LBF20406AM33: Difference between revisions

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|Chemical Synthesis=This compound was synthesized from arachidonic acid and isopropylamine. Yield 78 %. [[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 arachidonic acid and isopropylamine. Yield 78 %. [[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 to the brain cannabinoid receptor (CBl), Ki(nM)= 7.2±0.1 [[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



N-isopropyl α,α-dimethylarachidonoyl amide
LBF20406AM33.png
Structural Information
N-isopropyl α,α-dimethylarachidonoyl amide
  • N-isopropyl α,α-dimethylarachidonoyl amide
Formula C25H43NO
Exact Mass 373.334465003
Average Mass 373.61505999999997
SMILES C(=CCC=CCC=CCC=CCCCCC)CCC(C)(C)C(NC(C)C)=O
Physicochemical Information
colorless oil Sheskin_T et al.
This compound was synthesized from arachidonic acid and isopropylamine. Yield 78 %. Sheskin_T et al.
Binding to the brain cannabinoid receptor (CBl), Ki(nM)= 7.2±0.1 Sheskin_T et al.
Spectral Information
Mass Spectra
UV Spectra
IR Spectra
NMR Spectra 1H NMR (CDCl3) d5.20-5.50 (m, 9H), 4.04-4.14 (m, lH), 2.76-2.90 (m, 6H), 1.90-2.15 (m, 4H), 1.10-1.60 (series of m, 20H), 0.90 (t, J=6.9Hz, 3H). SheskinTet al.
Other Spectra
Chromatograms
Reported Metabolites, References
Biospecies ID Compound Name Reference Comment
n.a. LBF20406AM33 See above. Sheskin_T et al. 1997