p38 MAP 激酶抑制剂的历程:从治疗炎症性疾病的工作台到病床旁

IF 6 2区 医学 Q1 CHEMISTRY, MEDICINAL European Journal of Medicinal Chemistry Pub Date : 2024-10-11 DOI:10.1016/j.ejmech.2024.116950
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引用次数: 0

摘要

p38 丝裂原活化蛋白激酶 (MAPK) 通路在调节炎症反应中起着关键作用,已成为开发小分子抑制剂治疗炎症性疾病的关键靶点。在关节炎,尤其是类风湿性关节炎(RA)中,p38 MAPK 通路通过促进促炎细胞因子的产生,导致慢性炎症和关节破坏。临床前研究表明,靶向 p38 MAPK 通路的小分子抑制剂前景广阔,具有减轻炎症和保护关节完整性的潜力。靶向这一通路为缓解炎症提供了一种新的治疗方法。本综述追溯了 p38 MAP 激酶抑制剂从最初的实验室研究到临床候选药物的演变过程,强调了其显著改变炎症性疾病治疗方法的潜力。
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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The journey of p38 MAP kinase inhibitors: From bench to bedside in treating inflammatory diseases
The p38 mitogen-activated protein kinase (MAPK) pathway is pivotal in regulating inflammatory responses and has emerged as a key target for the development of small-molecule inhibitors aimed at treating inflammatory diseases. In arthritis, especially rheumatoid arthritis (RA), the p38 MAPK pathway contributes to chronic inflammation and joint destruction by promoting the production of pro-inflammatory cytokines. Preclinical studies have shown that small-molecule inhibitors targeting the p38 MAPK pathway hold significant promise, exhibiting the potential to reduce inflammation and preserve joint integrity. Targeting this pathway presents a novel therapeutic approach to mitigating inflammation. This review traces the evolution of p38 MAP kinase inhibitors from initial laboratory studies to clinical candidates, underscoring their potential to significantly alter the treatment approach for inflammatory diseases.
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来源期刊
CiteScore
11.70
自引率
9.00%
发文量
863
审稿时长
29 days
期刊介绍: The European Journal of Medicinal Chemistry is a global journal that publishes studies on all aspects of medicinal chemistry. It provides a medium for publication of original papers and also welcomes critical review papers. A typical paper would report on the organic synthesis, characterization and pharmacological evaluation of compounds. Other topics of interest are drug design, QSAR, molecular modeling, drug-receptor interactions, molecular aspects of drug metabolism, prodrug synthesis and drug targeting. The journal expects manuscripts to present the rational for a study, provide insight into the design of compounds or understanding of mechanism, or clarify the targets.
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