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Physiologically Based Modeling of Pravastatin Transporter-Mediated Hepatobiliary Disposition and Drug-Drug Interactions

Pharmaceutical research, 2012-10, Vol.29 (10), p.2860-2873

2012

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Metabolic disposition of the EGFR covalent inhibitor furmonertinib in humans

Acta pharmacologica Sinica, 2022-02, Vol.43 (2), p.494-503

2022

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Metabolism and disposition of pyrotinib in healthy male volunteers: covalent binding with human plasma protein

Acta pharmacologica Sinica, 2019-07, Vol.40 (7), p.980-988

2019

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Pharmacokinetics and disposition of anlotinib, an oral tyrosine kinase inhibitor, in experimental animal species

Acta pharmacologica Sinica, 2018-06, Vol.39 (6), p.1048-1063

2018

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Curcumin Affects Phase II Disposition of Resveratrol Through Inhibiting Efflux Transporters MRP2 and BCRP

Pharmaceutical research, 2016-03, Vol.33 (3), p.590-602

2016

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Metabolism and disposition of N,N-dimethyltryptamine and harmala alkaloids after oral administration of ayahuasca

Drug testing and analysis, 2012-07, Vol.4 (7-8), p.610-616

2012

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Enantioselective disposition of (R,R)‐formoterol, (S,S)‐formoterol and their respective glucuronides in urine following single inhaled dosing and application to doping control

Drug testing and analysis, 2019-07, Vol.11 (7), p.950-956

2019

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Pharmacokinetic Modeling of the Impact of P-glycoprotein on Ondansetron Disposition in the Central Nervous System

Pharmaceutical research, 2020-10, Vol.37 (10), p.205-205, Article 205

2020

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Dynamic Contrast-Enhanced Magnetic Resonance Imaging for the Prediction of Monoclonal Antibody Tumor Disposition

International journal of molecular sciences, 2022-01, Vol.23 (2), p.679

2022

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Confocal Imaging with a Fluorescent Bile Acid Analogue Closely Mimicking Hepatic Taurocholate Disposition

Journal of pharmaceutical sciences, 2014-06, Vol.103 (6), p.1872-1881

2014

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Disposition of Astragaloside IV via Enterohepatic Circulation Is Affected by the Activity of the Intestinal Microbiome

Journal of agricultural and food chemistry, 2015-07, Vol.63 (26), p.6084-6093

2015

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Tissue Disposition of 2′‐O‐(2‐methoxy) ethyl Modified Antisense Oligonucleotides in Monkeys

Journal of pharmaceutical sciences, 2004-01, Vol.93 (1), p.48-59

2004

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Disposition of ON 01210.Na (Ex-RAD(R)), a Novel Radioprotectant, in the Isolated Perfused Rat Liver: Probing Metabolic Inhibition to Increase Systemic Exposure

Journal of pharmaceutical sciences, 2013-02, Vol.102 (2), p.732-740

2013

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Metabolic Disposition and Elimination of Cyadox in Pigs, Chickens, Carp, and Rats

Journal of agricultural and food chemistry, 2015-06, Vol.63 (22), p.5557-5569

2015

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Mechanisms responsible for poor oral bioavailability of paeoniflorin : Role of intestinal disposition and interactions with sinomenine

Pharmaceutical research, 2006-12, Vol.23 (12), p.2768-2780

2006

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Breast Cancer Resistance Protein and Multidrug Resistance Protein 2 Regulate the Disposition of Acacetin Glucuronides

Pharmaceutical research, 2017-07, Vol.34 (7), p.1402-1415

2017

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Enantioselective disposition of PCB 136 (2,2′,3,3′,6,6′-hexachlorobiphenyl) in C57BL/6 mice after oral and intraperitoneal administration

Chirality (New York, N.Y.), 2007, Vol.19 (1), p.56-66

2007

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Paclitaxel Prodrugs with Sustained Release and High Solubility in Poly(ethylene glycol)-b-poly(ε-caprolactone) Micelle Nanocarriers: Pharmacokinetic Disposition, Tolerability, and Cytotoxicity

Pharmaceutical research, 2008-01, Vol.25 (1), p.194-206

2008

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FG-3019, a Human Monoclonal Antibody Recognizing Connective Tissue Growth Factor, is Subject to Target-Mediated Drug Disposition

Pharmaceutical research, 2016-08, Vol.33 (8), p.1833-1849

2016

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Pharmacokinetics and disposition of monoterpene glycosides derived from Paeonia lactiflora roots (Chishao) after intravenous dosing of antiseptic XueBiJing injection in human subjects and rats

