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Cefodizime is a new cephalosporin antibiotic with a wide range of biological activities.Cefodizime is non-toxic to the kidneys and is well tolerated with immunomodulatory activity.Cefodizime has antimicrobial activity and is used in the study of serious infections of the respiratory and urinary systems.

| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 10 mg | $39 | In Stock | In Stock | |
| 25 mg | $53 | In Stock | In Stock | |
| 50 mg | $64 | In Stock | In Stock | |
| 100 mg | $89 | In Stock | In Stock | |
| 500 mg | $219 | - | In Stock | |
| 1 mL x 10 mM (in DMSO) | $43 | In Stock | In Stock |
| Description | Cefodizime is a new cephalosporin antibiotic with a wide range of biological activities.Cefodizime is non-toxic to the kidneys and is well tolerated with immunomodulatory activity.Cefodizime has antimicrobial activity and is used in the study of serious infections of the respiratory and urinary systems. |
| In vitro | Cefodizime is a bactericidal antibiotic having a high affinity for penicillin-binding proteins lA/B, 2, and 3 of E. coli. Cefodizime inhibits other Gram-negative bacteria including Haemophilus irifluenzae, Neisseria gonorrhoeae, Moraxella catarrhalis, and Neisseria meningitidis. Cefodizime has marginal but variable inhibitory activity against Citrobacter species including Serratia marcescens and Citrobacter freundii. The in vitro concentrations of Cefodizime resulting in bactericidal activity against susceptible strains of Gram-positive and Gram-negative bacteria are generally similar to the minimum inhibitory concentrations [1]. |
| In vivo | Cefodizime exhibits comparable efficacy to Cefotaxime and Ceftazidime, and surpasses Cefoperazone, Latamoxef, Cefuroxime, and Cefazolin in combating K. pneumoniae respiratory tract infections in mice, following a single subcutaneous dose of 50 mg/kg, maintaining significant bactericidal activity up to 48 hours post-administration. This is unlike the aforementioned cephalosporins, as Cefodizime ensures bacterial eradication from the lungs within 48 hours in half of the treated mice, even when no longer present in the serum [1]. |
| Molecular Weight | 584.67 |
| Formula | C20H20N6O7S4 |
| Cas No. | 69739-16-8 |
| Smiles | C(O)(=O)C=1N2[C@@]([C@H](NC(/C(=N\OC)/C=3N=C(N)SC3)=O)C2=O)(SCC1CSC=4SC(CC(O)=O)=C(C)N4)[H] |
| Relative Density. | 1.86 g/cm3 |
| Storage | keep away from direct sunlight | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. | ||||||||||||||||||||||||||||||
| Solubility Information | DMSO: 40 mg/mL (68.41 mM), Sonication is recommended. | ||||||||||||||||||||||||||||||
| In Vivo Formulation | 10% DMSO+40% PEG300+5% Tween 80+45% Saline: 2 mg/mL (3.42 mM), Sonication is recommended. Please add the solvents sequentially, clarifying the solution as much as possible before adding the next one. Dissolve by heating and/or sonication if necessary. Working solution is recommended to be prepared and used immediately. The formulation provided above is for reference purposes only. In vivo formulations may vary and should be modified based on specific experimental conditions. | ||||||||||||||||||||||||||||||
Solution Preparation Table | |||||||||||||||||||||||||||||||
DMSO
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