Bolognesi Maria Laura, Lizzi Federica, Perozzo Remo, Brun Reto, Cavalli Andrea
Department of Pharmaceutical Sciences, Alma Mater Studiorum, Bologna University, Via Belmeloro 6, I-40126 Bologna, Italy.
Bioorg Med Chem Lett. 2008 Apr 1;18(7):2272-6. doi: 10.1016/j.bmcl.2008.03.009. Epub 2008 Mar 7.
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 (IC(50)=50nM, IC(50)=0.28microM, and IC(50)=1.26microM, respectively).
利用显示抗锥虫活性的天然产物的结构特征,我们设计并合成了一个由2-苯氧基-1,4-萘醌和2-苯氧基-1,4-蒽醌衍生物组成的小型文库。该文库采用平行方法并使用易于获得的合成子获得。所有衍生物对锥虫或利什曼原虫物种均表现出抑制活性,其中8、10和16是对罗德西亚布氏锥虫、杜氏利什曼原虫和克氏锥虫细胞活性最高的化合物(IC(50)分别为50 nM、0.28 μM和1.26 μM)。