CAS 23643-36-9
:2,4(1H,3H)-Pyrimidinedione, 1-(2,3,5-tri-O-benzoyl-2-C-methyl-b-D-ribofuranosyl)-
Description:
2,4(1H,3H)-Pyrimidinedione, 1-(2,3,5-tri-O-benzoyl-2-C-methyl-b-D-ribofuranosyl)-, commonly referred to by its CAS number 23643-36-9, is a complex organic compound characterized by its pyrimidinedione core structure, which features two carbonyl groups and nitrogen atoms in a six-membered ring. This compound is notable for its glycosylated form, where a ribofuranosyl moiety is substituted with multiple benzoyl groups, enhancing its lipophilicity and stability. The presence of these benzoyl groups can influence the compound's solubility and reactivity, making it potentially useful in pharmaceutical applications. The compound may exhibit biological activity due to its structural similarity to nucleosides, which are essential in various biochemical processes. Its synthesis and characterization typically involve organic synthesis techniques, including protection and deprotection strategies for the ribofuranosyl unit. Overall, this compound represents a significant interest in medicinal chemistry, particularly in the development of antiviral or anticancer agents.
Formula:C31H26N2O9
Synonyms:- Uridine,2'-C-methyl-, 2',3',5'-tribenzoate
- 2'-C-methyl-,2',3',5'-tribenzoateuridine
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Found 5 products.
2'-C-Methyl -2',3',5'-tri-O-benzoyluridine
CAS:2'-C-Methyl -2',3',5'-tri-O-benzoyluridine is a 2'-C-Methyl nucleoside.Formula:C31H26N2O9Color and Shape:SolidMolecular weight:570.55Ref: TM-TNU0771
5mgTo inquire10mgTo inquire25mgTo inquire50mgTo inquire100mgTo inquire500mgTo inquire2',3',5'-Tri-O-benzoyl-2'-C-methyluridine
CAS:<p>2',3',5'-Tri-O-benzoyl-2'-C-methyluridine is a modified nucleoside that can be used as an antiviral and anticancer agent. It is synthesized by reacting 2-amino-5-(3,4,5,6-tetrahydropyrimidin-2(1H)-yl)benzoic acid with methyl 2',3',5'-tri-O-benzoylcytidine 5'-monophosphate in the presence of triethylamine. This compound has been shown to inhibit DNA synthesis by inhibiting the activity of DNA polymerase. The modification of the uracil ring with 3,4,5,6 tetrahydropyrimidine (THP) moieties provides additional stability to the molecule and confers antiviral activity.</p>Formula:C31H26N2O9Purity:Min. 95%Molecular weight:570.55 g/mol




