Gastrointestinal prokinetic drugs have different affinity for the human cardiac human ether-à-gogo K+ channel

Journal of Pharmacology and Experimental Therapeutics

Volumn 299, Issue 3, 2001, Pages 1007-1012

  Potet, Franck ^a   Bouyssou, Thierry ^b   Escande, Denis ^a   Baró, Isabelle ^a  

^a HÔTEL DIEU   (France)

^b CHIESI SA   (France)

Author keywords

[No Author keywords available]

Indexed keywords

CISAPRIDE; MOSAPRIDE CITRATE; POTASSIUM CHANNEL; PROKINETIC AGENT; PRUCALOPRIDE; RENZAPRIDE; SEROTONIN 4 AGONIST;

ANIMAL CELL; ARTICLE; BINDING AFFINITY; CELL STRAIN COS1; CONCENTRATION RESPONSE; CONTROLLED STUDY; DEPOLARIZATION; DRUG BINDING; DRUG POTENCY; ELECTROPHYSIOLOGY; GASTROINTESTINAL TRACT; HEART ARRHYTHMIA; HEART MUSCLE POTENTIAL; NONHUMAN; PATCH CLAMP; POTASSIUM CURRENT; PRIORITY JOURNAL;

ANIMALS; ARRHYTHMIA; BENZAMIDES; BENZOFURANS; BICYCLO COMPOUNDS, HETEROCYCLIC; CATION TRANSPORT PROTEINS; CISAPRIDE; DNA-BINDING PROTEINS; ELECTROPHYSIOLOGY; ETHER-A-GO-GO POTASSIUM CHANNELS; GASTROINTESTINAL AGENTS; GLYCOSAMINOGLYCANS; HUMANS; MORPHOLINES; POTASSIUM CHANNELS; POTASSIUM CHANNELS, VOLTAGE-GATED; RECOMBINANT PROTEINS; SEROTONIN ANTAGONISTS; TRANS-ACTIVATORS;

EID: 0035197735     PISSN: 00223565     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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