• 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

肌苷单磷酸脱氢酶作为抗病毒药物研发的探针。

Inosine monophosphate dehydrogenase as a probe in antiviral drug discovery.

作者信息

Nair Vasu, Shu Qingning

机构信息

The Center for Drug Discovery, Department of Pharmaceutical and Biomedical Sciences, The University of Georgia, Athens, GA, USA.

出版信息

Antivir Chem Chemother. 2007;18(5):245-58. doi: 10.1177/095632020701800501.

DOI:10.1177/095632020701800501
PMID:18046958
Abstract

Inosine monophosphate (IMP) dehydrogenase (IMPDH) is a significant enzyme in the purine nucleotide biosynthetic pathway. IMPDH is viewed as an important biological target in the quest for drugs in the antiviral therapeutic area. This review article is focused on the chemistry and biology of IMPDH inhibitors and the use of IMPDH inhibition data as a probe in antiviral drug discovery. Examples of both inosine 5' monophosphate and NAD+ site-directed inhibitors are presented. Correlation of antiviral activities with IMPDH inhibition is discussed.

摘要

肌苷一磷酸(IMP)脱氢酶(IMPDH)是嘌呤核苷酸生物合成途径中的一种重要酶。在抗病毒治疗领域寻找药物的过程中,IMPDH被视为一个重要的生物学靶点。这篇综述文章聚焦于IMPDH抑制剂的化学和生物学特性,以及将IMPDH抑制数据用作抗病毒药物发现中的一种探针。文中展示了肌苷5'-单磷酸和NAD⁺位点定向抑制剂的实例。还讨论了抗病毒活性与IMPDH抑制之间的相关性。

相似文献

1
Inosine monophosphate dehydrogenase as a probe in antiviral drug discovery.肌苷单磷酸脱氢酶作为抗病毒药物研发的探针。
Antivir Chem Chemother. 2007;18(5):245-58. doi: 10.1177/095632020701800501.
2
Inhibitors of inosine monophosphate dehydrogenase: probes for antiviral drug discovery.肌苷单磷酸脱氢酶抑制剂:抗病毒药物研发的探针
Nucleosides Nucleotides Nucleic Acids. 2005;24(5-7):717-20. doi: 10.1081/ncn-200060308.
3
Inosine monophosphate dehydrogenase (IMPDH) as a target in drug discovery.肌苷单磷酸脱氢酶(IMPDH)作为药物研发的靶点。
Med Res Rev. 2008 Mar;28(2):219-32. doi: 10.1002/med.20104.
4
IMPDH as a biological probe for RNA antiviral drug discovery: synthesis, enzymology, molecular docking, and antiviral activity of new ribonucleosides with surrogate bases.肌苷-5'-单磷酸脱氢酶作为RNA抗病毒药物发现的生物探针:具有替代碱基的新型核糖核苷的合成、酶学、分子对接及抗病毒活性
Nucleosides Nucleotides Nucleic Acids. 2007;26(6-7):651-4. doi: 10.1080/15257770701490506.
5
The structure of inosine 5'-monophosphate dehydrogenase and the design of novel inhibitors.肌苷5'-单磷酸脱氢酶的结构与新型抑制剂的设计。
Immunopharmacology. 2000 May;47(2-3):163-84. doi: 10.1016/s0162-3109(00)00193-4.
6
Inactivation of inosine 5'-monophosphate dehydrogenase by the antiviral agent 5-ethynyl-1-beta-D-ribofuranosylimidazole-4-carboxamide 5'-monophosphate.抗病毒药物5-乙炔基-1-β-D-呋喃核糖基咪唑-4-甲酰胺5'-单磷酸酯对肌苷5'-单磷酸脱氢酶的失活作用
Biochemistry. 1996 Jan 9;35(1):95-101. doi: 10.1021/bi951499q.
7
[The basic functions of inosine 5'-monophosphate dehydrogenase and its application in drug discovery].[5'-肌苷酸脱氢酶的基本功能及其在药物研发中的应用]
Yao Xue Xue Bao. 2014 Mar;49(3):285-92.
8
Bacillus anthracis inosine 5'-monophosphate dehydrogenase in action: the first bacterial series of structures of phosphate ion-, substrate-, and product-bound complexes.炭疽芽孢杆菌肌苷 5′-单磷酸脱氢酶的作用机制:首个结合磷酸盐离子、底物和产物的系列细菌结构复合物。
Biochemistry. 2012 Aug 7;51(31):6148-63. doi: 10.1021/bi300511w. Epub 2012 Jul 25.
9
Covalent inactivation of Mycobacterium thermoresistibile inosine-5'-monophosphate dehydrogenase (IMPDH).结核分枝杆菌肌苷-5'-单磷酸脱氢酶(IMPDH)的共价失活。
Bioorg Med Chem Lett. 2020 Jan 15;30(2):126792. doi: 10.1016/j.bmcl.2019.126792. Epub 2019 Nov 9.
10
Novel inhibitors of inosine monophosphate dehydrogenase in patent literature of the last decade.近十年专利文献中肌苷单磷酸脱氢酶的新型抑制剂
Recent Pat Anticancer Drug Discov. 2013 May;8(2):103-25.

