Krahn Andrea I, Wells Carrow, Drewry David H, Beitel Lenore K, Durcan Thomas M, Axtman Alison D
Early Drug Discovery Unit, Montreal Neurological Institute-Hospital, McGill University, Montreal, QC, Canada H3A 2B4.
Structural Genomics Consortium, UNC Eshelman School of Pharmacy, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599, United States.
ACS Chem Neurosci. 2020 Jul 1;11(13):1871-1886. doi: 10.1021/acschemneuro.0c00176. Epub 2020 Jun 11.
Kinases are highly tractable drug targets that have reached unparalleled success in fields such as cancer but whose potential has not yet been realized in neuroscience. There are currently 55 approved small molecule kinase-targeting drugs, 48 of which have an anticancer indication. The intrinsic complexity linked to central nervous system (CNS) drug development and a lack of validated targets has hindered progress in developing kinase inhibitors for CNS disorders when compared to other therapeutic areas such as oncology. Identification and/or characterization of new kinases as potential drug targets for neurodegenerative diseases will create opportunities for the development of CNS drugs in the future. The track record of kinase inhibitors in other disease indications supports the idea that with the best targets identified small molecule kinase modulators will become impactful therapeutics for neurodegenerative diseases. This Review highlights the imminent need for new therapeutics to treat the most prevalent neurodegenerative diseases as well as the promise of kinase inhibitors to address this need. With a focus on kinases that remain largely unexplored after decades of dedicated research in the kinase field, we offer specific examples of understudied kinases that are supported by patient-derived data as linked to Alzheimer's disease, Parkinson's disease, and/or amyotrophic lateral sclerosis. Finally, we show literature-reported high-quality inhibitors for several understudied kinases and suggest other kinases that merit additional medicinal chemistry efforts to elucidate their therapeutic potential.
激酶是高度易于处理的药物靶点,在癌症等领域已取得了无与伦比的成功,但在神经科学领域其潜力尚未得到充分发挥。目前有55种已获批的靶向激酶的小分子药物,其中48种具有抗癌适应症。与肿瘤学等其他治疗领域相比,与中枢神经系统(CNS)药物开发相关的内在复杂性以及缺乏经过验证的靶点,阻碍了用于中枢神经系统疾病的激酶抑制剂的开发进展。鉴定和/或表征新的激酶作为神经退行性疾病的潜在药物靶点,将为未来中枢神经系统药物的开发创造机会。激酶抑制剂在其他疾病适应症中的记录支持这样一种观点,即一旦确定了最佳靶点,小分子激酶调节剂将成为治疗神经退行性疾病的有效疗法。本综述强调了迫切需要新的疗法来治疗最常见的神经退行性疾病,以及激酶抑制剂满足这一需求的前景。我们聚焦于在激酶领域经过数十年专门研究后仍基本未被探索的激酶,提供了一些研究不足的激酶的具体例子,这些例子有来自患者的数据支持,且与阿尔茨海默病、帕金森病和/或肌萎缩侧索硬化症相关。最后,我们展示了文献报道的针对几种研究不足的激酶的高质量抑制剂,并提出了其他值得进一步开展药物化学研究以阐明其治疗潜力的激酶。