Exploring the Dual Inhibitory Activity of Novel Anthranilic Acid Derivatives towards α-Glucosidase and Glycogen Phosphorylase Antidiabetic Targets: Design, In Vitro Enzyme Assay, and Docking Studies

Molecules : a Journal of Synthetic Chemistry and Natural Product Chemistry
Saleh Ihmaid

Abstract

A few new anthranilate diamide derivatives, 3a⁻e, 5a⁻c and 7a⁻d, were designed, synthesized, and evaluated for their inhibitory activity against two interesting antidiabetic targets, α-glucosidase and glycogen phosphorylase enzymes. Different instrumental analytical tools were applied in identification and conformation of their structures like; 13C NMR, ¹H NMR and elemental analysis. The screening of the novel compounds showed potent inhibitory activity with nanomolar concentration values. The most active compounds (5c) and (7b) showed the highest inhibitory activity against α-glucosidase and glycogen phosphorylase enzymes IC50 = 0.01247 ± 0.01 µM and IC50 = 0.01372 ± 0.03 µM, respectively. In addition, in vivo testing of the highly potent α-glucosidase inhibitor (7b) on rats with DTZ-induced diabetes was done and showed significant reduction of blood glucose levels compared to the reference drug. Furthermore, a molecular docking study was performed to help understand the binding interactions of the most active analogs with these two enzymes. The data obtained from the molecular modeling were correlated with those obtained from the biological screening. These data showed considerable antidiabetic activity for these newly synthe...Continue Reading

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Citations

Jun 13, 2021·Drug Development Research·Parteek Prasher, Mousmee Sharma

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Methods Mentioned

BETA
nuclear magnetic resonance
Assay
X-ray

Software Mentioned

AutoDock
MOE
AutoDock Tools ( ADT )
GraphPad Prism
GraphPad

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