(R)-2-Amino-3-(5-methyl-1H-indol-3-yl)propanoic acid
≥95%
- Product Code: 49164
CAS:
99295-79-1
| Molecular Weight: | 218.25 g./mol | Molecular Formula: | C₁₂H₁₄N₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09841957 | |
| Melting Point: | Boiling Point: | 455.1°C at 760 mmHg | |
| Density: | Storage Condition: | Room temperature, dry and sealed |
Product Description:
This compound is primarily utilized in biochemical research due to its role as a chiral building block in the synthesis of peptides and other biologically active molecules. It is particularly valuable in studies involving enzyme mechanisms and receptor interactions, where its specific stereochemistry can influence binding and activity. Additionally, it serves as a precursor in the development of pharmaceuticals targeting neurological disorders, leveraging its structural similarity to naturally occurring amino acids that play critical roles in brain function. Its indole moiety also makes it a candidate for research in the field of tryptophan metabolism and related pathways.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿14,319.00 |
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| 0.250 | 10-20 days | ฿28,638.00 |
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(R)-2-Amino-3-(5-methyl-1H-indol-3-yl)propanoic acid
This compound is primarily utilized in biochemical research due to its role as a chiral building block in the synthesis of peptides and other biologically active molecules. It is particularly valuable in studies involving enzyme mechanisms and receptor interactions, where its specific stereochemistry can influence binding and activity. Additionally, it serves as a precursor in the development of pharmaceuticals targeting neurological disorders, leveraging its structural similarity to naturally occurring amino acids that play critical roles in brain function. Its indole moiety also makes it a candidate for research in the field of tryptophan metabolism and related pathways.
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