H-4-Phenyl-D-Phe-OH, also known as a phenylalanine derivative, is a synthetic peptide that features a phenyl group attached to the D-phenylalanine amino acid. This compound is characterized by its structural properties, which include a phenyl ring that contributes to its hydrophobic characteristics, influencing its interactions in biological systems. The presence of the D-configuration of phenylalanine suggests that it may exhibit different biological activities compared to its L-counterpart, potentially affecting its role in peptide synthesis and receptor binding. H-4-Phenyl-D-Phe-OH is often studied in the context of drug design and development, particularly in the field of peptide therapeutics, due to its potential to mimic natural peptides while providing enhanced stability and bioactivity. Its CAS number, 170080-13-4, allows for easy identification in chemical databases, facilitating research and application in various scientific fields, including medicinal chemistry and biochemistry. Overall, this compound exemplifies the intricate relationship between molecular structure and biological function.

H-4-Phenyl-D-Phe-OH

170080-13-4: H-4-Phenyl-D-Phe-OH, also known as a phenylalanine derivative, is a synthetic peptide that features a phenyl group attached to the D-phenylalanine amino acid. This compound is characterized by its structural properties, which include a phenyl ring that contributes to its hydrophobic characteristics, influencing its interactions in biological systems. The presence of the D-configuration of phenylalanine suggests that it may exhibit different biological activities compared to its L-counterpart, potentially affecting its role in peptide synthesis and receptor binding. H-4-Phenyl-D-Phe-OH is often studied in the context of drug design and development, particularly in the field of peptide therapeutics, due to its potential to mimic natural peptides while providing enhanced stability and bioactivity. Its CAS number, 170080-13-4, allows for easy identification in chemical databases, facilitating research and application in various scientific fields, including medicinal chemistry and biochemistry. Overall, this compound exemplifies the intricate relationship between molecular structure and biological function.

CAS 170080-13-4

H-4-Phenyl-D-Phe-OH

[1,1'-Biphenyl]-4-propanoic acid, a-amino-, (R)-

Ref: IN-DA00HZD6

4-Phenyl-D-phenyalanine

Ref: 54-OR14745

(R)-3-([1,1′-Biphenyl]-4-yl)-2-aminopropanoic acid

Ref: 10-F228183