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抗结核双取代环脒衍生物:结构-活性关系和体内研究。

Antitubercular Bis-Substituted Cyclam Derivatives: Structure-Activity Relationships and in Vivo Studies.

机构信息

School of Chemistry , The University of Sydney , Sydney , NSW 2006 , Australia.

Microbial Immunity and Pathogenesis Group, Department of Infectious Diseases and Immunology, Sydney Medical School , The University of Sydney , Sydney , NSW 2006 , Australia.

出版信息

J Med Chem. 2018 Apr 26;61(8):3595-3608. doi: 10.1021/acs.jmedchem.7b01569. Epub 2018 Apr 5.

Abstract

We recently reported the discovery of nontoxic cyclam-derived compounds that are active against drug-resistant Mycobacterium tuberculosis. In this paper we report exploration of the structure-activity relationship for this class of compounds, identifying several simpler compounds with comparable activity. The most promising compound identified, possessing significantly improved water solubility, displayed high levels of bacterial clearance in an in vivo zebrafish embryo model, suggesting this compound series has promise for in vivo treatment of tuberculosis.

摘要

我们最近报道了一种非毒性的环脒衍生化合物的发现,该化合物对耐药性结核分枝杆菌具有活性。在本文中,我们报告了对该类化合物的构效关系的探索,确定了几种具有相当活性的更简单的化合物。所鉴定的最有前途的化合物具有明显提高的水溶性,在体内斑马鱼胚胎模型中显示出高水平的细菌清除率,这表明该化合物系列具有治疗结核病的体内治疗的潜力。

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