Fmoc-β-(3-pyridyl)-Ala-OH
98%
- Product Code: 105004
CAS:
175453-07-3
| Molecular Weight: | 388.42 g./mol | Molecular Formula: | C₂₃H₂₀N₂O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00144887 | |
| Melting Point: | 155.3 °C | Boiling Point: | |
| Density: | Storage Condition: | 2~8°C |
Product Description:
This chemical is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) methods. It serves as a protected amino acid derivative, where the Fmoc (fluorenylmethyloxycarbonyl) group acts as a temporary protecting group for the amino functionality. The presence of the 3-pyridyl side chain in the structure makes it valuable for introducing specific interactions or functionalities into peptide sequences, such as metal coordination or binding sites. It is often employed in the development of bioactive peptides, enzyme inhibitors, and peptide-based drugs, where the pyridyl group can enhance binding affinity or modulate activity. Additionally, it is utilized in research to study peptide-protein interactions and to design peptides with tailored properties for therapeutic or diagnostic applications.
Product Specification:
| Test | Specification |
|---|---|
| Purity (HPLC) | 98-100 |
| Appearance | White To Light Yellow Powder |
| Infrared Spectrum | Conforms To Structure |
| Proton NMR Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿2,560.00 |
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| 5.000 | 10-20 days | ฿11,980.00 |
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Fmoc-β-(3-pyridyl)-Ala-OH
This chemical is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) methods. It serves as a protected amino acid derivative, where the Fmoc (fluorenylmethyloxycarbonyl) group acts as a temporary protecting group for the amino functionality. The presence of the 3-pyridyl side chain in the structure makes it valuable for introducing specific interactions or functionalities into peptide sequences, such as metal coordination or binding sites. It is often employed in the development of bioactive peptides, enzyme inhibitors, and peptide-based drugs, where the pyridyl group can enhance binding affinity or modulate activity. Additionally, it is utilized in research to study peptide-protein interactions and to design peptides with tailored properties for therapeutic or diagnostic applications.
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