U 37883A

Known as: U 37883, U-37883, U-37883A 
 
National Institutes of Health

Papers overview

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Review
2006
Review
2006
U-37883A (PNU-37883A, guanidine; 4-morpholinecarboximidine-N-1-adamantyl-N'-cyclohexyl hydrochloride) was originally developed as… (More)
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2005
2005
The effects of U-37883A, a vascular ATP-sensitive K(+) channel (K(ATP) channel) blocker, on membrane currents were investigated… (More)
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1999
1999
1 The aim of this study was to investigate the selectivity of the ATP-sensitive potassium (K(ATP)) channel inhibitor U-37883A (4… (More)
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1998
1998
An 85 pS K+ channel of rat caudate-putamen neurons, which is activated by dopamine D2 receptors and inhibited by sulfonylurea… (More)
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1998
1998
In this study we have investigated the interaction of the loop diuretics torasemide and furosemide and of the eukalemic diuretic… (More)
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1996
1996
The effects of the vascular selective nonsulfonylurea guanidine ATP-sensitive K+ (KATP+) channel-blocking agent U-37883A on… (More)
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1996
1996
The cardiovascular effects of the K-ATP channel blocker U-37883A and 5 related morpholinoguanidines were determined in 6… (More)
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1995
1995
The activity of potassium uniport in rat liver mitochondria was measured using light scattering technique (mitochondrial swelling… (More)
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1995
1995
U-37883A is a K+ sparing diuretic which selectively blocks openers of vascular ATP-sensitive K channels. Many N'-disubstituted… (More)
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1993
1993
This study describes the in vitro and in vivo characteristics of a guanidine 4-morpholinecarboximidine-N-1-adamantyl-N… (More)
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