Autor: |
P. R. Findell, Richard I. Weiner, J. C. Craig, S. M. Torkelson |
Rok vydání: |
1989 |
Předmět: |
|
Zdroj: |
ChemInform. 20 |
ISSN: |
0931-7597 |
DOI: |
10.1002/chin.198939192 |
Popis: |
A series of 2-substituted octahydrobenzo[f]quinolines has been synthesized and assayed for dopamine agonist activity. Only the compounds corresponding to the beta-rotameric conformation of dopamine showed biphasic activity in competition binding studies with the radioligand [3H]spiroperidol. These findings suggest that the congeners possessing the beta-rotamer conformation show receptor-binding characteristics that resemble those of the ergolines more closely than do those of the corresponding alpha-rotamer congeners. |
Databáze: |
OpenAIRE |
Externí odkaz: |
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