LBF20406AM12

LipidBank Top (トップ)

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)

How to edit (ページの書き方)

Upper classes: LB LBF

IDs and Links
LipidBank	XPR7028
LipidMaps	LMFA08020014
CAS
KEGG	{{{KEGG}}}
KNApSAcK	{{{KNApSAcK}}}
mol	LBF20406AM12

N- (3-Methylbutyl)arachidonoylamide
Structural Information
Systematic Name	N- (3-Methylbutyl)- (cis-5,cis-8,cis-11,cis-14) -eicosatetraenoylamine
Common Name	N- (3-Methylbutyl)arachidonoylamide N- (3-Methylbutyl)- (5Z,8Z,11Z,14Z) -eicosatetraenoylamine
Symbol
Formula	C25H43NO
Exact Mass	373.334465003
Average Mass	373.61505999999997
SMILES	O=C(NCCC(C)C)CCCC=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 arachidonoylchloride and isoamylamine.Yield 7l % Sheskin_T et al.
Metabolism
Biological Activity	Binding of this compound to the brain cannabinoid receptor (CBl),Ki(nM)= 575.1±35.3 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), 3.26 (q, J=3Hz, 2H), 2.76-2.86 (m, 6H), 2.02-2.20 (m, 6H), 1.68-1.78 (m, 2H), 1.54-1.64 (m, lH), 1.26-1.40 (m, 8H), 0.82-0.96 (m, 9H) SheskinTet al.
Other Spectra
Chromatograms

Reported Metabolites, References
Biospecies ID Compound Name Reference Comment n.a. LBF20406AM12 See above. Sheskin_T et al. 1997