Saltar al contenido
Merck

Effects of Tenapanor on Cytochrome P450-Mediated Drug-Drug Interactions.

Clinical pharmacology in drug development (2017-03-17)
Susanne Johansson, David P Rosenbaum, Marie Ahlqvist, Helen Rollison, Mikael Knutsson, Bergur Stefansson, Marie Elebring
RESUMEN

Tenapanor (RDX5791, AZD1722) is an inhibitor of sodium/hydrogen exchanger isoform 3 in development for the treatment of constipation-predominant irritable bowel syndrome and the treatment of hyperphosphatemia in patients with chronic kidney disease on dialysis. We aimed to investigate whether tenapanor inhibits or induces cytochrome P450s (CYPs). In vitro experiments assessing the potential of tenapanor to affect various CYPs indicated that it could inhibit CYP3A4/5 (IC

MATERIALES
Referencia del producto
Marca
Descripción del producto

Sigma-Aldrich
CITCO, ≥98% (HPLC), solid