LBF18303SC03: Difference between revisions

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|Solubility=[[Reference:Kass_JP:Burr_GO:,J. Am. Chem. Soc.,1939,61,3292|{{RelationTable/GetFirstAuthor|Reference:Kass_JP:Burr_GO:,J. Am. Chem. Soc.,1939,61,3292}}]]
|Solubility=[[Reference:Kass_JP:Burr_GO:,J. Am. Chem. Soc.,1939,61,3292|{{RelationTable/GetFirstAuthor|Reference:Kass_JP:Burr_GO:,J. Am. Chem. Soc.,1939,61,3292}}]]
|Source=
|Source=
|Chemical Synthesis=Synthetic, by alkali isomerization of alpha-linolenic acid.
|Chemical Synthesis=Synthetic, by alkali isomerization of alpha -linolenic acid.
|Metabolism=
|Metabolism=
|Symbol=C18:3
|Symbol=C18:3

Latest revision as of 21:00, 14 April 2010

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(脂肪酸)
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Upper classes: LB LBF



10, 12 ,15-Octadecatrienoic acid
LBF18303SC03.png
Structural Information
10, 12 ,15-Octadecatrienoic acid
  • 10, 12 ,15-Octadecatrienoic acid
C18:3
Formula C18H30O2
Exact Mass 278.224580204
Average Mass 278.4296
SMILES CCC=CCC=CC=CCCCCCCCCC(O)=O
Physicochemical Information
Kass_JP et al.
Synthetic, by alkali isomerization of alpha -linolenic acid.
Spectral Information
Mass Spectra
UV Spectra
IR Spectra
NMR Spectra
Other Spectra
Chromatograms
Reported Metabolites, References
Biospecies ID Compound Name Reference Comment
n.a. LBF18303SC03 See above. Kass_JP et al. 1939