European Journal of Medicinal Chemistry p. 869 - 874 (1991)
Update date:2022-09-26
Topics:
Perrone, R
Berardi, F
Tortorella, V
Govoni, S
Lograno, MD
Daniele, E
A series of 1-aminoethylhetero-tetralines 3-6, which can be considered as opened-structure analogues of previously studied dopaminergic compounds 2, were synthesized.In the binding studies, to evaluate D-1 and D-2 activity, no significant affinity was observed towards both dopaminergic receptors.D-1 receptors / D-2 receptors / dopamine / binding / tetralines
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