
Bioorganic and Medicinal Chemistry p. 2245 - 2249 (1997)
Update date:2022-07-31
Topics:
Uchimura, Akira
Shimizu, Toshiyuki
Morita, Masahiro
Ueno, Hitomi
Motoki, Kazuhiro
Fukushima, Hideaki
Natori, Takenori
Koezuka, Yasuhiko
We compared the immunostimulatory effects of chemically synthesized α-galactosylceramides (α-GalCers), α-glucosylceramides (α-GluCers), 6''- monoglycosylated α-GalCer and 6''- or 4''-monoglycosylated α-GluCer and made the following observations: (1) the length of the fatty acid side chain in the ceramide portions greatly affects the immunostimulatory effects of α-GalCers and α-GluCers; (2) the configuration of the 4''-hydroxyl group of the inner pyranose moiety plays an important role in the immunostimulatory effects of monoglycosylated α-D-pyranosylceramides; (3) the free 4''-hydroxyl group of the inner pyranose of monoglycosylated α-D-pyranosylceramides plays a more important role in their immunostimulatory effects than the free 6''-hydroxyl group.
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