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TargetLactoylglutathione lyase
LigandBDBM50295287
Substrate/Competitorn/a
Meas. Tech.ChEMBL_716549 (CHEMBL1670273)
Ki 87800±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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BDBM50295287
n/a
NameBDBM50295287
Synonyms:2-(1-methyl-5-(4-methylbenzoyl)-1H-pyrrol-2-yl)acetic acid | CHEMBL1020 | MCN-2559 | TOLMETIN | Tolectin | [1-Methyl-5-(4-methyl-benzoyl)-1H-pyrrol-2-yl]-acetic acid | [1-Methyl-5-(4-methyl-benzoyl)-1H-pyrrol-2-yl]-acetic acid(tolmetin)
TypeSmall organic molecule
Emp. Form.C15H15NO3
Mol. Mass.257.2845
SMILESCc1ccc(cc1)C(=O)c1ccc(CC(O)=O)n1C
Structure
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