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Neurogenic Dural Protein Extravasation Induced by Meta-Chlorophenylpiperazine (Mcpp) Involves Nitric Oxide and 5-HT2B Receptor Activation

Cephalalgia, 2003-03, Vol.23 (2), p.117-123

2003

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Comparisons of hallucinogenic phenylisopropylamine binding affinities at cloned human 5-HT2A, 5-HT2B and 5-HT2C receptors

Naunyn-Schmiedeberg's archives of pharmacology, 1999-01, Vol.359 (1), p.1-6

1999

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Potent, Selective Tetrahydro-β-carboline Antagonists of the Serotonin 2B (5HT2B) Contractile Receptor in the Rat Stomach Fundus

Journal of medicinal chemistry, 1996-07, Vol.39 (14), p.2773-2780

1996

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Thieno[3,2-b]- and Thieno[2,3-b]pyrrole Bioisosteric Analogues of the Hallucinogen and Serotonin Agonist N,N-Dimethyltryptamine

Journal of medicinal chemistry, 1999-03, Vol.42 (6), p.1106-1111

1999

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A Novel (Benzodifuranyl)aminoalkane with Extremely Potent Activity at the 5-HT2A Receptor

Journal of medicinal chemistry, 1998-12, Vol.41 (26), p.5148-5149

1998

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Pharmacological characteristics of the newly cloned rat 5-hydroxytryptamine2F receptor

Molecular pharmacology, 1993-03, Vol.43 (3), p.419-426

1993

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Synthesis and Serotonin Receptor Affinities of a Series of trans-2-(Indol-3-yl)cyclopropylamine Derivatives

Journal of medicinal chemistry, 1998-12, Vol.41 (25), p.4995-5001

1998

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Species differences in the pharmacology of the 5-hydroxytryptamine2 receptor: structurally specific differentiation by ergolines and tryptamines

The Journal of pharmacology and experimental therapeutics, 1993-06, Vol.265 (3), p.1272

1993

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CCK-8, CCK-4 and gastrin-induced contractions in guinea pig ileum: evidence for differential release of acetylcholine and substance P by CCK-A and CCK-B receptors

The Journal of pharmacology and experimental therapeutics, 1991-02, Vol.256 (2), p.695

1991

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Pharmacologic characterization of the human 5-hydroxytryptamine2B receptor: evidence for species differences

The Journal of pharmacology and experimental therapeutics, 1996-02, Vol.276 (2), p.720

1996

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Protein kinase C translocation in rat stomach fundus: effects of serotonin, carbamylcholine and phorbol dibutyrate

The Journal of pharmacology and experimental therapeutics, 1991-01, Vol.256 (1), p.103

1991

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LY367265, an inhibitor of the 5-hydroxytryptamine transporter and 5-hydroxytryptamine(2A) receptor antagonist: a comparison with the antidepressant, nefazodone

European journal of pharmacology, 2000-10, Vol.407 (1-2), p.39-46

2000

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Receptor subtype and density determine the coupling repertoire of the 5-HT2 receptor subfamily

Life sciences (1973), 1996-08, Vol.59 (13), p.1081-1095

1996

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Mutations of transmembrane IV and V serines indicate that all tryptamines do not bind to the rat 5-HT2A receptor in the same manner

Brain research. Molecular brain research., 1997-10, Vol.49 (1-2), p.1-6

1997

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Autoradiographic localization of insulin-like growth factor II receptors in cerebellar cortex of weaver and Purkinje cell degeneration mutant mice

Brain research, 1988-08, Vol.458 (2), p.361-366

1988

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Antagonism by olanzapine of dopamine D1, serotonin2, muscarinic, histamine H1 and α1-adrenergic receptors in vitro

Schizophrenia research, 1999-05, Vol.37 (1), p.107-122

1999

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A novel class of 5-HT2A receptor antagonists: aryl aminoguanidines

Life sciences (1973), 1996-09, Vol.59 (15), p.1259-1268

1996

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[3H]LY334370, a novel radioligand for the 5-HT1F receptor. II. Autoradiographic localization in rat, guinea pig, monkey and human brain

Naunyn-Schmiedeberg's archives of pharmacology, 2005-03, Vol.371 (3), p.178-184

2005

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m-CPP hypolocomotion is selectively antagonized by compounds with high affinity for 5-HT2C receptors but not 5-HT2A or 5-HT2B receptors

Behavioural pharmacology, 2001-12, Vol.12 (8), p.613-620

2001

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[3H]LY334370, a novel radioligand for the 5-HT1F receptor. I. In vitro characterization of binding properties

