c2ncnn2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
44190266 193775 0 None - 1 Human 5.6 pIC50 = 5.6 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 435 4 0 5 6.6 Cc1cc(-c2scnc2Cl)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL552442 193775 0 None - 1 Human 5.6 pIC50 = 5.6 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 435 4 0 5 6.6 Cc1cc(-c2scnc2Cl)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
44191138 194232 0 None - 1 Human 5.6 pIC50 = 5.6 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 384 4 0 5 5.0 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL559273 194232 0 None - 1 Human 5.6 pIC50 = 5.6 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 384 4 0 5 5.0 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
44190943 194269 0 None - 1 Human 6.6 pIC50 = 6.6 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 471 7 0 7 5.5 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3COc3ccccn3)c2n1 10.1021/jm9002445
CHEMBL559564 194269 0 None - 1 Human 6.6 pIC50 = 6.6 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 471 7 0 7 5.5 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3COc3ccccn3)c2n1 10.1021/jm9002445
45267862 194636 0 None - 1 Human 6.6 pIC50 = 6.6 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 434 5 0 7 4.3 CC(=O)OCc1cncc(Cl)c1C(=O)c1cccc2c(-c3ccnn3C)cc(C)nc12 10.1021/jm9002445
CHEMBL562296 194636 0 None - 1 Human 6.6 pIC50 = 6.6 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 434 5 0 7 4.3 CC(=O)OCc1cncc(Cl)c1C(=O)c1cccc2c(-c3ccnn3C)cc(C)nc12 10.1021/jm9002445
44190751 193665 0 None - 1 Human 7.5 pIC50 = 7.5 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 479 6 0 8 6.2 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3Sc3nccs3)c2n1 10.1021/jm9002445
CHEMBL551758 193665 0 None - 1 Human 7.5 pIC50 = 7.5 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 479 6 0 8 6.2 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3Sc3nccs3)c2n1 10.1021/jm9002445
44190942 194543 0 None - 1 Human 8.4 pIC50 = 8.4 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 471 6 0 7 4.8 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3Cn3ccccc3=O)c2n1 10.1021/jm9002445
CHEMBL561634 194543 0 None - 1 Human 8.4 pIC50 = 8.4 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 471 6 0 7 4.8 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3Cn3ccccc3=O)c2n1 10.1021/jm9002445
44190581 194260 0 None - 1 Human 8.4 pIC50 = 8.4 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 443 7 1 6 4.5 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(C)ccnc3CNC(=O)C(C)C)c2n1 10.1021/jm9002445
CHEMBL559506 194260 0 None - 1 Human 8.4 pIC50 = 8.4 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 443 7 1 6 4.5 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(C)ccnc3CNC(=O)C(C)C)c2n1 10.1021/jm9002445
44190267 193456 0 None - 1 Human 6.5 pIC50 = 6.5 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 401 4 0 5 5.9 Cc1cc(-c2cscn2)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL550143 193456 0 None - 1 Human 6.5 pIC50 = 6.5 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 401 4 0 5 5.9 Cc1cc(-c2cscn2)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
44190168 193438 0 None - 1 Human 6.5 pIC50 = 6.5 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 415 4 0 5 6.3 Cc1cc(-c2csnc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL550016 193438 0 None - 1 Human 6.5 pIC50 = 6.5 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 415 4 0 5 6.3 Cc1cc(-c2csnc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
44191224 194577 0 None - 1 Human 5.5 pIC50 = 5.5 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 412 4 0 5 5.5 Cc1cc(-c2ncc(C)n2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL561839 194577 0 None - 1 Human 5.5 pIC50 = 5.5 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 412 4 0 5 5.5 Cc1cc(-c2ncc(C)n2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
44191226 193622 0 None - 1 Human 6.5 pIC50 = 6.5 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 384 4 1 4 5.2 Cc1cc(-c2ccn[nH]2)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL551435 193622 0 None - 1 Human 6.5 pIC50 = 6.5 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 384 4 1 4 5.2 Cc1cc(-c2ccn[nH]2)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
44190361 193125 0 None - 1 Human 5.4 pIC50 = 5.4 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 399 4 0 5 5.8 Cc1cc(-c2conc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL538865 193125 0 None - 1 Human 5.4 pIC50 = 5.4 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 399 4 0 5 5.8 Cc1cc(-c2conc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
44189789 194469 0 None - 1 Human 6.4 pIC50 = 6.4 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 398 4 1 4 5.5 Cc1cc(-c2n[nH]cc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL561223 194469 0 None - 1 Human 6.4 pIC50 = 6.4 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 398 4 1 4 5.5 Cc1cc(-c2n[nH]cc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
44190167 194804 0 None - 1 Human 6.4 pIC50 = 6.4 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 415 4 0 5 6.3 Cc1cc(-c2ncsc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL563391 194804 0 None - 1 Human 6.4 pIC50 = 6.4 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 415 4 0 5 6.3 Cc1cc(-c2ncsc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
44189792 193455 0 None - 1 Human 6.4 pIC50 = 6.4 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 401 4 0 5 5.9 Cc1cc(-c2cncs2)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL550142 193455 0 None - 1 Human 6.4 pIC50 = 6.4 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 401 4 0 5 5.9 Cc1cc(-c2cncs2)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
44190752 193666 0 None - 1 Human 7.4 pIC50 = 7.4 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 476 6 0 8 5.5 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3Sc3nccn3C)c2n1 10.1021/jm9002445
CHEMBL551759 193666 0 None - 1 Human 7.4 pIC50 = 7.4 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 476 6 0 8 5.5 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3Sc3nccn3C)c2n1 10.1021/jm9002445
44190165 194279 0 None - 1 Human 6.3 pIC50 = 6.3 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 401 4 0 5 5.9 Cc1cc(-c2nccs2)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL559645 194279 0 None - 1 Human 6.3 pIC50 = 6.3 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 401 4 0 5 5.9 Cc1cc(-c2nccs2)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
667 1934 32 None 2 2 Guinea pig 8.3 pIC50 = 8.3 Functional
In vitro antagonistic activity for Bradykinin receptor B2 by guinea pig pulmonary artery assay.In vitro antagonistic activity for Bradykinin receptor B2 by guinea pig pulmonary artery assay.
ChEMBL None None None None 10.1021/jm00015a001
71364 1934 32 None 2 2 Guinea pig 8.3 pIC50 = 8.3 Functional
In vitro antagonistic activity for Bradykinin receptor B2 by guinea pig pulmonary artery assay.In vitro antagonistic activity for Bradykinin receptor B2 by guinea pig pulmonary artery assay.
ChEMBL None None None None 10.1021/jm00015a001
CHEMBL2028850 1934 32 None 2 2 Guinea pig 8.3 pIC50 = 8.3 Functional
In vitro antagonistic activity for Bradykinin receptor B2 by guinea pig pulmonary artery assay.In vitro antagonistic activity for Bradykinin receptor B2 by guinea pig pulmonary artery assay.
ChEMBL None None None None 10.1021/jm00015a001
DB06196 1934 32 None 2 2 Guinea pig 8.3 pIC50 = 8.3 Functional
In vitro antagonistic activity for Bradykinin receptor B2 by guinea pig pulmonary artery assay.In vitro antagonistic activity for Bradykinin receptor B2 by guinea pig pulmonary artery assay.
ChEMBL None None None None 10.1021/jm00015a001
10327403 78160 0 None -1 2 Human 7.3 pIC50 = 7.3 Functional
Antagonism of the [Ca2+] efflux actions of the human Bradykinin receptor B2 (WI38 fibroblasts)Antagonism of the [Ca2+] efflux actions of the human Bradykinin receptor B2 (WI38 fibroblasts)
ChEMBL 702 14 4 10 3.8 CN(C)CCCN(C)CCNC(=O)c1cccn1S(=O)(=O)c1ccc(NNC(=O)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL2112220 78160 0 None -1 2 Human 7.3 pIC50 = 7.3 Functional
Antagonism of the [Ca2+] efflux actions of the human Bradykinin receptor B2 (WI38 fibroblasts)Antagonism of the [Ca2+] efflux actions of the human Bradykinin receptor B2 (WI38 fibroblasts)
ChEMBL 702 14 4 10 3.8 CN(C)CCCN(C)CCNC(=O)c1cccn1S(=O)(=O)c1ccc(NNC(=O)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
44189790 194957 0 None - 1 Human 5.2 pIC50 = 5.2 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 398 4 1 4 5.5 Cc1cc(-c2cn[nH]c2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL564341 194957 0 None - 1 Human 5.2 pIC50 = 5.2 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 398 4 1 4 5.5 Cc1cc(-c2cn[nH]c2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
44190166 194949 0 None - 1 Human 7.2 pIC50 = 7.2 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 415 4 0 5 6.3 Cc1cc(-c2scnc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL564294 194949 0 None - 1 Human 7.2 pIC50 = 7.2 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 415 4 0 5 6.3 Cc1cc(-c2scnc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
44190269 194512 0 None - 1 Human 7.2 pIC50 = 7.2 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 415 4 0 5 6.3 Cc1cc(-c2nscc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL561415 194512 0 None - 1 Human 7.2 pIC50 = 7.2 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 415 4 0 5 6.3 Cc1cc(-c2nscc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
44190756 193756 0 None - 1 Human 7.1 pIC50 = 7.1 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 463 7 0 6 4.6 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3CCC(=O)N(C)C)c2n1 10.1021/jm9002445
CHEMBL552359 193756 0 None - 1 Human 7.1 pIC50 = 7.1 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 463 7 0 6 4.6 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3CCC(=O)N(C)C)c2n1 10.1021/jm9002445
44190268 194826 0 None - 1 Human 6.1 pIC50 = 6.1 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 435 4 0 5 6.6 Cc1cc(-c2ncsc2Cl)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL563516 194826 0 None - 1 Human 6.1 pIC50 = 6.1 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 435 4 0 5 6.6 Cc1cc(-c2ncsc2Cl)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
44190754 194764 0 None - 1 Human 7.1 pIC50 = 7.1 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 497 7 0 7 3.8 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3[S+]([O-])CC(=O)N(C)C)c2n1 10.1021/jm9002445
CHEMBL563068 194764 0 None - 1 Human 7.1 pIC50 = 7.1 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 497 7 0 7 3.8 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3[S+]([O-])CC(=O)N(C)C)c2n1 10.1021/jm9002445
44191223 194583 0 None - 1 Human 6.1 pIC50 = 6.1 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 398 4 0 5 5.2 Cc1cc(-c2nccn2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL561899 194583 0 None - 1 Human 6.1 pIC50 = 6.1 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 398 4 0 5 5.2 Cc1cc(-c2nccn2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL2370243 208057 0 None - 1 Guinea pig 8.1 pIC50 = 8.1 Functional
In vitro antagonistic activity for Bradykinin receptor B2 by guinea pig ileal membrane receptor assay.In vitro antagonistic activity for Bradykinin receptor B2 by guinea pig ileal membrane receptor assay.
ChEMBL None None None N=C(N)NCCC[C@H](NC(=O)[C@@H]1C2CCCCC2CN1C(=O)[C@H]1Cc2ccccc2CN1C(=O)[C@H](CO)NC(=O)[C@H](NC(=O)CNC(=O)[C@@H]1C[C@@H](O)CN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H](CCCNC(=N)N)NC(=O)c1ccc(CN2CCCNCCNCCCNCC2)cc1)c1cccs1)C(=O)O 10.1021/jm00015a001
9987299 78176 0 None -2 2 Human 7.0 pIC50 = 7.0 Functional
Antagonism of the [Ca2+] efflux actions of human Bradykinin receptor B2 (SK-N-SH neuroblastoma)Antagonism of the [Ca2+] efflux actions of human Bradykinin receptor B2 (SK-N-SH neuroblastoma)
ChEMBL 706 14 4 9 3.3 CN(C)CCCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(NNC(=O)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL2112283 78176 0 None -2 2 Human 7.0 pIC50 = 7.0 Functional
Antagonism of the [Ca2+] efflux actions of human Bradykinin receptor B2 (SK-N-SH neuroblastoma)Antagonism of the [Ca2+] efflux actions of human Bradykinin receptor B2 (SK-N-SH neuroblastoma)
ChEMBL 706 14 4 9 3.3 CN(C)CCCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(NNC(=O)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
44190755 194144 0 None - 1 Human 7.0 pIC50 = 7.0 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 465 7 0 7 4.0 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3OCC(=O)N(C)C)c2n1 10.1021/jm9002445
CHEMBL558279 194144 0 None - 1 Human 7.0 pIC50 = 7.0 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 465 7 0 7 4.0 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3OCC(=O)N(C)C)c2n1 10.1021/jm9002445
44191225 194712 0 None - 1 Human 6.0 pIC50 = 6.0 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 384 4 0 5 5.0 Cc1cc(-n2cccn2)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL562747 194712 0 None - 1 Human 6.0 pIC50 = 6.0 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 384 4 0 5 5.0 Cc1cc(-n2cccn2)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
10463883 83405 0 None - 0 Guinea pig 10.4 pKd = 10.4 Functional
Antagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscleAntagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscle
ChEMBL 746 13 2 8 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[C@@H](N)CCCN(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL220596 83405 0 None - 0 Guinea pig 10.4 pKd = 10.4 Functional
Antagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscleAntagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscle
ChEMBL 746 13 2 8 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[C@@H](N)CCCN(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
11498853 82761 9 None - 1 Human 10.3 pKd = 10.3 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 763 12 2 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL218427 82761 9 None - 1 Human 10.3 pKd = 10.3 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 763 12 2 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL541758 82761 9 None - 1 Human 10.3 pKd = 10.3 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 763 12 2 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
11498853 82761 9 None - 1 Human 10.3 pKd = 10.3 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 763 12 2 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL218427 82761 9 None - 1 Human 10.3 pKd = 10.3 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 763 12 2 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL541758 82761 9 None - 1 Human 10.3 pKd = 10.3 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 763 12 2 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1021/jm061143k
57345657 71233 0 None - 0 Guinea pig 10.2 pKd = 10.2 Functional
Antagonist activity at guinea pig bradykinin B2 receptor in longitudinal smooth muscle assessed as inhibition of bradykinin-induced contractile responsesAntagonist activity at guinea pig bradykinin B2 receptor in longitudinal smooth muscle assessed as inhibition of bradykinin-induced contractile responses
ChEMBL 748 12 1 7 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956722 71233 0 None - 0 Guinea pig 10.2 pKd = 10.2 Functional
Antagonist activity at guinea pig bradykinin B2 receptor in longitudinal smooth muscle assessed as inhibition of bradykinin-induced contractile responsesAntagonist activity at guinea pig bradykinin B2 receptor in longitudinal smooth muscle assessed as inhibition of bradykinin-induced contractile responses
ChEMBL 748 12 1 7 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963183 71233 0 None - 0 Guinea pig 10.2 pKd = 10.2 Functional
Antagonist activity at guinea pig bradykinin B2 receptor in longitudinal smooth muscle assessed as inhibition of bradykinin-induced contractile responsesAntagonist activity at guinea pig bradykinin B2 receptor in longitudinal smooth muscle assessed as inhibition of bradykinin-induced contractile responses
ChEMBL 748 12 1 7 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
10439868 75558 0 None - 0 Guinea pig 10.0 pKd = 10 Functional
Antagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscleAntagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscle
ChEMBL 720 13 2 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)C[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL205093 75558 0 None - 0 Guinea pig 10.0 pKd = 10 Functional
Antagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscleAntagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscle
ChEMBL 720 13 2 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)C[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm061143k
10373970 137076 0 None - 0 Guinea pig 10.0 pKd = 10 Functional
Antagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscleAntagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscle
ChEMBL 760 13 5 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCNC(=N)N)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL375689 137076 0 None - 0 Guinea pig 10.0 pKd = 10 Functional
Antagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscleAntagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscle
ChEMBL 760 13 5 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCNC(=N)N)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
10032895 137093 0 None - 0 Guinea pig 10.0 pKd = 10 Functional
Antagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscleAntagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscle
ChEMBL 734 13 5 8 3.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCCNC(=N)N)CC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL375820 137093 0 None - 0 Guinea pig 10.0 pKd = 10 Functional
Antagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscleAntagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscle
ChEMBL 734 13 5 8 3.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCCNC(=N)N)CC4)c3Cl)c2n1 10.1021/jm061143k
10101294 139611 0 None - 0 Guinea pig 10.0 pKd = 10 Functional
Antagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscleAntagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscle
ChEMBL 706 12 2 8 4.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL380273 139611 0 None - 0 Guinea pig 10.0 pKd = 10 Functional
Antagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscleAntagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscle
ChEMBL 706 12 2 8 4.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm061143k
57403503 71306 0 None - 0 Human 9.9 pKd = 9.9 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 748 12 2 9 3.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCN(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956856 71306 0 None - 0 Human 9.9 pKd = 9.9 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 748 12 2 9 3.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCN(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963651 71306 0 None - 0 Human 9.9 pKd = 9.9 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 748 12 2 9 3.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCN(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
16105746 161369 0 None - 0 Human 9.8 pKd = 9.8 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 779 12 2 8 4.8 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCSCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL415366 161369 0 None - 0 Human 9.8 pKd = 9.8 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 779 12 2 8 4.8 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCSCC4)c3Cl)c2n1 10.1021/jm061143k
9988753 83404 0 None - 0 Guinea pig 9.8 pKd = 9.8 Functional
Antagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscleAntagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscle
ChEMBL 746 13 2 8 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCN(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL220595 83404 0 None - 0 Guinea pig 9.8 pKd = 9.8 Functional
Antagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscleAntagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscle
ChEMBL 746 13 2 8 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCN(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
10010104 140730 0 None - 0 Guinea pig 9.7 pKd = 9.7 Functional
Antagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscleAntagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscle
ChEMBL 720 13 2 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL383167 140730 0 None - 0 Guinea pig 9.7 pKd = 9.7 Functional
Antagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscleAntagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscle
ChEMBL 720 13 2 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm061143k
16105703 135944 0 None - 0 Human 9.6 pKd = 9.6 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 776 12 2 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCN(C)CC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL373607 135944 0 None - 0 Human 9.6 pKd = 9.6 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 776 12 2 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCN(C)CC4)c3Cl)c2n1 10.1021/jm061143k
10373970 137076 0 None - 0 Human 9.6 pKd = 9.6 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 760 13 5 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCNC(=N)N)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL375689 137076 0 None - 0 Human 9.6 pKd = 9.6 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 760 13 5 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCNC(=N)N)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
44378635 168171 0 None - 0 Human 9.6 pKd = 9.6 Functional
Antagonist effect against bradykinin B2 receptor was determined in rabbit jugular veinAntagonist effect against bradykinin B2 receptor was determined in rabbit jugular vein
ChEMBL 1351 29 15 18 -2.0 C[C@@]12CCCC[C@]1(C)N(C(=O)[C@H]1Cc3ccccc3CN1C(=O)[C@H](CO)NC(=O)[C@H](Cc1cccs1)NC(=O)CNC(=O)[C@@H]1C[C@@H](O)CN1C(=O)[C@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)c1ccc(NC(N)C=N)cc1)[C@H](C(=O)N[C@@H](CCCN=C(N)N)C(=O)O)C2 10.1016/S0960-894X(01)80847-7
CHEMBL437155 168171 0 None - 0 Human 9.6 pKd = 9.6 Functional
Antagonist effect against bradykinin B2 receptor was determined in rabbit jugular veinAntagonist effect against bradykinin B2 receptor was determined in rabbit jugular vein
ChEMBL 1351 29 15 18 -2.0 C[C@@]12CCCC[C@]1(C)N(C(=O)[C@H]1Cc3ccccc3CN1C(=O)[C@H](CO)NC(=O)[C@H](Cc1cccs1)NC(=O)CNC(=O)[C@@H]1C[C@@H](O)CN1C(=O)[C@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)c1ccc(NC(N)C=N)cc1)[C@H](C(=O)N[C@@H](CCCN=C(N)N)C(=O)O)C2 10.1016/S0960-894X(01)80847-7
667 1934 32 None -2 2 Human 9.6 pKd = 9.6 Functional
Antagonist activity against bradykinin B2 receptorAntagonist activity against bradykinin B2 receptor
ChEMBL None None None None 10.1016/j.bmcl.2006.01.125
71364 1934 32 None -2 2 Human 9.6 pKd = 9.6 Functional
Antagonist activity against bradykinin B2 receptorAntagonist activity against bradykinin B2 receptor
ChEMBL None None None None 10.1016/j.bmcl.2006.01.125
CHEMBL2028850 1934 32 None -2 2 Human 9.6 pKd = 9.6 Functional
Antagonist activity against bradykinin B2 receptorAntagonist activity against bradykinin B2 receptor
ChEMBL None None None None 10.1016/j.bmcl.2006.01.125
DB06196 1934 32 None -2 2 Human 9.6 pKd = 9.6 Functional
Antagonist activity against bradykinin B2 receptorAntagonist activity against bradykinin B2 receptor
ChEMBL None None None None 10.1016/j.bmcl.2006.01.125
57345657 71233 0 None - 0 Human 9.5 pKd = 9.5 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 748 12 1 7 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956722 71233 0 None - 0 Human 9.5 pKd = 9.5 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 748 12 1 7 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963183 71233 0 None - 0 Human 9.5 pKd = 9.5 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 748 12 1 7 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
11600324 141452 0 None - 0 Human 9.5 pKd = 9.5 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 747 12 2 7 4.8 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL387452 141452 0 None - 0 Human 9.5 pKd = 9.5 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 747 12 2 7 4.8 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
44412007 76843 1 None - 0 Guinea pig 9.5 pKd = 9.5 Functional
Antagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscleAntagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscle
ChEMBL 710 12 4 7 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)N4CCC[C@@H]4C(=O)NCCCNC(=O)c4ccc(C(=N)N)cc4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL207939 76843 1 None - 0 Guinea pig 9.5 pKd = 9.5 Functional
Antagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscleAntagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscle
ChEMBL 710 12 4 7 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)N4CCC[C@@H]4C(=O)NCCCNC(=O)c4ccc(C(=N)N)cc4)c3Cl)c2n1 10.1021/jm061143k
667 1934 32 None - 2 Rat 9.5 pKd = 9.5 Functional
In vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assayIn vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assay
ChEMBL None None None None 10.1021/jm950716i
71364 1934 32 None - 2 Rat 9.5 pKd = 9.5 Functional
In vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assayIn vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assay
ChEMBL None None None None 10.1021/jm950716i
CHEMBL2028850 1934 32 None - 2 Rat 9.5 pKd = 9.5 Functional
In vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assayIn vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assay
ChEMBL None None None None 10.1021/jm950716i
DB06196 1934 32 None - 2 Rat 9.5 pKd = 9.5 Functional
In vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assayIn vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assay
ChEMBL None None None None 10.1021/jm950716i
57399983 71216 0 None - 0 Human 9.4 pKd = 9.4 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 777 13 2 8 4.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956859 71216 0 None - 0 Human 9.4 pKd = 9.4 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 777 13 2 8 4.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963149 71216 0 None - 0 Human 9.4 pKd = 9.4 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 777 13 2 8 4.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57401772 71229 0 None - 0 Human 9.4 pKd = 9.4 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 734 12 3 9 3.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCN)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956857 71229 0 None - 0 Human 9.4 pKd = 9.4 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 734 12 3 9 3.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCN)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963175 71229 0 None - 0 Human 9.4 pKd = 9.4 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 734 12 3 9 3.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCN)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
44412007 76843 1 None - 0 Human 9.4 pKd = 9.4 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 710 12 4 7 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)N4CCC[C@@H]4C(=O)NCCCNC(=O)c4ccc(C(=N)N)cc4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL207939 76843 1 None - 0 Human 9.4 pKd = 9.4 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 710 12 4 7 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)N4CCC[C@@H]4C(=O)NCCCNC(=O)c4ccc(C(=N)N)cc4)c3Cl)c2n1 10.1021/jm061143k
57401770 71224 0 None - 0 Human 9.4 pKd = 9.4 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 733 12 1 8 5.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCN(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956853 71224 0 None - 0 Human 9.4 pKd = 9.4 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 733 12 1 8 5.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCN(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963162 71224 0 None - 0 Human 9.4 pKd = 9.4 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 733 12 1 8 5.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCN(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57396534 71305 0 None - 0 Human 9.3 pKd = 9.3 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 705 11 2 8 4.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCN)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956854 71305 0 None - 0 Human 9.3 pKd = 9.3 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 705 11 2 8 4.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCN)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963650 71305 0 None - 0 Human 9.3 pKd = 9.3 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 705 11 2 8 4.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCN)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL3038099 209177 0 None - 0 Rat 9.3 pKd = 9.3 Functional
In vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assayIn vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assay
ChEMBL None None None NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N(CC(=O)N[C@@H](CCCN=C(N)N)C(=O)O)C1CCCCC1 10.1021/jm950716i
10079793 93673 0 None - 0 Human 9.3 pKd = 9.3 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 717 11 3 7 4.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=N)NCCCN(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL249235 93673 0 None - 0 Human 9.3 pKd = 9.3 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 717 11 3 7 4.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=N)NCCCN(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
16105698 135810 0 None - 0 Human 9.3 pKd = 9.3 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 747 12 2 7 4.8 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@H](CCCN)[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL373459 135810 0 None - 0 Human 9.3 pKd = 9.3 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 747 12 2 7 4.8 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@H](CCCN)[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
10079797 137059 0 None - 0 Human 9.3 pKd = 9.3 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 718 12 3 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[C@@H](N)CCCN)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL375576 137059 0 None - 0 Human 9.3 pKd = 9.3 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 718 12 3 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[C@@H](N)CCCN)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
16105734 83842 0 None - 0 Human 9.2 pKd = 9.2 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 803 14 4 7 4.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@H](CCCCNC(=N)N)[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL221285 83842 0 None - 0 Human 9.2 pKd = 9.2 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 803 14 4 7 4.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@H](CCCCNC(=N)N)[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
57394782 71284 0 None - 0 Human 9.1 pKd = 9.1 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 720 11 3 9 3.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCN)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956855 71284 0 None - 0 Human 9.1 pKd = 9.1 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 720 11 3 9 3.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCN)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963557 71284 0 None - 0 Human 9.1 pKd = 9.1 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 720 11 3 9 3.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCN)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
10101294 139611 0 None - 0 Human 9.1 pKd = 9.1 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 706 12 2 8 4.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL380273 139611 0 None - 0 Human 9.1 pKd = 9.1 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 706 12 2 8 4.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
57399228 71213 0 None - 0 Human 9.1 pKd = 9.1 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 706 9 1 7 3.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956720 71213 0 None - 0 Human 9.1 pKd = 9.1 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 706 9 1 7 3.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963146 71213 0 None - 0 Human 9.1 pKd = 9.1 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 706 9 1 7 3.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57402746 71214 0 None - 0 Human 9.1 pKd = 9.1 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 734 11 1 7 4.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956721 71214 0 None - 0 Human 9.1 pKd = 9.1 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 734 11 1 7 4.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963147 71214 0 None - 0 Human 9.1 pKd = 9.1 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 734 11 1 7 4.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57401778 71219 0 None - 0 Human 9.1 pKd = 9.1 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 748 14 1 7 6.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(CCCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956870 71219 0 None - 0 Human 9.1 pKd = 9.1 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 748 14 1 7 6.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(CCCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963152 71219 0 None - 0 Human 9.1 pKd = 9.1 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 748 14 1 7 6.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(CCCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57400986 71223 0 None - 0 Human 9.1 pKd = 9.1 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 762 13 1 7 5.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956723 71223 0 None - 0 Human 9.1 pKd = 9.1 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 762 13 1 7 5.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963161 71223 0 None - 0 Human 9.1 pKd = 9.1 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 762 13 1 7 5.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
9988753 83404 0 None - 0 Human 9.1 pKd = 9.1 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 746 13 2 8 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCN(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL220595 83404 0 None - 0 Human 9.1 pKd = 9.1 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 746 13 2 8 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCN(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
10418701 96642 0 None - 0 Human 9.1 pKd = 9.1 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 760 13 5 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[C@@H](N)CCCNC(=N)N)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL267493 96642 0 None - 0 Human 9.1 pKd = 9.1 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 760 13 5 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[C@@H](N)CCCNC(=N)N)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
10032895 137093 0 None - 0 Human 9.1 pKd = 9.1 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 734 13 5 8 3.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCCNC(=N)N)CC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL375820 137093 0 None - 0 Human 9.1 pKd = 9.1 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 734 13 5 8 3.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCCNC(=N)N)CC4)c3Cl)c2n1 10.1021/jm061143k
10101294 139611 0 None - 0 Human 9.1 pKd = 9.1 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 706 12 2 8 4.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL380273 139611 0 None - 0 Human 9.1 pKd = 9.1 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 706 12 2 8 4.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL3038100 209178 0 None - 0 Rat 9.1 pKd = 9.1 Functional
In vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assayIn vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assay
ChEMBL None None None N=C(N)NCCCCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N1CCC[C@@H]1C(=O)N1C[C@@H](O)C[C@@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N(CC(=O)N[C@@H](CCCNC(=N)N)C(=O)O)C1CCCCC1 10.1021/jm950716i
667 1934 32 None -2 2 Human 9.0 pKd = 9.0 Functional
Antagonist effect against bradykinin B2 receptor was determined in rabbit jugular veinAntagonist effect against bradykinin B2 receptor was determined in rabbit jugular vein
ChEMBL None None None None 10.1016/S0960-894X(01)80847-7
71364 1934 32 None -2 2 Human 9.0 pKd = 9.0 Functional
Antagonist effect against bradykinin B2 receptor was determined in rabbit jugular veinAntagonist effect against bradykinin B2 receptor was determined in rabbit jugular vein
ChEMBL None None None None 10.1016/S0960-894X(01)80847-7
CHEMBL2028850 1934 32 None -2 2 Human 9.0 pKd = 9.0 Functional
Antagonist effect against bradykinin B2 receptor was determined in rabbit jugular veinAntagonist effect against bradykinin B2 receptor was determined in rabbit jugular vein
ChEMBL None None None None 10.1016/S0960-894X(01)80847-7
DB06196 1934 32 None -2 2 Human 9.0 pKd = 9.0 Functional
Antagonist effect against bradykinin B2 receptor was determined in rabbit jugular veinAntagonist effect against bradykinin B2 receptor was determined in rabbit jugular vein
ChEMBL None None None None 10.1016/S0960-894X(01)80847-7
57396538 71230 0 None - 0 Human 9.0 pKd = 9 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 721 11 1 6 5.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956861 71230 0 None - 0 Human 9.0 pKd = 9 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 721 11 1 6 5.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963176 71230 0 None - 0 Human 9.0 pKd = 9 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 721 11 1 6 5.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57394780 71283 0 None - 0 Human 8.9 pKd = 8.9 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 776 14 1 7 5.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956852 71283 0 None - 0 Human 8.9 pKd = 8.9 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 776 14 1 7 5.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963556 71283 0 None - 0 Human 8.9 pKd = 8.9 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 776 14 1 7 5.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
16105751 82802 0 None - 0 Human 8.9 pKd = 8.9 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 804 12 2 8 3.9 CC(=O)N1CCC(NS(=O)(=O)c2ccc(Cl)c(COc3cccc4c(C)cc(C)nc34)c2Cl)(C(=O)N2CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC2)CC1 10.1021/jm061143k
CHEMBL218636 82802 0 None - 0 Human 8.9 pKd = 8.9 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 804 12 2 8 3.9 CC(=O)N1CCC(NS(=O)(=O)c2ccc(Cl)c(COc3cccc4c(C)cc(C)nc34)c2Cl)(C(=O)N2CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC2)CC1 10.1021/jm061143k
16105690 83207 0 None - 0 Human 8.9 pKd = 8.9 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 761 13 2 7 5.2 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[C@H](CCCN)[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL220478 83207 0 None - 0 Human 8.9 pKd = 8.9 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 761 13 2 7 5.2 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[C@H](CCCN)[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
16105729 136398 0 None - 0 Human 8.9 pKd = 8.9 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 761 13 2 7 5.2 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL374273 136398 0 None - 0 Human 8.9 pKd = 8.9 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 761 13 2 7 5.2 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL3038095 209174 0 None - 0 Rat 8.9 pKd = 8.9 Functional
In vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assayIn vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assay
ChEMBL None None None NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N(CC(=O)N[C@@H](CCCN=C(N)N)C(=O)O)c1ccccc1 10.1021/jm950716i
CHEMBL2371961 208403 0 None - 0 Guinea pig 8.8 pKd = 8.8 Functional
Antagonism against bradykinin receptor B2 in guinea pig ileal tissueAntagonism against bradykinin receptor B2 in guinea pig ileal tissue
ChEMBL None None None NC(N)=NCCC[C@H](NC(=O)[C@@H]1CN(C(=O)[C@H]2c3ccccc3CCN2C(=O)[C@H](CO)NC(=O)[C@H](Cc2ccccc2)NC(=O)CNC(=O)[C@@H]2C[C@@H](O)CN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C2CCCCC21)C(=O)O 10.1021/jm00069a016
57401776 71217 0 None - 0 Human 8.8 pKd = 8.8 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 690 7 1 7 4.2 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+]6(CCN(C)CC6)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956866 71217 0 None - 0 Human 8.8 pKd = 8.8 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 690 7 1 7 4.2 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+]6(CCN(C)CC6)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963150 71217 0 None - 0 Human 8.8 pKd = 8.8 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 690 7 1 7 4.2 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+]6(CCN(C)CC6)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57401782 71227 0 None - 0 Human 8.8 pKd = 8.8 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 705 11 1 6 6.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956873 71227 0 None - 0 Human 8.8 pKd = 8.8 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 705 11 1 6 6.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963165 71227 0 None - 0 Human 8.8 pKd = 8.8 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 705 11 1 6 6.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
10463883 83405 0 None - 0 Human 8.8 pKd = 8.8 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 746 13 2 8 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[C@@H](N)CCCN(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL220596 83405 0 None - 0 Human 8.8 pKd = 8.8 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 746 13 2 8 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[C@@H](N)CCCN(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
16105701 83541 0 None - 0 Human 8.8 pKd = 8.8 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 762 12 3 8 3.6 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCNCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL220693 83541 0 None - 0 Human 8.8 pKd = 8.8 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 762 12 3 8 3.6 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCNCC4)c3Cl)c2n1 10.1021/jm061143k
10441167 96527 0 None - 0 Human 8.8 pKd = 8.8 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 732 11 3 6 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=N)NCCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL266493 96527 0 None - 0 Human 8.8 pKd = 8.8 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 732 11 3 6 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=N)NCCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
10102701 136900 0 None - 0 Human 8.8 pKd = 8.8 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 761 13 2 7 5.2 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@H](CCCCN)[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL375354 136900 0 None - 0 Human 8.8 pKd = 8.8 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 761 13 2 7 5.2 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@H](CCCCN)[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
16105694 141350 0 None - 0 Human 8.8 pKd = 8.8 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 732 12 1 6 5.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL386794 141350 0 None - 0 Human 8.8 pKd = 8.8 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 732 12 1 6 5.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
9897921 161340 0 None - 0 Human 8.8 pKd = 8.8 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 761 13 2 7 5.2 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[C@@H](N)CCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL415151 161340 0 None - 0 Human 8.8 pKd = 8.8 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 761 13 2 7 5.2 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[C@@H](N)CCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL2372283 208454 0 None - 0 Rat 8.8 pKd = 8.8 Functional
In vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assayIn vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assay
ChEMBL None None None NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@@H]1C(=O)N1C[C@@H](O)C[C@@H]1C(=O)NCC(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N(CC(=O)N[C@@H](CCCN=C(N)N)C(=O)O)C1CCCCC1 10.1021/jm950716i
57398324 71226 0 None - 0 Human 8.7 pKd = 8.7 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 735 12 1 6 5.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956862 71226 0 None - 0 Human 8.7 pKd = 8.7 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 735 12 1 6 5.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963164 71226 0 None - 0 Human 8.7 pKd = 8.7 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 735 12 1 6 5.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
16105727 83383 0 None - 0 Human 8.7 pKd = 8.7 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 718 12 3 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCN)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL220591 83383 0 None - 0 Human 8.7 pKd = 8.7 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 718 12 3 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCN)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
10396101 83911 0 None - 0 Human 8.7 pKd = 8.7 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 718 11 1 6 5.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL221683 83911 0 None - 0 Human 8.7 pKd = 8.7 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 718 11 1 6 5.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
10441194 84185 0 None - 0 Human 8.7 pKd = 8.7 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 745 13 4 7 5.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCCNC(=N)N)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL222156 84185 0 None - 0 Human 8.7 pKd = 8.7 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 745 13 4 7 5.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCCNC(=N)N)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
16105742 137613 0 None - 0 Human 8.7 pKd = 8.7 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 733 11 2 7 4.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL376866 137613 0 None - 0 Human 8.7 pKd = 8.7 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 733 11 2 7 4.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
10418495 77507 0 None - 0 Human 8.0 pKd = 8.0 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 649 10 4 7 3.5 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=N)NCCCN)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL209346 77507 0 None - 0 Human 8.0 pKd = 8.0 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 649 10 4 7 3.5 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=N)NCCCN)CC4)c3Cl)c2n1 10.1021/jm060137l
44354187 116287 0 None - 0 Guinea pig 6.0 pKd = 6 Functional
Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.
ChEMBL 925 29 11 10 0.2 NC(N)=NCCC[C@H](NC(=O)[C@H](N)CCCN=C(N)N)C(=O)NCCCCCCCCCCC(=O)N[C@@H](CO)C(=O)N[C@@H](C(=O)N1[C@@H](C(=O)O)C[C@H]2CCCC[C@H]21)C1Cc2ccccc2C1 10.1021/jm980495r
CHEMBL337833 116287 0 None - 0 Guinea pig 6.0 pKd = 6 Functional
Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.
ChEMBL 925 29 11 10 0.2 NC(N)=NCCC[C@H](NC(=O)[C@H](N)CCCN=C(N)N)C(=O)NCCCCCCCCCCC(=O)N[C@@H](CO)C(=O)N[C@@H](C(=O)N1[C@@H](C(=O)O)C[C@H]2CCCC[C@H]21)C1Cc2ccccc2C1 10.1021/jm980495r
CHEMBL410363 211059 17 None - 0 Guinea pig 6.0 pKd = 6 Functional
Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@@H](Cc1ccc2ccccc2c1)NC(=O)[C@H](CO)NC(=O)[C@H](Cc1ccccc1)NC(=O)CNC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CCCCN)NC(C)=O)C(=O)O 10.1021/jm980495r
10010669 76443 0 None - 0 Human 8.0 pKd = 8.0 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 706 13 2 8 4.2 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL206938 76443 0 None - 0 Human 8.0 pKd = 8.0 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 706 13 2 8 4.2 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
70685700 74139 0 None - 0 Rabbit 6.9 pKd = 6.9 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 670 6 6 6 0.7 N=C(N)NCCC[C@@H]1NC(=O)[C@@H]2CC3CCCCC3N2C(=O)[C@H]2Cc3ccccc3CN2C(=O)[C@H](Cc2ccccc2)NC(=O)CNC1=O 10.1021/jm950682e
CHEMBL2028840 74139 0 None - 0 Rabbit 6.9 pKd = 6.9 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 670 6 6 6 0.7 N=C(N)NCCC[C@@H]1NC(=O)[C@@H]2CC3CCCCC3N2C(=O)[C@H]2Cc3ccccc3CN2C(=O)[C@H](Cc2ccccc2)NC(=O)CNC1=O 10.1021/jm950682e
CHEMBL2370040 208018 0 None - 0 Guinea pig 7.9 pKd = 7.9 Functional
Antagonism against bradykinin receptor B2 in guinea pig ileal tissueAntagonism against bradykinin receptor B2 in guinea pig ileal tissue
ChEMBL None None None C[C@@](Cc1ccccc1)(NC(=O)CNC(=O)[C@@H]1C[C@H](O)CN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O 10.1021/jm00069a016
44354059 116545 0 None - 0 Guinea pig 5.9 pKd = 5.9 Functional
Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.
ChEMBL 925 34 11 10 1.8 CC[C@H](C)[C@H](NC(=O)[C@@H](Cc1ccc2ccccc2c1)NC(=O)[C@H](CO)NC(=O)CCCCCCCCCCNC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CCCCN)NC(C)=O)C(=O)O 10.1021/jm980495r
CHEMBL339159 116545 0 None - 0 Guinea pig 5.9 pKd = 5.9 Functional
Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.
ChEMBL 925 34 11 10 1.8 CC[C@H](C)[C@H](NC(=O)[C@@H](Cc1ccc2ccccc2c1)NC(=O)[C@H](CO)NC(=O)CCCCCCCCCCNC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CCCCN)NC(C)=O)C(=O)O 10.1021/jm980495r
CHEMBL3038103 209181 0 None - 1 Rat 5.9 pKd = 5.9 Functional
In vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assayIn vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assay
ChEMBL None None None NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N[C@@H](C(=O)N(CC(=O)N[C@@H](CCCN=C(N)N)C(=O)O)C1CCCCC1)C1CCCC1 10.1021/jm950716i
70685699 74133 0 None - 0 Rabbit 6.8 pKd = 6.8 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 747 10 6 9 1.1 NCCCC[C@@H]1N[C@@H](Cc2cccs2)C(=O)N2Cc3ccccc3C[C@@H]2C(=O)N2C3CCCCC3C[C@H]2C(=O)N[C@@H](CCCN=C(N)N)C(=O)NC1=O 10.1021/jm950682e
CHEMBL2028835 74133 0 None - 0 Rabbit 6.8 pKd = 6.8 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 747 10 6 9 1.1 NCCCC[C@@H]1N[C@@H](Cc2cccs2)C(=O)N2Cc3ccccc3C[C@@H]2C(=O)N2C3CCCCC3C[C@H]2C(=O)N[C@@H](CCCN=C(N)N)C(=O)NC1=O 10.1021/jm950682e
CHEMBL3038104 209182 0 None - 1 Rat 6.8 pKd = 6.8 Functional
In vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assayIn vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assay
ChEMBL None None None NC(N)=NCCC[C@@H](N)C(=O)N[C@@H](CCCNC(N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N(CC(=O)O)C1CCCCC1 10.1021/jm950716i
CHEMBL3038096 209175 0 None - 1 Rat 7.7 pKd = 7.7 Functional
In vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assayIn vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assay
ChEMBL None None None NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N[C@H](Cc1ccccc1)C(=O)N(CC(=O)N[C@@H](CCCN=C(N)N)C(=O)O)C1CCCCC1 10.1021/jm950716i
10056816 77381 0 None - 0 Human 7.7 pKd = 7.7 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 649 13 2 7 5.1 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(CCCCCCN)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL209038 77381 0 None - 0 Human 7.7 pKd = 7.7 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 649 13 2 7 5.1 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(CCCCCCN)CC4)c3Cl)c2n1 10.1021/jm060137l
11513471 138105 0 None - 0 Human 7.7 pKd = 7.7 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 748 14 2 8 4.4 CC(=O)N[C@@H](CCCCN(C)C)C(=O)N1CCN(C(=O)C(C)(C)NS(=O)(=O)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)CC1 10.1021/jm060137l
CHEMBL377612 138105 0 None - 0 Human 7.7 pKd = 7.7 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 748 14 2 8 4.4 CC(=O)N[C@@H](CCCCN(C)C)C(=O)N1CCN(C(=O)C(C)(C)NS(=O)(=O)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)CC1 10.1021/jm060137l
56668285 62973 0 None - 0 Guinea pig 5.7 pKd = 5.7 Functional
Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.
ChEMBL 1145 26 13 15 -1.1 C=C([C@H]1Cc2ccccc2CN1C(=O)[C@H](CO)CC(=O)[C@H](Cc1cccs1)NC(=O)CNC(=O)[C@@H]1C[C@@H](O)CN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](N)CCCNC(=N)N)N1[C@H](C(=O)O)C[C@@H]2CCCC[C@@H]21 10.1021/jm980495r
CHEMBL1793829 62973 0 None - 0 Guinea pig 5.7 pKd = 5.7 Functional
Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.
ChEMBL 1145 26 13 15 -1.1 C=C([C@H]1Cc2ccccc2CN1C(=O)[C@H](CO)CC(=O)[C@H](Cc1cccs1)NC(=O)CNC(=O)[C@@H]1C[C@@H](O)CN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](N)CCCNC(=N)N)N1[C@H](C(=O)O)C[C@@H]2CCCC[C@@H]21 10.1021/jm980495r
10439868 75558 0 None - 0 Human 8.6 pKd = 8.6 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 720 13 2 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)C[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL205093 75558 0 None - 0 Human 8.6 pKd = 8.6 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 720 13 2 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)C[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
11600186 77879 0 None - 0 Human 8.6 pKd = 8.6 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 734 14 2 8 4.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)C[C@@H](N)CCCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL210788 77879 0 None - 0 Human 8.6 pKd = 8.6 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 734 14 2 8 4.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)C[C@@H](N)CCCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
10418252 138349 0 None - 0 Human 8.6 pKd = 8.6 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 663 10 4 7 3.8 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=N)NCCCN)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL378237 138349 0 None - 0 Human 8.6 pKd = 8.6 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 663 10 4 7 3.8 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=N)NCCCN)CC4)c3Cl)c2n1 10.1021/jm060137l
57401774 71234 0 None - 0 Human 8.6 pKd = 8.6 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 749 13 1 6 5.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956863 71234 0 None - 0 Human 8.6 pKd = 8.6 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 749 13 1 6 5.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963184 71234 0 None - 0 Human 8.6 pKd = 8.6 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 749 13 1 6 5.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57391279 71235 0 None - 0 Human 8.6 pKd = 8.6 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 748 14 2 7 5.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CNCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956876 71235 0 None - 0 Human 8.6 pKd = 8.6 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 748 14 2 7 5.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CNCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963185 71235 0 None - 0 Human 8.6 pKd = 8.6 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 748 14 2 7 5.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CNCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57401784 71280 0 None - 0 Human 8.6 pKd = 8.6 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 734 13 2 7 5.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CNCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956875 71280 0 None - 0 Human 8.6 pKd = 8.6 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 734 13 2 7 5.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CNCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963532 71280 0 None - 0 Human 8.6 pKd = 8.6 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 734 13 2 7 5.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CNCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57392147 71310 0 None - 0 Human 8.6 pKd = 8.6 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 720 12 2 7 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CNCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1955876 71310 0 None - 0 Human 8.6 pKd = 8.6 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 720 12 2 7 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CNCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963660 71310 0 None - 0 Human 8.6 pKd = 8.6 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 720 12 2 7 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CNCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
10439868 75558 0 None - 0 Human 8.6 pKd = 8.6 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 720 13 2 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)C[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL205093 75558 0 None - 0 Human 8.6 pKd = 8.6 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 720 13 2 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)C[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm061143k
16105696 82781 0 None - 0 Human 8.6 pKd = 8.6 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 790 13 1 6 5.6 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@H](CCC[N+](C)(C)C)[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL218540 82781 0 None - 0 Human 8.6 pKd = 8.6 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 790 13 1 6 5.6 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@H](CCC[N+](C)(C)C)[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
57403505 71286 0 None - 0 Human 8.6 pKd = 8.6 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 675 7 1 6 5.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+]6(CCCCC6)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956865 71286 0 None - 0 Human 8.6 pKd = 8.6 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 675 7 1 6 5.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+]6(CCCCC6)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963559 71286 0 None - 0 Human 8.6 pKd = 8.6 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 675 7 1 6 5.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+]6(CCCCC6)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL3038101 209179 0 None - 0 Rat 7.7 pKd = 7.7 Functional
In vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assayIn vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assay
ChEMBL None None None NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N[C@H](Cc1ccccc1)C(=O)N(CC(=O)N[C@@H](CCCN=C(N)N)C(=O)O)c1ccccc1 10.1021/jm950716i
CHEMBL3038105 209183 0 None - 1 Rat 5.7 pKd = 5.7 Functional
In vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assayIn vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assay
ChEMBL None None None NC(N)=NCCC[C@@H](N)C(=O)N[C@@H](CCCNC(N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N(CC(=O)N1C2CCCCC2C[C@H]1C(=O)O)Cc1ccccc1 10.1021/jm950716i
70696204 74134 0 None - 0 Rabbit 6.7 pKd = 6.7 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 690 6 4 7 0.9 CN1CC(=O)N[C@@H](Cc2cccs2)C(=O)N2Cc3ccccc3C[C@@H]2C(=O)N2C3CCCCC3C[C@H]2C(=O)N[C@@H](CCCN=C(N)N)C1=O 10.1021/jm950682e
CHEMBL2028836 74134 0 None - 0 Rabbit 6.7 pKd = 6.7 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 690 6 4 7 0.9 CN1CC(=O)N[C@@H](Cc2cccs2)C(=O)N2Cc3ccccc3C[C@@H]2C(=O)N2C3CCCCC3C[C@H]2C(=O)N[C@@H](CCCN=C(N)N)C1=O 10.1021/jm950682e
CHEMBL2372278 208452 0 None - 0 Rat 7.7 pKd = 7.7 Functional
In vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assayIn vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assay
ChEMBL None None None N=C(N)NCCCCC(=O)N1CCC[C@@H]1C(=O)N1C[C@@H](O)C[C@@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N(CC(=O)N[C@@H](CCCNC(=N)N)C(=O)O)C1CCCCC1 10.1021/jm950716i
CHEMBL2370010 208012 0 None - 0 Guinea pig 6.6 pKd = 6.6 Functional
Antagonism against bradykinin receptor B2 in guinea pig ileal tissueAntagonism against bradykinin receptor B2 in guinea pig ileal tissue
ChEMBL None None None NC(N)=NCCC[C@H](NC(=O)[C@@H]1C2CCCCC2CN1C(=O)[C@@H]1Cc2ccccc2CN1C(=O)[C@H](CO)NC(=O)[C@@H]1CSSC[C@H](NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N2CCC[C@H]2C(=O)NCC(=O)N1)C(=O)O 10.1021/jm00069a016
70687850 74140 0 None - 0 Rabbit 6.6 pKd = 6.6 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 594 4 5 6 -0.7 C[C@@H]1NC(=O)CNC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@@H]2CC3CCCCC3N2C(=O)[C@H]2Cc3ccccc3CN2C1=O 10.1021/jm950682e
CHEMBL2028841 74140 0 None - 0 Rabbit 6.6 pKd = 6.6 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 594 4 5 6 -0.7 C[C@@H]1NC(=O)CNC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@@H]2CC3CCCCC3N2C(=O)[C@H]2Cc3ccccc3CN2C1=O 10.1021/jm950682e
11506007 77642 0 None - 0 Human 7.6 pKd = 7.6 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 676 9 2 8 3.1 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)CN5CCNCC5)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL209773 77642 0 None - 0 Human 7.6 pKd = 7.6 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 676 9 2 8 3.1 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)CN5CCNCC5)CC4)c3Cl)c2n1 10.1021/jm060137l
10463758 138329 0 None - 0 Human 7.6 pKd = 7.6 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 692 12 2 8 3.8 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL378189 138329 0 None - 0 Human 7.6 pKd = 7.6 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 692 12 2 8 3.8 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
90662813 106072 0 None - 0 Rabbit 6.6 pKd = 6.6 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 722 15 6 8 1.3 NCCCC(=O)N[C@@H](Cc1cccs1)C(=O)N1Cc2ccccc2C[C@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O 10.1021/jm950682e
CHEMBL3142191 106072 0 None - 0 Rabbit 6.6 pKd = 6.6 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 722 15 6 8 1.3 NCCCC(=O)N[C@@H](Cc1cccs1)C(=O)N1Cc2ccccc2C[C@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O 10.1021/jm950682e
CHEMBL2370042 208020 0 None - 0 Guinea pig 5.6 pKd = 5.6 Functional
Antagonism against bradykinin receptor B2 in guinea pig ileal tissueAntagonism against bradykinin receptor B2 in guinea pig ileal tissue
ChEMBL None None None CN(C(=O)CNC(=O)[C@@H]1C[C@H](O)CN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)[C@@H](Cc1ccccc1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O 10.1021/jm00069a016
44410425 96678 0 None - 0 Human 5.6 pKd = 5.6 Functional
Antagonist activity against bradykinin B2 receptorAntagonist activity against bradykinin B2 receptor
ChEMBL 1332 32 16 17 -4.3 NC(N)=NCCC[C@H](NC(=O)[C@@H]1CC2(CCCC2)C2CCC[C@](Cc3ccccc3)(NC(=O)[C@H](CO)NC(=O)[C@H](Cc3cccs3)NC(=O)CNC(=O)[C@@H]3CC(O)CN3C(=O)[C@@H]3CCCN3C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N21)C(=O)O 10.1016/j.bmcl.2006.01.125
CHEMBL267822 96678 0 None - 0 Human 5.6 pKd = 5.6 Functional
Antagonist activity against bradykinin B2 receptorAntagonist activity against bradykinin B2 receptor
ChEMBL 1332 32 16 17 -4.3 NC(N)=NCCC[C@H](NC(=O)[C@@H]1CC2(CCCC2)C2CCC[C@](Cc3ccccc3)(NC(=O)[C@H](CO)NC(=O)[C@H](Cc3cccs3)NC(=O)CNC(=O)[C@@H]3CC(O)CN3C(=O)[C@@H]3CCCN3C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N21)C(=O)O 10.1016/j.bmcl.2006.01.125
10010104 140730 0 None - 0 Human 8.5 pKd = 8.5 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 720 13 2 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL383167 140730 0 None - 0 Human 8.5 pKd = 8.5 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 720 13 2 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
57396536 71225 0 None - 0 Human 8.5 pKd = 8.5 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 707 10 1 6 4.6 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956860 71225 0 None - 0 Human 8.5 pKd = 8.5 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 707 10 1 6 4.6 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963163 71225 0 None - 0 Human 8.5 pKd = 8.5 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 707 10 1 6 4.6 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57393060 71228 0 None - 0 Human 8.5 pKd = 8.5 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 661 7 1 6 5.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+]6(CCCC6)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956851 71228 0 None - 0 Human 8.5 pKd = 8.5 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 661 7 1 6 5.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+]6(CCCC6)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963174 71228 0 None - 0 Human 8.5 pKd = 8.5 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 661 7 1 6 5.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+]6(CCCC6)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57398326 71285 0 None - 0 Human 8.5 pKd = 8.5 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 763 14 1 6 6.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CCCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956864 71285 0 None - 0 Human 8.5 pKd = 8.5 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 763 14 1 6 6.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CCCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963558 71285 0 None - 0 Human 8.5 pKd = 8.5 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 763 14 1 6 6.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CCCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
11766718 136397 0 None - 0 Human 8.5 pKd = 8.5 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 774 14 1 8 5.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@H](CCCCN(C)C)N(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL374272 136397 0 None - 0 Human 8.5 pKd = 8.5 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 774 14 1 8 5.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@H](CCCCN(C)C)N(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
10010104 140730 0 None - 0 Human 8.5 pKd = 8.5 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 720 13 2 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL383167 140730 0 None - 0 Human 8.5 pKd = 8.5 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 720 13 2 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL3038094 209173 0 None - 0 Rat 8.5 pKd = 8.5 Functional
In vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assayIn vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assay
ChEMBL None None None NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N(CC(=O)N[C@@H](CCCN=C(N)N)C(=O)O)C1CCCC1 10.1021/jm950716i
CHEMBL3038106 209184 0 None - 0 Rat 8.5 pKd = 8.5 Functional
In vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assayIn vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assay
ChEMBL None None None NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1C[C@@H](O)C[C@@H]1C(=O)N1C[C@@H](O)C[C@@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N(CC(=O)N[C@@H](CCCN=C(N)N)C(=O)O)C1CCCCC1 10.1021/jm950716i
57401780 71220 0 None - 0 Human 8.4 pKd = 8.4 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 691 10 1 6 5.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956872 71220 0 None - 0 Human 8.4 pKd = 8.4 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 691 10 1 6 5.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963153 71220 0 None - 0 Human 8.4 pKd = 8.4 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 691 10 1 6 5.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57398328 71309 0 None - 0 Human 8.4 pKd = 8.4 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 719 12 1 6 6.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956874 71309 0 None - 0 Human 8.4 pKd = 8.4 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 719 12 1 6 6.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963659 71309 0 None - 0 Human 8.4 pKd = 8.4 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 719 12 1 6 6.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
90662795 106069 0 None - 0 Rabbit 5.5 pKd = 5.5 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 778 17 9 8 1.4 N=C(N)NCCCCC(=O)N[C@@H](Cc1cccs1)C(=O)N1Cc2ccccc2C[C@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCNC(=N)N)C(=O)O 10.1021/jm950682e
CHEMBL3142173 106069 0 None - 0 Rabbit 5.5 pKd = 5.5 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 778 17 9 8 1.4 N=C(N)NCCCCC(=O)N[C@@H](Cc1cccs1)C(=O)N1Cc2ccccc2C[C@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCNC(=N)N)C(=O)O 10.1021/jm950682e
70681476 74142 0 None - 0 Rabbit 6.5 pKd = 6.5 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 709 5 7 8 -1.5 C[C@@H]1NC(=O)CCCNC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@@H]2CC3CCCCC3N2C(=O)[C@H]2Cc3ccccc3CN2C(=O)[C@H](CO)NC1=O 10.1021/jm950682e
CHEMBL2028844 74142 0 None - 0 Rabbit 6.5 pKd = 6.5 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 709 5 7 8 -1.5 C[C@@H]1NC(=O)CCCNC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@@H]2CC3CCCCC3N2C(=O)[C@H]2Cc3ccccc3CN2C(=O)[C@H](CO)NC1=O 10.1021/jm950682e
44354175 96447 0 None - 0 Guinea pig 5.5 pKd = 5.5 Functional
Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.
ChEMBL 1025 35 12 12 0.8 NCCCC[C@H](N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCCN=C(N)N)C(=O)NCCCCCCCCCCC(=O)N[C@@H](CO)C(=O)N[C@@H](C(=O)N1[C@H]2CCCC[C@H]2C[C@@H]1C(=O)O)C1Cc2ccccc2C1 10.1021/jm980495r
CHEMBL265814 96447 0 None - 0 Guinea pig 5.5 pKd = 5.5 Functional
Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.
ChEMBL 1025 35 12 12 0.8 NCCCC[C@H](N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCCN=C(N)N)C(=O)NCCCCCCCCCCC(=O)N[C@@H](CO)C(=O)N[C@@H](C(=O)N1[C@H]2CCCC[C@H]2C[C@@H]1C(=O)O)C1Cc2ccccc2C1 10.1021/jm980495r
CHEMBL2370700 208161 0 None - 0 Guinea pig 5.5 pKd = 5.5 Functional
Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.
ChEMBL None None None NCCCC[C@H](N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@H](C(=O)N[C@@H](CO)C(=O)N[C@@H](C(=O)N1[C@H](C(=O)O)C[C@@H]2CCCC[C@@H]21)C1Cc2ccccc2C1)C1Cc2ccccc2C1 10.1021/jm980495r
70696205 74137 0 None - 0 Rabbit 6.5 pKd = 6.5 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 704 6 6 7 1.5 N=C(N)NCCC[C@@H]1NC(=O)[C@@H]2CC3CCCCC3N2C(=O)[C@H]2Cc3ccccc3CN2C(=O)[C@H](Cc2cccs2)NC(=O)CCCNC1=O 10.1021/jm950682e
CHEMBL2028839 74137 0 None - 0 Rabbit 6.5 pKd = 6.5 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 704 6 6 7 1.5 N=C(N)NCCC[C@@H]1NC(=O)[C@@H]2CC3CCCCC3N2C(=O)[C@H]2Cc3ccccc3CN2C(=O)[C@H](Cc2cccs2)NC(=O)CCCNC1=O 10.1021/jm950682e
90662796 106070 0 None - 0 Rabbit 5.5 pKd = 5.5 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 792 18 9 8 1.8 N=C(N)NCCCCCC(=O)N[C@@H](Cc1cccs1)C(=O)N1Cc2ccccc2C[C@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCNC(=N)N)C(=O)O 10.1021/jm950682e
CHEMBL3142174 106070 0 None - 0 Rabbit 5.5 pKd = 5.5 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 792 18 9 8 1.8 N=C(N)NCCCCCC(=O)N[C@@H](Cc1cccs1)C(=O)N1Cc2ccccc2C[C@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCNC(=N)N)C(=O)O 10.1021/jm950682e
90662812 106071 0 None - 0 Rabbit 6.4 pKd = 6.4 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 716 15 6 7 1.2 NCCCC(=O)N[C@@H](Cc1ccccc1)C(=O)N1Cc2ccccc2C[C@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O 10.1021/jm950682e
CHEMBL3142190 106071 0 None - 0 Rabbit 6.4 pKd = 6.4 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 716 15 6 7 1.2 NCCCC(=O)N[C@@H](Cc1ccccc1)C(=O)N1Cc2ccccc2C[C@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O 10.1021/jm950682e
11527838 77940 0 None - 0 Human 7.4 pKd = 7.4 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 635 10 3 7 2.9 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(CCN=C(N)N)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL211017 77940 0 None - 0 Human 7.4 pKd = 7.4 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 635 10 3 7 2.9 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(CCN=C(N)N)CC4)c3Cl)c2n1 10.1021/jm060137l
10008626 138136 0 None - 0 Human 7.4 pKd = 7.4 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 592 7 3 6 3.5 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=N)N)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL377800 138136 0 None - 0 Human 7.4 pKd = 7.4 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 592 7 3 6 3.5 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=N)N)CC4)c3Cl)c2n1 10.1021/jm060137l
10463818 138729 0 None - 0 Human 7.4 pKd = 7.4 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 720 14 2 8 4.6 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)C[C@@H](N)CCCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL379063 138729 0 None - 0 Human 7.4 pKd = 7.4 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 720 14 2 8 4.6 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)C[C@@H](N)CCCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
10102599 140860 0 None - 0 Human 7.4 pKd = 7.4 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 706 13 2 8 4.2 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)C[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL383989 140860 0 None - 0 Human 7.4 pKd = 7.4 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 706 13 2 8 4.2 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)C[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
44354176 96294 0 None - 0 Guinea pig 5.4 pKd = 5.4 Functional
Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.
ChEMBL 925 28 10 10 0.6 NC(N)=NCCC[C@H](NC(=O)[C@H](N)CCCN=C(N)N)C(=O)NCCCCCCCCCCCC(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N1[C@H](C(=O)O)C[C@@H]2CCCC[C@@H]21 10.1021/jm980495r
CHEMBL264517 96294 0 None - 0 Guinea pig 5.4 pKd = 5.4 Functional
Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.
ChEMBL 925 28 10 10 0.6 NC(N)=NCCC[C@H](NC(=O)[C@H](N)CCCN=C(N)N)C(=O)NCCCCCCCCCCCC(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N1[C@H](C(=O)O)C[C@@H]2CCCC[C@@H]21 10.1021/jm980495r
10032469 74136 0 None - 0 Rabbit 7.4 pKd = 7.4 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 676 6 6 7 0.8 N=C(N)NCCC[C@@H]1NC(=O)[C@@H]2CC3CCCCC3N2C(=O)[C@H]2Cc3ccccc3CN2C(=O)[C@H](Cc2cccs2)NC(=O)CNC1=O 10.1021/jm950682e
CHEMBL2028838 74136 0 None - 0 Rabbit 7.4 pKd = 7.4 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 676 6 6 7 0.8 N=C(N)NCCC[C@@H]1NC(=O)[C@@H]2CC3CCCCC3N2C(=O)[C@H]2Cc3ccccc3CN2C(=O)[C@H](Cc2cccs2)NC(=O)CNC1=O 10.1021/jm950682e
70696206 74145 0 None - 0 Rabbit 6.4 pKd = 6.4 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 797 5 7 8 0.2 N=C(N)NCCC[C@@H]1NC(=O)[C@@H]2CC3CCCCC3N2C(=O)[C@H]2Cc3ccccc3CN2C(=O)[C@H](CO)NC(=O)[C@@H]2Cc3ccccc3CN2C(=O)CCCNC1=O 10.1021/jm950682e
CHEMBL2028847 74145 0 None - 0 Rabbit 6.4 pKd = 6.4 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 797 5 7 8 0.2 N=C(N)NCCC[C@@H]1NC(=O)[C@@H]2CC3CCCCC3N2C(=O)[C@H]2Cc3ccccc3CN2C(=O)[C@H](CO)NC(=O)[C@@H]2Cc3ccccc3CN2C(=O)CCCNC1=O 10.1021/jm950682e
70696207 74147 0 None - 0 Rabbit 7.3 pKd = 7.3 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 791 7 8 9 0.0 N=C(N)NCCC[C@@H]1NC(=O)[C@@H]2CC3CCCCC3N2C(=O)[C@H]2Cc3ccccc3CN2C(=O)[C@H](CO)NC(=O)[C@H](Cc2cccs2)NC(=O)CCCNC1=O 10.1021/jm950682e
CHEMBL2028849 74147 0 None - 0 Rabbit 7.3 pKd = 7.3 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 791 7 8 9 0.0 N=C(N)NCCC[C@@H]1NC(=O)[C@@H]2CC3CCCCC3N2C(=O)[C@H]2Cc3ccccc3CN2C(=O)[C@H](CO)NC(=O)[C@H](Cc2cccs2)NC(=O)CCCNC1=O 10.1021/jm950682e
90662814 106073 0 None - 0 Rabbit 6.3 pKd = 6.3 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 806 21 6 8 3.6 NCCCCCCCCCC(=O)N[C@@H](Cc1cccs1)C(=O)N1Cc2ccccc2C[C@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O 10.1021/jm950682e
CHEMBL3142192 106073 0 None - 0 Rabbit 6.3 pKd = 6.3 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 806 21 6 8 3.6 NCCCCCCCCCC(=O)N[C@@H](Cc1cccs1)C(=O)N1Cc2ccccc2C[C@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O 10.1021/jm950682e
70694084 74141 0 None - 0 Rabbit 6.3 pKd = 6.3 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 808 6 7 7 1.3 C[C@@H]1NC(=O)[C@H](Cc2cc3ccccc3[nH]2)NC(=O)CCCNC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@@H]2CC3CCCCC3N2C(=O)[C@H]2Cc3ccccc3CN2C1=O 10.1021/jm950682e
CHEMBL2028843 74141 0 None - 0 Rabbit 6.3 pKd = 6.3 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 808 6 7 7 1.3 C[C@@H]1NC(=O)[C@H](Cc2cc3ccccc3[nH]2)NC(=O)CCCNC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@@H]2CC3CCCCC3N2C(=O)[C@H]2Cc3ccccc3CN2C1=O 10.1021/jm950682e
57396540 71231 0 None - 0 Human 8.3 pKd = 8.3 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 705 7 1 6 4.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+]6(CC5)CC[N+](C)(C)CC6)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956867 71231 0 None - 0 Human 8.3 pKd = 8.3 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 705 7 1 6 4.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+]6(CC5)CC[N+](C)(C)CC6)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963177 71231 0 None - 0 Human 8.3 pKd = 8.3 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 705 7 1 6 4.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+]6(CC5)CC[N+](C)(C)CC6)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57394784 71308 0 None - 0 Human 8.3 pKd = 8.3 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 677 9 1 6 5.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(C[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956871 71308 0 None - 0 Human 8.3 pKd = 8.3 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 677 9 1 6 5.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(C[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963658 71308 0 None - 0 Human 8.3 pKd = 8.3 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 677 9 1 6 5.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(C[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
10350966 84187 0 None - 0 Human 8.3 pKd = 8.3 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 746 13 1 6 6.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL222167 84187 0 None - 0 Human 8.3 pKd = 8.3 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 746 13 1 6 6.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
10102296 161341 0 None - 0 Human 8.3 pKd = 8.3 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 690 9 1 6 4.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL415152 161341 0 None - 0 Human 8.3 pKd = 8.3 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 690 9 1 6 4.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL3038102 209180 0 None - 0 Rat 7.3 pKd = 7.3 Functional
In vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assayIn vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assay
ChEMBL None None None NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N(CC(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O)Cc1ccccc1 10.1021/jm950716i
CHEMBL2370011 208013 0 None - 0 Guinea pig 6.3 pKd = 6.3 Functional
Antagonism against bradykinin receptor B2 in guinea pig ileal tissueAntagonism against bradykinin receptor B2 in guinea pig ileal tissue
ChEMBL None None None NC(N)=NCCC[C@H](NC(=O)[C@@H]1C2CCCCC2CN1C(=O)[C@H]1Cc2ccccc2CN1C(=O)[C@@H]1CSSC[C@H](NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N2CCC[C@H]2C(=O)NCC(=O)N[C@@H](Cc2ccccc2)C(=O)N1)C(=O)O 10.1021/jm00069a016
CHEMBL2372276 208451 0 None - 1 Rat 7.3 pKd = 7.3 Functional
In vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assayIn vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assay
ChEMBL None None None NC(N)=NCCC[C@H](N)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1CCC[C@H]1C(=O)NCC(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](CO)C(=O)[C@@H]1CCCN1C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@H](CCCN=C(N)N)C(=O)O 10.1021/jm950716i
70694085 74144 0 None - 0 Rabbit 6.3 pKd = 6.3 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 771 6 8 8 0.1 N=C(N)NCCC[C@@H]1NC(=O)[C@@H]2CC3CCCCC3N2C(=O)[C@H]2Cc3ccccc3CN2C(=O)[C@H](CO)NC(=O)[C@H](c2ccccc2)NC(=O)CCCNC1=O 10.1021/jm950682e
CHEMBL2028846 74144 0 None - 0 Rabbit 6.3 pKd = 6.3 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 771 6 8 8 0.1 N=C(N)NCCC[C@@H]1NC(=O)[C@@H]2CC3CCCCC3N2C(=O)[C@H]2Cc3ccccc3CN2C(=O)[C@H](CO)NC(=O)[C@H](c2ccccc2)NC(=O)CCCNC1=O 10.1021/jm950682e
10441297 136352 0 None - 0 Human 8.2 pKd = 8.2 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 804 14 1 6 6.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@H](CCCC[N+](C)(C)C)[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL374224 136352 0 None - 0 Human 8.2 pKd = 8.2 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 804 14 1 6 6.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@H](CCCC[N+](C)(C)C)[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL2370699 208160 4 None - 0 Guinea pig 8.2 pKd = 8.2 Functional
Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.
