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Apoptosis inducer 46

Catalog No. T213336 Copy Product Info
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Apoptosis inducer46 is an apoptosis (apoptosis) inducer that exhibits potent and selective growth inhibitory effects on metastatic triple-negative breast cancer (TNBC) cells. It induces G2/M phase cell cycle arrest and apoptosis (apoptosis) cell death in MDA-MB-231 cells and blocks the nuclear translocation of NF-κB. Apoptosis inducer46 is useful for TNBC research.

Apoptosis inducer 46

Copy Product Info
🥰Excellent
Catalog No. T213336

Apoptosis inducer46 is an apoptosis (apoptosis) inducer that exhibits potent and selective growth inhibitory effects on metastatic triple-negative breast cancer (TNBC) cells. It induces G2/M phase cell cycle arrest and apoptosis (apoptosis) cell death in MDA-MB-231 cells and blocks the nuclear translocation of NF-κB. Apoptosis inducer46 is useful for TNBC research.

Apoptosis inducer 46
Cas No. 3085356-41-5
Pack SizePriceUSA StockGlobal StockQuantity
10 mgInquiry10-14 weeks10-14 weeks
50 mgInquiry10-14 weeks10-14 weeks
For In stock only · Estimated delivery: USA Stock (1-2 days) Global Stock (5-7 days)
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For research use only—not for human use. No sales to individuals. Use as intended only.
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Product Introduction

Bioactivity
Description
Apoptosis inducer46 is an apoptosis (apoptosis) inducer that exhibits potent and selective growth inhibitory effects on metastatic triple-negative breast cancer (TNBC) cells. It induces G2/M phase cell cycle arrest and apoptosis (apoptosis) cell death in MDA-MB-231 cells and blocks the nuclear translocation of NF-κB. Apoptosis inducer46 is useful for TNBC research.
In vitro
Apoptosis inducer 46 (Compound 5d) demonstrates potent growth inhibitory effects on metastatic triple-negative breast cancer (TNBC) cells, including MDA-MB-231, HCC 1806, MCF-7, and BEAS 2B cells, with IC 50 values of 0.38 μM, 0.31 μM, 0.39 μM, and 0.7 μM, respectively. Furthermore, at concentrations of 5-40 μM over 2-4 hours, it significantly reduces proteasome activity in MDA-MB-231 cells, with an IC 50 of 37.0 μM for proteasome inhibition, and leads to the accumulation of ubiquitinated proteins. At 5 μM across 24-72 hours, the compound elevates apoptosis rates and causes cell cycle arrest at the G2/M phase in MDA-MB-231 cells. Additionally, concentrations of 5-20 μM stabilize cyclin D1, p53, and p21 proteins, prevent the degradation of IκBα, IκBε, and IκKγ, and inhibit the nuclear translocation of NF-κB in MDA-MB-231 cells.
Chemical Properties
Molecular Weight375.47
FormulaC24H25NO3
Cas No.3085356-41-5
SmilesO=C1C(=CC2=CC=C(C=C2)C)CN(CC1=CC3=CC=C(O)C(OC)=C3)C4CC4
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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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.

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