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Chk1-IN-5 is a highly effective inhibitor of checkpoint kinase 1 (Chk1), which hinders the phosphorylation of Chk1 and effectively suppresses tumor growth in a colon cancer xenograft model[1].

| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 25 mg | $2,270 | 10-14 weeks | 10-14 weeks | |
| 50 mg | $2,980 | 10-14 weeks | 10-14 weeks | |
| 100 mg | $4,000 | 10-14 weeks | 10-14 weeks |
| Description | Chk1-IN-5 is a highly effective inhibitor of checkpoint kinase 1 (Chk1), which hinders the phosphorylation of Chk1 and effectively suppresses tumor growth in a colon cancer xenograft model[1]. |
| In vitro | Chk1-IN-5 (compound 3; concentrations of 0.4, 1.2, 3.7, 11.1, 33.3, and 100 nM) effectively inhibits Chk1 phosphorylation in HT-29 colon cells[1]. |
| In vivo | Chk1-IN-5 (compound 3; 40 mg/kg; IV; twice a week for 21 days) inhibits tumor growth in Baib/c nude mice with HT-29 colon cancer cells. Chk1-IN-5 (10 mg/kg; via tail vein intravenous injection) demonstrates a longer half-life (T1/2=3.8 hours) and higher systemic exposure (CL=2.3 L/hr⋅kg; Vss=6.4 L/kg; AUC=4531 ng⋅ml⋅h)[1]. [Animal Model: Baib/c nude mice with HT-29 colon cancer cells][1]. |
| Synonyms | Chk1-IN-5 |
| Molecular Weight | 383.38 |
| Formula | C18H18FN7O2 |
| Cas No. | 2120398-39-0 |
| Smiles | O(CCCN)C1=C(C(OC)=CC(F)=C1)C2=CC(NC=3C=NC(C#N)=CN3)=NN2 |
| 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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