LBF20107PG06: Difference between revisions

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|SysName=9alpha,11alpha-dihydroxy-15-oxo-prost-13E-en-1-oic acid
|SysName=9alpha,11alpha-dihydroxy-15-oxo-prost-13E-en-1-oic acid
|Common Name=&&15-keto Prostaglandin F_1alpha&&9alpha,11alpha-dihydroxy-15-oxo-prost-13E-en-1-oic acid&&
|Common Name=&&15-keto Prostaglandin F_1alpha&&9alpha,11alpha-dihydroxy-15-oxo-prost-13E-en-1-oic acid&&
|Source=15-keto PGF1alpha is the initial metabolite of PGF1alpha via PG 15-dehydrogenase.
|Source=15-keto PGF1 alpha  is the initial metabolite of PGF1 alpha  via PG 15-dehydrogenase.
|Chemical Synthesis=
|Chemical Synthesis=
|Metabolism=
|Metabolism=
|Biological Activity=In fish, the 15-keto compounds (including 15-keto PGF1alpha) serve as post-ovulatory pheromones and are more active tha the parent prostaglandins.[[Reference:Sorensen_PW:Hara_TJ:Stacey_NE:Goetz_FW:,Biol Reprod.,1988,39,1039|{{RelationTable/GetFirstAuthor|Reference:Sorensen_PW:Hara_TJ:Stacey_NE:Goetz_FW:,Biol Reprod.,1988,39,1039}}]]
|Biological Activity=In fish, the 15-keto compounds (including 15-keto PGF1 alpha ) serve as post-ovulatory pheromones and are more active tha the parent prostaglandins.[[Reference:Sorensen_PW:Hara_TJ:Stacey_NE:Goetz_FW:,Biol Reprod.,1988,39,1039|{{RelationTable/GetFirstAuthor|Reference:Sorensen_PW:Hara_TJ:Stacey_NE:Goetz_FW:,Biol Reprod.,1988,39,1039}}]]
}}
}}


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Revision as of 14:00, 19 February 2010

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Upper classes: LB LBF



15-keto Prostaglandin F_1α
LBF20107PG06.png
Structural Information
9α,11α-dihydroxy-15-oxo-prost-13E-en-1-oic acid
  • 15-keto Prostaglandin F_1α
  • 9α,11α-dihydroxy-15-oxo-prost-13E-en-1-oic acid
Formula C20H34O5
Exact Mass 354.240624198
Average Mass 354.48096000000004
SMILES C(CCC(=O)C=C[C@H]([C@H]1CCCCCCC(O)=O)[C@@H](C[C@@H]1O)O)CC
Physicochemical Information
15-keto PGF1 alpha is the initial metabolite of PGF1 alpha via PG 15-dehydrogenase.
In fish, the 15-keto compounds (including 15-keto PGF1 alpha ) serve as post-ovulatory pheromones and are more active tha the parent prostaglandins. Sorensen_PW 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. LBF20107PG06 See above. Sorensen_PW et al. 1988