S. Bae

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Physiologically-based pharmacokinetic predictions of intestinal BCRP-mediated drug interactions of rosuvastatin in Koreans

Jongtae Lee, D. Yim, Seunghoon Han, 2018, The Korean journal of physiology & pharmacology : official journal of the Korean Physiological Society and the Korean Society of Pharmacology.

Application of physiologically based pharmacokinetic modeling in predicting drug–drug interactions for sarpogrelate hydrochloride in humans

Doyun Kim, J. Seo, S. Bae, 2016, Drug design, development and therapy.

Application of physiologically based pharmacokinetic modeling in predicting drug–drug interactions for sarpogrelate hydrochloride in humans

Doyun Kim, J. Seo, S. Bae, 2016, Drug design, development and therapy.

Prediction of metabolizing enzyme-mediated clinical drug interactions using in vitro information

D. Yim, S. Bae, Suein Choi, 2022, Translational and clinical pharmacology.

Evaluation of the in vitro/in vivo drug interaction potential of BST204, a purified dry extract of ginseng, and its four bioactive ginsenosides through cytochrome P450 inhibition/induction and UDP-glucuronosyltransferase inhibition.

Gyu Hwan Park, W. Shin, S. O. Kim, 2014, Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association.

Direct measurement of active thiol metabolite levels of clopidogrel in human plasma using tris(2-carboxyethyl)phosphine as a reducing agent by LC-MS/MS.

S. Bae, J. Park, S. Bae, 2013, Journal of separation science.

Pharmacokinetic properties of trifolirhizin, (–)-maackiain, (–)-sophoranone and 2-(2,4-dihydroxyphenyl)-5,6-methylenedioxybenzofuran after intravenous and oral administration of Sophora tonkinensis extract in rats

Minseok Kang, Doyun Kim, S. Jang, 2015, Xenobiotica; the fate of foreign compounds in biological systems.

Simultaneous determination of metoprolol and its metabolites, α-hydroxymetoprolol and O-desmethylmetoprolol, in human plasma by liquid chromatography with tandem mass spectrometry: Application to the pharmacokinetics of metoprolol associated with CYP2D6 genotypes.

S. Bae, S. Bae, Doo-Yeoun Cho, 2014, Journal of separation science.

Quantitation and pharmacokinetics of 1,4-diamino-2,3-dicyano-1,4-bis (2-aminophenylthio) butadiene (U0126) in rat plasma by liquid chromatography-tandem mass spectrometry.

Gyu Hwan Park, J. Hwang, S. Shin, 2013, Journal of separation science.

Evaluation of the Effect of CYP2D6 Genotypes on Tramadol and O-Desmethyltramadol Pharmacokinetic Profiles in a Korean Population Using Physiologically-Based Pharmacokinetic Modeling

Sooyeun Lee, S. Bae, Anhye Kim, 2019, Pharmaceutics.

DallphinAtoM: Physiologically based pharmacokinetics software predicting human PK parameters based on physicochemical properties, in vitro and animal in vivo data

So Jin Lee, D. Yim, Seunghoon Han, 2022, Comput. Methods Programs Biomed..

Stereoselective determination of ginsenosides Rg3 and Rh2 epimers in rat plasma by LC-MS/MS: application to a pharmacokinetic study.

Jeom-Yong Kim, J. Seo, S. O. Kim, 2013, Journal of separation science.

Population pharmacokinetics and inter-laboratory variability of sildenafil and its metabolite after oral administration in Korean healthy male volunteers

D. Yim, Seunghoon Han, S. Bae, 2016 .

Simultaneous quantification of caffeine and its three primary metabolites in rat plasma by liquid chromatography-tandem mass spectrometry.

Su-Jun Lee, S. Bae, J. Park, 2013, Food chemistry.

Pharmacokinetics of sildenafil and its metabolite, N-desmethylsildenafil, in rats with liver cirrhosis and diabetes mellitus, alone and in combination

W. Shin, S. Bae, H. Kang, 2011, Xenobiotica; the fate of foreign compounds in biological systems.

Effect of hepatic CYP inhibitors on the metabolism of sildenafil and formation of its metabolite, N‐desmethylsildenafil, in rats in vitro and in vivo

M. Lee, S. Bae, S. Bae, 2009, The Journal of pharmacy and pharmacology.

Lack of Correlation between In Vitro and In Vivo Studies on the Inhibitory Effects of (‒)-Sophoranone on CYP2C9 Is Attributable to Low Oral Absorption and Extensive Plasma Protein Binding of (‒)-Sophoranone

Hyung Joon Shim, Doyun Kim, S. Bae, 2020, Pharmaceutics.

