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Development of Highly Potent Noncovalent Inhibitors of SARS-CoV-2 3CLpro.

Ningke HouLei ShuaiLijing ZhangXuping XieKaiming TangYunkai ZhuYin YuWenyi ZhangQiaozhu TanGongxun ZhongZhiyuan WenChong WangXijun HeHong HuoHaishan GaoYou XuJing XueChen PengJing ZouCraig SchindewolfVineet MenacheryWenji SuYoulang YuanZuyuan ShenRong ZhangShuo-Feng YuanHongtao YuPei-Yong ShiZhigao BuJing HuangQi Hu
Published in: ACS central science (2023)
The 3C-like protease (3CLpro) is an essential enzyme for the replication of SARS-CoV-2 and other coronaviruses and thus is a target for coronavirus drug discovery. Nearly all inhibitors of coronavirus 3CLpro reported so far are covalent inhibitors. Here, we report the development of specific, noncovalent inhibitors of 3CLpro. The most potent one, WU-04, effectively blocks SARS-CoV-2 replications in human cells with EC 50 values in the 10-nM range. WU-04 also inhibits the 3CLpro of SARS-CoV and MERS-CoV with high potency, indicating that it is a pan-inhibitor of coronavirus 3CLpro. WU-04 showed anti-SARS-CoV-2 activity similar to that of PF-07321332 (Nirmatrelvir) in K18-hACE2 mice when the same dose was administered orally. Thus, WU-04 is a promising drug candidate for coronavirus treatment.
Keyphrases
  • sars cov
  • respiratory syndrome coronavirus
  • drug discovery
  • emergency department
  • metabolic syndrome
  • photodynamic therapy
  • skeletal muscle
  • coronavirus disease
  • electronic health record
  • adverse drug