ChEMBL None None None NC(N)=NCCC[C@H](NC(=O)[C@@H]1C[C@@H]2CCCC[C@@H]2N1C(=O)[C@H](NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)CNC(=O)[C@@H]1C[C@@H](O)CN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C1Cc2ccccc2C1)C1Cc2ccccc2C1)C(=O)O 10.1021/jm980495r
70681477 74143 0 None - 0 Rabbit 7.2 pKd = 7.2 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 775 6 6 8 0.8 C[C@@H]1NC(=O)[C@H](Cc2cccs2)NC(=O)CCCNC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@@H]2CC3CCCCC3N2C(=O)[C@H]2Cc3ccccc3CN2C1=O 10.1021/jm950682e
CHEMBL2028845 74143 0 None - 0 Rabbit 7.2 pKd = 7.2 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 775 6 6 8 0.8 C[C@@H]1NC(=O)[C@H](Cc2cccs2)NC(=O)CCCNC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@@H]2CC3CCCCC3N2C(=O)[C@H]2Cc3ccccc3CN2C1=O 10.1021/jm950682e
10349694 76215 0 None - 0 Human 8.1 pKd = 8.1 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 691 13 4 7 4.7 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=N)NCCCCCCN)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL206312 76215 0 None - 0 Human 8.1 pKd = 8.1 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 691 13 4 7 4.7 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=N)NCCCCCCN)CC4)c3Cl)c2n1 10.1021/jm060137l
10055774 76335 0 None - 0 Human 8.1 pKd = 8.1 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 734 14 4 8 3.3 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)C[C@@H](N)CCCCN=C(N)N)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL206474 76335 0 None - 0 Human 8.1 pKd = 8.1 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 734 14 4 8 3.3 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)C[C@@H](N)CCCCN=C(N)N)CC4)c3Cl)c2n1 10.1021/jm060137l
10260476 77628 0 None - 0 Human 8.1 pKd = 8.1 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 691 14 3 7 4.5 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(CCCCCCN=C(N)N)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL209719 77628 0 None - 0 Human 8.1 pKd = 8.1 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 691 14 3 7 4.5 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(CCCCCCN=C(N)N)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL2372276 208451 0 None - 1 Rabbit 5.1 pKd = 5.1 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL None None None NC(N)=NCCC[C@H](N)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1CCC[C@H]1C(=O)NCC(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](CO)C(=O)[C@@H]1CCCN1C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@H](CCCN=C(N)N)C(=O)O 10.1021/jm950682e
70692045 74135 0 None - 0 Rabbit 7.1 pKd = 7.1 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 775 10 9 8 0.4 N=C(N)NCCC[C@@H]1NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H]2CC3CCCCC3N2C(=O)[C@H]2Cc3ccccc3CN2C(=O)[C@H](Cc2cccs2)NC1=O 10.1021/jm950682e
CHEMBL2028837 74135 0 None - 0 Rabbit 7.1 pKd = 7.1 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 775 10 9 8 0.4 N=C(N)NCCC[C@@H]1NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H]2CC3CCCCC3N2C(=O)[C@H]2Cc3ccccc3CN2C(=O)[C@H](Cc2cccs2)NC1=O 10.1021/jm950682e
70689879 74146 0 None - 0 Rabbit 7.1 pKd = 7.1 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 777 7 7 9 -0.6 C[C@@H]1NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@@H]2CC3CCCCC3N2C(=O)[C@H]2Cc3ccccc3CN2C(=O)[C@H](CO)NC(=O)[C@H](Cc2cccs2)NC1=O 10.1021/jm950682e
CHEMBL2028848 74146 0 None - 0 Rabbit 7.1 pKd = 7.1 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 777 7 7 9 -0.6 C[C@@H]1NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@@H]2CC3CCCCC3N2C(=O)[C@H]2Cc3ccccc3CN2C(=O)[C@H](CO)NC(=O)[C@H](Cc2cccs2)NC1=O 10.1021/jm950682e
44354174 141015 0 None - 0 Guinea pig 6.1 pKd = 6.1 Functional
Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.
ChEMBL 1081 35 14 12 -1.3 NC(N)=NCCC[C@H](NC(=O)[C@@H]1C[C@@H]2CCCC[C@@H]2N1C(=O)[C@H](NC(=O)[C@H](CO)NC(=O)CCCCCCCCCCNC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C1Cc2ccccc2C1)C(=O)O 10.1021/jm980495r
CHEMBL384846 141015 0 None - 0 Guinea pig 6.1 pKd = 6.1 Functional
Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.
ChEMBL 1081 35 14 12 -1.3 NC(N)=NCCC[C@H](NC(=O)[C@@H]1C[C@@H]2CCCC[C@@H]2N1C(=O)[C@H](NC(=O)[C@H](CO)NC(=O)CCCCCCCCCCNC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C1Cc2ccccc2C1)C(=O)O 10.1021/jm980495r
73345363 88897 0 None - 0 Rabbit 6.1 pKd = 6.1 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 793 17 8 9 -0.1 NC(N)=NCCC[C@H](N)C(=O)N[C@@H](Cc1cccs1)C(=O)N1Cc2ccccc2C[C@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O 10.1021/jm950682e
CHEMBL2369364 88897 0 None - 0 Rabbit 6.1 pKd = 6.1 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 793 17 8 9 -0.1 NC(N)=NCCC[C@H](N)C(=O)N[C@@H](Cc1cccs1)C(=O)N1Cc2ccccc2C[C@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O 10.1021/jm950682e
73354461 88908 0 None - 0 Rabbit 6.1 pKd = 6.1 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 688 13 6 7 0.4 NCC(=O)N[C@@H](Cc1ccccc1)C(=O)N1Cc2ccccc2C[C@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O 10.1021/jm950682e
CHEMBL2369400 88908 0 None - 0 Rabbit 6.1 pKd = 6.1 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 688 13 6 7 0.4 NCC(=O)N[C@@H](Cc1ccccc1)C(=O)N1Cc2ccccc2C[C@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O 10.1021/jm950682e
73354460 88906 0 None - 0 Rabbit 6.0 pKd = 6.0 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 718 14 7 8 -0.2 NC(N)=NCCC[C@H](NC(=O)[C@@H]1CC2CCCCC2N1C(=O)[C@@H]1Cc2ccccc2CN1C(=O)[C@H](CO)NC(=O)[C@@H](N)Cc1ccccc1)C(=O)O 10.1021/jm950682e
CHEMBL2369392 88906 0 None - 0 Rabbit 6.0 pKd = 6.0 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 718 14 7 8 -0.2 NC(N)=NCCC[C@H](NC(=O)[C@@H]1CC2CCCCC2N1C(=O)[C@@H]1Cc2ccccc2CN1C(=O)[C@H](CO)NC(=O)[C@@H](N)Cc1ccccc1)C(=O)O 10.1021/jm950682e
119343 2818 18 None -30 2 Human 5.2 pA2 = 5.2 Functional
Apparent affinity for bradykinin B<sub>2</sub> receptor in human umbilical veinApparent affinity for bradykinin B<sub>2</sub> receptor in human umbilical vein
Guide to Pharmacology None None None None 9650825
676 2818 18 None -30 2 Human 5.2 pA2 = 5.2 Functional
Apparent affinity for bradykinin B<sub>2</sub> receptor in human umbilical veinApparent affinity for bradykinin B<sub>2</sub> receptor in human umbilical vein
Guide to Pharmacology None None None None 9650825
CHEMBL446325 2818 18 None -30 2 Human 5.2 pA2 = 5.2 Functional
Apparent affinity for bradykinin B<sub>2</sub> receptor in human umbilical veinApparent affinity for bradykinin B<sub>2</sub> receptor in human umbilical vein
Guide to Pharmacology None None None None 9650825
653 559 0 None 5 3 Human 8.4 pA2 = 8.4 Functional
Apparent affinity for bradykinin B<sub>2</sub> receptor in human umbilical veinApparent affinity for bradykinin B<sub>2</sub> receptor in human umbilical vein
Guide to Pharmacology None None None None 9650825
5311108 1648 13 None -9 2 Human 8.2 pA2 = 8.2 Functional
UnclassifiedUnclassified
Guide to Pharmacology 591 9 2 6 5.6 CC(=O)Nc1ccc(cn1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2)Cl)C 9095082
674 1648 13 None -9 2 Human 8.2 pA2 = 8.2 Functional
UnclassifiedUnclassified
Guide to Pharmacology 591 9 2 6 5.6 CC(=O)Nc1ccc(cn1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2)Cl)C 9095082
CHEMBL130517 1648 13 None -9 2 Human 8.2 pA2 = 8.2 Functional
UnclassifiedUnclassified
Guide to Pharmacology 591 9 2 6 5.6 CC(=O)Nc1ccc(cn1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2)Cl)C 9095082
667 1934 32 None -2 2 Human 8.4 pA2 = 8.4 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8735629
71364 1934 32 None -2 2 Human 8.4 pA2 = 8.4 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8735629
CHEMBL2028850 1934 32 None -2 2 Human 8.4 pA2 = 8.4 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8735629
DB06196 1934 32 None -2 2 Human 8.4 pA2 = 8.4 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8735629
5128451 1348 0 None -1 2 Human 5.1 pIC50 = 5.1 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
646 1348 0 None -1 2 Human 5.1 pIC50 = 5.1 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
5128451 1348 0 None 1 2 Mouse 5.2 pIC50 = 5.2 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
646 1348 0 None 1 2 Mouse 5.2 pIC50 = 5.2 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
672 2227 17 None - 1 Human 7.5 pIC50 = 7.5 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 23362191
6918284 2227 17 None - 1 Human 7.5 pIC50 = 7.5 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 23362191
CHEMBL2105864 2227 17 None - 1 Human 7.5 pIC50 = 7.5 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 23362191
DB06549 2227 17 None - 1 Human 7.5 pIC50 = 7.5 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 23362191
5311108 1648 13 None -9 2 Human 8.1 pIC50 = 8.1 Functional
UnclassifiedUnclassified
Guide to Pharmacology 591 9 2 6 5.6 CC(=O)Nc1ccc(cn1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2)Cl)C 9203620
674 1648 13 None -9 2 Human 8.1 pIC50 = 8.1 Functional
UnclassifiedUnclassified
Guide to Pharmacology 591 9 2 6 5.6 CC(=O)Nc1ccc(cn1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2)Cl)C 9203620
CHEMBL130517 1648 13 None -9 2 Human 8.1 pIC50 = 8.1 Functional
UnclassifiedUnclassified
Guide to Pharmacology 591 9 2 6 5.6 CC(=O)Nc1ccc(cn1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2)Cl)C 9203620
3812 708 37 None -1 3 Human 8.2 pIC50 = 8.2 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
3812 708 37 None -1 3 Human 8.2 pIC50 = 8.2 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 9203620
439201 708 37 None -1 3 Human 8.2 pIC50 = 8.2 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
439201 708 37 None -1 3 Human 8.2 pIC50 = 8.2 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 9203620
649 708 37 None -1 3 Human 8.2 pIC50 = 8.2 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
649 708 37 None -1 3 Human 8.2 pIC50 = 8.2 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 9203620
CHEMBL406291 708 37 None -1 3 Human 8.2 pIC50 = 8.2 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
CHEMBL406291 708 37 None -1 3 Human 8.2 pIC50 = 8.2 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 9203620
DB12126 708 37 None -1 3 Human 8.2 pIC50 = 8.2 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
DB12126 708 37 None -1 3 Human 8.2 pIC50 = 8.2 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 9203620
667 1934 32 None -2 2 Human 8.7 pIC50 = 8.7 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
667 1934 32 None -2 2 Human 8.7 pIC50 = 8.7 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 9203620
71364 1934 32 None -2 2 Human 8.7 pIC50 = 8.7 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
71364 1934 32 None -2 2 Human 8.7 pIC50 = 8.7 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 9203620
CHEMBL2028850 1934 32 None -2 2 Human 8.7 pIC50 = 8.7 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
CHEMBL2028850 1934 32 None -2 2 Human 8.7 pIC50 = 8.7 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 9203620
DB06196 1934 32 None -2 2 Human 8.7 pIC50 = 8.7 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
DB06196 1934 32 None -2 2 Human 8.7 pIC50 = 8.7 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 9203620
10255 2766 0 None - 1 Human 8.7 pIC50 = 8.7 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 19111586
5311111 2135 0 None -1 2 Mouse 9.3 pIC50 = 9.3 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
650 2135 0 None -1 2 Mouse 9.3 pIC50 = 9.3 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
122227 1346 27 None -28840 3 Mouse 4.6 pIC50 None 4.6 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
3825 1346 27 None -28840 3 Mouse 4.6 pIC50 None 4.6 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
644 1346 27 None -28840 3 Mouse 4.6 pIC50 None 4.6 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
CHEMBL264100 1346 27 None -28840 3 Mouse 4.6 pIC50 None 4.6 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
678 3736 0 None -5 2 Human 6.3 pIC50 None 6.3 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
119343 2818 18 None -30 2 Human 6.9 pIC50 None 6.9 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
676 2818 18 None -30 2 Human 6.9 pIC50 None 6.9 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
CHEMBL446325 2818 18 None -30 2 Human 6.9 pIC50 None 6.9 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
123973 2817 0 None -79 2 Human 7.0 pIC50 None 7 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
675 2817 0 None -79 2 Human 7.0 pIC50 None 7 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
678 3736 0 None 5 2 Mouse 7.0 pIC50 None 7 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
673 1647 12 None -8 2 Human 7.2 pIC50 None 7.2 Functional
UnclassifiedUnclassified
Guide to Pharmacology 671 9 1 6 5.8 O=C(/C=C/c1ccc(cc1)C(=O)N(C)C)NCC(=O)N(c1ccc(c(c1Cl)COc1cccn2c1nc(c2Br)C)Cl)C 9203620
9810391 1647 12 None -8 2 Human 7.2 pIC50 None 7.2 Functional
UnclassifiedUnclassified
Guide to Pharmacology 671 9 1 6 5.8 O=C(/C=C/c1ccc(cc1)C(=O)N(C)C)NCC(=O)N(c1ccc(c(c1Cl)COc1cccn2c1nc(c2Br)C)Cl)C 9203620
CHEMBL1192627 1647 12 None -8 2 Human 7.2 pIC50 None 7.2 Functional
UnclassifiedUnclassified
Guide to Pharmacology 671 9 1 6 5.8 O=C(/C=C/c1ccc(cc1)C(=O)N(C)C)NCC(=O)N(c1ccc(c(c1Cl)COc1cccn2c1nc(c2Br)C)Cl)C 9203620
671 3822 0 None -1 2 Human 8.0 pIC50 None 8 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
671 3822 0 None 1 2 Mouse 8.1 pIC50 None 8.1 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
3035449 2470 0 None -1 3 Mouse 8.4 pIC50 None 8.4 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
638 2470 0 None -1 3 Mouse 8.4 pIC50 None 8.4 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
3035449 2470 0 None 1 3 Human 8.7 pIC50 None 8.7 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
638 2470 0 None 1 3 Human 8.7 pIC50 None 8.7 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
119343 2818 18 None 30 2 Mouse 8.7 pIC50 None 8.7 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
676 2818 18 None 30 2 Mouse 8.7 pIC50 None 8.7 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
CHEMBL446325 2818 18 None 30 2 Mouse 8.7 pIC50 None 8.7 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
123973 2817 0 None 79 2 Mouse 8.9 pIC50 None 8.9 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
675 2817 0 None 79 2 Mouse 8.9 pIC50 None 8.9 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
10394861 1651 3 None 9 2 Human 9.2 pIC50 None 9.2 Functional
UnclassifiedUnclassified
Guide to Pharmacology 687 12 2 9 5.5 COc1nc2c(n1Cc1ccccn1)cccc2OCc1c(Cl)ccc(c1Cl)N(C(=O)CNC(=O)/C=C/c1ccc(nc1)NC(=O)C)C 15139763
669 1651 3 None 9 2 Human 9.2 pIC50 None 9.2 Functional
UnclassifiedUnclassified
Guide to Pharmacology 687 12 2 9 5.5 COc1nc2c(n1Cc1ccccn1)cccc2OCc1c(Cl)ccc(c1Cl)N(C(=O)CNC(=O)/C=C/c1ccc(nc1)NC(=O)C)C 15139763
CHEMBL329762 1651 3 None 9 2 Human 9.2 pIC50 None 9.2 Functional
UnclassifiedUnclassified
Guide to Pharmacology 687 12 2 9 5.5 COc1nc2c(n1Cc1ccccn1)cccc2OCc1c(Cl)ccc(c1Cl)N(C(=O)CNC(=O)/C=C/c1ccc(nc1)NC(=O)C)C 15139763
3812 708 37 None 1 3 Mouse 9.3 pIC50 None 9.3 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
439201 708 37 None 1 3 Mouse 9.3 pIC50 None 9.3 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
649 708 37 None 1 3 Mouse 9.3 pIC50 None 9.3 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
CHEMBL406291 708 37 None 1 3 Mouse 9.3 pIC50 None 9.3 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
DB12126 708 37 None 1 3 Mouse 9.3 pIC50 None 9.3 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
5311111 2135 0 None 1 2 Human 9.3 pIC50 None 9.3 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
650 2135 0 None 1 2 Human 9.3 pIC50 None 9.3 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267




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
11498853 82761 9 None - 1 Human 10.3 pIC50 = 10.3 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 763 12 2 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1021/jm9002445
CHEMBL218427 82761 9 None - 1 Human 10.3 pIC50 = 10.3 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 763 12 2 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1021/jm9002445
CHEMBL541758 82761 9 None - 1 Human 10.3 pIC50 = 10.3 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 763 12 2 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1021/jm9002445
667 1934 32 None 1 6 Guinea pig 10.1 pIC50 = 10.1 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL None None None None 10.1021/jm980300f
71364 1934 32 None 1 6 Guinea pig 10.1 pIC50 = 10.1 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL None None None None 10.1021/jm980300f
CHEMBL2028850 1934 32 None 1 6 Guinea pig 10.1 pIC50 = 10.1 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL None None None None 10.1021/jm980300f
DB06196 1934 32 None 1 6 Guinea pig 10.1 pIC50 = 10.1 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL None None None None 10.1021/jm980300f
667 1934 32 None 1 6 Guinea pig 10.1 pIC50 = 10.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL None None None None 10.1021/jm980214f
71364 1934 32 None 1 6 Guinea pig 10.1 pIC50 = 10.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL None None None None 10.1021/jm980214f
CHEMBL2028850 1934 32 None 1 6 Guinea pig 10.1 pIC50 = 10.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL None None None None 10.1021/jm980214f
DB06196 1934 32 None 1 6 Guinea pig 10.1 pIC50 = 10.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL None None None None 10.1021/jm980214f
667 1934 32 None 1 6 Guinea pig 10.1 pIC50 = 10.1 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL None None None None 10.1021/jm030159x
71364 1934 32 None 1 6 Guinea pig 10.1 pIC50 = 10.1 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL None None None None 10.1021/jm030159x
CHEMBL2028850 1934 32 None 1 6 Guinea pig 10.1 pIC50 = 10.1 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL None None None None 10.1021/jm030159x
DB06196 1934 32 None 1 6 Guinea pig 10.1 pIC50 = 10.1 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL None None None None 10.1021/jm030159x
CHEMBL2370160 208047 0 None - 0 Guinea pig 10.1 pIC50 = 10.1 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL None None None NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CS)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N1c2ccccc2C[C@@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O 10.1021/jm030326t
11801968 13584 0 None - 0 Guinea pig 9.9 pIC50 = 9.9 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 617 9 1 6 5.7 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)nc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL1194974 13584 0 None - 0 Guinea pig 9.9 pIC50 = 9.9 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 617 9 1 6 5.7 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)nc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL553614 13584 0 None - 0 Guinea pig 9.9 pIC50 = 9.9 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 617 9 1 6 5.7 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)nc4)c3Cl)c2n1 10.1021/jm980300f
11250851 13491 0 None - 0 Human 9.8 pIC50 = 9.8 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 656 10 2 7 5.8 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(-n5cccn5)cc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL1194270 13491 0 None - 0 Human 9.8 pIC50 = 9.8 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 656 10 2 7 5.8 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(-n5cccn5)cc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL3216880 13491 0 None - 0 Human 9.8 pIC50 = 9.8 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 656 10 2 7 5.8 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(-n5cccn5)cc(C)nc34)c2Cl)cc1 10.1021/jm030159x
9874617 13180 0 None - 0 Human 9.7 pIC50 = 9.7 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 670 10 1 7 6.1 Cc1cc(-n2cccn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL1191908 13180 0 None - 0 Human 9.7 pIC50 = 9.7 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 670 10 1 7 6.1 Cc1cc(-n2cccn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL543070 13180 0 None - 0 Human 9.7 pIC50 = 9.7 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 670 10 1 7 6.1 Cc1cc(-n2cccn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
11250929 13708 0 None - 0 Guinea pig 9.7 pIC50 = 9.7 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 634 11 2 6 6.0 CCOc1cc(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc12 10.1021/jm030468n
CHEMBL1195824 13708 0 None - 0 Guinea pig 9.7 pIC50 = 9.7 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 634 11 2 6 6.0 CCOc1cc(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc12 10.1021/jm030468n
CHEMBL555403 13708 0 None - 0 Guinea pig 9.7 pIC50 = 9.7 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 634 11 2 6 6.0 CCOc1cc(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc12 10.1021/jm030468n
11158089 12793 0 None - 0 Guinea pig 9.6 pIC50 = 9.6 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 620 10 2 6 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OC)cc(C)nc34)c2Cl)cc1 10.1021/jm030468n
CHEMBL1189084 12793 0 None - 0 Guinea pig 9.6 pIC50 = 9.6 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 620 10 2 6 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OC)cc(C)nc34)c2Cl)cc1 10.1021/jm030468n
CHEMBL538022 12793 0 None - 0 Guinea pig 9.6 pIC50 = 9.6 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 620 10 2 6 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OC)cc(C)nc34)c2Cl)cc1 10.1021/jm030468n
18704946 13044 0 None - 0 Human 9.6 pIC50 = 9.6 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 657 10 2 8 5.2 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(-n5cncn5)cc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL1190879 13044 0 None - 0 Human 9.6 pIC50 = 9.6 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 657 10 2 8 5.2 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(-n5cncn5)cc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL3217081 13044 0 None - 0 Human 9.6 pIC50 = 9.6 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 657 10 2 8 5.2 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(-n5cncn5)cc(C)nc34)c2Cl)cc1 10.1021/jm030159x
44214214 13135 0 None - 0 Human 9.6 pIC50 = 9.6 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 708 10 3 8 7.0 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL1191492 13135 0 None - 0 Human 9.6 pIC50 = 9.6 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 708 10 3 8 7.0 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL542598 13135 0 None - 0 Human 9.6 pIC50 = 9.6 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 708 10 3 8 7.0 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030159x
44360533 12768 0 None - 0 Guinea pig 9.6 pIC50 = 9.6 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 686 11 1 7 5.3 Cc1ccc2cccc(OCc3c(C(=O)N(C)C)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3C(=O)N(C)C)c2n1 10.1021/jm980330i
CHEMBL1188925 12768 0 None - 0 Guinea pig 9.6 pIC50 = 9.6 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 686 11 1 7 5.3 Cc1ccc2cccc(OCc3c(C(=O)N(C)C)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3C(=O)N(C)C)c2n1 10.1021/jm980330i
CHEMBL537683 12768 0 None - 0 Guinea pig 9.6 pIC50 = 9.6 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 686 11 1 7 5.3 Cc1ccc2cccc(OCc3c(C(=O)N(C)C)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3C(=O)N(C)C)c2n1 10.1021/jm980330i
10009762 12805 0 None - 0 Human 9.6 pIC50 = 9.6 Binding
Displacement of [3H]bradykinin from human recombinant bradykinin B2 receptor expressed in CHO cells incubated for 2 hrs by liquid scintillation counterDisplacement of [3H]bradykinin from human recombinant bradykinin B2 receptor expressed in CHO cells incubated for 2 hrs by liquid scintillation counter
ChEMBL 678 10 1 7 7.4 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1016/j.ejmech.2019.07.064
CHEMBL1189175 12805 0 None - 0 Human 9.6 pIC50 = 9.6 Binding
Displacement of [3H]bradykinin from human recombinant bradykinin B2 receptor expressed in CHO cells incubated for 2 hrs by liquid scintillation counterDisplacement of [3H]bradykinin from human recombinant bradykinin B2 receptor expressed in CHO cells incubated for 2 hrs by liquid scintillation counter
ChEMBL 678 10 1 7 7.4 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1016/j.ejmech.2019.07.064
CHEMBL3217072 12805 0 None - 0 Human 9.6 pIC50 = 9.6 Binding
Displacement of [3H]bradykinin from human recombinant bradykinin B2 receptor expressed in CHO cells incubated for 2 hrs by liquid scintillation counterDisplacement of [3H]bradykinin from human recombinant bradykinin B2 receptor expressed in CHO cells incubated for 2 hrs by liquid scintillation counter
ChEMBL 678 10 1 7 7.4 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1016/j.ejmech.2019.07.064
10009762 12805 0 None - 0 Human 9.6 pIC50 = 9.6 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 678 10 1 7 7.4 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL1189175 12805 0 None - 0 Human 9.6 pIC50 = 9.6 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 678 10 1 7 7.4 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL3217072 12805 0 None - 0 Human 9.6 pIC50 = 9.6 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 678 10 1 7 7.4 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
10627384 13611 0 None - 0 Human 9.6 pIC50 = 9.6 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 598 9 2 5 6.9 CNC(=O)c1ccc(/C=C/C(=O)NCc2cccn2-c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980330i
CHEMBL1195129 13611 0 None - 0 Human 9.6 pIC50 = 9.6 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 598 9 2 5 6.9 CNC(=O)c1ccc(/C=C/C(=O)NCc2cccn2-c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980330i
CHEMBL553911 13611 0 None - 0 Human 9.6 pIC50 = 9.6 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 598 9 2 5 6.9 CNC(=O)c1ccc(/C=C/C(=O)NCc2cccn2-c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980330i
11490839 13043 0 None - 0 Human 9.6 pIC50 = 9.6 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 671 10 1 8 5.5 Cc1cc(-n2ccnn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL1190878 13043 0 None - 0 Human 9.6 pIC50 = 9.6 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 671 10 1 8 5.5 Cc1cc(-n2ccnn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL541805 13043 0 None - 0 Human 9.6 pIC50 = 9.6 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 671 10 1 8 5.5 Cc1cc(-n2ccnn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
11273808 13671 0 None - 0 Human 9.6 pIC50 = 9.6 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 656 10 2 7 5.8 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(-n5ccnc5)cc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL1195573 13671 0 None - 0 Human 9.6 pIC50 = 9.6 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 656 10 2 7 5.8 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(-n5ccnc5)cc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL3215979 13671 0 None - 0 Human 9.6 pIC50 = 9.6 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 656 10 2 7 5.8 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(-n5ccnc5)cc(C)nc34)c2Cl)cc1 10.1021/jm030159x
22008895 110056 0 None - 1 Guinea pig 9.5 pIC50 = 9.5 Binding
Displacement of [3H]bradykinin from guinea pig B2 receptorDisplacement of [3H]bradykinin from guinea pig B2 receptor
ChEMBL 592 8 1 5 6.5 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(F)(F)F)cc4)c3C#N)c2n1 10.1021/jm9002445
CHEMBL325255 110056 0 None - 1 Guinea pig 9.5 pIC50 = 9.5 Binding
Displacement of [3H]bradykinin from guinea pig B2 receptorDisplacement of [3H]bradykinin from guinea pig B2 receptor
ChEMBL 592 8 1 5 6.5 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(F)(F)F)cc4)c3C#N)c2n1 10.1021/jm9002445
11445288 13748 0 None - 0 Human 9.5 pIC50 = 9.5 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 670 10 1 7 6.1 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL1196072 13748 0 None - 0 Human 9.5 pIC50 = 9.5 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 670 10 1 7 6.1 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL3217085 13748 0 None - 0 Human 9.5 pIC50 = 9.5 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 670 10 1 7 6.1 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
11262728 137922 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
Agonist activity at bradykinin B2 receptor (unknown origin)Agonist activity at bradykinin B2 receptor (unknown origin)
ChEMBL 744 13 1 8 8.2 Cc1cc(OCc2ccccn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(/C=C/c5ccncc5)nc4)c3Cl)c2n1 10.1016/j.ejmech.2020.112948
CHEMBL3774617 137922 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
Agonist activity at bradykinin B2 receptor (unknown origin)Agonist activity at bradykinin B2 receptor (unknown origin)
ChEMBL 744 13 1 8 8.2 Cc1cc(OCc2ccccn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(/C=C/c5ccncc5)nc4)c3Cl)c2n1 10.1016/j.ejmech.2020.112948
11802489 13606 0 None - 0 Guinea pig 9.4 pIC50 = 9.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 658 9 2 7 4.8 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cn1 10.1021/jm980214f
CHEMBL1195106 13606 0 None - 0 Guinea pig 9.4 pIC50 = 9.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 658 9 2 7 4.8 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cn1 10.1021/jm980214f
CHEMBL553844 13606 0 None - 0 Guinea pig 9.4 pIC50 = 9.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 658 9 2 7 4.8 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cn1 10.1021/jm980214f
11262728 137922 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
Displacement of [3H]BK from cloned human B2 bradykinin receptor expressed in CHO cells after 2 hrs by liquid scintillation counterDisplacement of [3H]BK from cloned human B2 bradykinin receptor expressed in CHO cells after 2 hrs by liquid scintillation counter
ChEMBL 744 13 1 8 8.2 Cc1cc(OCc2ccccn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(/C=C/c5ccncc5)nc4)c3Cl)c2n1 10.1021/acs.jmedchem.5b00982
CHEMBL3774617 137922 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
Displacement of [3H]BK from cloned human B2 bradykinin receptor expressed in CHO cells after 2 hrs by liquid scintillation counterDisplacement of [3H]BK from cloned human B2 bradykinin receptor expressed in CHO cells after 2 hrs by liquid scintillation counter
ChEMBL 744 13 1 8 8.2 Cc1cc(OCc2ccccn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(/C=C/c5ccncc5)nc4)c3Cl)c2n1 10.1021/acs.jmedchem.5b00982
44329173 167238 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 787 14 2 9 7.4 Cc1cc(OCc2ccccn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N/C=C/c5ccncc5)nc4)c3Cl)c2n1 10.1021/jm030468n
CHEMBL430652 167238 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 787 14 2 9 7.4 Cc1cc(OCc2ccccn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N/C=C/c5ccncc5)nc4)c3Cl)c2n1 10.1021/jm030468n
44360597 13756 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 645 11 4 8 5.5 CC(=O)Nc1ccc(/C=C/C(=O)NCc2cccn2-c2ccc(NC(C)=O)c(COc3cccc4ccc(C)nc34)c2NC(C)=O)cn1 10.1021/jm980330i
CHEMBL1196121 13756 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 645 11 4 8 5.5 CC(=O)Nc1ccc(/C=C/C(=O)NCc2cccn2-c2ccc(NC(C)=O)c(COc3cccc4ccc(C)nc34)c2NC(C)=O)cn1 10.1021/jm980330i
CHEMBL555976 13756 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 645 11 4 8 5.5 CC(=O)Nc1ccc(/C=C/C(=O)NCc2cccn2-c2ccc(NC(C)=O)c(COc3cccc4ccc(C)nc34)c2NC(C)=O)cn1 10.1021/jm980330i
10349737 12990 0 None - 0 Guinea pig 9.4 pIC50 = 9.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 658 9 2 7 5.4 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cn1 10.1021/jm980214f
CHEMBL1190430 12990 0 None - 0 Guinea pig 9.4 pIC50 = 9.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 658 9 2 7 5.4 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cn1 10.1021/jm980214f
CHEMBL540840 12990 0 None - 0 Guinea pig 9.4 pIC50 = 9.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 658 9 2 7 5.4 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cn1 10.1021/jm980214f
11411675 96035 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 760 13 2 8 7.8 Cc1cc(OCc2ccccn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030468n
CHEMBL262507 96035 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 760 13 2 8 7.8 Cc1cc(OCc2ccccn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030468n
5311114 1650 6 None - 1 Human 9.4 pIC50 = 9.4 Binding
Agonist activity at bradykinin B2 receptor (unknown origin)Agonist activity at bradykinin B2 receptor (unknown origin)
ChEMBL 697 12 2 7 6.6 CNC(=O)c1ccc(cc1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2OCc1ccccn1)Cl)C 10.1016/j.ejmech.2020.112948
668 1650 6 None - 1 Human 9.4 pIC50 = 9.4 Binding
Agonist activity at bradykinin B2 receptor (unknown origin)Agonist activity at bradykinin B2 receptor (unknown origin)
ChEMBL 697 12 2 7 6.6 CNC(=O)c1ccc(cc1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2OCc1ccccn1)Cl)C 10.1016/j.ejmech.2020.112948
CHEMBL99869 1650 6 None - 1 Human 9.4 pIC50 = 9.4 Binding
Agonist activity at bradykinin B2 receptor (unknown origin)Agonist activity at bradykinin B2 receptor (unknown origin)
ChEMBL 697 12 2 7 6.6 CNC(=O)c1ccc(cc1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2OCc1ccccn1)Cl)C 10.1016/j.ejmech.2020.112948
5311114 1650 6 None - 1 Human 9.4 pIC50 = 9.4 Binding
Displacement of [3H]BK from cloned human B2 bradykinin receptor expressed in CHO cells after 2 hrs by liquid scintillation counterDisplacement of [3H]BK from cloned human B2 bradykinin receptor expressed in CHO cells after 2 hrs by liquid scintillation counter
ChEMBL 697 12 2 7 6.6 CNC(=O)c1ccc(cc1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2OCc1ccccn1)Cl)C 10.1021/acs.jmedchem.5b00982
668 1650 6 None - 1 Human 9.4 pIC50 = 9.4 Binding
Displacement of [3H]BK from cloned human B2 bradykinin receptor expressed in CHO cells after 2 hrs by liquid scintillation counterDisplacement of [3H]BK from cloned human B2 bradykinin receptor expressed in CHO cells after 2 hrs by liquid scintillation counter
ChEMBL 697 12 2 7 6.6 CNC(=O)c1ccc(cc1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2OCc1ccccn1)Cl)C 10.1021/acs.jmedchem.5b00982
CHEMBL99869 1650 6 None - 1 Human 9.4 pIC50 = 9.4 Binding
Displacement of [3H]BK from cloned human B2 bradykinin receptor expressed in CHO cells after 2 hrs by liquid scintillation counterDisplacement of [3H]BK from cloned human B2 bradykinin receptor expressed in CHO cells after 2 hrs by liquid scintillation counter
ChEMBL 697 12 2 7 6.6 CNC(=O)c1ccc(cc1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2OCc1ccccn1)Cl)C 10.1021/acs.jmedchem.5b00982
5311114 1650 6 None - 1 Human 9.4 pIC50 = 9.4 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 697 12 2 7 6.6 CNC(=O)c1ccc(cc1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2OCc1ccccn1)Cl)C 10.1021/jm030468n
668 1650 6 None - 1 Human 9.4 pIC50 = 9.4 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 697 12 2 7 6.6 CNC(=O)c1ccc(cc1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2OCc1ccccn1)Cl)C 10.1021/jm030468n
CHEMBL99869 1650 6 None - 1 Human 9.4 pIC50 = 9.4 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 697 12 2 7 6.6 CNC(=O)c1ccc(cc1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2OCc1ccccn1)Cl)C 10.1021/jm030468n
44360533 12768 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 686 11 1 7 5.3 Cc1ccc2cccc(OCc3c(C(=O)N(C)C)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3C(=O)N(C)C)c2n1 10.1021/jm980330i
CHEMBL1188925 12768 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 686 11 1 7 5.3 Cc1ccc2cccc(OCc3c(C(=O)N(C)C)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3C(=O)N(C)C)c2n1 10.1021/jm980330i
CHEMBL537683 12768 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 686 11 1 7 5.3 Cc1ccc2cccc(OCc3c(C(=O)N(C)C)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3C(=O)N(C)C)c2n1 10.1021/jm980330i
44360877 13560 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 722 11 1 7 6.6 Cc1ccc2cccc(OCc3c(N4CCCC4=O)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3N3CCCC3=O)c2n1 10.1021/jm980330i
CHEMBL1194797 13560 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 722 11 1 7 6.6 Cc1ccc2cccc(OCc3c(N4CCCC4=O)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3N3CCCC3=O)c2n1 10.1021/jm980330i
CHEMBL553315 13560 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 722 11 1 7 6.6 Cc1ccc2cccc(OCc3c(N4CCCC4=O)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3N3CCCC3=O)c2n1 10.1021/jm980330i
11491041 13330 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 719 11 2 8 7.1 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL1193122 13330 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 719 11 2 8 7.1 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL544480 13330 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 719 11 2 8 7.1 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030159x
11227974 13179 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 741 12 2 8 8.1 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(C(=O)NCc5ccccn5)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL1191906 13179 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 741 12 2 8 8.1 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(C(=O)NCc5ccccn5)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL543068 13179 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 741 12 2 8 8.1 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(C(=O)NCc5ccccn5)cc4)c3Cl)c2n1 10.1021/jm030159x
10652092 12892 0 None - 0 Guinea pig 9.4 pIC50 = 9.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 672 9 1 7 5.2 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)nc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL1189828 12892 0 None - 0 Guinea pig 9.4 pIC50 = 9.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 672 9 1 7 5.2 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)nc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL539550 12892 0 None - 0 Guinea pig 9.4 pIC50 = 9.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 672 9 1 7 5.2 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)nc4)c3Cl)cccn2c1Br 10.1021/jm980214f
5311108 1648 13 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 591 9 2 6 5.6 CC(=O)Nc1ccc(cn1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2)Cl)C 10.1021/jm980300f
674 1648 13 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 591 9 2 6 5.6 CC(=O)Nc1ccc(cn1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2)Cl)C 10.1021/jm980300f
CHEMBL130517 1648 13 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 591 9 2 6 5.6 CC(=O)Nc1ccc(cn1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2)Cl)C 10.1021/jm980300f
10531497 13087 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Displacement of [3H]BK from Bradykinin B2 Receptor in guinea pig ileum by liquid scintillation counterDisplacement of [3H]BK from Bradykinin B2 Receptor in guinea pig ileum by liquid scintillation counter
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cn1 10.1016/j.ejmech.2019.07.064
CHEMBL1191172 13087 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Displacement of [3H]BK from Bradykinin B2 Receptor in guinea pig ileum by liquid scintillation counterDisplacement of [3H]BK from Bradykinin B2 Receptor in guinea pig ileum by liquid scintillation counter
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cn1 10.1016/j.ejmech.2019.07.064
CHEMBL542232 13087 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Displacement of [3H]BK from Bradykinin B2 Receptor in guinea pig ileum by liquid scintillation counterDisplacement of [3H]BK from Bradykinin B2 Receptor in guinea pig ileum by liquid scintillation counter
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cn1 10.1016/j.ejmech.2019.07.064
5311108 1648 13 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 591 9 2 6 5.6 CC(=O)Nc1ccc(cn1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2)Cl)C 10.1021/jm980330i
674 1648 13 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 591 9 2 6 5.6 CC(=O)Nc1ccc(cn1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2)Cl)C 10.1021/jm980330i
CHEMBL130517 1648 13 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 591 9 2 6 5.6 CC(=O)Nc1ccc(cn1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2)Cl)C 10.1021/jm980330i
10674687 13501 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 576 9 1 5 5.7 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3C)c2n1 10.1021/jm980300f
CHEMBL1194363 13501 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 576 9 1 5 5.7 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3C)c2n1 10.1021/jm980300f
CHEMBL552543 13501 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 576 9 1 5 5.7 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3C)c2n1 10.1021/jm980300f
11251046 13079 0 None - 0 Human 9.3 pIC50 = 9.3 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 696 11 2 7 6.9 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1191121 13079 0 None - 0 Human 9.3 pIC50 = 9.3 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 696 11 2 7 6.9 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL542173 13079 0 None - 0 Human 9.3 pIC50 = 9.3 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 696 11 2 7 6.9 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
667 1934 32 None -1 6 Human 9.3 pIC50 = 9.3 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL None None None None 10.1021/jm030159x
71364 1934 32 None -1 6 Human 9.3 pIC50 = 9.3 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL None None None None 10.1021/jm030159x
CHEMBL2028850 1934 32 None -1 6 Human 9.3 pIC50 = 9.3 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL None None None None 10.1021/jm030159x
DB06196 1934 32 None -1 6 Human 9.3 pIC50 = 9.3 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL None None None None 10.1021/jm030159x
CHEMBL2370160 208047 0 None - 0 Human 9.3 pIC50 = 9.3 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL None None None NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CS)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N1c2ccccc2C[C@@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O 10.1021/jm030326t
667 1934 32 None -1 6 Human 9.3 pIC50 = 9.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL None None None None 10.1021/jm980300f
71364 1934 32 None -1 6 Human 9.3 pIC50 = 9.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL None None None None 10.1021/jm980300f
CHEMBL2028850 1934 32 None -1 6 Human 9.3 pIC50 = 9.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL None None None None 10.1021/jm980300f
DB06196 1934 32 None -1 6 Human 9.3 pIC50 = 9.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL None None None None 10.1021/jm980300f
11802476 12840 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 657 9 2 6 5.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL1189415 12840 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 657 9 2 6 5.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL538732 12840 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 657 9 2 6 5.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980300f
10698671 13342 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 590 9 2 5 6.2 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL1193229 13342 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 590 9 2 5 6.2 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL544599 13342 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 590 9 2 5 6.2 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980300f
11802476 12840 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 657 9 2 6 5.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
CHEMBL1189415 12840 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 657 9 2 6 5.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
CHEMBL538732 12840 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 657 9 2 6 5.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
11802476 12840 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 657 9 2 6 5.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL1189415 12840 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 657 9 2 6 5.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL538732 12840 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 657 9 2 6 5.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm030159x
10348414 168496 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL439737 168496 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL542096 168496 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980300f
10348414 168496 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2 in guinea pig ileum membraneConcentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2 in guinea pig ileum membrane
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm030468n
CHEMBL439737 168496 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2 in guinea pig ileum membraneConcentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2 in guinea pig ileum membrane
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm030468n
CHEMBL542096 168496 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2 in guinea pig ileum membraneConcentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2 in guinea pig ileum membrane
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm030468n
10348414 168496 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL439737 168496 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL542096 168496 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm030159x
10348414 168496 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL439737 168496 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL542096 168496 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm030326t
10348414 168496 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980330i
CHEMBL439737 168496 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980330i
CHEMBL542096 168496 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980330i
44360968 120558 0 None - 0 Human 9.3 pIC50 = 9.3 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 775 14 1 8 9.0 Cc1ccc2cccc(OCc3c(/C=C/c4ccncc4)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(/C=C/c5ccncc5)nc4)c3/C=C/c3ccncc3)c2n1 10.1021/jm980330i
CHEMBL357075 120558 0 None - 0 Human 9.3 pIC50 = 9.3 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 775 14 1 8 9.0 Cc1ccc2cccc(OCc3c(/C=C/c4ccncc4)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(/C=C/c5ccncc5)nc4)c3/C=C/c3ccncc3)c2n1 10.1021/jm980330i
10371910 19919 1 None - 0 Human 9.3 pIC50 = 9.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 637 10 1 6 7.2 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(/C=C/c5ccncc5)nc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL130436 19919 1 None - 0 Human 9.3 pIC50 = 9.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 637 10 1 6 7.2 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(/C=C/c5ccncc5)nc4)c3Cl)c2n1 10.1021/jm980300f
11411594 12784 0 None - 0 Human 9.3 pIC50 = 9.3 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 736 11 2 7 7.9 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1189023 12784 0 None - 0 Human 9.3 pIC50 = 9.3 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 736 11 2 7 7.9 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL537927 12784 0 None - 0 Human 9.3 pIC50 = 9.3 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 736 11 2 7 7.9 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
44360818 13352 0 None - 0 Human 9.3 pIC50 = 9.3 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 783 14 1 8 10.3 Cc1ccc2cccc(OCc3c(/C=C/c4ccncc4)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(/C=C/c5ccncc5)nc4)c3/C=C/c3ccncc3)c2n1 10.1021/jm980330i
CHEMBL1193250 13352 0 None - 0 Human 9.3 pIC50 = 9.3 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 783 14 1 8 10.3 Cc1ccc2cccc(OCc3c(/C=C/c4ccncc4)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(/C=C/c5ccncc5)nc4)c3/C=C/c3ccncc3)c2n1 10.1021/jm980330i
CHEMBL544623 13352 0 None - 0 Human 9.3 pIC50 = 9.3 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 783 14 1 8 10.3 Cc1ccc2cccc(OCc3c(/C=C/c4ccncc4)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(/C=C/c5ccncc5)nc4)c3/C=C/c3ccncc3)c2n1 10.1021/jm980330i
10555818 13558 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 616 9 1 5 6.3 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL1194778 13558 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 616 9 1 5 6.3 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL553293 13558 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 616 9 1 5 6.3 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)c2n1 10.1021/jm980300f
10675847 13291 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 657 9 2 6 6.0 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
CHEMBL1192831 13291 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 657 9 2 6 6.0 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
CHEMBL544134 13291 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 657 9 2 6 6.0 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
44361029 13240 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 714 11 1 7 5.3 Cc1ccc2cccc(OCc3c(N4CCCC4=O)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3N3CCCC3=O)c2n1 10.1021/jm980330i
CHEMBL1192448 13240 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 714 11 1 7 5.3 Cc1ccc2cccc(OCc3c(N4CCCC4=O)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3N3CCCC3=O)c2n1 10.1021/jm980330i
CHEMBL543685 13240 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 714 11 1 7 5.3 Cc1ccc2cccc(OCc3c(N4CCCC4=O)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3N3CCCC3=O)c2n1 10.1021/jm980330i
11479739 206452 0 None - 0 Human 9.3 pIC50 = 9.3 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 760 13 2 8 7.8 Cc1cc(OCc2ccccn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030468n
CHEMBL98460 206452 0 None - 0 Human 9.3 pIC50 = 9.3 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 760 13 2 8 7.8 Cc1cc(OCc2ccccn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030468n
44360597 13756 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 645 11 4 8 5.5 CC(=O)Nc1ccc(/C=C/C(=O)NCc2cccn2-c2ccc(NC(C)=O)c(COc3cccc4ccc(C)nc34)c2NC(C)=O)cn1 10.1021/jm980330i
CHEMBL1196121 13756 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 645 11 4 8 5.5 CC(=O)Nc1ccc(/C=C/C(=O)NCc2cccn2-c2ccc(NC(C)=O)c(COc3cccc4ccc(C)nc34)c2NC(C)=O)cn1 10.1021/jm980330i
CHEMBL555976 13756 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 645 11 4 8 5.5 CC(=O)Nc1ccc(/C=C/C(=O)NCc2cccn2-c2ccc(NC(C)=O)c(COc3cccc4ccc(C)nc34)c2NC(C)=O)cn1 10.1021/jm980330i
44360877 13560 0 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 722 11 1 7 6.6 Cc1ccc2cccc(OCc3c(N4CCCC4=O)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3N3CCCC3=O)c2n1 10.1021/jm980330i
CHEMBL1194797 13560 0 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 722 11 1 7 6.6 Cc1ccc2cccc(OCc3c(N4CCCC4=O)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3N3CCCC3=O)c2n1 10.1021/jm980330i
CHEMBL553315 13560 0 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 722 11 1 7 6.6 Cc1ccc2cccc(OCc3c(N4CCCC4=O)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3N3CCCC3=O)c2n1 10.1021/jm980330i
10604613 12987 0 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 683 9 1 6 6.2 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL1190420 12987 0 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 683 9 1 6 6.2 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL540828 12987 0 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 683 9 1 6 6.2 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)cccn2c1Br 10.1021/jm980214f
10580156 12985 0 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 653 10 2 6 6.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5cccnc5)cc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL1190412 12985 0 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 653 10 2 6 6.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5cccnc5)cc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL540819 12985 0 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 653 10 2 6 6.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5cccnc5)cc4)c3Cl)c2n1 10.1021/jm980300f
11239595 13596 0 None - 0 Human 9.2 pIC50 = 9.2 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 738 11 2 8 6.7 Cc1cc(N2CCOCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1195041 13596 0 None - 0 Human 9.2 pIC50 = 9.2 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 738 11 2 8 6.7 Cc1cc(N2CCOCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL553762 13596 0 None - 0 Human 9.2 pIC50 = 9.2 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 738 11 2 8 6.7 Cc1cc(N2CCOCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
10627384 13611 0 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 598 9 2 5 6.9 CNC(=O)c1ccc(/C=C/C(=O)NCc2cccn2-c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980330i
CHEMBL1195129 13611 0 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 598 9 2 5 6.9 CNC(=O)c1ccc(/C=C/C(=O)NCc2cccn2-c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980330i
CHEMBL553911 13611 0 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 598 9 2 5 6.9 CNC(=O)c1ccc(/C=C/C(=O)NCc2cccn2-c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980330i
10675243 96319 0 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 610 10 2 8 4.6 COc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(C)=O)nc4)c3Cl)cccc2n1C 10.1021/jm980300f
CHEMBL264751 96319 0 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 610 10 2 8 4.6 COc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(C)=O)nc4)c3Cl)cccc2n1C 10.1021/jm980300f
10675243 96319 0 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 610 10 2 8 4.6 COc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(C)=O)nc4)c3Cl)cccc2n1C 10.1021/jm030468n
CHEMBL264751 96319 0 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 610 10 2 8 4.6 COc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(C)=O)nc4)c3Cl)cccc2n1C 10.1021/jm030468n
673 1647 12 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 671 9 1 6 5.8 O=C(/C=C/c1ccc(cc1)C(=O)N(C)C)NCC(=O)N(c1ccc(c(c1Cl)COc1cccn2c1nc(c2Br)C)Cl)C 10.1021/jm980300f
9810391 1647 12 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 671 9 1 6 5.8 O=C(/C=C/c1ccc(cc1)C(=O)N(C)C)NCC(=O)N(c1ccc(c(c1Cl)COc1cccn2c1nc(c2Br)C)Cl)C 10.1021/jm980300f
CHEMBL1192627 1647 12 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 671 9 1 6 5.8 O=C(/C=C/c1ccc(cc1)C(=O)N(C)C)NCC(=O)N(c1ccc(c(c1Cl)COc1cccn2c1nc(c2Br)C)Cl)C 10.1021/jm980300f
673 1647 12 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 671 9 1 6 5.8 O=C(/C=C/c1ccc(cc1)C(=O)N(C)C)NCC(=O)N(c1ccc(c(c1Cl)COc1cccn2c1nc(c2Br)C)Cl)C 10.1021/jm980214f
9810391 1647 12 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 671 9 1 6 5.8 O=C(/C=C/c1ccc(cc1)C(=O)N(C)C)NCC(=O)N(c1ccc(c(c1Cl)COc1cccn2c1nc(c2Br)C)Cl)C 10.1021/jm980214f
CHEMBL1192627 1647 12 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 671 9 1 6 5.8 O=C(/C=C/c1ccc(cc1)C(=O)N(C)C)NCC(=O)N(c1ccc(c(c1Cl)COc1cccn2c1nc(c2Br)C)Cl)C 10.1021/jm980214f
45269613 193175 0 None - 0 Human 9.2 pIC50 = 9.2 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 695 12 3 7 6.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)N4CCC[C@H]4C(=O)CCCNC(=O)c4ccc(C(=N)N)cc4)c3Cl)c2n1 10.1021/jm9002445
CHEMBL539924 193175 0 None - 0 Human 9.2 pIC50 = 9.2 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 695 12 3 7 6.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)N4CCC[C@H]4C(=O)CCCNC(=O)c4ccc(C(=N)N)cc4)c3Cl)c2n1 10.1021/jm9002445
10531497 13087 0 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cn1 10.1021/jm980300f
CHEMBL1191172 13087 0 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cn1 10.1021/jm980300f
CHEMBL542232 13087 0 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cn1 10.1021/jm980300f
10394861 1651 3 None - 0 Human 9.2 pIC50 = 9.2 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 687 12 2 9 5.5 COc1nc2c(n1Cc1ccccn1)cccc2OCc1c(Cl)ccc(c1Cl)N(C(=O)CNC(=O)/C=C/c1ccc(nc1)NC(=O)C)C 10.1021/jm030468n
669 1651 3 None - 0 Human 9.2 pIC50 = 9.2 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 687 12 2 9 5.5 COc1nc2c(n1Cc1ccccn1)cccc2OCc1c(Cl)ccc(c1Cl)N(C(=O)CNC(=O)/C=C/c1ccc(nc1)NC(=O)C)C 10.1021/jm030468n
CHEMBL329762 1651 3 None - 0 Human 9.2 pIC50 = 9.2 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 687 12 2 9 5.5 COc1nc2c(n1Cc1ccccn1)cccc2OCc1c(Cl)ccc(c1Cl)N(C(=O)CNC(=O)/C=C/c1ccc(nc1)NC(=O)C)C 10.1021/jm030468n
44360879 12847 0 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 637 11 4 8 2.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C(=O)NC)c(COc3cccc4ccc(C)nc34)c2C(=O)NC)cn1 10.1021/jm980330i
CHEMBL1189464 12847 0 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 637 11 4 8 2.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C(=O)NC)c(COc3cccc4ccc(C)nc34)c2C(=O)NC)cn1 10.1021/jm980330i
CHEMBL538784 12847 0 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 637 11 4 8 2.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C(=O)NC)c(COc3cccc4ccc(C)nc34)c2C(=O)NC)cn1 10.1021/jm980330i
10394861 1651 3 None - 0 Human 9.2 pIC50 = 9.2 Binding
Agonist activity at bradykinin B2 receptor (unknown origin)Agonist activity at bradykinin B2 receptor (unknown origin)
ChEMBL 687 12 2 9 5.5 COc1nc2c(n1Cc1ccccn1)cccc2OCc1c(Cl)ccc(c1Cl)N(C(=O)CNC(=O)/C=C/c1ccc(nc1)NC(=O)C)C 10.1016/j.ejmech.2020.112948
669 1651 3 None - 0 Human 9.2 pIC50 = 9.2 Binding
Agonist activity at bradykinin B2 receptor (unknown origin)Agonist activity at bradykinin B2 receptor (unknown origin)
ChEMBL 687 12 2 9 5.5 COc1nc2c(n1Cc1ccccn1)cccc2OCc1c(Cl)ccc(c1Cl)N(C(=O)CNC(=O)/C=C/c1ccc(nc1)NC(=O)C)C 10.1016/j.ejmech.2020.112948
CHEMBL329762 1651 3 None - 0 Human 9.2 pIC50 = 9.2 Binding
Agonist activity at bradykinin B2 receptor (unknown origin)Agonist activity at bradykinin B2 receptor (unknown origin)
ChEMBL 687 12 2 9 5.5 COc1nc2c(n1Cc1ccccn1)cccc2OCc1c(Cl)ccc(c1Cl)N(C(=O)CNC(=O)/C=C/c1ccc(nc1)NC(=O)C)C 10.1016/j.ejmech.2020.112948
9958759 13345 0 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 533 8 1 4 6.2 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccccc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL1193231 13345 0 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 533 8 1 4 6.2 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccccc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL544601 13345 0 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 533 8 1 4 6.2 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccccc4)c3Cl)c2n1 10.1021/jm980300f
11445540 167599 0 None - 0 Human 9.2 pIC50 = 9.2 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 727 13 2 8 6.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OCc5ccccn5)cc(C)nc34)c2Cl)cc1OC 10.1021/jm030468n
CHEMBL433214 167599 0 None - 0 Human 9.2 pIC50 = 9.2 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 727 13 2 8 6.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OCc5ccccn5)cc(C)nc34)c2Cl)cc1OC 10.1021/jm030468n
10032884 13339 0 None - 0 Human 9.2 pIC50 = 9.2 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 696 11 2 7 6.9 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1193185 13339 0 None - 0 Human 9.2 pIC50 = 9.2 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 696 11 2 7 6.9 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL544549 13339 0 None - 0 Human 9.2 pIC50 = 9.2 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 696 11 2 7 6.9 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
10257108 9723 0 None - 1 Guinea pig 9.2 pIC50 = 9.2 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 554 9 1 6 5.4 COc1cccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2C#N)c1 10.1016/s0960-894x(98)00736-7
CHEMBL113963 9723 0 None - 1 Guinea pig 9.2 pIC50 = 9.2 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 554 9 1 6 5.4 COc1cccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2C#N)c1 10.1016/s0960-894x(98)00736-7
10371910 19919 1 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 637 10 1 6 7.2 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(/C=C/c5ccncc5)nc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL130436 19919 1 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 637 10 1 6 7.2 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(/C=C/c5ccncc5)nc4)c3Cl)c2n1 10.1021/jm980300f
10651980 13292 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 660 8 2 6 5.8 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(C(=O)N(C)C)c4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL1192832 13292 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 660 8 2 6 5.8 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(C(=O)N(C)C)c4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL544135 13292 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 660 8 2 6 5.8 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(C(=O)N(C)C)c4)c3Cl)cccn2c1Br 10.1021/jm980214f
11365972 13517 0 None - 0 Human 9.1 pIC50 = 9.1 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 687 10 1 6 6.9 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1194477 13517 0 None - 0 Human 9.1 pIC50 = 9.1 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 687 10 1 6 6.9 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL3216391 13517 0 None - 0 Human 9.1 pIC50 = 9.1 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 687 10 1 6 6.9 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030326t
44360968 120558 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 775 14 1 8 9.0 Cc1ccc2cccc(OCc3c(/C=C/c4ccncc4)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(/C=C/c5ccncc5)nc4)c3/C=C/c3ccncc3)c2n1 10.1021/jm980330i
CHEMBL357075 120558 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 775 14 1 8 9.0 Cc1ccc2cccc(OCc3c(/C=C/c4ccncc4)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(/C=C/c5ccncc5)nc4)c3/C=C/c3ccncc3)c2n1 10.1021/jm980330i
44353012 13263 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 600 8 1 5 6.1 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C\c4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL1192626 13263 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 600 8 1 5 6.1 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C\c4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL543898 13263 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 600 8 1 5 6.1 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C\c4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
10721082 13169 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 534 8 1 5 5.6 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4cccnc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL1191809 13169 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 534 8 1 5 5.6 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4cccnc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL542958 13169 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 534 8 1 5 5.6 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4cccnc4)c3Cl)c2n1 10.1021/jm980300f
10818426 13235 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 690 11 3 7 5.5 COCCNC(=O)c1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
CHEMBL1192425 13235 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 690 11 3 7 5.5 COCCNC(=O)c1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
CHEMBL543657 13235 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 690 11 3 7 5.5 COCCNC(=O)c1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
10746610 13290 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 631 8 2 6 6.3 CC(=O)c1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
CHEMBL1192829 13290 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 631 8 2 6 6.3 CC(=O)c1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
CHEMBL544132 13290 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 631 8 2 6 6.3 CC(=O)c1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
10578612 13605 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 551 9 2 6 4.9 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cn1 10.1021/jm980300f
CHEMBL1195105 13605 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 551 9 2 6 4.9 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cn1 10.1021/jm980300f
CHEMBL553843 13605 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 551 9 2 6 4.9 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cn1 10.1021/jm980300f
10722424 170382 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 609 10 2 7 4.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c3nc(OC)n4C)c2Cl)cc1 10.1021/jm980300f
CHEMBL44557 170382 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 609 10 2 7 4.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c3nc(OC)n4C)c2Cl)cc1 10.1021/jm980300f
10722424 170382 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 609 10 2 7 4.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c3nc(OC)n4C)c2Cl)cc1 10.1021/jm030159x
CHEMBL44557 170382 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 609 10 2 7 4.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c3nc(OC)n4C)c2Cl)cc1 10.1021/jm030159x
11491055 206450 0 None - 0 Human 9.1 pIC50 = 9.1 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 723 12 1 7 7.3 Cc1cc(OCc2ccccn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)c2n1 10.1021/jm030468n
CHEMBL98459 206450 0 None - 0 Human 9.1 pIC50 = 9.1 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 723 12 1 7 7.3 Cc1cc(OCc2ccccn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)c2n1 10.1021/jm030468n
44360553 13679 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 645 11 4 8 3.7 CNC(=O)c1ccc(/C=C/C(=O)NCc2cccn2-c2ccc(C(=O)NC)c(COc3cccc4ccc(C)nc34)c2C(=O)NC)cn1 10.1021/jm980330i
CHEMBL1195619 13679 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 645 11 4 8 3.7 CNC(=O)c1ccc(/C=C/C(=O)NCc2cccn2-c2ccc(C(=O)NC)c(COc3cccc4ccc(C)nc34)c2C(=O)NC)cn1 10.1021/jm980330i
CHEMBL555006 13679 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 645 11 4 8 3.7 CNC(=O)c1ccc(/C=C/C(=O)NCc2cccn2-c2ccc(C(=O)NC)c(COc3cccc4ccc(C)nc34)c2C(=O)NC)cn1 10.1021/jm980330i
11377448 12929 0 None - 0 Human 9.1 pIC50 = 9.1 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 689 10 1 7 5.8 Cc1cc(N2CCOCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1190058 12929 0 None - 0 Human 9.1 pIC50 = 9.1 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 689 10 1 7 5.8 Cc1cc(N2CCOCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL3216622 12929 0 None - 0 Human 9.1 pIC50 = 9.1 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 689 10 1 7 5.8 Cc1cc(N2CCOCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030326t
10842202 13719 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 672 9 3 6 5.8 CNC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
CHEMBL1195903 13719 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 672 9 3 6 5.8 CNC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
CHEMBL555555 13719 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 672 9 3 6 5.8 CNC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
9831859 9599 0 None - 1 Guinea pig 9.1 pIC50 = 9.1 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 508 10 3 6 3.6 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)NCCCCN)c3C#N)c2n1 10.1016/s0960-894x(98)00736-7
CHEMBL113169 9599 0 None - 1 Guinea pig 9.1 pIC50 = 9.1 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 508 10 3 6 3.6 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)NCCCCN)c3C#N)c2n1 10.1016/s0960-894x(98)00736-7
11422541 206416 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 682 13 2 10 4.6 CCOC(=O)Cn1c(OC)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(C)=O)nc4)c3Cl)cccc21 10.1021/jm030468n
CHEMBL98292 206416 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 682 13 2 10 4.6 CCOC(=O)Cn1c(OC)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(C)=O)nc4)c3Cl)cccc21 10.1021/jm030468n
10627732 22252 0 None - 0 Guinea pig 9.0 pIC50 = 9.0 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 623 10 1 7 5.0 COc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)cccc2n1C 10.1021/jm980300f
CHEMBL132510 22252 0 None - 0 Guinea pig 9.0 pIC50 = 9.0 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 623 10 1 7 5.0 COc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)cccc2n1C 10.1021/jm980300f
10769383 22648 0 None - 0 Guinea pig 9.0 pIC50 = 9.0 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 570 10 2 8 3.9 COc1nc2c(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(C)=O)nc4)c3C)cccc2n1C 10.1021/jm980300f
CHEMBL132860 22648 0 None - 0 Guinea pig 9.0 pIC50 = 9.0 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 570 10 2 8 3.9 COc1nc2c(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(C)=O)nc4)c3C)cccc2n1C 10.1021/jm980300f
10745254 35086 0 None - 0 Guinea pig 9.0 pIC50 = 9.0 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 550 9 2 5 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm980300f
CHEMBL143697 35086 0 None - 0 Guinea pig 9.0 pIC50 = 9.0 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 550 9 2 5 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm980300f
CHEMBL543781 35086 0 None - 0 Guinea pig 9.0 pIC50 = 9.0 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 550 9 2 5 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm980300f
10745254 35086 0 None - 0 Guinea pig 9.0 pIC50 = 9.0 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 550 9 2 5 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm030159x
CHEMBL143697 35086 0 None - 0 Guinea pig 9.0 pIC50 = 9.0 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 550 9 2 5 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm030159x
CHEMBL543781 35086 0 None - 0 Guinea pig 9.0 pIC50 = 9.0 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 550 9 2 5 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm030159x
10745254 35086 0 None - 0 Guinea pig 9.0 pIC50 = 9.0 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 550 9 2 5 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm980330i
CHEMBL143697 35086 0 None - 0 Guinea pig 9.0 pIC50 = 9.0 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 550 9 2 5 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm980330i
CHEMBL543781 35086 0 None - 0 Guinea pig 9.0 pIC50 = 9.0 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 550 9 2 5 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm980330i
10579332 13627 0 None - 0 Guinea pig 9.0 pIC50 = 9 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ncc(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL1195281 13627 0 None - 0 Guinea pig 9.0 pIC50 = 9 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ncc(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL554206 13627 0 None - 0 Guinea pig 9.0 pIC50 = 9 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ncc(C)nc34)c2Cl)cc1 10.1021/jm980300f
10579332 13627 0 None - 0 Guinea pig 9.0 pIC50 = 9 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ncc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL1195281 13627 0 None - 0 Guinea pig 9.0 pIC50 = 9 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ncc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL554206 13627 0 None - 0 Guinea pig 9.0 pIC50 = 9 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ncc(C)nc34)c2Cl)cc1 10.1021/jm030159x
11239019 13361 0 None - 0 Human 9.0 pIC50 = 9 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 626 10 2 5 6.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c(-c5ccccc5)cc(C)nc34)c2C)cc1 10.1021/jm030159x
CHEMBL1193332 13361 0 None - 0 Human 9.0 pIC50 = 9 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 626 10 2 5 6.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c(-c5ccccc5)cc(C)nc34)c2C)cc1 10.1021/jm030159x
CHEMBL544720 13361 0 None - 0 Human 9.0 pIC50 = 9 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 626 10 2 5 6.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c(-c5ccccc5)cc(C)nc34)c2C)cc1 10.1021/jm030159x
11468276 13387 0 None - 0 Human 9.0 pIC50 = 9 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 738 11 2 8 6.7 Cc1cc(N2CCOCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1193590 13387 0 None - 0 Human 9.0 pIC50 = 9 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 738 11 2 8 6.7 Cc1cc(N2CCOCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL545021 13387 0 None - 0 Human 9.0 pIC50 = 9 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 738 11 2 8 6.7 Cc1cc(N2CCOCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
10651897 12876 0 None - 0 Guinea pig 9.0 pIC50 = 9.0 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 653 10 2 6 6.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL1189702 12876 0 None - 0 Guinea pig 9.0 pIC50 = 9.0 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 653 10 2 6 6.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL539294 12876 0 None - 0 Guinea pig 9.0 pIC50 = 9.0 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 653 10 2 6 6.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm980300f
10841531 20343 0 None - 0 Guinea pig 9.0 pIC50 = 9.0 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 617 9 1 6 5.7 Cc1cnc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL130782 20343 0 None - 0 Guinea pig 9.0 pIC50 = 9.0 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 617 9 1 6 5.7 Cc1cnc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)c2n1 10.1021/jm980300f
11801800 20945 0 None - 0 Guinea pig 9.0 pIC50 = 9.0 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 604 9 1 5 5.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4cccc(C(=O)N(C)C)c4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL131263 20945 0 None - 0 Guinea pig 9.0 pIC50 = 9.0 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 604 9 1 5 5.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4cccc(C(=O)N(C)C)c4)c3Cl)c2n1 10.1021/jm980300f
10699672 12833 0 None - 0 Guinea pig 9.0 pIC50 = 9.0 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 671 9 1 6 6.1 CC(=O)N(C)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
CHEMBL1189342 12833 0 None - 0 Guinea pig 9.0 pIC50 = 9.0 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 671 9 1 6 6.1 CC(=O)N(C)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
CHEMBL538531 12833 0 None - 0 Guinea pig 9.0 pIC50 = 9.0 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 671 9 1 6 6.1 CC(=O)N(C)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
10348414 168496 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
Displacement of [3H]BK from cloned human B2 bradykinin receptor expressed in CHO cells after 2 hrs by liquid scintillation counterDisplacement of [3H]BK from cloned human B2 bradykinin receptor expressed in CHO cells after 2 hrs by liquid scintillation counter
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/acs.jmedchem.5b00982
CHEMBL439737 168496 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
Displacement of [3H]BK from cloned human B2 bradykinin receptor expressed in CHO cells after 2 hrs by liquid scintillation counterDisplacement of [3H]BK from cloned human B2 bradykinin receptor expressed in CHO cells after 2 hrs by liquid scintillation counter
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/acs.jmedchem.5b00982
CHEMBL542096 168496 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
Displacement of [3H]BK from cloned human B2 bradykinin receptor expressed in CHO cells after 2 hrs by liquid scintillation counterDisplacement of [3H]BK from cloned human B2 bradykinin receptor expressed in CHO cells after 2 hrs by liquid scintillation counter
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/acs.jmedchem.5b00982
10348414 168496 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL439737 168496 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL542096 168496 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm030159x
10348414 168496 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm030468n
CHEMBL439737 168496 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm030468n
CHEMBL542096 168496 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm030468n
11456652 13081 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 676 10 2 8 4.8 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCOCC5)cc(C)nc34)c2Cl)cn1 10.1021/jm030326t
CHEMBL1191124 13081 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 676 10 2 8 4.8 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCOCC5)cc(C)nc34)c2Cl)cn1 10.1021/jm030326t
CHEMBL542176 13081 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 676 10 2 8 4.8 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCOCC5)cc(C)nc34)c2Cl)cn1 10.1021/jm030326t
11468051 13563 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 673 10 2 6 6.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCCCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL1194820 13563 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 673 10 2 6 6.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCCCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL3215558 13563 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 673 10 2 6 6.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCCCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
10348414 168496 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL439737 168496 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL542096 168496 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm030326t
10348414 168496 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980330i
CHEMBL439737 168496 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980330i
CHEMBL542096 168496 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980330i
10348414 168496 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL439737 168496 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL542096 168496 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980300f
11216111 13164 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 648 12 2 6 6.4 CCCOc1cc(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc12 10.1021/jm030468n
CHEMBL1191769 13164 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 648 12 2 6 6.4 CCCOc1cc(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc12 10.1021/jm030468n
CHEMBL542911 13164 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 648 12 2 6 6.4 CCCOc1cc(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc12 10.1021/jm030468n
11169915 13413 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 648 11 2 6 6.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OC(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030468n
CHEMBL1193789 13413 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 648 11 2 6 6.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OC(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030468n
CHEMBL545255 13413 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 648 11 2 6 6.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OC(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030468n
