LBF20406AM11

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Fatty acid (脂肪酸)

Glycerolipid (グリセロ脂質)

Sphingolipid (スフィンゴ脂質)

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Upper classes: LB LBF

IDs and Links
LipidBank	XPR7027
LipidMaps	LMFA08020013
CAS
KEGG	{{{KEGG}}}
KNApSAcK	{{{KNApSAcK}}}
mol	LBF20406AM11

N-Amylarachidohoylamide
Structural Information
Systematic Name	N- (cis-5,cis-8,cis-11,cis-14) -Eicosatetraenoylamine
Common Name	N-Amylarachidohoylamide N- (5Z,8Z,11Z,14Z) -Eicosatetraenoylamine
Symbol
Formula	C25H43NO
Exact Mass	373.334465003
Average Mass	373.61505999999997
SMILES	C(CCCNC(CCCC=CCC=CCC=CCC=CCCCCC)=O)C
Physicochemical Information
Melting Point	colorless oil Sheskin_T et al.
Boiling Point
Density
Optical Rotation
Refractive Index
Solubility
Source
Chemical Synthesis	This compound was synthesized from arachidonoylchloride and amylamine.Yield 70 % Sheskin_T et al.
Metabolism
Biological Activity	Binding of this compound to the brain cannabinoid receptor (CBl),Ki(nM)>l000 Sheskin_T et al.
Genetic Information
Note
Spectral Information
Mass Spectra
UV Spectra
IR Spectra
NMR Spectra	1H NMR (CDCl3) δ 5.70 (br s lH), 5.23-5.33 (m, 8H), 3.15 (q, J=3Hz, 2H), 2.71-2.77(m, 6H), 1.97-2.16 (m, 6H), 1.58-1.68 (m, 2H), 1.18-1.42 (m, l2H), 0.79-0.85 (m, 6H). SheskinTet al.
Other Spectra
Chromatograms

Reported Metabolites, References
Biospecies ID Compound Name Reference Comment n.a. LBF20406AM11 See above. Sheskin_T et al. 1997