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Journal Abstract Search
191 related items for PubMed ID: 24316025
1. Synthesis and biological evaluation of a series of aminoalkyl-tetralones and tetralols as dual dopamine/serotonin ligands. Carro L, Torrado M, Raviña E, Masaguer CF, Lage S, Brea J, Loza MI. Eur J Med Chem; 2014 Jan; 71():237-49. PubMed ID: 24316025 [Abstract] [Full Text] [Related]
3. Synthesis and biological investigation of new equatorial (β) stereoisomers of 3-aminotropane arylamides with atypical antipsychotic profile. Stefanowicz J, Słowiński T, Wróbel MZ, Herold F, Gomółka AE, Wesołowska A, Jastrzębska-Więsek M, Partyka A, Andres-Mach M, Czuczwar SJ, Łuszczki JJ, Zagaja M, Siwek A, Nowak G, Żołnierek M, Bączek T, Ulenberg S, Belka M, Turło J. Bioorg Med Chem; 2016 Sep 15; 24(18):3994-4007. PubMed ID: 27377863 [Abstract] [Full Text] [Related]
6. Chemoenzymatic synthesis and binding affinity of novel (R)- and (S)-3-aminomethyl-1-tetralones, potential atypical antipsychotics. Caro Y, Torrado M, Masaguer CF, Raviña E, Padín F, Brea J, Loza MI. Bioorg Med Chem Lett; 2004 Feb 09; 14(3):585-9. PubMed ID: 14741248 [Abstract] [Full Text] [Related]
16. Long-term effects of JL 13, a potential atypical antipsychotic, on rat dopamine and serotonin receptor subtypes. Moran-Gates T, Massari C, Graulich A, Liégeois JF, Tarazi FI. J Neurosci Res; 2006 Aug 15; 84(3):675-82. PubMed ID: 16810690 [Abstract] [Full Text] [Related]
17. Design, synthesis and evaluation of benzo[a]thieno[3,2-g]quinolizines as novel l-SPD derivatives possessing dopamine D1, D2 and serotonin 5-HT1A multiple action profiles. Li Z, Huang J, Sun H, Zhou S, Guo L, Zhou Y, Zhen X, Liu H. Bioorg Med Chem; 2014 Nov 01; 22(21):5838-46. PubMed ID: 25308766 [Abstract] [Full Text] [Related]
18. Comparative effect of lurasidone and blonanserin on cortical glutamate, dopamine, and acetylcholine efflux: role of relative serotonin (5-HT)2A and DA D2 antagonism and 5-HT1A partial agonism. Huang M, Panos JJ, Kwon S, Oyamada Y, Rajagopal L, Meltzer HY. J Neurochem; 2014 Mar 01; 128(6):938-49. PubMed ID: 24164459 [Abstract] [Full Text] [Related]