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抗生素的重新编程以对抗抗微生物药物耐药性。

Reprogramming of antibiotics to combat antimicrobial resistance.

机构信息

Bioprocess Engineering Laboratory, Department of Biotechnology, Central University of Haryana, Mahendergarh, Haryana, India.

School of Biotechnology, Jawaharlal Nehru University, New Delhi, India.

出版信息

Arch Pharm (Weinheim). 2020 Nov;353(11):e2000168. doi: 10.1002/ardp.202000168. Epub 2020 Aug 10.

Abstract

This review outlines a literature-based approach with illustrative examples of drug repurposing (one molecule, multiple targets), which will be useful in tackling the problem of antimicrobial resistance (AMR). Globally, the demands for new drugs have increased due to multidrug-resistant pathogens and emerging viruses. Keeping these facts in view, drug repurposing started for utilization of a drug in a different way from a preexisting drug, which reduces the time and cost of development of a new drug. Repurposing increases the potency of a drug and reduces its toxicity level, as it is required in lower amounts, supporting the utilization of the drug as a new therapeutic option. This will be further explored to highlight the application in AMR.

摘要

本文概述了一种基于文献的方法,并通过药物重定位(一种分子,多个靶点)的实例进行说明,这对于解决抗菌药物耐药性(AMR)问题将非常有用。在全球范围内,由于多药耐药病原体和新出现的病毒,对抗菌药物的需求不断增加。鉴于这些事实,药物重定位开始用于以不同于现有药物的方式利用药物,从而缩短了新药开发的时间和成本。药物重定位提高了药物的效力,降低了其毒性水平,因为所需的药物剂量较低,支持将药物作为新的治疗选择进行利用。本文将进一步探讨其在 AMR 中的应用。

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