Cefpodoxime proxetil

BR

Reagent Code: #96377
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CAS Number 87239-81-4

science Other reagents with same CAS 87239-81-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 557.5972 g/mol
Formula C₂₁H₂₇N₅O₉S₂
badge Registry Numbers
MDL Number MFCD00865088
inventory_2 Storage & Handling
Density 1.58g/ml
Storage -20℃

description Product Description

Cefpodoxime proxetil is an oral prodrug of the third-generation cephalosporin antibiotic cefpodoxime, which is hydrolyzed in vivo to the active form. It exhibits broad-spectrum activity against Gram-positive and Gram-negative bacteria by inhibiting bacterial cell wall synthesis. This pharmaceutical intermediate is used in the formulation of medications for treating respiratory tract infections (e.g., bronchitis, pneumonia, sinusitis), urinary tract infections (e.g., cystitis, pyelonephritis), skin and soft tissue infections (e.g., wounds, abscesses), and ear infections (e.g., otitis media), including in pediatric applications. Supplied as a faint yellow powder, it conforms to the reference structure as confirmed by infrared spectroscopy and NMR.

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Test Parameter Specification
Appearance Faint Yellow Powder
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿490.00
inventory 25mg
10-20 days ฿2,200.00
inventory 100mg
10-20 days ฿4,600.00
inventory 1mg
10-20 days ฿320.00

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Cefpodoxime proxetil
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Cefpodoxime proxetil is an oral prodrug of the third-generation cephalosporin antibiotic cefpodoxime, which is hydrolyzed in vivo to the active form. It exhibits broad-spectrum activity against Gram-positive and Gram-negative bacteria by inhibiting bacterial cell wall synthesis. This pharmaceutical intermediate is used in the formulation of medications for treating respiratory tract infections (e.g., bronchitis, pneumonia, sinusitis), urinary tract infections (e.g., cystitis, pyelonephritis), skin and so

Cefpodoxime proxetil is an oral prodrug of the third-generation cephalosporin antibiotic cefpodoxime, which is hydrolyzed in vivo to the active form. It exhibits broad-spectrum activity against Gram-positive and Gram-negative bacteria by inhibiting bacterial cell wall synthesis. This pharmaceutical intermediate is used in the formulation of medications for treating respiratory tract infections (e.g., bronchitis, pneumonia, sinusitis), urinary tract infections (e.g., cystitis, pyelonephritis), skin and soft tissue infections (e.g., wounds, abscesses), and ear infections (e.g., otitis media), including in pediatric applications. Supplied as a faint yellow powder, it conforms to the reference structure as confirmed by infrared spectroscopy and NMR.

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