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Inhibition of dopamine beta-oxidase in vivo by benzyloxyamine and benzylhydrazine analogs.

作者信息

NIKODIJEVIC B, CREVELING C R, UDENFRIEND S

出版信息

J Pharmacol Exp Ther. 1963 May;140:224-8.

PMID:13938656
Abstract
摘要

相似文献

1
Inhibition of dopamine beta-oxidase in vivo by benzyloxyamine and benzylhydrazine analogs.苄氧基胺和苄基肼类似物对体内多巴胺β-氧化酶的抑制作用。
J Pharmacol Exp Ther. 1963 May;140:224-8.
2
On the mechanism of inhibition of dopamine-beta-oxidase by benzyloxyamines.关于苄氧基胺对多巴胺-β-氧化酶的抑制机制
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Dynamic kinetic asymmetric allylation of hydrazines and hydroxylamines.
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An amine oxidase inhibitor in angina. A preliminary study.一种用于心绞痛的胺氧化酶抑制剂。一项初步研究。
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[Comparison of the amine oxidase-inhibiting and hypotensive effects of hydrazinophthalazines].[肼酞嗪类药物的胺氧化酶抑制作用与降压作用的比较]
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Therapeutic re-orientation in some depressive states: clinical evaluation of a new mono-amine oxidase inhibitor (W-1554-A, phenelzine, Nardil).
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DISSOCIATION OF THE DECARBOXYLASE-INHIBITING AND NOREPINEPHRINE-DEPLETING EFFECTS OF ALPHA-METHYL-DOPA, ALPHA-ETHYL-DOPA, 4-BROMO-3-HYDROXY-BENZYLOXYAMINE AND RELATED SUBSTANCES.α-甲基多巴、α-乙基多巴、4-溴-3-羟基苄氧基胺及相关物质的脱羧酶抑制作用与去甲肾上腺素耗竭作用的解离
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A comparison of the in vivo inhibition of brain and liver monoamine oxidase as produced by beta-phenylisopropylhydrazine (PIH) and iproniazid.
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STRUCTURE-ACTIVITY RELATIONSHIP OF ALIPHATIC AMINES AND CARDIAC STIMULATION.脂肪胺与心脏刺激的构效关系
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1
The synthesis of noradrenaline by isolated guinea-pig atria.豚鼠离体心房去甲肾上腺素的合成
Biochem J. 1966 Jun;99(3):538-45. doi: 10.1042/bj0990538.
2
Mechanism of the hypotensive action of methyldopa in normal and immunosympathectomized rats.甲基多巴在正常大鼠和免疫交感神经切除大鼠中的降压作用机制。
Br J Pharmacol. 1970 Oct;40(2):186-93. doi: 10.1111/j.1476-5381.1970.tb09912.x.
3
Autonomic reflexes and vascular reactivity in experimental scurvy in man.人体实验性坏血病中的自主反射与血管反应性
J Clin Invest. 1970 Feb;49(2):298-307. doi: 10.1172/JCI106239.
4
Inhibition of noradrenaline biosynthesis and the level of blood pressure in spontaneously hypertensive rats and metacorticoid rats.去甲肾上腺素生物合成的抑制与自发性高血压大鼠和盐皮质激素过多大鼠的血压水平
Naunyn Schmiedebergs Arch Pharmakol. 1971;268(2):185-91. doi: 10.1007/BF01020073.