Acta pharmacologica Sinica, 2016-04, Vol.37 (4), p.530-544

2016

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Role of the OATP Transporter Family and a Benzbromarone-SensitiveEfflux Transporter in the Hepatocellular Disposition of Vincristine

Pharmaceutical research, 2017-11, Vol.34 (11), p.2336-2348

2017

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Exploring the links between dispositions, romantic relationships, support networks and community inclusion in men and women

PloS one, 2019-05, Vol.14 (5), p.e0216210-e0216210

2019

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Inferring individual sexual action dispositions from egocentric network data on dyadic sexual outcomes

PloS one, 2018, Vol.13 (11), p.e0207116-e0207116

2018

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Investigation of the disposition of loxapine, amoxapine and their hydroxylated metabolites in different brain regions, CSF and plasma of rat by LC–MS/MS

Journal of pharmaceutical and biomedical analysis, 2012-01, Vol.58 (25), p.83-93

2012

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Enantioselective disposition of (R)‐salmeterol and (S)‐salmeterol in urine following inhaled dosing and application to doping control

Drug testing and analysis, 2017-08, Vol.9 (8), p.1262-1266

2017

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Physiologically Based Modeling of Pravastatin Transporter-Mediated Hepatobiliary Disposition and Drug-Drug Interactions

Metabolic disposition of the EGFR covalent inhibitor furmonertinib in humans

Metabolism and disposition of pyrotinib in healthy male volunteers: covalent binding with human plasma protein

Pharmacokinetics and disposition of anlotinib, an oral tyrosine kinase inhibitor, in experimental animal species

Curcumin Affects Phase II Disposition of Resveratrol Through Inhibiting Efflux Transporters MRP2 and BCRP

Metabolism and disposition of N,N-dimethyltryptamine and harmala alkaloids after oral administration of ayahuasca

Enantioselective disposition of (R,R)‐formoterol, (S,S)‐formoterol and their respective glucuronides in urine following single inhaled dosing and application to doping control

Pharmacokinetic Modeling of the Impact of P-glycoprotein on Ondansetron Disposition in the Central Nervous System

Dynamic Contrast-Enhanced Magnetic Resonance Imaging for the Prediction of Monoclonal Antibody Tumor Disposition

Confocal Imaging with a Fluorescent Bile Acid Analogue Closely Mimicking Hepatic Taurocholate Disposition

Disposition of Astragaloside IV via Enterohepatic Circulation Is Affected by the Activity of the Intestinal Microbiome

Tissue Disposition of 2′‐O‐(2‐methoxy) ethyl Modified Antisense Oligonucleotides in Monkeys

Disposition of ON 01210.Na (Ex-RAD(R)), a Novel Radioprotectant, in the Isolated Perfused Rat Liver: Probing Metabolic Inhibition to Increase Systemic Exposure

Metabolic Disposition and Elimination of Cyadox in Pigs, Chickens, Carp, and Rats

Mechanisms responsible for poor oral bioavailability of paeoniflorin : Role of intestinal disposition and interactions with sinomenine

Breast Cancer Resistance Protein and Multidrug Resistance Protein 2 Regulate the Disposition of Acacetin Glucuronides

Enantioselective disposition of PCB 136 (2,2′,3,3′,6,6′-hexachlorobiphenyl) in C57BL/6 mice after oral and intraperitoneal administration

Paclitaxel Prodrugs with Sustained Release and High Solubility in Poly(ethylene glycol)-b-poly(ε-caprolactone) Micelle Nanocarriers: Pharmacokinetic Disposition, Tolerability, and Cytotoxicity

FG-3019, a Human Monoclonal Antibody Recognizing Connective Tissue Growth Factor, is Subject to Target-Mediated Drug Disposition

Pharmacokinetics and disposition of monoterpene glycosides derived from Paeonia lactiflora roots (Chishao) after intravenous dosing of antiseptic XueBiJing injection in human subjects and rats

Role of the OATP Transporter Family and a Benzbromarone-SensitiveEfflux Transporter in the Hepatocellular Disposition of Vincristine

Exploring the links between dispositions, romantic relationships, support networks and community inclusion in men and women

Inferring individual sexual action dispositions from egocentric network data on dyadic sexual outcomes

Investigation of the disposition of loxapine, amoxapine and their hydroxylated metabolites in different brain regions, CSF and plasma of rat by LC–MS/MS

Enantioselective disposition of (R)‐salmeterol and (S)‐salmeterol in urine following inhaled dosing and application to doping control

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