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Kota Toshimoto

Showing results (11-20 of 23) with videos related to

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CPT: Pharmacometrics & Systems Pharmacology|March 2, 2019
Physiologically-Based Pharmacokinetic Modeling Analysis for Quantitative Prediction of Renal Transporter-Mediated Interactions Between Metformin and CimetidineKotaro Nishiyama, Kota Toshimoto, Wooin Lee, et al.
CPT: Pharmacometrics & Systems Pharmacology|June 20, 2018
Application of PBPK Modeling and Virtual Clinical Study Approaches to Predict the Outcomes of CYP2D6 Genotype-Guided Dosing of TamoxifenToshimichi Nakamura, Kota Toshimoto, Wooin Lee, et al.
Pharmaceutical Research|August 26, 2018
In Silico Prediction of Major Clearance Pathways of Drugs among 9 Routes with Two-Step Support Vector MachinesNaomi Wakayama, Kota Toshimoto, Kazuya Maeda, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|May 5, 2017
Comparison of Methods for Estimating Unbound Intracellular-to-Medium Concentration Ratios in Rat and Human Hepatocytes Using StatinsTakashi Yoshikado, Kota Toshimoto, Tomohisa Nakada, et al.
Journal of Pharmaceutical Sciences|October 15, 2020
Improved Prediction of the Drug-Drug Interactions of Pemafibrate Caused by Cyclosporine A and Rifampicin via PBPK Modeling: Consideration of the Albumin-Mediated Hepatic Uptake of Pemafibrate and Inhibition Constants With Preincubation Against OATP1BJi Eun Park, Yoshihisa Shitara, Wooin Lee, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|February 25, 2018
Physiologically Based Pharmacokinetic Modeling of Bosentan Identifies the Saturable Hepatic Uptake As a Major Contributor to Its Nonlinear PharmacokineticsMasanobu Sato, Kota Toshimoto, Atsuko Tomaru, et al.
CPT: Pharmacometrics & Systems Pharmacology|January 26, 2018
Comprehensive PBPK Model of Rifampicin for Quantitative Prediction of Complex Drug-Drug Interactions: CYP3A/2C9 Induction and OATP Inhibition EffectsRyuta Asaumi, Kota Toshimoto, Yoshifusa Tobe, et al.
CPT: Pharmacometrics & Systems Pharmacology|September 4, 2018
PBPK Modeling of Coproporphyrin I as an Endogenous Biomarker for Drug Interactions Involving Inhibition of Hepatic OATP1B1 and OATP1B3Takashi Yoshikado, Kota Toshimoto, Kazuya Maeda, et al.
European Journal of Pharmaceutical Sciences : Official Journal of the European Federation for Pharmaceutical Sciences|October 6, 2018
Strategies to improve the prediction accuracy of hepatic intrinsic clearance of three antidiabetic drugs: Application of the extended clearance concept and consideration of the effect of albumin on CYP2C metabolism and OATP1B-mediated hepatic uptakeRyo Fujino, Kenta Hashizume, Shinsuke Aoyama, et al.
Journal of Pharmaceutical Sciences|June 6, 2016
Development of a Support Vector Machine-Based System to Predict Whether a Compound Is a Substrate of a Given Drug Transporter Using Its Chemical StructureAtsushi Ose, Kota Toshimoto, Kazushi Ikeda, et al.
Pageof 3

Showing results (11-20 of 23) with videos related to

Sort By:
Pageof 3
CPT: Pharmacometrics & Systems Pharmacology|March 2, 2019
Physiologically-Based Pharmacokinetic Modeling Analysis for Quantitative Prediction of Renal Transporter-Mediated Interactions Between Metformin and CimetidineKotaro Nishiyama, Kota Toshimoto, Wooin Lee, et al.
CPT: Pharmacometrics & Systems Pharmacology|June 20, 2018
Application of PBPK Modeling and Virtual Clinical Study Approaches to Predict the Outcomes of CYP2D6 Genotype-Guided Dosing of TamoxifenToshimichi Nakamura, Kota Toshimoto, Wooin Lee, et al.
Pharmaceutical Research|August 26, 2018
In Silico Prediction of Major Clearance Pathways of Drugs among 9 Routes with Two-Step Support Vector MachinesNaomi Wakayama, Kota Toshimoto, Kazuya Maeda, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|May 5, 2017
Comparison of Methods for Estimating Unbound Intracellular-to-Medium Concentration Ratios in Rat and Human Hepatocytes Using StatinsTakashi Yoshikado, Kota Toshimoto, Tomohisa Nakada, et al.
Journal of Pharmaceutical Sciences|October 15, 2020
Improved Prediction of the Drug-Drug Interactions of Pemafibrate Caused by Cyclosporine A and Rifampicin via PBPK Modeling: Consideration of the Albumin-Mediated Hepatic Uptake of Pemafibrate and Inhibition Constants With Preincubation Against OATP1BJi Eun Park, Yoshihisa Shitara, Wooin Lee, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|February 25, 2018
Physiologically Based Pharmacokinetic Modeling of Bosentan Identifies the Saturable Hepatic Uptake As a Major Contributor to Its Nonlinear PharmacokineticsMasanobu Sato, Kota Toshimoto, Atsuko Tomaru, et al.
CPT: Pharmacometrics & Systems Pharmacology|January 26, 2018
Comprehensive PBPK Model of Rifampicin for Quantitative Prediction of Complex Drug-Drug Interactions: CYP3A/2C9 Induction and OATP Inhibition EffectsRyuta Asaumi, Kota Toshimoto, Yoshifusa Tobe, et al.
CPT: Pharmacometrics & Systems Pharmacology|September 4, 2018
PBPK Modeling of Coproporphyrin I as an Endogenous Biomarker for Drug Interactions Involving Inhibition of Hepatic OATP1B1 and OATP1B3Takashi Yoshikado, Kota Toshimoto, Kazuya Maeda, et al.
European Journal of Pharmaceutical Sciences : Official Journal of the European Federation for Pharmaceutical Sciences|October 6, 2018
Strategies to improve the prediction accuracy of hepatic intrinsic clearance of three antidiabetic drugs: Application of the extended clearance concept and consideration of the effect of albumin on CYP2C metabolism and OATP1B-mediated hepatic uptakeRyo Fujino, Kenta Hashizume, Shinsuke Aoyama, et al.
Journal of Pharmaceutical Sciences|June 6, 2016
Development of a Support Vector Machine-Based System to Predict Whether a Compound Is a Substrate of a Given Drug Transporter Using Its Chemical StructureAtsushi Ose, Kota Toshimoto, Kazushi Ikeda, et al.
Pageof 3