Z-His-p-nitro-Phe-Phe-OMe, also known by its CAS number 15574-28-4, is a synthetic peptide derivative characterized by its specific amino acid sequence and modifications. The "Z" indicates the presence of a benzyloxycarbonyl (Z) protecting group on the N-terminus, which enhances stability and solubility. The inclusion of p-nitrophenylalanine (p-nitro-Phe) introduces an electron-withdrawing nitro group, which can influence the compound's reactivity and interactions, particularly in biochemical assays. The presence of two phenylalanine residues (Phe) contributes to the hydrophobic character of the molecule, potentially affecting its folding and binding properties. The "OMe" at the C-terminus signifies a methoxy group, which can also impact solubility and biological activity. Overall, Z-His-p-nitro-Phe-Phe-OMe is often utilized in research settings, particularly in studies involving peptide synthesis, enzyme inhibition, and drug design, due to its unique structural features and functional groups that facilitate various chemical interactions.

Z-His-p-nitro-Phe-Phe-OMe

15574-28-4: Z-His-p-nitro-Phe-Phe-OMe, also known by its CAS number 15574-28-4, is a synthetic peptide derivative characterized by its specific amino acid sequence and modifications. The "Z" indicates the presence of a benzyloxycarbonyl (Z) protecting group on the N-terminus, which enhances stability and solubility. The inclusion of p-nitrophenylalanine (p-nitro-Phe) introduces an electron-withdrawing nitro group, which can influence the compound's reactivity and interactions, particularly in biochemical assays. The presence of two phenylalanine residues (Phe) contributes to the hydrophobic character of the molecule, potentially affecting its folding and binding properties. The "OMe" at the C-terminus signifies a methoxy group, which can also impact solubility and biological activity. Overall, Z-His-p-nitro-Phe-Phe-OMe is often utilized in research settings, particularly in studies involving peptide synthesis, enzyme inhibition, and drug design, due to its unique structural features and functional groups that facilitate various chemical interactions.

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CAS 15574-28-4

Z-His-p-nitro-Phe-Phe-OMe

Z-His-p-nitro-Phe-Phe-OMe

Ref: 3D-FH111489