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Cyclotheonellazoles A-C, potent protease inhibitors from the marine sponge Theonella aff. swinhoei
Issac, M.; Aknin, M.; Gauvin-Bialecki, A.; De Voogd, N.; Ledoux, A.; Frederich, M.; Kashman, Y.; Carmeli, S. (2017). Cyclotheonellazoles A-C, potent protease inhibitors from the marine sponge Theonella aff. swinhoei. J. Nat. Prod. 80(4): 1110-1116. https://dx.doi.org/10.1021/acs.jnatprod.7b00028
In: Journal of Natural Products. American Chemical Society/American Society of Pharmacognosy: Washington DC. ISSN 0163-3864; e-ISSN 1520-6025, meer
Peer reviewed article  
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    Marien/Kust
Auteurs  Top 
  • Issac, M.
  • Aknin, M.
  • Gauvin-Bialecki, A.
  • De Voogd, N., meer
  • Ledoux, A., meer
  • Frederich, M., meer
  • Kashman, Y.
  • Carmeli, S.
Abstract
    The extract of a sample of the sponge Theonella aff. swinhoei collected in Madagascar exhibited promising in vitro antiplasmodial activity. The antiplasmodial activity was ascribed in part to the known metabolite swinholide A. Further investigation of the extract afforded three unusual cyclic peptides, cyclotheonellazoles A–C, which contain six nonproteinogenic amino acids out of the eight acid units that compose these natural products. Among these acids the most novel were 4-propenoyl-2-tyrosylthiazole and 3-amino-4-methyl-2-oxohexanoic acid. The structure of the compounds was elucidated by interpretation of the 1D and 2D NMR data, HRESIMS, and advanced Merfay’s techniques. The new compounds were found to be nanomolar inhibitors of chymotrypsin and sub-nanomolar inhibitors of elastase, but did not present antiplasmodial activity.
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