LBF20406AM30: Difference between revisions

Revision as of 14:00, 19 February 2010

Upper classes: LB LBF

N-propyl α-methyl arachidonoyl amide

Structural Information
	N-propyl α-methyl arachidonoyl amide
	N-propyl α-methyl arachidonoyl amide

Formula	C24H41NO
Exact Mass	359.318814939
Average Mass	359.58847999999995
SMILES	`C(C=CCCC(C)C(=O)NCCC)C=CCC=CCC=CCCCCC`
Physicochemical Information
	colorless oil Sheskin_T et al.






	This compound was synthesized from arachidonic acid and propylamine. Yield 84 %. Sheskin_T et al.

	Binding to the brain cannabinoid receptor (CBl), Ki(nM)= 7.4±0.2 Sheskin_T et al.


Spectral Information
Mass Spectra
UV Spectra
IR Spectra
NMR Spectra	¹H NMR (CDCl3) δ5.20-5.45 (m,
Other Spectra
Chromatograms

Reported Metabolites, References

Biospecies	ID	Compound Name	Reference	Comment
n.a.	LBF20406AM30	See above.	Sheskin_T et al. 1997

@@ Line 9: / Line 9: @@
 |Common Name=&&N-propyl alpha-methyl 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=<SUP><FONT SIZE=-1>1</FONT></SUP>H NMR (CDCl3) <FONT FACE="Symbol">d</FONT>5.20-5.45 (m,
+|NMR Spectra=^1 H NMR (CDCl3) delta5.20-5.45 (m,
 |Source=
 |Chemical Synthesis=This compound was synthesized from arachidonic acid and propylamine. Yield 84 %. [[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}}]]