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基于吡嗪的小分子激酶抑制剂:临床应用和专利审查(2019-2023)。

Pyrazine-based small molecule kinase inhibitors: clinical applications and patent review (2019-2023).

机构信息

Department of Pharmaceutical Sciences, College of Pharmacy, Princess Nourah bint Abdulrahman University, Riyadh, 11671, Saudi Arabia.

出版信息

Future Med Chem. 2024;16(18):1899-1921. doi: 10.1080/17568919.2024.2385293. Epub 2024 Aug 27.

Abstract

Protein kinases play a key role in cellular signaling pathways including proliferation, apoptosis, inflammation and immune regulation. Therefore, targeting kinases with small molecules has emerged as a therapeutic potential in cancers and other diseases including inflammatory and autoimmune disorders. The main chemical motifs of the available small molecule kinase inhibitors are heterocyclic, nitrogen-containing and six-membered rings including pyrazine. Several potent and selective pyrazine-based kinase inhibitors have been developed and progressed into clinical trials. The data of clinical application of kinase inhibitors demonstrate good clinical activity with manageable toxicity in several relapse-resistant malignancies and severe to moderate immunological disorders. All pyrazine-based kinase inhibitors are orally active. This paper reviews the most recent kinase literature (2019-2023) related to pyrazine-based small molecule inhibitors. This review includes the FDA (Food and Drug Administration)-approved and patent agents along with their targeted kinase, scaffold, potency, selectivity profile, assignee and biological results in clinical and preclinical studies.

摘要

蛋白激酶在包括增殖、凋亡、炎症和免疫调节在内的细胞信号通路中发挥着关键作用。因此,用小分子靶向激酶已成为癌症和其他疾病(包括炎症和自身免疫性疾病)的一种治疗潜力。现有小分子激酶抑制剂的主要化学结构基序为杂环、含氮和六元环,包括吡嗪。已经开发出了几种有效的、选择性的吡嗪基激酶抑制剂,并已进入临床试验。激酶抑制剂的临床应用数据表明,在几种复发耐药性恶性肿瘤和严重至中度免疫性疾病中,这些药物具有良好的临床活性和可管理的毒性。所有基于吡嗪的激酶抑制剂均为口服活性药物。本文综述了 2019 年至 2023 年与基于吡嗪的小分子抑制剂相关的最新激酶文献。本综述包括 FDA(美国食品和药物管理局)批准的药物和专利药物,以及它们在临床前和临床试验中的靶向激酶、支架、效力、选择性概况、受让人以及生物学结果。

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