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Labelling of “Peripheral‐Type” Benzodiazepine Binding Sites in the Rat Brain By Using [3H]PK 11195, an Isoquinoline Carboxamide Derivative: Kinetic Studies and Autoradiographic Localization

Journal of neurochemistry, 1983-12, Vol.41 (6), p.1744-1750

1983

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Pharmacological characterization of RP 62203, a novel 5‐hydroxytryptamine 5‐HT2 receptor antagonist

British journal of pharmacology, 1992-01, Vol.105 (1), p.27-36

1992

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Photoaffinity labeling of peripheral-type benzodiazepine-binding sites

Molecular pharmacology, 1987-01, Vol.31 (1), p.42-49

1987

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A diastereoselective synthesis of girolline

Tetrahedron letters, 1991-03, Vol.32 (11), p.1419-1422

1991

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2-Amino-6-trifluoromethoxy benzothiazole, a possible antagonist of excitatory amino acid neurotransmission—II: Biochemical properties

Neuropharmacology, 1985-11, Vol.24 (11), p.1085-1092

1985

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2-Amino-6-trifluoromethoxy benzothiazole, a possible antagonist of excitatory amino acid neurotransmission—I: Anticonvulsant properties

Neuropharmacology, 1985, Vol.24 (8), p.767-773

1985

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Opposite effects of two ligands for peripheral type benzodiazepine binding sites, PK 11195 and RO5-4864, in a conflict situation in the rat

Life sciences (1973), 1985-03, Vol.36 (11), p.1059-1068

1985

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Opposite effects of an agonist, RO5-4864, and an antagonist, PK 11195, of the peripheral type benzodiazepine binding sites on audiogenic seizures in DBA/2J mice

Life sciences (1973), 1984-06, Vol.34 (26), p.2613-2620

1984

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PK 11195, an antagonist of peripheral benzodiazepine receptors, reduces ventricular arrhythmias during myocardial ischemia and reperfusion in the dog

European journal of pharmacology, 1985-06, Vol.112 (2), p.257-260

1985

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Characterization of solubilized “peripheral type” benzodiazepine binding sites from rat adrenals by using [ 3H]PK 11195, an isoquinoline carboxamide derivative

Biochemical pharmacology, 1985-01, Vol.34 (2), p.167-170

1985

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Modulation of voltage-operated, but not receptor-operated, calcium channels in the rabbit aorta by PK 11195, an antagonist of peripheral-type benzodiazepine receptors

Journal of cardiovascular pharmacology, 1986-07, Vol.8 (4), p.729-734

1986

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1-[4-(2-ter-butyl-quinolyl)]-3-(4-piperidyl)propanol (PK 10139): a new potent and long-acting antiarrhythmic agent

The Journal of pharmacology and experimental therapeutics, 1983-04, Vol.225 (1), p.158

1983

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Electrophysiological and pharmacological characterization of peripheral benzodiazepine receptors in a guinea pig heart preparation

Life sciences (1973), 1984-08, Vol.35 (9), p.953-962

1984

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Histidine modification with diethylpyrocarbonate induces a decrease in the binding of an antagonist, PK 11195, but not of an agonist, RO5-4864, of the peripheral benzodiazepine receptors

Life sciences (1973), 1984-09, Vol.35 (12), p.1249-1256

1984

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Stereoselective inhibition of the binding of [ 3H]PK 11195 to peripheral-type benzodiazepine binding sites by a quinolinepropanamide derivative

European journal of pharmacology, 1986-09, Vol.128 (3), p.269-272

1986

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Binding sites for a peripheral type benzodiazepine antagonist ([ 3H] PK 11195) in human iris

Neuropharmacology, 1987-06, Vol.26 (6), p.549-552

1987

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Electrophysiological and pharmacological evidence that peripheral type benzodiazepine receptors are coupled to calcium channels in the heart

Life sciences (1973), 1985-01, Vol.36 (4), p.391-400

1985

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Biochemical evidence that 2-phenyl-4[2-(4-piperidinyl) ethyl]quinoline, a quinoline derivative with pure anticonflict properties, is a partial agonist of benzodiazepine receptors

Neuropharmacology, 1984-10, Vol.23 (10), p.1129-1136

1984

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Labelling of peripheral-type benzodiazepine binding sites in human brain with [ 3H]PK 11195: Anatomical and subcellular distribution

Brain research bulletin, 1987, Vol.18 (1), p.49-61

1987

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New indole derivatives as potent and selective serotonin uptake inhibitors

