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.
Copyright © 2017 Elsevier Inc. All rights reserved.