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GW768505A free base is a potent dual inhibitor of VEGFR2 (KDR) and Tie-2 (pIC50: 7.81 for VEGFR2) with anti-angiogenic activity.

| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 25 mg | $688 | 6-8 weeks | 6-8 weeks | |
| 50 mg | $913 | 6-8 weeks | 6-8 weeks | |
| 100 mg | $1,360 | 6-8 weeks | 6-8 weeks |
| Description | GW768505A free base is a potent dual inhibitor of VEGFR2 (KDR) and Tie-2 (pIC50: 7.81 for VEGFR2) with anti-angiogenic activity. |
| In vitro | GW768505A free base acts as an inhibitor of both KDR and TIE2, demonstrating significant inhibition (71–88% inhibition at 100 nM) of tropomyosin-related kinases, including TRKA, TRKB, and TRKC. Furthermore, it exhibits inhibitory effects on the growth of cancer cells in the NCI-60 panel screening. |
| Molecular Weight | 537.47 |
| Formula | C27H19F4N5O3 |
| Cas No. | 501693-25-0 |
| Smiles | Cl.COc1ccc(cc1)-c1oc2ncnc(N)c2c1-c1ccc(NC(=O)Nc2cc(ccc2F)C(F)(F)F)cc1 |
| 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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