KATP channel openers of the benzopyran type reach their binding site via the cytosol.

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Some cannabinoid receptor ligands and their distomers are direct-acting openers of SUR1 K(ATP) channels.

P2860

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KATP channel openers of the benzopyran type reach their binding site via the cytosol.

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2006 nî lūn-bûn

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KATP channel openers of the benzopyran type reach their binding site via the cytosol.

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KATP channel openers of the benzopyran type reach their binding site via the cytosol.

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KATP channel openers of the benzopyran type reach their binding site via the cytosol.

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P1476

KATP channel openers of the benzopyran type reach their binding site via the cytosol.

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D Stephan

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E Salamon

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H Lemoine

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H Weber

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U Quast

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U Russ

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Protein measurement with the Folin phenol reagent

Relationship between the inhibition constant (K1) and the concentration of inhibitor which causes 50 per cent inhibition (I50) of an enzymatic reaction

Physiological and pathophysiological roles of ATP-sensitive K+ channels

Membrane topology distinguishes a subfamily of the ATP-binding cassette (ABC) transporters

KATP channel openers: structure-activity relationships and therapeutic potential.

Identification of the potassium channel opener site on sulfonylurea receptors.

Potassium channel openers require ATP to bind to and act through sulfonylurea receptors

Recent developments in the biology and medicinal chemistry of potassium channel modulators: update from a decade of progress.

Local anesthetics: hydrophilic and hydrophobic pathways for the drug-receptor reaction.

The molecular basis of the specificity of action of K(ATP) channel openers.

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199-205

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scholarly article

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10.1038/SJ.BJP.0706858

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English

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149

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2006-08-14T00:00:00Z

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6867588

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16921394

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2013803

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KATP channel openers of the benzopyran type reach their binding site via the cytosol.

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P2860

P2860

KATP channel openers of the benzopyran type reach their binding site via the cytosol.

description

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P1476

P2093

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