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Conformationally constrained butyrophenones with mixed dopaminergic (D-2) and serotoninergic (5-HT2A, 5-HT2C) affinities: Synthesis, pharmacology, 3D-QSAR, and molecular modeling of (aminoalkyl)benzo- and -thienocycloalkanones as putative atypical antipsychotics (vol 42, pg 2775, 1999)
Authors: Ravina, E Negreira, J Cid, J Masaguer, CF Rosa, E Rivas, ME Fontenla, JA Loza, MI Tristan, H Cadavid, MI Sanz, F Lozoya, E Carotti, A Carrieri, A
Citation: E. Ravina et al., Conformationally constrained butyrophenones with mixed dopaminergic (D-2) and serotoninergic (5-HT2A, 5-HT2C) affinities: Synthesis, pharmacology, 3D-QSAR, and molecular modeling of (aminoalkyl)benzo- and -thienocycloalkanones as putative atypical antipsychotics (vol 42, pg 2775, 1999), J MED CHEM, 43(6), 2000, pp. 1250-1250
Conformationally constrained butyrophenones with mixed dopaminergic (D-2) and serotoninergic (5-HT2A, 5-HT2C) affinities: Synthesis, pharmacology, 3D-QSAR, and molecular modeling of (aminoalkyl)benzo- and -thienocycloalkanones as putative atypical antipsychotics
Authors: Ravina, E Negreira, J Cid, J Masaguer, CP Rosa, E Rivas, ME Fontenla, JA Loza, MI Tristan, H Cadavid, MI Sanz, F Lozoya, E Carotti, A Carrieri, A
Citation: E. Ravina et al., Conformationally constrained butyrophenones with mixed dopaminergic (D-2) and serotoninergic (5-HT2A, 5-HT2C) affinities: Synthesis, pharmacology, 3D-QSAR, and molecular modeling of (aminoalkyl)benzo- and -thienocycloalkanones as putative atypical antipsychotics, J MED CHEM, 42(15), 1999, pp. 2774-2797
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