null

SMILES: COc1ccc(cc1)-c1csc(COc2ccc(OCC(O)=O)c(C)c2)n1

InChI Key: InChIKey=LFWPUOKHJZLFMV-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50312390   

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))	BDBM50312390 (2-(4-((4-(4-methoxyphenyl)thiazol-2-yl)methoxy)-2-...) Show SMILES COc1ccc(cc1)-c1csc(COc2ccc(OCC(O)=O)c(C)c2)n1 Show InChI InChI=1S/C20H19NO5S/c1-13-9-16(7-8-18(13)26-11-20(22)23)25-10-19-21-17(12-27-19)14-3-5-15(24-2)6-4-14/h3-9,12H,10-11H2,1-2H3,(H,22,23)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	4.06E+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))	BDBM50312390 (2-(4-((4-(4-methoxyphenyl)thiazol-2-yl)methoxy)-2-...) Show SMILES COc1ccc(cc1)-c1csc(COc2ccc(OCC(O)=O)c(C)c2)n1 Show InChI InChI=1S/C20H19NO5S/c1-13-9-16(7-8-18(13)26-11-20(22)23)25-10-19-21-17(12-27-19)14-3-5-15(24-2)6-4-14/h3-9,12H,10-11H2,1-2H3,(H,22,23)	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))	BDBM50312390 (2-(4-((4-(4-methoxyphenyl)thiazol-2-yl)methoxy)-2-...) Show SMILES COc1ccc(cc1)-c1csc(COc2ccc(OCC(O)=O)c(C)c2)n1 Show InChI InChI=1S/C20H19NO5S/c1-13-9-16(7-8-18(13)26-11-20(22)23)25-10-19-21-17(12-27-19)14-3-5-15(24-2)6-4-14/h3-9,12H,10-11H2,1-2H3,(H,22,23)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	4.08E+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 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