N-Benzoyl 7-deaza-2'-deoxyadenosine is a modified nucleoside that features a benzoyl group at the nitrogen position of the adenine base, specifically at the 7-position, and lacks the nitrogen atom at the 7-position of the purine ring, which is characteristic of 7-deaza derivatives. This compound is part of a class of nucleoside analogs that can be utilized in various biochemical and pharmaceutical applications, particularly in the study of nucleic acid interactions and as potential antiviral or anticancer agents. The modification of the adenine structure can influence its binding affinity to nucleic acids and enzymes, potentially altering its biological activity. N-Benzoyl 7-deaza-2'-deoxyadenosine is typically characterized by its solubility in organic solvents, stability under physiological conditions, and specific spectral properties that can be analyzed using techniques such as NMR and UV-Vis spectroscopy. Its unique structure allows researchers to explore the role of nucleobase modifications in nucleic acid function and drug design.

N-Benzoyl 7-deaza-2'-deoxyadenosine

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N6-Benzoyl-7-deaza-2'-deoxyadenosine is a novel synthetic monophosphate activator that can be used to induce cell death in cancer cells. It is structurally similar to the natural nucleotide adenosine, and it binds to the same receptors on cells as adenosine. N6-Benzoyl-7-deaza-2'-deoxyadenosine has been shown to inhibit viral replication by interfering with DNA synthesis and RNA transcription, which are essential for viral reproduction.

CAS 95261-09-9: N-Benzoyl 7-deaza-2'-deoxyadenosine

N6-Benzoyl-7-deaza-2'-deoxyadenosine

Ref: 3D-NB74991