Interaction of D(3) preferring agonist (−)-N(6)-(2-(4-(Biphenyl-4-yl)piperazin-1-yl)ethyl)-N(6)-propyl-4,5,6,7-tetrahydrobenzo[d]thiazole-2,6-diamine (D-264) with cloned human D(2L), D(2S) and D(3) receptors: Potent stimulation of mitogen-activated protein kinases and G-protein coupled inward rectifier potassium channels

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