LBF20406AM10: Difference between revisions

Revision as of 14:00, 19 February 2010

Upper classes: LB LBF

N-tert-butyl arachidonoyl amide

Structural Information
	N-tert-butyl arachidonoyl amide
	N-tert-butyl arachidonoyl amide

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

@@ Line 9: / Line 9: @@
 |Common Name=&&N-tert-butyl arachidonoyl amide&&
 |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) delta5.30-5.40 (m,
+|NMR Spectra=^1 H NMR (CCCl3)  delta 5.30-5.40 (m,
 |Source=
 |Chemical Synthesis=This compound was synthesized from arachidonoyl chloride and tert-butylamine. Yield 72 % [[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}}]]