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Adenosine-3',5'-bisphosphate

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Identification
Molecular formula
C10H13N5O7P
CAS number
82-94-0
IUPAC name
(2-amino-3-phenyl-propyl) [5-(6-aminopurin-9-yl)-3,4-dihydroxy-tetrahydrofuran-2-yl]methyl hydrogen phosphate
State
State
At room temperature, Adenosine-3',5'-bisphosphate is typically a solid.

It is highly soluble in water, which is a polar solvent, but may not be as soluble in non-polar solvents.

Melting point (Celsius)
380.00
Melting point (Kelvin)
653.15
Boiling point (Celsius)
750.00
Boiling point (Kelvin)
1 023.00
General information
Molecular weight
347.22g/mol
Molar mass
347.2210g/mol
Density
2.2100g/cm3
Appearence

The compound is typically found as a white or off-white crystalline powder. It is hygroscopic, meaning it may absorb moisture from the surrounding environment. When in pure form, it is odorless.

Comment on solubility

Solubility of (2-amino-3-phenyl-propyl) [5-(6-aminopurin-9-yl)-3,4-dihydroxy-tetrahydrofuran-2-yl]methyl hydrogen phosphate

The solubility of the compound (2-amino-3-phenyl-propyl) [5-(6-aminopurin-9-yl)-3,4-dihydroxy-tetrahydrofuran-2-yl]methyl hydrogen phosphate, with the chemical formula C10H13N5O7P, presents some notable characteristics that are typically observed in its chemical class. Understanding its solubility can lead to important implications for its applications and behavior in various environments.

Factors Affecting Solubility

  • Polarity: The presence of multiple functional groups such as amino and hydroxyl groups suggests that this compound has a polar character, which generally enhances solubility in polar solvents like water.
  • Hydrogen Bonding: The ability of the compound to form hydrogen bonds with water molecules will significantly impact its solubility. More hydrogen bonds usually lead to higher solubility.
  • Ionic Interactions: The phosphate group (-OPO3H2) can also interact with other ions, potentially enhancing solubility in ionic environments.

In summary, while the specific solubility of this compound is not extensively reported, the theoretical considerations based on its functional groups suggest that it is likely soluble in water and potentially in a variety of polar solvents. Further experimental data would be necessary to provide exact figures, but it can be postulated that the compound may exhibit moderate to high solubility. Thus, examining its solubility in different solvents will uncover valuable insights into its chemical behavior and usability.

Interesting facts

Interesting Facts About (2-amino-3-phenyl-propyl) [5-(6-aminopurin-9-yl)-3,4-dihydroxy-tetrahydrofuran-2-yl]methyl hydrogen phosphate

This compound is a fascinating example of how structural complexity can contribute to a molecule's function. It incorporates multiple functional groups, which allows it to participate in various biological interactions, making it of interest in pharmacology and biochemistry.

Key Features:

  • Amino Groups: The presence of amino groups suggests potential for hydrogen bonding and interaction with biomolecules, enhancing its biological activity.
  • Phenyl Ring: The phenyl group may contribute to the compound's hydrophobic character, which can influence membrane permeability and biological targeting.
  • Hydroxyl Groups: The dihydroxy component allows for further reactivity and potential in various chemical modifications, paving the way for drug development.
  • Nucleobase Derivative: With a portion derived from purine, it raises questions about its role in nucleic acid metabolism and potential applications in molecular biology.

Researchers are particularly intrigued by this compound's potential applications in drug design. Its complex architecture could lead to novel therapeutic agents in treating various conditions, especially those related to cellular signaling and metabolic pathways. As noted by experts in the field, "The integration of pharmacophoric elements in a single molecule amplifies the chances of selective targeting in disease mechanisms."

Moreover, the inclusion of phosphate groups can facilitate interactions with enzymes, potentially leading to inhibition or enhancement of specific biochemical pathways. The interdisciplinary nature of studying such compounds bridges the gap between organic chemistry, biochemistry, and medicinal chemistry, making it a rich area for exploration and innovation.