MAPK/ERK通路
激酶
p38丝裂原活化蛋白激酶
丝裂原活化蛋白激酶
药物发现
临床试验
基因亚型
药物开发
药理学
计算生物学
医学
癌症研究
生物信息学
药品
生物
细胞生物学
生物化学
基因
作者
Valentin Wydra,Raphael Ditzinger,Nico J. Seidler,Frederik W Hacker,Stefan Laufer
标识
DOI:10.1080/13543776.2023.2242584
摘要
Introduction The mitogen-activated protein kinase (MAPK) family consist of p38 MAP kinases, c-Jun N-terminal kinases (JNKs) and extracellular signal-regulated kinases (ERKs). They are involved in a multitude of diseases, including inflammatory, autoimmune, neurodegenerative, and metabolic diseases as well as cancer. In recent years further developments in the field of MAPK-inhibitors have been reported, including an isoform or downstream target selective inhibition of MAPKs as well as target protein degradation approaches.Areas covered This review summarizes newly patented MAPK-inhibitors that were claimed between 2018 and early 2023. Presented are the patents as well as their corresponding publications, the storyline of development, and clinical trials involving these compounds. This article elaborates a total of 27 patents, which were identified using established search engines.Expert opinion Although industrial research on MAPK-inhibitors has been ongoing for more than 20 years, novel clinical trials of MAPK-inhibitors as potential drug candidates are still being conducted in the period under review. Recently reported inhibitors show an excellent selectivity profile and are even achieving selectivity between close related isoforms. This progression offers the possibility to eliminate unwanted side effects and may finally lead to the approval of the first MAPK-inhibitor.
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