Naunyn-Schmiedeberg's archives of pharmacology, 2005-03, Vol.371 (3), p.169-177

2005

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Pharmacological characterization of enantiomers of 8-thiomethyl-2-(di-n-propylamino)tetralin, potent and selective 5-HT1A receptor agonists

Drug development research, 1995-01, Vol.34 (1), p.66-85

1995

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m-CPP hypolocomotion is selectively antagonized by compounds with high affinity for 5-HT(2C) receptors but not 5-HT(2A) or 5-HT(2B) receptors

Behavioural pharmacology, 2001-12, Vol.12 (8), p.613-620

2001

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In vitro activity of LY393558, an inhibitor of the 5-hydroxytryptamine transporter with 5-HT(1B/1D/2) receptor antagonist properties

European journal of pharmacology, 2001-11, Vol.432 (1), p.9

2001

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In vitro activity of LY393558, an inhibitor of the 5-hydroxytryptamine transporter with 5-HT1B/1D/2 receptor antagonist properties

European journal of pharmacology, 2001-11, Vol.432 (1), p.9-17

2001

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Comparisons of hallucinogenic phenylisopropylamine binding affinities at cloned human 5-HT2A, -HT(2B) and 5-HT2C receptors

Naunyn-Schmiedeberg's archives of pharmacology, 1999-01, Vol.359 (1), p.1-6

1999

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Neurogenic Dural Protein Extravasation Induced by Meta-Chlorophenylpiperazine (Mcpp) Involves Nitric Oxide and 5-HT2B Receptor Activation

Comparisons of hallucinogenic phenylisopropylamine binding affinities at cloned human 5-HT2A, 5-HT2B and 5-HT2C receptors

Potent, Selective Tetrahydro-β-carboline Antagonists of the Serotonin 2B (5HT2B) Contractile Receptor in the Rat Stomach Fundus

Thieno[3,2-b]- and Thieno[2,3-b]pyrrole Bioisosteric Analogues of the Hallucinogen and Serotonin Agonist N,N-Dimethyltryptamine

A Novel (Benzodifuranyl)aminoalkane with Extremely Potent Activity at the 5-HT2A Receptor

Pharmacological characteristics of the newly cloned rat 5-hydroxytryptamine2F receptor

Synthesis and Serotonin Receptor Affinities of a Series of trans-2-(Indol-3-yl)cyclopropylamine Derivatives

Species differences in the pharmacology of the 5-hydroxytryptamine2 receptor: structurally specific differentiation by ergolines and tryptamines

CCK-8, CCK-4 and gastrin-induced contractions in guinea pig ileum: evidence for differential release of acetylcholine and substance P by CCK-A and CCK-B receptors

Pharmacologic characterization of the human 5-hydroxytryptamine2B receptor: evidence for species differences

Protein kinase C translocation in rat stomach fundus: effects of serotonin, carbamylcholine and phorbol dibutyrate

LY367265, an inhibitor of the 5-hydroxytryptamine transporter and 5-hydroxytryptamine(2A) receptor antagonist: a comparison with the antidepressant, nefazodone

Receptor subtype and density determine the coupling repertoire of the 5-HT2 receptor subfamily

Mutations of transmembrane IV and V serines indicate that all tryptamines do not bind to the rat 5-HT2A receptor in the same manner

Autoradiographic localization of insulin-like growth factor II receptors in cerebellar cortex of weaver and Purkinje cell degeneration mutant mice

Antagonism by olanzapine of dopamine D1, serotonin2, muscarinic, histamine H1 and α1-adrenergic receptors in vitro

A novel class of 5-HT2A receptor antagonists: aryl aminoguanidines

[3H]LY334370, a novel radioligand for the 5-HT1F receptor. II. Autoradiographic localization in rat, guinea pig, monkey and human brain

m-CPP hypolocomotion is selectively antagonized by compounds with high affinity for 5-HT2C receptors but not 5-HT2A or 5-HT2B receptors

[3H]LY334370, a novel radioligand for the 5-HT1F receptor. I. In vitro characterization of binding properties

Pharmacological characterization of enantiomers of 8-thiomethyl-2-(di-n-propylamino)tetralin, potent and selective 5-HT1A receptor agonists

m-CPP hypolocomotion is selectively antagonized by compounds with high affinity for 5-HT(2C) receptors but not 5-HT(2A) or 5-HT(2B) receptors

In vitro activity of LY393558, an inhibitor of the 5-hydroxytryptamine transporter with 5-HT(1B/1D/2) receptor antagonist properties

In vitro activity of LY393558, an inhibitor of the 5-hydroxytryptamine transporter with 5-HT1B/1D/2 receptor antagonist properties

Comparisons of hallucinogenic phenylisopropylamine binding affinities at cloned human 5-HT2A, -HT(2B) and 5-HT2C receptors

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