Faculty of Pharmacy, University of Ljubljana, Aškerčeva 7, SI-1000 Ljubljana, Slovenia.
Faculty of Pharmacy, University of Ljubljana, Aškerčeva 7, SI-1000 Ljubljana, Slovenia.
Bioorg Med Chem Lett. 2021 May 15;40:127966. doi: 10.1016/j.bmcl.2021.127966. Epub 2021 Mar 17.
Antibiotic resistance represents one of the biggest public health challenges in the last few years. Mur ligases (MurC-MurF) are involved in the synthesis of UDP-N-acetylmuramyl-pentapeptide, the main building block of bacterial peptidoglycan polymer. They are essential for the survival of bacteria and therefore important antibacterial targets. We report herein the synthesis and structure-activity relationships of Mur ligases inhibitors with an azastilbene scaffold. Several compounds showed promising inhibitory potencies against multiple ligases and one compound also possessed moderate antibacterial activity. These results represent a solid ground for further development and optimization of structurally novel antimicrobial agents to combat the rising bacterial resistance.
抗生素耐药性是近年来面临的最大公共卫生挑战之一。Mur 连接酶(MurC-MurF)参与 UDP-N-乙酰胞壁酰五肽的合成,该五肽是细菌肽聚糖聚合物的主要结构单元。Mur 连接酶对于细菌的生存至关重要,因此是重要的抗菌靶点。本研究报告了以氮杂二苯乙烯为骨架的 Mur 连接酶抑制剂的合成和构效关系。几种化合物对多种连接酶表现出有希望的抑制活性,其中一种化合物还具有中等的抗菌活性。这些结果为进一步开发和优化结构新颖的抗菌剂以应对日益严重的细菌耐药性提供了坚实的基础。