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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

🥰Excellent
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 SizePriceAvailabilityQuantity
10 mg$29In Stock
25 mg$39In Stock
50 mg$55In Stock
100 mg$79In Stock
200 mg$124In Stock
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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), Streptococcus viridans:0.125 μg/ml (MIC), S. aureus:0.25 μg/mL (MIC), methicillin-susceptible Staphylococcus aureus:0.25 μg/ml (MIC), Enterococcus faecalis:>125.0 μg/ml (MIC), Clostridium difficile:1.2 μg/ml (MIC), Streptococcus pneumoniae:0.125 μg/ml (MIC), Streptococcus pyogenes:0.125 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]
AliasKetocef, 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.
Solubility Information
DMSO: 100 mg/mL (235.63 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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Please enter your animal experiment information in the following box and click Calculate to obtain the mother liquor preparation method and in vivo formula preparation method:
TargetMol | Animal experimentsFor example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . TargetMol | Animal experiments A total of 10 animals were administered, and the formula you used is 5% TargetMol | reagent DMSO+30% PEG300+5% Tween 80+60% ddH2O. So your working solution concentration is 2 mg/mL。
Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSOTargetMol | reagent (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2OTargetMol | reagent mix well and clarify
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