Universite Paris Descartes, UMR 8601 CNRS, Laboratoire de Chimie et Biochimie Pharmacologiques et Toxicologiques, 45 rue des Saints Peres 75006 Paris, France.
Team Chemistry and Biology, Modeling & Immunology for Therapy, CBMIT, 2MI Platform, Paris, France.
Curr Med Chem. 2018;25(42):6013-6029. doi: 10.2174/0929867325666180330095154.
The bacterial resistance to antibiotics constitutes more than ever a severe public health problem. The enzymes involved in bacterial peptidoglycan biosynthesis are pertinent targets for developing new antibiotics, notably the MraY transferase that is not targeted by any marketed drug. Many research groups are currently working on the study or the inhibition of this enzyme. After a concise overview of the role, mechanism and inhibition of MraY, the structure-activity relationships of 5'-triazole-containing aminoribosyluridine inhibitors, we previously synthetized, will be presented. The recently published MraY X-ray structures allowed us to achieve a molecular virtual high-throughput screening of commercial databases and our in-house library resulting in the identification of promising compounds for the further development of new antibiotics.
细菌对抗生素的耐药性比以往任何时候都更成为严重的公共卫生问题。参与细菌肽聚糖生物合成的酶是开发新抗生素的重要靶点,特别是 MraY 转移酶,目前还没有任何市售药物针对该酶。目前,许多研究小组正在研究或抑制这种酶。在简要概述 MraY 的作用、机制和抑制作用之后,将介绍我们之前合成的含有 5'-三唑的氨基核糖核苷抑制剂的结构-活性关系。最近发表的 MraY X 射线结构使我们能够对商业数据库和我们的内部文库进行分子虚拟高通量筛选,从而鉴定出有希望的化合物,用于进一步开发新的抗生素。