Laurendecumallenes A-B and laurendecumenynes A-B, halogenated nonterpenoid C15-Acetogenins from the marine red alga Laurencia decumbens

被引:49
作者
Ji, Nai-Yun
Li, Xiao-Ming
Li, Ke
Wang, Bin-Gui [1 ]
机构
[1] Chinese Acad Sci, Inst Oceanog, Key Lab Expt Marine Biol, Qingdao 266071, Peoples R China
[2] Chinese Acad Sci, Grad Sch, Beijing 100049, Peoples R China
来源
JOURNAL OF NATURAL PRODUCTS | 2007年 / 70卷 / 09期
关键词
D O I
10.1021/np0701172
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Four new halogenated nonterpenoid C-15-acetogenins, 4:7,6:13-bisepoxy-9,10-diol-1,12-dibromopentadeca-1,2-diene (1, laurendecumallene A), 4:7,6:12-bisepoxy-9,10-diol-1,13-dibromopentadeca-1,2-diene (2, laurendecumallene 13), (3Z)-6:10,7:13-bisepoxy-12-bromo-9-hydroperoxylpentadeca-3-en-1-yne (3, laurendecumenyne A), and (3Z)-6:10,9:13-bisepoxy-12-bromo-7-chloropentadeca-3-en-1-yne (4, laurendecumenyne 13), together with one known halogenated C-15-acetogenin elatenyne (5) were isolated and identified from the organic extract of the marine red alga Laurencia decumbens. Their structures and relative stereochemistry were established by means of spectroscopic analysis including UV, IR, high-resolution electrospray ionization mass spectrometry (HRESIMS), and ID and 2D NMR techniques. All these metabolites were submitted for the cytotoxic assay against tumor cell line A549 (human lung adenocarcinoma), but all of them were found inactive (IC50 > 10 mu g/mL).
引用
收藏
页码:1499 / 1502
页数:4
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