硝唑烷
奥司他韦
病毒学
病毒
抗病毒药物
甲型流感病毒
广谱
大流行
药品
生物
抗药性
正粘病毒科
微生物学
2019年冠状病毒病(COVID-19)
医学
药理学
免疫学
化学
传染病(医学专业)
内科学
疾病
组合化学
作者
Lei Zhao,Yunzheng Yan,Qingsong Dai,Xingzhou Li,Ke Xu,Gang Zou,Keyu Yang,Wei Li,Xiaojia Guo,Jingjing Yang,Yuexiang Li,Qing Xia,Ruiyuan Cao,Wu Zhong
摘要
Seasonal and pandemic influenza causes 650,000 deaths annually in the world. The emergence of drug resistance to specific anti-influenza virus drugs such as oseltamivir and baloxavir marboxil highlights the urgency of novel anti-influenza chemical entity discovery. In this study, we report a series of novel thiazolides derived from an FDA-approved drug, nitazoxanide, with antiviral activity against influenza and a broad range of viruses. The preferred candidates 4a and 4d showed significantly enhanced anti-influenza virus potentials, with 10-fold improvement compared to results with nitazoxanide, and were effective against a variety of influenza virus subtypes including oseltamivir-resistant strains. Notably, the combination using compounds 4a/4d and oseltamivir carboxylate or zanamivir displayed synergistic antiviral effects against oseltamivir-resistant strains. Mode-of-action analysis demonstrated that compounds 4a/4d acted at the late phase of the viral infection cycle through inhibiting viral RNA transcription and replication. Further experiments showed that treatment with compounds 4a/4d significantly inhibited influenza virus infection in human lung organoids, suggesting the druggability of the novel thiazolides. In-depth transcriptome analysis revealed a series of upregulated cellular genes that may contribute to the antiviral activities of 4a/4d. Together, the results of our study indicated the direction to optimize nitazoxanide as an anti-influenza drug and discovered two candidates with novel structures, compounds 4a/4d, that have relatively broad-spectrum antiviral potentials.
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