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Characterization of recombinant human orexin receptor pharmacology in a Chinese hamster ovary cell‐line using FLIPR

British journal of pharmacology, 1999-09, Vol.128 (1), p.1-3

1999

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Molecular Cloning and Characterization of Two Novel Retinoic Acid-Inducible Orphan G-Protein-Coupled Receptors (GPRC5B and GPRC5C)

Genomics (San Diego, Calif.), 2000-07, Vol.67 (1), p.8-18

2000

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[3H]-SB-269970 radiolabels 5-HT7 receptors in rodent, pig and primate brain tissues

Neuropharmacology, 2002, Vol.42 (1), p.74-81

2002

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The behavioural effects of corticotropin-releasing factor-related peptides in rats

Psychopharmacologia, 1998-07, Vol.138 (2), p.124-132

1998

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Functional characterisation of the human cloned 5‐HT7 receptor (long form); antagonist profile of SB‐258719

British journal of pharmacology, 1998-07, Vol.124 (6), p.1300-1306

1998

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Cannabinoid activation of recombinant and endogenous vanilloid receptors

European journal of pharmacology, 2001-07, Vol.424 (3), p.211-219

2001

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(R)-3,N-Dimethyl-N-[1-methyl-3-(4-methylpiperidin-1-yl)propyl]benzenesulfonamide: The First Selective 5-HT7 Receptor Antagonist

Journal of medicinal chemistry, 1998-02, Vol.41 (5), p.655-657

1998

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Pharmacological characterization of extracellular acidification rate responses in human D 2(long) , D 3 and D 4.4 receptors expressed in Chinese hamster ovary cells

British journal of pharmacology, 2009-01, Vol.127 (5), p.1135-1144

2009

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SB‐224289–a novel selective (human) 5‐HT1B receptor antagonist with negative intrinsic activity

British journal of pharmacology, 1998-09, Vol.125 (1), p.202-208

1998

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Proposals for the classification and nomenclature of functional receptors for 5-hydroxytryptamine

Neuropharmacology, 1986-06, Vol.25 (6), p.563-576

1986

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Molecular Cloning of a Serotonin Receptor from Human Brain (5HT1E): A Fifth 5HT1-Like Subtype

Proceedings of the National Academy of Sciences - PNAS, 1992-06, Vol.89 (12), p.5517-5521

1992

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Characterization of SB‐269970‐A, a selective 5‐HT7 receptor antagonist

British journal of pharmacology, 2000-06, Vol.130 (3), p.539-548

2000

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SB-216641 and BRL-15572--compounds to pharmacologically discriminate h5-HT1B and h5-HT1D receptors

Naunyn-Schmiedeberg's archives of pharmacology, 1997-09, Vol.356 (3), p.312-320

1997

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Effects of selective h5-HT1B (SB-216641) and h5-HT1D (BRL-15572) receptor ligands on guinea-pig and human 5-HT auto- and heteroreceptors

Naunyn-Schmiedeberg's archives of pharmacology, 1997-09, Vol.356 (3), p.321-327

1997

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SB‐272183, a selective 5‐HT1A, 5‐HT1B and 5‐HT1D receptor antagonist in native tissue

British journal of pharmacology, 2001-07, Vol.133 (6), p.797-806

2001

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Spiropiperidines as high-affinity, selective .sigma. ligands

Journal of medicinal chemistry, 1992-05, Vol.35 (11), p.2033-2039

1992

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SB-236057, a selective 5-HT1B receptor inverse agonist, blocks the 5-HT human terminal autoreceptor

European journal of pharmacology, 1999-06, Vol.375 (1-3), p.359-365

1999

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Characterization of SB‐271046: A potent, selective and orally active 5‐HT6 receptor antagonist

British journal of pharmacology, 2000-08, Vol.130 (7), p.1606-1612

2000

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Characterization of [125I]‐SB‐258585 binding to human recombinant and native 5‐HT6 receptors in rat, pig and human brain tissue

