3-((2S,4S)-4-Mercapto-1-(((4-nitrobenzyl)oxy)carbonyl)pyrrolidine-2-carboxamido)benzoic acid

97%

Reagent Code: #51698
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CAS Number 202467-69-4

science Other reagents with same CAS 202467-69-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 445.45 g/mol
Formula C₂₀H₁₉N₃O₇S
badge Registry Numbers
MDL Number MFCD09263754
thermostat Physical Properties
Boiling Point 749.6°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry and sealed

description 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.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿21,294.00
inventory 100mg
10-20 days ฿1,323.00
inventory 1g
10-20 days ฿6,084.00
inventory 250mg
10-20 days ฿2,250.00

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3-((2S,4S)-4-Mercapto-1-(((4-nitrobenzyl)oxy)carbonyl)pyrrolidine-2-carboxamido)benzoic acid
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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

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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