• 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

咔唑基三环类化合物的抗癌活性研究综述。

A Review on the Anticancer Activity of Carbazole-based Tricyclic Compounds.

机构信息

Lab of Chemical Biology and Molecular Drug Design, College of Pharmaceutical Science, Zhejiang University of Technology, Hangzhou, 310014, China.

Institute of Drug Development & Chemical Biology, Zhejiang University of Technology, Hangzhou, 310014, China.

出版信息

Curr Med Chem. 2024;31(30):4826-4849. doi: 10.2174/0929867331666230825104254.

DOI:10.2174/0929867331666230825104254
PMID:37622700
Abstract

Cancers are a huge threat to human life and health. Every year, many people suffer and die from various cancers, and numerous resources have been used to combat cancer. Due to several disadvantages of anticancer agents, such as drug-induced side effects, drug resistance, etc., there are still wide gaps in their ability to conquer cancer. Therefore, there is an urgent need to discover and develop many novel chemotypes to suppress cancer. In this review, we mainly focus on the anticancer potency of two representative sorts of carbazole-based compounds: carboline derivatives and diazacarbazole derivatives. Diazacarbazole derivatives, which have not been fully explored yet, might bring us a new vision and a valuable opportunity for overcoming the enormous hurdle we are now facing in the cancer campaign. We also provide several synthetic approaches for constructing the critical skeletons of the carbazole-based tricyclic compounds.

摘要

癌症是对人类生命和健康的巨大威胁。每年,许多人因各种癌症而遭受痛苦和死亡,大量资源都被用于对抗癌症。由于抗癌药物存在一些缺点,如药物诱导的副作用、耐药性等,它们在攻克癌症方面的能力仍存在很大差距。因此,迫切需要发现和开发许多新型的化学结构来抑制癌症。在这篇综述中,我们主要关注两种具有代表性的咔唑类化合物的抗癌活性:卡洛啉衍生物和二氮杂咔唑衍生物。二氮杂咔唑衍生物尚未得到充分探索,可能为我们提供新的视角和克服癌症研究中面临的巨大障碍的宝贵机会。我们还提供了几种构建咔唑三环化合物关键骨架的合成方法。

相似文献

1
A Review on the Anticancer Activity of Carbazole-based Tricyclic Compounds.咔唑基三环类化合物的抗癌活性研究综述。
Curr Med Chem. 2024;31(30):4826-4849. doi: 10.2174/0929867331666230825104254.
2
Current status of carbazole hybrids as anticancer agents.咔唑杂化物作为抗癌剂的研究现状。
Eur J Med Chem. 2022 Feb 5;229:113999. doi: 10.1016/j.ejmech.2021.113999. Epub 2021 Nov 20.
3
Carbazole scaffolds in cancer therapy: a review from 2012 to 2018.咔唑骨架在癌症治疗中的应用:2012 年至 2018 年的综述。
J Enzyme Inhib Med Chem. 2019 Dec;34(1):1321-1346. doi: 10.1080/14756366.2019.1640692.
4
Biological potential of carbazole derivatives.咔唑衍生物的生物活性
Eur J Med Chem. 2015 Apr 13;94:405-26. doi: 10.1016/j.ejmech.2015.02.059. Epub 2015 Mar 3.
5
The anticancer activity of carbazole alkaloids.咔唑生物碱的抗癌活性。
Arch Pharm (Weinheim). 2022 Jan;355(1):e2100277. doi: 10.1002/ardp.202100277. Epub 2021 Sep 6.
6
Selective and effective anticancer agents: Synthesis, biological evaluation and structure-activity relationships of novel carbazole derivatives.选择性和有效的抗癌药物:新型咔唑衍生物的合成、生物评价和构效关系。
Bioorg Chem. 2021 Aug;113:104991. doi: 10.1016/j.bioorg.2021.104991. Epub 2021 May 18.
7
Synthesis and structure-activity relationship study of water-soluble carbazole sulfonamide derivatives as new anticancer agents.水溶性咔唑磺酰胺衍生物作为新型抗癌剂的合成及构效关系研究。
Eur J Med Chem. 2020 Apr 1;191:112181. doi: 10.1016/j.ejmech.2020.112181. Epub 2020 Feb 22.
8
Synthesis and biological evaluation of novel 3,9-substituted β-carboline derivatives as anticancer agents.新型3,9-取代β-咔啉衍生物作为抗癌剂的合成及生物学评价
Bioorg Med Chem Lett. 2015 Sep 15;25(18):3873-7. doi: 10.1016/j.bmcl.2015.07.058. Epub 2015 Jul 26.
9
Current perspective of natural alkaloid carbazole and its derivatives as antitumor agents.天然生物碱咔唑及其衍生物作为抗肿瘤药物的当前研究视角。
Anticancer Agents Med Chem. 2015;15(8):1049-65. doi: 10.2174/1871520615666150113105405.
10
Design, synthesis and biological evaluation of substituted 11H-benzo[a]carbazole-5-carboxamides as novel antitumor agents.取代 11H-苯并[a]咔唑-5-甲酰胺类化合物的设计、合成与生物评价作为新型抗肿瘤剂。
Eur J Med Chem. 2011 Dec;46(12):5878-84. doi: 10.1016/j.ejmech.2011.09.050. Epub 2011 Oct 4.

引用本文的文献

1
Design, synthesis and biological studies of carbazole-thiosemicarbazone hybrids as potential topoisomerase II catalytic inhibitors.咔唑-缩氨基硫脲杂化物作为潜在拓扑异构酶II催化抑制剂的设计、合成及生物学研究
RSC Med Chem. 2025 May 9. doi: 10.1039/d5md00234f.