LBF20303PG05: Difference between revisions
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|LipidBank=XPR1705 | |LipidBank=XPR1705 | ||
|LipidMaps=LMFA03010142 | |LipidMaps=LMFA03010142 | ||
|SysName=9alpha,15S- | |SysName=(9alpha,15S) -Dihydroxy-11-oxo-prosta- (cis-5,trans-13,cis-17) -trien-1-oic acid | ||
|Common Name=&&Prostaglandin D_3&&9alpha,15S- | |Common Name=&&Prostaglandin D_3&&(9alpha,15S) -Dihydroxy-11-oxo-prosta- (5Z,13E,17Z) -trien-1-oic acid&& | ||
|Source=PGD3 is produced by the metabolism of EPA via the cyclooxygenase pathway.[[Reference:Kulkarni_PS:Kaufman_PL:Srinivasan_BD:,J. Ocul. Pharmacol.,1987,3,349|{{RelationTable/GetFirstAuthor|Reference:Kulkarni_PS:Kaufman_PL:Srinivasan_BD:,J. Ocul. Pharmacol.,1987,3,349}}]] | |Source=PGD3 is produced by the metabolism of EPA via the cyclooxygenase pathway.[[Reference:Kulkarni_PS:Kaufman_PL:Srinivasan_BD:,J. Ocul. Pharmacol.,1987,3,349|{{RelationTable/GetFirstAuthor|Reference:Kulkarni_PS:Kaufman_PL:Srinivasan_BD:,J. Ocul. Pharmacol.,1987,3,349}}]] | ||
|Chemical Synthesis= | |Chemical Synthesis= | ||
|Metabolism= | |Metabolism= | ||
|Biological Activity=PGD3 has almost same ability to decrease systemic blood pressure in rats and to decrease intraocular pressure in rabbits.[[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}}]][[Reference:Goh_Y:Nakajima_M:Azuma_I:Hayaishi_O:,Jpn. J. Ophthalmol.,1988,32,471|{{RelationTable/GetFirstAuthor|Reference:Goh_Y:Nakajima_M:Azuma_I:Hayaishi_O:,Jpn. J. Ophthalmol.,1988,32,471}}]][[Reference:Kulkarni_PS:Srinivasan_BD:,Invest. Ophthalmol. Vis. Sci.,1985,26,1178|{{RelationTable/GetFirstAuthor|Reference:Kulkarni_PS:Srinivasan_BD:,Invest. Ophthalmol. Vis. Sci.,1985,26,1178}}]] However, it is 3 to 5 times more potent than PGD2 in the inhibition of ADP-induced human platelet aggregation.[[Reference:Herschman_HR:,Biochim._Biophys._Acta,1996,1299,125|{{RelationTable/GetFirstAuthor|Reference:Herschman_HR:,Biochim._Biophys._Acta,1996,1299,125}}]] [[Reference:Smith_WL:Garavito_RM:DeWitt_DL:,J. Biol. Chem.,1996,271,33157|{{RelationTable/GetFirstAuthor|Reference:Smith_WL:Garavito_RM:DeWitt_DL:,J. Biol. Chem.,1996,271,33157}}]] | |||
}} | }} | ||
{{Lipid/Footer}} | {{Lipid/Footer}} | ||
Latest revision as of 15:39, 8 November 2010
| 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 | |
|---|---|
| LipidBank | XPR1705 |
| LipidMaps | LMFA03010142 |
| CAS | |
| KEGG | {{{KEGG}}} |
| KNApSAcK | {{{KNApSAcK}}} |
| mol | LBF20303PG05 |
| Prostaglandin D3 | |
|---|---|
| |
| Structural Information | |
| (9α,15S) -Dihydroxy-11-oxo-prosta- (cis-5,trans-13,cis-17) -trien-1-oic acid | |
| |
| Formula | C20H30O5 |
| Exact Mass | 350.20932407 |
| Average Mass | 350.4492 |
| SMILES | C(=CC[C@@H](O)C=C[C@H]([C@H]1CC=CCCCC(O)=O)C(C[C@@H]1O)=O)CC |
| Physicochemical Information | |
| PGD3 is produced by the metabolism of EPA via the cyclooxygenase pathway. Kulkarni_PS et al. | |
| PGD3 has almost same ability to decrease systemic blood pressure in rats and to decrease intraocular pressure in rabbits. Bundy_GL et al. Goh_Y et al. Kulkarni_PS et al. However, it is 3 to 5 times more potent than PGD2 in the inhibition of ADP-induced human platelet aggregation. Herschman_HR Smith_WL et al. | |
| Spectral Information | |
| Mass Spectra | |
| UV Spectra | |
| IR Spectra | |
| NMR Spectra | |
| Other Spectra | |
| Chromatograms | |
| Reported Metabolites, References | |||||||||||||||||||||||||||||||||||
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