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Literature summary for 4.4.1.5 extracted from

  • Allen, R.E.; Lo, T.W.C.; Thornalley, P.J.
    Inhibitors of glyoxalase I: design, synthesis, inhibitory characteristics and biological evaluation (1993), Biochem. Soc. Trans., 21, 535-540.
    View publication on PubMed

Inhibitors

Inhibitors Comment Organism Structure
3-hydroxyflavone
-
Saccharomyces cerevisiae
Cbz-GSH
-
Homo sapiens
chrysin
-
Homo sapiens
chrysin
-
Saccharomyces cerevisiae
coumarin-10
-
Homo sapiens
coumarin-10
-
Saccharomyces cerevisiae
coumarin-4
-
Homo sapiens
coumarin-4
-
Saccharomyces cerevisiae
coumarin-5
-
Homo sapiens
coumarin-5
-
Saccharomyces cerevisiae
coumarin-8
-
Homo sapiens
coumarin-8
-
Saccharomyces cerevisiae
coumarin-9
-
Homo sapiens
coumarin-9
-
Saccharomyces cerevisiae
fisetin
-
Homo sapiens
fisetin
-
Saccharomyces cerevisiae
Lapachol
-
Homo sapiens
Lapachol
-
Saccharomyces cerevisiae
Lawsone
-
Homo sapiens
Lawsone
-
Saccharomyces cerevisiae
additional information substrate-analogue inhibitors and transition-state inhibitors Homo sapiens
additional information substrate-analogue inhibitors and transition-state inhibitors Saccharomyces cerevisiae
morin
-
Homo sapiens
morin
-
Saccharomyces cerevisiae
myricetin
-
Saccharomyces cerevisiae
norlapachol
-
Homo sapiens
norlapachol
-
Saccharomyces cerevisiae
para-substituted S-benzylglutathione
-
Saccharomyces cerevisiae
phthicol
-
Homo sapiens
phthicol
-
Saccharomyces cerevisiae
purpurogallin
-
Saccharomyces cerevisiae
quercetin
-
Homo sapiens
quercetin
-
Saccharomyces cerevisiae
S-(4-nitrobenzyloxycarbonyl)glutathione
-
Homo sapiens
S-(p-bromobenzyl)glutathione
-
Homo sapiens
S-(p-bromobenzyl)glutathione
-
Saccharomyces cerevisiae

Organism

Organism UniProt Comment Textmining
Homo sapiens
-
-
-
Saccharomyces cerevisiae
-
-
-