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Synonyms:
| Pack Size | Price | USA Stock | Global Stock | Quantity |
|---|---|---|---|---|
| 10 mg | Inquiry | 10-14 weeks | 10-14 weeks | |
| 50 mg | Inquiry | 10-14 weeks | 10-14 weeks |
| Description | ON 01500 is a tubulin inhibitor with a dissociation constant (Kd) of 21 nM. It acts by depolymerizing microtubules within cells and is utilized in cancer research. |
| In vitro | ON 01500 (1 μM) completely inhibits microtubule polymerization in samples enriched with MAP microtubule proteins. At concentrations of 7-15 nM over 3-5 days, ON 01500 sensitizes cells to TACC3 knockdown or KIF2C overexpression and protects cells from TACC3 overexpression or KIF2C knockdown, demonstrating high toxicity. Additionally, ON 01500 (10 nM, 3-7 days) induces the enrichment of K562 cells expressing L240F TUBB (mCherry positive) compared to wild-type cells. |
| Molecular Weight | 393.45 |
| Formula | C19H23NO6S |
| Cas No. | 592542-50-2 |
| Smiles | C(=C/S(CC1=CC(N)=C(OC)C=C1)(=O)=O)\C2=C(OC)C=C(OC)C=C2OC |
| 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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