4-Amino-N-((2R,3S)-3-amino-2-hydroxy-4-phenylbutyl)-N-isobutylbenzenesulfonamide
95%
- Product Code: 71143
CAS:
169280-56-2
| Molecular Weight: | 391.53 g./mol | Molecular Formula: | C₂₀H₂₉N₃O₃S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD16251177 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, protected from light, dry, sealed |
Product Description:
This compound is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various therapeutic agents. Its structure, featuring both amino and sulfonamide groups, makes it valuable in the development of protease inhibitors, which are crucial in treating diseases such as HIV and hepatitis C. Additionally, its stereochemistry allows for the creation of enantiomerically pure drugs, enhancing their efficacy and reducing potential side effects. The compound is also explored in research for its potential antimicrobial properties, contributing to the development of new antibiotics targeting resistant bacterial strains. Its application extends to the study of enzyme mechanisms, where it serves as a model compound to understand the interaction between inhibitors and enzymes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿909.00 |
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| 5.000 | 10-20 days | ฿2,844.00 |
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| 25.000 | 10-20 days | ฿6,813.00 |
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4-Amino-N-((2R,3S)-3-amino-2-hydroxy-4-phenylbutyl)-N-isobutylbenzenesulfonamide
This compound is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various therapeutic agents. Its structure, featuring both amino and sulfonamide groups, makes it valuable in the development of protease inhibitors, which are crucial in treating diseases such as HIV and hepatitis C. Additionally, its stereochemistry allows for the creation of enantiomerically pure drugs, enhancing their efficacy and reducing potential side effects. The compound is also explored in research for its potential antimicrobial properties, contributing to the development of new antibiotics targeting resistant bacterial strains. Its application extends to the study of enzyme mechanisms, where it serves as a model compound to understand the interaction between inhibitors and enzymes.
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