null

SMILES: CCC(C1CCc2cc(OCCn3ncc4ccccc4c3=O)ccc12)C(O)=O

InChI Key: InChIKey=NRMZHZYCKVOUPX-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50176625   

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 alpha (Homo sapiens (Human))	BDBM50176625 (2-(5-(2-(1-oxophthalazin-2(1H)-yl)ethoxy)-2,3-dihy...) Show SMILES CCC(C1CCc2cc(OCCn3ncc4ccccc4c3=O)ccc12)C(O)=O Show InChI InChI=1S/C23H24N2O4/c1-2-18(23(27)28)21-9-7-15-13-17(8-10-19(15)21)29-12-11-25-22(26)20-6-4-3-5-16(20)14-24-25/h3-6,8,10,13-14,18,21H,2,7,9,11-12H2,1H3,(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	>1.00E+4	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
Peroxisome proliferator-activated receptor gamma (Homo sapiens (Human))	BDBM50176625 (2-(5-(2-(1-oxophthalazin-2(1H)-yl)ethoxy)-2,3-dihy...) Show SMILES CCC(C1CCc2cc(OCCn3ncc4ccccc4c3=O)ccc12)C(O)=O Show InChI InChI=1S/C23H24N2O4/c1-2-18(23(27)28)21-9-7-15-13-17(8-10-19(15)21)29-12-11-25-22(26)20-6-4-3-5-16(20)14-24-25/h3-6,8,10,13-14,18,21H,2,7,9,11-12H2,1H3,(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	>1.00E+4	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