Metabolic Drug-Drug Interaction Potential of Macrolactin A and 7-O-Succinyl Macrolactin A Assessed by Evaluating Cytochrome P450 Inhibition and Induction and UDP-Glucuronosyltransferase Inhibition In Vitro

Doyun Kim, J. Kang, S. Bae, 2014, Antimicrobial Agents and Chemotherapy.

GAB2 Amplification in Squamous Cell Lung Cancer of Non-Smokers

Jae Cheol Lee, S. Jang, Y. Park, 2017, Journal of Korean medical science.

Potent inhibition of cytochrome P450 2B6 by sibutramine in human liver microsomes.

Kwang-Hyeon Liu, S. Bae, S. Bae, 2013, Chemico-biological interactions.

In vitro stereoselective inhibition of ginsenosides toward UDP-glucuronosyltransferase (UGT) isoforms.

Doyun Kim, Y. Chin, S. Bae, 2016, Toxicology letters.

Pharmacokinetics and tissue distribution of ginsenoside Rh2 and Rg3 epimers after oral administration of BST204, a purified ginseng dry extract, in rats

Jeom-Yong Kim, S. Bae, J. Park, 2014, Xenobiotica; the fate of foreign compounds in biological systems.

Effect of the potent CYP2D6 inhibitor sarpogrelate on the pharmacokinetics and pharmacodynamics of metoprolol in healthy male Korean volunteers

Bom-taeck Kim, S. Bae, J. Park, 2015, Xenobiotica; the fate of foreign compounds in biological systems.

Selective Inhibition of Cytochrome P450 2D6 by Sarpogrelate and Its Active Metabolite, M-1, in Human Liver Microsomes

Bom-taeck Kim, S. Bae, S. Bae, 2014, Drug Metabolism and Disposition.

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Bom-taeck Kim, S. Bae, S. Bae, 2013 .

and its Active Metabolite, M-1, in Human Liver Microsomes

Bom-taeck Kim, S. Bae, S. Bae, 2013 .

Retracted: Physiologically based pharmacokinetic predictions of intestinal BCRP‐mediated effect of telmisartan on the pharmacokinetics of rosuvastatin in humans

Jongtae Lee, D. Yim, Seunghoon Han, 2017, Biopharmaceutics & drug disposition.

Inhibitory effects of astaxanthin, β-cryptoxanthin, canthaxanthin, lutein, and zeaxanthin on cytochrome P450 enzyme activities.

W. Shin, S. Bae, J. Park, 2013, Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association.

Analytical Method Development of Benzisothiazolinone, a Biocide, Using LC–MS/MS and a Pharmacokinetic Application in Rat Biological Matrices

S. Bae, S. Bae, Chae Bin Lee, 2023, Molecules.

In vitro selective inhibition of human UDP-glucuronosyltransferase (UGT) 1A4 by finasteride, and prediction of in vivo drug-drug interactions.

Doyun Kim, Y. Chin, S. Bae, 2015, Toxicology letters.

Simultaneous determination of sarpogrelate and its active metabolite in human plasma by liquid chromatography with tandem mass spectrometry and its application to a pharmacokinetic study.

S. Bae, J. Park, E. Oh, 2015, Journal of separation science.

Drug–drug interaction of microdose and regular-dose omeprazole with a CYP2C19 inhibitor and inducer

Min-Ho Park, Seunghoon Han, Dong-Seok Yim, 2017, Drug design, development and therapy.

Application of Pharmacometrics in Pharmacotherapy: Open-Source Software for Vancomycin Therapeutic Drug Management

D. Yim, Seunghoon Han, S. Bae, 2019, Pharmaceutics.

High-sensitive LC-MS/MS method for the simultaneous determination of mirodenafil and its major metabolite, SK-3541, in human plasma: application to microdose clinical trials of mirodenafil.

Doo-Yeoun Cho, Soo Kyung Bae, Ji-Hong Shon, 2013, Journal of separation science.