LBF20406AM35

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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	XPR7052
LipidMaps	LMFA08020038
CAS
KEGG	{{{KEGG}}}
KNApSAcK	{{{KNApSAcK}}}
mol	LBF20406AM35

N- ( (R) - (-) -1-methyl-2-hydroxyethyl) a ,a -dimethylarachidonoyl amide
Structural Information
Systematic Name	N- ( (R) - (-) -1-methyl-2-hydroxyethyl) a ,a -dimethylarachidonoyl amide
Common Name	N- ( (R) - (-) -1-methyl-2-hydroxyethyl) a ,a -dimethylarachidonoyl amide
Symbol
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
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 (R)-(-)-2-amino-l-propanol. Yield is 45 %. Sheskin_T et al.;>
Metabolism
Biological Activity
Genetic Information
Note
Spectral Information
Mass Spectra
UV Spectra
IR Spectra
NMR Spectra	1H NMR (CDCl3) d5.80 (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