Microbial transformation of (+)-nootkatone and the antiproliferative activity of its metabolites

Bioorg Med Chem. 2011 Apr 1;19(7):2464-9. doi: 10.1016/j.bmc.2011.01.062. Epub 2011 Mar 4.

Abstract

Six metabolites were obtained as a result of microbial transformation of (+)-nootkatone (1) by the fungal strains: Botrytis, Didymosphaeria, Aspergillus, Chaetomium and Fusarium. Their structure were established as (+)-(4R,5S,7R,9R)-9α-hydroxynootkatone (2), (+)-(4R,5S,7R)-13-hydroxynootkatone (3) and (+)-(4R,5S,7R,9R,11S)-11,12-epoxy-9α-hydroxynootkatone (4), (+)-(4R,5S,7R,11S)-11,12-epoksynootkatone (5), (+)-(4R,5S,7R)-11,12-dihydroxynootkatone (6) and (+)-(4R,5S,7R)-7,11,12-trihydroxynootkatone (7) on the basis of their spectral data. Two products: (4) and (7) were not previously reported in the literature. The antiproliferative activity of (+)-nootkatone (1) and isolated metabolites (2-7) of its biotransformation has been evaluated.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenocarcinoma / drug therapy
  • Adenocarcinoma / pathology
  • Adenocarcinoma of Lung
  • Antineoplastic Agents / chemistry
  • Antineoplastic Agents / metabolism*
  • Antineoplastic Agents / pharmacology*
  • Biotransformation
  • Cell Growth Processes / drug effects
  • Cell Line, Tumor
  • Fungi / metabolism*
  • HL-60 Cells
  • Humans
  • Lung Neoplasms / drug therapy
  • Lung Neoplasms / pathology
  • Molecular Conformation
  • Molecular Structure
  • Polycyclic Sesquiterpenes
  • Sesquiterpenes / chemistry
  • Sesquiterpenes / metabolism*
  • Sesquiterpenes / pharmacology*
  • Stereoisomerism

Substances

  • Antineoplastic Agents
  • Polycyclic Sesquiterpenes
  • Sesquiterpenes
  • nootkatone