Facultad de Ciencias Quimicas, Benemerita Universidad Autonoma de Puebla, Pue, 72570, Mexico.
Mini Rev Med Chem. 2020;20(7):584-600. doi: 10.2174/1389557519666191205124050.
The resistance among various microbial species (infectious agents) to different antimicrobial drugs has emerged as a cause of serious public health problem all over the world. In this sense, natural products have been a rich source of compounds for drug discovery with antibiotic activity. Macrolactins are amazing structures which have antibiotic activity against some clinically relevant pathogens. In addition, they have anti-inflammatory, antifungal, antimicrobial, and antitumor activities. They are macrolides containing 24-membered lactone ring with some differences in their chemical structures. The synthesis of these compounds is a difficult task which has attracted attention of researchers; however few syntheses have been reported. In this review, the isolation of all reported macrolactins, their syntheses and biological activities are revisited.
各种微生物物种(感染因子)对不同抗菌药物的耐药性已成为全世界严重的公共卫生问题。从这个意义上说,天然产物是具有抗生素活性的化合物的重要来源。大环内酯类化合物是具有抗生素活性的神奇结构,可以对抗一些临床相关的病原体。此外,它们还具有抗炎、抗真菌、抗菌和抗肿瘤活性。它们是含有 24 元内酯环的大环内酯类化合物,其化学结构存在一些差异。这些化合物的合成是一项艰巨的任务,引起了研究人员的关注;然而,报道的合成方法却很少。在这篇综述中,重新考察了所有报道的大环内酯类化合物的分离、合成和生物活性。