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Tubulin/HDAC-IN-3

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Catalog No. T78880

Tubulin/HDAC-IN-3 (compound 12a) is a potent dual inhibitor of tubulin polymerization and HDAC1/8, with IC50 values of 5.4 μM for tubulin polymerization, and 0.155 and 0.177 μM for HDAC1 and HDAC8, respectively. It obstructs the cell cycle, triggers apoptosis, and suppresses colony formation [1].

Tubulin/HDAC-IN-3

Tubulin/HDAC-IN-3

😃Good
Catalog No. T78880
Tubulin/HDAC-IN-3 (compound 12a) is a potent dual inhibitor of tubulin polymerization and HDAC1/8, with IC50 values of 5.4 μM for tubulin polymerization, and 0.155 and 0.177 μM for HDAC1 and HDAC8, respectively. It obstructs the cell cycle, triggers apoptosis, and suppresses colony formation [1].
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Product Introduction

Bioactivity
Description
Tubulin/HDAC-IN-3 (compound 12a) is a potent dual inhibitor of tubulin polymerization and HDAC1/8, with IC50 values of 5.4 μM for tubulin polymerization, and 0.155 and 0.177 μM for HDAC1 and HDAC8, respectively. It obstructs the cell cycle, triggers apoptosis, and suppresses colony formation [1].
Targets&IC50
HDAC1:0.155 μM, HDAC6:1.037 μM, HDAC8:0.177 μM
In vitro
Tubulin/HDAC-IN-3 (compound 12a) exhibited antiproliferative activity in vitro against the cancer cell lines BE-(2)-C, A549, U87MG, and HCT116, with IC50 values of 0.017 ± 0.002, 0.053 ± 0.003, 0.056 ± 0.005, and 0.051 ± 0.003 μM, respectively [1].
In vivo
Tubulin/HDAC-IN-3 (compound 12a), administered intraperitoneally at 25 mg/kg every three days, demonstrated significant antitumor efficacy in mice [1].
Chemical Properties
Molecular Weight552.53
FormulaC28H28N2O10
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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Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc
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