BDBM50440279 CHEMBL470939

SMILES: CC\C(=C/c1cc(OC)cc(OC)c1)c1ccc(OC)c(OC)c1

InChI Key: InChIKey=SRWVTGHUQSILFT-OQLLNIDSSA-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 = 50440279   

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
Ribosyldihydronicotinamide dehydrogenase [quinone] (Homo sapiens (Human))	BDBM50440279 (CHEMBL470939) Show SMILES CC\C(=C/c1cc(OC)cc(OC)c1)c1ccc(OC)c(OC)c1 Show InChI InChI=1S/C20H24O4/c1-6-15(16-7-8-19(23-4)20(12-16)24-5)9-14-10-17(21-2)13-18(11-14)22-3/h7-13H,6H2,1-5H3/b15-9+	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.63E+4	n/a	n/a	n/a	n/a	n/a	n/a
Purdue University Curated by ChEMBL					Assay Description Inhibition of human quinone reductase 2 expressed in Escherichia coli BL21(DE3) using N-methyldihydronicotinamide as co-substrate				Bioorg Med Chem 21: 6022-37 (2013) Article DOI: 10.1016/j.bmc.2013.07.037 BindingDB Entry DOI: 10.7270/Q21R6RX0
					More data for this Ligand-Target Pair