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SCH 50911

Known as: SCH-50911 
National Institutes of Health

Papers overview

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Highly Cited
2010
Highly Cited
2010
Acupuncture suppresses morphine self-administration through the GABA receptors
2010
2010
Effects of imipramine or GABA(B) receptor ligands on the immobility, swimming and climbing in the forced swim test in rats following discontinuation of cocaine self-administration.
Highly Cited
2007
Highly Cited
2007
Effects of GABA(B) receptor agents on cocaine priming, discrete contextual cue and food induced relapses.
Highly Cited
2007
Highly Cited
2007
Effects of GABA(B) receptor antagonist, agonists and allosteric positive modulator on the cocaine-induced self-administration and drug discrimination.
Highly Cited
2004
Highly Cited
2004
Acupuncture-mediated inhibition of ethanol-induced dopamine release in the rat nucleus accumbens through the GABAB receptor
2004
2004
Gabapentin activates presynaptic GABAB heteroreceptors in rat cortical slices.
Highly Cited
2001
Highly Cited
2001
Presynaptic mechanisms underlying cannabinoid inhibition of excitatory synaptic transmission in rat striatal neurons
1 The striatum is a crucial site of action for the motor effects of cannabinoids (CBs). However, the electrophysiological… 
1999
1999
Activation of nigral dopamine neurons by the selective GABAB-receptor antagonist SCH 50911
Summary. Previous studies have shown that systemic as well as local administration of the GABAB-receptor agonist baclofen is… 
Highly Cited
1995
Highly Cited
1995
The pharmacology of SCH 50911: a novel, orally-active GABA-beta receptor antagonist.
Experiments were conducted to characterize the pharmacology of SCH 50911 ((+)-5,5-dimethyl-2-morpholineacetic acid hydrochloride… 
Highly Cited
1995
Highly Cited
1995
Characterization of the antiabsence effects of SCH 50911, a GABA-B receptor antagonist, in the lethargic mouse, gamma-hydroxybutyrate, and pentylenetetrazole models.
Recent studies have shown that gamma-aminobutyric acidB (GABAB) receptor antagonists suppress absence seizures in animal models… 
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