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S33005, a novel ligand at both serotonin and norepinephrine transporters: II. Behavioral profile in comparison with venlafaxine, reboxetine, citalopram, and clomipramine
The Journal of pharmacology and experimental therapeutics, 2001-08, Vol.298 (2), p.581
2001
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Neurokinin1 antagonists potentiate antidepressant properties of serotonin reuptake inhibitors, yet blunt their anxiogenic actions: a neurochemical, electrophysiological, and behavioral characterization
Neuropsychopharmacology (New York, N.Y.), 2009-03, Vol.34 (4), p.1039-1056
2009
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S33138 [N-[4-[2-[(3aS,9bR)-8-cyano-1,3a,4,9b-tetrahydro[1]-benzopyrano[3,4-c]pyrrol-2(3H)-yl)-ethyl]phenylacetamide], a preferential dopamine D3 versus D2 receptor antagonist and potential antipsychotic agent. II. A neurochemical, electrophysiological and behavioral characterization in vivo
The Journal of pharmacology and experimental therapeutics, 2008-02, Vol.324 (2), p.600
2008
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S 18126 ([2-[4-(2,3-dihydrobenzo[1,4]dioxin-6-yl)piperazin-1-yl methyl]indan-2-yl]), a potent, selective and competitive antagonist at dopamine D4 receptors: an in vitro and in vivo comparison with L 745,870 (3-(4-[4-chlorophenyl]piperazin-1-yl)methyl-1H-pyrrolo[2, 3b]pyridine) and raclopride
The Journal of pharmacology and experimental therapeutics, 1998-10, Vol.287 (1), p.167
1998
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S18327 (1-[2-[4-(6-fluoro-1, 2-benzisoxazol-3-yl)piperid-1-yl]ethyl]3-phenyl imidazolin-2-one), a novel, potential antipsychotic displaying marked antagonist properties at alpha(1)- and alpha(2)-adrenergic receptors: II. Functional profile and a multiparametric comparison with haloperidol, clozapine, and 11 other antipsychotic agents
The Journal of pharmacology and experimental therapeutics, 2000-01, Vol.292 (1), p.54
2000
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WAY 100,635 enhances both the `antidepressant' actions of duloxetine and its influence on dialysate levels of serotonin in frontal cortex
European journal of pharmacology, 1998-01, Vol.341 (2), p.165-167
1998
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Characterization of Potent and Selective Antagonists at Postsynaptic 5-HT1A Receptors in a Series of N4-Substituted Arylpiperazines
Journal of medicinal chemistry, 1995-09, Vol.38 (20), p.4044-4055
1995
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Novel benzodioxopiperazines acting as antagonists at postsynaptic 5-HT1A receptors and as agonists at 5-HT1A autoreceptors: a comparative pharmacological characterization with proposed 5-HT1A antagonists
The Journal of pharmacology and experimental therapeutics, 1994-01, Vol.268 (1), p.337
1994
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S 15535 : a highly selective benzodioxopiperazine 5-HT1A receptor ligand which acts as an agonist and an antagonist at presynaptic and postsynaptic sites respectively
European journal of pharmacology, 1993-01, Vol.230 (1), p.99-102
1993
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A drug discrimination analysis of the actions of novel serotonin1A receptor ligands in the rat using the 5-HT1A receptor agonist, 8-hydroxy-2-(di-n-propylamino)tetralin
The Journal of pharmacology and experimental therapeutics, 1995-11, Vol.275 (2), p.822
1995
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S 15535, a novel benzodioxopiperazine ligand of serotonin (5-HT)1A receptors: II. Modulation of hippocampal serotonin release in relation to potential anxiolytic properties
The Journal of pharmacology and experimental therapeutics, 1997-07, Vol.282 (1), p.148
1997
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S18327 (1-[2-[4-(6-fluoro-1, 2-benzisoxazol-3-yl)piperid-1-yl]ethyl]3-phenyl imidazolin-2-one), a novel, potential antipsychotic displaying marked antagonist properties at alpha(1)- and alpha(2)-adrenergic receptors: I. Receptorial, neurochemical, and electrophysiological profile
The Journal of pharmacology and experimental therapeutics, 2000-01, Vol.292 (1), p.38
2000
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Involvement of 5-HT1A receptors in the anxiolytic action of S 14671 in the pigeon conflict test
Pharmacology, biochemistry and behavior, 1995-06, Vol.51 (2-3), p.211-215
1995
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S 15535, a novel benzodioxopiperazine ligand of serotonin (5-HT)1A receptors: I. Interaction with cloned human (h)5-HT1A, dopamine hD2/hD3 and h alpha2A-adrenergic receptors in relation to modulation of cortical monoamine release and activity in models of potential antidepressant activity
The Journal of pharmacology and experimental therapeutics, 1997-07, Vol.282 (1), p.132
1997
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Functional correlates of dopamine D3 receptor activation in the rat in vivo and their modulation by the selective antagonist, (+)-S 14297: 1. Activation of postsynaptic D3 receptors mediates hypothermia, whereas blockade of D2 receptors elicits prolactin secretion and catalepsy
The Journal of pharmacology and experimental therapeutics, 1995-11, Vol.275 (2), p.885
1995
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