EMBL-EBI | Chemical Biology | ChEBI
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| Formula | C24H49NO3 |
| Net Charge | 0 |
| Average Mass | 399.660 |
| Monoisotopic Mass | 399.37124 |
| SMILES | CCCCCCCCCCCCCCC[C@@H](O)[C@H](CO)NC(=O)CCCCC |
| InChI | InChI=1S/C24H49NO3/c1-3-5-7-8-9-10-11-12-13-14-15-16-18-19-23(27)22(21-26)25-24(28)20-17-6-4-2/h22-23,26-27H,3-21H2,1-2H3,(H,25,28)/t22-,23+/m0/s1 |
| InChIKey | VUMHYWBWYSPQMM-XZOQPEGZSA-N |
| Roles Classification |
|---|
| Biological Roles: | 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). |
| ChEBI Ontology |
|---|
| Outgoing Relation(s) |
| N-hexanoyldihydroceramide (CHEBI:76226) has functional parent hexanoic acid (CHEBI:30776) |
| N-hexanoyldihydroceramide (CHEBI:76226) is a N-acylsphinganine (CHEBI:31488) |
| IUPAC Name |
|---|
| N-[(2S,3R)-1,3-dihydroxyoctadecan-2-yl]hexanamide |
| Synonyms | Source |
|---|---|
| N-hexanoyldihydrosphingosine | SUBMITTER |
| N-hexanoylsphinganine | ChEBI |
| C6-dihydroceramide | ChEBI |
| UniProt Name | Source |
|---|---|
| N-hexanoyl-sphinganine | UniProt |
| Registry Numbers | Sources |
|---|---|
| Reaxys:10125652 | Reaxys |
| Citations |
|---|