N-Cbz-L-Histidine Hydrazide: A Versatile Building Block for Peptide Synthesis

Explore advanced peptide chemistry with our high-purity N-Cbz-L-histidine hydrazide, a key intermediate for novel therapeutic discovery.

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Key Advantages

Enhanced Versatility

The ability to convert N-Cbz-L-histidine hydrazide to both peptide acids and amides provides researchers with versatile options for structure-activity relationship studies in drug discovery chemistry.

Improved Peptide Stability

Hydrazide modifications have been hypothesized to improve peptide stability against enzymatic degradation, potentially leading to enhanced therapeutic efficacy and longer shelf life.

Facilitated Library Synthesis

This building block is key for efficient solid-phase peptide synthesis, allowing for the creation of diverse peptide libraries for screening and lead optimization in the field of peptide therapeutics.

Key Applications

Peptide Synthesis Reagents

Essential component for synthesizing a wide range of peptides, including complex sequences and modified peptides, crucial for amino acid building blocks research.

Drug Discovery

Facilitates the exploration of novel peptide-based drug candidates by enabling late-stage modifications to optimize pharmacological properties and bioavailability.

Chemical Synthesis

A valuable tool in organic synthesis for researchers developing new chemical methodologies and creating diverse molecular structures.

Antimicrobial Peptide Research

Its derivatives have shown potent antimicrobial activity, making it a focus for research into new treatments for bacterial infections, a key area in antimicrobial peptide research.