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Cell Rep Med ; 4(8): 101127, 2023 08 15.
Article in English | MEDLINE | ID: mdl-37463584

ABSTRACT

The COVID-19 pandemic highlights an urgent need for effective antivirals. Targeting host processes co-opted by viruses is an attractive antiviral strategy with a high resistance barrier. Picolinic acid (PA) is a tryptophan metabolite endogenously produced in mammals. Here, we report the broad-spectrum antiviral activity of PA against enveloped viruses, including severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), influenza A virus (IAV), flaviviruses, herpes simplex virus, and parainfluenza virus. Mechanistic studies reveal that PA inhibits enveloped virus entry by compromising viral membrane integrity, inhibiting virus-cellular membrane fusion, and interfering with cellular endocytosis. More importantly, in pre-clinical animal models, PA exhibits promising antiviral efficacy against SARS-CoV-2 and IAV. Overall, our data establish PA as a broad-spectrum antiviral with promising pre-clinical efficacy against pandemic viruses SARS-CoV-2 and IAV.


Subject(s)
COVID-19 , Influenza A virus , Animals , Humans , SARS-CoV-2/metabolism , Virus Internalization , Pandemics , Virus Replication , Antiviral Agents/pharmacology , Antiviral Agents/therapeutic use , Mammals/metabolism
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