• 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

含磺乙基胺部分的嘌呤核苷衍生物:设计、合成、抗病毒活性和机制。

Purine Nucleoside Derivatives Containing a Sulfa Ethylamine Moiety: Design, Synthesis, Antiviral Activity, and Mechanism.

机构信息

State Key Laboratory Breeding Base of Green Pesticide and Agricultural Bioengineering, Key Laboratory of Green Pesticide and Agricultural Bioengineering, Ministry of Education, Guizhou University, Huaxi District, Guiyang 550025, P. R. China.

出版信息

J Agric Food Chem. 2021 May 26;69(20):5575-5582. doi: 10.1021/acs.jafc.0c06612. Epub 2021 May 14.

DOI:10.1021/acs.jafc.0c06612
PMID:33988985
Abstract

To find efficient and broad-spectrum viral agents, a series of purine nucleoside derivatives containing sulfa ethylamine moieties was designed and synthesized, and their antiviral activities against tobacco mosaic virus (TMV), cucumber mosaic virus (CMV), and potato virus Y (PVY) were evaluated. Some target compounds displayed good antiviral activities. Among them, compound showed excellent protective activity against CMV and PVY with 50% effective concentration values (EC) of 137 and 209 μg/mL, respectively, which were better than that of the control agent ningnanmycin (508 and 431 μg/mL). Moreover, the EC value of compound for the inactivating activity against TMV was 48 μg/mL, which was better than that of ningnanmycin (88 μg/mL). In addition, compound not only destroyed the structure of the TMV virus but also had a good interaction with the coat protein of the TMV virus. Therefore, compound may further destroy the structure of the virus by binding to the coat protein of the TMV virus, thereby weakening the infectivity of the virus.

摘要

为了寻找高效广谱的病毒制剂,设计并合成了一系列含磺乙基胺结构的嘌呤核苷衍生物,并评价了它们对烟草花叶病毒(TMV)、黄瓜花叶病毒(CMV)和马铃薯 Y 病毒(PVY)的抗病毒活性。部分目标化合物表现出良好的抗病毒活性。其中,化合物 对 CMV 和 PVY 显示出优异的保护活性,其对 CMV 和 PVY 的 50%有效浓度(EC)值分别为 137 和 209μg/mL,优于对照药剂宁南霉素(508 和 431μg/mL)。此外,化合物 对 TMV 的灭活活性的 EC 值为 48μg/mL,优于宁南霉素(88μg/mL)。此外,化合物 不仅破坏了 TMV 病毒的结构,而且与 TMV 病毒的外壳蛋白具有良好的相互作用。因此,化合物 可能通过与 TMV 病毒的外壳蛋白结合进一步破坏病毒的结构,从而减弱病毒的感染力。

相似文献

1
Purine Nucleoside Derivatives Containing a Sulfa Ethylamine Moiety: Design, Synthesis, Antiviral Activity, and Mechanism.含磺乙基胺部分的嘌呤核苷衍生物:设计、合成、抗病毒活性和机制。
J Agric Food Chem. 2021 May 26;69(20):5575-5582. doi: 10.1021/acs.jafc.0c06612. Epub 2021 May 14.
2
Synthesis, Antiviral Activity, and Mechanisms of Purine Nucleoside Derivatives Containing a Sulfonamide Moiety.含磺酰胺结构的嘌呤核苷衍生物的合成、抗病毒活性及作用机制。
J Agric Food Chem. 2019 Aug 7;67(31):8459-8467. doi: 10.1021/acs.jafc.9b02681. Epub 2019 Jul 24.
3
Synthesis of Anthranilic Diamide Derivatives Containing Moieties of Trifluoromethylpyridine and Hydrazone as Potential Anti-Viral Agents for Plants.含三氟甲基吡啶和腙部分的邻氨基甲酰胺衍生物的合成作为植物抗病毒剂的潜在药物。
J Agric Food Chem. 2019 Dec 4;67(48):13344-13352. doi: 10.1021/acs.jafc.9b05441. Epub 2019 Nov 19.
4
Design, Synthesis, Antiviral Bioactivity, and Defense Mechanisms of Novel Dithioacetal Derivatives Bearing a Strobilurin Moiety.新型含(strobilurin)部分二硫代缩醛衍生物的设计、合成、抗病毒活性和防御机制。
J Agric Food Chem. 2018 May 30;66(21):5335-5345. doi: 10.1021/acs.jafc.8b01297. Epub 2018 May 16.
5
Synthesis, anti-tobacco mosaic virus and cucumber mosaic virus activity, and 3D-QSAR study of novel 1,4-pentadien-3-one derivatives containing 4-thioquinazoline moiety.含4-硫代喹唑啉部分的新型1,4-戊二烯-3-酮衍生物的合成、抗烟草花叶病毒和黄瓜花叶病毒活性及3D-QSAR研究
Eur J Med Chem. 2015 Sep 18;102:639-47. doi: 10.1016/j.ejmech.2015.08.029. Epub 2015 Aug 19.
6
Design, Synthesis, and Mechanism of Antiviral Acylurea Derivatives Containing a Trifluoromethylpyridine Moiety.含三氟甲基吡啶基的抗病毒酰脲衍生物的设计、合成及作用机制。
J Agric Food Chem. 2021 Nov 3;69(43):12891-12899. doi: 10.1021/acs.jafc.1c03586. Epub 2021 Oct 25.
7
Facile Synthesis of Novel Vanillin Derivatives Incorporating a Bis(2-hydroxyethyl)dithhioacetal Moiety as Antiviral Agents.新型香草醛衍生物的简便合成:含双(2-羟乙基)二硫缩醛部分作为抗病毒剂
J Agric Food Chem. 2017 Jun 14;65(23):4582-4588. doi: 10.1021/acs.jafc.7b01035. Epub 2017 Jun 5.
8
Antiviral properties and interaction of novel chalcone derivatives containing a purine and benzenesulfonamide moiety.含嘌呤和苯磺酰胺部分的新型查尔酮衍生物的抗病毒特性及相互作用
Bioorg Med Chem Lett. 2018 Jun 15;28(11):2091-2097. doi: 10.1016/j.bmcl.2018.04.042. Epub 2018 Apr 17.
9
Design, synthesis and anti-TMV activities of novel chromone derivatives containing dithioacetal moiety.新型含二硫缩醛部分的色酮衍生物的设计、合成及抗 TMV 活性。
Bioorg Med Chem Lett. 2020 Mar 1;30(5):126945. doi: 10.1016/j.bmcl.2019.126945. Epub 2020 Jan 2.
10
Design, synthesis, and antiviral activity of novel rutin derivatives containing 1, 4-pentadien-3-one moiety.新型含有 1,4-戊二烯-3-酮部分的芦丁衍生物的设计、合成与抗病毒活性。
Eur J Med Chem. 2015 Mar 6;92:732-7. doi: 10.1016/j.ejmech.2015.01.017. Epub 2015 Jan 10.

