Methoxylation of 3β,7α-dihydroxychol-5-en-24-oic acid, a key intermediate of chenodeoxycholic acid biogenesis, compared with that of its 7β-epimer
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Clinical Biochemistry,Pharmacology,Endocrinology,Molecular Biology,Biochemistry
Reference15 articles.
1. Isolation of 33, 7α-Dihydroxychol-5-en-24-oic Acid, an Intermediate of Chenodeoxycholic Acid Biogenesis, from Fistula Bile of the Rat and Hen
2. Identification of 3β, 7α-Dihydroxychol-5-enoic Acid in Fistula Bile of the Rat Given Cholesterol-4-14C and DL-Mevalonate-2-14C
3. In vivo Metabolism of 3β 7α-Dihydroxychol-5-enoic-(14C-24) Acid in Carp (Cyprinus carpio)
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1. Mass Spectrometry of Bile Acids;The Bile Acids: Chemistry, Physiology, and Metabolism;1988
2. Nuclear Magnetic Resonance Spectroscopy of Bile Acids;The Bile Acids: Chemistry, Physiology, and Metabolism;1988
3. Techniques for Extraction and Group Separation of Bile Acids;The Bile Acids: Chemistry, Physiology, and Metabolism;1988
4. Determination of 3β,12α-dihydroxy-5-cholen-24-oic acid and related bile acids in human serum by gas chromatography-mass spectrometry;Journal of Chromatography B: Biomedical Sciences and Applications;1987-01
5. [4] Mass spectrometry of bile acids;Methods in Enzymology;1985
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