23199-56-6Relevant articles and documents
Synthesis and Structural Requirements of N-Substituted Norapomorphines for Affinity and Activity at Dopamine D-1, D-2, and Agonist Receptor Sites in Rat Brain
Gao, Yigong,Ram, Vishnu J.,Campbell, Alexander,Kula, Nora S.,Baldessarini, Ross J.,Neumeyer, Johm L.
, p. 39 - 44 (1990)
A series of N-substituted analogues of (R)-(-)-naorapomorphine were synthesized to study the optimal structural requirements of the N-alkyl side chain to interact with D-1 and D-2 dopaminergic receptors as well as dopamine (DA) agonist binding sites.Evaluation included testing the affinity of these compounds for DA receptor sites in rat striatal tissue and assessing stereotypy as a behavioral index of dopaminergic activity.The electronic, steric, and lipohilic properties of the N-alkyl side chain were found to be related to affinity, D-2 selectivity, and dopaminergic activity.All 11 compounds evaluated had relatively low affinity at D-1 sites.Optimum D-2 and agonist-site affinity as well as agonist activity were exhibited by N-cyclopropylmethyl (7) N-allyl N-propyl (4) or N-ethyl (3) substituted compounds.Branching of the N-alkyl side chain as in N-isopropyl (5) and N-isobutyl (6) markedly reduced the D-2 affinity and activity, presumably due to steric effects.The N-trifluoroethyl (10) and N-pentafluoropropyl (11) derivatives had low affinity for all their dopamine receptor sites and no agonistic activity; evidently, the highly electronegative F atoms decrease basicity of the N atom and therefore decrease the ability of the N atom to be cationic at physiological pH, a proposed requirement for high-affinity binding to DA receptors.