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      Sesquiterpene metabolites of the antarctic gorgonian Dasystenella acanthina.

      Journal of Natural Products
      Animals, Antarctic Regions, Anthozoa, chemistry, Cyprinodontiformes, Feeding Behavior, drug effects, Goldfish, Molecular Structure, Nuclear Magnetic Resonance, Biomolecular, Sesquiterpenes, Eudesmane, isolation & purification, pharmacology, Stereoisomerism

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          Abstract

          The ethereal extract of the Antarctic gorgonian Dasystenella acanthina was found to contain three main nonpolar and relatively transient sesquiterpene metabolites (1-3), which were isolated and submitted to spectral analysis. Two of them were identified as the previously reported compounds trans-beta-farnesene (1) and isofuranodiene (3), whereas the third metabolite, the furanoeudesmane 2, was unknown. The structure elucidation of this new sesquiterpene was solved mainly on the basis of its spectral properties and correlation with known compounds.

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