Bosentan is a substrate of human OATP1B1 and OATP1B3: inhibition of hepatic uptake as the common mechanism of its interactions with cyclosporin A, rifampicin, and sildenafil.

Publication

Citation: Treiber A, Schneiter R, Häusler S, Stieger B.: Bosentan is a substrate of human OATP1B1 and OATP1B3: inhibition of hepatic uptake as the common mechanism of its interactions with cyclosporin A, rifampicin, and sildenafil. Drug Metab Dispos, Volume 35 (8), 2007
Authors: Häusler S, Schneiter R, Stieger B., Treiber A
Journal: Drug Metab Dispos
Year: 2007
DOI: 10.1124/dmd.106.013615
PubMed: 17496208
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