激酶
药物发现
药理学
试验药物
小分子
化学
极光激酶
药品
医学
临床试验
细胞周期
生物化学
细胞
内科学
作者
Cecilia C. Ayala-Aguilera,Teresa Valero,Álvaro Lorente‐Macías,Daniel J. Baillache,Stephen Croke,Asier Unciti‐Broceta
标识
DOI:10.1021/acs.jmedchem.1c00963
摘要
The central role of dysregulated kinase activity in the etiology of progressive disorders, including cancer, has fostered incremental efforts on drug discovery programs over the past 40 years. As a result, kinase inhibitors are today one of the most important classes of drugs. The FDA approved 73 small molecule kinase inhibitor drugs until September 2021, and additional inhibitors were approved by other regulatory agencies during that time. To complement the published literature on clinical kinase inhibitors, we have prepared a review that recaps this large data set into an accessible format for the medicinal chemistry community. Along with the therapeutic and pharmacological properties of each kinase inhibitor approved across the world until 2020, we provide the synthesis routes originally used during the discovery phase, many of which were only available in patent applications. In the last section, we also provide an update on kinase inhibitor drugs approved in 2021.
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