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Inhibition of mammalian S-adenosylmethionine decarboxylase activity by 1,1'-((methylethanediylidene)-dinitrilo)bis(3-aminoguanidine).

作者信息

Pegg A E

出版信息

J Biol Chem. 1978 Jan 25;253(2):539-42.

PMID:618884
Abstract
摘要

相似文献

1
Inhibition of mammalian S-adenosylmethionine decarboxylase activity by 1,1'-((methylethanediylidene)-dinitrilo)bis(3-aminoguanidine).1,1'-((甲基亚乙基二亚基)-二腈基)双(3-氨基胍)对哺乳动物S-腺苷甲硫氨酸脱羧酶活性的抑制作用。
J Biol Chem. 1978 Jan 25;253(2):539-42.
2
Inhibition by derivatives of diguanidines of cell proliferation in Ehrlich ascites cells grown in cultures.双胍衍生物对培养的艾氏腹水癌细胞增殖的抑制作用。
Biochem J. 1980 May 15;188(2):491-501. doi: 10.1042/bj1880491.
3
Metabolic consequences of inhibition of cerebral adenosylmethionine decarboxylase by methylglyoxal bis(Guanylhydrazone).甲基乙二醛双（脒腙）抑制脑腺苷甲硫氨酸脱羧酶的代谢后果
J Neurochem. 1983 Sep;41(3):801-8. doi: 10.1111/j.1471-4159.1983.tb04811.x.
4
Methylglyoxal bis(butylamidinohydrazone), a new inhibitor of polyamine biosynthesis that simultaneously inhibits ornithine decarboxylase, adenosylmethionine decarboxylase and spermidine synthase.甲基乙二醛双（丁脒腙），一种新型多胺生物合成抑制剂，可同时抑制鸟氨酸脱羧酶、腺苷甲硫氨酸脱羧酶和亚精胺合酶。
Biochem Pharmacol. 1986 Sep 1;35(17):2982-3. doi: 10.1016/0006-2952(86)90499-5.
5
Inhibition of S-adenosylmethionine decarboxylase and diamine oxidase activities by analogues of methylglyoxal bis(guanylhydrazone) and their cellular uptake during lymphocyte activation.甲基乙二醛双（胍腙）类似物对S-腺苷甲硫氨酸脱羧酶和二胺氧化酶活性的抑制作用及其在淋巴细胞激活过程中的细胞摄取
Biochem J. 1984 Mar 15;218(3):947-51. doi: 10.1042/bj2180947.
6
Inhibitors of S-adenosylmethionine decarboxylase.S-腺苷甲硫氨酸脱羧酶抑制剂
Methods Enzymol. 1983;94:239-47. doi: 10.1016/s0076-6879(83)94042-9.
7
Inhibition of diamine oxidase by 1,1-[(methylethanediylidene)-dinitrilo]-bis-(3-aminoguanidine) and 1,1'-[(methylethanediylidene)-dinitrilo]-diguanidine.1,1-[(甲基亚乙基二亚基)-二腈基]-双-(3-氨基胍)和1,1'-[(甲基亚乙基二亚基)-二腈基]-双胍对二胺氧化酶的抑制作用
Biochem Pharmacol. 1978;27(12):1625-9. doi: 10.1016/0006-2952(78)90170-3.
8
Irreversible inhibition of mamalian and yeast S-adenosylmethionine decarboxylase by 1,1'- (methylethanediylidenedinitrilo)-bis (3-aminoguanidine).1,1'-（甲基乙二亚基二腈基）-双（3-氨基胍）对哺乳动物和酵母S-腺苷甲硫氨酸脱羧酶的不可逆抑制作用
Biochem Biophys Res Commun. 1976 Apr 5;69(3):766-74. doi: 10.1016/0006-291x(76)90941-4.
9
Methylglyoxal bis(cyclohexylamidinohydrazone), a novel inhibitor of polyamine biosynthesis that simultaneously inhibits S-adenosylmethionine decarboxylase and spermidine synthase.甲基乙二醛双（环己基脒腙），一种新型的多胺生物合成抑制剂，可同时抑制S-腺苷甲硫氨酸脱羧酶和亚精胺合酶。
Biochem Pharmacol. 1988 Jan 15;37(2):364-5. doi: 10.1016/0006-2952(88)90744-7.
10
Effects of inhibitors of S-adenosylmethionine decarboxylase and ornithine decarboxylase on DNA synthesis in rat liver after partial hepatectomy.S-腺苷甲硫氨酸脱羧酶和鸟氨酸脱羧酶抑制剂对大鼠部分肝切除术后肝脏DNA合成的影响。
Biochim Biophys Acta. 1978 Jan 26;517(1):169-80. doi: 10.1016/0005-2787(78)90044-8.

引用本文的文献

1
Inhibition by derivatives of diguanidines of cell proliferation in Ehrlich ascites cells grown in cultures.双胍衍生物对培养的艾氏腹水癌细胞增殖的抑制作用。
Biochem J. 1980 May 15;188(2):491-501. doi: 10.1042/bj1880491.
2
Effects of inhibitors of spermidine and spermine synthesis on polyamine concentrations and growth of transformed mouse fibroblasts.亚精胺和精胺合成抑制剂对转化小鼠成纤维细胞多胺浓度及生长的影响
Biochem J. 1981 Jan 15;194(1):79-89. doi: 10.1042/bj1940079.
3
Irreversible inhibition of putrescine-stimulated S-adenosyl-L-methionine decarboxylase by berenil and pentamidine.
贝尼尔和喷他脒对腐胺刺激的S-腺苷-L-蛋氨酸脱羧酶的不可逆抑制作用。
Biochem J. 1985 Oct 1;231(1):165-9. doi: 10.1042/bj2310165.
4
Effect of inhibitors of S-adenosylmethionine decarboxylase on the contents of ornithine decarboxylase and S-adenosylmethionine decarboxylase in L1210 cells.S-腺苷甲硫氨酸脱羧酶抑制剂对L1210细胞中鸟氨酸脱羧酶和S-腺苷甲硫氨酸脱羧酶含量的影响。
Biochem J. 1988 Aug 15;254(1):45-50. doi: 10.1042/bj2540045.