Xanthosine, 6-O-methyl- is a modified nucleoside that features a xanthine base linked to a ribose sugar, with a methoxy group (-OCH3) attached at the 6-position of the xanthine moiety. This structural modification can influence its biochemical properties and interactions. Xanthosine derivatives are often studied for their potential roles in cellular metabolism and signaling pathways, particularly in relation to purine metabolism. The presence of the methoxy group may enhance its stability and solubility compared to its unmodified counterparts. Additionally, xanthosine derivatives can exhibit various biological activities, including potential antioxidant properties and effects on nucleotide synthesis. The compound is typically characterized by its molecular weight, solubility in polar solvents, and its behavior in biochemical assays. As with many nucleosides, it may also be involved in various enzymatic reactions, making it of interest in both pharmacological and biochemical research. Further studies are often required to elucidate its specific biological roles and potential applications in medicine or biotechnology.

Xanthosine, 6-O-methyl-

88508-71-8: Xanthosine, 6-O-methyl- is a modified nucleoside that features a xanthine base linked to a ribose sugar, with a methoxy group (-OCH3) attached at the 6-position of the xanthine moiety. This structural modification can influence its biochemical properties and interactions. Xanthosine derivatives are often studied for their potential roles in cellular metabolism and signaling pathways, particularly in relation to purine metabolism. The presence of the methoxy group may enhance its stability and solubility compared to its unmodified counterparts. Additionally, xanthosine derivatives can exhibit various biological activities, including potential antioxidant properties and effects on nucleotide synthesis. The compound is typically characterized by its molecular weight, solubility in polar solvents, and its behavior in biochemical assays. As with many nucleosides, it may also be involved in various enzymatic reactions, making it of interest in both pharmacological and biochemical research. Further studies are often required to elucidate its specific biological roles and potential applications in medicine or biotechnology.

CAS 88508-71-8

Xanthosine, 6-O-methyl-

Nelarabine Impurity 4

Ref: 4Z-N-529

6-O-Methylxanthosine

Ref: ST-EA-CP-N38007