
CAS 1106012-39-8
:8-Chloro-2’-beta-C-methyl inosine
Description:
8-Chloro-2’-beta-C-methyl inosine is a modified nucleoside that exhibits unique structural and functional characteristics. As a derivative of inosine, it features a chlorine atom at the 8-position and a beta-C-methyl group at the 2’-position of the ribose sugar. This modification can influence its biological activity, particularly in relation to its interaction with nucleic acid structures and enzymes. The presence of the chlorine atom may enhance its stability and alter its binding affinity to various biological targets, potentially making it useful in therapeutic applications, such as antiviral or anticancer treatments. Additionally, the beta-C-methyl modification can affect the nucleoside's metabolic pathways and its incorporation into RNA. The compound is of interest in medicinal chemistry and biochemistry for its potential roles in modulating biological processes and as a tool for studying nucleic acid function. Its specific properties, such as solubility, reactivity, and pharmacokinetics, would depend on the surrounding conditions and the presence of other chemical entities.
Formula:C11H13ClN4O5
Synonyms:- 8-Chloro-2’-beta-C-methylinosine
- 8-Chloro-2’-beta-C-methyl inosine
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8-Chloro-2'-β-C-methyl inosine
CAS:<p>Nucleoside Derivatives - 2’-Modified nucleosides; 8-Modified purine nucleosides; Halo-nucleosides</p>Formula:C11H13ClN4O5Color and Shape:SolidMolecular weight:316.7
