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Updated: May 3, 2026

Mass Spectrometric Analysis of Glycosphingolipid Antigens
Published on: April 16, 2013
Synthesis of neoglycosphingolipid from methoxyamino-functionalized ceramide
Junya Ishida1, Hiroshi Hinou2, Kentaro Naruchi3
1Graduate School of Life Science and Faculty of Advanced Life Science, Hokkaido University, N21, W11, Kita-ku, Sapporo 001-0021, Japan.
Abstract:
An efficient approach for the synthesis of a methoxyamino-functionalized ceramide was established from phytosphingosine using specific Nβ→Nα acyl migration of the octadecanoyl group during the removal of Nα-Fmoc protective group. One step glycoblotting reaction of the ceramide mimic with lactose afforded a neoglycosphingolipid showing potent inhibitory activity against recombinant endoglycoceramidase II from Rhodococcus sp.
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