Green David W
Cubist Pharmaceuticals, Inc., 65 Hayden Ave., Lexington, MA 02421, USA.
Expert Opin Ther Targets. 2002 Feb;6(1):1-19. doi: 10.1517/14728222.6.1.1.
This review focuses on target-based approaches for developing new chemical classes of antibacterial agents aimed at the bacterial cell wall. The clinical success of antibiotics such as beta-lactams and glycopeptides validates this chemotherapeutic strategy and emerging resistance to these agents warrants the development of new antibacterial drugs. Understanding the mechanism of action and resistance to beta-lactams and glycopeptides at a molecular level has supported the development of new agents that prevent transpeptidation and transglycosylation reactions of peptidoglycan polymerisation. The enzymes involved in the synthesis of the peptidoglycan structural unit have also been targeted for antibacterial discovery. The influence of bacterial genetics and genomics, structural biology, assay development and the properties of known inhibitors on these approaches will be discussed in the context of drug discovery.
本综述聚焦于开发针对细菌细胞壁的新型抗菌化学类别基于靶点的方法。β-内酰胺类和糖肽类等抗生素的临床成功证实了这种化疗策略,而这些药物出现的耐药性促使人们研发新型抗菌药物。在分子水平上理解β-内酰胺类和糖肽类的作用机制及耐药性,为开发阻止肽聚糖聚合的转肽化和转糖基化反应的新型药物提供了支持。参与肽聚糖结构单元合成的酶也已成为抗菌药物发现的靶点。细菌遗传学和基因组学、结构生物学、检测方法开发以及已知抑制剂的特性对这些方法的影响将在药物发现的背景下进行讨论。