35085-18-8

Usage

Molecular Structure

2-ACETAMIDO-9-(2,3,5-TRI-O-BENZYL-BETA-D-ARABINOFURANOSYL)-6-CHLORO-9H-PURINE has a complex molecular structure that includes a purine base, a 2,3,5-tri-O-benzyl-beta-D-arabinofuranosyl moiety, an acetamido group, and a chloride substitution at specific positions.

Purine Base

The compound contains a purine base, which is a heterocyclic aromatic organic compound and a fundamental structure found in many important biological molecules, such as nucleotides and nucleic acids.

Chloride Substitution

The 6 position of the purine base features a chloride substitution, which can affect the compound's reactivity, stability, and interactions with other molecules.

Acetamino Group

At the 2 position, the compound has an acetamido group, which is an amide derivative of acetic acid and can form hydrogen bonds and coordinate with other molecules, influencing the compound's biological activity.

2,3,5-Tri-O-benzyl-Beta-D-arabinofuranosyl Moiety

The 9 position of the purine base is attached to a 2,3,5-tri-O-benzyl-beta-D-arabinofuranosyl moiety, which is a modified sugar component that can influence the compound's solubility, stability, and bioavailability.

Purine Nucleoside Class

2-ACETAMIDO-9-(2,3,5-TRI-O-BENZYL-BETA-D-ARABINOFURANOSYL)-6-CHLORO-9H-PURINE belongs to the class of purine nucleosides, which are derivatives of purine bases and play essential roles in various biological processes, such as DNA and RNA synthesis, energy transfer, and signal transduction.

Pharmaceutical and Biological Applications

Due to its unique structure and ability to interact with various cellular targets and enzymes, 2-ACETAMIDO-9-(2,3,5-TRI-O-BENZYL-BETA-D-ARABINOFURANOSYL)-6-CHLORO-9H-PURINE has potential importance in pharmaceutical and biological applications, although its specific uses and properties are still under investigation and study.