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Tubulin Polymerization-IN-40 is an acridane-based inhibitor that potently disrupts tubulin polymerization, exhibiting an IC50 of 1.5 μM. It halts cancer cell progression at the G2/M phase, triggers apoptosis, and possesses anti-cancer properties along with immunopotentiating effects [1].

| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 25 mg | $1,520 | 6-8 weeks | 6-8 weeks | |
| 50 mg | $1,980 | 6-8 weeks | 6-8 weeks | |
| 100 mg | $2,500 | 6-8 weeks | 6-8 weeks |
| Description | Tubulin Polymerization-IN-40 is an acridane-based inhibitor that potently disrupts tubulin polymerization, exhibiting an IC50 of 1.5 μM. It halts cancer cell progression at the G2/M phase, triggers apoptosis, and possesses anti-cancer properties along with immunopotentiating effects [1]. |
| In vitro | Tubulin polymerization-IN-40 (Compound NT-6) exhibited significant antiproliferative efficacy against four cancer cell lines (HCT-116, B16-F10, HeLa, HepG2), with an average IC50 of 30 nM [1]. At concentrations of 10, 25, and 50 nM administered over 48 hours, it effectively induced apoptosis in B16-F10 cells [1]. Furthermore, Tubulin polymerization-IN-40 caused a G2/M phase arrest in B16-F10 cells at the same concentrations after 24 hours [1]. The compound also significantly inhibited colony formation of B16-F10 cells at 50 nM, reducing formation almost completely after 24 hours of treatment [1]. Additionally, Tubulin polymerization-IN-40 dose-dependently inhibited the migration of B16-F10 cells at concentrations of 10, 25, and 50 nM over 24 hours [1]. |
| In vivo | Tubulin polymerization-IN-40 (Compound NT-6; 10 mg/kg; intraperitoneal administration; daily; for 14 days) demonstrated remarkable antitumor efficacy in a melanoma model. When combined with NP-19 (10 mg/kg; intraperitoneal administration), Tubulin polymerization-IN-40 significantly reduced tumor burden (TGI%=77.6%) and enhanced antitumor immune responses [1]. |
| Formula | C24H22FNO5 |
| Cas No. | 2921670-94-0 |
| Smiles | COC1=C(C2=C(C=C1)N(C3=CC=CC=C3C2)C(=O)C4=CC(=C(C(=C4)OC)OC)OC)F |
| 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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