Inquiry Basket
N-α-Carbobenzoxy-S-trityl-L-cysteine, a derivative of the amino acid L-cysteine, boasts noteworthy applications in bioscience and chemical industries. Here are four key applications:
Protein Synthesis: Serving as a crucial safeguard in peptide synthesis, N-α-Carbobenzoxy-S-trityl-L-cysteine shields the thiol group of cysteine, warding off undesired side reactions amidst peptide chain construction. This protective measure guarantees the production of pristine polypeptides and proteins, catering to the demands of cutting-edge research and pharmaceutical pursuits.
Drug Development: Positioned at the forefront of pharmaceutical innovation, N-α-Carbobenzoxy-S-trityl-L-cysteine assumes a pivotal role in shaping and synthesizing novel drugs. Through its adeptness in modifying cysteine residues, it bolsters the stability of drug molecules, elevating their specificity and efficacy. This characteristic renders it an indispensable asset in the fabrication of peptide-based drug contenders, propelling advancements in therapeutic solutions.
Bioconjugation: Embraced in bioconjugation methodologies, N-α-Carbobenzoxy-S-trityl-L-cysteine facilitates the fusion of cysteine-laden peptides with diverse molecules like fluorophores or affinity tags. This merger empowers researchers to delve into protein interactions, localization, and function with heightened precision. Leveraging this derivative streamlines the conjugation process, fortifying the stability of the final bioconjugate, thereby expanding avenues for meticulous research exploration.
Analytical Chemistry: Within the realm of analytical chemistry, N-α-Carbobenzoxy-S-trityl-L-cysteine emerges as a requisite asset for sample preparation and derivative-driven procedures. Its protective groups enable the selective assessment of cysteine-enriched compounds within intricate mixtures, underscoring its role in accurate quantification and identification of peptides and proteins in biochemical assays, thus driving forward the frontiers of analytical precision.
