A series of 5-hydroxy- and 5,6-dihydroxy- 1,2,3,7,12,12a-hexahydrobenzo[5,6]cyclohepta[1,2,3-iJ]isoquinoline derivatives (5a-e and 6a-e) were synthesized as conformationally rigid analogues of 1-benzyltetrahydroisoquinoline and evaluated for their affinity at D-1 and D-2 dopamine receptors. All compounds showed lower D1 and D affinities than dopamine. The 5-hydroxy-1-methyl-2,3,12,12a-hexahydrobenzo[5,6]cyclohepta[1,2,3-ij] 5a and the 5,6dihydroxy analogue 6a showed D-2 agonist activity. This was proved by their effects on prolactin release from primary cultures of rat anterior pituitary cells. Molecular modeling studies showed that the geometric parameters (namely the distances from meta and para hydroxyl oxygens to the nitrogen and the height of nitrogen from the hydroxylated phenyl ring plane) of the dopaminergic pharmacophore embedded in our compounds have lower values in comparison with those observed in D-1 and D-2 selective ligands. (C) 2001 Elsevier Science Ltd. All rights reserved.
|Autori interni:||COSTA, BARBARA|
|Autori:||CINGOLANI G.M.; DI STEFANO A.; NAPOLETANI F.; MOSCIATTI B.; GIORGIONI G.; CINONE N.; BRUNETTI L.; LUISI G.; MICHELOTTO B.; ORLANDO G.; COSTA B; LUCACCHINI A.; MARTINI C.; CLAUDI F.|
|Titolo:||Synthesis and preliminary pharmacological evaluation of 5-hydroxy-and 5,6-dihydroxy-1,2,3,7,12,12a-hexahydrobenzo [5,6]cycloheptal [1,2,3-ij]isoquinoline derivatives as dopamine receptor ligands|
|Anno del prodotto:||2001|
|Digital Object Identifier (DOI):||10.1016/S0968-0896(01)00016-5|
|Appare nelle tipologie:||1.1 Articolo in rivista|