Compile Data Set for Download or QSAR

Found 2 hits Enz. Inhib. hit(s) with Target = 'Type-1 angiotensin II receptor' and Ligand = 'BDBM50335929'   

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
Type-1 angiotensin II receptor (Homo sapiens (Human))	BDBM50335929 (2-((2'-(1H-tetrazol-5-yl)biphenyl-4-yl)methyl)-3-b...) Show SMILES CCCCN1CC2(CN1Cc1ccc(cc1)-c1ccccc1-c1nnn[nH]1)C(=O)CCC2=O Show InChI InChI=1S/C25H28N6O2/c1-2-3-14-30-16-25(22(32)12-13-23(25)33)17-31(30)15-18-8-10-19(11-9-18)20-6-4-5-7-21(20)24-26-28-29-27-24/h4-11H,2-3,12-17H2,1H3,(H,26,27,28,29)	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	25	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The M. S. University of Baroda Curated by ChEMBL					Assay Description Displacement of [3H]-angiotensin 2 from angiotensin AT1 receptor in human PLC-PRF5 cells				Bioorg Med Chem 18: 8418-56 (2010) Article DOI: 10.1016/j.bmc.2010.10.043 BindingDB Entry DOI: 10.7270/Q2H70G3T
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor (Homo sapiens (Human))	BDBM50335929 (2-((2'-(1H-tetrazol-5-yl)biphenyl-4-yl)methyl)-3-b...) Show SMILES CCCCN1CC2(CN1Cc1ccc(cc1)-c1ccccc1-c1nnn[nH]1)C(=O)CCC2=O Show InChI InChI=1S/C25H28N6O2/c1-2-3-14-30-16-25(22(32)12-13-23(25)33)17-31(30)15-18-8-10-19(11-9-18)20-6-4-5-7-21(20)24-26-28-29-27-24/h4-11H,2-3,12-17H2,1H3,(H,26,27,28,29)	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	22	n/a	n/a	n/a	n/a	n/a	n/a
The M. S. University of Baroda Curated by ChEMBL					Assay Description Antagonist activity at angiotensin AT1 receptor in human PLC-PRF5 cells				Bioorg Med Chem 18: 8418-56 (2010) Article DOI: 10.1016/j.bmc.2010.10.043 BindingDB Entry DOI: 10.7270/Q2H70G3T
					More data for this Ligand-Target Pair