LBF16000PG01: Difference between revisions

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|Solubility=ETHYL ACETATE [[Reference:Hamberg_M:Samuelsson_B:,J. Am. Chem. Soc.,1969,91,2177|{{RelationTable/GetFirstAuthor|Reference:Hamberg_M:Samuelsson_B:,J. Am. Chem. Soc.,1969,91,2177}}]]
|Solubility=ETHYL ACETATE [[Reference:Hamberg_M:Samuelsson_B:,J. Am. Chem. Soc.,1969,91,2177|{{RelationTable/GetFirstAuthor|Reference:Hamberg_M:Samuelsson_B:,J. Am. Chem. Soc.,1969,91,2177}}]]
|Mass Spectra=DIMETHYL ESTER DI-O-METHYLOXIME TMS ETHER DERIVATIVE ; m/e 486, 455, 369, 365, 355, 286, 279, 268, 265, 196, 115 [[Reference:Hamberg_M:Samuelsson_B:,J. Am. Chem. Soc.,1969,91,2177|{{RelationTable/GetFirstAuthor|Reference:Hamberg_M:Samuelsson_B:,J. Am. Chem. Soc.,1969,91,2177}}]]
|Mass Spectra=DIMETHYL ESTER DI-O-METHYLOXIME TMS ETHER DERIVATIVE ; m/e 486, 455, 369, 365, 355, 286, 279, 268, 265, 196, 115 [[Reference:Hamberg_M:Samuelsson_B:,J. Am. Chem. Soc.,1969,91,2177|{{RelationTable/GetFirstAuthor|Reference:Hamberg_M:Samuelsson_B:,J. Am. Chem. Soc.,1969,91,2177}}]]
|Source=When prostaglandin E2 or E1 was administered intravenously to man, 7<FONT FACE="Symbol">a</FONT>-hydroxy-5,11-diketo-tetranor-prosta-1,16-dioic acid was found as a major urinary metabolite (PGE-MUM) [[Reference:Hamberg_M:Samuelsson_B:,J. Biol. Chem.,1971,246,6713|{{RelationTable/GetFirstAuthor|Reference:Hamberg_M:Samuelsson_B:,J. Biol. Chem.,1971,246,6713}}]];>.
|Chemical Synthesis=
|Metabolism=
}}
}}


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{{Lipid/Footer}}

Revision as of 22:00, 24 November 2009

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Upper classes: LB LBF



8-[2(R)-(2-Carboxyethyl)-5(R)-hydroxy-3-oxocyclopentan-1(R)-yl]-6-oxooctanoic acid
LBF16000PG01.png
Structural Information
8-[2(R)-(2-Carboxyethyl)-5(R)-hydroxy-3-oxocyclopentan-1(R)-yl]-6-oxooctanoic acid
  • 8-[2(R)-(2-Carboxyethyl)-5(R)-hydroxy-3-oxocyclopentan-1(R)-yl]-6-oxooctanoic acid
Formula C16H24O7
Exact Mass 328.152203122
Average Mass 328.35756000000003
SMILES OC(=O)CCCCC(=O)CC[C@@H]([C@H](O)1)[C@@H](CCC(O)=O)C(=O)C1
Physicochemical Information
ETHYL ACETATE HambergMet al.
When prostaglandin E2 or E1 was administered intravenously to man, 7a-hydroxy-5,11-diketo-tetranor-prosta-1,16-dioic acid was found as a major urinary metabolite (PGE-MUM) Hamberg_M et al.;>.
Spectral Information
Mass Spectra DIMETHYL ESTER DI-O-METHYLOXIME TMS ETHER DERIVATIVE ; m/e 486, 455, 369, 365, 355, 286, 279, 268, 265, 196, 115 HambergMet al.
UV Spectra
IR Spectra
NMR Spectra
Other Spectra
Chromatograms
Reported Metabolites, References
Biospecies ID Compound Name Reference Comment
n.a. LBF16000PG01 See above. Hamberg_M et al. 1969
n.a. LBF16000PG01 See above. Hamberg_M et al. 1971