• 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

S-adenosyl-L-homocysteine hydrolase as a target for antiviral chemotherapy.

作者信息

Wolfe M S, Borchardt R T

机构信息

Department of Medicinal Chemistry, University of Kansas, Lawrence 66045.

出版信息

J Med Chem. 1991 May;34(5):1521-30. doi: 10.1021/jm00109a001.

DOI:10.1021/jm00109a001
PMID:2033576
Abstract
摘要

相似文献

1
S-adenosyl-L-homocysteine hydrolase as a target for antiviral chemotherapy.
J Med Chem. 1991 May;34(5):1521-30. doi: 10.1021/jm00109a001.
2
Rational approaches to the design of antiviral agents based on S-adenosyl-L-homocysteine hydrolase as a molecular target.基于S-腺苷-L-高半胱氨酸水解酶作为分子靶点设计抗病毒药物的合理方法。
Antiviral Res. 1992 Sep;19(3):247-65. doi: 10.1016/0166-3542(92)90083-h.
3
Synthesis of S-adenosyl-L-homocysteine hydrolase inhibitors and their biological activities.S-腺苷-L-高半胱氨酸水解酶抑制剂的合成及其生物活性。
Nucleic Acids Symp Ser. 1999(42):25-6. doi: 10.1093/nass/42.1.25.
4
Inactivation of S-adenosyl-L-homocysteine hydrolase and antiviral activity with 5',5',6',6'-tetradehydro-6'-deoxy-6'-halohomoadenosine analogues (4'-haloacetylene analogues derived from adenosine).S-腺苷-L-高半胱氨酸水解酶的失活以及5',5',6',6'-四脱氢-6'-脱氧-6'-卤代高腺苷类似物(源自腺苷的4'-卤代乙炔类似物)的抗病毒活性。
J Med Chem. 1998 Sep 24;41(20):3857-64. doi: 10.1021/jm980163m.
5
S-adenosylhomocysteine hydrolase inhibitors as broad-spectrum antiviral agents.作为广谱抗病毒剂的S-腺苷同型半胱氨酸水解酶抑制剂
Biochem Pharmacol. 1987 Aug 15;36(16):2567-75. doi: 10.1016/0006-2952(87)90533-8.
6
Nucleic acid related compounds. 74. Synthesis and biological activity of 2'(and 3')-deoxy-2'(and 3')-methylenenucleoside analogues that function as mechanism-based inhibitors of S-adenosyl-L-homocysteine hydrolase and/or ribonucleotide reductase.
J Med Chem. 1992 Jun 12;35(12):2283-93. doi: 10.1021/jm00090a020.
7
Elucidation of the mechanism by which homocysteine potentiates the anti-vaccinia virus effects of the S-adenosylhomocysteine hydrolase inhibitor 9-(trans-2',trans-3'-dihydroxycyclopent-4'-enyl)-adenine.阐明同型半胱氨酸增强S-腺苷同型半胱氨酸水解酶抑制剂9-(反式-2',反式-3'-二羟基环戊-4'-烯基)-腺嘌呤抗痘苗病毒作用的机制。
Mol Pharmacol. 1989 Sep;36(3):490-6.
8
Treatment of lethal Ebola virus infection in mice with a single dose of an S-adenosyl-L-homocysteine hydrolase inhibitor.用单剂量S-腺苷-L-高半胱氨酸水解酶抑制剂治疗小鼠致死性埃博拉病毒感染。
Antiviral Res. 2000 Feb;45(2):135-47. doi: 10.1016/s0166-3542(00)00066-8.
9
Homocysteine potentiates the antiviral and cytostatic activity of those nucleoside analogues that are targeted at S-adenosylhomocysteine hydrolase.
Biochem Pharmacol. 1989 Jun 1;38(11):1771-8. doi: 10.1016/0006-2952(89)90411-5.
10
[Synthesis of S-9-(2,3-dihydroxypropyl)adenine (DHPA) analogs and their inhibition of S-adenosyl-L-homocysteine (SAH) hydrolase].[S-9-(2,3-二羟基丙基)腺嘌呤(DHPA)类似物的合成及其对S-腺苷-L-高半胱氨酸(SAH)水解酶的抑制作用]
Yao Xue Xue Bao. 1997;32(3):188-92.

