Kinetic and pharmacological profiles of the in vitro binding of the potent dopamine agonist [3H]N,N-dipropyl-5,6-dihydroxy-2-aminotetralin to rat striatal membranes
Author:
Publisher
Elsevier BV
Subject
Pharmacology
Reference29 articles.
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1. Pharmacological profile of non-hydroxylated and ether derivatives of the potent D2-selective agonist N-0437;Naunyn-Schmiedeberg's Archives of Pharmacology;1991-02
2. Drugs acting on brain dopamine receptors: A conceptual re-evaluation five years after the first selective D-1 antagonist;Pharmacology & Therapeutics;1989-01
3. Synthesis and pharmacology of trans-4-n-propyl-3,4,4a,10b-tetrahydro-2H,5H-1-benzopyrano[4,3-b]1,4-oxazin-7- and -9-ols. The significance of nitrogen pka values for central dopamine receptor activation;Journal of Medicinal Chemistry;1988-11
4. Pharmacological profile of a chromanamine analogue (DP-6OH-3CA) of the selective presynaptic dopamine agonist N, N-dipropyl-7-hydroxy-2-aminotetralin;Journal of Pharmacy and Pharmacology;1988-08
5. Synthesis and dopaminergic activity of a new oxygen isostere of the 2-aminotetralins: N,N-dipropyl-8-hydroxy-3-chromanamine;European Journal of Medicinal Chemistry;1988-07
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