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TNP-2198 的设计、合成与表征:一种具有潜在活性的靶向利福霉素-硝基咪唑双药物偶联物,针对微需氧和厌氧细菌病原体。

Design, Synthesis, and Characterization of TNP-2198, a Dual-Targeted Rifamycin-Nitroimidazole Conjugate with Potent Activity against Microaerophilic and Anaerobic Bacterial Pathogens.

机构信息

TenNor Therapeutics Ltd, 218 Xinghu Street, Suzhou Industrial Park, Suzhou 215123, China.

Waksman Institute and Department of Chemistry and Chemical Biology, Rutgers University, Piscataway, New Jersey 08854, United States.

出版信息

J Med Chem. 2022 Mar 24;65(6):4481-4495. doi: 10.1021/acs.jmedchem.1c02045. Epub 2022 Feb 17.

Abstract

TNP-2198, a stable conjugate of a rifamycin pharmacophore and a nitroimidazole pharmacophore, has been designed, synthesized, and evaluated as a novel dual-targeted antibacterial agent for the treatment of microaerophilic and anaerobic bacterial infections. TNP-2198 exhibits greater activity than a 1:1 molar mixture of the parent drugs and exhibits activity against strains resistant to both rifamycins and nitroimidazoles. A crystal structure of TNP-2198 bound to a RNA polymerase transcription initiation complex reveals that the rifamycin portion of TNP-2198 binds to the rifamycin binding site on RNAP and the nitroimidazole portion of TNP-2198 interacts directly with the DNA template-strand in the RNAP active-center cleft, forming a hydrogen bond with a base of the DNA template strand. TNP-2198 is currently in Phase 2 clinical development for the treatment of infection, infection, and bacterial vaginosis.

摘要

TNP-2198 是利福霉素药效团和硝基咪唑药效团的稳定缀合物,被设计、合成并评估为用于治疗微需氧和厌氧细菌感染的新型双重靶向抗菌剂。TNP-2198 的活性大于母体药物 1:1 摩尔混合物的活性,并且对既抗利福霉素又抗硝基咪唑的菌株具有活性。TNP-2198 与 RNA 聚合酶转录起始复合物的晶体结构表明,TNP-2198 的利福霉素部分与 RNAP 上的利福霉素结合位点结合,而 TNP-2198 的硝基咪唑部分与 RNAP 活性中心裂缝中的 DNA 模板链直接相互作用,与 DNA 模板链的碱基形成氢键。TNP-2198 目前处于治疗 感染、 感染和细菌性阴道病的 2 期临床开发阶段。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c6f/8958509/d6e79f4193c9/jm1c02045_0001.jpg

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