N-Cbz-ala-ala-lys 4-methoxy-B-naphthylamide is a synthetic compound primarily used in biochemical research and peptide synthesis. The "N-Cbz" designation indicates that the amino group of the alanine residue is protected by a carbobenzyloxy (Cbz) group, which is commonly used to prevent unwanted reactions during peptide synthesis. The compound features two alanine residues and a lysine residue, contributing to its structure and functionality in biological systems. The presence of the 4-methoxy-B-naphthylamide moiety suggests that it may exhibit specific interactions with biological targets, potentially influencing its activity in assays or therapeutic applications. This compound is characterized by its stability under standard laboratory conditions, although it may require careful handling due to the presence of reactive functional groups. Its unique structure allows for potential applications in drug development, particularly in the design of peptide-based therapeutics. As with many synthetic peptides, purity and characterization through techniques such as HPLC and mass spectrometry are essential for ensuring its suitability for research purposes.

N-cbz-ala-ala-lys 4-methoxy-B-*naphthylamide form

100900-14-9: N-Cbz-ala-ala-lys 4-methoxy-B-naphthylamide is a synthetic compound primarily used in biochemical research and peptide synthesis. The "N-Cbz" designation indicates that the amino group of the alanine residue is protected by a carbobenzyloxy (Cbz) group, which is commonly used to prevent unwanted reactions during peptide synthesis. The compound features two alanine residues and a lysine residue, contributing to its structure and functionality in biological systems. The presence of the 4-methoxy-B-naphthylamide moiety suggests that it may exhibit specific interactions with biological targets, potentially influencing its activity in assays or therapeutic applications. This compound is characterized by its stability under standard laboratory conditions, although it may require careful handling due to the presence of reactive functional groups. Its unique structure allows for potential applications in drug development, particularly in the design of peptide-based therapeutics. As with many synthetic peptides, purity and characterization through techniques such as HPLC and mass spectrometry are essential for ensuring its suitability for research purposes.

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CAS 100900-14-9

N-cbz-ala-ala-lys 4-methoxy-B-*naphthylamide form

Z-Ala-Ala-Lys-4MbetaNA formiate salt

Ref: 3D-FA110620