BDBM50184650 CHEMBL381066::[4-(4,4''-bis-trifluoromethoxy-[1,1';2',1'']terphenyl-4'-ylmethoxy)-2-methyl-phenoxy]-acetic acid

SMILES: Cc1cc(OCc2ccc(-c3ccc(OC(F)(F)F)cc3)c(c2)-c2ccc(OC(F)(F)F)cc2)ccc1OCC(O)=O

InChI Key: InChIKey=WXVKNMWJOXNNFD-UHFFFAOYSA-N

Data: 3 EC50

Find this compound or compounds like it in BindingDB or PDB:

Substructure Similarity at least:  must be >=0.5 Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50184650   

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))	BDBM50184650 (CHEMBL381066 | [4-(4,4''-bis-trifluoromethoxy-[1,1...) Show SMILES Cc1cc(OCc2ccc(-c3ccc(OC(F)(F)F)cc3)c(c2)-c2ccc(OC(F)(F)F)cc2)ccc1OCC(O)=O Show InChI InChI=1S/C30H22F6O6/c1-18-14-24(11-13-27(18)40-17-28(37)38)39-16-19-2-12-25(20-3-7-22(8-4-20)41-29(31,32)33)26(15-19)21-5-9-23(10-6-21)42-30(34,35)36/h2-15H,16-17H2,1H3,(H,37,38)	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 Effect on human PPARdelta transactivation in 293T cells				Bioorg Med Chem Lett 16: 2969-73 (2006) Article DOI: 10.1016/j.bmcl.2006.02.079 BindingDB Entry DOI: 10.7270/Q2XW4JDG
					More data for this Ligand-Target Pair
Peroxisome proliferator-activated receptor alpha (Homo sapiens (Human))	BDBM50184650 (CHEMBL381066 | [4-(4,4''-bis-trifluoromethoxy-[1,1...) Show SMILES Cc1cc(OCc2ccc(-c3ccc(OC(F)(F)F)cc3)c(c2)-c2ccc(OC(F)(F)F)cc2)ccc1OCC(O)=O Show InChI InChI=1S/C30H22F6O6/c1-18-14-24(11-13-27(18)40-17-28(37)38)39-16-19-2-12-25(20-3-7-22(8-4-20)41-29(31,32)33)26(15-19)21-5-9-23(10-6-21)42-30(34,35)36/h2-15H,16-17H2,1H3,(H,37,38)	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 Effect on human PPARalpha transactivation in 293T cells				Bioorg Med Chem Lett 16: 2969-73 (2006) Article DOI: 10.1016/j.bmcl.2006.02.079 BindingDB Entry DOI: 10.7270/Q2XW4JDG
					More data for this Ligand-Target Pair
Peroxisome proliferator-activated receptor gamma (Homo sapiens (Human))	BDBM50184650 (CHEMBL381066 | [4-(4,4''-bis-trifluoromethoxy-[1,1...) Show SMILES Cc1cc(OCc2ccc(-c3ccc(OC(F)(F)F)cc3)c(c2)-c2ccc(OC(F)(F)F)cc2)ccc1OCC(O)=O Show InChI InChI=1S/C30H22F6O6/c1-18-14-24(11-13-27(18)40-17-28(37)38)39-16-19-2-12-25(20-3-7-22(8-4-20)41-29(31,32)33)26(15-19)21-5-9-23(10-6-21)42-30(34,35)36/h2-15H,16-17H2,1H3,(H,37,38)	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 Effect on human PPARgamma transactivation in 293T cells				Bioorg Med Chem Lett 16: 2969-73 (2006) Article DOI: 10.1016/j.bmcl.2006.02.079 BindingDB Entry DOI: 10.7270/Q2XW4JDG
					More data for this Ligand-Target Pair