Dopaminergic activity of four analogs of butaclamol

Abstract The displacing potency of four analogs of the neuroleptic drug butaclamol were evaluated using dog striatal tissue and [ 3 H]-Spiroperidol as ligand. Although significantly less powerful than the parent compound, two of them (N-isobutyl butaclamol equatorial; N-methyl butaclamol equatorial) could be used for dopaminergic receptor studies.