N-alpha-Boc-N-epsilon-benzyloxycarbonyl-D-lysine: A Cornerstone in Peptide Synthesis

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Advantages Offered

Precise Peptide Assembly

The dual protection system of Boc and Z groups on N-alpha-Boc-N-epsilon-benzyloxycarbonyl-D-lysine enables precise control over amino acid coupling during peptide synthesis, minimizing side reactions and ensuring high yields.

Versatile Application in SPPS

As a cornerstone in Boc strategy, this D-lysine derivative is indispensable for researchers and chemists engaged in solid-phase peptide synthesis, supporting the creation of a wide range of peptide structures.

Enables Structural Diversity

The incorporation of the D-isomer of lysine allows for the synthesis of peptides with unique conformational properties, which can be critical for therapeutic efficacy and stability in drug discovery.

Key Applications

Peptide Synthesis

N-alpha-Boc-N-epsilon-benzyloxycarbonyl-D-lysine serves as a fundamental building block for synthesizing a vast array of peptides, from simple sequences to complex therapeutic peptides.

Drug Discovery

Its utility in creating novel peptide-based therapeutics makes it invaluable for drug discovery programs aiming to develop new treatments for various diseases.

Biochemical Research

Researchers utilize this protected amino acid to construct peptides for studying protein-protein interactions, enzyme mechanisms, and other critical biological processes.

Custom Peptide Synthesis

It is a key reagent for custom peptide synthesis services, enabling the precise design and production of peptides tailored to specific research or commercial needs.