| Identification | Back Directory | [Name]
9(S)-HODE CHOLESTERYL ESTER | [CAS]
143442-54-0 | [Synonyms]
9(S)-HODE CHOLESTERYL ESTER
ALWABJCAEDQEGO-CNCQKSCYSA-N
9S-HYDROXY-10E,12Z-OCTADECADIENOIC ACID, CHOLESTERYL ESTER
Cholest-5-en-3-ol (3β)-, (9S,10E,12Z)-9-hydroxy-10,12-octadecadienoate (9CI) | [Molecular Formula]
C45H76O3 | [MDL Number]
MFCD00216100 | [MOL File]
143442-54-0.mol | [Molecular Weight]
665.08 |
| Chemical Properties | Back Directory | [Boiling point ]
705.137±55.00 °C(Press: 760.00 Torr)(predicted) | [density ]
0.992±0.10 g/cm3(Temp: 25 °C; Press: 760 Torr)(predicted) | [storage temp. ]
Store at -20°C | [solubility ]
DMF: >50 mg/ml; DMSO: >50 mg/ml; Ethanol: >50 mg/ml; Ethanol:PBS (1:10): <10 μg/ml | [pka]
14.225±0.20(predicted) |
| Hazard Information | Back Directory | [Description]
9(S)-HODE cholesteryl ester was originally extracted from atherosclerotic lesions.1 It remains uncertain whether the oxidized fatty acid portion of the molecule results from enzymatic lipoxygenation or from random lipid peroxidation.2 9(S)-HODE cholesteryl ester can be used as a standard for analysis of chiral HODE cholesteryl esters. | [Uses]
9(S)-HODE cholesteryl ester is originally extracted from atherosclerotic lesions. It remains uncertain whether the oxidized fatty acid portion of the molecule results from enzymatic lipoxygenation or from random lipid peroxidation.2 9(S)-HODE cholesteryl ester can be used as a standard for analysis of chiral HODE cholesteryl esters. | [References]
1. Brooks, C.J.W., Harland, W.A., Steel, G., et al. Lipids of human atheroma: Isolation of hydroxyoctadecadienoic acids from advanced aortal lesions Biochim. Biophys. Acta 202(3),563-566(1970).
2. Belkner, J., Wiesner, R., Kühn, H., et al. The oxygenation of cholesterol esters by the reticulocyte lipoxygenase FEBS Lett. 279(1),110-114(1991). |
|
|