4.6 Article

Human Enterovirus B: Selective Inhibition by Quinoxaline Derivatives and Bioinformatic RNA-Motif Identification as New Targets

期刊

PHARMACEUTICALS
卷 15, 期 2, 页码 -

出版社

MDPI
DOI: 10.3390/ph15020181

关键词

enterovirus; antiviral activity; quinoxaline derivatives; coxsackievirus B; time of drug addiction; RNA-binding protein database

资金

  1. PRIN 2017 Natural and pharmacological inhibition of the early phase of viral replication (Vir-SudNet) [Nffi 2017M8R7N9]
  2. Valere project of the University of Campania Luigi Vanvitelli
  3. University of Sassari, Fondo di ateneo per la ricerca (COEP): FAR2020CARTAA
  4. University of Sassari, Fondo di ateneo per la ricerca (COEP): FAR2020PIRASS

向作者/读者索取更多资源

Enteroviruses pose a significant threat to public health and effective antiviral drugs are currently lacking. Quinoxaline derivatives have been identified as potent inhibitors of the most common Coxsackie virus, B5, and interfere with early stages of viral replication. This study investigates the antiviral activity and mechanism of action of these compounds against other Enterovirus species.
The Enterovirus genus includes many viruses that are pathogenic in humans, including Coxsackie viruses and rhinoviruses, as well as the emerging enteroviruses D68 and A71. Currently, effective antiviral agents are not available for the treatment or prevention of enterovirus infections, which remain an important threat to public health. We recently identified a series of quinoxaline derivatives that were provento be potent inhibitors of coxsackievirus B5, the most common and a very important human pathogen belonging to the enterovirus genus. We have shown how most active derivatives interfere with the earliest stages of viral replication, blocking infection. Considering the broad antiviral spectrum, a very attractive property for an antiviral drug, we aimed to investigate the antiviral activity of the most promising compounds against other Enterovirus species. Here, we investigated the susceptibility of a panel of representatives of Enterovirus genus (enterovirus A71, belonging to A species; coxsackieviruses B4 and B3; echovirus 9, belonging to B species; and enterovirus D68, belonging to D species) to quinoxaline inhibitors. We also tested cytotoxicity and selectivity indices of the selected compounds, as well as their effects on virus yield. We also investigated their potential mechanism of action by a time course assay. In addition, a bioinformatic analysis was carried out to discover potential new conserved motifs in CVB3 and CVB4 compared to the other enterovirus species that can be used as new targets.

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