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FQI2-34 is an orally active small-molecule allosteric inhibitor of TFCP2 (LSF). It binds directly to the LSF protein (Ki = 63 nM), inhibits LSF oligomerization, and effectively suppresses LSF transcriptional activity (IC₅₀ = 48 nM), thereby disrupting the SF-DNA interaction. FQI2-34 exhibits significant antiproliferative effects on Huh7 cells and induces tumor regression in mouse models. This compound can be utilized for hepatocellular carcinoma research.
| Pack Size | Price | USA Stock | Global Stock | Quantity |
|---|---|---|---|---|
| 10 mg | Inquiry | 10-14 weeks | 10-14 weeks | |
| 50 mg | Inquiry | 10-14 weeks | 10-14 weeks |
| Description | FQI2-34 is an orally active small-molecule allosteric inhibitor of TFCP2 (LSF). It binds directly to the LSF protein (Ki = 63 nM), inhibits LSF oligomerization, and effectively suppresses LSF transcriptional activity (IC₅₀ = 48 nM), thereby disrupting the SF-DNA interaction. FQI2-34 exhibits significant antiproliferative effects on Huh7 cells and induces tumor regression in mouse models. This compound can be utilized for hepatocellular carcinoma research. |
| Molecular Weight | 352.39 |
| Formula | C20H20N2O4 |
| Cas No. | 2762499-38-5 |
| Smiles | O=C1C=C(C=2C=CC(=CC2OCC)N(C)C)C=3C=C4OCOC4=CC3N1 |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature. |
Dissolve 2 mg of the compound in 100 μL DMSO
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.
1) Add 100 μL of the DMSO
stock solution to 400 μL PEG300
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 ddH2O
and mix thoroughly until a homogeneous solution is obtained.
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