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Pharmacological specificity of novel, synthetic, cyclic peptides as antagonists at tachykinin receptors

British journal of pharmacology, 1991-10, Vol.104 (2), p.355-360

1991

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Identification of nociceptin in human cerebrospinal fluid: comparison of levels in pain and non-pain states

Pain (Amsterdam), 1998-10, Vol.78 (1), p.71-73

1998

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Evidence that cholecystokinin induces immediate early gene expression in the brainstem, hypothalamus and amygdala of the rat by a CCKA receptor mechanism

Neuropharmacology, 1994-06, Vol.33 (6), p.719-727

1994

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PD 176252 — The first high affinity non-peptide gastrin-releasing peptide (BB 2) receptor antagonist

Bioorganic & medicinal chemistry letters, 1998-09, Vol.8 (18), p.2589-2594

1998

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Nociceptin hyperpolarises neurones in the rat ventromedial hypothalamus

Neuroscience letters, 1997-12, Vol.239 (1), p.37-40

1997

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High performance liquid chromatography in neuroscience research (methods in the neurosciences, vol. 15): edited by R. B. Holman, A. J. Cross and M. H. Joseph, Wiley, 1993. £49.95 (xvii + 369 pages) ISBN 0 471 93813 0

Trends in neurosciences (Regular ed.), 1994, Vol.17 (1), p.44-45

1994

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High performance liquid chromatography in neuroscience research (methods in the neurosciences, vol. 15)

Trends in neurosciences (Regular ed.), 1994-01, Vol.17 (1), p.44-45

1994

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Pharmacological specificity of synthetic peptides as antagonists at tachykinin receptors

Regulatory peptides, 1988-07, Vol.22 (1), p.127-127

1988

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In vitro characterization of Ac-RYYRWK-NH2, Ac-RYYRIK-NH2 and [Phe1CΨ(CH2-NH)Gly2] nociceptin(1-13)NH2 at rat native and recombinant ORL1 receptors

Neuropeptides (Edinburgh), 2001-10, Vol.35 (5-6), p.244-256

2001

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Prolonged Changes in Neurochemistry of Dopamine Neurones After Chronic Ethanol Consumption

Pharmacology, biochemistry and behavior, 2000-05, Vol.66 (1), p.153-161

2000

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The interaction of the NK1 receptor antagonist CP‐96,345 with L‐type calcium channels and its functional consequences

British journal of pharmacology, 1993-09, Vol.110 (1), p.385-391

1993

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Rat central ORL-1 receptor uncouples from adenylyl cyclase during membrane preparation

Neuroscience letters, 1998-04, Vol.246 (1), p.49-52

1998

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PD 165929 — the first high affinity non-peptide neuromedin-B (NMB) receptor selective antagonist

Bioorganic & medicinal chemistry letters, 1996-11, Vol.6 (21), p.2617-2622

1996

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transN-Methyl- N-[2-(1-pyrrolidinyl)cyclohexyl] cycloprop-2-ene-1-carboxamides: Novel lipophilic kappa opioid agonists

Bioorganic & medicinal chemistry letters, 1997, Vol.7 (3), p.291-296

1997

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Trans N-methyl-N-[2-(1-pyrrolidinyl)cyclohexyl]cycloprop-2-ene-1-carboxamides : Novel lipophilic kappa opioid agonists

Bioorganic & medicinal chemistry letters, 1997-02, Vol.7 (3), p.291-296

1997

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Selectivities of opioid peptide analogues as agonists and antagonists at the δ‐receptor

British journal of pharmacology, 1984-09, Vol.83 (1), p.271-279

1984

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The rational development of small molecule tachykinin NK3 receptor selective antagonists - the utilisation of a dipeptide chemical library in drug design

Bioorganic & medicinal chemistry letters, 1994-07, Vol.4 (14), p.1679-1684

1994

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Evidence that cholecystokinin induces immediate early gene expression in the brainstem, hypothalamus and amygdala of the rat by a CCK A receptor mechanism

Neuropharmacology, 1994, Vol.33 (6), p.719-727

1994

Volltextzugriff (PDF)

The interaction of the NK 1 receptor antagonist CP‐96,345 with L‐type calcium channels and its functional consequences