11169975 206449 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 698 12 2 8 6.5 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OCc5ccccn5)cc(C)nc34)c2Cl)cn1 10.1021/jm030468n
CHEMBL98458 206449 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 698 12 2 8 6.5 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OCc5ccccn5)cc(C)nc34)c2Cl)cn1 10.1021/jm030468n
11169975 206449 0 None - 0 Human 8.9 pIC50 = 8.9 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 698 12 2 8 6.5 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OCc5ccccn5)cc(C)nc34)c2Cl)cn1 10.1021/jm030468n
CHEMBL98458 206449 0 None - 0 Human 8.9 pIC50 = 8.9 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 698 12 2 8 6.5 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OCc5ccccn5)cc(C)nc34)c2Cl)cn1 10.1021/jm030468n
11445066 13285 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 634 10 2 7 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cn1 10.1021/jm030326t
CHEMBL1192789 13285 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 634 10 2 7 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cn1 10.1021/jm030326t
CHEMBL544087 13285 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 634 10 2 7 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cn1 10.1021/jm030326t
11456756 13682 0 None - 0 Human 8.9 pIC50 = 8.9 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 699 10 1 6 7.3 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1195624 13682 0 None - 0 Human 8.9 pIC50 = 8.9 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 699 10 1 6 7.3 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL3216405 13682 0 None - 0 Human 8.9 pIC50 = 8.9 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 699 10 1 6 7.3 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)c2n1 10.1021/jm030326t
22008895 110056 0 None - 1 Guinea pig 8.9 pIC50 = 8.9 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 592 8 1 5 6.5 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(F)(F)F)cc4)c3C#N)c2n1 10.1016/s0960-894x(98)00736-7
CHEMBL325255 110056 0 None - 1 Guinea pig 8.9 pIC50 = 8.9 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 592 8 1 5 6.5 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(F)(F)F)cc4)c3C#N)c2n1 10.1016/s0960-894x(98)00736-7
10603710 13535 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 604 9 1 5 5.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL1194615 13535 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 604 9 1 5 5.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL552986 13535 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 604 9 1 5 5.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm980300f
10348414 168496 0 None - 0 Human 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL439737 168496 0 None - 0 Human 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL542096 168496 0 None - 0 Human 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980300f
10603710 13535 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 604 9 1 5 5.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL1194615 13535 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 604 9 1 5 5.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL552986 13535 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 604 9 1 5 5.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
44360617 13351 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 678 11 1 7 4.0 Cc1ccc2cccc(OCc3c(C(=O)N(C)C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3C(=O)N(C)C)c2n1 10.1021/jm980330i
CHEMBL1193249 13351 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 678 11 1 7 4.0 Cc1ccc2cccc(OCc3c(C(=O)N(C)C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3C(=O)N(C)C)c2n1 10.1021/jm980330i
CHEMBL544622 13351 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 678 11 1 7 4.0 Cc1ccc2cccc(OCc3c(C(=O)N(C)C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3C(=O)N(C)C)c2n1 10.1021/jm980330i
10555195 13118 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 577 9 1 6 5.1 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)nc4)c3C)c2n1 10.1021/jm980300f
CHEMBL1191388 13118 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 577 9 1 6 5.1 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)nc4)c3C)c2n1 10.1021/jm980300f
CHEMBL542479 13118 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 577 9 1 6 5.1 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)nc4)c3C)c2n1 10.1021/jm980300f
673 1647 12 None - 0 Human 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 671 9 1 6 5.8 O=C(/C=C/c1ccc(cc1)C(=O)N(C)C)NCC(=O)N(c1ccc(c(c1Cl)COc1cccn2c1nc(c2Br)C)Cl)C 10.1021/jm980300f
9810391 1647 12 None - 0 Human 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 671 9 1 6 5.8 O=C(/C=C/c1ccc(cc1)C(=O)N(C)C)NCC(=O)N(c1ccc(c(c1Cl)COc1cccn2c1nc(c2Br)C)Cl)C 10.1021/jm980300f
CHEMBL1192627 1647 12 None - 0 Human 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 671 9 1 6 5.8 O=C(/C=C/c1ccc(cc1)C(=O)N(C)C)NCC(=O)N(c1ccc(c(c1Cl)COc1cccn2c1nc(c2Br)C)Cl)C 10.1021/jm980300f
11801941 13720 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 614 7 2 6 5.9 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(C#N)c4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL1195904 13720 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 614 7 2 6 5.9 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(C#N)c4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL555556 13720 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 614 7 2 6 5.9 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(C#N)c4)c3Cl)cccn2c1Br 10.1021/jm980214f
10698666 13878 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 589 7 2 5 6.1 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL1197062 13878 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 589 7 2 5 6.1 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL559195 13878 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 589 7 2 5 6.1 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
10627456 19935 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 602 9 1 5 6.0 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)CCc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL130452 19935 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 602 9 1 5 6.0 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)CCc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
673 1647 12 None - 0 Human 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 671 9 1 6 5.8 O=C(/C=C/c1ccc(cc1)C(=O)N(C)C)NCC(=O)N(c1ccc(c(c1Cl)COc1cccn2c1nc(c2Br)C)Cl)C 10.1021/jm980214f
9810391 1647 12 None - 0 Human 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 671 9 1 6 5.8 O=C(/C=C/c1ccc(cc1)C(=O)N(C)C)NCC(=O)N(c1ccc(c(c1Cl)COc1cccn2c1nc(c2Br)C)Cl)C 10.1021/jm980214f
CHEMBL1192627 1647 12 None - 0 Human 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 671 9 1 6 5.8 O=C(/C=C/c1ccc(cc1)C(=O)N(C)C)NCC(=O)N(c1ccc(c(c1Cl)COc1cccn2c1nc(c2Br)C)Cl)C 10.1021/jm980214f
5311108 1648 13 None - 0 Human 8.9 pIC50 = 8.9 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 591 9 2 6 5.6 CC(=O)Nc1ccc(cn1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2)Cl)C 10.1021/jm9002445
674 1648 13 None - 0 Human 8.9 pIC50 = 8.9 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 591 9 2 6 5.6 CC(=O)Nc1ccc(cn1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2)Cl)C 10.1021/jm9002445
CHEMBL130517 1648 13 None - 0 Human 8.9 pIC50 = 8.9 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 591 9 2 6 5.6 CC(=O)Nc1ccc(cn1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2)Cl)C 10.1021/jm9002445
11204833 111130 1 None - 0 Human 8.9 pIC50 = 8.9 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 711 12 1 7 6.9 Cc1cc(OCc2ccccn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030468n
CHEMBL328509 111130 1 None - 0 Human 8.9 pIC50 = 8.9 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 711 12 1 7 6.9 Cc1cc(OCc2ccccn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030468n
11433973 111889 0 None - 0 Human 8.9 pIC50 = 8.9 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 698 12 2 8 6.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OCc5ccccn5)cc(C)nc34)c2Cl)cn1 10.1021/jm030468n
CHEMBL329701 111889 0 None - 0 Human 8.9 pIC50 = 8.9 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 698 12 2 8 6.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OCc5ccccn5)cc(C)nc34)c2Cl)cn1 10.1021/jm030468n
5311108 1648 13 None - 0 Human 8.9 pIC50 = 8.9 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 591 9 2 6 5.6 CC(=O)Nc1ccc(cn1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2)Cl)C 10.1021/jm980330i
674 1648 13 None - 0 Human 8.9 pIC50 = 8.9 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 591 9 2 6 5.6 CC(=O)Nc1ccc(cn1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2)Cl)C 10.1021/jm980330i
CHEMBL130517 1648 13 None - 0 Human 8.9 pIC50 = 8.9 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 591 9 2 6 5.6 CC(=O)Nc1ccc(cn1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2)Cl)C 10.1021/jm980330i
5311108 1648 13 None - 0 Human 8.9 pIC50 = 8.9 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 591 9 2 6 5.6 CC(=O)Nc1ccc(cn1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2)Cl)C 10.1021/jm980300f
674 1648 13 None - 0 Human 8.9 pIC50 = 8.9 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 591 9 2 6 5.6 CC(=O)Nc1ccc(cn1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2)Cl)C 10.1021/jm980300f
CHEMBL130517 1648 13 None - 0 Human 8.9 pIC50 = 8.9 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 591 9 2 6 5.6 CC(=O)Nc1ccc(cn1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2)Cl)C 10.1021/jm980300f
11802476 12840 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 657 9 2 6 5.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL1189415 12840 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 657 9 2 6 5.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL538732 12840 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 657 9 2 6 5.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980300f
11802476 12840 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 657 9 2 6 5.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
CHEMBL1189415 12840 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 657 9 2 6 5.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
CHEMBL538732 12840 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 657 9 2 6 5.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
44360553 13679 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 645 11 4 8 3.7 CNC(=O)c1ccc(/C=C/C(=O)NCc2cccn2-c2ccc(C(=O)NC)c(COc3cccc4ccc(C)nc34)c2C(=O)NC)cn1 10.1021/jm980330i
CHEMBL1195619 13679 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 645 11 4 8 3.7 CNC(=O)c1ccc(/C=C/C(=O)NCc2cccn2-c2ccc(C(=O)NC)c(COc3cccc4ccc(C)nc34)c2C(=O)NC)cn1 10.1021/jm980330i
CHEMBL555006 13679 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 645 11 4 8 3.7 CNC(=O)c1ccc(/C=C/C(=O)NCc2cccn2-c2ccc(C(=O)NC)c(COc3cccc4ccc(C)nc34)c2C(=O)NC)cn1 10.1021/jm980330i
10721752 168641 0 None - 0 Guinea pig 8.8 pIC50 = 8.8 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 569 10 2 7 3.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(OC)n4C)c2C)cc1 10.1021/jm980300f
CHEMBL44087 168641 0 None - 0 Guinea pig 8.8 pIC50 = 8.8 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 569 10 2 7 3.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(OC)n4C)c2C)cc1 10.1021/jm980300f
10675847 13291 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 657 9 2 6 6.0 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
CHEMBL1192831 13291 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 657 9 2 6 6.0 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
CHEMBL544134 13291 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 657 9 2 6 6.0 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
10721752 168641 0 None - 0 Guinea pig 8.8 pIC50 = 8.8 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 569 10 2 7 3.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(OC)n4C)c2C)cc1 10.1021/jm030159x
CHEMBL44087 168641 0 None - 0 Guinea pig 8.8 pIC50 = 8.8 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 569 10 2 7 3.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(OC)n4C)c2C)cc1 10.1021/jm030159x
11308648 12910 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 736 11 2 7 7.9 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1189935 12910 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 736 11 2 7 7.9 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL539792 12910 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 736 11 2 7 7.9 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
11445066 13285 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 634 10 2 7 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cn1 10.1021/jm030326t
CHEMBL1192789 13285 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 634 10 2 7 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cn1 10.1021/jm030326t
CHEMBL544087 13285 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 634 10 2 7 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cn1 10.1021/jm030326t
122189857 122885 0 None - 2 Guinea pig 8.8 pIC50 = 8.8 Binding
Antagonist activity against B2R in Hartley guinea pig ileum assessed as reduction in electrically-induced responseAntagonist activity against B2R in Hartley guinea pig ileum assessed as reduction in electrically-induced response
ChEMBL 1742 42 23 22 -4.6 C[C@@H](NC(=O)[C@@H](N)Cc1ccc(O)cc1)C(=O)NCC(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@H](CCCNC(=N)N)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N1CCC[C@H]1C(=O)N1CC(O)CC1C(=O)NCC(=O)NC(Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N1C(C(=O)N[C@@H](CCCNC(=N)N)C(=O)O)CC2CCCCC21 10.1016/j.bmcl.2015.08.014
CHEMBL3616881 122885 0 None - 2 Guinea pig 8.8 pIC50 = 8.8 Binding
Antagonist activity against B2R in Hartley guinea pig ileum assessed as reduction in electrically-induced responseAntagonist activity against B2R in Hartley guinea pig ileum assessed as reduction in electrically-induced response
ChEMBL 1742 42 23 22 -4.6 C[C@@H](NC(=O)[C@@H](N)Cc1ccc(O)cc1)C(=O)NCC(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@H](CCCNC(=N)N)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N1CCC[C@H]1C(=O)N1CC(O)CC1C(=O)NCC(=O)NC(Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N1C(C(=O)N[C@@H](CCCNC(=N)N)C(=O)O)CC2CCCCC21 10.1016/j.bmcl.2015.08.014
122189855 122883 0 None - 3 Guinea pig 8.7 pIC50 = 8.7 Binding
Antagonist activity against B2R in Hartley guinea pig ileum assessed as reduction in electrically-induced responseAntagonist activity against B2R in Hartley guinea pig ileum assessed as reduction in electrically-induced response
ChEMBL 1816 45 23 23 -3.5 CSCC[C@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](C)NC(=O)[C@@H](N)Cc1ccc(O)cc1)C(=O)N[C@H](CCCNC(=N)N)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N1CCC[C@H]1C(=O)N1CC(O)CC1C(=O)NCC(=O)NC(Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N1C(C(=O)N[C@@H](CCCNC(=N)N)C(=O)O)CC2CCCCC21 10.1016/j.bmcl.2015.08.014
CHEMBL3616879 122883 0 None - 3 Guinea pig 8.7 pIC50 = 8.7 Binding
Antagonist activity against B2R in Hartley guinea pig ileum assessed as reduction in electrically-induced responseAntagonist activity against B2R in Hartley guinea pig ileum assessed as reduction in electrically-induced response
ChEMBL 1816 45 23 23 -3.5 CSCC[C@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](C)NC(=O)[C@@H](N)Cc1ccc(O)cc1)C(=O)N[C@H](CCCNC(=N)N)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N1CCC[C@H]1C(=O)N1CC(O)CC1C(=O)NCC(=O)NC(Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N1C(C(=O)N[C@@H](CCCNC(=N)N)C(=O)O)CC2CCCCC21 10.1016/j.bmcl.2015.08.014
3812 708 37 None 1 6 Human 8.7 pIC50 = 8.7 Binding
Displacement of [3H]Bradykinin from human recombinant bradykinin B2 receptor expressed in CHEM1 cells after 60 minsDisplacement of [3H]Bradykinin from human recombinant bradykinin B2 receptor expressed in CHEM1 cells after 60 mins
ChEMBL None None None None 10.1016/j.bmcl.2013.01.025
439201 708 37 None 1 6 Human 8.7 pIC50 = 8.7 Binding
Displacement of [3H]Bradykinin from human recombinant bradykinin B2 receptor expressed in CHEM1 cells after 60 minsDisplacement of [3H]Bradykinin from human recombinant bradykinin B2 receptor expressed in CHEM1 cells after 60 mins
ChEMBL None None None None 10.1016/j.bmcl.2013.01.025
649 708 37 None 1 6 Human 8.7 pIC50 = 8.7 Binding
Displacement of [3H]Bradykinin from human recombinant bradykinin B2 receptor expressed in CHEM1 cells after 60 minsDisplacement of [3H]Bradykinin from human recombinant bradykinin B2 receptor expressed in CHEM1 cells after 60 mins
ChEMBL None None None None 10.1016/j.bmcl.2013.01.025
CHEMBL406291 708 37 None 1 6 Human 8.7 pIC50 = 8.7 Binding
Displacement of [3H]Bradykinin from human recombinant bradykinin B2 receptor expressed in CHEM1 cells after 60 minsDisplacement of [3H]Bradykinin from human recombinant bradykinin B2 receptor expressed in CHEM1 cells after 60 mins
ChEMBL None None None None 10.1016/j.bmcl.2013.01.025
DB12126 708 37 None 1 6 Human 8.7 pIC50 = 8.7 Binding
Displacement of [3H]Bradykinin from human recombinant bradykinin B2 receptor expressed in CHEM1 cells after 60 minsDisplacement of [3H]Bradykinin from human recombinant bradykinin B2 receptor expressed in CHEM1 cells after 60 mins
ChEMBL None None None None 10.1016/j.bmcl.2013.01.025
11399463 13331 0 None - 0 Guinea pig 8.7 pIC50 = 8.7 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 633 10 2 6 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL1193123 13331 0 None - 0 Guinea pig 8.7 pIC50 = 8.7 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 633 10 2 6 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL3143949 13331 0 None - 0 Guinea pig 8.7 pIC50 = 8.7 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 633 10 2 6 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030159x
11399463 13331 0 None - 0 Guinea pig 8.7 pIC50 = 8.7 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 633 10 2 6 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL1193123 13331 0 None - 0 Guinea pig 8.7 pIC50 = 8.7 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 633 10 2 6 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL3143949 13331 0 None - 0 Guinea pig 8.7 pIC50 = 8.7 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 633 10 2 6 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
11445445 13591 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 701 10 1 7 6.2 Cc1cc(N2CCOCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1195018 13591 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 701 10 1 7 6.2 Cc1cc(N2CCOCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL3215999 13591 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 701 10 1 7 6.2 Cc1cc(N2CCOCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)c2n1 10.1021/jm030326t
11204664 111072 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 676 10 2 8 5.4 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCOCC5)cc(C)nc34)c2Cl)cn1 10.1021/jm030326t
CHEMBL328131 111072 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 676 10 2 8 5.4 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCOCC5)cc(C)nc34)c2Cl)cn1 10.1021/jm030326t
10651897 12876 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 653 10 2 6 6.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL1189702 12876 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 653 10 2 6 6.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL539294 12876 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 653 10 2 6 6.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm980300f
122189856 122884 0 None - 1 Guinea pig 8.7 pIC50 = 8.7 Binding
Antagonist activity against B2R in Hartley guinea pig ileum assessed as reduction in electrically-induced responseAntagonist activity against B2R in Hartley guinea pig ileum assessed as reduction in electrically-induced response
ChEMBL 1858 43 22 22 -2.5 N=C(N)NCCC[C@H](NC(=O)C1CC2CCCCC2N1C(=O)[C@H]1Cc2ccccc2CN1C(=O)[C@H](CO)NC(=O)C(Cc1cccs1)NC(=O)CNC(=O)C1CC(O)CN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H](CCCNC(=N)N)NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H]1CCCN1C(=O)[C@@H](N)Cc1ccc(O)cc1)C(=O)O 10.1016/j.bmcl.2015.08.014
CHEMBL3616880 122884 0 None - 1 Guinea pig 8.7 pIC50 = 8.7 Binding
Antagonist activity against B2R in Hartley guinea pig ileum assessed as reduction in electrically-induced responseAntagonist activity against B2R in Hartley guinea pig ileum assessed as reduction in electrically-induced response
ChEMBL 1858 43 22 22 -2.5 N=C(N)NCCC[C@H](NC(=O)C1CC2CCCCC2N1C(=O)[C@H]1Cc2ccccc2CN1C(=O)[C@H](CO)NC(=O)C(Cc1cccs1)NC(=O)CNC(=O)C1CC(O)CN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H](CCCNC(=N)N)NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H]1CCCN1C(=O)[C@@H](N)Cc1ccc(O)cc1)C(=O)O 10.1016/j.bmcl.2015.08.014
10531744 115830 0 None - 0 Guinea pig 8.7 pIC50 = 8.7 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 605 9 1 6 5.3 Cc1cnc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL335946 115830 0 None - 0 Guinea pig 8.7 pIC50 = 8.7 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 605 9 1 6 5.3 Cc1cnc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm980300f
10698671 13342 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 590 9 2 5 6.2 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL1193229 13342 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 590 9 2 5 6.2 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL544599 13342 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 590 9 2 5 6.2 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980300f
119343 2818 18 None - 0 Human 8.0 pIC50 = 8 Binding
Binding affinity to human bradykinin B2 receptor by radioligand displacement assayBinding affinity to human bradykinin B2 receptor by radioligand displacement assay
ChEMBL None None None None 10.1016/j.bmc.2013.03.016
676 2818 18 None - 0 Human 8.0 pIC50 = 8 Binding
Binding affinity to human bradykinin B2 receptor by radioligand displacement assayBinding affinity to human bradykinin B2 receptor by radioligand displacement assay
ChEMBL None None None None 10.1016/j.bmc.2013.03.016
CHEMBL446325 2818 18 None - 0 Human 8.0 pIC50 = 8 Binding
Binding affinity to human bradykinin B2 receptor by radioligand displacement assayBinding affinity to human bradykinin B2 receptor by radioligand displacement assay
ChEMBL None None None None 10.1016/j.bmc.2013.03.016
45272156 193379 0 None - 0 Human 8.0 pIC50 = 8 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 556 6 0 7 6.8 Cc1cc(-c2ncsc2Cl)c2cccc(OCc3c(C)ccnc3Cn3cccc(C(F)(F)F)c3=O)c2n1 10.1021/jm9002445
CHEMBL549534 193379 0 None - 0 Human 8.0 pIC50 = 8 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 556 6 0 7 6.8 Cc1cc(-c2ncsc2Cl)c2cccc(OCc3c(C)ccnc3Cn3cccc(C(F)(F)F)c3=O)c2n1 10.1021/jm9002445
44190263 194270 0 None - 0 Human 8.0 pIC50 = 8 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 483 7 1 6 5.4 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(C)ccnc3CNC(=O)C3CCCCC3)c2n1 10.1021/jm9002445
CHEMBL559565 194270 0 None - 0 Human 8.0 pIC50 = 8 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 483 7 1 6 5.4 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(C)ccnc3CNC(=O)C3CCCCC3)c2n1 10.1021/jm9002445
18941145 9854 0 None - 1 Guinea pig 8.0 pIC50 = 8.0 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 569 9 1 6 6.3 COc1cccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4sc(C)nc34)c2Cl)c1 10.1016/s0960-894x(98)00736-7
CHEMBL114732 9854 0 None - 1 Guinea pig 8.0 pIC50 = 8.0 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 569 9 1 6 6.3 COc1cccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4sc(C)nc34)c2Cl)c1 10.1016/s0960-894x(98)00736-7
10627129 101063 0 None - 0 Guinea pig 6.0 pIC50 = 6 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 583 11 2 7 4.1 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(COC)n4C)c2C)cc1 10.1021/jm980300f
CHEMBL298320 101063 0 None - 0 Guinea pig 6.0 pIC50 = 6 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 583 11 2 7 4.1 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(COC)n4C)c2C)cc1 10.1021/jm980300f
10627129 101063 0 None - 0 Guinea pig 6.0 pIC50 = 6 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 583 11 2 7 4.1 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(COC)n4C)c2C)cc1 10.1021/jm030159x
CHEMBL298320 101063 0 None - 0 Guinea pig 6.0 pIC50 = 6 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 583 11 2 7 4.1 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(COC)n4C)c2C)cc1 10.1021/jm030159x
10663541 119004 1 None - 0 Guinea pig 5.0 pIC50 = 5 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 320 4 0 3 4.8 CCc1cn2cccc(OCc3c(Cl)cccc3Cl)c2n1 10.1021/jm970591c
CHEMBL345670 119004 1 None - 0 Guinea pig 5.0 pIC50 = 5 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 320 4 0 3 4.8 CCc1cn2cccc(OCc3c(Cl)cccc3Cl)c2n1 10.1021/jm970591c
10818058 116071 0 None - 0 Guinea pig 8.0 pIC50 = 8.0 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 653 10 2 6 6.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccccn5)cc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL336574 116071 0 None - 0 Guinea pig 8.0 pIC50 = 8.0 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 653 10 2 6 6.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccccn5)cc4)c3Cl)c2n1 10.1021/jm980300f
10579547 13450 0 None - 0 Guinea pig 8.0 pIC50 = 8.0 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 603 8 2 5 5.8 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)NCc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL1194034 13450 0 None - 0 Guinea pig 8.0 pIC50 = 8.0 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 603 8 2 5 5.8 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)NCc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL545534 13450 0 None - 0 Guinea pig 8.0 pIC50 = 8.0 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 603 8 2 5 5.8 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)NCc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
10556247 22811 0 None - 0 Human 8.0 pIC50 = 8.0 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 652 10 2 5 7.5 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccccc5)cc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL133005 22811 0 None - 0 Human 8.0 pIC50 = 8.0 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 652 10 2 5 7.5 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccccc5)cc4)c3Cl)c2n1 10.1021/jm980300f
44341039 9405 0 None - 1 Guinea pig 7.9 pIC50 = 7.9 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 597 9 1 5 6.6 COc1ccc(N(C)C(=O)CNC(=O)/C=C/c2ccc(C(F)(F)F)cc2)c(Cl)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
CHEMBL112140 9405 0 None - 1 Guinea pig 7.9 pIC50 = 7.9 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 597 9 1 5 6.6 COc1ccc(N(C)C(=O)CNC(=O)/C=C/c2ccc(C(F)(F)F)cc2)c(Cl)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
22008892 109660 0 None - 1 Guinea pig 7.9 pIC50 = 7.9 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 561 8 1 4 6.6 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(F)(F)F)cc4)c3C)c2n1 10.1016/s0960-894x(98)00736-7
CHEMBL323693 109660 0 None - 1 Guinea pig 7.9 pIC50 = 7.9 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 561 8 1 4 6.6 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(F)(F)F)cc4)c3C)c2n1 10.1016/s0960-894x(98)00736-7
10651074 101078 0 None - 0 Guinea pig 7.0 pIC50 = 7.0 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4cnc(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL298463 101078 0 None - 0 Guinea pig 7.0 pIC50 = 7.0 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4cnc(C)nc34)c2Cl)cc1 10.1021/jm980300f
44189789 194469 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 398 4 1 4 5.5 Cc1cc(-c2n[nH]cc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL561223 194469 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 398 4 1 4 5.5 Cc1cc(-c2n[nH]cc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
44190166 194949 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 415 4 0 5 6.3 Cc1cc(-c2scnc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL564294 194949 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 415 4 0 5 6.3 Cc1cc(-c2scnc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
10651074 101078 0 None - 0 Guinea pig 7.0 pIC50 = 7.0 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4cnc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL298463 101078 0 None - 0 Guinea pig 7.0 pIC50 = 7.0 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4cnc(C)nc34)c2Cl)cc1 10.1021/jm030159x
10626618 33241 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 556 9 2 5 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2)cc1 10.1021/jm980330i
CHEMBL142015 33241 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 556 9 2 5 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2)cc1 10.1021/jm980330i
10603982 79660 0 None - 0 Guinea pig 6.0 pIC50 = 6.0 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 625 12 2 8 4.0 CCOC(=O)Cc1nc2c(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3C)cccc2n1C 10.1021/jm980300f
CHEMBL21311 79660 0 None - 0 Guinea pig 6.0 pIC50 = 6.0 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 625 12 2 8 4.0 CCOC(=O)Cc1nc2c(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3C)cccc2n1C 10.1021/jm980300f
10603982 79660 0 None - 0 Guinea pig 6.0 pIC50 = 6.0 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 625 12 2 8 4.0 CCOC(=O)Cc1nc2c(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3C)cccc2n1C 10.1021/jm030159x
CHEMBL21311 79660 0 None - 0 Guinea pig 6.0 pIC50 = 6.0 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 625 12 2 8 4.0 CCOC(=O)Cc1nc2c(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3C)cccc2n1C 10.1021/jm030159x
10579143 167888 0 None - 0 Human 6.0 pIC50 = 6.0 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 580 9 2 6 5.2 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4oc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL43510 167888 0 None - 0 Human 6.0 pIC50 = 6.0 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 580 9 2 6 5.2 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4oc(C)nc34)c2Cl)cc1 10.1021/jm030159x
10579143 167888 0 None - 0 Human 6.0 pIC50 = 6.0 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 580 9 2 6 5.2 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4oc(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL43510 167888 0 None - 0 Human 6.0 pIC50 = 6.0 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 580 9 2 6 5.2 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4oc(C)nc34)c2Cl)cc1 10.1021/jm980300f
18941161 9622 0 None - 1 Guinea pig 5.0 pIC50 = 5.0 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 615 9 1 5 8.0 Cc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4sc(-c5ccccc5)nc34)c2Cl)cc1 10.1016/s0960-894x(98)00736-7
CHEMBL113320 9622 0 None - 1 Guinea pig 5.0 pIC50 = 5.0 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 615 9 1 5 8.0 Cc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4sc(-c5ccccc5)nc34)c2Cl)cc1 10.1016/s0960-894x(98)00736-7
10675163 13116 0 None - 0 Guinea pig 7.9 pIC50 = 7.9 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 603 7 2 5 6.4 Cc1ccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
CHEMBL1191383 13116 0 None - 0 Guinea pig 7.9 pIC50 = 7.9 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 603 7 2 5 6.4 Cc1ccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
CHEMBL542472 13116 0 None - 0 Guinea pig 7.9 pIC50 = 7.9 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 603 7 2 5 6.4 Cc1ccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
44190854 193764 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 435 6 1 6 4.2 CC(=O)NCc1cncc(Cl)c1COc1cccc2c(-c3ccnn3C)cc(C)nc12 10.1021/jm9002445
CHEMBL552384 193764 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 435 6 1 6 4.2 CC(=O)NCc1cncc(Cl)c1COc1cccc2c(-c3ccnn3C)cc(C)nc12 10.1021/jm9002445
19603349 13082 0 None - 0 Guinea pig 7.9 pIC50 = 7.9 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 685 10 3 7 6.9 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(C(=O)Nc5ccncc5)c4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1191125 13082 0 None - 0 Guinea pig 7.9 pIC50 = 7.9 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 685 10 3 7 6.9 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(C(=O)Nc5ccncc5)c4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL542177 13082 0 None - 0 Guinea pig 7.9 pIC50 = 7.9 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 685 10 3 7 6.9 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(C(=O)Nc5ccncc5)c4)c3Cl)c2n1 10.1021/jm030326t
11296863 13284 0 None - 0 Guinea pig 7.9 pIC50 = 7.9 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 675 10 2 7 5.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCOCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL1192787 13284 0 None - 0 Guinea pig 7.9 pIC50 = 7.9 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 675 10 2 7 5.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCOCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL3216859 13284 0 None - 0 Guinea pig 7.9 pIC50 = 7.9 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 675 10 2 7 5.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCOCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
44353012 13263 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 600 8 1 5 6.1 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C\c4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL1192626 13263 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 600 8 1 5 6.1 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C\c4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL543898 13263 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 600 8 1 5 6.1 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C\c4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
10854681 119503 0 None - 0 Guinea pig 5.9 pIC50 = 5.9 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 339 3 1 3 5.2 Cc1nc2c(NCc3c(Cl)cccc3Cl)cccn2c1Cl 10.1021/jm970591c
CHEMBL350232 119503 0 None - 0 Guinea pig 5.9 pIC50 = 5.9 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 339 3 1 3 5.2 Cc1nc2c(NCc3c(Cl)cccc3Cl)cccn2c1Cl 10.1021/jm970591c
176 394 63 None -5 31 Human 4.9 pIC50 = 4.9 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
ChEMBL 645 11 0 4 6.9 CCCCc1oc2c(c1C(=O)c1cc(I)c(c(c1)I)OCCN(CC)CC)cccc2 nan
2157 394 63 None -5 31 Human 4.9 pIC50 = 4.9 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
ChEMBL 645 11 0 4 6.9 CCCCc1oc2c(c1C(=O)c1cc(I)c(c(c1)I)OCCN(CC)CC)cccc2 nan
2566 394 63 None -5 31 Human 4.9 pIC50 = 4.9 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
ChEMBL 645 11 0 4 6.9 CCCCc1oc2c(c1C(=O)c1cc(I)c(c(c1)I)OCCN(CC)CC)cccc2 nan
CHEMBL633 394 63 None -5 31 Human 4.9 pIC50 = 4.9 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
ChEMBL 645 11 0 4 6.9 CCCCc1oc2c(c1C(=O)c1cc(I)c(c(c1)I)OCCN(CC)CC)cccc2 nan
DB01118 394 63 None -5 31 Human 4.9 pIC50 = 4.9 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
ChEMBL 645 11 0 4 6.9 CCCCc1oc2c(c1C(=O)c1cc(I)c(c(c1)I)OCCN(CC)CC)cccc2 nan
11169915 13413 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 648 11 2 6 6.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OC(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030468n
CHEMBL1193789 13413 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 648 11 2 6 6.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OC(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030468n
CHEMBL545255 13413 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 648 11 2 6 6.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OC(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030468n
11445445 13591 0 None - 0 Guinea pig 7.9 pIC50 = 7.9 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 701 10 1 7 6.2 Cc1cc(N2CCOCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1195018 13591 0 None - 0 Guinea pig 7.9 pIC50 = 7.9 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 701 10 1 7 6.2 Cc1cc(N2CCOCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL3215999 13591 0 None - 0 Guinea pig 7.9 pIC50 = 7.9 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 701 10 1 7 6.2 Cc1cc(N2CCOCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)c2n1 10.1021/jm030326t
11801083 114736 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 565 9 1 6 4.6 Cc1cnc2cccc(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3C)c2n1 10.1021/jm980300f
CHEMBL334753 114736 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 565 9 1 6 4.6 Cc1cnc2cccc(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3C)c2n1 10.1021/jm980300f
10530740 165029 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 552 9 2 7 4.3 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ncc(C)nc34)c2C)cn1 10.1021/jm980300f
CHEMBL424268 165029 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 552 9 2 7 4.3 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ncc(C)nc34)c2C)cn1 10.1021/jm980300f
44189792 193455 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 401 4 0 5 5.9 Cc1cc(-c2cncs2)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL550142 193455 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 401 4 0 5 5.9 Cc1cc(-c2cncs2)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
44340818 110107 0 None - 1 Guinea pig 5.9 pIC50 = 5.9 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 539 8 1 5 6.3 Cc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4scnc34)c2Cl)cc1 10.1016/s0960-894x(98)00736-7
CHEMBL325624 110107 0 None - 1 Guinea pig 5.9 pIC50 = 5.9 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 539 8 1 5 6.3 Cc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4scnc34)c2Cl)cc1 10.1016/s0960-894x(98)00736-7
11801800 20945 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 604 9 1 5 5.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4cccc(C(=O)N(C)C)c4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL131263 20945 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 604 9 1 5 5.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4cccc(C(=O)N(C)C)c4)c3Cl)c2n1 10.1021/jm980300f
119343 2818 18 None - 0 Human 7.9 pIC50 = 7.9 Binding
Displacement of [3H]bradykinin from human recombinant B2 bradykinin receptorDisplacement of [3H]bradykinin from human recombinant B2 bradykinin receptor
ChEMBL None None None None 10.1016/j.bmc.2016.03.006
676 2818 18 None - 0 Human 7.9 pIC50 = 7.9 Binding
Displacement of [3H]bradykinin from human recombinant B2 bradykinin receptorDisplacement of [3H]bradykinin from human recombinant B2 bradykinin receptor
ChEMBL None None None None 10.1016/j.bmc.2016.03.006
CHEMBL446325 2818 18 None - 0 Human 7.9 pIC50 = 7.9 Binding
Displacement of [3H]bradykinin from human recombinant B2 bradykinin receptorDisplacement of [3H]bradykinin from human recombinant B2 bradykinin receptor
ChEMBL None None None None 10.1016/j.bmc.2016.03.006
44190941 193750 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 471 7 1 7 3.6 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3CNS(C)(=O)=O)c2n1 10.1021/jm9002445
CHEMBL552296 193750 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 471 7 1 7 3.6 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3CNS(C)(=O)=O)c2n1 10.1021/jm9002445
119343 2818 18 None - 0 Human 7.9 pIC50 = 7.9 Binding
Displacement of [3H]bradykinin from human recombinant bradykinin B2 receptor expressed in CHO cells measured after 60 mins by scintillation counting methodDisplacement of [3H]bradykinin from human recombinant bradykinin B2 receptor expressed in CHO cells measured after 60 mins by scintillation counting method
ChEMBL None None None None 10.1016/j.bmc.2016.11.014
676 2818 18 None - 0 Human 7.9 pIC50 = 7.9 Binding
Displacement of [3H]bradykinin from human recombinant bradykinin B2 receptor expressed in CHO cells measured after 60 mins by scintillation counting methodDisplacement of [3H]bradykinin from human recombinant bradykinin B2 receptor expressed in CHO cells measured after 60 mins by scintillation counting method
ChEMBL None None None None 10.1016/j.bmc.2016.11.014
CHEMBL446325 2818 18 None - 0 Human 7.9 pIC50 = 7.9 Binding
Displacement of [3H]bradykinin from human recombinant bradykinin B2 receptor expressed in CHO cells measured after 60 mins by scintillation counting methodDisplacement of [3H]bradykinin from human recombinant bradykinin B2 receptor expressed in CHO cells measured after 60 mins by scintillation counting method
ChEMBL None None None None 10.1016/j.bmc.2016.11.014
11800992 118264 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 559 9 2 4 6.6 CNC(=O)c1ccc(/C=C/C(=O)NC/C=C\c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980330i
CHEMBL342016 118264 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 559 9 2 4 6.6 CNC(=O)c1ccc(/C=C/C(=O)NC/C=C\c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980330i
10627732 22252 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 623 10 1 7 5.0 COc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)cccc2n1C 10.1021/jm980300f
CHEMBL132510 22252 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 623 10 1 7 5.0 COc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)cccc2n1C 10.1021/jm980300f
18941160 9807 0 None - 1 Guinea pig 7.9 pIC50 = 7.9 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 553 8 1 5 6.6 Cc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4sc(C)nc34)c2Cl)cc1 10.1016/s0960-894x(98)00736-7
CHEMBL114401 9807 0 None - 1 Guinea pig 7.9 pIC50 = 7.9 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 553 8 1 5 6.6 Cc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4sc(C)nc34)c2Cl)cc1 10.1016/s0960-894x(98)00736-7
10651302 13191 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 603 7 2 5 6.4 Cc1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
CHEMBL1192012 13191 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 603 7 2 5 6.4 Cc1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
CHEMBL543188 13191 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 603 7 2 5 6.4 Cc1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
44190943 194269 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 471 7 0 7 5.5 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3COc3ccccn3)c2n1 10.1021/jm9002445
CHEMBL559564 194269 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 471 7 0 7 5.5 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3COc3ccccn3)c2n1 10.1021/jm9002445
10743094 45034 0 None - 0 Guinea pig 5.9 pIC50 = 5.9 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 471 4 0 5 5.5 COC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
CHEMBL152650 45034 0 None - 0 Guinea pig 5.9 pIC50 = 5.9 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 471 4 0 5 5.5 COC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
CHEMBL2392354 208660 0 None - 1 Human 7.8 pIC50 = 7.8 Binding
Binding affinity to human bradykinin B2 receptor by radioligand displacement assayBinding affinity to human bradykinin B2 receptor by radioligand displacement assay
ChEMBL None None None N=C(N)NCCC[C@H](N)C(=O)N[C@H](CCCNC(=N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](CO)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](CCCNC(=N)N)C(=O)O 10.1016/j.ejmech.2013.01.044
10818067 13236 0 None - 0 Guinea pig 7.8 pIC50 = 7.8 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 654 10 2 7 6.3 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)nc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL1192427 13236 0 None - 0 Guinea pig 7.8 pIC50 = 7.8 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 654 10 2 7 6.3 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)nc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL543659 13236 0 None - 0 Guinea pig 7.8 pIC50 = 7.8 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 654 10 2 7 6.3 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)nc4)c3Cl)c2n1 10.1021/jm980300f
10722378 21125 0 None - 0 Guinea pig 7.8 pIC50 = 7.8 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 604 7 3 6 5.7 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(N)c4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL131404 21125 0 None - 0 Guinea pig 7.8 pIC50 = 7.8 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 604 7 3 6 5.7 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(N)c4)c3Cl)cccn2c1Br 10.1021/jm980214f
10698666 13878 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 589 7 2 5 6.1 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL1197062 13878 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 589 7 2 5 6.1 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL559195 13878 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 589 7 2 5 6.1 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
10651301 116015 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 603 7 2 5 6.4 Cc1ccccc1NC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm980214f
CHEMBL336209 116015 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 603 7 2 5 6.4 Cc1ccccc1NC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm980214f
10604425 164584 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 661 9 2 7 6.3 CCOC(=O)c1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
CHEMBL422794 164584 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 661 9 2 7 6.3 CCOC(=O)c1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
10552342 47289 0 None - 0 Guinea pig 6.8 pIC50 = 6.8 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 469 5 0 4 5.7 CCN(C(C)=O)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
CHEMBL154625 47289 0 None - 0 Guinea pig 6.8 pIC50 = 6.8 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 469 5 0 4 5.7 CCN(C(C)=O)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
10744917 118318 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 536 9 2 5 4.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2cccc(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm980330i
CHEMBL342195 118318 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 536 9 2 5 4.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2cccc(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm980330i
10503130 12879 0 None - 0 Guinea pig 5.8 pIC50 = 5.8 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 399 3 1 4 4.9 Cc1nc2c(OCc3c(Cl)ccc(N)c3Cl)cccn2c1Br 10.1021/jm970591c
CHEMBL1189725 12879 0 None - 0 Guinea pig 5.8 pIC50 = 5.8 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 399 3 1 4 4.9 Cc1nc2c(OCc3c(Cl)ccc(N)c3Cl)cccn2c1Br 10.1021/jm970591c
CHEMBL539324 12879 0 None - 0 Guinea pig 5.8 pIC50 = 5.8 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 399 3 1 4 4.9 Cc1nc2c(OCc3c(Cl)ccc(N)c3Cl)cccn2c1Br 10.1021/jm970591c
10737855 45725 0 None - 0 Guinea pig 5.8 pIC50 = 5.8 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 368 3 0 3 4.8 Cc1nc2c(OCc3c(F)cccc3Cl)cccn2c1Br 10.1021/jm970591c
CHEMBL153271 45725 0 None - 0 Guinea pig 5.8 pIC50 = 5.8 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 368 3 0 3 4.8 Cc1nc2c(OCc3c(F)cccc3Cl)cccn2c1Br 10.1021/jm970591c
11239381 13018 0 None - 0 Guinea pig 5.8 pIC50 = 5.8 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 688 10 2 7 5.3 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCN(C)CC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL1190638 13018 0 None - 0 Guinea pig 5.8 pIC50 = 5.8 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 688 10 2 7 5.3 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCN(C)CC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL3215541 13018 0 None - 0 Guinea pig 5.8 pIC50 = 5.8 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 688 10 2 7 5.3 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCN(C)CC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
10601892 46752 0 None - 0 Guinea pig 7.8 pIC50 = 7.8 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%
ChEMBL 512 6 1 5 4.4 CC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm980214f
CHEMBL154188 46752 0 None - 0 Guinea pig 7.8 pIC50 = 7.8 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%
ChEMBL 512 6 1 5 4.4 CC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm980214f
CHEMBL558018 46752 0 None - 0 Guinea pig 7.8 pIC50 = 7.8 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%
ChEMBL 512 6 1 5 4.4 CC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm980214f
10699672 12833 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 671 9 1 6 6.1 CC(=O)N(C)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
CHEMBL1189342 12833 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 671 9 1 6 6.1 CC(=O)N(C)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
CHEMBL538531 12833 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 671 9 1 6 6.1 CC(=O)N(C)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
10601892 46752 0 None - 0 Guinea pig 7.8 pIC50 = 7.8 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 512 6 1 5 4.4 CC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
CHEMBL154188 46752 0 None - 0 Guinea pig 7.8 pIC50 = 7.8 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 512 6 1 5 4.4 CC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
CHEMBL558018 46752 0 None - 0 Guinea pig 7.8 pIC50 = 7.8 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 512 6 1 5 4.4 CC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
10531338 91261 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 582 10 2 7 4.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(N(C)C)n4C)c2C)cc1 10.1021/jm030159x
CHEMBL240875 91261 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 582 10 2 7 4.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(N(C)C)n4C)c2C)cc1 10.1021/jm030159x
10531338 91261 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 582 10 2 7 4.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(N(C)C)n4C)c2C)cc1 10.1021/jm980300f
CHEMBL240875 91261 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 582 10 2 7 4.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(N(C)C)n4C)c2C)cc1 10.1021/jm980300f
10506334 119121 0 None - 0 Guinea pig 5.8 pIC50 = 5.8 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 526 6 0 5 4.7 CC(=O)N(C)CC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
CHEMBL346718 119121 0 None - 0 Guinea pig 5.8 pIC50 = 5.8 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 526 6 0 5 4.7 CC(=O)N(C)CC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
11491041 13330 0 None - 0 Guinea pig 7.8 pIC50 = 7.8 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 719 11 2 8 7.1 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL1193122 13330 0 None - 0 Guinea pig 7.8 pIC50 = 7.8 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 719 11 2 8 7.1 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL544480 13330 0 None - 0 Guinea pig 7.8 pIC50 = 7.8 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 719 11 2 8 7.1 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030159x
11800992 118264 0 None - 0 Guinea pig 7.8 pIC50 = 7.8 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 559 9 2 4 6.6 CNC(=O)c1ccc(/C=C/C(=O)NC/C=C\c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980330i
CHEMBL342016 118264 0 None - 0 Guinea pig 7.8 pIC50 = 7.8 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 559 9 2 4 6.6 CNC(=O)c1ccc(/C=C/C(=O)NC/C=C\c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980330i
10744917 118318 0 None - 0 Guinea pig 7.8 pIC50 = 7.8 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 536 9 2 5 4.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2cccc(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm980330i
CHEMBL342195 118318 0 None - 0 Guinea pig 7.8 pIC50 = 7.8 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 536 9 2 5 4.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2cccc(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm980330i
10579159 118789 0 None - 0 Guinea pig 7.8 pIC50 = 7.8 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 582 11 2 7 4.3 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(OC)c(COc3cccc4ccc(C)nc34)c2OC)cc1 10.1021/jm980330i
CHEMBL344021 118789 0 None - 0 Guinea pig 7.8 pIC50 = 7.8 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 582 11 2 7 4.3 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(OC)c(COc3cccc4ccc(C)nc34)c2OC)cc1 10.1021/jm980330i
10674242 23938 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 551 9 2 6 4.3 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ncc(C)nc34)c2C)cc1 10.1021/jm980300f
CHEMBL133913 23938 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 551 9 2 6 4.3 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ncc(C)nc34)c2C)cc1 10.1021/jm980300f
11801594 99953 0 None - 0 Guinea pig 6.8 pIC50 = 6.8 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4nc(C)cnc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL290431 99953 0 None - 0 Guinea pig 6.8 pIC50 = 6.8 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4nc(C)cnc34)c2Cl)cc1 10.1021/jm980300f
11801594 99953 0 None - 0 Guinea pig 6.8 pIC50 = 6.8 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4nc(C)cnc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL290431 99953 0 None - 0 Guinea pig 6.8 pIC50 = 6.8 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4nc(C)cnc34)c2Cl)cc1 10.1021/jm030159x
10693943 119092 0 None - 0 Guinea pig 5.8 pIC50 = 5.8 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 428 3 0 3 5.4 Cc1nc2c(OCc3c(Br)cccc3Br)cccn2c1Cl 10.1021/jm970591c
CHEMBL346458 119092 0 None - 0 Guinea pig 5.8 pIC50 = 5.8 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 428 3 0 3 5.4 Cc1nc2c(OCc3c(Br)cccc3Br)cccn2c1Cl 10.1021/jm970591c
10554743 114643 0 None - 0 Guinea pig 7.8 pIC50 = 7.8 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 552 9 2 7 3.7 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ncc(C)nc34)c2C)cn1 10.1021/jm980300f
CHEMBL334421 114643 0 None - 0 Guinea pig 7.8 pIC50 = 7.8 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 552 9 2 7 3.7 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ncc(C)nc34)c2C)cn1 10.1021/jm980300f
44190752 193666 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 476 6 0 8 5.5 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3Sc3nccn3C)c2n1 10.1021/jm9002445
CHEMBL551759 193666 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 476 6 0 8 5.5 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3Sc3nccn3C)c2n1 10.1021/jm9002445
10508305 13483 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 634 8 2 7 6.0 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc([N+](=O)[O-])c4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL1194233 13483 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 634 8 2 7 6.0 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc([N+](=O)[O-])c4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL545765 13483 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 634 8 2 7 6.0 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc([N+](=O)[O-])c4)c3Cl)cccn2c1Br 10.1021/jm980214f
10836951 47211 0 None - 0 Guinea pig 5.8 pIC50 = 5.8 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 441 4 1 4 5.2 CC(=O)Nc1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
CHEMBL154558 47211 0 None - 0 Guinea pig 5.8 pIC50 = 5.8 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 441 4 1 4 5.2 CC(=O)Nc1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
10518915 119046 0 None - 0 Guinea pig 5.8 pIC50 = 5.8 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 308 3 0 3 4.2 Cc1nc2c(OCc3c(F)cccc3F)cccn2c1Cl 10.1021/jm970591c
CHEMBL346034 119046 0 None - 0 Guinea pig 5.8 pIC50 = 5.8 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 308 3 0 3 4.2 Cc1nc2c(OCc3c(F)cccc3F)cccn2c1Cl 10.1021/jm970591c
10649831 13243 0 None - 0 Guinea pig 7.7 pIC50 = 7.7 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 526 7 1 5 4.8 CCC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
CHEMBL1192462 13243 0 None - 0 Guinea pig 7.7 pIC50 = 7.7 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 526 7 1 5 4.8 CCC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
CHEMBL543700 13243 0 None - 0 Guinea pig 7.7 pIC50 = 7.7 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 526 7 1 5 4.8 CCC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
11262636 13710 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 721 16 2 8 5.7 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(CCOC)CCOC)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL1195841 13710 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 721 16 2 8 5.7 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(CCOC)CCOC)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL3215972 13710 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 721 16 2 8 5.7 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(CCOC)CCOC)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
11801941 13720 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 614 7 2 6 5.9 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(C#N)c4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL1195904 13720 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 614 7 2 6 5.9 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(C#N)c4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL555556 13720 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 614 7 2 6 5.9 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(C#N)c4)c3Cl)cccn2c1Br 10.1021/jm980214f
10841637 13791 0 None - 0 Human 5.7 pIC50 = 5.7 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 623 7 2 5 6.7 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(Cl)c4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL1196403 13791 0 None - 0 Human 5.7 pIC50 = 5.7 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 623 7 2 5 6.7 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(Cl)c4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL556816 13791 0 None - 0 Human 5.7 pIC50 = 5.7 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 623 7 2 5 6.7 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(Cl)c4)c3Cl)cccn2c1Br 10.1021/jm980214f
11181406 12814 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 663 11 2 7 5.7 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cc1OC 10.1021/jm030326t
CHEMBL1189212 12814 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 663 11 2 7 5.7 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cc1OC 10.1021/jm030326t
CHEMBL3217073 12814 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 663 11 2 7 5.7 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cc1OC 10.1021/jm030326t
11479285 13029 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 647 10 1 6 6.0 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL1190741 13029 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 647 10 1 6 6.0 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL3143958 13029 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 647 10 1 6 6.0 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
11479285 13029 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 647 10 1 6 6.0 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1190741 13029 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 647 10 1 6 6.0 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL3143958 13029 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 647 10 1 6 6.0 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030326t
10650330 13034 0 None - 0 Guinea pig 8.7 pIC50 = 8.7 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 551 9 2 6 4.3 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cn1 10.1021/jm980300f
CHEMBL1190789 13034 0 None - 0 Guinea pig 8.7 pIC50 = 8.7 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 551 9 2 6 4.3 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cn1 10.1021/jm980300f
CHEMBL541590 13034 0 None - 0 Guinea pig 8.7 pIC50 = 8.7 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 551 9 2 6 4.3 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cn1 10.1021/jm980300f
10604425 164584 0 None - 0 Guinea pig 8.7 pIC50 = 8.7 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 661 9 2 7 6.3 CCOC(=O)c1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
CHEMBL422794 164584 0 None - 0 Guinea pig 8.7 pIC50 = 8.7 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 661 9 2 7 6.3 CCOC(=O)c1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
10722424 170382 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 609 10 2 7 4.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c3nc(OC)n4C)c2Cl)cc1 10.1021/jm030159x
CHEMBL44557 170382 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 609 10 2 7 4.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c3nc(OC)n4C)c2Cl)cc1 10.1021/jm030159x
19603349 13082 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 685 10 3 7 6.9 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(C(=O)Nc5ccncc5)c4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1191125 13082 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 685 10 3 7 6.9 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(C(=O)Nc5ccncc5)c4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL542177 13082 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 685 10 3 7 6.9 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(C(=O)Nc5ccncc5)c4)c3Cl)c2n1 10.1021/jm030326t
673 1647 12 None - 0 Human 8.7 pIC50 = 8.7 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 671 9 1 6 5.8 O=C(/C=C/c1ccc(cc1)C(=O)N(C)C)NCC(=O)N(c1ccc(c(c1Cl)COc1cccn2c1nc(c2Br)C)Cl)C 10.1021/jm980300f
9810391 1647 12 None - 0 Human 8.7 pIC50 = 8.7 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 671 9 1 6 5.8 O=C(/C=C/c1ccc(cc1)C(=O)N(C)C)NCC(=O)N(c1ccc(c(c1Cl)COc1cccn2c1nc(c2Br)C)Cl)C 10.1021/jm980300f
CHEMBL1192627 1647 12 None - 0 Human 8.7 pIC50 = 8.7 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 671 9 1 6 5.8 O=C(/C=C/c1ccc(cc1)C(=O)N(C)C)NCC(=O)N(c1ccc(c(c1Cl)COc1cccn2c1nc(c2Br)C)Cl)C 10.1021/jm980300f
10722424 170382 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 609 10 2 7 4.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c3nc(OC)n4C)c2Cl)cc1 10.1021/jm980300f
CHEMBL44557 170382 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 609 10 2 7 4.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c3nc(OC)n4C)c2Cl)cc1 10.1021/jm980300f
5311114 1650 6 None - 1 Guinea pig 8.6 pIC50 = 8.6 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 697 12 2 7 6.6 CNC(=O)c1ccc(cc1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2OCc1ccccn1)Cl)C 10.1021/jm030468n
668 1650 6 None - 1 Guinea pig 8.6 pIC50 = 8.6 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 697 12 2 7 6.6 CNC(=O)c1ccc(cc1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2OCc1ccccn1)Cl)C 10.1021/jm030468n
CHEMBL99869 1650 6 None - 1 Guinea pig 8.6 pIC50 = 8.6 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 697 12 2 7 6.6 CNC(=O)c1ccc(cc1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2OCc1ccccn1)Cl)C 10.1021/jm030468n
10841582 13117 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 619 8 2 6 6.1 COc1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
CHEMBL1191384 13117 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 619 8 2 6 6.1 COc1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
CHEMBL542473 13117 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 619 8 2 6 6.1 COc1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
9894265 31308 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 569 9 2 4 7.1 CNC(=O)c1ccc(/C=C/C(=O)NCc2ccccc2-c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm980330i
CHEMBL140383 31308 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 569 9 2 4 7.1 CNC(=O)c1ccc(/C=C/C(=O)NCc2ccccc2-c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm980330i
10793563 13713 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 591 9 2 6 5.6 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ncc(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL1195858 13713 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 591 9 2 6 5.6 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ncc(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL555465 13713 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 591 9 2 6 5.6 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ncc(C)nc34)c2Cl)cc1 10.1021/jm980300f
10769517 23238 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 577 9 1 6 5.1 Cc1cnc2cccc(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3C)c2n1 10.1021/jm980300f
CHEMBL133339 23238 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 577 9 1 6 5.1 Cc1cnc2cccc(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3C)c2n1 10.1021/jm980300f
10840534 22358 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 555 8 1 6 3.9 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)CN(C)C)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL132620 22358 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 555 8 1 6 3.9 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)CN(C)C)c3Cl)cccn2c1Br 10.1021/jm980214f
10349737 12990 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 658 9 2 7 5.4 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cn1 10.1021/jm980214f
CHEMBL1190430 12990 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 658 9 2 7 5.4 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cn1 10.1021/jm980214f
CHEMBL540840 12990 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 658 9 2 7 5.4 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cn1 10.1021/jm980214f
10840534 22358 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 555 8 1 6 3.9 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)CN(C)C)c3Cl)cccn2c1Br 10.1021/jm970591c
CHEMBL132620 22358 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 555 8 1 6 3.9 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)CN(C)C)c3Cl)cccn2c1Br 10.1021/jm970591c
11320262 206428 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 775 14 2 9 7.2 Cc1cc(OCc2ccccn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)Cc5ccncc5)nc4)c3Cl)c2n1 10.1021/jm030468n
CHEMBL98349 206428 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 775 14 2 9 7.2 Cc1cc(OCc2ccccn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)Cc5ccncc5)nc4)c3Cl)c2n1 10.1021/jm030468n
11181524 206271 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 686 12 2 8 6.1 COc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(C)=O)nc4)c3Cl)cccc2n1Cc1ccccc1 10.1021/jm030468n
CHEMBL97393 206271 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 686 12 2 8 6.1 COc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(C)=O)nc4)c3Cl)cccc2n1Cc1ccccc1 10.1021/jm030468n
11193509 13610 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 750 12 2 7 7.5 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NCc5ccccn5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1195125 13610 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 750 12 2 7 7.5 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NCc5ccccn5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL553897 13610 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 750 12 2 7 7.5 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NCc5ccccn5)cc4)c3Cl)c2n1 10.1021/jm030326t
10818067 13236 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 654 10 2 7 6.3 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)nc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL1192427 13236 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 654 10 2 7 6.3 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)nc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL543659 13236 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 654 10 2 7 6.3 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)nc4)c3Cl)c2n1 10.1021/jm980300f
10793563 13713 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 591 9 2 6 5.6 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ncc(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL1195858 13713 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 591 9 2 6 5.6 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ncc(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL555465 13713 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 591 9 2 6 5.6 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ncc(C)nc34)c2Cl)cc1 10.1021/jm980300f
10842202 13719 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 672 9 3 6 5.8 CNC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
CHEMBL1195903 13719 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 672 9 3 6 5.8 CNC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
CHEMBL555555 13719 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 672 9 3 6 5.8 CNC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
11343115 12948 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 692 13 2 8 5.5 CCOC(=O)COc1cc(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc12 10.1021/jm030468n
CHEMBL1190165 12948 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 692 13 2 8 5.5 CCOC(=O)COc1cc(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc12 10.1021/jm030468n
CHEMBL540300 12948 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 692 13 2 8 5.5 CCOC(=O)COc1cc(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc12 10.1021/jm030468n
44360818 13352 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 783 14 1 8 10.3 Cc1ccc2cccc(OCc3c(/C=C/c4ccncc4)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(/C=C/c5ccncc5)nc4)c3/C=C/c3ccncc3)c2n1 10.1021/jm980330i
CHEMBL1193250 13352 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 783 14 1 8 10.3 Cc1ccc2cccc(OCc3c(/C=C/c4ccncc4)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(/C=C/c5ccncc5)nc4)c3/C=C/c3ccncc3)c2n1 10.1021/jm980330i
CHEMBL544623 13352 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 783 14 1 8 10.3 Cc1ccc2cccc(OCc3c(/C=C/c4ccncc4)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(/C=C/c5ccncc5)nc4)c3/C=C/c3ccncc3)c2n1 10.1021/jm980330i
9894265 31308 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 569 9 2 4 7.1 CNC(=O)c1ccc(/C=C/C(=O)NCc2ccccc2-c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm980330i
CHEMBL140383 31308 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 569 9 2 4 7.1 CNC(=O)c1ccc(/C=C/C(=O)NCc2ccccc2-c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm980330i
10651302 13191 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 603 7 2 5 6.4 Cc1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
CHEMBL1192012 13191 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 603 7 2 5 6.4 Cc1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
CHEMBL543188 13191 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 603 7 2 5 6.4 Cc1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
10604560 20190 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 676 10 3 7 5.7 COCC(=O)Nc1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
CHEMBL130660 20190 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 676 10 3 7 5.7 COCC(=O)Nc1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
11250851 13491 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 656 10 2 7 5.8 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(-n5cccn5)cc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL1194270 13491 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 656 10 2 7 5.8 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(-n5cccn5)cc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL3216880 13491 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 656 10 2 7 5.8 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(-n5cccn5)cc(C)nc34)c2Cl)cc1 10.1021/jm030159x
11296863 13284 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 675 10 2 7 5.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCOCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL1192787 13284 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 675 10 2 7 5.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCOCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL3216859 13284 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 675 10 2 7 5.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCOCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
10769485 20335 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 575 9 2 5 7.2 CNC(=O)c1ccc(/C=C/C(=O)NCc2sccc2-c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm980330i
CHEMBL130775 20335 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 575 9 2 5 7.2 CNC(=O)c1ccc(/C=C/C(=O)NCc2sccc2-c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm980330i
10746877 13691 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 654 10 2 7 6.3 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)nc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL1195721 13691 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 654 10 2 7 6.3 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)nc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL555202 13691 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 654 10 2 7 6.3 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)nc4)c3Cl)c2n1 10.1021/jm980300f
11479285 13029 0 None - 0 Guinea pig 8.5 pIC50 = 8.5 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 647 10 1 6 6.0 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL1190741 13029 0 None - 0 Guinea pig 8.5 pIC50 = 8.5 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 647 10 1 6 6.0 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL3143958 13029 0 None - 0 Guinea pig 8.5 pIC50 = 8.5 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 647 10 1 6 6.0 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
11479285 13029 0 None - 0 Guinea pig 8.5 pIC50 = 8.5 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 647 10 1 6 6.0 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1190741 13029 0 None - 0 Guinea pig 8.5 pIC50 = 8.5 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 647 10 1 6 6.0 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL3143958 13029 0 None - 0 Guinea pig 8.5 pIC50 = 8.5 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 647 10 1 6 6.0 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030326t
11343115 12948 0 None - 0 Guinea pig 7.7 pIC50 = 7.7 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 692 13 2 8 5.5 CCOC(=O)COc1cc(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc12 10.1021/jm030468n
CHEMBL1190165 12948 0 None - 0 Guinea pig 7.7 pIC50 = 7.7 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 692 13 2 8 5.5 CCOC(=O)COc1cc(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc12 10.1021/jm030468n
CHEMBL540300 12948 0 None - 0 Guinea pig 7.7 pIC50 = 7.7 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 692 13 2 8 5.5 CCOC(=O)COc1cc(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc12 10.1021/jm030468n
10818426 13235 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 690 11 3 7 5.5 COCCNC(=O)c1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
CHEMBL1192425 13235 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 690 11 3 7 5.5 COCCNC(=O)c1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
CHEMBL543657 13235 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 690 11 3 7 5.5 COCCNC(=O)c1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
10651980 13292 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 660 8 2 6 5.8 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(C(=O)N(C)C)c4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL1192832 13292 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 660 8 2 6 5.8 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(C(=O)N(C)C)c4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL544135 13292 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 660 8 2 6 5.8 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(C(=O)N(C)C)c4)c3Cl)cccn2c1Br 10.1021/jm980214f
44190269 194512 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 415 4 0 5 6.3 Cc1cc(-c2nscc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL561415 194512 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 415 4 0 5 6.3 Cc1cc(-c2nscc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
10555263 100614 0 None - 0 Guinea pig 6.7 pIC50 = 6.7 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 581 10 2 7 4.1 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(C(C)=O)n4C)c2C)cc1 10.1021/jm980300f
CHEMBL295005 100614 0 None - 0 Guinea pig 6.7 pIC50 = 6.7 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 581 10 2 7 4.1 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(C(C)=O)n4C)c2C)cc1 10.1021/jm980300f
10841582 13117 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 619 8 2 6 6.1 COc1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
CHEMBL1191384 13117 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 619 8 2 6 6.1 COc1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
CHEMBL542473 13117 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 619 8 2 6 6.1 COc1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
44191220 193350 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 398 4 0 5 5.3 Cc1cc(-n2ccnc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL549337 193350 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 398 4 0 5 5.3 Cc1cc(-n2ccnc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
44190168 193438 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 415 4 0 5 6.3 Cc1cc(-c2csnc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL550016 193438 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 415 4 0 5 6.3 Cc1cc(-c2csnc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
44191224 194577 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 412 4 0 5 5.5 Cc1cc(-c2ncc(C)n2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL561839 194577 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 412 4 0 5 5.5 Cc1cc(-c2ncc(C)n2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
10569271 49701 0 None - 0 Guinea pig 6.7 pIC50 = 6.7 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 340 3 0 3 5.2 Cc1nc2c(OCc3c(Cl)cccc3Cl)cccn2c1Cl 10.1021/jm970591c
CHEMBL156902 49701 0 None - 0 Guinea pig 6.7 pIC50 = 6.7 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 340 3 0 3 5.2 Cc1nc2c(OCc3c(Cl)cccc3Cl)cccn2c1Cl 10.1021/jm970591c
10555263 100614 0 None - 0 Guinea pig 6.7 pIC50 = 6.7 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 581 10 2 7 4.1 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(C(C)=O)n4C)c2C)cc1 10.1021/jm030159x
CHEMBL295005 100614 0 None - 0 Guinea pig 6.7 pIC50 = 6.7 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 581 10 2 7 4.1 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(C(C)=O)n4C)c2C)cc1 10.1021/jm030159x
10699094 23043 0 None - 0 Human 5.7 pIC50 = 5.7 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 619 10 2 6 5.5 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccnc3-n3c(C)ccc3C)c2Cl)cc1 10.1021/jm980300f
CHEMBL133186 23043 0 None - 0 Human 5.7 pIC50 = 5.7 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 619 10 2 6 5.5 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccnc3-n3c(C)ccc3C)c2Cl)cc1 10.1021/jm980300f
