LBF20406AM43: Difference between revisions

Latest revision as of 04:51, 21 October 2010

Upper classes: LB LBF

N- (2-Phenoxyethyl) -arachidonoylamide

Structural Information
	N- (2-Phenoxyethyl) - (cis-5,cis-8,cis-11,cis-14) -eicosatetraenoylamine
	N- (2-Phenoxyethyl) -arachidonoylamide N- (2-Phenoxyethyl) - (5Z,8Z,11Z,14Z) -eicosatetraenoylamine

Formula	C28H41NO2
Exact Mass	423.313729561
Average Mass	423.63068
SMILES	`C(=CCCCC(NCCOc(c1)cccc1)=O)CC=CCC=CCC=CCCCCC`
Physicochemical Information







	This compound was synthesized from arachidonoylchloride and phenoxyethylamine. 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.	LBF20406AM43	See above.	Adams_IB et al. 1995

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+{{Lipid/Header}}
 {{Hierarchy|{{PAGENAME}}}}
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 |LipidBank=XPR7068
 |LipidMaps=LMFA08020054
-|SysName=arachidonoyl- (2'-phenoxyethyl) amide
+|SysName=N- (2-Phenoxyethyl) - (cis-5,cis-8,cis-11,cis-14) -eicosatetraenoylamine
-|Common Name=&&arachidonoyl- (2'-phenoxyethyl) amide&&
+|Common Name=&&N- (2-Phenoxyethyl) -arachidonoylamide&&N- (2-Phenoxyethyl) - (5Z,8Z,11Z,14Z) -eicosatetraenoylamine&&
+|Source=
+|Chemical Synthesis=This compound was synthesized from arachidonoylchloride and phenoxyethylamine. [[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|LBF20406AM43FT7068.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}}