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CHEBI:134548 - N-pentacosanoylsphingosine

ChEBI IDCHEBI:134548
ChEBI NameN-pentacosanoylsphingosine
Stars
ASCII NameN-pentacosanoylsphingosine
DefinitionA N-acylsphingosine in which the ceramide N-acyl group is specified as pentacosanoyl.
Last Modified6 July 2017
Submittermwilliams
DownloadsMolfile
FormulaC43H85NO3
Net Charge0
Average Mass664.157
Monoisotopic Mass663.65295
SMILESCCCCCCCCCCCCC/C=C/[C@@H](O)[C@H](CO)NC(=O)CCCCCCCCCCCCCCCCCCCCCCCC
InChIInChI=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
InChIKeyQHPYSHVSWAOLHS-PVNBSDFKSA-N
Species of MetaboliteComponentSourceComments
Papio hamadryas (ncbitaxon:9557) - MetaboLights (MTBLS426)
Rattus norvegicus (ncbitaxon:10116) - PubMed (18835123)
Roles Classification
Biological Roles:
rat metabolite  Any mammalian metabolite produced during a metabolic reaction in rat (Rattus norvegicus).
Papio hamadryas metabolite  Any mammalian metabolite produced during a metabolic reaction in Papio hamadryas.
human metabolite  Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens).
ChEBI Ontology
Outgoing Relation(s)
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  Source
Cer(d18:1/25:0)LIPID MAPS
N-pentacosanoylsphing-4-enineChEBI
N-(pentacosanoyl)-ceramideLIPID MAPS
N-(pentacosanoyl)-sphing-4-enineLIPID MAPS
ceramide (d18:1/25:0)ChEBI
C25 ceramideChEBI
Manual XrefsDatabases
LMSP02010013LIPID MAPS
HMDB0004957HMDB
Registry NumbersSources
Reaxys:31222671Reaxys
CAS:104404-17-3HMDB
Citations