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A 5-HT2A and dopamine D2 receptor antagonist, selective for the 5-HT2A receptor over 5-HT2B and 5-HT1C receptors (Kis = 22.39, 977.24, and 1,548.82 nM, respectively) but does bind to the 5-HT1A receptor (Ki = 50 nM), selectively binds to the dopamine D2 receptor over the dopamine D1 receptor (Kis = 3 and 2,530 nM, respectively), completely inhibits amphetamine-induced increases in locomotor activity and rearing behavior in rats for at least three hours at 0.05 mg/kg, reduces amphetamine-induced increases in locomotor activity and rearing behavior in mice when used at doses of 0.15 and 0.2 mg/kg but the effects only last for 30 minutes. Formulation: A solid. InChI: InChI=1S/C22H26FN3O2/c23-18-7-9-20(10-8-18)28-16-4-13-25-14-11-22(12-15-25)21(27)24-17-26(22)19-5-2-1-3-6-19/h1-3,5-10H,4,11-17H2,(H,24,27). InChIKey: FJUKDAZEABGEIH-UHFFFAOYSA-N. SMILES: FC(C=C1)=CC=C1OCCCN2CCC(C3=O)(N(C4=CC=CC=C4)CN3)CC2
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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