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1 chain ceramide, free sphingosine, and O-acyl-N-acetylsphingosine.
3 nhibited by the short chain ceramide analogs N-acetylsphingosine and N-hexanoylsphingosine (5-15 micr
7 acetylsphinganine (C2-DHCer) is as potent as N-acetylsphingosine (C2-Cer) in suppression of CYP2C11;
11 displayed increased resistance to exogenous N-acetylsphingosine (C2-ceramide) or N-hexanoylsphingosi
13 ve phosphorylation occurs in the presence of N-acetylsphingosine (C2-ceramide), a synthetic cell-perm
18 :30) were incubated with the supernatant and N-acetylsphingosine, the formation of free arachidonic a
20 enzyme that catalyzes the esterification of N-acetylsphingosine was purified from the postmitochondr
22 es esterification of a short chain ceramide, N-acetylsphingosine, was found in Madin-Darby canine kid
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