(4R)-4-amino-4-phenylbutanoic acid, also known as phenylalanine derivative, is an amino acid characterized by its chiral center at the fourth carbon, which is crucial for its biological activity. This compound features an amino group (-NH2) and a carboxylic acid group (-COOH), typical of amino acids, allowing it to participate in peptide bond formation. The presence of a phenyl group contributes to its hydrophobic characteristics, influencing its solubility and interaction with other biomolecules. As a chiral molecule, it exists in two enantiomeric forms, but the (R) configuration is specifically associated with certain biological functions. This compound may play a role in various biochemical pathways, including protein synthesis and neurotransmitter regulation. Its unique structure allows it to interact with specific receptors and enzymes, making it of interest in pharmaceutical research and potential therapeutic applications. Additionally, its stability and reactivity can be influenced by environmental factors such as pH and temperature, which are important considerations in both laboratory and biological contexts.

(4R)-4-amino-4-phenylbutanoic acid

201863-97-0: benzenebutanoic acid, gamma-amino-, (gammaR)-, (4R)-4-Amino-4-phenylbutanoic acid

CAS 201863-97-0: (4R)-4-amino-4-phenylbutanoic acid

(R)-4-Amino-4-phenylbutanoic acid

Ref: 10-F234629

Benzenebutanoic acid, γ-amino-, (γR)-

Ref: IN-DA0027W8

(4R)-4-Amino-4-phenylbutanoic acid

Ref: 3D-BIA86397