Record Information
Version1.0
Created at2020-03-19 00:33:55 UTC
Updated at2020-11-18 16:35:08 UTC
CannabisDB IDCDB000379
Secondary Accession NumbersNot Available
Cannabis Compound Identification
Common NameLignoceric acid
DescriptionLignoceric acid or tetracosanoate, also known as lignocerat, with formula C23H47COOH, belongs to the class of organic compounds known as very long-chain fatty acids. These are fatty acids with an aliphatic tail that contains at least 22 carbon atoms. Lignoceric acid is a fatty acid lipid molecule. Lignoceric acid is practically insoluble in water and a weakly acidic compound. It is found in wood tar, various cerebrosides, and in small amounts in most natural fats. The fatty acids of peanut oil contain 1.1% – 2.2% of lignoceric acid. This fatty acid is also a by product of lignin production. Lignoceric acid is one of the saturated fatty acids identified in the oil of cannabis seed (PMID: 6991645 ). In humans, Lignoceric acid, one of the very long chain fatty acids, is associate with the X-chromosome linked disease, adrenoleukodystrophy (ALD), marked by a deficiency in peroxisomal fatty acid beta oxidation. ALD is caused by mutations in ABCD1, a gene that encodes for ALD, a peroxisomal membrane transporter protein. Those with ALD build-up long chain fatty acids, affecting myelin in the central nervous system, the adrenal cortex, and the Leydig cells in the testes. Lignoceric acid is also involved in carnitine-acylcarnitine translocase deficiency, which is a metabolic disorder.
Structure
Thumb
Synonyms
ValueSource
CH3-[CH2]22-COO(-)ChEBI
LignoceratChEBI
LignocerateChEBI
N-TetracosanoateChEBI
TetracosanateChEBI
TetracosanoatChEBI
TetracosoateChEBI
TetraeicosanoateChEBI
Lignoceric acidGenerator
N-Tetracosanoic acidGenerator
Tetracosanic acidGenerator
Tetracosoic acidGenerator
Tetraeicosanoic acidGenerator
Tetracosanoic acidGenerator
TetracosanoateChEBI
Chemical FormulaC24H47O2
Average Molecular Weight367.63
Monoisotopic Molecular Weight367.3576
IUPAC Nametetracosanoate
Traditional Namelignocerate
CAS Registry Number46927-71-3
SMILES
CCCCCCCCCCCCCCCCCCCCCCCC([O-])=O
InChI Identifier
InChI=1S/C24H48O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-24(25)26/h2-23H2,1H3,(H,25,26)/p-1
InChI KeyQZZGJDVWLFXDLK-UHFFFAOYSA-M
Chemical Taxonomy
Description Belongs to the class of organic compounds known as very long-chain fatty acids. These are fatty acids with an aliphatic tail that contains at least 22 carbon atoms.
KingdomOrganic compounds
Super ClassLipids and lipid-like molecules
ClassFatty Acyls
Sub ClassFatty acids and conjugates
Direct ParentVery long-chain fatty acids
Alternative Parents
Substituents
  • Very long-chain fatty acid
  • Straight chain fatty acid
  • Monocarboxylic acid or derivatives
  • Carboxylic acid
  • Carboxylic acid derivative
  • Organic oxygen compound
  • Organic oxide
  • Hydrocarbon derivative
  • Organooxygen compound
  • Carbonyl group
  • Organic anion
  • Aliphatic acyclic compound
Molecular FrameworkAliphatic acyclic compounds
External Descriptors
Ontology
Not Available
Physical Properties
StateSolid
Experimental Properties
PropertyValueReference
Melting Point84.2 °CWikipedia
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
logPNot AvailableNot Available
Predicted Properties
PropertyValueSource
logP9.89ALOGPS
logP9.81ChemAxon
logS-7.5ALOGPS
pKa (Strongest Acidic)4.95ChemAxon
Physiological Charge-1ChemAxon
Hydrogen Acceptor Count2ChemAxon
Hydrogen Donor Count0ChemAxon
Polar Surface Area40.13 ŲChemAxon
Rotatable Bond Count22ChemAxon
Refractivity124.73 m³·mol⁻¹ChemAxon
Polarizability51.07 ųChemAxon
Number of Rings0ChemAxon
BioavailabilityNoChemAxon
Rule of FiveNoChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Spectra
EI-MS/GC-MSNot Available
MS/MS
TypeDescriptionSplash KeyView
Predicted MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-0gb9-0009000000-fc10fec73a55a97959f82016-09-12View Spectrum
Predicted MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-0lk9-3339000000-b899443a95b5b926e6142016-09-12View Spectrum
Predicted MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-052f-9462000000-f09e84add1074f3e21102016-09-12View Spectrum
Predicted MS/MSPredicted LC-MS/MS Spectrum - 10V, Negativesplash10-014i-0009000000-1237c0652fcc50cc23ad2016-09-12View Spectrum
Predicted MS/MSPredicted LC-MS/MS Spectrum - 20V, Negativesplash10-01b9-0009000000-df22e761529a8f1dad172016-09-12View Spectrum
Predicted MS/MSPredicted LC-MS/MS Spectrum - 40V, Negativesplash10-00di-3339000000-361addf1b848f3eca0052016-09-12View Spectrum
NMRNot Available
Pathways
Pathways
Protein Targets
EnzymesNot Available
TransportersNot Available
Metal BindingsNot Available
ReceptorsNot Available
Transcriptional FactorsNot Available
Concentrations Data
Not Available
HMDB IDNot Available
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FoodDB IDNot Available
KNApSAcK IDNot Available
Chemspider IDNot Available
KEGG Compound IDNot Available
BioCyc IDTETRACOSANOATE
BiGG IDNot Available
Wikipedia LinkLignoceric acid
METLIN IDNot Available
PubChem Compound5461021
PDB IDNot Available
ChEBI ID31014
References
General References
  1. Turner CE, Elsohly MA, Boeren EG: Constituents of Cannabis sativa L. XVII. A review of the natural constituents. J Nat Prod. 1980 Mar-Apr;43(2):169-234. doi: 10.1021/np50008a001. [PubMed:6991645 ]