LBF20308PG03: Difference between revisions
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|IR Spectra=<FONT FACE="Symbol">n</FONT> : 2930, 1700, 1640, 1580, 1232, 028 cm<SUP><FONT SIZE=-1>-</FONT></SUP><SUP><FONT SIZE=-1>1</FONT></SUP> [[Reference:Kikawa_Y:Narumiya_S:Fukushima_M:Wakatsuka_H:Hayaishi_O:,Proc. Natl. Acad. Sci. U. S. A.,1984,81,1317|{{RelationTable/GetFirstAuthor|Reference:Kikawa_Y:Narumiya_S:Fukushima_M:Wakatsuka_H:Hayaishi_O:,Proc. Natl. Acad. Sci. U. S. A.,1984,81,1317}}]] | |IR Spectra=<FONT FACE="Symbol">n</FONT> : 2930, 1700, 1640, 1580, 1232, 028 cm<SUP><FONT SIZE=-1>-</FONT></SUP><SUP><FONT SIZE=-1>1</FONT></SUP> [[Reference:Kikawa_Y:Narumiya_S:Fukushima_M:Wakatsuka_H:Hayaishi_O:,Proc. Natl. Acad. Sci. U. S. A.,1984,81,1317|{{RelationTable/GetFirstAuthor|Reference:Kikawa_Y:Narumiya_S:Fukushima_M:Wakatsuka_H:Hayaishi_O:,Proc. Natl. Acad. Sci. U. S. A.,1984,81,1317}}]] | ||
|NMR Spectra=<SUP><FONT SIZE=-1>1</FONT></SUP>H-NMR(CDCl<SUB><FONT SIZE=-1>3</FONT></SUB>) : <FONT FACE="Symbol">d</FONT> 7.5(dd, 1H, 9-CH), 6.56(t, 1H, 13-CH), 6.35(dd,1 H, 10-CH), 5.48(m, 2H, 5,6-CH), 3.88(m, 1H, 15-CH), 3.44(m, 1H, 8-CH) [[Reference:Kikawa_Y:Narumiya_S:Fukushima_M:Wakatsuka_H:Hayaishi_O:,Proc. Natl. Acad. Sci. U. S. A.,1984,81,1317|{{RelationTable/GetFirstAuthor|Reference:Kikawa_Y:Narumiya_S:Fukushima_M:Wakatsuka_H:Hayaishi_O:,Proc. Natl. Acad. Sci. U. S. A.,1984,81,1317}}]] | |NMR Spectra=<SUP><FONT SIZE=-1>1</FONT></SUP>H-NMR(CDCl<SUB><FONT SIZE=-1>3</FONT></SUB>) : <FONT FACE="Symbol">d</FONT> 7.5(dd, 1H, 9-CH), 6.56(t, 1H, 13-CH), 6.35(dd,1 H, 10-CH), 5.48(m, 2H, 5,6-CH), 3.88(m, 1H, 15-CH), 3.44(m, 1H, 8-CH) [[Reference:Kikawa_Y:Narumiya_S:Fukushima_M:Wakatsuka_H:Hayaishi_O:,Proc. Natl. Acad. Sci. U. S. A.,1984,81,1317|{{RelationTable/GetFirstAuthor|Reference:Kikawa_Y:Narumiya_S:Fukushima_M:Wakatsuka_H:Hayaishi_O:,Proc. Natl. Acad. Sci. U. S. A.,1984,81,1317}}]] | ||
|Source= | |||
|Chemical Synthesis=[[Reference:Bundy_GL:Morton_DR:Peterson_DC:Nishizawa_EE:Miller_WL:,J. Med. Chem.,1983,26,790|{{RelationTable/GetFirstAuthor|Reference:Bundy_GL:Morton_DR:Peterson_DC:Nishizawa_EE:Miller_WL:,J. Med. Chem.,1983,26,790}}]];> {{Image200|XPR1911FT0001.gif}} | |||
|Metabolism=In human plasma prostaglandin D2 is dehydrated and converted to 9-deoxy-<FONT FACE="Symbol">D</FONT>9,12-13,14-dihydro-prostaglandin D2 (<FONT FACE="Symbol">D</FONT>12-prostaglandin J2) catalyzedby serum albumin [[Reference:Narumiya_S:Fukushima_M:,Biochem. Biophys. Res. Commun.,1985,127,739|{{RelationTable/GetFirstAuthor|Reference:Narumiya_S:Fukushima_M:,Biochem. Biophys. Res. Commun.,1985,127,739}}]];>. | |||
}} | }} | ||
{{Lipid/Footer}} | {{Lipid/Footer}} |
Revision as of 22:00, 24 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 | XPR1911 |
LipidMaps | - |
CAS | |
KEGG | {{{KEGG}}} |
KNApSAcK | {{{KNApSAcK}}} |
mol | LBF20308PG03 |
7- [ 2 (E) - (3 (S) -Hydroxyoctylidene) -3-oxo-4-cyclopenten-1 (R) -yl ] -5 (Z) -heptenoic acid | |
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Structural Information | |
7- [ 2 (E) - (3 (S) -Hydroxyoctylidene) -3-oxo-4-cyclopenten-1 (R) -yl ] -5 (Z) -heptenoic acid | |
| |
Formula | C20H30O4 |
Exact Mass | 334.21440944799997 |
Average Mass | 334.4498 |
SMILES | C(CC[C@@H](O)CC=C(C(=O)1)[C@@H](CC=CCCCC(O)=O)C=C1)CC |
Physicochemical Information | |
METHANOL Fitzpatrick_FA et al.ETHANOL, CHLOROFORM, ETHYL ACETATE KikawaYet al. | |
Bundy_GL et al.;> File:XPR1911FT0001.gif | |
In human plasma prostaglandin D2 is dehydrated and converted to 9-deoxy-D9,12-13,14-dihydro-prostaglandin D2 (D12-prostaglandin J2) catalyzedby serum albumin Narumiya_S et al.;>. | |
Spectral Information | |
Mass Spectra | m/e 334(M+), 316, 245, 236 KikawaYet al. |
UV Spectra | l EtOHmax = 244(e 6100)nm KikawaYet al. |
IR Spectra | n : 2930, 1700, 1640, 1580, 1232, 028 cm-1 KikawaYet al. |
NMR Spectra | 1H-NMR(CDCl3) : d 7.5(dd, 1H, 9-CH), 6.56(t, 1H, 13-CH), 6.35(dd,1 H, 10-CH), 5.48(m, 2H, 5,6-CH), 3.88(m, 1H, 15-CH), 3.44(m, 1H, 8-CH) KikawaYet al. |
Other Spectra | |
Chromatograms |
Reported Metabolites, References | ||||||||||||||||||||||||||||||
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