N-Acetylaspartylglutamic acid
- Molecular formula
- C11H16N2O8
- CAS Number
- 99941-00-3
- IUPAC Name
- 2-[(2-acetamido-3-carboxy-propanoyl)amino]pentanedioic acid
- Molecular Weight
- 290.26g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.5800g/cm3
- Synonyms
- N-Acetyl-Asp-Glu-OH
Identification
Interesting Facts about 2-[(2-acetamido-3-carboxy-propanoyl)amino]pentanedioic acid
2-[(2-acetamido-3-carboxy-propanoyl)amino]pentanedioic acid is a fascinating compound that falls under the category of amino acids, specifically a derivative of L-aspartic acid. Here are some intriguing aspects of this compound:
- Biosynthesis: It plays a crucial role in various metabolic pathways, especially in amino acid biosynthesis.
- pH Sensitivity: Its behavior can vary significantly with pH changes, making it essential in biochemical applications where pH stability is crucial.
- Enzyme Substrate: This compound can act as a substrate for specific enzymes, illustrating its importance in enzymatic reactions and metabolic processes.
- Therapeutic Potential: Due to its structure, it has been researched for potential therapeutic applications in treating metabolic disorders.
Notable Functional Groups
The compound contains several functional groups including:
- Amide groups that contribute to its chemical reactivity and stability.
- Carboxylic acid groups that play a vital role in acid-base behavior.
“Understanding the properties and reactions of such compounds opens doors to advancements in pharmaceuticals and biochemistry.” This quote encapsulates the significance of studying compounds like 2-[(2-acetamido-3-carboxy-propanoyl)amino]pentanedioic acid, which not only enhance our understanding of biochemistry but also hold potential for innovative therapeutic solutions.
In summary, this compound is not just a simple molecule; it is a crucial element in the biochemical landscape, paving the way for future discoveries and applications in health and medicine.