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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
12
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pubmed:dateCreated |
1995-4-25
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pubmed:abstractText |
In a previous paper, it had been found that completely aliphatic 3-(methylene aminoxy)propanolamine derivatives showed a good beta-blocking adrenergic activity directed prevalently towards beta 2-tracheal receptors. In an attempt to change the beta-adrenergic properties of these compounds from antagonist to agonist, while still retaining the beta 2-selectivity, a series of new completely aliphatic 3-(methyleneaminoxy)propanolamine derivatives were designed in which either a hydroxylic or a methoxylic group was present on the aliphatic portion linked to the oximic carbon. The synthesis of the new compounds and their beta-adrenergic activity, evaluated by means of functional tests on isolated preparations, are described and discussed; the results obtained are then rationalised on the basis of their conformational and reactivity characteristics, determined by means of theoretical methods.
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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
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pubmed:month |
Dec
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pubmed:issn |
0014-827X
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
49
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
759-66
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:7893332-Adrenergic Agents,
pubmed-meshheading:7893332-Adrenergic beta-Agonists,
pubmed-meshheading:7893332-Adrenergic beta-Antagonists,
pubmed-meshheading:7893332-Animals,
pubmed-meshheading:7893332-Guinea Pigs,
pubmed-meshheading:7893332-Molecular Conformation,
pubmed-meshheading:7893332-Muscle, Smooth,
pubmed-meshheading:7893332-Propanolamines,
pubmed-meshheading:7893332-Structure-Activity Relationship
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pubmed:year |
1994
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pubmed:articleTitle |
Synthesis and beta-adrenergic activity of new completely aliphatic 3-(methyleneaminoxy)propanolamine derivatives.
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pubmed:affiliation |
Dipartimento di Scienze Farmaceutiche, Università di Pisa, Italy.
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pubmed:publicationType |
Journal Article,
Comparative Study,
In Vitro
|