Journal of medicinal chemistry, 1993-04, Vol.36 (9), p.1194-1202

1993

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Partial Purification and Pharmacology of Peripheral-Type Benzodiazepine Receptors

Journal of receptor research, 1987, Vol.7 (1-4), p.55-70

1987

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The 5-hydroxytryptamine-releasing properties of two epimer quinoline derivatives

Neuropharmacology, 1984-02, Vol.23 (2), p.169-173

1984

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Caractérisation biochimique et étude par autoradiographie quantitative des sites de fixation de l'indalpine, un inhibiteur de la récapture de 5-HT, dans le cerveau de chat

Encéphale, 1985, Vol.11 (6), p.247-254

1985

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QUANTITATIVE AUTORADIOGRAPHIC DETERMINATION OF BINDING SITES FOR A PERIPHERAL BENZODIAZEPINE LIGAND ([3H]PK 11195) IN HUMAN IRIS

Fundamental & clinical pharmacology, 1987-01, Vol.1 (3), p.161-167

1987

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Labelling of “Peripheral‐Type” Benzodiazepine Binding Sites in the Rat Brain By Using [3H]PK 11195, an Isoquinoline Carboxamide Derivative: Kinetic Studies and Autoradiographic Localization

Riluzole Series. Synthesis and in Vivo “Antiglutamate” Activity of 6-Substituted-2-benzothiazolamines and 3-Substituted-2-imino-benzothiazolines

Pharmacological characterization of RP 62203, a novel 5‐hydroxytryptamine 5‐HT2 receptor antagonist

Photoaffinity labeling of peripheral-type benzodiazepine-binding sites

A diastereoselective synthesis of girolline

2-Amino-6-trifluoromethoxy benzothiazole, a possible antagonist of excitatory amino acid neurotransmission—II: Biochemical properties

2-Amino-6-trifluoromethoxy benzothiazole, a possible antagonist of excitatory amino acid neurotransmission—I: Anticonvulsant properties

Opposite effects of two ligands for peripheral type benzodiazepine binding sites, PK 11195 and RO5-4864, in a conflict situation in the rat

Opposite effects of an agonist, RO5-4864, and an antagonist, PK 11195, of the peripheral type benzodiazepine binding sites on audiogenic seizures in DBA/2J mice

PK 11195, an antagonist of peripheral benzodiazepine receptors, reduces ventricular arrhythmias during myocardial ischemia and reperfusion in the dog

Characterization of solubilized “peripheral type” benzodiazepine binding sites from rat adrenals by using [ 3H]PK 11195, an isoquinoline carboxamide derivative

Modulation of voltage-operated, but not receptor-operated, calcium channels in the rabbit aorta by PK 11195, an antagonist of peripheral-type benzodiazepine receptors

1-[4-(2-ter-butyl-quinolyl)]-3-(4-piperidyl)propanol (PK 10139): a new potent and long-acting antiarrhythmic agent

Electrophysiological and pharmacological characterization of peripheral benzodiazepine receptors in a guinea pig heart preparation

Histidine modification with diethylpyrocarbonate induces a decrease in the binding of an antagonist, PK 11195, but not of an agonist, RO5-4864, of the peripheral benzodiazepine receptors

Stereoselective inhibition of the binding of [ 3H]PK 11195 to peripheral-type benzodiazepine binding sites by a quinolinepropanamide derivative

Binding sites for a peripheral type benzodiazepine antagonist ([ 3H] PK 11195) in human iris

Electrophysiological and pharmacological evidence that peripheral type benzodiazepine receptors are coupled to calcium channels in the heart

Biochemical evidence that 2-phenyl-4[2-(4-piperidinyl) ethyl]quinoline, a quinoline derivative with pure anticonflict properties, is a partial agonist of benzodiazepine receptors

Labelling of peripheral-type benzodiazepine binding sites in human brain with [ 3H]PK 11195: Anatomical and subcellular distribution

New indole derivatives as potent and selective serotonin uptake inhibitors

Partial Purification and Pharmacology of Peripheral-Type Benzodiazepine Receptors

The 5-hydroxytryptamine-releasing properties of two epimer quinoline derivatives

Caractérisation biochimique et étude par autoradiographie quantitative des sites de fixation de l'indalpine, un inhibiteur de la récapture de 5-HT, dans le cerveau de chat

QUANTITATIVE AUTORADIOGRAPHIC DETERMINATION OF BINDING SITES FOR A PERIPHERAL BENZODIAZEPINE LIGAND ([3H]PK 11195) IN HUMAN IRIS

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