Compile Data Set for Download or QSAR

Found 2 hits of ic50 for monomerid = 50285819   

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 A/B (RAT)	BDBM50285819 (CHEMBL315401 | {2-Butyl-4-oxo-3-[2'-(1H-tetrazol-5...) Show SMILES CCCCc1nc2ccn(C(C(=O)OC(C)C)c3ccccc3Cl)c(=O)c2n1Cc1ccc(cc1)-c1ccccc1-c1nnn[nH]1 Show InChI InChI=1S/C35H34ClN7O3/c1-4-5-14-30-37-29-19-20-42(31(35(45)46-22(2)3)27-12-8-9-13-28(27)36)34(44)32(29)43(30)21-23-15-17-24(18-16-23)25-10-6-7-11-26(25)33-38-40-41-39-33/h6-13,15-20,22,31H,4-5,14,21H2,1-3H3,(H,38,39,40,41)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	11	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description In vitro binding affinity determined against angiotensin II AT1 receptor in rat adrenal cortex preparation				Bioorg Med Chem Lett 5: 2665-2670 (1995) Article DOI: 10.1016/0960-894X(95)00477-B BindingDB Entry DOI: 10.7270/Q2ZW1KVW
					More data for this Ligand-Target Pair
Type-2 angiotensin II receptor (RAT)	BDBM50285819 (CHEMBL315401 | {2-Butyl-4-oxo-3-[2'-(1H-tetrazol-5...) Show SMILES CCCCc1nc2ccn(C(C(=O)OC(C)C)c3ccccc3Cl)c(=O)c2n1Cc1ccc(cc1)-c1ccccc1-c1nnn[nH]1 Show InChI InChI=1S/C35H34ClN7O3/c1-4-5-14-30-37-29-19-20-42(31(35(45)46-22(2)3)27-12-8-9-13-28(27)36)34(44)32(29)43(30)21-23-15-17-24(18-16-23)25-10-6-7-11-26(25)33-38-40-41-39-33/h6-13,15-20,22,31H,4-5,14,21H2,1-3H3,(H,38,39,40,41)	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	570	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description In vitro binding affinity determined against angiotensin II AT2 receptor in rat adrenal medulla preparation				Bioorg Med Chem Lett 5: 2665-2670 (1995) Article DOI: 10.1016/0960-894X(95)00477-B BindingDB Entry DOI: 10.7270/Q2ZW1KVW
					More data for this Ligand-Target Pair