BDBM50415824 CHEMBL1090569

SMILES: Fc1ccc(CN(Cc2ccc(cc2)-c2ccccc2)S(=O)(=O)c2ccccc2)c(Cl)c1

InChI Key: InChIKey=INHFGMLOZMSHPE-UHFFFAOYSA-N

Data: 1 IC50

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 = 50415824   

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
Oxysterols receptor LXR-beta (Homo sapiens (Human))	BDBM50415824 (CHEMBL1090569) Show SMILES Fc1ccc(CN(Cc2ccc(cc2)-c2ccccc2)S(=O)(=O)c2ccccc2)c(Cl)c1 Show InChI InChI=1S/C26H21ClFNO2S/c27-26-17-24(28)16-15-23(26)19-29(32(30,31)25-9-5-2-6-10-25)18-20-11-13-22(14-12-20)21-7-3-1-4-8-21/h1-17H,18-19H2	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.16E+3	n/a	n/a	n/a	n/a	n/a	n/a
GlaxoSmithKline Curated by ChEMBL					Assay Description Displacement of [N-methyl-3H]T1317 from human biotinylated LXRbeta LBD after 3 hrs by LEAD seeker binding assay				J Med Chem 53: 3412-6 (2010) Article DOI: 10.1021/jm901797p BindingDB Entry DOI: 10.7270/Q2NP25P6
					More data for this Ligand-Target Pair