Structure Database (LMSD)

Common Name
Lignoceroyl-EA
Systematic Name
N-(Tetracosanoyl)-ethanolamine
Synonyms
  • Lignoceroyl-ethanolamine
LM ID
LMFA08040054
Formula
C26H53NO2
Exact Mass
Calculate m/z
411.407629
Sum Composition
NAE 24:0
Status
Active
Show lipids differing only in stereochemistry/bond geometry

Classification

Category
Main Class
Sub Class
Fatty Acyls [FA]
Fatty amides [FA08]
N-acyl ethanolamines (endocannabinoids) [FA0804]

References

Taxonomy Information

Curated from
NCBI taxonomy class
Reference
Rattus norvegicus (#10116)
Mammalia (#40674)
Inflammatory hyperalgesia induces essential bioactive lipid production in the spinal cord.,
J Neurochem, 2010
Pubmed ID: 20492349

String Representations

InChiKey (Click to copy)
HJPVEPFLQVCCLM-UHFFFAOYSA-N
InChi (Click to copy)
InChI=1S/C26H53NO2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-26(29)27-24-25-28/h28H,2-25H2,1H3,(H,27,29)
SMILES (Click to copy)
C(CCCCCCCCCCCCC(=O)NCCO)CCCCCCCCCC

Other Databases

CHEBI ID
165586
PubChem CID
14455161
SwissLipids ID
SLM:000598133
Cayman ID
9001744

Calculated Physicochemical Properties

Heavy Atoms 29
Rings 0
Aromatic Rings 0
Rotatable Bonds 24
Van der Waals Molecular Volume 484.30
Topological Polar Surface Area 49.33
Hydrogen Bond Donors 2
Hydrogen Bond Acceptors 3
logP 8.27
Molar Refractivity 128.32

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Updated at
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