Department of Medicinal Chemistry, School of Pharmaceutical Sciences, Shandong University, Jinan 250012, P.R. China.
Mini Rev Med Chem. 2011 Oct;11(12):1009-18. doi: 10.2174/138955711797247734.
The continuing emergence of bacterial resistance has provided an incentive for recent intensified research on macrolide antibiotics. Belonging to the macrolide family, 16-membered macrolides also experience a renewed interest in further exploration. The medicinal potential of 16-membered macrolides in search for new antibacterials stems from some advantages over 14-membered macrolides, such as gastrointestinal tolerability, structural flexibility, and lack of inducible resistance. Thus, compared with abundant articles on various 14-membered macrolide derivatives in the literature, this review will highlight some representative 16-membered macrolide antibiotics and their recently discovered analogs. Furthermore, the action and resistance mechanisms of 16-membered macrolide antibiotics will be elucidated as well to assist the drug design.
细菌耐药性的不断出现为近年来对大环内酯类抗生素的深入研究提供了动力。属于大环内酯类的 16 元大环内酯类也引起了进一步探索的兴趣。16 元大环内酯类在寻找新的抗菌药物方面的药用潜力源于其相对于 14 元大环内酯类的一些优势,如胃肠道耐受性、结构灵活性和缺乏诱导耐药性。因此,与文献中大量关于各种 14 元大环内酯类衍生物的文章相比,本综述将重点介绍一些代表性的 16 元大环内酯类抗生素及其最近发现的类似物。此外,还将阐明 16 元大环内酯类抗生素的作用和耐药机制,以协助药物设计。