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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
9
|
pubmed:dateCreated |
1982-12-21
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pubmed:abstractText |
The title compound was prepared to complete a series of small ring (cyclopropane, cyclobutane) cis/trans 1,2-disubstituted semirigid congeners of acetylcholine. A multistep synthetic sequence, beginning with cis-cyclobutane-1,2-dicarboxylic anhydride, permitted unequivocal preparation of the (+/-)-cis target compound 4. The geometry of 4 was confirmed by comparison with an authentic sample of the (+/-)-trans isomer. The cis and trans isomers were equipotent as muscarinic agonists, but they were much weaker than acetyl-beta-methylcholine.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Sep
|
pubmed:issn |
0022-2623
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pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
25
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
1091-4
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pubmed:dateRevised |
2008-11-21
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pubmed:meshHeading |
pubmed-meshheading:7131487-Acetylcholine,
pubmed-meshheading:7131487-Animals,
pubmed-meshheading:7131487-Chemical Phenomena,
pubmed-meshheading:7131487-Chemistry,
pubmed-meshheading:7131487-Cyclobutanes,
pubmed-meshheading:7131487-Guinea Pigs,
pubmed-meshheading:7131487-Isomerism,
pubmed-meshheading:7131487-Muscle, Smooth,
pubmed-meshheading:7131487-Muscle Contraction,
pubmed-meshheading:7131487-Receptors, Muscarinic
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pubmed:year |
1982
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pubmed:articleTitle |
(+/-)-cis-2-acetoxycyclobutyltrimethylammonium iodide: a semirigid analogue of acetylcholine.
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pubmed:publicationType |
Journal Article,
In Vitro
|