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Mupirocin

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Catalog No. T1465Cas No. 12650-69-0
Alias Pseudomonic acid, BRL-4910A

Mupirocin (BRL-4910A) is a RNA synthetase inhibitor antibacterial. It has shown excellent activity against gram-positive staphylococci and streptococci.

Mupirocin

Mupirocin

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Purity: 97.46%
Catalog No. T1465Alias Pseudomonic acid, BRL-4910ACas No. 12650-69-0
Mupirocin (BRL-4910A) is a RNA synthetase inhibitor antibacterial. It has shown excellent activity against gram-positive staphylococci and streptococci.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
10 mg$32In StockIn Stock
25 mg$67In StockIn Stock
50 mg$103In StockIn Stock
100 mg$163In StockIn Stock
500 mg$375-In 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:97.46%
Color:White
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Product Introduction

Mupirocin AI Summary
Mupirocin exhibits broad-spectrum antibacterial activity against a variety of bacterial strains, including Staphylococcus aureus, Streptococcus pyogenes, Streptococcus pneumoniae, Haemophilus influenzae, and Moraxella catarrhalis, with minimum inhibitory concentrations (MIC) ranging from <= 0.06 to 0.25 ug/mL. It demonstrates potent effects against methicillin-resistant Staphylococcus aureus (MRSA), with MIC values as low as 0.12 ug/mL for some strains. Additionally, Mupirocin has been shown to inhibit isoleucyl-tRNA synthetase with IC50 values as low as 0.8 nM and competitive inhibition (Ki = 2.5 nM). Notably, it also displays significant activity against mupirocin-susceptible MRSA and has shown efficacy in a BALB/c mouse model of skin infection caused by MRSA. However, its efficacy against gram-negative Bacilli species and certain other strains such as Pseudomonas aeruginosa and Klebsiella pneumoniae is relatively limited, with higher MIC values. The compound demonstrates low cytotoxicity against human cells, and it has shown minimal potential for liver-related toxicity. Mupirocin also exhibits antiviral and antifungal activities, though with varying degrees of efficacy across different pathogens..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Mupirocin (BRL-4910A) is a RNA synthetase inhibitor antibacterial. It has shown excellent activity against gram-positive staphylococci and streptococci.
SynonymsPseudomonic acid, BRL-4910A
Chemical Properties
Molecular Weight500.62
FormulaC26H44O9
Cas No.12650-69-0
SmilesC([C@H]1[C@]([C@H]([C@H](C)O)C)(O1)[H])[C@@H]2[C@@H](O)[C@@H](O)[C@H](C/C(=C/C(OCCCCCCCCC(O)=O)=O)/C)OC2
Relative Density.1.183 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
Ethanol: 93 mg/mL (185.77 mM), Sonication is recommended.
H2O: 42 mg/mL (83.9 mM), Sonication is recommended.
DMSO: 240 mg/mL (479.41 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 5 mg/mL (9.99 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
H2O/Ethanol/DMSO
1mg5mg10mg50mg
1 mM1.9975 mL9.9876 mL19.9752 mL99.8762 mL
5 mM0.3995 mL1.9975 mL3.9950 mL19.9752 mL
10 mM0.1998 mL0.9988 mL1.9975 mL9.9876 mL
20 mM0.0999 mL0.4994 mL0.9988 mL4.9938 mL
50 mM0.0400 mL0.1998 mL0.3995 mL1.9975 mL
Ethanol/DMSO
1mg5mg10mg50mg
100 mM0.0200 mL0.0999 mL0.1998 mL0.9988 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

You can also refer to dose conversion for different animals. More Dose Conversion

Tech Support

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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