CAS 282727-46-2
:Talose,2-(acetylamino)-2-deoxy-
Description:
Talose, 2-(acetylamino)-2-deoxy- is a synthetic derivative of talose, a sugar that belongs to the class of aldohexoses. This compound features an acetylamino group at the second carbon position, which distinguishes it from its parent sugar. The presence of the acetylamino group enhances its solubility and reactivity, making it useful in various biochemical applications. Talose derivatives are often studied for their potential roles in glycosylation reactions and as building blocks in the synthesis of more complex carbohydrates or glycoproteins. The compound is typically characterized by its molecular structure, which includes a six-membered ring with hydroxyl groups and an amine functional group. Its properties, such as melting point, solubility, and reactivity, can vary based on the specific conditions and solvents used. Talose derivatives may also exhibit biological activity, making them of interest in pharmaceutical and medicinal chemistry research. Overall, this compound represents a significant area of study within carbohydrate chemistry and its applications in biochemistry.
Formula:C8H15NO6
Synonyms:- N-Acetyl-D-Talosamine
- Talnac
- 2-Acetamido-2-deoxy-D-talopyranose
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Found 2 products.
2-Acetamido-2-deoxy-D-talopyranose
CAS:<p>2-Acetamido-2-deoxy-D-talopyranose is a noncompetitive inhibitor of the enzyme glycosidase. It has been shown to inhibit the enzymatic cleavage of glycoconjugates, such as glycoproteins and glycolipids, as well as antigen binding. 2-Acetamido-2-deoxy-D-talopyranose binds to the receptor binding domain on the surface of cancer cells and inhibits the growth of these cells in vitro. This compound also has potent inhibitory activity against influenza virus and is used in the synthesis of glycans for use in vaccines. 2-Acetamido-2-deoxy-D-talopyranose can be produced through acid hydrolysis or enzymatic methods.</p>Formula:C8H15NO6Purity:Min. 95%Color and Shape:PowderMolecular weight:221.2 g/mol

