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TargetLactoylglutathione lyase
LigandBDBM50569124
Substrate/Competitorn/a
Meas. Tech.ChEMBL_2108109 (CHEMBL4816784)
IC50 5500±n/a nM
Citation Azuma, MInoue, MNishida, AAkahane, HKitajima, MNatani, SChimori, RYoshimori, AMano, YUchiro, HTanuma, SITakasawa, R Addition of hydrophobic side chains improve the apoptosis inducibility of the human glyoxalase I inhibitor, TLSC702. Bioorg Med Chem Lett40:0 (2021) [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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BDBM50569124
n/a
NameBDBM50569124
Synonyms:CHEMBL4877073
TypeSmall organic molecule
Emp. Form.C19H15NO5S
Mol. Mass.369.391
SMILESOC(=O)COc1ccc(\C=C(/CC(O)=O)c2nc3ccccc3s2)cc1
Structure
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