• 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

新一代更强效的合成抗鼻病毒化合物:其最低抑菌浓度及协同相互作用的比较

A 'new' generation of more potent synthetic antirhinovirus compounds: comparison of their MICs and their synergistic interactions.

作者信息

Al-Nakib W, Tyrrell D A

机构信息

MRC Common Cold Unit, Harvard Hospital, Salisbury, Wiltshire, U.K.

出版信息

Antiviral Res. 1987 Nov;8(4):179-87. doi: 10.1016/0166-3542(87)90072-6.

DOI:10.1016/0166-3542(87)90072-6
PMID:2833156
Abstract

A 'new' generation of synthetic antirhinovirus compounds has recently become available for in vitro evaluation. Thus a new group of compounds from Janssen was found to be 10-fold more active than enviroxime or 57-fold more active than dichloroflavan (DCF), against human rhinovirus 9 (HRV-9). In addition, they were also some 5- and 10-fold more potent than enviroxime and DCF, respectively, against HRV-2. Similarly, a 'new' series of antirhinovirus compounds from Roche, although as active as enviroxime against HRV-9, were found to be 4-fold more potent than DCF against the same virus. Moreover, they were 45- and 90-fold more active than enviroxime and DCF, respectively, when tested against HRV-2. We found that generally HRV-2 was more sensitive to these new compounds than HRV-9. In this study we also report on the synergistic interaction between these new synthetic substances and also with some of the earlier compounds such as DCF and enviroxime and we discuss the possible implication of this synergistic activity regarding the future prevention and treatment of common colds caused by rhinoviruses.

摘要

新一代合成抗鼻病毒化合物最近已可用于体外评估。因此,发现杨森公司的一组新化合物对人鼻病毒9(HRV - 9)的活性比恩韦肟高10倍,比二氯黄烷(DCF)高57倍。此外,它们对HRV - 2的效力分别比恩韦肟和DCF约高5倍和10倍。同样,罗氏公司的一系列“新”抗鼻病毒化合物,虽然对HRV - 9的活性与恩韦肟相同,但发现对同一病毒的效力比DCF高4倍。此外,在针对HRV - 2进行测试时,它们的活性分别比恩韦肟和DCF高45倍和90倍。我们发现,一般来说,HRV - 2对这些新化合物比HRV - 9更敏感。在本研究中,我们还报告了这些新合成物质之间以及与一些早期化合物(如DCF和恩韦肟)之间的协同相互作用,并讨论了这种协同活性对未来预防和治疗由鼻病毒引起的普通感冒的可能意义。

