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Novel capsid binder and PI4KIIIbeta inhibitors for EV-A71 replication inhibition
Yong Wah Tan1, Wan Keat Yam1, Rachel Jia Wen Kooi1
1Collaborative and Translation Unit for HFMD, Institute of Molecular and Cell Biology, Agency for Science, Technology and Research (A*STAR), Singapore, Singapore.
Abstract:
The Hand, Foot and Mouth Disease (HFMD) is a highly contagious viral illness generally manifests as a mild disease in young children and immunocompromised adults. It has however emerged as a significant public health threat in recent years as outbreaks have been occurring regularly, especially in the Asia-Pacific. The disease can result from infections by a wide variety of human enteroviruses, particularly, Enterovirus A71 (EV-A71) has garnered more attention due to its association with severe disease in infected patients. Despite the potential to result severe neurological complications or even fatality, there is currently no effective antiviral for treatment of EV-A71 infections and the only vaccines available are restricted to distribution in China. In this study, we report the in vitro and in vivo evaluation of two candidate antiviral compounds active against EV-A71, a viral capsid inhibitor (G197) and a novel host-targeting phosphatidylinositol 4-kinase III beta inhibitor (N373) which, especially when used in combination, can significantly improve the survival and pathology of infected mice.
Insights
Two new antiviral compounds, G197 and N373, show promise in treating Enterovirus A71 (EV-A71) infections. Combined treatment significantly improved survival rates and reduced pathology in mice infected with EV-A71.
Area of Science:
- Virology
- Infectious Diseases
- Pharmacology
Background:
- Hand, Foot and Mouth Disease (HFMD) is a contagious viral illness.
- Enterovirus A71 (EV-A71) causes severe neurological complications and fatalities.
- No effective antivirals or widely available vaccines exist for EV-A71.
Purpose of the Study:
- Evaluate two novel antiviral compounds against EV-A71.
- Assess the efficacy of a viral capsid inhibitor (G197) and a host-targeting inhibitor (N373).
- Investigate the combined therapeutic potential of G197 and N373.
Main Methods:
- In vitro and in vivo studies were conducted.
- Compounds G197 and N373 were tested against EV-A71.
- Efficacy was evaluated in infected mouse models.
Main Results:
- Both G197 and N373 demonstrated antiviral activity against EV-A71.
- Combination therapy significantly improved survival rates in infected mice.
- Combined treatment reduced disease pathology in the animal model.
Conclusions:
- G197 and N373 represent potential therapeutic agents for EV-A71 infections.
- Combination therapy offers a promising strategy to combat EV-A71.
- Further research is warranted to develop treatments for EV-A71.
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