(S)-3-Phenyl-2-(pyrazine-2-carboxamido)propanoic acid
98%
- Product Code: 54573
Alias:
N-(pyrazinylcarbonyl)-L-phenylalanine
CAS:
114457-94-2
| Molecular Weight: | 271.27 g./mol | Molecular Formula: | C₁₄H₁₃N₃O₃ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | 166-169°C | Boiling Point: | |
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of novel drug candidates. Its structure, featuring a phenyl group and a pyrazine ring, makes it a valuable intermediate in the design of molecules targeting specific biological pathways. It is often explored for its potential in creating enzyme inhibitors or receptor modulators, which can be applied in treating conditions like inflammation, cancer, or metabolic disorders. Additionally, its chiral center allows for the development of enantioselective drugs, enhancing specificity and reducing side effects in therapeutic applications. Researchers also study its properties to optimize bioavailability and pharmacokinetics in drug formulations.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White Solid |
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | $12.56 |
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| 1.000 | 10-20 days | $21.60 |
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| 5.000 | 10-20 days | $54.24 |
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| 25.000 | 10-20 days | $254.14 |
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| 100.000 | 10-20 days | $883.98 |
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(S)-3-Phenyl-2-(pyrazine-2-carboxamido)propanoic acid
This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of novel drug candidates. Its structure, featuring a phenyl group and a pyrazine ring, makes it a valuable intermediate in the design of molecules targeting specific biological pathways. It is often explored for its potential in creating enzyme inhibitors or receptor modulators, which can be applied in treating conditions like inflammation, cancer, or metabolic disorders. Additionally, its chiral center allows for the development of enantioselective drugs, enhancing specificity and reducing side effects in therapeutic applications. Researchers also study its properties to optimize bioavailability and pharmacokinetics in drug formulations.
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