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Inhibitory effects of (E)-5-(2-bromovinyl)-2'-deoxyuridine (BVDU) and related compounds on herpes simplex virus (HSV)-infected cells and HSV thymidine kinase gene-transformed cells.

作者信息

Balzarini J, De Clercq E

机构信息

Rega Institute for Medical Research, Katholieke Universiteit Leuven, Belgium.

出版信息

Methods Find Exp Clin Pharmacol. 1989 Jun;11(6):379-89.

PMID:2545982
Abstract
摘要

相似文献

1
Inhibitory effects of (E)-5-(2-bromovinyl)-2'-deoxyuridine (BVDU) and related compounds on herpes simplex virus (HSV)-infected cells and HSV thymidine kinase gene-transformed cells.(E)-5-(2-溴乙烯基)-2'-脱氧尿苷(BVDU)及相关化合物对单纯疱疹病毒(HSV)感染细胞和HSV胸苷激酶基因转化细胞的抑制作用。
Methods Find Exp Clin Pharmacol. 1989 Jun;11(6):379-89.
2
Thymidylate synthase is the principal target enzyme for the cytostatic activity of (E)-5-(2-bromovinyl)-2'-deoxyuridine against murine mammary carcinoma (FM3A) cells transformed with the herpes simplex virus type 1 or type 2 thymidine kinase gene.胸苷酸合成酶是(E)-5-(2-溴乙烯基)-2'-脱氧尿苷对用1型或2型单纯疱疹病毒胸苷激酶基因转化的小鼠乳腺癌(FM3A)细胞的细胞生长抑制活性的主要靶酶。
Mol Pharmacol. 1987 Sep;32(3):410-6.
3
Selective inhibition of the proliferation of herpes simplex virus type 1 thymidine kinase gene-transformed murine mammary FM3A carcinoma cells by (E)-5-(2-bromovinyl)-2'-deoxyuridine and related compounds.(E)-5-(2-溴乙烯基)-2'-脱氧尿苷及相关化合物对单纯疱疹病毒1型胸苷激酶基因转化的小鼠乳腺FM3A癌细胞增殖的选择性抑制作用
Nucleic Acids Symp Ser. 1985(16):283-6.
4
Highly selective cytostatic activity of (E)-5-(2-bromovinyl)-2'-deoxyuridine derivatives for murine mammary carcinoma (FM3A) cells transformed with the herpes simplex virus type 1 thymidine kinase gene.(E)-5-(2-溴乙烯基)-2'-脱氧尿苷衍生物对用1型单纯疱疹病毒胸苷激酶基因转化的小鼠乳腺癌(FM3A)细胞具有高度选择性的细胞生长抑制活性。
Mol Pharmacol. 1985 Dec;28(6):581-7.
5
Carbocyclic 5-iodo-2'-deoxyuridine (C-IDU) and carbocyclic (E)-5-(2-bromovinyl)-2'-deoxyuridine (C-BVDU) as unique examples of chiral molecules where the two enantiomeric forms are biologically active: interaction of the (+)- and (-)-enantiomers of C-IDU and C-BVDU with the thymidine kinase of herpes simplex virus type 1.碳环5-碘-2'-脱氧尿苷(C-IDU)和碳环(E)-5-(2-溴乙烯基)-2'-脱氧尿苷(C-BVDU)是手性分子的独特例子,其中两种对映体形式都具有生物活性:C-IDU和C-BVDU的(+)-和(-)-对映体与单纯疱疹病毒1型胸苷激酶的相互作用。
Mol Pharmacol. 1990 Mar;37(3):395-401.
6
Comparative in vitro and in vivo cytotoxic activity of (E)-5-(2-bromovinyl)-2'-deoxyuridine (BVDU) and its arabinosyl derivative, (E)-5-(2-bromovinyl)-1-beta-D-arabinofuranosyluracil (BVaraU), against tumor cells expressing either the Varicella zoster or the Herpes simplex virus thymidine kinase.(E)-5-(2-溴乙烯基)-2'-脱氧尿苷(BVDU)及其阿拉伯糖基衍生物(E)-5-(2-溴乙烯基)-1-β-D-阿拉伯呋喃糖基尿嘧啶(BVaraU)对表达水痘带状疱疹病毒或单纯疱疹病毒胸苷激酶的肿瘤细胞的体外和体内比较细胞毒性活性。
Cancer Gene Ther. 2000 Feb;7(2):215-23. doi: 10.1038/sj.cgt.7700108.
7
(E)-5-(2-bromovinyl)-2'-deoxyuridine potentiates ganciclovir-mediated cytotoxicity on herpes simplex virus-thymidine kinase--expressing cells.(E)-5-(2-溴乙烯基)-2'-脱氧尿苷增强更昔洛韦对表达单纯疱疹病毒胸苷激酶细胞的细胞毒性作用。
Cancer Gene Ther. 2001 May;8(5):388-96. doi: 10.1038/sj.cgt.7700322.
8
Murine mammary FM3A carcinoma cells transformed with the herpes simplex virus type 1 thymidine kinase gene are highly sensitive to the growth-inhibitory properties of (E)-5-(2-bromovinyl)-2'-deoxyuridine and related compounds.用1型单纯疱疹病毒胸苷激酶基因转化的小鼠乳腺FM3A癌细胞对(E)-5-(2-溴乙烯基)-2'-脱氧尿苷及相关化合物的生长抑制特性高度敏感。
FEBS Lett. 1985 Jun 3;185(1):95-100. doi: 10.1016/0014-5793(85)80747-x.
9
Herpes simplex virus type 1 that exhibits herpes simplex virus type 2 sensitivity to (E)-5-(2-bromovinyl)-2'-deoxyuridine.对(E)-5-(2-溴乙烯基)-2'-脱氧尿苷表现出2型单纯疱疹病毒敏感性的1型单纯疱疹病毒。
Intervirology. 1991;32(5):308-15. doi: 10.1159/000150213.
10
Selection of HSV-1 TK gene-transfected murine mammary carcinoma cells resistant to (E)-5-(2-bromovinyl)-2'-deoxyuridine (BVDU) and ganciclovir (GCV).对(E)-5-(2-溴乙烯基)-2'-脱氧尿苷(BVDU)和更昔洛韦(GCV)耐药的单纯疱疹病毒1型胸苷激酶(HSV-1 TK)基因转染的小鼠乳腺癌细胞的筛选。
Gene Ther. 2000 Sep;7(18):1543-52. doi: 10.1038/sj.gt.3301278.

引用本文的文献

1
Anti-(herpes simplex virus) activity of 4'-thio-2'-deoxyuridines: a biochemical investigation for viral and cellular target enzymes.4'-硫代-2'-脱氧尿苷的抗(单纯疱疹病毒)活性:针对病毒和细胞靶酶的生化研究
Biochem J. 2000 Oct 15;351 Pt 2(Pt 2):319-26.
2
Relaxed enantioselectivity of human mitochondrial thymidine kinase and chemotherapeutic uses of L-nucleoside analogues.人线粒体胸苷激酶的宽松对映选择性及L-核苷类似物的化疗用途。
Biochem J. 1997 Nov 15;328 ( Pt 1)(Pt 1):317-20. doi: 10.1042/bj3280317.