Isoswinholide B and swinholide K, potently cytotoxic dimeric macrolides from Theonella swinhoei

Bioorg Med Chem. 2013 Sep 1;21(17):5332-8. doi: 10.1016/j.bmc.2013.06.015. Epub 2013 Jun 15.

Abstract

Chemical investigation of an Indonesian specimen of Theonella swinhoei afforded the new dimeric macrolides isoswinholide B (5) and swinholide K (6), along with the known swinholides A (1), B (2) and D (3) and isoswinholide A (4). Isoswinholide B showed an unprecedented 21/19' lactonization pattern, while swinholide K included an sp(2) methylene attached at C-4 and an additional oxymethine group at C-5, whose configuration has been determined through application of J-based configuration analysis. The isolated swinholides (1-6), with the exception of isoswinholide B, showed a cytotoxic activity on HepG2 (hepatocarcinoma cell line) in the nanomolar range.

Keywords: Actin-binding cytotoxins; Macrolides; Swinholides; Theonella swinhoei.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Survival / drug effects
  • Dimerization
  • Hep G2 Cells
  • Humans
  • Macrolides / chemistry*
  • Macrolides / isolation & purification
  • Macrolides / toxicity
  • Magnetic Resonance Spectroscopy
  • Marine Toxins / chemistry*
  • Marine Toxins / isolation & purification
  • Marine Toxins / toxicity
  • Molecular Conformation
  • Theonella / chemistry*

Substances

  • Macrolides
  • Marine Toxins
  • isoswinholide B
  • swinholide B