Acetylene compounds of potential pharmacological value. XXX. Synthesis and pharmacological properties of N-(4-pyrrolidino-2-pentynyl)-substituted 2-pyrrolidone and succinimide. - Suppr | 超能文献

Acetylene compounds of potential pharmacological value. XXX. Synthesis and pharmacological properties of N-(4-pyrrolidino-2-pentynyl)-substituted 2-pyrrolidone and succinimide.

作者信息

Resul B, Ringdahl B, Dahlbom R

出版信息

Acta Pharm Suec. 1979;16(3):161-5.

Abstract

摘要

相似文献

1

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.

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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。

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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。

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Acetylene compounds of potential pharmacological value. XXVIII. Oxotremorine analogues substituted with a methyl group in the lactam ring.

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Acetylene compounds of potential pharmacological value. XVI. N-(perhydroazepinoalkynyl)- and N-(perhydroazocinoalkynyl)succinimides.具有潜在药理价值的乙炔化合物。十六。N-（全氢氮杂环庚三烯炔基）-和N-（全氢氮杂环辛四烯炔基）琥珀酰亚胺。

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Acetylene compounds of potential pharmacological value. XXII. Base strength and biological activity in oxotremorine antagonists.

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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.

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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.

引用本文的文献

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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.

2

Muscarinic receptor binding and activation of second messengers by substituted N-methyl-N-[4-(1-azacycloalkyl)-2-butynyl]acetamides.取代的N-甲基-N-[4-(1-氮杂环烷基)-2-丁炔基]乙酰胺对毒蕈碱受体的结合及第二信使的激活作用

J Med Chem. 1991 Mar;34(3):1073-9. doi: 10.1021/jm00107a029.

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