CAS 103884-97-5
:9H-Purine-2,6-diamine, 9-(2-deoxy-2-fluoro-β-D-arabinofuranosyl)-
Description:
9H-Purine-2,6-diamine, 9-(2-deoxy-2-fluoro-β-D-arabinofuranosyl)-, commonly known as a nucleoside analog, is characterized by its structural features that include a purine base and a modified sugar moiety. This compound is notable for the presence of a fluorine atom at the 2-deoxy position of the β-D-arabinofuranosyl sugar, which can influence its biological activity and stability. The purine base contributes to its potential role in nucleic acid synthesis and function, making it of interest in medicinal chemistry, particularly in the development of antiviral and anticancer agents. The compound's unique structure may enhance its ability to interfere with nucleic acid metabolism in target organisms or cells. Additionally, its solubility, stability, and interaction with biological macromolecules are critical factors that determine its pharmacological properties. Overall, this compound exemplifies the modifications made to nucleosides to improve therapeutic efficacy and reduce resistance in various biological contexts.
Formula:C10H13FN6O3
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Found 2 products.
2,6-Diaminopurine -9-β-D-(2'-deoxy-2'-fluoro)-arabinoriboside
CAS:Fluoro-modified nucleoside; arabino-nucleosideFormula:C10H13FN6O3Color and Shape:SolidMolecular weight:284.252,6-Diamino-9-(2'-deoxy-2'-fluoro-b-D-arabinofuranosyl)purine
CAS:<p>2,6-Diamino-9-(2'-deoxy-2'-fluoro-b-D-arabinofuranosyl)purine is a synthetic purine nucleoside analog. The fluorine substitution and sugar modification allow it to mimic natural nucleosides but disrupt DNA or RNA synthesis when incorporated. The fluorine makes the molecule more chemically stable and can influence how enzymes interact with it. Like other nucleoside analogs, it has the potential to act as a chain terminator or inhibit key enzymes like polymerases or reverse transcriptases.</p>Formula:C10H13FN6O3Purity:Min. 95%Color and Shape:White PowderMolecular weight:284.25 g/mol
