null

SMILES: COc1ccc(cc1)-c1nc(CSc2ccc(OCC(O)=O)cc2Cl)oc1-c1ccc(OC)cc1

InChI Key: InChIKey=LLMINKODSCABRE-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50312456   

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
Peroxisome proliferator-activated receptor alpha (Homo sapiens (Human))	BDBM50312456 (2-(4-((4,5-Bis(4-methoxyphenyl)oxazol-2-yl)methylt...) Show SMILES COc1ccc(cc1)-c1nc(CSc2ccc(OCC(O)=O)cc2Cl)oc1-c1ccc(OC)cc1 Show InChI InChI=1S/C26H22ClNO6S/c1-31-18-7-3-16(4-8-18)25-26(17-5-9-19(32-2)10-6-17)34-23(28-25)15-35-22-12-11-20(13-21(22)27)33-14-24(29)30/h3-13H,14-15H2,1-2H3,(H,29,30)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	>1.00E+4	n/a	n/a	n/a	n/a
The Genomics Institute of the Novartis Research Foundation Curated by ChEMBL					Assay Description Agonist activity at human PPARalpha ligand binding domain expressed in human 293T cells cotransfected with Gal4-DBD by luciferase transactivation ass...				J Med Chem 53: 77-105 (2010) Article DOI: 10.1021/jm9007399 BindingDB Entry DOI: 10.7270/Q28052RP
					More data for this Ligand-Target Pair
Peroxisome proliferator-activated receptor delta (Homo sapiens (Human))	BDBM50312456 (2-(4-((4,5-Bis(4-methoxyphenyl)oxazol-2-yl)methylt...) Show SMILES COc1ccc(cc1)-c1nc(CSc2ccc(OCC(O)=O)cc2Cl)oc1-c1ccc(OC)cc1 Show InChI InChI=1S/C26H22ClNO6S/c1-31-18-7-3-16(4-8-18)25-26(17-5-9-19(32-2)10-6-17)34-23(28-25)15-35-22-12-11-20(13-21(22)27)33-14-24(29)30/h3-13H,14-15H2,1-2H3,(H,29,30)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	250	n/a	n/a	n/a	n/a
The Genomics Institute of the Novartis Research Foundation Curated by ChEMBL					Assay Description Agonist activity at human PPARdelta ligand binding domain expressed in human 293T cells cotransfected with Gal4-DBD by luciferase transactivation ass...				J Med Chem 53: 77-105 (2010) Article DOI: 10.1021/jm9007399 BindingDB Entry DOI: 10.7270/Q28052RP
					More data for this Ligand-Target Pair
Peroxisome proliferator-activated receptor gamma (Homo sapiens (Human))	BDBM50312456 (2-(4-((4,5-Bis(4-methoxyphenyl)oxazol-2-yl)methylt...) Show SMILES COc1ccc(cc1)-c1nc(CSc2ccc(OCC(O)=O)cc2Cl)oc1-c1ccc(OC)cc1 Show InChI InChI=1S/C26H22ClNO6S/c1-31-18-7-3-16(4-8-18)25-26(17-5-9-19(32-2)10-6-17)34-23(28-25)15-35-22-12-11-20(13-21(22)27)33-14-24(29)30/h3-13H,14-15H2,1-2H3,(H,29,30)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	>1.00E+4	n/a	n/a	n/a	n/a
The Genomics Institute of the Novartis Research Foundation Curated by ChEMBL					Assay Description Agonist activity at human PPARgamma ligand binding domain expressed in human 293T cells cotransfected with Gal4-DBD by luciferase transactivation ass...				J Med Chem 53: 77-105 (2010) Article DOI: 10.1021/jm9007399 BindingDB Entry DOI: 10.7270/Q28052RP
					More data for this Ligand-Target Pair