Z-S-4-methoxybenzyl-L-cysteine
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Z-S-4-methoxybenzyl-L-cysteine

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Category
CBZ-Amino Acids
Catalog number
BAT-000481
CAS number
816446-81-8
Molecular Formula
C19H21NO5S
Molecular Weight
375.30
IUPAC Name
(2R)-3-[(4-methoxyphenyl)methylsulfanyl]-2-(phenylmethoxycarbonylamino)propanoic acid
Synonyms
Z-L-Cys(pMeOBzl)-OH
Purity
≥ 98% (HPLC)
Melting Point
63-72 °C
Storage
Store at 2-8 °C
InChI
InChI=1S/C19H21NO5S/c1-24-16-9-7-15(8-10-16)12-26-13-17(18(21)22)20-19(23)25-11-14-5-3-2-4-6-14/h2-10,17H,11-13H2,1H3,(H,20,23)(H,21,22)/t17-/m0/s1
InChI Key
ITIVJYICKMMKHE-KRWDZBQOSA-N
Canonical SMILES
COC1=CC=C(C=C1)CSCC(C(=O)O)NC(=O)OCC2=CC=CC=C2

Z-S-4-methoxybenzyl-L-cysteine, a specialized chemical compound with diverse applications in bioscience, presents myriad opportunities for innovative research and development. Here are four key applications:

Peptide Synthesis: Serving as a cornerstone in peptide synthesis, Z-S-4-methoxybenzyl-L-cysteine plays a pivotal role in constructing peptide chains with intricate structures. Its unique features enable the incorporation of methoxybenzyl and cysteine residues, facilitating the development of peptides with customized biological activities and heightened stability. This capacity sparks creativity in designing peptides with specific functionalities and properties.

Enzyme Inhibition Studies: Embarking on the exploration of enzyme inhibition studies, researchers leverage the distinct properties of Z-S-4-methoxybenzyl-L-cysteine to uncover the interactions between enzymes and cysteine-containing inhibitors. By dissecting how this compound binds to and obstructs specific enzymatic activities, scientists glean valuable insights for designing novel inhibitors to revolutionize therapeutic interventions. This profound investigation propels the growth of innovative approaches in enzyme inhibition research.

Pharmaceutical Development: In the dynamic landscape of pharmaceutical research, Z-S-4-methoxybenzyl-L-cysteine emerges as a pivotal player in synthesizing bioactive molecules. Serving as a precursor or intermediate, it streamlines the creation of potential drug candidates imbued with cysteine-like characteristics. By furnishing a sturdy and adaptable scaffold, this compound drives the exploration of novel pharmacological properties, setting the stage for groundbreaking advancements in drug discovery and development. This compound serves as a catalyst for pioneering pharmaceutical breakthroughs.

Protein Modification: Unleashing the potential of Z-S-4-methoxybenzyl-L-cysteine for site-specific protein modification opens up a realm of possibilities in protein engineering and therapeutics. By strategically integrating this compound into proteins, researchers can introduce targeted functional groups at specific cysteine residues, paving the way for in-depth studies on protein function and the development of protein-based therapies. This innovative technique propels the field of protein modification research towards new frontiers, enabling the customization of proteins with enhanced properties and functionalities.

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