Adenosine
- Molecular formula
- C10H13N5O4
- CAS Number
- 58-61-7
- IUPAC Name
- 2-(7H-purin-6-ylamino)ethanol
- Molecular Weight
- 267.24g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.6100g/cm3
- Synonyms
- 4551-95-5
Identification
Interesting Facts About 2-(7H-purin-6-ylamino)ethanol
The compound 2-(7H-purin-6-ylamino)ethanol is a fascinating molecule that has piqued the interest of chemists and biochemists alike due to its structural characteristics and biological significance.
Biological Role
This compound is known to be involved in important biological processes. Here are some key roles it plays:
- Nucleic Acid Synthesis: 2-(7H-purin-6-ylamino)ethanol is a potential precursor in the synthesis of nucleotides, the building blocks of DNA and RNA.
- Enzyme Regulation: It can influence enzymatic functions, acting as an important cofactor in several metabolic pathways.
- Cell Signaling: The compound has been studied for its role in cellular signaling, potentially impacting various physiological responses.
Chemical Properties
Despite its relatively simple structure, 2-(7H-purin-6-ylamino)ethanol exhibits interesting chemical properties:
- Amine and Alcohol Functional Groups: The presence of both amine and alcohol groups in its structure allows for diverse chemical reactivity, including hydrogen bonding and nucleophilic attacks.
- Stability: This compound has shown chemical stability under various conditions, which is an essential factor when considering its applications in pharmaceuticals.
Applications
With its unique properties, the compound has several potential applications:
- Pharmaceutical Development: Its biological relevance makes it a candidate for the development of drugs targeting specific proteins or pathways.
- Research Tool: This compound can be utilized in biochemical assays and experiments to study enzyme interactions and metabolic pathways.
In summary, 2-(7H-purin-6-ylamino)ethanol is more than just a chemical; it is a vital player in biochemical processes and a promising avenue for research in medicinal chemistry. Its intricate relationship with biological systems makes it a compelling subject of study for both scientists and chemistry students alike.