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发现用于治疗手足口病的强效肠道病毒71型衣壳抑制剂。

Discovery of Potent EV71 Capsid Inhibitors for Treatment of HFMD.

作者信息

Li Peng, Yu Jun, Hao Fei, He Haiying, Shi Xuyang, Hu Jiao, Wang Li, Du Chunyan, Zhang Xiao, Sun Ya, Lin Fusen, Gu Zhengxian, Xu Deming, Chen Xinsheng, Shen Liang, Hu Guoping, Li Jian, Chen Shuhui, Xiao Wei, Wang Zhenzhong, Guo Qingming, Chang Xiujuan, Tian Xuyang, Lin Tianwei

机构信息

WuXi AppTec (Shanghai) Co., Ltd., 288 FuTe Zhong Road, Shanghai 200131, People's Republic of China.

State Key Laboratory of Cellular Stress Biology, School of Life Sciences, Xiamen University, Xiamen, Fujian 361102, People's Republic of China.

出版信息

ACS Med Chem Lett. 2017 Jul 10;8(8):841-846. doi: 10.1021/acsmedchemlett.7b00188. eCollection 2017 Aug 10.

Abstract

Enterovirus 71 (EV71) is a major causative agent of hand, foot, and mouth disease (HFMD), which can spread its infections to the central nervous and other systems with severe consequences. The viral caspid protein VP1 is a well-known target for antiviral efficacy because its occupancy by suitable compounds could stabilize the virus capsid, thus preventing uncoating of virus for RNA release. In this Letter, design, synthesis, and biological evaluation of novel anti-EV71 agents (aminopyridyl 1,2,5-thiadiazolidine 1,1-dioxides) are described. One of the most promising compounds () showed excellent antiviral activity against EV71 (EC = 4 nM) and exhibited excellent efficacy in the EV71 infected mouse model.

摘要

肠道病毒71型(EV71)是手足口病(HFMD)的主要病原体,它可将感染扩散至中枢神经系统和其他系统,后果严重。病毒衣壳蛋白VP1是抗病毒疗效的一个众所周知的靶点,因为合适的化合物与之结合可稳定病毒衣壳,从而防止病毒脱壳释放RNA。在本信函中,描述了新型抗EV71药物(氨基吡啶基1,2,5-噻二唑烷1,1-二氧化物)的设计、合成及生物学评价。其中最有前景的一种化合物()对EV71显示出优异的抗病毒活性(半数有效浓度=4 nM),并在EV71感染的小鼠模型中表现出优异的疗效。

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Discovery of Potent EV71 Capsid Inhibitors for Treatment of HFMD.发现用于治疗手足口病的强效肠道病毒71型衣壳抑制剂。
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本文引用的文献

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Design, synthesis, and biological evaluation of anti-EV71 agents.抗EV71药物的设计、合成及生物学评价
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