LBF20406HO17: Difference between revisions

No edit summary
No edit summary
Line 9: Line 9:
|Common Name=&&11S-hydroxy-5Z,8Z,12E,14Z-eicosatetraenoic acid&&
|Common Name=&&11S-hydroxy-5Z,8Z,12E,14Z-eicosatetraenoic acid&&
|UV Spectra=<FONT FACE="Symbol">l</FONT>max: 236nm <FONT FACE="Symbol">e</FONT>: 27,000
|UV Spectra=<FONT FACE="Symbol">l</FONT>max: 236nm <FONT FACE="Symbol">e</FONT>: 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.
|Chemical Synthesis=
|Metabolism=
}}
}}


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

Revision as of 22:00, 24 November 2009

LipidBank Top
(トップ)
Fatty acid
(脂肪酸)
Glycerolipid
(グリセロ脂質)
Sphingolipid
(スフィンゴ脂質)
Journals
(雑誌一覧)
How to edit
(ページの書き方)


Upper classes: LB LBF



11S-hydroxy-5Z,8Z,12E,14Z-eicosatetraenoic acid
LBF20406HO17.png
Structural Information
11S-hydroxy-5Z,8Z,12E,14Z-eicosatetraenoic acid
  • 11S-hydroxy-5Z,8Z,12E,14Z-eicosatetraenoic acid
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 lmax: 236nm e: 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