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SR 47063

Known as: SR-47063, SR47063 
 
National Institutes of Health

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1 relation

Broader (1)

Chromans

Papers overview

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2011
2011
Recognition of sulfonylurea receptor (ABCC8/9) ligands by the multidrug resistance transporter P-glycoprotein (ABCB1): functional similarities based on common structural features between two…
ATP-sensitive K(+) (K(ATP)) channels are the target of a number of pharmacological agents, blockers like hypoglycemic… Expand
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2010
2010
Impact of disease-causing SUR1 mutations on the KATP channel subunit interface probed with a rhodamine protection assay.
The function of the ATP-sensitive potassium (K(ATP)) channel relies on the proper coupling between its two subunits: the pore… Expand
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2006
2006
Interaction of KATP Channels and Endothelin-1 in Lambs With Persistent Pulmonary Hypertension of the Newborn
Persistent pulmonary hypertension of the newborn is a life-threatening condition in which half of infants fail to respond to… Expand
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2005
2005
The size of a single residue of the sulfonylurea receptor dictates the effectiveness of K ATP channel openers.
K(ATP) channel openers are a diverse group of molecules able to activate ATP-sensitive K(+) channels in a tissue-dependent manner… Expand
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2000
2000
Vasorelaxant effects of the potassium channel opener SR 47063 on the isolated human saphenous vein and rat aorta.
The vasorelaxant effects of SR 47063 (4-(2-cyanimino-1, 2-dihydropyrid-1-yl)-2,2-dimethyl-6-nitr ochromene), a new K(+)-channel… Expand
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1994
1994
SR47063, A potent channel opener, activates KATP and a time-dependent current likely due to potassium accumulation
Abstract(i) We studied the effects of a new cromakalim analogue, SR47063, in guinea-pig ventricular cells. The experiments were… Expand
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