Biological evaluation of new imidazole derivatives tethered with indole moiety as potent α-glucosidase inhibitors

Bioorg Chem. 2018 Feb:76:365-369. doi: 10.1016/j.bioorg.2017.12.014. Epub 2017 Dec 5.

Abstract

A series of triarylimidazoles substituted with 2-arylindoles (4a-4j) were prepared and evaluated for their in vitro α-Glucosidase inhibition. α-Glucosidase inhibition assay displayed a new class of highly potent agents The new compounds showed significant α-glucosidase inhibitory activity as compared to the standard inhibitor acrabose. Structures of synthesized compounds were determined by using Mass spectrometry FT-IR, 1H NMR and 13C NMR.

Keywords: 2-Arylindoles; Diabetes; Multicomponent reactions; NMR spectra; α-Glucosidase inhibition.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Enzyme Assays
  • Glycoside Hydrolase Inhibitors / chemical synthesis
  • Glycoside Hydrolase Inhibitors / chemistry*
  • Imidazoles / chemical synthesis
  • Imidazoles / chemistry*
  • Indoles / chemical synthesis
  • Indoles / chemistry*
  • Molecular Structure

Substances

  • Glycoside Hydrolase Inhibitors
  • Imidazoles
  • Indoles