吡嗪和吡嗪酮在药物化学中的作用:合成和靶向TxA2、TNF-α和IL-6的抗炎途径。

IF 3.3 3区 医学 Q2 CHEMISTRY, MEDICINAL
Soha H Emam, Eman M Ahmed, Nadia A Khalil, Basma A Mohammad, Nirvana A Gohar
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引用次数: 0

摘要

炎症是对有害刺激的基本生物反应,在不同疾病的发生和发展中起着至关重要的作用,包括类风湿关节炎、心血管疾病、阿尔茨海默病和帕金森病等神经系统疾病以及多种癌症类型。慢性炎症,特别是,有助于不可逆的组织损伤和疾病的进展。因此,抑制关键炎症介质已成为一种很有前途的治疗方法。血栓素A2 (TxA2)、肿瘤坏死因子α (TNF-α)和白细胞介素6 (IL-6)是在调节免疫反应和维持炎症中的作用已被彻底研究的介质;因此,靶向这些介质提供了巨大的治疗潜力。近年来,杂环类化合物因其结构多样、具有广泛的生物活性而受到广泛关注,尤其是吡啶嗪和吡啶嗪酮衍生物。这些支架通过限制TxA2的产生、减少TNF-α的释放和破坏IL-6信号传导,在调节炎症途径方面显示出显著的有效性。本文综述了吡嗪和吡嗪酮类化合物作为潜在抗炎剂的研究进展。它强调了传统和当前在其发展中使用的合成策略,并探讨了它们在关键炎症靶点方面的作用机制。此外,该研究审查了最近的药理学评估和临床前结果,为这些物质的药用提供了见解。展望了未来的研究方向,强调了进一步的结构优化、体内验证和临床转化的必要性。总之,这些结果突出了吡啶嗪和吡啶嗪酮衍生物在开发高级抗炎药物方面的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pyridazine and Pyridazinone in Medicinal Chemistry: Synthesis and Antiinflammatory Pathways Targeting TxA2, TNF-α, and IL-6.

Inflammation is a fundamental biological reaction to harmful stimuli, which is crucial in the initiation and advancement of different diseases, including rheumatoid arthritis, cardiovascular conditions, neurological disorders such as Alzheimer's and Parkinson's, and multiple cancer types. Chronic inflammation, in particular, contributes to irreversible tissue damage and the progression of disease. Thus, the suppression of key inflammatory mediators has become a promising therapeutic approach. Thromboxane A2 (TxA2), tumor necrosis factor-alpha (TNF-α), and interleukin-6 (IL-6) are among the mediators that have been thoroughly investigated for their roles in regulating immune responses and sustaining inflammation; therefore, targeting these mediators offers substantial therapeutic potential. In recent years, significant attention has been focused on heterocyclic compounds, especially pyridazine and pyridazinone derivatives, owing to their structural diversity and extensive biological activity. These scaffolds have shown significant effectiveness in regulating inflammatory pathways by limiting TxA2 production, reducing TNF-α release, and disrupting IL-6 signaling. This review presents a comprehensive overview of pyridazine and pyridazinone-based compounds as potential anti-inflammatory agents. It highlights both traditional and current synthetic strategies used in their development and explores their mechanisms of action with respect to key inflammatory targets. Additionally, the study examines recent pharmacological assessments and preclinical results, offering insights into the medicinal uses of these substances. A brief perspective on future research directions is also included, emphasizing the need for further structural optimization, in vivo validation, and clinical translation. Collectively, these results highlight the potential of pyridazine and pyridazinone derivatives in the development of advanced anti-inflammatory pharmaceuticals.

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来源期刊
CiteScore
7.80
自引率
0.00%
发文量
231
审稿时长
6 months
期刊介绍: The aim of Mini-Reviews in Medicinal Chemistry is to publish short reviews on the important recent developments in medicinal chemistry and allied disciplines. Mini-Reviews in Medicinal Chemistry covers all areas of medicinal chemistry including developments in rational drug design, synthetic chemistry, bioorganic chemistry, high-throughput screening, combinatorial chemistry, drug targets, and natural product research and structure-activity relationship studies. Mini-Reviews in Medicinal Chemistry is an essential journal for every medicinal and pharmaceutical chemist who wishes to be kept informed and up-to-date with the latest and most important developments.
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