null

SMILES: Cc1cc(OCc2nc(cs2)-c2ccc(cc2)C(F)(F)F)ccc1OCC(O)=O

InChI Key: InChIKey=XLTUMQNQEDLBKM-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50312393   

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 delta (Homo sapiens (Human))	BDBM50312393 (2-(2-methyl-4-((4-(4-(trifluoromethyl)phenyl)thiaz...) Show SMILES Cc1cc(OCc2nc(cs2)-c2ccc(cc2)C(F)(F)F)ccc1OCC(O)=O Show InChI InChI=1S/C20H16F3NO4S/c1-12-8-15(6-7-17(12)28-10-19(25)26)27-9-18-24-16(11-29-18)13-2-4-14(5-3-13)20(21,22)23/h2-8,11H,9-10H2,1H3,(H,25,26)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	1.39E+3	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))	BDBM50312393 (2-(2-methyl-4-((4-(4-(trifluoromethyl)phenyl)thiaz...) Show SMILES Cc1cc(OCc2nc(cs2)-c2ccc(cc2)C(F)(F)F)ccc1OCC(O)=O Show InChI InChI=1S/C20H16F3NO4S/c1-12-8-15(6-7-17(12)28-10-19(25)26)27-9-18-24-16(11-29-18)13-2-4-14(5-3-13)20(21,22)23/h2-8,11H,9-10H2,1H3,(H,25,26)	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
Peroxisome proliferator-activated receptor alpha (Homo sapiens (Human))	BDBM50312393 (2-(2-methyl-4-((4-(4-(trifluoromethyl)phenyl)thiaz...) Show SMILES Cc1cc(OCc2nc(cs2)-c2ccc(cc2)C(F)(F)F)ccc1OCC(O)=O Show InChI InChI=1S/C20H16F3NO4S/c1-12-8-15(6-7-17(12)28-10-19(25)26)27-9-18-24-16(11-29-18)13-2-4-14(5-3-13)20(21,22)23/h2-8,11H,9-10H2,1H3,(H,25,26)	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