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Phenyltropanes & arylcyclohexylamines seem to span the same major euphoric / recreational receptors in humans: including NMDA antagonism, dopamine reuptake obstruction/blocking/inhibition, opioid agonism, etc., depending on the specific conformation of the individual SAR of the molecule belonging to a specific type of either class. Difluoropine seems to be in-between these two classes, but that is only from a layman's perspective, bridging certain characteristics. Am I mistaken? 65.102.8.249 (talk) 11:59, 29 March 2010 (UTC)[reply]
