艾美汀
法维皮拉维
洛比那韦
高三尖杉酯碱
维罗细胞
药理学
体外
病毒学
医学
利巴韦林
病毒复制
病毒
氯喹
病毒载量
化学
2019年冠状病毒病(COVID-19)
免疫学
内科学
生物化学
丙型肝炎病毒
传染病(医学专业)
疟疾
髓系白血病
疾病
抗逆转录病毒疗法
作者
Ka-Tim Choy,Alvina Yin-Lam Wong,Prathanporn Kaewpreedee,Sin Fun Sia,Dongdong Chen,Kenrie Pui Yan Hui,Daniel K. W. Chu,Mcw Chan,Peter Pak-Hang Cheung,Xuhui Huang,Malik Peiris,Hui‐Ling Yen
标识
DOI:10.1016/j.antiviral.2020.104786
摘要
An escalating pandemic by the novel SARS-CoV-2 virus is impacting global health and effective therapeutic options are urgently needed. We evaluated the in vitro antiviral effect of compounds that were previously reported to inhibit coronavirus replication and compounds that are currently under evaluation in clinical trials for SARS-CoV-2 patients. We report the antiviral effect of remdesivir, lopinavir, homorringtonine, and emetine against SARS-CoV-2 virus in Vero E6 cells with the estimated 50% effective concentration at 23.15 μM, 26.63 μM, 2.55 μM and 0.46 μM, respectively. Ribavirin or favipiravir that are currently evaluated under clinical trials showed no inhibition at 100 μM. Synergy between remdesivir and emetine was observed, and remdesivir at 6.25 μM in combination with emetine at 0.195 μM may achieve 64.9% inhibition in viral yield. Combinational therapy may help to reduce the effective concentration of compounds below the therapeutic plasma concentrations and provide better clinical benefits.
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