Structure determination of two new trichothecenes from a halotolerant fungus Myrothecium sp. GS-17 by NMR spectroscopy

Magn Reson Chem. 2012 Sep;50(9):632-6. doi: 10.1002/mrc.3845. Epub 2012 Jul 16.

Abstract

Two new trichothecenes, named 8α-hydroxyroridin H and myrothecin A, along with six known compounds, 8α-acetoxy roridin H, isororidin K, verrucarin A, verrucarin J, verrucarin L and 8α-acetoxy verrucarin L, were isolated from the fermentation broth of a halotolerant fungus Myrothecium sp. GS-17, which was separated from the soil sample of a salina. Structure elucidation and NMR signal assignments were achieved on the basis of spectroscopy. In addition, compounds 1 and 2 were active against plant pathogenic fungi Rhizoctonia solani and Fusarium oxysporum.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antifungal Agents / chemistry*
  • Antifungal Agents / isolation & purification
  • Antifungal Agents / pharmacology
  • Fusarium / drug effects
  • Hypocreales / chemistry*
  • Magnetic Resonance Spectroscopy
  • Microbial Sensitivity Tests
  • Molecular Structure
  • Rhizoctonia / drug effects
  • Structure-Activity Relationship
  • Trichothecenes / chemistry*
  • Trichothecenes / isolation & purification
  • Trichothecenes / pharmacology

Substances

  • 8alpha-hydroxyroridin H
  • Antifungal Agents
  • Trichothecenes
  • myrothecin A