作用于RNA靶点的治疗剂

J. P. Rife
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引用次数: 0

摘要

有许多靶向RNA的治疗药物,如链霉素、庆大霉素和四环素;其中一些已经存在了很多年。它们都与核糖体RNA结合并改变正常核糖体的功能。现代药物发现和设计的策略几乎完全与蛋白质靶点有关。然而,针对RNA靶点的药物发现领域正在迅速成熟,这主要是由于最近已经解决了令人兴奋的核糖体/药物复合物。潜在的RNA药物靶点在细菌、病毒和细胞系统中比比皆是。然而,是否可以找到同时满足RNA结合和药理学特性(如吸收和膜渗透)的化合物仍然存在问题。观察到的相互作用范围,从库仑到疏水,以及预测的几种核糖体结合抗生素的“药物样”特性,表明靶向RNA的药物的发现可能是一种普遍现象。关键词:氨基糖甙类;抗生素;药物发现;红霉素;oxazolidinones;核糖体;四环素
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Therapeutic Agents Acting on RNA Targets
There are many therapeutics that target RNA, such as streptomycin, gentamicin, and tetracycline; some of them have been in existence for many years. All of them bind to ribosomal RNA and alter normal ribosome function. The modern strategies of drug discovery and design pertain nearly exclusively to protein targets. However, the field of drug discovery for RNA targets is maturing rapidly, largely due to the exciting ribosome/drug complexes that have recently been solved. Potential RNA drug targets abound for bacterial, viral, and cellular systems. Nevertheless, questions remain as to whether or not compounds can be found that simultaneously satisfy RNA binding and pharmacological properties, such as absorption and membrane permeation. The range of interactions observed, from Coulombic to hydrophobic, and the predicted “drug-like” qualities of several ribosome binding antibiotics, suggest that the discovery of drugs that target RNA can be a general phenomenon. Keywords: aminoglycosides; antibiotics; drug discovery; erythromycin; oxazolidinones; ribosome; tetracyclines
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