Fmoc-β-(4-pyridyl)-D-Ala-OH
98%
- Product Code: 105025
Alias:
FMOC-D-3-(4-pyridyl)-alanine
CAS:
205528-30-9
| Molecular Weight: | 388.42 g./mol | Molecular Formula: | C₂₃H₂₀N₂O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00672567 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2~8°C |
Product Description:
This compound is primarily used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It serves as a protected amino acid derivative, where the Fmoc (fluorenylmethyloxycarbonyl) group acts as a temporary protecting group for the amine functionality during the synthesis process. The presence of the 4-pyridyl group in the β-position of the alanine side chain introduces a unique structural feature, which can be exploited to study interactions with proteins or other biomolecules. Its application is significant in the development of peptide-based drugs, where specific side-chain modifications are required to enhance binding affinity, stability, or bioavailability. Additionally, it can be used in the preparation of peptidomimetics or as a building block in the synthesis of complex organic molecules for medicinal chemistry research.
Product Specification:
| Test | Specification |
|---|---|
| Assay | 98-100 |
| Appearance | White To Light Yellow Powder |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.200 | 10-20 days | ฿621.00 |
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| 1.000 | 10-20 days | ฿2,200.00 |
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Fmoc-β-(4-pyridyl)-D-Ala-OH
This compound is primarily used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It serves as a protected amino acid derivative, where the Fmoc (fluorenylmethyloxycarbonyl) group acts as a temporary protecting group for the amine functionality during the synthesis process. The presence of the 4-pyridyl group in the β-position of the alanine side chain introduces a unique structural feature, which can be exploited to study interactions with proteins or other biomolecules. Its application is significant in the development of peptide-based drugs, where specific side-chain modifications are required to enhance binding affinity, stability, or bioavailability. Additionally, it can be used in the preparation of peptidomimetics or as a building block in the synthesis of complex organic molecules for medicinal chemistry research.
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