• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

异吲哚酮杂化物及其生物学特性的综述。

A survey of isatin hybrids and their biological properties.

作者信息

Shu Vanessa Asoh, Eni Donatus Bekindaka, Ntie-Kang Fidele

机构信息

Center for Drug Discovery, Faculty of Science, University of Buea, Buea, Cameroon.

Department of Chemistry, Faculty of Science, University of Buea, Buea, Cameroon.

出版信息

Mol Divers. 2025 Apr;29(2):1737-1760. doi: 10.1007/s11030-024-10883-z. Epub 2024 Jun 4.

DOI:10.1007/s11030-024-10883-z
PMID:38833124
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11909063/
Abstract

The emergence of diverse infections worldwide, which is a serious global threat to human existence, necessitates the urgent development of novel therapeutic candidates that can combat these diseases with efficacy. Molecular hybridization has been established as an efficient technique in designing bioactive molecules capable of fighting infections. Isatin, a core nucleus of an array of compounds with diverse biological properties can be modified at different positions leading to the creation of novel drug targets, is an active area of medicinal chemistry. This review containing published articles from 2005 to 2022 highlights isatin hybrids which have been synthesized and reported in the literature alongside a discussion on their biological properties. The enriched structure-activity relationship studies discussed provides insights for the rational design of novel isatin hybrids with tailored biological properties as effective therapeutic candidates inspired by nature.

摘要

全球范围内各种感染的出现对人类生存构成了严重的全球威胁,因此迫切需要开发能够有效对抗这些疾病的新型治疗候选药物。分子杂交已被确立为设计能够对抗感染的生物活性分子的有效技术。异吲哚酮是一系列具有多种生物学特性的化合物的核心结构,可在不同位置进行修饰以产生新的药物靶点,这是药物化学的一个活跃领域。这篇综述涵盖了2005年至2022年发表的文章,重点介绍了文献中已合成并报道的异吲哚酮杂化物,并讨论了它们的生物学特性。所讨论的丰富的构效关系研究为合理设计具有定制生物学特性的新型异吲哚酮杂化物提供了见解,这些杂化物可作为受自然启发的有效治疗候选药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c6a/11909063/b5d4d7918c40/11030_2024_10883_Fig24_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c6a/11909063/e8af8e054273/11030_2024_10883_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c6a/11909063/e5ac637bca1c/11030_2024_10883_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c6a/11909063/7f964a9ca6b8/11030_2024_10883_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c6a/11909063/1ecd79da40ea/11030_2024_10883_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c6a/11909063/9bc76ae30c85/11030_2024_10883_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c6a/11909063/361ded7c90b7/11030_2024_10883_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c6a/11909063/ad42924ae2c7/11030_2024_10883_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c6a/11909063/ad2d69f6a67c/11030_2024_10883_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c6a/11909063/02230e5f42ef/11030_2024_10883_Fig9_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c6a/11909063/283c2fbc3329/11030_2024_10883_Fig10_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c6a/11909063/cbb241adc38d/11030_2024_10883_Fig11_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c6a/11909063/16f206bf8d6a/11030_2024_10883_Fig12_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c6a/11909063/65948646f4c3/11030_2024_10883_Fig13_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c6a/11909063/b8e6dfb17dec/11030_2024_10883_Fig14_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c6a/11909063/bd66b3019e10/11030_2024_10883_Fig15_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c6a/11909063/c31ca4a37433/11030_2024_10883_Fig16_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c6a/11909063/fbe0ccb5ab27/11030_2024_10883_Fig17_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c6a/11909063/531d88909e8b/11030_2024_10883_Fig18_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c6a/11909063/e668ea87db62/11030_2024_10883_Fig19_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c6a/11909063/e176855bba31/11030_2024_10883_Fig20_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c6a/11909063/d61843a4a95a/11030_2024_10883_Fig21_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c6a/11909063/5f6452123dad/11030_2024_10883_Fig22_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c6a/11909063/4ecf92c1ffd4/11030_2024_10883_Fig23_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c6a/11909063/b5d4d7918c40/11030_2024_10883_Fig24_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c6a/11909063/e8af8e054273/11030_2024_10883_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c6a/11909063/e5ac637bca1c/11030_2024_10883_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c6a/11909063/7f964a9ca6b8/11030_2024_10883_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c6a/11909063/1ecd79da40ea/11030_2024_10883_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c6a/11909063/9bc76ae30c85/11030_2024_10883_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c6a/11909063/361ded7c90b7/11030_2024_10883_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c6a/11909063/ad42924ae2c7/11030_2024_10883_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c6a/11909063/ad2d69f6a67c/11030_2024_10883_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c6a/11909063/02230e5f42ef/11030_2024_10883_Fig9_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c6a/11909063/283c2fbc3329/11030_2024_10883_Fig10_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c6a/11909063/cbb241adc38d/11030_2024_10883_Fig11_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c6a/11909063/16f206bf8d6a/11030_2024_10883_Fig12_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c6a/11909063/65948646f4c3/11030_2024_10883_Fig13_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c6a/11909063/b8e6dfb17dec/11030_2024_10883_Fig14_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c6a/11909063/bd66b3019e10/11030_2024_10883_Fig15_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c6a/11909063/c31ca4a37433/11030_2024_10883_Fig16_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c6a/11909063/fbe0ccb5ab27/11030_2024_10883_Fig17_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c6a/11909063/531d88909e8b/11030_2024_10883_Fig18_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c6a/11909063/e668ea87db62/11030_2024_10883_Fig19_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c6a/11909063/e176855bba31/11030_2024_10883_Fig20_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c6a/11909063/d61843a4a95a/11030_2024_10883_Fig21_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c6a/11909063/5f6452123dad/11030_2024_10883_Fig22_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c6a/11909063/4ecf92c1ffd4/11030_2024_10883_Fig23_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c6a/11909063/b5d4d7918c40/11030_2024_10883_Fig24_HTML.jpg

