CHEBI:77413 - tetracosan-1-ol

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ChEBI Name tetracosan-1-ol
ChEBI ID CHEBI:77413
Definition A 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).
Stars This entity has been manually annotated by the ChEBI Team.
Submitter abridge
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Formula C24H50O
Net Charge 0
Average Mass 354.65320
Monoisotopic Mass 354.38617
InChI InChI=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
InChIKey TYWMIZZBOVGFOV-UHFFFAOYSA-N
SMILES CCCCCCCCCCCCCCCCCCCCCCCCO
Metabolite of Species Details
Ageratina adenophora (NCBI:txid176616) Found in leaf (BTO:0000713). Species also known as Eupatorium glandulosum. See: PubMed
Roles Classification
Biological Role(s): plant metabolite
Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
Application(s): vulnerary
A drug used in treating and healing of wounds.
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ChEBI Ontology
Outgoing 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 22-methyltetracosan-1-ol (CHEBI:84926) has functional parent tetracosan-1-ol (CHEBI:77413)
IUPAC Name
tetracosan-1-ol
Synonyms Sources
1-tetracosanol NIST Chemistry WebBook
lignoceric alcohol NIST Chemistry WebBook
lignocerol NIST Chemistry WebBook
lignoceryl alcohol ChemIDplus
n-tetracosanol MetaCyc
n-tetracosanol-1 NIST Chemistry WebBook
tetracosanol ChemIDplus
tetracosyl alcohol ChemIDplus
Manual Xrefs Databases
1-Tetracosanol Wikipedia
C00034311 KNApSAcK
CPD-7874 MetaCyc
FDB005216 FooDB
LMFA05000222 LIPID MAPS
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Registry Numbers Types Sources
1777129 Reaxys Registry Number Reaxys
506-51-4 CAS Registry Number ChemIDplus
506-51-4 CAS Registry Number NIST Chemistry WebBook
Citations Waiting for Citations Types Sources
14472947 PubMed citation Europe PMC
19716291 PubMed citation Europe PMC
22417487 PubMed citation Europe PMC
24239848 PubMed citation Europe PMC
24386928 PubMed citation Europe PMC
28874162 PubMed citation Europe PMC
321567 Chinese Abstracts citation Europe PMC
34579407 PubMed citation Europe PMC
35885338 PubMed citation Europe PMC
37225028 PubMed citation Europe PMC
834119 PubMed citation Europe PMC
IND605264960 Agricola citation Europe PMC
IND605526742 Agricola citation Europe PMC
Last Modified
30 October 2023