• 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

1-[ω-(溴苯氧基)烷基]-3-萘甲基尿嘧啶衍生物及其类似物的合成作为人巨细胞病毒复制的可能抑制剂。

Synthesis of 1-[ω-(Bromophenoxy)alkyl]-3-Naphthalenylmethyl Uracil Derivatives and Their Analogues as Probable Inhibitors of Human Cytomegalovirus Replication.

机构信息

Volgograd State Medical University, Volgograd, Russia.

Rega Institute for Medical Research, B-3000, Leuven, KU Leuven, Belgium.

出版信息

Dokl Biochem Biophys. 2022 Dec;507(1):357-362. doi: 10.1134/S1607672922340099. Epub 2023 Feb 14.

DOI:10.1134/S1607672922340099
PMID:36787002
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9926436/
Abstract

A new series of 1-[ω-(bromophenoxy)alkyl]-uracil derivatives containing naphthalen-1-yl, naphthalen-2-yl, 1-bromonaphthalen-2-ylmethyl, benzyl, and anthracene-9-ylmethyl fragments in position 3 of uracil residue was synthesized. The antiviral properties of the synthesized compounds against human cytomegalovirus were studied. It was found that the compound containing a bridge consisting of five methylene groups exhibits a high anti-cytomegalovirus activity in vitro.

摘要

合成了一系列含有萘-1-基、萘-2-基、1-溴-2-萘甲基、苄基和蒽-9-基甲基片段的 1-[ω-(溴苯氧基)烷基]-尿嘧啶衍生物。研究了合成化合物对人巨细胞病毒的抗病毒特性。结果发现,含有由五个亚甲基组成的桥的化合物在体外具有很高的抗巨细胞病毒活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2db5/9926436/3acc5da89f38/10628_2023_7362_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2db5/9926436/4a72772a0910/10628_2023_7362_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2db5/9926436/86edc6db0082/10628_2023_7362_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2db5/9926436/37de79fc8ac0/10628_2023_7362_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2db5/9926436/3acc5da89f38/10628_2023_7362_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2db5/9926436/4a72772a0910/10628_2023_7362_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2db5/9926436/86edc6db0082/10628_2023_7362_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2db5/9926436/37de79fc8ac0/10628_2023_7362_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2db5/9926436/3acc5da89f38/10628_2023_7362_Fig4_HTML.jpg

相似文献

1
Synthesis of 1-[ω-(Bromophenoxy)alkyl]-3-Naphthalenylmethyl Uracil Derivatives and Their Analogues as Probable Inhibitors of Human Cytomegalovirus Replication.1-[ω-(溴苯氧基)烷基]-3-萘甲基尿嘧啶衍生物及其类似物的合成作为人巨细胞病毒复制的可能抑制剂。
Dokl Biochem Biophys. 2022 Dec;507(1):357-362. doi: 10.1134/S1607672922340099. Epub 2023 Feb 14.
2
Synthesis of 1-[ω-(Bromophenoxy)alkyl]-3-naphthalenylmethyl Derivatives of Uracil and Their Analogues As Probable Inhibitors of Human Cytomegalovirus Replication.1-[ω-(溴苯氧基)烷基]-3-(萘-1-基甲基)尿嘧啶及其类似物的合成作为人巨细胞病毒复制的可能抑制剂。
Dokl Biochem Biophys. 2023 Apr;509(1):41-46. doi: 10.1134/S1607672923700151. Epub 2023 Jun 20.
3
Synthesis and anti-HCMV activity of 1-[ω-(phenoxy)alkyl]uracil derivatives and analogues thereof.1-[ω-(苯氧基)烷基]尿嘧啶衍生物及其类似物的合成及抗 HCMV 活性。
Bioorg Med Chem. 2013 Jul 15;21(14):4151-7. doi: 10.1016/j.bmc.2013.05.009. Epub 2013 May 16.
4
Toward the discovery of dual HCMV-VZV inhibitors: Synthesis, structure activity relationship analysis, and cytotoxicity studies of long chained 2-uracil-3-yl-N-(4-phenoxyphenyl)acetamides.迈向双 HCMV-VZV 抑制剂的发现:长链 2-尿嘧啶-3-基-N-(4-苯氧基苯基)乙酰胺的合成、构效关系分析及细胞毒性研究
Bioorg Med Chem. 2015 Nov 1;23(21):7035-44. doi: 10.1016/j.bmc.2015.09.033. Epub 2015 Sep 21.
5
Synthesis and Antiviral Properties of 1-Substituted 3-[ω-(4-Oxoquinazolin-4(3H)-yl)alkyl]uracil Derivatives.1-取代的3-[ω-(4-氧代喹唑啉-4(3H)-基)烷基]尿嘧啶衍生物的合成及抗病毒特性
Acta Naturae. 2020 Jul-Sep;12(3):134-139. doi: 10.32607/actanaturae.10983.
6
Antiviral activity of 3-(3,5-dimethylbenzyl)uracil derivatives against HIV-1 and HCMV.3-(3,5-二甲基苄基)尿嘧啶衍生物对HIV-1和人巨细胞病毒的抗病毒活性
Nucleosides Nucleotides Nucleic Acids. 2007;26(10-12):1553-8. doi: 10.1080/15257770701545424.
7
Synthesis and antiviral activity of 1-substituted 3-(3,5-dimethylbenzyl)uracil against HIV-1.1-取代-3-(3,5-二甲基苄基)尿嘧啶对HIV-1的合成及抗病毒活性
Nucleic Acids Symp Ser (Oxf). 2004(48):3-4. doi: 10.1093/nass/48.1.3.
8
Synthesis and antiviral activity of 1,3-disubstituted uracils against HIV-1 and HCMV.1,3 - 二取代尿嘧啶对HIV - 1和HCMV的合成及抗病毒活性
Antivir Chem Chemother. 2003 Sep;14(5):271-9. doi: 10.1177/095632020301400506.
9
Antiviral and Cytostatic Evaluation of 5-(1-Halo-2-sulfonylvinyl)- and 5-(2-Furyl)uracil Nucleosides.5-(1-卤代-2-磺酰乙烯基)-和5-(2-呋喃基)尿嘧啶核苷的抗病毒及细胞生长抑制活性评估
Arch Pharm (Weinheim). 2017 Apr;350(3-4). doi: 10.1002/ardp.201700023. Epub 2017 Mar 17.
10
Synthesis and antiviral activity of 1-cyclobutyl-5-(2-bromovinyl)uracil nucleoside analogues and related compounds.1-环丁基-5-(2-溴乙烯基)尿嘧啶核苷类似物及相关化合物的合成与抗病毒活性
J Med Chem. 1992 May 15;35(10):1799-806. doi: 10.1021/jm00088a015.

