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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 Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 25 mg | $39 | In Stock | In Stock | |
| 50 mg | $54 | In Stock | In Stock | |
| 100 mg | $77 | - | In Stock | |
| 1 mL x 10 mM (in DMSO) | $29 | In Stock | In Stock |
| 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] |
| Synonyms | Ketocef, Cephuroxime |
| Molecular Weight | 424.39 |
| Formula | C16H16N4O8S |
| Cas No. | 55268-75-2 |
| Smiles | C(O)(=O)C=1N2[C@@]([C@H](NC(/C(=N\OC)/C3=CC=CO3)=O)C2=O)(SCC1COC(N)=O)[H] |
| Storage | Powder: -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
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Dissolve 2 mg of the compound in 100 μL DMSO
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.
1) Add 100 μL of the DMSO
stock solution to 400 μL PEG300
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 ddH2O
and mix thoroughly until a homogeneous solution is obtained.
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