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Zeneca ZD 6169

Known as: ZD6169, ZD 6169, Zeneca ZD6169 
 
National Institutes of Health

Papers overview

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2014
2014
Pharmacologically, vasoactive agents targeting endothelial and/or smooth muscle cells (SMC) are known to cause acute drug-induced… Expand
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2003
2003
Although ATP-sensitive K+ channels continue to be explored for their therapeutic potential, developments in high-affinity… Expand
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2003
2003
OBJECTIVE To compare in vivo the potency and bladder-vascular selectivity of ATP-sensitive potassium channel openers (KCOs… Expand
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Highly Cited
2002
Highly Cited
2002
PURPOSE Adenosine triphosphate (ATP) (Sigma Chemical Co., St. Louis, Missouri) is known to contract animal as well as human… Expand
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2002
2002
ATP-sensitive potassium (K(ATP)) channel openers (KCOs) have been shown to inhibit spontaneous myogenic contractile activity of… Expand
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2001
2001
Activation of ATP-sensitive potassium (K(ATP)) channels can regulate smooth muscle function through membrane potential… Expand
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Highly Cited
2000
Highly Cited
2000
PURPOSE To investigate whether intravesical oxyhemoglobin, a nitric oxide scavenger, changes bladder activity in normal rats… Expand
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1999
1999
The effects of the ATP-dependent potassium channel agonists ZD6169, celikalim, and WAY-133537 on bladder contractile function… Expand
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1997
1997
ZD6169, the S-enantiomer of the racemic N-(4-benzoylphenyl)-3,3,3-trifluoro-2-hydroxy-2-methylpropionamide , was reported to… Expand
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1995
1995
(S)-N-(4-benzoylphenyl)-3,3,3-trifluoro-2-hydroxy-2-methyl-propionamide (ZD6169) is a novel ATP-sensitive potassium channel… Expand
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