LBF20406HO17: Difference between revisions

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|LipidBank=DFA8135
|LipidBank=DFA8135
|LipidMaps=-
|LipidMaps=-
|SysName=11S-hydroxy-5Z,8Z,12E,14Z-eicosatetraenoic acid
|SysName=11S-Hydroxy- (cis-5,cis-8,trans-12,cis-14) -eicosatetraenoic acid
|Common Name=&&11S-hydroxy-5Z,8Z,12E,14Z-eicosatetraenoic acid&&
|Common Name=&&11S-Hydroxy- (5Z,8Z,12E,14Z) -eicosatetraenoic acid&&
|UV Spectra= lambda max: 236nm  epsilon : 27,000
|UV Spectra= lambda max: 236nm  epsilon : 27,000
|Source=The synthesis of 11-HETE by rat polymorphonuclear neutrophils has been reported [[Reference:Myers_RF:Siegel_MI:,Biochem. Biophys. Res. Commun.,1983,112,586|{{RelationTable/GetFirstAuthor|Reference:Myers_RF:Siegel_MI:,Biochem. Biophys. Res. Commun.,1983,112,586}}]], but the stereochemistry of the 11-HETE produced was not defined.
|Source=The synthesis of 11-HETE by rat polymorphonuclear neutrophils has been reported [[Reference:Myers_RF:Siegel_MI:,Biochem. Biophys. Res. Commun.,1983,112,586|{{RelationTable/GetFirstAuthor|Reference:Myers_RF:Siegel_MI:,Biochem. Biophys. Res. Commun.,1983,112,586}}]], but the stereochemistry of the 11-HETE produced was not defined.

Latest revision as of 07:27, 21 October 2010

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Upper classes: LB LBF



11S-Hydroxy- (5Z,8Z,12E,14Z) -eicosatetraenoic acid
LBF20406HO17.png
Structural Information
11S-Hydroxy- (cis-5,cis-8,trans-12,cis-14) -eicosatetraenoic acid
  • 11S-Hydroxy- (5Z,8Z,12E,14Z) -eicosatetraenoic acid
11(S)-HETE
Formula C20H32O3
Exact Mass 320.23514489
Average Mass 320.46628
SMILES C(CC=CC=C[C@H](CC=CCC=CCCCC(O)=O)O)CCC
Physicochemical Information
The synthesis of 11-HETE by rat polymorphonuclear neutrophils has been reported Myers_RF et al., but the stereochemistry of the 11-HETE produced was not defined.
Spectral Information
Mass Spectra
UV Spectra λ max: 236nm ε : 27,000
IR Spectra
NMR Spectra
Other Spectra
Chromatograms
Reported Metabolites, References
Biospecies ID Compound Name Reference Comment
n.a. LBF20406HO17 See above. Myers_RF et al. 1983