LBF20307PG04: Difference between revisions
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|LipidBank=XPR1131 | |LipidBank=XPR1131 | ||
|LipidMaps=LMFA03010132 | |LipidMaps=LMFA03010132 | ||
|SysName=7- [ | |SysName=7- [2R- ((3S,7)-Dihydroxy-1-trans-octenyl) -5-oxo-1-cyclopenten-1R-yl] -5-cis-heptenoic acid | ||
|Common Name=&&19-hydroxy Prostaglandin B_2&&(15S,19)-Dihydroxy-9-oxo-5-cis-8(12),13-trans-prostadienoic acid&&7- [ | |Common Name=&&19-hydroxy Prostaglandin B_2&&(15S,19)-Dihydroxy-9-oxo-5-cis-8(12),13-trans-prostadienoic acid&&7- [2R- ((3S,7)-Dihydroxy-1-(E)-octenyl) -5-oxo-1-cyclopenten-1R-yl] -5-(Z)-heptenoic acid | ||
|Solubility=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}}]] | |Solubility=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}}]] | ||
|UV Spectra= lambda ^{EtOH}_{max} = 278 nm( epsilon ∼20,000) [[Reference:Hamberg_M:Samuelsson_B:,J. Biol. Chem.,1966,241,257|{{RelationTable/GetFirstAuthor|Reference:Hamberg_M:Samuelsson_B:,J. Biol. Chem.,1966,241,257}}]] | |UV Spectra= lambda ^{EtOH}_{max} = 278 nm( epsilon ∼20,000) [[Reference:Hamberg_M:Samuelsson_B:,J. Biol. Chem.,1966,241,257|{{RelationTable/GetFirstAuthor|Reference:Hamberg_M:Samuelsson_B:,J. Biol. Chem.,1966,241,257}}]] |
Revision as of 06:10, 28 May 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 | |
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LipidBank | XPR1131 |
LipidMaps | LMFA03010132 |
CAS | |
KEGG | {{{KEGG}}} |
KNApSAcK | {{{KNApSAcK}}} |
mol | LBF20307PG04 |
19-hydroxy Prostaglandin B2 | |
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Structural Information | |
7- [2R- ((3S,7)-Dihydroxy-1-trans-octenyl) -5-oxo-1-cyclopenten-1R-yl] -5-cis-heptenoic acid | |
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19-HYDROXY-PGB2 | |
Formula | C20H30O5 |
Exact Mass | 350.20932407 |
Average Mass | 350.4492 |
SMILES | O[C@H](CCC[C@H](C)O)C=CC(=C1CC=CCCCC(O)=O)CCC(=O)1 |
Physicochemical Information | |
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.. | |
19-Hydroxy-prostaglandin B2 relaxes uterine myometriuim Horton_EW . | |
Spectral Information | |
Mass Spectra | |
UV Spectra | λ EtOH max = 278 nm( ε ∼20,000) HambergMet al. |
IR Spectra | 5.92, 6.09, 6.26, 10.3 μ m HambergMet al. |
NMR Spectra | |
Other Spectra | |
Chromatograms |
Reported Metabolites, References | |||||||||||||||||||||||||
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