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A 5-HT2A, 5-HT2B, and 5-HT2C receptor agonist, induces calcium accumulation in CHO-K1 cells expressing 5-HT2A, 5-HT2B, or 5-HT2C receptors (EC50s = 309.03, 177.83, and 338.84 nM, respectively, for the human receptors), binds to the 5-HT3 receptor (Ki = 2.1 nM), decreases food intake in rats at 2.5, 5, or 10 mg/kg, restores spinal circuitry function, improves gait regularity, and increases interlimb coordination and limb weight-bearing in a rat model of spinal cord transection-induced hindlimb paralysis at 0.3 mg/kg per day in combination with 8-hydroxy DPAT, electrode stimulation of dorsal and lumbar spine regions, and locomotor training. Formulation: A solid. InChI: InChI=1S/C13H15N3.2C4H4O4/c1-2-4-12-11(3-1)5-6-13(15-12)16-9-7-14-8-10-16,2*5-3(6)1-2-4(7)8/h1-6,14H,7-10H2,2*1-2H,(H,5,6)(H,7,8)/b,2*2-1-. InChIKey: VAOSOCRJSSWBEQ-SPIKMXEPSA-N. SMILES: O=C(O)/C=C\C(O)=O.O=C(O)/C=C\C(O)=O.C1(N2CCNCC2)=NC3=C(C=CC=C3)C=C1
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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