pilsicainide

Known as: tetrahydro-1H-pyrrolizine-7a(5H)-aceto-2',6'-xylidide 
 
National Institutes of Health

Papers overview

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2010
2010
Peripheral branches of the trigeminal nerve may be damaged during maxillofacial injury or surgical procedures and trigeminal… (More)
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Highly Cited
2006
Highly Cited
2006
INTRODUCTION Autonomic modulation, particularly high vagal tone, plays an important role in the occurrence of ventricular… (More)
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Review
2006
Review
2006
Pilsicainide is a class IC antiarrhythmic drug, which has a pure sodium channel blocking action with slow recovery… (More)
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2005
2005
The new triterpene Delta1-lupenone (1), together with lupeol, beta-amyrin and betulin were isolated from the wood of Byrsonima… (More)
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2004
2004
Agonist-induced internalization of G protein-coupled receptors (GPCRs) is a well characterized phenomenon believed to contribute… (More)
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2003
2003
PURPOSE Pilsicainide, classified as a relatively pure Na+ channel blocker, occasionally causes QT prolongation, suggesting… (More)
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2001
2001
As a first step in structure-based design of highly selective and potent Cdk4 inhibitors, we performed structure-based generation… (More)
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1998
1998
The present study investigates the possibility that imidazoline receptors mediate modulation of cholinergic motor functions of… (More)
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1998
1998
The effects of pilsicainide on vagally induced atrial fibrillation and on electrophysiological parameters were compared with… (More)
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1996
1996
The present work reports the synthesis and preliminary pharmacological characterization of 8,9-dihydroxy-2,3,7,11b-tetrahydro-1H… (More)
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