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Research ArticleArticle

Interaction and Transport of Methamphetamine and its Primary Metabolites by Organic Cation and Multidrug and Toxin Extrusion Transporters

David J Wagner, Jennifer E Sager, Haichuan Duan, Nina Isoherranen and Joanne Wang
Drug Metabolism and Disposition April 20, 2017, dmd.116.074708; DOI: https://doi.org/10.1124/dmd.116.074708
David J Wagner
University of Washington
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  • ORCID record for David J Wagner
Jennifer E Sager
University of Washington
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Haichuan Duan
University of Washington
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Nina Isoherranen
University of Washington
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Joanne Wang
University of Washington
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  • For correspondence: jowang@u.washington.edu

Data Supplement

  • Supplemental Data -

    Supplemental Figure 1 - Metformin uptake by hOCT1, hOCT2, hOCT3, hMATE1, and hMATE2-K in Flp-in HEK293 cells in the presence or absence of the prototypical inhibitor cimetidine

    Supplemental Figure 2 - Replica studies of methamphetamine, amphetamine, and p-OHMA inhibition of hOCT1, hOCT2, hOCT3, hMATE1, and hMATE2-K

    Supplemental Figure 3 - Inhibition of hOCT1 and hOCT2 by methamphetamine and amphetamine fitted to a two binding site model

    Supplemental Figure 4 - Replica studies on methamphetamine, amphetamine, and p-OHMA uptake kinetics by hOCTs

    Supplemental Figure 5 - Replica studies of methamphetamine (A-D), amphetamine (E-F), and p-OHMA (I & J) uptake kinetics by hMATE1 and hMATE2-K

  View article

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