LBF20406HP01

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Upper classes: LB LBF



5-Hydroperoxy- 6,8,11,14 -eicosatetraenoic acid
LBF20406HP01.png
Structural Information
5-Hydroperoxy- 6,8,11,14 -eicosatetraenoic acid
  • 5-Hydroperoxy- 6,8,11,14 -eicosatetraenoic acid
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..
Isomerization of hydroperoxides : Both 5- and 15-hydroperoxide were generated predominantly by autooxidation or singlet-oxygen mediated oxidation Terao_J et al. Yamagata_S et al. Peers_KE et al.. However, the proportion of each isomer generated become almost equal by supplementation of hydrogen donor such as tocopherol Porter_NA et al. Terao_J et al. Peers_KE 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: λ max=235nm, UV(Me-ester) TeraoJet al. conjugated diene: λ max=232.5nm, UV(Me-ester; after reduction) Porter_NA et al. BorgeatPet al. conjugated trans, cis diene: λ max=235-236nm, conjugated trans, trans diene: λ max=232.5nm
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
Biospecies ID Compound Name Reference Comment
n.a. LBF20406HP01 See above. Borgeat_P et al. 1976
n.a. LBF20406HP01 See above. Furukawa_M et al. 1984
n.a. LBF20406HP01 See above. Koshihara_Y et al. 1982
n.a. LBF20406HP01 See above. Mayer_B et al. 1986
n.a. LBF20406HP01 See above. Ochi_K et al. 1983
n.a. LBF20406HP01 See above. Peers_KE et al. 1983
n.a. LBF20406HP01 See above. Porter_NA et al. 1981
n.a. LBF20406HP01 See above. Porter_NA et al. 1979
n.a. LBF20406HP01 See above. Porter_NA et al. 1979
n.a. LBF20406HP01 See above. Rabinovitch_H et al. 1981
n.a. LBF20406HP01 See above. Spector_AA et al. 1988
n.a. LBF20406HP01 See above. Terao_J et al. 1981
n.a. LBF20406HP01 See above. Terao_J et al. 1981