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Irreversible inhibition of mamalian and yeast S-adenosylmethionine decarboxylase by 1,1'- (methylethanediylidenedinitrilo)-bis (3-aminoguanidine).

作者信息

Pegg A E, Conover C

出版信息

Biochem Biophys Res Commun. 1976 Apr 5;69(3):766-74. doi: 10.1016/0006-291x(76)90941-4.

DOI:10.1016/0006-291x(76)90941-4
PMID:773381
Abstract
摘要

相似文献

1
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.
2
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.
3
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.
4
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.
5
Comparison of inhibitors of S-adenosylmethionine decarboxylase from different species.不同物种间S-腺苷甲硫氨酸脱羧酶抑制剂的比较。
Biochem J. 1983 Aug 1;213(2):495-502. doi: 10.1042/bj2130495.
6
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.
7
Inhibitors of polyamine biosynthesis. 8. Irreversible inhibition of mammalian S-adenosyl-L-methionine decarboxylase by substrate analogues.多胺生物合成抑制剂。8. 底物类似物对哺乳动物S-腺苷-L-甲硫氨酸脱羧酶的不可逆抑制作用。
J Med Chem. 1980 Feb;23(2):121-7. doi: 10.1021/jm00176a004.
8
Inhibition of S-adenosylmethionine decarboxylase from rat liver by synthetic decarboxylated S-adenosylmethionine and its analogs.合成的脱羧S-腺苷甲硫氨酸及其类似物对大鼠肝脏S-腺苷甲硫氨酸脱羧酶的抑制作用。
Chem Pharm Bull (Tokyo). 1980 Jul;28(7):2232-4. doi: 10.1248/cpb.28.2232.
9
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.
10
Effect of methylglyoxal bis(guanylhydrazone) on S-adenosylmethionine decarboxylase in the isolated perfused rat.甲基乙二醛双(脒腙)对离体灌注大鼠体内S-腺苷甲硫氨酸脱羧酶的影响。
FEBS Lett. 1974 Apr 1;40(2):321-4. doi: 10.1016/0014-5793(74)80254-1.

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
Role of pyridoxal phosphate in mammalian polyamine biosynthesis. Lack of requirement for mammalian S-adenosylmethionine decarboxylase activity.磷酸吡哆醛在哺乳动物多胺生物合成中的作用。对哺乳动物S-腺苷甲硫氨酸脱羧酶活性的需求缺失。
Biochem J. 1977 Jul 15;166(1):81-8. doi: 10.1042/bj1660081.
5
Effects of aliphatic diamines on rat liver ornithine decarboxylase activity.脂肪族二胺对大鼠肝脏鸟氨酸脱羧酶活性的影响。
Biochem J. 1978 Mar 15;170(3):651-60. doi: 10.1042/bj1700651.