General Information of MET (ID: META00597) |
Name |
CerP(d18:1/16:0)
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Synonyms |
Click to Show/Hide Synonyms of This Metabolite
Ceramide phosphate; Ceramide phosphate(D18:1/16:0); N-(Hexadecanoyl)-1-phosphate-4-sphingenine; N-(Hexadecanoyl)-1-phosphate-D-erythro-sphingosine; N-(Hexadecanoyl)-1-phosphate-D-sphingosine; N-(Hexadecanoyl)-1-phosphate-erythro-4-sphingenine; N-(Hexadecanoyl)-1-phosphate-sphing-4-enine; N-(Hexadecanoyl)-1-phosphate-sphingenine; N-(Hexadecanoyl)-1-phosphate-sphingosine; N-(Hexadecanoyl)-sphing-4-enine-1-phosphate; N-Hexadecanoylsphing-4-enine-1-phosphate; N-Hexadecanoylsphing-4-enine-1-phosphoric acid; N-Palmitoylsphing-4-enine-1-phosphate; N-Palmitoylsphing-4-enine-1-phosphoric acid; N-Palmitoylsphingosine 1-phosphate; N-Palmitoylsphingosine 1-phosphoric acid; [(e,2S,3R)-2-(Hexadecanoylamino)-3-hydroxyoctadec-4-enyl] dihydrogen phosphate
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Source |
Aliphatic acyclic compounds
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Structure Type |
Phosphosphingolipids (Click to Show/Hide the Complete Structure Type Hierarchy)
Lipids and lipid-like molecules
Sphingolipids
Phosphosphingolipids
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PubChem CID |
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HMDB ID |
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Formula |
C34H68NO6P
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Structure |
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3D MOL is unavailable
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2D MOL
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Click to Show/Hide the Molecular/Functional Data (External Links/Property/Function) of This Metabolite
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ChEBI ID |
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FooDB ID |
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ChemSpider ID |
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Physicochemical Properties |
Molecular Weight |
617.9 |
Topological Polar Surface Area |
116 |
XlogP |
11.8 |
Complexity |
668 |
Heavy Atom Count |
42 |
Rotatable Bond Count |
32 |
Hydrogen Bond Donor Count |
4 |
Hydrogen Bond Acceptor Count |
6 |
Function |
CerP(d18:1/16:0) is a ceramide 1-phosphate belonging to the sphingolipid class of molecules. Ceramides are amides of fatty acids with long-chain di- or trihydroxy bases, the commonest in animals being sphingosine and in plants phytosphingosine. The acyl group of ceramides is generally a long-chain saturated or monounsaturated fatty acid. The most frequent fatty acids found in animal ceramides are 18:0, 24:0 and 24:1(n-9). Ceramide 1-phosphates are produced by phosphorylation of ceramide by a specific ceramide kinase. Ceramide-1-phosphate was shown to be a specific and potent inducer of arachidonic acid and prostanoid synthesis in cells through the translocation and activation of the cytoplasmic phospholipase A2.
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Regulatory Network
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