LBF20406AM10: Difference between revisions

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|LipidBank=XPR7026
|LipidBank=XPR7026
|LipidMaps=LMFA08020012
|LipidMaps=LMFA08020012
|SysName=N-Tert-butylarachidonoyl amide
|SysName=N-Tert-butylarachidonoylamide
|Common Name=&&N-Tert-butylarachidonoyl amide&&
|Common Name=&&N-Tert-butylarachidonoylamide&&
|Melting Point=colorless oil [[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}}]]
|Melting Point=colorless oil [[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}}]]
|NMR Spectra=^1 H NMR (CCCl3)  delta 5.30-5.40 (m,
|NMR Spectra=^1 H NMR (CCCl3)  delta 5.30-5.40 (m,

Revision as of 07:07, 28 May 2010

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Upper classes: LB LBF



N-Tert-butylarachidonoylamide
LBF20406AM10.png
Structural Information
N-Tert-butylarachidonoylamide
  • N-Tert-butylarachidonoylamide
Formula C24H41NO
Exact Mass 359.318814939
Average Mass 359.58847999999995
SMILES C(=CCCCC(NC(C)(C)C)=O)CC=CCC=CCC=CCCCCC
Physicochemical Information
colorless oil Sheskin_T et al.
This compound was synthesized from arachidonoyl chloride and tert-butylamine. Yield 72 % Sheskin_T et al.
Binding of this compound to the brain cannabinoid receptor (CBl),Ki(nM)>1000 Sheskin_T et al.
Spectral Information
Mass Spectra
UV Spectra
IR Spectra
NMR Spectra 1H NMR (CCCl3) δ 5.30-5.40 (m,
Other Spectra
Chromatograms
Reported Metabolites, References
Biospecies ID Compound Name Reference Comment
n.a. LBF20406AM10 See above. Sheskin_T et al. 1997