Alanine, N-phenylalanyl-

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Identification

Molecular formula
C12H14N2O3
CAS Number
3061-88-9
IUPAC Name
2-(2-aminopropanoylamino)-3-phenyl-propanoic acid
Molecular Weight
237.28g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.3500g/cm3
Synonyms
dl-Alanyl-dl-phenylalanine
Interesting facts

Interesting Facts about 2-(2-aminopropanoylamino)-3-phenyl-propanoic acid

This compound, often referred to as a specialized amino acid derivative, showcases the complexity and versatility of amino acids in biochemical processes. Here are some intriguing aspects to consider:

  • Structure & Function: The compound's structure features both an amino group and a propanoic acid moiety, which contribute to its potential functionality in various biochemical pathways.
  • Biological Significance: Amino acids play critical roles in protein synthesis. The unique configuration of this compound suggests it could be pivotal for understanding enzyme interactions and metabolic pathways.
  • Potential Applications: Due to its structure, this compound could be explored in drug design, especially in the realms of neurotransmitter function and hormonal regulation.
  • Research Implications: The study of derivatives like this can lead to advances in medicinal chemistry, providing insights into antioxidant properties, anti-inflammatory potential, and their roles in disease prevention.
  • Common Analogs: Many amino acid derivatives have been adapted for enhanced stability or bioavailability in pharmaceuticals, highlighting an ongoing trend in the modification of natural compounds for improved efficacy.

In conclusion, 2-(2-aminopropanoylamino)-3-phenyl-propanoic acid represents a fascinating intersection of organic chemistry and biotechnology, making it a compound of interest for ongoing research and innovation. As we continue to uncover the properties and implications of such compounds, the boundaries of drug development and therapeutic applications are continually expanded.

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