• 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

三芳基吡啶:用于识别G-四链体的多功能小分子骨架

Triarylpyridines: a versatile small molecule scaffold for G-quadruplex recognition.

作者信息

Waller Zoë A E, Shirude Pravin S, Rodriguez Raphaël, Balasubramanian Shankar

机构信息

The University Chemical Laboratory, Lensfield Road, Cambridge, CB2 1EW, UK.

出版信息

Chem Commun (Camb). 2008 Mar 28(12):1467-9. doi: 10.1039/b718854d. Epub 2008 Jan 29.

DOI:10.1039/b718854d
PMID:18338058
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2527513/
Abstract

The triarylpyridines are potent G-quadruplex ligands that are highly discriminating against duplex DNA and show promising selectivity between intramolecular quadruplexes.

摘要

三芳基吡啶是有效的G-四链体配体,对双链DNA具有高度选择性,并且在分子内四链体之间表现出有前景的选择性。

相似文献

1
Triarylpyridines: a versatile small molecule scaffold for G-quadruplex recognition.三芳基吡啶:用于识别G-四链体的多功能小分子骨架
Chem Commun (Camb). 2008 Mar 28(12):1467-9. doi: 10.1039/b718854d. Epub 2008 Jan 29.
2
Synthesis and binding studies of novel diethynyl-pyridine amides with genomic promoter DNA G-quadruplexes.新型二乙炔基-吡啶酰胺与基因组启动子 DNA G-四链体的合成及结合研究。
Chemistry. 2011 Apr 11;17(16):4571-81. doi: 10.1002/chem.201003157. Epub 2011 Mar 8.
3
Unraveling the relationship between structure and stabilization of triarylpyridines as G-quadruplex binding ligands.解析三芳基吡啶作为 G-四链体结合配体的结构与稳定性关系。
Org Biomol Chem. 2011 Sep 7;9(17):6154-62. doi: 10.1039/c1ob05560g. Epub 2011 Jul 13.
4
Novel G-quadruplex stabilizing agents: in-silico approach and dynamics.新型 G-四链体稳定剂:计算机模拟方法与动力学。
J Biomol Struct Dyn. 2013 Dec;31(12):1497-518. doi: 10.1080/07391102.2012.742246. Epub 2012 Dec 17.
5
A comparative study of the interaction of two structurally analogous ruthenium complexes with human telomeric G-quadruplex DNA.两种结构类似的钌配合物与人端粒 G-四链体 DNA 相互作用的比较研究。
J Inorg Biochem. 2013 Apr;121:19-27. doi: 10.1016/j.jinorgbio.2012.12.011. Epub 2012 Dec 29.
6
A small molecule that disrupts G-quadruplex DNA structure and enhances gene expression.一种破坏G-四链体DNA结构并增强基因表达的小分子。
J Am Chem Soc. 2009 Sep 9;131(35):12628-33. doi: 10.1021/ja901892u.
7
DNA G-Quadruplex in Human Telomeres and Oncogene Promoters: Structures, Functions, and Small Molecule Targeting.人类端粒和癌基因启动子中的 DNA G-四链体:结构、功能和小分子靶向。
Acc Chem Res. 2022 Sep 20;55(18):2628-2646. doi: 10.1021/acs.accounts.2c00337. Epub 2022 Sep 2.
8
The importance of metal geometry in the recognition of G-quadruplex-DNA by metal-terpyridine complexes.金属三联吡啶配合物识别G-四链体DNA过程中金属几何结构的重要性。
Org Biomol Chem. 2007 Aug 21;5(16):2555-9. doi: 10.1039/b708635k.
9
Tetramethylpyridiniumporphyrazines--a new class of G-quadruplex inducing and stabilising ligands.四甲基吡啶卟吩嗪——一类新型的诱导和稳定G-四链体的配体。
Chem Commun (Camb). 2006 Dec 7(45):4685-7. doi: 10.1039/b611731g. Epub 2006 Sep 27.
10
The role of thermodynamics and kinetics in ligand binding to G-quadruplex DNA.热力学和动力学在配体与 G-四链体 DNA 结合中的作用。
Chem Commun (Camb). 2012 Sep 14;48(71):8958-60. doi: 10.1039/c2cc32240d. Epub 2012 Jul 27.