127034153 138022 0 None - 0 Human 4.7 pIC50 = 4.7 Binding
Inhibition of recombinant human bradykinin receptor 2 expressed in CHO cellsInhibition of recombinant human bradykinin receptor 2 expressed in CHO cells
ChEMBL 365 5 2 3 4.5 CC(C)CN1[C@H](C)Cc2cc(O)ccc2[C@H]1c1ccc(/C=C/C(=O)O)cc1 10.1021/acsmedchemlett.5b00413
CHEMBL3775378 138022 0 None - 0 Human 4.7 pIC50 = 4.7 Binding
Inhibition of recombinant human bradykinin receptor 2 expressed in CHO cellsInhibition of recombinant human bradykinin receptor 2 expressed in CHO cells
ChEMBL 365 5 2 3 4.5 CC(C)CN1[C@H](C)Cc2cc(O)ccc2[C@H]1c1ccc(/C=C/C(=O)O)cc1 10.1021/acsmedchemlett.5b00413
1016 3678 75 None -46 35 Human 4.7 pIC50 = 4.7 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
ChEMBL 371 8 0 2 6.0 CC/C(=C(\c1ccccc1)/c1ccc(cc1)OCCN(C)C)/c1ccccc1 nan
2561 3678 75 None -46 35 Human 4.7 pIC50 = 4.7 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
ChEMBL 371 8 0 2 6.0 CC/C(=C(\c1ccccc1)/c1ccc(cc1)OCCN(C)C)/c1ccccc1 nan
2733526 3678 75 None -46 35 Human 4.7 pIC50 = 4.7 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
ChEMBL 371 8 0 2 6.0 CC/C(=C(\c1ccccc1)/c1ccc(cc1)OCCN(C)C)/c1ccccc1 nan
5384 3678 75 None -46 35 Human 4.7 pIC50 = 4.7 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
ChEMBL 371 8 0 2 6.0 CC/C(=C(\c1ccccc1)/c1ccc(cc1)OCCN(C)C)/c1ccccc1 nan
CHEMBL83 3678 75 None -46 35 Human 4.7 pIC50 = 4.7 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
ChEMBL 371 8 0 2 6.0 CC/C(=C(\c1ccccc1)/c1ccc(cc1)OCCN(C)C)/c1ccccc1 nan
DB00675 3678 75 None -46 35 Human 4.7 pIC50 = 4.7 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
ChEMBL 371 8 0 2 6.0 CC/C(=C(\c1ccccc1)/c1ccc(cc1)OCCN(C)C)/c1ccccc1 nan
72548703 161007 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor after 60 mins by scintillation counting analysisDisplacement of [3H]bradykinin from human recombinant B2 receptor after 60 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 7.7 pIC50 = 7.7 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor after 60 mins by scintillation counting analysisDisplacement of [3H]bradykinin from human recombinant B2 receptor after 60 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
11296704 13698 0 None - 0 Guinea pig 7.7 pIC50 = 7.7 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 647 10 2 6 6.6 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cc1C 10.1021/jm030326t
CHEMBL1195759 13698 0 None - 0 Guinea pig 7.7 pIC50 = 7.7 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 647 10 2 6 6.6 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cc1C 10.1021/jm030326t
CHEMBL3216408 13698 0 None - 0 Guinea pig 7.7 pIC50 = 7.7 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 647 10 2 6 6.6 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cc1C 10.1021/jm030326t
22008929 9643 0 None - 1 Guinea pig 7.7 pIC50 = 7.7 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 597 9 1 5 6.6 COc1c(N(C)C(=O)CNC(=O)/C=C/c2ccc(C(F)(F)F)cc2)ccc(Cl)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
CHEMBL113465 9643 0 None - 1 Guinea pig 7.7 pIC50 = 7.7 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 597 9 1 5 6.6 COc1c(N(C)C(=O)CNC(=O)/C=C/c2ccc(C(F)(F)F)cc2)ccc(Cl)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
44190268 194826 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 435 4 0 5 6.6 Cc1cc(-c2ncsc2Cl)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL563516 194826 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 435 4 0 5 6.6 Cc1cc(-c2ncsc2Cl)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
10579159 118789 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 582 11 2 7 4.3 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(OC)c(COc3cccc4ccc(C)nc34)c2OC)cc1 10.1021/jm980330i
CHEMBL344021 118789 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 582 11 2 7 4.3 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(OC)c(COc3cccc4ccc(C)nc34)c2OC)cc1 10.1021/jm980330i
10791325 44494 0 None - 0 Guinea pig 5.7 pIC50 = 5.7 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 491 5 0 5 4.7 Cc1nc2c(OCc3c(Cl)ccc(N(C)S(C)(=O)=O)c3Cl)cccn2c1Br 10.1021/jm970591c
CHEMBL152158 44494 0 None - 0 Guinea pig 5.7 pIC50 = 5.7 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 491 5 0 5 4.7 Cc1nc2c(OCc3c(Cl)ccc(N(C)S(C)(=O)=O)c3Cl)cccn2c1Br 10.1021/jm970591c
10841393 13157 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 607 10 2 6 5.2 CCc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc2n1C 10.1021/jm030159x
CHEMBL1191700 13157 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 607 10 2 6 5.2 CCc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc2n1C 10.1021/jm030159x
CHEMBL542836 13157 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 607 10 2 6 5.2 CCc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc2n1C 10.1021/jm030159x
10841393 13157 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 607 10 2 6 5.2 CCc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc2n1C 10.1021/jm980300f
CHEMBL1191700 13157 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 607 10 2 6 5.2 CCc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc2n1C 10.1021/jm980300f
CHEMBL542836 13157 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 607 10 2 6 5.2 CCc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc2n1C 10.1021/jm980300f
10792967 78103 0 None - 0 Guinea pig 6.7 pIC50 = 6.7 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 559 9 2 4 6.6 CNC(=O)c1ccc(/C=C/C(=O)NC/C=C/c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980330i
CHEMBL2111974 78103 0 None - 0 Guinea pig 6.7 pIC50 = 6.7 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 559 9 2 4 6.6 CNC(=O)c1ccc(/C=C/C(=O)NC/C=C/c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980330i
10507708 161262 0 None - 0 Guinea pig 7.6 pIC50 = 7.6 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 593 9 2 5 6.1 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(C)c(C)oc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL41446 161262 0 None - 0 Guinea pig 7.6 pIC50 = 7.6 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 593 9 2 5 6.1 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(C)c(C)oc34)c2Cl)cc1 10.1021/jm980300f
10507708 161262 0 None - 0 Guinea pig 7.6 pIC50 = 7.6 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 593 9 2 5 6.1 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(C)c(C)oc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL41446 161262 0 None - 0 Guinea pig 7.6 pIC50 = 7.6 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 593 9 2 5 6.1 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(C)c(C)oc34)c2Cl)cc1 10.1021/jm030159x
9851817 9574 0 None - 1 Guinea pig 7.6 pIC50 = 7.6 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 607 8 1 5 7.3 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(F)(F)F)cc4)c3Cl)cccc2s1 10.1016/s0960-894x(98)00736-7
CHEMBL112991 9574 0 None - 1 Guinea pig 7.6 pIC50 = 7.6 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 607 8 1 5 7.3 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(F)(F)F)cc4)c3Cl)cccc2s1 10.1016/s0960-894x(98)00736-7
10762703 46976 0 None - 0 Guinea pig 6.6 pIC50 = 6.6 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 384 3 0 3 5.3 Cc1nc2c(OCc3c(Cl)cccc3Cl)cccn2c1Br 10.1021/jm970591c
CHEMBL154386 46976 0 None - 0 Guinea pig 6.6 pIC50 = 6.6 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 384 3 0 3 5.3 Cc1nc2c(OCc3c(Cl)cccc3Cl)cccn2c1Br 10.1021/jm970591c
44323787 12891 0 None - 0 Guinea pig 5.6 pIC50 = 5.6 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 659 10 2 6 6.2 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL1189812 12891 0 None - 0 Guinea pig 5.6 pIC50 = 5.6 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 659 10 2 6 6.2 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL3215529 12891 0 None - 0 Guinea pig 5.6 pIC50 = 5.6 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 659 10 2 6 6.2 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
11468071 12912 0 None - 0 Guinea pig 5.6 pIC50 = 5.6 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 676 13 3 7 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(NCCN(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL1189943 12912 0 None - 0 Guinea pig 5.6 pIC50 = 5.6 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 676 13 3 7 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(NCCN(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL539800 12912 0 None - 0 Guinea pig 5.6 pIC50 = 5.6 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 676 13 3 7 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(NCCN(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
10555061 116452 0 None - 0 Human 6.6 pIC50 = 6.6 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 568 10 1 5 6.0 CCCCCC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm980214f
CHEMBL338682 116452 0 None - 0 Human 6.6 pIC50 = 6.6 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 568 10 1 5 6.0 CCCCCC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm980214f
11411594 12784 0 None - 0 Guinea pig 6.6 pIC50 = 6.6 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 736 11 2 7 7.9 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1189023 12784 0 None - 0 Guinea pig 6.6 pIC50 = 6.6 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 736 11 2 7 7.9 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL537927 12784 0 None - 0 Guinea pig 6.6 pIC50 = 6.6 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 736 11 2 7 7.9 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
11239502 13576 0 None - 0 Guinea pig 7.6 pIC50 = 7.6 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 674 11 2 6 6.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OC5CCCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030468n
CHEMBL1194911 13576 0 None - 0 Guinea pig 7.6 pIC50 = 7.6 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 674 11 2 6 6.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OC5CCCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030468n
CHEMBL553530 13576 0 None - 0 Guinea pig 7.6 pIC50 = 7.6 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 674 11 2 6 6.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OC5CCCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030468n
44340760 110006 0 None - 1 Guinea pig 7.6 pIC50 = 7.6 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 523 10 3 6 3.8 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)NCCCC(=O)O)c3C#N)c2n1 10.1016/s0960-894x(98)00736-7
CHEMBL324950 110006 0 None - 1 Guinea pig 7.6 pIC50 = 7.6 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 523 10 3 6 3.8 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)NCCCC(=O)O)c3C#N)c2n1 10.1016/s0960-894x(98)00736-7
11468071 12912 0 None - 0 Human 5.6 pIC50 = 5.6 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 676 13 3 7 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(NCCN(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL1189943 12912 0 None - 0 Human 5.6 pIC50 = 5.6 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 676 13 3 7 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(NCCN(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL539800 12912 0 None - 0 Human 5.6 pIC50 = 5.6 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 676 13 3 7 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(NCCN(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
11181524 206271 0 None - 0 Guinea pig 7.6 pIC50 = 7.6 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 686 12 2 8 6.1 COc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(C)=O)nc4)c3Cl)cccc2n1Cc1ccccc1 10.1021/jm030468n
CHEMBL97393 206271 0 None - 0 Guinea pig 7.6 pIC50 = 7.6 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 686 12 2 8 6.1 COc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(C)=O)nc4)c3Cl)cccc2n1Cc1ccccc1 10.1021/jm030468n
10816636 13640 0 None - 0 Guinea pig 7.6 pIC50 = 7.6 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 555 8 2 5 5.0 CCCNC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
CHEMBL1195365 13640 0 None - 0 Guinea pig 7.6 pIC50 = 7.6 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 555 8 2 5 5.0 CCCNC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
CHEMBL554412 13640 0 None - 0 Guinea pig 7.6 pIC50 = 7.6 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 555 8 2 5 5.0 CCCNC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
10841531 20343 0 None - 0 Human 7.6 pIC50 = 7.6 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 617 9 1 6 5.7 Cc1cnc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL130782 20343 0 None - 0 Human 7.6 pIC50 = 7.6 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 617 9 1 6 5.7 Cc1cnc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)c2n1 10.1021/jm980300f
44214279 9609 0 None - 1 Guinea pig 7.6 pIC50 = 7.6 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 489 8 1 5 5.3 C=C/C=C/C(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccc3sc(C)nc23)c1Cl 10.1016/s0960-894x(98)00736-7
CHEMBL113222 9609 0 None - 1 Guinea pig 7.6 pIC50 = 7.6 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 489 8 1 5 5.3 C=C/C=C/C(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccc3sc(C)nc23)c1Cl 10.1016/s0960-894x(98)00736-7
10675163 13116 0 None - 0 Human 6.6 pIC50 = 6.6 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 603 7 2 5 6.4 Cc1ccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
CHEMBL1191383 13116 0 None - 0 Human 6.6 pIC50 = 6.6 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 603 7 2 5 6.4 Cc1ccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
CHEMBL542472 13116 0 None - 0 Human 6.6 pIC50 = 6.6 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 603 7 2 5 6.4 Cc1ccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
10507708 161262 0 None - 0 Human 6.6 pIC50 = 6.6 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 593 9 2 5 6.1 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(C)c(C)oc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL41446 161262 0 None - 0 Human 6.6 pIC50 = 6.6 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 593 9 2 5 6.1 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(C)c(C)oc34)c2Cl)cc1 10.1021/jm030159x
10507708 161262 0 None - 0 Human 6.6 pIC50 = 6.6 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 593 9 2 5 6.1 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(C)c(C)oc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL41446 161262 0 None - 0 Human 6.6 pIC50 = 6.6 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 593 9 2 5 6.1 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(C)c(C)oc34)c2Cl)cc1 10.1021/jm980300f
11422667 12861 0 None - 0 Guinea pig 7.6 pIC50 = 7.6 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 710 12 2 7 6.6 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NCc5ccccn5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1189575 12861 0 None - 0 Guinea pig 7.6 pIC50 = 7.6 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 710 12 2 7 6.6 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NCc5ccccn5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL539023 12861 0 None - 0 Guinea pig 7.6 pIC50 = 7.6 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 710 12 2 7 6.6 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NCc5ccccn5)cc4)c3Cl)c2n1 10.1021/jm030326t
11456756 13682 0 None - 0 Guinea pig 7.6 pIC50 = 7.6 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 699 10 1 6 7.3 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1195624 13682 0 None - 0 Guinea pig 7.6 pIC50 = 7.6 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 699 10 1 6 7.3 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL3216405 13682 0 None - 0 Guinea pig 7.6 pIC50 = 7.6 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 699 10 1 6 7.3 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)c2n1 10.1021/jm030326t
10555202 116239 0 None - 0 Guinea pig 6.6 pIC50 = 6.6 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 577 9 3 6 5.6 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)Nc2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cn1 10.1021/jm980330i
CHEMBL337555 116239 0 None - 0 Guinea pig 6.6 pIC50 = 6.6 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 577 9 3 6 5.6 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)Nc2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cn1 10.1021/jm980330i
11468276 13387 0 None - 0 Guinea pig 7.5 pIC50 = 7.5 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 738 11 2 8 6.7 Cc1cc(N2CCOCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1193590 13387 0 None - 0 Guinea pig 7.5 pIC50 = 7.5 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 738 11 2 8 6.7 Cc1cc(N2CCOCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL545021 13387 0 None - 0 Guinea pig 7.5 pIC50 = 7.5 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 738 11 2 8 6.7 Cc1cc(N2CCOCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
15388873 114220 0 None - 1 Guinea pig 7.5 pIC50 = 7.5 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 529 8 1 6 5.9 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccco4)c3Cl)cccc2s1 10.1016/s0960-894x(98)00736-7
CHEMBL333832 114220 0 None - 1 Guinea pig 7.5 pIC50 = 7.5 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 529 8 1 6 5.9 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccco4)c3Cl)cccc2s1 10.1016/s0960-894x(98)00736-7
11801594 99953 0 None - 0 Human 5.5 pIC50 = 5.5 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4nc(C)cnc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL290431 99953 0 None - 0 Human 5.5 pIC50 = 5.5 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4nc(C)cnc34)c2Cl)cc1 10.1021/jm030159x
11801594 99953 0 None - 0 Human 5.5 pIC50 = 5.5 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4nc(C)cnc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL290431 99953 0 None - 0 Human 5.5 pIC50 = 5.5 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4nc(C)cnc34)c2Cl)cc1 10.1021/jm980300f
10009762 12805 0 None - 0 Guinea pig 8.5 pIC50 = 8.5 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 678 10 1 7 7.4 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL1189175 12805 0 None - 0 Guinea pig 8.5 pIC50 = 8.5 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 678 10 1 7 7.4 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL3217072 12805 0 None - 0 Guinea pig 8.5 pIC50 = 8.5 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 678 10 1 7 7.4 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
10579332 13627 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ncc(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL1195281 13627 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ncc(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL554206 13627 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ncc(C)nc34)c2Cl)cc1 10.1021/jm980300f
11239019 13361 0 None - 0 Guinea pig 8.5 pIC50 = 8.5 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 626 10 2 5 6.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c(-c5ccccc5)cc(C)nc34)c2C)cc1 10.1021/jm030159x
CHEMBL1193332 13361 0 None - 0 Guinea pig 8.5 pIC50 = 8.5 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 626 10 2 5 6.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c(-c5ccccc5)cc(C)nc34)c2C)cc1 10.1021/jm030159x
CHEMBL544720 13361 0 None - 0 Guinea pig 8.5 pIC50 = 8.5 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 626 10 2 5 6.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c(-c5ccccc5)cc(C)nc34)c2C)cc1 10.1021/jm030159x
11399463 13331 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 633 10 2 6 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL1193123 13331 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 633 10 2 6 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL3143949 13331 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 633 10 2 6 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030159x
11399463 13331 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 633 10 2 6 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL1193123 13331 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 633 10 2 6 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL3143949 13331 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 633 10 2 6 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
44361029 13240 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 714 11 1 7 5.3 Cc1ccc2cccc(OCc3c(N4CCCC4=O)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3N3CCCC3=O)c2n1 10.1021/jm980330i
CHEMBL1192448 13240 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 714 11 1 7 5.3 Cc1ccc2cccc(OCc3c(N4CCCC4=O)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3N3CCCC3=O)c2n1 10.1021/jm980330i
CHEMBL543685 13240 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 714 11 1 7 5.3 Cc1ccc2cccc(OCc3c(N4CCCC4=O)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3N3CCCC3=O)c2n1 10.1021/jm980330i
10555818 13558 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 616 9 1 5 6.3 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL1194778 13558 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 616 9 1 5 6.3 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL553293 13558 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 616 9 1 5 6.3 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)c2n1 10.1021/jm980300f
10746877 13691 0 None - 0 Guinea pig 8.5 pIC50 = 8.5 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 654 10 2 7 6.3 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)nc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL1195721 13691 0 None - 0 Guinea pig 8.5 pIC50 = 8.5 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 654 10 2 7 6.3 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)nc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL555202 13691 0 None - 0 Guinea pig 8.5 pIC50 = 8.5 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 654 10 2 7 6.3 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)nc4)c3Cl)c2n1 10.1021/jm980300f
667 1934 32 None -1 6 Human 8.5 pIC50 = 8.5 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL None None None None 10.1021/jm980300f
71364 1934 32 None -1 6 Human 8.5 pIC50 = 8.5 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL None None None None 10.1021/jm980300f
CHEMBL2028850 1934 32 None -1 6 Human 8.5 pIC50 = 8.5 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL None None None None 10.1021/jm980300f
DB06196 1934 32 None -1 6 Human 8.5 pIC50 = 8.5 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL None None None None 10.1021/jm980300f
667 1934 32 None -1 6 Human 8.5 pIC50 = 8.5 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL None None None None 10.1021/jm980214f
71364 1934 32 None -1 6 Human 8.5 pIC50 = 8.5 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL None None None None 10.1021/jm980214f
CHEMBL2028850 1934 32 None -1 6 Human 8.5 pIC50 = 8.5 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL None None None None 10.1021/jm980214f
DB06196 1934 32 None -1 6 Human 8.5 pIC50 = 8.5 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL None None None None 10.1021/jm980214f
9874617 13180 0 None - 0 Guinea pig 8.5 pIC50 = 8.5 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 670 10 1 7 6.1 Cc1cc(-n2cccn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL1191908 13180 0 None - 0 Guinea pig 8.5 pIC50 = 8.5 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 670 10 1 7 6.1 Cc1cc(-n2cccn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL543070 13180 0 None - 0 Guinea pig 8.5 pIC50 = 8.5 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 670 10 1 7 6.1 Cc1cc(-n2cccn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
10674242 23938 0 None - 0 Guinea pig 8.5 pIC50 = 8.5 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 551 9 2 6 4.3 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ncc(C)nc34)c2C)cc1 10.1021/jm980300f
CHEMBL133913 23938 0 None - 0 Guinea pig 8.5 pIC50 = 8.5 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 551 9 2 6 4.3 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ncc(C)nc34)c2C)cc1 10.1021/jm980300f
11169752 111903 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 654 13 2 9 4.7 COCCn1c(OC)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(C)=O)nc4)c3Cl)cccc21 10.1021/jm030468n
CHEMBL329758 111903 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 654 13 2 9 4.7 COCCn1c(OC)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(C)=O)nc4)c3Cl)cccc21 10.1021/jm030468n
10652092 12892 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 672 9 1 7 5.2 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)nc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL1189828 12892 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 672 9 1 7 5.2 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)nc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL539550 12892 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 672 9 1 7 5.2 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)nc4)c3Cl)cccn2c1Br 10.1021/jm980214f
11273808 13671 0 None - 0 Guinea pig 8.4 pIC50 = 8.4 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 656 10 2 7 5.8 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(-n5ccnc5)cc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL1195573 13671 0 None - 0 Guinea pig 8.4 pIC50 = 8.4 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 656 10 2 7 5.8 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(-n5ccnc5)cc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL3215979 13671 0 None - 0 Guinea pig 8.4 pIC50 = 8.4 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 656 10 2 7 5.8 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(-n5ccnc5)cc(C)nc34)c2Cl)cc1 10.1021/jm030159x
11491069 12792 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 691 12 2 7 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OCC(=O)N(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030468n
CHEMBL1189082 12792 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 691 12 2 7 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OCC(=O)N(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030468n
CHEMBL538020 12792 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 691 12 2 7 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OCC(=O)N(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030468n
10841637 13791 0 None - 0 Guinea pig 8.4 pIC50 = 8.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 623 7 2 5 6.7 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(Cl)c4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL1196403 13791 0 None - 0 Guinea pig 8.4 pIC50 = 8.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 623 7 2 5 6.7 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(Cl)c4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL556816 13791 0 None - 0 Guinea pig 8.4 pIC50 = 8.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 623 7 2 5 6.7 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(Cl)c4)c3Cl)cccn2c1Br 10.1021/jm980214f
10580536 12816 0 None - 0 Guinea pig 8.4 pIC50 = 8.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 693 10 2 7 5.5 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NS(C)(=O)=O)cc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL1189218 12816 0 None - 0 Guinea pig 8.4 pIC50 = 8.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 693 10 2 7 5.5 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NS(C)(=O)=O)cc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL538281 12816 0 None - 0 Guinea pig 8.4 pIC50 = 8.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 693 10 2 7 5.5 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NS(C)(=O)=O)cc4)c3Cl)cccn2c1Br 10.1021/jm980214f
10603710 13535 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 604 9 1 5 5.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL1194615 13535 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 604 9 1 5 5.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL552986 13535 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 604 9 1 5 5.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
44360617 13351 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 678 11 1 7 4.0 Cc1ccc2cccc(OCc3c(C(=O)N(C)C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3C(=O)N(C)C)c2n1 10.1021/jm980330i
CHEMBL1193249 13351 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 678 11 1 7 4.0 Cc1ccc2cccc(OCc3c(C(=O)N(C)C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3C(=O)N(C)C)c2n1 10.1021/jm980330i
CHEMBL544622 13351 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 678 11 1 7 4.0 Cc1ccc2cccc(OCc3c(C(=O)N(C)C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3C(=O)N(C)C)c2n1 10.1021/jm980330i
10603710 13535 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 604 9 1 5 5.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL1194615 13535 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 604 9 1 5 5.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL552986 13535 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 604 9 1 5 5.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm980300f
11491069 12792 0 None - 0 Guinea pig 7.5 pIC50 = 7.5 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 691 12 2 7 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OCC(=O)N(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030468n
CHEMBL1189082 12792 0 None - 0 Guinea pig 7.5 pIC50 = 7.5 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 691 12 2 7 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OCC(=O)N(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030468n
CHEMBL538020 12792 0 None - 0 Guinea pig 7.5 pIC50 = 7.5 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 691 12 2 7 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OCC(=O)N(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030468n
11365972 13517 0 None - 0 Guinea pig 7.5 pIC50 = 7.5 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 687 10 1 6 6.9 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1194477 13517 0 None - 0 Guinea pig 7.5 pIC50 = 7.5 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 687 10 1 6 6.9 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL3216391 13517 0 None - 0 Guinea pig 7.5 pIC50 = 7.5 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 687 10 1 6 6.9 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030326t
10818058 116071 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 653 10 2 6 6.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccccn5)cc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL336574 116071 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 653 10 2 6 6.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccccn5)cc4)c3Cl)c2n1 10.1021/jm980300f
10840241 115956 0 None - 0 Human 5.5 pIC50 = 5.5 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 541 7 2 5 4.6 CCNC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm980214f
CHEMBL336116 115956 0 None - 0 Human 5.5 pIC50 = 5.5 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 541 7 2 5 4.6 CCNC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm980214f
44191226 193622 0 None - 0 Human 6.5 pIC50 = 6.5 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 384 4 1 4 5.2 Cc1cc(-c2ccn[nH]2)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL551435 193622 0 None - 0 Human 6.5 pIC50 = 6.5 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 384 4 1 4 5.2 Cc1cc(-c2ccn[nH]2)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
10756101 45806 4 None - 0 Guinea pig 4.5 pIC50 = 4.5 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 292 3 0 3 4.2 Clc1cccc(Cl)c1COc1cccn2ccnc12 10.1021/jm970591c
CHEMBL153344 45806 4 None - 0 Guinea pig 4.5 pIC50 = 4.5 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 292 3 0 3 4.2 Clc1cccc(Cl)c1COc1cccn2ccnc12 10.1021/jm970591c
44369201 120930 0 None - 0 Guinea pig 4.5 pIC50 = 4.5 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 381 5 0 4 5.8 CCn1c(C)cc(C#N)c1-c1ccc(COc2cc(C)nc3ccccc23)cc1 10.1021/jm970591c
CHEMBL358232 120930 0 None - 0 Guinea pig 4.5 pIC50 = 4.5 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 381 5 0 4 5.8 CCn1c(C)cc(C#N)c1-c1ccc(COc2cc(C)nc3ccccc23)cc1 10.1021/jm970591c
44191225 194712 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 384 4 0 5 5.0 Cc1cc(-n2cccn2)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL562747 194712 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 384 4 0 5 5.0 Cc1cc(-n2cccn2)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL2372276 208451 0 None 3 3 Human 7.5 pIC50 = 7.5 Binding
Displacement of radiolabeled NPC 567 from human bradykinin B2 receptorDisplacement of radiolabeled NPC 567 from human bradykinin B2 receptor
ChEMBL None None None NC(N)=NCCC[C@H](N)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1CCC[C@H]1C(=O)NCC(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](CO)C(=O)[C@@H]1CCCN1C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@H](CCCN=C(N)N)C(=O)O 10.1021/jm8007618
44341214 109928 0 None - 1 Guinea pig 7.5 pIC50 = 7.5 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 621 12 1 6 6.7 CCCOc1c(N(C)C(=O)CNC(=O)/C=C/c2ccc(C(F)(F)F)cc2)ccc(OC)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
CHEMBL324575 109928 0 None - 1 Guinea pig 7.5 pIC50 = 7.5 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 621 12 1 6 6.7 CCCOc1c(N(C)C(=O)CNC(=O)/C=C/c2ccc(C(F)(F)F)cc2)ccc(OC)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
44190853 194605 4 None - 0 Human 7.5 pIC50 = 7.5 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 435 7 1 6 4.0 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3CCC(N)=O)c2n1 10.1021/jm9002445
CHEMBL562097 194605 4 None - 0 Human 7.5 pIC50 = 7.5 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 435 7 1 6 4.0 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3CCC(N)=O)c2n1 10.1021/jm9002445
11250929 13708 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Displacement of [3H]BK from cloned human B2 bradykinin receptor expressed in CHO cells after 2 hrs by liquid scintillation counterDisplacement of [3H]BK from cloned human B2 bradykinin receptor expressed in CHO cells after 2 hrs by liquid scintillation counter
ChEMBL 634 11 2 6 6.0 CCOc1cc(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc12 10.1021/acs.jmedchem.5b00982
CHEMBL1195824 13708 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Displacement of [3H]BK from cloned human B2 bradykinin receptor expressed in CHO cells after 2 hrs by liquid scintillation counterDisplacement of [3H]BK from cloned human B2 bradykinin receptor expressed in CHO cells after 2 hrs by liquid scintillation counter
ChEMBL 634 11 2 6 6.0 CCOc1cc(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc12 10.1021/acs.jmedchem.5b00982
CHEMBL555403 13708 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Displacement of [3H]BK from cloned human B2 bradykinin receptor expressed in CHO cells after 2 hrs by liquid scintillation counterDisplacement of [3H]BK from cloned human B2 bradykinin receptor expressed in CHO cells after 2 hrs by liquid scintillation counter
ChEMBL 634 11 2 6 6.0 CCOc1cc(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc12 10.1021/acs.jmedchem.5b00982
11250929 13708 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 634 11 2 6 6.0 CCOc1cc(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc12 10.1021/jm030468n
CHEMBL1195824 13708 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 634 11 2 6 6.0 CCOc1cc(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc12 10.1021/jm030468n
CHEMBL555403 13708 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 634 11 2 6 6.0 CCOc1cc(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc12 10.1021/jm030468n
10579723 21102 0 None - 0 Guinea pig 6.5 pIC50 = 6.5 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 617 7 2 6 5.4 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)NC(=O)c4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL131380 21102 0 None - 0 Guinea pig 6.5 pIC50 = 6.5 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 617 7 2 6 5.4 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)NC(=O)c4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
9958759 13345 0 None - 0 Human 6.5 pIC50 = 6.5 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 533 8 1 4 6.2 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccccc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL1193231 13345 0 None - 0 Human 6.5 pIC50 = 6.5 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 533 8 1 4 6.2 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccccc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL544601 13345 0 None - 0 Human 6.5 pIC50 = 6.5 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 533 8 1 4 6.2 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccccc4)c3Cl)c2n1 10.1021/jm980300f
10699094 23043 0 None - 0 Guinea pig 6.5 pIC50 = 6.5 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 619 10 2 6 5.5 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccnc3-n3c(C)ccc3C)c2Cl)cc1 10.1021/jm980300f
CHEMBL133186 23043 0 None - 0 Guinea pig 6.5 pIC50 = 6.5 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 619 10 2 6 5.5 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccnc3-n3c(C)ccc3C)c2Cl)cc1 10.1021/jm980300f
10627456 19935 0 None - 0 Human 6.5 pIC50 = 6.5 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 602 9 1 5 6.0 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)CCc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL130452 19935 0 None - 0 Human 6.5 pIC50 = 6.5 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 602 9 1 5 6.0 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)CCc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
10504612 120604 0 None - 0 Guinea pig 6.5 pIC50 = 6.5 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 470 4 1 4 5.1 CNC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
CHEMBL357530 120604 0 None - 0 Guinea pig 6.5 pIC50 = 6.5 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 470 4 1 4 5.1 CNC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
10699094 23043 0 None - 0 Human 5.5 pIC50 = 5.5 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 619 10 2 6 5.5 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccnc3-n3c(C)ccc3C)c2Cl)cc1 10.1021/jm980300f
CHEMBL133186 23043 0 None - 0 Human 5.5 pIC50 = 5.5 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 619 10 2 6 5.5 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccnc3-n3c(C)ccc3C)c2Cl)cc1 10.1021/jm980300f
44190756 193756 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 463 7 0 6 4.6 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3CCC(=O)N(C)C)c2n1 10.1021/jm9002445
CHEMBL552359 193756 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 463 7 0 6 4.6 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3CCC(=O)N(C)C)c2n1 10.1021/jm9002445
44189790 194957 0 None - 0 Human 5.4 pIC50 = 5.4 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 398 4 1 4 5.5 Cc1cc(-c2cn[nH]c2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL564341 194957 0 None - 0 Human 5.4 pIC50 = 5.4 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 398 4 1 4 5.5 Cc1cc(-c2cn[nH]c2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
44190754 194764 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 497 7 0 7 3.8 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3[S+]([O-])CC(=O)N(C)C)c2n1 10.1021/jm9002445
CHEMBL563068 194764 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 497 7 0 7 3.8 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3[S+]([O-])CC(=O)N(C)C)c2n1 10.1021/jm9002445
11239595 13596 0 None - 0 Guinea pig 7.4 pIC50 = 7.4 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 738 11 2 8 6.7 Cc1cc(N2CCOCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1195041 13596 0 None - 0 Guinea pig 7.4 pIC50 = 7.4 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 738 11 2 8 6.7 Cc1cc(N2CCOCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL553762 13596 0 None - 0 Guinea pig 7.4 pIC50 = 7.4 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 738 11 2 8 6.7 Cc1cc(N2CCOCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
11433935 13080 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 687 10 2 6 7.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCCCCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL1191123 13080 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 687 10 2 6 7.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCCCCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL3215986 13080 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 687 10 2 6 7.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCCCCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
10531338 91261 0 None - 0 Guinea pig 7.4 pIC50 = 7.4 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 582 10 2 7 4.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(N(C)C)n4C)c2C)cc1 10.1021/jm980300f
CHEMBL240875 91261 0 None - 0 Guinea pig 7.4 pIC50 = 7.4 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 582 10 2 7 4.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(N(C)C)n4C)c2C)cc1 10.1021/jm980300f
10531338 91261 0 None - 0 Guinea pig 7.4 pIC50 = 7.4 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 582 10 2 7 4.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(N(C)C)n4C)c2C)cc1 10.1021/jm030159x
CHEMBL240875 91261 0 None - 0 Guinea pig 7.4 pIC50 = 7.4 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 582 10 2 7 4.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(N(C)C)n4C)c2C)cc1 10.1021/jm030159x
10579143 167888 0 None - 0 Guinea pig 6.4 pIC50 = 6.4 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 580 9 2 6 5.2 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4oc(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL43510 167888 0 None - 0 Guinea pig 6.4 pIC50 = 6.4 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 580 9 2 6 5.2 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4oc(C)nc34)c2Cl)cc1 10.1021/jm980300f
10790603 44894 0 None - 0 Guinea pig 6.4 pIC50 = 6.4 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 470 5 1 5 4.2 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CN)c3Cl)cccn2c1Br 10.1021/jm970591c
CHEMBL152542 44894 0 None - 0 Guinea pig 6.4 pIC50 = 6.4 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 470 5 1 5 4.2 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CN)c3Cl)cccn2c1Br 10.1021/jm970591c
10579143 167888 0 None - 0 Guinea pig 6.4 pIC50 = 6.4 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 580 9 2 6 5.2 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4oc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL43510 167888 0 None - 0 Guinea pig 6.4 pIC50 = 6.4 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 580 9 2 6 5.2 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4oc(C)nc34)c2Cl)cc1 10.1021/jm030159x
10555195 13118 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 577 9 1 6 5.1 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)nc4)c3C)c2n1 10.1021/jm980300f
CHEMBL1191388 13118 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 577 9 1 6 5.1 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)nc4)c3C)c2n1 10.1021/jm980300f
CHEMBL542479 13118 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 577 9 1 6 5.1 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)nc4)c3C)c2n1 10.1021/jm980300f
44346506 11319 0 None - 0 Guinea pig 5.4 pIC50 = 5.4 Binding
Compound was evaluated for competitive [3H]bradykinin binding to guinea pig ileum homogenatesCompound was evaluated for competitive [3H]bradykinin binding to guinea pig ileum homogenates
ChEMBL 545 29 0 0 12.9 CCCC[P+](CCCC)(CCCC)CCCCCCCCCC[P+](CCCC)(CCCC)CCCC 10.1016/0960-894X(95)00035-R
CHEMBL1180320 11319 0 None - 0 Guinea pig 5.4 pIC50 = 5.4 Binding
Compound was evaluated for competitive [3H]bradykinin binding to guinea pig ileum homogenatesCompound was evaluated for competitive [3H]bradykinin binding to guinea pig ileum homogenates
ChEMBL 545 29 0 0 12.9 CCCC[P+](CCCC)(CCCC)CCCCCCCCCC[P+](CCCC)(CCCC)CCCC 10.1016/0960-894X(95)00035-R
CHEMBL121851 11319 0 None - 0 Guinea pig 5.4 pIC50 = 5.4 Binding
Compound was evaluated for competitive [3H]bradykinin binding to guinea pig ileum homogenatesCompound was evaluated for competitive [3H]bradykinin binding to guinea pig ileum homogenates
ChEMBL 545 29 0 0 12.9 CCCC[P+](CCCC)(CCCC)CCCCCCCCCC[P+](CCCC)(CCCC)CCCC 10.1016/0960-894X(95)00035-R
44340964 9600 0 None - 1 Guinea pig 6.4 pIC50 = 6.4 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 609 10 1 6 6.7 COc1c(N(C)C(=O)CNC(=O)/C=C/c2ccc(C(F)(F)F)cc2)ccc(SC)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
CHEMBL113176 9600 0 None - 1 Guinea pig 6.4 pIC50 = 6.4 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 609 10 1 6 6.7 COc1c(N(C)C(=O)CNC(=O)/C=C/c2ccc(C(F)(F)F)cc2)ccc(SC)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
44190944 194249 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 539 6 0 7 5.8 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3Cn3cccc(C(F)(F)F)c3=O)c2n1 10.1021/jm9002445
CHEMBL559436 194249 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 539 6 0 7 5.8 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3Cn3cccc(C(F)(F)F)c3=O)c2n1 10.1021/jm9002445
11479294 13697 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 648 10 1 7 5.4 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)nc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1195758 13697 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 648 10 1 7 5.4 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)nc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL3216404 13697 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 648 10 1 7 5.4 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)nc4)c3Cl)c2n1 10.1021/jm030326t
11801083 114736 0 None - 0 Guinea pig 8.4 pIC50 = 8.4 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 565 9 1 6 4.6 Cc1cnc2cccc(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3C)c2n1 10.1021/jm980300f
CHEMBL334753 114736 0 None - 0 Guinea pig 8.4 pIC50 = 8.4 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 565 9 1 6 4.6 Cc1cnc2cccc(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3C)c2n1 10.1021/jm980300f
10604613 12987 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 683 9 1 6 6.2 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL1190420 12987 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 683 9 1 6 6.2 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL540828 12987 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 683 9 1 6 6.2 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)cccn2c1Br 10.1021/jm980214f
11422541 206416 0 None - 0 Guinea pig 8.4 pIC50 = 8.4 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 682 13 2 10 4.6 CCOC(=O)Cn1c(OC)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(C)=O)nc4)c3Cl)cccc21 10.1021/jm030468n
CHEMBL98292 206416 0 None - 0 Guinea pig 8.4 pIC50 = 8.4 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 682 13 2 10 4.6 CCOC(=O)Cn1c(OC)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(C)=O)nc4)c3Cl)cccc21 10.1021/jm030468n
10508305 13483 0 None - 0 Guinea pig 8.4 pIC50 = 8.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 634 8 2 7 6.0 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc([N+](=O)[O-])c4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL1194233 13483 0 None - 0 Guinea pig 8.4 pIC50 = 8.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 634 8 2 7 6.0 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc([N+](=O)[O-])c4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL545765 13483 0 None - 0 Guinea pig 8.4 pIC50 = 8.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 634 8 2 7 6.0 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc([N+](=O)[O-])c4)c3Cl)cccn2c1Br 10.1021/jm980214f
18923274 19610 0 None - 0 Guinea pig 8.4 pIC50 = 8.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 604 9 1 6 5.4 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)COc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL130196 19610 0 None - 0 Guinea pig 8.4 pIC50 = 8.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 604 9 1 6 5.4 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)COc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
10675243 96319 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 610 10 2 8 4.6 COc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(C)=O)nc4)c3Cl)cccc2n1C 10.1021/jm030468n
CHEMBL264751 96319 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 610 10 2 8 4.6 COc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(C)=O)nc4)c3Cl)cccc2n1C 10.1021/jm030468n
11490605 13624 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 634 10 2 7 5.6 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cn1 10.1021/jm030326t
CHEMBL1195242 13624 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 634 10 2 7 5.6 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cn1 10.1021/jm030326t
CHEMBL554127 13624 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 634 10 2 7 5.6 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cn1 10.1021/jm030326t
10675243 96319 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 610 10 2 8 4.6 COc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(C)=O)nc4)c3Cl)cccc2n1C 10.1021/jm980300f
CHEMBL264751 96319 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 610 10 2 8 4.6 COc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(C)=O)nc4)c3Cl)cccc2n1C 10.1021/jm980300f
11445288 13748 0 None - 0 Guinea pig 8.4 pIC50 = 8.4 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 670 10 1 7 6.1 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL1196072 13748 0 None - 0 Guinea pig 8.4 pIC50 = 8.4 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 670 10 1 7 6.1 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL3217085 13748 0 None - 0 Guinea pig 8.4 pIC50 = 8.4 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 670 10 1 7 6.1 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
18704946 13044 0 None - 0 Guinea pig 8.4 pIC50 = 8.4 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 657 10 2 8 5.2 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(-n5cncn5)cc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL1190879 13044 0 None - 0 Guinea pig 8.4 pIC50 = 8.4 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 657 10 2 8 5.2 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(-n5cncn5)cc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL3217081 13044 0 None - 0 Guinea pig 8.4 pIC50 = 8.4 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 657 10 2 8 5.2 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(-n5cncn5)cc(C)nc34)c2Cl)cc1 10.1021/jm030159x
11169752 111903 0 None - 0 Guinea pig 8.3 pIC50 = 8.3 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 654 13 2 9 4.7 COCCn1c(OC)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(C)=O)nc4)c3Cl)cccc21 10.1021/jm030468n
CHEMBL329758 111903 0 None - 0 Guinea pig 8.3 pIC50 = 8.3 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 654 13 2 9 4.7 COCCn1c(OC)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(C)=O)nc4)c3Cl)cccc21 10.1021/jm030468n
44360879 12847 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 637 11 4 8 2.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C(=O)NC)c(COc3cccc4ccc(C)nc34)c2C(=O)NC)cn1 10.1021/jm980330i
CHEMBL1189464 12847 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 637 11 4 8 2.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C(=O)NC)c(COc3cccc4ccc(C)nc34)c2C(=O)NC)cn1 10.1021/jm980330i
CHEMBL538784 12847 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 637 11 4 8 2.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C(=O)NC)c(COc3cccc4ccc(C)nc34)c2C(=O)NC)cn1 10.1021/jm980330i
10531497 13087 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cn1 10.1021/jm980300f
CHEMBL1191172 13087 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cn1 10.1021/jm980300f
CHEMBL542232 13087 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cn1 10.1021/jm980300f
10580536 12816 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 693 10 2 7 5.5 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NS(C)(=O)=O)cc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL1189218 12816 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 693 10 2 7 5.5 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NS(C)(=O)=O)cc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL538281 12816 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 693 10 2 7 5.5 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NS(C)(=O)=O)cc4)c3Cl)cccn2c1Br 10.1021/jm980214f
10745254 35086 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 550 9 2 5 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm030159x
CHEMBL143697 35086 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 550 9 2 5 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm030159x
CHEMBL543781 35086 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 550 9 2 5 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm030159x
11296704 13698 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 647 10 2 6 6.6 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cc1C 10.1021/jm030326t
CHEMBL1195759 13698 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 647 10 2 6 6.6 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cc1C 10.1021/jm030326t
CHEMBL3216408 13698 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 647 10 2 6 6.6 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cc1C 10.1021/jm030326t
10745254 35086 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 550 9 2 5 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm980330i
CHEMBL143697 35086 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 550 9 2 5 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm980330i
CHEMBL543781 35086 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 550 9 2 5 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm980330i
10745254 35086 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 550 9 2 5 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm980300f
CHEMBL143697 35086 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 550 9 2 5 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm980300f
CHEMBL543781 35086 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 550 9 2 5 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm980300f
11193509 13610 0 None - 0 Guinea pig 7.4 pIC50 = 7.4 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 750 12 2 7 7.5 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NCc5ccccn5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1195125 13610 0 None - 0 Guinea pig 7.4 pIC50 = 7.4 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 750 12 2 7 7.5 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NCc5ccccn5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL553897 13610 0 None - 0 Guinea pig 7.4 pIC50 = 7.4 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 750 12 2 7 7.5 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NCc5ccccn5)cc4)c3Cl)c2n1 10.1021/jm030326t
11331301 13161 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 663 13 3 7 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(NCCOC)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL1191763 13161 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 663 13 3 7 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(NCCOC)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL3215537 13161 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 663 13 3 7 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(NCCOC)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
44375675 56197 0 None - 0 Rat 6.4 pIC50 = 6.4 Binding
In vitro binding affinity against Bradykinin receptor B2 in rat NG 108-15 neuroblastoma-glioma hybrid cell membranes using [3H]BK binding assayIn vitro binding affinity against Bradykinin receptor B2 in rat NG 108-15 neuroblastoma-glioma hybrid cell membranes using [3H]BK binding assay
ChEMBL 605 12 4 7 4.9 O=C(O)CN(Cc1ccccc1)S(=O)(=O)c1ccc(N/N=C(/S)NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1016/s0960-894x(01)00044-0
CHEMBL163506 56197 0 None - 0 Rat 6.4 pIC50 = 6.4 Binding
In vitro binding affinity against Bradykinin receptor B2 in rat NG 108-15 neuroblastoma-glioma hybrid cell membranes using [3H]BK binding assayIn vitro binding affinity against Bradykinin receptor B2 in rat NG 108-15 neuroblastoma-glioma hybrid cell membranes using [3H]BK binding assay
ChEMBL 605 12 4 7 4.9 O=C(O)CN(Cc1ccccc1)S(=O)(=O)c1ccc(N/N=C(/S)NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1016/s0960-894x(01)00044-0
10789357 47294 0 None - 0 Guinea pig 6.4 pIC50 = 6.4 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 441 5 0 4 5.7 CCN(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
CHEMBL154633 47294 0 None - 0 Guinea pig 6.4 pIC50 = 6.4 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 441 5 0 4 5.7 CCN(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
10601892 46752 0 None - 0 Human 5.4 pIC50 = 5.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 512 6 1 5 4.4 CC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm980214f
CHEMBL154188 46752 0 None - 0 Human 5.4 pIC50 = 5.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 512 6 1 5 4.4 CC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm980214f
CHEMBL558018 46752 0 None - 0 Human 5.4 pIC50 = 5.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 512 6 1 5 4.4 CC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm980214f
11796916 49695 0 None - 0 Guinea pig 7.4 pIC50 = 7.4 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 429 4 0 5 5.2 Cc1nc2c(OCc3c(Cl)ccc([N+](=O)[O-])c3Cl)cccn2c1Br 10.1021/jm970591c
CHEMBL156899 49695 0 None - 0 Guinea pig 7.4 pIC50 = 7.4 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 429 4 0 5 5.2 Cc1nc2c(OCc3c(Cl)ccc([N+](=O)[O-])c3Cl)cccn2c1Br 10.1021/jm970591c
44190165 194279 0 None - 0 Human 6.4 pIC50 = 6.4 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 401 4 0 5 5.9 Cc1cc(-c2nccs2)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL559645 194279 0 None - 0 Human 6.4 pIC50 = 6.4 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 401 4 0 5 5.9 Cc1cc(-c2nccs2)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
11799290 49640 0 None - 0 Guinea pig 6.4 pIC50 = 6.4 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 489 4 0 4 5.9 CC(=O)N(C)c1c(Cl)cc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
CHEMBL156847 49640 0 None - 0 Guinea pig 6.4 pIC50 = 6.4 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 489 4 0 4 5.9 CC(=O)N(C)c1c(Cl)cc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
10555202 116239 0 None - 0 Human 5.4 pIC50 = 5.4 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 577 9 3 6 5.6 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)Nc2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cn1 10.1021/jm980330i
CHEMBL337555 116239 0 None - 0 Human 5.4 pIC50 = 5.4 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 577 9 3 6 5.6 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)Nc2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cn1 10.1021/jm980330i
9916589 99761 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 593 9 2 6 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c3nc(C)n4C)c2Cl)cc1 10.1021/jm980300f
CHEMBL288603 99761 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 593 9 2 6 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c3nc(C)n4C)c2Cl)cc1 10.1021/jm980300f
11377448 12929 0 None - 0 Guinea pig 7.4 pIC50 = 7.4 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 689 10 1 7 5.8 Cc1cc(N2CCOCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1190058 12929 0 None - 0 Guinea pig 7.4 pIC50 = 7.4 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 689 10 1 7 5.8 Cc1cc(N2CCOCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL3216622 12929 0 None - 0 Guinea pig 7.4 pIC50 = 7.4 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 689 10 1 7 5.8 Cc1cc(N2CCOCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030326t
44190361 193125 0 None - 0 Human 6.4 pIC50 = 6.4 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 399 4 0 5 5.8 Cc1cc(-c2conc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL538865 193125 0 None - 0 Human 6.4 pIC50 = 6.4 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 399 4 0 5 5.8 Cc1cc(-c2conc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
11801594 99953 0 None - 0 Human 5.4 pIC50 = 5.4 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4nc(C)cnc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL290431 99953 0 None - 0 Human 5.4 pIC50 = 5.4 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4nc(C)cnc34)c2Cl)cc1 10.1021/jm980300f
10531744 115830 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 605 9 1 6 5.3 Cc1cnc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL335946 115830 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 605 9 1 6 5.3 Cc1cnc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm980300f
44191221 194553 0 None - 0 Human 5.4 pIC50 = 5.4 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 398 4 0 5 5.2 Cc1cc(-c2cncn2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL561701 194553 0 None - 0 Human 5.4 pIC50 = 5.4 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 398 4 0 5 5.2 Cc1cc(-c2cncn2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
10852230 49335 0 None - 0 Guinea pig 5.4 pIC50 = 5.4 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 306 3 0 3 4.5 Cc1cn2cccc(OCc3c(Cl)cccc3Cl)c2n1 10.1021/jm970591c
CHEMBL156606 49335 0 None - 0 Guinea pig 5.4 pIC50 = 5.4 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 306 3 0 3 4.5 Cc1cn2cccc(OCc3c(Cl)cccc3Cl)c2n1 10.1021/jm970591c
10792291 13767 0 None - 0 Guinea pig 7.3 pIC50 = 7.3 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 527 6 2 5 4.2 CNC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
CHEMBL1196218 13767 0 None - 0 Guinea pig 7.3 pIC50 = 7.3 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 527 6 2 5 4.2 CNC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
CHEMBL556176 13767 0 None - 0 Guinea pig 7.3 pIC50 = 7.3 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 527 6 2 5 4.2 CNC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
10769517 23238 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 577 9 1 6 5.1 Cc1cnc2cccc(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3C)c2n1 10.1021/jm980300f
CHEMBL133339 23238 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 577 9 1 6 5.1 Cc1cnc2cccc(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3C)c2n1 10.1021/jm980300f
44214619 110103 0 None - 1 Guinea pig 7.3 pIC50 = 7.3 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 553 13 1 8 4.7 COC(=O)CCCCC(=O)NCC(=O)N(C)c1ccc(OC)c(COc2cccc3ccc(C)nc23)c1SC 10.1016/s0960-894x(98)00736-7
CHEMBL325601 110103 0 None - 1 Guinea pig 7.3 pIC50 = 7.3 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 553 13 1 8 4.7 COC(=O)CCCCC(=O)NCC(=O)N(C)c1ccc(OC)c(COc2cccc3ccc(C)nc23)c1SC 10.1016/s0960-894x(98)00736-7
44190751 193665 0 None - 0 Human 6.3 pIC50 = 6.3 Binding
Displacement of [3H]bradykinin from wild-type B2 receptorDisplacement of [3H]bradykinin from wild-type B2 receptor
ChEMBL 479 6 0 8 6.2 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3Sc3nccs3)c2n1 10.1021/jm9002445
CHEMBL551758 193665 0 None - 0 Human 6.3 pIC50 = 6.3 Binding
Displacement of [3H]bradykinin from wild-type B2 receptorDisplacement of [3H]bradykinin from wild-type B2 receptor
ChEMBL 479 6 0 8 6.2 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3Sc3nccs3)c2n1 10.1021/jm9002445
10721082 13169 0 None - 0 Human 6.3 pIC50 = 6.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 534 8 1 5 5.6 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4cccnc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL1191809 13169 0 None - 0 Human 6.3 pIC50 = 6.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 534 8 1 5 5.6 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4cccnc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL542958 13169 0 None - 0 Human 6.3 pIC50 = 6.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 534 8 1 5 5.6 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4cccnc4)c3Cl)c2n1 10.1021/jm980300f
10530740 165029 0 None - 0 Guinea pig 7.3 pIC50 = 7.3 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 552 9 2 7 4.3 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ncc(C)nc34)c2C)cn1 10.1021/jm980300f
CHEMBL424268 165029 0 None - 0 Guinea pig 7.3 pIC50 = 7.3 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 552 9 2 7 4.3 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ncc(C)nc34)c2C)cn1 10.1021/jm980300f
10675204 168204 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 607 10 2 6 5.4 CCn1c(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc21 10.1021/jm030159x
CHEMBL43746 168204 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 607 10 2 6 5.4 CCn1c(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc21 10.1021/jm030159x
10675204 168204 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 607 10 2 6 5.4 CCn1c(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc21 10.1021/jm980300f
CHEMBL43746 168204 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 607 10 2 6 5.4 CCn1c(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc21 10.1021/jm980300f
10603884 19922 0 None - 0 Human 6.3 pIC50 = 6.3 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 616 10 1 5 6.4 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)CCCc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL130438 19922 0 None - 0 Human 6.3 pIC50 = 6.3 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 616 10 1 5 6.4 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)CCCc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
11331301 13161 0 None - 0 Guinea pig 7.3 pIC50 = 7.3 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 663 13 3 7 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(NCCOC)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL1191763 13161 0 None - 0 Guinea pig 7.3 pIC50 = 7.3 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 663 13 3 7 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(NCCOC)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL3215537 13161 0 None - 0 Guinea pig 7.3 pIC50 = 7.3 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 663 13 3 7 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(NCCOC)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
11796407 47496 0 None - 0 Guinea pig 6.3 pIC50 = 6.3 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 418 3 0 3 5.9 Cc1nc2c(OCc3c(Cl)ccc(Cl)c3Cl)cccn2c1Br 10.1021/jm970591c
CHEMBL154823 47496 0 None - 0 Guinea pig 6.3 pIC50 = 6.3 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 418 3 0 3 5.9 Cc1nc2c(OCc3c(Cl)ccc(Cl)c3Cl)cccn2c1Br 10.1021/jm970591c
44190942 194543 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 471 6 0 7 4.8 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3Cn3ccccc3=O)c2n1 10.1021/jm9002445
CHEMBL561634 194543 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 471 6 0 7 4.8 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3Cn3ccccc3=O)c2n1 10.1021/jm9002445
10032884 13339 0 None - 0 Guinea pig 8.3 pIC50 = 8.3 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 696 11 2 7 6.9 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1193185 13339 0 None - 0 Guinea pig 8.3 pIC50 = 8.3 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 696 11 2 7 6.9 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL544549 13339 0 None - 0 Guinea pig 8.3 pIC50 = 8.3 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 696 11 2 7 6.9 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
10626618 33241 0 None - 0 Guinea pig 8.3 pIC50 = 8.3 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 556 9 2 5 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2)cc1 10.1021/jm980330i
CHEMBL142015 33241 0 None - 0 Guinea pig 8.3 pIC50 = 8.3 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 556 9 2 5 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2)cc1 10.1021/jm980330i
10579332 13627 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ncc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL1195281 13627 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ncc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL554206 13627 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ncc(C)nc34)c2Cl)cc1 10.1021/jm030159x
44340859 9933 0 None - 1 Guinea pig 8.3 pIC50 = 8.3 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 599 11 2 8 5.0 COc1ccc(N(C)C(=O)CNC(=O)/C=C/c2ccc(NC(C)=O)nc2)c(SC)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
CHEMBL115163 9933 0 None - 1 Guinea pig 8.3 pIC50 = 8.3 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 599 11 2 8 5.0 COc1ccc(N(C)C(=O)CNC(=O)/C=C/c2ccc(NC(C)=O)nc2)c(SC)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
11801968 13584 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 617 9 1 6 5.7 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)nc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL1194974 13584 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 617 9 1 6 5.7 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)nc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL553614 13584 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 617 9 1 6 5.7 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)nc4)c3Cl)c2n1 10.1021/jm980300f
10579332 13627 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ncc(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL1195281 13627 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ncc(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL554206 13627 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ncc(C)nc34)c2Cl)cc1 10.1021/jm980300f
10793528 13344 0 None - 0 Guinea pig 8.3 pIC50 = 8.3 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 588 8 1 5 5.6 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Cc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL1193230 13344 0 None - 0 Guinea pig 8.3 pIC50 = 8.3 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 588 8 1 5 5.6 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Cc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL544600 13344 0 None - 0 Guinea pig 8.3 pIC50 = 8.3 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 588 8 1 5 5.6 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Cc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
44190581 194260 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 443 7 1 6 4.5 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(C)ccnc3CNC(=O)C(C)C)c2n1 10.1021/jm9002445
CHEMBL559506 194260 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 443 7 1 6 4.5 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(C)ccnc3CNC(=O)C(C)C)c2n1 10.1021/jm9002445
10555061 116452 0 None - 0 Guinea pig 8.3 pIC50 = 8.3 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 568 10 1 5 6.0 CCCCCC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm980214f
CHEMBL338682 116452 0 None - 0 Guinea pig 8.3 pIC50 = 8.3 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 568 10 1 5 6.0 CCCCCC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm980214f
11181406 12814 0 None - 0 Guinea pig 8.3 pIC50 = 8.3 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 663 11 2 7 5.7 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cc1OC 10.1021/jm030326t
CHEMBL1189212 12814 0 None - 0 Guinea pig 8.3 pIC50 = 8.3 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 663 11 2 7 5.7 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cc1OC 10.1021/jm030326t
CHEMBL3217073 12814 0 None - 0 Guinea pig 8.3 pIC50 = 8.3 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 663 11 2 7 5.7 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cc1OC 10.1021/jm030326t
10769485 20335 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 575 9 2 5 7.2 CNC(=O)c1ccc(/C=C/C(=O)NCc2sccc2-c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm980330i
CHEMBL130775 20335 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 575 9 2 5 7.2 CNC(=O)c1ccc(/C=C/C(=O)NCc2sccc2-c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm980330i
11422667 12861 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 710 12 2 7 6.6 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NCc5ccccn5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1189575 12861 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 710 12 2 7 6.6 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NCc5ccccn5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL539023 12861 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 710 12 2 7 6.6 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NCc5ccccn5)cc4)c3Cl)c2n1 10.1021/jm030326t
11158136 206692 0 None - 0 Guinea pig 7.3 pIC50 = 7.3 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 664 12 3 7 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OCC(=O)O)cc(C)nc34)c2Cl)cc1 10.1021/jm030468n
CHEMBL99978 206692 0 None - 0 Guinea pig 7.3 pIC50 = 7.3 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 664 12 3 7 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OCC(=O)O)cc(C)nc34)c2Cl)cc1 10.1021/jm030468n
44190751 193665 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 479 6 0 8 6.2 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3Sc3nccs3)c2n1 10.1021/jm9002445
CHEMBL551758 193665 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 479 6 0 8 6.2 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3Sc3nccs3)c2n1 10.1021/jm9002445
44189787 194660 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 398 4 0 5 5.2 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL562434 194660 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 398 4 0 5 5.2 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
10553878 47351 0 None - 0 Guinea pig 6.3 pIC50 = 6.3 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 513 6 0 6 4.8 CC(=O)OCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
CHEMBL154682 47351 0 None - 0 Guinea pig 6.3 pIC50 = 6.3 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 513 6 0 6 4.8 CC(=O)OCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
10842026 96261 0 None - 0 Guinea pig 6.3 pIC50 = 6.3 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 655 10 2 6 6.3 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c3nc(-c3ccccc3)n4C)c2Cl)cc1 10.1021/jm980300f
CHEMBL264259 96261 0 None - 0 Guinea pig 6.3 pIC50 = 6.3 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 655 10 2 6 6.3 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c3nc(-c3ccccc3)n4C)c2Cl)cc1 10.1021/jm980300f
18923274 19610 0 None - 0 Human 6.3 pIC50 = 6.3 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 604 9 1 6 5.4 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)COc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL130196 19610 0 None - 0 Human 6.3 pIC50 = 6.3 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 604 9 1 6 5.4 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)COc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
10579723 21102 0 None - 0 Human 6.3 pIC50 = 6.3 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 617 7 2 6 5.4 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)NC(=O)c4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL131380 21102 0 None - 0 Human 6.3 pIC50 = 6.3 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 617 7 2 6 5.4 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)NC(=O)c4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
44190672 193664 0 None - 0 Human 6.3 pIC50 = 6.3 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 364 4 0 5 4.6 Cc1cc(-c2ccnn2C)c2cccc(OCc3ccncc3Cl)c2n1 10.1021/jm9002445
CHEMBL551757 193664 0 None - 0 Human 6.3 pIC50 = 6.3 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 364 4 0 5 4.6 Cc1cc(-c2ccnn2C)c2cccc(OCc3ccncc3Cl)c2n1 10.1021/jm9002445
10722735 19849 0 None - 0 Human 5.3 pIC50 = 5.3 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 633 8 3 6 5.8 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(C(=O)O)c4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL130379 19849 0 None - 0 Human 5.3 pIC50 = 5.3 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 633 8 3 6 5.8 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(C(=O)O)c4)c3Cl)cccn2c1Br 10.1021/jm980214f
22008916 9655 0 None - 1 Guinea pig 7.3 pIC50 = 7.3 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 461 8 2 6 3.3 CCNC(=O)NCC(=O)N(C)c1ccc(OC)c(COc2cccc3ccc(C)nc23)c1C#N 10.1016/s0960-894x(98)00736-7
CHEMBL113502 9655 0 None - 1 Guinea pig 7.3 pIC50 = 7.3 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 461 8 2 6 3.3 CCNC(=O)NCC(=O)N(C)c1ccc(OC)c(COc2cccc3ccc(C)nc23)c1C#N 10.1016/s0960-894x(98)00736-7
44190363 193623 0 None - 0 Human 5.3 pIC50 = 5.3 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 318 3 0 3 4.8 Cc1ccc2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL551436 193623 0 None - 0 Human 5.3 pIC50 = 5.3 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 318 3 0 3 4.8 Cc1ccc2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
10575810 120951 0 None - 0 Guinea pig 7.3 pIC50 = 7.3 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 455 4 0 4 5.3 CC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
CHEMBL358234 120951 0 None - 0 Guinea pig 7.3 pIC50 = 7.3 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 455 4 0 4 5.3 CC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
10693220 47088 0 None - 0 Guinea pig 6.3 pIC50 = 6.3 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 414 4 0 4 5.3 COc1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
CHEMBL154465 47088 0 None - 0 Guinea pig 6.3 pIC50 = 6.3 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 414 4 0 4 5.3 COc1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
10651074 101078 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4cnc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL298463 101078 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4cnc(C)nc34)c2Cl)cc1 10.1021/jm030159x
10651074 101078 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4cnc(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL298463 101078 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4cnc(C)nc34)c2Cl)cc1 10.1021/jm980300f
44340951 9892 0 None - 1 Guinea pig 7.3 pIC50 = 7.3 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 587 11 1 7 6.4 COc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(SC)c(COc3cccc4ccc(C)nc34)c2SC)cc1 10.1016/s0960-894x(98)00736-7
CHEMBL114915 9892 0 None - 1 Guinea pig 7.3 pIC50 = 7.3 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 587 11 1 7 6.4 COc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(SC)c(COc3cccc4ccc(C)nc34)c2SC)cc1 10.1016/s0960-894x(98)00736-7
