BDBM50430581 CHEMBL2337789

SMILES: CCOc1ccc2\C(=C/c3ccc(cc3)C(C)C)C(C)=C(CC(O)=O)c2c1

InChI Key: InChIKey=NRSSQZXATYHVTO-MTJSOVHGSA-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 = 50430581   

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))	BDBM50430581 (CHEMBL2337789) Show SMILES CCOc1ccc2\C(=C/c3ccc(cc3)C(C)C)C(C)=C(CC(O)=O)c2c1 |t:20| Show InChI InChI=1S/C24H26O3/c1-5-27-19-10-11-20-21(12-17-6-8-18(9-7-17)15(2)3)16(4)22(14-24(25)26)23(20)13-19/h6-13,15H,5,14H2,1-4H3,(H,25,26)/b21-12-	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	3.08E+3	n/a	n/a	n/a	n/a	n/a	n/a
Xiamen University Curated by ChEMBL					Assay Description Displacement of [3H]-9-cis-RA from human GST-tagged N-terminal truncated RXRalpha after 1 hr by liquid scintillation counting				Eur J Med Chem 62: 632-48 (2013) Article DOI: 10.1016/j.ejmech.2013.01.012 BindingDB Entry DOI: 10.7270/Q2J104JR
					More data for this Ligand-Target Pair