LBF20307PG04: Difference between revisions

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|LipidBank=XPR1131
|LipidBank=XPR1131
|LipidMaps=LMFA03010132
|LipidMaps=LMFA03010132
|SysName=7- [2- ((3S,7)-Dihydroxy-1-trans-octenyl) -5-oxo-1-cyclopenten-1-yl] -5-cis-heptenoic acid
|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- [2- ((3S,7)-Dihydroxy-1(E)-octenyl) -5-oxo-1-cyclopenten-1-yl] -5-(Z)-heptenoic acid&&
|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

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Upper classes: LB LBF



19-hydroxy Prostaglandin B2
LBF20307PG04.png
Structural Information
7- [2R- ((3S,7)-Dihydroxy-1-trans-octenyl) -5-oxo-1-cyclopenten-1R-yl] -5-cis-heptenoic acid
  • 19-hydroxy Prostaglandin B2
  • (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
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
Biospecies ID Compound Name Reference Comment
n.a. LBF20307PG04 See above. Bergstrom_S 1967
n.a. LBF20307PG04 See above. Hamberg_M et al. 1966
n.a. LBF20307PG04 See above. Horton_EW 1969
n.a. LBF20307PG04 See above. Taylor_PL et al. 1974