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发现一种大环流感帽依赖性内切酶抑制剂。

Discovery of a Macrocyclic Influenza Cap-Dependent Endonuclease Inhibitor.

机构信息

WuXi AppTec Co., Ltd., Shanghai 200131, China.

Pharmaceutical Research Institute, Cisen Pharmaceutical Co., Ltd., Jining 272000, China.

出版信息

J Med Chem. 2024 Feb 22;67(4):2570-2583. doi: 10.1021/acs.jmedchem.3c01715. Epub 2024 Feb 1.

Abstract

Influenza viruses (IFVs) have caused several pandemics and have claimed numerous lives since their first record in the early 20th century. While the outbreak of COVID-19 seemed to expel influenza from the sight of people for a short period of time, it is not surprising that it will recirculate around the globe after the coronavirus has mutated into a less fatal variant. Baloxavir marboxil (), the prodrug of baloxavir () and a cap-dependent endonuclease (CEN) inhibitor, were approved by the FDA for the first treatment in almost 20 years. Despite their high antiviral potency, drug-resistant variants have been observed in clinical trials. Herein, we report a novel CEN inhibitor with a delicately designed macrocyclic scaffold that exhibits a significantly smaller shift of inhibitory activity toward baloxavir-resistant variants.

摘要

流感病毒(IFVs)自 20 世纪初首次记录以来,已经引发了多次大流行,并夺走了许多人的生命。虽然 COVID-19 的爆发似乎在短时间内将流感从人们的视线中驱逐出去,但在冠状病毒变异为致命性较弱的变体后,它在全球范围内再次传播也就不足为奇了。巴洛沙韦马波西利(),巴洛沙韦()的前药和帽依赖性内切酶(CEN)抑制剂,是近 20 年来首次获得 FDA 批准的治疗药物。尽管它们具有很高的抗病毒活性,但在临床试验中已经观察到耐药变体。在此,我们报告了一种新型的 CEN 抑制剂,它具有精心设计的大环支架,对巴洛沙韦耐药变体的抑制活性变化很小。

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