Suppr超能文献

具有抗锥虫和抗利什曼原虫活性的2-苯氧基-1,4-萘醌和2-苯氧基-1,4-蒽醌衍生物的小型文库的合成。

Synthesis of a small library of 2-phenoxy-1,4-naphthoquinone and 2-phenoxy-1,4-anthraquinone derivatives bearing anti-trypanosomal and anti-leishmanial activity.

作者信息

Bolognesi Maria Laura, Lizzi Federica, Perozzo Remo, Brun Reto, Cavalli Andrea

机构信息

Department of Pharmaceutical Sciences, Alma Mater Studiorum, Bologna University, Via Belmeloro 6, I-40126 Bologna, Italy.

出版信息

Bioorg Med Chem Lett. 2008 Apr 1;18(7):2272-6. doi: 10.1016/j.bmcl.2008.03.009. Epub 2008 Mar 7.

Abstract

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).

摘要

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)。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验