11262636 13710 0 None - 0 Guinea pig 6.3 pIC50 = 6.3 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 721 16 2 8 5.7 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(CCOC)CCOC)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL1195841 13710 0 None - 0 Guinea pig 6.3 pIC50 = 6.3 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 721 16 2 8 5.7 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(CCOC)CCOC)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL3215972 13710 0 None - 0 Guinea pig 6.3 pIC50 = 6.3 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 721 16 2 8 5.7 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(CCOC)CCOC)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
10579547 13450 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 603 8 2 5 5.8 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)NCc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL1194034 13450 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 603 8 2 5 5.8 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)NCc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL545534 13450 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 603 8 2 5 5.8 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)NCc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
10650330 13034 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 551 9 2 6 4.3 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cn1 10.1021/jm980300f
CHEMBL1190789 13034 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 551 9 2 6 4.3 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cn1 10.1021/jm980300f
CHEMBL541590 13034 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 551 9 2 6 4.3 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cn1 10.1021/jm980300f
44191138 194232 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 384 4 0 5 5.0 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL559273 194232 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 384 4 0 5 5.0 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
10578574 13457 0 None - 0 Guinea pig 6.2 pIC50 = 6.2 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 548 7 1 6 3.8 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNS(C)(=O)=O)c3Cl)cccn2c1Br 10.1021/jm970591c
CHEMBL1194067 13457 0 None - 0 Guinea pig 6.2 pIC50 = 6.2 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 548 7 1 6 3.8 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNS(C)(=O)=O)c3Cl)cccn2c1Br 10.1021/jm970591c
CHEMBL545573 13457 0 None - 0 Guinea pig 6.2 pIC50 = 6.2 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 548 7 1 6 3.8 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNS(C)(=O)=O)c3Cl)cccn2c1Br 10.1021/jm970591c
10743570 46666 0 None - 0 Guinea pig 6.2 pIC50 = 6.2 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 485 6 0 5 4.9 COCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
CHEMBL154122 46666 0 None - 0 Guinea pig 6.2 pIC50 = 6.2 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 485 6 0 5 4.9 COCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
10651074 101078 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4cnc(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL298463 101078 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4cnc(C)nc34)c2Cl)cc1 10.1021/jm980300f
10554743 114643 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 552 9 2 7 3.7 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ncc(C)nc34)c2C)cn1 10.1021/jm980300f
CHEMBL334421 114643 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 552 9 2 7 3.7 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ncc(C)nc34)c2C)cn1 10.1021/jm980300f
45267862 194636 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 434 5 0 7 4.3 CC(=O)OCc1cncc(Cl)c1C(=O)c1cccc2c(-c3ccnn3C)cc(C)nc12 10.1021/jm9002445
CHEMBL562296 194636 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 434 5 0 7 4.3 CC(=O)OCc1cncc(Cl)c1C(=O)c1cccc2c(-c3ccnn3C)cc(C)nc12 10.1021/jm9002445
11227974 13179 0 None - 0 Guinea pig 8.2 pIC50 = 8.2 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 741 12 2 8 8.1 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(C(=O)NCc5ccccn5)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL1191906 13179 0 None - 0 Guinea pig 8.2 pIC50 = 8.2 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 741 12 2 8 8.1 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(C(=O)NCc5ccccn5)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL543068 13179 0 None - 0 Guinea pig 8.2 pIC50 = 8.2 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 741 12 2 8 8.1 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(C(=O)NCc5ccccn5)cc4)c3Cl)c2n1 10.1021/jm030159x
11479739 206452 0 None - 0 Guinea pig 8.2 pIC50 = 8.2 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the B2 receptor in guinea pig ileum membrane;Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the B2 receptor in guinea pig ileum membrane;
ChEMBL 760 13 2 8 7.8 Cc1cc(OCc2ccccn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030468n
CHEMBL98460 206452 0 None - 0 Guinea pig 8.2 pIC50 = 8.2 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the B2 receptor in guinea pig ileum membrane;Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the B2 receptor in guinea pig ileum membrane;
ChEMBL 760 13 2 8 7.8 Cc1cc(OCc2ccccn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030468n
10556247 22811 0 None - 0 Guinea pig 8.2 pIC50 = 8.2 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 652 10 2 5 7.5 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccccc5)cc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL133005 22811 0 None - 0 Guinea pig 8.2 pIC50 = 8.2 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 652 10 2 5 7.5 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccccc5)cc4)c3Cl)c2n1 10.1021/jm980300f
10394861 1651 3 None - 0 Guinea pig 8.2 pIC50 = 8.2 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 687 12 2 9 5.5 COc1nc2c(n1Cc1ccccn1)cccc2OCc1c(Cl)ccc(c1Cl)N(C(=O)CNC(=O)/C=C/c1ccc(nc1)NC(=O)C)C 10.1021/jm030468n
669 1651 3 None - 0 Guinea pig 8.2 pIC50 = 8.2 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 687 12 2 9 5.5 COc1nc2c(n1Cc1ccccn1)cccc2OCc1c(Cl)ccc(c1Cl)N(C(=O)CNC(=O)/C=C/c1ccc(nc1)NC(=O)C)C 10.1021/jm030468n
CHEMBL329762 1651 3 None - 0 Guinea pig 8.2 pIC50 = 8.2 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 687 12 2 9 5.5 COc1nc2c(n1Cc1ccccn1)cccc2OCc1c(Cl)ccc(c1Cl)N(C(=O)CNC(=O)/C=C/c1ccc(nc1)NC(=O)C)C 10.1021/jm030468n
11490605 13624 0 None - 0 Guinea pig 8.2 pIC50 = 8.2 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 634 10 2 7 5.6 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cn1 10.1021/jm030326t
CHEMBL1195242 13624 0 None - 0 Guinea pig 8.2 pIC50 = 8.2 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 634 10 2 7 5.6 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cn1 10.1021/jm030326t
CHEMBL554127 13624 0 None - 0 Guinea pig 8.2 pIC50 = 8.2 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 634 10 2 7 5.6 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cn1 10.1021/jm030326t
44190755 194144 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 465 7 0 7 4.0 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3OCC(=O)N(C)C)c2n1 10.1021/jm9002445
CHEMBL558279 194144 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 465 7 0 7 4.0 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3OCC(=O)N(C)C)c2n1 10.1021/jm9002445
44190851 194885 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 464 6 1 6 4.3 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3CNC(=O)N(C)C)c2n1 10.1021/jm9002445
CHEMBL563878 194885 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 464 6 1 6 4.3 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3CNC(=O)N(C)C)c2n1 10.1021/jm9002445
44214214 13135 0 None - 0 Guinea pig 8.2 pIC50 = 8.2 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 708 10 3 8 7.0 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL1191492 13135 0 None - 0 Guinea pig 8.2 pIC50 = 8.2 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 708 10 3 8 7.0 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL542598 13135 0 None - 0 Guinea pig 8.2 pIC50 = 8.2 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 708 10 3 8 7.0 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030159x
11251046 13079 0 None - 0 Guinea pig 8.2 pIC50 = 8.2 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 696 11 2 7 6.9 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1191121 13079 0 None - 0 Guinea pig 8.2 pIC50 = 8.2 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 696 11 2 7 6.9 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL542173 13079 0 None - 0 Guinea pig 8.2 pIC50 = 8.2 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 696 11 2 7 6.9 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
44190169 193608 0 None - 0 Human 5.2 pIC50 = 5.2 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 399 4 0 5 5.8 Cc1cc(-c2ocnc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL551354 193608 0 None - 0 Human 5.2 pIC50 = 5.2 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 399 4 0 5 5.8 Cc1cc(-c2ocnc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
10746610 13290 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 631 8 2 6 6.3 CC(=O)c1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
CHEMBL1192829 13290 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 631 8 2 6 6.3 CC(=O)c1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
CHEMBL544132 13290 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 631 8 2 6 6.3 CC(=O)c1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
11239502 13576 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 674 11 2 6 6.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OC5CCCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030468n
CHEMBL1194911 13576 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 674 11 2 6 6.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OC5CCCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030468n
CHEMBL553530 13576 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 674 11 2 6 6.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OC5CCCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030468n
10506663 21217 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 540 8 1 5 5.2 CCCC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm980214f
CHEMBL131517 21217 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 540 8 1 5 5.2 CCCC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm980214f
10722735 19849 0 None - 0 Guinea pig 7.2 pIC50 = 7.2 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 633 8 3 6 5.8 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(C(=O)O)c4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL130379 19849 0 None - 0 Guinea pig 7.2 pIC50 = 7.2 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 633 8 3 6 5.8 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(C(=O)O)c4)c3Cl)cccn2c1Br 10.1021/jm980214f
44190167 194804 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 415 4 0 5 6.3 Cc1cc(-c2ncsc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL563391 194804 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 415 4 0 5 6.3 Cc1cc(-c2ncsc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
10895913 9761 0 None - 1 Guinea pig 7.2 pIC50 = 7.2 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 465 7 2 5 3.9 CCNC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccc3ccc(C)nc23)c1C#N 10.1016/s0960-894x(98)00736-7
CHEMBL114180 9761 0 None - 1 Guinea pig 7.2 pIC50 = 7.2 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 465 7 2 5 3.9 CCNC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccc3ccc(C)nc23)c1C#N 10.1016/s0960-894x(98)00736-7
11204664 111072 0 None - 0 Guinea pig 7.2 pIC50 = 7.2 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 676 10 2 8 5.4 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCOCC5)cc(C)nc34)c2Cl)cn1 10.1021/jm030326t
CHEMBL328131 111072 0 None - 0 Guinea pig 7.2 pIC50 = 7.2 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 676 10 2 8 5.4 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCOCC5)cc(C)nc34)c2Cl)cn1 10.1021/jm030326t
9916589 99761 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 593 9 2 6 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c3nc(C)n4C)c2Cl)cc1 10.1021/jm030159x
CHEMBL288603 99761 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 593 9 2 6 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c3nc(C)n4C)c2Cl)cc1 10.1021/jm030159x
9916589 99761 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 593 9 2 6 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c3nc(C)n4C)c2Cl)cc1 10.1021/jm980300f
CHEMBL288603 99761 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 593 9 2 6 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c3nc(C)n4C)c2Cl)cc1 10.1021/jm980300f
10793528 13344 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 588 8 1 5 5.6 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Cc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL1193230 13344 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 588 8 1 5 5.6 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Cc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL544600 13344 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 588 8 1 5 5.6 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Cc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
10793125 99701 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 568 10 3 7 4.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(NC)n4C)c2C)cc1 10.1021/jm030159x
CHEMBL288079 99701 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 568 10 3 7 4.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(NC)n4C)c2C)cc1 10.1021/jm030159x
10793125 99701 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 568 10 3 7 4.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(NC)n4C)c2C)cc1 10.1021/jm980300f
CHEMBL288079 99701 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 568 10 3 7 4.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(NC)n4C)c2C)cc1 10.1021/jm980300f
44190077 194786 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 399 4 0 6 4.6 Cc1cc(-c2ncnn2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL563254 194786 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 399 4 0 6 4.6 Cc1cc(-c2ncnn2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
11468051 13563 0 None - 0 Guinea pig 7.2 pIC50 = 7.2 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 673 10 2 6 6.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCCCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL1194820 13563 0 None - 0 Guinea pig 7.2 pIC50 = 7.2 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 673 10 2 6 6.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCCCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL3215558 13563 0 None - 0 Guinea pig 7.2 pIC50 = 7.2 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 673 10 2 6 6.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCCCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
119343 2818 18 None - 0 Human 8.2 pIC50 = 8.2 Binding
Inhibition of human bradykinin B2 receptorInhibition of human bradykinin B2 receptor
ChEMBL None None None None 10.1021/jm701575k
676 2818 18 None - 0 Human 8.2 pIC50 = 8.2 Binding
Inhibition of human bradykinin B2 receptorInhibition of human bradykinin B2 receptor
ChEMBL None None None None 10.1021/jm701575k
CHEMBL446325 2818 18 None - 0 Human 8.2 pIC50 = 8.2 Binding
Inhibition of human bradykinin B2 receptorInhibition of human bradykinin B2 receptor
ChEMBL None None None None 10.1021/jm701575k
10721752 168641 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 569 10 2 7 3.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(OC)n4C)c2C)cc1 10.1021/jm030159x
CHEMBL44087 168641 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 569 10 2 7 3.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(OC)n4C)c2C)cc1 10.1021/jm030159x
10721752 168641 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 569 10 2 7 3.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(OC)n4C)c2C)cc1 10.1021/jm980300f
CHEMBL44087 168641 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 569 10 2 7 3.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(OC)n4C)c2C)cc1 10.1021/jm980300f
44190753 195018 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 481 7 0 7 4.8 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3SCC(=O)N(C)C)c2n1 10.1021/jm9002445
CHEMBL564841 195018 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 481 7 0 7 4.8 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3SCC(=O)N(C)C)c2n1 10.1021/jm9002445
10580156 12985 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 653 10 2 6 6.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5cccnc5)cc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL1190412 12985 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 653 10 2 6 6.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5cccnc5)cc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL540819 12985 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 653 10 2 6 6.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5cccnc5)cc4)c3Cl)c2n1 10.1021/jm980300f
44190850 193543 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 463 7 1 6 4.8 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3CNC(=O)C(C)C)c2n1 10.1021/jm9002445
CHEMBL550827 193543 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 463 7 1 6 4.8 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3CNC(=O)C(C)C)c2n1 10.1021/jm9002445
10816618 13647 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 554 9 1 5 5.6 CCCCC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
CHEMBL1195382 13647 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 554 9 1 5 5.6 CCCCC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
CHEMBL554431 13647 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 554 9 1 5 5.6 CCCCC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
10792967 78103 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 559 9 2 4 6.6 CNC(=O)c1ccc(/C=C/C(=O)NC/C=C/c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980330i
CHEMBL2111974 78103 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 559 9 2 4 6.6 CNC(=O)c1ccc(/C=C/C(=O)NC/C=C/c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980330i
44189791 194881 0 None - 0 Human 5.2 pIC50 = 5.2 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 399 4 0 6 4.6 Cc1cc(-c2nncn2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL563861 194881 0 None - 0 Human 5.2 pIC50 = 5.2 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 399 4 0 6 4.6 Cc1cc(-c2nncn2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
10672078 48005 0 None - 0 Guinea pig 7.1 pIC50 = 7.1 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 469 5 0 4 5.7 CCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
CHEMBL155339 48005 0 None - 0 Guinea pig 7.1 pIC50 = 7.1 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 469 5 0 4 5.7 CCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
11801411 100861 0 None - 0 Human 6.1 pIC50 = 6.1 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 583 11 2 7 4.3 CCOc1nc2c(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3C)cccc2n1C 10.1021/jm030159x
CHEMBL296865 100861 0 None - 0 Human 6.1 pIC50 = 6.1 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 583 11 2 7 4.3 CCOc1nc2c(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3C)cccc2n1C 10.1021/jm030159x
11801411 100861 0 None - 0 Human 6.1 pIC50 = 6.1 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 583 11 2 7 4.3 CCOc1nc2c(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3C)cccc2n1C 10.1021/jm980300f
CHEMBL296865 100861 0 None - 0 Human 6.1 pIC50 = 6.1 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 583 11 2 7 4.3 CCOc1nc2c(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3C)cccc2n1C 10.1021/jm980300f
10604560 20190 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 676 10 3 7 5.7 COCC(=O)Nc1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
CHEMBL130660 20190 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 676 10 3 7 5.7 COCC(=O)Nc1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
11308648 12910 0 None - 0 Guinea pig 7.1 pIC50 = 7.1 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 736 11 2 7 7.9 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1189935 12910 0 None - 0 Guinea pig 7.1 pIC50 = 7.1 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 736 11 2 7 7.9 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL539792 12910 0 None - 0 Guinea pig 7.1 pIC50 = 7.1 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 736 11 2 7 7.9 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
10568916 46390 0 None - 0 Guinea pig 5.1 pIC50 = 5.1 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 336 4 1 4 4.0 Cc1nc2c(OCc3c(Cl)cccc3Cl)cccn2c1CO 10.1021/jm970591c
CHEMBL153890 46390 0 None - 0 Guinea pig 5.1 pIC50 = 5.1 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 336 4 1 4 4.0 Cc1nc2c(OCc3c(Cl)cccc3Cl)cccn2c1CO 10.1021/jm970591c
13825921 44791 0 None - 0 Guinea pig 5.1 pIC50 = 5.1 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 374 6 0 4 4.7 C#CCOCc1c(C)nc2c(OCc3c(Cl)cccc3Cl)cccn12 10.1021/jm970591c
CHEMBL152439 44791 0 None - 0 Guinea pig 5.1 pIC50 = 5.1 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 374 6 0 4 4.7 C#CCOCc1c(C)nc2c(OCc3c(Cl)cccc3Cl)cccn12 10.1021/jm970591c
11216111 13164 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 648 12 2 6 6.4 CCCOc1cc(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc12 10.1021/jm030468n
CHEMBL1191769 13164 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 648 12 2 6 6.4 CCCOc1cc(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc12 10.1021/jm030468n
CHEMBL542911 13164 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 648 12 2 6 6.4 CCCOc1cc(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc12 10.1021/jm030468n
15388870 110131 0 None - 1 Guinea pig 7.1 pIC50 = 7.1 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 543 8 1 6 6.4 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)OCc4ccccc4)c3Cl)cccc2s1 10.1016/s0960-894x(98)00736-7
CHEMBL325742 110131 0 None - 1 Guinea pig 7.1 pIC50 = 7.1 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 543 8 1 6 6.4 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)OCc4ccccc4)c3Cl)cccc2s1 10.1016/s0960-894x(98)00736-7
10768499 46674 0 None - 0 Guinea pig 6.1 pIC50 = 6.1 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 526 6 1 5 4.8 CC(=O)NC(C)C(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
CHEMBL154130 46674 0 None - 0 Guinea pig 6.1 pIC50 = 6.1 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 526 6 1 5 4.8 CC(=O)NC(C)C(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
10745895 100673 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 585 10 2 7 4.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(SC)n4C)c2C)cc1 10.1021/jm030159x
CHEMBL295428 100673 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 585 10 2 7 4.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(SC)n4C)c2C)cc1 10.1021/jm030159x
10745895 100673 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 585 10 2 7 4.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(SC)n4C)c2C)cc1 10.1021/jm980300f
CHEMBL295428 100673 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 585 10 2 7 4.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(SC)n4C)c2C)cc1 10.1021/jm980300f
11158089 12793 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 620 10 2 6 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OC)cc(C)nc34)c2Cl)cc1 10.1021/jm030468n
CHEMBL1189084 12793 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 620 10 2 6 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OC)cc(C)nc34)c2Cl)cc1 10.1021/jm030468n
CHEMBL538022 12793 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 620 10 2 6 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OC)cc(C)nc34)c2Cl)cc1 10.1021/jm030468n
11479294 13697 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 648 10 1 7 5.4 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)nc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1195758 13697 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 648 10 1 7 5.4 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)nc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL3216404 13697 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 648 10 1 7 5.4 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)nc4)c3Cl)c2n1 10.1021/jm030326t
44190852 193725 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 465 6 0 7 4.8 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3COC(=O)N(C)C)c2n1 10.1021/jm9002445
CHEMBL552090 193725 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 465 6 0 7 4.8 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3COC(=O)N(C)C)c2n1 10.1021/jm9002445
10578612 13605 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 551 9 2 6 4.9 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cn1 10.1021/jm980300f
CHEMBL1195105 13605 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 551 9 2 6 4.9 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cn1 10.1021/jm980300f
CHEMBL553843 13605 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 551 9 2 6 4.9 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cn1 10.1021/jm980300f
10769383 22648 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 570 10 2 8 3.9 COc1nc2c(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(C)=O)nc4)c3C)cccc2n1C 10.1021/jm980300f
CHEMBL132860 22648 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 570 10 2 8 3.9 COc1nc2c(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(C)=O)nc4)c3C)cccc2n1C 10.1021/jm980300f
10841393 13157 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 607 10 2 6 5.2 CCc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc2n1C 10.1021/jm980300f
CHEMBL1191700 13157 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 607 10 2 6 5.2 CCc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc2n1C 10.1021/jm980300f
CHEMBL542836 13157 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 607 10 2 6 5.2 CCc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc2n1C 10.1021/jm980300f
25019714 194898 1 None - 0 Human 8.1 pIC50 = 8.1 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 519 6 1 6 5.8 Cc1cc(-c2[nH]ncc2C)c2cccc(OCc3c(C)ccnc3Cn3cccc(C(F)(F)F)c3=O)c2n1 10.1021/jm9002445
CHEMBL563956 194898 1 None - 0 Human 8.1 pIC50 = 8.1 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 519 6 1 6 5.8 Cc1cc(-c2[nH]ncc2C)c2cccc(OCc3c(C)ccnc3Cn3cccc(C(F)(F)F)c3=O)c2n1 10.1021/jm9002445
10841393 13157 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 607 10 2 6 5.2 CCc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc2n1C 10.1021/jm030159x
CHEMBL1191700 13157 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 607 10 2 6 5.2 CCc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc2n1C 10.1021/jm030159x
CHEMBL542836 13157 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 607 10 2 6 5.2 CCc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc2n1C 10.1021/jm030159x
44191040 194300 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 519 6 0 7 5.5 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(C)ccnc3Cn3cccc(C(F)(F)F)c3=O)c2n1 10.1021/jm9002445
CHEMBL559825 194300 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 519 6 0 7 5.5 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(C)ccnc3Cn3cccc(C(F)(F)F)c3=O)c2n1 10.1021/jm9002445
10675204 168204 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 607 10 2 6 5.4 CCn1c(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc21 10.1021/jm980300f
CHEMBL43746 168204 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 607 10 2 6 5.4 CCn1c(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc21 10.1021/jm980300f
10603884 19922 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 616 10 1 5 6.4 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)CCCc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL130438 19922 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 616 10 1 5 6.4 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)CCCc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
10506663 21217 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 540 8 1 5 5.2 CCCC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm980214f
CHEMBL131517 21217 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 540 8 1 5 5.2 CCCC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm980214f
10506663 21217 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 540 8 1 5 5.2 CCCC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
CHEMBL131517 21217 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 540 8 1 5 5.2 CCCC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
10675204 168204 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 607 10 2 6 5.4 CCn1c(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc21 10.1021/jm030159x
CHEMBL43746 168204 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 607 10 2 6 5.4 CCn1c(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc21 10.1021/jm030159x
44190267 193456 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 401 4 0 5 5.9 Cc1cc(-c2cscn2)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL550143 193456 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 401 4 0 5 5.9 Cc1cc(-c2cscn2)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
44341060 9454 0 None - 1 Guinea pig 7.1 pIC50 = 7.1 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 539 10 1 6 5.2 COc1ccc(N(C)C(=O)CNC(=O)/C=C/c2cccc(C)c2)c(OC)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
CHEMBL112360 9454 0 None - 1 Guinea pig 7.1 pIC50 = 7.1 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 539 10 1 6 5.2 COc1ccc(N(C)C(=O)CNC(=O)/C=C/c2cccc(C)c2)c(OC)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
10625996 120482 0 None - 0 Guinea pig 6.1 pIC50 = 6.1 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 526 7 1 5 4.8 CC(=O)NCCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
CHEMBL356480 120482 0 None - 0 Guinea pig 6.1 pIC50 = 6.1 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 526 7 1 5 4.8 CC(=O)NCCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
10651301 116015 0 None - 0 Guinea pig 7.1 pIC50 = 7.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 603 7 2 5 6.4 Cc1ccccc1NC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm980214f
CHEMBL336209 116015 0 None - 0 Guinea pig 7.1 pIC50 = 7.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 603 7 2 5 6.4 Cc1ccccc1NC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm980214f
10840534 22358 0 None - 0 Human 6.1 pIC50 = 6.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 555 8 1 6 3.9 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)CN(C)C)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL132620 22358 0 None - 0 Human 6.1 pIC50 = 6.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 555 8 1 6 3.9 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)CN(C)C)c3Cl)cccn2c1Br 10.1021/jm980214f
11433935 13080 0 None - 0 Guinea pig 6.1 pIC50 = 6.1 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 687 10 2 6 7.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCCCCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL1191123 13080 0 None - 0 Guinea pig 6.1 pIC50 = 6.1 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 687 10 2 6 7.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCCCCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL3215986 13080 0 None - 0 Guinea pig 6.1 pIC50 = 6.1 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 687 10 2 6 7.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCCCCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
10603982 79660 0 None - 0 Human 5.1 pIC50 = 5.1 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 625 12 2 8 4.0 CCOC(=O)Cc1nc2c(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3C)cccc2n1C 10.1021/jm030159x
CHEMBL21311 79660 0 None - 0 Human 5.1 pIC50 = 5.1 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 625 12 2 8 4.0 CCOC(=O)Cc1nc2c(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3C)cccc2n1C 10.1021/jm030159x
10603982 79660 0 None - 0 Human 5.1 pIC50 = 5.1 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 625 12 2 8 4.0 CCOC(=O)Cc1nc2c(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3C)cccc2n1C 10.1021/jm980300f
CHEMBL21311 79660 0 None - 0 Human 5.1 pIC50 = 5.1 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 625 12 2 8 4.0 CCOC(=O)Cc1nc2c(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3C)cccc2n1C 10.1021/jm980300f
11456652 13081 0 None - 0 Guinea pig 7.1 pIC50 = 7.1 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 676 10 2 8 4.8 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCOCC5)cc(C)nc34)c2Cl)cn1 10.1021/jm030326t
CHEMBL1191124 13081 0 None - 0 Guinea pig 7.1 pIC50 = 7.1 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 676 10 2 8 4.8 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCOCC5)cc(C)nc34)c2Cl)cn1 10.1021/jm030326t
CHEMBL542176 13081 0 None - 0 Guinea pig 7.1 pIC50 = 7.1 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 676 10 2 8 4.8 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCOCC5)cc(C)nc34)c2Cl)cn1 10.1021/jm030326t
10579143 167888 0 None - 0 Human 6.1 pIC50 = 6.1 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 580 9 2 6 5.2 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4oc(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL43510 167888 0 None - 0 Human 6.1 pIC50 = 6.1 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 580 9 2 6 5.2 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4oc(C)nc34)c2Cl)cc1 10.1021/jm980300f
44323787 12891 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 659 10 2 6 6.2 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL1189812 12891 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 659 10 2 6 6.2 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL3215529 12891 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 659 10 2 6 6.2 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
10840241 115956 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 541 7 2 5 4.6 CCNC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm980214f
CHEMBL336116 115956 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 541 7 2 5 4.6 CCNC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm980214f
10840241 115956 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 541 7 2 5 4.6 CCNC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
CHEMBL336116 115956 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 541 7 2 5 4.6 CCNC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
11802476 12840 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 657 9 2 6 5.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL1189415 12840 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 657 9 2 6 5.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL538732 12840 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 657 9 2 6 5.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm030159x
11802476 12840 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 657 9 2 6 5.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL1189415 12840 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 657 9 2 6 5.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL538732 12840 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 657 9 2 6 5.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980300f
9916589 99761 0 None - 0 Guinea pig 8.0 pIC50 = 8.0 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 593 9 2 6 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c3nc(C)n4C)c2Cl)cc1 10.1021/jm980300f
CHEMBL288603 99761 0 None - 0 Guinea pig 8.0 pIC50 = 8.0 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 593 9 2 6 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c3nc(C)n4C)c2Cl)cc1 10.1021/jm980300f
11802489 13606 0 None - 0 Human 8.0 pIC50 = 8.0 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 658 9 2 7 4.8 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cn1 10.1021/jm980214f
CHEMBL1195106 13606 0 None - 0 Human 8.0 pIC50 = 8.0 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 658 9 2 7 4.8 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cn1 10.1021/jm980214f
CHEMBL553844 13606 0 None - 0 Human 8.0 pIC50 = 8.0 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 658 9 2 7 4.8 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cn1 10.1021/jm980214f
11490839 13043 0 None - 0 Guinea pig 8.0 pIC50 = 8.0 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 671 10 1 8 5.5 Cc1cc(-n2ccnn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL1190878 13043 0 None - 0 Guinea pig 8.0 pIC50 = 8.0 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 671 10 1 8 5.5 Cc1cc(-n2ccnn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL541805 13043 0 None - 0 Guinea pig 8.0 pIC50 = 8.0 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 671 10 1 8 5.5 Cc1cc(-n2ccnn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
9916589 99761 0 None - 0 Guinea pig 8.0 pIC50 = 8.0 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 593 9 2 6 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c3nc(C)n4C)c2Cl)cc1 10.1021/jm030159x
CHEMBL288603 99761 0 None - 0 Guinea pig 8.0 pIC50 = 8.0 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 593 9 2 6 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c3nc(C)n4C)c2Cl)cc1 10.1021/jm030159x
10674687 13501 0 None - 0 Human 8.0 pIC50 = 8.0 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 576 9 1 5 5.7 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3C)c2n1 10.1021/jm980300f
CHEMBL1194363 13501 0 None - 0 Human 8.0 pIC50 = 8.0 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 576 9 1 5 5.7 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3C)c2n1 10.1021/jm980300f
CHEMBL552543 13501 0 None - 0 Human 8.0 pIC50 = 8.0 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 576 9 1 5 5.7 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3C)c2n1 10.1021/jm980300f
10745895 100673 0 None - 0 Guinea pig 8.0 pIC50 = 8.0 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 585 10 2 7 4.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(SC)n4C)c2C)cc1 10.1021/jm980300f
CHEMBL295428 100673 0 None - 0 Guinea pig 8.0 pIC50 = 8.0 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 585 10 2 7 4.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(SC)n4C)c2C)cc1 10.1021/jm980300f
10745895 100673 0 None - 0 Guinea pig 8.0 pIC50 = 8.0 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 585 10 2 7 4.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(SC)n4C)c2C)cc1 10.1021/jm030159x
CHEMBL295428 100673 0 None - 0 Guinea pig 8.0 pIC50 = 8.0 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 585 10 2 7 4.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(SC)n4C)c2C)cc1 10.1021/jm030159x
11801411 100861 0 None - 0 Guinea pig 7.1 pIC50 = 7.1 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 583 11 2 7 4.3 CCOc1nc2c(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3C)cccc2n1C 10.1021/jm980300f
CHEMBL296865 100861 0 None - 0 Guinea pig 7.1 pIC50 = 7.1 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 583 11 2 7 4.3 CCOc1nc2c(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3C)cccc2n1C 10.1021/jm980300f
44191223 194583 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 398 4 0 5 5.2 Cc1cc(-c2nccn2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL561899 194583 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 398 4 0 5 5.2 Cc1cc(-c2nccn2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
11801411 100861 0 None - 0 Guinea pig 7.1 pIC50 = 7.1 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 583 11 2 7 4.3 CCOc1nc2c(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3C)cccc2n1C 10.1021/jm030159x
CHEMBL296865 100861 0 None - 0 Guinea pig 7.1 pIC50 = 7.1 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 583 11 2 7 4.3 CCOc1nc2c(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3C)cccc2n1C 10.1021/jm030159x
10627129 101063 0 None - 0 Human 5.0 pIC50 = 5.0 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 583 11 2 7 4.1 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(COC)n4C)c2C)cc1 10.1021/jm030159x
CHEMBL298320 101063 0 None - 0 Human 5.0 pIC50 = 5.0 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 583 11 2 7 4.1 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(COC)n4C)c2C)cc1 10.1021/jm030159x
10627129 101063 0 None - 0 Human 5.0 pIC50 = 5.0 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 583 11 2 7 4.1 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(COC)n4C)c2C)cc1 10.1021/jm980300f
CHEMBL298320 101063 0 None - 0 Human 5.0 pIC50 = 5.0 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 583 11 2 7 4.1 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(COC)n4C)c2C)cc1 10.1021/jm980300f
10793125 99701 0 None - 0 Guinea pig 7.0 pIC50 = 7.0 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 568 10 3 7 4.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(NC)n4C)c2C)cc1 10.1021/jm980300f
CHEMBL288079 99701 0 None - 0 Guinea pig 7.0 pIC50 = 7.0 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 568 10 3 7 4.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(NC)n4C)c2C)cc1 10.1021/jm980300f
10793125 99701 0 None - 0 Guinea pig 7.0 pIC50 = 7.0 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 568 10 3 7 4.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(NC)n4C)c2C)cc1 10.1021/jm030159x
CHEMBL288079 99701 0 None - 0 Guinea pig 7.0 pIC50 = 7.0 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 568 10 3 7 4.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(NC)n4C)c2C)cc1 10.1021/jm030159x
10555263 100614 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 581 10 2 7 4.1 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(C(C)=O)n4C)c2C)cc1 10.1021/jm030159x
CHEMBL295005 100614 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 581 10 2 7 4.1 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(C(C)=O)n4C)c2C)cc1 10.1021/jm030159x
10626599 30756 0 None - 0 Guinea pig 7.0 pIC50 = 7.0 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 555 8 2 4 7.4 CNC(=O)c1ccc(/C=C/C(=O)Nc2cccc(-c3ccc(C)c(COc4cccc5ccc(C)nc45)c3C)c2)cc1 10.1021/jm980330i
CHEMBL139870 30756 0 None - 0 Guinea pig 7.0 pIC50 = 7.0 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 555 8 2 4 7.4 CNC(=O)c1ccc(/C=C/C(=O)Nc2cccc(-c3ccc(C)c(COc4cccc5ccc(C)nc45)c3C)c2)cc1 10.1021/jm980330i
10555263 100614 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 581 10 2 7 4.1 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(C(C)=O)n4C)c2C)cc1 10.1021/jm980300f
CHEMBL295005 100614 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 581 10 2 7 4.1 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(C(C)=O)n4C)c2C)cc1 10.1021/jm980300f
11239381 13018 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 688 10 2 7 5.3 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCN(C)CC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL1190638 13018 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 688 10 2 7 5.3 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCN(C)CC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL3215541 13018 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 688 10 2 7 5.3 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCN(C)CC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
44190266 193775 0 None - 0 Human 6.0 pIC50 = 6.0 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 435 4 0 5 6.6 Cc1cc(-c2scnc2Cl)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL552442 193775 0 None - 0 Human 6.0 pIC50 = 6.0 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 435 4 0 5 6.6 Cc1cc(-c2scnc2Cl)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
44317520 104397 0 None - 1 Human 4.9 pKd = 4.9 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 601 12 5 5 3.6 N=C(N)NCC1N=C(c2ccccc2)c2cc(N(Cc3ccccc3)Cc3ccccc3)ccc2N(CCCN=C(N)N)C1=O 10.1016/s0960-894x(00)00482-0
CHEMBL311191 104397 0 None - 1 Human 4.9 pKd = 4.9 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 601 12 5 5 3.6 N=C(N)NCC1N=C(c2ccccc2)c2cc(N(Cc3ccccc3)Cc3ccccc3)ccc2N(CCCN=C(N)N)C1=O 10.1016/s0960-894x(00)00482-0
44317577 203922 0 None - 1 Human 4.9 pKd = 4.9 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 382 9 2 4 5.2 CCCCC1(CCCC)Oc2cccc(NC(=O)c3ccc(CN)cc3)c2O1 10.1016/s0960-894x(00)00482-0
CHEMBL81864 203922 0 None - 1 Human 4.9 pKd = 4.9 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 382 9 2 4 5.2 CCCCC1(CCCC)Oc2cccc(NC(=O)c3ccc(CN)cc3)c2O1 10.1016/s0960-894x(00)00482-0
44317502 204009 0 None - 1 Human 4.9 pKd = 4.9 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 439 12 2 5 5.0 CCCCC1(CCCC)Oc2cccc(N(CCCN)C(=O)c3ccc(CN)cc3)c2O1 10.1016/s0960-894x(00)00482-0
CHEMBL82600 204009 0 None - 1 Human 4.9 pKd = 4.9 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 439 12 2 5 5.0 CCCCC1(CCCC)Oc2cccc(N(CCCN)C(=O)c3ccc(CN)cc3)c2O1 10.1016/s0960-894x(00)00482-0
44317490 104204 0 None - 1 Human 4.8 pKd = 4.8 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 402 6 3 3 3.1 N=C(N)NC[C@H]1C[C@@H](OCc2ccccc2)CN1C(=O)c1ccc2ccccc2c1 10.1016/s0960-894x(00)00482-0
CHEMBL310531 104204 0 None - 1 Human 4.8 pKd = 4.8 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 402 6 3 3 3.1 N=C(N)NC[C@H]1C[C@@H](OCc2ccccc2)CN1C(=O)c1ccc2ccccc2c1 10.1016/s0960-894x(00)00482-0
44317519 105246 0 None - 1 Human 4.8 pKd = 4.8 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 531 11 2 5 5.1 NCCCN1C(=O)C(CCN)N=C(c2ccccc2)c2cc(N(Cc3ccccc3)Cc3ccccc3)ccc21 10.1016/s0960-894x(00)00482-0
CHEMBL312658 105246 0 None - 1 Human 4.8 pKd = 4.8 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 531 11 2 5 5.1 NCCCN1C(=O)C(CCN)N=C(c2ccccc2)c2cc(N(Cc3ccccc3)Cc3ccccc3)ccc21 10.1016/s0960-894x(00)00482-0
44317631 104633 0 None - 1 Human 4.8 pKd = 4.8 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 501 11 4 5 3.7 NCc1ccc(CNC(=O)[C@@H](CN)n2cccc2CNC(=O)C(c2ccccc2)C2CCCCC2)cc1 10.1016/s0960-894x(00)00482-0
CHEMBL311420 104633 0 None - 1 Human 4.8 pKd = 4.8 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 501 11 4 5 3.7 NCc1ccc(CNC(=O)[C@@H](CN)n2cccc2CNC(=O)C(c2ccccc2)C2CCCCC2)cc1 10.1016/s0960-894x(00)00482-0
73351522 88945 0 None - 1 Human 6.7 pKd = 6.7 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells; 0.2-16Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells; 0.2-16
ChEMBL 861 10 7 9 0.9 NCCCC[C@@H]1NC(=O)[C@H](c2ccccc2)NC(=O)[C@H](CNC(=O)Cc2ccccc2)NC(=O)[C@H]2Cc3ccccc3CN2C(=O)[C@@H]2CC3CCCCC3N2C(=O)[C@H](CN)NC1=O 10.1016/s0960-894x(00)00482-0
CHEMBL2369879 88945 0 None - 1 Human 6.7 pKd = 6.7 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells; 0.2-16Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells; 0.2-16
ChEMBL 861 10 7 9 0.9 NCCCC[C@@H]1NC(=O)[C@H](c2ccccc2)NC(=O)[C@H](CNC(=O)Cc2ccccc2)NC(=O)[C@H]2Cc3ccccc3CN2C(=O)[C@@H]2CC3CCCCC3N2C(=O)[C@H](CN)NC1=O 10.1016/s0960-894x(00)00482-0
90662959 106092 0 None - 1 Human 6.7 pKd = 6.7 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells; 0.2-16Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells; 0.2-16
ChEMBL 769 8 7 7 1.6 N=C(N)NCCC[C@@H]1NC(=O)N2C3CCCCC3C[C@H]2C(=O)N2Cc3ccccc3C[C@@H]2C(=O)NCC[C@@H](NC(=O)CCc2ccccc2)C(=O)CCNC1=O 10.1016/s0960-894x(00)00482-0
CHEMBL3142416 106092 0 None - 1 Human 6.7 pKd = 6.7 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells; 0.2-16Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells; 0.2-16
ChEMBL 769 8 7 7 1.6 N=C(N)NCCC[C@@H]1NC(=O)N2C3CCCCC3C[C@H]2C(=O)N2Cc3ccccc3C[C@@H]2C(=O)NCC[C@@H](NC(=O)CCc2ccccc2)C(=O)CCNC1=O 10.1016/s0960-894x(00)00482-0
44317544 203965 0 None - 1 Human 4.6 pKd = 4.6 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 471 18 1 3 7.6 CCCCc1ccnc([C@H](CC2CCCCC2)NC(=O)CCCCN(CCCC)CCCC)c1 10.1016/s0960-894x(00)00482-0
CHEMBL82249 203965 0 None - 1 Human 4.6 pKd = 4.6 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 471 18 1 3 7.6 CCCCc1ccnc([C@H](CC2CCCCC2)NC(=O)CCCCN(CCCC)CCCC)c1 10.1016/s0960-894x(00)00482-0
44317810 105138 0 None - 1 Human 4.6 pKd = 4.6 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 537 14 4 5 4.6 NCCCC[C@H](C(=O)NCc1ccc(CN)cc1)n1cccc1C(=O)NC(Cc1ccccc1)c1ccccc1 10.1016/s0960-894x(00)00482-0
CHEMBL312374 105138 0 None - 1 Human 4.6 pKd = 4.6 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 537 14 4 5 4.6 NCCCC[C@H](C(=O)NCc1ccc(CN)cc1)n1cccc1C(=O)NC(Cc1ccccc1)c1ccccc1 10.1016/s0960-894x(00)00482-0
90663066 106093 0 None - 1 Guinea pig 5.5 pKd = 5.5 Binding
Functional antagonism against BK-induced contractions in the classical guinea pig ileum B2 binding assayFunctional antagonism against BK-induced contractions in the classical guinea pig ileum B2 binding assay
ChEMBL 1081 34 14 12 -0.5 N=C(N)NCCC[C@H](NC(=O)[C@H](N)CCCN=C(N)N)C(=O)NCCCCCCCCCCCC(=O)N[C@@H](CO)C(=O)N1CCc2ccccc2[C@@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O 10.1016/S0960-894X(97)10042-7
CHEMBL3142595 106093 0 None - 1 Guinea pig 5.5 pKd = 5.5 Binding
Functional antagonism against BK-induced contractions in the classical guinea pig ileum B2 binding assayFunctional antagonism against BK-induced contractions in the classical guinea pig ileum B2 binding assay
ChEMBL 1081 34 14 12 -0.5 N=C(N)NCCC[C@H](NC(=O)[C@H](N)CCCN=C(N)N)C(=O)NCCCCCCCCCCCC(=O)N[C@@H](CO)C(=O)N1CCc2ccccc2[C@@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O 10.1016/S0960-894X(97)10042-7
10481702 103913 0 None - 1 Human 5.4 pKd = 5.4 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 517 10 2 5 4.8 NCCCN1C(=O)C(CN)N=C(c2ccccc2)c2cc(N(Cc3ccccc3)Cc3ccccc3)ccc21 10.1016/s0960-894x(00)00482-0
CHEMBL310300 103913 0 None - 1 Human 5.4 pKd = 5.4 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 517 10 2 5 4.8 NCCCN1C(=O)C(CN)N=C(c2ccccc2)c2cc(N(Cc3ccccc3)Cc3ccccc3)ccc21 10.1016/s0960-894x(00)00482-0
10371624 104932 0 None - 1 Human 5.4 pKd = 5.4 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 615 13 5 5 4.0 N=C(N)NCCC1N=C(c2ccccc2)c2cc(N(Cc3ccccc3)Cc3ccccc3)ccc2N(CCCN=C(N)N)C1=O 10.1016/s0960-894x(00)00482-0
CHEMBL311969 104932 0 None - 1 Human 5.4 pKd = 5.4 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 615 13 5 5 4.0 N=C(N)NCCC1N=C(c2ccccc2)c2cc(N(Cc3ccccc3)Cc3ccccc3)ccc2N(CCCN=C(N)N)C1=O 10.1016/s0960-894x(00)00482-0
44317826 203554 0 None - 1 Human 5.3 pKd = 5.3 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 435 10 3 3 4.6 CCCCc1ccnc([C@H](CC2CCCCC2)NC(=O)c2ccc(CN=C(N)N)cc2)c1 10.1016/s0960-894x(00)00482-0
CHEMBL79057 203554 0 None - 1 Human 5.3 pKd = 5.3 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 435 10 3 3 4.6 CCCCc1ccnc([C@H](CC2CCCCC2)NC(=O)c2ccc(CN=C(N)N)cc2)c1 10.1016/s0960-894x(00)00482-0
44317458 203476 0 None - 1 Human 4.2 pKd = 4.2 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 359 11 2 3 4.7 CCCCc1ccnc([C@H](CC2CCCCC2)NC(=O)CCCCN)c1 10.1016/s0960-894x(00)00482-0
CHEMBL78487 203476 0 None - 1 Human 4.2 pKd = 4.2 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 359 11 2 3 4.7 CCCCc1ccnc([C@H](CC2CCCCC2)NC(=O)CCCCN)c1 10.1016/s0960-894x(00)00482-0
44317602 203954 0 None - 1 Human 4.2 pKd = 4.2 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 360 5 1 3 3.6 NC[C@H]1C[C@@H](OCc2ccccc2)CN1C(=O)c1ccc2ccccc2c1 10.1016/s0960-894x(00)00482-0
CHEMBL82194 203954 0 None - 1 Human 4.2 pKd = 4.2 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 360 5 1 3 3.6 NC[C@H]1C[C@@H](OCc2ccccc2)CN1C(=O)c1ccc2ccccc2c1 10.1016/s0960-894x(00)00482-0
44317543 104833 0 None - 1 Human 5.1 pKd = 5.1 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 393 9 2 3 5.3 CCCCc1ccnc([C@H](CC2CCCCC2)NC(=O)c2ccc(CN)cc2)c1 10.1016/s0960-894x(00)00482-0
CHEMBL311593 104833 0 None - 1 Human 5.1 pKd = 5.1 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 393 9 2 3 5.3 CCCCc1ccnc([C@H](CC2CCCCC2)NC(=O)c2ccc(CN)cc2)c1 10.1016/s0960-894x(00)00482-0
44317849 103412 0 None - 1 Human 5.1 pKd = 5.1 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 434 7 1 3 5.6 NCc1cccc(Cn2ccc3c2C(=O)C(Cc2ccccc2)(Cc2ccccc2)CC3)c1 10.1016/s0960-894x(00)00482-0
CHEMBL309221 103412 0 None - 1 Human 5.1 pKd = 5.1 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 434 7 1 3 5.6 NCc1cccc(Cn2ccc3c2C(=O)C(Cc2ccccc2)(Cc2ccccc2)CC3)c1 10.1016/s0960-894x(00)00482-0
11050762 67318 0 None 5248 2 Rat 10.6 pKi = 10.6 Binding
Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesInhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranes
ChEMBL 696 16 4 9 3.7 CN(C)CCCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(N/N=C(\S)NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL1907651 67318 0 None 5248 2 Rat 10.6 pKi = 10.6 Binding
Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesInhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranes
ChEMBL 696 16 4 9 3.7 CN(C)CCCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(N/N=C(\S)NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1021/jm0111088
667 1934 32 None -1 6 Human 10.6 pKi = 10.6 Binding
Binding affinity to human bradykinin B2 receptor transfected in CHO cellsBinding affinity to human bradykinin B2 receptor transfected in CHO cells
ChEMBL None None None None 10.1016/j.bmcl.2006.01.125
71364 1934 32 None -1 6 Human 10.6 pKi = 10.6 Binding
Binding affinity to human bradykinin B2 receptor transfected in CHO cellsBinding affinity to human bradykinin B2 receptor transfected in CHO cells
ChEMBL None None None None 10.1016/j.bmcl.2006.01.125
CHEMBL2028850 1934 32 None -1 6 Human 10.6 pKi = 10.6 Binding
Binding affinity to human bradykinin B2 receptor transfected in CHO cellsBinding affinity to human bradykinin B2 receptor transfected in CHO cells
ChEMBL None None None None 10.1016/j.bmcl.2006.01.125
DB06196 1934 32 None -1 6 Human 10.6 pKi = 10.6 Binding
Binding affinity to human bradykinin B2 receptor transfected in CHO cellsBinding affinity to human bradykinin B2 receptor transfected in CHO cells
ChEMBL None None None None 10.1016/j.bmcl.2006.01.125
57398326 71285 0 None - 1 Human 10.4 pKi = 10.4 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 763 14 1 6 6.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CCCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956864 71285 0 None - 1 Human 10.4 pKi = 10.4 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 763 14 1 6 6.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CCCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963558 71285 0 None - 1 Human 10.4 pKi = 10.4 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 763 14 1 6 6.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CCCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57401774 71234 0 None - 1 Human 10.3 pKi = 10.3 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 749 13 1 6 5.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956863 71234 0 None - 1 Human 10.3 pKi = 10.3 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 749 13 1 6 5.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963184 71234 0 None - 1 Human 10.3 pKi = 10.3 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 749 13 1 6 5.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57391279 71235 0 None - 1 Human 10.3 pKi = 10.3 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 748 14 2 7 5.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CNCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956876 71235 0 None - 1 Human 10.3 pKi = 10.3 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 748 14 2 7 5.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CNCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963185 71235 0 None - 1 Human 10.3 pKi = 10.3 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 748 14 2 7 5.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CNCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57394782 71284 0 None - 1 Human 10.3 pKi = 10.3 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 720 11 3 9 3.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCN)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956855 71284 0 None - 1 Human 10.3 pKi = 10.3 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 720 11 3 9 3.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCN)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963557 71284 0 None - 1 Human 10.3 pKi = 10.3 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 720 11 3 9 3.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCN)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57403503 71306 0 None - 1 Human 10.3 pKi = 10.3 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 748 12 2 9 3.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCN(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956856 71306 0 None - 1 Human 10.3 pKi = 10.3 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 748 12 2 9 3.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCN(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963651 71306 0 None - 1 Human 10.3 pKi = 10.3 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 748 12 2 9 3.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCN(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
11498853 82761 9 None - 1 Human 10.3 pKi = 10.3 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 763 12 2 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL218427 82761 9 None - 1 Human 10.3 pKi = 10.3 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 763 12 2 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL541758 82761 9 None - 1 Human 10.3 pKi = 10.3 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 763 12 2 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
11498853 82761 9 None - 1 Human 10.3 pKi = 10.3 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 763 12 2 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL218427 82761 9 None - 1 Human 10.3 pKi = 10.3 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 763 12 2 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL541758 82761 9 None - 1 Human 10.3 pKi = 10.3 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 763 12 2 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1021/jm061143k
11600324 141452 0 None - 1 Human 10.3 pKi = 10.3 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 747 12 2 7 4.8 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL387452 141452 0 None - 1 Human 10.3 pKi = 10.3 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 747 12 2 7 4.8 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
16105746 161369 0 None - 1 Human 10.3 pKi = 10.3 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 779 12 2 8 4.8 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCSCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL415366 161369 0 None - 1 Human 10.3 pKi = 10.3 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 779 12 2 8 4.8 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCSCC4)c3Cl)c2n1 10.1021/jm061143k
667 1934 32 None -1 6 Human 10.2 pKi = 10.2 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL None None None None 10.1021/jm9901531
71364 1934 32 None -1 6 Human 10.2 pKi = 10.2 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL None None None None 10.1021/jm9901531
CHEMBL2028850 1934 32 None -1 6 Human 10.2 pKi = 10.2 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL None None None None 10.1021/jm9901531
DB06196 1934 32 None -1 6 Human 10.2 pKi = 10.2 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL None None None None 10.1021/jm9901531
57399981 71215 0 None - 1 Human 10.2 pKi = 10.2 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 762 13 2 9 4.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCN(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956858 71215 0 None - 1 Human 10.2 pKi = 10.2 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 762 13 2 9 4.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCN(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963148 71215 0 None - 1 Human 10.2 pKi = 10.2 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 762 13 2 9 4.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCN(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57401778 71219 0 None - 1 Human 10.2 pKi = 10.2 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 748 14 1 7 6.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(CCCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956870 71219 0 None - 1 Human 10.2 pKi = 10.2 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 748 14 1 7 6.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(CCCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963152 71219 0 None - 1 Human 10.2 pKi = 10.2 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 748 14 1 7 6.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(CCCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57390466 71281 0 None - 1 Human 10.2 pKi = 10.2 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 776 13 5 9 3.2 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCNC(=N)N)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956719 71281 0 None - 1 Human 10.2 pKi = 10.2 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 776 13 5 9 3.2 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCNC(=N)N)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963540 71281 0 None - 1 Human 10.2 pKi = 10.2 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 776 13 5 9 3.2 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCNC(=N)N)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
667 1934 32 None -1 6 Human 10.2 pKi = 10.2 Binding
Binding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligandBinding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligand
ChEMBL None None None None 10.1021/jm9901529
71364 1934 32 None -1 6 Human 10.2 pKi = 10.2 Binding
Binding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligandBinding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligand
ChEMBL None None None None 10.1021/jm9901529
CHEMBL2028850 1934 32 None -1 6 Human 10.2 pKi = 10.2 Binding
Binding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligandBinding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligand
ChEMBL None None None None 10.1021/jm9901529
DB06196 1934 32 None -1 6 Human 10.2 pKi = 10.2 Binding
Binding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligandBinding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligand
ChEMBL None None None None 10.1021/jm9901529
3812 708 37 None 1 6 Human 10.2 pKi = 10.2 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL None None None None 10.1021/jm9901531
439201 708 37 None 1 6 Human 10.2 pKi = 10.2 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL None None None None 10.1021/jm9901531
649 708 37 None 1 6 Human 10.2 pKi = 10.2 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL None None None None 10.1021/jm9901531
CHEMBL406291 708 37 None 1 6 Human 10.2 pKi = 10.2 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL None None None None 10.1021/jm9901531
DB12126 708 37 None 1 6 Human 10.2 pKi = 10.2 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL None None None None 10.1021/jm9901531
44355428 168557 0 None - 1 Human 10.2 pKi = 10.2 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1200 31 15 18 -5.4 NCCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1CC(O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)NC1CSc2ccccc2N(CC(=O)N[C@H](CCCN=C(N)N)C(=O)O)C1=O 10.1021/jm9901531
CHEMBL440257 168557 0 None - 1 Human 10.2 pKi = 10.2 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1200 31 15 18 -5.4 NCCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1CC(O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)NC1CSc2ccccc2N(CC(=O)N[C@H](CCCN=C(N)N)C(=O)O)C1=O 10.1021/jm9901531
667 1934 32 None -1 6 Rat 10.1 pKi = 10.1 Binding
Binding affinity against rat bradykinin B2 receptors expressed in CHO cells using [3H]bradykinin as radioligandBinding affinity against rat bradykinin B2 receptors expressed in CHO cells using [3H]bradykinin as radioligand
ChEMBL None None None None 10.1021/jm9901529
71364 1934 32 None -1 6 Rat 10.1 pKi = 10.1 Binding
Binding affinity against rat bradykinin B2 receptors expressed in CHO cells using [3H]bradykinin as radioligandBinding affinity against rat bradykinin B2 receptors expressed in CHO cells using [3H]bradykinin as radioligand
ChEMBL None None None None 10.1021/jm9901529
CHEMBL2028850 1934 32 None -1 6 Rat 10.1 pKi = 10.1 Binding
Binding affinity against rat bradykinin B2 receptors expressed in CHO cells using [3H]bradykinin as radioligandBinding affinity against rat bradykinin B2 receptors expressed in CHO cells using [3H]bradykinin as radioligand
ChEMBL None None None None 10.1021/jm9901529
DB06196 1934 32 None -1 6 Rat 10.1 pKi = 10.1 Binding
Binding affinity against rat bradykinin B2 receptors expressed in CHO cells using [3H]bradykinin as radioligandBinding affinity against rat bradykinin B2 receptors expressed in CHO cells using [3H]bradykinin as radioligand
ChEMBL None None None None 10.1021/jm9901529
57399228 71213 0 None - 1 Human 10.1 pKi = 10.1 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 706 9 1 7 3.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956720 71213 0 None - 1 Human 10.1 pKi = 10.1 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 706 9 1 7 3.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963146 71213 0 None - 1 Human 10.1 pKi = 10.1 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 706 9 1 7 3.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57398324 71226 0 None - 1 Human 10.1 pKi = 10.1 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 735 12 1 6 5.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956862 71226 0 None - 1 Human 10.1 pKi = 10.1 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 735 12 1 6 5.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963164 71226 0 None - 1 Human 10.1 pKi = 10.1 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 735 12 1 6 5.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57345657 71233 0 None -2 2 Human 10.1 pKi = 10.1 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 748 12 1 7 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956722 71233 0 None -2 2 Human 10.1 pKi = 10.1 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 748 12 1 7 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963183 71233 0 None -2 2 Human 10.1 pKi = 10.1 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 748 12 1 7 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57396534 71305 0 None - 1 Human 10.1 pKi = 10.1 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 705 11 2 8 4.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCN)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956854 71305 0 None - 1 Human 10.1 pKi = 10.1 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 705 11 2 8 4.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCN)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963650 71305 0 None - 1 Human 10.1 pKi = 10.1 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 705 11 2 8 4.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCN)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
16105703 135944 0 None - 1 Human 10.1 pKi = 10.1 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 776 12 2 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCN(C)CC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL373607 135944 0 None - 1 Human 10.1 pKi = 10.1 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 776 12 2 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCN(C)CC4)c3Cl)c2n1 10.1021/jm061143k
90662945 106091 0 None - 1 Human 10.1 pKi = 10.1 Binding
Ability to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykininAbility to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykinin
ChEMBL 1298 30 15 17 -5.2 NC(N)=NCCC[C@H](N)C(=O)N[C@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1CC(O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@H]1C(=O)N1c2ccccc2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O 10.1021/jm990961s
CHEMBL3142396 106091 0 None - 1 Human 10.1 pKi = 10.1 Binding
Ability to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykininAbility to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykinin
ChEMBL 1298 30 15 17 -5.2 NC(N)=NCCC[C@H](N)C(=O)N[C@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1CC(O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@H]1C(=O)N1c2ccccc2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O 10.1021/jm990961s
CHEMBL2371961 208403 0 None - 1 Guinea pig 10.1 pKi = 10.1 Binding
Binding affinity against [3H]bradykinin binding to bradykinin receptor B2 in guinea pig ileal membraneBinding affinity against [3H]bradykinin binding to bradykinin receptor B2 in guinea pig ileal membrane
ChEMBL None None None NC(N)=NCCC[C@H](NC(=O)[C@@H]1CN(C(=O)[C@H]2c3ccccc3CCN2C(=O)[C@H](CO)NC(=O)[C@H](Cc2ccccc2)NC(=O)CNC(=O)[C@@H]2C[C@@H](O)CN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C2CCCCC21)C(=O)O 10.1021/jm00069a016
57401770 71224 0 None - 1 Human 10.0 pKi = 10 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 733 12 1 8 5.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCN(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956853 71224 0 None - 1 Human 10.0 pKi = 10 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 733 12 1 8 5.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCN(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963162 71224 0 None - 1 Human 10.0 pKi = 10 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 733 12 1 8 5.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCN(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57401772 71229 0 None - 1 Human 10.0 pKi = 10 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 734 12 3 9 3.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCN)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956857 71229 0 None - 1 Human 10.0 pKi = 10 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 734 12 3 9 3.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCN)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963175 71229 0 None - 1 Human 10.0 pKi = 10 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 734 12 3 9 3.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCN)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57396538 71230 0 None - 1 Human 10.0 pKi = 10 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 721 11 1 6 5.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956861 71230 0 None - 1 Human 10.0 pKi = 10 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 721 11 1 6 5.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963176 71230 0 None - 1 Human 10.0 pKi = 10 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 721 11 1 6 5.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
16105734 83842 0 None - 1 Human 10.0 pKi = 10 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 803 14 4 7 4.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@H](CCCCNC(=N)N)[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL221285 83842 0 None - 1 Human 10.0 pKi = 10 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 803 14 4 7 4.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@H](CCCCNC(=N)N)[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
9831859 9599 0 None - 1 Guinea pig 10.0 pKi = 10 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 508 10 3 6 3.6 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)NCCCCN)c3C#N)c2n1 10.1016/s0960-894x(98)00736-7
CHEMBL113169 9599 0 None - 1 Guinea pig 10.0 pKi = 10 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 508 10 3 6 3.6 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)NCCCCN)c3C#N)c2n1 10.1016/s0960-894x(98)00736-7
10257108 9723 0 None - 1 Guinea pig 10.0 pKi = 10 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 554 9 1 6 5.4 COc1cccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2C#N)c1 10.1016/s0960-894x(98)00736-7
CHEMBL113963 9723 0 None - 1 Guinea pig 10.0 pKi = 10 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 554 9 1 6 5.4 COc1cccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2C#N)c1 10.1016/s0960-894x(98)00736-7
3812 708 37 None 1 6 Human 10.0 pKi = 10.0 Binding
Ability to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykininAbility to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykinin
ChEMBL None None None None 10.1021/jm990961s
439201 708 37 None 1 6 Human 10.0 pKi = 10.0 Binding
Ability to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykininAbility to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykinin
ChEMBL None None None None 10.1021/jm990961s
649 708 37 None 1 6 Human 10.0 pKi = 10.0 Binding
Ability to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykininAbility to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykinin
ChEMBL None None None None 10.1021/jm990961s
CHEMBL406291 708 37 None 1 6 Human 10.0 pKi = 10.0 Binding
Ability to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykininAbility to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykinin
ChEMBL None None None None 10.1021/jm990961s
DB12126 708 37 None 1 6 Human 10.0 pKi = 10.0 Binding
Ability to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykininAbility to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykinin
ChEMBL None None None None 10.1021/jm990961s
CHEMBL2371961 208403 0 None - 1 Guinea pig 10.0 pKi = 10.0 Binding
Binding affinity towards bradykinin receptor B2 using [3H]bradykininBinding affinity towards bradykinin receptor B2 using [3H]bradykinin
ChEMBL None None None NC(N)=NCCC[C@H](NC(=O)[C@@H]1CN(C(=O)[C@H]2c3ccccc3CCN2C(=O)[C@H](CO)NC(=O)[C@H](Cc2ccccc2)NC(=O)CNC(=O)[C@@H]2C[C@@H](O)CN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C2CCCCC21)C(=O)O 10.1021/jm00035a015
667 1934 32 None 1 6 Guinea pig 10.0 pKi = 10.0 Binding
In vitro binding affinity against bradykinin receptor B2 from guinea pig ileum.In vitro binding affinity against bradykinin receptor B2 from guinea pig ileum.
ChEMBL None None None None 10.1021/jm00062a018
71364 1934 32 None 1 6 Guinea pig 10.0 pKi = 10.0 Binding
In vitro binding affinity against bradykinin receptor B2 from guinea pig ileum.In vitro binding affinity against bradykinin receptor B2 from guinea pig ileum.
ChEMBL None None None None 10.1021/jm00062a018
CHEMBL2028850 1934 32 None 1 6 Guinea pig 10.0 pKi = 10.0 Binding
In vitro binding affinity against bradykinin receptor B2 from guinea pig ileum.In vitro binding affinity against bradykinin receptor B2 from guinea pig ileum.
ChEMBL None None None None 10.1021/jm00062a018
DB06196 1934 32 None 1 6 Guinea pig 10.0 pKi = 10.0 Binding
In vitro binding affinity against bradykinin receptor B2 from guinea pig ileum.In vitro binding affinity against bradykinin receptor B2 from guinea pig ileum.
ChEMBL None None None None 10.1021/jm00062a018
57402746 71214 0 None - 1 Human 9.9 pKi = 9.9 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 734 11 1 7 4.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956721 71214 0 None - 1 Human 9.9 pKi = 9.9 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 734 11 1 7 4.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963147 71214 0 None - 1 Human 9.9 pKi = 9.9 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 734 11 1 7 4.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57402744 71222 0 None - 1 Human 9.9 pKi = 9.9 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 762 12 5 9 2.8 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCNC(=N)N)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956718 71222 0 None - 1 Human 9.9 pKi = 9.9 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 762 12 5 9 2.8 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCNC(=N)N)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963160 71222 0 None - 1 Human 9.9 pKi = 9.9 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 762 12 5 9 2.8 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCNC(=N)N)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57400986 71223 0 None - 1 Human 9.9 pKi = 9.9 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 762 13 1 7 5.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956723 71223 0 None - 1 Human 9.9 pKi = 9.9 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 762 13 1 7 5.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963161 71223 0 None - 1 Human 9.9 pKi = 9.9 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 762 13 1 7 5.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
16105690 83207 0 None - 1 Human 9.9 pKi = 9.9 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 761 13 2 7 5.2 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[C@H](CCCN)[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL220478 83207 0 None - 1 Human 9.9 pKi = 9.9 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 761 13 2 7 5.2 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[C@H](CCCN)[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
10102701 136900 0 None - 1 Human 9.9 pKi = 9.9 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 761 13 2 7 5.2 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@H](CCCCN)[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL375354 136900 0 None - 1 Human 9.9 pKi = 9.9 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 761 13 2 7 5.2 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@H](CCCCN)[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
44337475 7984 0 None - 1 Human 9.8 pKi = 9.8 Binding
Affinity to human Bradykinin receptor B2 in CHO cell membranes determined by displacement of [3H]-NPC 17731Affinity to human Bradykinin receptor B2 in CHO cell membranes determined by displacement of [3H]-NPC 17731
ChEMBL 329 5 0 4 1.4 CC(=O)CN1CN(CCc2ccccc2)C2(CCN(C)CC2)C1=O 10.1021/jm950676i
CHEMBL109123 7984 0 None - 1 Human 9.8 pKi = 9.8 Binding
Affinity to human Bradykinin receptor B2 in CHO cell membranes determined by displacement of [3H]-NPC 17731Affinity to human Bradykinin receptor B2 in CHO cell membranes determined by displacement of [3H]-NPC 17731
ChEMBL 329 5 0 4 1.4 CC(=O)CN1CN(CCc2ccccc2)C2(CCN(C)CC2)C1=O 10.1021/jm950676i
57401784 71280 0 None - 1 Human 9.8 pKi = 9.8 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 734 13 2 7 5.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CNCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956875 71280 0 None - 1 Human 9.8 pKi = 9.8 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 734 13 2 7 5.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CNCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963532 71280 0 None - 1 Human 9.8 pKi = 9.8 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 734 13 2 7 5.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CNCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
16105751 82802 0 None - 1 Human 9.8 pKi = 9.8 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 804 12 2 8 3.9 CC(=O)N1CCC(NS(=O)(=O)c2ccc(Cl)c(COc3cccc4c(C)cc(C)nc34)c2Cl)(C(=O)N2CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC2)CC1 10.1021/jm061143k
CHEMBL218636 82802 0 None - 1 Human 9.8 pKi = 9.8 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 804 12 2 8 3.9 CC(=O)N1CCC(NS(=O)(=O)c2ccc(Cl)c(COc3cccc4c(C)cc(C)nc34)c2Cl)(C(=O)N2CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC2)CC1 10.1021/jm061143k
CHEMBL2369941 207982 0 None - 1 Guinea pig 9.8 pKi = 9.8 Binding
In vitro binding affinity against bradykinin receptor B2 from guinea pig ileum.In vitro binding affinity against bradykinin receptor B2 from guinea pig ileum.
