LBF18109AM01: Difference between revisions

Revision as of 07:06, 26 May 2010

Upper classes: LB LBF

Oleoylamide

Structural Information
	Octadecenoic acidamide
	Oleoylamide Octadecenamide

Formula	C18H35NO
Exact Mass	281.271864747
Average Mass	281.47664
SMILES	`CCCCCCCCC=CCCCCCCCC(N)=O`
Physicochemical Information
	74-75°C Sheskin_T et al.






	This compound was synthesized from oleic acid and ammonium hydroxide in 60 % yield. Sheskin_T et al.

	Binding of this compound to the brain cannabinoid receptor (CBl)was not found. Sheskin_T et al.


Spectral Information
Mass Spectra
UV Spectra
IR Spectra
NMR Spectra	¹H NMR (CDCl3) δ 5.42 (br s, 2H), 5.32-5.36 (m, 2H), 2.22 (t, J=7.8 Hz 2H), 1.98-2.02 (m,6H), 1.62-1.66 (m, 4H), 1.27-1.31 (m, 16H), 0.88 (t, J=6.9Hz, 3H). Sheskin_Tet al.
Other Spectra
Chromatograms

Reported Metabolites, References

Biospecies	ID	Compound Name	Reference	Comment
n.a.	LBF18109AM01	See above.	Sheskin_T et al. 1997

@@ Line 6: / Line 6: @@
 |LipidBank=XPR7014
 |LipidMaps=-
-|SysName=Oleoylamide
+|SysName=Octadecenoic acidamide
-|Common Name=&&Oleoylamide&&
+|Common Name=&&Oleoylamide&&Octadecenamide&&
 |Melting Point=74-75°C[[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 (CDCl3)  delta 5.42 (br s, 2H), 5.32-5.36 (m, 2H), 2.22 (t, J=7.8 Hz 2H), 1.98-2.02 (m,6H), 1.62-1.66 (m, 4H), 1.27-1.31 (m, 16H), 0.88 (t, J=6.9Hz, 3H). [[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}}]]