• 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

卡波韦尔:其左旋对映体在体外是一种针对人类免疫缺陷病毒的强效且选择性抗病毒剂。

Carbovir: the (-) enantiomer is a potent and selective antiviral agent against human immunodeficiency virus in vitro.

作者信息

Coates J A, Inggall H J, Pearson B A, Penn C R, Storer R, Williamson C, Cameron J M

机构信息

Department of Virology, Glaxo Group Research Limited, Greenford, U.K.

出版信息

Antiviral Res. 1991 Feb;15(2):161-8. doi: 10.1016/0166-3542(91)90033-n.

DOI:10.1016/0166-3542(91)90033-n
PMID:1677557
Abstract

In this paper we describe the in vitro antiviral activity of the (-) enantiomer of carbocyclic 2',3'-deoxydidehydroguanosine, (-) carbovir, a nucleoside analogue that has selective and potent anti-HIV activity in a series of lymphocyte culture systems. The cellular cytotoxicity of this compound has also been evaluated in a number of systems and compared to the saturated dideoxynucleoside analogues AZT and ddC.

摘要

在本文中,我们描述了碳环2',3'-二脱氧脱氢鸟苷的(-)对映体(-)卡波韦的体外抗病毒活性,卡波韦是一种核苷类似物,在一系列淋巴细胞培养系统中具有选择性和强效的抗HIV活性。还在多个系统中评估了该化合物的细胞毒性,并与饱和双脱氧核苷类似物齐多夫定和双脱氧胞苷进行了比较。

相似文献

1
Carbovir: the (-) enantiomer is a potent and selective antiviral agent against human immunodeficiency virus in vitro.卡波韦尔:其左旋对映体在体外是一种针对人类免疫缺陷病毒的强效且选择性抗病毒剂。
Antiviral Res. 1991 Feb;15(2):161-8. doi: 10.1016/0166-3542(91)90033-n.
2
Potent and selective activity of a new carbocyclic nucleoside analog (carbovir: NSC 614846) against human immunodeficiency virus in vitro.一种新型碳环核苷类似物(卡波韦:NSC 614846)在体外对人类免疫缺陷病毒具有强效和选择性活性。
Biochem Biophys Res Commun. 1988 Oct 31;156(2):1046-53. doi: 10.1016/s0006-291x(88)80950-1.
3
Activities of (-)-carbovir and 3'-azido-3'-deoxythymidine against human immunodeficiency virus in vitro.(-)-卡波韦和3'-叠氮-3'-脱氧胸苷在体外对人类免疫缺陷病毒的活性。
Antimicrob Agents Chemother. 1990 Jun;34(6):1297-300. doi: 10.1128/AAC.34.6.1297.
4
Inhibition of human immunodeficiency virus (HIV-1/HTLV-IIIBa-L) replication in fresh and cultured human peripheral blood monocytes/macrophages by azidothymidine and related 2',3'-dideoxynucleosides.叠氮胸苷及相关的2',3'-双脱氧核苷对新鲜的和培养的人外周血单核细胞/巨噬细胞中人类免疫缺陷病毒(HIV-1/HTLV-IIIBa-L)复制的抑制作用
J Exp Med. 1988 Sep 1;168(3):1111-25. doi: 10.1084/jem.168.3.1111.
5
Human immunodeficiency virus inhibition is prolonged by 3'-azido-3'-deoxythymidine alternating with 2',3'-dideoxycytidine compared with 3'-azido-3'-deoxythymidine alone.与单独使用3'-叠氮-3'-脱氧胸苷相比,3'-叠氮-3'-脱氧胸苷与2',3'-二脱氧胞苷交替使用可延长对人类免疫缺陷病毒的抑制作用。
Antimicrob Agents Chemother. 1989 Jun;33(6):920-3. doi: 10.1128/AAC.33.6.920.
6
Effects of bone marrow stimulatory cytokines on human immunodeficiency virus replication and the antiviral activity of dideoxynucleosides in cultures of monocyte/macrophages.骨髓刺激细胞因子对人免疫缺陷病毒复制及双脱氧核苷在单核细胞/巨噬细胞培养物中的抗病毒活性的影响。
Blood. 1992 Aug 15;80(4):995-1003.
7
Evaluation of synergy between carbovir and 3'-azido-2',3'-deoxythymidine for inhibition of human immunodeficiency virus type 1.卡波韦和3'-叠氮-2',3'-双脱氧胸苷协同抑制1型人类免疫缺陷病毒的评估。
Antimicrob Agents Chemother. 1993 Jan;37(1):144-7. doi: 10.1128/AAC.37.1.144.
8
Decreased anti-human immunodeficiency virus type-1 activities of 2',3'-dideoxynucleoside analogs in MOLT-4 cell sublines resistant to 2',3'-dideoxynucleoside analogs.
Acta Virol. 1993 Oct;37(5):360-8.
9
The antiretroviral and cytostatic activity, and metabolism of 3'-azido-2',3'-dideoxythymidine, 3'-fluoro-2',3'-dideoxythymidine and 2',3'-dideoxycytidine are highly cell type-dependent.
Adv Exp Med Biol. 1989;253B:407-13. doi: 10.1007/978-1-4684-5676-9_60.
10
(-)-2'-deoxy-3'-thiacytidine is a potent, highly selective inhibitor of human immunodeficiency virus type 1 and type 2 replication in vitro.(-)-2'-脱氧-3'-硫代胞苷是一种在体外对1型和2型人类免疫缺陷病毒复制具有强效、高度选择性的抑制剂。
Antimicrob Agents Chemother. 1992 Apr;36(4):733-9. doi: 10.1128/AAC.36.4.733.

引用本文的文献

1
Synthesis of Cyclobutane Analogue 4: Preparation of Purine and Pyrimidine Carbocyclic Nucleoside Derivatives.合成环丁烷类似物 4:嘌呤和嘧啶碳环核苷衍生物的制备。
Molecules. 2019 Sep 5;24(18):3235. doi: 10.3390/molecules24183235.
2
Metabolism of carbovir, a potent inhibitor of human immunodeficiency virus type 1, and its effects on cellular metabolism.卡波韦(一种强效的人类免疫缺陷病毒1型抑制剂)的代谢及其对细胞代谢的影响。
Antimicrob Agents Chemother. 1993 May;37(5):1004-9. doi: 10.1128/AAC.37.5.1004.
3
Zalcitabine. A review of its pharmacology and clinical potential in acquired immunodeficiency syndrome (AIDS).
扎西他滨。对其在获得性免疫缺陷综合征(艾滋病)中的药理学及临床潜力的综述。
Drugs. 1992 Oct;44(4):656-83. doi: 10.2165/00003495-199244040-00009.