Sulfonamide chalcone as a new class of alpha-glucosidase inhibitors

Bioorg Med Chem Lett. 2005 Dec 15;15(24):5514-6. doi: 10.1016/j.bmcl.2005.08.087. Epub 2005 Oct 3.

Abstract

Chalcones 1-20, a new class of glycosidase inhibitors, were synthesized, and their glycosidase inhibitory activities were investigated. Non-aminochalcones 1-12 had no inhibitory activity, however, aminochalcones 13-20 had strong glycosidase (alpha-glucosidase, alpha-amylase, and beta-amylase) inhibitory activities. In particular, sulfonamide chalcones 17-20 had more potent alpha-glucosidase inhibitory activity than aminated chalcone 13-16. 4'-(p-Toluenesulfonamide)-3,4-dihydroxy chalcone 20 (IC(50)=0.4microM) was the best inhibitor against alpha-glucosidase, and these sulfonamide chalcones showed non-competitive inhibition.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Chalcones / chemical synthesis*
  • Chalcones / pharmacology
  • Enzyme Inhibitors / chemical synthesis
  • Enzyme Inhibitors / pharmacology*
  • Glycoside Hydrolase Inhibitors*
  • Kinetics
  • Models, Molecular
  • Structure-Activity Relationship
  • Sulfonamides / chemical synthesis*
  • Sulfonamides / pharmacology
  • alpha-Amylases / metabolism
  • beta-Amylase / metabolism

Substances

  • Chalcones
  • Enzyme Inhibitors
  • Glycoside Hydrolase Inhibitors
  • Sulfonamides
  • alpha-Amylases
  • beta-Amylase