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Tubulin inhibitor 40 (compound 45) is a tubulin inhibitor with an IC50 value of 1.2 μM. It exhibits selective cytotoxicity against cancer cells and possesses antitumor activity.
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| 10 mg | Inquiry | Inquiry | Inquiry | |
| 50 mg | Inquiry | Inquiry | Inquiry |
| Description | Tubulin inhibitor 40 (compound 45) is a tubulin inhibitor with an IC50 value of 1.2 μM. It exhibits selective cytotoxicity against cancer cells and possesses antitumor activity. |
| In vitro | Tubulin inhibitor 40 exhibits cytotoxic effects on A549, VA13, MCF7, and HEK293T cell lines with IC 50 values of 0.005 μM, 0.008 μM, 0.009 μM, and 0.008 μM, respectively. It impedes tubulin polymerization with an IC 50 of 1.2 μM. Additionally, Tubulin inhibitor 40 (1-25 μM, 24 h) induces changes in cell morphology and tubulin polymerization in A549 cells. |
| In vivo | Tubulin inhibitor 40 (administered intravenously at 20 mg/kg for 5 days) demonstrates antitumor activity. |
| Formula | C19H20N2O5 |
| 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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