LBF20207PG50: Difference between revisions

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|LipidBank=XPR8048
|LipidBank=XPR8048
|LipidMaps=LMFA03010094
|LipidMaps=LMFA03010094
|SysName= (5Z, 13E) - (8R,11R,12R,15R) -11,15-dihydroxy-9-oxoprost-5,13-dienoic acid
|SysName=(cis-5,trans-13) - (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_2  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_2  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=

Latest revision as of 08:37, 21 October 2010

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Upper classes: LB LBF



15-epi Prostaglandin E2 acetate, methyl ester
LBF20207PG50.png
Structural Information
(cis-5,trans-13) - (8R,11R,12R,15R) -11,15-Dihydroxy-9-oxoprost-5,13-dienoic acid
  • 15-epi Prostaglandin E2 acetate, methyl ester
  • (5Z, 13E) - (8R,11R,12R,15R) -11,15-Dihydroxy-9-oxoprost-5,13-dienoic acid
(15R)-PGE_2
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 E_2 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
Biospecies ID Compound Name Reference Comment
n.a. LBF20207PG50 See above. Light_RJ et al. 1972