WuXi AppTec Co., Ltd., Shanghai 200131, China.
Pharmaceutical Research Institute, Cisen Pharmaceutical Co., Ltd., Jining 272000, China.
J Med Chem. 2024 Feb 22;67(4):2570-2583. doi: 10.1021/acs.jmedchem.3c01715. Epub 2024 Feb 1.
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.
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。