Adenosine triphosphate

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Identification

Molecular formula
C10H16N5O13P3
CAS Number
56-65-5
IUPAC Name
[[5-(2-amino-6-oxo-3H-purin-9-yl)tetrahydrofuran-2-yl]methoxy-hydroxy-phosphoryl] phosphono hydrogen phosphate
Molecular Weight
507.18g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.5000g/cm3
Interesting facts

Interesting Facts about [5-(2-amino-6-oxo-3H-purin-9-yl)tetrahydrofuran-2-yl]methoxy-hydroxy-phosphoryl phosphono hydrogen phosphate

This compound is a fascinating example of nucleoside derivatives, which play critical roles in biological systems. Here are some intriguing aspects:

  • Biological Significance: This compound features a purine base, which is foundational for the structure of nucleotides, the building blocks of DNA and RNA. The modification with phosphoryl groups enhances its functionality in various biochemical reactions.
  • Enzymatic Interactions: Its structure resembles substrates for key enzymes, potentially making it a target for enzymatic activity studies or drug design in biochemistry.
  • Phosphorylation: Phosphoryl groups are vital in energy transfer within cells via adenosine triphosphate (ATP). This compound may exhibit similar properties, which can lead to innovative applications in bioenergetics.
  • Synthetic Pathways: The synthesis of this compound often involves sophisticated organic synthesis techniques, showcasing the ingenuity present in modern chemistry.
  • Analytical Applications: The compound can be utilized in various analytical methods, including high-performance liquid chromatography (HPLC), due to its distinct chromophores.

In summary, this compound not only furthers our understanding of nucleoside biochemistry but also represents a synthesis challenge in organic chemistry. Its multifaceted roles and potential applications may inspire future research and pharmaceutical developments:

"The beauty of chemistry lies in the synthesis and understanding of complex structures that can unlock the mysteries of life itself."

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