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Cefotetan

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Catalog No. T7043Cas No. 69712-56-7
Alias Apacef

Cefotetan (Apacef) Sodium (ICI-156834, YM-09330) is a second-generation cephalosporin, cephamycin antibiotic that is active against a wide range of both aerobic and anaerobic gram-positive and gram-negative bacteria. Cefotetan binds to penicillin-binding proteins and disrupts the cell wall synthesis.

Cefotetan

Cefotetan

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Purity: 99.38%
Catalog No. T7043Alias ApacefCas No. 69712-56-7
Cefotetan (Apacef) Sodium (ICI-156834, YM-09330) is a second-generation cephalosporin, cephamycin antibiotic that is active against a wide range of both aerobic and anaerobic gram-positive and gram-negative bacteria. Cefotetan binds to penicillin-binding proteins and disrupts the cell wall synthesis.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
5 mg$39In StockIn Stock
10 mg$59In StockIn Stock
25 mg$93In StockIn Stock
50 mg$139In StockIn Stock
100 mg$185In StockIn Stock
200 mg$278-In Stock
1 mL x 10 mM (in DMSO)$48In StockIn Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
All TargetMol products are for research purposes only and cannot be used for human consumption. We do not provide products or services to individuals. Please comply with the intended use and do not use TargetMol products for any other purpose.
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Purity:99.38%
Appearance:solid
Color:White
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Product Introduction

Cefotetan AI Summary
Cefotetan exhibits a wide range of biological activities, including potent antibacterial and antiviral properties. Its antimicrobial effects include high potency against aerobic bacteria such as Escherichia coli and Klebsiella pneumoniae with minimum inhibitory concentrations (MIC) as low as 0.031 ug/mL. It is effective against anaerobic bacteria like Clostridium perfringens and Bacteroides thetaiotaomicron with MIC values ranging from 1.0 to 16.0 ug/mL, though it shows limited activity against others such as Bacteroides melaninogenicus with MIC values greater than 128.0 ug/mL. Additionally, Cefotetan has shown efficacy in inhibiting resistant strains of Escherichia coli and Shigella sonnei expressing beta-lactamase enzymes, with MIC values as low as 0.5 ug/mL. In pharmacokinetic studies, Cefotetan demonstrates species-specific distribution and clearance rates. In humans, it has a low volume of distribution (0.13 L.kg-1) and a short half-life of 4.5 hours, indicating moderate bioavailability and fast elimination. In animal models such as rats, dogs, and monkeys, the compound shows higher distribution volumes and faster clearance rates, suggesting variable bioavailability across species. Cefotetan also exhibits moderate hepatotoxicity with elevated levels of liver enzymes (ALT, AST, and alkaline phosphatase), albeit without severe liver damage. It also shows inhibitory activity on human bile salt export pump (BSEP) and multidrug resistance-associated proteins (MRP) with relatively low potency (IC50 values greater than 135,000 nM). In antiviral studies, Cefotetan demonstrates activity against SARS-CoV-2 by inhibiting the 3CL-Pro protease and decreasing viral-induced cytotoxicity in cell lines. However, its potency appears to be relatively low, with an IC50 value greater than 20,000 nM. Overall, Cefotetan is a multifaceted compound with notable antibacterial and antiviral activities, moderate hepatotoxicity, and specific pharmacokinetic profiles across different species..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Cefotetan (Apacef) Sodium (ICI-156834, YM-09330) is a second-generation cephalosporin, cephamycin antibiotic that is active against a wide range of both aerobic and anaerobic gram-positive and gram-negative bacteria. Cefotetan binds to penicillin-binding proteins and disrupts the cell wall synthesis.
SynonymsApacef
Chemical Properties
Molecular Weight575.62
FormulaC17H17N7O8S4
Cas No.69712-56-7
SmilesCO[C@]1(NC(=O)C2SC(S2)=C(C(N)=O)C(O)=O)[C@H]2SCC(CSc3nnnn3C)=C(N2C1=O)C(O)=O
Relative Density.2.07 g/cm3
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 (434.31 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 1 mg/mL (1.74 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
1mg5mg10mg50mg
1 mM1.7373 mL8.6863 mL17.3726 mL86.8629 mL
5 mM0.3475 mL1.7373 mL3.4745 mL17.3726 mL
10 mM0.1737 mL0.8686 mL1.7373 mL8.6863 mL
20 mM0.0869 mL0.4343 mL0.8686 mL4.3431 mL
50 mM0.0347 mL0.1737 mL0.3475 mL1.7373 mL
100 mM0.0174 mL0.0869 mL0.1737 mL0.8686 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:
mg/kg
g
μL
2 Enter the in vivo formulation:
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

Dose Conversion

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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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