BDBM50282616 6-{2-Cyclopropyl-3-[2'-(1H-tetrazol-5-yl)-biphenyl-4-ylmethyl]-3H-benzoimidazol-5-yl}-5-methyl-2H-pyridazin-3-one::CHEMBL24266

SMILES: Cc1cc(=O)[nH]nc1-c1ccc2nc(C3CC3)n(Cc3ccc(cc3)-c3ccccc3-c3nnn[nH]3)c2c1

InChI Key: InChIKey=KIDSBZQLILXVNO-UHFFFAOYSA-N

Data: 1 IC50

Find this compound or compounds like it in BindingDB or PDB:

Substructure Similarity at least:  must be >=0.5 Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50282616   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kcal/mole	IC50 nM	Kd nM	EC50/IC50 nM	koff s-1	kon M-1s-1	pH	Temp °C
Angiotensin II type 1a (AT-1a) receptor (RABBIT)	BDBM50282616 (6-{2-Cyclopropyl-3-[2'-(1H-tetrazol-5-yl)-biphenyl...) Show SMILES Cc1cc(=O)[nH]nc1-c1ccc2nc(C3CC3)n(Cc3ccc(cc3)-c3ccccc3-c3nnn[nH]3)c2c1 Show InChI InChI=1S/C29H24N8O/c1-17-14-26(38)31-32-27(17)21-12-13-24-25(15-21)37(29(30-24)20-10-11-20)16-18-6-8-19(9-7-18)22-4-2-3-5-23(22)28-33-35-36-34-28/h2-9,12-15,20H,10-11,16H2,1H3,(H,31,38)(H,33,34,35,36)	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article	n/a	n/a	3	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity against Angiotensin II receptor, type 1 induced contractions in isolated rabbit aortic rings				Bioorg Med Chem Lett 4: 1297-1302 (1994) Article DOI: 10.1016/S0960-894X(01)80348-6 BindingDB Entry DOI: 10.7270/Q2G44QRD
					More data for this Ligand-Target Pair