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首页> 外文期刊>Journal of Medicinal Chemistry >Two Decades of Successful SAR-Grounded Stories of the Novel Bacterial Topoisomerase Inhibitors (NBTIs)
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Two Decades of Successful SAR-Grounded Stories of the Novel Bacterial Topoisomerase Inhibitors (NBTIs)

机译:新型细菌拓扑异构酶抑制剂(NBTIS)的二十年成功的SAR接地故事

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摘要

The emergence of bacterial resistance against life-saving medicines has forced the scientific community and pharmaceutical industry to take actions in the quest for novel antibacterials. These should not only overcome the existing bacterial resistance but also provide at least interim effective protection against emerging bacterial infections. Research into DNA gyrase and topoisomerase IV inhibitors has become a particular focus, with the description of a new class of bacterial topoisomerase type II inhibitors known as "novel bacterial topoisomerase inhibitors", NBTIs. Elucidation of the key structural modifications incorporated into these inhibitors and the impact these can have on their general physicochemical properties are detailed in this review. This defines novel bacterial topoisomerase inhibitors with promising antibacterial activities and potencies, which thus represent one potential example of the future "drugs for bad bugs", as identified by the World Health Organization.
机译:对救生药物的细菌性抗性的出现已迫使科学界和制药行业采取行动寻求新型抗菌。 这些不仅应克服现有的细菌耐药性,而且还提供至少临时有效保护免受新出现的细菌感染。 DNA乙酶和拓扑异构酶IV抑制剂的研究已成为特定的重点,具有新的细菌拓扑异构酶II型II型抑制剂,称为“新型细菌拓扑酶抑制剂”,NBTIS。 阐明掺入这些抑制剂中的关键结构改性和这些抑制作用的影响在本综述中详述了它们的一般物理化学特性。 这使新的细菌拓扑异构酶抑制剂定义了具有有前途的抗菌活性和职能,因此由世界卫生组织所确定的,因此代表了未来“坏虫药的药物”的潜在例子。

著录项

  • 来源
    《Journal of Medicinal Chemistry》 |2020年第11期|共11页
  • 作者单位

    Univ Ljubljana Chair Pharmaceut Chem Fac Pharm SI-1000 Ljubljana Slovenia;

    Univ Ljubljana Chair Pharmaceut Chem Fac Pharm SI-1000 Ljubljana Slovenia;

    Natl Inst Chem Lab Cheminformat Theory Dept SI-1001 Ljubljana Slovenia;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 药学;
  • 关键词

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