CHEBI:134548 - N-pentacosanoylsphingosine

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ChEBI Name N-pentacosanoylsphingosine
ChEBI ID CHEBI:134548
ChEBI ASCII Name N-pentacosanoylsphingosine
Definition A N-acylsphingosine in which the ceramide N-acyl group is specified as pentacosanoyl.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C43H85NO3
Net Charge 0
Average Mass 664.142
Monoisotopic Mass 663.65295
InChI InChI=1S/C43H85NO3/c1-3-5-7-9-11-13-15-17-18-19-20-21-22-23-24-25-27-29-31-33-35-37-39-43(47)44-41(40-45)42(46)38-36-34-32-30-28-26-16-14-12-10-8-6-4-2/h36,38,41-42,45-46H,3-35,37,39-40H2,1-2H3,(H,44,47)/b38-36+/t41-,42+/m0/s1
InChIKey QHPYSHVSWAOLHS-PVNBSDFKSA-N
SMILES C(=C/CCCCCCCCCCCCC)\[C@@H](O)[C@@H](NC(CCCCCCCCCCCCCCCCCCCCCCCC)=O)CO
Metabolite of Species Details
Rattus norvegicus (NCBI:txid10116) See: PubMed
Papio hamadryas (NCBI:txid9557) See: MetaboLights Study
Roles Classification
Biological Role(s): Papio hamadryas metabolite
Any mammalian metabolite produced during a metabolic reaction in Papio hamadryas.
rat metabolite
Any mammalian metabolite produced during a metabolic reaction in rat (Rattus norvegicus).
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-pentacosanoylsphingosine (CHEBI:134548) has functional parent pentacosanoic acid (CHEBI:39420)
N-pentacosanoylsphingosine (CHEBI:134548) has role Papio hamadryas metabolite (CHEBI:137684)
N-pentacosanoylsphingosine (CHEBI:134548) has role rat metabolite (CHEBI:86264)
N-pentacosanoylsphingosine (CHEBI:134548) is a N-acylsphingosine (CHEBI:52639)
N-pentacosanoylsphingosine (CHEBI:134548) is a Cer(d43:1) (CHEBI:137573)
IUPAC Name
N-[(2S,3R,4E)-1,3-dihydroxyoctadec-4-en-2-yl]pentacosanamide
Synonyms Sources
C25 ceramide ChEBI
Cer(d18:1/25:0) LIPID MAPS
ceramide (d18:1/25:0) ChEBI
N-(pentacosanoyl)-ceramide LIPID MAPS
N-(pentacosanoyl)-sphing-4-enine LIPID MAPS
N-pentacosanoylsphing-4-enine ChEBI
Manual Xrefs Databases
HMDB0004957 HMDB
LMSP02010013 LIPID MAPS
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Registry Numbers Types Sources
104404-17-3 CAS Registry Number HMDB
31222671 Reaxys Registry Number Reaxys
Citation Waiting for Citations Type Source
18835123 PubMed citation Europe PMC
Last Modified
06 July 2017