Author/Authors :
Richard Y. Kao، نويسنده , , Wayne H.W. Tsui، نويسنده , , Terri S.W. Lee، نويسنده , , Julian A. Tanner، نويسنده , , Rory M. Watt، نويسنده , , Jiandong Huang، نويسنده , , LiHong Hu، نويسنده , , Guanhua Chen، نويسنده , , Zhiwei Chen، نويسنده , , Linqi Zhang، نويسنده , , Tian He، نويسنده , , Kwok-hung Chan، نويسنده , , Herman Tse، نويسنده , , Amanda P.C. To، نويسنده , , Louisa W.Y. Ng، نويسنده , , Bonnie C.W. Wong، نويسنده , , Hoi-wah Tsoi، نويسنده , , Dan Y، نويسنده ,
Abstract :
The severe acute respiratory syndrome-associated coronavirus (SARS-CoV) infected more than 8,000 people across 29 countries and caused more than 900 fatalities. Based on the concept of chemical genetics, we screened 50,240 structurally diverse small molecules from which we identified 104 compounds with anti-SARS-CoV activity. Of these 104 compounds, 2 target the SARS-CoV main protease (Mpro), 7 target helicase (Hel), and 18 target spike (S) protein-angiotensin-converting enzyme 2 (ACE2)-mediated viral entry. The EC50 of the majority of the 104 compounds determined by SARS-CoV plaque reduction assay were found to be at low micromolar range. Three selected compounds, MP576, HE602, and VE607, validated to be inhibitors of SARS-CoV Mpro, Hel, and viral entry, respectively, exhibited potent antiviral activity (EC50 < 10 μM) and comparable inhibitory activities in target-specific in vitro assays.
