Reactions of nitroxides. Part X: antifungal activity of selected sulfur and selenium derivatives of 2,2,6,6-tetramethylpiperidine

Bioorg Med Chem Lett. 2011 Jan 1;21(1):514-6. doi: 10.1016/j.bmcl.2010.10.092. Epub 2010 Oct 25.

Abstract

The antifungal activity of nitroxyl radicals-derivatives of 2,2,6,6-tetramethylpiperidine-1-oxyl with reactive substituents 4-isothiocyanato-, 4-isocyano-, and 4-isoselenocyanato- and of N-formyl-, N-thioformyl-, N-selenoformyl-derivatives of 2,2,6,6-tetramethylpiperidine was investigated. Those of the above compounds, which contain a sulfur or selenium atom are the most active against four fungus plant patogens: Botrytiscinerea, Fusariumculmorum, Phytophthoracactorum, Rhizoctoniasolani. 4-Isoselenocyanato-2,2,6,6-tetramethylpiperidine-1-oxyl proved to be the most active compound.

MeSH terms

  • Antifungal Agents / chemical synthesis
  • Antifungal Agents / chemistry*
  • Antifungal Agents / pharmacology
  • Botrytis / drug effects
  • Cyclic N-Oxides / chemistry*
  • Fusarium / drug effects
  • Microbial Sensitivity Tests
  • Nitrogen Oxides / chemistry*
  • Phytophthora / drug effects
  • Rhizoctonia / drug effects
  • Selenium / chemistry*
  • Selenium / pharmacology
  • Spin Labels
  • Sulfur / chemistry*
  • Sulfur / pharmacology

Substances

  • Antifungal Agents
  • Cyclic N-Oxides
  • Nitrogen Oxides
  • Spin Labels
  • Sulfur
  • nitroxyl
  • Selenium
  • tempol