3-((2S,4S)-4-Mercapto-1-(((4-nitrobenzyl)oxy)carbonyl)pyrrolidine-2-carboxamido)benzoic acid
97%
- Product Code: 51698
CAS:
202467-69-4
| Molecular Weight: | 445.45 g./mol | Molecular Formula: | C₂₀H₁₉N₃O₇S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09263754 | |
| Melting Point: | Boiling Point: | 749.6°C at 760 mmHg | |
| Density: | Storage Condition: | Room temperature, dry and sealed |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry and drug development, particularly in the design of enzyme inhibitors. Its structure, featuring a mercapto group and a nitrobenzyl moiety, makes it a valuable intermediate for synthesizing targeted therapeutic agents. It is often employed in the development of protease inhibitors, which are crucial in treating diseases like HIV and hepatitis C. Additionally, the nitrobenzyl group allows for photolabile protection, enabling controlled release mechanisms in drug delivery systems. Its application extends to research involving cysteine protease studies, where it serves as a tool to investigate enzyme-substrate interactions and inhibition pathways.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿1,323.00 |
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| 0.250 | 10-20 days | ฿2,250.00 |
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| 1.000 | 10-20 days | ฿6,084.00 |
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| 5.000 | 10-20 days | ฿21,294.00 |
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3-((2S,4S)-4-Mercapto-1-(((4-nitrobenzyl)oxy)carbonyl)pyrrolidine-2-carboxamido)benzoic acid
This compound is primarily utilized in the field of medicinal chemistry and drug development, particularly in the design of enzyme inhibitors. Its structure, featuring a mercapto group and a nitrobenzyl moiety, makes it a valuable intermediate for synthesizing targeted therapeutic agents. It is often employed in the development of protease inhibitors, which are crucial in treating diseases like HIV and hepatitis C. Additionally, the nitrobenzyl group allows for photolabile protection, enabling controlled release mechanisms in drug delivery systems. Its application extends to research involving cysteine protease studies, where it serves as a tool to investigate enzyme-substrate interactions and inhibition pathways.
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