虚拟筛选
药物重新定位
重新调整用途
2019年冠状病毒病(COVID-19)
严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)
药效团
维罗细胞
药品
药理学
2019-20冠状病毒爆发
假阳性悖论
药物发现
病毒学
计算生物学
医学
生物
生物信息学
计算机科学
病毒
传染病(医学专业)
生态学
疾病
病理
机器学习
爆发
作者
Woo Dae Jang,Sangeun Jeon,Seungtaek Kim,Sang Yup Lee
标识
DOI:10.1073/pnas.2024302118
摘要
Significance Recent spread of SARS-CoV-2 has sparked significant health concerns of emerging infectious viruses. Drug repurposing is a tangible strategy for developing antiviral agents within a short period. In general, drug repurposing starts with virtual screening of approved drugs employing docking simulations. However, the actual hit rate is low, and most of the predicted compounds are false positives. To tackle the challenges, we report advanced virtual screening with pre- and postdocking pharmacophore filtering of 6,218 drugs for COVID-19. Notably, 7 out of 38 compounds showed efficacies in inhibiting SARS-CoV-2 in Vero cells. Three of these were also found to inhibit SARS-CoV-2 in human Calu-3 cells. Furthermore, three drug combinations showed strong synergistic effects in SARS-CoV-2 inhibition at their clinically achievable concentrations.
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