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ZK-261991 is an orally active inhibitor of VEGFR tyrosine kinase (IC50 of 5 nM, VEGFR2).

| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 25 mg | $1,520 | 6-8 weeks | 6-8 weeks | |
| 50 mg | $1,980 | 6-8 weeks | 6-8 weeks | |
| 100 mg | $2,500 | 6-8 weeks | 6-8 weeks |
| Description | ZK-261991 is an orally active inhibitor of VEGFR tyrosine kinase (IC50 of 5 nM, VEGFR2). |
| Targets&IC50 | VEGFR2:5 nM |
| In vitro | ZK-261991 inhibits cellular receptor autophosphorylation in KDR-PAECs (IC50 of 2 nM) and VEGFR-3 autophosphorylation in a concentration-dependent manner (IC50 of 20 nM). |
| Molecular Weight | 443.5 |
| Formula | C24H25N7O2 |
| Cas No. | 886563-25-3 |
| Smiles | N(C(=O)C1=C(NCC=2C=C(NC(N(C)C)=O)N=CC2)C=CC=C1)C3=CC=4C(C=C3)=CN(C)N4 |
| Relative Density. | no data available |
| 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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