CAS · 6254-48-4
Product Overview
3-Phenyl-L-serine is a high-purity amino-acids supplied for industrial and specialty chemical applications. Contact our team for specifications, packaging options and lead times.
Product Specifications
| Appearance: | White solid |
|---|---|
| Purity (HPLC, 210 nm): | 99.5% min |
| Optical Purity / Chiral HPLC: | EE 99.5% min |
| Mass Spectrum: | In accordance with the structure |
| NMR Spectrum: | In accordance with the structure |
Applications
1. Peptide and Protein Synthesis
3-Phenyl-L-serine is incorporated into peptides to study structure-activity relationships, modify biological activity, or improve peptide stability. Its phenyl side chain can influence peptide folding and interactions.
2. Pharmaceutical Intermediate
It serves as an intermediate in the synthesis of biologically active compounds, including drugs and enzyme inhibitors. Its unique structure aids in designing molecules with specific binding properties.
3. Chiral Building Block
Due to its stereochemistry, 3-Phenyl-L-serine is valuable in asymmetric synthesis, helping prepare chiral molecules important for drug development and fine chemical production.
4. Research Tool
Used in biochemical and pharmacological studies to explore enzyme specificity, receptor binding, and metabolic pathways involving serine derivatives.
Benefits
Chirality: The L-configuration allows for incorporation into chiral molecules with high stereochemical purity, crucial for biological activity.
Functional Diversity: The phenyl group adds hydrophobic and aromatic characteristics, enhancing molecular interactions in peptides and drugs.
Versatility: Its role as a building block allows for diverse chemical modifications and derivatizations.
Biological Relevance: Useful in creating analogs of natural amino acids to study protein function or develop novel therapeutics.
Conclusion
3-Phenyl-L-serine is a valuable amino acid derivative widely utilized in peptide synthesis, pharmaceutical intermediates, and asymmetric organic synthesis. Its unique structural features and chirality provide important advantages for creating biologically active compounds and studying protein interactions. As a versatile building block, it continues to support advances in medicinal chemistry and biochemical research, making it an essential component in the development of new drugs and therapeutic agents.
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