In vitro inhibition of 1,3-beta-glucan synthase by glycolipids from convolvulaceous species

Planta Med. 2002 Aug;68(8):739-42. doi: 10.1055/s-2002-33791.

Abstract

Sixteen convolvulaceous glycolipids selected from the tricolorin (1 - 7) and orizabin (8 - 16) series, proved to be strong in vitro inhibitors of the enzyme that catalyzes the synthesis of 1,3-beta-D-glucan, a major polymer of fungal cell-walls. Results provide an insight into function of the specific structures of these complex macrocyclic lactones as inhibitors of the 1,3-beta-D-glucan synthase and open the possibility of using these compounds as starting points for the development of antifungal agents that act by inhibiting fungal cell-wall synthesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antifungal Agents / pharmacology*
  • Convolvulaceae / chemistry*
  • Dose-Response Relationship, Drug
  • Glucosyltransferases / antagonists & inhibitors*
  • Glucosyltransferases / metabolism
  • Glycolipids / pharmacology*
  • Inhibitory Concentration 50
  • Membrane Proteins*
  • Molecular Structure
  • Schizosaccharomyces pombe Proteins*

Substances

  • Antifungal Agents
  • Glycolipids
  • Membrane Proteins
  • Schizosaccharomyces pombe Proteins
  • Glucosyltransferases
  • 1,3-beta-glucan synthase