Marine Drugs (Nov 2018)

Anti-<i>Acanthamoeba</i> Activity of Brominated Sesquiterpenes from <i>Laurencia johnstonii</i>

  • Sara García-Davis,
  • Ines Sifaoui,
  • María Reyes-Batlle,
  • Ezequiel Viveros-Valdez,
  • José E. Piñero,
  • Jacob Lorenzo-Morales,
  • José J. Fernández,
  • Ana R. Díaz-Marrero

DOI
https://doi.org/10.3390/md16110443
Journal volume & issue
Vol. 16, no. 11
p. 443

Abstract

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Focused on our interest to develop novel antiparasistic agents, the present study was aimed to evaluate the biological activity of an extract of Laurencia johnstonii collected in Baja California Sur, Mexico, against an Acantamoeba castellanii Neff strain. Bioassay-guided fractionation allowed us to identify the amoebicidal diastereoisomers α-bromocuparane (4) and α-isobromocuparane (5). Furthermore, bromination of the inactive laurinterol (1) and isolaurinterol (2) yielded four halogenated derivatives, (6)⁻(9), which improved the activity of the natural sesquiterpenes. Among them, the most active compound was 3α-bromojohnstane (7), a sesquiterpene derivative which possesses a novel carbon skeleton johnstane.

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