LBF20210PG01: Difference between revisions

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|LipidBank=XPR1729
|LipidBank=XPR1729
|LipidMaps=LMFA03010033
|LipidMaps=LMFA03010033
|SysName=9-Oxo-15R-hydroxy-prostsa- (5-cis,13-trans) -dien-1-oic acid
|SysName=9-Oxo-15R-hydroxy-prostsa- (10,13-trans) -dien-1-oic acid
|Common Name=&&13,14-dihydro-15-keto Prostaglandin A_2&&9-Oxo-15R-hydroxy-prostsa- (5Z,13E) -dien-1-oic acid&&
|Common Name=&&13,14-dihydro-15-keto Prostaglandin A_2&&9-Oxo-15R-hydroxy-prostsa- (10,13E) -dien-1-oic acid&&
|Source=13,14-dihydro-15-keto PGA2 is produced via non-enzymatic dehydration of 13,14-dihydro-15-keto PGE2, whose process is a ccelerated by the presence of albumin.[[Reference:Granstrom_E:Hamberg_M:Hansson_G:Kindahl_H:,Prostaglandins,1980,19,933|{{RelationTable/GetFirstAuthor|Reference:Granstrom_E:Hamberg_M:Hansson_G:Kindahl_H:,Prostaglandins,1980,19,933}}]][[Reference:Fitzpatrick_FA:Aguirre_R:Pike_JE:Lincoln_FH:,Prostaglandins,1980,19,917|{{RelationTable/GetFirstAuthor|Reference:Fitzpatrick_FA:Aguirre_R:Pike_JE:Lincoln_FH:,Prostaglandins,1980,19,917}}]]
|Source=13,14-dihydro-15-keto PGA2 is produced via non-enzymatic dehydration of 13,14-dihydro-15-keto PGE2, whose process is a ccelerated by the presence of albumin.[[Reference:Granstrom_E:Hamberg_M:Hansson_G:Kindahl_H:,Prostaglandins,1980,19,933|{{RelationTable/GetFirstAuthor|Reference:Granstrom_E:Hamberg_M:Hansson_G:Kindahl_H:,Prostaglandins,1980,19,933}}]][[Reference:Fitzpatrick_FA:Aguirre_R:Pike_JE:Lincoln_FH:,Prostaglandins,1980,19,917|{{RelationTable/GetFirstAuthor|Reference:Fitzpatrick_FA:Aguirre_R:Pike_JE:Lincoln_FH:,Prostaglandins,1980,19,917}}]]
|Chemical Synthesis=
|Chemical Synthesis=

Revision as of 03:33, 7 September 2010

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Upper classes: LB LBF



13,14-dihydro-15-keto Prostaglandin A2
LBF20210PG01.png
Structural Information
9-Oxo-15R-hydroxy-prostsa- (10,13-trans) -dien-1-oic acid
  • 13,14-dihydro-15-keto Prostaglandin A2
  • 9-Oxo-15R-hydroxy-prostsa- (10,13E) -dien-1-oic acid
Formula C20H30O4
Exact Mass 334.21440944799997
Average Mass 334.4498
SMILES C(CCC(=O)CC[C@H]([C@H]1CC=CCCCC(O)=O)C=CC(=O)1)CC
Physicochemical Information
13,14-dihydro-15-keto PGA2 is produced via non-enzymatic dehydration of 13,14-dihydro-15-keto PGE2, whose process is a ccelerated by the presence of albumin. Granstrom_E et al. Fitzpatrick_FA et al.
Spectral Information
Mass Spectra
UV Spectra
IR Spectra
NMR Spectra
Other Spectra
Chromatograms
Reported Metabolites, References
Biospecies ID Compound Name Reference Comment
n.a. LBF20210PG01 See above. Fitzpatrick_FA et al. 1980
n.a. LBF20210PG01 See above. Granstrom_E et al. 1980