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Preferential in vivo action of F15599, a novel 5‐HT1A receptor agonist, at postsynaptic 5‐HT1A receptors

British journal of pharmacology, 2010-08, Vol.160 (8), p.1929-1940

2010

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Design and Synthesis of a Series of 6-Substituted-2-pyridinylmethylamine Derivatives as Novel, High-Affinity, Selective Agonists at 5-HT1A Receptors

Journal of medicinal chemistry, 1998-12, Vol.41 (25), p.5070-5083

1998

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Signal transduction and functional selectivity of F15599, a preferential post‐synaptic 5‐HT 1A receptor agonist

British journal of pharmacology, 2009-01, Vol.156 (2), p.338-353

2009

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Rapid desensitization of somatodendritic 5‐HT 1A receptors by chronic administration of the high‐efficacy 5‐HT 1A agonist, F13714: a microdialysis study in the rat

British journal of pharmacology, 2009-01, Vol.149 (2), p.170-178

2009

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F15063, a potential antipsychotic with D2/D3 antagonist, 5‐HT1A agonist and D4 partial agonist properties: (I) in vitro receptor affinity and efficacy profile

British journal of pharmacology, 2007-05, Vol.151 (2), p.237-252

2007

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Correlation between low/high affinity ratios for 5-HT1A receptors and intrinsic activity

European journal of pharmacology, 1999-12, Vol.386 (1), p.97-103

1999

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[3H]‐8‐OH‐DPAT binding in the rat brain raphe area: involvement of 5‐HT1A and non‐5‐HT1A receptors

British journal of pharmacology, 2000-07, Vol.130 (6), p.1348-1352

2000

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F15063, a potential antipsychotic with D 2 /D 3 antagonist, 5‐HT 1A agonist and D 4 partial agonist properties: (I) in vitro receptor affinity and efficacy profile

British journal of pharmacology, 2009-01, Vol.151 (2), p.237-252

2009

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5‐HT 1A receptors are involved in the effects of xaliproden on G‐protein activation, neurotransmitter release and nociception

British journal of pharmacology, 2009-09, Vol.158 (1), p.232-242

2009

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In vivo [ 3H]ketanserin binding: effect of modifying synaptic serotonin levels

Neurochemistry international, 1988, Vol.12 (1), p.85-89

1988

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Large-amplitude 5-HT1A receptor activation: a new mechanism of profound, central analgesia

Neuropharmacology, 2002-11, Vol.43 (6), p.945-958

2002

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Rapid desensitization of somatodendritic 5-HT sub(1A)receptors by chronic administration of the high-efficacy 5-HT sub(1A) agonist, F13714: a microdialysis study in the rat

British journal of pharmacology, 2006-09, Vol.149 (2), p.170-178

2006

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F15063, a potential antipsychotic with D sub(2)/D sub(3) antagonist, 5-HT sub(1A) agonist and D sub(4) partial agonist properties: (I) in vitro receptor affinity and efficacy profile

British journal of pharmacology, 2007-05, Vol.151 (2), p.237-252

2007

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Repeated administration of milnacipran, a new antidepressant, has no effect on a functional β-adrenergic response in the rat brain

European journal of pharmacology, 1990, Vol.183 (3), p.741-742

1990

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Effects of 5-HT sub(1A) receptor antagonists on hippocampal 5-hydroxytryptamine levels: (S)-WAY100135, but not WAY100635, has partial agonist properties

European journal of pharmacology, 1996-05, Vol.304 (1-3), p.15-21

1996

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(-)-Pindolol and ( plus or minus )-tertatolol affect rat hippocampal 5-HT levels through mechanisms involving not only 5-HT sub(1A), but also 5-HT sub(1B) receptors

Neuropharmacology, 1996-02, Vol.35 (2), p.213-222

1996

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(−)-Pindolol and (±)-Tertatolol Affect Rat Hippocampal 5-HT Levels Through Mechanisms Involving Not Only 5-HT 1A, But Also 5-HT 1B Receptors

Neuropharmacology, 1996, Vol.35 (2), p.213-222

1996

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5-HT sub(1A) receptor agonist properties of the antipsychotic, nemonapride: Comparison with bromerguride and clozapine

European journal of pharmacology, 1997-09, Vol.334 (2-3), p.141-147

1997

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In vivo estimates of efficacy at 5-HT 1A receptors: effects of EEDQ on the ability of agonists to produce lower-lip retraction in rats

Psychopharmacology, 2000-05, Vol.149 (4), p.377-387

2000

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Preferential in vivo action of F15599, a novel 5‐HT 1A receptor agonist, at postsynaptic 5‐HT 1A receptors

British journal of pharmacology, 2010-08, Vol.160 (8), p.1929-1940

2010

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Large-amplitude 5-HT sub(1A) receptor activation: a new mechanism of profound, central analgesia

