Thiazol-5-ylmethyl ((2S,3S,5S)-5-amino-3-hydroxy-1,6-diphenylhexan-2-yl)carbamate
95%
- Product Code: 70867
CAS:
144164-11-4
| Molecular Weight: | 425.55 g./mol | Molecular Formula: | C₂₃H₂₇N₃O₃S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD07367634 | |
| Melting Point: | Boiling Point: | 656.1°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, protected from light, stored in an inert gas |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of protease inhibitors. Its structural features, including the thiazole ring and carbamate linkage, make it a valuable building block for developing drugs targeting viral proteases, particularly in the treatment of HIV and hepatitis C. The compound's stereochemistry and functional groups are crucial for its binding affinity and specificity to protease enzymes, enabling the design of potent inhibitors. Additionally, it has been explored in research for its potential application in cancer therapy, where protease inhibition plays a role in controlling tumor growth and metastasis. Its versatility and efficacy in drug development highlight its significance in pharmaceutical research.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to light-yellow powder or crystals |
| PURITY | 94.5-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿1,692.00 |
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| 1.000 | 10-20 days | ฿4,950.00 |
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| 5.000 | 10-20 days | ฿16,920.00 |
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Thiazol-5-ylmethyl ((2S,3S,5S)-5-amino-3-hydroxy-1,6-diphenylhexan-2-yl)carbamate
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of protease inhibitors. Its structural features, including the thiazole ring and carbamate linkage, make it a valuable building block for developing drugs targeting viral proteases, particularly in the treatment of HIV and hepatitis C. The compound's stereochemistry and functional groups are crucial for its binding affinity and specificity to protease enzymes, enabling the design of potent inhibitors. Additionally, it has been explored in research for its potential application in cancer therapy, where protease inhibition plays a role in controlling tumor growth and metastasis. Its versatility and efficacy in drug development highlight its significance in pharmaceutical research.
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