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为结核病药物研发注入新动力:新型抗分枝杆菌靶点和药物。

Priming the tuberculosis drug pipeline: new antimycobacterial targets and agents.

机构信息

SAMRC/NHLS/UCT Molecular Mycobacteriology Research Unit, DST/NRF Centre of Excellence for Biomedical TB Research & Wellcome Centre for Infectious Diseases Research in Africa, Institute of Infectious Disease and Molecular Medicine and Department of Pathology, Faculty of Health Sciences, University of Cape Town, Observatory 7925, South Africa.

SAMRC/NHLS/UCT Molecular Mycobacteriology Research Unit, DST/NRF Centre of Excellence for Biomedical TB Research & Wellcome Centre for Infectious Diseases Research in Africa, Institute of Infectious Disease and Molecular Medicine and Department of Pathology, Faculty of Health Sciences, University of Cape Town, Observatory 7925, South Africa.

出版信息

Curr Opin Microbiol. 2018 Oct;45:39-46. doi: 10.1016/j.mib.2018.02.006. Epub 2018 Feb 23.

Abstract

Claiming close to two million lives each year, tuberculosis is now the leading cause of death from an infectious disease. The rise in number of Mycobacterium tuberculosis (Mtb) strains resistant to existing TB drugs has underscored the urgent need to develop new antimycobacterials with novel mechanisms of action. To meet this need, a drug pipeline has been established that is populated with new and repurposed drugs. Recent advances in identifying molecules with inhibitory activity against Mtb under conditions modelled on those encountered during infection, and in elucidating their mechanisms of action, have primed the pipeline with promising drug/target couples, hit compounds and new targets. In this review, we highlight recent advances and emerging areas of opportunity in this field.

摘要

每年导致近 200 万人死亡,结核病现在是传染病导致死亡的主要原因。耐现有结核病药物的结核分枝杆菌(Mtb)菌株数量的增加,突显了迫切需要开发具有新型作用机制的新抗分枝杆菌药物。为了满足这一需求,已经建立了一个药物管道,其中包含新的和重新定位的药物。最近在鉴定在感染过程中遇到的条件下对 Mtb 具有抑制活性的分子方面取得了进展,并阐明了它们的作用机制,为有前途的药物/靶标对、命中化合物和新靶标充实了药物管道。在这篇综述中,我们强调了该领域的最新进展和新的机会领域。

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