LBF18109AM01: Difference between revisions

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|Chemical Synthesis=This compound was synthesized from oleic acid and ammonium hydroxide in 60 % yield.[[Reference:Sheskin_T:Hanus_L:Slager_J:Vogel_Z:Mechoulam_R:,J. Med. Chem.,1997,40,659|{{RelationTable/GetFirstAuthor|Reference:Sheskin_T:Hanus_L:Slager_J:Vogel_Z:Mechoulam_R:,J. Med. Chem.,1997,40,659}}]]
|Chemical Synthesis=This compound was synthesized from oleic acid and ammonium hydroxide in 60 % yield.[[Reference:Sheskin_T:Hanus_L:Slager_J:Vogel_Z:Mechoulam_R:,J. Med. Chem.,1997,40,659|{{RelationTable/GetFirstAuthor|Reference:Sheskin_T:Hanus_L:Slager_J:Vogel_Z:Mechoulam_R:,J. Med. Chem.,1997,40,659}}]]
|Metabolism=
|Metabolism=
|Biological Activity=Binding of this compound to the brain cannabinoid receptor (CBl)was not found. [[Reference:Sheskin_T:Hanus_L:Slager_J:Vogel_Z:Mechoulam_R:,J. Med. Chem.,1997,40,659|{{RelationTable/GetFirstAuthor|Reference:Sheskin_T:Hanus_L:Slager_J:Vogel_Z:Mechoulam_R:,J. Med. Chem.,1997,40,659}}]]
}}
}}


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{{Lipid/Footer}}

Revision as of 21:00, 6 January 2010

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(脂肪酸)
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Upper classes: LB LBF



oleoylamide
LBF18109AM01.png
Structural Information
oleoylamide
  • oleoylamide
Formula C18H35NO
Exact Mass 281.271864747
Average Mass 281.47664
SMILES CCCCCCCCC=CCCCCCCCC(N)=O
Physicochemical Information
74-75°C Sheskin_T et al.
This compound was synthesized from oleic acid and ammonium hydroxide in 60 % yield. Sheskin_T et al.
Binding of this compound to the brain cannabinoid receptor (CBl)was not found. Sheskin_T et al.
Spectral Information
Mass Spectra
UV Spectra
IR Spectra
NMR Spectra 1H NMR (CDCl3) d5.42 (br s, 2H), 5.32-5.36 (m, 2H), 2.22 (t, J=7.8 Hz 2H), 1.98-2.02 (m,6H), 1.62-1.66 (m, 4H), 1.27-1.31 (m, 16H), 0.88 (t, J=6.9Hz, 3H). SheskinTet al.
Other Spectra
Chromatograms
Reported Metabolites, References
Biospecies ID Compound Name Reference Comment
n.a. LBF18109AM01 See above. Sheskin_T et al. 1997