S-carboxymethyl-L-cysteine

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Identification

Molecular formula
C5H9NO4S
CAS Number
638-23-3
IUPAC Name
2-amino-4-(ethylsulfanylamino)-4-oxo-butanoic acid
Molecular Weight
179.21g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.2600g/cm3
Synonyms
Ethyl-scc
Interesting facts

Interesting Facts about 2-amino-4-(ethylsulfanylamino)-4-oxo-butanoic acid

This compound, often referred to in scientific literature, showcases an intriguing blend of functional groups that result in its unique chemical properties and potential applications. Here are some fascinating details:

  • Biochemical Significance: 2-amino-4-(ethylsulfanylamino)-4-oxo-butanoic acid is an analog of various amino acids, making it interesting for studies in biological systems, especially in protein synthesis and metabolism.
  • Potential Therapeutic Applications: The presence of the sulfanyl group suggests potential roles in enzyme inhibition, making this compound a candidate for drug development, particularly in targeting specific metabolic pathways.
  • Structure-Activity Relationship: This compound is an excellent model for understanding structure-activity relationships in medicinal chemistry. Researchers often explore how subtle changes in molecular structure can significantly impact biological activity.
  • Versatile Synthesis: The compound can be synthesized via various methods, providing chemists with the flexibility to modify its structure for research purposes. This can include changing substituents to enhance reactivity or selectivity.
  • Hydrophilic Nature: As an amino acid derivative, 2-amino-4-(ethylsulfanylamino)-4-oxo-butanoic acid likely exhibits hydrophilic characteristics, suggesting its potential for applications in aqueous environments, such as drug delivery systems.

In summary, the complex structure of 2-amino-4-(ethylsulfanylamino)-4-oxo-butanoic acid opens doors for diverse research avenues. Its role in biochemical processes, potential therapeutic implications, and unique chemical properties illustrate the beauty of organic chemistry.

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