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ST1936 is an agonist of the serotonin (5-HT) receptor subtype 5-HT6.1,2 It selectively binds to 5-HT6 (Ki = 31 nM) over 5-HT1A, 5-HT1B, 5-HT1D, 5-HT2A, 5-HT2B, 5-HT2C, 5-HT3, 5-HT4, 5-HT5A, and the serotonin transporter (SERT; Kis = >1,000 nM for all) but also binds to the 5-HT7 receptor (Ki = 168 nM).1 ST1936 induces cAMP accumulation in BHK fibroblasts (EC50 = 16 nM).2 It decreases the basal firing rate of dopaminergic neurons in the ventral tegmental area but not substantia nigra pars compacta in rats in a dose-dependent manner.3 ST1936 (10 and 30 mg/kg) prevents stress-induced decreases in vanilla sugar-sustained appetitive behavior, indicating anti-anhedonic-like activity, in rats.4 It induces self-administration in rats when administered at a dose of 1 mg/kg.5
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3. Effects of ST1936, a selective serotonin-
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5. Evidence for a role of a dopamine/5-