LBF20306HO02: Difference between revisions

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|Chemical Synthesis=
|Chemical Synthesis=
|Metabolism=
|Metabolism=
|Symbol=(±)8,9-DiHETrE
|Biological Activity=Epoxide hydrolases convert the EpETrEs into vicinal diols[[Reference:Oliw_EH:Guengerich_FP:Oates_JA:,J. Biol. Chem.,1982,257,3771|{{RelationTable/GetFirstAuthor|Reference:Oliw_EH:Guengerich_FP:Oates_JA:,J. Biol. Chem.,1982,257,3771}}]], with the concurrent loss of much of their biological activity. The 8(S),9(R)-EpETrE isomer is metabolized by platelet cyclooxygenase to form 8(S),9(R)-THETA, a trihydroxy fatty acid which may act as a renal vasoconstrictor[[Reference:Zhang_JY:Prakash_C:Yamashita_K:Blair_IA:,Biochem. Biophys. Res. Commun.,1992,183,138|{{RelationTable/GetFirstAuthor|Reference:Zhang_JY:Prakash_C:Yamashita_K:Blair_IA:,Biochem. Biophys. Res. Commun.,1992,183,138}}]].
}}
}}


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{{Lipid/Footer}}

Revision as of 21:00, 6 January 2010

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(脂肪酸)
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Upper classes: LB LBF



(+-) 8,9-dihydroxy-5Z,11Z,14Z-eicosatrienoic acid
LBF20306HO02.png
Structural Information
(+-) 8,9-dihydroxy-5Z,11Z,14Z-eicosatrienoic acid
  • (+-) 8,9-dihydroxy-5Z,11Z,14Z-eicosatrienoic acid
(±)8,9-DiHETrE
Formula C20H34O4
Exact Mass 338.24570957599997
Average Mass 338.48156
SMILES C(CC=CCC=CCC(O)C(O)CC=CCCCC(O)=O)CCC
Physicochemical Information
Epoxide hydrolases convert the EpETrEs into vicinal diols Oliw_EH et al., with the concurrent loss of much of their biological activity. The 8(S),9(R)-EpETrE isomer is metabolized by platelet cyclooxygenase to form 8(S),9(R)-THETA, a trihydroxy fatty acid which may act as a renal vasoconstrictor Zhang_JY et al..
Spectral Information
Mass Spectra
UV Spectra
IR Spectra
NMR Spectra
Other Spectra
Chromatograms
Reported Metabolites, References
Biospecies ID Compound Name Reference Comment
n.a. LBF20306HO02 See above. Oliw_EH et al. 1982
n.a. LBF20306HO02 See above. Zhang_JY et al. 1992