本文引用的文献

1
Synthesis and Antiviral Properties of 1-Substituted 3-[ω-(4-Oxoquinazolin-4(3H)-yl)alkyl]uracil Derivatives.1-取代的3-[ω-(4-氧代喹唑啉-4(3H)-基)烷基]尿嘧啶衍生物的合成及抗病毒特性
Acta Naturae. 2020 Jul-Sep;12(3):134-139. doi: 10.32607/actanaturae.10983.
2
Cytomegalovirus Infection Is a Risk Factor in Gastrointestinal Cancer: A Cross-Sectional and Meta-Analysis Study.巨细胞病毒感染是胃肠道癌症的一个危险因素:一项横断面和荟萃分析研究。
Intervirology. 2020;63(1-6):10-16. doi: 10.1159/000506683. Epub 2020 Aug 7.
3
Cytomegalovirus and Inflammatory Bowel Diseases (IBD) with a Special Focus on the Link with Ulcerative Colitis (UC).
巨细胞病毒与炎症性肠病(IBD),特别关注与溃疡性结肠炎(UC)的关联。
Microorganisms. 2020 Jul 20;8(7):1078. doi: 10.3390/microorganisms8071078.
4
A critical review of the relationship between post-transplant atherosclerotic events and cytomegalovirus exposure in kidney transplant recipients.肾移植受者移植后动脉粥样硬化事件与巨细胞病毒暴露之间关系的批判性回顾。
Expert Rev Anti Infect Ther. 2020 Feb;18(2):113-125. doi: 10.1080/14787210.2020.1707079. Epub 2019 Dec 25.
5
Breast cancer and cytomegalovirus.乳腺癌与巨细胞病毒。
Clin Transl Oncol. 2020 Apr;22(4):585-602. doi: 10.1007/s12094-019-02164-1. Epub 2019 Jun 29.
6
Letermovir for the prevention of cytomegalovirus infection and disease in transplant recipients: an evidence-based review.来特莫韦预防移植受者巨细胞病毒感染和疾病:一项循证综述
Infect Drug Resist. 2019 Jun 4;12:1481-1491. doi: 10.2147/IDR.S180908. eCollection 2019.
7
Updates on antiviral drugs for cytomegalovirus prevention and treatment.巨细胞病毒预防和治疗的抗病毒药物更新。
Curr Opin Organ Transplant. 2019 Aug;24(4):469-475. doi: 10.1097/MOT.0000000000000666.
8
Clinical development of letermovir and maribavir: Overview of human cytomegalovirus drug resistance.来特莫韦和马拉韦罗的临床研发:人巨细胞病毒耐药性概述。
Antiviral Res. 2019 Mar;163:91-105. doi: 10.1016/j.antiviral.2019.01.011. Epub 2019 Jan 25.
9
Maribavir for Refractory or Resistant Cytomegalovirus Infections in Hematopoietic-cell or Solid-organ Transplant Recipients: A Randomized, Dose-ranging, Double-blind, Phase 2 Study.马利巴韦治疗造血细胞或实体器官移植受者难治性或耐药性巨细胞病毒感染的随机、剂量范围、双盲、Ⅱ期研究。
Clin Infect Dis. 2019 Apr 8;68(8):1255-1264. doi: 10.1093/cid/ciy706.
10
Reply to Gantt et al., "Higher Expectations for a Vaccine To Prevent Congenital Cytomegalovirus Infection".对甘特等人《对预防先天性巨细胞病毒感染疫苗的更高期望》一文的回复
J Virol. 2018 Jul 17;92(15). doi: 10.1128/JVI.00771-18. Print 2018 Aug 1.