LBF20406HO17: Difference between revisions
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|LipidBank=DFA8135 | |LipidBank=DFA8135 | ||
|LipidMaps=- | |LipidMaps=- | ||
|SysName=11S- | |SysName=11S-Hydroxy- (cis-5,cis-8,trans-12,cis-14) -eicosatetraenoic acid | ||
|Common Name=&&11S- | |Common Name=&&11S-Hydroxy- (5Z,8Z,12E,14Z) -eicosatetraenoic acid&& | ||
|UV Spectra= | |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. | ||
|Chemical Synthesis= | |Chemical Synthesis= | ||
Latest revision as of 07:27, 21 October 2010
| 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) |
| IDs and Links | |
|---|---|
| LipidBank | DFA8135 |
| LipidMaps | - |
| CAS | |
| KEGG | {{{KEGG}}} |
| KNApSAcK | {{{KNApSAcK}}} |
| mol | LBF20406HO17 |
| 11S-Hydroxy- (5Z,8Z,12E,14Z) -eicosatetraenoic acid | |
|---|---|
| |
| Structural Information | |
| 11S-Hydroxy- (cis-5,cis-8,trans-12,cis-14) -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 | ||||||||||
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