LBF18304HP01: Difference between revisions

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|LipidBank=DFA8053
|LipidBank=DFA8053
|LipidMaps=LMFA01040016
|LipidMaps=LMFA01040016
|SysName=16-Hydroperoxy-9,12,14-Octadecatrienoic Acid/16-Hydroperoxy-9,12,14-Octadecatrienoate
|SysName=16-Hydroperoxy-9,12,14-octadecatrienoic acid
|Common Name=&&16-Hydroperoxy-9,12,14-Octadecatrienoic Acid&&16-Hydroperoxy-9,12,14-Octadecatrienoate&&
|Common Name=&&16-Hydroperoxy-9,12,14-octadecatrienoic acid&&
|Mass Spectra=EI-MS(Me-ester; after reduction and hydrogenation)[[Reference:Chan_HWS:,J. Am. Oil Chem. Soc.,1977,54,100|{{RelationTable/GetFirstAuthor|Reference:Chan_HWS:,J. Am. Oil Chem. Soc.,1977,54,100}}]][[Reference:Frankel_EN:Neff_WE:Rohwedder_WK:Khambay_BPS:Garwood_RF:Weedon_BCL:,Lipids,1977,12,1055|{{RelationTable/GetFirstAuthor|Reference:Frankel_EN:Neff_WE:Rohwedder_WK:Khambay_BPS:Garwood_RF:Weedon_BCL:,Lipids,1977,12,1055}}]]: m/e=285[O=CH(CH2)14C(=OH)OCH3]; 256[CH2(CH2)13C(=OH)OCH3]; 253[O=CH(CH2)14C=O], GC-EI-MS(Me-ester; after reduction,tms)[[Reference:Frankel_EN:Neff_WE:Rohwedder_WK:Khambay_BPS:Garwood_RF:Weedon_BCL:,Lipids,1977,12,1055|{{RelationTable/GetFirstAuthor|Reference:Frankel_EN:Neff_WE:Rohwedder_WK:Khambay_BPS:Garwood_RF:Weedon_BCL:,Lipids,1977,12,1055}}]]: m/e=380[M]; 365[M-CH3]; 351[SMTO=CH-CH=CH-CH=CH-CH2-CH=CH-(CH2)7-COOCH3]
|Mass Spectra=EI-MS(Me-ester; after reduction and hydrogenation)[[Reference:Chan_HWS:,J. Am. Oil Chem. Soc.,1977,54,100|{{RelationTable/GetFirstAuthor|Reference:Chan_HWS:,J. Am. Oil Chem. Soc.,1977,54,100}}]][[Reference:Frankel_EN:Neff_WE:Rohwedder_WK:Khambay_BPS:Garwood_RF:Weedon_BCL:,Lipids,1977,12,1055|{{RelationTable/GetFirstAuthor|Reference:Frankel_EN:Neff_WE:Rohwedder_WK:Khambay_BPS:Garwood_RF:Weedon_BCL:,Lipids,1977,12,1055}}]]: m/e=285[O=CH(CH2)14C(=OH)OCH3]; 256[CH2(CH2)13C(=OH)OCH3]; 253[O=CH(CH2)14C=O], GC-EI-MS(Me-ester; after reduction,tms)[[Reference:Frankel_EN:Neff_WE:Rohwedder_WK:Khambay_BPS:Garwood_RF:Weedon_BCL:,Lipids,1977,12,1055|{{RelationTable/GetFirstAuthor|Reference:Frankel_EN:Neff_WE:Rohwedder_WK:Khambay_BPS:Garwood_RF:Weedon_BCL:,Lipids,1977,12,1055}}]]: m/e=380[M]; 365[M-CH3]; 351[SMTO=CH-CH=CH-CH=CH-CH2-CH=CH-(CH2)7-COOCH3]
|UV Spectra=(Me-ester; after reduction; in ethanol)[[Reference:Chan_HWS:Levett_G:,Lipids,1977,12,837|{{RelationTable/GetFirstAuthor|Reference:Chan_HWS:Levett_G:,Lipids,1977,12,837}}]], cis, cis, trans isomer:  lambda max=236nm, cis, trans, trans isomer:  lambda max=232nm
|UV Spectra=(Me-ester; after reduction; in ethanol)[[Reference:Chan_HWS:Levett_G:,Lipids,1977,12,837|{{RelationTable/GetFirstAuthor|Reference:Chan_HWS:Levett_G:,Lipids,1977,12,837}}]], cis, cis, trans isomer:  lambda max=236nm, cis, trans, trans isomer:  lambda max=232nm

