LBF20407HO04: Difference between revisions

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{{Metabolite
{{Metabolite
|LipidBank=DFA8105
|LipidBank=DFA8105
|LipidMaps=-
|LipidMaps=LMFA03060050
|SysName=8S,15S-dihydroxy-5Z,9E,11Z,13E-eicosatetraenoic acid
|SysName=8S,15S-dihydroxy-5Z,9E,11Z,13E-eicosatetraenoic acid
|Common Name=&&8S,15S-dihydroxy-5Z,9E,11Z,13E-eicosatetraenoic acid&&
|Common Name=&&8S,15S-dihydroxy-5Z,9E,11Z,13E-eicosatetraenoic acid&&

Revision as of 02:59, 12 March 2010

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Fatty acid
(脂肪酸)
Glycerolipid
(グリセロ脂質)
Sphingolipid
(スフィンゴ脂質)
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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
8(S),15(S)-DiHETE
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..
8(S),15(S)-diHETE causes chemotaxis of human eosinophils with an ED _{50} of 1.5 mu M but is not chemotactic for neutrophils Morita_E et al.. 8(S),15(S)-diHETE exhibits hypoalgesic activity by antagonizing the hyperalgesic activity of 8(R),15(S)-diHETE and LTB 4 when measuring nociceptive activity in the rat hindpaw model of pain Oliw_EH .
Spectral Information
Mass Spectra
UV Spectra λ max: 269 nm ε : 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