Chemoenzymatic Synthesis of Ganglioside Gm4 Analogs as Potential Immunosuppressive Agents
Author:
Affiliation:
1. a Department of Applied Bioorganic Chemistry , Gifu University , Gifu, 501-1193, Japan
Publisher
Informa UK Limited
Subject
Organic Chemistry,Biochemistry
Link
https://www.tandfonline.com/doi/pdf/10.1080/07328309908543992
Reference11 articles.
1. Synthetic studies on sialoglycoconjugares. Part CVII. Synthetic Studies on Selectin Ligands/Inhibitors. Synthesis and Biological Evaluation of Sulfated and Phosphorylated .BETA.-D-Galacto- and Lactopyranosides Containing Fatty-Alkyl Residues of Different Carbon Chain Lengths.
2. Immunosuppressive Activity of Chemically Synthesized Gangliosides
3. 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
4. Synthetic Studies on Sialoglycoconjugates 88: Synthesis of Ganglioside GM3and GM4Analogs Containing 2- OR 3-Branched Fatty-Alkyl Residues in Place of Ceramide
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