Ancistrobenomine A, the first naphthylisoquinoline oxygenated at Me-3, and related 5,1′-coupled alkaloids, from the "new" plant species Ancistrocladus benomensis

被引:28
作者
Bringmann, G
Dreyer, M
Rischer, H
Wolf, K
Hadi, HA
Brun, R
Meimberg, H
Heubl, G
机构
[1] Univ Wurzburg, Inst Organ Chem, D-97074 Wurzburg, Germany
[2] Univ Malaya, Dept Chem, Kuala Lumpur 59100, Malaysia
[3] Swiss Trop Inst, CH-4002 Basel, Switzerland
[4] Univ Munich, Dept Biol 1, Sect Biodivers Res, D-80638 Munich, Germany
[5] Univ Munich, Dept Biol 1, Sect Systemat Bot, D-80638 Munich, Germany
来源
JOURNAL OF NATURAL PRODUCTS | 2004年 / 67卷 / 12期
关键词
D O I
10.1021/np0497651
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Three new 5,1'-coupled naphthylisoquinoline alkaloids, ancistrobenomine A (1), 6-O-demethylancistrobenomine A (2), and 5-O-demethylancistrocline (3), have been isolated from the stem bark of a botanically as yet undescribed highland liana Ancistrocladus sp., proposed to be named "A. benomensis" according to the region in Peninsular Malaysia where it has been discovered on the mountain of Ginning Benom. Two of the compounds possess an unprecedented structure with a novel hydroxymethylene group at C-3 of the fully dehydrogenated isoquinoline moiety. The structural elucidation was achieved by chemical, spectroscopic, and chiroptical methods. As typical of the so-called Ancistrocladaceae type, all of the compounds isolated bear an oxygen at C-6. Biological activities of these alkaloids against different protozoic pathogens are described.
引用
收藏
页码:2058 / 2062
页数:5
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