引用本文的文献

1
Discovery of highly effective antiviral agents based on flavonoid-benzothiazole against TMV.基于黄酮类-苯并噻唑的抗烟草花叶病毒高效抗病毒剂的发现。
Mol Divers. 2025 Feb 19. doi: 10.1007/s11030-025-11126-5.
2
Discovery of Crinasiadine, Trisphaeridine, Bicolorine, and Their Derivatives as Anti-Tobacco Mosaic Virus (TMV) Agents.发现海葱定碱、三棱碱、双色水仙碱及其衍生物作为抗烟草花叶病毒(TMV)制剂
Int J Mol Sci. 2025 Jan 27;26(3):1103. doi: 10.3390/ijms26031103.
3
Microwave-assisted synthesis of base-modified fluorescent 1,4-dihydropyridine nucleosides: photophysical characterization and insights.
微波辅助合成碱基修饰的荧光1,4-二氢吡啶核苷:光物理表征及见解
RSC Adv. 2024 Dec 18;14(54):39833-39843. doi: 10.1039/d4ra07295b. eCollection 2024 Dec 17.
4
Rational design of 2-chromene-based antiphytovirals that inhibit virion assembly by outcompeting virus capsid-RNA interactions.基于2-色烯的抗植物病毒剂的合理设计,通过竞争病毒衣壳与RNA的相互作用来抑制病毒粒子组装。
iScience. 2024 Oct 18;27(11):111210. doi: 10.1016/j.isci.2024.111210. eCollection 2024 Nov 15.
5
Antiviral Activity of Ailanthone from on the Rice Stripe Virus.苦木苦味素 A 对水稻条纹病毒的抗病毒活性。
Viruses. 2023 Dec 31;16(1):73. doi: 10.3390/v16010073.
6
Discovery of Novel -Aminophosphonates with Hydrazone as Potential Antiviral Agents Combined With Active Fragment and Molecular Docking.以腙为潜在抗病毒剂并结合活性片段和分子对接的新型氨基膦酸酯的发现
Front Chem. 2022 May 20;10:911453. doi: 10.3389/fchem.2022.911453. eCollection 2022.
7
Research Progress of Benzothiazole and Benzoxazole Derivatives in the Discovery of Agricultural Chemicals.苯并噻唑和苯并恶唑衍生物在农用化学品发现中的研究进展。
Int J Mol Sci. 2023 Jun 28;24(13):10807. doi: 10.3390/ijms241310807.
8
Design, Synthesis, and Bioactivity of Chalcone Derivatives Containing Indanone.含茚满酮查尔酮衍生物的设计、合成及生物活性
ACS Omega. 2023 Jan 4;8(2):2556-2563. doi: 10.1021/acsomega.2c07071. eCollection 2023 Jan 17.
9
Hydrazone modification of non-food natural product sclareolide as potential agents for plant disease.将非食用天然产物香紫苏内酯腙化修饰作为植物病害的潜在防治剂
Heliyon. 2022 Dec 22;8(12):e12391. doi: 10.1016/j.heliyon.2022.e12391. eCollection 2022 Dec.
10
Antibacterial Activity of Aureonuclemycin Produced by Strain SPRI-371.菌株 SPRI-371 产生的金核霉素的抗菌活性。
Molecules. 2022 Aug 8;27(15):5041. doi: 10.3390/molecules27155041.