恰加斯病
广告
药理学
克鲁兹锥虫
拓扑异构酶
表型筛选
中性粒细胞
化学
免疫学
疾病
杀锥虫剂
医学
锥虫病
鞘脂
寄生虫寄主
作者
Olivier René,Manuel Saldivia,Maxime Dauphinais,Lei Zhang,Scott A. Hollingsworth,Jan Jiříček,Dennis C. Koester,Sarah L. Miller,Sarah Williams,Pearly Shuyi Ng,Debjani Patra,Rajiv S. Jumani,Grace M. Baxley,Colin Osborne,Chen Ying-Bo,Yen‐Liang Chen,Harry Cheung,Suresh B. Lakshminarayana,Jean-René Galarneau,Thierry T. Diagana
标识
DOI:10.1021/acs.jmedchem.5c02459
摘要
Chagas Disease is a neglected tropical disease caused by the parasite Trypanosoma cruzi, affecting millions worldwide. Current treatments suffer from variable efficacy, long duration, and safety concerns, highlighting the need for better therapies. A phenotypic screening of the Novartis compound library against Trypanosoma brucei identified cyanotriazole (CT) compounds with rapid sterilizing activity across kinetoplastids via selective inhibition of parasite topoisomerase II. First-generation CTs had safety liabilities, including lymphopenia and neutrophilia due to sphingolipid pathway modulation. Medicinal chemistry optimization led to a tailored aminopyrrolidine core structure for Chagas Disease, improving ADME properties and reducing off-target effects. IID432 showed potent activity against T. cruzi (EC 50 = 8 nM) and achieved a relapse-free cure in a chronic mouse model of infection with shorter treatment duration. These findings support IID432 as a promising fast-acting, curative therapy for T. cruzi infections.
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