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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
11
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pubmed:dateCreated |
1989-3-30
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pubmed:abstractText |
Certain 1,2,3-triazole derivatives were prepared and tested for their ability to displace [3H]diazepam from bovine brain membranes. From these compounds, the quinolytriazole derivatives (14, 15, 16, 17) were clearly the most potent, while the naphthyl- and the naphthyridyl-triazoles were considerably less active. The p-nitrophenyl derivative (15) was the compound that bound with the highest affinity within the quinolyltriazole compounds class. The replacement of the p-nitrophenyl group with other substituents greatly decreased the binding activity. From a Lineweaver-Burk analysis of 11, it appears that the inhibition is competitive.
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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 |
Nov
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pubmed:issn |
0022-3549
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
77
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
977-80
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pubmed:dateRevised |
2008-11-21
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pubmed:meshHeading |
pubmed-meshheading:2852246-Animals,
pubmed-meshheading:2852246-Binding, Competitive,
pubmed-meshheading:2852246-Brain,
pubmed-meshheading:2852246-Cattle,
pubmed-meshheading:2852246-Chemical Phenomena,
pubmed-meshheading:2852246-Chemistry,
pubmed-meshheading:2852246-Diazepam,
pubmed-meshheading:2852246-Kinetics,
pubmed-meshheading:2852246-Receptors, GABA-A,
pubmed-meshheading:2852246-Spectrophotometry, Infrared,
pubmed-meshheading:2852246-Structure-Activity Relationship,
pubmed-meshheading:2852246-Triazoles
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pubmed:year |
1988
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pubmed:articleTitle |
Specific inhibition of benzodiazepine receptor binding by some 1,2,3-triazole derivatives.
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pubmed:affiliation |
Istituto Policattedra di Discipline Biologiche, Università di Pisa, Italy.
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pubmed:publicationType |
Journal Article,
In Vitro
|