A model of in vitro UDP-glucuronosyltransferase inhibition by bile acids predicts possible metabolic disorders-Reference-Cited by-同舟云学术

A model of in vitro UDP-glucuronosyltransferase inhibition by bile acids predicts possible metabolic disorders

Published:2013-12 Issue:12 Volume:54 Page:3334-3344
ISSN:0022-2275
Container-title:Journal of Lipid Research
language:en
Short-container-title:Journal of Lipid Research

Author:

Fang Zhong-Ze,He Rong-Rong,Cao Yun-Feng,Tanaka Naoki,Jiang Changtao,Krausz Kristopher W.,Qi Yunpeng,Dong Pei-Pei,Ai Chun-Zhi,Sun Xiao-Yu,Hong Mo,Ge Guang-Bo,Gonzalez Frank J.,Ma Xiao-Chi,Sun Hong-Zhi

Publisher

Elsevier BV

Subject

Cell Biology,Endocrinology,Biochemistry

Reference34 articles.

1. Bile acids metabolomic study on the CCl4- and α-naphthylisothiocyanate-induced animal models: quantitative analysis of 22 bile acids by ultraperformance liquid chromatography-mass spectrometry;Yang;Chem. Res. Toxicol.,2008

2. The enzymes, regulation, and genetics of bile acid synthesis;Russell;Annu. Rev. Biochem.,2003

3. Metabolic pathways of bile acid synthesis;Elliott;Am. J. Med.,1971

4. Mitochondrially-mediated toxicity of bile acids;Palmeira;Toxicology.,2004

5. UDP-glucuronosyltransferases and clinical drug-drug interactions;Kiang;Pharmacol. Ther.,2005

Cited by 31 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Drug disposition in cholestasis: An important concern;Pharmacology Research & Perspectives;2024-06-20

2. Metabolism characterization and toxicity of N-hydap, a marine candidate drug for lung cancer therapy by LC–MS method;Natural Products and Bioprospecting;2024-05-21

3. Characterisation of UDP-glucuronosyltransferase activity in sea turtle Chelonia mydas;Xenobiotica;2022-12-02

4. Evaluation for Potential Drug–Drug Interaction of MT921 Using In Vitro Studies and Physiologically–Based Pharmacokinetic Models;Pharmaceuticals;2021-07-07

5. Potent inhibition of tributyltin (TBT) and triphenyltin (TPT) against multiple UDP-glucuronosyltransferases (UGT): A new potential mechanism underlying endocrine disrupting actions;Food and Chemical Toxicology;2021-03