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pro vyhledávání: '"David, Rampe"'
Autor:
Ulrich Koert, Philipp Reiß
Publikováno v:
Angewandte Chemie. 118:5540-5540
Autor:
Ulrich Koert, Philipp Reiß
Publikováno v:
Angewandte Chemie International Edition. 45:5414-5414
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 28:446-451
Abuse of the common anti-diarrheal loperamide is associated with QT interval prolongation as well as development of the potentially fatal arrhythmia torsades de pointes. The mechanism underlying this cardiotoxicity is high affinity inhibition of the
Publikováno v:
Journal of Applied Toxicology. 37:445-453
Inhibition of the human ether-a-go-go-related gene (hERG) K+ channel by drugs leads to QT prolongation on the electrocardiogram and can result in serious cardiac arrhythmia. For this reason, screening of drugs on hERG is mandatory during the drug dev
Autor:
Reiß, Philipp, Koert, Ulrich
Publikováno v:
Angewandte Chemie. International Edition; August 2006, Vol. 45 Issue: 33 p5414-5414, 1p
Autor:
Reiß, Philipp, Koert, Ulrich
Publikováno v:
Angewandte Chemie; August 2006, Vol. 118 Issue: 33 p5540-5540, 1p
Publikováno v:
ASSAY and Drug Development Technologies. 12:352-360
Human stem cell-derived cardiomyocytes provide a cellular model for the study of electrophysiology in the human heart and are finding a niche in the field of safety pharmacology for predicting proarrhythmia. The cardiac L-type Ca2+ channel is an impo
Publikováno v:
Naunyn-Schmiedeberg's archives of pharmacology. 389(10)
Loperamide is a μ-opioid receptor agonist commonly used to treat diarrhea and often available as an over-the-counter medication. Recently, numerous reports of QRS widening accompanied by dramatic QT interval prolongation, torsades de pointe arrhythm
Publikováno v:
Journal of applied toxicology : JAT. 37(4)
Inhibition of the human ether-a-go-go-related gene (hERG) K
Publikováno v:
Journal of Pharmacology and Experimental Therapeutics. 341:510-517
Human stem cell-derived cardiomyocytes provide new models for studying the ion channel pharmacology of human cardiac cells for both drug discovery and safety pharmacology purposes. However, detailed pharmacological characterization of ion channels in