CAS 161110-00-5

N4-BENZOYL-3'-DEOXYCYTIDINE

Description:

N4-Benzoyl-3'-deoxycytidine is a modified nucleoside analog that features a benzoyl group at the N4 position of the cytidine base and lacks the hydroxyl group at the 3' position of the ribose sugar, which is characteristic of deoxycytidine. This compound is of interest in the field of medicinal chemistry and molecular biology due to its potential applications in antiviral and anticancer therapies. The modification enhances its stability and may influence its interaction with nucleic acid targets. N4-benzoyl-3'-deoxycytidine can be utilized in various biochemical assays and research studies aimed at understanding nucleoside function and metabolism. Its structural modifications may also affect its binding affinity and selectivity towards specific enzymes or receptors, making it a valuable tool for investigating nucleoside-related processes. As with many nucleoside analogs, the pharmacological properties, including bioavailability and toxicity, are critical factors that determine its therapeutic potential.

Formula: C₁₆H₁₇N₃O₅

Synonyms:

• N4-Benzoyl-3'-deoxy-D-cytidine

N4-Benzoyl-3’-deoxycytidine

CAS: 161110-00-5

Formula: C₁₆H₁₇N₃O₅

Molecular weight: 331.3233

Ref: IN-DA001S68

N4-Benzoyl-3''-deoxycytidine

CAS: 161110-00-5

Ref: 7W-GN1182

N4-Benzoyl-3'-deoxycytidine

CAS: 161110-00-5

Nucleoside Derivatives - 3’-Deoxy nucleosides

Formula: C₁₆H₁₇N₃O₅

Color and Shape: Solid

Molecular weight: 331.32

Ref: TM-TNU1415

N4-Benzoyl-3'-deoxycytidine

CAS: 161110-00-5

N4-Benzoyl-3'-deoxycytidine is a novel antiviral agent that has shown activity against DNA and RNA viruses. It is an activator of DNA polymerase, which is essential for replication of viral nucleic acids. The compound is a modified nucleoside with a benzoyl group at the 4' position of the ribose moiety. It also has phosphoramidite, monophosphate, and diphosphate analogues. N4-Benzoyl-3'-deoxycytidine binds to the enzyme DNA polymerase, thereby inhibiting its ability to synthesize deoxyribonucleotides from ribonucleotides. This results in inhibition of viral DNA synthesis and subsequent inhibition of viral replication.

Formula: C₁₆H₁₇N₃O₅

Purity: Min. 95%

Color and Shape: White To Off-White Solid

Molecular weight: 331.32 g/mol

Ref: 3D-NB02825