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N 0861

Known as: 9H-Purin-6-amine, N-bicyclo(2.2.1)hept-2-yl-9-methyl-, endo-(+-)-, N-0861, N0861 
 
National Institutes of Health

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Highly Cited
2001
Highly Cited
2001
We investigated whether activation of A(1) or A(3) adenosine receptors (ARs) induces late preconditioning (PC) against infarction… Expand
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1998
1998
Receptor antagonists can be classified as neutral antagonists or antagonists with inverse agonist activity based on their… Expand
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1996
1996
BACKGROUND To determine the adenosine receptor subtype selectivity of the novel antagonist N-0861, the A1 and A2 receptor… Expand
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1996
1996
Previous studies in our laboratory identified N6-endonorbornyl-9-methyladenine (N-0861) as a highly selective (100-fold) A1… Expand
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1995
1995
The objective of this study was to characterize the adenosine receptor (AdoR) antagonistic properties of a newly synthesized… Expand
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1993
1993
OBJECTIVE The aim was to study the mechanism of global hypoxia induced atrioventricular (AV) nodal conduction block in vivo using… Expand
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1993
1993
In this study, the hypothesis that mammalian ventricular myocytes possess A2-adenosine receptors was tested. Electrophysiological… Expand
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1992
1992
Activation of cardiac A1 adenosine receptors slows atrioventricular conduction and attenuates the effects of catecholamines… Expand
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1992
1992
This study examines the cellular basis and specificity of the effects of adenosine on early afterdepolarizations (EADs), delayed… Expand
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1992
1992
Experiments were performed to determine the antagonistic actions of (+/-)N6-endonorbornan-2-yl-9-methyladenine (N-0861) at A1 and… Expand
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