British journal of pharmacology, 1993-09, Vol.110 (1), p.385-391

1993

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L‐689,660, a novel cholinomimetic with functional selectivity for M1 and M3 muscarinic receptors

British journal of pharmacology, 1992-10, Vol.107 (2), p.494-501

1992

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A novel series of non‐quaternary oxadiazoles acting as full agonists at muscarinic receptors

British journal of pharmacology, 1990-11, Vol.101 (3), p.575-580

1990

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The effect of CCK B /gastrin antagonists on stimulated gastric acid secretion in the anaesthetized rat

British journal of pharmacology, 1991-12, Vol.104 (4), p.973-977

1991

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L‐689,660, a novel cholinomimetic with functional selectivity for M 1 and M 3 muscarinic receptors

British journal of pharmacology, 1992-10, Vol.107 (2), p.494-501

1992

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The opioid receptors in the hamster vas deferens are of the δ-type

Neuropharmacology, 1985-11, Vol.24 (11), p.1011-1017

1985

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The rational development of small molecule tachykinin NK 3 receptor selective antagonists - the utilisation of a dipeptide chemical library in drug design

Bioorganic & medicinal chemistry letters, 1994, Vol.4 (14), p.1679-1684

1994

Volltextzugriff (PDF)

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Pharmacological specificity of novel, synthetic, cyclic peptides as antagonists at tachykinin receptors

Identification of nociceptin in human cerebrospinal fluid: comparison of levels in pain and non-pain states

Evidence that cholecystokinin induces immediate early gene expression in the brainstem, hypothalamus and amygdala of the rat by a CCKA receptor mechanism

PD 176252 — The first high affinity non-peptide gastrin-releasing peptide (BB 2) receptor antagonist

Nociceptin hyperpolarises neurones in the rat ventromedial hypothalamus

High performance liquid chromatography in neuroscience research (methods in the neurosciences, vol. 15): edited by R. B. Holman, A. J. Cross and M. H. Joseph, Wiley, 1993. £49.95 (xvii + 369 pages) ISBN 0 471 93813 0

High performance liquid chromatography in neuroscience research (methods in the neurosciences, vol. 15)

Pharmacological specificity of synthetic peptides as antagonists at tachykinin receptors

In vitro characterization of Ac-RYYRWK-NH2, Ac-RYYRIK-NH2 and [Phe1CΨ(CH2-NH)Gly2] nociceptin(1-13)NH2 at rat native and recombinant ORL1 receptors

Prolonged Changes in Neurochemistry of Dopamine Neurones After Chronic Ethanol Consumption

The interaction of the NK1 receptor antagonist CP‐96,345 with L‐type calcium channels and its functional consequences

Rat central ORL-1 receptor uncouples from adenylyl cyclase during membrane preparation

PD 165929 — the first high affinity non-peptide neuromedin-B (NMB) receptor selective antagonist

transN-Methyl- N-[2-(1-pyrrolidinyl)cyclohexyl] cycloprop-2-ene-1-carboxamides: Novel lipophilic kappa opioid agonists

Trans N-methyl-N-[2-(1-pyrrolidinyl)cyclohexyl]cycloprop-2-ene-1-carboxamides : Novel lipophilic kappa opioid agonists

Selectivities of opioid peptide analogues as agonists and antagonists at the δ‐receptor

The rational development of small molecule tachykinin NK3 receptor selective antagonists - the utilisation of a dipeptide chemical library in drug design

Evidence that cholecystokinin induces immediate early gene expression in the brainstem, hypothalamus and amygdala of the rat by a CCK A receptor mechanism

The interaction of the NK 1 receptor antagonist CP‐96,345 with L‐type calcium channels and its functional consequences

L‐689,660, a novel cholinomimetic with functional selectivity for M1 and M3 muscarinic receptors

A novel series of non‐quaternary oxadiazoles acting as full agonists at muscarinic receptors

The effect of CCK B /gastrin antagonists on stimulated gastric acid secretion in the anaesthetized rat

L‐689,660, a novel cholinomimetic with functional selectivity for M 1 and M 3 muscarinic receptors

The opioid receptors in the hamster vas deferens are of the δ-type

The rational development of small molecule tachykinin NK 3 receptor selective antagonists - the utilisation of a dipeptide chemical library in drug design

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