5-Iodo-2'-O-methyl-cytidine is a modified nucleoside that features an iodine atom at the 5-position of the pyrimidine ring and a methoxy group at the 2'-position of the ribose sugar. This compound is part of the broader class of nucleosides, which are essential building blocks of nucleic acids like RNA and DNA. The introduction of the iodine atom can influence the compound's biological activity, potentially enhancing its stability and altering its interaction with nucleic acid targets. The 2'-O-methyl modification is known to confer resistance to nucleases, making it a valuable component in therapeutic applications, particularly in the development of antiviral and anticancer agents. Additionally, the presence of the methoxy group can affect the compound's solubility and binding affinity. Overall, 5-Iodo-2'-O-methyl-cytidine is of interest in medicinal chemistry and molecular biology for its potential roles in drug design and as a research tool in studying nucleic acid function and structure.

5-Iodo-2'-O-methyl-cytidine

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5-Iodo-2’-O-methylcytidine

5-Iodo-2’-O-methylcytidine is a nucleoside that is used as an activator for the synthesis of ribonucleosides. It is also used in the synthesis of DNA, RNA, and phosphoramidites. 5-Iodo-2’-O-methylcytidine has shown anticancer activity against a variety of cancer cell lines. This novel nucleotide exhibits high quality and purity, with an excellent yield and low impurities. The compound has been assigned CAS No. 847650-69-5 and its physical properties have been described in detail.

5-Iodo-2'-O-methylcytidine is a Halo-nucleoside; 2'-O-Methyl nucleoside.

CAS 847650-69-5: 5-Iodo-2'-O-methyl-cytidine

5-Iodo-2’-O-methylcytidine

Ref: IN-DA01E5FU

5-Iodo-2’-O-methylcytidine

Ref: 3D-NI144590

5-Iodo-2'-O-methylcytidine

Ref: TM-TNU0018