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铜结合配体对劳氏肉瘤病毒的失活和抑制作用:硫代氨基脲、8-羟基喹啉和异烟肼。

Inactivation and inhibition of Rous sarcoma virus by copper-binding ligands: thiosemicarbazones, 8-hydroxyquinolines, and isonicotinic acid hydrazide.

作者信息

Levinson W, Rohde W, Mikelens P, Jackson J, Antony A, Ramakrishnan T

出版信息

Ann N Y Acad Sci. 1977 Mar 4;284:525-32. doi: 10.1111/j.1749-6632.1977.tb21985.x.

DOI:10.1111/j.1749-6632.1977.tb21985.x
PMID:81642
Abstract

We have shown that three types of copper-binding ligands, thiosemicarbazones, 8-hydroxyquinolines, and isonicotinic acid hydrazide and their copper complexes, inactivate the transforming ability of RSV and inhibit its RNA-dependent DNA polymerases. Three other compounds, 2-pyridine thiosemicarbazone, 1-formyl isoquinoline thiosemicarbazone, and diphenyl thiocarbazone inhibit transformation by RSV intracellularly. Most but not all of these compounds bind to nucleic acids in the presence of copper, which may be important in their mode of action.

摘要

我们已经表明,三种类型的铜结合配体,即硫代氨基脲、8-羟基喹啉、异烟酸酰肼及其铜配合物,可使劳斯肉瘤病毒(RSV)的转化能力失活,并抑制其RNA依赖性DNA聚合酶。另外三种化合物,2-吡啶硫代氨基脲、1-甲酰基异喹啉硫代氨基脲和二苯基硫代卡巴腙在细胞内抑制RSV的转化。这些化合物中的大多数(但不是全部)在有铜存在的情况下与核酸结合,这可能对它们的作用方式很重要。

相似文献

1
Inactivation and inhibition of Rous sarcoma virus by copper-binding ligands: thiosemicarbazones, 8-hydroxyquinolines, and isonicotinic acid hydrazide.铜结合配体对劳氏肉瘤病毒的失活和抑制作用:硫代氨基脲、8-羟基喹啉和异烟肼。
Ann N Y Acad Sci. 1977 Mar 4;284:525-32. doi: 10.1111/j.1749-6632.1977.tb21985.x.
2
Anti-tumor virus activity of copper-binding drugs.铜结合药物的抗肿瘤病毒活性。
Adv Exp Med Biol. 1977;91:161-78. doi: 10.1007/978-1-4684-0796-9_12.
3
Hydroxyquinolines inhibit ribonucleic acid-dependent deoxyribonucleic acid polymerase and inactivate Rous sarcoma virus and herpes simplex virus.羟基喹啉可抑制核糖核酸依赖性脱氧核糖核酸聚合酶,并使劳氏肉瘤病毒和单纯疱疹病毒失活。
Antimicrob Agents Chemother. 1976 Aug;10(2):234-40. doi: 10.1128/AAC.10.2.234.
4
Inhibition of the RNA dependent DNA polymerase and the malignant transforming ability of Rous sarcoma virus by thiosemicarbazone-transition metal complexes.硫代氨基脲-过渡金属络合物对劳斯肉瘤病毒的RNA依赖性DNA聚合酶及恶性转化能力的抑制作用
Bioinorg Chem. 1978;8(3):225-36. doi: 10.1016/s0006-3061(00)80198-2.
5
Inhibition of RNA-dependent DNA polymerase of Rous sarcoma virus by thiosemicarbazones and several cations.硫代氨基脲和几种阳离子对劳氏肉瘤病毒RNA依赖性DNA聚合酶的抑制作用。
Proc Natl Acad Sci U S A. 1973 Jan;70(1):164-8. doi: 10.1073/pnas.70.1.164.
6
Effect of isonicotinic acid hydrazide-copper complex on Rous sarcoma virus and its genome RNA.异烟肼-铜络合物对劳斯肉瘤病毒及其基因组RNA的作用
Bioinorg Chem. 1978 Jul;9(1):23-34. doi: 10.1016/s0006-3061(00)82003-7.
7
Molecular mechanism for the specific inhibition of reverse transcriptase of Rous sarcoma virus by the copper complexes of isonicontinic acid hydrazide.异烟肼铜配合物对劳氏肉瘤病毒逆转录酶特异性抑制的分子机制
Biochem Pharmacol. 1978 Feb 15;27(4):579-84. doi: 10.1016/0006-2952(78)90398-2.
8
Inhibition of amino acyl tRNA synthetase activity by copper complexes of two metal binding ligands. N-Methyl isatin beta-thiosemicarbazone and 8-hydroxyquinoline.两种金属结合配体的铜配合物对氨酰tRNA合成酶活性的抑制作用。N-甲基异吲哚啉酮β-硫代半卡巴腙和8-羟基喹啉。
Biochim Biophys Acta. 1977 Jul 15;477(2):102-11. doi: 10.1016/0005-2787(77)90226-x.
9
N-Methyl isatin beta-thiosemicarbazone-copper complex inhibits RNA-dependent DNA polymerase but not ribonuclease H of Rous sarcoma virus.N-甲基异吲哚啉酮β-硫代半卡巴腙-铜配合物抑制劳氏肉瘤病毒的RNA依赖性DNA聚合酶,但不抑制其核糖核酸酶H。
Bioinorg Chem. 1978 Jun;8(6):535-40. doi: 10.1016/0006-3061(78)80007-6.
10
Effect of antabuse (disulfiram) on Rous sarcoma virus and on eukaryotic cells.安塔布司(双硫仑)对劳斯肉瘤病毒和真核细胞的作用。
Biochim Biophys Acta. 1978 Jun 22;519(1):65-75. doi: 10.1016/0005-2787(78)90062-x.

引用本文的文献

1
8-Hydroxyquinolines Are Boosting Agents of Copper-Related Toxicity in Mycobacterium tuberculosis.8-羟基喹啉是结核分枝杆菌中铜相关毒性的增强剂。
Antimicrob Agents Chemother. 2016 Sep 23;60(10):5765-76. doi: 10.1128/AAC.00325-16. Print 2016 Oct.
2
High-throughput screening for inhibitors of Mycobacterium tuberculosis H37Rv.结核分枝杆菌 H37Rv 抑制剂的高通量筛选。
Tuberculosis (Edinb). 2009 Sep;89(5):334-53. doi: 10.1016/j.tube.2009.05.008. Epub 2009 Sep 15.