Unlock the Power of Protected Amino Acids: H-Orn(Z)-OH for Advanced Peptide Synthesis

Discover the indispensable role of N-delta-Benzyloxycarbonyl-L-ornithine (H-Orn(Z)-OH) in crafting intricate peptide structures for cutting-edge research and development.

Get a Quote & Sample

Advantages of Using H-Orn(Z)-OH

Controlled Reactivity

The selective N-delta protection of H-Orn(Z)-OH prevents undesired side reactions, allowing for accurate stepwise synthesis, which is a core tenet of efficient custom peptide synthesis.

Enhanced Peptide Stability

Utilizing protected ornithine derivatives like H-Orn(Z)-OH can lead to peptides with improved resistance to enzymatic degradation, a key factor in developing stable therapeutic peptides.

Facilitated Research

As a vital component in the field of amino acid chemistry, H-Orn(Z)-OH empowers researchers to explore novel peptide sequences and structures, accelerating breakthroughs in drug discovery and development.

Key Applications

Peptide Synthesis

H-Orn(Z)-OH is fundamental in constructing complex peptide sequences, serving as a reliable building block in both solid-phase and solution-phase synthesis, critical for producing custom peptide synthesis building blocks.

Biochemical Research

Researchers utilize this protected amino acid in various biochemical studies, including the development of peptide-based diagnostics and tools for probing biological pathways, leveraging its specific chemical properties.

Drug Discovery

The compound plays a role in screening peptide libraries and identifying potential drug candidates. Its precise structure aids in structure-activity relationship studies, a key aspect of modern drug discovery.

Pharmaceutical Intermediates

As a pharmaceutical intermediate, H-Orn(Z)-OH is essential for the synthesis of active pharmaceutical ingredients (APIs) that incorporate modified ornithine residues, supporting the development of new medicines.