(S)-2-Amino-3-(2-methyl-1H-indol-3-yl)propanoic acid
95%
- Product Code: 57148
CAS:
33468-32-5
| Molecular Weight: | 218.25 g./mol | Molecular Formula: | C₁₂H₁₄N₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01318648 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Store at room temperature, away from light, inert atmosphere |
Product Description:
This compound is primarily utilized in biochemical research due to its role as a tryptophan derivative. It serves as a valuable substrate in enzymatic studies, particularly in investigations involving tryptophan metabolism and biosynthesis pathways. Researchers employ it to explore enzyme specificity and catalytic mechanisms, especially in the context of indole-containing amino acids. Additionally, it is used in the synthesis of peptide analogs and as a building block in the development of biologically active compounds, including potential pharmaceuticals targeting neurological and metabolic disorders. Its structural similarity to tryptophan makes it a useful tool in studying protein-ligand interactions and designing novel therapeutic agents.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to light-yellow solid |
| PURITY | 94.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿9,500.00 |
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| 0.250 | 10-20 days | ฿16,500.00 |
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(S)-2-Amino-3-(2-methyl-1H-indol-3-yl)propanoic acid
This compound is primarily utilized in biochemical research due to its role as a tryptophan derivative. It serves as a valuable substrate in enzymatic studies, particularly in investigations involving tryptophan metabolism and biosynthesis pathways. Researchers employ it to explore enzyme specificity and catalytic mechanisms, especially in the context of indole-containing amino acids. Additionally, it is used in the synthesis of peptide analogs and as a building block in the development of biologically active compounds, including potential pharmaceuticals targeting neurological and metabolic disorders. Its structural similarity to tryptophan makes it a useful tool in studying protein-ligand interactions and designing novel therapeutic agents.
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