Febrifugine analogue compounds: synthesis and antimalarial evaluation.
Febrifugine analogue compounds: synthesis and antimalarial evaluation.
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DOI：
10.1016/j.bmc.2011.11.053
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发表时间：
2012-01-15
影响因子：
3.5
通讯作者：
Chatterji, Dipsanker
中科院分区：
文献类型：
--
作者：
Zhu, Shuren;Chandrashekar, Gudise;Meng, Li;Robinson, Katie;Chatterji, Dipsanker
Febrifugine is an alkaloid isolated from Dichroa febrifuga Lour as the active component against Plasmodium falciparum, but exhibits toxic side effects. In this study novel febrifugine analogues were designed and efficiently synthesized. New compounds underwent efficacy and toxicity evaluation. Some compounds are much less toxic than the natural product febrifugine and existing antimalarial drugs and are expected to possess wide therapeutic windows. In Aotus monkeys infected with the chloroquine resistant FVO strain of P. falciparum, one interesting compound possesses a 50% curative dose of 2mg/kg/day and a 100% curative dose of 8mg/kg/day. These compounds, as well as the underlying design rationale, may find usefulness in the discovery and development of new antimalarial drugs.
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影响因子：
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通讯作者：
ROSSAN, R
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