N-Fmoc-(S)-4-fluorohomophenylalanine
97%
- Product Code: 38046
CAS:
1260608-85-2
| Molecular Weight: | 419.4449 g./mol | Molecular Formula: | C₂₅H₂₂FNO₄ |
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| Density: | Storage Condition: | room temperature |
Product Description:
N-Fmoc-(S)-4-fluorohomophenylalanine is primarily used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) methodologies. The Fmoc (fluorenylmethyloxycarbonyl) protecting group is crucial for its role in temporarily shielding the amino group during the peptide chain assembly, allowing for selective deprotection and elongation of the peptide sequence. The incorporation of the (S)-4-fluorohomophenylalanine moiety introduces a fluorinated aromatic side chain, which can enhance the peptide's stability, binding affinity, and metabolic resistance. This makes it valuable in the development of peptide-based pharmaceuticals, such as enzyme inhibitors, receptor agonists/antagonists, and diagnostic agents. Additionally, the fluorine atom can be utilized in structural studies, such as NMR spectroscopy, to provide insights into peptide conformation and interactions. Its application extends to research in medicinal chemistry, where fluorinated amino acids are explored for their potential to improve drug-like properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | Ft94,736.73 |
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N-Fmoc-(S)-4-fluorohomophenylalanine
N-Fmoc-(S)-4-fluorohomophenylalanine is primarily used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) methodologies. The Fmoc (fluorenylmethyloxycarbonyl) protecting group is crucial for its role in temporarily shielding the amino group during the peptide chain assembly, allowing for selective deprotection and elongation of the peptide sequence. The incorporation of the (S)-4-fluorohomophenylalanine moiety introduces a fluorinated aromatic side chain, which can enhance the peptide's stability, binding affinity, and metabolic resistance. This makes it valuable in the development of peptide-based pharmaceuticals, such as enzyme inhibitors, receptor agonists/antagonists, and diagnostic agents. Additionally, the fluorine atom can be utilized in structural studies, such as NMR spectroscopy, to provide insights into peptide conformation and interactions. Its application extends to research in medicinal chemistry, where fluorinated amino acids are explored for their potential to improve drug-like properties.
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