LBF20307PG41: Difference between revisions

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|Mass Spectra=HREIMS m/z 478.2998 for TMS derivative C<SUB><FONT SIZE=-1>2</FONT></SUB><SUB><FONT SIZE=-1>6</FONT></SUB>H<SUB><FONT SIZE=-1>4</FONT></SUB><SUB><FONT SIZE=-1>6</FONT></SUB>O<SUB><FONT SIZE=-1>4</FONT></SUB> Si<SUB><FONT SIZE=-1>2</FONT></SUB>, calcd 478.2932.[[Reference:Bundy_GL:Daniels_EG:Lincoln_FH:Pike_JE:,J. Am. Chem. Soc.,1972,94,2124|{{RelationTable/GetFirstAuthor|Reference:Bundy_GL:Daniels_EG:Lincoln_FH:Pike_JE:,J. Am. Chem. Soc.,1972,94,2124}}]]
|Mass Spectra=HREIMS m/z 478.2998 for TMS derivative C<SUB><FONT SIZE=-1>2</FONT></SUB><SUB><FONT SIZE=-1>6</FONT></SUB>H<SUB><FONT SIZE=-1>4</FONT></SUB><SUB><FONT SIZE=-1>6</FONT></SUB>O<SUB><FONT SIZE=-1>4</FONT></SUB> Si<SUB><FONT SIZE=-1>2</FONT></SUB>, calcd 478.2932.[[Reference:Bundy_GL:Daniels_EG:Lincoln_FH:Pike_JE:,J. Am. Chem. Soc.,1972,94,2124|{{RelationTable/GetFirstAuthor|Reference:Bundy_GL:Daniels_EG:Lincoln_FH:Pike_JE:,J. Am. Chem. Soc.,1972,94,2124}}]]
|UV Spectra=<FONT FACE="Symbol">l</FONT><SUB><FONT SIZE=-1>m</FONT></SUB><SUB><FONT SIZE=-1>a</FONT></SUB><SUB><FONT SIZE=-1>x</FONT></SUB> 217 nm(<FONT FACE="Symbol">e</FONT>9050))[[Reference:Bundy_GL:Daniels_EG:Lincoln_FH:Pike_JE:,J. Am. Chem. Soc.,1972,94,2124|{{RelationTable/GetFirstAuthor|Reference:Bundy_GL:Daniels_EG:Lincoln_FH:Pike_JE:,J. Am. Chem. Soc.,1972,94,2124}}]]
|UV Spectra=<FONT FACE="Symbol">l</FONT><SUB><FONT SIZE=-1>m</FONT></SUB><SUB><FONT SIZE=-1>a</FONT></SUB><SUB><FONT SIZE=-1>x</FONT></SUB> 217 nm(<FONT FACE="Symbol">e</FONT>9050))[[Reference:Bundy_GL:Daniels_EG:Lincoln_FH:Pike_JE:,J. Am. Chem. Soc.,1972,94,2124|{{RelationTable/GetFirstAuthor|Reference:Bundy_GL:Daniels_EG:Lincoln_FH:Pike_JE:,J. Am. Chem. Soc.,1972,94,2124}}]]
|Source=5-trans-Prostaglandin A<SUB><FONT SIZE=-1>2</FONT></SUB> was isolated from Gorgonian, Plexaura homomalla.[[Reference:Bundy_GL:Daniels_EG:Lincoln_FH:Pike_JE:,J. Am. Chem. Soc.,1972,94,2124|{{RelationTable/GetFirstAuthor|Reference:Bundy_GL:Daniels_EG:Lincoln_FH:Pike_JE:,J. Am. Chem. Soc.,1972,94,2124}}]];>
|Source=5-trans-Prostaglandin A<SUB><FONT SIZE=-1>2</FONT></SUB> was isolated from Gorgonian, Plexaura homomalla.[[Reference:Bundy_GL:Daniels_EG:Lincoln_FH:Pike_JE:,J. Am. Chem. Soc.,1972,94,2124|{{RelationTable/GetFirstAuthor|Reference:Bundy_GL:Daniels_EG:Lincoln_FH:Pike_JE:,J. Am. Chem. Soc.,1972,94,2124}}]]
|Chemical Synthesis=
|Chemical Synthesis=
|Metabolism=
|Metabolism=

Revision as of 11:55, 25 November 2009

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Upper classes: LB LBF



5-trans-prostaglandin A2
LBF20307PG41.png
Structural Information
(5E, 13E) - (8R,12S,15S) -15-hydroxy-9-oxoprost-5,10,13-trienoic acid
  • 5-trans-prostaglandin A2
  • (5E, 13E) - (8R,12S,15S) -15-hydroxy-9-oxoprost-5,10,13-trienoic acid
Formula C20H30O4
Exact Mass 334.21440944799997
Average Mass 334.4498
SMILES C(CC[C@H](O)C=C[C@H]([C@H]1CC=CCCCC(O)=O)C=CC(=O)1)CC
Physicochemical Information
5-trans-Prostaglandin A2 was isolated from Gorgonian, Plexaura homomalla. Bundy_GL et al.
Spectral Information
Mass Spectra HREIMS m/z 478.2998 for TMS derivative C26H46O4 Si2, calcd 478.2932. Bundy_GL et al.
UV Spectra lmax 217 nm(e9050)) Bundy_GL et al.
IR Spectra
NMR Spectra
Other Spectra
Chromatograms
Reported Metabolites, References
Biospecies ID Compound Name Reference Comment
n.a. LBF20307PG41 See above. Bundy_GL et al. 1972