LBF20406HP01
LipidBank Top (トップ) |
Fatty acid (脂肪酸) |
Glycerolipid (グリセロ脂質) |
Sphingolipid (スフィンゴ脂質) |
Journals (雑誌一覧) |
How to edit (ページの書き方) |
IDs and Links | |
---|---|
LipidBank | DFA8079 |
LipidMaps | - |
CAS | |
KEGG | {{{KEGG}}} |
KNApSAcK | {{{KNApSAcK}}} |
mol | LBF20406HP01 |
5-Hydroperoxy-6,8,11,14-Eicosatetraenoic Acid | |
---|---|
Structural Information | |
5-Hydroperoxy-6,8,11,14-Eicosatetraenoic Acid/5-Hydroperoxy-6,8,11,14-Eicosatetraenoate | |
| |
Formula | C20H32O4 |
Exact Mass | 336.23005951199997 |
Average Mass | 336.46567999999996 |
SMILES | C(CC=CCC=CCC=CC=CC(OO)CCCC(O)=O)CCC |
Physicochemical Information | |
Autooxidation of arachidonic acid Terao_J et al. Yamagata_S et al. Porter_NA et al.. Oxidation of arachidonic acid by singlet-oxygen Terao_J et al. Porter_NA et al.. Reaction products between arachidonic acid and lipoxygenase from living cells(5-HPETE) Spector_AA et al.. | |
5-HPETE generated by 5-lipoxygenase is enzymatically converted to bioactive compounds such as leukotriene and HETE Spector_AA et al.. | |
Spectral Information | |
Mass Spectra | GC-EI-MS(Me-ester; after reduction and TMS) TeraoJet al. TeraoJet al. BorgeatPet al. RabinovitchHet al. KoshiharaYet al. OchiKet al. FurukawaMet al.GC-EI-MS(Me-ester; after reduction and TBDMS)(114), GC-EI-MS(Me-ester; after reduction, hydrogenation and TMS) TeraoJet al. TeraoJet al. Porter_NA et al. Porter_NA et al. BorgeatPet al. RabinovitchHet al. MayerBet al. |
UV Spectra | UV Porter_NA et al.conjugated diene: lmax=235nm, UV(Me-ester) TeraoJet al. conjugated diene: lmax=232.5nm, UV(Me-ester; after reduction) Porter_NA et al. BorgeatPet al. conjugated trans, cis diene: lmax=235-236nm, conjugated trans, trans diene: lm |
IR Spectra | IR(Me-ester; after reduction) Porter_NA et al.conjugated trans, cis diene: 985, 950cm-1, conjugated trans, trans diene: 989cm-1 |
NMR Spectra | |
Other Spectra | |
Chromatograms |
Reported Metabolites, References | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|