Torezolid phosphate

98%

Reagent Code: #239514
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CAS Number 856867-55-5

science Other reagents with same CAS 856867-55-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 450.32 g/mol
Formula C₁₇H₁₆FN₆O₆P
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used in the treatment of acute bacterial skin and skin structure infections (ABSSSI) caused by susceptible gram-positive pathogens, including methicillin-resistant Staphylococcus aureus (MRSA). It is a prodrug that converts to the active form, tedizolid, inhibiting bacterial protein synthesis by binding to the 50S ribosomal subunit. Also shows potent activity against vancomycin-resistant enterococci (VRE). Being investigated for use in respiratory tract infections where conventional antibiotics fail. Its phosphate ester form improves oral bioavailability, making it suitable for outpatient therapy.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,390.00
inventory 1g
10-20 days ฿3,580.00
inventory 5g
10-20 days ฿12,720.00
Torezolid phosphate
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Used in the treatment of acute bacterial skin and skin structure infections (ABSSSI) caused by susceptible gram-positive pathogens, including methicillin-resistant Staphylococcus aureus (MRSA). It is a prodrug that converts to the active form, tedizolid, inhibiting bacterial protein synthesis by binding to the 50S ribosomal subunit. Also shows potent activity against vancomycin-resistant enterococci (VRE). Being investigated for use in respiratory tract infections where conventional antibiotics fa

Used in the treatment of acute bacterial skin and skin structure infections (ABSSSI) caused by susceptible gram-positive pathogens, including methicillin-resistant Staphylococcus aureus (MRSA). It is a prodrug that converts to the active form, tedizolid, inhibiting bacterial protein synthesis by binding to the 50S ribosomal subunit. Also shows potent activity against vancomycin-resistant enterococci (VRE). Being investigated for use in respiratory tract infections where conventional antibiotics fail. Its phosphate ester form improves oral bioavailability, making it suitable for outpatient therapy.

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