Compile Data Set for Download or QSAR

Found 3 hits Enz. Inhib. hit(s) with Target = 'Peroxisome proliferator-activated receptor gamma' and Ligand = 'BDBM50472014'   

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
Peroxisome proliferator-activated receptor gamma (Homo sapiens (Human))	BDBM50472014 (CHEMBL146530) Show SMILES Cc1oc(nc1CCOc1ccc(CC(Nc2ccccc2C(=O)c2cccc(CO)c2)C(O)=O)cc1)-c1ccccc1 Show InChI InChI=1S/C35H32N2O6/c1-23-30(37-34(43-23)26-9-3-2-4-10-26)18-19-42-28-16-14-24(15-17-28)21-32(35(40)41)36-31-13-6-5-12-29(31)33(39)27-11-7-8-25(20-27)22-38/h2-17,20,32,36,38H,18-19,21-22H2,1H3,(H,40,41)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	3.40	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Glaxo Wellcome Research and Development Curated by ChEMBL					Assay Description Binding affinity against peroxisome proliferator activated receptor gamma (PPAR-gamma)				J Med Chem 41: 5055-69 (1998) Article DOI: 10.1021/jm980414r BindingDB Entry DOI: 10.7270/Q2DB84MJ
					More data for this Ligand-Target Pair
Peroxisome proliferator-activated receptor gamma (Homo sapiens (Human))	BDBM50472014 (CHEMBL146530) Show SMILES Cc1oc(nc1CCOc1ccc(CC(Nc2ccccc2C(=O)c2cccc(CO)c2)C(O)=O)cc1)-c1ccccc1 Show InChI InChI=1S/C35H32N2O6/c1-23-30(37-34(43-23)26-9-3-2-4-10-26)18-19-42-28-16-14-24(15-17-28)21-32(35(40)41)36-31-13-6-5-12-29(31)33(39)27-11-7-8-25(20-27)22-38/h2-17,20,32,36,38H,18-19,21-22H2,1H3,(H,40,41)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	n/a	n/a	25	n/a	n/a	n/a	n/a
Glaxo Wellcome Research and Development Curated by ChEMBL					Assay Description in vitro agonist activity against peroxisome proliferator activated receptor-gamma (PPAR-gamma), using alkaline phosphatase activity transactivator a...				J Med Chem 41: 5055-69 (1998) Article DOI: 10.1021/jm980414r BindingDB Entry DOI: 10.7270/Q2DB84MJ
					More data for this Ligand-Target Pair
Peroxisome proliferator-activated receptor gamma (Homo sapiens (Human))	BDBM50472014 (CHEMBL146530) Show SMILES Cc1oc(nc1CCOc1ccc(CC(Nc2ccccc2C(=O)c2cccc(CO)c2)C(O)=O)cc1)-c1ccccc1 Show InChI InChI=1S/C35H32N2O6/c1-23-30(37-34(43-23)26-9-3-2-4-10-26)18-19-42-28-16-14-24(15-17-28)21-32(35(40)41)36-31-13-6-5-12-29(31)33(39)27-11-7-8-25(20-27)22-38/h2-17,20,32,36,38H,18-19,21-22H2,1H3,(H,40,41)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	n/a	n/a	759	n/a	n/a	n/a	n/a
Glaxo Wellcome Research and Development Curated by ChEMBL					Assay Description -log concentration required to induce 50% maximum lipogenic activity against Peroxisome proliferator activated receptor gamma				J Med Chem 41: 5055-69 (1998) Article DOI: 10.1021/jm980414r BindingDB Entry DOI: 10.7270/Q2DB84MJ
					More data for this Ligand-Target Pair