Your shopping cart is currently empty

VEGFR-2-IN-73 is a potent and highly selective inhibitor of VEGFR-2, demonstrating significantly stronger inhibition (IC50 = 0.0787 μM) compared to its effect on EGFR (IC50 = 1.31 μM). It exhibits strong antiproliferative activity across various cancer cell lines, induces cell cycle arrest at the G2/M and Pre-G1 phases, and significantly promotes apoptosis. This compound is applicable in cancer research, including studies on colorectal cancer, hepatocellular carcinoma, and breast cancer.
| Pack Size | Price | USA Stock | Global Stock | Quantity |
|---|---|---|---|---|
| 10 mg | Inquiry | Inquiry | Inquiry | |
| 50 mg | Inquiry | Inquiry | Inquiry |
| Description | VEGFR-2-IN-73 is a potent and highly selective inhibitor of VEGFR-2, demonstrating significantly stronger inhibition (IC50 = 0.0787 μM) compared to its effect on EGFR (IC50 = 1.31 μM). It exhibits strong antiproliferative activity across various cancer cell lines, induces cell cycle arrest at the G2/M and Pre-G1 phases, and significantly promotes apoptosis. This compound is applicable in cancer research, including studies on colorectal cancer, hepatocellular carcinoma, and breast cancer. |
| Targets&IC50 | VEGFR2:0.0787 μM |
| In vitro | VEGFR-2-IN-73 (compound 15) (2 days) demonstrates significant cytotoxicity against HCT-116, HepG-2, and MCF-7 cancer cell lines with IC₅₀ values of 3.66, 3.31, and 4.29 μM respectively, while exhibiting minimal cytotoxicity towards normal WI-38 cells (IC₅₀ > 69 μM), indicating strong selectivity. It effectively induces G2/M and Pre-G1 phase cell cycle arrest and significantly triggers apoptosis in HCT-116, HepG-2, and MCF-7 cells, with effects comparable to Doxorubicin. The predicted binding energy of VEGFR-2-IN-73 with VEGFR-2 is -24.27 kcal/mol, notably lower than that of Sorafenib at -20.88 kcal/mol, suggesting superior binding affinity. |
| 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.
| Size | Quantity | Unit Price | Amount | Operation |
|---|

Copyright © 2015-2026 TargetMol Chemicals Inc. All Rights Reserved.