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. 2004 Mar 1;101(10):3569–3574. doi: 10.1073/pnas.0304987101

Fig. 5.

Fig. 5.

Dose-dependent inhibition by various compounds on [3H]digoxin (a) or [125I]T3 (b) uptake via human OATP4C1. The OATP4C1-mediated 0.1 μM [3H]digoxin or 0.1 μM [125I]T3 uptake was determined in the absence or presence of unlabeled compounds for 30 min.