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6-Hydroxybenzbromarone
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Catalog No. T10182Cas No. 152831-00-0
6-Hydroxybenzbromarone is the major metabolite of Benzbromarone. 6-Hydroxybenzbromarone is a protein Eyes Absent 3 (EYA3) inhibitor (IC50: 21.5 μM). It is an angiogenic agent, has strong inhibitory effects on cell migration, tubulogenesis, and angiogenic sprouting.
6-Hydroxybenzbromarone
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Catalog No. T10182Cas No. 152831-00-0
6-Hydroxybenzbromarone is the major metabolite of Benzbromarone. 6-Hydroxybenzbromarone is a protein Eyes Absent 3 (EYA3) inhibitor (IC50: 21.5 μM). It is an angiogenic agent, has strong inhibitory effects on cell migration, tubulogenesis, and angiogenic sprouting.
| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 2 mg | $416 | 5 days | 5 days |
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Chemical Properties
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| Description | 6-Hydroxybenzbromarone is the major metabolite of Benzbromarone. 6-Hydroxybenzbromarone is a protein Eyes Absent 3 (EYA3) inhibitor (IC50: 21.5 μM). It is an angiogenic agent, has strong inhibitory effects on cell migration, tubulogenesis, and angiogenic sprouting. |
| Targets&IC50 | EYA3:21.5 μM |
| In vitro | 6-Hydroxybenzbromarone (7.5 μM; 72 hours) reduces cell proliferation by over 50%. Simultaneously, BBR and BZ treatments decrease cell viability, while other compounds tested do not affect cell viability or proliferation. 6-Hydroxybenzbromarone (7.5 μM; 1-20 hours) inhibits EC migration and tubulogenesis in HUVECs, but its impact on tube formation diminishes with high concentrations of fetal bovine serum (FBS), likely due to non-specific protein binding. |
| Cell Research | Cell Line: HUVEC cells. Concentration: 7.5 μM. Incubation Time: 72 hours |
| Molecular Weight | 440.08 |
| Formula | C17H12Br2O4 |
| Cas No. | 152831-00-0 |
| Smiles | CCc1oc2cc(O)ccc2c1C(=O)c1cc(Br)c(O)c(Br)c1 |
| Relative Density. | 1.785 g/cm3 (Predicted) |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. |
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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:
For example, if the intended dosage is 10 mg/kg for animals weighing 20 g , with a dosing volume of 100 μL per animal, and a total of 10 animals are to be administered, using a formulation of 
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 DMSO 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 DMSO stock solution to 400 μL PEG300 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 ddH2O 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.
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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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