CAS 214833-21-3

N6-Benzoyl-7-deaza-2'-deoxy-7-iodoadenosine

Description:

N6-Benzoyl-7-deaza-2'-deoxy-7-iodoadenosine is a modified nucleoside that exhibits unique structural and chemical characteristics. It is a derivative of adenosine, where the nitrogen at the 7-position is replaced by a carbon atom, resulting in the 7-deaza modification. The presence of a benzoyl group at the N6 position enhances its lipophilicity and may influence its biological activity, potentially affecting interactions with nucleic acid targets. The incorporation of iodine at the 7-position can impart distinct spectroscopic properties, making it useful in various biochemical applications, including imaging and labeling studies. This compound is often utilized in research related to nucleic acid chemistry, drug design, and molecular biology due to its ability to mimic natural nucleosides while providing additional functional properties. Its CAS number, 214833-21-3, allows for precise identification in chemical databases and literature. Overall, N6-Benzoyl-7-deaza-2'-deoxy-7-iodoadenosine serves as a valuable tool in the exploration of nucleoside analogs and their potential therapeutic applications.

Formula: C₁₈H₁₇IN₄O₄

Synonyms:

• N-(7-((2R,4S,5R)-4-hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-5-iodo-7H-pyrrolo[2,3-d]pyrimidin-4-yl)benzamide
• N6-Benzoyl-7-deaza-2'-deoxy-7-iodoadenosine
• Benzamide, N-[7-(2-deoxy-β-D-erythro-pentofuranosyl)-5-iodo-7H-pyrrolo[2,3-d]pyrimidin-4-yl]-

N6-Benzoyl-7-deaza-2'-deoxy-7-iodoadenosine

CAS: 214833-21-3

N6-Benzoyl-7-deaza-2'-deoxy-7-iodoadenosine is an antiviral compound that inhibits the synthesis of DNA and RNA. It is a synthetic, modified nucleoside with antiviral properties. The compound has been shown to be active against both animal and human tumor cells, as well as being effective in the treatment of viral infections.N6-Benzoyl-7-deaza-2'-deoxy-7-iodoadenosine is water soluble and biologically stable.

Purity: Min. 95%

Ref: 3D-NB137597