CHEBI:72965 - N-tetracosanoylsphingosine

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name N-tetracosanoylsphingosine
ChEBI ID CHEBI:72965
ChEBI ASCII Name N-tetracosanoylsphingosine
Definition A N-acylsphingosine in which the ceramide N-acyl group is specified as tetracosanoyl.
Stars This entity has been manually annotated by the ChEBI Team.
Submitter Alan Bridge
Supplier Information
Download Molfile XML SDF
Formula C42H83NO3
Net Charge 0
Average Mass 650.11330
Monoisotopic Mass 649.63730
InChI InChI=1S/C42H83NO3/c1-3-5-7-9-11-13-15-17-18-19-20-21-22-23-24-26-28-30-32-34-36-38-42(46)43-40(39-44)41(45)37-35-33-31-29-27-25-16-14-12-10-8-6-4-2/h35,37,40-41,44-45H,3-34,36,38-39H2,1-2H3,(H,43,46)/b37-35+/t40-,41+/m0/s1
InChIKey ZJVVOYPTFQEGPH-AUTSUKAISA-N
SMILES CCCCCCCCCCCCCCCCCCCCCCCC(=O)N[C@@H](CO)[C@H](O)\C=C\CCCCCCCCCCCCC
Metabolite of Species Details
Mus musculus (NCBI:txidtxid10090) See: MetaboLights Study
Roles Classification
Biological Role(s): mouse metabolite
Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens).
(via N-acylsphingosine )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing N-tetracosanoylsphingosine (CHEBI:72965) has functional parent tetracosanoic acid (CHEBI:28866)
N-tetracosanoylsphingosine (CHEBI:72965) has role mouse metabolite (CHEBI:75771)
N-tetracosanoylsphingosine (CHEBI:72965) is a N-(very-long-chain fatty acyl)-sphingoid base (CHEBI:144712)
N-tetracosanoylsphingosine (CHEBI:72965) is a N-acylsphingosine (CHEBI:52639)
N-tetracosanoylsphingosine (CHEBI:72965) is a Cer(d42:1) (CHEBI:85777)
IUPAC Name
N-[(2S,3R,4E)-1,3-dihydroxyoctadec-4-en-2-yl]tetracosanamide
Synonyms Sources
C24 Cer LIPID MAPS
Cer(d18:1/24:0) LIPID MAPS
Ceramide (d18:1/24:0) HMDB
N-(tetracosanoyl)-sphing-4-enine UniProt
N-(tetracosanoyl)ceramide LIPID MAPS
N-(tetracosanoyl)sphing-4-enine SUBMITTER
N-lignoceroylsphingosine LIPID MAPS
N-tetracosanoylsphing-4-enine SUBMITTER
Manual Xrefs Databases
HMDB0004956 HMDB
LMSP02010012 LIPID MAPS
View more database links
Registry Number Type Source
1730385 Reaxys Registry Number Reaxys
Citation Waiting for Citations Type Source
22677645 PubMed citation Europe PMC
Last Modified
30 June 2017