Zanamivir-Amantadine Conjugate: A Dual-Action Agent with Broad-Spectrum Synergistic Antiviral Efficacy

Influenza A virus is a highly contagious respiratory pathogen, and its rapid and continuous adaptive mutations for immune escape have limited the efficacy of existing vaccines and antiviral drugs. Here, we report a multimechanism anti-influenza platform based on the conjugation of zanamivir (ZMV) with amantadine (Aman). Aman acts as a hydrophobic tag that promotes the degradation of neuraminidase and concurrently enhances the physicochemical properties of ZMV, leading to improved membrane permeability and a significantly prolonged half-life. Meanwhile, the ZMV moiety counteracts Aman-induced cytotoxic autophagy. The resulting conjugate, compound <b>7j</b>, exhibits potent activity against a wide range of neuraminidase and M2 ion channel mutations. Notably, a single intravenous dose of <b>7j</b> fully protected mice from a lethal H1N1 challenge. Our work demonstrates that the rational fusion of ZMV and Aman achieves synergistic multimechanistic antiviral activity with enhanced efficacy and safety, offering a new strategy for the development of next-generation anti-influenza drugs.

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Publication Details

Journal
Journal of Medicinal Chemistry
Published
2026-02-26
DOI
https://doi.org/10.1021/acs.jmedchem.5c03547
Primary Topic
Influenza Virus Research Studies
Type
article
Field-Weighted Citation Impact
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article

Zanamivir-Amantadine Conjugate: A Dual-Action Agent with Broad-Spectrum Synergistic Antiviral Efficacy

Liwen Hua, Mengyang Wang, Yao Zhong, Ruiwen Liu et al.
Journal of Medicinal Chemistry
Influenza Virus Research Studies
article

Zanamivir-Amantadine Conjugate: A Dual-Action Agent with Broad-Spectrum Synergistic Antiviral Efficacy

Liwen Hua, Mengyang Wang, Yao Zhong, Ruiwen Liu, S. Y. Xiao, Demin Zhou, Y. Zhang, P Zhao, Honggao Duan, Rui Feng, Yiming Wang, Tao Yuan, Xingxing Zhu
article en

Abstract

Influenza A virus is a highly contagious respiratory pathogen, and its rapid and continuous adaptive mutations for immune escape have limited the efficacy of existing vaccines and antiviral drugs. Here, we report a multimechanism anti-influenza platform based on the conjugation of zanamivir (ZMV) with amantadine (Aman). Aman acts as a hydrophobic tag that promotes the degradation of neuraminidase and concurrently enhances the physicochemical properties of ZMV, leading to improved membrane permeability and a significantly prolonged half-life. Meanwhile, the ZMV moiety counteracts Aman-induced cytotoxic autophagy. The resulting conjugate, compound <b>7j</b>, exhibits potent activity against a wide range of neuraminidase and M2 ion channel mutations. Notably, a single intravenous dose of <b>7j</b> fully protected mice from a lethal H1N1 challenge. Our work demonstrates that the rational fusion of ZMV and Aman achieves synergistic multimechanistic antiviral activity with enhanced efficacy and safety, offering a new strategy for the development of next-generation anti-influenza drugs.

Journal of Medicinal ChemistryVol. 69(5)
Centre National de la Recherche Scientifique (FR), Ministry of Education of the People's Republic of China (CN), Beijing University of Posts and Telecommunications (CN), Southwest University (CN), Hainan Normal University (CN), Peking University (CN), Sorbonne Université (FR), Peking University International Hospital (CN), Institut Parisien de Chimie Moléculaire (FR)
Good health and well-being
Openalex Percentile: Top 43%
Influenza Virus Research Studies
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