Roseopurpurins: Chemical Diversity Enhanced by Convergent Biosynthesis and Forward and Reverse Michael Additions

Org Lett. 2016 Sep 2;18(17):4340-3. doi: 10.1021/acs.orglett.6b02099. Epub 2016 Aug 18.

Abstract

Cultures of the estuarine fungus Penicillium roseopurpureum (CMB-MF038) yielded a diverse array of polyketides, many of which were related via a highly convergent biosynthetic pathway. In addition to revising and assigning structures, and documenting chemical and biological properties, pro-drug cytotoxic properties were attributed to roseopurpurins H (10) and I (11) on the basis of in situ reverse Michael addition to a cytotoxic Michael acceptor (12).

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Line, Tumor
  • Cell Survival / drug effects
  • Dose-Response Relationship, Drug
  • Humans
  • Molecular Structure
  • Penicillium / chemistry
  • Penicillium / metabolism*
  • Polyketides / chemistry
  • Polyketides / metabolism
  • Polyketides / pharmacology*
  • Prodrugs / chemistry
  • Prodrugs / metabolism
  • Prodrugs / pharmacology*
  • Structure-Activity Relationship

Substances

  • Polyketides
  • Prodrugs