Pyrazinone Derivatives in Medicinal Chemistry: SAR Insights and Emerging Therapeutic Applications.

IF 2.5 4区 医学 Q3 CHEMISTRY, MEDICINAL
Neetu Agrawal, Priya Kushwah, Shilpi Pathak
{"title":"Pyrazinone Derivatives in Medicinal Chemistry: SAR Insights and Emerging Therapeutic Applications.","authors":"Neetu Agrawal, Priya Kushwah, Shilpi Pathak","doi":"10.2174/0115734064519985260907100959","DOIUrl":null,"url":null,"abstract":"<p><p>Pyrazinones remain a comparatively underexplored class of nitrogen heterocycles, despite their recurrence in bioactive natural products and their emergence as a privileged scaffold engaging viral polymerases, kinases, proteases, and G-protein-coupled receptors. Unlike prior reviews, typically confined to a single therapeutic class or to synthetic methodology alone, this review is the first to integrate the natural occurrence, synthetic access, structure-activity relationships, and clinical translatability of pyrazinone derivatives within a single framework, and in doing so identifies structural determinants that recur across nine otherwise unrelated therapeutic areas rather than being specific to any one target. Three such determinants emerge consistently: halogenation at C-3/C-5 improves potency and metabolic stability across kinase, protease, and antifungal series alike; hydrogen-bond donor/acceptor substituents are well tolerated at N-1/C-6 but sharply disruptive when placed adjacent to the lactam at N-3/C-2, reflecting a conserved role for this region in target recognition; and lipophilic extensions at N-1/C-6 raise cellular potency at the recurring cost of selectivity. Inherent limitations are critically examined, including lactam-lactim tautomeric equilibria, challenges in regioselective functionalization, and the trade-off between aqueous solubility and membrane permeability, alongside ADMET considerations such as metabolic stability and off-target toxicity. A central finding of this synthesis is that, across almost every therapeutic class surveyed, reported activity data remain confined to in vitro measurements, without matching pharmacokinetic or translatability data, indicating that the principal bottleneck to clinical progression is evaluative rather than a shortage of potent chemical matter. Clinically relevant examples, including the antiviral drug favipiravir and the clinical-stage candidates RWJ-671818 and BI 730357, nonetheless demonstrate that this bottleneck is surmountable and illustrate the scaffold's translational potential. Recent advances, emerging resistance mechanisms, and future directions, including multi-target-directed ligand design, structure-based optimization, and AI-assisted drug design, are also discussed. By consolidating this fragmented literature into a single cross-scaffold structure-activity framework and by pinpointing where pharmacokinetic and toxicological characterization, rather than potency optimization, most limits clinical translation, this review provides a practical, decisionoriented resource for researchers designing the next generation of pyrazinone-based therapeutics.</p>","PeriodicalId":18382,"journal":{"name":"Medicinal Chemistry","volume":" ","pages":""},"PeriodicalIF":2.5000,"publicationDate":"2026-09-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Medicinal Chemistry","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.2174/0115734064519985260907100959","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}
引用次数: 0

