LBF20207PG45: Difference between revisions

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|LipidBank=XPR1787
|LipidBank=XPR1787
|LipidMaps=-
|LipidMaps=-
|SysName=9a,11a,15R-trihydroxy-prosta-5Z,13E-dien-1-oic acid
|SysName=(9alpha,11alpha,15R) -Trihydroxy-prosta- (cis-5,trans-13) -dien-1-oic acid
|Common Name=&&15 (R) -Prostaglandin F_2alpha&&9a,11a,15R-trihydroxy-prosta-5Z,13E-dien-1-oic acid&&
|Common Name=&&15R- Prostaglandin F_2 alpha&&(9alpha,11alpha,15R) -Trihydroxy-prosta- (5Z,13E) -dien-1-oic acid&&
|Source=
|Chemical Synthesis=
|Metabolism=
|Biological Activity=In hamster antifertility study, 15(R)-PGF2 alpha  is reported quarter potency of PGF2 alpha , which is due to reduced affinity to FP receptors.[[Reference:Miller_WL:Sutton_MJ:,Prostaglandins,1976,11,77|{{RelationTable/GetFirstAuthor|Reference:Miller_WL:Sutton_MJ:,Prostaglandins,1976,11,77}}]]
}}
}}


{{Lipid/Footer}}
{{Lipid/Footer}}

Latest revision as of 08:36, 21 October 2010

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(脂肪酸)
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Upper classes: LB LBF



15R- Prostaglandin F2α
LBF20207PG45.png
Structural Information
(9α,11α,15R) -Trihydroxy-prosta- (cis-5,trans-13) -dien-1-oic acid
  • 15R- Prostaglandin F2α
  • (9α,11α,15R) -Trihydroxy-prosta- (5Z,13E) -dien-1-oic acid
Formula C20H34O5
Exact Mass 354.240624198
Average Mass 354.48096000000004
SMILES C(CC[C@@H](O)C=C[C@H]([C@H]1CC=CCCCC(O)=O)[C@@H](C[C@@H]1O)O)CC
Physicochemical Information
In hamster antifertility study, 15(R)-PGF2 alpha is reported quarter potency of PGF2 alpha , which is due to reduced affinity to FP receptors. Miller_WL 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. LBF20207PG45 See above. Miller_WL et al. 1976