LBF20406AM41: Difference between revisions

Latest revision as of 13:50, 21 October 2010

Upper classes: LB LBF

Arachidonoylmorpholine

Structural Information
	N-Morpholine- (cis-5,cis-8,cis-11,cis-14) -eicosatetraenoylamine
	Arachidonoylmorpholine N-Morpholine- (5Z,8Z,11Z,14Z) -eicosatetraenoylamine

Formula	C24H39NO2
Exact Mass	373.298079497
Average Mass	373.572
SMILES	`O=C(N(C1)CCOC1)CCCC=CCC=CCC=CCC=CCCCCC`
Physicochemical Information







	This compound was synthesized from arachidonoylchloride and morpholine. Adams_IB et al.

	Adams_IB et al.


Spectral Information
Mass Spectra
UV Spectra
IR Spectra
NMR Spectra
Other Spectra
Chromatograms

Reported Metabolites, References

Biospecies	ID	Compound Name	Reference	Comment
n.a.	LBF20406AM41	See above.	Adams_IB et al. 1995

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+{{Lipid/Header}}
 {{Hierarchy|{{PAGENAME}}}}
@@ Line 4: / Line 6: @@
 |LipidBank=XPR7066
 |LipidMaps=LMFA08020052
-|SysName=arachidonoylmorpholine
+|SysName=N-Morpholine- (cis-5,cis-8,cis-11,cis-14) -eicosatetraenoylamine
-|Common Name=&&arachidonoylmorpholine&&
+|Common Name=&&Arachidonoylmorpholine&&N-Morpholine- (5Z,8Z,11Z,14Z) -eicosatetraenoylamine&&
+|Source=
+|Chemical Synthesis=This compound was synthesized from arachidonoylchloride and morpholine. [[Reference:Adams_IB:Ryan_W:Singer_M:Thomas_BF:Compton_DR:Razdan_RK:Martin_BR:,J. Pharmacol. Exp. Ther.,1995,273,1172|{{RelationTable/GetFirstAuthor|Reference:Adams_IB:Ryan_W:Singer_M:Thomas_BF:Compton_DR:Razdan_RK:Martin_BR:,J. Pharmacol. Exp. Ther.,1995,273,1172}}]]
+|Metabolism=
+|Biological Activity={{Image200|LBF20406AM41FT7066.gif}} [[Reference:Adams_IB:Ryan_W:Singer_M:Thomas_BF:Compton_DR:Razdan_RK:Martin_BR:,J. Pharmacol. Exp. Ther.,1995,273,1172|{{RelationTable/GetFirstAuthor|Reference:Adams_IB:Ryan_W:Singer_M:Thomas_BF:Compton_DR:Razdan_RK:Martin_BR:,J. Pharmacol. Exp. Ther.,1995,273,1172}}]]
 }}
+{{Lipid/Footer}}