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[Structure-activity relationships of unsaturated esters of arecaidine and dihydroarecaidine].

作者信息

Mutschler E, Hultzsch K

出版信息

Arzneimittelforschung. 1973 May;23(5):732-7.

PMID:4740217
Abstract
摘要

相似文献

1
[Structure-activity relationships of unsaturated esters of arecaidine and dihydroarecaidine].[槟榔次碱和二氢槟榔次碱不饱和酯的构效关系]
Arzneimittelforschung. 1973 May;23(5):732-7.
2
[Structure-activity relations of arecaidines].[槟榔碱类的构效关系]
Arzneimittelforschung. 1966 Nov;16(11):1426-7.
3
The action of tertiary and quaternary arecaidine and dihydroarecaidine esters on the guinea pig isolated ileum.叔胺型和季铵型槟榔次碱及二氢槟榔次碱酯对豚鼠离体回肠的作用。
Br J Pharmacol Chemother. 1966 May;27(1):185-95. doi: 10.1111/j.1476-5381.1966.tb01654.x.
4
[Structure- and conformation-activity relationships of heterocyclic acetylcholine analogs. 17. Conformational behavior and cholinergic properties of arecaidine and sulfoarecaidine esters].[杂环乙酰胆碱类似物的结构与构象-活性关系。17. 槟榔次碱和磺基槟榔次碱酯的构象行为及胆碱能性质]
Arzneimittelforschung. 1983;33(6):806-12.
5
[Structure and conformation-activity relationships of cyclic acetylcholine analogues / 12th communication: Synthesis and cholinergic properties of stereoisomeric 3-acetoxythiacyclohexanes (author's transl)].环状乙酰胆碱类似物的结构与构效关系/第12篇通讯：立体异构的3-乙酰氧基硫杂环己烷的合成及胆碱能性质（作者译）
Arzneimittelforschung. 1981;31(4):634-40.
6
[Use of 14C-labelled arecaidine esters to estimate the number of acetylcholine receptors in muscle tissue].[使用¹⁴C标记的槟榔次碱酯来估计肌肉组织中乙酰胆碱受体的数量]
Naunyn Schmiedebergs Arch Exp Pathol Pharmakol. 1969;263(1):255-6.
7
[Structure-activity relationship of N-methyl-3-pyrroline and N-methyl-pyrrolidine-3-carboxylic acid].
Arzneimittelforschung. 1971 Dec;21(12):1979-84.
8
[Structure- and conformation-activity relationships of cyclic acetylcholine analogs of the piperidine and quinuclidine series].[哌啶和奎宁环系列环状乙酰胆碱类似物的结构与构象活性关系]
Arzneimittelforschung. 1974 Nov;24(11):1725-9.
9
The cholinergic effects and rates of hydrolysis of conformationally rigid analogs of acetylcholine.乙酰胆碱构象刚性类似物的胆碱能效应及水解速率。
J Pharmacol Exp Ther. 1969 Apr;166(2):243-8.
10
[Structure- and conformation-activity relationships of heterocyclic acetylcholine analogues. 16. Conformational behaviour and cholinergic properties of isoarecaidine and sulfoisoarecaidine esters].[杂环乙酰胆碱类似物的结构与构象-活性关系。16. 异槟榔次碱和磺基异槟榔次碱酯的构象行为及胆碱能性质]
Arzneimittelforschung. 1983;33(2):190-7.

引用本文的文献

1
Stereoselective recognition of the enantiomers of phenglutarimide and of six related compounds by four muscarinic receptor subtypes.四种毒蕈碱受体亚型对苯戊二酰亚胺对映体及六种相关化合物的立体选择性识别。
Br J Pharmacol. 1996 Dec;119(7):1319-30. doi: 10.1111/j.1476-5381.1996.tb16041.x.
2
Binding and functional properties of hexocyclium and sila-hexocyclium derivatives to muscarinic receptor subtypes.己环铵和硅己环铵衍生物与毒蕈碱受体亚型的结合及功能特性
Br J Pharmacol. 1994 Jun;112(2):505-14. doi: 10.1111/j.1476-5381.1994.tb13102.x.
3
Pre- and postsynaptic effects of muscarinic agonists in the guinea-pig ileum.
毒蕈碱激动剂对豚鼠回肠的突触前和突触后效应。
Naunyn Schmiedebergs Arch Pharmacol. 1980 Nov;314(3):259-66. doi: 10.1007/BF00498547.
4
The relative potencies of some agonists at M2 muscarinic receptors in guinea-pig ileum, atria and bronchi.某些激动剂对豚鼠回肠、心房和支气管中M2毒蕈碱受体的相对效价。
Br J Pharmacol. 1985 Jun;85(2):437-40. doi: 10.1111/j.1476-5381.1985.tb08879.x.
5
A search for selective antagonists at M2 muscarinic receptors.对M2毒蕈碱受体选择性拮抗剂的研究。
Br J Pharmacol. 1985 Jun;85(2):427-35. doi: 10.1111/j.1476-5381.1985.tb08878.x.
6
The selectivity of the (-)-and (+)-forms of hyoscine methiodide and of hyoscyamine camphorsulphonate for muscarinic (M2) receptors.东莨菪碱甲基碘化物的（-）-和（+）-形式以及莨菪碱樟脑磺酸盐对毒蕈碱（M2）受体的选择性。
Br J Pharmacol. 1986 Oct;89(2):439-44. doi: 10.1111/j.1476-5381.1986.tb10278.x.
7
Competitive and non-competitive antagonism exhibited by 'selective' antagonists at atrial and ileal muscarinic receptor subtypes.“选择性”拮抗剂对心房和回肠毒蕈碱受体亚型表现出的竞争性和非竞争性拮抗作用。
Br J Pharmacol. 1987 Apr;90(4):701-7. doi: 10.1111/j.1476-5381.1987.tb11223.x.
8
The affinity of some acetylenic analogues of 4-DAMP methobromide for muscarinic receptors in guinea-pig ileum and atria.4-二甲基氨基吡啶甲溴化物的一些乙炔类似物对豚鼠回肠和心房毒蕈碱受体的亲和力。
Br J Pharmacol. 1988 Jul;94(3):947-51. doi: 10.1111/j.1476-5381.1988.tb11608.x.
9
Structure-activity relationships of new analogues of arecaidine propargyl ester at muscarinic M1 and M2 receptor subtypes.槟榔次碱炔丙基酯新类似物在毒蕈碱M1和M2受体亚型上的构效关系。
Br J Pharmacol. 1989 Feb;96(2):319-24. doi: 10.1111/j.1476-5381.1989.tb11820.x.
10
Binding and functional properties of antimuscarinics of the hexocyclium/sila-hexocyclium and hexahydro-diphenidol/hexahydro-sila-diphenidol type to muscarinic receptor subtypes.六环铵/硅-六环铵和六氢双苯丙醇/六氢硅双苯丙醇型抗毒蕈碱药物与毒蕈碱受体亚型的结合及功能特性
Br J Pharmacol. 1989 Sep;98(1):197-205. doi: 10.1111/j.1476-5381.1989.tb16882.x.