STAT3-IN-54
STAT3-IN-54 is a STAT3 inhibitor. STAT3-IN-54 induces Apoptosis and G0/G1 cell cycle arrest. STAT3-IN-54 exhibits selective anticancer activity against non-small cell lung cancer cells. STAT3-IN-54 can be used for research on non-small cell lung cancer.
For research use only. We do not sell to patients.
- Formula: C17H10BrF2N3O2S
- Molecular Weight:438.25
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Storage:
Please store the product under the recommended conditions in the Certificate of Analysis.
Biological Activity
Description
IC50 & Target
[1]|
STAT3 |
Cellular Effect
|
Cell Line
|
Type | Value | Description | References |
|---|---|---|---|---|
| A549 | IC50 |
20.13 μM
|
Cytotoxicity against human A549 lung adenocarcinoma cells assessed as reduction in cell viability incubated for 24 hrs by MTT assay.
Cytotoxicity against human A549 lung adenocarcinoma cells assessed as reduction in cell viability incubated for 24 hrs by MTT assay.
|
42612271 |
| L929 | IC50 |
>500 μM
|
Cytotoxicity against mouse L929 embryonic fibroblast cells assessed as reduction in cell viability incubated for 24 hrs by MTT assay.
Cytotoxicity against mouse L929 embryonic fibroblast cells assessed as reduction in cell viability incubated for 24 hrs by MTT assay.
|
42612271 |
| A549 | IC50 |
2.04 μM
|
Inhibition of STAT3 (Tyr705) in human A549 lung adenocarcinoma cells incubated for 24 hrs by in-cell ELISA assay.
Inhibition of STAT3 (Tyr705) in human A549 lung adenocarcinoma cells incubated for 24 hrs by in-cell ELISA assay.
|
42612271 |
In Vitro
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Cell Line:A549, L929
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Concentration:Various concentrations
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Incubation Time:24 h
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Result:Exerted cytotoxicity against A549 cells with an IC50 of 20.13 μM.
Exhibited an IC50 of >500 μM against L929 cells.
Achieved a selectivity index of >24.84.
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Cell Line:A549
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Concentration:IC50 concentration
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Incubation Time:24 h
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Result:Induced early apoptosis in 12.95% of A549 cells.
Induced late apoptosis in 6.04% of A549 cells.
Induced total apoptosis of 18.99%.
Induced greater total apoptosis than erlotinib and GSK690693.
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Cell Line:A549
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Concentration:IC50 concentration
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Incubation Time:24 h
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Result:Induced a cell cycle distribution with 65.84% in G0/G1 phase, 21.01% in S phase, and 5.68% in G2/M phase.
Chemical Information
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Molecular Weight 438.25
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Formula C17H10BrF2N3O2S
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SMILES
FC1=CC=C(C2=CSC(N/N=C/C3=C(Br)C=C(OCO4)C4=C3)=N2)C(F)=C1
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Shipping
Room temperature in continental US; may vary elsewhere.
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Storage
Please store the product under the recommended conditions in the Certificate of Analysis.
Purity & Documentation
References
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)