DNA聚合酶抑制剂的最新进展。

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
Poonam Piplani, Ajay Kumar, Akanksha Kulshreshtha, Tamanna Vohra, Vritti Piplani
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引用次数: 0

摘要

当细菌或真菌感染对治疗这些感染的药物方案没有反应时,抗生素或抗微生物耐药性是一个紧迫的全球公共卫生威胁。因此,这些微生物没有被躲避,并继续生长。通过开发一种可以以不同方式发挥作用的药物,可以克服对环丙沙星和Novobicin等天然和已知抗生素的抗生素耐药性。Zodiflodacin和Zenoxacin等药物在针对作用于DNA旋转酶不同位点的DNA旋转酶抑制剂的临床试验中的成功,导致了对该靶点的进一步探索。然而,由于细菌对这些靶标产生了耐药性,因此非常需要设计能够克服这种耐药性并发挥更大功效的制剂。这篇综述提供了最近开发的合成和天然DNA旋转酶抑制剂的信息,以及它们在对抗抗微生物耐药性方面的潜在潜力。该综述还介绍了正在进行临床试验的分子及其现状的信息。它还分析了SAR研究和入伍特工的行动机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Recent Development of DNA Gyrase Inhibitors: An Update.

Antibiotic or antimicrobial resistance is an urgent global public health threat that occurs when bacterial or fungal infections do not respond to the drug regimen designed to treat these infections. As a result, these microbes are not evaded and continue to grow. Antibiotic resistance against natural and already-known antibiotics like Ciprofloxacin and Novobiocin can be overcome by developing an agent that can act in different ways. The success of agents like Zodiflodacin and Zenoxacin in clinical trials against DNA gyrase inhibitors that act on different sites of DNA gyrase has resulted in further exploration of this target. However, due to the emergence of bacterial resistance against these targets, there is a great need to design agents that can overcome this resistance and act with greater efficacy. This review provides information on the synthetic and natural DNA gyrase inhibitors that have been developed recently and their promising potential for combating antimicrobial resistance. The review also presents information on molecules that are in clinical trials and their current status. It also analysed the SAR studies and mechanisms of action of enlisted agents.

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来源期刊
CiteScore
7.20
自引率
4.30%
发文量
567
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