Isolation of swinholide A and related glycosylated derivatives from two field collections of marine cyanobacteria

Org Lett. 2005 Mar 31;7(7):1375-8. doi: 10.1021/ol050188x.

Abstract

[structure: see text] Chemical investigation of two field collections of marine cyanobacteria has led to the discovery of two new cytotoxic natural products, ankaraholides A (2) and B (3), along with the known compound swinholide A (1). Since swinholide-type compounds were previously localized to the heterotrophic bacteria of sponges, these findings raise intriguing questions about their true metabolic source.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Antineoplastic Agents / chemistry
  • Antineoplastic Agents / isolation & purification*
  • Antineoplastic Agents / pharmacology
  • Cyanobacteria / chemistry*
  • Fiji
  • Glycosylation
  • Marine Toxins / chemistry
  • Marine Toxins / isolation & purification*
  • Marine Toxins / pharmacology
  • Molecular Structure
  • Porifera / chemistry*
  • Pyrans / chemistry
  • Pyrans / isolation & purification*
  • Pyrans / pharmacology
  • Symbiosis

Substances

  • Antineoplastic Agents
  • Marine Toxins
  • Pyrans
  • ankaraholide A
  • ankaraholide B
  • swinholide A