变构调节
激酶
鉴定(生物学)
计算生物学
细胞生物学
蛋白激酶A
药理学
生物
生物化学
酶
植物
作者
Sandra W. Cowan‐Jacob,Wolfgang Jahnke,Stefan Knapp
出处
期刊:Future Medicinal Chemistry
[Newlands Press Ltd]
日期:2014-03-20
卷期号:6 (5): 541-561
被引量:85
摘要
Protein kinases are involved in many essential cellular processes and their deregulation can lead to a variety of diseases, including cancer. The pharmaceutical industry has invested heavily in the identification of kinase inhibitors to modulate these disease-promoting pathways, resulting in several successful drugs. However, the field is challenging as it is difficult to identify novel selective inhibitors with good pharmacokinetic/pharmacodynamic properties. In addition, resistance to kinase inhibitor treatment frequently arises. The identification of non-ATP site targeting ('allosteric') inhibitors, the identification of kinase activators and the expansion of kinase target space to include the less studied members of the family, including atypical- and pseudo-kinases, are potential avenues to overcome these challenges. In this perspective, the opportunities and challenges of following these approaches and others will be discussed.
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