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Ruiyuan Cao

Publications -  26
Citations -  7867

Ruiyuan Cao is an academic researcher. The author has contributed to research in topics: Biology & Virus. The author has an hindex of 8, co-authored 11 publications receiving 6158 citations.

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

TL;DR: This study evaluated the antiviral efficiency of five FAD-approved drugs including ribavirin, penciclovir, nitazoxanide, nafamostat, chloroquine and two well-known broad-spectrum antiviral drugs remdesivir and favipiravir against a clinical isolate of 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

TL;DR: Evaluated the antiviral effect of HCQ against SARS-CoV-2 infection in comparison to CQ in vitro and concluded that CQ appears to be the drug of choice for large-scale use due to its availability, proven safety record, and a relatively low cost.
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The anti-influenza virus drug, arbidol is an efficient inhibitor of SARS-CoV-2 in vitro

TL;DR: Six currently available and licensed anti-influenza drugs against SARS-CoV-2 are evaluated and it is suggested that arbidol treatment showed tendency to improve the discharging rate and decrease the mortality rate of COVID-19 patients.
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Anti-SARS-CoV-2 Potential of Artemisinins In Vitro.

TL;DR: Evaluated anti-SARS-CoV-2 activities of nine artemisinin-related compounds in vitro and carried out a time-of-drug-addition assay to explore their antiviral mode of action; a pharmacokinetic prediction model was established to predict the therapeutic potential of selected compounds against COVID-19 and revealed lumefantrine showed therapeutic promise due to high plasma and lung drug concentrations after multiple dosing.
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Pediatric Drug Nitazoxanide: A Potential Choice for Control of Zika.

TL;DR: Nitazoxanides and its bioactive metabolite, tizoxanide, have anti-ZIKV potential in vitro, and it is identified that they exerts antiviral effect possibly by targeting the viral postattachment step.