Neuropharmacology, 2002-11, Vol.43 (6), p.945-958

2002

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Neuropharmacology of a new potential anxiolytic compound, F 2692, 1-(3'-trifluoromethyl phenyl) 1, 4-dihydro 3-amino 4-oxo 6-methyl pyridazine. II: Evaluation of its tolerance and dependence producing potential and of its effects on benzodiazepine withdrawal in the elevated plus-maze test in rats

Psychopharmacologia, 1993, Vol.110 (1-2), p.19-26

1993

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Neuropharmacology of a new potential anxiolytic compound, F 2692, 1-(3'-trifluoromethyl phenyl) 1, 4-dihydro 3-amino 4-oxo 6-methyl pyridazine. I: Acute and in vitro effects

Psychopharmacologia, 1993, Vol.110 (1-2), p.13-18

1993

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In vivo ( super(3)H)ketanserin binding: Effect of modifying synaptic serotonin levels

Neurochemistry international, 1988-01, Vol.12 (1), p.85-89

1988

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Comparison between a complete preconditioning programme and conventional conduct on behaviour, health and performance of young bulls from small cow-calf herds

Animal (Cambridge, England), 2024-06, Vol.18 (6), p.101169, Article 101169

2024

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Preferential in vivo action of F15599, a novel 5‐HT1A receptor agonist, at postsynaptic 5‐HT1A receptors

Design and Synthesis of a Series of 6-Substituted-2-pyridinylmethylamine Derivatives as Novel, High-Affinity, Selective Agonists at 5-HT1A Receptors

Signal transduction and functional selectivity of F15599, a preferential post‐synaptic 5‐HT 1A receptor agonist

Rapid desensitization of somatodendritic 5‐HT 1A receptors by chronic administration of the high‐efficacy 5‐HT 1A agonist, F13714: a microdialysis study in the rat

F15063, a potential antipsychotic with D2/D3 antagonist, 5‐HT1A agonist and D4 partial agonist properties: (I) in vitro receptor affinity and efficacy profile

Correlation between low/high affinity ratios for 5-HT1A receptors and intrinsic activity

[3H]‐8‐OH‐DPAT binding in the rat brain raphe area: involvement of 5‐HT1A and non‐5‐HT1A receptors

F15063, a potential antipsychotic with D 2 /D 3 antagonist, 5‐HT 1A agonist and D 4 partial agonist properties: (I) in vitro receptor affinity and efficacy profile

5‐HT 1A receptors are involved in the effects of xaliproden on G‐protein activation, neurotransmitter release and nociception

In vivo [ 3H]ketanserin binding: effect of modifying synaptic serotonin levels

Large-amplitude 5-HT1A receptor activation: a new mechanism of profound, central analgesia

Rapid desensitization of somatodendritic 5-HT sub(1A)receptors by chronic administration of the high-efficacy 5-HT sub(1A) agonist, F13714: a microdialysis study in the rat

F15063, a potential antipsychotic with D sub(2)/D sub(3) antagonist, 5-HT sub(1A) agonist and D sub(4) partial agonist properties: (I) in vitro receptor affinity and efficacy profile

Repeated administration of milnacipran, a new antidepressant, has no effect on a functional β-adrenergic response in the rat brain

Effects of 5-HT sub(1A) receptor antagonists on hippocampal 5-hydroxytryptamine levels: (S)-WAY100135, but not WAY100635, has partial agonist properties

(-)-Pindolol and ( plus or minus )-tertatolol affect rat hippocampal 5-HT levels through mechanisms involving not only 5-HT sub(1A), but also 5-HT sub(1B) receptors

(−)-Pindolol and (±)-Tertatolol Affect Rat Hippocampal 5-HT Levels Through Mechanisms Involving Not Only 5-HT 1A, But Also 5-HT 1B Receptors

5-HT sub(1A) receptor agonist properties of the antipsychotic, nemonapride: Comparison with bromerguride and clozapine

In vivo estimates of efficacy at 5-HT 1A receptors: effects of EEDQ on the ability of agonists to produce lower-lip retraction in rats

Preferential in vivo action of F15599, a novel 5‐HT 1A receptor agonist, at postsynaptic 5‐HT 1A receptors

Large-amplitude 5-HT sub(1A) receptor activation: a new mechanism of profound, central analgesia

Neuropharmacology of a new potential anxiolytic compound, F 2692, 1-(3'-trifluoromethyl phenyl) 1, 4-dihydro 3-amino 4-oxo 6-methyl pyridazine. II: Evaluation of its tolerance and dependence producing potential and of its effects on benzodiazepine withdrawal in the elevated plus-maze test in rats

Neuropharmacology of a new potential anxiolytic compound, F 2692, 1-(3'-trifluoromethyl phenyl) 1, 4-dihydro 3-amino 4-oxo 6-methyl pyridazine. I: Acute and in vitro effects

In vivo ( super(3)H)ketanserin binding: Effect of modifying synaptic serotonin levels

Comparison between a complete preconditioning programme and conventional conduct on behaviour, health and performance of young bulls from small cow-calf herds

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