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Tubulin-IN-56 is a tubulin inhibitor with cytotoxic effects on colon cancer cell lines (LS180, HCT116, SW620, LoVo). It downregulates βIII-tubulin expression and upregulates βIVa-tubulin expression within these cell lines. Additionally, Tubulin-IN-56 inhibits cell invasiveness and elevates intracellular ROS levels in colon cancer cell lines. This compound is applicable in colon cancer research.
| Pack Size | Price | USA Stock | Global Stock | Quantity |
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| 10 mg | Inquiry | Inquiry | Inquiry | |
| 50 mg | Inquiry | Inquiry | Inquiry |
| Description | Tubulin-IN-56 is a tubulin inhibitor with cytotoxic effects on colon cancer cell lines (LS180, HCT116, SW620, LoVo). It downregulates βIII-tubulin expression and upregulates βIVa-tubulin expression within these cell lines. Additionally, Tubulin-IN-56 inhibits cell invasiveness and elevates intracellular ROS levels in colon cancer cell lines. This compound is applicable in colon cancer research. |
| In vitro | Tubulin-IN-56 (Compound 1b) induces an increase in the proportion of M phase-arrested and apoptotic cells in colon cancer cell lines (LS180, HCT116, SW620, LoVo) over time (12-48 h). It shows antiproliferative activity with IC50 values of 279 nM, 102 nM, 132 nM, and 45 nM for LS180, HCT116, SW620, and LoVo cells, respectively. At 3 μM concentration for 80 minutes, Tubulin-IN-56 alters the microtubule polymerization rate in HCT116 and LoVo cells. This compound significantly downregulates βIII-tubulin and upregulates βIVa-tubulin expression in SW620, HCT116, and LoVo cells. Tubulin-IN-56 inhibits invasion and reduces MMP-7 secretion in SW620, HCT116, and LoVo cells at 8 hours. It decreases cytoplasmic integrin-linked kinase (ILK) levels in LoVo cells. At 1 μM for 4 hours, it increases intracellular ROS levels in LS180, SW620, and LoVo cells. Additionally, Tubulin-IN-56 reduces the growth of LoVo cell spheroids in a 3D culture over 72 hours. |
| 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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