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STAT3-IN-47

Catalog No. T213720 Copy Product Info
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STAT3-IN-47 is an orally active STAT3 inhibitor. It exhibits broad-spectrum antitumor activity against HeLa, HepG2, U87, and LN229 cells. STAT3-IN-47 inhibits STAT3 activation in vitro. This compound is applicable for solid tumor research, particularly in studies of central nervous system (CNS) malignancies and hepatocellular carcinoma.

STAT3-IN-47

Copy Product Info
🥰Excellent
Catalog No. T213720

STAT3-IN-47 is an orally active STAT3 inhibitor. It exhibits broad-spectrum antitumor activity against HeLa, HepG2, U87, and LN229 cells. STAT3-IN-47 inhibits STAT3 activation in vitro. This compound is applicable for solid tumor research, particularly in studies of central nervous system (CNS) malignancies and hepatocellular carcinoma.

STAT3-IN-47
Cas No. 2787548-58-5
Pack SizePriceUSA StockGlobal StockQuantity
10 mgInquiry10-14 weeks10-14 weeks
50 mgInquiry10-14 weeks10-14 weeks
For In stock only · Estimated delivery: USA Stock (1-2 days) Global Stock (5-7 days)
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With extensive experience in compound synthesis, we can provide rapid custom synthesis services for this product according to your research needs.
For research use only—not for human use. No sales to individuals. Use as intended only.
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Product Introduction

Bioactivity
Description
STAT3-IN-47 is an orally active STAT3 inhibitor. It exhibits broad-spectrum antitumor activity against HeLa, HepG2, U87, and LN229 cells. STAT3-IN-47 inhibits STAT3 activation in vitro. This compound is applicable for solid tumor research, particularly in studies of central nervous system (CNS) malignancies and hepatocellular carcinoma.
In vitro
STAT3-IN-47 (Compound S1) exhibits broad-spectrum antitumor activity against HeLa, HepG2, U87, and LN229 cells, with IC50 values of 5.066 μM, 0.8089 μM, 1.970 μM, and 1.412 μM, respectively. At concentrations of 0.1-10 μM, STAT3-IN-47 inhibits STAT3 activation in these cell lines in a dose-dependent manner. Additionally, STAT3-IN-47 (0.5-2 μM) inhibits EGF-induced STAT3 phosphorylation (Y705) in HeLa cells and suppresses IL-6-induced STAT3 phosphorylation (Y705) in HepG2, U87, and LN229 cells in a dose-dependent fashion. Furthermore, it downregulates the expression of stemness-associated genes (Nanog, Oct4, β-catenin) in Huh7, LN229, and HepG2 cells.
Chemical Properties
Molecular Weight324.31
FormulaC15H8N4O3S
Cas No.2787548-58-5
SmilesO=C1C=2OC(C=NN3C=NNC3=S)=CC2C(=O)C=4C=CC=CC14
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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