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中国药学(英文版) ›› 2025, Vol. 34 ›› Issue (8): 798-800.

• 【新闻】 • 上一篇    

孙崎团队和黄卓团队合作在靶向αβ界面的GABAA受体正向变构调节剂及其治疗癫痫持续状态方面获得新进展

北京大学药学院天然药物及仿生药物全国重点实验室   

  1. 北京大学药学院天然药物及仿生药物全国重点实验室
  • 收稿日期:2025-07-31 修回日期:2025-07-31 接受日期:2025-07-31 出版日期:2025-08-29 发布日期:2025-08-29

The research teams of Prof. Qi Sun and Prof. Zhuo Huang have made new progress in the research of positive allosteric modulators targeting β+/α–subunit interface as GABAAR positive allosteric modulator for the treatment of status epilepticus in mouse

State Key Laboratory of Natural and Biomimetic Drugs, School of Pharmaceutical Sciences, Peking University Health Science Center   

  1. State Key Laboratory of Natural and Biomimetic Drugs, School of Pharmaceutical Sciences, Peking University Health Science Center
  • Received:2025-07-31 Revised:2025-07-31 Accepted:2025-07-31 Online:2025-08-29 Published:2025-08-29

摘要:

2025年7月11日, 北京大学药学院天然药物及仿生药物全国重点实验室孙崎教授和黄卓教授团队合作在Journal of Medicinal Chemistry上在线发表新型2-(2-噻吩基)噻唑并[4,5-d]嘧啶-7(6H)-酮类GABAAR正向变构调节剂通过靶向β+/α–亚基界面治疗小鼠癫痫持续状态的原创性研究工作。该研究针对临床治疗癫痫持续状态(Status Epilepticus, SE)面临的苯二氮䓬类药物耐药性难题, 开发了具有全新化学骨架的靶向疗法。

Abstract:

The research teams of Prof. Qi Sun and Prof. Zhuo Huang have made new progress in the research of positive allosteric modulators targeting β+/α–subunit interface as GABAAR positive allosteric modulator for the treatment of status epilepticus in mouse.

Supporting: