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STAT3-IN-12

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Catalog No. T62803Cas No. 2980758-31-2

STAT3-IN-12, a potent STAT3 signaling inhibitor, suppresses IL-6-induced JAK/STAT3 pathway activation. This compound inhibits cancer cell proliferation and migration while inducing apoptosis and cell cycle arrest, making it suitable for hepatocellular carcinoma (HCC) and esophageal cancer research.

STAT3-IN-12

STAT3-IN-12

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Purity: 99.19%
Catalog No. T62803Cas No. 2980758-31-2
STAT3-IN-12, a potent STAT3 signaling inhibitor, suppresses IL-6-induced JAK/STAT3 pathway activation. This compound inhibits cancer cell proliferation and migration while inducing apoptosis and cell cycle arrest, making it suitable for hepatocellular carcinoma (HCC) and esophageal cancer research.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 mg$52-In Stock
5 mg$123-In Stock
10 mg$189-In Stock
25 mg$396-In Stock
50 mg$569-In Stock
100 mg$745-In Stock
1 mL x 10 mM (in DMSO)$135-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:99.19%
Appearance:Solid
Color:Brown
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Product Introduction

Bioactivity
Description
STAT3-IN-12, a potent STAT3 signaling inhibitor, suppresses IL-6-induced JAK/STAT3 pathway activation. This compound inhibits cancer cell proliferation and migration while inducing apoptosis and cell cycle arrest, making it suitable for hepatocellular carcinoma (HCC) and esophageal cancer research.
Targets&IC50
HepG2 cells:4.32 μM, EC109 cells:3.63 μM
In vitro
Methods: HepG2 and EC109 cells were treated with STAT3-IN-12 (0, 1.25, 2.5, 5, 10 μM, 16-72 hours) and subjected to cell viability assays, cell migration assays, and Western blotting. Results: STAT3-IN-12 inhibited the growth of HepG2 and EC109 cells with IC50 values of 4.32 μM and 3.63 μM, respectively. It selectively inhibited STAT3 tyrosine 705 phosphorylation after 16 hours of treatment. [1]
In vivo
Methods: STAT3-IN-12 (20, 40 mg/kg intraperitoneal injection, daily for 24 days) was used to treat HepG2 cell xenograft tumor model mice to study its effect on tumor growth in mice. Results: STAT3-IN-12 was able to inhibit tumor growth in mice without affecting the body weight of the mice. [1]
Chemical Properties
Molecular Weight454.56
FormulaC28H30N4O2
Cas No.2980758-31-2
SmilesN=1C=2C=C3N=C(C=4C=CC=C(OC)C4)N(C3=CC2N(C1C=5C=CC=C(OC)C5)CCC)CCC
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
DMSO: 80 mg/mL (175.99 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.1999 mL10.9996 mL21.9993 mL109.9965 mL
5 mM0.4400 mL2.1999 mL4.3999 mL21.9993 mL
10 mM0.2200 mL1.1000 mL2.1999 mL10.9996 mL
20 mM0.1100 mL0.5500 mL1.1000 mL5.4998 mL
50 mM0.0440 mL0.2200 mL0.4400 mL2.1999 mL
100 mM0.0220 mL0.1100 mL0.2200 mL1.1000 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

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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