Autor: |
J Zhang, WJ Griffiths, T Bergman, J Sjövall |
Jazyk: |
angličtina |
Rok vydání: |
1993 |
Předmět: |
|
Zdroj: |
Journal of Lipid Research, Vol 34, Iss 11, Pp 1895-1900 (1993) |
Druh dokumentu: |
article |
ISSN: |
0022-2275 |
DOI: |
10.1016/S0022-2275(20)35107-5 |
Popis: |
When analyzed by fast atom bombardment mass spectrometry, taurine-conjugated bile acids give intense [M-H]-pseudomolecular ions that can be subjected to collision-induced fragmentation to give structural information. A method has been developed that permits rapid coupling of taurine to unconjugated, glycine-conjugated, sulfated, and glucuronidated bile acids. The reaction is performed for 2 h at room temperature in aqueous pyridine hydrochloride buffer, with or without dioxane, using 0.1 M 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide as the coupling agent and 0.2 M taurine. The yields are higher than 95%. In contrast to published coupling reactions, the method permits conjugation of bile acids with the labile 7 alpha-hydroxy-3-oxo-4-ene structure. |
Databáze: |
Directory of Open Access Journals |
Externí odkaz: |
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