In silico evaluation of phenolic compounds as inhibitors of Α-amylase and Α-glucosidase

J Biomol Struct Dyn. 2021 Feb;39(3):816-822. doi: 10.1080/07391102.2020.1718553. Epub 2020 Feb 10.

Abstract

The aim of the present study focuses on the molecular docking approach to screen alternative drug that can regulate the hyperglycemia by down-regulating α-glucosidase and α-amylase activity using phenolic compounds: tannic acid (L1), catechin (L2), gallic acid (L3), quercetin (L5) and epicatechin (L6). L1 gives the best docking scores, its interaction with α-amylase and α-glucosidase has the lowest energy score compared to the other complexes and to the acarbose (L4). L1 forms strong five H-donor interactions with residues of active site of α-amylase and three H-donor interactions with α-glucosidase. The in silico evaluation of the unfavorable absorption, distribution, metabolism, and elimination (ADME) properties and drug-likeness revealed that L5 has high absorption compared to tannic acid and to the other compounds. This study revealed for the first time that tannic acid is a functional inhibitor of α-glucosidase and α-amylase activities and can be used as alternative for the regulation of post-prandial hyperglycaemia. Communicated by Ramaswamy Sarma.

Keywords: Diabetes mellitus; docking; phenolic compounds; α-amylase; α-glucosidase.

MeSH terms

  • Computer Simulation
  • Glycoside Hydrolase Inhibitors / pharmacology
  • Molecular Docking Simulation
  • alpha-Amylases*
  • alpha-Glucosidases*

Substances

  • Glycoside Hydrolase Inhibitors
  • alpha-Amylases
  • alpha-Glucosidases