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Cefuroxime

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Catalog No. T65068Cas No. 55268-75-2
Alias Ketocef, Cephuroxime

Cefuroxime (Cephuroxime) is an orally active second-generation cephalosporin antibiotic with antimicrobial activity that inhibits both Gram-positive and Gram-negative bacteria, and is used in the study of soft tissue infections.

Cefuroxime

Cefuroxime

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Purity: 98.42%
Catalog No. T65068Alias Ketocef, CephuroximeCas No. 55268-75-2
Cefuroxime (Cephuroxime) is an orally active second-generation cephalosporin antibiotic with antimicrobial activity that inhibits both Gram-positive and Gram-negative bacteria, and is used in the study of soft tissue infections.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
25 mg$39In StockIn Stock
50 mg$54In StockIn Stock
100 mg$77-In Stock
1 mL x 10 mM (in DMSO)$29In StockIn Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Purity:98.42%
Appearance:Solid
Color:White
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Product Introduction

Bioactivity
Description
Cefuroxime (Cephuroxime) is an orally active second-generation cephalosporin antibiotic with antimicrobial activity that inhibits both Gram-positive and Gram-negative bacteria, and is used in the study of soft tissue infections.
Targets&IC50
methicillin-resistant Staphylococcus aureus:5.9 μg/ml (MIC), Clostridium difficile:1.2 μg/ml (MIC), methicillin-susceptible Staphylococcus aureus:0.25 μg/ml (MIC), Streptococcus pyogenes:0.125 μg/ml (MIC), Enterococcus faecalis:>125.0 μg/ml (MIC), Streptococcus viridans:0.125 μg/ml (MIC), Streptococcus pneumoniae:0.125 μg/ml (MIC), S. aureus:0.25 μg/mL (MIC)
In vitro
Regardless of whether S. aureus produces penicillinase or not, Cefuroxime showed strong antibacterial activity with a minimum inhibitory concentration (MIC) of 0.25 μg/ml.It exhibited significant antibacterial activity against methicillin-sensitive S. aureus, methicillin-resistant S. aureus, Streptococcus pyogenes, Streptococcus pneumoniae, Streptococcus viridans, Enterococcus faecalis, and Clostridium difficile. antimicrobial effect with MIC values of 0.25 μg/ml, 5.9 μg/ml, 0.125 μg/ml, 0.125 μg/ml, 0.125 μg/ml, >125.0 μg/ml and 1.2 μg/ml, respectively.
Cefuroxime (10-100 μg/ml, 2-6 hours of action) is rapidly bactericidal. Although it is relatively slow against S. aureus strains, it kills more than 99% of the initial inoculum within 6 hours. For Gram-negative bacteria, Cefuroxime is even faster, killing more than 99% of highly inoculated strains in just 2 hours in most cases. There is no significant difference in the speed of sterilization between β-lactamase-producing and non-enzyme-producing strains. [1]
In vivo
In rabbits (2.0 to 2.5 kg body weight) infected with 630 strains of penicillinase-producing Staphylococcus aureus by intravenous injection, a protection test showed a median effective dose of Cefuroxime of 3 mg/kg. [2]
SynonymsKetocef, Cephuroxime
Chemical Properties
Molecular Weight424.39
FormulaC16H16N4O8S
Cas No.55268-75-2
SmilesC(O)(=O)C=1N2[C@@]([C@H](NC(/C(=N\OC)/C3=CC=CO3)=O)C2=O)(SCC1COC(N)=O)[H]
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 250 mg/mL (589.08 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.3563 mL11.7816 mL23.5632 mL117.8162 mL
5 mM0.4713 mL2.3563 mL4.7126 mL23.5632 mL
10 mM0.2356 mL1.1782 mL2.3563 mL11.7816 mL
20 mM0.1178 mL0.5891 mL1.1782 mL5.8908 mL
50 mM0.0471 mL0.2356 mL0.4713 mL2.3563 mL
100 mM0.0236 mL0.1178 mL0.2356 mL1.1782 mL

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In Vivo Formulation Calculator (Clear solution)

Please enter your animal experiment information in the following box and click Calculate to obtain the stock solution preparation method and in vivo formula preparation method:
TargetMol | Animal experiments For example, if the intended dosage is 10 mg/kg for animals weighing 20 g , with a dosing volume of 100 μL per animal, TargetMol | Animal experiments and a total of 10 animals are to be administered, using a formulation of TargetMol | reagent 10% DMSO+ 40% PEG300+ 5% Tween 80+ 45% Saline/PBS/ddH2O , the resulting working solution concentration would be 2 mg/mL.
Stock Solution Preparation:

Dissolve 2 mg of the compound in 100 μL DMSOTargetMol | reagent to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.

Preparation of the In Vivo Formulation:

1) Add 100 μL of the DMSOTargetMol | reagent stock solution to 400 μL PEG300TargetMol | reagent and mix thoroughly until the solution becomes clear.

2) Add 50 μL Tween 80 and mix well until fully clarified.

3) Add 450 μL Saline,PBS or ddH2OTargetMol | reagent and mix thoroughly until a homogeneous solution is obtained.

This example is provided solely to demonstrate the use of the In Vivo Formulation Calculator and does not constitute a recommended formulation for any specific compound. Please select an appropriate dissolution and formulation strategy based on your experimental model and route of administration.
All co-solvents required for this protocol, includingDMSO, PEG300/PEG400, Tween 80, SBE-β-CD, and Corn oil, are available for purchase on the TargetMol website.
1 Enter information below:
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2 Enter the in vivo formulation:
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

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Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc
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