LBF20406HO19: Difference between revisions
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|LipidBank=DFA8141 | |LipidBank=DFA8141 | ||
|LipidMaps=LMFA03060009 | |LipidMaps=LMFA03060009 | ||
|SysName=20- | |SysName=20-Hydroxy- (cis-5,cis-8,cis-11,cis-14) -eicosatetraenoic acid | ||
|Common Name=&&20- | |Common Name=&&20-Hydroxy- (5Z,8Z,11Z,14Z) -eicosatetraenoic acid&& | ||
|Source= | |Source= | ||
|Chemical Synthesis= | |Chemical Synthesis= | ||
|Metabolism=20-HETE is a cytochrome P metabolite of arachidonic acid [[Reference:Hatzelmann_A:Ullrich_V:,Eur. J. Biochem.,1988,173,445|{{RelationTable/GetFirstAuthor|Reference:Hatzelmann_A:Ullrich_V:,Eur. J. Biochem.,1988,173,445}}]] | |Metabolism=20-HETE is a cytochrome P metabolite of arachidonic acid [[Reference:Hatzelmann_A:Ullrich_V:,Eur. J. Biochem.,1988,173,445|{{RelationTable/GetFirstAuthor|Reference:Hatzelmann_A:Ullrich_V:,Eur. J. Biochem.,1988,173,445}}]]. 20-HETE can be further metabolized to 20-hydroxy prostaglandin G2 and 20-hydroxy prostaglandin H2 [[Reference:Schwartzman_ML:Falck_JR:Yadagiri_P:Escalante_B:,J. Biol. Chem.,1989,264,11658|{{RelationTable/GetFirstAuthor|Reference:Schwartzman_ML:Falck_JR:Yadagiri_P:Escalante_B:,J. Biol. Chem.,1989,264,11658}}]]. | ||
|Symbol=20-HETE | |||
}} | }} | ||
{{Lipid/Footer}} | {{Lipid/Footer}} | ||
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 | DFA8141 |
| LipidMaps | LMFA03060009 |
| CAS | |
| KEGG | {{{KEGG}}} |
| KNApSAcK | {{{KNApSAcK}}} |
| mol | LBF20406HO19 |
| 20-Hydroxy- (5Z,8Z,11Z,14Z) -eicosatetraenoic acid | |
|---|---|
| |
| Structural Information | |
| 20-Hydroxy- (cis-5,cis-8,cis-11,cis-14) -eicosatetraenoic acid | |
| |
| 20-HETE | |
| Formula | C20H32O3 |
| Exact Mass | 320.23514489 |
| Average Mass | 320.46628 |
| SMILES | C(CCC=CCC=CCC=CCC=CCCCC(O)=O)CCO |
| Physicochemical Information | |
| 20-HETE is a cytochrome P metabolite of arachidonic acid Hatzelmann_A et al.. 20-HETE can be further metabolized to 20-hydroxy prostaglandin G2 and 20-hydroxy prostaglandin H2 Schwartzman_ML et al.. | |
| Spectral Information | |
| Mass Spectra | |
| UV Spectra | |
| IR Spectra | |
| NMR Spectra | |
| Other Spectra | |
| Chromatograms | |
| Reported Metabolites, References | |||||||||||||||
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