• 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

Inhibition of human T-cell lymphotropic virus type III in vitro by phosphonoformate.

作者信息

Sandstrom E G, Kaplan J C, Byington R E, Hirsch M S

出版信息

Lancet. 1985 Jun 29;1(8444):1480-2. doi: 10.1016/s0140-6736(85)92255-x.

DOI:10.1016/s0140-6736(85)92255-x
PMID:2409414
Abstract

Phosphonoformate, an inhibitor of reverse transcriptase in a number of retroviruses, was shown to have a dose-related inhibitory effect on human T-cell lymphotropic virus type III (HTLV-III) replication in the H9 cell line in vitro. HTLV-III replication was eliminated at a concentration of 680 mumol, a non-cytotoxic dose. A lower dose of 132 mumol inhibited HTLV-III replication by more than 98%, as measured by reverse transcriptase activity, compared with untreated infected cultures. Reverse transcriptase activity in HTLV-III particles was completely inhibited by 5.0 mumol phosphonoformate.

摘要

相似文献

1
Inhibition of human T-cell lymphotropic virus type III in vitro by phosphonoformate.
Lancet. 1985 Jun 29;1(8444):1480-2. doi: 10.1016/s0140-6736(85)92255-x.
2
Synergistic inhibition of human T-cell lymphotropic virus type III replication in vitro by phosphonoformate and recombinant alpha-A interferon.膦甲酸盐与重组α-A干扰素在体外对人嗜T细胞病毒III型复制的协同抑制作用
Antimicrob Agents Chemother. 1986 Jul;30(1):189-91. doi: 10.1128/AAC.30.1.189.
3
Inhibition of HTLV-III/LAV replication by foscarnet.膦甲酸对人嗜T淋巴细胞病毒III型/淋巴腺病相关病毒复制的抑制作用
Biochem Pharmacol. 1985 Nov 15;34(22):4075-9. doi: 10.1016/0006-2952(85)90392-2.
4
Prospects of therapy for infections with human T-lymphotropic virus type III.人类嗜T淋巴细胞病毒III型感染的治疗前景
Ann Intern Med. 1985 Nov;103(5):750-5. doi: 10.7326/0003-4819-103-5-750.
5
Combinations of 3'-azido-3'-deoxythymidine (zidovudine) and phosphonoformate (foscarnet) against human immunodeficiency virus type 1 and cytomegalovirus replication in vitro.3'-叠氮-3'-脱氧胸苷(齐多夫定)与膦甲酸盐(膦甲酸)联合用于抗1型人类免疫缺陷病毒及体外巨细胞病毒复制的研究
Antimicrob Agents Chemother. 1989 May;33(5):663-9. doi: 10.1128/AAC.33.5.663.
6
Mode of action of phosphonoformate as an anti-herpes simplex virus agent.膦甲酸作为抗单纯疱疹病毒药物的作用机制。
Biochim Biophys Acta. 1981 Jan 29;652(1):90-8. doi: 10.1016/0005-2787(81)90212-4.
7
Inhibitors of retroviral DNA polymerase: their implication in the treatment of AIDS.逆转录病毒DNA聚合酶抑制剂:它们在艾滋病治疗中的意义。
Cancer Res. 1985 Sep;45(9 Suppl):4677s-4684s.
8
Differential inhibition of DNA polymerase and RNase H activities of the reverse transcriptase by phosphonoformate.膦甲酸对逆转录酶的DNA聚合酶和核糖核酸酶H活性的差异性抑制作用
Mol Cell Biochem. 1982 Mar 19;43(2):97-103. doi: 10.1007/BF00423097.
9
Phosphonoformate inhibits reverse transcriptase.膦甲酸抑制逆转录酶。
J Gen Virol. 1979 Nov;45(2):273-81. doi: 10.1099/0022-1317-45-2-273.
10
In vitro inhibition of Herpesvirus sylvilagus by phosphonoacetic acid and phosphonoformate.膦甲酸钠和膦乙酸对兔疱疹病毒的体外抑制作用。
Arch Virol. 1980;66(3):261-4. doi: 10.1007/BF01314739.

引用本文的文献

1
Anti-retroviral strategies for AIDS and related diseases.用于治疗艾滋病及相关疾病的抗逆转录病毒策略。
Can J Infect Dis. 1991 Fall;2(3):121-8. doi: 10.1155/1991/487657.
2
Relationship between 3'-azido-3'-deoxythymidine resistance and primer unblocking activity in foscarnet-resistant mutants of human immunodeficiency virus type 1 reverse transcriptase.1型人类免疫缺陷病毒逆转录酶的膦甲酸钠抗性突变体中3'-叠氮-3'-脱氧胸苷抗性与引物解封活性之间的关系
J Virol. 2003 Jun;77(11):6127-37. doi: 10.1128/jvi.77.11.6127-6137.2003.
3
Viral skin infections in the elderly: diagnosis and management.
老年人的病毒性皮肤感染:诊断与管理
Drugs Aging. 2002;19(7):503-14. doi: 10.2165/00002512-200219070-00004.
4
Coresistance to zidovudine and foscarnet is associated with multiple mutations in the human immunodeficiency virus type 1 reverse transcriptase.对齐多夫定和膦甲酸的协同耐药与人类免疫缺陷病毒1型逆转录酶的多个突变相关。
Antimicrob Agents Chemother. 1998 Nov;42(11):3038-43. doi: 10.1128/AAC.42.11.3038.
5
Minimising the dosage-limiting toxicities of foscarnet induction therapy.尽量减少膦甲酸诱导疗法的剂量限制性毒性。
Drug Saf. 1997 Apr;16(4):258-66. doi: 10.2165/00002018-199716040-00003.
6
Zidovudine resistance is suppressed by mutations conferring resistance of human immunodeficiency virus type 1 to foscarnet.齐多夫定耐药性可被赋予人类免疫缺陷病毒1型对膦甲酸钠耐药性的突变所抑制。
J Virol. 1996 Oct;70(10):7171-81. doi: 10.1128/JVI.70.10.7171-7181.1996.
7
Foscarnet 5 versus 7 days a week treatment for severe gastrointestinal CMV disease in HIV-infected patients.每周5天与7天使用膦甲酸钠治疗HIV感染患者的严重胃肠道巨细胞病毒疾病
Infection. 1996 Mar-Apr;24(2):121-4. doi: 10.1007/BF01713315.
8
Foscarnet alters antidiuretic hormone-mediated transport.膦甲酸钠改变抗利尿激素介导的转运。
Antimicrob Agents Chemother. 1995 Sep;39(9):2008-12. doi: 10.1128/AAC.39.9.2008.
9
Liposomal encapsulation of foscarnet protects against hypocalcemia induced by free foscarnet.膦甲酸钠的脂质体包封可防止游离膦甲酸钠引起的低钙血症。
Antimicrob Agents Chemother. 1995 Sep;39(9):1973-8. doi: 10.1128/AAC.39.9.1973.
10
Penetration of foscarnet into cerebrospinal fluid of AIDS patients.膦甲酸钠在艾滋病患者脑脊液中的渗透情况。
Antimicrob Agents Chemother. 1993 Sep;37(9):1777-80. doi: 10.1128/AAC.37.9.1777.