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  2. In-vitro antiviral activity of doxepin hydrochloride against group B coxsackievirus

In-vitro antiviral activity of doxepin hydrochloride against group B coxsackievirus

  • Virus Res. 2022 Aug;317:198816. doi: 10.1016/j.virusres.2022.198816.
Yongqi Yang 1 Ge Liu 2 Jiaoyan Jia 1 Jianfeng Zhong 1 Ran Yan 1 Xiangyi Lin 1 Kai Zheng 1 Qinchang Zhu 3
Affiliations

Affiliations

  • 1 School of Pharmaceutical Sciences, Shenzhen University, Shenzhen, 518060, China.
  • 2 College of Pharmacy, Shenzhen Technology University, Shenzhen, 518118, China.
  • 3 School of Pharmaceutical Sciences, Shenzhen University, Shenzhen, 518060, China; College of Pharmacy, Shenzhen Technology University, Shenzhen, 518118, China. Electronic address: zhuqinchang@sztu.edu.cn.
Abstract

Group B coxsackievirus is an Enterovirus that can cause a variety of diseases, including myocarditis, aseptic meningitis, and hand, foot, and mouth disease. Currently, there is no effective Antiviral drug against this virus. In this study, we used a cytopathic effect-based viral inhibition assay to screen an FDA-approved drug library and found that doxepin hydrochloride had potential Antiviral activity. Doxepin hydrochloride exhibited strong Antiviral activity against coxsackievirus B types 1-3 with a 50% inhibitory concentration of 10.12 ± 0.85 μM. Moreover, doxepin hydrochloride did not exert Antiviral activity against Other enteroviruses, including Enterovirus A71 (subtypes BrCr/C4) and coxsackievirus A (subtypes 6/10/16). Furthermore, doxepin hydrochloride inhibited virus replication in the early stage of the Infection cycle rather than affecting the entry or assembly process. In addition, a few mechanism-related pharmacophores were discovered through gene association network analysis. These findings identify a possible lead compound for treating coxsackievirus B Infection and simultaneously offer valuable clues for drug repositioning.

Keywords

CVB; Coxsackievirus; Doxepin hydrochloride; Drug repositioning; HFMD.

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