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Research ArticleArticle

Identification of Intestinal UDP-Glucuronosyltransferase Inhibitors in Green Tea (Camellia sinensis) Using a Biochemometric Approach: Application to Raloxifene as a Test Drug via In Vitro to In Vivo Extrapolation

Dan-Dan Tian, Joshua J Kellogg, Neşe Okut, Nicholas H Oberlies, Nadja B Cech, Danny D Shen, Jeannine S McCune and Mary F Paine
Drug Metabolism and Disposition February 21, 2018, dmd.117.079491; DOI: https://doi.org/10.1124/dmd.117.079491
Dan-Dan Tian
1 Department of Pharmaceutical Sciences, College of Pharmacy, Washington State University, Spokane, WA;
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Joshua J Kellogg
2 Department of Chemistry & Biochemistry, University of North Carolina at Greensboro, Greensboro, NC;
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Neşe Okut
2 Department of Chemistry & Biochemistry, University of North Carolina at Greensboro, Greensboro, NC;
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Nicholas H Oberlies
2 Department of Chemistry & Biochemistry, University of North Carolina at Greensboro, Greensboro, NC;
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Nadja B Cech
2 Department of Chemistry & Biochemistry, University of North Carolina at Greensboro, Greensboro, NC;
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Danny D Shen
3 Department of Pharmaceutics, School of Pharmacy, University of Washington, Seattle, WA;
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Jeannine S McCune
4 Department of Population Sciences, City of Hope, Duarte, CA
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Mary F Paine
1 Department of Pharmaceutical Sciences, College of Pharmacy, Washington State University, Spokane, WA;
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  • For correspondence: mary.paine@wsu.edu

Data Supplement

  • Supplemental Figures -

    Supplemental Figure 1- Concentration-dependent inhibition of intestinal microsomal UGT activity (4-MU glucuronidation) by purified catechins

    Supplemental Figure 2 - Dixon plots showing inhibition of raloxifene-4'-glucuronide (R4G; left) or raloxifene-6-glucuronide (R6G; right) formation by ECG (upper) and EGCG (lower)

    Supplemental Figure 3 - Concentration-dependent inhibition of intestinal microsomal UGT activity (raloxifene glucuronidation) by purified catechins

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