Fmoc-Phe-Thr(psime,MePro)-OH
98%
- Product Code: 96126
CAS:
1196703-48-6
| Molecular Weight: | 528.60 g./mol | Molecular Formula: | C₃₁H₃₂N₂O₆ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD18427357 | |
| Melting Point: | Boiling Point: | 764.4±60.0 °C(Predicted) | |
| Density: | 1.258±0.06 g/cm3(Predicted) | Storage Condition: | 2-8°C, dry |
Product Description:
This compound is primarily utilized 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 during the peptide chain assembly. The inclusion of Thr(psime,MePro) indicates the presence of a pseudoproline dipeptide derivative, which is employed to reduce secondary structure formation during synthesis, thereby improving the efficiency and yield of the peptide assembly process. This compound is especially useful in synthesizing complex peptides with challenging sequences, as it helps to minimize aggregation and improve solubility. Its application is critical in the development of therapeutic peptides, research peptides, and peptide-based materials.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿1,791.00 |
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Fmoc-Phe-Thr(psime,MePro)-OH
This compound is primarily utilized 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 during the peptide chain assembly. The inclusion of Thr(psime,MePro) indicates the presence of a pseudoproline dipeptide derivative, which is employed to reduce secondary structure formation during synthesis, thereby improving the efficiency and yield of the peptide assembly process. This compound is especially useful in synthesizing complex peptides with challenging sequences, as it helps to minimize aggregation and improve solubility. Its application is critical in the development of therapeutic peptides, research peptides, and peptide-based materials.
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