L-Alanine
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- Molecular formula
- C3H7NO2
- CAS Number
- 56-41-7
- IUPAC Name
- (2S)-2-aminopropanoic acid
- Molecular Weight
- 89.09g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.4240g/cm3
- Synonyms
- L-alanine
Identification
Interesting facts
Interesting Facts About (2S)-2-Aminopropanoic Acid
(2S)-2-Aminopropanoic acid, commonly known as L-alanine, is one of the 20 standard amino acids vital for protein synthesis in living organisms. Here are some noteworthy points regarding this remarkable compound:
- Amino Acid Structure: L-alanine consists of an amino group, a carboxylic acid group, and a side chain that is simply a methyl group. This straightforward structure makes it a non-polar, aliphatic amino acid.
- Biological Role: As a key building block of proteins, L-alanine plays significant roles in metabolism. It is involved in the transamination process, indirectly contributing to glucose metabolism via gluconeogenesis.
- Energy Source: During prolonged fasting or intense exercise, L-alanine can be converted to glucose, serving as an important energy source for the body. Thus, it holds particular importance in muscle health and overall energy metabolism.
- Neurotransmitter Precursor: L-alanine is a precursor to other amino acids and neurotransmitters. It plays a vital role in neurotransmission, contributing to the central nervous system's overall balance.
- Food Sources: This amino acid is abundantly found in various protein-rich foods such as meat, poultry, fish, eggs, dairy products, and even in plant sources like soybeans and legumes.
- Supplement Use: Due to its essential roles in energy production and muscle recovery, L-alanine is often included in dietary supplements, especially those aimed at athletes.
As a simple yet essential amino acid, (2S)-2-aminopropanoic acid plays a multitude of roles both in the human body and in various biochemical processes. Its influence extends beyond just being a component of proteins, affecting metabolism, energy production, and overall health.