Compile Data Set for Download or QSAR

Found 3 hits Enz. Inhib. hit(s) with Target = 'B2 bradykinin receptor' and Ligand = 'BDBM50062878'   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kJ/mole	IC50 nM	Kd nM	EC50/IC50 nM	koff s-1	kon M-1s-1	pH	Temp °C
B2 bradykinin receptor (Cavia porcellus)	BDBM50062878 (CHEMBL131517 | N-({[3-(3-Bromo-2-methyl-imidazo[1,...) Show SMILES CCCC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl Show InChI InChI=1S/C22H23BrCl2N4O3/c1-4-6-18(30)26-11-19(31)28(3)16-9-8-15(24)14(20(16)25)12-32-17-7-5-10-29-21(23)13(2)27-22(17)29/h5,7-10H,4,6,11-12H2,1-3H3,(H,26,30)	MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	8.90	n/a	n/a	n/a	n/a	n/a	n/a
Fujisawa Pharmaceutical Company, Ltd. Curated by ChEMBL					Assay Description 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%.				J Med Chem 41: 4053-61 (1998) Article DOI: 10.1021/jm980214f BindingDB Entry DOI: 10.7270/Q2WQ04GV
					More data for this Ligand-Target Pair
B2 bradykinin receptor (Homo sapiens (Human))	BDBM50062878 (CHEMBL131517 | N-({[3-(3-Bromo-2-methyl-imidazo[1,...) Show SMILES CCCC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl Show InChI InChI=1S/C22H23BrCl2N4O3/c1-4-6-18(30)26-11-19(31)28(3)16-9-8-15(24)14(20(16)25)12-32-17-7-5-10-29-21(23)13(2)27-22(17)29/h5,7-10H,4,6,11-12H2,1-3H3,(H,26,30)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	8.90	n/a	n/a	n/a	n/a	n/a	n/a
Fujisawa Pharmaceutical Company, Ltd. Curated by ChEMBL					Assay Description 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%.				J Med Chem 41: 4053-61 (1998) Article DOI: 10.1021/jm980214f BindingDB Entry DOI: 10.7270/Q2WQ04GV
					More data for this Ligand-Target Pair
B2 bradykinin receptor (Cavia porcellus)	BDBM50062878 (CHEMBL131517 | N-({[3-(3-Bromo-2-methyl-imidazo[1,...) Show SMILES CCCC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl Show InChI InChI=1S/C22H23BrCl2N4O3/c1-4-6-18(30)26-11-19(31)28(3)16-9-8-15(24)14(20(16)25)12-32-17-7-5-10-29-21(23)13(2)27-22(17)29/h5,7-10H,4,6,11-12H2,1-3H3,(H,26,30)	MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	8.90	n/a	n/a	n/a	n/a	n/a	n/a
Fujisawa Pharmaceutical Co., Ltd. Curated by ChEMBL					Assay Description In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.				J Med Chem 41: 564-78 (1998) Article DOI: 10.1021/jm970591c BindingDB Entry DOI: 10.7270/Q2445N6P
					More data for this Ligand-Target Pair