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Remimazolam: Non-Clinical and Clinical Profile of a New Sedative/Anesthetic Agent

Frontiers in pharmacology, 2021-07, Vol.12, p.690875

Kilpatrick, Gavin J.

2021

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Morphine-6-glucuronide: Actions and mechanisms

Medicinal research reviews, 2005-09, Vol.25 (5), p.521-544

2005

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A Placebo- and Midazolam-Controlled Phase I Single Ascending-Dose Study Evaluating the Safety, Pharmacokinetics, and Pharmacodynamics of Remimazolam (CNS 7056): Part II. Population Pharmacokinetic and Pharmacodynamic Modeling and Simulation

Anesthesia and analgesia, 2012-08, Vol.115 (2), p.284-296

2012

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Orphanin FQ Acts as an Anxiolytic to Attenuate Behavioral Responses to Stress

Proceedings of the National Academy of Sciences - PNAS, 1997-12, Vol.94 (26), p.14854-14858

1997

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CNS 7056: a novel ultra-short-acting Benzodiazepine

Anesthesiology (Philadelphia), 2007-07, Vol.107 (1), p.60-66

2007

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Molecular biology of the CRH receptors— in the mood

Peptides (New York, N.Y. : 1980), 2001-05, Vol.22 (5), p.753-760

2001

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Pharmacological characterization of the novel nonpeptide orphanin FQ/nociceptin receptor agonist Ro 64-6198: rapid and reversible desensitization of the ORL1 receptor in vitro and lack of tolerance in vivo

The Journal of pharmacology and experimental therapeutics, 2001-08, Vol.298 (2), p.812

2001

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Drug development in anaesthesia: industrial perspective

Current opinion in anaesthesiology, 2006-08, Vol.19 (4), p.385-389

2006

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Thioperamide, the selective histamine H3 receptor antagonist, attenuates stimulant-induced locomotor activity in the mouse

European journal of pharmacology, 1994-07, Vol.259 (2), p.107-114

1994

Volltextzugriff (PDF)

CNS 7056

Anesthesiology (Philadelphia), 2007-07, Vol.107 (1), p.60-66

2007

Volltextzugriff (PDF)

Binding of the 5-HT3, ligand, [3H]GR65630, to rat area postrema, vagus nerve and the brains of several species

European journal of pharmacology, 1989-01, Vol.159 (2), p.157-164

1989

Volltextzugriff (PDF)

Memantine. Merz

Current opinion in investigational drugs (London, England : 2000), 2002-05, Vol.3 (5), p.798

2002

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Urocortin: slower dissociation than corticotropin releasing factor from the CRF binding protein

European journal of pharmacology, 1999-07, Vol.376 (3), p.321-324

1999

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The distribution of specific binding of the 5-HT3 receptor ligand [3H]GR65630 in rat brain using quantitative autoradiography

Neuroscience letters, 1988-11, Vol.94 (1-2), p.156-160

1988

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Consensus meeting agrees distribution of 5-HT3 receptors in mammalian hindbrain

Trends in pharmacological sciences (Regular ed.), 1990-04, Vol.11 (4), p.135-137

1990

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Pharmacological characterisation of the recombinant human CRF binding protein using a simple assay

Journal of neuroscience methods, 1998-03, Vol.80 (1), p.99-105

1998

Volltextzugriff (PDF)

Inter-species variants of the 5-HT3 receptor

Biochemical Society transactions, 1992-02, Vol.20 (1), p.118

1992

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7TM receptors: the splicing on the cake

Trends in Pharmacological Sciences, 1999-07, Vol.20 (7), p.294-301

1999

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Characterization of 5-HT3 receptors in intact N1E-115 neuroblastoma cells

European journal of pharmacology, 1990-09, Vol.189 (2-3), p.223-227

1990

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The distribution of 5-HT3 recognition sites in the marmoset brain

European journal of pharmacology, 1992-04, Vol.215 (1), p.63-67

1992

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Do thermodynamic studies provide information on both the binding to and the activation of dopaminergic and other receptors?

Biochemical pharmacology, 1987-12, Vol.36 (23), p.4041-4046

1987

Volltextzugriff (PDF)

Thioperamide, the selective histamine H 3 receptor antagonist, attenuates stimulant-induced locomotor activity in the mouse

European journal of pharmacology, 1994-07, Vol.259 (2), p.107-114

1994

Volltextzugriff (PDF)

Human CRF2 α and β splice variants : Pharmacological characterization using radioligand binding and a luciferase gene expression assay

Neuropharmacology, 1999-03, Vol.38 (3), p.441-448

1999

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The ligand-selective domains of corticotropin-releasing factor type 1 and type 2 receptor reside in different extracellular domains : Generation of chimeric receptors with a novel ligand-selective profile

Journal of neurochemistry, 1999-08, Vol.73 (2), p.821-829

1999

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Interaction of neuroleptic drugs with rat striatal D-1 and D-2 dopamine receptors: a quantitative structure—affinity relationship study

European journal of medicinal chemistry, 1988-03, Vol.23 (2), p.173-182

1988

Volltextzugriff (PDF)

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Remimazolam: Non-Clinical and Clinical Profile of a New Sedative/Anesthetic Agent

Morphine-6-glucuronide: Actions and mechanisms

A Placebo- and Midazolam-Controlled Phase I Single Ascending-Dose Study Evaluating the Safety, Pharmacokinetics, and Pharmacodynamics of Remimazolam (CNS 7056): Part II. Population Pharmacokinetic and Pharmacodynamic Modeling and Simulation

Orphanin FQ Acts as an Anxiolytic to Attenuate Behavioral Responses to Stress

CNS 7056: a novel ultra-short-acting Benzodiazepine

Molecular biology of the CRH receptors— in the mood

Pharmacological characterization of the novel nonpeptide orphanin FQ/nociceptin receptor agonist Ro 64-6198: rapid and reversible desensitization of the ORL1 receptor in vitro and lack of tolerance in vivo

Drug development in anaesthesia: industrial perspective

Thioperamide, the selective histamine H3 receptor antagonist, attenuates stimulant-induced locomotor activity in the mouse

CNS 7056

Binding of the 5-HT3, ligand, [3H]GR65630, to rat area postrema, vagus nerve and the brains of several species

Memantine. Merz

Urocortin: slower dissociation than corticotropin releasing factor from the CRF binding protein

The distribution of specific binding of the 5-HT3 receptor ligand [3H]GR65630 in rat brain using quantitative autoradiography

Consensus meeting agrees distribution of 5-HT3 receptors in mammalian hindbrain

Pharmacological characterisation of the recombinant human CRF binding protein using a simple assay

Inter-species variants of the 5-HT3 receptor

7TM receptors: the splicing on the cake

Characterization of 5-HT3 receptors in intact N1E-115 neuroblastoma cells

The distribution of 5-HT3 recognition sites in the marmoset brain

Do thermodynamic studies provide information on both the binding to and the activation of dopaminergic and other receptors?

Thioperamide, the selective histamine H 3 receptor antagonist, attenuates stimulant-induced locomotor activity in the mouse

Human CRF2 α and β splice variants : Pharmacological characterization using radioligand binding and a luciferase gene expression assay

The ligand-selective domains of corticotropin-releasing factor type 1 and type 2 receptor reside in different extracellular domains : Generation of chimeric receptors with a novel ligand-selective profile

Interaction of neuroleptic drugs with rat striatal D-1 and D-2 dopamine receptors: a quantitative structure—affinity relationship study

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