LBF20406PH01

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	XPR7016
LipidMaps	LMFA08020002
CAS
KEGG	{{{KEGG}}}
KNApSAcK	{{{KNApSAcK}}}
mol	LBF20406PH01

anandamide 0-phosphate
Structural Information
Systematic Name	anandamide 0-phosphate
Common Name	anandamide 0-phosphate
Symbol
Formula	C22H38NO5P
Exact Mass	427.2487598409999
Average Mass	427.51462100000003
SMILES	C(CCCC=CCC=CCC=CCC=CCCCCC)(NCCOP(O)(O)=O)=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 N-hydroxysuccinimide ester of arachidonic acid and O-phosphoethanolamine in 60% yield. Sheskin_T et al.
Metabolism
Biological Activity	Binding of this compound to the brain cannabinoid receptor (CBl),Ki(nM)= 190.8±11.1 Sheskin_T et al.
Genetic Information
Note
Spectral Information
Mass Spectra
UV Spectra
IR Spectra
NMR Spectra	1H NMR (CDCl3) δ 5.34-5.42 (m, 8H), 3.98 (br s 2H), 3.46 (br s 2H), 2.77-2.81 (m, 6H), 2.26 (t, J=6.8Hz, 2H), 2.00-2.06 (m, 4H), 1.60-1.69 (m, 2H), 1.29-1.42 (m, 6H), 0.88 (t, J=6.9Hz,3H) SheskinTet al.
Other Spectra
Chromatograms

Reported Metabolites, References
Biospecies ID Compound Name Reference Comment n.a. LBF20406PH01 See above. Sheskin_T et al. 1997