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TargetLactoylglutathione lyase
LigandBDBM50336253
Substrate/Competitorn/a
Meas. Tech.ChEMBL_716548 (CHEMBL1670272)
Ki 74000±n/a nM
Citation Yuan, MLuo, MSong, YXu, QWang, XCao, YBu, XRen, YHu, X Identification of curcumin derivatives as human glyoxalase I inhibitors: A combination of biological evaluation, molecular docking, 3D-QSAR and molecular dynamics simulation studies. Bioorg Med Chem19:1189-96 (2011) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Lactoylglutathione lyase
Name:Lactoylglutathione lyase
Synonyms:Aldoketomutase | GLO1 | Glx I | Glyoxalase 1 (GLO1) | Glyoxalase I | Ketone-aldehyde mutase | LGUL_HUMAN | Methylglyoxalase | S-D-lactoylglutathione methylglyoxal lyase
Type:Enzyme
Mol. Mass.:20772.95
Organism:Homo sapiens (Human)
Description:Q04760
Residue:184
Sequence:
MAEPQPPSGGLTDEAALSCCSDADPSTKDFLLQQTMLRVKDPKKSLDFYTRVLGMTLIQK
CDFPIMKFSLYFLAYEDKNDIPKEKDEKIAWALSRKATLELTHNWGTEDDETQSYHNGNS
DPRGFGHIGIAVPDVYSACKRFEELGVKFVKKPDDGKMKGLAFIQDPDGYWIEILNPNKM
ATLM
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BDBM50336253
n/a
NameBDBM50336253
Synonyms:5-hydroxy-7-(5-(hydroxymethyl)furan-2-yl)-1-(4-methoxyphenyl)hepta-1,4,6-trien-3-one | CHEMBL488901
TypeSmall organic molecule
Emp. Form.C19H18O5
Mol. Mass.326.3432
SMILESCOc1ccc(C=CC(=O)CC(=O)C=Cc2ccc(CO)o2)cc1 |w:14.14,7.7|
Structure
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