Thiaproline
- Molecular formula
- C4H9N2O3S
- CAS Number
- 6026-29-5
- IUPAC Name
- (2S)-2-amino-4-oxo-4-(sulfanylamino)butanoic acid
- Molecular Weight
- 163.19g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.5000g/cm3
- Synonyms
- (2S)-2-AMINO-3-(SULFANYLCARBAMOYL)PROPANOIC ACID
Identification
Interesting Facts about (2S)-2-amino-4-oxo-4-(sulfanylamino)butanoic acid
(2S)-2-amino-4-oxo-4-(sulfanylamino)butanoic acid, often referred to as a member of the amino acid family, has a variety of intriguing properties and applications in the field of biochemistry. Here are some engaging insights:
- Amino Acid Derivative: This compound is a derivative of the amino acid cysteine, which is essential for numerous biological functions, including protein synthesis and enzymatic reactions.
- Role in Metabolism: As an amino acid, it plays a crucial role in metabolic pathways where it is involved in the synthesis of proteins and other important biomolecules.
- Antioxidant Properties: Due to the presence of the thiol (-SH) group, this compound may exhibit antioxidant properties, which can help protect cells against oxidative stress.
- Structural Significance: The unique structure that features both an amino and keto group contributes to its diverse reactivity, allowing it to participate in various chemical reactions, including peptide bond formation.
- Biological Relevance: It can play a role in the structure and function of proteins that rely heavily on disulfide bonds, which are critical for maintaining protein stability.
In recent studies, the compound has attracted attention for its potential therapeutic applications. As scientists delve deeper into its biochemical pathways, they uncover its implications in:
- Drug Development: Investigating its role as a lead compound in pharmaceutical formulations aimed at treating various diseases.
- Nutritional Science: Assessing its benefits in nutritional supplements due to its amino acid profile.
- Genetic Engineering: Employing its properties in biotechnological applications for engineering protein function.
While (2S)-2-amino-4-oxo-4-(sulfanylamino)butanoic acid may not be as well-known as other amino acids, its fascinating chemistry continues to inspire researchers and chemists alike. In the words of one notable biochemist, "Understanding the complexity of amino acids is the key to unraveling the mysteries of life itself."