• 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

苯基苯并咪唑和苯并咪唑并[1,2-c]喹唑啉的合成及其对DNA的亲和力

Synthesis and affinity to DNA of phenylbenzoimidazoles and benzoimidazo[1,2-c]quinazolines.

作者信息

Lyakhova Elena A, Gusyeva Yulia A, Nekhoroshkova Julia V, Shafran Lev M, Lyakhov Sergey A

机构信息

AV Bogatsky Physico-Chemical Institute of NAS of Ukraine, Odessa, Ukraine.

出版信息

Eur J Med Chem. 2009 Aug;44(8):3305-12. doi: 10.1016/j.ejmech.2009.03.004. Epub 2009 Mar 21.

DOI:10.1016/j.ejmech.2009.03.004
PMID:19349097
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7115644/
Abstract

Novel N-(benzoimidazophenyl)dialkylaminoalkylamides and 6-dialkylaminoalkylbenzoimidazo[1,2-c]quinazolines were prepared as potential interferon inducers and antiviral agents. They were screened for the DNA affinity by the ethidium bromide displacement assay. It was shown that the lg K(a) values of the compounds containing tetracyclic benzoimidazo[1,2-c]quinazoline fragment are approximately one order magnitude greater than those of the corresponding acyclic phenylbenzoimidazole derivatives.

摘要

新型N-(苯并咪唑基苯基)二烷基氨基烷基酰胺和6-二烷基氨基烷基苯并咪唑并[1,2-c]喹唑啉被制备为潜在的干扰素诱导剂和抗病毒剂。通过溴化乙锭置换试验对它们的DNA亲和力进行了筛选。结果表明,含有四环苯并咪唑并[1,2-c]喹唑啉片段的化合物的lg K(a)值比相应的无环苯基苯并咪唑衍生物大约高一个数量级。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8114/7115644/e337778264d1/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8114/7115644/133636c359a6/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8114/7115644/ee7c5dcbb3b1/fx2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8114/7115644/0f555d66ddb3/fx3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8114/7115644/678beb591470/sc1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8114/7115644/eb40e180ca97/sc2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8114/7115644/4576b0b1afb7/sc3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8114/7115644/e337778264d1/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8114/7115644/133636c359a6/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8114/7115644/ee7c5dcbb3b1/fx2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8114/7115644/0f555d66ddb3/fx3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8114/7115644/678beb591470/sc1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8114/7115644/eb40e180ca97/sc2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8114/7115644/4576b0b1afb7/sc3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8114/7115644/e337778264d1/gr1.jpg

相似文献

1
Synthesis and affinity to DNA of phenylbenzoimidazoles and benzoimidazo[1,2-c]quinazolines.苯基苯并咪唑和苯并咪唑并[1,2-c]喹唑啉的合成及其对DNA的亲和力
Eur J Med Chem. 2009 Aug;44(8):3305-12. doi: 10.1016/j.ejmech.2009.03.004. Epub 2009 Mar 21.
2
Ligand design and synthesis of new imidazo[5,1-b]quinazoline derivatives as alpha1-adrenoceptor agonists and antagonists.新型咪唑并[5,1 - b]喹唑啉衍生物作为α1 - 肾上腺素能受体激动剂和拮抗剂的配体设计与合成
Bioorg Med Chem. 2006 Feb 15;14(4):898-910. doi: 10.1016/j.bmc.2005.07.037. Epub 2005 Dec 7.
3
Synthesis of condensed quinolines and quinazolines as DNA ligands.作为DNA配体的稠合喹啉和喹唑啉的合成。
Bioorg Med Chem. 2004 Feb 1;12(3):641-7. doi: 10.1016/j.bmc.2003.10.014.
4
Tyrosine kinase inhibitors. 9. Synthesis and evaluation of fused tricyclic quinazoline analogues as ATP site inhibitors of the tyrosine kinase activity of the epidermal growth factor receptor.酪氨酸激酶抑制剂。9. 稠合三环喹唑啉类似物作为表皮生长因子受体酪氨酸激酶活性的ATP位点抑制剂的合成与评价。
J Med Chem. 1996 Feb 16;39(4):918-28. doi: 10.1021/jm950692f.
5
Synthesis, molecular structure and reactivity of 5-methylidene-1,2,3,5-tetrahydroimidazo[2,1-b]quinazolines.5-亚甲基-1,2,3,5-四氢咪唑并[2,1-b]喹唑啉的合成、分子结构及反应活性
Molecules. 2004 Feb 28;9(3):86-101. doi: 10.3390/90300086.
6
1,2,3-triazolo[1.5-a]quinazolines: synthesis, benzodiazepine receptor binding and theoretical calculations.1,2,3-三唑并[1.5-a]喹唑啉类化合物:合成、苯二氮䓬受体结合及理论计算
Farmaco. 1996 Feb;51(2):131-6.
7
Mono and bis-6-arylbenzimidazo[1,2-c]quinazolines: a new class of antimicrobial agents.单-和双-6-芳基苯并咪唑并[1,2-c]喹唑啉类:一类新型抗菌剂。
Eur J Med Chem. 2009 Aug;44(8):3330-9. doi: 10.1016/j.ejmech.2009.03.022. Epub 2009 Mar 27.
8
Copper-catalyzed aerobic intramolecular carbo- and amino-oxygenation of alkynes for synthesis of azaheterocycles.铜催化炔烃的有氧分子内碳-和氨基-氧化反应合成氮杂杂环。
Org Lett. 2012 May 4;14(9):2290-2. doi: 10.1021/ol3007106. Epub 2012 Apr 10.
9
Synthesis, antimicrobial evaluation, and docking studies of novel 4-substituted quinazoline derivatives as DNA-gyrase inhibitors.新型 4-取代喹唑啉衍生物作为 DNA-拓扑异构酶抑制剂的合成、抗菌评价和对接研究。
Arch Pharm (Weinheim). 2010 Oct;343(10):570-6. doi: 10.1002/ardp.201000065.
10
Scaffold approach for solid-phase synthesis of 2,3-disubstituted 8-arylamino-3H-imidazo[4,5-g]quinazolines.用于固相合成2,3-二取代的8-芳基氨基-3H-咪唑并[4,5-g]喹唑啉的支架方法。
J Comb Chem. 2007 Jan-Feb;9(1):9-11. doi: 10.1021/cc0601231.

