Source:http://linkedlifedata.com/resource/pubmed/id/10741554
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
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pubmed:dateCreated |
2000-6-13
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pubmed:abstractText |
The heterocyclic analogues of 5,6-dihydroxy-2-aminotetralins (6) were synthesized and their in vitro dopaminergic activity was compared to that of (-)-DP-5,6-ADTN and the novel potent agonist Z12571. The results show that changing the cathecol ring for a heterocycle decreases the D1-like activity of the target molecules 6. However, the D2-like activity of tetrahydroquinoline (6j) was comparable to that of (-)-DP-5,6-ADTN.
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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 |
Mar
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pubmed:issn |
0960-894X
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
20
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pubmed:volume |
10
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
563-6
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:10741554-Acylation,
pubmed-meshheading:10741554-Amines,
pubmed-meshheading:10741554-Animals,
pubmed-meshheading:10741554-Arteries,
pubmed-meshheading:10741554-Dopamine Agents,
pubmed-meshheading:10741554-Muscle, Smooth, Vascular,
pubmed-meshheading:10741554-Muscle Relaxation,
pubmed-meshheading:10741554-Rabbits,
pubmed-meshheading:10741554-Receptors, Dopamine D1,
pubmed-meshheading:10741554-Receptors, Dopamine D2
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pubmed:year |
2000
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pubmed:articleTitle |
Synthesis and dopaminergic activity of heterocyclic analogues of 5,6-dihydroxy-2-aminotetralins.
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pubmed:affiliation |
Laboratory of Organic Chemistry, Faculty of Pharmacy, University of Barcelona, Spain. jbosch@farmacia.far.ub.es
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pubmed:publicationType |
Journal Article,
In Vitro,
Research Support, Non-U.S. Gov't
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