BDBM50396604 CHEMBL2171905

SMILES: CN1c2ccc(cc2C(=C)c2ccccc2C1=O)C(C)=O

InChI Key: InChIKey=XLPHZTCBPKMHIB-UHFFFAOYSA-N

Data: 2 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 2 hits for monomerid = 50396604   

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-alpha (Homo sapiens (Human))	BDBM50396604 (CHEMBL2171905) Show SMILES CN1c2ccc(cc2C(=C)c2ccccc2C1=O)C(C)=O Show InChI InChI=1S/C18H15NO2/c1-11-14-6-4-5-7-15(14)18(21)19(3)17-9-8-13(12(2)20)10-16(11)17/h4-10H,1H2,2-3H3	GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	4.90E+3	n/a	n/a	n/a	n/a	n/a	n/a
The University of Tokyo Curated by ChEMBL					Assay Description Transactivational antagonist activity at human LXRalpha transfected in HEK293 cells expressing CMX-Gal4N assessed as inhibition of T1317-induced luci...				J Med Chem 55: 7360-77 (2012) Article DOI: 10.1021/jm3002394 BindingDB Entry DOI: 10.7270/Q2NV9KCH
					More data for this Ligand-Target Pair
Oxysterols receptor LXR-beta (Homo sapiens (Human))	BDBM50396604 (CHEMBL2171905) Show SMILES CN1c2ccc(cc2C(=C)c2ccccc2C1=O)C(C)=O Show InChI InChI=1S/C18H15NO2/c1-11-14-6-4-5-7-15(14)18(21)19(3)17-9-8-13(12(2)20)10-16(11)17/h4-10H,1H2,2-3H3	GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	7.50E+3	n/a	n/a	n/a	n/a	n/a	n/a
The University of Tokyo Curated by ChEMBL					Assay Description Transactivational antagonist activity at human LXRbeta transfected in HEK293 cells expressing CMX-Gal4N assessed as inhibition of T1317-induced lucif...				J Med Chem 55: 7360-77 (2012) Article DOI: 10.1021/jm3002394 BindingDB Entry DOI: 10.7270/Q2NV9KCH
					More data for this Ligand-Target Pair