N-[(2R,3S)-3-Amino-2-hydroxy-4-phenylbutyl]-N-isobutyl-4-methoxybenzenesulfonamide hydrochloride
95%
- Product Code: 50507
CAS:
160232-87-1
| Molecular Weight: | 443.0 g./mol | Molecular Formula: | C₂₁H₃₁ClN₂O₄S |
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| Density: | Storage Condition: | 2-8°C, dry, sealed |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmaceutical agents. Its structure is particularly significant in the development of protease inhibitors, which are crucial in treating diseases such as HIV and hepatitis C. The presence of the amino and hydroxy groups allows for further chemical modifications, enabling the creation of compounds with enhanced binding affinity and specificity to viral proteases. Additionally, its sulfonamide moiety contributes to the overall stability and bioavailability of the final drug molecules. Researchers also explore its potential in designing novel therapeutics for other viral infections and certain types of cancer, leveraging its unique chemical framework to improve drug efficacy and reduce side effects.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.025 | 10-20 days | €709.94 |
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N-[(2R,3S)-3-Amino-2-hydroxy-4-phenylbutyl]-N-isobutyl-4-methoxybenzenesulfonamide hydrochloride
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmaceutical agents. Its structure is particularly significant in the development of protease inhibitors, which are crucial in treating diseases such as HIV and hepatitis C. The presence of the amino and hydroxy groups allows for further chemical modifications, enabling the creation of compounds with enhanced binding affinity and specificity to viral proteases. Additionally, its sulfonamide moiety contributes to the overall stability and bioavailability of the final drug molecules. Researchers also explore its potential in designing novel therapeutics for other viral infections and certain types of cancer, leveraging its unique chemical framework to improve drug efficacy and reduce side effects.
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