相似文献

1
A survey of isatin hybrids and their biological properties.异吲哚酮杂化物及其生物学特性的综述。
Mol Divers. 2025 Apr;29(2):1737-1760. doi: 10.1007/s11030-024-10883-z. Epub 2024 Jun 4.
2
Indole/isatin-containing hybrids as potential antibacterial agents.吲哚/色胺酮类杂合化合物作为潜在的抗菌剂。
Arch Pharm (Weinheim). 2020 Oct;353(10):e2000143. doi: 10.1002/ardp.202000143. Epub 2020 Jul 15.
3
Moxifloxacin-isatin Hybrids Tethered by 1,2,3-triazole and their Anticancer Activities.通过1,2,3-三唑连接的莫西沙星-异吲哚酮杂合物及其抗癌活性。
Curr Top Med Chem. 2020;20(16):1461-1467. doi: 10.2174/1568026620666200128144825.
4
Isatin-azole hybrids and their anticancer activities.靛红-唑类杂合体及其抗癌活性。
Arch Pharm (Weinheim). 2020 Jan;353(1):e1900272. doi: 10.1002/ardp.201900272. Epub 2019 Nov 6.
5
A Comprehensive Review of the Diverse Spectrum Activity of 1,2,3-Triazole-linked Isatin Hybrids.1,2,3-三唑连接的靛红杂合体的多样化光谱活性的综合评价。
Chem Biodivers. 2024 Apr;21(4):e202301612. doi: 10.1002/cbdv.202301612. Epub 2024 Mar 14.
6
A Mini Review on Pharmacological Significance of Isatin-1,2,3-Triazole Hybrids.关于色胺-1,2,3-三唑杂合体的药理学意义的小型综述。
Curr Top Med Chem. 2023;23(10):833-847. doi: 10.2174/1568026623666230202160925.
7
The Antibacterial Activity of Isatin Hybrids.靛红杂合体的抗菌活性。
Curr Top Med Chem. 2022;22(1):25-40. doi: 10.2174/1568026621666211116090456.
8
Isatin Hybrids and Their Pharmacological Investigations.靛红杂合体及其药理学研究。
Mini Rev Med Chem. 2021;21(10):1182-1225. doi: 10.2174/1389557520999201209213029.
9
Recent advances in isatin hybrids as potential anticancer agents.色胺酮杂合体作为潜在抗癌剂的最新进展。
Arch Pharm (Weinheim). 2020 Mar;353(3):e1900367. doi: 10.1002/ardp.201900367. Epub 2020 Jan 21.
10
Fluoroquinolone-isatin hybrids and their biological activities.氟喹诺酮-靛红杂合体及其生物活性。
Eur J Med Chem. 2019 Jan 15;162:396-406. doi: 10.1016/j.ejmech.2018.11.032. Epub 2018 Nov 12.

引用本文的文献

1
Epoxy-Functionalized Isatin Derivative: Synthesis, Computational Evaluation, and Antibacterial Analysis.环氧官能化异吲哚酮衍生物:合成、计算评估及抗菌分析
Antibiotics (Basel). 2025 Jun 9;14(6):595. doi: 10.3390/antibiotics14060595.
2
Synthesis, Biological Evaluation, and Molecular Docking Studies of Novel Coumarin-Triazole-Isatin Hybrids as Selective Butyrylcholinesterase Inhibitors.新型香豆素-三唑-异吲哚酮杂化物作为选择性丁酰胆碱酯酶抑制剂的合成、生物学评价及分子对接研究
Molecules. 2025 May 11;30(10):2121. doi: 10.3390/molecules30102121.
3
In Vitro Enzymatic and Computational Assessments of Pyrazole-Isatin and Pyrazole-Indole Conjugates as Anti-Diabetic, Anti-Arthritic, and Anti-Inflammatory Agents.

