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Article 2024 · 2 citations

Assessment of 3-Amino-Benzoic Acid Methyl Ester Derivatives as Glutathione S-Transferase and Glutathione Reductase Inhibitor: Supported by Molecular Docking Studies

Korkmaz, Isil Nihan, Guller, Pinar, Kalin, Ramazan, Ozdemir, Hasan

Abstract

GSTs catalyze detoxification reactions of harmful xenobiotics via conjugation with glutathione (GSH) while glutathione reductase (GR) is the sole enzyme that acts in the recovery reaction of GSH from oxidized glutathione (GSSG). In this study, in vitro inhibitory impacts of 3-amino-benzoic acid methyl ester compounds on GR and GST were investigated. For this firstly, GR and GST were obtained from human blood with specific activity of 6.26 EU/mg protein and 8.57 EU/mg protein respectively. Then, inhibition studies were performed. It was found that methyl 3-amino-5-chlorobenzoate had the highest inhibitory effect on hGR with Ki value of 0.524 +/- 0.109 mu M) and methyl 3-amino-4-nitrobenzoate was the most effective inhibitor on hGST with Ki value of 37.05 +/- 4.487 mu M. Besides, molecular docking analysis was used to estimate the binding energies of molecules. Methyl 3-amino-4-nitrobenzoate and methyl 3-amino-4-chlorobenzoate were predicted to have the highest binding affinity into GR and GST receptors respectively.

Keywords
Glutathione reductase Glutathione S-transferases In vitro inhibition Methyl 3-amino benzoates Molecular docking INDUCED OXIDATIVE STRESS MECHANISMS REDOX CARCINOMA PRODRUG
WoS Categories
Chemistry, Multidisciplinary
Sustainable Development Goals
Citation
Journal
CHEMISTRYSELECT
Year
2024
Volume
9
Issue
26
ISSN
2365-6549
DOI
10.1002/slct.202401362
WoS UID
WOS:001262681100001
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