D2 receptor genes--the cause or consequence of substance abuse?

SCH 39166, a potential antipsychotic drug, does not evoke movement disorders in cebus monkeys.

Neurochemistry international·1992

Effect of SCH 39166, a novel dopamine D1 receptor antagonist, on [3H]acetylcholine release in rat striatal slices.

European journal of pharmacology·1992

Selective up-regulation of D-1 dopamine receptors following chronic administration of SCH 39166 in primates.

Pharmacology, biochemistry, and behavior·1992

[3H]SCH 39166, a new D1-selective radioligand: in vitro and in vivo binding analyses.

Journal of neurochemistry·1991

In vivo binding of SCH 39166: a D-1 selective antagonist.

The Journal of pharmacology and experimental therapeutics·1991

Effects of [N-(L-(1-carboxy-2-phenyl)ethyl]-L-phenylalanyl-beta-alanine (SCH32615), a neutral endopeptidase (enkephalinase) inhibitor, on levels of enkephalin, encrypted enkephalins and substance P in cerebrospinal fluid and plasma of primates.

The Journal of pharmacology and experimental therapeutics·1991

Beyond Bayesian integration: how meaning shapes placebo effects.

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Chemical communications (Cambridge, England)·2026

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D2 receptor genes--the cause or consequence of substance abuse?

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SCH 39166, a potential antipsychotic drug, does not evoke movement disorders in cebus monkeys.

Effect of SCH 39166, a novel dopamine D1 receptor antagonist, on [3H]acetylcholine release in rat striatal slices.

Selective up-regulation of D-1 dopamine receptors following chronic administration of SCH 39166 in primates.

[3H]SCH 39166, a new D1-selective radioligand: in vitro and in vivo binding analyses.

In vivo binding of SCH 39166: a D-1 selective antagonist.

Effects of [N-(L-(1-carboxy-2-phenyl)ethyl]-L-phenylalanyl-beta-alanine (SCH32615), a neutral endopeptidase (enkephalinase) inhibitor, on levels of enkephalin, encrypted enkephalins and substance P in cerebrospinal fluid and plasma of primates.

Beyond Bayesian integration: how meaning shapes placebo effects.

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Fronto-striatal molecular convergence in eating and obsessive-compulsive disorders.

Electron-withdrawing group effects on the structural, electronic, reactivity, and binding characteristics of triazolopyrimidine herbicides: a comparative study of diclosulam, cloransulam-methyl, and cloransulam.

Multiple binding modes underlie Cannabis sativa cannabinoids recognition by peroxisome proliferator-activated receptor gamma.

Sulfonamide-Based 2-Amino-1,3,4-Oxadiazole Derivatives as Dual Cholinesterase and Carbonic Anhydrase Inhibitors: Design, Synthesis, Kinetic Characterization, Molecular Modeling, and ADMET Evaluation.

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