LBF20307PG02: Difference between revisions

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|IR Spectra= 5.87, 6.30, 10.3<FONT FACE="Symbol">m</FONT>m [[Reference:Hamberg_M:Samuelsson_B:,J. Biol. Chem.,1966,241,257|{{RelationTable/GetFirstAuthor|Reference:Hamberg_M:Samuelsson_B:,J. Biol. Chem.,1966,241,257}}]]
|IR Spectra= 5.87, 6.30, 10.3<FONT FACE="Symbol">m</FONT>m [[Reference:Hamberg_M:Samuelsson_B:,J. Biol. Chem.,1966,241,257|{{RelationTable/GetFirstAuthor|Reference:Hamberg_M:Samuelsson_B:,J. Biol. Chem.,1966,241,257}}]]
|NMR Spectra=<SUP><FONT SIZE=-1>1</FONT></SUP>H-NMR : <FONT FACE="Symbol">d</FONT> 5.75-5.50(m, 2H,13, 14-CH), 5.50-5.25(m, 2H, 5,6-CH), 1.15(d, 3H, 20-CH) [[Reference:Hamberg_M:Samuelsson_B:,J. Biol. Chem.,1966,241,257|{{RelationTable/GetFirstAuthor|Reference:Hamberg_M:Samuelsson_B:,J. Biol. Chem.,1966,241,257}}]]
|NMR Spectra=<SUP><FONT SIZE=-1>1</FONT></SUP>H-NMR : <FONT FACE="Symbol">d</FONT> 5.75-5.50(m, 2H,13, 14-CH), 5.50-5.25(m, 2H, 5,6-CH), 1.15(d, 3H, 20-CH) [[Reference:Hamberg_M:Samuelsson_B:,J. Biol. Chem.,1966,241,257|{{RelationTable/GetFirstAuthor|Reference:Hamberg_M:Samuelsson_B:,J. Biol. Chem.,1966,241,257}}]]
|Source=The compound is contained in human seminal plasma in a considerable amount [[Reference:Bergstrom_S:,Science,1967,157,382|{{RelationTable/GetFirstAuthor|Reference:Bergstrom_S:,Science,1967,157,382}}]];>, but it is attributed presumably to a degradation product of 19-hydroxy-prostagaldnin E2 [[Reference:Taylor_PL:Kelly_RW:,Nature,1974,250,665|{{RelationTable/GetFirstAuthor|Reference:Taylor_PL:Kelly_RW:,Nature,1974,250,665}}]];>.
|Source=The compound is contained in human seminal plasma in a considerable amount [[Reference:Bergstrom_S:,Science,1967,157,382|{{RelationTable/GetFirstAuthor|Reference:Bergstrom_S:,Science,1967,157,382}}]], but it is attributed presumably to a degradation product of 19-hydroxy-prostagaldnin E2 [[Reference:Taylor_PL:Kelly_RW:,Nature,1974,250,665|{{RelationTable/GetFirstAuthor|Reference:Taylor_PL:Kelly_RW:,Nature,1974,250,665}}]].
|Chemical Synthesis=
|Chemical Synthesis=
|Metabolism=
|Metabolism=

Revision as of 11:55, 25 November 2009

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Upper classes: LB LBF



19-HYDROXY-PROSTAGLANDIN A2
LBF20307PG02.png
Structural Information
7- [ 2 (R) - (3 (S) ,7-Dihydroxy-1 (E) -octenyl) -5-oxo-3-cyclopenten-1 (R) -yl ] -5 (Z) -heptenoic acid / 15 (S) ,19-Dihydroxy-9-oxo-8 (12) ,13-trans-prostadienoic acid
  • 19-HYDROXY-PROSTAGLANDIN A2
  • 7- [ 2 (R) - (3 (S) ,7-Dihydroxy-1 (E) -octenyl) -5-oxo-3-cyclopenten-1 (R) -yl ] -5 (Z) -heptenoic acid
  • 15 (S) ,19-Dihydroxy-9-oxo-8 (12) ,13-trans-prostadienoic acid
Formula C20H30O5
Exact Mass 350.20932407
Average Mass 350.4492
SMILES O[C@H](CCC[C@H](C)O)C=C[C@H]([C@H]1CC=CCCCC(O)=O)C=CC(=O)1
Physicochemical Information
DIETHYL ETHER, CHLOROFORM, ETHANOL HambergMet al.
The compound is contained in human seminal plasma in a considerable amount Bergstrom_S , but it is attributed presumably to a degradation product of 19-hydroxy-prostagaldnin E2 Taylor_PL et al..
Spectral Information
Mass Spectra METHYL ESTER ; m/e 364(M+), 246, 328, 315 HambergMet al.
UV Spectra l EtOHmax = 217 nm(e ?10,000) HambergMet al.
IR Spectra 5.87, 6.30, 10.3mm HambergMet al.
NMR Spectra 1H-NMR : d 5.75-5.50(m, 2H,13, 14-CH), 5.50-5.25(m, 2H, 5,6-CH), 1.15(d, 3H, 20-CH) HambergMet al.
Other Spectra
Chromatograms
Reported Metabolites, References
Biospecies ID Compound Name Reference Comment
n.a. LBF20307PG02 See above. Bergstrom_S 1967
n.a. LBF20307PG02 See above. Hamberg_M et al. 1966
n.a. LBF20307PG02 See above. Horton_EW 1969
n.a. LBF20307PG02 See above. Taylor_PL et al. 1974