LBF20406LT01: Difference between revisions
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|UV Spectra=METHYL ESTER ; <FONT FACE="Symbol">l</FONT> <SUP><FONT SIZE=-1>M</FONT></SUP><SUP><FONT SIZE=-1>e</FONT></SUP><SUP><FONT SIZE=-1>O</FONT></SUP><SUP><FONT SIZE=-1>H</FONT></SUP><SUB><FONT SIZE=-1>m</FONT></SUB><SUB><FONT SIZE=-1>a</FONT></SUB><SUB><FONT SIZE=-1>x</FONT></SUB> = 269(<FONT FACE="Symbol">e</FONT> 30,500), 278(<FONT FACE="Symbol">e</FONT> 40,000), 287(<FONT FACE="Symbol">e</FONT> 34,400) nm [[Reference:Corey_EJ:Arai_Y:Mioskowski_C:,J. Am. Chem. Soc.,1979,101,6748|{{RelationTable/GetFirstAuthor|Reference:Corey_EJ:Arai_Y:Mioskowski_C:,J. Am. Chem. Soc.,1979,101,6748}}]] | |UV Spectra=METHYL ESTER ; <FONT FACE="Symbol">l</FONT> <SUP><FONT SIZE=-1>M</FONT></SUP><SUP><FONT SIZE=-1>e</FONT></SUP><SUP><FONT SIZE=-1>O</FONT></SUP><SUP><FONT SIZE=-1>H</FONT></SUP><SUB><FONT SIZE=-1>m</FONT></SUB><SUB><FONT SIZE=-1>a</FONT></SUB><SUB><FONT SIZE=-1>x</FONT></SUB> = 269(<FONT FACE="Symbol">e</FONT> 30,500), 278(<FONT FACE="Symbol">e</FONT> 40,000), 287(<FONT FACE="Symbol">e</FONT> 34,400) nm [[Reference:Corey_EJ:Arai_Y:Mioskowski_C:,J. Am. Chem. Soc.,1979,101,6748|{{RelationTable/GetFirstAuthor|Reference:Corey_EJ:Arai_Y:Mioskowski_C:,J. Am. Chem. Soc.,1979,101,6748}}]] | ||
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Revision as of 22:00, 26 July 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 | |
|---|---|
| LipidBank | XPR3001 |
| LipidMaps | LMFA03020023 |
| CAS | |
| KEGG | {{{KEGG}}} |
| KNApSAcK | {{{KNApSAcK}}} |
| mol | LBF20406LT01 |
| LEUKOTRIENE A4 | |
|---|---|
| |
| Structural Information | |
| 5 (S) ,6 (S) -Epoxyeicosa-7 (E) ,9 (E) ,11 (Z) ,14 (Z) -tetraenoic acid | |
| |
| Formula | C20H30O3 |
| Exact Mass | 318.21949482599996 |
| Average Mass | 318.4504 |
| SMILES | C(CC=CCC=CC=CC=C[C@@H](O1)[C@@H]1CCCC(O)=O)CCC |
| Physicochemical Information | |
| SOL. IN CYCLOHEXANE,METHANOL Corey_EJ et al.. STABILITIES : to decompose to 5,12-DIHYDROXY-6,8,10,14-EICOSATETRAENOIC ACID and 5,6-DIHYDROXY-7,9,11,14-EICOSATETRAENOIC ACID under neutral aqueous solution at 37°C with one minite of half-life BorgeatPet al.. | |
| Spectral Information | |
| Mass Spectra | METHYL ESTER ; 332(M+), 316, 300, 221, 189, 181, 129, 101 Mckay_SW et al. |
| UV Spectra | METHYL ESTER ; l MeOHmax = 269(e 30,500), 278(e 40,000), 287(e 34,400) nm Corey_EJ et al. |
| IR Spectra | |
| NMR Spectra | |
| Other Spectra | |
| Chromatograms | |
| Reported Metabolites, References | |||||||||||||||||||||||||||||||||||||||||||||
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