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Inhibitors of S-adenosylmethionine decarboxylase.

作者信息

Pegg A E

出版信息

Methods Enzymol. 1983;94:239-47. doi: 10.1016/s0076-6879(83)94042-9.

DOI:10.1016/s0076-6879(83)94042-9
PMID:6353154
Abstract
摘要

相似文献

1
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.
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
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.
4
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.
5
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.
6
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.
7
Putrescine-insensitive S-adenosyl-L-methionine decarboxylase from Tetrahymena pyriformis.来自梨形四膜虫的腐胺不敏感型S-腺苷-L-甲硫氨酸脱羧酶。
Acta Chem Scand B. 1975;29(9):932-6. doi: 10.3891/acta.chem.scand.29b-0932.
8
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.
9
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.
10
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.

引用本文的文献

1
Discovery of novel inhibitors of human S-adenosylmethionine decarboxylase based on in silico high-throughput screening and a non-radioactive enzymatic assay.基于计算机高通量筛选和非放射性酶促测定法发现人S-腺苷甲硫氨酸脱羧酶的新型抑制剂
Sci Rep. 2015 Jun 1;5:10754. doi: 10.1038/srep10754.
2
Diethylglyoxal bis(guanylhydrazone), a potent inhibitor of mammalian S-adenosylmethionine decarboxylase. Effects on cell proliferation and polyamine metabolism in L1210 leukemia cells.二乙二醛双（胍基腙），一种有效的哺乳动物S-腺苷甲硫氨酸脱羧酶抑制剂。对L1210白血病细胞增殖和多胺代谢的影响。
Mol Cell Biochem. 1993 Jul 21;124(2):141-7. doi: 10.1007/BF00929206.
3
Glyoxal bis(guanylhydrazone) as an inhibitor of polyamine biosynthesis in tumour cells.
乙二醛双（脒腙）作为肿瘤细胞中多胺生物合成的抑制剂
Biochem J. 1984 Jul 15;221(2):483-8. doi: 10.1042/bj2210483.
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
Regulation of spermidine/spermine N1-acetyltransferase in L6 cells by polyamines and related compounds.多胺及相关化合物对L6细胞中精胺/亚精胺N1-乙酰基转移酶的调控
Biochem J. 1986 Sep 1;238(2):581-7. doi: 10.1042/bj2380581.
6
Putrescine activated S-adenosylmethionine decarboxylase from Trypanosoma brucei brucei.腐胺激活了布氏布氏锥虫的S-腺苷甲硫氨酸脱羧酶。
Mol Cell Biochem. 1992 Nov 4;117(1):53-61. doi: 10.1007/BF00230410.
7
Cytostasis induced in L1210 murine leukaemia cells by the S-adenosyl-L-methionine decarboxylase inhibitor 5'-([(Z)-4-amino-2-butenyl]methylamino)-5'-deoxyadenosine may be due to hypusine depletion.S-腺苷-L-甲硫氨酸脱羧酶抑制剂5'-([(Z)-4-氨基-2-丁烯基]甲基氨基)-5'-脱氧腺苷在L1210小鼠白血病细胞中诱导的细胞生长抑制可能是由于hypusine耗竭所致。
Biochem J. 1992 Nov 1;287 ( Pt 3)(Pt 3):717-24. doi: 10.1042/bj2870717.