(2R,4S)-H-D-Pro(4-N3)-OH hydrochloride Catalog number: BADC-01912

(2R,4S)-H-D-Pro(4-N3)-OH hydrochloride, a chiral chemical compound, finds specific applications in biochemistry and molecular biology. Here are four key applications, presented with high perplexity and burstiness:

Peptide Synthesis: A versatile building block in peptide and protein synthesis, (2R,4S)-H-D-Pro(4-N3)-OH hydrochloride plays a crucial role in creating peptide chains with azide groups, allowing for intricate conjugation reactions. This process leads to the formation of complex peptide-based molecules used for both research and therapeutic endeavors.

Bioconjugation Chemistry: The azide functionality of (2R,4S)-H-D-Pro(4-N3)-OH hydrochloride is essential in bioorthogonal click chemistry, facilitating the linking of peptides and proteins to various biomolecules, such as dyes, drugs, or other peptides. This capability enables researchers to explore biological systems and craft innovative biomaterials without disrupting natural biological processes.

Drug Development: Within the realm of drug discovery, (2R,4S)-H-D-Pro(4-N3)-OH hydrochloride plays a pivotal role in designing peptide-based drugs, enhancing drug stability, specificity, and delivery mechanisms. Incorporating this compound into peptide structures can pave the way for the development of novel therapeutic agents with heightened efficacy and minimized side effects.

Protein Engineering: Employed in protein engineering, (2R,4S)-H-D-Pro(4-N3)-OH hydrochloride facilitates the introduction of specific modifications to protein structures, including labeling, cross-linking, or protein immobilization for diverse applications, such as enzyme assays, structural studies, and biosensor development. These modifications offer insights into protein function and behavior, advancing our understanding of complex biological processes.