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Betavulgarin

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Catalog No. TN11392Cas No. 51068-94-1

Betavulgarin is an anticancer agent that can be isolated from beets (Beta vulgaris). It inhibits the proliferation, migration, colony formation, and mammosphere formation of breast cancer cells, while reducing the size of the CD44+/CD24− subpopulation and the expression of self-renewal-related genes C-Myc, Nanog, and Oct4. Betavulgarin promotes the death of breast cancer stem cells (BCSCs) by regulating Stat3/Sox2 signaling pathways.

Betavulgarin

Betavulgarin

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Catalog No. TN11392Cas No. 51068-94-1
Betavulgarin is an anticancer agent that can be isolated from beets (Beta vulgaris). It inhibits the proliferation, migration, colony formation, and mammosphere formation of breast cancer cells, while reducing the size of the CD44+/CD24− subpopulation and the expression of self-renewal-related genes C-Myc, Nanog, and Oct4. Betavulgarin promotes the death of breast cancer stem cells (BCSCs) by regulating Stat3/Sox2 signaling pathways.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
10 mgInquiry10-14 weeks10-14 weeks
50 mgInquiry10-14 weeks10-14 weeks
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Product Introduction

Bioactivity
Description
Betavulgarin is an anticancer agent that can be isolated from beets (Beta vulgaris). It inhibits the proliferation, migration, colony formation, and mammosphere formation of breast cancer cells, while reducing the size of the CD44+/CD24− subpopulation and the expression of self-renewal-related genes C-Myc, Nanog, and Oct4. Betavulgarin promotes the death of breast cancer stem cells (BCSCs) by regulating Stat3/Sox2 signaling pathways.
In vitro
Betavulgarin, when applied at concentrations of 50-500 μM for 24 hours, significantly inhibits the proliferation, migration, colony formation, and mammosphere formation of MDA-MB-231 and MCF-7 breast cancer cells. At 200 μM for 24 hours, it effectively reduces the size of the CD44+/CD24− subpopulation in MDA-MB-231 cells from 90.4% to 57.2%. Additionally, Betavulgarin at 200 μM for 48 hours inhibits Stat3 translocation and decreases both total and nuclear p-Stat3 protein levels along with mRNA and protein levels of SOX2 in mammospheres derived from MDA-MB-231 cells. It also significantly impairs the ability of Stat3 to bind DNA in these mammospheres. Over a period of 24-72 hours, Betavulgarin reduces the mRNA expression of self-renewal-related genes C-Myc, Nanog, and Oct4, and inhibits the growth of mammospheres derived from breast cancer stem cells (BCSCs).
Chemical Properties
Molecular Weight312.27
FormulaC17H12O6
Cas No.51068-94-1
SmilesO=C1C(=COC=2C=C3OCOC3=C(OC)C12)C=4C=CC=CC4O
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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