LBF20406AM28

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Fatty acid (脂肪酸)

Glycerolipid (グリセロ脂質)

Sphingolipid (スフィンゴ脂質)

Journals (雑誌一覧)

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Upper classes: LB LBF

IDs and Links
LipidBank	XPR7045
LipidMaps	LMFA08040016
CAS
KEGG	{{{KEGG}}}
KNApSAcK	{{{KNApSAcK}}}
mol	LBF20406AM28

α-Methylanandamide
Structural Information
Systematic Name	N-2-Methy- (cis-5,cis-8,cis-11,cis-14) -eicosatetraenoylethanolamine
Common Name	α-Methylanandamide N-2-Methy- (5Z,8Z,11Z,14Z) -eicosatetraenoylethanolamine
Symbol
Formula	C23H39NO2
Exact Mass	361.298079497
Average Mass	361.5613
SMILES	CC(C(=O)NCCO)CCC=CCC=CCC=CCC=CCCCCC
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 arachidonic acid and ethanolamine. Yield 82 %. Sheskin_T et al.
Metabolism
Biological Activity	Binding to the brain cannabinoid receptor (CBl), Ki(nM)= 32.5±5.1 Sheskin_T et al.
Genetic Information
Note
Spectral Information
Mass Spectra
UV Spectra
IR Spectra
NMR Spectra	1H NMR (CDCl3) δ 6.10 (br s lH), 5.22-5.40 (m, 8H), 3.75 (t, J=5.1Hz, 2H), 3.42 (q, J=4.9 Hz, 2H), 2.74-2.86 (m, 6H), 2.20-2.30 (m, lH), 2.00-2.12 (m, 4H), 1.68-1.80 (m, lH), 1.20-1.50 (m, 6H), 1.16 (d, J=6.6Hz, 3H), 0.89 (t, J=6.9Hz, 3H). SheskinTet al.
Other Spectra
Chromatograms

Reported Metabolites, References
Biospecies ID Compound Name Reference Comment n.a. LBF20406AM28 See above. Sheskin_T et al. 1997