SCH 23390

Known as: SCH-23390, SCH23390 
 
National Institutes of Health

Papers overview

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2007
2007
[11C]NNC 112 and [11C]SCH 23390 are selective positron emission tomography (PET) tracers for visualizing dopamine D1 receptors… (More)
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Highly Cited
2002
Highly Cited
2002
Hypertext poses new research challenges for text classification. Hyperlinks, HTML tags, category labels distributed over linked… (More)
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Review
2001
Review
2001
SCH 23390, the halobenzazepine (R)-(+)-7-chloro-8-hydroxy-3-methyl-1-phenyl-2,3,4,5- tetrahydro-1H-3-benzazepine, is a highly… (More)
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Highly Cited
1991
Highly Cited
1991
Previous work suggests that the dopamine agonist apomorphine decreases prepulse inhibition (PPI) of the acoustic startle response… (More)
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Highly Cited
1989
Highly Cited
1989
Pre-exposure of rats to systemic injections of D-amphetamine sulfate in the presence of bilateral injections of Sch-23390 (0.5 or… (More)
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1988
1988
Affinities and regional densities of the D1- and D2-dopamine receptor subtypes were studied in the human post-mortem brain in… (More)
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Highly Cited
1987
Highly Cited
1987
Tracer doses of 11C-SCH 23390 and 11C-raclopride, selective D1-dopamine and D2-dopamine receptor antagonists, respectively, were… (More)
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1985
1985
The ability of SCH 23390 as compared to haloperidol to produce catalepsy in rats was evaluated in three tests for catalepsy. SCH… (More)
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Highly Cited
1984
Highly Cited
1984
The selective D1 dopamine receptor agonist R-SK & F 38393 (20 mg/kg), but not its S-antipode, stereospecifically promoted… (More)
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Highly Cited
1983
Highly Cited
1983
SCH 23390 [R-(+)-8-chloro-2,3,4,5-tetrahydro-3-methyl-5-phenyl-1H-3-benzazepine-7-ol) possesses pharmacologic effects similar to… (More)
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