LBF20307PG02: Difference between revisions
No edit summary |
No edit summary |
||
| Line 6: | Line 6: | ||
|SysName=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 | |SysName=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 | ||
|Common Name=&&19-HYDROXY-PROSTAGLANDIN A2&& | |Common Name=&&19-HYDROXY-PROSTAGLANDIN A2&& | ||
|Solubility=DIETHYL ETHER, CHLOROFORM, ETHANOL | |Solubility=DIETHYL ETHER, CHLOROFORM, ETHANOL [[Reference:Hamberg_M:Samuelsson_B:,J. Biol. Chem.,1966,241,257|{{RelationTable/GetFirstAuthor|Reference:Hamberg_M:Samuelsson_B:,J. Biol. Chem.,1966,241,257}}]] | ||
|Mass Spectra=METHYL ESTER ; m/e 364(M<SUP><FONT SIZE=-1>+</FONT></SUP>), 246, 328, 315 | |Mass Spectra=METHYL ESTER ; m/e 364(M<SUP><FONT SIZE=-1>+</FONT></SUP>), 246, 328, 315 [[Reference:Hamberg_M:Samuelsson_B:,J. Biol. Chem.,1966,241,257|{{RelationTable/GetFirstAuthor|Reference:Hamberg_M:Samuelsson_B:,J. Biol. Chem.,1966,241,257}}]] | ||
|UV Spectra=<FONT FACE="Symbol">l</FONT> <SUP><FONT SIZE=-1>E</FONT></SUP><SUP><FONT SIZE=-1>t</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> = 217 nm(<FONT FACE="Symbol">e</FONT> ˜10,000) | |UV Spectra=<FONT FACE="Symbol">l</FONT> <SUP><FONT SIZE=-1>E</FONT></SUP><SUP><FONT SIZE=-1>t</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> = 217 nm(<FONT FACE="Symbol">e</FONT> ˜10,000) [[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 | |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) | |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}}]] | ||
}} | }} | ||
Revision as of 09:00, 12 December 2008
| IDs and Links | |
|---|---|
| LipidBank | XPR1031 |
| LipidMaps | LMFA03010130 |
| CAS | |
| KEGG | {{{KEGG}}} |
| KNApSAcK | {{{KNApSAcK}}} |
| mol | LBF20307PG02 |
| 19-HYDROXY-PROSTAGLANDIN A2 | |
|---|---|
| |
| 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 | |
| |
| 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. | |
| 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 | |||||||||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
