C1-Methylated 5-hydroxy-2-(dipropylamino)tetralins: central dopamine-receptor stimulating activity
- 31 July 1984
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of Medicinal Chemistry
- Vol. 27 (8) , 1003-1007
- https://doi.org/10.1021/jm00374a012
Abstract
C1-Methylated derivatives of the potent dopaminergic agonist 5-hydroxy-2-(di-n-propylamino)tetralin (6) were synthesized and tested for central dopamine (DA) receptor stimulating activity, by using biochemical and behavioral tests in rats. Both cis- and trans-5-hydroxy-1-methyl-2-(di-n-propylamino)tetralin (4 and 3) may be classified as central DA-receptor agonists, albeit of lower potency than 6. Both 4 and 3 display DA-autoreceptor stimulation capacity. Only 1 of the isomers, trans-3 is able to elicit clear-cut postsynaptic DA receptor agonist actions at larger doses. 5-Hydroxy-1,1-dimethyl-2-(n-propylamino)tetralin was inactive.This publication has 1 reference indexed in Scilit:
- Congeners of the .beta. conformer of dopamine derived from cis- and trans-octahydrobenzo[f]quinoline and trans-octahydrobenzo[g]quinolineJournal of Medicinal Chemistry, 1980