Interesting facts
Interesting Facts about 2-(2-aminopropanoylamino)-3-phenyl-propanoic acid
This compound, often referred to as a specialized amino acid derivative, showcases the complexity and versatility of amino acids in biochemical processes. Here are some intriguing aspects to consider:
- Structure & Function: The compound's structure features both an amino group and a propanoic acid moiety, which contribute to its potential functionality in various biochemical pathways.
- Biological Significance: Amino acids play critical roles in protein synthesis. The unique configuration of this compound suggests it could be pivotal for understanding enzyme interactions and metabolic pathways.
- Potential Applications: Due to its structure, this compound could be explored in drug design, especially in the realms of neurotransmitter function and hormonal regulation.
- Research Implications: The study of derivatives like this can lead to advances in medicinal chemistry, providing insights into antioxidant properties, anti-inflammatory potential, and their roles in disease prevention.
- Common Analogs: Many amino acid derivatives have been adapted for enhanced stability or bioavailability in pharmaceuticals, highlighting an ongoing trend in the modification of natural compounds for improved efficacy.
In conclusion, 2-(2-aminopropanoylamino)-3-phenyl-propanoic acid represents a fascinating intersection of organic chemistry and biotechnology, making it a compound of interest for ongoing research and innovation. As we continue to uncover the properties and implications of such compounds, the boundaries of drug development and therapeutic applications are continually expanded.
Synonyms
dl-Alanyl-dl-phenylalanine
1999-45-7
H-Ala-Phe-OH
2-(2-aminopropanamido)-3-phenylpropanoic acid
alanyl-DL-phenylalanine
2-(2-aminopropanoylamino)-3-phenylpropanoic acid
D-Alanyl-L-phenylalanine
L-Phenylalanine, N-L-alanyl-
CHEMBL161461
D-Ala-Phe-OH
59905-28-1
DL-Ala-DL-Phe
DL-Phenylalanine, N-DL-alanyl-
N-DL-Alanyl-DL-3-phenylalanine
Ala-Phe-OH
EINECS 217-885-6
MFCD00008074
Phenylalanine,alanyl-
Spectrum_000420
2-(2-Amino-propionylamino)-3-phenyl-propionic acid
dl-Alanyl-l-phenylalanine
Spectrum2_001347
H-DL-Ala-DL-Phe-OH
KBioSS_000900
DivK1c_000446
SPBio_001533
(2S)-2-[(2S)-2-AMINOPROPANAMIDO]-3-PHENYLPROPANOIC ACID
SCHEMBL2597740
HMS501G08
KBio1_000446
KBio2_000900
KBio2_003468
KBio2_006036
DTXSID40941963
CHEBI:137013
NINDS_000446
NSC89630
NSC89668
BDBM50085098
CCG-39285
N-(2-Aminopropanoyl)phenylalanine #
NSC-89630
NSC-89668
NSC118375
NSC339933
AKOS009157695
NSC 118375
NSC-118375
NSC-339933
IDI1_000446
LS-14092
DB-045054
DB-047816
DB-047817
DB-047818
DB-047819
A0223
NS00045642
N-(2-Amino-1-hydroxypropylidene)phenylalanine
T70522
Solubility of 2-(2-aminopropanoylamino)-3-phenyl-propanoic acid
The solubility of 2-(2-aminopropanoylamino)-3-phenyl-propanoic acid, with the chemical formula C12H14N2O3, can be influenced by several factors. Generally, this compound is expected to exhibit notable solubility characteristics due to its amino and carboxylic acid functional groups.
Overall, the compound is likely to be more soluble in polar solvents than in non-polar solvents. The balance between hydrophilic and hydrophobic characteristics will ultimately dictate the solubility behavior of the compound.
Understanding the solubility of this compound can provide significant insights into its practical applications and its behavior in different environments. As with many similar compounds, options for solubility testing might include:
In summary, while the initial insights into the solubility of this compound with C12H14N2O3 suggest a good potential for solubility in polar solvents, empirical testing remains crucial for precise characterization.