Cytotoxic anthraquinone derivatives from Picramnia antidesma

被引:12
作者
Hernández-Medel, MD
Pereda-Miranda, R [1 ]
机构
[1] Univ Nacl Autonoma Mexico, Dept Farm, Fac Quim, Mexico City 04510, DF, Mexico
[2] Univ Veracruzana, Inst Ciencias Basicas, Xalapa 91000, Veracruz, Mexico
关键词
D O I
10.1055/s-2002-32562
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Activity-guided investigation of crude extracts prepared from the root bark of Picramnia antidesma, a medicinal plant long used for the treatment of malaria in tropical areas of the Americas, when tested on KB cells led to the isolation of a new compound, 10-epi-uveoside, from a cytotoxic fraction containing a rich mixture of anthrone glycosides. The antiplasmodial activity proved to be a result of the high levels of cytotoxicity displayed by the anthraquinone derivatives and therefore infusions from this crude drug lack the selectivity index needed to be an effective antimalarial agent.
引用
收藏
页码:556 / 558
页数:3
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