Compile Data Set for Download or QSAR

Found 2 hits of ic50 for monomerid = 50039913   

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 (RABBIT)	BDBM50039913 (4'-[3-Butyl-5-oxo-1-(2-trifluoromethyl-phenyl)-1,5...) Show SMILES CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(cc1)-c1ccccc1S(=O)(=O)NC(=O)c1ccc(Br)o1 Show InChI InChI=1S/C31H26BrF3N4O5S/c1-2-3-12-28-36-39(24-10-6-5-9-23(24)31(33,34)35)30(41)38(28)19-20-13-15-21(16-14-20)22-8-4-7-11-26(22)45(42,43)37-29(40)25-17-18-27(32)44-25/h4-11,13-18H,2-3,12,19H2,1H3,(H,37,40)	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	0.400	n/a	n/a	n/a	n/a	n/a	n/a
Merck Research Laboratories Curated by ChEMBL					Assay Description In vitro inhibitory activity against angiotensin II rabbit aorta AT1 receptor using radioligand [125I]-Sar Ile-AII				J Med Chem 37: 2808-24 (1994) BindingDB Entry DOI: 10.7270/Q2M907QM
					More data for this Ligand-Target Pair
Type-2 angiotensin II receptor (RAT)	BDBM50039913 (4'-[3-Butyl-5-oxo-1-(2-trifluoromethyl-phenyl)-1,5...) Show SMILES CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(cc1)-c1ccccc1S(=O)(=O)NC(=O)c1ccc(Br)o1 Show InChI InChI=1S/C31H26BrF3N4O5S/c1-2-3-12-28-36-39(24-10-6-5-9-23(24)31(33,34)35)30(41)38(28)19-20-13-15-21(16-14-20)22-8-4-7-11-26(22)45(42,43)37-29(40)25-17-18-27(32)44-25/h4-11,13-18H,2-3,12,19H2,1H3,(H,37,40)	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	170	n/a	n/a	n/a	n/a	n/a	n/a
Merck Research Laboratories Curated by ChEMBL					Assay Description In vitro inhibitory activity against angiotensin II rat midbrain AT2 receptor using radioligand [125I]-Sar Ile-AII				J Med Chem 37: 2808-24 (1994) BindingDB Entry DOI: 10.7270/Q2M907QM
					More data for this Ligand-Target Pair