重新审视二肽基羧肽酶抑制剂卡托普利作为泛抗锥虫药物的来源。

IF 2.5 4区 医学 Q3 CHEMISTRY, MEDICINAL Bioorganic & Medicinal Chemistry Letters Pub Date : 2024-07-14 DOI:10.1016/j.bmcl.2024.129883
Jean-Baptiste Garsi , Sofiane Hocine , Raphaël Hensienne , Matthieu Moitessier , Helen Denton , Louise L. Major , Terry K. Smith , Stephen Hanessian
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引用次数: 0

摘要

原生动物寄生虫布氏锥虫、克氏锥虫和利什曼原虫分别是非洲昏睡病、南美锥虫病和利什曼病等被忽视的热带疾病持续传播的罪魁祸首。有报告称卡托普利能抑制利什曼原虫二肽基羧肽酶,随后合成了一系列简单的脯氨酸酰胺和卡托普利类似物,发现它们对布氏锥虫、克鲁兹锥虫和利什曼原虫具有 1-2 μM 的体外抑制和选择性。可以说,合成的脯氨酸酰胺是体外泛抗原虫化合物中结构最简单的例子。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Revisiting the dipeptidyl carboxypeptidase inhibitor captopril as a source of pan anti-trypanosomatid agents

The protozoan parasites Trypanosoma brucei, Trypanosoma cruzi and Leishmania spp. are responsible for continued propagation of neglected tropical diseases such as African sleeping sickness, Chagas disease and leishmaniasis respectively. Following a report that captopril targets Leishmania donovani dipeptidyl carboxypeptidase, a series of simple proline amides and captopril analogues were synthesized and found to exhibit 1–2 μM in vitro inhibition and selectivity against Trypanosoma brucei, Trypanosoma cruzi and Leishmania spp. The results were corroborated with computational docking studies. Arguably, the synthetic proline amides represent the structurally simplest examples of in vitro pan antiprotozoal compounds.

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来源期刊
CiteScore
5.70
自引率
3.70%
发文量
463
审稿时长
27 days
期刊介绍: Bioorganic & Medicinal Chemistry Letters presents preliminary experimental or theoretical research results of outstanding significance and timeliness on all aspects of science at the interface of chemistry and biology and on major advances in drug design and development. The journal publishes articles in the form of communications reporting experimental or theoretical results of special interest, and strives to provide maximum dissemination to a large, international audience.
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