- Author:
Quanjie LI
1
;
Dongrong YI
1
;
Xiaobo LEI
2
;
Jianyuan ZHAO
1
;
Yongxin ZHANG
1
;
Xiangling CUI
1
;
Xia XIAO
2
;
Tao JIAO
2
;
Xiaojing DONG
2
;
Xuesen ZHAO
3
;
Hui ZENG
3
;
Chen LIANG
4
;
Lili REN
2
;
Fei GUO
2
;
Xiaoyu LI
1
;
Jianwei WANG
2
;
Shan CEN
1
Author Information
- Publication Type:Journal Article
- Keywords: Corilagin; Drug combinations; Non-nucleoside inhibitor; RdRp; SARS-CoV-2; Structure-based virtual screening; Viral replication
- From: Acta Pharmaceutica Sinica B 2021;11(6):1555-1567
- CountryChina
- Language:English
- Abstract: Severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) has become one major threat to human population health. The RNA-dependent RNA polymerase (RdRp) presents an ideal target of antivirals, whereas nucleoside analogs inhibitor is hindered by the proofreading activity of coronavirus. Herein, we report that corilagin (RAI-S-37) as a non-nucleoside inhibitor of SARS-CoV-2 RdRp, binds directly to RdRp, effectively inhibits the polymerase activity in both cell-free and cell-based assays, fully resists the proofreading activity and potently inhibits SARS-CoV-2 infection with a low 50% effective concentration (EC