ChEMBL None None None CCCC1C[C@H](C(=O)N2C3CCCCC3C[C@H]2C(=O)N[C@@H](CCCN=C(N)N)C(=O)O)N(C(=O)[C@H](CO)NC(=O)[C@H](Cc2ccsc2)NC(=O)CNC(=O)[C@@H]2CC[C@H](O)N2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C1 10.1021/jm00062a018
CHEMBL3038098 209176 0 None - 1 Human 9.8 pKi = 9.8 Binding
Binding affinity towards Bradykinin receptor B2 in human S34 clone cellsBinding affinity towards Bradykinin receptor B2 in human S34 clone cells
ChEMBL None None None NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N(CC(=O)N[C@@H](CCCN=C(N)N)C(=O)O)CC1CCCCC1 10.1021/jm950716i
667 1934 32 None -1 6 Human 9.7 pKi = 9.7 Binding
Binding affinity towards Bradykinin receptor B2 in human S34 clone cellsBinding affinity towards Bradykinin receptor B2 in human S34 clone cells
ChEMBL None None None None 10.1021/jm950716i
71364 1934 32 None -1 6 Human 9.7 pKi = 9.7 Binding
Binding affinity towards Bradykinin receptor B2 in human S34 clone cellsBinding affinity towards Bradykinin receptor B2 in human S34 clone cells
ChEMBL None None None None 10.1021/jm950716i
CHEMBL2028850 1934 32 None -1 6 Human 9.7 pKi = 9.7 Binding
Binding affinity towards Bradykinin receptor B2 in human S34 clone cellsBinding affinity towards Bradykinin receptor B2 in human S34 clone cells
ChEMBL None None None None 10.1021/jm950716i
DB06196 1934 32 None -1 6 Human 9.7 pKi = 9.7 Binding
Binding affinity towards Bradykinin receptor B2 in human S34 clone cellsBinding affinity towards Bradykinin receptor B2 in human S34 clone cells
ChEMBL None None None None 10.1021/jm950716i
57394780 71283 0 None - 1 Human 9.7 pKi = 9.7 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 776 14 1 7 5.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956852 71283 0 None - 1 Human 9.7 pKi = 9.7 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 776 14 1 7 5.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963556 71283 0 None - 1 Human 9.7 pKi = 9.7 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 776 14 1 7 5.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57392147 71310 0 None - 1 Human 9.7 pKi = 9.7 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 720 12 2 7 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CNCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1955876 71310 0 None - 1 Human 9.7 pKi = 9.7 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 720 12 2 7 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CNCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963660 71310 0 None - 1 Human 9.7 pKi = 9.7 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 720 12 2 7 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CNCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
16105696 82781 0 None - 1 Human 9.7 pKi = 9.7 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 790 13 1 6 5.6 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@H](CCC[N+](C)(C)C)[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL218540 82781 0 None - 1 Human 9.7 pKi = 9.7 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 790 13 1 6 5.6 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@H](CCC[N+](C)(C)C)[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
10441297 136352 0 None - 1 Human 9.7 pKi = 9.7 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 804 14 1 6 6.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@H](CCCC[N+](C)(C)C)[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL374224 136352 0 None - 1 Human 9.7 pKi = 9.7 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 804 14 1 6 6.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@H](CCCC[N+](C)(C)C)[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
11766718 136397 0 None - 1 Human 9.7 pKi = 9.7 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 774 14 1 8 5.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@H](CCCCN(C)C)N(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL374272 136397 0 None - 1 Human 9.7 pKi = 9.7 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 774 14 1 8 5.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@H](CCCCN(C)C)N(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
9897921 161340 0 None - 1 Human 9.7 pKi = 9.7 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 761 13 2 7 5.2 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[C@@H](N)CCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL415151 161340 0 None - 1 Human 9.7 pKi = 9.7 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 761 13 2 7 5.2 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[C@@H](N)CCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL3038106 209184 0 None 16 2 Human 9.7 pKi = 9.7 Binding
Binding affinity towards Bradykinin receptor B2 in human S34 clone cellsBinding affinity towards Bradykinin receptor B2 in human S34 clone cells
ChEMBL None None None NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1C[C@@H](O)C[C@@H]1C(=O)N1C[C@@H](O)C[C@@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N(CC(=O)N[C@@H](CCCN=C(N)N)C(=O)O)C1CCCCC1 10.1021/jm950716i
CHEMBL3038099 209177 0 None 2 2 Human 9.6 pKi = 9.6 Binding
Binding affinity towards Bradykinin receptor B2 in human S34 clone cellsBinding affinity towards Bradykinin receptor B2 in human S34 clone cells
ChEMBL None None None NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N(CC(=O)N[C@@H](CCCN=C(N)N)C(=O)O)C1CCCCC1 10.1021/jm950716i
57399983 71216 0 None - 1 Human 9.6 pKi = 9.6 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 777 13 2 8 4.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956859 71216 0 None - 1 Human 9.6 pKi = 9.6 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 777 13 2 8 4.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963149 71216 0 None - 1 Human 9.6 pKi = 9.6 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 777 13 2 8 4.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57396536 71225 0 None - 1 Human 9.6 pKi = 9.6 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 707 10 1 6 4.6 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956860 71225 0 None - 1 Human 9.6 pKi = 9.6 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 707 10 1 6 4.6 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963163 71225 0 None - 1 Human 9.6 pKi = 9.6 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 707 10 1 6 4.6 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57396540 71231 0 None - 1 Human 9.6 pKi = 9.6 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 705 7 1 6 4.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+]6(CC5)CC[N+](C)(C)CC6)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956867 71231 0 None - 1 Human 9.6 pKi = 9.6 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 705 7 1 6 4.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+]6(CC5)CC[N+](C)(C)CC6)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963177 71231 0 None - 1 Human 9.6 pKi = 9.6 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 705 7 1 6 4.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+]6(CC5)CC[N+](C)(C)CC6)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
16105698 135810 0 None - 1 Human 9.6 pKi = 9.6 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 747 12 2 7 4.8 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@H](CCCN)[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL373459 135810 0 None - 1 Human 9.6 pKi = 9.6 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 747 12 2 7 4.8 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@H](CCCN)[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
16105694 141350 0 None - 1 Human 9.6 pKi = 9.6 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 732 12 1 6 5.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL386794 141350 0 None - 1 Human 9.6 pKi = 9.6 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 732 12 1 6 5.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
22008895 110056 0 None - 1 Guinea pig 9.5 pKi = 9.5 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 592 8 1 5 6.5 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(F)(F)F)cc4)c3C#N)c2n1 10.1016/s0960-894x(98)00736-7
CHEMBL325255 110056 0 None - 1 Guinea pig 9.5 pKi = 9.5 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 592 8 1 5 6.5 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(F)(F)F)cc4)c3C#N)c2n1 10.1016/s0960-894x(98)00736-7
10996140 67319 0 None 309 2 Rat 9.5 pKi = 9.5 Binding
Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesInhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranes
ChEMBL 710 17 4 9 4.1 CN(C)CCCN(C)CCCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(N/N=C(\S)NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL1907652 67319 0 None 309 2 Rat 9.5 pKi = 9.5 Binding
Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesInhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranes
ChEMBL 710 17 4 9 4.1 CN(C)CCCN(C)CCCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(N/N=C(\S)NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1021/jm0111088
57393062 71218 0 None - 1 Human 9.5 pKi = 9.5 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 706 11 1 7 4.8 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956869 71218 0 None - 1 Human 9.5 pKi = 9.5 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 706 11 1 7 4.8 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963151 71218 0 None - 1 Human 9.5 pKi = 9.5 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 706 11 1 7 4.8 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
16105727 83383 0 None - 1 Human 9.5 pKi = 9.5 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 718 12 3 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCN)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL220591 83383 0 None - 1 Human 9.5 pKi = 9.5 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 718 12 3 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCN)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
16105742 137613 0 None - 1 Human 9.5 pKi = 9.5 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 733 11 2 7 4.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL376866 137613 0 None - 1 Human 9.5 pKi = 9.5 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 733 11 2 7 4.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL3038094 209173 0 None 8 2 Human 9.4 pKi = 9.4 Binding
Binding affinity towards Bradykinin receptor B2 in human S34 clone cellsBinding affinity towards Bradykinin receptor B2 in human S34 clone cells
ChEMBL None None None NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N(CC(=O)N[C@@H](CCCN=C(N)N)C(=O)O)C1CCCC1 10.1021/jm950716i
CHEMBL3038095 209174 0 None 3 2 Human 9.4 pKi = 9.4 Binding
Binding affinity towards Bradykinin receptor B2 in human S34 clone cellsBinding affinity towards Bradykinin receptor B2 in human S34 clone cells
ChEMBL None None None NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N(CC(=O)N[C@@H](CCCN=C(N)N)C(=O)O)c1ccccc1 10.1021/jm950716i
57403505 71286 0 None - 1 Human 9.4 pKi = 9.4 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 675 7 1 6 5.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+]6(CCCCC6)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956865 71286 0 None - 1 Human 9.4 pKi = 9.4 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 675 7 1 6 5.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+]6(CCCCC6)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963559 71286 0 None - 1 Human 9.4 pKi = 9.4 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 675 7 1 6 5.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+]6(CCCCC6)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57394784 71308 0 None - 1 Human 9.4 pKi = 9.4 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 677 9 1 6 5.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(C[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956871 71308 0 None - 1 Human 9.4 pKi = 9.4 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 677 9 1 6 5.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(C[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963658 71308 0 None - 1 Human 9.4 pKi = 9.4 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 677 9 1 6 5.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(C[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
10463758 138329 0 None - 1 Human 9.4 pKi = 9.4 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 692 12 2 8 3.8 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL378189 138329 0 None - 1 Human 9.4 pKi = 9.4 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 692 12 2 8 3.8 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
10101294 139611 0 None -5 2 Human 9.4 pKi = 9.4 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 706 12 2 8 4.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL380273 139611 0 None -5 2 Human 9.4 pKi = 9.4 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 706 12 2 8 4.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
44412007 76843 1 None -1 2 Human 9.4 pKi = 9.4 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 710 12 4 7 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)N4CCC[C@@H]4C(=O)NCCCNC(=O)c4ccc(C(=N)N)cc4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL207939 76843 1 None -1 2 Human 9.4 pKi = 9.4 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 710 12 4 7 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)N4CCC[C@@H]4C(=O)NCCCNC(=O)c4ccc(C(=N)N)cc4)c3Cl)c2n1 10.1021/jm061143k
10396101 83911 0 None - 1 Human 9.4 pKi = 9.4 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 718 11 1 6 5.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL221683 83911 0 None - 1 Human 9.4 pKi = 9.4 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 718 11 1 6 5.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
10441167 96527 0 None - 1 Human 9.4 pKi = 9.4 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 732 11 3 6 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=N)NCCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL266493 96527 0 None - 1 Human 9.4 pKi = 9.4 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 732 11 3 6 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=N)NCCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
10101294 139611 0 None -5 2 Human 9.4 pKi = 9.4 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 706 12 2 8 4.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL380273 139611 0 None -5 2 Human 9.4 pKi = 9.4 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 706 12 2 8 4.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm061143k
10102296 161341 0 None - 1 Human 9.4 pKi = 9.4 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 690 9 1 6 4.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL415152 161341 0 None - 1 Human 9.4 pKi = 9.4 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 690 9 1 6 4.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
44316161 160957 0 None -1 2 Human 9.4 pKi = 9.4 Binding
Ability to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykininAbility to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykinin
ChEMBL 1043 25 12 16 -4.0 NCCCCC(N)C(=O)N[C@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1CC(O)C[C@H]1C(=O)NCC(=O)NC(Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N[C@@H]1CSc2ccccc2N(CC(=O)O)C1=O 10.1021/jm990961s
CHEMBL412824 160957 0 None -1 2 Human 9.4 pKi = 9.4 Binding
Ability to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykininAbility to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykinin
ChEMBL 1043 25 12 16 -4.0 NCCCCC(N)C(=O)N[C@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1CC(O)C[C@H]1C(=O)NCC(=O)NC(Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N[C@@H]1CSc2ccccc2N(CC(=O)O)C1=O 10.1021/jm990961s
122189902 122894 0 None 13489 2 Guinea pig 9.4 pKi = 9.4 Binding
Displacement of [3H]BK from B2R in guinea pig ileum membranes by liquid scintillation counting in based radioligand competition assayDisplacement of [3H]BK from B2R in guinea pig ileum membranes by liquid scintillation counting in based radioligand competition assay
ChEMBL 1304 30 18 17 -4.4 N=C(N)NCCC[C@H](NC(=O)C1CC2CCCCC2N1C(=O)[C@H]1Cc2ccccc2CN1C(=O)[C@H](CO)NC(=O)C(Cc1cccs1)NC(=O)CNC(=O)C1CC(O)CN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](N)CCCNC(=N)N)C(=O)O 10.1016/j.bmcl.2015.08.014
CHEMBL3616944 122894 0 None 13489 2 Guinea pig 9.4 pKi = 9.4 Binding
Displacement of [3H]BK from B2R in guinea pig ileum membranes by liquid scintillation counting in based radioligand competition assayDisplacement of [3H]BK from B2R in guinea pig ileum membranes by liquid scintillation counting in based radioligand competition assay
ChEMBL 1304 30 18 17 -4.4 N=C(N)NCCC[C@H](NC(=O)C1CC2CCCCC2N1C(=O)[C@H]1Cc2ccccc2CN1C(=O)[C@H](CO)NC(=O)C(Cc1cccs1)NC(=O)CNC(=O)C1CC(O)CN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](N)CCCNC(=N)N)C(=O)O 10.1016/j.bmcl.2015.08.014
3812 708 37 None -1 6 Rat 9.3 pKi = 9.3 Binding
Binding affinity against rat Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligandBinding affinity against rat Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligand
ChEMBL None None None None 10.1021/jm9901529
439201 708 37 None -1 6 Rat 9.3 pKi = 9.3 Binding
Binding affinity against rat Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligandBinding affinity against rat Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligand
ChEMBL None None None None 10.1021/jm9901529
649 708 37 None -1 6 Rat 9.3 pKi = 9.3 Binding
Binding affinity against rat Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligandBinding affinity against rat Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligand
ChEMBL None None None None 10.1021/jm9901529
CHEMBL406291 708 37 None -1 6 Rat 9.3 pKi = 9.3 Binding
Binding affinity against rat Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligandBinding affinity against rat Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligand
ChEMBL None None None None 10.1021/jm9901529
DB12126 708 37 None -1 6 Rat 9.3 pKi = 9.3 Binding
Binding affinity against rat Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligandBinding affinity against rat Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligand
ChEMBL None None None None 10.1021/jm9901529
5312119 709 4 None 1148 2 Rat 9.3 pKi = 9.3 Binding
Inhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranesInhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranes
ChEMBL 682 15 4 9 2.9 CN(CCN(C)C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(c(c1)[N+](=O)[O-])NNC(=S)NC(c1ccccc1)c1ccccc1 10.1021/jm991155o
680 709 4 None 1148 2 Rat 9.3 pKi = 9.3 Binding
Inhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranesInhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranes
ChEMBL 682 15 4 9 2.9 CN(CCN(C)C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(c(c1)[N+](=O)[O-])NNC(=S)NC(c1ccccc1)c1ccccc1 10.1021/jm991155o
CHEMBL308468 709 4 None 1148 2 Rat 9.3 pKi = 9.3 Binding
Inhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranesInhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranes
ChEMBL 682 15 4 9 2.9 CN(CCN(C)C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(c(c1)[N+](=O)[O-])NNC(=S)NC(c1ccccc1)c1ccccc1 10.1021/jm991155o
5312119 709 4 None 1148 2 Rat 9.3 pKi = 9.3 Binding
Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesInhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranes
ChEMBL 682 15 4 9 2.9 CN(CCN(C)C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(c(c1)[N+](=O)[O-])NNC(=S)NC(c1ccccc1)c1ccccc1 10.1021/jm0111088
680 709 4 None 1148 2 Rat 9.3 pKi = 9.3 Binding
Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesInhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranes
ChEMBL 682 15 4 9 2.9 CN(CCN(C)C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(c(c1)[N+](=O)[O-])NNC(=S)NC(c1ccccc1)c1ccccc1 10.1021/jm0111088
CHEMBL308468 709 4 None 1148 2 Rat 9.3 pKi = 9.3 Binding
Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesInhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranes
ChEMBL 682 15 4 9 2.9 CN(CCN(C)C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(c(c1)[N+](=O)[O-])NNC(=S)NC(c1ccccc1)c1ccccc1 10.1021/jm0111088
57401782 71227 0 None - 1 Human 9.3 pKi = 9.3 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 705 11 1 6 6.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956873 71227 0 None - 1 Human 9.3 pKi = 9.3 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 705 11 1 6 6.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963165 71227 0 None - 1 Human 9.3 pKi = 9.3 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 705 11 1 6 6.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
11600186 77879 0 None - 1 Human 9.3 pKi = 9.3 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 734 14 2 8 4.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)C[C@@H](N)CCCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL210788 77879 0 None - 1 Human 9.3 pKi = 9.3 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 734 14 2 8 4.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)C[C@@H](N)CCCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
16105701 83541 0 None - 1 Human 9.3 pKi = 9.3 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 762 12 3 8 3.6 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCNCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL220693 83541 0 None - 1 Human 9.3 pKi = 9.3 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 762 12 3 8 3.6 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCNCC4)c3Cl)c2n1 10.1021/jm061143k
10350966 84187 0 None - 1 Human 9.3 pKi = 9.3 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 746 13 1 6 6.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL222167 84187 0 None - 1 Human 9.3 pKi = 9.3 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 746 13 1 6 6.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL2370040 208018 0 None - 1 Guinea pig 9.3 pKi = 9.3 Binding
Binding affinity against [3H]bradykinin binding to bradykinin receptor B2 in guinea pig ileal membraneBinding affinity against [3H]bradykinin binding to bradykinin receptor B2 in guinea pig ileal membrane
ChEMBL None None None C[C@@](Cc1ccccc1)(NC(=O)CNC(=O)[C@@H]1C[C@H](O)CN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O 10.1021/jm00069a016
44337490 9063 0 None - 1 Human 9.2 pKi = 9.2 Binding
Affinity to human Bradykinin receptor B2 in CHO cell membranes determined by displacement of [3H]-NPC 17731Affinity to human Bradykinin receptor B2 in CHO cell membranes determined by displacement of [3H]-NPC 17731
ChEMBL 307 3 0 4 1.5 CC(=O)CN1CN(C2CCCCC2)C2(CCN(C)CC2)C1=O 10.1021/jm950676i
CHEMBL110188 9063 0 None - 1 Human 9.2 pKi = 9.2 Binding
Affinity to human Bradykinin receptor B2 in CHO cell membranes determined by displacement of [3H]-NPC 17731Affinity to human Bradykinin receptor B2 in CHO cell membranes determined by displacement of [3H]-NPC 17731
ChEMBL 307 3 0 4 1.5 CC(=O)CN1CN(C2CCCCC2)C2(CCN(C)CC2)C1=O 10.1021/jm950676i
10556495 167365 0 None 2398 2 Rat 9.2 pKi = 9.2 Binding
Inhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranesInhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranes
ChEMBL 682 15 4 9 2.9 CN(C)CCN(C)CCNC(=O)[C@H]1CCCN1S(=O)(=O)c1ccc(NNC(=S)NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1021/jm991155o
CHEMBL2112044 167365 0 None 2398 2 Rat 9.2 pKi = 9.2 Binding
Inhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranesInhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranes
ChEMBL 682 15 4 9 2.9 CN(C)CCN(C)CCNC(=O)[C@H]1CCCN1S(=O)(=O)c1ccc(NNC(=S)NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1021/jm991155o
CHEMBL431562 167365 0 None 2398 2 Rat 9.2 pKi = 9.2 Binding
Inhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranesInhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranes
ChEMBL 682 15 4 9 2.9 CN(C)CCN(C)CCNC(=O)[C@H]1CCCN1S(=O)(=O)c1ccc(NNC(=S)NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1021/jm991155o
10556495 167365 0 None 2398 2 Rat 9.2 pKi = 9.2 Binding
Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesInhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranes
ChEMBL 682 15 4 9 2.9 CN(C)CCN(C)CCNC(=O)[C@H]1CCCN1S(=O)(=O)c1ccc(NNC(=S)NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL2112044 167365 0 None 2398 2 Rat 9.2 pKi = 9.2 Binding
Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesInhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranes
ChEMBL 682 15 4 9 2.9 CN(C)CCN(C)CCNC(=O)[C@H]1CCCN1S(=O)(=O)c1ccc(NNC(=S)NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL431562 167365 0 None 2398 2 Rat 9.2 pKi = 9.2 Binding
Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesInhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranes
ChEMBL 682 15 4 9 2.9 CN(C)CCN(C)CCNC(=O)[C@H]1CCCN1S(=O)(=O)c1ccc(NNC(=S)NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1021/jm0111088
44340859 9933 0 None - 1 Guinea pig 9.2 pKi = 9.2 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 599 11 2 8 5.0 COc1ccc(N(C)C(=O)CNC(=O)/C=C/c2ccc(NC(C)=O)nc2)c(SC)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
CHEMBL115163 9933 0 None - 1 Guinea pig 9.2 pKi = 9.2 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 599 11 2 8 5.0 COc1ccc(N(C)C(=O)CNC(=O)/C=C/c2ccc(NC(C)=O)nc2)c(SC)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
57393060 71228 0 None - 1 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 661 7 1 6 5.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+]6(CCCC6)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956851 71228 0 None - 1 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 661 7 1 6 5.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+]6(CCCC6)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963174 71228 0 None - 1 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 661 7 1 6 5.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+]6(CCCC6)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57398328 71309 0 None - 1 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 719 12 1 6 6.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956874 71309 0 None - 1 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 719 12 1 6 6.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963659 71309 0 None - 1 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 719 12 1 6 6.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
10439868 75558 0 None -12 2 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 720 13 2 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)C[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL205093 75558 0 None -12 2 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 720 13 2 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)C[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
10463818 138729 0 None - 1 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 720 14 2 8 4.6 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)C[C@@H](N)CCCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL379063 138729 0 None - 1 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 720 14 2 8 4.6 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)C[C@@H](N)CCCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
10010104 140730 0 None -7 2 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 720 13 2 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL383167 140730 0 None -7 2 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 720 13 2 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
10439868 75558 0 None -12 2 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 720 13 2 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)C[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL205093 75558 0 None -12 2 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 720 13 2 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)C[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm061143k
10463883 83405 0 None -25 2 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 746 13 2 8 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[C@@H](N)CCCN(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL220596 83405 0 None -25 2 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 746 13 2 8 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[C@@H](N)CCCN(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
10079793 93673 0 None - 1 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 717 11 3 7 4.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=N)NCCCN(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL249235 93673 0 None - 1 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 717 11 3 7 4.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=N)NCCCN(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
16105729 136398 0 None - 1 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 761 13 2 7 5.2 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL374273 136398 0 None - 1 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 761 13 2 7 5.2 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
10079797 137059 0 None - 1 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 718 12 3 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[C@@H](N)CCCN)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL375576 137059 0 None - 1 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 718 12 3 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[C@@H](N)CCCN)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
10032895 137093 0 None -7 2 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 734 13 5 8 3.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCCNC(=N)N)CC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL375820 137093 0 None -7 2 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 734 13 5 8 3.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCCNC(=N)N)CC4)c3Cl)c2n1 10.1021/jm061143k
10010104 140730 0 None -7 2 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 720 13 2 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL383167 140730 0 None -7 2 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 720 13 2 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm061143k
3812 708 37 None 1 6 Human 9.2 pKi = 9.2 Binding
Binding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligandBinding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligand
ChEMBL None None None None 10.1021/jm9901529
439201 708 37 None 1 6 Human 9.2 pKi = 9.2 Binding
Binding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligandBinding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligand
ChEMBL None None None None 10.1021/jm9901529
649 708 37 None 1 6 Human 9.2 pKi = 9.2 Binding
Binding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligandBinding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligand
ChEMBL None None None None 10.1021/jm9901529
CHEMBL406291 708 37 None 1 6 Human 9.2 pKi = 9.2 Binding
Binding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligandBinding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligand
ChEMBL None None None None 10.1021/jm9901529
DB12126 708 37 None 1 6 Human 9.2 pKi = 9.2 Binding
Binding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligandBinding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligand
ChEMBL None None None None 10.1021/jm9901529
3812 708 37 None 1 6 Human 9.2 pKi = 9.2 Binding
Binding affinity towards Bradykinin receptor B2 in human S34 clone cellsBinding affinity towards Bradykinin receptor B2 in human S34 clone cells
ChEMBL None None None None 10.1021/jm950716i
439201 708 37 None 1 6 Human 9.2 pKi = 9.2 Binding
Binding affinity towards Bradykinin receptor B2 in human S34 clone cellsBinding affinity towards Bradykinin receptor B2 in human S34 clone cells
ChEMBL None None None None 10.1021/jm950716i
649 708 37 None 1 6 Human 9.2 pKi = 9.2 Binding
Binding affinity towards Bradykinin receptor B2 in human S34 clone cellsBinding affinity towards Bradykinin receptor B2 in human S34 clone cells
ChEMBL None None None None 10.1021/jm950716i
CHEMBL406291 708 37 None 1 6 Human 9.2 pKi = 9.2 Binding
Binding affinity towards Bradykinin receptor B2 in human S34 clone cellsBinding affinity towards Bradykinin receptor B2 in human S34 clone cells
ChEMBL None None None None 10.1021/jm950716i
DB12126 708 37 None 1 6 Human 9.2 pKi = 9.2 Binding
Binding affinity towards Bradykinin receptor B2 in human S34 clone cellsBinding affinity towards Bradykinin receptor B2 in human S34 clone cells
ChEMBL None None None None 10.1021/jm950716i
71450888 78368 0 None 8 2 Human 9.2 pKi = 9.2 Binding
Binding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligandBinding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligand
ChEMBL 1228 31 16 18 -6.5 NC(N)=NCCC[C@H](NC(=O)CN1C(=O)[C@H](NC(=O)[C@H](CO)NC(=O)[C@H](Cc2cccs2)NC(=O)CNC(=O)[C@@H]2CC(O)CN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)CSc2ccccc21)C(=O)O 10.1021/jm9901529
CHEMBL2112698 78368 0 None 8 2 Human 9.2 pKi = 9.2 Binding
Binding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligandBinding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligand
ChEMBL 1228 31 16 18 -6.5 NC(N)=NCCC[C@H](NC(=O)CN1C(=O)[C@H](NC(=O)[C@H](CO)NC(=O)[C@H](Cc2cccs2)NC(=O)CNC(=O)[C@@H]2CC(O)CN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)CSc2ccccc21)C(=O)O 10.1021/jm9901529
44355233 166092 0 None - 1 Human 9.2 pKi = 9.2 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1228 31 16 18 -6.5 NC(N)=NCCC[C@H](NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1CC(O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)NC1CSc2ccccc2N(CC(=O)N[C@H](CCCN=C(N)N)C(=O)O)C1=O 10.1021/jm9901531
CHEMBL428148 166092 0 None - 1 Human 9.2 pKi = 9.2 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1228 31 16 18 -6.5 NC(N)=NCCC[C@H](NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1CC(O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)NC1CSc2ccccc2N(CC(=O)N[C@H](CCCN=C(N)N)C(=O)O)C1=O 10.1021/jm9901531
70683601 74154 0 None - 1 Guinea pig 9.1 pKi = 9.1 Binding
In vitro binding affinity against bradykinin receptor B2 from guinea pig ileum.In vitro binding affinity against bradykinin receptor B2 from guinea pig ileum.
ChEMBL 1270 33 15 15 -4.3 NC(N)=NCCC[C@H](NC(=O)[C@@H]1CC2CCCCC2N1C(=O)[C@@H](Cc1ccccc1)NC(=O)[C@H](CO)NC(=O)[C@H](Cc1ccccc1)NC(=O)CNC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C(=O)O 10.1021/jm00062a018
CHEMBL2028979 74154 0 None - 1 Guinea pig 9.1 pKi = 9.1 Binding
In vitro binding affinity against bradykinin receptor B2 from guinea pig ileum.In vitro binding affinity against bradykinin receptor B2 from guinea pig ileum.
ChEMBL 1270 33 15 15 -4.3 NC(N)=NCCC[C@H](NC(=O)[C@@H]1CC2CCCCC2N1C(=O)[C@@H](Cc1ccccc1)NC(=O)[C@H](CO)NC(=O)[C@H](Cc1ccccc1)NC(=O)CNC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C(=O)O 10.1021/jm00062a018
9987299 78176 0 None 13 2 Human 9.1 pKi = 9.1 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 706 14 4 9 3.3 CN(C)CCCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(NNC(=O)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL2112283 78176 0 None 13 2 Human 9.1 pKi = 9.1 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 706 14 4 9 3.3 CN(C)CCCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(NNC(=O)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
57401780 71220 0 None - 1 Human 9.1 pKi = 9.1 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 691 10 1 6 5.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956872 71220 0 None - 1 Human 9.1 pKi = 9.1 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 691 10 1 6 5.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963153 71220 0 None - 1 Human 9.1 pKi = 9.1 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 691 10 1 6 5.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57391277 71307 0 None - 1 Human 9.1 pKi = 9.1 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 692 10 1 7 4.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(CC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956868 71307 0 None - 1 Human 9.1 pKi = 9.1 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 692 10 1 7 4.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(CC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963652 71307 0 None - 1 Human 9.1 pKi = 9.1 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 692 10 1 7 4.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(CC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
44412007 76843 1 None -1 2 Human 9.1 pKi = 9.1 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 710 12 4 7 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)N4CCC[C@@H]4C(=O)NCCCNC(=O)c4ccc(C(=N)N)cc4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL207939 76843 1 None -1 2 Human 9.1 pKi = 9.1 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 710 12 4 7 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)N4CCC[C@@H]4C(=O)NCCCNC(=O)c4ccc(C(=N)N)cc4)c3Cl)c2n1 10.1021/jm060137l
10102599 140860 0 None - 1 Human 9.1 pKi = 9.1 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 706 13 2 8 4.2 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)C[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL383989 140860 0 None - 1 Human 9.1 pKi = 9.1 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 706 13 2 8 4.2 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)C[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
10418701 96642 0 None - 1 Human 9.1 pKi = 9.1 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 760 13 5 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[C@@H](N)CCCNC(=N)N)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL267493 96642 0 None - 1 Human 9.1 pKi = 9.1 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 760 13 5 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[C@@H](N)CCCNC(=N)N)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
122189902 122894 0 None 13489 2 Guinea pig 9.0 pKi = 9 Binding
Binding affinity to B2R in guinea pig ileum membranesBinding affinity to B2R in guinea pig ileum membranes
ChEMBL 1304 30 18 17 -4.4 N=C(N)NCCC[C@H](NC(=O)C1CC2CCCCC2N1C(=O)[C@H]1Cc2ccccc2CN1C(=O)[C@H](CO)NC(=O)C(Cc1cccs1)NC(=O)CNC(=O)C1CC(O)CN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](N)CCCNC(=N)N)C(=O)O 10.1016/j.bmcl.2015.08.014
CHEMBL3616944 122894 0 None 13489 2 Guinea pig 9.0 pKi = 9 Binding
Binding affinity to B2R in guinea pig ileum membranesBinding affinity to B2R in guinea pig ileum membranes
ChEMBL 1304 30 18 17 -4.4 N=C(N)NCCC[C@H](NC(=O)C1CC2CCCCC2N1C(=O)[C@H]1Cc2ccccc2CN1C(=O)[C@H](CO)NC(=O)C(Cc1cccs1)NC(=O)CNC(=O)C1CC(O)CN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](N)CCCNC(=N)N)C(=O)O 10.1016/j.bmcl.2015.08.014
57401776 71217 0 None - 1 Human 9.0 pKi = 9 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 690 7 1 7 4.2 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+]6(CCN(C)CC6)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956866 71217 0 None - 1 Human 9.0 pKi = 9 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 690 7 1 7 4.2 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+]6(CCN(C)CC6)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963150 71217 0 None - 1 Human 9.0 pKi = 9 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 690 7 1 7 4.2 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+]6(CCN(C)CC6)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
10349694 76215 0 None - 1 Human 9.0 pKi = 9 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 691 13 4 7 4.7 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=N)NCCCCCCN)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL206312 76215 0 None - 1 Human 9.0 pKi = 9 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 691 13 4 7 4.7 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=N)NCCCCCCN)CC4)c3Cl)c2n1 10.1021/jm060137l
10418252 138349 0 None - 1 Human 9.0 pKi = 9 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 663 10 4 7 3.8 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=N)NCCCN)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL378237 138349 0 None - 1 Human 9.0 pKi = 9 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 663 10 4 7 3.8 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=N)NCCCN)CC4)c3Cl)c2n1 10.1021/jm060137l
10373970 137076 0 None -5 2 Human 9.0 pKi = 9 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 760 13 5 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCNC(=N)N)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL375689 137076 0 None -5 2 Human 9.0 pKi = 9 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 760 13 5 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCNC(=N)N)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
3812 708 37 None 1 6 Human 9.0 pKi = 9.0 Binding
Displacement of [3H]Bradykinin from human recombinant bradykinin B2 receptor expressed in CHEM1 cells after 60 minsDisplacement of [3H]Bradykinin from human recombinant bradykinin B2 receptor expressed in CHEM1 cells after 60 mins
ChEMBL None None None None 10.1016/j.bmcl.2013.01.025
439201 708 37 None 1 6 Human 9.0 pKi = 9.0 Binding
Displacement of [3H]Bradykinin from human recombinant bradykinin B2 receptor expressed in CHEM1 cells after 60 minsDisplacement of [3H]Bradykinin from human recombinant bradykinin B2 receptor expressed in CHEM1 cells after 60 mins
ChEMBL None None None None 10.1016/j.bmcl.2013.01.025
649 708 37 None 1 6 Human 9.0 pKi = 9.0 Binding
Displacement of [3H]Bradykinin from human recombinant bradykinin B2 receptor expressed in CHEM1 cells after 60 minsDisplacement of [3H]Bradykinin from human recombinant bradykinin B2 receptor expressed in CHEM1 cells after 60 mins
ChEMBL None None None None 10.1016/j.bmcl.2013.01.025
CHEMBL406291 708 37 None 1 6 Human 9.0 pKi = 9.0 Binding
Displacement of [3H]Bradykinin from human recombinant bradykinin B2 receptor expressed in CHEM1 cells after 60 minsDisplacement of [3H]Bradykinin from human recombinant bradykinin B2 receptor expressed in CHEM1 cells after 60 mins
ChEMBL None None None None 10.1016/j.bmcl.2013.01.025
DB12126 708 37 None 1 6 Human 9.0 pKi = 9.0 Binding
Displacement of [3H]Bradykinin from human recombinant bradykinin B2 receptor expressed in CHEM1 cells after 60 minsDisplacement of [3H]Bradykinin from human recombinant bradykinin B2 receptor expressed in CHEM1 cells after 60 mins
ChEMBL None None None None 10.1016/j.bmcl.2013.01.025
10055774 76335 0 None - 1 Human 8.9 pKi = 8.9 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 734 14 4 8 3.3 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)C[C@@H](N)CCCCN=C(N)N)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL206474 76335 0 None - 1 Human 8.9 pKi = 8.9 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 734 14 4 8 3.3 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)C[C@@H](N)CCCCN=C(N)N)CC4)c3Cl)c2n1 10.1021/jm060137l
10441194 84185 0 None - 1 Human 8.9 pKi = 8.9 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 745 13 4 7 5.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCCNC(=N)N)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL222156 84185 0 None - 1 Human 8.9 pKi = 8.9 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 745 13 4 7 5.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCCNC(=N)N)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
44341039 9405 0 None - 1 Guinea pig 8.9 pKi = 8.9 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 597 9 1 5 6.6 COc1ccc(N(C)C(=O)CNC(=O)/C=C/c2ccc(C(F)(F)F)cc2)c(Cl)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
CHEMBL112140 9405 0 None - 1 Guinea pig 8.9 pKi = 8.9 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 597 9 1 5 6.6 COc1ccc(N(C)C(=O)CNC(=O)/C=C/c2ccc(C(F)(F)F)cc2)c(Cl)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
18941145 9854 0 None - 1 Guinea pig 8.9 pKi = 8.9 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 569 9 1 6 6.3 COc1cccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4sc(C)nc34)c2Cl)c1 10.1016/s0960-894x(98)00736-7
CHEMBL114732 9854 0 None - 1 Guinea pig 8.9 pKi = 8.9 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 569 9 1 6 6.3 COc1cccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4sc(C)nc34)c2Cl)c1 10.1016/s0960-894x(98)00736-7
22008892 109660 0 None - 1 Guinea pig 8.9 pKi = 8.9 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 561 8 1 4 6.6 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(F)(F)F)cc4)c3C)c2n1 10.1016/s0960-894x(98)00736-7
CHEMBL323693 109660 0 None - 1 Guinea pig 8.9 pKi = 8.9 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 561 8 1 4 6.6 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(F)(F)F)cc4)c3C)c2n1 10.1016/s0960-894x(98)00736-7
11136263 78161 0 None 43 2 Human 8.8 pKi = 8.8 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 704 13 4 10 3.9 CN(C)CCN(C)CCNC(=O)c1cccn1S(=O)(=O)c1ccc(N/N=C(\S)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL2112221 78161 0 None 43 2 Human 8.8 pKi = 8.8 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 704 13 4 10 3.9 CN(C)CCN(C)CCNC(=O)c1cccn1S(=O)(=O)c1ccc(N/N=C(\S)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL2370010 208012 0 None - 1 Guinea pig 8.8 pKi = 8.8 Binding
Binding affinity against [3H]bradykinin binding to bradykinin receptor B2 in guinea pig ileal membraneBinding affinity against [3H]bradykinin binding to bradykinin receptor B2 in guinea pig ileal membrane
ChEMBL None None None NC(N)=NCCC[C@H](NC(=O)[C@@H]1C2CCCCC2CN1C(=O)[C@@H]1Cc2ccccc2CN1C(=O)[C@H](CO)NC(=O)[C@@H]1CSSC[C@H](NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N2CCC[C@H]2C(=O)NCC(=O)N1)C(=O)O 10.1021/jm00069a016
10418495 77507 0 None - 1 Human 8.8 pKi = 8.8 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 649 10 4 7 3.5 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=N)NCCCN)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL209346 77507 0 None - 1 Human 8.8 pKi = 8.8 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 649 10 4 7 3.5 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=N)NCCCN)CC4)c3Cl)c2n1 10.1021/jm060137l
10260476 77628 0 None - 1 Human 8.8 pKi = 8.8 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 691 14 3 7 4.5 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(CCCCCCN=C(N)N)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL209719 77628 0 None - 1 Human 8.8 pKi = 8.8 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 691 14 3 7 4.5 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(CCCCCCN=C(N)N)CC4)c3Cl)c2n1 10.1021/jm060137l
9988753 83404 0 None -7 2 Human 8.8 pKi = 8.8 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 746 13 2 8 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCN(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL220595 83404 0 None -7 2 Human 8.8 pKi = 8.8 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 746 13 2 8 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCN(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
10788314 119449 0 None - 1 Rat 8.7 pKi = 8.7 Binding
Inhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranesInhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranes
ChEMBL 421 7 4 5 3.7 NC(=O)c1ccc(N/N=C(/S)NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1021/jm991155o
CHEMBL349817 119449 0 None - 1 Rat 8.7 pKi = 8.7 Binding
Inhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranesInhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranes
ChEMBL 421 7 4 5 3.7 NC(=O)c1ccc(N/N=C(/S)NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1021/jm991155o
18941160 9807 0 None - 1 Guinea pig 8.7 pKi = 8.7 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 553 8 1 5 6.6 Cc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4sc(C)nc34)c2Cl)cc1 10.1016/s0960-894x(98)00736-7
CHEMBL114401 9807 0 None - 1 Guinea pig 8.7 pKi = 8.7 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 553 8 1 5 6.6 Cc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4sc(C)nc34)c2Cl)cc1 10.1016/s0960-894x(98)00736-7
10010669 76443 0 None - 1 Human 8.7 pKi = 8.7 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 706 13 2 8 4.2 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL206938 76443 0 None - 1 Human 8.7 pKi = 8.7 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 706 13 2 8 4.2 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
44276460 98769 0 None - 1 Human 8.0 pKi = 8 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 610 9 0 6 7.6 CCn1c(CC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)ccc1C(=O)c1ccc(C#N)cc1 10.1016/s0960-894x(03)00104-5
CHEMBL281706 98769 0 None - 1 Human 8.0 pKi = 8 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 610 9 0 6 7.6 CCn1c(CC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)ccc1C(=O)c1ccc(C#N)cc1 10.1016/s0960-894x(03)00104-5
11527838 77940 0 None - 1 Human 8.0 pKi = 8 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 635 10 3 7 2.9 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(CCN=C(N)N)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL211017 77940 0 None - 1 Human 8.0 pKi = 8 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 635 10 3 7 2.9 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(CCN=C(N)N)CC4)c3Cl)c2n1 10.1021/jm060137l
11513471 138105 0 None - 1 Human 8.0 pKi = 8 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 748 14 2 8 4.4 CC(=O)N[C@@H](CCCCN(C)C)C(=O)N1CCN(C(=O)C(C)(C)NS(=O)(=O)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)CC1 10.1021/jm060137l
CHEMBL377612 138105 0 None - 1 Human 8.0 pKi = 8 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 748 14 2 8 4.4 CC(=O)N[C@@H](CCCCN(C)C)C(=O)N1CCN(C(=O)C(C)(C)NS(=O)(=O)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)CC1 10.1021/jm060137l
9987299 78176 0 None -13 2 Rat 8.0 pKi = 8.0 Binding
Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesInhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranes
ChEMBL 706 14 4 9 3.3 CN(C)CCCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(NNC(=O)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL2112283 78176 0 None -13 2 Rat 8.0 pKi = 8.0 Binding
Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesInhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranes
ChEMBL 706 14 4 9 3.3 CN(C)CCCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(NNC(=O)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
44410425 96678 0 None - 1 Human 7.0 pKi = 7 Binding
Binding affinity to human bradykinin B2 receptor transfected in CHO cellsBinding affinity to human bradykinin B2 receptor transfected in CHO cells
ChEMBL 1332 32 16 17 -4.3 NC(N)=NCCC[C@H](NC(=O)[C@@H]1CC2(CCCC2)C2CCC[C@](Cc3ccccc3)(NC(=O)[C@H](CO)NC(=O)[C@H](Cc3cccs3)NC(=O)CNC(=O)[C@@H]3CC(O)CN3C(=O)[C@@H]3CCCN3C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N21)C(=O)O 10.1016/j.bmcl.2006.01.125
CHEMBL267822 96678 0 None - 1 Human 7.0 pKi = 7 Binding
Binding affinity to human bradykinin B2 receptor transfected in CHO cellsBinding affinity to human bradykinin B2 receptor transfected in CHO cells
ChEMBL 1332 32 16 17 -4.3 NC(N)=NCCC[C@H](NC(=O)[C@@H]1CC2(CCCC2)C2CCC[C@](Cc3ccccc3)(NC(=O)[C@H](CO)NC(=O)[C@H](Cc3cccs3)NC(=O)CNC(=O)[C@@H]3CC(O)CN3C(=O)[C@@H]3CCCN3C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N21)C(=O)O 10.1016/j.bmcl.2006.01.125
11699718 76719 0 None - 1 Human 7.0 pKi = 7 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 524 9 3 6 3.6 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCN)c3Cl)c2n1 10.1021/jm060137l
CHEMBL207465 76719 0 None - 1 Human 7.0 pKi = 7 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 524 9 3 6 3.6 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCN)c3Cl)c2n1 10.1021/jm060137l
11513163 77408 0 None - 1 Human 7.0 pKi = 7 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 578 7 2 6 4.7 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCCNCCC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL209130 77408 0 None - 1 Human 7.0 pKi = 7 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 578 7 2 6 4.7 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCCNCCC4)c3Cl)c2n1 10.1021/jm060137l
44320402 14218 0 None - 1 Human 6.0 pKi = 6 Binding
Binding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligandBinding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligand
ChEMBL 713 18 3 2 11.2 CCCC[PH](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2cccc3ccccc23)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1021/jm00069a021
CHEMBL1162589 14218 0 None - 1 Human 6.0 pKi = 6 Binding
Binding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligandBinding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligand
ChEMBL 713 18 3 2 11.2 CCCC[PH](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2cccc3ccccc23)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1021/jm00069a021
CHEMBL1200092 14218 0 None - 1 Human 6.0 pKi = 6 Binding
Binding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligandBinding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligand
ChEMBL 713 18 3 2 11.2 CCCC[PH](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2cccc3ccccc23)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1021/jm00069a021
44347466 14206 0 None - 1 Human 6.0 pKi = 6 Binding
Tested for binding affinity against human IMR-90 Bradykinin receptor B2Tested for binding affinity against human IMR-90 Bradykinin receptor B2
ChEMBL 836 20 3 3 11.4 CCCC[PH](CCCC)(CCCC)Cc1ccc(NC(=O)C2Cc3ccccc3CN2C(=O)[C@H](CCc2ccccc2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00037-T
CHEMBL1162799 14206 0 None - 1 Human 6.0 pKi = 6 Binding
Tested for binding affinity against human IMR-90 Bradykinin receptor B2Tested for binding affinity against human IMR-90 Bradykinin receptor B2
ChEMBL 836 20 3 3 11.4 CCCC[PH](CCCC)(CCCC)Cc1ccc(NC(=O)C2Cc3ccccc3CN2C(=O)[C@H](CCc2ccccc2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00037-T
CHEMBL1200034 14206 0 None - 1 Human 6.0 pKi = 6 Binding
Tested for binding affinity against human IMR-90 Bradykinin receptor B2Tested for binding affinity against human IMR-90 Bradykinin receptor B2
ChEMBL 836 20 3 3 11.4 CCCC[PH](CCCC)(CCCC)Cc1ccc(NC(=O)C2Cc3ccccc3CN2C(=O)[C@H](CCc2ccccc2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00037-T
44347552 12057 0 None - 1 Human 5.0 pKi = 5 Binding
Tested for binding affinity against human IMR-90 Bradykinin receptor B2Tested for binding affinity against human IMR-90 Bradykinin receptor B2
ChEMBL 613 17 1 2 9.5 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)C2Cc3ccccc3CN2C(=O)CCCc2ccccc2)cc1 10.1016/0960-894X(95)00037-T
CHEMBL1184218 12057 0 None - 1 Human 5.0 pKi = 5 Binding
Tested for binding affinity against human IMR-90 Bradykinin receptor B2Tested for binding affinity against human IMR-90 Bradykinin receptor B2
ChEMBL 613 17 1 2 9.5 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)C2Cc3ccccc3CN2C(=O)CCCc2ccccc2)cc1 10.1016/0960-894X(95)00037-T
CHEMBL339723 12057 0 None - 1 Human 5.0 pKi = 5 Binding
Tested for binding affinity against human IMR-90 Bradykinin receptor B2Tested for binding affinity against human IMR-90 Bradykinin receptor B2
ChEMBL 613 17 1 2 9.5 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)C2Cc3ccccc3CN2C(=O)CCCc2ccccc2)cc1 10.1016/0960-894X(95)00037-T
2324360 56882 12 None - 1 Rat 4.0 pKi = 4 Binding
Inhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranesInhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranes
ChEMBL 257 4 3 2 2.7 S=C(NCc1ccccc1)NNc1ccccc1 10.1021/jm991155o
CHEMBL164968 56882 12 None - 1 Rat 4.0 pKi = 4 Binding
Inhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranesInhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranes
ChEMBL 257 4 3 2 2.7 S=C(NCc1ccccc1)NNc1ccccc1 10.1021/jm991155o
44215785 95077 0 None - 1 Human 7.0 pKi = 7.0 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 557 8 0 7 5.8 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(C#N)nc5)n4C)c3C)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL25751 95077 0 None - 1 Human 7.0 pKi = 7.0 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 557 8 0 7 5.8 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(C#N)nc5)n4C)c3C)c2n1 10.1016/s0960-894x(03)00104-5
101653258 13655 0 None - 1 Human 6.0 pKi = 6.0 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 712 18 3 2 11.5 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2cccc3ccccc23)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
44320402 13655 0 None - 1 Human 6.0 pKi = 6.0 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 712 18 3 2 11.5 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2cccc3ccccc23)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL1195447 13655 0 None - 1 Human 6.0 pKi = 6.0 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 712 18 3 2 11.5 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2cccc3ccccc23)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL554592 13655 0 None - 1 Human 6.0 pKi = 6.0 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 712 18 3 2 11.5 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2cccc3ccccc23)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
44355241 168148 0 None - 1 Human 6.0 pKi = 6.0 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1134 31 16 17 -8.4 NC(N)=NCCC[C@H](NC(=O)CN1CC[C@H](NC(=O)[C@H](CO)NC(=O)[C@H](Cc2cccs2)NC(=O)CNC(=O)[C@@H]2CC(O)CN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C1=O)C(=O)O 10.1021/jm9901531
CHEMBL436963 168148 0 None - 1 Human 6.0 pKi = 6.0 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1134 31 16 17 -8.4 NC(N)=NCCC[C@H](NC(=O)CN1CC[C@H](NC(=O)[C@H](CO)NC(=O)[C@H](Cc2cccs2)NC(=O)CNC(=O)[C@@H]2CC(O)CN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C1=O)C(=O)O 10.1021/jm9901531
118719116 114932 0 None - 1 Human 6.0 pKi = 6.0 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1285 32 16 18 -5.8 NC(N)=NCCC[C@H](NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)NC1N=C(c2ccccc2)c2ccccc2N(CC(=O)N[C@H](CCCN=C(N)N)C(=O)O)C1=O 10.1021/jm9901531
CHEMBL3350763 114932 0 None - 1 Human 6.0 pKi = 6.0 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1285 32 16 18 -5.8 NC(N)=NCCC[C@H](NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)NC1N=C(c2ccccc2)c2ccccc2N(CC(=O)N[C@H](CCCN=C(N)N)C(=O)O)C1=O 10.1021/jm9901531
44346315 13714 0 None - 1 Human 7.0 pKi = 7.0 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 771 12 3 2 10.1 O=C(Nc1ccc(C[P+](c2ccccc2)(c2ccccc2)c2ccccc2)cc1)[C@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1016/0960-894X(95)00035-R
CHEMBL1195864 13714 0 None - 1 Human 7.0 pKi = 7.0 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 771 12 3 2 10.1 O=C(Nc1ccc(C[P+](c2ccccc2)(c2ccccc2)c2ccccc2)cc1)[C@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1016/0960-894X(95)00035-R
CHEMBL555493 13714 0 None - 1 Human 7.0 pKi = 7.0 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 771 12 3 2 10.1 O=C(Nc1ccc(C[P+](c2ccccc2)(c2ccccc2)c2ccccc2)cc1)[C@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1016/0960-894X(95)00035-R
44346282 12227 0 None - 1 Human 6.0 pKi = 6.0 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 712 30 1 1 15.1 CCCCC[P+](CCCCC)(CCCCC)Cc1ccc(NC(=O)c2ccc(C[P+](CCCCC)(CCCCC)CCCCC)cc2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL1185367 12227 0 None - 1 Human 6.0 pKi = 6.0 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 712 30 1 1 15.1 CCCCC[P+](CCCCC)(CCCCC)Cc1ccc(NC(=O)c2ccc(C[P+](CCCCC)(CCCCC)CCCCC)cc2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL409910 12227 0 None - 1 Human 6.0 pKi = 6.0 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 712 30 1 1 15.1 CCCCC[P+](CCCCC)(CCCCC)Cc1ccc(NC(=O)c2ccc(C[P+](CCCCC)(CCCCC)CCCCC)cc2)cc1 10.1016/0960-894X(95)00035-R
9919335 106090 1 None -489 2 Human 4.9 pKi = 4.9 Binding
Binding affinity towards human cloned B2 receptor was determined using [3H]BK as radioligandBinding affinity towards human cloned B2 receptor was determined using [3H]BK as radioligand
ChEMBL 922 22 9 13 -2.1 NCCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC2(CC1)C(=O)N(CC(=O)N[C@@H](CO)C(=O)N[C@@H]1CSc3ccccc3N(CC(=O)O)C1=O)CN2CCc1ccccc1 10.1021/jm990962k
CHEMBL3142392 106090 1 None -489 2 Human 4.9 pKi = 4.9 Binding
Binding affinity towards human cloned B2 receptor was determined using [3H]BK as radioligandBinding affinity towards human cloned B2 receptor was determined using [3H]BK as radioligand
ChEMBL 922 22 9 13 -2.1 NCCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC2(CC1)C(=O)N(CC(=O)N[C@@H](CO)C(=O)N[C@@H]1CSc3ccccc3N(CC(=O)O)C1=O)CN2CCc1ccccc1 10.1021/jm990962k
11050762 67318 0 None -5248 2 Human 6.9 pKi = 6.9 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 696 16 4 9 3.7 CN(C)CCCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(N/N=C(\S)NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL1907651 67318 0 None -5248 2 Human 6.9 pKi = 6.9 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 696 16 4 9 3.7 CN(C)CCCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(N/N=C(\S)NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1021/jm0111088
71456185 78105 0 None - 1 Human 4.9 pKi = 4.9 Binding
Binding affinity towards human bradykinin B2 receptor (membranes from Cos-7 cells expressing human B2 receptor) using [3H]-BK as radioligandBinding affinity towards human bradykinin B2 receptor (membranes from Cos-7 cells expressing human B2 receptor) using [3H]-BK as radioligand
ChEMBL 473 6 3 3 5.0 N=C(N)Nc1cccc(CN2C(=O)[C@@H](Cc3ccccc3)N=C(c3ccccc3)c3ccccc32)c1 10.1016/s0960-894x(99)00015-3
CHEMBL2111994 78105 0 None - 1 Human 4.9 pKi = 4.9 Binding
Binding affinity towards human bradykinin B2 receptor (membranes from Cos-7 cells expressing human B2 receptor) using [3H]-BK as radioligandBinding affinity towards human bradykinin B2 receptor (membranes from Cos-7 cells expressing human B2 receptor) using [3H]-BK as radioligand
ChEMBL 473 6 3 3 5.0 N=C(N)Nc1cccc(CN2C(=O)[C@@H](Cc3ccccc3)N=C(c3ccccc3)c3ccccc32)c1 10.1016/s0960-894x(99)00015-3
CHEMBL3038100 209178 0 None -14 2 Human 7.9 pKi = 7.9 Binding
Binding affinity towards Bradykinin receptor B2 in human S34 clone cellsBinding affinity towards Bradykinin receptor B2 in human S34 clone cells
ChEMBL None None None N=C(N)NCCCCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N1CCC[C@@H]1C(=O)N1C[C@@H](O)C[C@@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N(CC(=O)N[C@@H](CCCNC(=N)N)C(=O)O)C1CCCCC1 10.1021/jm950716i
CHEMBL2372276 208451 0 None 3 3 Human 7.9 pKi = 7.9 Binding
Binding affinity towards Bradykinin receptor B2 in human S34 clone cellsBinding affinity towards Bradykinin receptor B2 in human S34 clone cells
ChEMBL None None None NC(N)=NCCC[C@H](N)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1CCC[C@H]1C(=O)NCC(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](CO)C(=O)[C@@H]1CCCN1C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@H](CCCN=C(N)N)C(=O)O 10.1021/jm950716i
1016 3678 75 None -46 35 Human 4.9 pKi = 4.9 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
ChEMBL 371 8 0 2 6.0 CC/C(=C(\c1ccccc1)/c1ccc(cc1)OCCN(C)C)/c1ccccc1 nan
2561 3678 75 None -46 35 Human 4.9 pKi = 4.9 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
ChEMBL 371 8 0 2 6.0 CC/C(=C(\c1ccccc1)/c1ccc(cc1)OCCN(C)C)/c1ccccc1 nan
2733526 3678 75 None -46 35 Human 4.9 pKi = 4.9 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
ChEMBL 371 8 0 2 6.0 CC/C(=C(\c1ccccc1)/c1ccc(cc1)OCCN(C)C)/c1ccccc1 nan
5384 3678 75 None -46 35 Human 4.9 pKi = 4.9 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
ChEMBL 371 8 0 2 6.0 CC/C(=C(\c1ccccc1)/c1ccc(cc1)OCCN(C)C)/c1ccccc1 nan
CHEMBL83 3678 75 None -46 35 Human 4.9 pKi = 4.9 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
ChEMBL 371 8 0 2 6.0 CC/C(=C(\c1ccccc1)/c1ccc(cc1)OCCN(C)C)/c1ccccc1 nan
DB00675 3678 75 None -46 35 Human 4.9 pKi = 4.9 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
ChEMBL 371 8 0 2 6.0 CC/C(=C(\c1ccccc1)/c1ccc(cc1)OCCN(C)C)/c1ccccc1 nan
22288574 99104 0 None - 1 Human 6.9 pKi = 6.9 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 606 8 0 6 7.3 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(Cl)nc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL283824 99104 0 None - 1 Human 6.9 pKi = 6.9 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 606 8 0 6 7.3 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(Cl)nc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
11549560 77861 0 None - 1 Human 6.9 pKi = 6.9 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 671 14 4 7 4.9 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCNCc4ccc(C(N)=O)cc4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL210708 77861 0 None - 1 Human 6.9 pKi = 6.9 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 671 14 4 7 4.9 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCNCc4ccc(C(N)=O)cc4)c3Cl)c2n1 10.1021/jm060137l
44276438 98973 0 None - 1 Human 6.9 pKi = 6.9 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 580 9 0 6 7.0 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)CCc4ccc(C(=O)c5ccc(Cl)nc5)n4C)c3C)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL282981 98973 0 None - 1 Human 6.9 pKi = 6.9 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 580 9 0 6 7.0 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)CCc4ccc(C(=O)c5ccc(Cl)nc5)n4C)c3C)c2n1 10.1016/s0960-894x(03)00104-5
44355038 161133 0 None - 1 Human 7.9 pKi = 7.9 Binding
Binding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligandBinding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligand
ChEMBL 1065 25 13 15 -5.1 NC(N)=NCCC[C@H](N)C(=O)N1CCC[C@H]1C(=O)N1CC(O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](CO)C(=O)NC1CSc2ccccc2N(CC(=O)N[C@H](CCCN=C(N)N)C(=O)O)C1=O 10.1021/jm9901529
CHEMBL413386 161133 0 None - 1 Human 7.9 pKi = 7.9 Binding
Binding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligandBinding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligand
ChEMBL 1065 25 13 15 -5.1 NC(N)=NCCC[C@H](N)C(=O)N1CCC[C@H]1C(=O)N1CC(O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](CO)C(=O)NC1CSc2ccccc2N(CC(=O)N[C@H](CCCN=C(N)N)C(=O)O)C1=O 10.1021/jm9901529
70695304 77082 0 None 17 2 Human 6.9 pKi = 6.9 Binding
Binding affinity to B2 receptorBinding affinity to B2 receptor
ChEMBL 556 8 2 6 4.0 Cc1ccc2cccc(OCc3cc(S(=O)(=O)N4CCC[C@H]4C(=O)NCC4CCNCC4)ccc3Cl)c2n1 10.1021/jm2016057
CHEMBL2087027 77082 0 None 17 2 Human 6.9 pKi = 6.9 Binding
Binding affinity to B2 receptorBinding affinity to B2 receptor
ChEMBL 556 8 2 6 4.0 Cc1ccc2cccc(OCc3cc(S(=O)(=O)N4CCC[C@H]4C(=O)NCC4CCNCC4)ccc3Cl)c2n1 10.1021/jm2016057
44346367 10140 0 None - 1 Human 5.9 pKi = 5.9 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 547 7 3 3 7.1 O=C(Nc1cnc2ccccc2c1)[C@@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1016/0960-894X(95)00035-R
CHEMBL1160972 10140 0 None - 1 Human 5.9 pKi = 5.9 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 547 7 3 3 7.1 O=C(Nc1cnc2ccccc2c1)[C@@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1016/0960-894X(95)00035-R
18941161 9622 0 None - 1 Guinea pig 5.9 pKi = 5.9 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 615 9 1 5 8.0 Cc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4sc(-c5ccccc5)nc34)c2Cl)cc1 10.1016/s0960-894x(98)00736-7
