噻吩衍生物作为COX和LOX抑制剂的合成方法和治疗潜力。

IF 3.4 4区 医学 Q3 CHEMISTRY, MEDICINAL
Future medicinal chemistry Pub Date : 2025-09-01 Epub Date: 2025-09-07 DOI:10.1080/17568919.2025.2557184
Suman Lata, Shivani Bharti, Komalpreet Kaur, Amit Pandit, Vikrant Abbot
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引用次数: 0

摘要

噻吩衍生物由于其作为抗炎剂的潜力,最近获得了相当大的兴趣。它们的结构灵活性和与炎症过程中涉及的关键酶相互作用的能力使它们成为药物开发的有希望的候选者。本文综述了噻吩类化合物在环氧合氧酶(COX)和脂合氧酶(LOX)抑制剂方面的最新研究进展,重点介绍了噻吩类化合物的合成和疗效评价。它讨论了这些化合物的合成方法、构效关系(SAR)模式和生物活性,特别关注那些表现出双重COX/LOX抑制的化合物。通过巩固最近的发现,本综述旨在加强正在进行的开发更有效、更安全的抗炎药的努力,这些抗炎药利用噻吩作为核心支架。本文通过对谷歌Scholar、Web of Science、PubMed、Scopus等数据库2018 - 2025年的研究数据进行总结,旨在为新型先导分子的开发做出贡献,为未来的药物发现和炎症相关疾病的治疗创新提供有希望的途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synthetic approaches and therapeutic potential of thiophene derivatives as COX and LOX inhibitors.

Thiophene derivatives have gained considerable interest lately due to their potential as anti-inflammatory agents. Their structural flexibility and capacity to interact with key enzymes involved in inflammatory processes position them as promising candidates for drug development. This review provides a comprehensive overview of the latest research, focusing on the synthesis and therapeutic evaluation of thiophene-based compounds that act as inhibitors of cyclooxygenase (COX) and lipoxygenase (LOX) enzymes. It discusses synthetic methodologies, structure-activity relationship (SAR) patterns, and the biological activities of these compounds, with a particular focus on those demonstrating dual COX/LOX inhibition. By consolidating recent findings, the review aims to enhance ongoing efforts to develop more effective and safer anti-inflammatory agents that utilize thiophene as a core scaffold. By summarizing research data from 2018 to 2025 using databases such as Google Scholar, Web of Science, PubMed, and Scopus, this review article aims to contribute to the development of novel lead molecules, offer promising avenues for future drug discovery, and therapeutic innovation in inflammation-related diseases.

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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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