LBF20406HP03

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Upper classes: LB LBF



9-Hydroperoxy-5,7,11,14-Eicosatetraenoic Acid
LBF20406HP03.png
Structural Information
9-Hydroperoxy-5,7,11,14-Eicosatetraenoic Acid/9-Hydroperoxy-5,7,11,14-Eicosatetraenoate
  • 9-Hydroperoxy-5,7,11,14-Eicosatetraenoic Acid
  • 9-Hydroperoxy-5,7,11,14-Eicosatetraenoate
Formula C20H32O4
Exact Mass 336.23005951199997
Average Mass 336.46567999999996
SMILES C(CC=CCC=CCC(OO)C=CC=CCCCC(O)=O)CCC
Physicochemical Information
Spectral Information
Mass Spectra GC-EI-MS(Me-ester; after reduction and TMS) TeraoJet al. TeraoJet al. RabinovitchHet al.: m/e=406[M]; 316[M-HOTMS]; 255[SMTO=CHCH=CHCH=CH(CH2)3COOCH3]; GC-EI-MS(Me-ester; after reduction and TBDMS)(114): m/e=448[M], 391[M-(CH3)3C]; GC-EI-MS(Me-ester; after reduction hydrogenation and TMS)
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. conjugated cis, trans diene: lmax=236nm, conjugated trans, trans diene: lmax=232.
IR Spectra IR(me-ester; after reduction) Porter_NA et al. conjugated cis, trans 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. LBF20406HP03 See above. Peers_KE et al. 1983
n.a. LBF20406HP03 See above. Porter_NA et al. 1981
n.a. LBF20406HP03 See above. Porter_NA et al. 1979
n.a. LBF20406HP03 See above. Porter_NA et al. 1979
n.a. LBF20406HP03 See above. Rabinovitch_H et al. 1981
n.a. LBF20406HP03 See above. Terao_J et al. 1981
n.a. LBF20406HP03 See above. Terao_J et al. 1981
n.a. LBF20406HP03 See above. Yamagata_S et al. 1983