本文引用的文献

1
Exploring diverse frontiers: Advancements of bioactive 4-aminoquinoline-based molecular hybrids in targeted therapeutics and beyond.探索多样的前沿领域:基于生物活性 4-氨基喹啉的分子杂合体在靶向治疗及其他领域的进展。
Eur J Med Chem. 2024 Jan 15;264:116043. doi: 10.1016/j.ejmech.2023.116043. Epub 2023 Dec 14.
2
Triazole hybrid compounds: A new frontier in malaria treatment.三唑杂合物:疟疾治疗的新前沿。
Eur J Med Chem. 2023 Nov 5;259:115694. doi: 10.1016/j.ejmech.2023.115694. Epub 2023 Jul 29.
3
Recent developments in antimalarial activities of 4-aminoquinoline derivatives.
吡唑-异吲哚酮和吡唑-吲哚共轭物作为抗糖尿病、抗关节炎和抗炎剂的体外酶促和计算评估
Pharmaceutics. 2025 Feb 23;17(3):293. doi: 10.3390/pharmaceutics17030293.
4
From Structure to Function: Isatin Derivatives as a Promising Class of Antiviral Agents.从结构到功能:异吲哚酮衍生物作为一类有前景的抗病毒药物
Curr Drug Targets. 2025;26(7):470-488. doi: 10.2174/0113894501352560250115054156.
5
Novel isatin conjugates endowed with analgesic and anti-inflammatory properties: design, synthesis and biological evaluation.具有镇痛和抗炎特性的新型异吲哚酮共轭物:设计、合成及生物学评价
Future Med Chem. 2025 Jan;17(1):59-73. doi: 10.1080/17568919.2024.2437981. Epub 2024 Dec 16.
6
Biological Activity Evaluation of Phenolic Isatin-3-Hydrazones Containing a Quaternary Ammonium Center of Various Structures.各种结构季铵中心含酚异吲哚-3-腙的生物活性评价。
Int J Mol Sci. 2024 Oct 17;25(20):11130. doi: 10.3390/ijms252011130.
7
Isatin Bis-Imidathiazole Hybrids Identified as FtsZ Inhibitors with On-Target Activity Against .异吲哚酮双咪唑噻唑杂化物被鉴定为具有针对……的靶向活性的FtsZ抑制剂。
Antibiotics (Basel). 2024 Oct 19;13(10):992. doi: 10.3390/antibiotics13100992.
4-氨基喹啉衍生物抗疟活性的最新研究进展。
Eur J Med Chem. 2023 Aug 5;256:115458. doi: 10.1016/j.ejmech.2023.115458. Epub 2023 May 5.
4
A Mini Review on Isatin, an Anticancer Scaffold with Potential Activities against Neglected Tropical Diseases (NTDs).关于异吲哚酮的综述:一种具有抗被忽视热带病(NTDs)潜在活性的抗癌骨架
Pharmaceuticals (Basel). 2022 Apr 27;15(5):536. doi: 10.3390/ph15050536.
5
Promising bactericidal approach of dihydrazone analogues against bio-film forming Gram-negative bacteria and molecular mechanistic studies.双腙类似物对形成生物膜的革兰氏阴性菌的有前景的杀菌方法及分子机制研究
RSC Adv. 2018 Jan 31;8(10):5473-5483. doi: 10.1039/c7ra13661g. eCollection 2018 Jan 29.
6
Sulfonamide derivatives as potential anti-cancer agents and their SARs elucidation.磺胺衍生物作为有潜力的抗癌药物及其构效关系的阐明。
Eur J Med Chem. 2021 Dec 15;226:113837. doi: 10.1016/j.ejmech.2021.113837. Epub 2021 Sep 8.
7
Novel piperazine based compounds as potential inhibitors for SARS-CoV-2 Protease Enzyme: Synthesis and molecular docking study.新型基于哌嗪的化合物作为严重急性呼吸综合征冠状病毒2蛋白酶的潜在抑制剂:合成与分子对接研究
J Mol Struct. 2021 Dec 5;1245:131020. doi: 10.1016/j.molstruc.2021.131020. Epub 2021 Jul 4.
8
Chalcone Derivatives: Role in Anticancer Therapy.查尔酮衍生物:在抗癌治疗中的作用。
Biomolecules. 2021 Jun 16;11(6):894. doi: 10.3390/biom11060894.
9
Structural improvement of new thiazolyl-isatin derivatives produces potent and selective trypanocidal and leishmanicidal compounds.新型噻唑基异吲哚酮衍生物的结构改进产生了高效且具选择性的杀锥虫和杀利什曼原虫化合物。
Chem Biol Interact. 2021 Aug 25;345:109561. doi: 10.1016/j.cbi.2021.109561. Epub 2021 Jun 24.
10
Design, synthesis, studies and evaluation of isatin-pyridine oximes hybrids as novel acetylcholinesterase reactivators.设计、合成、研究和评价色酮-吡啶肟类化合物作为新型乙酰胆碱酯酶重激活剂。
J Enzyme Inhib Med Chem. 2021 Dec;36(1):1370-1377. doi: 10.1080/14756366.2021.1916009.