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378755-69-2

378755-69-2 Structure

378755-69-2 Structure
IdentificationBack Directory
[Name]

N-palMitoyl-1-deoxysphinganine (M18:0/16:0)
[CAS]

378755-69-2
[Synonyms]

N-C16-deoxysphinganine
N-palMitoyl-1-deoxysphinganine (M18:0/16:0)
Hexadecanamide, N-[(1S,2R)-2-hydroxy-1-methylheptadecyl]-
N-PALMITOYL-1-DEOXYSPHINGANINE (M18:0/16:0);N-C16-DEOXYSPHINGANINE
[Molecular Formula]

C34H69NO2
[MDL Number]

MFCD22416666
[MOL File]

378755-69-2.mol
[Molecular Weight]

523.92
Chemical PropertiesBack Directory
[Boiling point ]

635.5±38.0 °C(Predicted)
[density ]

0.882±0.06 g/cm3(Predicted)
[storage temp. ]

-20°C
[pka]

14.54±0.20(Predicted)
Hazard InformationBack Directory
[General Description]

N-C16-deoxysphinganine Commonly referred to as 1-deoxydihydroceramide (1-deoxyDHCer), is the N-acylated form of 1-deoxysphinganine, a potent inhibitor of sphingolipid metabolism. The N-acyl group can be 16, 20 and 24 carbon chain. N-acylsphinganines (dihydroceramides) are synthesized by the acylation of sphingoid bases in the presence of ceramide synthases (CerS).
[Biochem/physiol Actions]

N-acylsphinganines (dihydroceramides) levels are lower during ceramide synthase inhibition. They are intermediates of ceramide and dihydrosphingolipids synthesis. Treatment of MCF7 cancer cells with fenretinide alters sphingolipid metabolism.
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