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Neuromuscular blocking activities of some steroidal mono and bis-quaternary ammonium compounds with special reference to NN'-dimethylconessine.

作者信息

Busfield D, Child K J, Clarke A J, Davis B, Dodds M G

出版信息

Br J Pharmacol Chemother. 1968 Mar;32(3):609-23. doi: 10.1111/j.1476-5381.1968.tb00461.x.

DOI:10.1111/j.1476-5381.1968.tb00461.x
PMID:4966723
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1570313/
Abstract
摘要

相似文献

1
Neuromuscular blocking activities of some steroidal mono and bis-quaternary ammonium compounds with special reference to NN'-dimethylconessine.某些甾体单季铵盐和双季铵盐化合物的神经肌肉阻滞活性，特别提及N，N'-二甲基锥丝碱
Br J Pharmacol Chemother. 1968 Mar;32(3):609-23. doi: 10.1111/j.1476-5381.1968.tb00461.x.
2
Steroidal neuromuscular blocking agents.甾体类神经肌肉阻滞剂。
Adv Drug Res. 1975;10:53-92.
3
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C R Acad Hebd Seances Acad Sci D. 1968 Jul 22;267(4):448-51.
4
A comparison between the blocking actions of 2-(4-phenylpiperidino) cyclohexanol (AH 5183) and its N-methyl quaternary analogue (AH 5954).2-(4-苯基哌啶基)环己醇(AH 5183)及其N-甲基季铵类似物(AH 5954)阻断作用的比较。
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5
[Neuro-muscular and ganglionic effects of quaternary bis-ammonium compounds derived from phosphoric acid].[磷酸衍生的季铵双铵化合物的神经肌肉和神经节效应]
Arch Int Pharmacodyn Ther. 1969 Apr;178(2):269-84.
6
Neuromuscular blocking activity of 6-phenylphenanthridine-3,8-bis-(tri-methylammonium) iodide (compound 76-805).6-苯基菲啶-3,8-双（三甲基铵）碘化物（化合物76-805）的神经肌肉阻断活性。
Indian J Exp Biol. 1988 Jul;26(7):535-7.
7
Anaesthesia and temperature effect mechanism in neuromuscular blocking by N+ quaternary depolarizing drugs.N⁺ 季铵去极化药物神经肌肉阻滞中的麻醉和温度效应机制
Nature. 1965 Sep 11;207(5002):1149-52. doi: 10.1038/2071149a0.
8
[The effect of adamantyl radicals on the mechanism of the cholinergic action of mono-quaternary ammonium compounds].
Farmakol Toksikol. 1973 Mar-Apr;36(2):201-5.
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[The effect of adamantyl radicals on the mechanism of the cholinergic action of mono-quaternary ammonium compounds].[金刚烷基对单季铵化合物胆碱能作用机制的影响]
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The pharmacology of pancuronium bromide (Org.NA97), a new potent steroidal neuromuscular blocking agent.泮库溴铵（Org.NA97）的药理学，一种新型强效甾体类神经肌肉阻滞剂。
Br J Pharmacol Chemother. 1968 Mar;32(3):671-82. doi: 10.1111/j.1476-5381.1968.tb00466.x.

引用本文的文献

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Factors limiting the rate of termination of the neuromuscular blocking action of fazadinium dibromide.限制二溴法扎地铵神经肌肉阻滞作用终止速率的因素。
Br J Pharmacol. 1978 Jun;63(2):287-93. doi: 10.1111/j.1476-5381.1978.tb09759.x.

本文引用的文献

1
Equidistance concept and structure-activity relationship of curarizing drugs.箭毒类药物的等距概念及构效关系。
Naunyn Schmiedebergs Arch Exp Pathol Pharmakol. 1952;214(2):214-26. doi: 10.1007/BF00246056.
2
The action of d-tubocurarine and of decamethonium on respiratory and other muscles in the cat.d-筒箭毒碱和十烃季铵对猫呼吸肌及其他肌肉的作用。
J Physiol. 1951 Feb;112(3-4):311-31. doi: 10.1113/jphysiol.1951.sp004531.
3
RELAXANT ACTION IN MAN OF DIPYRANDIUM CHLORIDE (M&B 9105A). (A STEROID BIS-QUATERNARY AMMONIUM SALT).
Br J Anaesth. 1964 Dec;36:761-8. doi: 10.1093/bja/36.12.761.
4
SOME CHEMICAL ASPECTS OF NEUROMUSCULAR BLOCK.
Prog Med Chem. 1963;19:1-51. doi: 10.1016/s0079-6468(08)70115-2.
5
[CURARIZING ACTIVITY OF 3-BETA,20-ALPHA-BISTRIMETHYLAMMONIUM-5-ALPHA-PREGNANE DICHLORIDE (MALOUETINE) AND OF ITS STEREOISOMERS].[3-β,20-α-双三甲铵基-5-α-孕烷二氯化物（马洛替丁）及其立体异构体的箭毒样活性]
Arch Int Pharmacodyn Ther. 1964 Jan 1;147:209-19.
6
[Steroid alkaloids. V. Alkaloids of Malouetia bequaertiana E. Woodson (Apocynaceae): funtuphyllamine B and malouetine. Preliminary communication].
Ann Pharm Fr. 1960 Sep;18:673-7.
7
The initial transient stimulating action of neuromuscular blocking agents in the cat.神经肌肉阻滞剂对猫的初始短暂刺激作用。
Br J Anaesth. 1961 Jun;33:285-8. doi: 10.1093/bja/33.6.285.
8
A new biological method for the assay of depolarizing substances using the isolated semispinalis muscle of the chick.一种使用鸡的离体半棘肌测定去极化物质的新生物学方法。
Br J Pharmacol Chemother. 1960 Sep;15(3):412-6. doi: 10.1111/j.1476-5381.1960.tb01265.x.
9
[Pharmacological study of a new short-acting curarimimetic].一种新型短效类箭毒样作用药物的药理学研究
C R Hebd Seances Acad Sci. 1959 Mar 16;248(11):1723-5.
10
Neuromuscular blocking agnets of short duration.短效神经肌肉阻滞剂
Nature. 1959 Feb 21;183(4660):542-3. doi: 10.1038/183542a0.