BDBM50535440 CHEMBL4438226

SMILES: CC(C)(Oc1ccc(OCCc2ccc(cc2)\N=N\c2ccc(cc2)C(F)(F)F)cc1)C(O)=O

InChI Key: InChIKey=IVNPTURJCAQYEW-QVIHXGFCSA-N

Data: 1 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 1 hit for monomerid = 50535440   

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))	BDBM50535440 (CHEMBL4438226) Show SMILES CC(C)(Oc1ccc(OCCc2ccc(cc2)\N=N\c2ccc(cc2)C(F)(F)F)cc1)C(O)=O Show InChI InChI=1S/C25H23F3N2O4/c1-24(2,23(31)32)34-22-13-11-21(12-14-22)33-16-15-17-3-7-19(8-4-17)29-30-20-9-5-18(6-10-20)25(26,27)28/h3-14H,15-16H2,1-2H3,(H,31,32)/b30-29+	PDB UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	n/a	n/a	2.20E+3	n/a	n/a	n/a	n/a
University of Chieti "G. d.Annunzio" Curated by ChEMBL					Assay Description Transactivation of GAL4-tagged human PPARalpha LBD expressed in human HepG2 cells at 100 nM to 100 uM incubated for 20 to 22 hrs by luciferase report...				ACS Med Chem Lett 10: 545-551 (2019) Article DOI: 10.1021/acsmedchemlett.8b00574
					More data for this Ligand-Target Pair