LBF20308PG03: Difference between revisions

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|LipidBank=XPR1911
|LipidBank=XPR1911
|LipidMaps=-
|LipidMaps=-
|SysName=7- [ 2 (E) - (3 (S) -Hydroxyoctylidene) -3-oxo-4-cyclopenten-1 (R) -yl ] -5 (Z) -heptenoic acid
|SysName=7- [cis-2- (3S-Hydroxyoctylidene) -3-oxo-4-cyclopenten-1R-yl] -cis-5-heptenoic acid
|Common Name=&&7- [ 2 (E) - (3 (S) -Hydroxyoctylidene) -3-oxo-4-cyclopenten-1 (R) -yl ] -5 (Z) -heptenoic acid&&
|Common Name=&&7- [2-(E)- (3S-Hydroxyoctylidene) -3-oxo-4-cyclopenten-1R-yl] -5-(Z) -heptenoic acid&&
|Solubility=METHANOL[[Reference:Fitzpatrick_FA:Wynalda_MA:,J. Biol. Chem.,1983,258,11713|{{RelationTable/GetFirstAuthor|Reference:Fitzpatrick_FA:Wynalda_MA:,J. Biol. Chem.,1983,258,11713}}]]ETHANOL, CHLOROFORM, ETHYL ACETATE [[Reference:Kikawa_Y:Narumiya_S:Fukushima_M:Wakatsuka_H:Hayaishi_O:,Proc. Natl. Acad. Sci. U. S. A.,1984,81,1317|{{RelationTable/GetFirstAuthor|Reference:Kikawa_Y:Narumiya_S:Fukushima_M:Wakatsuka_H:Hayaishi_O:,Proc. Natl. Acad. Sci. U. S. A.,1984,81,1317}}]]
|Solubility=METHANOL[[Reference:Fitzpatrick_FA:Wynalda_MA:,J. Biol. Chem.,1983,258,11713|{{RelationTable/GetFirstAuthor|Reference:Fitzpatrick_FA:Wynalda_MA:,J. Biol. Chem.,1983,258,11713}}]]ETHANOL, CHLOROFORM, ETHYL ACETATE [[Reference:Kikawa_Y:Narumiya_S:Fukushima_M:Wakatsuka_H:Hayaishi_O:,Proc. Natl. Acad. Sci. U. S. A.,1984,81,1317|{{RelationTable/GetFirstAuthor|Reference:Kikawa_Y:Narumiya_S:Fukushima_M:Wakatsuka_H:Hayaishi_O:,Proc. Natl. Acad. Sci. U. S. A.,1984,81,1317}}]]
|Mass Spectra=m/e 334(M^+ ), 316, 245, 236 [[Reference:Kikawa_Y:Narumiya_S:Fukushima_M:Wakatsuka_H:Hayaishi_O:,Proc. Natl. Acad. Sci. U. S. A.,1984,81,1317|{{RelationTable/GetFirstAuthor|Reference:Kikawa_Y:Narumiya_S:Fukushima_M:Wakatsuka_H:Hayaishi_O:,Proc. Natl. Acad. Sci. U. S. A.,1984,81,1317}}]]
|Mass Spectra=m/e 334(M^+ ), 316, 245, 236 [[Reference:Kikawa_Y:Narumiya_S:Fukushima_M:Wakatsuka_H:Hayaishi_O:,Proc. Natl. Acad. Sci. U. S. A.,1984,81,1317|{{RelationTable/GetFirstAuthor|Reference:Kikawa_Y:Narumiya_S:Fukushima_M:Wakatsuka_H:Hayaishi_O:,Proc. Natl. Acad. Sci. U. S. A.,1984,81,1317}}]]

Latest revision as of 03:43, 29 November 2010

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Upper classes: LB LBF



7- [2-(E)- (3S-Hydroxyoctylidene) -3-oxo-4-cyclopenten-1R-yl] -5-(Z) -heptenoic acid
LBF20308PG03.png
Structural Information
7- [cis-2- (3S-Hydroxyoctylidene) -3-oxo-4-cyclopenten-1R-yl] -cis-5-heptenoic acid
  • 7- [2-(E)- (3S-Hydroxyoctylidene) -3-oxo-4-cyclopenten-1R-yl] -5-(Z) -heptenoic acid
Delta 12-PGJ2
Formula C20H30O4
Exact Mass 334.21440944799997
Average Mass 334.4498
SMILES C(CC[C@@H](O)CC=C(C(=O)1)[C@@H](CC=CCCCC(O)=O)C=C1)CC
Physicochemical Information
METHANOL Fitzpatrick_FA et al.ETHANOL, CHLOROFORM, ETHYL ACETATE KikawaYet al.
Bundy_GL et al.
LBF20308PG03FT0001.gif
In human plasma prostaglandin D2 is dehydrated and converted to 9-deoxy- Delta 9,12-13,14-dihydro-prostaglandin D2 ( Delta 12-prostaglandin J2) catalyzedby serum albumin Narumiya_S et al..
Delta 12-Prostaglandin J2 is considered to be an ultimate metabolite of prostaglandin D2 with anti-tumor and anti-viral activities Narumiya_S et al.. The compound has no cell surface recptor, but is transported into cells and then inot nuclei. The biological activities of Delta 12-prostaglandin J2 are due to the syntheses of various proteins including heat shock proteins, gamma -glutamylcysteine synthetase, collagen and heme oxygenase Negishi_M et al..
Spectral Information
Mass Spectra m/e 334(M+), 316, 245, 236 KikawaYet al.
UV Spectra λ EtOH
max
     = 244( ε 6100)nm KikawaYet al.
IR Spectra ν  : 2930, 1700, 1640, 1580, 1232, 028 cm-1 KikawaYet al.
NMR Spectra 1H-NMR(CDCl3) : δ 7.5(dd, 1H, 9-CH), 6.56(t, 1H, 13-CH), 6.35(dd,1 H, 10-CH), 5.48(m, 2H, 5,6-CH), 3.88(m, 1H, 15-CH), 3.44(m, 1H, 8-CH) KikawaYet al.
Other Spectra
Chromatograms
Reported Metabolites, References
Biospecies ID Compound Name Reference Comment
n.a. LBF20308PG03 See above. Bundy_GL et al. 1983
n.a. LBF20308PG03 See above. Fitzpatrick_FA et al. 1983
n.a. LBF20308PG03 See above. Kikawa_Y et al. 1984
n.a. LBF20308PG03 See above. Narumiya_S et al. 1985
n.a. LBF20308PG03 See above. Negishi_M et al. 1995