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TargetLactoylglutathione lyase
LigandBDBM50517464
Substrate/Competitorn/a
Meas. Tech.ChEMBL_1901787 (CHEMBL4404009)
Ki 230±n/a nM
Citation Jin, TZhao, LWang, HPHuang, MLYue, YLu, CZheng, ZB Recent advances in the discovery and development of glyoxalase I inhibitors. Bioorg Med Chem28:0 (2020) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Lactoylglutathione lyase
Name:Lactoylglutathione lyase
Synonyms:4.4.1.5 | Aldoketomutase | Glo1 | Glx I | Glyoxalase I | Ketone-aldehyde mutase | LGUL_MOUSE | Lactoylglutathione lyase | Methylglyoxalase | S-D-lactoylglutathione methylglyoxal lyase
Type:PROTEIN
Mol. Mass.:20805.83
Organism:Mus musculus
Description:ChEMBL_10270
Residue:184
Sequence:
MAEPQPASSGLTDETAFSCCSDPDPSTKDFLLQQTMLRIKDPKKSLDFYTRVLGLTLLQK
LDFPAMKFSLYFLAYEDKNDIPKDKSEKTAWTFSRKATLELTHNWGTEDDETQSYHNGNS
DPRGFGHIGIAVPDVYSACKRFEELGVKFVKKPDDGKMKGLAFIQDPDGYWIEILNPNKI
ATII
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BDBM50517464
n/a
NameBDBM50517464
Synonyms:CHEMBL1234300
TypeSmall organic molecule
Emp. Form.C16H16O6
Mol. Mass.304.2946
SMILESCOC(=O)c1c(C)cc(Oc2cc(C)cc(O)c2O)cc1O
Structure
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