Bile Acid Disposition and Drug Pharmacokinetic Implications

Molecular Pharmaceutics - United States
doi 10.1021/mp0600440
Full Text
Abstract

Available in full text

Date
Authors
Publisher

American Chemical Society (ACS)

Related search

A Pharmacokinetic Model for Percutaneous Absorption of Valproic Acid and Prediction of Drug Disposition.

Journal of Pharmacobio-Dynamics
1988English

P53-Mediated Regulation of Bile Acid Disposition Attenuates Cholic Acid-Induced Cholestasis in Mice

British Journal of Pharmacology
Pharmacology
2017English

Bile Acids Decrease Intracellular Bilirubin Levels in the Cholestatic Liver: Implications for Bile Acid-Mediated Oxidative Stress

Journal of Cellular and Molecular Medicine
Molecular MedicineCell Biology
2010English

Physiologically Based Pharmacokinetic Modeling of Chloroethane Disposition in Mice, Rats, and Women

Toxicological Sciences
Toxicology
2008English

Semiphysiologically Based Pharmacokinetic Model of Leflunomide Disposition in Rheumatoid Arthritis Patients

CPT: Pharmacometrics and Systems Pharmacology
ModelingSimulationCardiovascular MedicinePharmacologyCardiology
2015English

Disposition of Marograstim (KW-2228). (4). Pharmacokinetic Studies in Monkeys.

Drug Metabolism and Pharmacokinetics
1991English

Target‐mediated Drug Disposition Pharmacokinetic/Pharmacodynamic Model‐informed Dose Selection for the First‐in‐human Study of AVB‐S6‐500

Clinical and Translational Science
GeneticsMolecular BiologyPharmacologyBiochemistryNeuroscienceMedicineToxicologyPharmaceutics
2019English

Pharmacokinetic Drug-Drug Interaction and Responsible Mechanism Between Memantine and Cimetidine

Pharmaceutics
Pharmaceutical Science
2018English

Physiologically Based Pharmacokinetic Model of Rifapentine and 25-Desacetyl Rifapentine Disposition in Humans

Antimicrobial Agents and Chemotherapy
Infectious DiseasesPharmacology
2016English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy