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Cefsulodin sodium

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Catalog No. T0827Cas No. 52152-93-9
Alias Sulcephalosporin, Cefsulodine sodium

Cefsulodin sodium (Sulcephalosporin) hydrate is a β lactam antibiotic.

Cefsulodin sodium

Cefsulodin sodium

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Purity: 99.3%
Catalog No. T0827Alias Sulcephalosporin, Cefsulodine sodiumCas No. 52152-93-9
Cefsulodin sodium (Sulcephalosporin) hydrate is a β lactam antibiotic.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
25 mg$30In StockIn Stock
50 mg$41In StockIn Stock
100 mg$59In StockIn Stock
200 mg$83In StockIn Stock
1 mL x 10 mM (in DMSO)$66In 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:99.3%
Color:Yellow
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Product Introduction

Cefsulodin sodium AI Summary
Cefsulodin sodium exhibits significant bioactivity across a range of biological targets, demonstrating diverse inhibitory effects. It exerts inhibitory activity on human Jumonji Domain Containing 2E (JMJD2E), MLL CXXC domain-DNA interaction, Tyrosyl-DNA Phosphodiesterase (TDP1), Tau fibril formation, DNA Polymerase Beta, and several other molecular targets including enzymes and proteins involved in DNA repair, epigenetic regulation, and cellular transport processes. The compound's potency varies widely, from 199.5 nM to 56234.1 nM, depending on the specific target. Additionally, Cefsulodin sodium shows a high level of inhibition (91.84% and 101.2%) in the sodium fluorescein uptake assay in OATP1B1- and OATP1B3-transfected CHO cells at a concentration of 10 µM, suggesting interference with sodium fluorescein transport. In the context of infectious diseases, Cefsulodin sodium inhibits Mycobacterium tuberculosis PTPB with an IC50 value of 16000.0 nM. It also exhibits trypanocidal activity against Trypanosoma cruzi, the causative agent of Chagas disease, displaying moderate activity against the INC-5 strain (14%) and strong activity against the NINOA strain (87%) at 50 µg/mL, with an LC50 value of 16.6 µg/mL against the NINOA strain. Moreover, Cefsulodin sodium shows activity against SARS-CoV-2 in Vero E6 cells, reducing cell viability with an inhibition index of 0.2889 after 72 hours at a MOI of 0.002, indicating potential antiviral properties. Overall, Cefsulodin sodium is a bioactive molecule with inhibitory effects on a variety of biological targets, making it a notable candidate for further investigation in multiple therapeutic areas..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Cefsulodin sodium (Sulcephalosporin) hydrate is a β lactam antibiotic.
Targets&IC50
mPTPB:16 μM
SynonymsSulcephalosporin, Cefsulodine sodium
Chemical Properties
Molecular Weight554.52
FormulaC22H19N4NaO8S2
Cas No.52152-93-9
Smiles[Na+].NC(=O)c1cc[n+](CC2=C(N3[C@H](SC2)[C@H](NC(=O)[C@@H](c2ccccc2)S([O-])(=O)=O)C3=O)C([O-])=O)cc1
Relative Density.no data available
Storage & Solubility Information
Storagestore at low temperature,store under nitrogen | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 55 mg/mL (99.18 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 2 mg/mL (3.61 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 mM1.8034 mL9.0168 mL18.0336 mL90.1681 mL
5 mM0.3607 mL1.8034 mL3.6067 mL18.0336 mL
10 mM0.1803 mL0.9017 mL1.8034 mL9.0168 mL
20 mM0.0902 mL0.4508 mL0.9017 mL4.5084 mL
50 mM0.0361 mL0.1803 mL0.3607 mL1.8034 mL

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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:
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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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