CAS 22882-02-6
:2'-deoxy-N-methylcytidine
Description:
2'-Deoxy-N-methylcytidine is a modified nucleoside that is a derivative of cytidine, where a methyl group is attached to the nitrogen atom at the 5-position of the pyrimidine ring. This compound is characterized by its structural components, which include a deoxyribose sugar and a nitrogenous base. The presence of the methyl group can influence the nucleoside's biochemical properties, such as its stability and interaction with nucleic acids. 2'-Deoxy-N-methylcytidine is often used in research, particularly in studies related to DNA synthesis and modification, as well as in the development of nucleoside analogs for therapeutic applications. Its CAS number, 22882-02-6, is a unique identifier that facilitates the cataloging and referencing of this specific chemical substance in scientific literature and databases. Overall, this compound plays a significant role in molecular biology and medicinal chemistry, contributing to our understanding of nucleic acid function and the development of novel therapeutic agents.
Formula:C10H15N3O4
InChI:InChI=1/C10H15N3O4/c1-11-8-2-3-13(10(16)12-8)9-4-6(15)7(5-14)17-9/h2-3,6-7,9,14-15H,4-5H2,1H3,(H,11,12,16)/t6-,7+,9+/m0/s1
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Found 6 products.
2'-Deoxy-N-methyl-cytidine
CAS:Controlled Product<p>Applications 2'-Deoxy-N-methyl-cytidine is a nucleotide derivative used as an analytical reagent.<br>References Dupret, D.: Biomed. Health. Res., 23(Human Genome Analysis), 244-255 (1998)<br></p>Formula:C10H15N3O4Color and Shape:NeatMolecular weight:241.2442'-Deoxy-N4-methylcytidine
CAS:<p>2’-Deoxy-N4-methylcytidine (N(3)-Methyl-2'-deoxycytidine) is a purine nucleoside analog with potential antitumor activity for the study of apoptosis.</p>Formula:C10H15N3O4Purity:99.61%Color and Shape:SolidMolecular weight:241.242'-Deoxy-N4-methylcytidine
CAS:<p>2'-Deoxy-N4-methylcytidine is a modified nucleoside that is used to inhibit the activity of protein kinases. It has been shown to inhibit the function of two different types of enzymes, eukaryotic protein kinase and bacterial RNA polymerase. 2'-Deoxy-N4-methylcytidine inhibits the activity of these enzymes by modifying their structure, which in turn prevents them from carrying out their normal functions. This modification can be achieved through deamination or protonation reactions with this drug. The effects of this drug are nonparametric and are observed at transcript levels.</p>Formula:C10H15N3O4Purity:Min. 97 Area-%Color and Shape:White PowderMolecular weight:241.24 g/mol2'-Deoxy-N-methyl-cytidine-d3
CAS:Controlled ProductFormula:C10H12D3N3O4Color and Shape:NeatMolecular weight:244.26




