Zitao Guo
State Key Laboratory Of Drug Research
Shanghai, China
Shanghai, China
Last Updated: 09/26/2026
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Found 12 publications
Species difference in the excretion routes of Ciprofol (HSK3486) in rats and humans: Contribution of hepatic transporters and renal UDP-glucuronosyltransferase enzymes.
Journal: Drug metabolism and disposition: the biological fate of chemicals
Published: February 14, 2025
Changes in Disposition of Ezetimibe and Its Active Metabolites Induced by Impaired Hepatic Function: The Influence of Enzyme and Transporter Activities.
Journal: Pharmaceutics
Published: November 07, 2022
Mechanistic Study on the Effect of Renal Impairment on the Pharmacokinetics of Vildagliptin and its Carboxylic Acid Metabolite.
Journal: Pharmaceutical research
Published: March 01, 2022
Mechanistic Study on the Species Differences in Excretion Pathway of HR011303 in Humans and Rats.
Journal: Drug metabolism and disposition: the biological fate of chemicals
Published: June 14, 2021
Drug interaction of ningetinib and gefitinib involving CYP1A1 and efflux transporters in non-small cell lung cancer patients.
Journal: British journal of clinical pharmacology
Published: March 30, 2020
Carboxylesterase 2 and Intestine Transporters Contribute to the Low Bioavailability of Allisartan, a Prodrug of Exp3174 for Hypertension Treatment in Humans.
Journal: Drug metabolism and disposition: the biological fate of chemicals
Published: October 24, 2018
Pharmacokinetic Drug Interactions of Apatinib With Rifampin and Itraconazole.
Journal: Journal of clinical pharmacology
Published: July 21, 2017
Impact of curcumin on the pharmacokinetics of rosuvastatin in rats and dogs based on the conjugated metabolites.
Journal: Xenobiotica; the fate of foreign compounds in biological systems
Published: May 14, 2016
Fasiglifam (TAK-875) Inhibits Hepatobiliary Transporters: A Possible Factor Contributing to Fasiglifam-Induced Liver Injury.
Journal: Drug metabolism and disposition: the biological fate of chemicals
Published: March 03, 2015
Bioactivation of 3-n-butylphthalide via sulfation of its major metabolite 3-hydroxy-NBP: mediated mainly by sulfotransferase 1A1.
Journal: Drug metabolism and disposition: the biological fate of chemicals
Published: January 29, 2014
Metabolism and bioactivation of famitinib, a novel inhibitor of receptor tyrosine kinase, in cancer patients.
Journal: British journal of pharmacology
Published: September 04, 2012
Mechanistic studies on the absorption and disposition of scutellarin in humans: selective OATP2B1-mediated hepatic uptake is a likely key determinant for its unique pharmacokinetic characteristics.
Journal: Drug metabolism and disposition: the biological fate of chemicals
Published: July 24, 2012
Showing 1-12 of 12
Last Updated: 09/26/2026