4-Nitrobenzyl 2-(3-benzyl-7-oxo-4-thia-2,6-diazabicyclo[3.2.0]hept-2-en-6-yl)-3-methylbut-3-enoate

97%

Reagent Code: #131857
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CAS Number 50272-96-3

science Other reagents with same CAS 50272-96-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 451.49 g/mol
Formula C₂₃H₂₁N₃O₅S
badge Registry Numbers
MDL Number MFCD28166554
thermostat Physical Properties
Boiling Point 658.9±55.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.39±0.1 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used in pharmaceutical research as a beta-lactamase inhibitor scaffold. Shows potential in enhancing antibiotic efficacy by blocking bacterial enzyme activity that causes drug resistance. Investigated for combination therapies against multidrug-resistant pathogens. Also applied in prodrug design due to its nitrobenzyl-based photocleavable properties, enabling controlled release of active compounds upon light exposure.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,520.00
inventory 250mg
10-20 days ฿7,690.00
inventory 1g
10-20 days ฿20,750.00

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4-Nitrobenzyl 2-(3-benzyl-7-oxo-4-thia-2,6-diazabicyclo[3.2.0]hept-2-en-6-yl)-3-methylbut-3-enoate
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Used in pharmaceutical research as a beta-lactamase inhibitor scaffold. Shows potential in enhancing antibiotic efficacy by blocking bacterial enzyme activity that causes drug resistance. Investigated for combination therapies against multidrug-resistant pathogens. Also applied in prodrug design due to its nitrobenzyl-based photocleavable properties, enabling controlled release of active compounds upon light exposure.

Used in pharmaceutical research as a beta-lactamase inhibitor scaffold. Shows potential in enhancing antibiotic efficacy by blocking bacterial enzyme activity that causes drug resistance. Investigated for combination therapies against multidrug-resistant pathogens. Also applied in prodrug design due to its nitrobenzyl-based photocleavable properties, enabling controlled release of active compounds upon light exposure.

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