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Amphilectene Diterpene Isonitriles and Formamido Derivatives from the Hainan Nudibranch Phyllidia Coelestis.


ABSTRACT: Terpene content of two distinct collections of the nudibranch Phyllidia coelestis from the South China Sea has been chemically analyzed. A series of amphilectene diterpenes, most likely of dietary origin, with isocyano and formamido functionalities have been isolated from both collections and spectroscopically characterized by an exhaustive nuclear magnetic resonance (NMR) analysis. Interestingly, the structural architecture of compounds 5-7 and 9 with both 8,13-cis and 12,13-cis ring junctions is unprecedented in the amphilectene skeleton. Metabolite 3, which was the most abundant in the nudibranch's mantle, has been shown to deter feeding by a generalist predator, supporting its involvement in chemical defense.

SUBMITTER: Carbone M 

PROVIDER: S-EPMC6891729 | biostudies-literature | 2019 Oct

REPOSITORIES: biostudies-literature

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Amphilectene Diterpene Isonitriles and Formamido Derivatives from the Hainan Nudibranch <i>Phyllidia Coelestis</i>.

Carbone Marianna M   Ciavatta Maria Letizia ML   Manzo Emiliano E   Li Xiao-Lu XL   Mollo Ernesto E   Mudianta I Wayan IW   Guo Yue-Wei YW   Gavagnin Margherita M  

Marine drugs 20191024 11


Terpene content of two distinct collections of the nudibranch <i>Phyllidia coelestis</i> from the South China Sea has been chemically analyzed. A series of amphilectene diterpenes, most likely of dietary origin, with isocyano and formamido functionalities have been isolated from both collections and spectroscopically characterized by an exhaustive nuclear magnetic resonance (NMR) analysis. Interestingly, the structural architecture of compounds <b>5</b>-<b>7</b> and <b>9</b> with both 8,13-<i>ci  ...[more]

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