2-Indolinone: An Anticancer Scaffold, Overview of the Studies and Approaches (2017–2024)

IF 1.9 4区 化学 Q3 CHEMISTRY, MULTIDISCIPLINARY ChemistrySelect Pub Date : 2025-02-05 DOI:10.1002/slct.202405357
Taha Koulani, Asu Busra Temizer, Prof. Dr. Nilgun Karali
{"title":"2-Indolinone: An Anticancer Scaffold, Overview of the Studies and Approaches (2017–2024)","authors":"Taha Koulani,&nbsp;Asu Busra Temizer,&nbsp;Prof. Dr. Nilgun Karali","doi":"10.1002/slct.202405357","DOIUrl":null,"url":null,"abstract":"<p>2-Indolinone is a versatile scaffold that has been the central moiety in the structure of various drugs. Since the introduction of sunitinib malate, 2-indolinones have been a principal pharmacophoric building block in many drug discovery studies, especially in the last few years. Compounds bearing the 2-indolinone ring system have shown various therapeutic effects, including but not limited to, antidiabetic, antioxidant, anti-inflammatory, anti-HIV, antimicrobial, antipsychotic, antiparkinson, and anticancer activities. Considering that cancer is among the major global causes of death, the antiproliferative activities of these compounds have been the goal of numerous studies. The present review presents an overview of the approaches and advances made during the last eight years (2017–2024) regarding the development of 2-indolinone derivatives within the field of anticancer drug discovery. The derivates gathered herein are classified according to the therapeutic target of the developed compounds, and notable structure-activity relationships as well as significant molecular docking interactions with the target enzymes have been highlighted in each instance. Accordingly, special attention has been paid to reporting derivatives with superior antiproliferative and enzymatic inhibitory effects that have emerged as lead compounds within each respective study.</p>","PeriodicalId":146,"journal":{"name":"ChemistrySelect","volume":"10 5","pages":""},"PeriodicalIF":1.9000,"publicationDate":"2025-02-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ChemistrySelect","FirstCategoryId":"92","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/slct.202405357","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

Abstract

2-Indolinone is a versatile scaffold that has been the central moiety in the structure of various drugs. Since the introduction of sunitinib malate, 2-indolinones have been a principal pharmacophoric building block in many drug discovery studies, especially in the last few years. Compounds bearing the 2-indolinone ring system have shown various therapeutic effects, including but not limited to, antidiabetic, antioxidant, anti-inflammatory, anti-HIV, antimicrobial, antipsychotic, antiparkinson, and anticancer activities. Considering that cancer is among the major global causes of death, the antiproliferative activities of these compounds have been the goal of numerous studies. The present review presents an overview of the approaches and advances made during the last eight years (2017–2024) regarding the development of 2-indolinone derivatives within the field of anticancer drug discovery. The derivates gathered herein are classified according to the therapeutic target of the developed compounds, and notable structure-activity relationships as well as significant molecular docking interactions with the target enzymes have been highlighted in each instance. Accordingly, special attention has been paid to reporting derivatives with superior antiproliferative and enzymatic inhibitory effects that have emerged as lead compounds within each respective study.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
求助全文
约1分钟内获得全文 去求助
来源期刊
ChemistrySelect
ChemistrySelect Chemistry-General Chemistry
CiteScore
3.30
自引率
4.80%
发文量
1809
审稿时长
1.6 months
期刊介绍: ChemistrySelect is the latest journal from ChemPubSoc Europe and Wiley-VCH. It offers researchers a quality society-owned journal in which to publish their work in all areas of chemistry. Manuscripts are evaluated by active researchers to ensure they add meaningfully to the scientific literature, and those accepted are processed quickly to ensure rapid online publication.
期刊最新文献
2-Indolinone: An Anticancer Scaffold, Overview of the Studies and Approaches (2017–2024) Theoretical Study on Interaction of Fluorine-Containing Compounds Involving the Fourth Period Metal Elements With N-base: Comparison With Halogen Bonds Green Synthesis of Pachyrhizus erosus-Derived Carbon Aerogels for Adsorption of Oil and Organic Solvents and Investigation of Their Electrochemical Properties Aminocatalytic, Stereoselective Synthesis of Tetrahydrocarbazole Spiropyrazolones via Remote [4 + 2] Annulation of Indole Tethered Enal With Olefinic Pyrazolones Recent Developments in Catalytic CO2-to-Ethanol Conversion Technologies
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1