Synthetic Studies on Sialoglycoconjugates 89: Synthesis of Ganglioside GM3and KDN-GM3Containing Different Carbon-Chain Length Fatty Acyl Groups at the Ceramide Residue-Reference-Cited by-同舟云学术

Synthetic Studies on Sialoglycoconjugates 89: Synthesis of Ganglioside GM3and KDN-GM3Containing Different Carbon-Chain Length Fatty Acyl Groups at the Ceramide Residue

Published:1996-07 Issue:5 Volume:15 Page:639-648
ISSN:0732-8303
Container-title:Journal of Carbohydrate Chemistry
language:en
Short-container-title:Journal of Carbohydrate Chemistry

Author:

Hasegawa Akira,Suzuki Naomi,Kozawa Fumitaka,Ishida Hideharu,Kiso Makoto

Publisher

Informa UK Limited

Subject

Organic Chemistry,Biochemistry

Link

http://www.tandfonline.com/doi/pdf/10.1080/10256018808623883

Reference8 articles.

1. Ceramide structure predicts tumor ganglioside immunosuppressive activity.

2. A Chemically Synthesized Sialic Acid-Containing Glycoconjugate, 2-(tetradecylhexadecyl)-O-(5-acetamido-3,5-dideoxy-D-glycero-α-D-galacto-2-nonulopyranosylonic acid)-(2→3)-O-β-D-galactopyrannosyl-(1→4)-β-D-glucopyrannoside, Is a Potent Inhibitor of Cellular Immune Responses

3. Immunosuppressive Activity of Chemically Synthesized Gangliosides

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