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 $54.94
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0.250 10-20 days $93.44
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1.000 10-20 days $252.66
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5.000 10-20 days $884.32
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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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