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Butaclamol Hydrochloride

Known as: Hydrochloride, Butaclamol 
 
National Institutes of Health

Papers overview

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2007
2007
Drugs targeting dopamine receptors have been the focus of much research over the past 30 years, in large part because of their… Expand
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1999
1999
RAT dopamine D2short receptors expressed in CHO cells were characterized by activation of [35S]GTPgammaS binding. There were no… Expand
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1998
1998
[11C]A-84543, 3-[(1-[11C]methyl-2(S)-pyrrolidinyl)methoxy]pyridine, is a specific and enantioselective neuronal nicotinic… Expand
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1995
1995
Quinelorane is a BCD partial ergoline with potent dopaminergic effects in vitro and in vivo. Partial ergoline compounds of this… Expand
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1993
1993
We have previously identified [3H]quinpirole-labeled dopamine receptors in the molecular layer of cerebellar lobule 10 which have… Expand
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Highly Cited
1989
Highly Cited
1989
3-(2'-[18F]fluoroethyl)spiperone (FESP), a recently developed dopamine D2-receptor binding radiopharmaceutical, was used for… Expand
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1989
1989
N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline (EEDQ) inactivates a variety of monoamine neurotransmitter receptors. In this… Expand
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1988
1988
In primary culture of anterior pituitary cells, BAY-K-8644, a calcium channel agonist, stimulated PRL secretion by 83% with EC50… Expand
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1981
1981
Tail vein injections of [3H]N-propylnorapomorphine ([3H]NPA) in male mice resulted in a dose-related accumulaton of radioactivity… Expand
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Highly Cited
1976
Highly Cited
1976
  • J. Walters, R. Roth
  • Naunyn-Schmiedeberg's Archives of Pharmacology
  • 1976
  • Corpus ID: 22266663
SummaryAn in vivo system has been used to investigate the ability of dopamine agonists and antagonists to alter dopamine… Expand
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