LBF20406HO07: Difference between revisions
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|Source=5S,6R-DiHETE is a dihydroxy polyunsaturated fatty acid and a nonenzymatic hydrolysis product of leukotriene A 4 . | |Source=5S,6R-DiHETE is a dihydroxy polyunsaturated fatty acid and a nonenzymatic hydrolysis product of leukotriene A 4 . | ||
|Chemical Synthesis= | |Chemical Synthesis= | ||
|Metabolism=Mouse liver cytosolic epoxide hydrolase catalyzes the conversion of LTA to 5,6-DiHETE[[Reference:Haeggstrom_J:Wetterholm_A:Hamberg_M:Meijer_J:Zipkin_R:Radmark_O:,Biochim. Biophys. Acta,1988,958,469|{{RelationTable/GetFirstAuthor|Reference:Haeggstrom_J:Wetterholm_A:Hamberg_M:Meijer_J:Zipkin_R:Radmark_O:,Biochim. Biophys. Acta,1988,958,469}}]] | |Metabolism=Mouse liver cytosolic epoxide hydrolase catalyzes the conversion of LTA to 5,6-DiHETE[[Reference:Haeggstrom_J:Wetterholm_A:Hamberg_M:Meijer_J:Zipkin_R:Radmark_O:,Biochim. Biophys. Acta,1988,958,469|{{RelationTable/GetFirstAuthor|Reference:Haeggstrom_J:Wetterholm_A:Hamberg_M:Meijer_J:Zipkin_R:Radmark_O:,Biochim. Biophys. Acta,1988,958,469}}]]. | ||
}} | }} | ||
{{Lipid/Footer}} | {{Lipid/Footer}} |
Revision as of 11:55, 25 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) |
IDs and Links | |
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LipidBank | DFA8102 |
LipidMaps | - |
CAS | |
KEGG | {{{KEGG}}} |
KNApSAcK | {{{KNApSAcK}}} |
mol | LBF20406HO07 |
5S,6R-dihydroxy-7E,9E,11Z,14Z-eicosatetraenoic acid | |
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Structural Information | |
5S,6R-dihydroxy-7E,9E,11Z,14Z-eicosatetraenoic acid | |
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Formula | C20H32O4 |
Exact Mass | 336.23005951199997 |
Average Mass | 336.46567999999996 |
SMILES | C(CC=CCC=CC=CC=C[C@@H](O)[C@@H](O)CCCC(O)=O)CCC |
Physicochemical Information | |
Soluble in ethanol. | |
5S,6R-DiHETE is a dihydroxy polyunsaturated fatty acid and a nonenzymatic hydrolysis product of leukotriene A 4 . | |
Mouse liver cytosolic epoxide hydrolase catalyzes the conversion of LTA to 5,6-DiHETE Haeggstrom_J et al.. | |
Spectral Information | |
Mass Spectra | |
UV Spectra | lmax:273nm e:40,000 |
IR Spectra | |
NMR Spectra | |
Other Spectra | |
Chromatograms |
Reported Metabolites, References | |||||||||||||||
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