3,4-Dimethyl-L-phenylalanine, identified by its CAS number 142995-28-6, is an amino acid derivative that features a phenylalanine backbone with two methyl groups attached to the 3 and 4 positions of the aromatic ring. This modification can influence its biochemical properties, including its solubility, stability, and interaction with biological systems. The presence of the methyl groups may enhance lipophilicity, potentially affecting its absorption and distribution in biological contexts. As a non-standard amino acid, it may be utilized in various applications, including peptide synthesis and as a building block in drug development. The compound's chirality, being an L-isomer, is significant for its biological activity, as amino acids often exhibit different properties based on their stereochemistry. Additionally, the compound's structural characteristics may allow it to participate in specific interactions with enzymes or receptors, making it of interest in medicinal chemistry and biochemistry research. However, detailed studies on its pharmacokinetics and biological effects are essential for understanding its full potential and applications.

3,4-Dimethy-L-Phenylalanine

142995-28-6: 3,4-Dimethyl-L-phenylalanine, identified by its CAS number 142995-28-6, is an amino acid derivative that features a phenylalanine backbone with two methyl groups attached to the 3 and 4 positions of the aromatic ring. This modification can influence its biochemical properties, including its solubility, stability, and interaction with biological systems. The presence of the methyl groups may enhance lipophilicity, potentially affecting its absorption and distribution in biological contexts. As a non-standard amino acid, it may be utilized in various applications, including peptide synthesis and as a building block in drug development. The compound's chirality, being an L-isomer, is significant for its biological activity, as amino acids often exhibit different properties based on their stereochemistry. Additionally, the compound's structural characteristics may allow it to participate in specific interactions with enzymes or receptors, making it of interest in medicinal chemistry and biochemistry research. However, detailed studies on its pharmacokinetics and biological effects are essential for understanding its full potential and applications.

CAS 142995-28-6

3,4-Dimethy-L-Phenylalanine

L-Phenylalanine,3,4-dimethyl-

Ref: IN-DA007Z6K

3,4-Dimethyl-L-phenylalanine

Ref: 54-OR452017

(S)-2-amino-3-(3,4-dimethylphenyl)propanoic acid

Ref: 10-F721756