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Product Categories:

Amino Acid Derivatives;

Amino Acid Esters

Application:

Peptide Synthesis: H-D-Phe(4-NO2)-Ome·HCl is often employed as a building block in solid-phase peptide synthesis. The methyl ester moiety stabilizes the amino acid, allowing for efficient coupling reactions and peptide chain elongation. The D-configuration of the phenylglycine residue ensures that the resulting peptides have the desired stereochemistry.

Structure-Activity Relationship Studies: The 4-nitrobenzoyl moiety introduces a specific chemical functionality into the peptide or protein, enabling researchers to investigate the effects of this modification on biological activity. Such studies are crucial in understanding the role of amino acid side chains in protein function and for designing novel therapeutic agents.

Protein Engineering and Modification: H-D-Phe(4-NO2)-Ome·HCl can be used to introduce modified amino acid residues into proteins, either during chemical synthesis or through post-translational modification. This allows for the creation of mutant proteins with altered properties or the attachment of specific labels or probes for bioconjugation and imaging applications.

Bioconjugation and Biomaterial Synthesis: The reactive functionalities present in H-D-Phe(4-NO2)-Ome·HCl enable its use in bioconjugation reactions. This compound can be covalently attached to other biomolecules, such as proteins, peptides, or polymers, to create functionalized biomaterials with unique properties and applications.

Manufacturer:

Sichuan HongRi Pharma-Tech Co., Ltd.