null

SMILES: Cc1oc(nc1CCOc1ccc2C(CCc2c1)C(C)(C)C(O)=O)-c1ccccc1

InChI Key: InChIKey=JEFUCHIBJHJCTM-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50176657   

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 gamma (Homo sapiens (Human))	BDBM50176657 (2-methyl-2-(5-(2-(5-methyl-2-phenyloxazol-4-yl)eth...) Show SMILES Cc1oc(nc1CCOc1ccc2C(CCc2c1)C(C)(C)C(O)=O)-c1ccccc1 Show InChI InChI=1S/C25H27NO4/c1-16-22(26-23(30-16)17-7-5-4-6-8-17)13-14-29-19-10-11-20-18(15-19)9-12-21(20)25(2,3)24(27)28/h4-8,10-11,15,21H,9,12-14H2,1-3H3,(H,27,28)	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	5.64E+3	n/a	n/a	n/a	n/a
Bayer Research Center Curated by ChEMBL					Assay Description Activity against PPAR gamma in human by FRET assay				Bioorg Med Chem Lett 16: 297-301 (2005) Article DOI: 10.1016/j.bmcl.2005.10.008 BindingDB Entry DOI: 10.7270/Q28P6025
					More data for this Ligand-Target Pair
Peroxisome proliferator-activated receptor alpha (Homo sapiens (Human))	BDBM50176657 (2-methyl-2-(5-(2-(5-methyl-2-phenyloxazol-4-yl)eth...) Show SMILES Cc1oc(nc1CCOc1ccc2C(CCc2c1)C(C)(C)C(O)=O)-c1ccccc1 Show InChI InChI=1S/C25H27NO4/c1-16-22(26-23(30-16)17-7-5-4-6-8-17)13-14-29-19-10-11-20-18(15-19)9-12-21(20)25(2,3)24(27)28/h4-8,10-11,15,21H,9,12-14H2,1-3H3,(H,27,28)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	6.00E+3	n/a	n/a	n/a	n/a
Bayer Research Center Curated by ChEMBL					Assay Description Activity against PPAR alpha in human by FRET assay				Bioorg Med Chem Lett 16: 297-301 (2005) Article DOI: 10.1016/j.bmcl.2005.10.008 BindingDB Entry DOI: 10.7270/Q28P6025
					More data for this Ligand-Target Pair