BDBM50415822 CHEMBL1091958

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

InChI Key: InChIKey=SISXRZFAYYJKHJ-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 = 50415822   

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))	BDBM50415822 (CHEMBL1091958) Show SMILES Fc1ccc(CN(Cc2ccc(cc2)-c2ccccc2)C(=O)c2ccccc2)c(Cl)c1 Show InChI InChI=1S/C27H21ClFNO/c28-26-17-25(29)16-15-24(26)19-30(27(31)23-9-5-2-6-10-23)18-20-11-13-22(14-12-20)21-7-3-1-4-8-21/h1-17H,18-19H2	UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	<1.00E+4	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