BDBM50396235 CHEMBL2172299

SMILES: CC(=O)NCCCn1c2-c3ccccc3C(=O)c2c2ccc(N)cc2c1=O

InChI Key: InChIKey=NRPQUZCFMRCDRJ-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 = 50396235   

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))	BDBM50396235 (CHEMBL2172299) Show SMILES CC(=O)NCCCn1c2-c3ccccc3C(=O)c2c2ccc(N)cc2c1=O Show InChI InChI=1S/C21H19N3O3/c1-12(25)23-9-4-10-24-19-15-5-2-3-6-16(15)20(26)18(19)14-8-7-13(22)11-17(14)21(24)27/h2-3,5-8,11H,4,9-10,22H2,1H3,(H,23,25)	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	2.09E+4	n/a	n/a	n/a	n/a
The University of Illinois at Chicago Curated by ChEMBL					Assay Description Agonist activity at human RXRalpha expressed in african green monkey COS1 cells assessed as induction of RXRE transcriptional activity after 12 hrs b...				J Med Chem 55: 5965-81 (2012) Article DOI: 10.1021/jm3006806 BindingDB Entry DOI: 10.7270/Q2QR4Z7Z
					More data for this Ligand-Target Pair