Tricyclic thienopyridine–pyrimidones/thienopyrimidine–pyrimidones as orally efficacious mGluR1 antagonists for neuropathic pain

Bioorganic & Medicinal Chemistry Letters（2009）

引用 32|浏览33

暂无评分

摘要

A series of highly potent and selective mGluR1 antagonists have been discovered and demonstrated efficacy in animal model for pain.

查看译文

关键词

Tricyclic thienopyridine–pyrimidone,Thienopyrimidine–pyrimidone,Triazafluorenone,mGluR1 antagonist,Neuropathic pain

AI 理解论文

溯源树

样例

生成溯源树，研究论文发展脉络

Chat Paper

正在生成论文摘要