相似文献

1
A 'new' generation of more potent synthetic antirhinovirus compounds: comparison of their MICs and their synergistic interactions.新一代更强效的合成抗鼻病毒化合物:其最低抑菌浓度及协同相互作用的比较
Antiviral Res. 1987 Nov;8(4):179-87. doi: 10.1016/0166-3542(87)90072-6.
2
Comparative studies on the modes of action of the antirhinovirus agents Ro 09-0410, Ro 09-0179, RMI-15,731, 4',6-dichloroflavan, and enviroxime.抗鼻病毒药物Ro 09-0410、Ro 09-0179、RMI-15731、4',6-二氯黄烷和恩韦肟作用模式的比较研究
Antimicrob Agents Chemother. 1985 Apr;27(4):595-9. doi: 10.1128/AAC.27.4.595.
3
Synergism between anti-rhinovirus antivirals: various human interferons and a number of synthetic compounds.
Antiviral Res. 1986 Jul;6(4):241-52. doi: 10.1016/0166-3542(86)90005-7.
4
Comparative studies on the antirhinovirus activity and the mode of action of the rhinovirus capsid binding agents, chalcone amides.鼻病毒衣壳结合剂查耳酮酰胺的抗鼻病毒活性及作用模式的比较研究
Antiviral Res. 1990 Feb;13(2):61-74. doi: 10.1016/0166-3542(90)90022-y.
5
Synthesis and antirhinovirus activity of 3-(diethylamino)-5-phenylisoxazole derivatives.3-(二乙氨基)-5-苯基异恶唑衍生物的合成及其抗鼻病毒活性
Farmaco. 1996 May;51(5):351-9.
6
9-Benzyl-6-(dimethylamino)-9H-purines with antirhinovirus activity.具有抗鼻病毒活性的9-苄基-6-(二甲基氨基)-9H-嘌呤。
J Med Chem. 1988 Oct;31(10):2001-4. doi: 10.1021/jm00118a025.
7
Synthesis and antirhinovirus activity of new 3-benzyl chromene and chroman derivatives.新型3-苄基色烯和色满衍生物的合成及其抗鼻病毒活性
Bioorg Med Chem. 2009 May 15;17(10):3720-7. doi: 10.1016/j.bmc.2009.03.051. Epub 2009 Apr 1.
8
Molecular basis of drug resistance to new antirhinovirus agents.新型抗鼻病毒药物耐药性的分子基础
J Antimicrob Chemother. 1986 Oct;18 Suppl B:11-8. doi: 10.1093/jac/18.supplement_b.11.
9
Activity against rhinoviruses, toxicity, and delivery in aerosol of enviroxime in liposomes.脂质体中恩韦肟对鼻病毒的活性、毒性及气雾剂递送
Antimicrob Agents Chemother. 1988 Jun;32(6):890-5. doi: 10.1128/AAC.32.6.890.
10
Synthesis and evaluation of antirhinovirus activity of 3-hydroxy and 3-methoxy 2-styrylchromones.3-羟基和3-甲氧基-2-苯乙烯基色酮的抗鼻病毒活性的合成与评价
Antivir Chem Chemother. 2003 Jul;14(4):195-203. doi: 10.1177/095632020301400404.

引用本文的文献

1
Chalcone-amide, a privileged backbone for the design and development of selective SARS-CoV/SARS-CoV-2 papain-like protease inhibitors.查尔酮酰胺,一种用于设计和开发选择性 SARS-CoV/SARS-CoV-2 木瓜蛋白酶样蛋白酶抑制剂的优势骨架。
Eur J Med Chem. 2022 Oct 5;240:114572. doi: 10.1016/j.ejmech.2022.114572. Epub 2022 Jul 3.
2
Selective human enterovirus and rhinovirus inhibitors: An overview of capsid-binding and protease-inhibiting molecules.选择性人肠道病毒和鼻病毒抑制剂:衣壳结合分子与蛋白酶抑制分子综述
Med Res Rev. 2004 Jul;24(4):449-74. doi: 10.1002/med.10067.
3
Chemotherapy of rhinovirus colds.
鼻病毒感冒的化学疗法。
Antimicrob Agents Chemother. 1988 Apr;32(4):409-19. doi: 10.1128/AAC.32.4.409.
4
In vitro and in vivo activities of WIN 54954, a new broad-spectrum antipicornavirus drug.新型广谱抗微小核糖核酸病毒药物WIN 54954的体外和体内活性
Antimicrob Agents Chemother. 1989 Dec;33(12):2069-74. doi: 10.1128/AAC.33.12.2069.
5
Suppression of colds in human volunteers challenged with rhinovirus by a new synthetic drug (R61837).一种新型合成药物(R61837)对感染鼻病毒的人类志愿者感冒症状的抑制作用。
Antimicrob Agents Chemother. 1989 Apr;33(4):522-5. doi: 10.1128/AAC.33.4.522.
6
Pathogenicity for humans of human rhinovirus type 2 mutants resistant to or dependent on chalcone Ro 09-0410.对查耳酮Ro 09 - 0410耐药或依赖的2型人鼻病毒对人类的致病性
Antimicrob Agents Chemother. 1990 Jun;34(6):963-6. doi: 10.1128/AAC.34.6.963.
7
Binding affinities of structurally related human rhinovirus capsid-binding compounds are related to their activities against human rhinovirus type 14.结构相关的人鼻病毒衣壳结合化合物的结合亲和力与其对14型人鼻病毒的活性相关。
Antimicrob Agents Chemother. 1991 Jun;35(6):1040-7. doi: 10.1128/AAC.35.6.1040.