Boc-D-Phe(4-CN)-OH: A Key Component in Advanced Peptide Synthesis

Discover the synthesis, applications, and supply chain insights of this vital amino acid derivative.

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Key Advantages Offered

Enhanced Peptide Bioactivity

The strategic placement of the cyano group on the phenyl ring of D-phenylalanine, protected by the Boc group, significantly enhances the biological activity of synthesized peptides, making it a preferred choice for researchers aiming for potent and selective compounds.

Facilitates Targeted Drug Delivery

The compound's structure lends itself well to bioconjugation, enabling the precise attachment of biomolecules to therapeutic agents. This capability is fundamental in developing sophisticated targeted drug delivery systems, improving treatment efficacy and minimizing side effects.

Streamlined Synthesis Processes

The inclusion of the tert-butyloxycarbonyl (Boc) protecting group ensures orthogonal protection during peptide assembly. This facilitates controlled and efficient chain elongation, simplifying complex synthesis pathways and improving overall yields.

Key Applications

Peptide Synthesis

Serve as a key building block in solid-phase and solution-phase peptide synthesis, enabling the creation of novel peptide sequences with unique properties.

Drug Development

Utilized in the design and optimization of drug candidates, particularly in areas like cancer therapy and neuropharmacology, where modifying peptide properties is crucial.

Bioconjugation

Its structure supports bioconjugation techniques, allowing for the linking of peptides to other molecules for targeted therapeutic applications.

Analytical Chemistry

Employed as a standard in analytical methods to quantify similar compounds, ensuring quality control in pharmaceutical manufacturing and research settings.