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新型基于 3-硝基-1H-1,2,4-三唑的哌嗪和 2-氨基-1,3-苯并噻唑类化合物作为抗恰加斯病药物。

Novel 3-nitro-1H-1,2,4-triazole-based piperazines and 2-amino-1,3-benzothiazoles as antichagasic agents.

机构信息

NorthShore University HealthSystem, Department of Radiation Medicine, 2650 Ridge Ave., Evanston, IL 60201, USA.

出版信息

Bioorg Med Chem. 2013 Nov 1;21(21):6600-7. doi: 10.1016/j.bmc.2013.08.022. Epub 2013 Aug 20.

Abstract

We have previously shown that 3-nitro-1H-1,2,4-triazole-based amines demonstrate significant trypanocidal activity, in particular against Trypanosoma cruzi, the causative parasite of Chagas disease. In the present work we further expanded our research by evaluating in vitro the trypanocidal activity of nitrotriazole-based piperazines and nitrotriazole-based 2-amino-1,3-benzothiazoles to establish additional SARs. All nitrotriazole-based derivatives were active or moderately active against T. cruzi; however two of them did not fulfill the selectivity criteria. Five derivatives were active or moderately active against Trypanosoma brucei rhodesiense while one derivative was moderately active against Leishmania donovani. Active compounds against T. cruzi demonstrated selectivity indexes (toxicity to host cells/toxicity to T. cruzi amastigotes) from 117 to 1725 and 12 of 13 compounds were up to 39-fold more potent than the reference compound benznidazole. Detailed SARs are discussed.

摘要

我们之前已经表明,基于 3-硝基-1H-1,2,4-三唑的胺类化合物具有显著的杀锥虫活性,特别是针对引起恰加斯病的寄生虫克氏锥虫。在本工作中,我们通过评估基于硝三唑的哌嗪和基于硝三唑的 2-氨基-1,3-苯并噻唑的体外杀锥虫活性,进一步扩展了我们的研究,以建立其他 SAR。所有基于硝三唑的衍生物对 T. cruzi 均具有活性或中度活性;然而,其中两种不符合选择性标准。五种衍生物对罗得西亚锥虫具有活性或中度活性,而一种衍生物对利什曼原虫具有中度活性。对 T. cruzi 具有活性的化合物的选择性指数(对宿主细胞的毒性/对 T. cruzi 无鞭毛体的毒性)为 117 至 1725,其中 13 种化合物中有 12 种比参考化合物苯并硝唑的效力高 39 倍。详细的 SAR 讨论。

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