引用本文的文献

1
I-Catalyzed Oxidative Cross-Coupling Reaction of Methyl Ketones and 2-(2-Aminophenyl) Benzimidazole: Facile Access to Benzimidazo[1,2-]quinazoline.铱催化的甲基酮与2-(2-氨基苯基)苯并咪唑的氧化交叉偶联反应:便捷合成苯并咪唑并[1,2-]喹唑啉
ACS Omega. 2018 May 8;3(5):5021-5028. doi: 10.1021/acsomega.8b00067. eCollection 2018 May 31.

本文引用的文献

1
DNA binding of tilorone: 1H NMR and calorimetric studies of the intercalation.泰洛龙的DNA结合:嵌入作用的1H核磁共振和量热研究
Biochemistry. 2007 Jul 10;46(27):8156-63. doi: 10.1021/bi602402m. Epub 2007 Jun 16.
2
Antiviral activity of arbidol against influenza A virus, respiratory syncytial virus, rhinovirus, coxsackie virus and adenovirus in vitro and in vivo.阿比朵尔在体外和体内对甲型流感病毒、呼吸道合胞病毒、鼻病毒、柯萨奇病毒和腺病毒的抗病毒活性。
Arch Virol. 2007;152(8):1447-55. doi: 10.1007/s00705-007-0974-5. Epub 2007 May 14.
3
Arbidol: a broad-spectrum antiviral that inhibits acute and chronic HCV infection.
阿比朵尔:一种抑制急性和慢性丙型肝炎病毒感染的广谱抗病毒药物。
Virol J. 2006 Jul 19;3:56. doi: 10.1186/1743-422X-3-56.
4
A high-throughput, high-resolution strategy for the study of site-selective DNA binding agents: analysis of a "highly twisted" benzimidazole-diamidine.一种用于研究位点选择性DNA结合剂的高通量、高分辨率策略:对一种“高度扭曲”的苯并咪唑-二脒的分析。
J Am Chem Soc. 2006 Jun 21;128(24):7846-54. doi: 10.1021/ja0600936.
5
Design of new bidentate ligands constructed of two Hoechst 33258 units for discrimination of the length of two A3T3 binding motifs.由两个Hoechst 33258单元构建的新型双齿配体的设计,用于区分两个A3T3结合基序的长度。
J Org Chem. 2006 Jan 6;71(1):125-34. doi: 10.1021/jo051836t.
6
[Individual changes of gene expression in the interferon system in human blood cells due to amixin and cycloferon].[阿咪新和环磷酰胺对人体血细胞中干扰素系统基因表达的个体影响]
Vopr Virusol. 2005 Mar-Apr;50(2):32-6.
7
Thiophene-based diamidine forms a "super" at binding minor groove agent.基于噻吩的双脒形成一种结合小沟的“超级”试剂。
J Am Chem Soc. 2004 Oct 27;126(42):13659-69. doi: 10.1021/ja048175m.
8
Expanding the repertoire of heterocycle ring pairs for programmable minor groove DNA recognition.拓展用于可编程性小沟DNA识别的杂环环对库。
J Am Chem Soc. 2004 Aug 25;126(33):10339-49. doi: 10.1021/ja0486465.
9
Solid-phase synthesis of positively charged deoxynucleic guanidine (DNG) tethering a Hoechst 33258 analogue: triplex and duplex stabilization by simultaneous minor groove binding.连接Hoechst 33258类似物的带正电荷的脱氧核酸胍(DNG)的固相合成:通过同时小沟结合实现三链体和双链体稳定化
J Am Chem Soc. 2004 Mar 31;126(12):3736-47. doi: 10.1021/ja031557s.
10
Design and synthesis of DNA-intercalating 9-fluoren-beta-O-glycosides as potential IFN-inducers, and antiviral and cytostatic agents.作为潜在的干扰素诱导剂、抗病毒和细胞生长抑制剂的DNA嵌入型9-芴基-β-O-糖苷的设计与合成。
Bioorg Med Chem. 2004 Apr 1;12(7):1781-91. doi: 10.1016/j.bmc.2003.12.034.