Phe-D-met-arg-phe amide, also known by its CAS number 84313-43-9, is a synthetic peptide that exhibits characteristics typical of peptide compounds. It is composed of a sequence of amino acids, specifically phenylalanine (Phe), D-methionine (D-met), arginine (Arg), and another phenylalanine (Phe), with an amide functional 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-amino acids, such as D-methionine, can enhance stability against enzymatic degradation, making such peptides of interest in therapeutic applications. Additionally, the hydrophobic nature of phenylalanine may influence the peptide's solubility and interaction with lipid membranes. Overall, the characteristics of Phe-D-met-arg-phe amide suggest its relevance in pharmacological research and potential therapeutic uses.

phe-D-met-arg-phe amide

84313-43-9: Phe-D-met-arg-phe amide, also known by its CAS number 84313-43-9, is a synthetic peptide that exhibits characteristics typical of peptide compounds. It is composed of a sequence of amino acids, specifically phenylalanine (Phe), D-methionine (D-met), arginine (Arg), and another phenylalanine (Phe), with an amide functional 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-amino acids, such as D-methionine, can enhance stability against enzymatic degradation, making such peptides of interest in therapeutic applications. Additionally, the hydrophobic nature of phenylalanine may influence the peptide's solubility and interaction with lipid membranes. Overall, the characteristics of Phe-D-met-arg-phe amide suggest its relevance in pharmacological research and potential therapeutic uses.

H-Phe-D-Met-Arg-Phe-NH2

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CAS 84313-43-9

phe-D-met-arg-phe amide

H-Phe-D-Met-Arg-Phe-NH2

Ref: IN-DA00G2OM

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

Ref: 3D-FP108980