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Bromfenac Sodium

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Catalog No. T6424Cas No. 91714-93-1
Alias Bronuck, AHR 10282R, AHR 10282B

Bromfenac Sodium (AHR 10282R) is a nonsteroidal anti-inflammatory drug (NSAID), which has anti-inflammatory activity and may block prostaglandin synthesis by inhibiting cyclooxygenase 1 and 2.

Bromfenac Sodium

Bromfenac Sodium

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Purity: 99.93%
Catalog No. T6424Alias Bronuck, AHR 10282R, AHR 10282BCas No. 91714-93-1
Bromfenac Sodium (AHR 10282R) is a nonsteroidal anti-inflammatory drug (NSAID), which has anti-inflammatory activity and may block prostaglandin synthesis by inhibiting cyclooxygenase 1 and 2.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
25 mg$36In StockIn Stock
50 mg$56In StockIn Stock
100 mg$73In StockIn Stock
500 mg$178-In Stock
1 mL x 10 mM (in DMSO)$29In 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:99.93%
Appearance:Solid
Color:Yellow
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Product Introduction

Bromfenac Sodium AI Summary
Bromfenac Sodium exhibits context-dependent bioactivity, impacting cell viability and protein stability variably across different conditions. In HEK293T cells, it shows mixed effects on growth rates (0.43, -0.53, 0.98), while consistently enhancing growth in U2OS cells with rates ranging from 0.2 to 0.95. Conversely, it negatively affects human fibroblast cell growth with a rate of -0.66. Additionally, Bromfenac Sodium influences the thermal stability of various protein domains, stabilizing some (positive Delta TM values) and destabilizing others (negative Delta TM values). These findings indicate that Bromfenac Sodium's effects are highly dependent on the specific biological context..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Bromfenac Sodium (AHR 10282R) is a nonsteroidal anti-inflammatory drug (NSAID), which has anti-inflammatory activity and may block prostaglandin synthesis by inhibiting cyclooxygenase 1 and 2.
Targets&IC50
COX-2:7.45 nM (IC50), COX-1:5.56 nM (IC50)
SynonymsBronuck, AHR 10282R, AHR 10282B
Chemical Properties
Molecular Weight356.15
FormulaC15H11BrNO3·Na
Cas No.91714-93-1
Smiles[Na+].NC1=C(C=CC=C1CC([O-])=O)C(=O)C1=CC=C(Br)C=C1
Relative Density.no data available
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
H2O: 65 mg/mL (182.51 mM), Sonication is recommended.
Ethanol: 2 mg/mL (5.62 mM), Sonication is recommended.
DMSO: 55 mg/mL (154.43 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 1 mg/mL (2.81 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
Ethanol/DMSO/H2O
1mg5mg10mg50mg
1 mM2.8078 mL14.0390 mL28.0781 mL140.3903 mL
5 mM0.5616 mL2.8078 mL5.6156 mL28.0781 mL
DMSO/H2O
1mg5mg10mg50mg
10 mM0.2808 mL1.4039 mL2.8078 mL14.0390 mL
20 mM0.1404 mL0.7020 mL1.4039 mL7.0195 mL
50 mM0.0562 mL0.2808 mL0.5616 mL2.8078 mL
100 mM0.0281 mL0.1404 mL0.2808 mL1.4039 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

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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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