H-Cys(Acm)-OH·HCl: A Key Building Block for Peptide Synthesis and Disulfide Bond Formation
Discover the essential role of H-Cys(Acm)-OH·HCl in advanced peptide synthesis, enabling precise control over disulfide bond formation and unlocking new possibilities in drug discovery and biochemical research.
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H-Cys(Acm)-OH·HCl
As a reliable supplier in China, we offer H-Cys(Acm)-OH·HCl, a crucial protected D-cysteine derivative vital for sophisticated peptide synthesis. Its unique acetamidomethyl (Acm) protecting group on the sulfur atom allows for selective disulfide bond formation, a critical step in creating functional peptides. This compound is instrumental for researchers aiming to build complex peptide structures with high precision and purity, making it a cornerstone for innovative biochemical applications and drug discovery efforts.
- Facilitating Selective Disulfide Bond Formation: H-Cys(Acm)-OH·HCl is indispensable for achieving controlled and site-specific disulfide bridges in peptides, a key aspect of achieving desired biological activity.
- Orthogonal Protection Strategy: This compound's Acm group offers an orthogonal protection strategy, remaining stable while other protecting groups are removed, enabling sequential modifications in complex peptide sequences.
- Building Blocks for Peptide Synthesis: As a high-purity amino acid derivative, it serves as a fundamental building block in solid-phase and solution-phase peptide synthesis, supporting the creation of novel therapeutic peptides.
- Enhancing Peptide Stability and Function: The incorporation of D-amino acids, as in this D-cysteine derivative, can lead to peptides with increased resistance to enzymatic degradation, improving their pharmacokinetic profiles and therapeutic potential.
Key Advantages You Gain
High Purity and Reliability
Sourced from reputable manufacturers, our H-Cys(Acm)-OH·HCl is guaranteed for high purity (≥95%), ensuring consistent and reproducible results in your critical peptide synthesis projects.
Enabling Complex Peptide Architectures
The compound's specific protective group allows chemists to precisely control the assembly of complex peptides, including those with multiple cysteine residues and intricate disulfide linkages, significantly advancing research in this field.
Versatility in Research Applications
Whether for academic research or pharmaceutical development, this protected amino acid is a versatile tool, supporting advancements in drug discovery, protein engineering, and the study of bioactive peptides.
Key Applications
Peptide Synthesis
Essential for solid-phase and solution-phase synthesis, providing a reliable method for incorporating protected cysteine residues into peptide chains.
Disulfide Bond Engineering
Crucial for researchers focusing on selective disulfide bond formation, a key factor in the structure and function of many bioactive peptides and proteins.
Biochemical Research
Used in laboratories for a wide range of biochemical studies, including protein folding, enzyme mechanisms, and the development of peptide-based therapeutics.
Pharmaceutical Development
Serves as a vital intermediate in the synthesis of peptide drugs and other pharmaceutical compounds, contributing to the advancement of medicinal chemistry.