The anti-influenza virus drug, arbidol is an efficient inhibitor of SARS-CoV-2 in vitro

Remdesivir and chloroquine effectively inhibit the recently emerged novel coronavirus (2019-nCoV) in vitro

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Hydroxychloroquine, a less toxic derivative of chloroquine, is effective in inhibiting SARS-CoV-2 infection in vitro

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Remdesivir, lopinavir, emetine, and homoharringtonine inhibit SARS-CoV-2 replication in vitro

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Triterpenoids manipulate a broad range of virus-host fusion via wrapping the HR2 domain prevalent in viral envelopes

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Approved Antiviral Drugs over the Past 50 Years

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Structural basis of influenza virus fusion inhibition by the antiviral drug Arbidol

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Arbidol as a broad-spectrum antiviral: An update

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Antiviral and anti-inflammatory activity of arbidol hydrochloride in influenza A (H1N1) virus infection

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Arbidol inhibits viral entry by interfering with clathrin-dependent trafficking

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Pharmacokinetics of single and multiple oral doses of arbidol in healthy Chinese volunteers

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Conventional and unconventional mechanisms for capping viral mRNA

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