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STX-721 is an irreversible EGFR inhibitor targeting the exon 20 insertion (ex20ins) mutation. It specifically inhibits the proliferation of Ba/F3 cells with EGFR exon20 A769_V770 insASV and EGFR exon20 D770_N771 insSVD mutations, demonstrating IC50 values of 5.4 and 5.8 nM, respectively, while showing much less inhibition of cells expressing wild-type EGFR (IC50 = 127.365 nM). Additionally, STX-721, administered at 50 mg/kg once daily, induces tumor regression in a mouse xenograft model utilizing NCI H2073 non-small cell lung cancer (NSCLC) cells with the EGFR exon20 D770_N771 insSVD mutation.
| Pack Size | Price | USA Stock | Global Stock | Quantity |
|---|---|---|---|---|
| 10 mg | Inquiry | Inquiry | Inquiry | |
| 50 mg | Inquiry | Inquiry | Inquiry |
| Description | STX-721 is an irreversible EGFR inhibitor targeting the exon 20 insertion (ex20ins) mutation. It specifically inhibits the proliferation of Ba/F3 cells with EGFR exon20 A769_V770 insASV and EGFR exon20 D770_N771 insSVD mutations, demonstrating IC50 values of 5.4 and 5.8 nM, respectively, while showing much less inhibition of cells expressing wild-type EGFR (IC50 = 127.365 nM). Additionally, STX-721, administered at 50 mg/kg once daily, induces tumor regression in a mouse xenograft model utilizing NCI H2073 non-small cell lung cancer (NSCLC) cells with the EGFR exon20 D770_N771 insSVD mutation. |
| 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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