CHEBI:77413 - tetracosan-1-ol

ChEBI IDCHEBI:77413
ChEBI Nametetracosan-1-ol
Stars
DefinitionA very long-chain primary fatty alcohol that is tetracosane in which a hydrogen attached to one of the terminal carbons is replaced by a hydroxy group. It has been isolated from a variety of plants, including grape seeds, evening primrose (Oenothera biennis), pitaya fruits (Hylocereus polyrhizus and Hylocereus undatus), and the flowers of Arabian jasmine ( Jasminum sambac).
Last Modified24 September 2024
Submitterabridge
DownloadsMolfile
FormulaC24H50O
Net Charge0
Average Mass354.663
Monoisotopic Mass354.38617
SMILESCCCCCCCCCCCCCCCCCCCCCCCCO
InChIInChI=1S/C24H50O/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/h25H,2-24H2,1H3
InChIKeyTYWMIZZBOVGFOV-UHFFFAOYSA-N
Wikipedia
Species of MetaboliteComponentSourceComments
Ageratina adenophora (ncbitaxon:176616) leaf (BTO:0000713) PubMed (37225028) Species also known as Eupatorium glandulosum.
Roles Classification
Biological Role:
plant metabolite  Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
Application:
vulnerary  A drug used in treating and healing of wounds.
ChEBI Ontology
Outgoing Relation(s)
tetracosan-1-ol (CHEBI:77413) has role plant metabolite (CHEBI:76924)
tetracosan-1-ol (CHEBI:77413) has role vulnerary (CHEBI:73336)
tetracosan-1-ol (CHEBI:77413) is a tetracosanol (CHEBI:205576)
tetracosan-1-ol (CHEBI:77413) is a very long-chain primary fatty alcohol (CHEBI:138741)
Incoming Relation(s)
22-methyltetracosan-1-ol (CHEBI:84926) has functional parent tetracosan-1-ol (CHEBI:77413)
IUPAC Name 
tetracosan-1-ol
Synonyms  Source
tetracosanolChemIDplus
lignoceryl alcoholChemIDplus
tetracosyl alcoholChemIDplus
1-tetracosanolNIST Chemistry WebBook
n-tetracosanolMetaCyc
n-tetracosanol-1NIST Chemistry WebBook
UniProt Name  Source
tetracosan-1-olUniProt
Manual XrefsDatabases
LMFA05000222LIPID MAPS
1-TetracosanolWikipedia
CPD-7874MetaCyc
FDB005216FooDB
C00034311KNApSAcK
Registry NumbersSources
Reaxys:1777129Reaxys
CAS:506-51-4NIST Chemistry WebBook
CAS:506-51-4ChemIDplus
Citations