杜氏利什曼原虫
化学
萘醌
克鲁兹锥虫
布氏锥虫
合成子
蒽醌
罗得西亚布氏锥虫
锥虫
IC50型
利什曼原虫
杀虫药
立体化学
1,4-萘醌
醌
天然产物
体外
生物化学
有机化学
生物
病毒学
寄生虫寄主
万维网
计算机科学
基因
作者
María Laura Bolognesi,Federica Lizzi,Remo Perozzo,Reto Brun,Andrea Cavalli
标识
DOI:10.1016/j.bmcl.2008.03.009
摘要
Taking advantage of the structural features of natural products showing anti-trypanosomatid activity, we designed and synthesized a small library of 2-phenoxy-1,4-naphthoquinone and 2-phenoxy-1,4-anthraquinone derivatives. The library was obtained following a parallel approach and using readily available synthons. All the derivatives showed inhibitory activity toward either Trypanosoma or Leishmania species, with 8, 10, and 16 being the most active compounds against Trypanosoma brucei rhodesiense, Leishmania donovani, and Trypanosoma cruzi cells (IC50 = 50 nM, IC50 = 0.28 μM, and IC50 = 1.26 μM, respectively).
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