Interesting facts
Interesting Facts about 2-(3-aminopropanoylamino)-4-methyl-pentanoic acid
2-(3-aminopropanoylamino)-4-methyl-pentanoic acid, often referred to as a derivative of amino acids, is a fascinating compound that intersects various fields like biochemistry, medicinal chemistry, and nutrition. Here are some intriguing highlights:
- Amino Acid Connection: This compound can be categorized as an α-amino acid, meaning it contains both an amino group and a carboxylic acid group. Such structural features allow this compound to participate in many biological reactions.
- Structural Diversity: The presence of both an amino group (-NH2) and an additional functional group contributes to its unique structural properties. This intricacy supports diverse biological functions, playing a crucial role in protein synthesis and metabolism.
- Potential Therapeutic Uses: Similar to other amino acid derivatives, 2-(3-aminopropanoylamino)-4-methyl-pentanoic acid holds promise in pharmaceutical research. Researchers are investigating potential applications such as neuroprotective agents and metabolic modulating drugs.
- Natural Sources: Many amino acid derivatives have been sourced from natural proteins and peptides, hinting at a deeper biochemical significance in organisms. Exploring these natural origins can pave the way for new findings in biochemistry.
- Research Feasibility: Scientists are constantly exploring amino acid derivatives due to their abundance and diverse reactivity. This compound is likely being investigated in laboratories worldwide for its role in various biochemical pathways.
Overall, 2-(3-aminopropanoylamino)-4-methyl-pentanoic acid exemplifies the remarkable complexity and utility of amino acid derivatives in both nature and scientific research. As chemists continue to unlock its potential, the implications for health and industry could be significant.
Synonyms
H-BETA-ALA-DL-LEU-OH
102029-56-1
2-(3-aminopropanoylamino)-4-methylpentanoic acid
2-(3-aminopropanamido)-4-methylpentanoic acid
Beta-alanyl-dl-leucine
N-(3-aminopropanoyl)leucine
SPBio_001567
Spectrum2_001354
Spectrum4_000816
Spectrum4_001195
KBioGR_001331
KBioGR_001889
DivK1c_000223
SCHEMBL6447009
CHEMBL3039404
HMS500L05
KBio1_000223
NINDS_000223
CCG-39292
AKOS010404076
IDI1_000223
PD118920
DB-043863
Solubility of 2-(3-aminopropanoylamino)-4-methyl-pentanoic acid
The solubility of 2-(3-aminopropanoylamino)-4-methyl-pentanoic acid (C9H18N2O3) is influenced by its molecular structure and functional groups.
Key Factors Affecting Solubility:
Overall, it is anticipated that this compound is moderately soluble in water while displaying reduced solubility in non-polar organic solvents. According to the principles of solubility, “like dissolves like,” thus polar solvents will dissolve this compound more readily than non-polar substances.