British journal of pharmacology, 2000-08, Vol.130 (7), p.1597-1605

2000

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5-chloro-N-(4-methoxy-3-piperazin-1-yl-phenyl)-3-methyl-2-benzothiophenesulfonamide (SB-271046) : A potent, selective, and orally bioavailable 5-HT6 receptor antagonist

Journal of medicinal chemistry, 1999-01, Vol.42 (2), p.202-205

1999

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(-)Baclofen decreases neurotransmitter release in the mammalian CNS by an action at a novel GABA receptor

Nature (London), 1980-01, Vol.283 (5742), p.92-94

1980

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Pharmacological characterisation of human 5-HT2 receptor subtypes

European journal of pharmacology, 2001-02, Vol.414 (1), p.23-30

2001

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Graphics computer-aided receptor mapping as a predictive tool for drug design: development of potent, selective, and stereospecific ligands for the 5-HT1A receptor

Journal of medicinal chemistry, 1988-06, Vol.31 (6), p.1087-1093

1988

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The 5-HT hypothesis of depression revisited

Molecular psychiatry, 1996-12, Vol.1 (6), p.437

1996

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Influence of peptide CRF receptor antagonists upon the behavioural effects of human/rat CRF

European journal of pharmacology, 1999-06, Vol.373 (2), p.141-145

1999

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Characterization of recombinant human orexin receptor pharmacology in a Chinese hamster ovary cell‐line using FLIPR

Molecular Cloning and Characterization of Two Novel Retinoic Acid-Inducible Orphan G-Protein-Coupled Receptors (GPRC5B and GPRC5C)

[3H]-SB-269970 radiolabels 5-HT7 receptors in rodent, pig and primate brain tissues

The behavioural effects of corticotropin-releasing factor-related peptides in rats

Functional characterisation of the human cloned 5‐HT7 receptor (long form); antagonist profile of SB‐258719

Cannabinoid activation of recombinant and endogenous vanilloid receptors

(R)-3,N-Dimethyl-N-[1-methyl-3-(4-methylpiperidin-1-yl)propyl]benzenesulfonamide: The First Selective 5-HT7 Receptor Antagonist

Pharmacological characterization of extracellular acidification rate responses in human D 2(long) , D 3 and D 4.4 receptors expressed in Chinese hamster ovary cells

SB‐224289–a novel selective (human) 5‐HT1B receptor antagonist with negative intrinsic activity

Proposals for the classification and nomenclature of functional receptors for 5-hydroxytryptamine

Molecular Cloning of a Serotonin Receptor from Human Brain (5HT1E): A Fifth 5HT1-Like Subtype

Characterization of SB‐269970‐A, a selective 5‐HT7 receptor antagonist

SB-216641 and BRL-15572--compounds to pharmacologically discriminate h5-HT1B and h5-HT1D receptors

Effects of selective h5-HT1B (SB-216641) and h5-HT1D (BRL-15572) receptor ligands on guinea-pig and human 5-HT auto- and heteroreceptors

SB‐272183, a selective 5‐HT1A, 5‐HT1B and 5‐HT1D receptor antagonist in native tissue

Spiropiperidines as high-affinity, selective .sigma. ligands

SB-236057, a selective 5-HT1B receptor inverse agonist, blocks the 5-HT human terminal autoreceptor

Characterization of SB‐271046: A potent, selective and orally active 5‐HT6 receptor antagonist

Characterization of [125I]‐SB‐258585 binding to human recombinant and native 5‐HT6 receptors in rat, pig and human brain tissue

5-chloro-N-(4-methoxy-3-piperazin-1-yl-phenyl)-3-methyl-2-benzothiophenesulfonamide (SB-271046) : A potent, selective, and orally bioavailable 5-HT6 receptor antagonist

(-)Baclofen decreases neurotransmitter release in the mammalian CNS by an action at a novel GABA receptor

Pharmacological characterisation of human 5-HT2 receptor subtypes

Graphics computer-aided receptor mapping as a predictive tool for drug design: development of potent, selective, and stereospecific ligands for the 5-HT1A receptor

The 5-HT hypothesis of depression revisited

Influence of peptide CRF receptor antagonists upon the behavioural effects of human/rat CRF

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