Cysteine
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- Molecular formula
- C6H11NO2S
- CAS Number
- 52-90-4
- IUPAC Name
- 3-(2-amino-2-carboxy-ethyl)sulfanylbutanoic acid
- Molecular Weight
- 121.16g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.4600g/cm3
- Synonyms
- S-(2-CARBOXY-1-METHYLETHYL)-L-CYSTEINE
Identification
Interesting facts
Interesting Facts about 3-(2-amino-2-carboxy-ethyl)sulfanylbutanoic acid
3-(2-amino-2-carboxy-ethyl)sulfanylbutanoic acid, commonly referred to by its more approachable name, is an intriguing compound with various applications in biochemistry and nutrition. Below are some interesting highlights about this compound:
- Biochemical Role: This compound plays a critical role in the synthesis of peptides and proteins. Its structure allows it to serve as a building block, contributing to the overall functionality of biological molecules.
- Supplemental Significance: It is often included in dietary supplements aimed at enhancing muscle recovery and promoting overall health, especially in athletes.
- Amino Acid Derivative: This compound can be considered a derivative of amino acids, enriched with both carboxyl and amino groups, making it integral to metabolic processes.
- Mechanistic Interest: Researchers are particularly interested in its potential mechanisms within cellular signaling pathways, shedding light on how it may influence growth and repair.
- Potential Therapeutics: Preliminary studies suggest that this compound may hold promise for therapeutic uses, particularly in amino acid replacement therapies.
In conclusion, 3-(2-amino-2-carboxy-ethyl)sulfanylbutanoic acid exemplifies the fascinating world of biochemically significant compounds. Its versatile roles and potential health benefits make it a key subject of study for scientists and health enthusiasts alike. As scientists continue to explore its properties, we can anticipate even greater insights into this remarkable compound.