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甲基乙二醛双(脒腙)及其两种苯基化类似物对斯氏艾美耳球虫(顶复门)S-腺苷甲硫氨酸脱羧酶活性的影响

Effects of methylglyoxal bis(guanylhydrazone) and two phenylated analogues on S-adenosylmethionine decarboxylase activity from Eimeria stiedai (Apicomplexa).

作者信息

San-Martín Núñez B, Alunda J M, Balaña-Fouce R, Ordóñez Escudero D

机构信息

Departamento de Toxicología y Farmacología, Facultad de Veterinaria Universidad Complutense de Madrid, Spain.

出版信息

Comp Biochem Physiol B. 1987;87(4):863-6. doi: 10.1016/0305-0491(87)90403-2.

DOI:10.1016/0305-0491(87)90403-2
PMID:3665433
Abstract
  1. Activity of S-adenosylmethionine decarboxylase, one of the rate-limiting enzymes of polyamine biosynthesis, was determined in oocysts of Eimeria stiedai, a coccidian parasite of the rabbit. 2. Several properties of the enzyme were compared to the mammalian enzyme. It showed considerably less substrate affinity than the analog enzyme from the rabbit. 3. The E. stiedai enzyme showed a low sensitivity to methylglyoxal bis(guanylhydrazone), a frequently used inhibitor of the enzyme in mammals, and two phenylated derivatives. 4. Results with the inhibitors are discussed in view of their potential use in chemotherapy.
摘要
  1. 测定了艾美耳球虫(兔的一种球虫寄生虫)斯氏艾美耳球虫卵囊中多胺生物合成的限速酶之一S-腺苷甲硫氨酸脱羧酶的活性。2. 将该酶的几个特性与哺乳动物的酶进行了比较。它显示出的底物亲和力比来自兔的类似酶低得多。3. 斯氏艾美耳球虫的酶对甲基乙二醛双(脒腙)(一种在哺乳动物中常用的该酶抑制剂)和两种苯基化衍生物的敏感性较低。4. 鉴于抑制剂在化疗中的潜在用途,对抑制剂的结果进行了讨论。

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1
Effects of methylglyoxal bis(guanylhydrazone) and two phenylated analogues on S-adenosylmethionine decarboxylase activity from Eimeria stiedai (Apicomplexa).甲基乙二醛双(脒腙)及其两种苯基化类似物对斯氏艾美耳球虫(顶复门)S-腺苷甲硫氨酸脱羧酶活性的影响
Comp Biochem Physiol B. 1987;87(4):863-6. doi: 10.1016/0305-0491(87)90403-2.
2
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.
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Properties of S-adenosylmethionine decarboxylase from rabbit liver: effects of some hydrazone compounds on its activity.兔肝脏S-腺苷甲硫氨酸脱羧酶的性质:某些腙类化合物对其活性的影响。
Comp Biochem Physiol B. 1986;83(1):221-5. doi: 10.1016/0305-0491(86)90356-1.
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Effect of methylglyoxal bis (guanylhydrazone) (MGBG) in vivo on the decarboxylation of s-adenosylmethionine and synthesis of spermidine in the rat and guinea pig.甲基乙二醛双(脒腙)(MGBG)在体内对大鼠和豚鼠S-腺苷甲硫氨酸脱羧作用及亚精胺合成的影响。
Life Sci. 1976 Apr 15;18(8):879-86. doi: 10.1016/0024-3205(76)90015-1.
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Regulation of S-adenosylmethionine decarboxylase activity in rat liver and prostate.大鼠肝脏和前列腺中S-腺苷甲硫氨酸脱羧酶活性的调节
J Biol Chem. 1985 Aug 15;260(17):9583-8.
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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.
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Plasmodium falciparum: S-adenosyl-L-methionine decarboxylase.恶性疟原虫:S-腺苷-L-甲硫氨酸脱羧酶。
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Detection of proenzyme form of S-adenosylmethionine decarboxylase in extracts from rat prostate.大鼠前列腺提取物中S-腺苷甲硫氨酸脱羧酶原酶形式的检测
Biochem Biophys Res Commun. 1988 Jan 29;150(2):788-93. doi: 10.1016/0006-291x(88)90460-3.
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Exp Parasitol. 1988 Apr;65(2):277-81. doi: 10.1016/0014-4894(88)90132-4.
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S-adenosylmethionine decarboxylase as target of chemotherapy.作为化疗靶点的S-腺苷甲硫氨酸脱羧酶
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