Microbiology Spectrum · 2023 · 18 citations · 38 references
Life SciencesInfectious DiseasesPharmacologyDrug DiscoveryMolecular VirologyVirologyAntiviral AgentsAntiviral PharmacologyAntiviral PharmacotherapyAntiviral TherapyEnzyme InhibitionViral InfectionsAntiviral Drug DesignAntiviral Structure-activity RelationshipsAntiviral TherapeuticsGuanosine Triphosphate MetabolismMycophenolic Acid TherapyRate-limiting EnzymesViral Entry InhibitorsViral Therapeutic Targets
Mpox is a zoonotic disease caused by infection with the mpox virus, and a worldwide outbreak occurred in May 2022. The smallpox vaccine has recently been approved for clinical use against mpox in the United States. Although brincidofovir and tecovirimat are drugs approved for the treatment of smallpox by the U.S. Food and Drug Administration, their efficacy against mpox has not been established. Moreover, these drugs may present negative side effects. Therefore, new anti-mpox virus agents are needed. This study revealed that gemcitabine, trifluridine, and mycophenolic acid inhibited mpox virus propagation and exhibited broad-spectrum anti-orthopoxvirus activities. We also suggested IMP dehydrogenase as a potential target for the development of anti-mpox virus agents. By targeting this molecule, we identified a series of compounds with stronger anti-mpox virus activity than mycophenolic acid.
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Guang Yang, Daniel C. Pevear, Marc H. Davies et al. · Journal of Virology · 2005 · 457 citations · Full text
Life Sciences, Infectious Diseases, Host-pathogen Interactions +12
Characterization of human type I and type II IMP dehydrogenases.
Stephen F. Carr, Eva Papp, J. Wu et al. · Journal of Biological Chemistry · 1993 · 425 citations · Full text
Oral Tecovirimat for the Treatment of Smallpox
Douglas W. Grosenbach, Kady M. Honeychurch, Eric A. Rose et al. · New England Journal of Medicine · 2018 · 416 citations · Full text