Phe-met-D-arg-phe amide, also known by its CAS number 84313-44-0, is a synthetic peptide that exhibits characteristics typical of peptide compounds. It is composed of four amino acids: phenylalanine (Phe), methionine (Met), D-arginine (D-Arg), and another phenylalanine (Phe), with an amide group at the terminal end. This structure contributes to its potential biological activity, particularly in the context of receptor binding and signaling pathways. Peptides like this one often demonstrate specific interactions with biological targets, which can include hormones, neurotransmitters, or other signaling molecules. The presence of D-arginine, a non-natural amino acid, may enhance stability against enzymatic degradation, making it of interest in pharmaceutical applications. Additionally, the hydrophobic nature of phenylalanine and methionine can influence the peptide's solubility and interaction with lipid membranes. Overall, the unique sequence and structure of phe-met-D-arg-phe amide suggest potential utility in research and therapeutic contexts, particularly in areas related to peptide-based drug design and development.

phe-met-D-arg-phe amide

84313-44-0: Phe-met-D-arg-phe amide, also known by its CAS number 84313-44-0, is a synthetic peptide that exhibits characteristics typical of peptide compounds. It is composed of four amino acids: phenylalanine (Phe), methionine (Met), D-arginine (D-Arg), and another phenylalanine (Phe), with an amide group at the terminal end. This structure contributes to its potential biological activity, particularly in the context of receptor binding and signaling pathways. Peptides like this one often demonstrate specific interactions with biological targets, which can include hormones, neurotransmitters, or other signaling molecules. The presence of D-arginine, a non-natural amino acid, may enhance stability against enzymatic degradation, making it of interest in pharmaceutical applications. Additionally, the hydrophobic nature of phenylalanine and methionine can influence the peptide's solubility and interaction with lipid membranes. Overall, the unique sequence and structure of phe-met-D-arg-phe amide suggest potential utility in research and therapeutic contexts, particularly in areas related to peptide-based drug design and development.

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CAS 84313-44-0

phe-met-D-arg-phe amide

H-Phe-Met-D-Arg-Phe-NH2 acetate salt

Ref: 3D-FP110007