H-p-Me-D-Phe-OH, also known as 4-(p-methylphenyl)-D-phenylalanine, is a synthetic amino acid derivative characterized by its unique structural features. It contains a phenylalanine backbone with a para-methylphenyl group attached to the aromatic ring, which influences its hydrophobicity and steric properties. This compound is often studied in the context of peptide synthesis and drug design due to its potential to enhance the biological activity of peptides. The presence of the D-configuration of phenylalanine allows for specific interactions in biological systems, making it relevant in the development of pharmaceuticals, particularly in the field of neurobiology and receptor binding studies. Additionally, its solubility and stability can vary based on the pH and solvent conditions, which is crucial for its application in various biochemical assays. Overall, H-p-Me-D-Phe-OH serves as an important building block in medicinal chemistry and peptide research, contributing to the understanding of structure-activity relationships in drug development.

H-p-Me-D-Phe-OH

49759-61-7: H-p-Me-D-Phe-OH, also known as 4-(p-methylphenyl)-D-phenylalanine, is a synthetic amino acid derivative characterized by its unique structural features. It contains a phenylalanine backbone with a para-methylphenyl group attached to the aromatic ring, which influences its hydrophobicity and steric properties. This compound is often studied in the context of peptide synthesis and drug design due to its potential to enhance the biological activity of peptides. The presence of the D-configuration of phenylalanine allows for specific interactions in biological systems, making it relevant in the development of pharmaceuticals, particularly in the field of neurobiology and receptor binding studies. Additionally, its solubility and stability can vary based on the pH and solvent conditions, which is crucial for its application in various biochemical assays. Overall, H-p-Me-D-Phe-OH serves as an important building block in medicinal chemistry and peptide research, contributing to the understanding of structure-activity relationships in drug development.

CAS 49759-61-7

H-p-Me-D-Phe-OH

H-D-Phe(4-Me)-OH

Ref: IN-DA003LRX

4-Methyl-D-phenylalanine

Ref: 7W-GM4889

4-Methyl-D-phenylalanine

Ref: 54-OR14704

4-Methyl-D-phenylalanine

Ref: 10-M03245