Synthesis and examination of 1,2,4‐triazine‐sulfonamide hybrids as potential inhibitory drugs: Inhibition effects on AChE and GST enzymes in silico and in vitro conditions
Przemysław Rozbicki(University of Siedlce), Danuta Branowska(University of Siedlce), Ewa Wolińska(University of Siedlce), Ercan Oğuz(Department of Health Services), Fikret Türkan(University of Turku), Adnan Çetin(Van Yüzüncü Yıl Üniversitesi)
Cited by 36
Related Papers
Rosmarinic acid inhibits some metabolic enzymes including glutathione<i>S</i>-transferase, lactoperoxidase, acetylcholinesterase, butyrylcholinesterase and carbonic anhydrase isoenzymes
|Journal of Enzyme Inhibition and Medicinal Chemistry|2016|228
Antidiabetic and antiparasitic potentials: Inhibition effects of some natural antioxidant compounds on α-glycosidase, α-amylase and human glutathione S-transferase enzymes
|International Journal of Biological Macromolecules|2018|215
Synthesis, biological evaluation and molecular docking of novel pyrazole derivatives as potent carbonic anhydrase and acetylcholinesterase inhibitors
|Bioorganic Chemistry|2019|202
The effect of caffeic acid phenethyl ester (CAPE) on metabolic enzymes including acetylcholinesterase, butyrylcholinesterase, glutathione S-transferase, lactoperoxidase, and carbonic anhydrase isoenzymes I, II, IX, and XII
|Journal of Enzyme Inhibition and Medicinal Chemistry|2015|180
Benzenesulfonamide derivatives as potent acetylcholinesterase, α-glycosidase, and glutathione S-transferase inhibitors: biological evaluation and molecular docking studies
|Journal of Biomolecular Structure and Dynamics|2020|107