BDBM50349443 CHEMBL1808555

SMILES: CCCCCCC(Sc1nc2cc(Cl)ccc2s1)C(=O)NS(=O)(=O)c1ccccc1

InChI Key: InChIKey=ZUXZKZCYIPMAJX-UHFFFAOYSA-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 = 50349443   

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))	BDBM50349443 (CHEMBL1808555) Show SMILES CCCCCCC(Sc1nc2cc(Cl)ccc2s1)C(=O)NS(=O)(=O)c1ccccc1 Show InChI InChI=1S/C21H23ClN2O3S3/c1-2-3-4-8-11-19(20(25)24-30(26,27)16-9-6-5-7-10-16)29-21-23-17-14-15(22)12-13-18(17)28-21/h5-7,9-10,12-14,19H,2-4,8,11H2,1H3,(H,24,25)	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	5.06E+4	n/a	n/a	n/a	n/a
Universit£ degli Studi G. d'Annunzio Curated by ChEMBL					Assay Description Agonist activity at PPARalpha ligand binding domain expressed in HEK293 cells co-expressing GAL4 after 18 hrs by dual-luciferase activity based trans...				Bioorg Med Chem Lett 21: 4869-72 (2011) Article DOI: 10.1016/j.bmcl.2011.06.028 BindingDB Entry DOI: 10.7270/Q2DN45F9
					More data for this Ligand-Target Pair