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Tubulin polymerization-IN-40

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Catalog No. T72169Cas No. 2921670-94-0

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].

Tubulin polymerization-IN-40

Tubulin polymerization-IN-40

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Catalog No. T72169Cas No. 2921670-94-0
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 SizePriceUSA WarehouseGlobal WarehouseQuantity
25 mg$1,5206-8 weeks6-8 weeks
50 mg$1,9806-8 weeks6-8 weeks
100 mg$2,5006-8 weeks6-8 weeks
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
All TargetMol products are for research purposes only and cannot be used for human consumption. We do not provide products or services to individuals. Please comply with the intended use and do not use TargetMol products for any other purpose.
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Product Introduction

Bioactivity
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].
Chemical Properties
FormulaC24H22FNO5
Cas No.2921670-94-0
SmilesCOC1=C(C2=C(C=C1)N(C3=CC=CC=C3C2)C(=O)C4=CC(=C(C(=C4)OC)OC)OC)F
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.

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Please enter your animal experiment information in the following box and click Calculate to obtain the stock solution preparation method and in vivo formula preparation method:
TargetMol | Animal experiments For example, if the intended dosage is 10 mg/kg for animals weighing 20 g , with a dosing volume of 100 μL per animal, TargetMol | Animal experiments and a total of 10 animals are to be administered, using a formulation of TargetMol | reagent 10% DMSO+ 40% PEG300+ 5% Tween 80+ 45% Saline/PBS/ddH2O , the resulting working solution concentration would be 2 mg/mL.
Stock Solution Preparation:

Dissolve 2 mg of the compound in 100 μL DMSOTargetMol | reagent 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.

Preparation of the In Vivo Formulation:

1) Add 100 μL of the DMSOTargetMol | reagent stock solution to 400 μL PEG300TargetMol | reagent 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 ddH2OTargetMol | reagent and mix thoroughly until a homogeneous solution is obtained.

This example is provided solely to demonstrate the use of the In Vivo Formulation Calculator and does not constitute a recommended formulation for any specific compound. Please select an appropriate dissolution and formulation strategy based on your experimental model and route of administration.
All co-solvents required for this protocol, includingDMSO, PEG300/PEG400, Tween 80, SBE-β-CD, and Corn oil, are available for purchase on the TargetMol website.
1 Enter information below:
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2 Enter the in vivo formulation:
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