Chemical synthesis of N-acetylcysteine conjugates of bile acids and in vivo formation in cholestatic rats as shown by liquid chromatography/electrospray ionization-linear ion trap mass spectrometry-Reference-Cited by-同舟云学术

Chemical synthesis of N-acetylcysteine conjugates of bile acids and in vivo formation in cholestatic rats as shown by liquid chromatography/electrospray ionization-linear ion trap mass spectrometry

Published:2009-09 Issue:25 Volume:877 Page:2630-2638
ISSN:1570-0232
Container-title:Journal of Chromatography B
language:en
Short-container-title:Journal of Chromatography B

Author:

Mitamura Kuniko,Watanabe Saai,Sakai Toshihiro,Okihara Rika,Sogabe Mitsuru,Wakamiya Tateaki,Hofmann Alan F.,Ikegawa Shigeo

Publisher

Elsevier BV

Subject

Cell Biology,Clinical Biochemistry,Biochemistry,General Medicine,Analytical Chemistry

Reference33 articles.

1. Separation and Characterization of Carboxyl-linked Glucuronides of Bile Acids in Incubation Mixture of Rat Liver Microsomes

2. A method for the determination of the hepatic enzyme activity catalyzing bile acid acyl glucuronide formation by high-performance liquid chromatography with pulsed amperometric detection

3. Characterization of rat liver bile acid acyl glucuronosyltransferase

4. Differential glucuronidation of bile acids, androgens and estrogens by human UGT1A3 and 2B7

5. Human UDP-glucuronosyltransferase (UGT)1A3 enzyme conjugates chenodeoxycholic acid in the liver

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