化学
扎那米韦
神经氨酸酶
金刚烷胺
神经氨酸酶抑制剂
病毒
药理学
部分
脂质双层融合
结构-活动关系
细胞毒性
细胞毒性T细胞
合理设计
甲型流感病毒
免疫系统
膜透性
药品
病毒学
生物活性
毒性
铅化合物
病毒进入
奥司他韦
呼吸系统
抗病毒药物
作者
Yiming Wang,Liwen Hua,Honggao Duan,Ruiwen Liu,Mengyang Wang,P Zhao,Tao Yuan,Yiping Zhong,Rui Feng,Xingxing Zhu,Y. Zhang,Demin Zhou,S. Y. Xiao
标识
DOI:10.1021/acs.jmedchem.5c03547
摘要
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 7j, exhibits potent activity against a wide range of neuraminidase and M2 ion channel mutations. Notably, a single intravenous dose of 7j 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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