激酶
现存分类群
药物发现
药理学
药物开发
药品
机制(生物学)
医学
计算生物学
生物
生物信息学
细胞生物学
进化生物学
认识论
哲学
作者
Zheng Zhao,Philip E. Bourne
出处
期刊:Springer eBooks
[Springer Nature]
日期:2020-01-01
卷期号:: 13-28
被引量:14
标识
DOI:10.1007/978-3-030-48283-1_2
摘要
Research on kinase-targeting drugs has made great strides over the last 30 years and is attracting greater attention for the treatment of yet more kinase-related diseases. Currently, 42 kinase drugs have been approved by the FDA, most of which (39) are Type I/II inhibitors. Notwithstanding these advances, it is desirable to target additional kinases for drug development as more than 200 diseases, particularly cancers, are directly associated with aberrant kinase regulation and signaling. Here, we review the extant Type I/II drugs systematically to obtain insights into the binding pocket characteristics, the associated features of Type I/II drugs, and the mechanism of action to facilitate future kinase drug design and discovery. We conclude by summarizing the main successes and limitations of targeting kinase for the development of drugs.
科研通智能强力驱动
Strongly Powered by AbleSci AI