| Autor: |
R Kumar, S T Weintraub, D J Hanahan |
| Jazyk: |
angličtina |
| Rok vydání: |
1983 |
| Předmět: |
|
| Zdroj: |
Journal of Lipid Research, Vol 24, Iss 7, Pp 930-937 (1983) |
| Druh dokumentu: |
article |
| ISSN: |
0022-2275 |
| DOI: |
10.1016/S0022-2275(20)37939-6 |
| Popis: |
The effectiveness of acetolysis as a tool in structural characterization of mono- and di-O-alkyl phosphoglycerides was investigated. Surprisingly, it was found that the di-O-alkyl phosphoglycerides were resistant to attack during acetolysis, whereas the mono-ether types, with a free hydroxyl function or an ester on carbon-2, were easily attacked at the glycerol-phosphate bond. On the other hand, Vitride reduction occurred readily with the mono-ether or di-ether phosphoglycerides. The implications of these findings as they relate to identification of ether phospholipids in tissues are discussed. |
| Databáze: |
Directory of Open Access Journals |
| Externí odkaz: |
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