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Oxazolidinone compounds and methods of use thereof as antibacterial agents

机译:恶唑烷酮化合物及其使用方法作为抗菌剂

摘要

The present invention relates to oxazolidinone compounds of Formula (I):; embedded image and pharmaceutically acceptable salts thereof, wherein A, E, and R1 are as defined herein. The present invention also relates to compositions which comprise at least one oxazolidinone compound of the invention. The invention also provides methods for inhibiting growth of mycobacterial cells as well as a method of treating mycobacterial infections by Mycobacterium tuberculosis comprising administering a therapeutically effective amount of an oxazolidinone of the invention and/or a pharmaceutically acceptable salt thereof, or a composition comprising such compound and/or salt.
机译:本发明涉及式(I)的恶唑烷酮化合物: <化学ID =“Chem-US-00001”> “嵌入式图像”文件=“US10947205-20210316-C00001.gif”他=“24.89mm”imgContent 和药学上可接受的盐,其中a,e和r 1 如本文所定义。本发明还涉及包含至少一种本发明恶唑烷酮化合物的组合物。本发明还提供了抑制分枝杆菌细胞生长的方法以及通过结核分枝杆菌治疗分枝杆菌感染的方法,包括给予治疗有效量的本发明的恶唑烷酮和/或其药学上可接受的盐或包含这种化合物和/或盐的组合物。

著录项

  • 公开/公告号US10947205B2

    专利类型

  • 公开/公告日2021-03-16

    原文格式PDF

  • 申请/专利权人 MERCK SHARP & DOHME CORP.;

    申请/专利号US201916397172

  • 申请日2019-04-29

  • 分类号A61K31/422;A61K31/541;C07D401/14;C07D413/14;C07D417/14;C07D417/10;C07D413/10;C07D471/04;C07D487/04;C07D263/20;A61K31/421;A61K45/06;A61K31/427;A61K31/4439;C07D413/06;A61K31/437;A61K31/4985;A61K31/506;A61K31/5377;A61K31/553;C07D413/04;

  • 国家 US

  • 入库时间 2022-08-24 17:43:20

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