Z-Leu-Phe-NH2, also known as Z-Leucyl-Phenylalanine amide, is a synthetic dipeptide derivative characterized by the presence of a Z (benzyloxycarbonyl) protecting group on the leucine residue. This compound features a sequence of leucine (Leu) and phenylalanine (Phe) linked by a peptide bond, with an amide group at the terminal end. The Z group enhances the stability and solubility of the peptide, making it useful in various biochemical applications, particularly in peptide synthesis and drug development. Z-Leu-Phe-NH2 exhibits properties typical of peptides, such as the ability to form secondary structures and engage in specific interactions with biological targets. Its CAS number, 13171-96-5, allows for easy identification in chemical databases. This compound may be utilized in research related to protein synthesis, enzyme activity, and as a potential lead in therapeutic applications due to its structural characteristics and biological relevance.

Z-Leu-Phe-NH2

13171-96-5: Z-Leu-Phe-NH2, also known as Z-Leucyl-Phenylalanine amide, is a synthetic dipeptide derivative characterized by the presence of a Z (benzyloxycarbonyl) protecting group on the leucine residue. This compound features a sequence of leucine (Leu) and phenylalanine (Phe) linked by a peptide bond, with an amide group at the terminal end. The Z group enhances the stability and solubility of the peptide, making it useful in various biochemical applications, particularly in peptide synthesis and drug development. Z-Leu-Phe-NH2 exhibits properties typical of peptides, such as the ability to form secondary structures and engage in specific interactions with biological targets. Its CAS number, 13171-96-5, allows for easy identification in chemical databases. This compound may be utilized in research related to protein synthesis, enzyme activity, and as a potential lead in therapeutic applications due to its structural characteristics and biological relevance.

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CAS 13171-96-5

Z-Leu-Phe-NH2

Z-Leu-Phe-NH2

Ref: 3D-FL111498