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唑烷酮类药物的并排分析,以估计针对分枝杆菌感染的治疗窗。

Side-by-Side Profiling of Oxazolidinones to Estimate the Therapeutic Window against Mycobacterial Infections.

机构信息

Center for Discovery and Innovation, Hackensack Meridian Health, Nutley, New Jersey, USA.

Center for Innovative Drug Development and Therapeutic Trials for Africa (CDT-Africa), Addis Ababa University, Addis Ababa, Ethiopia.

出版信息

Antimicrob Agents Chemother. 2023 Apr 18;67(4):e0165522. doi: 10.1128/aac.01655-22. Epub 2023 Mar 15.

Abstract

New oxazolidinones are in clinical development for the treatment of tuberculosis and nontuberculous mycobacterial (NTM) infections, as a replacement for linezolid and tedizolid, which cause mitochondrial toxicity after prolonged treatment. Here, we carried out side-by-side measurements of mitochondrial protein synthesis inhibition and activity against clinically relevant mycobacterial pathogens of approved and novel oxazolidinones. We found a large range of selectivity indices suggesting TBI-223 and sutezolid as promising candidates against tuberculosis and NTM lung disease caused by Mycobacterium kansasii.

摘要

新型恶唑烷酮类药物正处于结核病和非结核分枝杆菌(NTM)感染的临床开发阶段,用以替代利奈唑胺和替加环素,后者长期治疗后会引起线粒体毒性。在此,我们对已批准和新型恶唑烷酮类药物的线粒体蛋白合成抑制和针对临床相关分枝杆菌病原体的活性进行了平行测量。我们发现了一系列广泛的选择性指数,提示 TBI-223 和 sutezolid 有望成为治疗由堪萨斯分枝杆菌引起的结核病和 NTM 肺病的候选药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1db9/10112060/3da8d7c04468/aac.01655-22-f001.jpg

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