Beilstein Journal of Organic Chemistry (Aug 2014)

Synthesis and bioactivity of analogues of the marine antibiotic tropodithietic acid

  • Patrick Rabe,
  • Tim A. Klapschinski,
  • Nelson L. Brock,
  • Christian A. Citron,
  • Paul D’Alvise,
  • Lone Gram,
  • Jeroen S. Dickschat

DOI
https://doi.org/10.3762/bjoc.10.188
Journal volume & issue
Vol. 10, no. 1
pp. 1796 – 1801

Abstract

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Tropodithietic acid (TDA) is a structurally unique sulfur-containing antibiotic from the Roseobacter clade bacterium Phaeobacter inhibens DSM 17395 and a few other related species. We have synthesised several structural analogues of TDA and used them in bioactivity tests against Staphylococcus aureus and Vibrio anguillarum for a structure–activity relationship (SAR) study, revealing that the sulfur-free analogue of TDA, tropone-2-carboxylic acid, has an antibiotic activity that is even stronger than the bioactivity of the natural product. The synthesis of this compound and of several analogues is presented and the bioactivity of the synthetic compounds is discussed.

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