Gould Eoin R, King Elizabeth F B, Menzies Stefanie K, Fraser Andrew L, Tulloch Lindsay B, Zacharova Marija K, Smith Terry K, Florence Gordon J
EaStChem School of Chemistry, Biomedical Science Research Complex, University of St Andrews, North Haugh, St Andrews, Fife KY16 9ST, UK.
EaStChem School of Chemistry, Biomedical Science Research Complex, University of St Andrews, North Haugh, St Andrews, Fife KY16 9ST, UK.
Bioorg Med Chem. 2017 Nov 15;25(22):6126-6136. doi: 10.1016/j.bmc.2017.01.021. Epub 2017 Jan 28.
The need for new treatments for the neglected tropical diseases African sleeping sickness, Chagas disease and Leishmaniasis remains urgent with the diseases widespread in tropical regions, affecting the world's very poorest. We have previously reported bis-tetrahydropyran 1,4-triazole analogues designed as mimics of the annonaceous acetogenin natural product chamuvarinin, which maintained trypanocidal activity. Building upon these studies, we here report related triazole compounds with pendant heterocycles, mimicking the original butenolide of the natural product. Analogues were active against T. brucei, with a nitrofuran compound displaying nanomolar trypanocidal activity. Several analogues also showed strong activity against T. cruzi and L. major. Importantly, select compounds gave excellent selectivity over mammalian cells with a furan-based analogue highly selective while remaining active against all three cell lines, thus representing a potential lead for a new broad spectrum kinetoplastid inhibitor.
对于非洲昏睡病、恰加斯病和利什曼病等被忽视的热带疾病,新治疗方法的需求仍然迫切,这些疾病在热带地区广泛传播,影响着世界上最贫困的人群。我们之前报道过设计为番荔枝内酯天然产物查木瓦林宁类似物的双四氢吡喃1,4 - 三唑类似物,其保持了杀锥虫活性。基于这些研究,我们在此报告具有侧链杂环的相关三唑化合物,模拟天然产物的原始丁烯内酯。类似物对布氏锥虫有活性,一种硝基呋喃化合物显示出纳摩尔级的杀锥虫活性。几种类似物对克氏锥虫和硕大利什曼原虫也表现出很强的活性。重要的是,特定化合物对哺乳动物细胞具有优异的选择性,一种基于呋喃的类似物具有高度选择性,同时对所有三种细胞系仍有活性,因此代表了一种新型广谱动基体抑制剂的潜在先导物。