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

被引:79
作者
Rashid, MA
Gustafson, KR
Cartner, AK
Shigematsu, N
Pannell, LK
Boyd, MR
机构
[1] NCI, Frederick Canc Res & Dev Ctr, Lab Drug Discovery Res & Dev, Dev Therapeut Program,Div Canc Treatment & Canc, Frederick, MD 21702 USA
[2] Frederick Canc Res & Dev Ctr, SAIC Frederick, Frederick, MD 21701 USA
[3] NIDDK, Lab Bioorgan Chem, Bethesda, MD 20892 USA
来源
JOURNAL OF NATURAL PRODUCTS | 2001年 / 64卷 / 01期
关键词
D O I
10.1021/np0002379
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
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.
引用
收藏
页码:117 / 121
页数:5
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