基于吡嗪的小分子激酶抑制剂:临床应用和专利回顾(2019-2023 年)。

IF 3.2 4区 医学 Q3 CHEMISTRY, MEDICINAL
Aisha Alsfouk
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引用次数: 0

摘要

蛋白激酶在增殖、凋亡、炎症和免疫调节等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)的一种潜在疗法。现有小分子激酶抑制剂的主要化学结构为杂环、含氮和六元环,包括吡嗪。目前已开发出几种强效和选择性的吡嗪类激酶抑制剂,并已进入临床试验阶段。激酶抑制剂的临床应用数据表明,它们对几种耐复发的恶性肿瘤和重度至中度免疫性疾病具有良好的临床活性和可控的毒性。所有基于吡嗪的激酶抑制剂都具有口服活性。本文回顾了与吡嗪类小分子抑制剂相关的最新激酶文献(2019-2023年)。该综述包括经 FDA(美国食品和药物管理局)批准的制剂和专利制剂,以及它们的靶激酶、支架、效力、选择性特征、受让人以及临床和临床前研究中的生物学结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pyrazine-based small molecule kinase inhibitors: clinical applications and patent review (2019-2023).

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.

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来源期刊
Future medicinal chemistry
Future medicinal chemistry CHEMISTRY, MEDICINAL-
CiteScore
5.80
自引率
2.40%
发文量
118
审稿时长
4-8 weeks
期刊介绍: Future Medicinal Chemistry offers a forum for the rapid publication of original research and critical reviews of the latest milestones in the field. Strong emphasis is placed on ensuring that the journal stimulates awareness of issues that are anticipated to play an increasingly central role in influencing the future direction of pharmaceutical chemistry. Where relevant, contributions are also actively encouraged on areas as diverse as biotechnology, enzymology, green chemistry, genomics, immunology, materials science, neglected diseases and orphan drugs, pharmacogenomics, proteomics and toxicology.
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