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S33005, a novel ligand at both serotonin and norepinephrine transporters: I. Receptor binding, electrophysiological, and neurochemical profile in comparison with venlafaxine, reboxetine, citalopram, and clomipramine

The Journal of pharmacology and experimental therapeutics, 2001-08, Vol.298 (2), p.565

2001

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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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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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Anti-Ischemic Effects of Ivabradine, a Selective Heart Rate-Reducing Agent, in Exercise-Induced Myocardial Ischemia in Pigs

Journal of cardiovascular pharmacology, 2003-11, Vol.42 (5), p.688-696

2003

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A Short and Efficient Stereoselective Synthesis of the Octalactin Lactone Using Enantioselective Crotyltitanations and a Cross-Metathesis Reaction

Synlett, 2005-11, Vol.2005 (18), p.2851-2853

2005

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5-HT2C receptors mediate penile erections in rats : actions of novel and selective agonists and antagonists

European journal of pharmacology, 1997-04, Vol.325 (1), p.9-12

1997

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Stereospecific in vitro and in vivo effects of the new sinus node inhibitor (+)-S 16257

European journal of pharmacology, 1997-11, Vol.339 (1), p.43-51

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: 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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Improvement in the Selectivity and Metabolic Stability of the Serotonin 5-HT1A Ligand, S 15535: A Series of cis- and trans-2-(Arylcycloalkylamine) 1-Indanols

Journal of medicinal chemistry, 2002-01, Vol.45 (1), p.165-176

2002

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S32504, a Novel Naphtoxazine Agonist at Dopamine D 3 /D 2 Receptors: III. Actions in Models of Potential Antidepressive and Anxiolytic Activity in Comparison with Ropinirole

The Journal of pharmacology and experimental therapeutics, 2004-06, Vol.309 (3), p.936-950

2004

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Short Synthesis of the Selective Rho-Kinase Inhibitor Y-27632 and of Its Enantiomer

Letters in organic chemistry, 2005-11, Vol.2 (7), p.634-636

2005

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S32504, a Novel Naphtoxazine Agonist at Dopamine D 3 /D 2 Receptors: I. Cellular, Electrophysiological, and Neurochemical Profile in Comparison with Ropinirole

The Journal of pharmacology and experimental therapeutics, 2004-06, Vol.309 (3), p.903-920

2004

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Modulation of mesolimbic dopamine release by the selective dopamine D 3 receptor antagonist, (+)-S 14297

European journal of pharmacology, 1994-11, Vol.265 (3), p.175-177

1994

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Synthesis of Spiro[benzazepine-2,4‘-piperidine]

Journal of organic chemistry, 1998-06, Vol.63 (13), p.4554-4557

1998

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In Vivo Quantification of Myocardial Dihydropyridine Binding Sites: A PET Study in Dogs

The Journal of nuclear medicine (1978), 2002-09, Vol.43 (9), p.1227-1233

2002

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Synthesis of spiro[quinoline-2,4′-piperidines] Heck versus radical reaction

Tetrahedron letters, 1998-05, Vol.39 (19), p.2965-2968

1998

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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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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 14297, a novel selective ligand at cloned human dopamine D 3 receptors, blocks 7-OH-DPAT-induced hypothermia in rats

European journal of pharmacology, 1994-08, Vol.260 (2), p.R3-R5

1994

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Highly efficient synthesis of [11C]S12968 and [11C]S12967, for the in vivo imaging of the cardiac calcium channels using PET

Journal of labelled compounds & radiopharmaceuticals, 2001-06, Vol.44 (7), p.481-499

2001

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Synthesis of two optically active calcium channel antagonists labelled with carbon-11 for in vivo cardiac PET imaging

Bioorganic & medicinal chemistry, 1997-04, Vol.5 (4), p.749-764

1997

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Ca2+ channel inhibition in a rat osteoblast-like cell line, UMR 106, by a new dihydropyridine derivative, S11568

European journal of pharmacology, 1992-09, Vol.220 (1), p.11-17

1992

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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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Synthesis of 2-(Alkylamino)benzonitriles from α-(Bromoarylamino)nitriles

Synthesis (Stuttgart), 1995-11, Vol.1995 (11), p.1368-1370

1995

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The calcium channel antagonist S 11568 causes endothelium-dependent relaxation in canine arteries

European journal of pharmacology, 1991-05, Vol.197 (1), p.41-48

1991

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S33005, a novel ligand at both serotonin and norepinephrine transporters: I. Receptor binding, electrophysiological, and neurochemical profile in comparison with venlafaxine, reboxetine, citalopram, and clomipramine

S33005, a novel ligand at both serotonin and norepinephrine transporters: II. Behavioral profile in comparison with venlafaxine, reboxetine, citalopram, and clomipramine

Characterization of Potent and Selective Antagonists at Postsynaptic 5-HT1A Receptors in a Series of N4-Substituted Arylpiperazines

Anti-Ischemic Effects of Ivabradine, a Selective Heart Rate-Reducing Agent, in Exercise-Induced Myocardial Ischemia in Pigs

A Short and Efficient Stereoselective Synthesis of the Octalactin Lactone Using Enantioselective Crotyltitanations and a Cross-Metathesis Reaction

5-HT2C receptors mediate penile erections in rats : actions of novel and selective agonists and antagonists

Stereospecific in vitro and in vivo effects of the new sinus node inhibitor (+)-S 16257

Improvement in the Selectivity and Metabolic Stability of the Serotonin 5-HT1A Ligand, S 15535: A Series of cis- and trans-2-(Arylcycloalkylamine) 1-Indanols

S32504, a Novel Naphtoxazine Agonist at Dopamine D 3 /D 2 Receptors: III. Actions in Models of Potential Antidepressive and Anxiolytic Activity in Comparison with Ropinirole

Short Synthesis of the Selective Rho-Kinase Inhibitor Y-27632 and of Its Enantiomer

S32504, a Novel Naphtoxazine Agonist at Dopamine D 3 /D 2 Receptors: I. Cellular, Electrophysiological, and Neurochemical Profile in Comparison with Ropinirole

Modulation of mesolimbic dopamine release by the selective dopamine D 3 receptor antagonist, (+)-S 14297

Synthesis of Spiro[benzazepine-2,4‘-piperidine]

In Vivo Quantification of Myocardial Dihydropyridine Binding Sites: A PET Study in Dogs

Synthesis of spiro[quinoline-2,4′-piperidines] Heck versus radical reaction

S 15535 : a highly selective benzodioxopiperazine 5-HT1A receptor ligand which acts as an agonist and an antagonist at presynaptic and postsynaptic sites respectively

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

S 14297, a novel selective ligand at cloned human dopamine D 3 receptors, blocks 7-OH-DPAT-induced hypothermia in rats

Highly efficient synthesis of [11C]S12968 and [11C]S12967, for the in vivo imaging of the cardiac calcium channels using PET

Synthesis of two optically active calcium channel antagonists labelled with carbon-11 for in vivo cardiac PET imaging

Ca2+ channel inhibition in a rat osteoblast-like cell line, UMR 106, by a new dihydropyridine derivative, S11568

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

Synthesis of 2-(Alkylamino)benzonitriles from α-(Bromoarylamino)nitriles

The calcium channel antagonist S 11568 causes endothelium-dependent relaxation in canine arteries

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