4.7 Article

Small Molecule Kinase Inhibitor Drugs (1995-2021): Medical Indication, Pharmacology, and Synthesis

期刊

JOURNAL OF MEDICINAL CHEMISTRY
卷 65, 期 2, 页码 1047-1131

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.jmedchem.1c00963

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资金

  1. CONACyT
  2. H2020 Marie Sklodowska-Curie actions through Grant BRAINHIB [H2020-MSCA-IF-2016749299]
  3. H2020 Marie Sklodowska-Curie actions through Grant THERACAT [H2020-MSCA-ITN-2017765497]
  4. Institute of Genetics Cancer
  5. Grant TARGETOF [H2020-MSCA-IF-2019-895664]
  6. Medical Research Scotland [PhD-1046-2016]

向作者/读者索取更多资源

Kinase inhibitors play a central role in the treatment of progressive disorders, with FDA approving 73 small molecule kinase inhibitor drugs by September 2021. This review summarizes the therapeutic and pharmacological properties of approved kinase inhibitors, as well as their synthesis routes, with an update on drugs approved in 2021.
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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