LBF20406AM35

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Upper classes: LB LBF



N- (R) - (-) -1-Methyl-2-hydroxyethyl-α,α-dimethylarachidonoylamide
LBF20406AM35.png
Structural Information
N-l-1R-Methyl-2-hydroxyethyl-α,α-dimethyl- (cis-5,cis-8,cis-11,cis-14) -eicosatetraenoylamine
  • N- (R) - (-) -1-Methyl-2-hydroxyethyl-α,α-dimethylarachidonoylamide
  • N- (R) - (-) -1-Methyl-2-hydroxyethyl-α,α-dimethyl- (5Z,8Z,11Z,14Z) -eicosatetraenoylamine
Formula C25H43NO2
Exact Mass 389.329379625
Average Mass 389.61446
SMILES C(=CCC=CCC=CCC=CCCCCC)CCC(C)(C)C(N[C@H](CO)C)=O
Physicochemical Information
colorless oil Sheskin_T et al.
This compound was synthesized from arachidonic acid and (R)-(-)-2-amino-l-propanol. Yield is 45 %. Sheskin_T et al.
Binding to the brain cannabinoid receptor (CBl), Ki(nM)= 3l.l±1.0 Sheskin_T et al.
Spectral Information
Mass Spectra
UV Spectra
IR Spectra
NMR Spectra 1H NMR (CDCl3) δ 5.80 (br s, lH), 5.30-5.42 (m, 8H), 4.01-4.12 (m, lH), 3.60-3.68 (m, lH), 3.50-3.55 (m, lH), 2.98-3.01 (m, lH), 2.76-2.84 (m, 6H), 1.90-2.10 (m, 4H), 1.15-1.62 (series of m, l7H), 0.90 (t, J=7.1Hz, 3H). SheskinTet al.
Other Spectra
Chromatograms
Reported Metabolites, References
Biospecies ID Compound Name Reference Comment
n.a. LBF20406AM35 See above. Sheskin_T et al. 1997