Publication date: Jul 05, 2025
The coronavirus disease 2019 (COVID-19) pandemic crisis has been mitigated by worldwide efforts to develop vaccines and therapeutic drugs. However, there remains concern regarding public health and an unmet need for therapeutic options. Herein, we report the discovery of S-892216, a second-generation SARS-CoV-2 3C-like protease (3CL) inhibitor, to treat COVID-19. S-892216 is a reversible covalent 3CL inhibitor with highly potent antiviral activity and an EC value of 2. 48 nM against SARS-CoV-2 infected cells. Structure-based design of a covalent modifier for compound 1 revealed that introducing a nitrile warhead increased 3CL inhibition activity by 180-fold. Subsequent optimization efforts yielded S-892216, which combined a favorable pharmacokinetic profile and high off-target selectivity. S-892216 exhibited antiviral activity against diverse SARS-CoV-2 variants, including major mutations reducing antiviral activities of nirmatrelvir and ensitrelvir. In SARS-CoV-2-infected mice, S-892216 inhibited viral replication in the lungs similar to ensitrelvir, although at a 30-fold lower dose.
| Concepts | Keywords |
|---|---|
| Mice | 3cl |
| Pandemic | Activity |
| Pharmacokinetic | Antiviral |
| Vaccines | Cov |
| Covalent | |
| Covid | |
| Efforts | |
| Generation | |
| Infected | |
| Inhibitor | |
| Protease | |
| Sars | |
| Second | |
| Therapeutic |
Semantics
| Type | Source | Name |
|---|---|---|
| disease | MESH | COVID-19 |
| pathway | KEGG | Viral replication |