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Synthesis,<i>in vitro</i>inhibitory activity, kinetic study and molecular docking of novel<i>N</i>-alkyl–deoxynojirimycin derivatives as potential α-glucosidase inhibitors

Ping Lin, Jiacheng Zeng, Jiguang Chen, Xu‐Liang Nie, En Yuan, Xiaoqiang Wang, Da‐Yong Peng, Zhongping Yin

2020Journal of Enzyme Inhibition and Medicinal Chemistry20 citationsDOIOpen Access PDF

Abstract

of 10 µM, 52 µM, and 150 µM, respectively. Molecular docking demonstrated that the high active inhibitors interacted with α-glucosidase by four types of interactions, including hydrogen bonds, π-π stacking interactions, hydrophobic interactions, and electrostatic interaction. Among all the interactions, the π-π stacking interaction and hydrogen bond played a significant role in a various range of activities of the compounds.

Topics & Concepts

AcarboseChemistryHydrogen bondAlkylStereochemistryDocking (animal)Active siteIC50StackingHydrophobic effectIn vitroMolecular modelInhibitory postsynaptic potentialEnzymeBiochemistryOrganic chemistryMoleculeBiologyNursingNeuroscienceMedicineNatural Antidiabetic Agents StudiesCarbohydrate Chemistry and SynthesisEnzyme Production and Characterization
Synthesis,<i>in vitro</i>inhibitory activity, kinetic study and molecular docking of novel<i>N</i>-alkyl–deoxynojirimycin derivatives as potential α-glucosidase inhibitors | Litcius