N-Fmoc-5-methoxy-D-tryptophan
98%
- Product Code: 104178
CAS:
1353018-42-4
| Molecular Weight: | 456.49 g./mol | Molecular Formula: | C₂₇H₂₄N₂O₅ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28166523 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, sealed, dry |
Product Description:
N-Fmoc-5-methoxy-D-tryptophan is primarily 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 amine functionality. This allows for the sequential addition of amino acids to build peptides with high precision. The 5-methoxy group on the tryptophan side chain can influence the peptide's biological activity, making it valuable in the development of bioactive peptides, enzyme inhibitors, or receptor ligands. Its application is especially relevant in pharmaceutical research and the design of peptide-based drugs, where specific modifications like methoxylation can enhance stability, binding affinity, or selectivity. Additionally, it is used in the study of peptide structure-activity relationships (SAR) to understand the role of tryptophan derivatives in biological systems.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿44,217.00 |
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N-Fmoc-5-methoxy-D-tryptophan
N-Fmoc-5-methoxy-D-tryptophan is primarily 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 amine functionality. This allows for the sequential addition of amino acids to build peptides with high precision. The 5-methoxy group on the tryptophan side chain can influence the peptide's biological activity, making it valuable in the development of bioactive peptides, enzyme inhibitors, or receptor ligands. Its application is especially relevant in pharmaceutical research and the design of peptide-based drugs, where specific modifications like methoxylation can enhance stability, binding affinity, or selectivity. Additionally, it is used in the study of peptide structure-activity relationships (SAR) to understand the role of tryptophan derivatives in biological systems.
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