rdf:type |
|
lifeskim:mentions |
|
pubmed:issue |
11
|
pubmed:dateCreated |
1987-12-9
|
pubmed:abstractText |
C1-Methylated derivatives of the potent 5-hydroxytryptamine (5-HT) receptor agonist 8-hydroxy-2-(di-n-propylamino)tetralin (8-OH-DPAT, 1) were synthesized and tested for central 5-HT and dopamine receptor activity by use of a biochemical test method in rats. cis-8-Hydroxy-1-methyl-2-(di-n-propylamino)tetralin (8) was found to be a 5-HT receptor agonist. The (+)-enantiomer of 8 had a potency equal to that of 1, whereas (-)-8 and the trans isomer (+/-)-9 were inactive.
|
pubmed:language |
eng
|
pubmed:journal |
|
pubmed:citationSubset |
IM
|
pubmed:chemical |
|
pubmed:status |
MEDLINE
|
pubmed:month |
Nov
|
pubmed:issn |
0022-2623
|
pubmed:author |
|
pubmed:issnType |
Print
|
pubmed:volume |
30
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
2105-9
|
pubmed:dateRevised |
2006-11-15
|
pubmed:meshHeading |
pubmed-meshheading:2959776-8-Hydroxy-2-(di-n-propylamino)tetralin,
pubmed-meshheading:2959776-Animals,
pubmed-meshheading:2959776-Male,
pubmed-meshheading:2959776-Molecular Conformation,
pubmed-meshheading:2959776-Naphthalenes,
pubmed-meshheading:2959776-Rats,
pubmed-meshheading:2959776-Rats, Inbred Strains,
pubmed-meshheading:2959776-Receptors, Dopamine,
pubmed-meshheading:2959776-Receptors, Serotonin,
pubmed-meshheading:2959776-Serotonin,
pubmed-meshheading:2959776-Stereoisomerism,
pubmed-meshheading:2959776-Structure-Activity Relationship,
pubmed-meshheading:2959776-Tetrahydronaphthalenes
|
pubmed:year |
1987
|
pubmed:articleTitle |
(+)-cis-8-Hydroxy-1-methyl-2-(di-n-propylamino)tetralin: a potent and highly stereoselective 5-hydroxytryptamine receptor agonist.
|
pubmed:affiliation |
Department of Organic Pharmaceutical Chemistry, University of Uppsala,Sweden.
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|