The following articles (labelled with PubMed ID or TBD) are for your review
PMID | Data | Article Title | Organization |
28169168 |
1 |
Piceatannol, a natural trans-stilbene compound, inhibits human glyoxalase I. |
Tokyo University of Science |
3290487 |
113 |
The hypothetical active site lattice. An approach to modelling active sites from data on inhibitor molecules. |
Uniroyal Chemical |
26320622 |
10 |
Novel bivalent inhibitors with sub-nanomolar affinities towards human glyoxalase I. |
Chengdu University |
24856185 |
2 |
Inhibition by active site directed covalent modification of human glyoxalase I. |
University of Maryland |
903914 |
7 |
Synthesis and evaluation of alpha-hydroxythiol esters as antitumor agents and glyoxalase I inhibitors. |
TBA |
23122816 |
18 |
Design and evaluation of azaindole-substituted N-hydroxypyridones as glyoxalase I inhibitors. |
Chugai Pharmaceutical |
8035422 |
17 |
S-(N-aryl-N-hydroxycarbamoyl)glutathione derivatives are tight-binding inhibitors of glyoxalase I and slow substrates for glyoxalase II. |
University of Maryland |
21669529 |
5 |
Discovery of a new type inhibitor of human glyoxalase I by myricetin-based 4-point pharmacophore. |
Tokyo University of Science |
21689932 |
7 |
Structural investigation into the inhibitory mechanisms of indomethacin and its analogues towards human glyoxalase I. |
Sun Yat-Sen University |
21237663 |
38 |
Identification of curcumin derivatives as human glyoxalase I inhibitors: A combination of biological evaluation, molecular docking, 3D-QSAR and molecular dynamics simulation studies. |
Sun Yat-Sen University |
20801663 |
4 |
Delphinidin, a dietary anthocyanidin in berry fruits, inhibits human glyoxalase I. |
Tokyo University of Science |
18258440 |
6 |
Structure-activity relationship of human GLO I inhibitory natural flavonoids and their growth inhibitory effects. |
Tokyo University of Science |
15686923 |
1 |
Reversal of anticancer drug resistance by COTC based on intracellular glutathione and glyoxalase I. |
Keio University |
32299660 |
3 |
Induction of enantio-selective apoptosis in human leukemia HL-60 cells by (S)-erypoegin K, an isoflavone isolated from Erythrina poeppigiana. |
Meijo University |
11052803 |
19 |
Role of hydrophobic interactions in binding S-(N-aryl/alkyl-N-hydroxycarbamoyl)glutathiones to the active site of the antitumor target enzyme glyoxalase I. |
University of Maryland |
31879183 |
15 |
Recent advances in the discovery and development of glyoxalase I inhibitors. |
Chengdu University |
10206549 |
2 |
Synthesis and activity of gamma-(L-gamma-azaglutamyl)-S-(p-bromobenzyl)-L-cysteinylglycine: a metabolically stable inhibitor of glyoxalase I. |
University of Minnesota |
30628789 |
63 |
Metal-Binding Pharmacophore Library Yields the Discovery of a Glyoxalase 1 Inhibitor. |
TBA |
9871526 |
8 |
Syntheses and kinetic evaluation of hydroxamate-based peptide inhibitors of glyoxalase I. |
University of Waterloo |