L-Alanyl-D-glutamic acid
- Molecular formula
- C8H15N2O4
- CAS Number
- 3383-45-9
- IUPAC Name
- 2-(1-carboxyethylamino)pentanoic acid
- Molecular Weight
- 189.20g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.4095g/cm3
- Synonyms
- SCHEMBL5940872
Identification
Interesting Facts About 2-(1-Carboxyethylamino)pentanoic Acid
2-(1-Carboxyethylamino)pentanoic acid, often referred to as a derivative of amino acids, exhibits intriguing characteristics that highlight its importance in both biological systems and potential applications. Here are some compelling facts about this compound:
- Amino Acid Derivative: This compound can be classified as an amino acid due to its amine and carboxylic acid functional groups, which play a crucial role in various metabolic processes.
- Biological Significance: Amino acids are vital for the synthesis of proteins, and derivatives like this one can serve as intermediates in metabolic pathways, potentially influencing the body's physiology.
- Synthesis Routes: Scientists often explore various synthesis pathways to create this compound, making it a point of interest for research in organic chemistry and pharmaceutical applications.
- Potential Therapeutic Uses: Compounds with similar structures are being investigated for their therapeutic properties, including roles in treating metabolic disorders and neurological conditions.
- Structural Diversity: The unique structure, with the branched chain and the carboxyethylamino group, allows for various interactions in biochemical systems, making it a subject of study.
As a student or a scientist delving into the realm of organic and medicinal chemistry, the exploration of 2-(1-carboxyethylamino)pentanoic acid opens up discussions about:
- How slight modifications to a compound's structure can drastically alter its biological function.
- The role of amino acid derivatives in protein folding and function.
- Contributions to the development of new drugs targeting specific metabolic pathways.
In conclusion, the study of 2-(1-carboxyethylamino)pentanoic acid not only enhances our understanding of organic chemistry but also bridges the gap between chemical structure and biological function, emphasizing the intricate relationships within biochemistry.