引用本文的文献

1
Major Achievements in the Design of Quadruplex-Interactive Small Molecules.四链体相互作用小分子设计的主要成就
Pharmaceuticals (Basel). 2022 Feb 28;15(3):300. doi: 10.3390/ph15030300.
2
Modulation of DNA structure formation using small molecules.利用小分子调节 DNA 结构形成。
Biochim Biophys Acta Mol Cell Res. 2019 Dec;1866(12):118539. doi: 10.1016/j.bbamcr.2019.118539. Epub 2019 Sep 3.
3
4,6-Dihydroxysalicylic Acid-Catalyzed Oxidative Condensation of Benzylic Amines and Aromatic Ketones for the Preparation of 2,4,6-Trisubstituted Pyridines and Its Application to Metal-Free Synthesis of G-Quadruplex Binding Ligands.4,6-二羟基水杨酸催化苄胺与芳香酮的氧化缩合反应制备2,4,6-三取代吡啶及其在无金属合成G-四链体结合配体中的应用
ACS Omega. 2019 May 23;4(5):9029-9040. doi: 10.1021/acsomega.9b00999. eCollection 2019 May 31.
4
In Silico Screening and Binding Characterization of Small Molecules toward a G-Quadruplex Structure Formed in the Promoter Region of Oncogene.小分子对癌基因启动子区域形成的G-四链体结构的计算机筛选及结合表征
ACS Omega. 2017 Aug 31;2(8):4382-4397. doi: 10.1021/acsomega.6b00531. Epub 2017 Aug 9.
5
G-quadruplex virtual drug screening: A review.四链体虚拟药物筛选:综述。
Biochimie. 2018 Sep;152:134-148. doi: 10.1016/j.biochi.2018.06.024. Epub 2018 Jun 30.
6
Precision engineering of targeted nanocarriers.靶向纳米载体的精密工程
Wiley Interdiscip Rev Nanomed Nanobiotechnol. 2018 Sep;10(5):e1511. doi: 10.1002/wnan.1511. Epub 2018 Feb 13.
7
In silico identification of novel ligands for G-quadruplex in the c-MYC promoter.在计算机上鉴定c-MYC启动子中G-四链体的新型配体。
J Comput Aided Mol Des. 2015 Apr;29(4):339-48. doi: 10.1007/s10822-014-9826-z. Epub 2014 Dec 20.
8
Targeting the c-Kit Promoter G-quadruplexes with 6-Substituted Indenoisoquinolines.用6-取代茚并异喹啉靶向c-Kit启动子G-四链体
ACS Med Chem Lett. 2010 Jul 1;1(7):306-10. doi: 10.1021/ml100062z. eCollection 2010 Oct 14.
9
Pyridostatin analogues promote telomere dysfunction and long-term growth inhibition in human cancer cells.吡啶硫酮类似物促进人类癌细胞中端粒功能障碍和长期生长抑制。
Org Biomol Chem. 2012 Aug 28;10(32):6537-46. doi: 10.1039/c2ob25830g. Epub 2012 Jul 13.
10
G-quadruplex-binding benzo[a]phenoxazines down-regulate c-KIT expression in human gastric carcinoma cells.苯并[a]吩嗪类化合物与 G-四链体结合可下调人胃癌细胞中 c-KIT 的表达。
J Am Chem Soc. 2011 Mar 2;133(8):2658-63. doi: 10.1021/ja109474c. Epub 2011 Feb 4.

本文引用的文献

1
Trisubstituted isoalloxazines as a new class of G-quadruplex binding ligands: small molecule regulation of c-kit oncogene expression.三取代异咯嗪作为一类新型的G-四链体结合配体:c-kit癌基因表达的小分子调控
J Am Chem Soc. 2007 Oct 31;129(43):12926-7. doi: 10.1021/ja075881p. Epub 2007 Oct 5.
2
Macrocyclic and helical oligoamides as a new class of G-quadruplex ligands.大环和螺旋状低聚酰胺作为一类新型的G-四链体配体。
J Am Chem Soc. 2007 Oct 3;129(39):11890-1. doi: 10.1021/ja073775h. Epub 2007 Sep 11.
3
Single-molecule conformational analysis of G-quadruplex formation in the promoter DNA duplex of the proto-oncogene c-kit.原癌基因c-kit启动子DNA双链中G-四链体形成的单分子构象分析
J Am Chem Soc. 2007 Jun 20;129(24):7484-5. doi: 10.1021/ja070497d. Epub 2007 May 25.
4
Tetraplex DNA and its interacting proteins.四链体DNA及其相互作用蛋白。
Front Biosci. 2007 May 1;12:4336-51. doi: 10.2741/2391.
5
Fluorescence-based melting assays for studying quadruplex ligands.用于研究四链体配体的基于荧光的熔解分析。
Methods. 2007 Jun;42(2):183-95. doi: 10.1016/j.ymeth.2006.10.004.
6
Stabilization of G-quadruplex DNA and down-regulation of oncogene c-myc by quindoline derivatives.喹啉衍生物对G-四链体DNA的稳定作用及癌基因c-myc的下调
J Med Chem. 2007 Apr 5;50(7):1465-74. doi: 10.1021/jm0610088. Epub 2007 Mar 9.
7
G-quadruplexes in promoters throughout the human genome.人类基因组中启动子区域的G-四链体
Nucleic Acids Res. 2007;35(2):406-13. doi: 10.1093/nar/gkl1057. Epub 2006 Dec 14.
8
Structure-specific recognition of quadruplex DNA by organic cations: influence of shape, substituents and charge.有机阳离子对四链体DNA的结构特异性识别:形状、取代基和电荷的影响
Biophys Chem. 2007 Mar;126(1-3):140-53. doi: 10.1016/j.bpc.2006.06.006. Epub 2006 Jun 20.
9
A conserved quadruplex motif located in a transcription activation site of the human c-kit oncogene.位于人类c-kit癌基因转录激活位点的一个保守四链体基序。
Biochemistry. 2006 Jun 27;45(25):7854-60. doi: 10.1021/bi0601510.
10
G-quadruplex formation within the promoter of the KRAS proto-oncogene and its effect on transcription.KRAS原癌基因启动子内G-四链体的形成及其对转录的影响。
Nucleic Acids Res. 2006 May 10;34(9):2536-49. doi: 10.1093/nar/gkl286. Print 2006.