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Bekanamycin

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Catalog No. T8118Cas No. 4696-76-8
Alias Kanamycin B

Bekanamycin (Kanamycin B) is an aminoglycoside antibiotic extracted from Streptomyces kanamyceticus, which inhibits a range of Gram-positive and Gram-negative bacteria.

Bekanamycin

Bekanamycin

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Purity: 99.97%
Catalog No. T8118Alias Kanamycin BCas No. 4696-76-8
Bekanamycin (Kanamycin B) is an aminoglycoside antibiotic extracted from Streptomyces kanamyceticus, which inhibits a range of Gram-positive and Gram-negative bacteria.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
50 mg$34In StockIn Stock
100 mg$48In 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:99.97%
Color:White
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Product Introduction

Bekanamycin AI Summary
Bekanamycin exhibits broad-spectrum antibacterial activity against various bacterial strains, including Escherichia coli, Staphylococcus aureus, Pseudomonas aeruginosa, Bacillus subtilis, Klebsiella pneumoniae, Salmonella Typhimurium, Enterobacter cloacae, and Serratia marcescens. The compound shows potent activity with Minimum Inhibitory Concentrations (MIC) ranging from 0.39 to 3.125 ug/mL. Notably, it has MIC values of 0.39 ug/mL against Bacillus subtilis, 1.56 ug/mL against Staphylococcus aureus and Escherichia coli, and 3.13 ug/mL against Pseudomonas aeruginosa. Additionally, Bekanamycin demonstrates a binding affinity to various RNA constructs and the 16S ribosomal RNA A-site, suggesting potential mechanisms of action related to interference with bacterial protein synthesis and RNA binding. Furthermore, it shows moderate activity against lysosomal phospholipase A1 with an IC50 value of 110000.0 nM and inhibition metrics in various enzymatic and cellular assays. This combination of properties highlights Bekanamycin's potential as a robust antimicrobial agent targeting both Gram-positive and Gram-negative bacteria..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Bekanamycin (Kanamycin B) is an aminoglycoside antibiotic extracted from Streptomyces kanamyceticus, which inhibits a range of Gram-positive and Gram-negative bacteria.
Targets&IC50
HEK293 cells:> 500 μg/mL, NIH3T3 cells:139.6 μM
In vitro
METHODS: : HEK293 and NIH3T3 were treated with Bekanamycin for 24 hours, and the cell growth inhibition was detected by MTT assay.
RESULTS: Bekanamycin did not inhibit the growth of HEK293, with an IC50> 500 μg/mL. Bekanamycin inhibited the growth of NIH3T3, with an IC50=139.6 μM. [1] [2]
SynonymsKanamycin B
Chemical Properties
Molecular Weight483.51
FormulaC18H37N5O10
Cas No.4696-76-8
SmilesO([C@H]1[C@H](O)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](N)[C@H]2O)[C@H](N)C[C@@H]1N)[C@H]3O[C@H](CN)[C@@H](O)[C@H](O)[C@H]3N
Relative Density.1.59g/cm3
Storage & Solubility Information
Storagestore under nitrogen | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 1 mg/mL (2.07 mM), Sonication and heating to 80℃ are recommended.
H2O: 247.5 mg/mL (511.88 mM), Sonication is recommended.
Solution Preparation Table
DMSO/H2O
1mg5mg10mg50mg
1 mM2.0682 mL10.3410 mL20.6821 mL103.4105 mL
H2O
1mg5mg10mg50mg
5 mM0.4136 mL2.0682 mL4.1364 mL20.6821 mL
10 mM0.2068 mL1.0341 mL2.0682 mL10.3410 mL
20 mM0.1034 mL0.5171 mL1.0341 mL5.1705 mL
50 mM0.0414 mL0.2068 mL0.4136 mL2.0682 mL
100 mM0.0207 mL0.1034 mL0.2068 mL1.0341 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
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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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