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SHP2-IN-26 (Compound 4b) is a highly selective allosteric inhibitor of SHP2, with an IC50 of 3.2 nM. It effectively inhibits the phosphorylation levels of ERK and AKT in NCI-H358 cells and demonstrates antitumor activity.
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| 10 mg | Inquiry | Inquiry | Inquiry | |
| 50 mg | Inquiry | Inquiry | Inquiry |
| Description | SHP2-IN-26 (Compound 4b) is a highly selective allosteric inhibitor of SHP2, with an IC50 of 3.2 nM. It effectively inhibits the phosphorylation levels of ERK and AKT in NCI-H358 cells and demonstrates antitumor activity. |
| In vitro | SHP2-IN-26 inhibits the proliferation of various cancer cells, with IC50 values of 0.58, 5.36, 5.88, and 4.35 μM against NCI-H358, A549, MDA-MB-231, and MDA-MB468, respectively. Additionally, SHP2-IN-26 significantly reduces the phosphorylation levels of ERK and AKT in NCI-H358 cells when applied at concentrations of 0, 0.25, 0.5, 1, and 2 μM for 12 hours. |
| Formula | C20H22Cl2N6OS |
| 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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