CHEMBL113320 9622 0 None - 1 Guinea pig 5.9 pKi = 5.9 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 615 9 1 5 8.0 Cc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4sc(-c5ccccc5)nc34)c2Cl)cc1 10.1016/s0960-894x(98)00736-7
11342079 161225 0 None - 1 Human 4.9 pKi = 4.9 Binding
Displacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cellsDisplacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cells
ChEMBL 567 9 2 4 6.0 O=C(C[C@@H](NS(=O)(=O)c1ccc2ccccc2c1)c1ccccc1)N[C@H]1CCc2cc(CN3CCCCC3)ccc21 10.1021/jm061224g
CHEMBL414091 161225 0 None - 1 Human 4.9 pKi = 4.9 Binding
Displacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cellsDisplacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cells
ChEMBL 567 9 2 4 6.0 O=C(C[C@@H](NS(=O)(=O)c1ccc2ccccc2c1)c1ccccc1)N[C@H]1CCc2cc(CN3CCCCC3)ccc21 10.1021/jm061224g
44355196 140980 0 None - 1 Human 7.9 pKi = 7.9 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1328 35 16 18 -6.0 NC(N)=NCCC[C@H](NC(=O)CN1C(=O)[C@](Cc2ccccc2)(NC(=O)[C@H](CO)NC(=O)[C@H](Cc2cccs2)NC(=O)CNC(=O)[C@@H]2CC(O)CN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C(=O)C1Cc1ccccc1)C(=O)O 10.1021/jm9901531
CHEMBL384617 140980 0 None - 1 Human 7.9 pKi = 7.9 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1328 35 16 18 -6.0 NC(N)=NCCC[C@H](NC(=O)CN1C(=O)[C@](Cc2ccccc2)(NC(=O)[C@H](CO)NC(=O)[C@H](Cc2cccs2)NC(=O)CNC(=O)[C@@H]2CC(O)CN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C(=O)C1Cc1ccccc1)C(=O)O 10.1021/jm9901531
CHEMBL3038101 209179 0 None 1 2 Human 7.8 pKi = 7.8 Binding
Binding affinity towards Bradykinin receptor B2 in human S34 clone cellsBinding affinity towards Bradykinin receptor B2 in human S34 clone cells
ChEMBL None None None NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N[C@H](Cc1ccccc1)C(=O)N(CC(=O)N[C@@H](CCCN=C(N)N)C(=O)O)c1ccccc1 10.1021/jm950716i
57393602 67323 0 None -3 2 Rat 7.8 pKi = 7.8 Binding
Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesInhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranes
ChEMBL 708 13 4 9 3.0 CN(C)CCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(NNC(=S)NC2Cc3ccccc3Cc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL1907656 67323 0 None -3 2 Rat 7.8 pKi = 7.8 Binding
Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesInhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranes
ChEMBL 708 13 4 9 3.0 CN(C)CCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(NNC(=S)NC2Cc3ccccc3Cc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL2370011 208013 0 None - 1 Guinea pig 7.8 pKi = 7.8 Binding
Binding affinity against [3H]bradykinin binding to bradykinin receptor B2 in guinea pig ileal membraneBinding affinity against [3H]bradykinin binding to bradykinin receptor B2 in guinea pig ileal membrane
ChEMBL None None None NC(N)=NCCC[C@H](NC(=O)[C@@H]1C2CCCCC2CN1C(=O)[C@H]1Cc2ccccc2CN1C(=O)[C@@H]1CSSC[C@H](NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N2CCC[C@H]2C(=O)NCC(=O)N[C@@H](Cc2ccccc2)C(=O)N1)C(=O)O 10.1021/jm00069a016
44346372 12978 0 None - 1 Human 6.9 pKi = 6.9 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 727 18 3 2 12.3 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@@H](Cc2ccc3ccccc3c2)N/C(=N/c2ccc(C)cc2)Nc2ccc(C)cc2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL1190356 12978 0 None - 1 Human 6.9 pKi = 6.9 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 727 18 3 2 12.3 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@@H](Cc2ccc3ccccc3c2)N/C(=N/c2ccc(C)cc2)Nc2ccc(C)cc2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL540643 12978 0 None - 1 Human 6.9 pKi = 6.9 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 727 18 3 2 12.3 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@@H](Cc2ccc3ccccc3c2)N/C(=N/c2ccc(C)cc2)Nc2ccc(C)cc2)cc1 10.1016/0960-894X(95)00035-R
71456177 78082 0 None - 1 Human 6.9 pKi = 6.9 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1222 30 16 17 -6.7 NC(N)=NCCC[C@H](NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1CC(O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N[C@@H]1CCc2cccc3c2N(C1=O)[C@@H](C(=O)N[C@H](CCCN=C(N)N)C(=O)O)C3 10.1021/jm9901531
CHEMBL2111891 78082 0 None - 1 Human 6.9 pKi = 6.9 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1222 30 16 17 -6.7 NC(N)=NCCC[C@H](NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1CC(O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N[C@@H]1CCc2cccc3c2N(C1=O)[C@@H](C(=O)N[C@H](CCCN=C(N)N)C(=O)O)C3 10.1021/jm9901531
11284303 65995 0 None 2 2 Human 5.9 pKi = 5.9 Binding
Binding affinity for Bradykinin receptor B2 expressed in COS7 cellsBinding affinity for Bradykinin receptor B2 expressed in COS7 cells
ChEMBL 553 15 1 7 4.7 CN(C)CCCN(CCCN(C)C)S(=O)(=O)c1ccc(NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1021/jm049747g
CHEMBL185068 65995 0 None 2 2 Human 5.9 pKi = 5.9 Binding
Binding affinity for Bradykinin receptor B2 expressed in COS7 cellsBinding affinity for Bradykinin receptor B2 expressed in COS7 cells
ChEMBL 553 15 1 7 4.7 CN(C)CCCN(CCCN(C)C)S(=O)(=O)c1ccc(NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1021/jm049747g
44276461 97808 0 None - 1 Human 6.9 pKi = 6.9 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 551 9 0 6 7.0 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)CCc4ccc(C(=O)c5cccs5)n4C)c3C)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL27461 97808 0 None - 1 Human 6.9 pKi = 6.9 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 551 9 0 6 7.0 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)CCc4ccc(C(=O)c5cccs5)n4C)c3C)c2n1 10.1016/s0960-894x(03)00104-5
10556495 167365 0 None -2398 2 Human 5.8 pKi = 5.8 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 682 15 4 9 2.9 CN(C)CCN(C)CCNC(=O)[C@H]1CCCN1S(=O)(=O)c1ccc(NNC(=S)NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL2112044 167365 0 None -2398 2 Human 5.8 pKi = 5.8 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 682 15 4 9 2.9 CN(C)CCN(C)CCNC(=O)[C@H]1CCCN1S(=O)(=O)c1ccc(NNC(=S)NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL431562 167365 0 None -2398 2 Human 5.8 pKi = 5.8 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 682 15 4 9 2.9 CN(C)CCN(C)CCNC(=O)[C@H]1CCCN1S(=O)(=O)c1ccc(NNC(=S)NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1021/jm0111088
10770256 56855 0 None - 1 Rat 6.8 pKi = 6.8 Binding
Inhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranesInhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranes
ChEMBL 627 16 3 8 4.5 CN(C)CCCN(CCCN(C)C)S(=O)(=O)c1ccc(N/N=C(/S)NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1021/jm991155o
CHEMBL164754 56855 0 None - 1 Rat 6.8 pKi = 6.8 Binding
Inhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranesInhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranes
ChEMBL 627 16 3 8 4.5 CN(C)CCCN(CCCN(C)C)S(=O)(=O)c1ccc(N/N=C(/S)NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1021/jm991155o
44276793 99048 0 None - 1 Human 7.8 pKi = 7.8 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 586 9 0 6 7.0 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CCc4ccc(C(=O)c5cccnc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL283394 99048 0 None - 1 Human 7.8 pKi = 7.8 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 586 9 0 6 7.0 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CCc4ccc(C(=O)c5cccnc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
11467345 161390 0 None -489 2 Human 4.8 pKi = 4.8 Binding
Displacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cellsDisplacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cells
ChEMBL 581 9 2 4 6.4 O=C(C[C@@H](NS(=O)(=O)c1ccc2ccccc2c1)c1ccccc1)N[C@H]1CCCc2cc(CN3CCCCC3)ccc21 10.1021/jm061224g
CHEMBL415629 161390 0 None -489 2 Human 4.8 pKi = 4.8 Binding
Displacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cellsDisplacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cells
ChEMBL 581 9 2 4 6.4 O=C(C[C@@H](NS(=O)(=O)c1ccc2ccccc2c1)c1ccccc1)N[C@H]1CCCc2cc(CN3CCCCC3)ccc21 10.1021/jm061224g
11549562 77144 0 None - 1 Human 6.8 pKi = 6.8 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 671 14 3 7 5.8 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCNCc4ccc(N(C)C)cc4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL208738 77144 0 None - 1 Human 6.8 pKi = 6.8 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 671 14 3 7 5.8 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCNCc4ccc(N(C)C)cc4)c3Cl)c2n1 10.1021/jm060137l
11549335 139606 0 None - 1 Human 6.8 pKi = 6.8 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 578 9 3 6 4.6 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCC4CCNCC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL380260 139606 0 None - 1 Human 6.8 pKi = 6.8 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 578 9 3 6 4.6 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCC4CCNCC4)c3Cl)c2n1 10.1021/jm060137l
11621618 139614 0 None - 1 Human 6.8 pKi = 6.8 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 538 10 3 6 4.0 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCN)c3Cl)c2n1 10.1021/jm060137l
CHEMBL380282 139614 0 None - 1 Human 6.8 pKi = 6.8 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 538 10 3 6 4.0 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCN)c3Cl)c2n1 10.1021/jm060137l
11621850 165754 0 None - 1 Human 6.8 pKi = 6.8 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 618 13 4 7 4.5 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCNCc4c[nH]cn4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL427217 165754 0 None - 1 Human 6.8 pKi = 6.8 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 618 13 4 7 4.5 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCNCc4c[nH]cn4)c3Cl)c2n1 10.1021/jm060137l
51351563 58185 0 None - 1 Human 4.8 pKi = 4.8 Binding
Binding affinity towards human bradykinin B2 receptor (membranes from Cos-7 cells expressing human B2 receptor) using [3H]-BK as radioligandBinding affinity towards human bradykinin B2 receptor (membranes from Cos-7 cells expressing human B2 receptor) using [3H]-BK as radioligand
ChEMBL 473 6 3 3 5.0 N=C(N)Nc1cccc(CN2C(=O)[C@H](Cc3ccccc3)N=C(c3ccccc3)c3ccccc32)c1 10.1016/s0960-894x(99)00015-3
CHEMBL1683738 58185 0 None - 1 Human 4.8 pKi = 4.8 Binding
Binding affinity towards human bradykinin B2 receptor (membranes from Cos-7 cells expressing human B2 receptor) using [3H]-BK as radioligandBinding affinity towards human bradykinin B2 receptor (membranes from Cos-7 cells expressing human B2 receptor) using [3H]-BK as radioligand
ChEMBL 473 6 3 3 5.0 N=C(N)Nc1cccc(CN2C(=O)[C@H](Cc3ccccc3)N=C(c3ccccc3)c3ccccc32)c1 10.1016/s0960-894x(99)00015-3
71450890 78370 0 None - 1 Human 6.8 pKi = 6.8 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1222 30 16 17 -6.7 NC(N)=NCCC[C@H](NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1CC(O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N[C@H]1CCc2cccc3c2N(C1=O)[C@@H](C(=O)N[C@H](CCCN=C(N)N)C(=O)O)C3 10.1021/jm9901531
CHEMBL2112709 78370 0 None - 1 Human 6.8 pKi = 6.8 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1222 30 16 17 -6.7 NC(N)=NCCC[C@H](NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1CC(O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N[C@H]1CCc2cccc3c2N(C1=O)[C@@H](C(=O)N[C@H](CCCN=C(N)N)C(=O)O)C3 10.1021/jm9901531
44340818 110107 0 None - 1 Guinea pig 6.8 pKi = 6.8 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 539 8 1 5 6.3 Cc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4scnc34)c2Cl)cc1 10.1016/s0960-894x(98)00736-7
CHEMBL325624 110107 0 None - 1 Guinea pig 6.8 pKi = 6.8 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 539 8 1 5 6.3 Cc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4scnc34)c2Cl)cc1 10.1016/s0960-894x(98)00736-7
10662116 56240 0 None - 1 Rat 5.8 pKi = 5.8 Binding
Inhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranesInhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranes
ChEMBL 302 5 3 4 3.0 O=[N+]([O-])c1ccccc1N/N=C(/S)NCc1ccccc1 10.1021/jm991155o
CHEMBL163956 56240 0 None - 1 Rat 5.8 pKi = 5.8 Binding
Inhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranesInhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranes
ChEMBL 302 5 3 4 3.0 O=[N+]([O-])c1ccccc1N/N=C(/S)NCc1ccccc1 10.1021/jm991155o
16108965 160771 0 None -1000 2 Human 4.8 pKi = 4.8 Binding
Displacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cellsDisplacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cells
ChEMBL 646 9 2 6 4.9 CN1c2cc(CN3CCCCC3)ccc2[C@H](NC(=O)C[C@@H](NS(=O)(=O)c2ccc3ccccc3c2)c2ccccc2)CS1(=O)=O 10.1021/jm061224g
CHEMBL412552 160771 0 None -1000 2 Human 4.8 pKi = 4.8 Binding
Displacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cellsDisplacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cells
ChEMBL 646 9 2 6 4.9 CN1c2cc(CN3CCCCC3)ccc2[C@H](NC(=O)C[C@@H](NS(=O)(=O)c2ccc3ccccc3c2)c2ccccc2)CS1(=O)=O 10.1021/jm061224g
71459890 78081 0 None - 1 Human 6.8 pKi = 6.8 Binding
Binding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligandBinding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligand
ChEMBL 1228 31 16 18 -6.5 NC(N)=NCCC[C@H](NC(=O)CN1C(=O)[C@@H](NC(=O)[C@H](CO)NC(=O)[C@H](Cc2cccs2)NC(=O)CNC(=O)[C@@H]2CC(O)CN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)CSc2ccccc21)C(=O)O 10.1021/jm9901529
CHEMBL2111889 78081 0 None - 1 Human 6.8 pKi = 6.8 Binding
Binding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligandBinding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligand
ChEMBL 1228 31 16 18 -6.5 NC(N)=NCCC[C@H](NC(=O)CN1C(=O)[C@@H](NC(=O)[C@H](CO)NC(=O)[C@H](Cc2cccs2)NC(=O)CNC(=O)[C@@H]2CC(O)CN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)CSc2ccccc21)C(=O)O 10.1021/jm9901529
CHEMBL2370038 208017 0 None - 1 Guinea pig 5.8 pKi = 5.8 Binding
Binding affinity against [3H]bradykinin binding to bradykinin receptor B2 in guinea pig ileal membraneBinding affinity against [3H]bradykinin binding to bradykinin receptor B2 in guinea pig ileal membrane
ChEMBL None None None CN(CC(=O)N(C)[C@@H](Cc1ccccc1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O)C(=O)[C@@H]1C[C@H](O)CN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N 10.1021/jm00069a016
44276753 164764 0 None - 1 Human 5.8 pKi = 5.8 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 551 7 0 5 7.2 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)C(C)(C)C)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL423482 164764 0 None - 1 Human 5.8 pKi = 5.8 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 551 7 0 5 7.2 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)C(C)(C)C)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
10327403 78160 0 None -63 2 Rat 6.8 pKi = 6.8 Binding
Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesInhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranes
ChEMBL 702 14 4 10 3.8 CN(C)CCCN(C)CCNC(=O)c1cccn1S(=O)(=O)c1ccc(NNC(=O)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL2112220 78160 0 None -63 2 Rat 6.8 pKi = 6.8 Binding
Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesInhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranes
ChEMBL 702 14 4 10 3.8 CN(C)CCCN(C)CCNC(=O)c1cccn1S(=O)(=O)c1ccc(NNC(=O)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
44276287 164256 0 None - 1 Human 5.8 pKi = 5.8 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 577 8 0 5 7.7 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)C5CCCCC5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL421863 164256 0 None - 1 Human 5.8 pKi = 5.8 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 577 8 0 5 7.7 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)C5CCCCC5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
44346451 10143 0 None - 1 Human 4.8 pKi = 4.8 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 695 10 3 3 8.4 O=C(NC1C2CCN(CC2)C1C(c1ccccc1)c1ccccc1)[C@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1016/0960-894X(95)00035-R
CHEMBL1160979 10143 0 None - 1 Human 4.8 pKi = 4.8 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 695 10 3 3 8.4 O=C(NC1C2CCN(CC2)C1C(c1ccccc1)c1ccccc1)[C@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1016/0960-894X(95)00035-R
44355256 156669 0 None - 1 Human 4.7 pKi = 4.7 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1148 31 16 17 -8.0 NC(N)=NCCC[C@H](NC(=O)CN1CCC[C@H](NC(=O)[C@H](CO)NC(=O)[C@H](Cc2cccs2)NC(=O)CNC(=O)[C@@H]2CC(O)CN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C1=O)C(=O)O 10.1021/jm9901531
CHEMBL407626 156669 0 None - 1 Human 4.7 pKi = 4.7 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1148 31 16 17 -8.0 NC(N)=NCCC[C@H](NC(=O)CN1CCC[C@H](NC(=O)[C@H](CO)NC(=O)[C@H](Cc2cccs2)NC(=O)CNC(=O)[C@@H]2CC(O)CN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C1=O)C(=O)O 10.1021/jm9901531
672 2227 17 None -1 2 Human 7.7 pKi = 7.7 Binding
Binding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligandBinding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligand
ChEMBL None None None None 10.1021/jm9901529
6918284 2227 17 None -1 2 Human 7.7 pKi = 7.7 Binding
Binding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligandBinding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligand
ChEMBL None None None None 10.1021/jm9901529
CHEMBL2105864 2227 17 None -1 2 Human 7.7 pKi = 7.7 Binding
Binding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligandBinding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligand
ChEMBL None None None None 10.1021/jm9901529
DB06549 2227 17 None -1 2 Human 7.7 pKi = 7.7 Binding
Binding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligandBinding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligand
ChEMBL None None None None 10.1021/jm9901529
44276550 96836 0 None - 1 Human 7.7 pKi = 7.7 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 570 9 0 6 6.8 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)CCc4ccc(C(=O)c5ccc(C#N)cc5)n4C)c3C)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL26908 96836 0 None - 1 Human 7.7 pKi = 7.7 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 570 9 0 6 6.8 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)CCc4ccc(C(=O)c5ccc(C#N)cc5)n4C)c3C)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL2370748 208163 0 None - 1 Human 7.7 pKi = 7.7 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL None None None Cc1ccc(C[C@@H](CN[C@@H](CCCN=C(N)N)C(=O)O)NC(=O)[C@@H]2CCCN2C(=O)[C@H](CO)NC(=O)[C@H](Cc2cccs2)NC(=O)CNC(=O)[C@@H]2C[C@@H](O)CN2C(=O)[C@@H]2CCCN2C(=O)[C@@H](N)CCCN=C(N)N)cc1 10.1021/jm9901531
11577748 77728 0 None - 1 Human 7.7 pKi = 7.7 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 566 10 4 6 2.9 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCN=C(N)N)c3Cl)c2n1 10.1021/jm060137l
CHEMBL210217 77728 0 None - 1 Human 7.7 pKi = 7.7 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 566 10 4 6 2.9 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCN=C(N)N)c3Cl)c2n1 10.1021/jm060137l
11505970 77801 0 None - 1 Human 7.7 pKi = 7.7 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 656 13 5 7 5.4 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCNc4ccc(C(=N)N)cc4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL210472 77801 0 None - 1 Human 7.7 pKi = 7.7 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 656 13 5 7 5.4 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCNc4ccc(C(=N)N)cc4)c3Cl)c2n1 10.1021/jm060137l
11585604 76759 0 None - 1 Human 6.7 pKi = 6.7 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 566 11 2 6 4.6 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCN(C)C)c3Cl)c2n1 10.1021/jm060137l
CHEMBL207692 76759 0 None - 1 Human 6.7 pKi = 6.7 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 566 11 2 6 4.6 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCN(C)C)c3Cl)c2n1 10.1021/jm060137l
11672243 77813 0 None - 1 Human 6.7 pKi = 6.7 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 658 14 3 7 5.8 COc1ccc(CNCCCNC(=O)C(C)(C)NS(=O)(=O)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm060137l
CHEMBL210524 77813 0 None - 1 Human 6.7 pKi = 6.7 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 658 14 3 7 5.8 COc1ccc(CNCCCNC(=O)C(C)(C)NS(=O)(=O)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm060137l
11600235 137870 0 None - 1 Human 6.7 pKi = 6.7 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 642 13 3 6 6.1 Cc1ccc(CNCCCNC(=O)C(C)(C)NS(=O)(=O)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm060137l
CHEMBL377370 137870 0 None - 1 Human 6.7 pKi = 6.7 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 642 13 3 6 6.1 Cc1ccc(CNCCCNC(=O)C(C)(C)NS(=O)(=O)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm060137l
11707335 138776 0 None - 1 Human 6.7 pKi = 6.7 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 552 11 3 6 4.3 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCCN)c3Cl)c2n1 10.1021/jm060137l
CHEMBL379259 138776 0 None - 1 Human 6.7 pKi = 6.7 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 552 11 3 6 4.3 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCCN)c3Cl)c2n1 10.1021/jm060137l
11672186 139152 0 None - 1 Human 6.7 pKi = 6.7 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 628 13 3 6 5.8 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCNCc4ccccc4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL379806 139152 0 None - 1 Human 6.7 pKi = 6.7 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 628 13 3 6 5.8 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCNCc4ccccc4)c3Cl)c2n1 10.1021/jm060137l
44355427 141333 0 None - 1 Human 8.6 pKi = 8.6 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1212 31 16 18 -7.2 NC(N)=NCCC[C@H](NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1CC(O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)NC1COc2ccccc2N(CC(=O)N[C@H](CCCN=C(N)N)C(=O)O)C1=O 10.1021/jm9901531
CHEMBL386697 141333 0 None - 1 Human 8.6 pKi = 8.6 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1212 31 16 18 -7.2 NC(N)=NCCC[C@H](NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1CC(O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)NC1COc2ccccc2N(CC(=O)N[C@H](CCCN=C(N)N)C(=O)O)C1=O 10.1021/jm9901531
22008929 9643 0 None - 1 Guinea pig 8.6 pKi = 8.6 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 597 9 1 5 6.6 COc1c(N(C)C(=O)CNC(=O)/C=C/c2ccc(C(F)(F)F)cc2)ccc(Cl)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
CHEMBL113465 9643 0 None - 1 Guinea pig 8.6 pKi = 8.6 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 597 9 1 5 6.6 COc1c(N(C)C(=O)CNC(=O)/C=C/c2ccc(C(F)(F)F)cc2)ccc(Cl)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
10056816 77381 0 None - 1 Human 8.6 pKi = 8.6 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 649 13 2 7 5.1 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(CCCCCCN)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL209038 77381 0 None - 1 Human 8.6 pKi = 8.6 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 649 13 2 7 5.1 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(CCCCCCN)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL3038096 209175 0 None 6 2 Human 8.6 pKi = 8.6 Binding
Binding affinity towards Bradykinin receptor B2 in human S34 clone cellsBinding affinity towards Bradykinin receptor B2 in human S34 clone cells
ChEMBL None None None NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N[C@H](Cc1ccccc1)C(=O)N(CC(=O)N[C@@H](CCCN=C(N)N)C(=O)O)C1CCCCC1 10.1021/jm950716i
10327403 78160 0 None 63 2 Human 8.6 pKi = 8.6 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 702 14 4 10 3.8 CN(C)CCCN(C)CCNC(=O)c1cccn1S(=O)(=O)c1ccc(NNC(=O)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL2112220 78160 0 None 63 2 Human 8.6 pKi = 8.6 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 702 14 4 10 3.8 CN(C)CCCN(C)CCNC(=O)c1cccn1S(=O)(=O)c1ccc(NNC(=O)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
9851817 9574 0 None - 1 Guinea pig 8.6 pKi = 8.6 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 607 8 1 5 7.3 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(F)(F)F)cc4)c3Cl)cccc2s1 10.1016/s0960-894x(98)00736-7
CHEMBL112991 9574 0 None - 1 Guinea pig 8.6 pKi = 8.6 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 607 8 1 5 7.3 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(F)(F)F)cc4)c3Cl)cccc2s1 10.1016/s0960-894x(98)00736-7
44340760 110006 0 None - 1 Guinea pig 8.5 pKi = 8.5 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 523 10 3 6 3.8 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)NCCCC(=O)O)c3C#N)c2n1 10.1016/s0960-894x(98)00736-7
CHEMBL324950 110006 0 None - 1 Guinea pig 8.5 pKi = 8.5 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 523 10 3 6 3.8 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)NCCCC(=O)O)c3C#N)c2n1 10.1016/s0960-894x(98)00736-7
CHEMBL2372276 208451 0 None 3 3 Human 7.7 pKi = 7.7 Binding
Displacement of radiolabeled NPC 567 from human bradykinin B2 receptorDisplacement of radiolabeled NPC 567 from human bradykinin B2 receptor
ChEMBL None None None NC(N)=NCCC[C@H](N)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1CCC[C@H]1C(=O)NCC(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](CO)C(=O)[C@@H]1CCCN1C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@H](CCCN=C(N)N)C(=O)O 10.1021/jm8007618
22288598 96706 0 None - 1 Human 6.7 pKi = 6.7 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 642 9 0 6 6.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(C(=O)N(C)C)cc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL26810 96706 0 None - 1 Human 6.7 pKi = 6.7 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 642 9 0 6 6.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(C(=O)N(C)C)cc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
44355288 96313 0 None - 1 Human 5.7 pKi = 5.7 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1224 33 16 17 -6.8 NC(N)=NCCC[C@H](NC(=O)[C@H](Cc1ccccc1)N1CC[C@@H](NC(=O)[C@H](CO)NC(=O)[C@H](Cc2cccs2)NC(=O)CNC(=O)[C@@H]2CC(O)CN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C1=O)C(=O)O 10.1021/jm9901531
CHEMBL264712 96313 0 None - 1 Human 5.7 pKi = 5.7 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1224 33 16 17 -6.8 NC(N)=NCCC[C@H](NC(=O)[C@H](Cc1ccccc1)N1CC[C@@H](NC(=O)[C@H](CO)NC(=O)[C@H](Cc2cccs2)NC(=O)CNC(=O)[C@@H]2CC(O)CN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C1=O)C(=O)O 10.1021/jm9901531
44346465 11313 0 None - 1 Human 4.7 pKi = 4.7 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 584 23 0 0 13.2 CCCC[P+](CCCC)(CCCC)Cc1ccc(-c2ccc(C[P+](CCCC)(CCCC)CCCC)cc2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL1180311 11313 0 None - 1 Human 4.7 pKi = 4.7 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 584 23 0 0 13.2 CCCC[P+](CCCC)(CCCC)Cc1ccc(-c2ccc(C[P+](CCCC)(CCCC)CCCC)cc2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL121350 11313 0 None - 1 Human 4.7 pKi = 4.7 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 584 23 0 0 13.2 CCCC[P+](CCCC)(CCCC)Cc1ccc(-c2ccc(C[P+](CCCC)(CCCC)CCCC)cc2)cc1 10.1016/0960-894X(95)00035-R
44346306 10136 0 None - 1 Human 6.7 pKi = 6.7 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 529 7 3 3 5.2 O=C(NC1CN2CCC1CC2)C(Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1016/0960-894X(95)00035-R
CHEMBL1160968 10136 0 None - 1 Human 6.7 pKi = 6.7 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 529 7 3 3 5.2 O=C(NC1CN2CCC1CC2)C(Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1016/0960-894X(95)00035-R
44320168 10137 0 None - 1 Human 6.7 pKi = 6.7 Binding
Binding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligandBinding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligand
ChEMBL 529 7 3 3 5.2 O=C(NC1CN2CCC1CC2)[C@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1021/jm00069a021
CHEMBL1160969 10137 0 None - 1 Human 6.7 pKi = 6.7 Binding
Binding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligandBinding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligand
ChEMBL 529 7 3 3 5.2 O=C(NC1CN2CCC1CC2)[C@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1021/jm00069a021
CHEMBL444322 10137 0 None - 1 Human 6.7 pKi = 6.7 Binding
Binding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligandBinding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligand
ChEMBL 529 7 3 3 5.2 O=C(NC1CN2CCC1CC2)[C@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1021/jm00069a021
9826248 33845 0 None - 1 Human 4.7 pKi = 4.7 Binding
Binding affinity towards human bradykinin B2 receptor (membranes from Cos-7 cells expressing human B2 receptor) using [3H]-BK as radioligandBinding affinity towards human bradykinin B2 receptor (membranes from Cos-7 cells expressing human B2 receptor) using [3H]-BK as radioligand
ChEMBL 439 8 3 3 3.7 N=C(N)NCCCCN1C(=O)C(Cc2ccccc2)N=C(c2ccccc2)c2ccccc21 10.1016/s0960-894x(99)00015-3
CHEMBL142515 33845 0 None - 1 Human 4.7 pKi = 4.7 Binding
Binding affinity towards human bradykinin B2 receptor (membranes from Cos-7 cells expressing human B2 receptor) using [3H]-BK as radioligandBinding affinity towards human bradykinin B2 receptor (membranes from Cos-7 cells expressing human B2 receptor) using [3H]-BK as radioligand
ChEMBL 439 8 3 3 3.7 N=C(N)NCCCCN1C(=O)C(Cc2ccccc2)N=C(c2ccccc2)c2ccccc21 10.1016/s0960-894x(99)00015-3
CHEMBL3038103 209181 0 None 61 2 Human 7.6 pKi = 7.6 Binding
Binding affinity towards Bradykinin receptor B2 in human S34 clone cellsBinding affinity towards Bradykinin receptor B2 in human S34 clone cells
ChEMBL None None None NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N[C@@H](C(=O)N(CC(=O)N[C@@H](CCCN=C(N)N)C(=O)O)C1CCCCC1)C1CCCC1 10.1021/jm950716i
44276711 96470 0 None - 1 Human 5.6 pKi = 5.6 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 571 8 0 5 7.2 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccccc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL26604 96470 0 None - 1 Human 5.6 pKi = 5.6 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 571 8 0 5 7.2 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccccc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
15952860 98778 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 596 8 0 6 7.1 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(C#N)cc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL281756 98778 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 596 8 0 6 7.1 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(C#N)cc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
11050689 101784 0 None - 1 Human 6.6 pKi = 6.6 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 678 15 4 10 3.8 CN(C)CCN(C)CCNC(=O)c1cccn1S(=O)(=O)c1ccc(N/N=C(\S)NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL303258 101784 0 None - 1 Human 6.6 pKi = 6.6 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 678 15 4 10 3.8 CN(C)CCN(C)CCNC(=O)c1cccn1S(=O)(=O)c1ccc(N/N=C(\S)NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1021/jm0111088
44276375 96259 0 None - 1 Human 5.6 pKi = 5.6 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 585 9 0 5 7.4 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)Cc5ccccc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL26422 96259 0 None - 1 Human 5.6 pKi = 5.6 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 585 9 0 5 7.4 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)Cc5ccccc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
44276380 98947 0 None - 1 Human 6.6 pKi = 6.6 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 577 8 0 6 7.3 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)c5cccs5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL28282 98947 0 None - 1 Human 6.6 pKi = 6.6 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 577 8 0 6 7.3 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)c5cccs5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
44320404 12997 0 None - 1 Human 4.6 pKi = 4.6 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 581 18 3 2 8.5 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2ccccc2)N/C(=N/C(C)C)NC(C)C)cc1 10.1016/0960-894X(95)00035-R
CHEMBL1190474 12997 0 None - 1 Human 4.6 pKi = 4.6 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 581 18 3 2 8.5 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2ccccc2)N/C(=N/C(C)C)NC(C)C)cc1 10.1016/0960-894X(95)00035-R
CHEMBL540896 12997 0 None - 1 Human 4.6 pKi = 4.6 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 581 18 3 2 8.5 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2ccccc2)N/C(=N/C(C)C)NC(C)C)cc1 10.1016/0960-894X(95)00035-R
11679144 76928 0 None - 1 Human 7.6 pKi = 7.6 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 552 10 3 6 4.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCN)c3Cl)c2n1 10.1021/jm060137l
CHEMBL208223 76928 0 None - 1 Human 7.6 pKi = 7.6 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 552 10 3 6 4.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCN)c3Cl)c2n1 10.1021/jm060137l
11636121 138469 0 None - 1 Human 7.6 pKi = 7.6 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 564 7 2 6 4.3 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCCNCC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL378567 138469 0 None - 1 Human 7.6 pKi = 7.6 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 564 7 2 6 4.3 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCCNCC4)c3Cl)c2n1 10.1021/jm060137l
44412412 168209 0 None - 1 Human 7.6 pKi = 7.6 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 550 7 2 6 3.9 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCNCC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL437491 168209 0 None - 1 Human 7.6 pKi = 7.6 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 550 7 2 6 3.9 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCNCC4)c3Cl)c2n1 10.1021/jm060137l
44346682 14113 0 None - 1 Human 6.6 pKi = 6.6 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 696 18 2 1 12.3 CCCC[PH](CCCC)(CCCC)Cc1ccc(/C=C/[C@H](Cc2ccc3ccccc3c2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL1162798 14113 0 None - 1 Human 6.6 pKi = 6.6 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 696 18 2 1 12.3 CCCC[PH](CCCC)(CCCC)Cc1ccc(/C=C/[C@H](Cc2ccc3ccccc3c2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL1199421 14113 0 None - 1 Human 6.6 pKi = 6.6 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 696 18 2 1 12.3 CCCC[PH](CCCC)(CCCC)Cc1ccc(/C=C/[C@H](Cc2ccc3ccccc3c2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
44320404 14219 0 None - 1 Human 4.6 pKi = 4.6 Binding
Binding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligandBinding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligand
ChEMBL 582 18 3 2 8.2 CCCC[PH](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2ccccc2)N/C(=N/C(C)C)NC(C)C)cc1 10.1021/jm00069a021
CHEMBL1162590 14219 0 None - 1 Human 4.6 pKi = 4.6 Binding
Binding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligandBinding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligand
ChEMBL 582 18 3 2 8.2 CCCC[PH](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2ccccc2)N/C(=N/C(C)C)NC(C)C)cc1 10.1021/jm00069a021
CHEMBL1200093 14219 0 None - 1 Human 4.6 pKi = 4.6 Binding
Binding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligandBinding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligand
ChEMBL 582 18 3 2 8.2 CCCC[PH](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2ccccc2)N/C(=N/C(C)C)NC(C)C)cc1 10.1021/jm00069a021
11707528 77403 0 None - 1 Human 6.6 pKi = 6.6 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 621 11 2 7 4.2 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCN4CCN(C)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL209117 77403 0 None - 1 Human 6.6 pKi = 6.6 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 621 11 2 7 4.2 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCN4CCN(C)CC4)c3Cl)c2n1 10.1021/jm060137l
11657717 139524 0 None - 1 Human 5.6 pKi = 5.6 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 594 10 2 7 3.9 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCN4CCOCC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL380045 139524 0 None - 1 Human 5.6 pKi = 5.6 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 594 10 2 7 3.9 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCN4CCOCC4)c3Cl)c2n1 10.1021/jm060137l
10876210 78159 0 None - 1 Human 6.6 pKi = 6.6 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 691 13 4 8 4.5 CN(C)CCCN(C)CCNC(=O)c1cccn1S(=O)(=O)c1ccc(NNC(=O)NC2c3ccccc3CCc3ccccc32)c(Cl)c1 10.1021/jm0111088
CHEMBL2112219 78159 0 None - 1 Human 6.6 pKi = 6.6 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 691 13 4 8 4.5 CN(C)CCCN(C)CCNC(=O)c1cccn1S(=O)(=O)c1ccc(NNC(=O)NC2c3ccccc3CCc3ccccc32)c(Cl)c1 10.1021/jm0111088
44346347 10138 0 None - 1 Human 5.6 pKi = 5.6 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 547 7 3 3 7.1 O=C(Nc1cccc2ccncc12)[C@@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1016/0960-894X(95)00035-R
CHEMBL1160970 10138 0 None - 1 Human 5.6 pKi = 5.6 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 547 7 3 3 7.1 O=C(Nc1cccc2ccncc12)[C@@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1016/0960-894X(95)00035-R
44346416 12976 0 None - 1 Human 5.6 pKi = 5.6 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 667 18 3 3 10.4 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2cccs2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL1190354 12976 0 None - 1 Human 5.6 pKi = 5.6 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 667 18 3 3 10.4 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2cccs2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL540641 12976 0 None - 1 Human 5.6 pKi = 5.6 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 667 18 3 3 10.4 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2cccs2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL2370042 208020 0 None - 1 Guinea pig 7.6 pKi = 7.6 Binding
Binding affinity against [3H]bradykinin binding to bradykinin receptor B2 in guinea pig ileal membraneBinding affinity against [3H]bradykinin binding to bradykinin receptor B2 in guinea pig ileal membrane
ChEMBL None None None CN(C(=O)CNC(=O)[C@@H]1C[C@H](O)CN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)[C@@H](Cc1ccccc1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O 10.1021/jm00069a016
44337466 5328 0 None - 1 Human 7.6 pKi = 7.6 Binding
Affinity to human Bradykinin receptor B2 in CHO cell membranes determined by displacement of [3H]-NPC 17731Affinity to human Bradykinin receptor B2 in CHO cell membranes determined by displacement of [3H]-NPC 17731
ChEMBL 267 4 0 4 0.6 CCCN1CN(CC(C)=O)C(=O)C12CCN(C)CC2 10.1021/jm950676i
CHEMBL107234 5328 0 None - 1 Human 7.6 pKi = 7.6 Binding
Affinity to human Bradykinin receptor B2 in CHO cell membranes determined by displacement of [3H]-NPC 17731Affinity to human Bradykinin receptor B2 in CHO cell membranes determined by displacement of [3H]-NPC 17731
ChEMBL 267 4 0 4 0.6 CCCN1CN(CC(C)=O)C(=O)C12CCN(C)CC2 10.1021/jm950676i
44276482 99030 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 624 10 0 6 7.9 CCCn1c(CC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)ccc1C(=O)c1ccc(C#N)cc1 10.1016/s0960-894x(03)00104-5
CHEMBL283295 99030 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 624 10 0 6 7.9 CCCn1c(CC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)ccc1C(=O)c1ccc(C#N)cc1 10.1016/s0960-894x(03)00104-5
44346410 13656 0 None - 1 Human 5.6 pKi = 5.6 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 701 18 4 2 10.8 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2c[nH]c3ccccc23)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL1195448 13656 0 None - 1 Human 5.6 pKi = 5.6 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 701 18 4 2 10.8 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2c[nH]c3ccccc23)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL554593 13656 0 None - 1 Human 5.6 pKi = 5.6 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 701 18 4 2 10.8 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2c[nH]c3ccccc23)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
44215784 99523 0 None - 1 Human 6.6 pKi = 6.6 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 566 8 0 6 6.6 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(Cl)nc5)n4C)c3C)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL286710 99523 0 None - 1 Human 6.6 pKi = 6.6 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 566 8 0 6 6.6 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(Cl)nc5)n4C)c3C)c2n1 10.1016/s0960-894x(03)00104-5
44276513 99495 0 None - 1 Human 7.5 pKi = 7.5 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 638 11 0 6 8.3 CCCCn1c(CC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)ccc1C(=O)c1ccc(C#N)cc1 10.1016/s0960-894x(03)00104-5
CHEMBL286520 99495 0 None - 1 Human 7.5 pKi = 7.5 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 638 11 0 6 8.3 CCCCn1c(CC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)ccc1C(=O)c1ccc(C#N)cc1 10.1016/s0960-894x(03)00104-5
57395311 67322 0 None 2 2 Human 6.5 pKi = 6.5 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 580 7 4 7 2.9 NC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(NNC(=S)NC2Cc3ccccc3Cc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL1907655 67322 0 None 2 2 Human 6.5 pKi = 6.5 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 580 7 4 7 2.9 NC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(NNC(=S)NC2Cc3ccccc3Cc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
44214279 9609 0 None - 1 Guinea pig 8.5 pKi = 8.5 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 489 8 1 5 5.3 C=C/C=C/C(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccc3sc(C)nc23)c1Cl 10.1016/s0960-894x(98)00736-7
CHEMBL113222 9609 0 None - 1 Guinea pig 8.5 pKi = 8.5 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 489 8 1 5 5.3 C=C/C=C/C(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccc3sc(C)nc23)c1Cl 10.1016/s0960-894x(98)00736-7
15388873 114220 0 None - 1 Guinea pig 8.5 pKi = 8.5 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 529 8 1 6 5.9 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccco4)c3Cl)cccc2s1 10.1016/s0960-894x(98)00736-7
CHEMBL333832 114220 0 None - 1 Guinea pig 8.5 pKi = 8.5 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 529 8 1 6 5.9 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccco4)c3Cl)cccc2s1 10.1016/s0960-894x(98)00736-7
44341214 109928 0 None - 1 Guinea pig 8.4 pKi = 8.4 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 621 12 1 6 6.7 CCCOc1c(N(C)C(=O)CNC(=O)/C=C/c2ccc(C(F)(F)F)cc2)ccc(OC)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
CHEMBL324575 109928 0 None - 1 Guinea pig 8.4 pKi = 8.4 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 621 12 1 6 6.7 CCCOc1c(N(C)C(=O)CNC(=O)/C=C/c2ccc(C(F)(F)F)cc2)ccc(OC)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
11506007 77642 0 None - 1 Human 8.4 pKi = 8.4 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 676 9 2 8 3.1 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)CN5CCNCC5)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL209773 77642 0 None - 1 Human 8.4 pKi = 8.4 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 676 9 2 8 3.1 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)CN5CCNCC5)CC4)c3Cl)c2n1 10.1021/jm060137l
10008626 138136 0 None - 1 Human 8.4 pKi = 8.4 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 592 7 3 6 3.5 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=N)N)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL377800 138136 0 None - 1 Human 8.4 pKi = 8.4 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 592 7 3 6 3.5 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=N)N)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL2370028 208015 0 None - 1 Guinea pig 7.5 pKi = 7.5 Binding
Binding affinity against [3H]bradykinin binding to bradykinin receptor B2 in guinea pig ileal membraneBinding affinity against [3H]bradykinin binding to bradykinin receptor B2 in guinea pig ileal membrane
ChEMBL None None None CN(CC(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O)C(=O)[C@@H]1C[C@H](O)CN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N 10.1021/jm00069a016
22288562 162392 0 None - 1 Human 6.5 pKi = 6.5 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 586 8 1 6 6.8 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(N)cc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL417474 162392 0 None - 1 Human 6.5 pKi = 6.5 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 586 8 1 6 6.8 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(N)cc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL2370035 208016 0 None - 1 Guinea pig 5.5 pKi = 5.5 Binding
Binding affinity against [3H]bradykinin binding to bradykinin receptor B2 in guinea pig ileal membraneBinding affinity against [3H]bradykinin binding to bradykinin receptor B2 in guinea pig ileal membrane
ChEMBL None None None CC(NC(=O)[C@@H]1C[C@H](O)CN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N[C@@](C)(Cc1ccccc1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O 10.1021/jm00069a016
44276439 96503 0 None - 1 Human 6.5 pKi = 6.5 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 546 9 0 6 6.3 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)CCc4ccc(C(=O)c5cccnc5)n4C)c3C)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL26629 96503 0 None - 1 Human 6.5 pKi = 6.5 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 546 9 0 6 6.3 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)CCc4ccc(C(=O)c5cccnc5)n4C)c3C)c2n1 10.1016/s0960-894x(03)00104-5
44276474 96928 0 None - 1 Human 6.5 pKi = 6.5 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 591 9 0 6 7.7 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CCc4ccc(C(=O)c5cccs5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL26976 96928 0 None - 1 Human 6.5 pKi = 6.5 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 591 9 0 6 7.7 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CCc4ccc(C(=O)c5cccs5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
10504589 56866 0 None - 1 Rat 6.5 pKi = 6.5 Binding
Inhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranesInhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranes
ChEMBL 471 9 4 6 3.5 O=[N+]([O-])c1cc(S(=O)(=O)NCc2ccccc2)ccc1N/N=C(/S)NCc1ccccc1 10.1021/jm991155o
CHEMBL164848 56866 0 None - 1 Rat 6.5 pKi = 6.5 Binding
Inhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranesInhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranes
ChEMBL 471 9 4 6 3.5 O=[N+]([O-])c1cc(S(=O)(=O)NCc2ccccc2)ccc1N/N=C(/S)NCc1ccccc1 10.1021/jm991155o
44346389 10141 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 497 7 3 3 6.0 O=C(Nc1cccnc1)[C@@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1016/0960-894X(95)00035-R
CHEMBL1160975 10141 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 497 7 3 3 6.0 O=C(Nc1cccnc1)[C@@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1016/0960-894X(95)00035-R
11614670 77286 0 None - 1 Human 6.5 pKi = 6.5 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 618 13 3 7 5.4 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCNCc4ccoc4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL208859 77286 0 None - 1 Human 6.5 pKi = 6.5 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 618 13 3 7 5.4 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCNCc4ccoc4)c3Cl)c2n1 10.1021/jm060137l
11571204 138168 0 None - 1 Human 6.5 pKi = 6.5 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 592 10 2 6 5.1 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCN4CCCCC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL377966 138168 0 None - 1 Human 6.5 pKi = 6.5 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 592 10 2 6 5.1 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCN4CCCCC4)c3Cl)c2n1 10.1021/jm060137l
44410526 82829 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity to human bradykinin B2 receptor transfected in CHO cellsBinding affinity to human bradykinin B2 receptor transfected in CHO cells
ChEMBL 1332 32 16 17 -4.3 NC(N)=NCCC[C@H](NC(=O)[C@@H]1CC2(CCCC2)C2CCC[C@@](Cc3ccccc3)(NC(=O)[C@H](CO)NC(=O)[C@H](Cc3cccs3)NC(=O)CNC(=O)[C@@H]3CC(O)CN3C(=O)[C@@H]3CCCN3C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N21)C(=O)O 10.1016/j.bmcl.2006.01.125
CHEMBL218749 82829 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity to human bradykinin B2 receptor transfected in CHO cellsBinding affinity to human bradykinin B2 receptor transfected in CHO cells
ChEMBL 1332 32 16 17 -4.3 NC(N)=NCCC[C@H](NC(=O)[C@@H]1CC2(CCCC2)C2CCC[C@@](Cc3ccccc3)(NC(=O)[C@H](CO)NC(=O)[C@H](Cc3cccs3)NC(=O)CNC(=O)[C@@H]3CC(O)CN3C(=O)[C@@H]3CCCN3C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N21)C(=O)O 10.1016/j.bmcl.2006.01.125
44316621 81690 0 None -57 2 Human 6.5 pKi = 6.5 Binding
Ability to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykininAbility to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykinin
ChEMBL 1091 24 13 15 -4.9 NC(N)=NCCCC(N)C(=O)N[C@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1CC(O)C[C@H]1C(=O)NCC(=O)NC(C(=O)N[C@@H](CO)C(=O)N[C@@H]1CSc2ccccc2N(CC(=O)O)C1=O)C1Cc2ccccc2C1 10.1021/jm990961s
CHEMBL216618 81690 0 None -57 2 Human 6.5 pKi = 6.5 Binding
Ability to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykininAbility to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykinin
ChEMBL 1091 24 13 15 -4.9 NC(N)=NCCCC(N)C(=O)N[C@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1CC(O)C[C@H]1C(=O)NCC(=O)NC(C(=O)N[C@@H](CO)C(=O)N[C@@H]1CSc2ccccc2N(CC(=O)O)C1=O)C1Cc2ccccc2C1 10.1021/jm990961s
101653256 12977 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 661 18 3 2 10.4 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2ccccc2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
44320170 12977 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 661 18 3 2 10.4 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2ccccc2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL1190355 12977 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 661 18 3 2 10.4 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2ccccc2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL540642 12977 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 661 18 3 2 10.4 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2ccccc2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
44298960 193955 0 None - 1 Human 7.5 pKi = 7.5 Binding
In vitro binding affinity against Bradykinin receptor B2In vitro binding affinity against Bradykinin receptor B2
ChEMBL 563 9 2 6 5.9 CC(=O)Nc1ccc(/C=C/C(=O)NC[C@@H]2CCCN2c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cn1 10.1016/s0960-894x(03)00309-3
CHEMBL55632 193955 0 None - 1 Human 7.5 pKi = 7.5 Binding
In vitro binding affinity against Bradykinin receptor B2In vitro binding affinity against Bradykinin receptor B2
ChEMBL 563 9 2 6 5.9 CC(=O)Nc1ccc(/C=C/C(=O)NC[C@@H]2CCCN2c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cn1 10.1016/s0960-894x(03)00309-3
44346104 11304 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 643 28 0 0 15.0 CCCCC[P+](CCCCC)(CCCCC)Cc1ccc2cc(C[P+](CCCCC)(CCCCC)CCCCC)ccc2c1 10.1016/0960-894X(95)00035-R
CHEMBL1180289 11304 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 643 28 0 0 15.0 CCCCC[P+](CCCCC)(CCCCC)Cc1ccc2cc(C[P+](CCCCC)(CCCCC)CCCCC)ccc2c1 10.1016/0960-894X(95)00035-R
CHEMBL120282 11304 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 643 28 0 0 15.0 CCCCC[P+](CCCCC)(CCCCC)Cc1ccc2cc(C[P+](CCCCC)(CCCCC)CCCCC)ccc2c1 10.1016/0960-894X(95)00035-R
44320170 14162 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligandBinding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligand
ChEMBL 663 18 3 2 10.1 CCCC[PH](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2ccccc2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1021/jm00069a021
CHEMBL1162585 14162 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligandBinding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligand
ChEMBL 663 18 3 2 10.1 CCCC[PH](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2ccccc2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1021/jm00069a021
CHEMBL1199851 14162 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligandBinding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligand
ChEMBL 663 18 3 2 10.1 CCCC[PH](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2ccccc2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1021/jm00069a021
22288578 98642 0 None - 1 Human 7.5 pKi = 7.5 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 649 9 0 7 6.6 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(S(C)(=O)=O)cc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL280869 98642 0 None - 1 Human 7.5 pKi = 7.5 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 649 9 0 7 6.6 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(S(C)(=O)=O)cc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
10930680 67321 0 None -6 2 Human 7.5 pKi = 7.5 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 750 15 4 9 4.7 CN(C)CCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(N/N=C(\S)NC(c2ccccc2Cl)c2ccccc2Cl)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL1907654 67321 0 None -6 2 Human 7.5 pKi = 7.5 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 750 15 4 9 4.7 CN(C)CCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(N/N=C(\S)NC(c2ccccc2Cl)c2ccccc2Cl)c([N+](=O)[O-])c1 10.1021/jm0111088
10100960 16297 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 669 29 0 0 15.5 CCCCC[P+](CCCCC)(CCCCC)Cc1ccc(-c2ccc(C[P+](CCCCC)(CCCCC)CCCCC)cc2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL123548 16297 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 669 29 0 0 15.5 CCCCC[P+](CCCCC)(CCCCC)Cc1ccc(-c2ccc(C[P+](CCCCC)(CCCCC)CCCCC)cc2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL333705 16297 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 669 29 0 0 15.5 CCCCC[P+](CCCCC)(CCCCC)Cc1ccc(-c2ccc(C[P+](CCCCC)(CCCCC)CCCCC)cc2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL539629 16297 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 669 29 0 0 15.5 CCCCC[P+](CCCCC)(CCCCC)Cc1ccc(-c2ccc(C[P+](CCCCC)(CCCCC)CCCCC)cc2)cc1 10.1016/0960-894X(95)00035-R
10100960 16297 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity against human IMR90 fetal lung fibroblast bradykinin B2 receptor was evaluatedBinding affinity against human IMR90 fetal lung fibroblast bradykinin B2 receptor was evaluated
ChEMBL 669 29 0 0 15.5 CCCCC[P+](CCCCC)(CCCCC)Cc1ccc(-c2ccc(C[P+](CCCCC)(CCCCC)CCCCC)cc2)cc1 10.1016/0960-894X(95)00036-S
CHEMBL123548 16297 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity against human IMR90 fetal lung fibroblast bradykinin B2 receptor was evaluatedBinding affinity against human IMR90 fetal lung fibroblast bradykinin B2 receptor was evaluated
ChEMBL 669 29 0 0 15.5 CCCCC[P+](CCCCC)(CCCCC)Cc1ccc(-c2ccc(C[P+](CCCCC)(CCCCC)CCCCC)cc2)cc1 10.1016/0960-894X(95)00036-S
CHEMBL333705 16297 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity against human IMR90 fetal lung fibroblast bradykinin B2 receptor was evaluatedBinding affinity against human IMR90 fetal lung fibroblast bradykinin B2 receptor was evaluated
ChEMBL 669 29 0 0 15.5 CCCCC[P+](CCCCC)(CCCCC)Cc1ccc(-c2ccc(C[P+](CCCCC)(CCCCC)CCCCC)cc2)cc1 10.1016/0960-894X(95)00036-S
CHEMBL539629 16297 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity against human IMR90 fetal lung fibroblast bradykinin B2 receptor was evaluatedBinding affinity against human IMR90 fetal lung fibroblast bradykinin B2 receptor was evaluated
ChEMBL 669 29 0 0 15.5 CCCCC[P+](CCCCC)(CCCCC)Cc1ccc(-c2ccc(C[P+](CCCCC)(CCCCC)CCCCC)cc2)cc1 10.1016/0960-894X(95)00036-S
44346418 13631 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 697 17 3 2 11.6 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)C(N/C(=N/C2CCCCC2)NC2CCCCC2)c2ccc3ccccc3c2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL1195322 13631 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 697 17 3 2 11.6 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)C(N/C(=N/C2CCCCC2)NC2CCCCC2)c2ccc3ccccc3c2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL554254 13631 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 697 17 3 2 11.6 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)C(N/C(=N/C2CCCCC2)NC2CCCCC2)c2ccc3ccccc3c2)cc1 10.1016/0960-894X(95)00035-R
11215913 136003 0 None -26915 2 Human 4.5 pKi = 4.5 Binding
Displacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cellsDisplacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cells
ChEMBL 646 9 2 6 4.9 CN1c2cc(CN3CCCCC3)ccc2[C@@H](NC(=O)C[C@@H](NS(=O)(=O)c2ccc3ccccc3c2)c2ccccc2)CS1(=O)=O 10.1021/jm061224g
CHEMBL373654 136003 0 None -26915 2 Human 4.5 pKi = 4.5 Binding
Displacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cellsDisplacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cells
ChEMBL 646 9 2 6 4.9 CN1c2cc(CN3CCCCC3)ccc2[C@@H](NC(=O)C[C@@H](NS(=O)(=O)c2ccc3ccccc3c2)c2ccccc2)CS1(=O)=O 10.1021/jm061224g
44276975 96055 0 None - 1 Guinea pig 6.4 pKi = 6.4 Binding
Binding affinity towards bradykinin receptor B2 using [3H]bradykininBinding affinity towards bradykinin receptor B2 using [3H]bradykinin
ChEMBL 1081 34 13 12 -0.8 NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)NCCCCCCCCCCCC(=O)N[C@@H](CO)C(=O)N1CCc2ccccc2C1C(=O)N1CC(C(=O)N[C@@H](CCCN=C(N)N)C(=O)O)C2CCCCC21 10.1021/jm00035a015
CHEMBL262639 96055 0 None - 1 Guinea pig 6.4 pKi = 6.4 Binding
Binding affinity towards bradykinin receptor B2 using [3H]bradykininBinding affinity towards bradykinin receptor B2 using [3H]bradykinin
ChEMBL 1081 34 13 12 -0.8 NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)NCCCCCCCCCCCC(=O)N[C@@H](CO)C(=O)N1CCc2ccccc2C1C(=O)N1CC(C(=O)N[C@@H](CCCN=C(N)N)C(=O)O)C2CCCCC21 10.1021/jm00035a015
90663066 106093 0 None - 1 Guinea pig 6.4 pKi = 6.4 Binding
Compound was evaluated for inhibitory activity against [3H]BK in the classical guinea pig ileum B2 binding assayCompound was evaluated for inhibitory activity against [3H]BK in the classical guinea pig ileum B2 binding assay
ChEMBL 1081 34 14 12 -0.5 N=C(N)NCCC[C@H](NC(=O)[C@H](N)CCCN=C(N)N)C(=O)NCCCCCCCCCCCC(=O)N[C@@H](CO)C(=O)N1CCc2ccccc2[C@@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O 10.1016/S0960-894X(97)10042-7
CHEMBL3142595 106093 0 None - 1 Guinea pig 6.4 pKi = 6.4 Binding
Compound was evaluated for inhibitory activity against [3H]BK in the classical guinea pig ileum B2 binding assayCompound was evaluated for inhibitory activity against [3H]BK in the classical guinea pig ileum B2 binding assay
ChEMBL 1081 34 14 12 -0.5 N=C(N)NCCC[C@H](NC(=O)[C@H](N)CCCN=C(N)N)C(=O)NCCCCCCCCCCCC(=O)N[C@@H](CO)C(=O)N1CCc2ccccc2[C@@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O 10.1016/S0960-894X(97)10042-7
22288581 98813 0 None - 1 Human 7.4 pKi = 7.4 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 582 8 1 5 7.1 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(C#N)cc5)[nH]4)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL281951 98813 0 None - 1 Human 7.4 pKi = 7.4 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 582 8 1 5 7.1 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(C#N)cc5)[nH]4)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
9830551 99573 0 None - 1 Human 7.4 pKi = 7.4 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 620 9 0 6 7.6 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CCc4ccc(C(=O)c5ccc(Cl)nc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL287018 99573 0 None - 1 Human 7.4 pKi = 7.4 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 620 9 0 6 7.6 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CCc4ccc(C(=O)c5ccc(Cl)nc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
10571699 56842 0 None - 1 Rat 7.4 pKi = 7.4 Binding
Inhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranesInhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranes
ChEMBL 378 6 3 4 4.6 O=[N+]([O-])c1ccccc1N/N=C(/S)NC(c1ccccc1)c1ccccc1 10.1021/jm991155o
CHEMBL164636 56842 0 None - 1 Rat 7.4 pKi = 7.4 Binding
Inhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranesInhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranes
ChEMBL 378 6 3 4 4.6 O=[N+]([O-])c1ccccc1N/N=C(/S)NC(c1ccccc1)c1ccccc1 10.1021/jm991155o
22288602 99255 0 None - 1 Human 5.4 pKi = 5.4 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 624 10 0 6 7.9 CCCN(C(=O)Cc1ccc(C(=O)c2ccc(C#N)cc2)n1C)c1ccc(Cl)c(COc2cccc3ccc(C)nc23)c1Cl 10.1016/s0960-894x(03)00104-5
CHEMBL284865 99255 0 None - 1 Human 5.4 pKi = 5.4 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 624 10 0 6 7.9 CCCN(C(=O)Cc1ccc(C(=O)c2ccc(C#N)cc2)n1C)c1ccc(Cl)c(COc2cccc3ccc(C)nc23)c1Cl 10.1016/s0960-894x(03)00104-5
11707423 77662 0 None - 1 Human 7.4 pKi = 7.4 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 580 11 4 6 3.3 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCN=C(N)N)c3Cl)c2n1 10.1021/jm060137l
CHEMBL209873 77662 0 None - 1 Human 7.4 pKi = 7.4 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 580 11 4 6 3.3 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCN=C(N)N)c3Cl)c2n1 10.1021/jm060137l
11592927 138734 0 None - 1 Human 7.4 pKi = 7.4 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 629 13 3 7 5.2 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCNCc4ccccn4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL379083 138734 0 None - 1 Human 7.4 pKi = 7.4 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 629 13 3 7 5.2 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCNCc4ccccn4)c3Cl)c2n1 10.1021/jm060137l
11636064 77651 0 None - 1 Human 6.4 pKi = 6.4 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 553 11 2 6 4.6 COCCCNC(=O)C(C)(C)NS(=O)(=O)c1ccc(Cl)c(COc2cccc3ccc(C)nc23)c1Cl 10.1021/jm060137l
CHEMBL209819 77651 0 None - 1 Human 6.4 pKi = 6.4 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 553 11 2 6 4.6 COCCCNC(=O)C(C)(C)NS(=O)(=O)c1ccc(Cl)c(COc2cccc3ccc(C)nc23)c1Cl 10.1021/jm060137l
11498691 77851 0 None - 1 Human 6.4 pKi = 6.4 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 646 13 3 6 5.9 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCNCc4ccc(F)cc4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL210662 77851 0 None - 1 Human 6.4 pKi = 6.4 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 646 13 3 6 5.9 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCNCc4ccc(F)cc4)c3Cl)c2n1 10.1021/jm060137l
9916936 99237 0 None - 1 Human 8.4 pKi = 8.4 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 610 9 0 6 7.5 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CCc4ccc(C(=O)c5ccc(C#N)cc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL284727 99237 0 None - 1 Human 8.4 pKi = 8.4 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 610 9 0 6 7.5 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CCc4ccc(C(=O)c5ccc(C#N)cc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
10790025 57142 0 None - 1 Rat 8.4 pKi = 8.4 Binding
Inhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranesInhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranes
ChEMBL 457 7 4 6 3.2 NS(=O)(=O)c1ccc(N/N=C(/S)NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1021/jm991155o
CHEMBL165627 57142 0 None - 1 Rat 8.4 pKi = 8.4 Binding
Inhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranesInhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranes
ChEMBL 457 7 4 6 3.2 NS(=O)(=O)c1ccc(N/N=C(/S)NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1021/jm991155o
44316620 2081 0 None 19 2 Human 8.4 pKi = 8.4 Binding
Ability to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykininAbility to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykinin
ChEMBL None None None None 10.1021/jm990961s
656 2081 0 None 19 2 Human 8.4 pKi = 8.4 Binding
Ability to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykininAbility to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykinin
ChEMBL None None None None 10.1021/jm990961s
CHEMBL408846 2081 0 None 19 2 Human 8.4 pKi = 8.4 Binding
Ability to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykininAbility to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykinin
ChEMBL None None None None 10.1021/jm990961s
57393602 67323 0 None 3 2 Human 8.3 pKi = 8.3 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 708 13 4 9 3.0 CN(C)CCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(NNC(=S)NC2Cc3ccccc3Cc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL1907656 67323 0 None 3 2 Human 8.3 pKi = 8.3 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 708 13 4 9 3.0 CN(C)CCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(NNC(=S)NC2Cc3ccccc3Cc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
44320168 10137 0 None - 1 Human 6.4 pKi = 6.4 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 529 7 3 3 5.2 O=C(NC1CN2CCC1CC2)[C@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1016/0960-894X(95)00035-R
CHEMBL1160969 10137 0 None - 1 Human 6.4 pKi = 6.4 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 529 7 3 3 5.2 O=C(NC1CN2CCC1CC2)[C@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1016/0960-894X(95)00035-R
CHEMBL444322 10137 0 None - 1 Human 6.4 pKi = 6.4 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 529 7 3 3 5.2 O=C(NC1CN2CCC1CC2)[C@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1016/0960-894X(95)00035-R
44320168 10137 0 None - 1 Human 6.4 pKi = 6.4 Binding
Binding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligandBinding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligand
ChEMBL 529 7 3 3 5.2 O=C(NC1CN2CCC1CC2)[C@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1021/jm00069a021
CHEMBL1160969 10137 0 None - 1 Human 6.4 pKi = 6.4 Binding
Binding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligandBinding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligand
ChEMBL 529 7 3 3 5.2 O=C(NC1CN2CCC1CC2)[C@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1021/jm00069a021
CHEMBL444322 10137 0 None - 1 Human 6.4 pKi = 6.4 Binding
Binding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligandBinding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligand
ChEMBL 529 7 3 3 5.2 O=C(NC1CN2CCC1CC2)[C@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1021/jm00069a021
44346412 12974 0 None - 1 Human 6.4 pKi = 6.4 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 717 18 3 3 11.6 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2cc3ccccc3s2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL1190352 12974 0 None - 1 Human 6.4 pKi = 6.4 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 717 18 3 3 11.6 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2cc3ccccc3s2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL540639 12974 0 None - 1 Human 6.4 pKi = 6.4 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 717 18 3 3 11.6 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2cc3ccccc3s2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
70688994 77083 0 None -18 2 Human 4.4 pKi = 4.4 Binding
Binding affinity to B2 receptorBinding affinity to B2 receptor
ChEMBL 433 5 2 4 2.6 Cc1c(Cl)ccc(S(=O)(=O)N2CCC[C@H]2C(=O)NCC2CCNCC2)c1Cl 10.1021/jm2016057
