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Selective inhibition of the replication of herpes simplex virus by 5-halogenated analogues of deoxycytidine.

作者信息

Schildkraut I, Cooper G M, Greer S

出版信息

Mol Pharmacol. 1975 Mar;11(2):153-8.

PMID:164617
Abstract
摘要

相似文献

1
Selective inhibition of the replication of herpes simplex virus by 5-halogenated analogues of deoxycytidine.
Mol Pharmacol. 1975 Mar;11(2):153-8.
2
5-Substituted 2'-deoxyuridines which selectively inhibit herpes simplex virus replication.选择性抑制单纯疱疹病毒复制的5-取代2'-脱氧尿苷。
Adv Ophthalmol. 1979;38:204-13.
3
Inhibition of Herpes simplex virus replication by cordycepin.虫草素对单纯疱疹病毒复制的抑制作用。
Isr J Med Sci. 1973 Nov-Dec;9(11):1581-5.
4
Inhibition of Herpes simplex virus replication by camptothecin.喜树碱对单纯疱疹病毒复制的抑制作用。
Isr J Med Sci. 1973 Nov-Dec;9(11):1578-81.
5
Mechanism of action of 5-(2-chloroethyl)-2'-deoxyuridine, a selective inhibitor of herpes simplex virus replication.5-(2-氯乙基)-2'-脱氧尿苷(一种单纯疱疹病毒复制的选择性抑制剂)的作用机制
Mol Pharmacol. 1990 May;37(5):658-64.
6
Capacity of deoxycytidine to selectively antagonize cytotoxicity of 5-halogenated analogs of deoxycytidine without loss of antiherpetic activity.脱氧胞苷在不丧失抗疱疹活性的情况下,选择性拮抗脱氧胞苷5-卤代类似物细胞毒性的能力。
Antimicrob Agents Chemother. 1982 Sep;22(3):431-41. doi: 10.1128/AAC.22.3.431.
7
5-Halogenated analogs of deoxycytidine as selective inhibitors of the replication of herpes simplex viruses in cell culture and related studies of intracranial herpes simplex virus infections in mice.脱氧胞苷的5-卤代类似物作为单纯疱疹病毒在细胞培养中复制的选择性抑制剂以及小鼠颅内单纯疱疹病毒感染的相关研究
Ann N Y Acad Sci. 1975 Aug 8;255:359-65. doi: 10.1111/j.1749-6632.1975.tb29243.x.
8
5-(2-Chloroethyl)-2'-deoxyuridine: a potent and selective inhibitor of herpes viruses in vitro and in vivo.5-(2-氯乙基)-2'-脱氧尿苷:一种在体外和体内均有效的疱疹病毒选择性抑制剂。
Antiviral Res. 1985;Suppl 1:20-8.
9
Reactivation of herpes simplex virus in nonpermissive cells: dependence on cell fusion.单纯疱疹病毒在非允许细胞中的重新激活:对细胞融合的依赖性。
Trans Am Neurol Assoc. 1973;98:174-7.
10
The effect of cytosine arabinoside on virus production in various cells infected with herpes simplex virus types 1 and 2.阿糖胞苷对感染1型和2型单纯疱疹病毒的各种细胞中病毒产生的影响。
Cancer Res. 1973 Jan;33(1):166-70.

引用本文的文献

1
Chapter 3 Antiviral drugs: general considerations.第3章 抗病毒药物:一般考虑因素。
Perspect Med Virol. 1985;1:93-126. doi: 10.1016/S0168-7069(08)70011-9. Epub 2008 May 29.
2
Incorporation of 5-substituted analogs of deoxycytidine into DNA of herpes simplex virus-infected or - transformed cells without deamination to the thymidine analog.将脱氧胞苷的5-取代类似物掺入单纯疱疹病毒感染或转化细胞的DNA中,而不会脱氨基形成胸苷类似物。
Antimicrob Agents Chemother. 1983 Mar;23(3):465-76. doi: 10.1128/AAC.23.3.465.
3
Synthesis and biological properties of 2'-deoxy-5-vinyluridine and 2'deoxy-5-vinylcytidine.
2'-脱氧-5-乙烯基尿苷和2'-脱氧-5-乙烯基胞苷的合成及生物学特性
Nucleic Acids Res. 1982 Sep 11;10(17):5285-95. doi: 10.1093/nar/10.17.5285.
4
Capacity of deoxycytidine to selectively antagonize cytotoxicity of 5-halogenated analogs of deoxycytidine without loss of antiherpetic activity.脱氧胞苷在不丧失抗疱疹活性的情况下,选择性拮抗脱氧胞苷5-卤代类似物细胞毒性的能力。
Antimicrob Agents Chemother. 1982 Sep;22(3):431-41. doi: 10.1128/AAC.22.3.431.
5
Acyclovir inhibition of Epstein-Barr virus replication.阿昔洛韦对EB病毒复制的抑制作用。
Proc Natl Acad Sci U S A. 1980 Sep;77(9):5163-6. doi: 10.1073/pnas.77.9.5163.
6
Specific targets for antiviral drugs.抗病毒药物的特定靶点。
Biochem J. 1982 Jul 1;205(1):1-13. doi: 10.1042/bj2050001.
7
N-Mannich-base prodrugs of 5-iodo-2'-deoxycytidine as topical delivery enhancers.5-碘-2'-脱氧胞苷的N-曼尼希碱前药作为局部给药增强剂。
Pharm Res. 1987 Aug;4(4):317-20. doi: 10.1023/a:1016497204211.
8
5-Propyl-2'-deoxyuridine: a specific anti-herpes agent.5-丙基-2'-脱氧尿苷:一种特异性抗疱疹剂。
Antimicrob Agents Chemother. 1978 Mar;13(3):545-7. doi: 10.1128/AAC.13.3.545.
9
Inhibition of herpes simplex virus-induced DNA polymerase activity and viral DNA replication by 9-(2-hydroxyethoxymethyl)guanine and its triphosphate.9-(2-羟乙氧甲基)鸟嘌呤及其三磷酸酯对单纯疱疹病毒诱导的DNA聚合酶活性和病毒DNA复制的抑制作用。
J Virol. 1979 Oct;32(1):72-7. doi: 10.1128/JVI.32.1.72-77.1979.
10
(E)-5-(2-Bromovinyl)-2'-deoxyuridine: a potent and selective anti-herpes agent.(E)-5-(2-溴乙烯基)-2'-脱氧尿苷:一种高效且选择性的抗疱疹药物。
Proc Natl Acad Sci U S A. 1979 Jun;76(6):2947-51. doi: 10.1073/pnas.76.6.2947.