LBF20407HO04: Difference between revisions

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|Common Name=&&8S,15S-dihydroxy-5Z,9E,11Z,13E-eicosatetraenoic acid&&
|Common Name=&&8S,15S-dihydroxy-5Z,9E,11Z,13E-eicosatetraenoic acid&&
|UV Spectra=<FONT FACE="Symbol">l</FONT>max: 269 nm <FONT FACE="Symbol">e</FONT>: 40,000
|UV Spectra=<FONT FACE="Symbol">l</FONT>max: 269 nm <FONT FACE="Symbol">e</FONT>: 40,000
|Source=8(S),15(S)-DiHETE is formed when15(S)-HETE is subjected to further oxidation by 15-lipoxygenase [[Reference:Morita_E:Schroder_JM:Christophers_E:,J. Immunol.,1990,144,1893|{{RelationTable/GetFirstAuthor|Reference:Morita_E:Schroder_JM:Christophers_E:,J. Immunol.,1990,144,1893}}]];>.
|Chemical Synthesis=
|Metabolism=
}}
}}


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Revision as of 22:00, 24 November 2009

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Upper classes: LB LBF



8S,15S-dihydroxy-5Z,9E,11Z,13E-eicosatetraenoic acid
LBF20407HO04.png
Structural Information
8S,15S-dihydroxy-5Z,9E,11Z,13E-eicosatetraenoic acid
  • 8S,15S-dihydroxy-5Z,9E,11Z,13E-eicosatetraenoic acid
Formula C20H32O4
Exact Mass 336.23005951199997
Average Mass 336.46567999999996
SMILES C(CCC(C=CC=CC=CC(CC=CCCCC(O)=O)O)O)CC
Physicochemical Information
8(S),15(S)-DiHETE is formed when15(S)-HETE is subjected to further oxidation by 15-lipoxygenase Morita_E et al.;>.
Spectral Information
Mass Spectra
UV Spectra lmax: 269 nm e: 40,000
IR Spectra
NMR Spectra
Other Spectra
Chromatograms
Reported Metabolites, References
Biospecies ID Compound Name Reference Comment
n.a. LBF20407HO04 See above. Morita_E et al. 1990