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Butaclamol Hydrochloride

Known as: Hydrochloride, Butaclamol 
National Institutes of Health

Papers overview

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Highly Cited
2004
Highly Cited
2004
  • J. Walters, R. Roth
  • Naunyn-Schmiedeberg's Archives of Pharmacology
  • 2004
  • 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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1999
1999
RAT dopamine D2short receptors expressed in CHO cells were characterized by activation of [35S]GTPgammaS binding. There were no… Expand
1995
1995
Quinelorane is a BCD partial ergoline with potent dopaminergic effects in vitro and in vivo. Partial ergoline compounds of this… Expand
1993
1993
We have previously identified [3H]quinpirole‐labeled dopamine receptors in the molecular layer of cerebellar lobule 10 which have… Expand
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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Highly Cited
1989
Highly Cited
1989
N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline (EEDQ) inactivates a variety of monoamine neurotransmitter receptors. In this… Expand
Highly Cited
1988
Highly Cited
1988
In primary culture of anterior pituitary cells, BAY-K-8644, a calcium channel agonist, stimulated PRL secretion by 83% with EC50… Expand
Highly Cited
1981
Highly Cited
1981
Tail vein injections of [3H]N-propylnorapomorphine ([3H]NPA) in male mice resulted in a dose-related accumulaton of radioactivity… Expand
1980
1980
Unanesthetized adult male rats with indwelling right atrial cannulae were used in the majority of experiments. Morphine (MOR, 3.0… Expand
1975
1975
: The syntheses and the structural and stereochemical requirements for antagonism of (+)-amphetamine-induced sterotypy are… Expand