O-glycosyl compounds
O-Glycosyl compounds are a class of glycoconjugates where the sugar moiety is linked to an organic compound via an oxygen atom at the 1-position of the sugar. These compounds play crucial roles in biological systems, often serving as intermediates in carbohydrate metabolism or acting as key components in signaling pathways. O-Glycosylation can be found in various biomolecules such as proteins, lipids, and nucleic acids, contributing to their structural stability and functional diversity.
The synthesis of O-glycosyl compounds involves the coupling of a sugar donor with an acceptor molecule through an enzymatic or chemical process. This reaction typically requires a specific enzyme known as glycosyltransferase for biological systems, whereas chemical methods may involve harsher conditions such as acid catalysis or use of protecting groups.
O-Glycosylated molecules are extensively studied in the fields of biochemistry and medicinal chemistry due to their potential applications in drug design. They can serve as valuable tools for understanding complex biological processes and developing therapeutic agents targeting glycan-related diseases, including cancer, inflammation, and viral infections.
| Structure | Chemical Name | CAS | MF |
|---|---|---|---|
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D-(+)-Cellobiose Octaacetate | 3616-19-1 | C28H38O19 |
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Pteroside C | 35910-17-9 | C20H28O8 |
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(2S)-2-(Hydroxymethyl)-2,5,7-trimethyl-6-[2-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyethyl]-3H-inden-1-one | 35910-15-7 | C21H30O8 |
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D-chiro-Inositol, 2-O-.beta.-D-galactopyranosyl-4-O-methyl- | 88199-72-8 | C13H24O11 |
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(2R,3R,4S,5R,6S)-2-(hydroxymethyl)-6-methoxyoxane-3,4,5-triol | 3396-99-4 | C7H14O6 |
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Methyl α-D-mannopyranoside | 617-04-9 | C7H14O6 |
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β-Lactose | 5965-66-2 | C12H22O11 |
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Sucrose-1-13Cfru | 154368-11-3 | C12H22O11 |
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Cellulose | 9004-34-6 | C12H22O11 |
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Cornstarch | 9005-25-8 | C6H12O6 |
Related Literature
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Ivor Lon?ari? Phys. Chem. Chem. Phys., 2015,17, 9436-9445
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Joseph H. Bisesi,Tara Sabo-Attwood Environ. Sci.: Nano, 2014,1, 574-583
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Eléonore Resongles,Corinne Casiot,Fran?oise Elbaz-Poulichet,Rémi Freydier,Odile Bruneel,Christine Piot,Sophie Delpoux,Aurélie Volant,Angélique Desoeuvre Environ. Sci.: Processes Impacts, 2013,15, 1536-1544
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Yaling Zhang,Chunhui Dai,Shiwei Zhou,Bin Liu Chem. Commun., 2018,54, 10092-10095
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