Recent advances of quinoline-based small molecules as kinase inhibitors (2020-2024).

IF 3.6 4区 医学 Q2 CHEMISTRY, MEDICINAL
ChemMedChem Pub Date : 2025-05-13 DOI:10.1002/cmdc.202500279
Sara Sultan, Ruba A Zenati, Hanan S Anbar, Mohammed I El-Gamal, Mohammad H Semreen
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引用次数: 0

Abstract

Quinoline-containing compounds have gained prominence in drug discovery as versatile scaffolds. These compounds have shown promise in the development of kinase inhibitors, which are crucial treatment options used in various cancer cases. This review explores the recent advances from 2020 to 2024 in the design, synthesis, and optimization of quinoline-based kinase inhibitors, focusing on their role in targeting key kinases, implicated in cancer signaling pathways. Quinoline derivatives exhibit significant inhibitory activity across a broad spectrum of kinases, highlighting their potential to disrupt aberrant signaling that drives tumor growth and progression. Several FDA-approved quinoline-containing compounds are utilized in clinical settings as kinase inhibitors, reinforcing their importance and relevance in clinical oncology. This review compiles the pharmacological profiles of these inhibitors spotlighting key compounds that have demonstrated potent inhibitory activities, excellent selectivity profiles, and promising preclinical or clinical outcomes. The review also addresses the challenges associated with their development and discusses future directions for optimizing quinoline-based kinase inhibitors, such as leveraging advanced drug design techniques, exploring novel targets, and expanding their use in combination therapies. By summarizing recent advancements, this review aims to provide insights into the evolving landscape of quinoline-based kinase inhibitors and their potential as next-generation anticancer therapies.

喹啉类小分子激酶抑制剂研究进展(2020-2024)。
含喹啉的化合物作为多功能支架在药物发现中获得突出地位。这些化合物在开发激酶抑制剂方面显示出了希望,激酶抑制剂是用于各种癌症病例的关键治疗选择。本文综述了从2020年到2024年喹诺啉类激酶抑制剂的设计、合成和优化方面的最新进展,重点关注它们在癌症信号通路中涉及的关键激酶中的作用。喹啉衍生物在广泛的激酶中表现出显著的抑制活性,突出了它们破坏驱动肿瘤生长和进展的异常信号的潜力。一些fda批准的含有喹啉的化合物在临床环境中用作激酶抑制剂,加强了它们在临床肿瘤学中的重要性和相关性。本文综述了这些抑制剂的药理学特征,重点介绍了具有有效抑制活性、良好选择性和有希望的临床前或临床结果的关键化合物。这篇综述还讨论了与它们的发展相关的挑战,并讨论了优化喹啉类激酶抑制剂的未来方向,例如利用先进的药物设计技术,探索新的靶点,扩大它们在联合治疗中的应用。通过总结最近的进展,本综述旨在深入了解喹诺啉类激酶抑制剂的发展前景及其作为下一代抗癌疗法的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
ChemMedChem
ChemMedChem 医学-药学
CiteScore
6.70
自引率
2.90%
发文量
280
审稿时长
1 months
期刊介绍: Quality research. Outstanding publications. With an impact factor of 3.124 (2019), ChemMedChem is a top journal for research at the interface of chemistry, biology and medicine. It is published on behalf of Chemistry Europe, an association of 16 European chemical societies. ChemMedChem publishes primary as well as critical secondary and tertiary information from authors across and for the world. Its mission is to integrate the wide and flourishing field of medicinal and pharmaceutical sciences, ranging from drug design and discovery to drug development and delivery, from molecular modeling to combinatorial chemistry, from target validation to lead generation and ADMET studies. ChemMedChem typically covers topics on small molecules, therapeutic macromolecules, peptides, peptidomimetics, and aptamers, protein-drug conjugates, nucleic acid therapies, and beginning 2017, nanomedicine, particularly 1) targeted nanodelivery, 2) theranostic nanoparticles, and 3) nanodrugs. Contents ChemMedChem publishes an attractive mixture of: Full Papers and Communications Reviews and Minireviews Patent Reviews Highlights and Concepts Book and Multimedia Reviews.
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