4-[(2,4-Dimethoxyphenyl)(Fmoc-amino)methyl]phenoxyacetic Acid: A Key Linker in Peptide Synthesis and Drug Development

Explore the versatile applications of this critical chemical intermediate in advancing peptide synthesis and targeted drug delivery.

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Advantages of Utilizing This Intermediate

Enhanced Peptide Assembly

The Fmoc group provides UV-detectable amine protection, facilitating selective deprotection during peptide chain elongation in solid-phase peptide synthesis linkers.

Targeted Drug Delivery Capabilities

Its role as a linker is vital in drug development, allowing for the conjugation of therapeutic agents to targeting moieties for improved efficacy.

Versatile Bioconjugation Applications

The compound's structure is key for chemical linker for bioconjugation, enabling the stable attachment of biomolecules for research and diagnostic purposes.

Key Applications

Peptide Synthesis

This compound is a cornerstone for Rink amide linker peptide synthesis, enabling the creation of complex and biologically active peptides.

Drug Development

As an Fmoc-protected linker in drug delivery, it assists in creating conjugates with improved therapeutic profiles and targeted action.

Bioconjugation

Crucial for chemical linker for bioconjugation, it facilitates the conjugation of diverse molecules for advanced bioanalytical applications.

Anticancer Research

The compound's derivatives show potential in anticancer peptide linker applications, targeting specific cell pathways for therapeutic intervention.