撤回:用天然产物靶向分枝杆菌酶。

Chemistry & biology Pub Date : 2015-10-22 Epub Date: 2015-10-01 DOI:10.1016/j.chembiol.2015.08.012
Elwira Sieniawska
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引用次数: 9

摘要

结核病(TB)是对当代文明的经常性威胁。它不仅影响发展中国家,而且还再次出现在曾经被认为已被根除的地方。在撰写本文时,艾滋病毒感染者的结核病合并感染是最常见的死亡原因。在寻找新的抗真菌药物先导物方面,天然化合物仍是一个有希望的来源。本综述旨在收集有关天然产物(植物、真菌、细菌和海洋海绵的代谢物)对分枝杆菌酶具有活性的信息。在这里,天然代谢物被认为是分枝杆菌酶在体外(ClpC1, ClpP, MurE连接酶,真菌硫醇s偶联氨基酶,β-酮酰基- acp合成酶,InhA)和体内的抑制剂/激活剂,涉及到宿主细胞(PtpB)。每一种酶都被简要地描述,以产生其在分枝杆菌生长中的作用的理解,并产生对所研究的天然化合物的作用机制的认识。此外,在引入酶后,它的抑制剂被列出并准确表征。
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RETRACTED: Targeting Mycobacterial Enzymes with Natural Products.

Tuberculosis (TB) is a recurring threat to contemporary civilization. It affects not only those within developing countries, but has also appeared again in places where it was once considered eradicated. TB co-infection in patients infected by HIV is, at the time of writing, the most common cause of death. In the field of searching for new antimycobacterial drug leads, compounds of natural origin still remain a promising source. The review is intended to gather information about natural products (metabolites of plants, fungi, bacteria, and marine sponges) that show activity against mycobacterial enzymes. Here, natural metabolites are presented as being inhibitors/activators of the mycobacterial enzymes involved in mycobacterial growth in vitro (ClpC1, ClpP, MurE ligase, mycothiol S-conjugate amidase, β-ketoacyl-ACP synthase, InhA) and in vivo, as regards the host cell (PtpB). Each enzyme is briefly described so as to generate an understanding of its role in mycobacterial growth and engender a perception of the mechanism of action of the studied natural compounds. Furthermore, after the introduction of the enzyme, its inhibitors are listed and exactly characterized.

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来源期刊
Chemistry & biology
Chemistry & biology 生物-生化与分子生物学
自引率
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0
审稿时长
4-8 weeks
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