LBF20210PG01: Difference between revisions

Latest revision as of 20:14, 2 November 2010

Upper classes: LB LBF

113,14-dihydro-15-keto Prostaglandin A₂

Structural Information
	9,15-Dioxo- (cis-5,10) -prostadienoic acid
	113,14-dihydro-15-keto Prostaglandin A₂ 9,15-Dioxo- (5Z,10) -prostadienoic 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

@@ Line 1: / Line 1: @@
+{{Lipid/Header}}
 {{Hierarchy|{{PAGENAME}}}}
@@ Line 4: / Line 6: @@
 |LipidBank=XPR1729
 |LipidMaps=LMFA03010033
-|SysName=9-oxo-15R-hydroxy-prostsa-10,13E-dien-1-oic acid
+|SysName=9,15-Dioxo- (cis-5,10) -prostadienoic acid
-|Common Name=&&13,14-dihydro-15-keto Prostaglandin A2&&
+|Common Name=&&113,14-dihydro-15-keto Prostaglandin A_2&&9,15-Dioxo- (5Z,10) -prostadienoic 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}}]]
+|Chemical Synthesis=
+|Metabolism=
 }}
+{{Lipid/Footer}}