Thiazol-5-ylmethyl ((2S,3S,5S)-5-amino-3-hydroxy-1,6-diphenylhexan-2-yl)carbamate
98%
- Product Code: 36544
Alias:
利托那韦中间6;N-(5-amino-3-hydroxy-1,6-diphenylhexan-2-yl)carbamic acid 5-thiazolylmethyl ester;Thiazol-5-ylMethyl ((2S,3S,5S)-5-aMino-3-hydroxy-1,6-diphenylhexan-2-yl)carbaMate
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: | 1.251±0.06 g/cm3(Predicted) | Storage Condition: | 2-8°C, inert gas, protected from light |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of potent protease inhibitors. Its structure is particularly valuable in the development of antiviral and antiretroviral drugs, targeting enzymes like HIV protease, which is crucial for the replication of the HIV virus. Additionally, its stereochemistry and functional groups make it a candidate for designing inhibitors that can selectively bind to specific protein targets, offering potential therapeutic applications in treating viral infections and related diseases. Its role in drug development underscores its importance in advancing treatments for complex medical conditions.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to light-yellow powder or crystals |
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | $93.86 |
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| 1.000 | 10-20 days | $253.33 |
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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 potent protease inhibitors. Its structure is particularly valuable in the development of antiviral and antiretroviral drugs, targeting enzymes like HIV protease, which is crucial for the replication of the HIV virus. Additionally, its stereochemistry and functional groups make it a candidate for designing inhibitors that can selectively bind to specific protein targets, offering potential therapeutic applications in treating viral infections and related diseases. Its role in drug development underscores its importance in advancing treatments for complex medical conditions.
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