Hydroxycoumarin derivatives: novel and potent α-glucosidase inhibitors

J Med Chem. 2010 Dec 9;53(23):8252-9. doi: 10.1021/jm100757r. Epub 2010 Nov 5.

Abstract

A novel class of hydroxycoumarin derivatives were found to be potent α-glucosidase inhibitors. Their syntheses were reported and the structure-activity relationship was established. Kinetic enzymatic assays indicated that compound 10 was a slow-binding and noncompetitive inhibitor with a Ki value of 589 nM, while compound 11 was a competitive inhibitor with a Ki value of 4.810 μM. Among all hydroxycoumarin derivatives studied, compounds 10 and 11 exhibited the highest activities, were specific inhibitors of α-glucosidase, and could be exploited as the lead compounds for the development of potent α-glucosidase inhibitors. Compounds 10 and 11 were also selected for further discussion for the mechanism of enzymatic inhibition.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Circular Dichroism
  • Coumarins / chemistry
  • Coumarins / pharmacology*
  • Enzyme Inhibitors / chemistry
  • Enzyme Inhibitors / pharmacology*
  • Glycoside Hydrolase Inhibitors*
  • Hydrogen Bonding
  • Kinetics
  • Magnetic Resonance Spectroscopy
  • Models, Molecular
  • Spectrometry, Mass, Electrospray Ionization
  • Structure-Activity Relationship
  • alpha-Glucosidases / metabolism

Substances

  • Coumarins
  • Enzyme Inhibitors
  • Glycoside Hydrolase Inhibitors
  • alpha-Glucosidases