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针对药物发现的靶向 CDK5 的新型药物化学策略。

Novel Medicinal Chemistry Strategies Targeting CDK5 for Drug Discovery.

机构信息

Department of Biotherapy, Cancer Center and State Key Laboratory of Biotherapy and Joint Research Institution of Altitude Health and National Clinical Research Center for Geriatrics, West China Hospital, Sichuan University, Chengdu 610041, China.

Department of Medicinal Chemistry and Natural Medicine Chemistry, College of Pharmacy, Harbin Medical University, Harbin 150081, China.

出版信息

J Med Chem. 2023 Jun 8;66(11):7140-7161. doi: 10.1021/acs.jmedchem.3c00566. Epub 2023 May 26.

Abstract

Cyclin-dependent kinase 5 (CDK5) protein plays an important role not only in the central nervous system but also in the periphery, including immune response, regulation of insulin secretion, and cancer development and progression. Consequently, targeting the CDK5 protein is a potential strategy for the treatment of many diseases, especially cancer and neurodegenerative diseases. To date, numerous pan-CDK inhibitors have entered clinical trials. Nevertheless, limited clinical efficacy and severe adverse effects have prompted the application of new techniques to optimize clinical efficacy and minimize adverse events. In this Perspective, we highlight the protein properties, biofunctions, relevant signaling pathways, and associations with cancer development and proliferation of CDK5, and analyze the clinical status of pan-CDK inhibitors and the preclinical status of CDK5-specific inhibitors. In addition, CDK5-selective inhibitors, protein-protein interaction inhibitors, proteolytic-targeting chimera (PROTAC) degraders, and dual-target CDK5 inhibitors are discussed.

摘要

细胞周期蛋白依赖性激酶 5(CDK5)蛋白不仅在中枢神经系统中发挥着重要作用,在免疫系统、胰岛素分泌的调节以及癌症的发生和发展等外周组织中也发挥着重要作用。因此,靶向 CDK5 蛋白是治疗多种疾病,尤其是癌症和神经退行性疾病的潜在策略。迄今为止,已有许多泛 CDK 抑制剂进入临床试验。然而,有限的临床疗效和严重的不良反应促使人们应用新技术来优化临床疗效并最小化不良反应。在本述评中,我们重点介绍了 CDK5 的蛋白特性、生物功能、相关信号通路以及与癌症发生和增殖的关系,并分析了泛 CDK 抑制剂的临床现状和 CDK5 特异性抑制剂的临床前现状。此外,还讨论了 CDK5 选择性抑制剂、蛋白-蛋白相互作用抑制剂、靶向蛋白水解嵌合体(PROTAC)降解剂和双靶 CDK5 抑制剂。

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