Structure-activity relationships of bergenin derivatives effect on α-glucosidase inhibition

J Enzyme Inhib Med Chem. 2013 Dec;28(6):1162-70. doi: 10.3109/14756366.2012.719503. Epub 2012 Sep 26.

Abstract

The α-glucosidase inhibitory activities of bergenin derivatives were evaluated. Bergenin derivatives were synthesized from bergenin which is a characteristic compound of B. ligulata. A new bergenin derivative, 11-O-(3',4'-dimethoxybenzoyl)-bergenin showed the highest potent inhibitory activity among those of bergenin derivatives. The presence of substituents at 3',4'-position in bergenin derivatives altered the α-glucosidase inhibitory activity. 11-O-(3',4'-dimethoxybenzoyl)-bergenin was noncompetitive inhibitor for α-glucosidase. The present study reveals that bergenin derivatives could be classified as a new group of α-glucosidase inhibitors.

MeSH terms

  • Benzopyrans / chemistry*
  • Benzopyrans / isolation & purification
  • Benzopyrans / pharmacology*
  • Dose-Response Relationship, Drug
  • Enzyme Inhibitors / chemistry
  • Enzyme Inhibitors / isolation & purification
  • Enzyme Inhibitors / pharmacology*
  • Glycoside Hydrolase Inhibitors*
  • Molecular Structure
  • Saccharomyces cerevisiae / enzymology
  • Saxifragaceae / chemistry*
  • Structure-Activity Relationship
  • alpha-Glucosidases / metabolism

Substances

  • Benzopyrans
  • Enzyme Inhibitors
  • Glycoside Hydrolase Inhibitors
  • alpha-Glucosidases
  • bergenin