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[On the pharmacology of 2-(2,6-dimethylphenylamino)-4H-5,6-dihydro-1,3-thiazine (Bayer 1470), a substance inhibitory for adrenergic and cholinergic neurons].

作者信息

Kroneberg G, Oberdorf A, Hoffmeister F, Wirth W

出版信息

Naunyn Schmiedebergs Arch Exp Pathol Pharmakol. 1967;256(2):257-80.

PMID:4233002
Abstract
摘要

相似文献

1
[On the pharmacology of 2-(2,6-dimethylphenylamino)-4H-5,6-dihydro-1,3-thiazine (Bayer 1470), a substance inhibitory for adrenergic and cholinergic neurons].关于2-(2,6-二甲基苯基氨基)-4H-5,6-二氢-1,3-噻嗪(拜耳1470)的药理学,一种对肾上腺素能和胆碱能神经元有抑制作用的物质
Naunyn Schmiedebergs Arch Exp Pathol Pharmakol. 1967;256(2):257-80.
2
[On the mechanism of action of new drugs effective upon the autonomic and central nervous system].[关于对自主神经系统和中枢神经系统有效的新药的作用机制]
Naunyn Schmiedebergs Arch Exp Pathol Pharmakol. 1967;257(1):48-9.
3
[On the teaching of pharmacology. (I. Lecture program)].[论药理学教学。(一、课程大纲)]
Farmakol Toksikol. 1968 Sep-Oct;31(5):628-34.
4
[Further studies on the mechanism of action of 2-(2,6-dimethylphenylamino)-4H-5,6-dihydro-1,3-thiazine (BAY 1470) on the isolated guinea pig ileum according to Paton].[根据帕顿对2-(2,6-二甲基苯胺基)-4H-5,6-二氢-1,3-噻嗪(BAY 1470)对离体豚鼠回肠作用机制的进一步研究]
Naunyn Schmiedebergs Arch Exp Pathol Pharmakol. 1968;260(2):183-4.
5
[Combination effects. 3. Special questions of combination research in antineuralgic mixed preparations, other combination preparations and in anesthetic combinations].
Arzneimittelforschung. 1966 Oct;16(10):1297-304.
6
Adrenergic neurone blocking agents: effects and site of action.
Acta Med Acad Sci Hung. 1968;25(3):409-20.
7
Pharmacological studies of new indole alkaloids, rugulovasine A and B hydrochloride. II. Hypotensive mechanism of both alkaloids in the anesthetized cats.新型吲哚生物碱盐酸鲁古洛瓦辛A和B的药理学研究。II. 两种生物碱对麻醉猫的降压机制。
Arzneimittelforschung. 1972 Jan;22(1):143-6.
8
[Peripheral and central circulatory effect of the alpha-sympathomimetic 2-(2,6-xylidino)-5,6-dihydro-4H-1,3-thiazine-HCl (BAY 1470)].
Naunyn Schmiedebergs Arch Pharmakol. 1970;266(4):350-1.
9
[Pressor and depressor action of BAY 1470 (2-(2,6-Xylidino)-5,6-dihydro-4H-1,3-thiazinehydrochloride) as a consequence of its -receptor-stimulating properties].[由于BAY 1470(2-(2,6-二甲基苯胺基)-5,6-二氢-4H-1,3-噻嗪盐酸盐)具有β-受体刺激特性而产生的升压和降压作用]
Naunyn Schmiedebergs Arch Pharmakol. 1971;268(3):348-60.
10
Adrenergic neurone blocking agents: tolerance and hypersensitivity to adrenaline and noradrenaline.肾上腺素能神经元阻断剂:对肾上腺素和去甲肾上腺素的耐受性及超敏反应。
Br J Pharmacol Chemother. 1965 Oct;25(2):497-506. doi: 10.1111/j.1476-5381.1965.tb02067.x.

引用本文的文献

1
[Peripheral sympathetic depressant effect of clonidine].可乐定的外周交感神经抑制作用
Experientia. 1971 Jan 15;27(1):70-1. doi: 10.1007/BF02137748.
2
Alpha sympathomimetic inhibition of adrenergic and cholinergic transmission in the rabbit heart.α拟交感神经药对兔心脏肾上腺素能和胆碱能传递的抑制作用。
Naunyn Schmiedebergs Arch Pharmacol. 1972;274(1):18-45. doi: 10.1007/BF00501004.
3
Effects of centrally applied drugs on pressor responses to hypothalamic stimulation.中枢给药对下丘脑刺激所致升压反应的影响。
Naunyn Schmiedebergs Arch Pharmacol. 1974;282(4):389-400. doi: 10.1007/BF00500987.
4
Effect of duration and frequency of stimulation on the presynaptic inhibition by alpha-adrenoceptor stimulation of the adrenergic transmission.刺激持续时间和频率对肾上腺素能传递中α-肾上腺素能受体刺激引起的突触前抑制的影响。
Naunyn Schmiedebergs Arch Pharmacol. 1973;280(1):79-91. doi: 10.1007/BF00505357.
5
Central nervous alpha-adrenergic receptors and the mode of action of alpha-methyldopa.中枢神经系统α-肾上腺素能受体与α-甲基多巴的作用方式
Naunyn Schmiedebergs Arch Pharmacol. 1973;279(3):285-300. doi: 10.1007/BF00500607.
6
The effect of oxotremorine on the acetylcholine output from the CSF containing spaces.
Experientia. 1975 Jan 15;31(1):88-9. doi: 10.1007/BF01924694.
7
Clonidine antinociceptive activity: effects of drugs influencing central monoaminergic and cholinergic mechanisms in the rat.可乐定的抗伤害感受活性:影响大鼠中枢单胺能和胆碱能机制的药物的作用
Naunyn Schmiedebergs Arch Pharmacol. 1976;292(2):119-26. doi: 10.1007/BF00498581.
8
Investigation into some imidazoline compounds, with respect to peripheral alpha-adrenoceptor stimulation and depression of cardiovascular centers.关于外周α-肾上腺素能受体刺激及心血管中枢抑制作用,对某些咪唑啉化合物展开的研究。
Naunyn Schmiedebergs Arch Pharmacol. 1975;291(2):175-91. doi: 10.1007/BF00500048.