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A 68930

Known as: A-68930, A68930 
 
National Institutes of Health

Papers overview

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2012
2012
RationaleAdult rats emit ultrasonic calls at around 22 and 50 kHz, which are often elicited by aversive and rewarding stimuli… Expand
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Highly Cited
2005
Highly Cited
2005
Structurally dissimilar dopamine D1 receptor agonists were compared with dopamine in their ability to activate adenylate cyclase… Expand
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Highly Cited
2004
Highly Cited
2004
N-methyl-D-aspartate (NMDA) receptor antagonists have antiakinetic and antidyskinetic effects in animals models of Parkinson's… Expand
Highly Cited
1998
Highly Cited
1998
The role of drug efficacy in agonist-induced desensitization was studied in C-6 glioma cells transfected with the monkey dopamine… Expand
Highly Cited
1995
Highly Cited
1995
The intrinsic activities of selected dopamine D1 receptor agonists were compared in three distinct molecular expression systems… Expand
Highly Cited
1994
Highly Cited
1994
We compared the effect of two selective dopamine D1 receptor agonists, SKF 38393 ((+/-)-1-phenyl-2,3,4,5-tetrahydro-(1H)-3… Expand
Highly Cited
1993
Highly Cited
1993
The effects of the dopamine D1 receptor full agonist, A68930, on sleep-wake patterns and grooming behaviour were studied in the… Expand
Highly Cited
1993
Highly Cited
1993
Adenylyl cyclase activity was stimulated by dopamine to approximately 200% over basal activity in both squirrel monkey caudate… Expand
1992
1992
Administration of the selective D1-dopamine receptor agonist 2,3,4,5-tetrahydro-7,8-dihydroxy-1-phenyl-1H-3-benzazepine (SKF… Expand
Highly Cited
1991
Highly Cited
1991
A68930, (1R,3S)-1-aminomethyl-5,6-dihydroxy-3-phenylisochroman HCl, is a potent (EC50 = 2.5 nM), partial (intrinsic activity = 66… Expand