Boc-D-Pro-OSu CAS:102185-34-2

Boc-D-Pro-OSu is widely employed in peptide synthesis to introduce D-proline residues into peptide sequences. As an N-hydroxysuccinimide (NHS) ester derivative, it selectively reacts with amino groups of other amino acids, facilitating the controlled and efficient formation of peptide bonds. This reactivity enables its use in both solution-phase peptide synthesis and solid-phase peptide synthesis (SPPS), where it aids in the stepwise assembly of peptide chains. Researchers and pharmaceutical scientists utilize Boc-D-Pro-OSu to create tailored peptides with specific D-amino acid sequences optimized for biological assays, structural studies, and drug development. By leveraging the reactivity of the NHS ester group, they achieve efficient coupling with amino groups, leading to the controlled elongation of peptide chains and the production of diverse peptide structures. The versatility of Boc-D-Pro-OSu makes it an invaluable tool in various fields such as biochemistry, pharmacology, and biotechnology. Its compatibility with standard peptide synthesis protocols, high yield, and reliable performance contribute to its widespread use in academic and industrial settings. Whether applied in basic research or drug discovery efforts, Boc-D-Pro-OSu facilitates the creation of peptides that underpin pivotal advancements in biomedical science and therapeutic innovation.