Small-molecule inhibitors of GSK3β: Therapeutic potential and structure-activity relationship in multiple systems.

IF 4.7 2区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Jiale Wang, Dan Wang, Fanfei Liu, Yan Ji, Xuling Peng, Gen Li
{"title":"Small-molecule inhibitors of GSK3β: Therapeutic potential and structure-activity relationship in multiple systems.","authors":"Jiale Wang, Dan Wang, Fanfei Liu, Yan Ji, Xuling Peng, Gen Li","doi":"10.1016/j.bioorg.2025.109053","DOIUrl":null,"url":null,"abstract":"<p><p>Protein kinases (PK) are a class of enzymes that phosphorylate protein molecules and play crucial roles in various biological processes, including cell proliferation, apoptosis, cell cycle regulation, differentiation, and signalling pathways. As essential components of the human body, they have become a major focus in drug development. Consequently, protein kinase inhibitors have emerged as a prominent area of clinical medicine. In recent years, small molecule inhibitors targeting glycogen synthase kinase-3 (GSK3), a representative protein kinase, have been increasingly used in clinical settings. This review comprehensively summarises 26 GSK3β small molecule inhibitors, categorizing them by their therapeutic applications across nine major systemic diseases. It also summarises the structure-activity relationships of several common compounds and examines, through molecular docking, the protein-binding capabilities of highly selective and specific inhibitors, many of which are already in clinical use or nearing clinical entry. By proposing promising research directions and establishing a solid foundation, this work paves the way for developing GSK3β small molecule inhibitors tailored to diverse diseases.</p>","PeriodicalId":257,"journal":{"name":"Bioorganic Chemistry","volume":"165 ","pages":"109053"},"PeriodicalIF":4.7000,"publicationDate":"2025-09-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Bioorganic Chemistry","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1016/j.bioorg.2025.109053","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Protein kinases (PK) are a class of enzymes that phosphorylate protein molecules and play crucial roles in various biological processes, including cell proliferation, apoptosis, cell cycle regulation, differentiation, and signalling pathways. As essential components of the human body, they have become a major focus in drug development. Consequently, protein kinase inhibitors have emerged as a prominent area of clinical medicine. In recent years, small molecule inhibitors targeting glycogen synthase kinase-3 (GSK3), a representative protein kinase, have been increasingly used in clinical settings. This review comprehensively summarises 26 GSK3β small molecule inhibitors, categorizing them by their therapeutic applications across nine major systemic diseases. It also summarises the structure-activity relationships of several common compounds and examines, through molecular docking, the protein-binding capabilities of highly selective and specific inhibitors, many of which are already in clinical use or nearing clinical entry. By proposing promising research directions and establishing a solid foundation, this work paves the way for developing GSK3β small molecule inhibitors tailored to diverse diseases.

GSK3β小分子抑制剂:在多系统中的治疗潜力和构效关系
蛋白激酶(PK)是一类磷酸化蛋白分子的酶,在多种生物过程中发挥重要作用,包括细胞增殖、细胞凋亡、细胞周期调节、分化和信号通路。作为人体的重要组成部分,它们已成为药物开发的主要焦点。因此,蛋白激酶抑制剂已成为临床医学的一个突出领域。近年来,靶向糖原合成酶激酶-3 (GSK3)的小分子抑制剂越来越多地应用于临床。本文综合总结了26种GSK3β小分子抑制剂,并根据其在9种主要系统性疾病中的治疗应用对其进行了分类。它还总结了几种常见化合物的结构-活性关系,并通过分子对接检查了高选择性和特异性抑制剂的蛋白质结合能力,其中许多抑制剂已经在临床使用或即将进入临床。本研究提出了有前景的研究方向,奠定了坚实的基础,为开发针对多种疾病的GSK3β小分子抑制剂铺平了道路。
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
Bioorganic Chemistry
Bioorganic Chemistry 生物-生化与分子生物学
CiteScore
9.70
自引率
3.90%
发文量
679
审稿时长
31 days
期刊介绍: Bioorganic Chemistry publishes research that addresses biological questions at the molecular level, using organic chemistry and principles of physical organic chemistry. The scope of the journal covers a range of topics at the organic chemistry-biology interface, including: enzyme catalysis, biotransformation and enzyme inhibition; nucleic acids chemistry; medicinal chemistry; natural product chemistry, natural product synthesis and natural product biosynthesis; antimicrobial agents; lipid and peptide chemistry; biophysical chemistry; biological probes; bio-orthogonal chemistry and biomimetic chemistry. For manuscripts dealing with synthetic bioactive compounds, the Journal requires that the molecular target of the compounds described must be known, and must be demonstrated experimentally in the manuscript. For studies involving natural products, if the molecular target is unknown, some data beyond simple cell-based toxicity studies to provide insight into the mechanism of action is required. Studies supported by molecular docking are welcome, but must be supported by experimental data. The Journal does not consider manuscripts that are purely theoretical or computational in nature. The Journal publishes regular articles, short communications and reviews. Reviews are normally invited by Editors or Editorial Board members. Authors of unsolicited reviews should first contact an Editor or Editorial Board member to determine whether the proposed article is within the scope of the Journal.
×
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