(7R,8aS)-2-Benzyl-7-hydroxyhexahydropyrrolo[1,2-a]pyrazine-1,4-dione
98%
- Product Code: 82085
CAS:
132714-97-7
| Molecular Weight: | 260.29 g./mol | Molecular Formula: | C₁₄H₁₆N₂O₃ |
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| EC Number: | MDL Number: | MFCD28132965 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research due to its complex structure, which makes it a valuable candidate for drug development. Its pyrrolo[1,2-a]pyrazine-dione core is of particular interest in the design of protease inhibitors, which are crucial in treating diseases like HIV, hepatitis, and certain cancers. The benzyl group attached to the structure enhances its binding affinity to specific enzyme targets, making it a promising scaffold for the synthesis of novel therapeutic agents. Additionally, its hydroxyl group provides a site for further chemical modifications, allowing researchers to fine-tune its pharmacological properties. This compound is also explored in the development of antimicrobial agents, as its structure exhibits potential activity against resistant bacterial strains. Overall, it serves as a versatile intermediate in the synthesis of biologically active molecules.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.250 | 10-20 days | $431.69 |
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| 1.000 | 10-20 days | $863.39 |
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| 5.000 | 10-20 days | $2,586.43 |
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(7R,8aS)-2-Benzyl-7-hydroxyhexahydropyrrolo[1,2-a]pyrazine-1,4-dione
This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research due to its complex structure, which makes it a valuable candidate for drug development. Its pyrrolo[1,2-a]pyrazine-dione core is of particular interest in the design of protease inhibitors, which are crucial in treating diseases like HIV, hepatitis, and certain cancers. The benzyl group attached to the structure enhances its binding affinity to specific enzyme targets, making it a promising scaffold for the synthesis of novel therapeutic agents. Additionally, its hydroxyl group provides a site for further chemical modifications, allowing researchers to fine-tune its pharmacological properties. This compound is also explored in the development of antimicrobial agents, as its structure exhibits potential activity against resistant bacterial strains. Overall, it serves as a versatile intermediate in the synthesis of biologically active molecules.
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