• 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

硝吖啶及其同类物——综述。

Nitracrine and its congeners--an overview.

作者信息

Gniazdowski M, Szmigiero L

机构信息

Department of General Chemistry, Medical University in Lódź, Poland.

出版信息

Gen Pharmacol. 1995 May;26(3):473-81. doi: 10.1016/0306-3623(94)00143-b.

DOI:10.1016/0306-3623(94)00143-b
PMID:7789719
Abstract
  1. An anticancer drug, nitracrine 1-nitro-9(3'3'-dimethylaminopropylamino)acridine (Ledakrin, C-283) exhibits potent cytostatic effects which can be ascribed to interactions of the drug with DNA. 2. The reduction of the nitro group of nitracrine is one of the activation steps leading to the drug covalent binding to DNA and proteins both in subcellular systems and in the cell. 3. DNA-drug non-covalent interactions and covalent complexes are examined in several model systems and compared with the properties of a number of derivatives with programmed structural changes. 4. DNA-protein crosslinks and interstrand crosslinks are detected in the cells following exposition to the drug. 5. The drug exhibits selective toxicity and radiosensitization effects to hypoxic mammalian cells.
摘要
  1. 一种抗癌药物,硝吖啶1-硝基-9(3'3'-二甲基氨基丙基氨基)吖啶(利达克林,C-283)具有强大的细胞生长抑制作用,这可归因于该药物与DNA的相互作用。2. 硝吖啶硝基的还原是导致该药物在亚细胞系统和细胞中与DNA和蛋白质共价结合的激活步骤之一。3. 在几个模型系统中研究了DNA-药物非共价相互作用和共价复合物,并与一些具有特定结构变化的衍生物的性质进行了比较。4. 细胞在接触该药物后可检测到DNA-蛋白质交联和链间交联。5. 该药物对缺氧的哺乳动物细胞表现出选择性毒性和放射增敏作用。

相似文献

1
Nitracrine and its congeners--an overview.硝吖啶及其同类物——综述。
Gen Pharmacol. 1995 May;26(3):473-81. doi: 10.1016/0306-3623(94)00143-b.
2
Crosslinking of cellular DNA by nitracrine and furocoumarin derivatives.硝吖啶和呋喃香豆素衍生物对细胞DNA的交联作用。
Neoplasma. 1999;46(1):50-3.
3
Anaerobic incubation and mutagenicity of nitracrine analogues in Salmonella typhimurium.硝吖啶类似物在鼠伤寒沙门氏菌中的厌氧培养及致突变性
Mutagenesis. 1987 Jul;2(4):253-7. doi: 10.1093/mutage/2.4.253.
4
Induction of DNA-protein crosslinks by antitumor 1-nitro-9-aminoacridines in L1210 leukemia cells.抗肿瘤1-硝基-9-氨基吖啶诱导L1210白血病细胞中DNA-蛋白质交联
Biochem Pharmacol. 1989 Nov 15;38(22):4095-101. doi: 10.1016/0006-2952(89)90691-6.
5
The mode of action of cytotoxic and antitumor 1-nitroacridines. II. In vivo enzyme-mediated covalent binding of a 1-nitroacridine derivative, Ledakrin or Nitracrine, with dna and other macromolecules of mammalian or bacterial cells.细胞毒性和抗肿瘤1-硝基吖啶的作用模式。II. 1-硝基吖啶衍生物(雷达克林或硝吖啶)在体内通过酶介导与哺乳动物或细菌细胞的DNA及其他大分子的共价结合
Chem Biol Interact. 1983 Feb;43(2):151-73. doi: 10.1016/0009-2797(83)90093-5.
6
Hypoxia-selective antitumor agents. 13. Effects of acridine substitution on the hypoxia-selective cytotoxicity and metabolic reduction of the bis-bioreductive agent nitracrine N-oxide.缺氧选择性抗肿瘤剂。13. 吖啶取代对双生物还原剂硝吖啶N-氧化物的缺氧选择性细胞毒性和代谢还原的影响。
J Med Chem. 1996 Jun 21;39(13):2508-17. doi: 10.1021/jm9600104.
7
Are lethal effects of nitracrine on L5178Y cell sublines associated with DNA-protein crosslinks?硝吖啶对L5178Y细胞亚系的致死效应与DNA-蛋白质交联有关吗?
Biochem Pharmacol. 1993 Aug 17;46(4):615-20. doi: 10.1016/0006-2952(93)90546-9.
8
Selective toxicity of nitracrine to hypoxic mammalian cells.硝吖啶对缺氧哺乳动物细胞的选择性毒性。
Br J Cancer. 1984 Feb;49(2):215-23. doi: 10.1038/bjc.1984.34.
9
Ledakrin--anticancerous medicine 1-nitro-9(3-dimethylaminopropylamino)-acridine -2HCl-H2O.来达克林——抗癌药物1-硝基-9(3-二甲氨基丙基氨基)吖啶-2盐酸盐-水合物
Mater Med Pol. 1976 Jul-Sep;8(3):237-51.
10
32P-post-labeling analysis of DNA adduct formation by antitumor drug nitracrine (Ledakrin) and other nitroacridines in different biological systems.用32P后标记分析法研究抗肿瘤药物硝吖啶(雷得菌素)及其他硝基吖啶在不同生物系统中形成DNA加合物的情况。
Biochem Pharmacol. 1989 Apr 15;38(8):1301-12. doi: 10.1016/0006-2952(89)90337-7.

引用本文的文献

1
The interactions of Pu22 G-quadruplex, derived from promoter sequence, with antitumor acridine derivatives-An NMR/MD combined study.源自启动子序列的Pu22 G-四链体与抗肿瘤吖啶衍生物的相互作用——一项核磁共振/分子动力学联合研究
Mol Ther Nucleic Acids. 2025 Mar 13;36(2):102513. doi: 10.1016/j.omtn.2025.102513. eCollection 2025 Jun 10.
2
The interactions of monomeric acridines and unsymmetrical bisacridines (UAs) with DNA duplexes: an insight provided by NMR and MD studies.单体吖啶和不对称双吖啶(UAs)与 DNA 双链体的相互作用:NMR 和 MD 研究提供的深入了解。
Sci Rep. 2023 Mar 1;13(1):3431. doi: 10.1038/s41598-023-30587-y.
3
Acid-Base Equilibrium and Self-Association in Relation to High Antitumor Activity of Selected Unsymmetrical Bisacridines Established by Extensive Chemometric Analysis.
通过广泛的化学计量学分析确定选定的不对称双吖啶的抗肿瘤高活性与酸碱平衡和自缔合的关系。
Molecules. 2022 Jun 21;27(13):3995. doi: 10.3390/molecules27133995.
4
Pre-clinical evaluation of 1-nitroacridine derived chemotherapeutic agent that has preferential cytotoxic activity towards prostate cancer.对一种对前列腺癌具有优先细胞毒性活性的1-硝基吖啶衍生化疗药物的临床前评估。
Cancer Biol Ther. 2007 Oct;6(10):1632-7. doi: 10.4161/cbt.6.10.4790. Epub 2007 Jul 24.