BDBM50171905 (S)-2-(4-Acetyl-phenoxy)-3-phenyl-propionic acid::CHEMBL190368

SMILES: CC(=O)c1ccc(O[C@@H](Cc2ccccc2)C(O)=O)cc1

InChI Key: InChIKey=WDFFIFRBPUFLPS-INIZCTEOSA-N

Data: 4 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 4 hits for monomerid = 50171905   

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 (Homo sapiens (Human))	BDBM50171905 ((S)-2-(4-Acetyl-phenoxy)-3-phenyl-propionic acid |...) Show SMILES CC(=O)c1ccc(O[C@@H](Cc2ccccc2)C(O)=O)cc1 Show InChI InChI=1S/C17H16O4/c1-12(18)14-7-9-15(10-8-14)21-16(17(19)20)11-13-5-3-2-4-6-13/h2-10,16H,11H2,1H3,(H,19,20)/t16-/m0/s1	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	1.24E+4	n/a	n/a	n/a	n/a
Università degli Studi di Milano Curated by ChEMBL					Assay Description Effective concentration against human PPARgamma expressed in HepG2 cells				J Med Chem 48: 5509-19 (2005) Article DOI: 10.1021/jm0502844 BindingDB Entry DOI: 10.7270/Q2PV6JXF
					More data for this Ligand-Target Pair
Peroxisome proliferator-activated receptor (Homo sapiens (Human))	BDBM50171905 ((S)-2-(4-Acetyl-phenoxy)-3-phenyl-propionic acid |...) Show SMILES CC(=O)c1ccc(O[C@@H](Cc2ccccc2)C(O)=O)cc1 Show InChI InChI=1S/C17H16O4/c1-12(18)14-7-9-15(10-8-14)21-16(17(19)20)11-13-5-3-2-4-6-13/h2-10,16H,11H2,1H3,(H,19,20)/t16-/m0/s1	PDB UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	1.35E+4	n/a	n/a	n/a	n/a
Universit£ degli studi di Bari 'Aldo Moro' Curated by ChEMBL					Assay Description Agonist activity at GAL4-fused PPARalpha (unknown origin) expressed in human HepG2 cells by transactivation assay				Eur J Med Chem 63: 321-32 (2013) Article DOI: 10.1016/j.ejmech.2013.02.015 BindingDB Entry DOI: 10.7270/Q29G5QRP
					More data for this Ligand-Target Pair
Peroxisome proliferator-activated receptor (Homo sapiens (Human))	BDBM50171905 ((S)-2-(4-Acetyl-phenoxy)-3-phenyl-propionic acid |...) Show SMILES CC(=O)c1ccc(O[C@@H](Cc2ccccc2)C(O)=O)cc1 Show InChI InChI=1S/C17H16O4/c1-12(18)14-7-9-15(10-8-14)21-16(17(19)20)11-13-5-3-2-4-6-13/h2-10,16H,11H2,1H3,(H,19,20)/t16-/m0/s1	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	1.23E+4	n/a	n/a	n/a	n/a
Universit£ degli studi di Bari 'Aldo Moro' Curated by ChEMBL					Assay Description Agonist activity at GAL4-fused PPARgamma (unknown origin) expressed in human HepG2 cells by transactivation assay				Eur J Med Chem 63: 321-32 (2013) Article DOI: 10.1016/j.ejmech.2013.02.015 BindingDB Entry DOI: 10.7270/Q29G5QRP
					More data for this Ligand-Target Pair
Peroxisome proliferator-activated receptor alpha (PPAR alpha) (Homo sapiens (Human))	BDBM50171905 ((S)-2-(4-Acetyl-phenoxy)-3-phenyl-propionic acid |...) Show SMILES CC(=O)c1ccc(O[C@@H](Cc2ccccc2)C(O)=O)cc1 Show InChI InChI=1S/C17H16O4/c1-12(18)14-7-9-15(10-8-14)21-16(17(19)20)11-13-5-3-2-4-6-13/h2-10,16H,11H2,1H3,(H,19,20)/t16-/m0/s1	PDB UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	1.35E+4	n/a	n/a	n/a	n/a
Università degli Studi di Milano Curated by ChEMBL					Assay Description Effective concentration against human PPARalpha expressed in HepG2 cells				J Med Chem 48: 5509-19 (2005) Article DOI: 10.1021/jm0502844 BindingDB Entry DOI: 10.7270/Q2PV6JXF
					More data for this Ligand-Target Pair