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Research ArticleArticle

Discovery and Validation of Pyridoxic Acid and Homovanillic Acid as Novel Endogenous Plasma Biomarkers of Organic Anion Transporter (OAT) 1 and OAT3 in Cynomolgus Monkeys

Hong Shen, David M. Nelson, Regina V. Oliveira, Yueping Zhang, Colleen A. Mcnaney, Xiaomei Gu, Weiqi Chen, Ching Su, Michael D. Reily, Petia A. Shipkova, Jinping Gan, Yurong Lai, Punit Marathe and W. Griffith Humphreys
Drug Metabolism and Disposition November 21, 2017, dmd.117.077586; DOI: https://doi.org/10.1124/dmd.117.077586
Hong Shen
1 Bristol-Myers Squibb;
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  • For correspondence: hong.shen1@bms.com
David M. Nelson
2 Bristol-Myers Squib
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Regina V. Oliveira
2 Bristol-Myers Squib
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Yueping Zhang
2 Bristol-Myers Squib
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Colleen A. Mcnaney
2 Bristol-Myers Squib
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Xiaomei Gu
2 Bristol-Myers Squib
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Weiqi Chen
2 Bristol-Myers Squib
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Ching Su
2 Bristol-Myers Squib
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Michael D. Reily
2 Bristol-Myers Squib
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Petia A. Shipkova
2 Bristol-Myers Squib
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Jinping Gan
2 Bristol-Myers Squib
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Yurong Lai
2 Bristol-Myers Squib
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Punit Marathe
2 Bristol-Myers Squib
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W. Griffith Humphreys
2 Bristol-Myers Squib
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Data Supplement

  • Supplemental Data -

    Supplementary Table 1 - Comparison of Plasma Concentrations of Selected Endogenous Metabolites between a Single or Combined IV Administration of PROB (40 mg/kg) and FSM with a Single IV Administration of 2 mg/kg FSM in 3 Cynomolgus Monkeys

    Supplementary Table 2 - Comparison of Inhibition Potency of PROB Towards Various Human Transporters

    Supplementary Figure 1 - Time course of uptake of PDA (1 μM) by OAT1 (A) and OAT3 (B), and HVA (5 μM) by OAT1

    Supplementary Figure 2 - Profiling of the transport of PDA and HVA by major drug transporters expressed at the basolateral membrane of human hepatocytes

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