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Comparative studies of the antineoplastic activity of 5-hydroxy-2-formylpyridine thiosemicarbazone and its seleno-semicarbazone, guanylhydrazone and semicarbazone analogs.

作者信息

Agrawal K C, Booth B A, Michaud R L, Moore E C, Sartorelli A C

出版信息

Biochem Pharmacol. 1974 Sep 1;23(17):2421-9. doi: 10.1016/0006-2952(74)90233-0.

DOI:10.1016/0006-2952(74)90233-0
PMID:4429575
Abstract
摘要

相似文献

1
Comparative studies of the antineoplastic activity of 5-hydroxy-2-formylpyridine thiosemicarbazone and its seleno-semicarbazone, guanylhydrazone and semicarbazone analogs.5-羟基-2-甲酰基吡啶硫代半卡巴腙及其硒代半卡巴腙、胍基腙和半卡巴腙类似物的抗肿瘤活性比较研究。
Biochem Pharmacol. 1974 Sep 1;23(17):2421-9. doi: 10.1016/0006-2952(74)90233-0.
2
Alpha-(N)-heterocyclic carboxaldehyde thiosemicarbazone inhibitors of ribonucleoside diphosphate reductase.核糖核苷二磷酸还原酶的α-(N)-杂环羧醛缩氨基硫脲抑制剂
Cancer Res. 1974 Jun;34(6):1308-14.
3
Metabolic effects of some tumor-inhibitory pyridine carboxaldehyde thiosemicarbazones.某些具有肿瘤抑制作用的吡啶羧醛缩氨基硫脲的代谢效应
Cancer Res. 1971 Mar;31(3):228-34.
4
Sites of inhibition of DNA synthesis by kethoxal bis(thiosemicarbazone).乙二醛双(硫代半卡巴腙)对DNA合成的抑制位点。
Nature. 1968 Jan 20;217(5125):250-1. doi: 10.1038/217250a0.
5
Effect of chelating agents upon the synthesis of nucleic acids and protein: inhibition of DNA synthesis by 1-formylisoquinoline thiosemicarbazone.螯合剂对核酸和蛋白质合成的影响:1-甲酰基异喹啉硫代半卡巴腙对DNA合成的抑制作用。
Biochem Biophys Res Commun. 1967 Apr 7;27(1):26-32. doi: 10.1016/s0006-291x(67)80034-2.
6
Comparative cytotoxic and biochemical effects of ligands and metal complexes of alpha-N-heterocyclic carboxaldehyde thiosemicarbazones.α-N-杂环羧醛缩氨基硫脲的配体和金属配合物的细胞毒性及生化效应比较
J Med Chem. 1979 Oct;22(10):1218-21. doi: 10.1021/jm00196a013.
7
Inhibitors of ribonucleotide reductase. Comparative effects of amino- and hydroxy-substituted pyridine-2-carboxaldehyde thiosemicarbazones.核糖核苷酸还原酶抑制剂。氨基和羟基取代的吡啶-2-甲醛缩氨基硫脲的比较效应。
Biochem Pharmacol. 1994 Jul 19;48(2):335-44. doi: 10.1016/0006-2952(94)90105-8.
8
Cytotoxicity of imides-N-alkyl semicarbazones, thiosemicarbazones, acetylhydrazones and related derivatives.
Anticancer Drugs. 1995 Feb;6(1):147-53. doi: 10.1097/00001813-199502000-00017.
9
Antitumor effects of bis-thiosemicarbazones--inhibition of deoxyribonucleic acid synthesis in vitro.
Biochem Pharmacol. 1975 Jan 1;24(1):133-7. doi: 10.1016/0006-2952(75)90325-1.
10
Synthesis, characterization and biological activities of semicarbazones and their copper complexes.氨基脲及其铜配合物的合成、表征与生物活性
J Inorg Biochem. 2016 Sep;162:295-308. doi: 10.1016/j.jinorgbio.2016.04.006. Epub 2016 Apr 8.

引用本文的文献

1
(Chalcogen)semicarbazones and their cobalt complexes differentiate HL-60 myeloid leukaemia cells and are cytotoxic towards tumor cell lines.(硫属元素)氨基脲及其钴配合物可区分HL-60髓系白血病细胞,并且对肿瘤细胞系具有细胞毒性。
Medchemcomm. 2016 Oct 20;8(1):103-111. doi: 10.1039/c6md00501b. eCollection 2017 Jan 1.
2
A selenosemicarbazone complex with copper efficiently down-regulates the 90-kDa heat shock protein HSP90AA1 and its client proteins in cancer cells.一种与铜形成的硒代氨基脲配合物可有效下调癌细胞中90 kDa热休克蛋白HSP90AA1及其客户蛋白。
BMC Cancer. 2014 Aug 29;14:629. doi: 10.1186/1471-2407-14-629.