4.7 Article

Cyclotheonellazoles A-C, Potent Protease Inhibitors from the Marine Sponge Theonella aff. swinhoei

Journal

JOURNAL OF NATURAL PRODUCTS
Volume 80, Issue 4, Pages 1110-1116

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.jnatprod.7b00028

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Funding

  1. Tel Aviv University
  2. School of Chemistry of Tel Aviv University
  3. European Commission
  4. Regional Council of Reunion Island: BIOMOL-TCN program (Activites Therapeutiques, Cosmetologiques et Nutraceutiques de Molecules Issues de la Biodiversite Terrestre, Marine et Microbienne de la Zone Sud-Ouest de l'Ocean Indien)
  5. ERDF (European Regional Development Fund)

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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 (1-3), 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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