4.7 Article

Microspinosamide, a new HIV-inhibitory cyclic depsipeptide from the marine sponge Sidonops microspinosa

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JOURNAL OF NATURAL PRODUCTS
卷 64, 期 1, 页码 117-121

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AMER CHEMICAL SOC
DOI: 10.1021/np0002379

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  1. NCI NIH HHS [N01-CO-56000] Funding Source: Medline
  2. NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES [Z01DK032102] Funding Source: NIH RePORTER
  3. OFFICE OF THE DIRECTOR, NCI [N01CO056000] Funding Source: NIH RePORTER

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Microspinosamide (1), a new cyclic depsipeptide incorporating 13 amino acid residues, was isolated from extracts of an Indonesian collection of the marine sponge Sidonops microspinosa. Its structure was elucidated by extensive NMR and mass spectral analyses, and by chemical degradation and derivatization studies. The tridecapeptide 1 incorporates numerous uncommon amino acids, and it is the first naturally occurring peptide to contain a beta -hydroxy-p-bromophenylalanine residue. Microspinosamide (1) inhibited the cytopathic effect of HIV-1 infection in an XTT-based in vitro assay with an EC50 value of approximately 0.2 mug/mL.

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