引用本文的文献

1
Role of the Mobile Active Site Flap in IMP Dehydrogenase Inhibitor Binding.移动活性位点瓣在肌苷酸脱氢酶抑制剂结合中的作用。
ACS Infect Dis. 2025 Feb 14;11(2):442-452. doi: 10.1021/acsinfecdis.4c00636. Epub 2025 Jan 29.
2
Fragment-Based Lead Discovery Strategies in Antimicrobial Drug Discovery.抗菌药物发现中的基于片段的先导化合物发现策略
Antibiotics (Basel). 2023 Feb 3;12(2):315. doi: 10.3390/antibiotics12020315.
3
Identification of a potent dual-function inhibitor for hIMPDH isoforms by computer-aided drug discovery approaches.
通过计算机辅助药物发现方法鉴定一种针对人肌苷-5'-单磷酸脱氢酶同工型的强效双功能抑制剂。
Front Pharmacol. 2022 Oct 26;13:977568. doi: 10.3389/fphar.2022.977568. eCollection 2022.
4
Inhibitors of Nucleotide Biosynthesis as Candidates for a Wide Spectrum of Antiviral Chemotherapy.作为广谱抗病毒化疗候选药物的核苷酸生物合成抑制剂
Microorganisms. 2022 Aug 12;10(8):1631. doi: 10.3390/microorganisms10081631.
5
Structures, functions, and mechanisms of filament forming enzymes: a renaissance of enzyme filamentation.丝状形成酶的结构、功能及机制:酶丝状化的复兴
Biophys Rev. 2019 Dec;11(6):927-994. doi: 10.1007/s12551-019-00602-6. Epub 2019 Nov 16.
6
Purine-Metabolising Enzymes and Apoptosis in Cancer.癌症中的嘌呤代谢酶与细胞凋亡
Cancers (Basel). 2019 Sep 12;11(9):1354. doi: 10.3390/cancers11091354.
7
Newer human inosine 5'-monophosphate dehydrogenase 2 (hIMPDH2) inhibitors as potential anticancer agents.新型人肌苷 5'-单磷酸脱氢酶 2(hIMPDH2)抑制剂作为潜在的抗癌药物。
J Enzyme Inhib Med Chem. 2018 Dec;33(1):972-977. doi: 10.1080/14756366.2018.1474211.
8
Fragment-Based Approach to Targeting Inosine-5'-monophosphate Dehydrogenase (IMPDH) from Mycobacterium tuberculosis.基于片段的结核分枝杆菌肌苷 5'-单磷酸脱氢酶(IMPDH)靶向方法。
J Med Chem. 2018 Apr 12;61(7):2806-2822. doi: 10.1021/acs.jmedchem.7b01622. Epub 2018 Mar 23.
9
Synthesis of carbocyclic nucleoside analogs with five-membered heterocyclic nucleobases.具有五元杂环核苷碱基的碳环核苷类似物的合成。
Tetrahedron Lett. 2015 Jun 3;56(23):3587-3590. doi: 10.1016/j.tetlet.2015.01.051.
10
Antiviral activity of an N-allyl acridone against dengue virus.一种N-烯丙基吖啶酮对登革病毒的抗病毒活性。
J Biomed Sci. 2015 Apr 17;22(1):29. doi: 10.1186/s12929-015-0134-2.