Adenosine monophosphate
- Molecular formula
- C10H14N5O7P
- CAS Number
- 61-19-8
- IUPAC Name
- [3,4-dihydroxy-2-(hydroxymethyl)-5-(phosphonooxymethyl)tetrahydrofuran-2-yl] dihydrogen phosphate
- Molecular Weight
- 347.22g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 2.1303g/cm3
- Synonyms
- 77164-51-3
Identification
Interesting Facts About [3,4-dihydroxy-2-(hydroxymethyl)-5-(phosphonooxymethyl)tetrahydrofuran-2-yl] dihydrogen phosphate
This intriguing compound, known as [3,4-dihydroxy-2-(hydroxymethyl)-5-(phosphonooxymethyl)tetrahydrofuran-2-yl] dihydrogen phosphate, has captured the interest of scientists due to its unique structure and potential applications. Here are some noteworthy aspects:
- Biochemical Significance: This compound is related to sugars and nucleotides, suggesting a role in energy transfer and biochemical pathways.
- Phosphorylation: The presence of phosphate groups highlights its importance in biological processes, especially in energy metabolism and signaling.
- Hydroxymethyl Groups: Hydroxymethyl functionalities can enhance the solubility and activity of the compound, making it potentially useful in pharmaceutical applications.
- Stereochemistry: The tetrahydrofuran ring introduces chirality into the molecule, which could lead to different biological activities depending on the stereoisomer.
- Research Applications: Due to its structural characteristics, this compound may serve as a model for studying nucleotide analogs in drug development.
As a researcher or chemistry student delving into the intricacies of this compound, one might ponder:
"How can the modification of such phosphorylated sugars lead to novel therapeutic agents?"
Understanding the chemical behavior and interactions of such compounds can pave the way for advancements in medicinal chemistry and biochemistry. This compound's complex structure provides a valuable opportunity for exploration and innovation in drug synthesis and design.