N-α-Carbobenzoxy-S-octyl-L-cysteine
Need Assistance?
  • US & Canada:
    +
  • UK: +

N-α-Carbobenzoxy-S-octyl-L-cysteine

* Please kindly note that our products are not to be used for therapeutic purposes and cannot be sold to patients.

Category
CBZ-Amino Acids
Catalog number
BAT-001467
Molecular Formula
C19H29NO4S
Molecular Weight
367.51
Synonyms
Z-Cys(Octyl)-OH; Z-Cys{(CH2)7-CH3}-OH

N-α-Carbobenzoxy-S-octyl-L-cysteine, a synthetic derivative of amino acid, finds applications in biochemical research and pharmaceutical development.

Peptide Synthesis: Serving as a shielded amino acid in peptide synthesis, N-α-Carbobenzoxy-S-octyl-L-cysteine plays a pivotal role in maintaining stability throughout synthesis stages. Its carbobenzoxy (Z) protecting group safeguards the cysteine residue, facilitating the formation of longer peptide chains without unintended side reactions. This intricate process ensures precise peptide assembly, with intricate protection mechanisms in place.

Enzyme Inhibition Studies: Unraveling the mysteries of enzyme inhibition mechanisms, N-α-Carbobenzoxy-S-octyl-L-cysteine is instrumental in research endeavors. By incorporating this derivative into enzyme substrates, scientists embark on a journey to explore how modifications impact enzyme activity. This exploration is fundamental in designing inhibitors for therapeutic enzymes or gaining insights into enzyme functionality within metabolic pathways, fostering a nuanced understanding of biochemical reactions.

Protein Structure Analysis: Delving into crystallographic studies, N-α-Carbobenzoxy-S-octyl-L-cysteine becomes a valuable asset for probing protein-ligand complex structures. Its distinctive side chain and protective group make it a potent tool for creating targeted protein modifications. This strategic approach aids in dissecting intricate interactions between proteins and their ligands, offering a glimpse into the intricacies of protein structure with an emphasis on detailed molecular interplay.

Drug Development: Unveiling new horizons in drug discovery, N-α-Carbobenzoxy-S-octyl-L-cysteine emerges as a catalyst in the synthesis of bioactive compounds. Its meticulously protected cysteine residue serves as a foundation for further modifications, paving the way for potential therapeutic agents. This modular approach accelerates the drug development process by providing a versatile array of chemical building blocks, catalyzing the creation of novel drugs with diverse therapeutic potentials.

Online Inquiry
Verification code
Inquiry Basket