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A 5-HT6 receptor agonist, increases intracellular cAMP levels in HeLa cells expressing 5-HT6 (EC50 = 6.5 nM), selectively binds to 5-HT6 over 5-HT2B, 5-HT2C, and 5-HT7 (Kis = 2,458, 124, and 679 nM, respectively), selective for 5-HT6 over a panel of 31 receptors and ion channels at 100 nM, increases extracellular GABA levels in the rat frontal cortex at 10 mg/kg, reduces schedule-induced polydipsia, an adjunctive model of compulsive disorder, in rats at 178 mg/kg, has antidepressant-like activity in rats at 17 mg/kg and anxiolytic-like activity in rats at 10 and 17 mg/kg. Formulation: A solid. InChI: InChI=1S/C15H13ClN4O2S2/c16-13-14(19-7-8-23-15(19)18-13)24(21,22)20-9-10(5-6-17)11-3-1-2-4-12(11)20/h1-4,7-9H,5-6,17H2. InChIKey: RYBOXBBYCVOYNO-UHFFFAOYSA-N. SMILES: NCCC1=CN(S(=O)(C2=C(Cl)N=C3N2C=CS3)=O)C4=C1C=CC=C4
This website uses cookies, which are necessary for the technical operation of the website and are always set. Other cookies, which increase the usability of this website, serve for direct advertising or simplify interaction with other websites and social networks, will only be used with your consent.
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