α-L-Glucopyranose, 2-deoxy-2-(methylamino)-, also known by its CAS number 42852-95-9, is a derivative of glucose characterized by the presence of a methylamino group at the 2-position of the glucopyranose ring. This modification alters its chemical properties and biological activity compared to standard glucose. The compound is typically a white to off-white solid and is soluble in water due to the presence of hydroxyl groups, which facilitate hydrogen bonding. It exhibits characteristics common to amino sugars, including potential roles in biological processes such as cell signaling and metabolism. The methylamino group can influence the compound's reactivity and interaction with biological molecules, making it of interest in pharmaceutical and biochemical research. Additionally, its structural features may allow it to participate in various chemical reactions, including glycosylation and other modifications relevant in synthetic organic chemistry. Overall, α-L-Glucopyranose, 2-deoxy-2-(methylamino)- is a significant compound in the study of carbohydrate chemistry and its applications in medicinal chemistry.

a-L-Glucopyranose,2-deoxy-2-(methylamino)-

42852-95-9: α-L-Glucopyranose, 2-deoxy-2-(methylamino)-, also known by its CAS number 42852-95-9, is a derivative of glucose characterized by the presence of a methylamino group at the 2-position of the glucopyranose ring. This modification alters its chemical properties and biological activity compared to standard glucose. The compound is typically a white to off-white solid and is soluble in water due to the presence of hydroxyl groups, which facilitate hydrogen bonding. It exhibits characteristics common to amino sugars, including potential roles in biological processes such as cell signaling and metabolism. The methylamino group can influence the compound's reactivity and interaction with biological molecules, making it of interest in pharmaceutical and biochemical research. Additionally, its structural features may allow it to participate in various chemical reactions, including glycosylation and other modifications relevant in synthetic organic chemistry. Overall, α-L-Glucopyranose, 2-deoxy-2-(methylamino)- is a significant compound in the study of carbohydrate chemistry and its applications in medicinal chemistry.

<p>N-Methyl-L-glucosamine is a monosaccharide that is used as a building block for glycosaminoglycans. It can be synthesized by the enzyme glucoamylase from glucose and UDP-N-acetylglucosamine, or supplied exogenously as a dietary supplement. N-Methyl-L-glucosamine is stable in the presence of light and resistant to microbial degradation. This agent has been shown to be effective in inhibiting skin cancer in mice when combined with other agents such as hydroquinone, retinoic acid, and tretinoin. N-Methyl-L-glucosamine has been shown to have antiangiogenic properties on tubule cells, which may be due to its ability to inhibit the production of vascular endothelial growth factor (VEGF) in these cells.</p>

CAS 42852-95-9

a-L-Glucopyranose,2-deoxy-2-(methylamino)-

N-Methyl-L-glucosamine

Ref: 3D-MM157100