2'-Deoxy-5-methylisocytidine is a nucleoside analog characterized by its structural modification of the standard nucleoside framework. It features a deoxyribose sugar, which lacks an oxygen atom at the 2' position, and a methyl group attached to the 5-position of the isocytidine base. This modification can influence its biological activity, particularly in nucleic acid synthesis and interactions with enzymes. The compound is often studied for its potential applications in molecular biology and medicinal chemistry, particularly in the context of antiviral and anticancer research. Its unique structure may affect its binding affinity to nucleic acid targets and its stability in biological systems. The CAS number 19316-88-2 serves as a unique identifier for this compound, facilitating its identification in chemical databases and literature. Overall, 2'-deoxy-5-methylisocytidine represents an important tool in the study of nucleoside function and the development of therapeutic agents.

2'-DEOXY-5-METHYLISOCYTIDINE

19316-88-2: 5-Methyl-2'-Deoxyisocytidine, 2'-Decxy-5-methylisocytidine

5-Methyl-2'-deoxyisouridine

2'-Deoxy-5-methyl-isocytidine is an analog of cytidine that is used in the synthesis of oligodeoxynucleotides. It has shown to be complementary to dsDNA and to inhibit hepatitis B virus replication in cell culture. 2'-Deoxy-5-methyl-isocytidine is synthesized by solid phase chemistry on a polystyrene support with monomers, depyrimidination, and purification by column chromatography. The chemical stability of this compound has been shown by its ability to withstand heating at 100°C for 10 minutes without decomposition.

CAS 19316-88-2: 2'-DEOXY-5-METHYLISOCYTIDINE

5-Methyl-2'-deoxyisouridine

Ref: TM-TNU0711

2'-Deoxy-5-methyl-isocytidine

Ref: 3D-ND76392