BDBM50427896 CHEMBL2326683

SMILES: CN(C)CCCn1c2-c3ccccc3C(=O)c2c2ccc(N)cc2c1=O

InChI Key: InChIKey=NABOZFKQMMKPEB-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 = 50427896   

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
Retinoic acid receptor RXR-alpha (Homo sapiens (Human))	BDBM50427896 (CHEMBL2326683) Show SMILES CN(C)CCCn1c2-c3ccccc3C(=O)c2c2ccc(N)cc2c1=O Show InChI InChI=1S/C21H21N3O2/c1-23(2)10-5-11-24-19-15-6-3-4-7-16(15)20(25)18(19)14-9-8-13(22)12-17(14)21(24)26/h3-4,6-9,12H,5,10-11,22H2,1-2H3	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	7.00E+3	n/a	n/a	n/a	n/a
Purdue University Curated by ChEMBL					Assay Description Activation of human RXRalpha activity expressed in COS1 cells after 12 hrs by RXRE-luciferase reporter gene assay				J Med Chem 56: 2581-605 (2013) Article DOI: 10.1021/jm400026k BindingDB Entry DOI: 10.7270/Q2G44RNG
					More data for this Ligand-Target Pair