LBF20406AM10: Difference between revisions

Latest revision as of 04:41, 21 October 2010

Upper classes: LB LBF

N-Tert-butylarachidonoylamide

Structural Information
	N-Tert-butyl- (cis-5,cis-8,cis-11,cis-14) -eicosatetraenoylamine
	N-Tert-butylarachidonoylamide N-Tert-butyl- (5Z,8Z,11Z,14Z) -eicosatetraenoylamine

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 1: / Line 1: @@
+{{Lipid/Header}}
 {{Hierarchy|{{PAGENAME}}}}
@@ Line 4: / Line 6: @@
 |LipidBank=XPR7026
 |LipidMaps=LMFA08020012
-|SysName=N-tert-butyl arachidonoyl amide
+|SysName=N-Tert-butyl- (cis-5,cis-8,cis-11,cis-14) -eicosatetraenoylamine
-|Melting Point=colorless oil <<7001>>
+|Common Name=&&N-Tert-butylarachidonoylamide&&N-Tert-butyl- (5Z,8Z,11Z,14Z) -eicosatetraenoylamine&&
-|NMR Spectra=<SUP><FONT SIZE=-1>1</FONT></SUP>H NMR (CCCl3) <FONT FACE="Symbol">d</FONT>5.30-5.40 (m,
+|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,
+|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}}]]
+|Metabolism=
+|Biological Activity=Binding of this compound to the brain cannabinoid receptor (CBl),Ki(nM)>1000 [[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}}]]
 }}
+{{Lipid/Footer}}