null

SMILES: CCc1nc2c(C)cc(C)nc2n1Cc1ccc(OC(C(O)=O)c2ccccc2)c(c1)C(C)C

InChI Key: InChIKey=YXCTZWLWOZHFGW-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50284442   

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-2 angiotensin II receptor (RAT)	BDBM50284442 (CHEMBL15882 | [4-(2-Ethyl-5,7-dimethyl-imidazo[4,5...) Show SMILES CCc1nc2c(C)cc(C)nc2n1Cc1ccc(OC(C(O)=O)c2ccccc2)c(c1)C(C)C Show InChI InChI=1S/C28H31N3O3/c1-6-24-30-25-18(4)14-19(5)29-27(25)31(24)16-20-12-13-23(22(15-20)17(2)3)34-26(28(32)33)21-10-8-7-9-11-21/h7-15,17,26H,6,16H2,1-5H3,(H,32,33)	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	3.30E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rat midbrain membrane (AT2 receptor)				Bioorg Med Chem Lett 5: 1151-1154 (1995) Article DOI: 10.1016/0960-894X(95)00185-V BindingDB Entry DOI: 10.7270/Q2J67GV9
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor (RABBIT)	BDBM50284442 (CHEMBL15882 | [4-(2-Ethyl-5,7-dimethyl-imidazo[4,5...) Show SMILES CCc1nc2c(C)cc(C)nc2n1Cc1ccc(OC(C(O)=O)c2ccccc2)c(c1)C(C)C Show InChI InChI=1S/C28H31N3O3/c1-6-24-30-25-18(4)14-19(5)29-27(25)31(24)16-20-12-13-23(22(15-20)17(2)3)34-26(28(32)33)21-10-8-7-9-11-21/h7-15,17,26H,6,16H2,1-5H3,(H,32,33)	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	30	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Tested for its ability to displace the specific binding ligand [125I]-Sar 1,lle8-AlI from rabbit aortic membrane (AT1 receptor)				Bioorg Med Chem Lett 5: 1151-1154 (1995) Article DOI: 10.1016/0960-894X(95)00185-V BindingDB Entry DOI: 10.7270/Q2J67GV9
					More data for this Ligand-Target Pair