LBF20406AM37: Difference between revisions

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|LipidMaps=LMFA08020040
|LipidMaps=LMFA08020040
|SysName=N- (1-methyl-2-hydroxyethyl) arachidonoylamide (R)  
|SysName=N- (1-methyl-2-hydroxyethyl) arachidonoylamide (R)  
|Common Name=&&N- (1-methyl-2-hydroxyethyl) arachidonoylamide (R) &&
|Common Name=&&N- (1-methyl-2-hydroxyethyl) arachidonoylamide (R)&&
|Melting Point=colorless liquid [[Reference:Abadji_V:Lin_S:Taha_G:Griffin_G:Stevenson_LA:Pertwee_RG:Makriyannis_A:,J. Med. Chem.,1994,37,1889|{{RelationTable/GetFirstAuthor|Reference:Abadji_V:Lin_S:Taha_G:Griffin_G:Stevenson_LA:Pertwee_RG:Makriyannis_A:,J. Med. Chem.,1994,37,1889}}]].
|Melting Point=colorless liquid [[Reference:Abadji_V:Lin_S:Taha_G:Griffin_G:Stevenson_LA:Pertwee_RG:Makriyannis_A:,J. Med. Chem.,1994,37,1889|{{RelationTable/GetFirstAuthor|Reference:Abadji_V:Lin_S:Taha_G:Griffin_G:Stevenson_LA:Pertwee_RG:Makriyannis_A:,J. Med. Chem.,1994,37,1889}}]].
|Reflactive=dX<sub>4</sub><sup>25</sup>= +10.9° [[Reference:Abadji_V:Lin_S:Taha_G:Griffin_G:Stevenson_LA:Pertwee_RG:Makriyannis_A:,J. Med. Chem.,1994,37,1889|{{RelationTable/GetFirstAuthor|Reference:Abadji_V:Lin_S:Taha_G:Griffin_G:Stevenson_LA:Pertwee_RG:Makriyannis_A:,J. Med. Chem.,1994,37,1889}}]]
|Reflactive=dX<sub>4</sub><sup>25</sup>= +10.9° [[Reference:Abadji_V:Lin_S:Taha_G:Griffin_G:Stevenson_LA:Pertwee_RG:Makriyannis_A:,J. Med. Chem.,1994,37,1889|{{RelationTable/GetFirstAuthor|Reference:Abadji_V:Lin_S:Taha_G:Griffin_G:Stevenson_LA:Pertwee_RG:Makriyannis_A:,J. Med. Chem.,1994,37,1889}}]]

Revision as of 00:02, 20 December 2008


Upper classes: LB LBF



N- (1-methyl-2-hydroxyethyl) arachidonoylamide (R)
LBF20406AM37.png
Structural Information
N- (1-methyl-2-hydroxyethyl) arachidonoylamide (R)
  • N- (1-methyl-2-hydroxyethyl) arachidonoylamide (R)
Formula C23H39NO2
Exact Mass 361.298079497
Average Mass 361.5613
SMILES C(CCC(=O)N[C@@H](CO)C)C=CCC=CCC=CCC=CCCCCC
Physicochemical Information
colorless liquid Abadji_V et al..
Spectral Information
Mass Spectra
UV Spectra
IR Spectra
NMR Spectra 1H NMR (200 MHz, CDCl3) d(TMS)5.57 (m, 1H), 5.47-5.30 (m, 8H), 4.14-4.02 (m, 1H), 3.71-3.48 (m, 2H), 2.84-2.81 (m, 6H), 2.24-2.01 (m, 6H), 1.77-1.65 (m, 2H), 1.39-1.26 (m, 6H), 1.17 (d, J=3.46Hz, 3H), 0.89 (t, J=6.12Hz, 3H) AbadjiVet al.
Other Spectra
Chromatograms Rf 0.3(5% MeOH/CHCl3) HayaishiO
Reported Metabolites, References
Biospecies ID Compound Name Reference Comment
n.a. LBF20406AM37 See above. Abadji_V et al. 1994
n.a. LBF20406AM37 See above. Hayaishi_O 1988
n.a. LBF20406AM37 See above. Seltzman_HH et al. 1997