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Upper classes: LB LBF



16-Hydroperoxy-9,12,14-octadecatrienoic acid
LBF18304HP01.png
Structural Information
16-Hydroperoxy-9,12,14-octadecatrienoic acid
  • 16-Hydroperoxy-9,12,14-octadecatrienoic acid
Formula C18H30O4
Exact Mass 310.21440944799997
Average Mass 310.4284
SMILES CCC(OO)C=CC=CCC=CCCCCCCCC(O)=O
Physicochemical Information
Auto oxidation of linoleate Frankel_EN Frankel_EN Frankel_EN Chan_HWS et al.. Oxidation of linoleate by singlet oxygen Frankel_EN Frankel_EN Frankel_EN .
Pysiological damages are induced by these hydroperoxides which are incorporated into bodies or synthesized endogenously. Logani_MK et al. Sevanian_A et al. Fujimoto_K . It reacts with DNA in the presence of Fe ions and ascorbic acid Fujimoto_K et al..
Isomerization of hydroperoxides: Positional isomers at 9, 12, 13, and 16 and their geometric isomers of cis, cis, trans- or cis, trans, trans are formed. The proportion of 9-, 16- isomers is higher than that of 12-, 13- isomers.
Spectral Information
Mass Spectra EI-MS(Me-ester; after reduction and hydrogenation) Chan_HWS Frankel_EN et al.: m/e=285[O=CH(CH2)14C(=OH)OCH3]; 256[CH2(CH2)13C(=OH)OCH3]; 253[O=CH(CH2)14C=O], GC-EI-MS(Me-ester; after reduction,tms) Frankel_EN et al.: m/e=380[M]; 365[M-CH3]; 351[SMTO=CH-CH=CH-CH=CH-CH2-CH=CH-(CH2)7-COOCH3]
UV Spectra (Me-ester; after reduction; in ethanol) Chan_HWS et al., cis, cis, trans isomer: λ max=236nm, cis, trans, trans isomer: λ max=232nm
IR Spectra (Me-ester; after reduction) Chan_HWS et al. Frankel_EN et al., cis, cis, trans isomer: 989-983 and 951-945cm-1; cis, trans, trans isomer: 991-983cm-1, (Me-ester) ToyodaIet al., OOH group: 3400cm-1
NMR Spectra
Other Spectra
Chromatograms
Reported Metabolites, References
Biospecies ID Compound Name Reference Comment
n.a. LBF18304HP01 See above. Chan_HWS 1977
n.a. LBF18304HP01 See above. Chan_HWS et al. 1982
n.a. LBF18304HP01 See above. Chan_HWS et al. 1977
n.a. LBF18304HP01 See above. Frankel_EN 1980
n.a. LBF18304HP01 See above. Frankel_EN 1983
n.a. LBF18304HP01 See above. Frankel_EN 1984
n.a. LBF18304HP01 See above. Frankel_EN et al. 1977
n.a. LBF18304HP01 See above. Fujimoto_K 1986
n.a. LBF18304HP01 See above. Fujimoto_K et al. 1984
n.a. LBF18304HP01 See above. Logani_MK et al. 1980
n.a. LBF18304HP01 See above. Sevanian_A et al. 1985
n.a. LBF18304HP01 See above. Toyoda_I et al. 1982