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Kinase targets in CNS drug discovery

机译:CNS药物发现中的激酶靶标

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摘要

Originally thought to be nondruggable, kinases represent attractive drug targets for pharmaceutical companies and academia. To date, there are over 40 kinase inhibitors approved by the US FDA, with 32 of these being small molecules, in addition to the three mammalian target of rapamycin inhibitor macrolides ( sirolimus, temsirolimus and everolimus). Despite the rapid development of kinase inhibitors for cancer, presently none of these agents are approved for CNS indications. This mini perspective highlights selected kinase targets for CNS disorders, of which brain-permeable small-molecule inhibitors are reported, with demonstrated preclinical proof-of-concept efficacy. This is followed by a brief discussion on the key challenges of blood-brain barrier penetration and selectivity profiles in developing kinase inhibitors for CNS disorders.
机译:最初被认为是不懈的,激酶代表了制药公司和学术界的吸引力药物目标。 迄今为止,除了雷帕霉素抑制剂大溴化胶(西罗莫司,Temsirolimus和Everolimus)的三个哺乳动物靶外,美国FDA批准的40多种激酶抑制剂,其中32个是小分子。 尽管癌症激酶抑制剂的快速发展,但目前没有这些代理商被批准用于CNS适应症。 该迷你透视突出显示CNS疾病的选定激酶靶标,其中报道了脑渗透性的小分子抑制剂,具有突出的概念验证效果。 随后是浅谈血脑屏障渗透和选择性谱对CNS疾病开发激酶抑制剂的关键挑战。

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