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WRN inhibitor 6 (compound 3ci) is an effective inhibitor of WRN, inducing apoptosis and increasing the expression of p-p53, P-Chk2, and γH2AX.
| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
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| 10 mg | Inquiry | Inquiry | Inquiry | |
| 50 mg | Inquiry | Inquiry | Inquiry |
| Description | WRN inhibitor 6 (compound 3ci) is an effective inhibitor of WRN, inducing apoptosis and increasing the expression of p-p53, P-Chk2, and γH2AX. |
| In vitro | WRN inhibitor 6 (compound 3ci) induces DNA damage and apoptosis in HCT116 and SW620 cells, with IC50 values of 2.305 µM and 16.58 µM, respectively, when used at concentrations of 0-100 µM for 72 hours. Additionally, WRN inhibitor 6 at concentrations of 0, 2.5, 5, and 10 µM over 3 and 27 hours increases the expression of p-p53, P-Chk2, and γH2AX in a dose-dependent manner in HCT116 cells. |
| In vivo | WRN inhibitor 6 has low oral bioavailability in mice, recorded at 11.43%, and a short half-life of 0.17 hours when administered intravenously (20 mg/kg for p.o.; 5 mg/kg for i.v.). |
| Formula | C29H34O5S |
| 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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