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TargetLactoylglutathione lyase
LigandBDBM50336259
Substrate/Competitorn/a
Meas. Tech.ChEMBL_716548 (CHEMBL1670272)
Ki 3600±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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  Blast E-value cutoff:
BDBM50336259
n/a
NameBDBM50336259
Synonyms:4-(5-(3,4-dimethoxyphenyl)-2-(-3-(3,4-dimethoxyphenyl)acryloyl)-3-oxopenta-1,4-dienyl)phthalaldehyde | CHEMBL1669730
TypeSmall organic molecule
Emp. Form.C32H28O8
Mol. Mass.540.5599
SMILES[#6]-[#8]-c1ccc(\[#6]=[#6]\[#6](=O)-[#6](=[#6]/c2ccc(-[#6]=O)c(-[#6]=O)c2)\[#6](=O)\[#6]=[#6]\c2ccc(-[#8]-[#6])c(-[#8]-[#6])c2)cc1-[#8]-[#6]
Structure
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