N-Acetyl-L-ornithine

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Identification

Molecular formula
C7H14N2O3
CAS Number
1949-84-8
IUPAC Name
2-acetamido-5-amino-pentanoic acid
Molecular Weight
188.21g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.2900g/cm3
Synonyms
N-Acetyl-ornithine
Interesting facts

Interesting Facts about 2-Acetamido-5-amino-pentanoic acid

2-Acetamido-5-amino-pentanoic acid, commonly known in the scientific community as a derivative of amino acids, is notable for its unique structural characteristics and functions. Here are several intriguing facts about this compound:

  • Amino Acid Precursor: This compound acts as a precursor to essential amino acids, playing a critical role in protein synthesis and metabolism.
  • Biological Importance: It is key in several biochemical pathways, particularly those involving the synthesis of other biologically active molecules.
  • Research Applications: Scientists have studied 2-acetamido-5-amino-pentanoic acid in various research contexts, particularly in pharmaceutical chemistry and biochemistry, investigating its potential therapeutic effects.
  • Structural Insights: The compound features an acetamido group, which contributes to its reactivity and interactions with biological systems.
  • Conformational Flexibility: The presence of multiple amino and carboxyl groups allows for significant conformational variability, impacting how it interacts with enzymes or receptor sites.

As chemists delve deeper into derivatives like 2-acetamido-5-amino-pentanoic acid, they reveal not only its unique properties but also its potential contributions to health and medicine. In the words of one researcher, “The understanding of amino acid derivatives like this compound opens new avenues for the development of targeted therapies.”

Exploring these compounds further may lead to advancements in fields such as nutrition and drug development, with implications too significant to overlook.

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