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Brittonin A (Synonyms: 1,2-Bis(3,4,5-trimethoxyphenyl)ethane | NSC 600172)

Catalog No. TN13574 Copy Product Info
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Brittonin A, a methoxylated bibenzyl compound discovered in the liverwort F. inouei, exhibits anticancer properties. It demonstrates cytotoxic effects on KB cells and vincristine-resistant KB/VCR cells with IC50 values of 42.1 and 33.7 µM, respectively, as well as on K562 cells and adriamycin-resistant K562/A02 cells with IC50 values of 49.6 and 30.9 µM, respectively. At a concentration of 5 µM, Brittonin A enhances vincristine-induced cell death in KB/VCR cells and adriamycin-induced cell death in K562/A02 cells.

Brittonin A

Copy Product Info
🥰Excellent
Catalog No. TN13574
Synonyms 1,2-Bis(3,4,5-trimethoxyphenyl)ethane | NSC 600172

Brittonin A, a methoxylated bibenzyl compound discovered in the liverwort F. inouei, exhibits anticancer properties. It demonstrates cytotoxic effects on KB cells and vincristine-resistant KB/VCR cells with IC50 values of 42.1 and 33.7 µM, respectively, as well as on K562 cells and adriamycin-resistant K562/A02 cells with IC50 values of 49.6 and 30.9 µM, respectively. At a concentration of 5 µM, Brittonin A enhances vincristine-induced cell death in KB/VCR cells and adriamycin-induced cell death in K562/A02 cells.

Brittonin A
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Product Introduction

Bioactivity
Description
Brittonin A, a methoxylated bibenzyl compound discovered in the liverwort F. inouei, exhibits anticancer properties. It demonstrates cytotoxic effects on KB cells and vincristine-resistant KB/VCR cells with IC50 values of 42.1 and 33.7 µM, respectively, as well as on K562 cells and adriamycin-resistant K562/A02 cells with IC50 values of 49.6 and 30.9 µM, respectively. At a concentration of 5 µM, Brittonin A enhances vincristine-induced cell death in KB/VCR cells and adriamycin-induced cell death in K562/A02 cells.
Synonyms1,2-Bis(3,4,5-trimethoxyphenyl)ethane | NSC 600172
Chemical Properties
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature.

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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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