N-Acetylaspartylglutamic acid

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Identification

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
Interesting facts

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.

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