Chapter One - Exploration of the Sialic Acid World
-
Add time:09/07/2019 Source:sciencedirect.com
Sialic acids are cytoprotectors, mainly localized on the surface of cell membranes with multiple and outstanding cell biological functions. The history of their structural analysis, occurrence, and functions is fascinating and described in this review. Reports from different researchers on apparently similar substances from a variety of biological materials led to the identification of a 9-carbon monosaccharide, which in 1957 was designated “sialic acid.” The most frequently occurring member of the sialic acid family is N-acetylneuraminic acid, followed by N-glycolylneuraminic acid and O-acetylated derivatives, and up to now over about 80 neuraminic acid derivatives have been described. They appeared first in the animal kingdom, ranging from echinoderms up to higher animals, in many microorganisms, and are also expressed in insects, but are absent in higher plants. Sialic acids are masks and ligands and play as such dual roles in biology. Their involvement in immunology and tumor biology, as well as in hereditary diseases, cannot be underestimated. N-Glycolylneuraminic acid is very special, as this sugar cannot be expressed by humans, but is a xenoantigen with pathogenetic potential. Sialidases (neuraminidases), which liberate sialic acids from cellular compounds, had been known from very early on from studies with influenza viruses. Sialyltransferases, which are responsible for the sialylation of glycans and elongation of polysialic acids, are studied because of their significance in development and, for instance, in cancer. As more information about the functions in health and disease is acquired, the use of sialic acids in the treatment of diseases is also envisaged.
We also recommend Trading Suppliers and Manufacturers of 8-O-acetyl-N-acetylneuraminic acid (cas 18529-64-1). Pls Click Website Link as below: cas 18529-64-1 suppliers
Prev:Sialic acids in the extracellular polymeric substances of seawater-adapted aerobic granular sludge
Next:Syntheses of (α2–9) and (α2–8) linked dineuraminyl saccharides by use of 2β-bromo-3β-hydroxy-4,7,8,9-tetra-o-acetyl-n-acetylneuraminic acid methyl ester1) - 【Back】【Close 】【Print】【Add to favorite 】
- Related Information
- Molecular dynamics simulation and quantum mechanical calculations on α-d-N-acetylneuraminic acid09/25/2019
- Short communicationN-Acetylneuraminic acid aldolase-catalyzed synthesis of acyclic nucleoside analogues carrying a 4-hydroxy-2-oxoacid moiety09/24/2019
- ArticleN-Glycolylneuraminic Acid as a Receptor for Influenza A Viruses09/10/2019
- Characterization of Escherichia coli K1 colominic acid-specific murine antibodies that are cross-protective against Neisseria meningitidis groups B, C, and Y09/09/2019
- Syntheses of (α2–9) and (α2–8) linked dineuraminyl saccharides by use of 2β-bromo-3β-hydroxy-4,7,8,9-tetra-o-acetyl-n-acetylneuraminic acid methyl ester109/08/2019
- Sialic acids in the extracellular polymeric substances of seawater-adapted aerobic granular sludge09/06/2019
- Concise synthesis of 2,7-anhydrosialic acid derivatives and its application09/05/2019
-
Health and Chemical more >


