null

SMILES: CCCCc1cc(=O)n2nc(nc2n1Cc1ccc(cc1)-c1ccccc1-c1nnn[nH]1)-c1ccccc1

InChI Key: InChIKey=NYRQQEFQBCBNOY-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50285162   

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
Type-1 angiotensin II receptor B (RAT)	BDBM50285162 (5-Butyl-2-phenyl-4-[2'-(1H-tetrazol-5-yl)-biphenyl...) Show SMILES CCCCc1cc(=O)n2nc(nc2n1Cc1ccc(cc1)-c1ccccc1-c1nnn[nH]1)-c1ccccc1 Show InChI InChI=1S/C29H26N8O/c1-2-3-11-23-18-26(38)37-29(30-27(33-37)22-9-5-4-6-10-22)36(23)19-20-14-16-21(17-15-20)24-12-7-8-13-25(24)28-31-34-35-32-28/h4-10,12-18H,2-3,11,19H2,1H3,(H,31,32,34,35)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article	n/a	n/a	83	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Tested for binding affinity against angiotensin II receptor in rat adrenal cortex				Bioorg Med Chem Lett 5: 2071-2076 (1995) Article DOI: 10.1016/0960-894X(95)00370-9 BindingDB Entry DOI: 10.7270/Q2SF2W4J
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor (Bos taurus)	BDBM50285162 (5-Butyl-2-phenyl-4-[2'-(1H-tetrazol-5-yl)-biphenyl...) Show SMILES CCCCc1cc(=O)n2nc(nc2n1Cc1ccc(cc1)-c1ccccc1-c1nnn[nH]1)-c1ccccc1 Show InChI InChI=1S/C29H26N8O/c1-2-3-11-23-18-26(38)37-29(30-27(33-37)22-9-5-4-6-10-22)36(23)19-20-14-16-21(17-15-20)24-12-7-8-13-25(24)28-31-34-35-32-28/h4-10,12-18H,2-3,11,19H2,1H3,(H,31,32,34,35)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article	n/a	n/a	520	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Tested for binding affinity against angiotensin II receptor in bovine adrenal cortex				Bioorg Med Chem Lett 5: 2071-2076 (1995) Article DOI: 10.1016/0960-894X(95)00370-9 BindingDB Entry DOI: 10.7270/Q2SF2W4J
					More data for this Ligand-Target Pair