Glycosyl compounds
Glycosyl compounds are a class of organic molecules characterized by the presence of a glycosidic bond, which links a carbohydrate (sugar) to another molecule such as an alcohol, amine, or even another sugar. These compounds play crucial roles in various biological processes and have diverse applications in both pharmaceutical and industrial fields. Structurally, glycosyl compounds can be mono-, oligo-, or polysaccharides depending on the number of monosaccharide units they contain. They are essential components in plant and animal cell walls and are involved in energy storage, immune responses, and cellular communication. In the medical field, certain glycosyl compounds exhibit potent therapeutic properties and have shown promise in treatments for diabetes, inflammation, and cancer. Their ability to modulate biological interactions makes them valuable tools in drug discovery and development.
| Structure | Chemical Name | CAS | MF |
|---|---|---|---|
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4-Nitrophenyl β-D-xylopyranoside | 2001-96-9 | C11H13NO7 |
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3-Ketotrehalose | 24885-76-5 | C12H20O11 |
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6-Aza-2-thiouridine | 27089-56-1 | C8H11N3O5S |
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4-Methylphenylthio-b-D-galactopyranoside | 28244-98-6 | C13H18O5S |
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Benzoic acid, p-(b-D-glucopyranosylamino)-, ethylester (8CI) | 28315-50-6 | C15H21NO7 |
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b-D-Glucopyranose,6-O-(2,3,4,6-tetra-O-acetyl-a-D-galactopyranosyl)-, 1,2,3,4-tetraacetate | 29873-67-4 | C28H38O19 |
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8-Hydroxyquinoline-β-D-glucopyranoside | 29266-96-4 | C15H17NO6 |
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1,3,5-Triazin-2(1H)-one,4-(dimethylamino)-1-b-D-ribofuranosyl- | 27826-77-3 | C10H16N4O5 |
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Trehalose octaacetate | 25018-27-3 | C28H38O19 |
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2',3',5'-Tri-O-Benzoyl-5-Azacytidine | 28998-36-9 | C29H24N4O8 |
Related Literature
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Byungho Lim,Jaewon Jin,Jin Yoo,Seung Yong Han,Kyeongyeol Kim,Sungah Kang,Nojin Park,Sang Moon Lee,Hae Jin Kim,Seung Uk Son Chem. Commun., 2014,50, 7723-7726
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3. Fe3O4/Au/Fe3O4 nanoflowers exhibiting tunable saturation magnetization and enhanced bioconjugationFeng Shi,Kunping Yan,Mingli Peng,Xiao Cheng,Yanling Luo,Xuemei Chen,V. A. L. Roy,Zuankai Wang Nanoscale, 2012,4, 747-751
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J. Xu,T. J. Carrocci,A. A. Hoskins Chem. Commun., 2016,52, 549-552
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