LBF20406AM32

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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	XPR7049
LipidMaps	LMFA08020035
CAS
KEGG	{{{KEGG}}}
KNApSAcK	{{{KNApSAcK}}}
mol	LBF20406AM32

N-Isopropyl-α-methylarachidonoylamide
Structural Information
Systematic Name	N-Isopropyl-α-methyl- (cis-5,cis-8,cis-11,cis-14) -eicosatetraenoylamine
Common Name	N-Isopropyl-α-methylarachidonoylamide N-Isopropyl-α-methyl- (5Z,8Z,11Z,14Z) -eicosatetraenoylamine
Symbol
Formula	C24H41NO
Exact Mass	359.318814939
Average Mass	359.58847999999995
SMILES	N(C(C(C)CCC=CCC=CCC=CCC=CCCCCC)=O)C(C)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 arachidonic acid and isopropylamine. Yield 85 %. Sheskin_T et al.
Metabolism
Biological Activity	Binding to the brain cannabinoid receptor (CBl), Ki(nM)= 8.4±1.1 Sheskin_T et al.
Genetic Information
Note
Spectral Information
Mass Spectra
UV Spectra
IR Spectra
NMR Spectra	1H NMR (CDCl3) δ 5.30-5.42 (m, 8H), 4.02-4.14 (m, lH), 2.76-2.90 (m, 6H), 1.92-2.12 (m, 5H), 1.10-1.60 (series of m, 17H), 0.89 (t, J=6.9Hz, 3H). SheskinTet al.
Other Spectra
Chromatograms

Reported Metabolites, References
Biospecies ID Compound Name Reference Comment n.a. LBF20406AM32 See above. Sheskin_T et al. 1997