Stereoselective synthesis of 7 alpha- and 7 beta-aminocholestanol as potent fungicidal drugs

Bioorg Med Chem Lett. 2001 Dec 3;11(23):3011-4. doi: 10.1016/s0960-894x(01)00609-6.

Abstract

Potentially lymphotropic 7 alpha- and 7 beta-aminocholestanol were stereoselectively synthesized. In vitro bioassay studies have shown that these fungicidal lipidic derivatives possess strong antifungal activity against Candida spp resistant strains to amphotericin B, 5-fluorocytosine and azoles.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amphotericin B / pharmacology
  • Antifungal Agents / chemical synthesis
  • Antifungal Agents / chemistry*
  • Antifungal Agents / pharmacology*
  • Biochemistry / methods
  • Candida / drug effects
  • Cholestanols / chemical synthesis
  • Cholestanols / pharmacology
  • Drug Evaluation, Preclinical
  • Flucytosine / pharmacology
  • Microbial Sensitivity Tests
  • Stereoisomerism

Substances

  • Antifungal Agents
  • Cholestanols
  • Amphotericin B
  • Flucytosine