2-羟基-5-甲氧基羰基苄氧基胺：一种新型强效组氨酸脱羧酶抑制剂。 - Suppr

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超能文献

2-hydroxy-5-carbomethoxybenzyloxyamine: a new potent inhibitor of histidine decarboxylase.

作者信息

Huszti Z, Kasztreiner E, Kürti M, Fekete M, Borsy J

出版信息

Biochem Pharmacol. 1973 Sep 15;22(18):2253-65. doi: 10.1016/0006-2952(73)90006-3.

DOI:10.1016/0006-2952(73)90006-3

PMID:4200282

Abstract

摘要

相似文献

2-hydroxy-5-carbomethoxybenzyloxyamine: a new potent inhibitor of histidine decarboxylase.2-羟基-5-甲氧基羰基苄氧基胺：一种新型强效组氨酸脱羧酶抑制剂。

Biochem Pharmacol. 1973 Sep 15;22(18):2253-65. doi: 10.1016/0006-2952(73)90006-3.

Decarboxylase inhibition and structure-activity relationship studies with some newly synthetized benzyloxyamine and pyridylmethoxyamine derivatives.

Biochem Pharmacol. 1973 Sep 15;22(18):2267-75. doi: 10.1016/0006-2952(73)90007-5.

Inhibition of histidine, decarboxylation in vivo by 2-hydroxy-5-carbomethoxybenzyloxyamine, a new, potent inhibitor of histidine decarboxylase.新型强效组氨酸脱羧酶抑制剂2-羟基-5-甲氧羰基苄氧胺对体内组氨酸脱羧作用的抑制

J Pharmacol Exp Ther. 1975 Feb;192(2):432-40.

Inhibition of histidine decarboxylase and diamine oxidase by 4-bromo-3-hydroxybenzyloxyamine.4-溴-3-羟基苄氧胺对组氨酸脱羧酶和二胺氧化酶的抑制作用。

Biochem Pharmacol. 1970 May;19(5):1761-70. doi: 10.1016/0006-2952(70)90168-1.

[Effect of the histidine decarboxylase inhibitor brocresine (NSD-1055) on gastric histidine decarboxylase and hydrochloric acid secretion in rats].[组氨酸脱羧酶抑制剂布罗克辛（NSD-1055）对大鼠胃组氨酸脱羧酶及盐酸分泌的影响]

Naunyn Schmiedebergs Arch Pharmakol. 1970;266(4):402-3.

Inhibition of histidine decarboxylases in vitro.

Arch Int Pharmacodyn Ther. 1972 Jan;195(1):109-47.

Structure-action relationships of histidine decarboxylase inhibitors.组氨酸脱羧酶抑制剂的构效关系

Arch Int Pharmacodyn Ther. 1975 Aug;216(2):192-6.

Nonmast-cell histamine kinetics--II. Effect of histidine decarboxylase inhibitors on rates of decline of tissue 3H-histamine in the female rat.非肥大细胞组胺动力学——II. 组氨酸脱羧酶抑制剂对雌性大鼠组织3H-组胺下降速率的影响。

Biochem Pharmacol. 1969 Mar;18(3):651-8. doi: 10.1016/0006-2952(69)90090-2.

Mechanism of inhibition of histidine decarboxylase by rhodanines.罗丹宁对组氨酸脱羧酶的抑制机制

Biochem Pharmacol. 1971 Jul;20(7):1421-8. doi: 10.1016/0006-2952(71)90269-3.

4-imidazolyl-3-amino-2-butanone (McN-A-1293), a new specific inhibitor of histidine decarboxylase.

Biochem Pharmacol. 1973 Sep 15;22(18):2299-310. doi: 10.1016/0006-2952(73)90011-7.

引用本文的文献

Induction of gastric histamine synthesis by H2-receptor antagonists: potentiation of their antisecretory activity by histidine decarboxylase inhibitors.

Agents Actions. 1980 Sep;10(4):302-8. doi: 10.1007/BF01971429.

Effects of L-histidine administration on the concentrations histidine and histamine in various tissues.给予L-组氨酸对各组织中组氨酸和组胺浓度的影响。

Agents Actions. 1974 Aug;4(3):183. doi: 10.1007/BF01970262.

Regulation of histamine synthesis: metiamide-induced synthesis of histamine in the rat stomach and the effect of histidine decarboxylase inhibitors on the elevated 14C-histamine level and histidine decarboxylase activity [proceedings].组胺合成的调节：甲硫米特诱导大鼠胃中组胺的合成以及组氨酸脱羧酶抑制剂对升高的14C-组胺水平和组氨酸脱羧酶活性的影响[会议论文集]

Agents Actions. 1978 Jun;8(4):393-4. doi: 10.1007/BF01968637.

Peptide inhibition of mammalian histidine decarboxylase.

Agents Actions. 1979 Oct;9(4):314-8. doi: 10.1007/BF01970654.

Possible involvement of endogenous histamine in the myotropic effect of clonidine on the isolated rabbit aorta.内源性组胺可能参与可乐定对离体兔主动脉的肌otropic作用。（注：这里“myotropic”可能有误，推测正确单词或许是“myotropic”，若有误请按正确内容调整翻译，整体翻译思路是先直译每个单词，再根据语境调整通顺表述）

Agents Actions. 1978 Oct;8(5):478-83. doi: 10.1007/BF02111432.

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