Cysteine

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Identification

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
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.

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