Therapeutic Potentials of Pyridine Derivatives, Highlighting the Synthetic Pathway, Biological Activity, and Structure-activity Relationship: A Mini- Review.

IF 3.3 3区 医学 Q2 CHEMISTRY, MEDICINAL
Muhammad Majed Abdin, Mustapha Suleiman, Syazwani Itri Amran, Helmi Mohammed Al-Maqtari, Sarkar M A Kawsar, Joazaizulfazli Jamalis
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引用次数: 0

Abstract

Heterocyclic compounds constitute the largest family in organic chemistry. Their potential to treat and deter various types of diseases renders them essential compounds. Moreover, their extensive implementations in drug discovery and development are significantly contributing to the current state of medicinal chemistry. Pyridine is one of the most fundamental heterocyclic compounds. Pyridine-based compounds are structurally diverse and have been utilized to tackle various challenges in pharmaceuticals and medicinal chemistry, providing novel approaches for enhanced health accomplishments. The main objective of this review is to comprehensively clarify the crucial role of pyridine derivatives in drug discovery between 2015 and 2025 by summarizing the various synthetic pathways and evaluating their therapeutic relevance. In addition, it highlights the outstanding pharmacological applications of pyridine-containing compounds across a broad range of therapeutic areas, such as oncology, infectious diseases, inflammatory disorders, oxidative stress-related conditions, metabolic disorders, and neurodegenerative diseases, emphasizing their prominence among clinically approved drugs. Furthermore, structure-activity relationship analyses are investigated to illustrate how particular substitutions, electronic effects, and positional modifications on the pyridine ring affect biological potency, selectivity, and pharmacokinetic behavior. Finally, by integrating synthetic approaches, biological evaluations, and structure-activity relationship insights, this review aims to support the rational design and optimization of more potent, selective, and safer pyridine- based therapeutic agents for future drug development.

吡啶衍生物的治疗潜力,重点是合成途径、生物活性和构效关系:综述。
杂环化合物是有机化学中最大的一类化合物。它们治疗和阻止各种疾病的潜力使它们成为必不可少的化合物。此外,它们在药物发现和开发中的广泛应用对药物化学的现状做出了重大贡献。吡啶是最基本的杂环化合物之一。吡啶基化合物结构多样,已被用于解决制药和药物化学中的各种挑战,为提高健康成就提供了新的途径。本综述的主要目的是通过总结各种合成途径并评估其治疗相关性,全面阐明2015年至2025年间吡啶衍生物在药物发现中的关键作用。此外,它还强调了含吡啶化合物在广泛治疗领域的杰出药理学应用,如肿瘤学、传染病、炎症性疾病、氧化应激相关疾病、代谢紊乱和神经退行性疾病,强调了它们在临床批准药物中的突出地位。此外,研究人员还研究了结构-活性关系分析,以说明吡啶环上的特定取代、电子效应和位置修饰如何影响生物效力、选择性和药代动力学行为。最后,通过综合合成方法、生物学评价和构效关系的见解,本文旨在为未来药物开发提供更有效、更有选择性和更安全的吡啶类治疗药物的合理设计和优化。
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
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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