LBF20207PG50: Difference between revisions
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|SysName= (5Z, 13E) - (8R,11R,12R,15R) -11,15-dihydroxy-9-oxoprost-5,13-dienoic acid | |SysName= (5Z, 13E) - (8R,11R,12R,15R) -11,15-dihydroxy-9-oxoprost-5,13-dienoic acid | ||
|Common Name=&&15-epi-prostaglandin E_2 acetate, methyl ester&&(5Z, 13E) - (8R,11R,12R,15R) -11,15-dihydroxy-9-oxoprost-5,13-dienoic acid&& | |Common Name=&&15-epi-prostaglandin E_2 acetate, methyl ester&&(5Z, 13E) - (8R,11R,12R,15R) -11,15-dihydroxy-9-oxoprost-5,13-dienoic acid&& | ||
|Source=15-Epi-prostaglandin E<SUB><FONT SIZE=-1>2</FONT></SUB> and its methyl ester were isolated from Gorgonian, Plexaura homomalla.[[Reference:Light_RJ:Samuelsson_B:,Eur. J. Biochem.,1972,28,232|{{RelationTable/GetFirstAuthor|Reference:Light_RJ:Samuelsson_B:,Eur. J. Biochem.,1972,28,232}}]] | |Source=15-Epi-prostaglandin E<SUB><FONT SIZE=-1>2</FONT></SUB> and its methyl ester were isolated from Gorgonian, Plexaura homomalla.[[Reference:Light_RJ:Samuelsson_B:,Eur. J. Biochem.,1972,28,232|{{RelationTable/GetFirstAuthor|Reference:Light_RJ:Samuelsson_B:,Eur. J. Biochem.,1972,28,232}}]] | ||
|Chemical Synthesis= | |Chemical Synthesis= | ||
|Metabolism= | |Metabolism= |
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 | XPR8048 |
LipidMaps | LMFA03010094 |
CAS | |
KEGG | {{{KEGG}}} |
KNApSAcK | {{{KNApSAcK}}} |
mol | LBF20207PG50 |
15-epi-prostaglandin E2acetate, methyl ester | |
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Structural Information | |
(5Z, 13E) - (8R,11R,12R,15R) -11,15-dihydroxy-9-oxoprost-5,13-dienoic acid | |
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Formula | C20H32O5 |
Exact Mass | 352.224974134 |
Average Mass | 352.46508 |
SMILES | C(CC[C@@H](O)C=C[C@H]([C@H]1CC=CCCCC(O)=O)[C@@H](CC1=O)O)CC |
Physicochemical Information | |
15-Epi-prostaglandin E2 and its methyl ester were isolated from Gorgonian, Plexaura homomalla. Light_RJ et al. | |
Spectral Information | |
Mass Spectra | |
UV Spectra | |
IR Spectra | |
NMR Spectra | |
Other Spectra | |
Chromatograms |
Reported Metabolites, References | ||||||||||
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