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c-Met-IN-2 is a selective and orally available c-Met inhibitor (IC50: 0.6 nM) exhibiting antitumor activity.

| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 25 mg | $2,270 | 3-6 months | 3-6 months | |
| 50 mg | $2,980 | 3-6 months | 3-6 months | |
| 100 mg | $4,000 | 3-6 months | 3-6 months |
| Description | c-Met-IN-2 is a selective and orally available c-Met inhibitor (IC50: 0.6 nM) exhibiting antitumor activity. |
| Targets&IC50 | c-Met:0.6 nM |
| In vitro | c-Met-IN-2 (Compound 14) exhibits weak activity on other kinases, with IC50 values of 731 nM [RON], 1075 nM [AxI], 18364 nM [VEGFR2], 2357 nM [PDGFRa], 5396 nM [c-Kit], and 17056 nM [c-Src]. |
| In vivo | In mice bearing H1993 tumors, c-Met-IN-2 (0.1, 1, 10 mg/kg, p.o., once daily) significantly reduces the volume of tumors. c-Met-IN-2 has a similar effect in SNU-5 xenograft model via oral administration at 0.3, 1 and 3 mg/kg. |
| Molecular Weight | 484.49 |
| Formula | C24H21FN10O |
| Cas No. | 1635406-73-3 |
| Smiles | C(C)(N1C=2C(N=N1)=NC=C(N2)C3=CN(CCO)N=C3)C4=CC5=C(C=C4F)N=CC(=C5)C=6C=NN(C)C6 |
| Relative Density. | 1.55 g/cm3 (Predicted) |
| 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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