Stereospecificity of oxotremorine antagonists.

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作者信息

Dahlbom R, Lindquist A, Lindgren S, Svensson U, Ringdahl B, Blair M R

出版信息

Experientia. 1974 Oct 15;30(10):1165-7. doi: 10.1007/BF01923668.

DOI:10.1007/BF01923668

PMID:4435124

Abstract

摘要

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Stereospecificity of oxotremorine antagonists.

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引用本文的文献

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Configurations of amino-compounds and the steric course of deamination.氨基化合物的构型与脱氨基作用的立体过程。

Nature. 1950 Jul 29;166(4213):179-80. doi: 10.1038/166179a0.

Acetylene compounds of potential pharmacological value. 8. N-(4-dialkylamino-2-butynyl)-substituted cyclic imides.具有潜在药理价值的乙炔化合物。8. N-（4-二烷基氨基-2-丁炔基）取代的环状酰亚胺。

J Med Chem. 1966 Nov;9(6):843-6. doi: 10.1021/jm00324a014.

N-(t-aminoalkynyl)-substituted pyrrolidones as oxotremorine antagonists.作为毒蕈碱拮抗剂的N-（叔氨基炔基）取代吡咯烷酮

Experientia. 1970 Nov 15;26(11):1232-3. doi: 10.1007/BF01897984.

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J Med Chem. 1970 Jul;13(4):651-7. doi: 10.1021/jm00298a017.

Acta Pharm Suec. 1972 Apr;9(2):93-8.

Acta Pharm Suec. 1973 Dec;10(6):435-40.

N-(perhydroazepinoalkynyl)- and N-(perhydroazocinoalkynyl) succinimides as oxotremorine antagonists.N-（全氢氮杂环庚三烯基炔基）-和N-（全氢氮杂环辛四烯基炔基）琥珀酰亚胺作为氧化震颤素拮抗剂。

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