Effect of O-methylated and glucuronosylated flavonoids from Tamarix gallica on α-glucosidase inhibitory activity: structure-activity relationship and synergistic potential

Biosci Biotechnol Biochem. 2017 Mar;81(3):445-448. doi: 10.1080/09168451.2016.1254538. Epub 2016 Nov 14.

Abstract

O-Methylated and glucuronosylated flavonoids were isolated from Tamarix gallica as α-glucosidase inhibitors. Structure-activity relationship of these flavonoids suggests that catechol moiety and glucuronic acid at C-3 are factors in the increase in α-glucosidase inhibitory activity. Furthermore, rhamnetin, tamarixetin, rhamnazin, KGlcA, KGlcA-Me, QGlcA, and QGlcA-Me exhibit synergistic potential when applied with a very low concentration of acarbose to α-glucosidase from rat intestine.

Keywords: O-methylated and glucuronosylated flavonoids; Tamarix gallica; structure–activity relationship and synergistic potential; α-glucosidase inhibitors.

MeSH terms

  • Dose-Response Relationship, Drug
  • Flavonoids / chemistry*
  • Flavonoids / pharmacology*
  • Glycoside Hydrolase Inhibitors / chemistry
  • Glycoside Hydrolase Inhibitors / pharmacology*
  • Molecular Structure
  • Structure-Activity Relationship
  • Tamaricaceae / chemistry*
  • alpha-Glucosidases / metabolism

Substances

  • Flavonoids
  • Glycoside Hydrolase Inhibitors
  • alpha-Glucosidases