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Atomfair 2-amino-9-[(2R,4S,5R)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-5H-purin-6-one;hydrate C10H15N5O5

Description 2-amino-9-[(2R,4S,5R)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-5H-purin-6-one hydrate is a high-purity nucleoside analog with the molecular formula C10H15N5O5(CAS No. 312693-72-4). This compound features a modified purine base linked to a ribose-like sugar moiety, making it valuable for biochemical and pharmaceutical research. The product is supplied as a hydrate to ensure stability and is characterized by rigorous quality control, including HPLC and NMR analysis. Ideal for nucleotide synthesis, enzyme studies, and antiviral research, this compound is packaged under inert conditions to maintain purity. Each batch is accompanied by comprehensive analytical data for research reproducibility.

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Description

Description

2-amino-9-[(2R,4S,5R)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-5H-purin-6-one hydrate is a high-purity nucleoside analog with the molecular formula C10H15N5O5 (CAS No. 312693-72-4). This compound features a modified purine base linked to a ribose-like sugar moiety, making it valuable for biochemical and pharmaceutical research. The product is supplied as a hydrate to ensure stability and is characterized by rigorous quality control, including HPLC and NMR analysis. Ideal for nucleotide synthesis, enzyme studies, and antiviral research, this compound is packaged under inert conditions to maintain purity. Each batch is accompanied by comprehensive analytical data for research reproducibility.

  • CAS No: 312693-72-4
  • Molecular Formula: C10H15N5O5
  • Molecular Weight: 285.26
  • Exact Mass: 285.10731860
  • Monoisotopic Mass: 285.10731860
  • IUPAC Name: 2-amino-9-[(2R,4S,5R)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-5H-purin-6-one;hydrate
  • SMILES: C1[C@@H]([C@H](O[C@H]1N2C=NC3C2=NC(=NC3=O)N)CO)O.O

Application

This nucleoside analog is widely used in biochemical research for studying enzyme mechanisms, particularly those involving purine metabolism. It serves as a precursor in the synthesis of modified nucleotides for antiviral and anticancer drug development. Researchers also utilize it to investigate RNA/DNA interactions and polymerase activities in molecular biology studies.

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