引用本文的文献

1
The chemistry and biology of natural ribomimetics and related compounds.天然核酶模拟物及相关化合物的化学与生物学
RSC Chem Biol. 2022 Apr 7;3(5):519-538. doi: 10.1039/d2cb00019a. eCollection 2022 May 11.
2
Antivirals against the Chikungunya Virus.抗基孔肯雅病毒药物。
Viruses. 2021 Jul 5;13(7):1307. doi: 10.3390/v13071307.
3
5'-Nor-3-Deaza-1',6'-Isoneplanocin, the Synthesis and Antiviral Study.5'-去氮-3-去氮杂-1',6'-异鸟嘌呤核苷,合成与抗病毒研究。
Molecules. 2020 Aug 25;25(17):3865. doi: 10.3390/molecules25173865.
4
Antiproliferative and Antimigration Activities of Fluoro-Neplanocin A via Inhibition of Histone H3 Methylation in Triple-Negative Breast Cancer.氟代新培高利特 A 通过抑制三阴性乳腺癌中的组蛋白 H3 甲基化发挥抗增殖和抗迁移作用。
Biomolecules. 2020 Mar 31;10(4):530. doi: 10.3390/biom10040530.
5
6'-β-Fluoro-Homoaristeromycin and 6'-Fluoro-Homoneplanocin A Are Potent Inhibitors of Chikungunya Virus Replication through Their Direct Effect on Viral Nonstructural Protein 1.6'-β-氟霍巴他汀和 6'-氟霍巴他霉素是通过直接作用于病毒非结构蛋白 1 而对基孔肯雅病毒复制具有强大抑制作用的药物。
Antimicrob Agents Chemother. 2020 Mar 24;64(4). doi: 10.1128/AAC.02532-19.
6
Identification of 6'-β-fluoro-homoaristeromycin as a potent inhibitor of chikungunya virus replication.鉴定 6'-β-氟-homoaristeromycin 为一种有效的基孔肯雅病毒复制抑制剂。
Eur J Med Chem. 2020 Feb 1;187:111956. doi: 10.1016/j.ejmech.2019.111956. Epub 2019 Dec 9.
7
Design, Synthesis, and Anti-RNA Virus Activity of 6'-Fluorinated-Aristeromycin Analogues.6'-氟代阿利斯特霉素类似物的设计、合成及抗 RNA 病毒活性。
J Med Chem. 2019 Jul 11;62(13):6346-6362. doi: 10.1021/acs.jmedchem.9b00781. Epub 2019 Jun 20.
8
The evolution of nucleoside analogue antivirals: A review for chemists and non-chemists. Part 1: Early structural modifications to the nucleoside scaffold.核苷类似物抗病毒药物的演进:化学家与非化学家的综述。第 1 部分:核苷骨架的早期结构修饰。
Antiviral Res. 2018 Jun;154:66-86. doi: 10.1016/j.antiviral.2018.04.004. Epub 2018 Apr 10.
9
3,7-Dideazaneplanocin: Synthesis and antiviral analysis.3,7-二去氮奈普洛诺辛:合成与抗病毒分析。
Antivir Chem Chemother. 2017 Dec;25(3):90-93. doi: 10.1177/2040206617742561.
10
Characterization of human S-adenosyl-homocysteine hydrolase in vitro and identification of its potential inhibitors.人S-腺苷同型半胱氨酸水解酶的体外特性及其潜在抑制剂的鉴定。
J Enzyme Inhib Med Chem. 2017 Dec;32(1):1209-1215. doi: 10.1080/14756366.2017.1370584.