Antimicrobial Agents and Chemotherapy · 2014 · 118 citations · 10 references
Life SciencesInfectious DiseasesMedicinal ChemistryDrug DiscoveryMolecular VirologyVirologyAntiviral PharmacologyHost-virus InteractionsViral HepatitisViral InfectionsViral PathologyViral StructureAntiviral Drug DesignAntiviral TherapeuticsBinding Pocket GeometryMiddle East Respiratory Syndrome CoronavirusSevere Acute Respiratory SyndromeViral Helicase InhibitorsViral Therapeutic Targets
We have previously shown that SSYA10-001 blocks severe acute respiratory syndrome coronavirus (SARS-CoV) replication by inhibiting SARS-CoV helicase (nsp13). Here, we show that SSYA10-001 also inhibits replication of two other coronaviruses, mouse hepatitis virus (MHV) and Middle Eastern respiratory syndrome coronavirus (MERS-CoV). A putative binding pocket for SSYA10-001 was identified and shown to be similar in SARS-CoV, MERS-CoV, and MHV helicases. These studies show that it is possible to target multiple coronaviruses through broad-spectrum inhibitors.
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Dipeptidyl peptidase 4 is a functional receptor for the emerging human coronavirus-EMC
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