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TPBM

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Catalog No. T60827Cas No. 6466-43-9

TPBM is a potent estrogen receptor α (ERα) inhibitor with an IC50 value of 9 μM for disruption of 17β-estradiol–ERα interaction, effectively reducing E2·ERα recruitment to endogenous estrogen-responsive genes and inhibiting E2-dependent proliferation of ERα-positive cancer cells with an IC50 of 5 μM, while remaining non-toxic and not affecting estrogen-independent cell growth, making it a selective probe for ERα signaling research.

TPBM

TPBM

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Purity: 99.64%
Catalog No. T60827Cas No. 6466-43-9
TPBM is a potent estrogen receptor α (ERα) inhibitor with an IC50 value of 9 μM for disruption of 17β-estradiol–ERα interaction, effectively reducing E2·ERα recruitment to endogenous estrogen-responsive genes and inhibiting E2-dependent proliferation of ERα-positive cancer cells with an IC50 of 5 μM, while remaining non-toxic and not affecting estrogen-independent cell growth, making it a selective probe for ERα signaling research.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 mg$68-In Stock
5 mg$163-In Stock
10 mg$263-In Stock
25 mg$529-In Stock
50 mg$853-In Stock
100 mg$1,360-In Stock
1 mL x 10 mM (in DMSO)$179-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:99.64%
Appearance:Solid
Color:White
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Product Introduction

Bioactivity
Description
TPBM is a potent estrogen receptor α (ERα) inhibitor with an IC50 value of 9 μM for disruption of 17β-estradiol–ERα interaction, effectively reducing E2·ERα recruitment to endogenous estrogen-responsive genes and inhibiting E2-dependent proliferation of ERα-positive cancer cells with an IC50 of 5 μM, while remaining non-toxic and not affecting estrogen-independent cell growth, making it a selective probe for ERα signaling research.
In vitro
TPBM inhibits the binding of E2-liganded ERα to EREs with an IC₅₀ of 9 μM. By obstructing this interaction, the molecule blocks estrogen-dependent transcriptional activity.
Chemical Properties
Molecular Weight316.38
FormulaC15H16N4O2S
Cas No.6466-43-9
SmilesO=C1C=2NC(=NC2N(C(=O)N1C)C)CSCC=3C=CC=CC3
Storage & Solubility Information
StorageIn solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 80 mg/mL (252.86 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM3.1608 mL15.8038 mL31.6076 mL158.0378 mL
5 mM0.6322 mL3.1608 mL6.3215 mL31.6076 mL
10 mM0.3161 mL1.5804 mL3.1608 mL15.8038 mL
20 mM0.1580 mL0.7902 mL1.5804 mL7.9019 mL
50 mM0.0632 mL0.3161 mL0.6322 mL3.1608 mL
100 mM0.0316 mL0.1580 mL0.3161 mL1.5804 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:
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g
μL
2 Enter the in vivo formulation:
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

Dose Conversion

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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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