F13459, a new derivative of mycophenolic acid. I. Taxonomy, isolation, and biological properties

J Antibiot (Tokyo). 2001 Jun;54(6):489-93. doi: 10.7164/antibiotics.54.489.

Abstract

In the course of screening for inhibitors of intracellular trafficking of glycoprotein, a new inhibitor, F13459 was isolated from the culture broth of a Penicillium sp. It was purified using solvent extraction, silica gel, Sephadex LH-20 and ODS column chromatography. From structural analysis, F13459 was a derivative of mycophenolic acid, an inhibitor of inosine 5'-monophosphate dehydrogenase. F13459 inhibited hemagglutinin synthesis of NDV at concentrations more than 25 microg/ml. However, syncytium formation as a result of cell surface expression of F-glycoprotein of NDV was inhibited at concentrations of F13459 lower than those required for appreciable inhibition of glycoprotein synthesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antiviral Agents / isolation & purification*
  • Antiviral Agents / pharmacology
  • Cells, Cultured
  • Cricetinae
  • Enzyme Inhibitors / isolation & purification
  • Enzyme Inhibitors / pharmacology
  • Giant Cells / drug effects
  • Hemagglutinins / biosynthesis
  • Kidney / cytology
  • Microscopy, Electron, Scanning
  • Mycophenolic Acid / analogs & derivatives*
  • Mycophenolic Acid / isolation & purification*
  • Mycophenolic Acid / pharmacology*
  • Newcastle disease virus / drug effects
  • Newcastle disease virus / metabolism
  • Penicillium / chemistry*
  • Penicillium / classification
  • Viral Fusion Proteins / antagonists & inhibitors
  • Viral Fusion Proteins / biosynthesis

Substances

  • Antiviral Agents
  • Enzyme Inhibitors
  • F13459
  • Hemagglutinins
  • Viral Fusion Proteins
  • Mycophenolic Acid