Application of astragalus acid in the preparation of inhibitors of core protease I7L activity and drugs against orthopoxvirus infections
High-throughput drug screening identified urushiol as an inhibitor of the core protease I7L, solving a challenge in the treatment of monkeypox virus. It achieved the dual effects of effectively inhibiting viral replication and alleviating inflammation, providing a safe treatment option.
Patent Information
- Authority / Receiving Office
- CN · China
- Patent Type
- Applications(China)
- Current Assignee / Owner
- SHANGHAI INSTITUTE OF INFECTIOUS DISEASE & BIOSECURITY
- Filing Date
- 2026-04-15
- Publication Date
- 2026-05-26
AI Technical Summary
Currently, there is a lack of effective vaccines or drugs for the prevention and treatment of monkeypox virus. Existing drugs such as Tecovirimat have not shown significant effects in clinical treatment, and there is an urgent need to develop new and highly effective anti-monkeypox virus drugs.
High-throughput drug screening technology was used to discover and confirm that urushiol can effectively inhibit the activity of the core protease I7L. Rushiol was developed as an inhibitor of the core protease I7L activity to block viral replication and alleviate inflammatory response, and to prepare an anti-orchioplasmosis virus infection drug.
Ascorbic acid inhibits monkeypox virus core protease I7L by 70%, exhibiting significant dual antiviral and anti-inflammatory effects, thus improving the safety and efficiency of treatment.
Smart Images

Figure CN122075461A_ABST