(S)-2-(((S)-1-Ethoxy-1-oxo-4-phenylbutan-2-yl)amino)-6-(2,2,2-trifluoroacetamido)hexanoic acid
≥95%
- Product Code: 50698
CAS:
116169-90-5
| Molecular Weight: | 432.43 g./mol | Molecular Formula: | C₂₀H₂₇F₃N₂O₅ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD06658211 | |
| Melting Point: | Boiling Point: | 586.987°C at 760 mmHg | |
| Density: | Storage Condition: | Room temperature, dry and sealed |
Product Description:
This compound is primarily utilized in the field of peptide synthesis and pharmaceutical research. It serves as a key intermediate in the production of peptide-based drugs, particularly those targeting specific biological pathways. Its structure allows for the incorporation of unique amino acid sequences, enhancing the stability and efficacy of the resulting peptides. Additionally, it is employed in the development of enzyme inhibitors and receptor modulators, contributing to advancements in treatments for various diseases, including cancer and metabolic disorders. The trifluoroacetamido group in its structure plays a crucial role in improving the compound's binding affinity and selectivity, making it valuable in drug design and optimization.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 5.000 | 10-20 days | ฿387.00 |
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| 10.000 | 10-20 days | ฿576.00 |
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| 25.000 | 10-20 days | ฿1,170.00 |
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(S)-2-(((S)-1-Ethoxy-1-oxo-4-phenylbutan-2-yl)amino)-6-(2,2,2-trifluoroacetamido)hexanoic acid
This compound is primarily utilized in the field of peptide synthesis and pharmaceutical research. It serves as a key intermediate in the production of peptide-based drugs, particularly those targeting specific biological pathways. Its structure allows for the incorporation of unique amino acid sequences, enhancing the stability and efficacy of the resulting peptides. Additionally, it is employed in the development of enzyme inhibitors and receptor modulators, contributing to advancements in treatments for various diseases, including cancer and metabolic disorders. The trifluoroacetamido group in its structure plays a crucial role in improving the compound's binding affinity and selectivity, making it valuable in drug design and optimization.
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