Abstract

Pyrazinones remain a comparatively underexplored class of nitrogen heterocycles, despite their recurrence in bioactive natural products and their emergence as a privileged scaffold engaging viral polymerases, kinases, proteases, and G-protein-coupled receptors. Unlike prior reviews, typically confined to a single therapeutic class or to synthetic methodology alone, this review is the first to integrate the natural occurrence, synthetic access, structure-activity relationships, and clinical translatability of pyrazinone derivatives within a single framework, and in doing so identifies structural determinants that recur across nine otherwise unrelated therapeutic areas rather than being specific to any one target. Three such determinants emerge consistently: halogenation at C-3/C-5 improves potency and metabolic stability across kinase, protease, and antifungal series alike; hydrogen-bond donor/acceptor substituents are well tolerated at N-1/C-6 but sharply disruptive when placed adjacent to the lactam at N-3/C-2, reflecting a conserved role for this region in target recognition; and lipophilic extensions at N-1/C-6 raise cellular potency at the recurring cost of selectivity. Inherent limitations are critically examined, including lactam-lactim tautomeric equilibria, challenges in regioselective functionalization, and the trade-off between aqueous solubility and membrane permeability, alongside ADMET considerations such as metabolic stability and off-target toxicity. A central finding of this synthesis is that, across almost every therapeutic class surveyed, reported activity data remain confined to in vitro measurements, without matching pharmacokinetic or translatability data, indicating that the principal bottleneck to clinical progression is evaluative rather than a shortage of potent chemical matter. Clinically relevant examples, including the antiviral drug favipiravir and the clinical-stage candidates RWJ-671818 and BI 730357, nonetheless demonstrate that this bottleneck is surmountable and illustrate the scaffold's translational potential. Recent advances, emerging resistance mechanisms, and future directions, including multi-target-directed ligand design, structure-based optimization, and AI-assisted drug design, are also discussed. By consolidating this fragmented literature into a single cross-scaffold structure-activity framework and by pinpointing where pharmacokinetic and toxicological characterization, rather than potency optimization, most limits clinical translation, this review provides a practical, decisionoriented resource for researchers designing the next generation of pyrazinone-based therapeutics.

吡嗪酮衍生物在药物化学:SAR的见解和新兴的治疗应用。
尽管吡嗪酮类化合物在具有生物活性的天然产物中反复出现,并且作为一种特殊的支架与病毒聚合酶、激酶、蛋白酶和g蛋白偶联受体结合,但它们仍然是一类相对未被充分开发的氮杂环化合物。与以往的综述不同,以往的综述通常局限于单一的治疗类别或单独的合成方法,本综述首次将吡嗪酮衍生物的自然发生、合成途径、结构-活性关系和临床可翻译性整合在一个框架内,并通过这样做确定了在九个其他不相关的治疗领域中反复出现的结构决定因素,而不是特定于任何一个靶标。三个这样的决定因素一致地出现:C-3/C-5的卤化提高了激酶、蛋白酶和抗真菌系列的效力和代谢稳定性;氢键供体/受体取代基在N-1/C-6位点耐受性良好,但在N-3/C-2位点与内酰胺相邻时具有明显的破坏作用,反映了该区域在目标识别中的保守作用;在N-1/C-6上的亲脂性延伸提高了细胞效力,但反复付出了选择性的代价。固有的局限性被严格审查,包括内酰胺-乳酸互变异构平衡,区域选择性功能化的挑战,水溶解度和膜渗透性之间的权衡,以及ADMET的考虑,如代谢稳定性和脱靶毒性。这项综合研究的一个中心发现是,在几乎所有被调查的治疗类别中,报告的活性数据仍然局限于体外测量,没有匹配的药代动力学或可翻译性数据,这表明临床进展的主要瓶颈是评估性的,而不是缺乏有效的化学物质。然而,包括抗病毒药物favipiravir和临床阶段候选药物RWJ-671818和BI 730357在内的临床相关实例表明,这一瓶颈是可以克服的,并说明了支架的转化潜力。本文还讨论了近年来的研究进展、新出现的耐药机制和未来的发展方向,包括多靶点定向配体设计、基于结构的优化和人工智能辅助药物设计。通过将这些零散的文献整合到一个单一的交叉支架结构-活性框架中,并通过确定药代动力学和毒理学特征,而不是效价优化,大多数限制临床翻译,本综述为研究人员设计下一代吡嗪酮为基础的治疗方法提供了实用的、面向决策的资源。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Medicinal Chemistry
Medicinal Chemistry 医学-医药化学
CiteScore
4.30
自引率
4.30%
发文量
109
审稿时长
12 months
期刊介绍: Aims & Scope Medicinal Chemistry a peer-reviewed journal, aims to cover all the latest outstanding developments in medicinal chemistry and rational drug design. The journal publishes original research, mini-review articles and guest edited thematic issues covering recent research and developments in the field. Articles are published rapidly by taking full advantage of Internet technology for both the submission and peer review of manuscripts. Medicinal Chemistry is an essential journal for all involved in drug design and discovery.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书