LBF20306HO05: Difference between revisions

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|LipidBank=DFA8143
|LipidBank=DFA8143
|LipidMaps=LMFA03050011
|LipidMaps=LMFA03050011
|SysName=8S-hydroxy-9E,11Z,14Z-eicosatrienoic acid
|SysName=8S-Hydroxy- (trans-9,cis-11,cis-14) -eicosatrienoic acid
|Common Name=&&8S-hydroxy-9E,11Z,14Z-eicosatrienoic acid&&
|Common Name=&&8S-Hydroxy- (9E,11Z,14Z) -eicosatrienoic acid&&
|UV Spectra=<FONT FACE="Symbol">l</FONT>max: 235nm <FONT FACE="Symbol">e</FONT>: 23,000
|UV Spectra= lambda max: 235nm epsilon : 23,000
|Source=8(S)-HETrE is a monohydroxy polyunsaturated fatty acid produced by rabbit neutrophil lipoxygenase when dihomo-<FONT FACE="Symbol">g</FONT>-linolenic acid is used as a substrate [[Reference:Shak_S:Goldstein_IM:,J. Biol. Chem.,1984,259,10181|{{RelationTable/GetFirstAuthor|Reference:Shak_S:Goldstein_IM:,J. Biol. Chem.,1984,259,10181}}]];>.
|Source=8(S)-HETrE is a monohydroxy polyunsaturated fatty acid produced by rabbit neutrophil lipoxygenase when dihomo- &gamma; -linolenic acid is used as a substrate [[Reference:Shak_S:Goldstein_IM:,J. Biol. Chem.,1984,259,10181|{{RelationTable/GetFirstAuthor|Reference:Shak_S:Goldstein_IM:,J. Biol. Chem.,1984,259,10181}}]].
|Chemical Synthesis=
|Chemical Synthesis=
|Metabolism=
|Metabolism=
|Symbol=8(S)-HETrE
}}
}}


{{Lipid/Footer}}
{{Lipid/Footer}}

Latest revision as of 07:20, 21 October 2010

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Upper classes: LB LBF



8S-Hydroxy- (9E,11Z,14Z) -eicosatrienoic acid
LBF20306HO05.png
Structural Information
8S-Hydroxy- (trans-9,cis-11,cis-14) -eicosatrienoic acid
  • 8S-Hydroxy- (9E,11Z,14Z) -eicosatrienoic acid
8(S)-HETrE
Formula C20H34O3
Exact Mass 322.25079495399996
Average Mass 322.48216
SMILES C(CC=CCC=CC=CC(CCCCCCC(O)=O)O)CCC
Physicochemical Information
8(S)-HETrE is a monohydroxy polyunsaturated fatty acid produced by rabbit neutrophil lipoxygenase when dihomo- γ -linolenic acid is used as a substrate Shak_S et al..
Spectral Information
Mass Spectra
UV Spectra λ max: 235nm ε : 23,000
IR Spectra
NMR Spectra
Other Spectra
Chromatograms
Reported Metabolites, References
Biospecies ID Compound Name Reference Comment
n.a. LBF20306HO05 See above. Shak_S et al. 1984