BDBM50402203 CHEMBL2203963

SMILES: COCCn1ccc2cc(ccc12)-c1cc(cc(=O)n1O)-c1ccccc1

InChI Key: InChIKey=YTMDLHHXJUCLGT-UHFFFAOYSA-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 = 50402203   

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
Glyoxalase 1 (GLO1) (Homo sapiens (Human))	BDBM50402203 (CHEMBL2203963) Show SMILES COCCn1ccc2cc(ccc12)-c1cc(cc(=O)n1O)-c1ccccc1 Show InChI InChI=1S/C22H20N2O3/c1-27-12-11-23-10-9-18-13-17(7-8-20(18)23)21-14-19(15-22(25)24(21)26)16-5-3-2-4-6-16/h2-10,13-15,26H,11-12H2,1H3	PDB UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	260	n/a	n/a	n/a	n/a	n/a	n/a
Chugai Pharmaceutical Co., Ltd Curated by ChEMBL					Assay Description Inhibition of human recombinant GLO1 expressed in Escherichia coli BL21 assessed as decrease in reduced glutathione level after 1 hr by Ellman's meth...				Bioorg Med Chem Lett 22: 7486-9 (2012) Article DOI: 10.1016/j.bmcl.2012.10.045 BindingDB Entry DOI: 10.7270/Q2RX9D8Q
					More data for this Ligand-Target Pair