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Acetylene compounds of potential pharmacological value. XXIX. Stereoselectivity of N-(1-alkyl-4-pyrrolidino-2-butynyl)-substituted 2-pyrrolidones and succinimides as oxotremorine antagonists.

作者信息

Ringdahl B, Dahlbom R

出版信息

Acta Pharm Suec. 1979;16(1):13-20.

PMID:452907
Abstract
摘要

相似文献

1
Acetylene compounds of potential pharmacological value. XXIX. Stereoselectivity of N-(1-alkyl-4-pyrrolidino-2-butynyl)-substituted 2-pyrrolidones and succinimides as oxotremorine antagonists.
Acta Pharm Suec. 1979;16(1):13-20.
2
Acetylene compounds of potential pharmacological value. XXI. Further studies on the effect of branching the intermediate chain of N-(t-aminoalkynyl)-substituted succinimides and 2-pyrrolidones.具有潜在药理价值的乙炔化合物。XXI. 关于N-（叔氨基炔基）取代琥珀酰亚胺和2-吡咯烷酮中间链支化效应的进一步研究。
Acta Pharm Suec. 1975;12(4):297-304.
3
Acetylene compounds of potential pharmacological value. XXX. Synthesis and pharmacological properties of N-(4-pyrrolidino-2-pentynyl)-substituted 2-pyrrolidone and succinimide.
Acta Pharm Suec. 1979;16(3):161-5.
4
Acetylene compounds of potential pharmacological value. XIX. N-(dialkylaminoalkynyl)-substituted succinimides and 2-pyrrolidones as partial cholinergic agonists.具有潜在药理价值的乙炔化合物。十九。N-（二烷基氨基炔基）取代的琥珀酰亚胺和2-吡咯烷酮作为部分胆碱能激动剂。
Acta Pharm Suec. 1975;12(3):209-14.
5
Acetylene compounds of potential pharmacological value. XXVII. Stereoselectivity of oxotremorine antagonists containing a chiral pyrrolidine group.具有潜在药理价值的乙炔化合物。XXVII. 含手性吡咯烷基的氧代震颤素拮抗剂的立体选择性。
Acta Pharm Suec. 1978;15(4):255-63.
6
Acetylene compounds of potential pharmacological value. XXIII. N-(1-Methyl-5-pyrrolidino-3-pentynyl)-substituted succinimide and 2-pyrrolidone.
Acta Pharm Suec. 1975;12(5-6):503-6.
7
Acetylene compounds of potential pharmacological value. 18. N-(t-aminoalkynyl)-substituted 2-pyrrolidones, a new series of potent oxotremorine antagonists.具有潜在药理价值的乙炔化合物。18. N-（叔氨基炔基）取代的2-吡咯烷酮，一类新型强效氧化震颤素拮抗剂。
Acta Pharm Suec. 1973 Dec;10(6):435-40.
8
Acetylene compounds of potential pharmacological value. XXXVI. N-(4-tert-Amino-2-butynyl)-substituted 2(3H)-thiazolones and 2(3H)-oxazolones.具有潜在药理价值的乙炔化合物。三十六。N-（4-叔氨基-2-丁炔基）取代的2（3H）-噻唑酮和2（3H）-恶唑酮。
Acta Pharm Suec. 1978;15(3):175-80.
9
Acetylene compounds of potential pharmacological value. XXII. Base strength and biological activity in oxotremorine antagonists.
Acta Pharm Suec. 1975;12(5-6):393-400.
10
Cyclopropane analogues to acetylenic oxotremorine antagonists.乙炔基氧震颤素拮抗剂的环丙烷类似物。
Acta Pharm Suec. 1972 Nov;9(5):491-8.

引用本文的文献

1
Stereochemical requirements for central and peripheral muscarinic and antimuscarinic activity of some acetylenic compounds related to oxotremorine.与氧化震颤素相关的一些炔类化合物的中枢及外周毒蕈碱能和抗毒蕈碱能活性的立体化学要求
Br J Pharmacol. 1982 Jun;76(2):299-304. doi: 10.1111/j.1476-5381.1982.tb09220.x.

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