21691-41-8 Cbz-N-Me-L-Ala-OH

Peptide Synthesis: Cbz-N-Me-L-Ala-OH serves as a building block in solid-phase peptide synthesis. The benzoxycarbonyl (Cbz) protecting group stabilizes the amino group of the amino acid during the synthesis process, ensuring specific and efficient reactions. The N-methylation modifies the chemical properties of alanine, thereby influencing the overall properties and functions of the resulting peptides.

Drug Discovery and Development: Cbz-N-Me-L-Ala-OH and its peptide conjugates play a pivotal role in drug design and development. Due to their unique chemical structures, they may exhibit specific pharmacological activities, making them potential enzyme inhibitors, receptor ligands, or signal transduction molecules. This opens up opportunities for developing novel therapeutics or optimizing the performance of existing drugs.

Biological Activity Studies: The introduction of N-methylation in Cbz-N-Me-L-Ala-OH modifies the biological activity of alanine, altering the interactions between peptides and biomolecules such as proteins, enzymes, or receptors. This makes Cbz-N-Me-L-Ala-OH a powerful tool for studying biological activities, protein functions, and signal transduction pathways.

Structural Biology Research: Cbz-N-Me-L-Ala-OH can also be utilized in structural biology research to investigate the conformation, stability, and interactions of peptides with other biological molecules. This information is crucial for understanding biological processes, disease mechanisms, and drug action mechanisms.