(-)-N6-Phenylisopropyl adenosine is a selective agonist for the A1 adenosine receptor. This compound effectively inhibits K+-induced Ca2+ uptake with an IC50 of 0.5 µM. It has been shown to protect against ischemia-induced ventricular arrhythmias and atrial fibrillation, while also exacerbating symptoms associated with ethanol withdrawal. Additionally, (-)-N6-phenylisopropyl adenosine exhibits notable analgesic properties, making it a valuable tool for research in cardiovascular and pain-related studies.
(-)-N6-Phenylisopropyl adenosine is a selective agonist for the A1 adenosine receptor. This compound effectively inhibits K+-induced Ca2+ uptake with an IC50 of 0.5 µM. It has been shown to protect against ischemia-induced ventricular arrhythmias and atrial fibrillation, while also exacerbating symptoms associated with ethanol withdrawal. Additionally, (-)-N6-phenylisopropyl adenosine exhibits notable analgesic properties, making it a valuable tool for research in cardiovascular and pain-related studies.
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