Targeting the r-spine: Design, synthesis, and biological evaluation of novel type I1/2 p38α MAP kinase inhibitors with excellent selectivity, high potency, and prolonged target residence time. Implication for cancer- and CNS-applications

被引：0

作者：

Laufer, Stefan ^{[1
]}

Wentsch, Heike ^{[1
]}

Walter, Niklas ^{[1
]}

Laemmerhofer, Michael ^{[1
]}

Buijsman, Roger ^{[2
]}

Rauh, Daniel ^{[3
]}

Zender, Lars ^{[4
]}

机构：

[1] Univ Tubingen, Dept Pharm & Biochem, Tubingen, Germany

[2] Netherlands Translat Res Ctr, NL-5342 Oss, Netherlands

[3] Tech Univ Dortmund, Chem Biol, Dortmund, Germany

[4] Univ Hosp Tubingen, Dept Internal Med 8, D-72076 Tubingen, Germany

来源：

ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY | 2019年 / 258卷

关键词：

D O I：

暂无

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

151-COMP

引用

页数：2