CHEMBL2087028 77083 0 None -18 2 Human 4.4 pKi = 4.4 Binding
Binding affinity to B2 receptorBinding affinity to B2 receptor
ChEMBL 433 5 2 4 2.6 Cc1c(Cl)ccc(S(=O)(=O)N2CCC[C@H]2C(=O)NCC2CCNCC2)c1Cl 10.1021/jm2016057
44276459 95897 0 None - 1 Human 7.4 pKi = 7.4 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 652 11 0 6 8.6 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(C#N)cc5)n4CCC(C)C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL26160 95897 0 None - 1 Human 7.4 pKi = 7.4 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 652 11 0 6 8.6 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(C#N)cc5)n4CCC(C)C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
90663068 106094 0 None - 1 Human 7.4 pKi = 7.4 Binding
Compound was evaluated for inhibitory activity against [3H]BK in membrane preparations from a stable cell line that expresses the human B2 receptorCompound was evaluated for inhibitory activity against [3H]BK in membrane preparations from a stable cell line that expresses the human B2 receptor
ChEMBL 1095 35 13 12 -0.3 NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)NCCCCCCCCCCCCC(=O)N[C@@H](CO)C(=O)N1CCc2ccccc2[C@@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O 10.1016/S0960-894X(97)10042-7
CHEMBL3142597 106094 0 None - 1 Human 7.4 pKi = 7.4 Binding
Compound was evaluated for inhibitory activity against [3H]BK in membrane preparations from a stable cell line that expresses the human B2 receptorCompound was evaluated for inhibitory activity against [3H]BK in membrane preparations from a stable cell line that expresses the human B2 receptor
ChEMBL 1095 35 13 12 -0.3 NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)NCCCCCCCCCCCCC(=O)N[C@@H](CO)C(=O)N1CCc2ccccc2[C@@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O 10.1016/S0960-894X(97)10042-7
44340964 9600 0 None - 1 Guinea pig 7.3 pKi = 7.3 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 609 10 1 6 6.7 COc1c(N(C)C(=O)CNC(=O)/C=C/c2ccc(C(F)(F)F)cc2)ccc(SC)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
CHEMBL113176 9600 0 None - 1 Guinea pig 7.3 pKi = 7.3 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 609 10 1 6 6.7 COc1c(N(C)C(=O)CNC(=O)/C=C/c2ccc(C(F)(F)F)cc2)ccc(SC)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
10482991 100170 0 None - 1 Human 7.3 pKi = 7.3 Binding
In vitro binding affinity against Bradykinin receptor B2In vitro binding affinity against Bradykinin receptor B2
ChEMBL 563 9 2 6 5.9 CC(=O)Nc1ccc(/C=C/C(=O)NC[C@H]2CCCN2c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cn1 10.1016/s0960-894x(03)00309-3
CHEMBL292181 100170 0 None - 1 Human 7.3 pKi = 7.3 Binding
In vitro binding affinity against Bradykinin receptor B2In vitro binding affinity against Bradykinin receptor B2
ChEMBL 563 9 2 6 5.9 CC(=O)Nc1ccc(/C=C/C(=O)NC[C@H]2CCCN2c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cn1 10.1016/s0960-894x(03)00309-3
44346414 13632 0 None - 1 Human 5.3 pKi = 5.3 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 676 19 3 2 10.7 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](CCc2ccccc2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL1195323 13632 0 None - 1 Human 5.3 pKi = 5.3 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 676 19 3 2 10.7 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](CCc2ccccc2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL554255 13632 0 None - 1 Human 5.3 pKi = 5.3 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 676 19 3 2 10.7 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](CCc2ccccc2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
44276666 98152 0 None - 1 Human 6.3 pKi = 6.3 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 639 8 0 5 8.2 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(C(F)(F)F)cc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL27701 98152 0 None - 1 Human 6.3 pKi = 6.3 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 639 8 0 5 8.2 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(C(F)(F)F)cc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
44355289 161343 0 None - 1 Human 5.3 pKi = 5.3 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1134 31 16 17 -8.4 NC(N)=NCCC[C@H](NC(=O)CN1CC[C@@H](NC(=O)[C@H](CO)NC(=O)[C@H](Cc2cccs2)NC(=O)CNC(=O)[C@@H]2CC(O)CN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C1=O)C(=O)O 10.1021/jm9901531
CHEMBL415209 161343 0 None - 1 Human 5.3 pKi = 5.3 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1134 31 16 17 -8.4 NC(N)=NCCC[C@H](NC(=O)CN1CC[C@@H](NC(=O)[C@H](CO)NC(=O)[C@H](Cc2cccs2)NC(=O)CNC(=O)[C@@H]2CC(O)CN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C1=O)C(=O)O 10.1021/jm9901531
16108960 168682 0 None -30902 2 Human 4.3 pKi = 4.3 Binding
Displacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cellsDisplacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cells
ChEMBL 567 9 2 4 6.0 O=C(C[C@@H](NS(=O)(=O)c1ccc2ccccc2c1)c1ccccc1)N[C@@H]1CCc2cc(CN3CCCCC3)ccc21 10.1021/jm061224g
CHEMBL441188 168682 0 None -30902 2 Human 4.3 pKi = 4.3 Binding
Displacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cellsDisplacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cells
ChEMBL 567 9 2 4 6.0 O=C(C[C@@H](NS(=O)(=O)c1ccc2ccccc2c1)c1ccccc1)N[C@@H]1CCc2cc(CN3CCCCC3)ccc21 10.1021/jm061224g
44300140 101125 0 None - 1 Human 5.3 pKi = 5.3 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 526 8 4 3 6.1 O=C(Nc1ccc(CO)cc1)[C@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1016/0960-894X(95)00035-R
CHEMBL298832 101125 0 None - 1 Human 5.3 pKi = 5.3 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 526 8 4 3 6.1 O=C(Nc1ccc(CO)cc1)[C@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1016/0960-894X(95)00035-R
44214619 110103 0 None - 1 Guinea pig 8.3 pKi = 8.3 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 553 13 1 8 4.7 COC(=O)CCCCC(=O)NCC(=O)N(C)c1ccc(OC)c(COc2cccc3ccc(C)nc23)c1SC 10.1016/s0960-894x(98)00736-7
CHEMBL325601 110103 0 None - 1 Guinea pig 8.3 pKi = 8.3 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 553 13 1 8 4.7 COC(=O)CCCCC(=O)NCC(=O)N(C)c1ccc(OC)c(COc2cccc3ccc(C)nc23)c1SC 10.1016/s0960-894x(98)00736-7
10930680 67321 0 None 6 2 Rat 8.3 pKi = 8.3 Binding
Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesInhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranes
ChEMBL 750 15 4 9 4.7 CN(C)CCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(N/N=C(\S)NC(c2ccccc2Cl)c2ccccc2Cl)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL1907654 67321 0 None 6 2 Rat 8.3 pKi = 8.3 Binding
Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesInhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranes
ChEMBL 750 15 4 9 4.7 CN(C)CCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(N/N=C(\S)NC(c2ccccc2Cl)c2ccccc2Cl)c([N+](=O)[O-])c1 10.1021/jm0111088
44276716 99236 0 None - 1 Human 6.3 pKi = 6.3 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 622 10 0 6 7.6 C=CCN(C(=O)Cc1ccc(C(=O)c2ccc(C#N)cc2)n1C)c1ccc(Cl)c(COc2cccc3ccc(C)nc23)c1Cl 10.1016/s0960-894x(03)00104-5
CHEMBL284726 99236 0 None - 1 Human 6.3 pKi = 6.3 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 622 10 0 6 7.6 C=CCN(C(=O)Cc1ccc(C(=O)c2ccc(C#N)cc2)n1C)c1ccc(Cl)c(COc2cccc3ccc(C)nc23)c1Cl 10.1016/s0960-894x(03)00104-5
44355287 161319 0 None - 1 Human 6.3 pKi = 6.3 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1162 31 16 17 -7.6 NC(N)=NCCC[C@H](NC(=O)CN1CCCC[C@H](NC(=O)[C@H](CO)NC(=O)[C@H](Cc2cccs2)NC(=O)CNC(=O)[C@@H]2CC(O)CN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C1=O)C(=O)O 10.1021/jm9901531
CHEMBL415032 161319 0 None - 1 Human 6.3 pKi = 6.3 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1162 31 16 17 -7.6 NC(N)=NCCC[C@H](NC(=O)CN1CCCC[C@H](NC(=O)[C@H](CO)NC(=O)[C@H](Cc2cccs2)NC(=O)CNC(=O)[C@@H]2CC(O)CN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C1=O)C(=O)O 10.1021/jm9901531
122189855 122883 0 None -75 3 Rat 5.3 pKi = 5.3 Binding
Displacement of [3H]BK from B2R in rat brain membranes by liquid scintillation counting in based radioligand competition assayDisplacement of [3H]BK from B2R in rat brain membranes by liquid scintillation counting in based radioligand competition assay
ChEMBL 1816 45 23 23 -3.5 CSCC[C@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](C)NC(=O)[C@@H](N)Cc1ccc(O)cc1)C(=O)N[C@H](CCCNC(=N)N)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N1CCC[C@H]1C(=O)N1CC(O)CC1C(=O)NCC(=O)NC(Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N1C(C(=O)N[C@@H](CCCNC(=N)N)C(=O)O)CC2CCCCC21 10.1016/j.bmcl.2015.08.014
CHEMBL3616879 122883 0 None -75 3 Rat 5.3 pKi = 5.3 Binding
Displacement of [3H]BK from B2R in rat brain membranes by liquid scintillation counting in based radioligand competition assayDisplacement of [3H]BK from B2R in rat brain membranes by liquid scintillation counting in based radioligand competition assay
ChEMBL 1816 45 23 23 -3.5 CSCC[C@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](C)NC(=O)[C@@H](N)Cc1ccc(O)cc1)C(=O)N[C@H](CCCNC(=N)N)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N1CCC[C@H]1C(=O)N1CC(O)CC1C(=O)NCC(=O)NC(Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N1C(C(=O)N[C@@H](CCCNC(=N)N)C(=O)O)CC2CCCCC21 10.1016/j.bmcl.2015.08.014
44346361 10139 0 None - 1 Human 5.3 pKi = 5.3 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 536 7 4 3 6.5 O=C(Nc1nc2ccccc2[nH]1)[C@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1016/0960-894X(95)00035-R
CHEMBL1160971 10139 0 None - 1 Human 5.3 pKi = 5.3 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 536 7 4 3 6.5 O=C(Nc1nc2ccccc2[nH]1)[C@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1016/0960-894X(95)00035-R
10742229 119750 0 None - 1 Rat 6.3 pKi = 6.3 Binding
Inhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranesInhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranes
ChEMBL 451 9 4 8 2.7 O=[N+]([O-])c1cc(S(=O)(=O)NCc2ccco2)ccc1N/N=C(/S)NCc1ccco1 10.1021/jm991155o
CHEMBL352459 119750 0 None - 1 Rat 6.3 pKi = 6.3 Binding
Inhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranesInhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranes
ChEMBL 451 9 4 8 2.7 O=[N+]([O-])c1cc(S(=O)(=O)NCc2ccco2)ccc1N/N=C(/S)NCc1ccco1 10.1021/jm991155o
44276455 97912 0 None - 1 Human 7.3 pKi = 7.3 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 610 9 0 6 7.5 CCN(C(=O)Cc1ccc(C(=O)c2ccc(C#N)cc2)n1C)c1ccc(Cl)c(COc2cccc3ccc(C)nc23)c1Cl 10.1016/s0960-894x(03)00104-5
CHEMBL27530 97912 0 None - 1 Human 7.3 pKi = 7.3 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 610 9 0 6 7.5 CCN(C(=O)Cc1ccc(C(=O)c2ccc(C#N)cc2)n1C)c1ccc(Cl)c(COc2cccc3ccc(C)nc23)c1Cl 10.1016/s0960-894x(03)00104-5
44346306 10136 0 None - 1 Human 6.3 pKi = 6.3 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 529 7 3 3 5.2 O=C(NC1CN2CCC1CC2)C(Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1016/0960-894X(95)00035-R
CHEMBL1160968 10136 0 None - 1 Human 6.3 pKi = 6.3 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 529 7 3 3 5.2 O=C(NC1CN2CCC1CC2)C(Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1016/0960-894X(95)00035-R
44320168 10137 0 None - 1 Human 6.3 pKi = 6.3 Binding
Binding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligandBinding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligand
ChEMBL 529 7 3 3 5.2 O=C(NC1CN2CCC1CC2)[C@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1021/jm00069a021
CHEMBL1160969 10137 0 None - 1 Human 6.3 pKi = 6.3 Binding
Binding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligandBinding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligand
ChEMBL 529 7 3 3 5.2 O=C(NC1CN2CCC1CC2)[C@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1021/jm00069a021
CHEMBL444322 10137 0 None - 1 Human 6.3 pKi = 6.3 Binding
Binding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligandBinding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligand
ChEMBL 529 7 3 3 5.2 O=C(NC1CN2CCC1CC2)[C@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1021/jm00069a021
44276487 99524 0 None - 1 Human 5.3 pKi = 5.3 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 582 8 1 6 7.1 Cc1ccc2cccc(OCc3c(Cl)ccc(NC(=O)Cc4ccc(C(=O)c5ccc(C#N)cc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL286711 99524 0 None - 1 Human 5.3 pKi = 5.3 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 582 8 1 6 7.1 Cc1ccc2cccc(OCc3c(Cl)ccc(NC(=O)Cc4ccc(C(=O)c5ccc(C#N)cc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
16108967 83912 0 None -147 2 Human 4.3 pKi = 4.3 Binding
Displacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cellsDisplacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cells
ChEMBL 541 10 2 4 5.6 O=C(CC(NS(=O)(=O)c1ccc2ccccc2c1)c1ccccc1)NCc1ccc(CN2CCCCC2)cc1 10.1021/jm061224g
CHEMBL221691 83912 0 None -147 2 Human 4.3 pKi = 4.3 Binding
Displacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cellsDisplacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cells
ChEMBL 541 10 2 4 5.6 O=C(CC(NS(=O)(=O)c1ccc2ccccc2c1)c1ccccc1)NCc1ccc(CN2CCCCC2)cc1 10.1021/jm061224g
10461651 98901 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 628 9 1 6 7.2 CC(=O)Nc1ccc(C(=O)c2ccc(CC(=O)N(C)c3ccc(Cl)c(COc4cccc5ccc(C)nc45)c3Cl)n2C)cc1 10.1016/s0960-894x(03)00104-5
CHEMBL282562 98901 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 628 9 1 6 7.2 CC(=O)Nc1ccc(C(=O)c2ccc(CC(=O)N(C)c3ccc(Cl)c(COc4cccc5ccc(C)nc45)c3Cl)n2C)cc1 10.1016/s0960-894x(03)00104-5
16108969 82604 0 None -239883 2 Human 4.2 pKi = 4.2 Binding
Displacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cellsDisplacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cells
ChEMBL 581 9 2 4 6.4 O=C(C[C@@H](NS(=O)(=O)c1ccc2ccccc2c1)c1ccccc1)N[C@@H]1CCCc2cc(CN3CCCCC3)ccc21 10.1021/jm061224g
CHEMBL218152 82604 0 None -239883 2 Human 4.2 pKi = 4.2 Binding
Displacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cellsDisplacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cells
ChEMBL 581 9 2 4 6.4 O=C(C[C@@H](NS(=O)(=O)c1ccc2ccccc2c1)c1ccccc1)N[C@@H]1CCCc2cc(CN3CCCCC3)ccc21 10.1021/jm061224g
CHEMBL3038105 209183 0 None 3 2 Human 6.2 pKi = 6.2 Binding
Binding affinity towards Bradykinin receptor B2 in human S34 clone cellsBinding affinity towards Bradykinin receptor B2 in human S34 clone cells
ChEMBL None None None NC(N)=NCCC[C@@H](N)C(=O)N[C@@H](CCCNC(N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N(CC(=O)N1C2CCCCC2C[C@H]1C(=O)O)Cc1ccccc1 10.1021/jm950716i
71450888 78368 0 None -8 2 Rat 8.2 pKi = 8.2 Binding
Binding affinity against rat bradykinin B2 receptors expressed in CHO cells using [3H]bradykinin as radioligandBinding affinity against rat bradykinin B2 receptors expressed in CHO cells using [3H]bradykinin as radioligand
ChEMBL 1228 31 16 18 -6.5 NC(N)=NCCC[C@H](NC(=O)CN1C(=O)[C@H](NC(=O)[C@H](CO)NC(=O)[C@H](Cc2cccs2)NC(=O)CNC(=O)[C@@H]2CC(O)CN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)CSc2ccccc21)C(=O)O 10.1021/jm9901529
CHEMBL2112698 78368 0 None -8 2 Rat 8.2 pKi = 8.2 Binding
Binding affinity against rat bradykinin B2 receptors expressed in CHO cells using [3H]bradykinin as radioligandBinding affinity against rat bradykinin B2 receptors expressed in CHO cells using [3H]bradykinin as radioligand
ChEMBL 1228 31 16 18 -6.5 NC(N)=NCCC[C@H](NC(=O)CN1C(=O)[C@H](NC(=O)[C@H](CO)NC(=O)[C@H](Cc2cccs2)NC(=O)CNC(=O)[C@@H]2CC(O)CN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)CSc2ccccc21)C(=O)O 10.1021/jm9901529
44355234 95998 0 None - 1 Human 8.2 pKi = 8.2 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1242 31 16 18 -6.2 Cc1ccc2c(c1)SCC(NC(=O)[C@H](CO)NC(=O)[C@H](Cc1cccs1)NC(=O)CNC(=O)[C@@H]1CC(O)CN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N2CC(=O)N[C@H](CCCN=C(N)N)C(=O)O 10.1021/jm9901531
CHEMBL262313 95998 0 None - 1 Human 8.2 pKi = 8.2 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1242 31 16 18 -6.2 Cc1ccc2c(c1)SCC(NC(=O)[C@H](CO)NC(=O)[C@H](Cc1cccs1)NC(=O)CNC(=O)[C@@H]1CC(O)CN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N2CC(=O)N[C@H](CCCN=C(N)N)C(=O)O 10.1021/jm9901531
22008916 9655 0 None - 1 Guinea pig 8.2 pKi = 8.2 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 461 8 2 6 3.3 CCNC(=O)NCC(=O)N(C)c1ccc(OC)c(COc2cccc3ccc(C)nc23)c1C#N 10.1016/s0960-894x(98)00736-7
CHEMBL113502 9655 0 None - 1 Guinea pig 8.2 pKi = 8.2 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 461 8 2 6 3.3 CCNC(=O)NCC(=O)N(C)c1ccc(OC)c(COc2cccc3ccc(C)nc23)c1C#N 10.1016/s0960-894x(98)00736-7
44337425 109376 0 None - 1 Human 8.2 pKi = 8.2 Binding
Affinity to human Bradykinin receptor B2 in CHO cell membranes determined by displacement of [3H]-NPC 17731Affinity to human Bradykinin receptor B2 in CHO cell membranes determined by displacement of [3H]-NPC 17731
ChEMBL 315 3 0 4 1.7 CC(=O)CN1CN(c2ccc(C)cc2)C2(CCN(C)CC2)C1=O 10.1021/jm950676i
CHEMBL323421 109376 0 None - 1 Human 8.2 pKi = 8.2 Binding
Affinity to human Bradykinin receptor B2 in CHO cell membranes determined by displacement of [3H]-NPC 17731Affinity to human Bradykinin receptor B2 in CHO cell membranes determined by displacement of [3H]-NPC 17731
ChEMBL 315 3 0 4 1.7 CC(=O)CN1CN(c2ccc(C)cc2)C2(CCN(C)CC2)C1=O 10.1021/jm950676i
44340951 9892 0 None - 1 Guinea pig 8.2 pKi = 8.2 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 587 11 1 7 6.4 COc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(SC)c(COc3cccc4ccc(C)nc34)c2SC)cc1 10.1016/s0960-894x(98)00736-7
CHEMBL114915 9892 0 None - 1 Guinea pig 8.2 pKi = 8.2 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 587 11 1 7 6.4 COc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(SC)c(COc3cccc4ccc(C)nc34)c2SC)cc1 10.1016/s0960-894x(98)00736-7
44337476 8029 0 None - 1 Human 8.2 pKi = 8.2 Binding
Affinity to human Bradykinin receptor B2 in CHO cell membranes determined by displacement of [3H]-NPC 17731Affinity to human Bradykinin receptor B2 in CHO cell membranes determined by displacement of [3H]-NPC 17731
ChEMBL 321 4 0 4 1.7 CC(=O)CN1CN(CC2CCCCC2)C2(CCN(C)CC2)C1=O 10.1021/jm950676i
CHEMBL109172 8029 0 None - 1 Human 8.2 pKi = 8.2 Binding
Affinity to human Bradykinin receptor B2 in CHO cell membranes determined by displacement of [3H]-NPC 17731Affinity to human Bradykinin receptor B2 in CHO cell membranes determined by displacement of [3H]-NPC 17731
ChEMBL 321 4 0 4 1.7 CC(=O)CN1CN(CC2CCCCC2)C2(CCN(C)CC2)C1=O 10.1021/jm950676i
132927 4009 3 None 6 2 Human 7.2 pKi = 7.2 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 746 18 3 2 8.5 CCCC[P+](Cc1ccc(cc1)NC(=O)[C@H](Cc1ccc2c(c1)cccc2)NC(=NC1CCCCC1)NC1CCCCC1)(CCCC)CCCC.[Cl-] 10.1016/0960-894X(95)00035-R
138398059 4009 3 None 6 2 Human 7.2 pKi = 7.2 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 746 18 3 2 8.5 CCCC[P+](Cc1ccc(cc1)NC(=O)[C@H](Cc1ccc2c(c1)cccc2)NC(=NC1CCCCC1)NC1CCCCC1)(CCCC)CCCC.[Cl-] 10.1016/0960-894X(95)00035-R
677 4009 3 None 6 2 Human 7.2 pKi = 7.2 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 746 18 3 2 8.5 CCCC[P+](Cc1ccc(cc1)NC(=O)[C@H](Cc1ccc2c(c1)cccc2)NC(=NC1CCCCC1)NC1CCCCC1)(CCCC)CCCC.[Cl-] 10.1016/0960-894X(95)00035-R
CHEMBL294453 4009 3 None 6 2 Human 7.2 pKi = 7.2 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 746 18 3 2 8.5 CCCC[P+](Cc1ccc(cc1)NC(=O)[C@H](Cc1ccc2c(c1)cccc2)NC(=NC1CCCCC1)NC1CCCCC1)(CCCC)CCCC.[Cl-] 10.1016/0960-894X(95)00035-R
CHEMBL551291 4009 3 None 6 2 Human 7.2 pKi = 7.2 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 746 18 3 2 8.5 CCCC[P+](Cc1ccc(cc1)NC(=O)[C@H](Cc1ccc2c(c1)cccc2)NC(=NC1CCCCC1)NC1CCCCC1)(CCCC)CCCC.[Cl-] 10.1016/0960-894X(95)00035-R
101005081 12975 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 754 21 3 2 12.7 CCCCC[P+](CCCCC)(CCCCC)Cc1ccc(NC(=O)[C@H](Cc2ccc3ccccc3c2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
44346317 12975 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 754 21 3 2 12.7 CCCCC[P+](CCCCC)(CCCCC)Cc1ccc(NC(=O)[C@H](Cc2ccc3ccccc3c2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL1190353 12975 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 754 21 3 2 12.7 CCCCC[P+](CCCCC)(CCCCC)Cc1ccc(NC(=O)[C@H](Cc2ccc3ccccc3c2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL540640 12975 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 754 21 3 2 12.7 CCCCC[P+](CCCCC)(CCCCC)Cc1ccc(NC(=O)[C@H](Cc2ccc3ccccc3c2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
132928 14167 3 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity against human IMR90 fetal lung fibroblast bradykinin B2 receptor was evaluatedBinding affinity against human IMR90 fetal lung fibroblast bradykinin B2 receptor was evaluated
ChEMBL 713 18 3 2 11.2 CCCC[PH](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2ccc3ccccc3c2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00036-S
CHEMBL1162586 14167 3 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity against human IMR90 fetal lung fibroblast bradykinin B2 receptor was evaluatedBinding affinity against human IMR90 fetal lung fibroblast bradykinin B2 receptor was evaluated
ChEMBL 713 18 3 2 11.2 CCCC[PH](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2ccc3ccccc3c2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00036-S
CHEMBL1199865 14167 3 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity against human IMR90 fetal lung fibroblast bradykinin B2 receptor was evaluatedBinding affinity against human IMR90 fetal lung fibroblast bradykinin B2 receptor was evaluated
ChEMBL 713 18 3 2 11.2 CCCC[PH](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2ccc3ccccc3c2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00036-S
132928 14167 3 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligandBinding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligand
ChEMBL 713 18 3 2 11.2 CCCC[PH](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2ccc3ccccc3c2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1021/jm00069a021
CHEMBL1162586 14167 3 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligandBinding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligand
ChEMBL 713 18 3 2 11.2 CCCC[PH](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2ccc3ccccc3c2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1021/jm00069a021
CHEMBL1199865 14167 3 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligandBinding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligand
ChEMBL 713 18 3 2 11.2 CCCC[PH](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2ccc3ccccc3c2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1021/jm00069a021
90662943 106089 0 None -1778 2 Human 7.2 pKi = 7.2 Binding
Ability to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykininAbility to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykinin
ChEMBL 1192 30 14 17 -4.3 NCCCC[C@H](N)C(=O)N[C@@H](CCCCN)C(=O)N[C@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1CC(O)C[C@H]1C(=O)NCC(=O)N[C@H](C(=O)N[C@@H](CO)C(=O)N[C@@H]1CSc2ccccc2N(CC(=O)O)C1=O)C1Cc2ccccc2C1 10.1021/jm990961s
CHEMBL3142391 106089 0 None -1778 2 Human 7.2 pKi = 7.2 Binding
Ability to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykininAbility to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykinin
ChEMBL 1192 30 14 17 -4.3 NCCCC[C@H](N)C(=O)N[C@@H](CCCCN)C(=O)N[C@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1CC(O)C[C@H]1C(=O)NCC(=O)N[C@H](C(=O)N[C@@H](CO)C(=O)N[C@@H]1CSc2ccccc2N(CC(=O)O)C1=O)C1Cc2ccccc2C1 10.1021/jm990961s
11650337 138145 0 None - 1 Human 7.2 pKi = 7.2 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 523 7 3 5 3.3 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N=C(N)N)c3Cl)c2n1 10.1021/jm060137l
CHEMBL377835 138145 0 None - 1 Human 7.2 pKi = 7.2 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 523 7 3 5 3.3 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N=C(N)N)c3Cl)c2n1 10.1021/jm060137l
11542210 77241 0 None - 1 Human 6.2 pKi = 6.2 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 608 11 2 7 4.3 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCN4CCOCC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL208807 77241 0 None - 1 Human 6.2 pKi = 6.2 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 608 11 2 7 4.3 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCN4CCOCC4)c3Cl)c2n1 10.1021/jm060137l
11136263 78161 0 None -43 2 Rat 7.2 pKi = 7.2 Binding
Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesInhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranes
ChEMBL 704 13 4 10 3.9 CN(C)CCN(C)CCNC(=O)c1cccn1S(=O)(=O)c1ccc(N/N=C(\S)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL2112221 78161 0 None -43 2 Rat 7.2 pKi = 7.2 Binding
Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesInhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranes
ChEMBL 704 13 4 10 3.9 CN(C)CCN(C)CCNC(=O)c1cccn1S(=O)(=O)c1ccc(N/N=C(\S)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
10952583 67324 0 None - 1 Human 6.2 pKi = 6.2 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 694 14 4 9 3.7 CN(C)CCCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(N/N=C(\S)NC2c3ccccc3-c3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL1907657 67324 0 None - 1 Human 6.2 pKi = 6.2 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 694 14 4 9 3.7 CN(C)CCCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(N/N=C(\S)NC2c3ccccc3-c3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
57395311 67322 0 None -2 2 Rat 6.2 pKi = 6.2 Binding
Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesInhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranes
ChEMBL 580 7 4 7 2.9 NC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(NNC(=S)NC2Cc3ccccc3Cc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL1907655 67322 0 None -2 2 Rat 6.2 pKi = 6.2 Binding
Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesInhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranes
ChEMBL 580 7 4 7 2.9 NC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(NNC(=S)NC2Cc3ccccc3Cc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
9915727 95068 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 556 8 0 6 6.4 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(C#N)cc5)n4C)c3C)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL25745 95068 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 556 8 0 6 6.4 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(C#N)cc5)n4C)c3C)c2n1 10.1016/s0960-894x(03)00104-5
10886849 67320 0 None - 1 Rat 8.1 pKi = 8.1 Binding
Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesInhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranes
ChEMBL 655 14 4 7 3.5 CN(C)CCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(NNC(=O)NC(c2ccccc2)c2ccccc2)c(Cl)c1 10.1021/jm0111088
CHEMBL1907653 67320 0 None - 1 Rat 8.1 pKi = 8.1 Binding
Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesInhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranes
ChEMBL 655 14 4 7 3.5 CN(C)CCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(NNC(=O)NC(c2ccccc2)c2ccccc2)c(Cl)c1 10.1021/jm0111088
44337489 9125 0 None - 1 Human 8.1 pKi = 8.1 Binding
Affinity to human Bradykinin receptor B2 in CHO cell membranes determined by displacement of [3H]-NPC 17731Affinity to human Bradykinin receptor B2 in CHO cell membranes determined by displacement of [3H]-NPC 17731
ChEMBL 301 3 0 4 1.3 CC(=O)CN1CN(c2ccccc2)C2(CCN(C)CC2)C1=O 10.1021/jm950676i
CHEMBL110652 9125 0 None - 1 Human 8.1 pKi = 8.1 Binding
Affinity to human Bradykinin receptor B2 in CHO cell membranes determined by displacement of [3H]-NPC 17731Affinity to human Bradykinin receptor B2 in CHO cell membranes determined by displacement of [3H]-NPC 17731
ChEMBL 301 3 0 4 1.3 CC(=O)CN1CN(c2ccccc2)C2(CCN(C)CC2)C1=O 10.1021/jm950676i
CHEMBL2392354 208660 0 None - 1 Human 8.1 pKi = 8.1 Binding
Binding affinity to human bradykinin B2 receptor by radioligand displacement assayBinding affinity to human bradykinin B2 receptor by radioligand displacement assay
ChEMBL None None None N=C(N)NCCC[C@H](N)C(=O)N[C@H](CCCNC(=N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](CO)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](CCCNC(=N)N)C(=O)O 10.1016/j.ejmech.2013.01.044
11527906 139575 0 None - 1 Human 8.1 pKi = 8.1 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 670 13 5 7 5.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCNc4ccc(C(=N)N)cc4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL380086 139575 0 None - 1 Human 8.1 pKi = 8.1 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 670 13 5 7 5.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCNc4ccc(C(=N)N)cc4)c3Cl)c2n1 10.1021/jm060137l
45266122 12979 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 726 18 2 2 11.9 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2ccc3ccccc3c2)N(C)/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL1190357 12979 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 726 18 2 2 11.9 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2ccc3ccccc3c2)N(C)/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL540644 12979 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 726 18 2 2 11.9 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2ccc3ccccc3c2)N(C)/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
44346679 12996 0 None - 1 Human 5.2 pKi = 5.2 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 631 18 3 2 9.7 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2ccc3ccccc3c2)N/C(=N/C(C)C)NC(C)C)cc1 10.1016/0960-894X(95)00035-R
CHEMBL1190473 12996 0 None - 1 Human 5.2 pKi = 5.2 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 631 18 3 2 9.7 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2ccc3ccccc3c2)N/C(=N/C(C)C)NC(C)C)cc1 10.1016/0960-894X(95)00035-R
CHEMBL540895 12996 0 None - 1 Human 5.2 pKi = 5.2 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 631 18 3 2 9.7 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2ccc3ccccc3c2)N/C(=N/C(C)C)NC(C)C)cc1 10.1016/0960-894X(95)00035-R
10542327 57097 0 None - 1 Rat 5.2 pKi = 5.2 Binding
Inhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranesInhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranes
ChEMBL 301 5 2 3 3.2 O=[N+]([O-])c1ccccc1C/N=C(\S)NCc1ccccc1 10.1021/jm991155o
CHEMBL165240 57097 0 None - 1 Rat 5.2 pKi = 5.2 Binding
Inhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranesInhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranes
ChEMBL 301 5 2 3 3.2 O=[N+]([O-])c1ccccc1C/N=C(\S)NCc1ccccc1 10.1021/jm991155o
44276840 99500 0 None - 1 Human 7.1 pKi = 7.1 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 628 9 1 6 7.2 CC(=O)Nc1cccc(C(=O)c2ccc(CC(=O)N(C)c3ccc(Cl)c(COc4cccc5ccc(C)nc45)c3Cl)n2C)c1 10.1016/s0960-894x(03)00104-5
CHEMBL286556 99500 0 None - 1 Human 7.1 pKi = 7.1 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 628 9 1 6 7.2 CC(=O)Nc1cccc(C(=O)c2ccc(CC(=O)N(C)c3ccc(Cl)c(COc4cccc5ccc(C)nc45)c3Cl)n2C)c1 10.1016/s0960-894x(03)00104-5
44276488 96748 0 None - 1 Human 7.1 pKi = 7.1 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 597 8 0 7 6.5 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(C#N)nc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL26847 96748 0 None - 1 Human 7.1 pKi = 7.1 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 597 8 0 7 6.5 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(C#N)nc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
44276624 96391 0 None - 1 Human 6.1 pKi = 6.1 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 605 8 0 5 7.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(Cl)cc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL26532 96391 0 None - 1 Human 6.1 pKi = 6.1 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 605 8 0 5 7.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(Cl)cc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
44276599 95948 0 None - 1 Human 7.1 pKi = 7.1 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 650 9 1 7 5.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(S(N)(=O)=O)cc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL26192 95948 0 None - 1 Human 7.1 pKi = 7.1 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 650 9 1 7 5.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(S(N)(=O)=O)cc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
44346387 14205 0 None - 1 Human 6.1 pKi = 6.1 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 696 18 2 1 12.3 CCCC[PH](CCCC)(CCCC)Cc1ccc(/C=C\[C@H](Cc2ccc3ccccc3c2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL1162797 14205 0 None - 1 Human 6.1 pKi = 6.1 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 696 18 2 1 12.3 CCCC[PH](CCCC)(CCCC)Cc1ccc(/C=C\[C@H](Cc2ccc3ccccc3c2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL1200033 14205 0 None - 1 Human 6.1 pKi = 6.1 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 696 18 2 1 12.3 CCCC[PH](CCCC)(CCCC)Cc1ccc(/C=C\[C@H](Cc2ccc3ccccc3c2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
176 394 63 None -5 31 Human 5.1 pKi = 5.1 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
ChEMBL 645 11 0 4 6.9 CCCCc1oc2c(c1C(=O)c1cc(I)c(c(c1)I)OCCN(CC)CC)cccc2 nan
2157 394 63 None -5 31 Human 5.1 pKi = 5.1 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
ChEMBL 645 11 0 4 6.9 CCCCc1oc2c(c1C(=O)c1cc(I)c(c(c1)I)OCCN(CC)CC)cccc2 nan
2566 394 63 None -5 31 Human 5.1 pKi = 5.1 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
ChEMBL 645 11 0 4 6.9 CCCCc1oc2c(c1C(=O)c1cc(I)c(c(c1)I)OCCN(CC)CC)cccc2 nan
CHEMBL633 394 63 None -5 31 Human 5.1 pKi = 5.1 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
ChEMBL 645 11 0 4 6.9 CCCCc1oc2c(c1C(=O)c1cc(I)c(c(c1)I)OCCN(CC)CC)cccc2 nan
DB01118 394 63 None -5 31 Human 5.1 pKi = 5.1 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
ChEMBL 645 11 0 4 6.9 CCCCc1oc2c(c1C(=O)c1cc(I)c(c(c1)I)OCCN(CC)CC)cccc2 nan
10373002 137770 0 None - 1 Human 6.1 pKi = 6.1 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 697 30 0 1 15.1 CCCCC[P+](CCCCC)(CCCCC)Cc1ccc(C(=O)c2ccc(C[P+](CCCCC)(CCCCC)CCCCC)cc2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL121565 137770 0 None - 1 Human 6.1 pKi = 6.1 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 697 30 0 1 15.1 CCCCC[P+](CCCCC)(CCCCC)Cc1ccc(C(=O)c2ccc(C[P+](CCCCC)(CCCCC)CCCCC)cc2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL377100 137770 0 None - 1 Human 6.1 pKi = 6.1 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 697 30 0 1 15.1 CCCCC[P+](CCCCC)(CCCCC)Cc1ccc(C(=O)c2ccc(C[P+](CCCCC)(CCCCC)CCCCC)cc2)cc1 10.1016/0960-894X(95)00035-R
10373002 137770 0 None - 1 Human 6.1 pKi = 6.1 Binding
Binding affinity against human IMR90 fetal lung fibroblast bradykinin B2 receptor was evaluatedBinding affinity against human IMR90 fetal lung fibroblast bradykinin B2 receptor was evaluated
ChEMBL 697 30 0 1 15.1 CCCCC[P+](CCCCC)(CCCCC)Cc1ccc(C(=O)c2ccc(C[P+](CCCCC)(CCCCC)CCCCC)cc2)cc1 10.1016/0960-894X(95)00036-S
CHEMBL121565 137770 0 None - 1 Human 6.1 pKi = 6.1 Binding
Binding affinity against human IMR90 fetal lung fibroblast bradykinin B2 receptor was evaluatedBinding affinity against human IMR90 fetal lung fibroblast bradykinin B2 receptor was evaluated
ChEMBL 697 30 0 1 15.1 CCCCC[P+](CCCCC)(CCCCC)Cc1ccc(C(=O)c2ccc(C[P+](CCCCC)(CCCCC)CCCCC)cc2)cc1 10.1016/0960-894X(95)00036-S
CHEMBL377100 137770 0 None - 1 Human 6.1 pKi = 6.1 Binding
Binding affinity against human IMR90 fetal lung fibroblast bradykinin B2 receptor was evaluatedBinding affinity against human IMR90 fetal lung fibroblast bradykinin B2 receptor was evaluated
ChEMBL 697 30 0 1 15.1 CCCCC[P+](CCCCC)(CCCCC)Cc1ccc(C(=O)c2ccc(C[P+](CCCCC)(CCCCC)CCCCC)cc2)cc1 10.1016/0960-894X(95)00036-S
44355257 165898 0 None - 1 Human 6.1 pKi = 6.1 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1162 31 16 17 -7.6 NC(N)=NCCC[C@H](NC(=O)CN1CCCC[C@@H](NC(=O)[C@H](CO)NC(=O)[C@H](Cc2cccs2)NC(=O)CNC(=O)[C@@H]2CC(O)CN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C1=O)C(=O)O 10.1021/jm9901531
CHEMBL427805 165898 0 None - 1 Human 6.1 pKi = 6.1 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1162 31 16 17 -7.6 NC(N)=NCCC[C@H](NC(=O)CN1CCCC[C@@H](NC(=O)[C@H](CO)NC(=O)[C@H](Cc2cccs2)NC(=O)CNC(=O)[C@@H]2CC(O)CN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C1=O)C(=O)O 10.1021/jm9901531
5312119 709 4 None -1148 2 Human 6.1 pKi = 6.1 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 682 15 4 9 2.9 CN(CCN(C)C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(c(c1)[N+](=O)[O-])NNC(=S)NC(c1ccccc1)c1ccccc1 10.1021/jm0111088
680 709 4 None -1148 2 Human 6.1 pKi = 6.1 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 682 15 4 9 2.9 CN(CCN(C)C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(c(c1)[N+](=O)[O-])NNC(=S)NC(c1ccccc1)c1ccccc1 10.1021/jm0111088
CHEMBL308468 709 4 None -1148 2 Human 6.1 pKi = 6.1 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 682 15 4 9 2.9 CN(CCN(C)C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(c(c1)[N+](=O)[O-])NNC(=S)NC(c1ccccc1)c1ccccc1 10.1021/jm0111088
11650783 52135 0 None - 1 Human 7.1 pKi = 7.1 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 706 14 3 8 5.2 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCNCc4ccc(S(C)(=O)=O)cc4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL159066 52135 0 None - 1 Human 7.1 pKi = 7.1 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 706 14 3 8 5.2 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCNCc4ccc(S(C)(=O)=O)cc4)c3Cl)c2n1 10.1021/jm060137l
11636119 77709 0 None - 1 Human 7.1 pKi = 7.1 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 564 8 3 6 4.4 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NC4CCNCC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL210100 77709 0 None - 1 Human 7.1 pKi = 7.1 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 564 8 3 6 4.4 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NC4CCNCC4)c3Cl)c2n1 10.1021/jm060137l
11686399 139594 0 None - 1 Human 7.1 pKi = 7.1 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 644 13 4 7 5.5 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCNCc4ccc(O)cc4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL380206 139594 0 None - 1 Human 7.1 pKi = 7.1 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 644 13 4 7 5.5 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCNCc4ccc(O)cc4)c3Cl)c2n1 10.1021/jm060137l
11527892 138985 0 None - 1 Human 6.1 pKi = 6.1 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 662 13 3 6 6.4 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCNCc4ccc(Cl)cc4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL379541 138985 0 None - 1 Human 6.1 pKi = 6.1 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 662 13 3 6 6.4 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCNCc4ccc(Cl)cc4)c3Cl)c2n1 10.1021/jm060137l
11671905 77391 0 None - 1 Human 5.1 pKi = 5.1 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 539 10 2 6 4.2 COCCNC(=O)C(C)(C)NS(=O)(=O)c1ccc(Cl)c(COc2cccc3ccc(C)nc23)c1Cl 10.1021/jm060137l
CHEMBL209068 77391 0 None - 1 Human 5.1 pKi = 5.1 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 539 10 2 6 4.2 COCCNC(=O)C(C)(C)NS(=O)(=O)c1ccc(Cl)c(COc2cccc3ccc(C)nc23)c1Cl 10.1021/jm060137l
11513104 77790 0 None - 1 Human 5.1 pKi = 5.1 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 557 8 2 5 6.1 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)Nc4ccccc4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL210427 77790 0 None - 1 Human 5.1 pKi = 5.1 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 557 8 2 5 6.1 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)Nc4ccccc4)c3Cl)c2n1 10.1021/jm060137l
10895913 9761 0 None - 1 Guinea pig 8.1 pKi = 8.1 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 465 7 2 5 3.9 CCNC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccc3ccc(C)nc23)c1C#N 10.1016/s0960-894x(98)00736-7
CHEMBL114180 9761 0 None - 1 Guinea pig 8.1 pKi = 8.1 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 465 7 2 5 3.9 CCNC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccc3ccc(C)nc23)c1C#N 10.1016/s0960-894x(98)00736-7
CHEMBL3038102 209180 0 None 5 2 Human 8.1 pKi = 8.1 Binding
Binding affinity towards Bradykinin receptor B2 in human S34 clone cellsBinding affinity towards Bradykinin receptor B2 in human S34 clone cells
ChEMBL None None None NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N(CC(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O)Cc1ccccc1 10.1021/jm950716i
44347466 14206 0 None - 1 Human 6.1 pKi = 6.1 Binding
Tested for binding affinity against human IMR-90 Bradykinin receptor B2Tested for binding affinity against human IMR-90 Bradykinin receptor B2
ChEMBL 836 20 3 3 11.4 CCCC[PH](CCCC)(CCCC)Cc1ccc(NC(=O)C2Cc3ccccc3CN2C(=O)[C@H](CCc2ccccc2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00037-T
CHEMBL1162799 14206 0 None - 1 Human 6.1 pKi = 6.1 Binding
Tested for binding affinity against human IMR-90 Bradykinin receptor B2Tested for binding affinity against human IMR-90 Bradykinin receptor B2
ChEMBL 836 20 3 3 11.4 CCCC[PH](CCCC)(CCCC)Cc1ccc(NC(=O)C2Cc3ccccc3CN2C(=O)[C@H](CCc2ccccc2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00037-T
CHEMBL1200034 14206 0 None - 1 Human 6.1 pKi = 6.1 Binding
Tested for binding affinity against human IMR-90 Bradykinin receptor B2Tested for binding affinity against human IMR-90 Bradykinin receptor B2
ChEMBL 836 20 3 3 11.4 CCCC[PH](CCCC)(CCCC)Cc1ccc(NC(=O)C2Cc3ccccc3CN2C(=O)[C@H](CCc2ccccc2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00037-T
44347757 11327 0 None - 1 Human 5.1 pKi = 5.1 Binding
Tested for binding affinity against human IMR-90 Bradykinin receptor B2Tested for binding affinity against human IMR-90 Bradykinin receptor B2
ChEMBL 728 18 2 4 10.0 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)C2Cc3ccccc3CN2C(=O)C(CCc2ccccc2)NC(=O)OC(C)(C)C)cc1 10.1016/0960-894X(95)00037-T
CHEMBL1180347 11327 0 None - 1 Human 5.1 pKi = 5.1 Binding
Tested for binding affinity against human IMR-90 Bradykinin receptor B2Tested for binding affinity against human IMR-90 Bradykinin receptor B2
ChEMBL 728 18 2 4 10.0 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)C2Cc3ccccc3CN2C(=O)C(CCc2ccccc2)NC(=O)OC(C)(C)C)cc1 10.1016/0960-894X(95)00037-T
CHEMBL123124 11327 0 None - 1 Human 5.1 pKi = 5.1 Binding
Tested for binding affinity against human IMR-90 Bradykinin receptor B2Tested for binding affinity against human IMR-90 Bradykinin receptor B2
ChEMBL 728 18 2 4 10.0 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)C2Cc3ccccc3CN2C(=O)C(CCc2ccccc2)NC(=O)OC(C)(C)C)cc1 10.1016/0960-894X(95)00037-T
CHEMBL2370041 208019 0 None - 1 Guinea pig 7.1 pKi = 7.1 Binding
Binding affinity against [3H]bradykinin binding to bradykinin receptor B2 in guinea pig ileal membraneBinding affinity against [3H]bradykinin binding to bradykinin receptor B2 in guinea pig ileal membrane
ChEMBL None None None CC(NC(=O)[C@@H]1C[C@H](O)CN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O 10.1021/jm00069a016
44346449 10142 0 None - 1 Human 6.1 pKi = 6.1 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 619 9 2 3 7.1 O=C([C@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1)N(Cc1ccccc1)C1CN2CCC1CC2 10.1016/0960-894X(95)00035-R
CHEMBL1160978 10142 0 None - 1 Human 6.1 pKi = 6.1 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 619 9 2 3 7.1 O=C([C@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1)N(Cc1ccccc1)C1CN2CCC1CC2 10.1016/0960-894X(95)00035-R
118719116 114932 0 None - 1 Human 7.1 pKi = 7.1 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1285 32 16 18 -5.8 NC(N)=NCCC[C@H](NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)NC1N=C(c2ccccc2)c2ccccc2N(CC(=O)N[C@H](CCCN=C(N)N)C(=O)O)C1=O 10.1021/jm9901531
CHEMBL3350763 114932 0 None - 1 Human 7.1 pKi = 7.1 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1285 32 16 18 -5.8 NC(N)=NCCC[C@H](NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)NC1N=C(c2ccccc2)c2ccccc2N(CC(=O)N[C@H](CCCN=C(N)N)C(=O)O)C1=O 10.1021/jm9901531
44276841 95072 0 None - 1 Human 6.1 pKi = 6.1 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 628 9 1 6 7.2 CC(=O)Nc1ccccc1C(=O)c1ccc(CC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)n1C 10.1016/s0960-894x(03)00104-5
CHEMBL25748 95072 0 None - 1 Human 6.1 pKi = 6.1 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 628 9 1 6 7.2 CC(=O)Nc1ccccc1C(=O)c1ccc(CC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)n1C 10.1016/s0960-894x(03)00104-5
10005078 33530 0 None - 1 Human 5.1 pKi = 5.1 Binding
Binding affinity towards human bradykinin B2 receptor (membranes from Cos-7 cells expressing human B2 receptor) using [3H]-BK as radioligandBinding affinity towards human bradykinin B2 receptor (membranes from Cos-7 cells expressing human B2 receptor) using [3H]-BK as radioligand
ChEMBL 473 6 3 3 5.0 N=C(N)Nc1cccc(CN2C(=O)C(Cc3ccccc3)N=C(c3ccccc3)c3ccccc32)c1 10.1016/s0960-894x(99)00015-3
CHEMBL142260 33530 0 None - 1 Human 5.1 pKi = 5.1 Binding
Binding affinity towards human bradykinin B2 receptor (membranes from Cos-7 cells expressing human B2 receptor) using [3H]-BK as radioligandBinding affinity towards human bradykinin B2 receptor (membranes from Cos-7 cells expressing human B2 receptor) using [3H]-BK as radioligand
ChEMBL 473 6 3 3 5.0 N=C(N)Nc1cccc(CN2C(=O)C(Cc3ccccc3)N=C(c3ccccc3)c3ccccc32)c1 10.1016/s0960-894x(99)00015-3
15388870 110131 0 None - 1 Guinea pig 8.0 pKi = 8.0 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 543 8 1 6 6.4 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)OCc4ccccc4)c3Cl)cccc2s1 10.1016/s0960-894x(98)00736-7
CHEMBL325742 110131 0 None - 1 Guinea pig 8.0 pKi = 8.0 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 543 8 1 6 6.4 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)OCc4ccccc4)c3Cl)cccc2s1 10.1016/s0960-894x(98)00736-7
CHEMBL3085458 209232 3 None -398 2 Human 8.0 pKi = 8.0 Binding
Binding affinity towards human cloned B2 receptor was determined using [3H]BK as radioligandBinding affinity towards human cloned B2 receptor was determined using [3H]BK as radioligand
ChEMBL None None None NCCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@H](C(=O)N[C@@H](CO)C(=O)N[C@@H]1CSc2ccccc2N(CC(=O)O)C1=O)C1Cc2ccccc2C1 10.1021/jm990962k
CHEMBL3085458 209232 3 None -398 2 Human 8.0 pKi = 8.0 Binding
Ability to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykininAbility to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykinin
ChEMBL None None None NCCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@H](C(=O)N[C@@H](CO)C(=O)N[C@@H]1CSc2ccccc2N(CC(=O)O)C1=O)C1Cc2ccccc2C1 10.1021/jm990961s
44341060 9454 0 None - 1 Guinea pig 8.0 pKi = 8.0 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 539 10 1 6 5.2 COc1ccc(N(C)C(=O)CNC(=O)/C=C/c2cccc(C)c2)c(OC)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
CHEMBL112360 9454 0 None - 1 Guinea pig 8.0 pKi = 8.0 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 539 10 1 6 5.2 COc1ccc(N(C)C(=O)CNC(=O)/C=C/c2cccc(C)c2)c(OC)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
122189902 122894 0 None -13489 2 Human 5.1 pKi = 5.1 Binding
Displacement of [3H]BK from human B2R expressed in HEK293 cell membranes by liquid scintillation counting in based radioligand competition assayDisplacement of [3H]BK from human B2R expressed in HEK293 cell membranes by liquid scintillation counting in based radioligand competition assay
ChEMBL 1304 30 18 17 -4.4 N=C(N)NCCC[C@H](NC(=O)C1CC2CCCCC2N1C(=O)[C@H]1Cc2ccccc2CN1C(=O)[C@H](CO)NC(=O)C(Cc1cccs1)NC(=O)CNC(=O)C1CC(O)CN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](N)CCCNC(=N)N)C(=O)O 10.1016/j.bmcl.2015.08.014
CHEMBL3616944 122894 0 None -13489 2 Human 5.1 pKi = 5.1 Binding
Displacement of [3H]BK from human B2R expressed in HEK293 cell membranes by liquid scintillation counting in based radioligand competition assayDisplacement of [3H]BK from human B2R expressed in HEK293 cell membranes by liquid scintillation counting in based radioligand competition assay
ChEMBL 1304 30 18 17 -4.4 N=C(N)NCCC[C@H](NC(=O)C1CC2CCCCC2N1C(=O)[C@H]1Cc2ccccc2CN1C(=O)[C@H](CO)NC(=O)C(Cc1cccs1)NC(=O)CNC(=O)C1CC(O)CN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](N)CCCNC(=N)N)C(=O)O 10.1016/j.bmcl.2015.08.014
44276667 98153 0 None - 1 Human 7.0 pKi = 7.0 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 601 9 0 6 7.2 COc1ccc(C(=O)c2ccc(CC(=O)N(C)c3ccc(Cl)c(COc4cccc5ccc(C)nc45)c3Cl)n2C)cc1 10.1016/s0960-894x(03)00104-5
CHEMBL27702 98153 0 None - 1 Human 7.0 pKi = 7.0 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 601 9 0 6 7.2 COc1ccc(C(=O)c2ccc(CC(=O)N(C)c3ccc(Cl)c(COc4cccc5ccc(C)nc45)c3Cl)n2C)cc1 10.1016/s0960-894x(03)00104-5
44361937 168827 0 None - 1 Human 5.0 pKi = 5.0 Binding
Binding affinity towards human bradykinin B2 receptor (membranes from Cos-7 cells expressing human B2 receptor) using [3H]-BK as radioligandBinding affinity towards human bradykinin B2 receptor (membranes from Cos-7 cells expressing human B2 receptor) using [3H]-BK as radioligand
ChEMBL 459 5 3 3 5.1 N=C(N)Nc1ccc(N2C(=O)C(Cc3ccccc3)N=C(c3ccccc3)c3ccccc32)cc1 10.1016/s0960-894x(99)00015-3
CHEMBL442294 168827 0 None - 1 Human 5.0 pKi = 5.0 Binding
Binding affinity towards human bradykinin B2 receptor (membranes from Cos-7 cells expressing human B2 receptor) using [3H]-BK as radioligandBinding affinity towards human bradykinin B2 receptor (membranes from Cos-7 cells expressing human B2 receptor) using [3H]-BK as radioligand
ChEMBL 459 5 3 3 5.1 N=C(N)Nc1ccc(N2C(=O)C(Cc3ccccc3)N=C(c3ccccc3)c3ccccc32)cc1 10.1016/s0960-894x(99)00015-3
10996140 67319 0 None -309 2 Human 7.0 pKi = 7.0 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 710 17 4 9 4.1 CN(C)CCCN(C)CCCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(N/N=C(\S)NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL1907652 67319 0 None -309 2 Human 7.0 pKi = 7.0 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 710 17 4 9 4.1 CN(C)CCCN(C)CCCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(N/N=C(\S)NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1021/jm0111088
3812 708 37 None -1 6 Mouse 9.4 pKd = 9.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 9333122
439201 708 37 None -1 6 Mouse 9.4 pKd = 9.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 9333122
649 708 37 None -1 6 Mouse 9.4 pKd = 9.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 9333122
CHEMBL406291 708 37 None -1 6 Mouse 9.4 pKd = 9.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 9333122
DB12126 708 37 None -1 6 Mouse 9.4 pKd = 9.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 9333122
122173054 216002 0 None -1 6 Rat 8.0 pKi = 8 Binding
Binding affinity against rat bradykinin B2 receptors expressed in CHO cells using [3H]bradykinin as radioligandBinding affinity against rat bradykinin B2 receptors expressed in CHO cells using [3H]bradykinin as radioligand
Drug Central 1304 30 18 17 -4.4 N[C@H](CCCNC(N)=N)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](CC1=CC=CS1)C(=O)N[C@@H](CO)C(=O)N1CC2=C(C[C@@H]1C(=O)N1[C@H]3CCCC[C@H]3C[C@H]1C(=O)N[C@@H](CCCNC(N)=N)C(O)=O)C=CC=C2 None
122173054 216002 0 None -1 6 Human 8.0 pKi = 8.0 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
Drug Central 1304 30 18 17 -4.4 N[C@H](CCCNC(N)=N)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](CC1=CC=CS1)C(=O)N[C@@H](CO)C(=O)N1CC2=C(C[C@@H]1C(=O)N1[C@H]3CCCC[C@H]3C[C@H]1C(=O)N[C@@H](CCCNC(N)=N)C(O)=O)C=CC=C2 None
3075702 215584 0 3H-NPC 17731 -2 37 Human 6.0 pKi = 6 Binding
NoneNone
PDSP KiDatabase 198 3 1 3 1.5 C1CNC1COC2=CN=C(C=C2)Cl None
243 3141 85 3H-BRADYKININ -1096 34 Human 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 367 6 2 5 2.1 COCCCN1CCC(CC1)NC(=O)c1cc(Cl)c(c2c1OCC2)N None
3052762 3141 85 3H-BRADYKININ -1096 34 Human 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 367 6 2 5 2.1 COCCCN1CCC(CC1)NC(=O)c1cc(Cl)c(c2c1OCC2)N None
3502 3141 85 3H-BRADYKININ -1096 34 Human 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 367 6 2 5 2.1 COCCCN1CCC(CC1)NC(=O)c1cc(Cl)c(c2c1OCC2)N None
CHEMBL117287 3141 85 3H-BRADYKININ -1096 34 Human 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 367 6 2 5 2.1 COCCCN1CCC(CC1)NC(=O)c1cc(Cl)c(c2c1OCC2)N None
DB06480 3141 85 3H-BRADYKININ -1096 34 Human 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 367 6 2 5 2.1 COCCCN1CCC(CC1)NC(=O)c1cc(Cl)c(c2c1OCC2)N None
44208932 140163 6 UNDEFINED -120226 37 Human 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 475 5 1 3 6.8 Cc1ccc(Cn2nc(C(=O)NC3C4(C)CCC(C4)C3(C)C)cc2-c2ccc(Cl)c(C)c2)cc1 None
CHEMBL381689 140163 6 UNDEFINED -120226 37 Human 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 475 5 1 3 6.8 Cc1ccc(Cn2nc(C(=O)NC3C4(C)CCC(C4)C3(C)C)cc2-c2ccc(Cl)c(C)c2)cc1 None
1973 201781 12 3H-NPC 17731 -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 3H-NPC 17731 -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 3H-NPC 17731 -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
None 214742 0 3H-BRADYKININ -10471285 17 Rat 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 372 2 1 3 4.4 CC(C)(C)C1=CC=C(C=C1)NC(=O)N2CCN(CC2)C3=C(C=CC=N3)Cl None
1016 3678 75 None -46 35 Human 8.3 pKi = 8.3 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
Drug Central 371 8 0 2 6.0 CC/C(=C(\c1ccccc1)/c1ccc(cc1)OCCN(C)C)/c1ccccc1 None
2561 3678 75 None -46 35 Human 8.3 pKi = 8.3 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
Drug Central 371 8 0 2 6.0 CC/C(=C(\c1ccccc1)/c1ccc(cc1)OCCN(C)C)/c1ccccc1 None
2733526 3678 75 None -46 35 Human 8.3 pKi = 8.3 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
Drug Central 371 8 0 2 6.0 CC/C(=C(\c1ccccc1)/c1ccc(cc1)OCCN(C)C)/c1ccccc1 None
5384 3678 75 None -46 35 Human 8.3 pKi = 8.3 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
Drug Central 371 8 0 2 6.0 CC/C(=C(\c1ccccc1)/c1ccc(cc1)OCCN(C)C)/c1ccccc1 None
CHEMBL83 3678 75 None -46 35 Human 8.3 pKi = 8.3 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
Drug Central 371 8 0 2 6.0 CC/C(=C(\c1ccccc1)/c1ccc(cc1)OCCN(C)C)/c1ccccc1 None
DB00675 3678 75 None -46 35 Human 8.3 pKi = 8.3 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
Drug Central 371 8 0 2 6.0 CC/C(=C(\c1ccccc1)/c1ccc(cc1)OCCN(C)C)/c1ccccc1 None
176 394 63 None -5 31 Human 8.3 pKi = 8.3 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
Drug Central 645 11 0 4 6.9 CCCCc1oc2c(c1C(=O)c1cc(I)c(c(c1)I)OCCN(CC)CC)cccc2 None
2157 394 63 None -5 31 Human 8.3 pKi = 8.3 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
Drug Central 645 11 0 4 6.9 CCCCc1oc2c(c1C(=O)c1cc(I)c(c(c1)I)OCCN(CC)CC)cccc2 None
2566 394 63 None -5 31 Human 8.3 pKi = 8.3 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
Drug Central 645 11 0 4 6.9 CCCCc1oc2c(c1C(=O)c1cc(I)c(c(c1)I)OCCN(CC)CC)cccc2 None
CHEMBL633 394 63 None -5 31 Human 8.3 pKi = 8.3 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
Drug Central 645 11 0 4 6.9 CCCCc1oc2c(c1C(=O)c1cc(I)c(c(c1)I)OCCN(CC)CC)cccc2 None
DB01118 394 63 None -5 31 Human 8.3 pKi = 8.3 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
Drug Central 645 11 0 4 6.9 CCCCc1oc2c(c1C(=O)c1cc(I)c(c(c1)I)OCCN(CC)CC)cccc2 None
122173054 216002 0 None -1 6 Mouse 8.0 pKi = 8.0 Binding
NoneNone
Drug Central 1304 30 18 17 -4.4 N[C@H](CCCNC(N)=N)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](CC1=CC=CS1)C(=O)N[C@@H](CO)C(=O)N1CC2=C(C[C@@H]1C(=O)N1[C@H]3CCCC[C@H]3C[C@H]1C(=O)N[C@@H](CCCNC(N)=N)C(O)=O)C=CC=C2 None
122173054 216002 0 None -1 6 Guinea pig 8.0 pKi = 8 Binding
In vitro binding affinity against bradykinin receptor B2 from guinea pig ileum.In vitro binding affinity against bradykinin receptor B2 from guinea pig ileum.
Drug Central 1304 30 18 17 -4.4 N[C@H](CCCNC(N)=N)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](CC1=CC=CS1)C(=O)N[C@@H](CO)C(=O)N1CC2=C(C[C@@H]1C(=O)N1[C@H]3CCCC[C@H]3C[C@H]1C(=O)N[C@@H](CCCNC(N)=N)C(O)=O)C=CC=C2 None
12421 1367 0 None - 1 Human 9.3 pKi = 9.3 Binding
Binding affinity to human bradykinin B<sub>2</sub> receptor derived from a [<sup>3</sup>H]BK binding competition assay.Binding affinity to human bradykinin B<sub>2</sub> receptor derived from a [<sup>3</sup>H]BK binding competition assay.
Guide to Pharmacology 534 9 1 7 5.1 [2H][C@](C)(C1=C(C(=CC(=C1)F)Cl)COC=2C=CC=C3C(=CC(=NC23)C)C4=NC=NN4C)NC(COC(F)F)=O 32636746
12421 1367 0 None - 1 Human 9.3 pKi = 9.3 Binding
Binding affinity to human bradykinin B<sub>2</sub> receptor derived from a [<sup>3</sup>H]BK binding competition assay.Binding affinity to human bradykinin B<sub>2</sub> receptor derived from a [<sup>3</sup>H]BK binding competition assay.
Guide to Pharmacology 534 9 1 7 5.1 [2H][C@](C)(C1=C(C(=CC(=C1)F)Cl)COC=2C=CC=C3C(=CC(=NC23)C)C4=NC=NN4C)NC(COC(F)F)=O 35086057
154623230 1367 0 None - 1 Human 9.3 pKi = 9.3 Binding
Binding affinity to human bradykinin B<sub>2</sub> receptor derived from a [<sup>3</sup>H]BK binding competition assay.Binding affinity to human bradykinin B<sub>2</sub> receptor derived from a [<sup>3</sup>H]BK binding competition assay.
Guide to Pharmacology 534 9 1 7 5.1 [2H][C@](C)(C1=C(C(=CC(=C1)F)Cl)COC=2C=CC=C3C(=CC(=NC23)C)C4=NC=NN4C)NC(COC(F)F)=O 32636746
154623230 1367 0 None - 1 Human 9.3 pKi = 9.3 Binding
Binding affinity to human bradykinin B<sub>2</sub> receptor derived from a [<sup>3</sup>H]BK binding competition assay.Binding affinity to human bradykinin B<sub>2</sub> receptor derived from a [<sup>3</sup>H]BK binding competition assay.
Guide to Pharmacology 534 9 1 7 5.1 [2H][C@](C)(C1=C(C(=CC(=C1)F)Cl)COC=2C=CC=C3C(=CC(=NC23)C)C4=NC=NN4C)NC(COC(F)F)=O 35086057
11159 1071 0 None - 1 Human 9.3 pKi = 9.3 Binding
Ki values at the human B2 receptor derived from a [3H]BK binding competition assay.Ki values at the human B2 receptor derived from a [3H]BK binding competition assay.
Guide to Pharmacology 533 9 1 7 5.1 FC(OCC(=O)N[C@H](c1cc(F)cc(c1COc1cccc2c1nc(C)cc2c1ncnn1C)Cl)C)F 32636746
138634054 1071 0 None - 1 Human 9.3 pKi = 9.3 Binding
Ki values at the human B2 receptor derived from a [3H]BK binding competition assay.Ki values at the human B2 receptor derived from a [3H]BK binding competition assay.
Guide to Pharmacology 533 9 1 7 5.1 FC(OCC(=O)N[C@H](c1cc(F)cc(c1COc1cccc2c1nc(C)cc2c1ncnn1C)Cl)C)F 32636746
667 1934 32 None -1 6 Human 10.2 pKi = 10.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 10514288
71364 1934 32 None -1 6 Human 10.2 pKi = 10.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 10514288
CHEMBL2028850 1934 32 None -1 6 Human 10.2 pKi = 10.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 10514288
DB06196 1934 32 None -1 6 Human 10.2 pKi = 10.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 10514288
679 410 0 None 2 2 Human 8.2 pKi = 8.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology 710 12 4 7 5.1 Cc1cc(C)c2c(n1)c(ccc2)OCc1c(Cl)ccc(c1Cl)S(=O)(=O)N1CCC[C@H]1C(=O)NCCCNC(=O)c1ccc(cc1)C(=N)N 10596852
9831652 410 0 None 2 2 Human 8.2 pKi = 8.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology 710 12 4 7 5.1 Cc1cc(C)c2c(n1)c(ccc2)OCc1c(Cl)ccc(c1Cl)S(=O)(=O)N1CCC[C@H]1C(=O)NCCCNC(=O)c1ccc(cc1)C(=N)N 10596852
CHEMBL2107725 410 0 None 2 2 Human 8.2 pKi = 8.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology 710 12 4 7 5.1 Cc1cc(C)c2c(n1)c(ccc2)OCc1c(Cl)ccc(c1Cl)S(=O)(=O)N1CCC[C@H]1C(=O)NCCCNC(=O)c1ccc(cc1)C(=N)N 10596852
DB05038 410 0 None 2 2 Human 8.2 pKi = 8.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology 710 12 4 7 5.1 Cc1cc(C)c2c(n1)c(ccc2)OCc1c(Cl)ccc(c1Cl)S(=O)(=O)N1CCC[C@H]1C(=O)NCCCNC(=O)c1ccc(cc1)C(=N)N 10596852
670 2080 0 None 8 2 Rat 10.1 pKi None 10.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 10514288
667 1934 32 None -1 6 Rat 10.2 pKi None 10.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 10694205
71364 1934 32 None -1 6 Rat 10.2 pKi None 10.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 10694205
CHEMBL2028850 1934 32 None -1 6 Rat 10.2 pKi None 10.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 10694205
DB06196 1934 32 None -1 6 Rat 10.2 pKi None 10.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 10694205
5312119 709 4 None -1148 2 Human 6.4 pKi None 6.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 682 15 4 9 2.9 CN(CCN(C)C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(c(c1)[N+](=O)[O-])NNC(=S)NC(c1ccccc1)c1ccccc1 10694205
680 709 4 None -1148 2 Human 6.4 pKi None 6.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 682 15 4 9 2.9 CN(CCN(C)C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(c(c1)[N+](=O)[O-])NNC(=S)NC(c1ccccc1)c1ccccc1 10694205
CHEMBL308468 709 4 None -1148 2 Human 6.4 pKi None 6.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 682 15 4 9 2.9 CN(CCN(C)C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(c(c1)[N+](=O)[O-])NNC(=S)NC(c1ccccc1)c1ccccc1 10694205
658 2816 0 None -3981 2 Human 6.6 pKi None 6.6 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8995263
132927 4009 3 None 6 2 Human 6.7 pKi None 6.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 746 18 3 2 8.5 CCCC[P+](Cc1ccc(cc1)NC(=O)[C@H](Cc1ccc2c(c1)cccc2)NC(=NC1CCCCC1)NC1CCCCC1)(CCCC)CCCC.[Cl-] 8197121
132927 4009 3 None 6 2 Human 6.7 pKi None 6.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 746 18 3 2 8.5 CCCC[P+](Cc1ccc(cc1)NC(=O)[C@H](Cc1ccc2c(c1)cccc2)NC(=NC1CCCCC1)NC1CCCCC1)(CCCC)CCCC.[Cl-] 8394936
138398059 4009 3 None 6 2 Human 6.7 pKi None 6.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 746 18 3 2 8.5 CCCC[P+](Cc1ccc(cc1)NC(=O)[C@H](Cc1ccc2c(c1)cccc2)NC(=NC1CCCCC1)NC1CCCCC1)(CCCC)CCCC.[Cl-] 8197121
138398059 4009 3 None 6 2 Human 6.7 pKi None 6.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 746 18 3 2 8.5 CCCC[P+](Cc1ccc(cc1)NC(=O)[C@H](Cc1ccc2c(c1)cccc2)NC(=NC1CCCCC1)NC1CCCCC1)(CCCC)CCCC.[Cl-] 8394936
677 4009 3 None 6 2 Human 6.7 pKi None 6.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 746 18 3 2 8.5 CCCC[P+](Cc1ccc(cc1)NC(=O)[C@H](Cc1ccc2c(c1)cccc2)NC(=NC1CCCCC1)NC1CCCCC1)(CCCC)CCCC.[Cl-] 8197121
677 4009 3 None 6 2 Human 6.7 pKi None 6.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 746 18 3 2 8.5 CCCC[P+](Cc1ccc(cc1)NC(=O)[C@H](Cc1ccc2c(c1)cccc2)NC(=NC1CCCCC1)NC1CCCCC1)(CCCC)CCCC.[Cl-] 8394936
CHEMBL294453 4009 3 None 6 2 Human 6.7 pKi None 6.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 746 18 3 2 8.5 CCCC[P+](Cc1ccc(cc1)NC(=O)[C@H](Cc1ccc2c(c1)cccc2)NC(=NC1CCCCC1)NC1CCCCC1)(CCCC)CCCC.[Cl-] 8197121
CHEMBL294453 4009 3 None 6 2 Human 6.7 pKi None 6.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 746 18 3 2 8.5 CCCC[P+](Cc1ccc(cc1)NC(=O)[C@H](Cc1ccc2c(c1)cccc2)NC(=NC1CCCCC1)NC1CCCCC1)(CCCC)CCCC.[Cl-] 8394936
CHEMBL551291 4009 3 None 6 2 Human 6.7 pKi None 6.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 746 18 3 2 8.5 CCCC[P+](Cc1ccc(cc1)NC(=O)[C@H](Cc1ccc2c(c1)cccc2)NC(=NC1CCCCC1)NC1CCCCC1)(CCCC)CCCC.[Cl-] 8197121
CHEMBL551291 4009 3 None 6 2 Human 6.7 pKi None 6.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 746 18 3 2 8.5 CCCC[P+](Cc1ccc(cc1)NC(=O)[C@H](Cc1ccc2c(c1)cccc2)NC(=NC1CCCCC1)NC1CCCCC1)(CCCC)CCCC.[Cl-] 8394936
5311114 1650 6 None - 1 Human 7.3 pKi None 7.3 Binding
UnclassifiedUnclassified
Guide to Pharmacology 697 12 2 7 6.6 CNC(=O)c1ccc(cc1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2OCc1ccccn1)Cl)C 9224807
668 1650 6 None - 1 Human 7.3 pKi None 7.3 Binding
UnclassifiedUnclassified
Guide to Pharmacology 697 12 2 7 6.6 CNC(=O)c1ccc(cc1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2OCc1ccccn1)Cl)C 9224807
CHEMBL99869 1650 6 None - 1 Human 7.3 pKi None 7.3 Binding
UnclassifiedUnclassified
Guide to Pharmacology 697 12 2 7 6.6 CNC(=O)c1ccc(cc1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2OCc1ccccn1)Cl)C 9224807
679 410 0 None -2 2 Rat 7.8 pKi None 7.8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 710 12 4 7 5.1 Cc1cc(C)c2c(n1)c(ccc2)OCc1c(Cl)ccc(c1Cl)S(=O)(=O)N1CCC[C@H]1C(=O)NCCCNC(=O)c1ccc(cc1)C(=N)N 10596852
9831652 410 0 None -2 2 Rat 7.8 pKi None 7.8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 710 12 4 7 5.1 Cc1cc(C)c2c(n1)c(ccc2)OCc1c(Cl)ccc(c1Cl)S(=O)(=O)N1CCC[C@H]1C(=O)NCCCNC(=O)c1ccc(cc1)C(=N)N 10596852
CHEMBL2107725 410 0 None -2 2 Rat 7.8 pKi None 7.8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 710 12 4 7 5.1 Cc1cc(C)c2c(n1)c(ccc2)OCc1c(Cl)ccc(c1Cl)S(=O)(=O)N1CCC[C@H]1C(=O)NCCCNC(=O)c1ccc(cc1)C(=N)N 10596852
DB05038 410 0 None -2 2 Rat 7.8 pKi None 7.8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 710 12 4 7 5.1 Cc1cc(C)c2c(n1)c(ccc2)OCc1c(Cl)ccc(c1Cl)S(=O)(=O)N1CCC[C@H]1C(=O)NCCCNC(=O)c1ccc(cc1)C(=N)N 10596852
672 2227 17 None 1 2 Rat 7.9 pKi None 7.9 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 10514288
672 2227 17 None 1 2 Rat 7.9 pKi None 7.9 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 7965719
6918284 2227 17 None 1 2 Rat 7.9 pKi None 7.9 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 10514288
6918284 2227 17 None 1 2 Rat 7.9 pKi None 7.9 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 7965719
CHEMBL2105864 2227 17 None 1 2 Rat 7.9 pKi None 7.9 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 10514288
CHEMBL2105864 2227 17 None 1 2 Rat 7.9 pKi None 7.9 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 7965719
DB06549 2227 17 None 1 2 Rat 7.9 pKi None 7.9 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 10514288
DB06549 2227 17 None 1 2 Rat 7.9 pKi None 7.9 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 7965719
3081308 2815 0 None 15 2 Human 8.1 pKi None 8.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8995263
657 2815 0 None 15 2 Human 8.1 pKi None 8.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8995263
44316620 2081 0 None 19 2 Human 8.4 pKi None 8.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 10882364
656 2081 0 None 19 2 Human 8.4 pKi None 8.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 10882364
CHEMBL408846 2081 0 None 19 2 Human 8.4 pKi None 8.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 10882364
653 559 0 None -1 4 Mouse 9.0 pKi None 9 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 9276157
653 559 0 None 1 4 Human 9.1 pKi None 9.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8856115
653 559 0 None 1 4 Human 9.1 pKi None 9.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 9276157
670 2080 0 None -8 2 Human 9.2 pKi None 9.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 10514288
5312119 709 4 None 1148 2 Rat 9.4 pKi None 9.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 682 15 4 9 2.9 CN(CCN(C)C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(c(c1)[N+](=O)[O-])NNC(=S)NC(c1ccccc1)c1ccccc1 10694205
680 709 4 None 1148 2 Rat 9.4 pKi None 9.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 682 15 4 9 2.9 CN(CCN(C)C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(c(c1)[N+](=O)[O-])NNC(=S)NC(c1ccccc1)c1ccccc1 10694205
CHEMBL308468 709 4 None 1148 2 Rat 9.4 pKi None 9.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 682 15 4 9 2.9 CN(CCN(C)C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(c(c1)[N+](=O)[O-])NNC(=S)NC(c1ccccc1)c1ccccc1 10694205
667 1934 32 None -2 6 Mouse 9.6 pKi None 9.6 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
71364 1934 32 None -2 6 Mouse 9.6 pKi None 9.6 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
CHEMBL2028850 1934 32 None -2 6 Mouse 9.6 pKi None 9.6 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
DB06196 1934 32 None -2 6 Mouse 9.6 pKi None 9.6 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267