alexa Halogenated secondary metabolites from Laurencia obtusa.
Psychiatry

Psychiatry

Journal of Addiction Research & Therapy

Author(s): Aydomu Z, Imre S, Ersoy L, Wray V

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Abstract A new sesquiterpene (1), and a halogenated C15 acetogenin (2), a stereoisomer of neoisoprelaurefucin were isolated from Laurencia obtusa. Four known compounds laurencienyne (3), rogiolenyne B (4), obtusenol (5), and (3E)-dactomelyne (6) were also isolated from this alga. Rogiolenyne B (4) and (3E)-dactomelyne (6) were found for the first from this species. The structures of these compounds were elucidated by spectroscopic methods. The unambiguous assignments of the 1H and 13C NMR spectral data of (5) and 13C NMR data of (6) were also reported for the first time. This article was published in Nat Prod Res and referenced in Journal of Addiction Research & Therapy

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