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Apoptosis inducer 41
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Catalog No. T212296Cas No. 3085940-57-1
Apoptosis inducer41 is an apoptosis-inducing agent that prompts cell death through the mitochondrial pathway. It exhibits significant inhibitory effects on MCF-7 cells, with an IC50 of 6.2 μM. Apoptosis inducer41 notably arrests MCF-7 cells in the G2/M phase, increases the accumulation of reactive oxygen species (ROS), and induces mitochondrial membrane potential depolarization. This compound is applicable in breast cancer research.
Apoptosis inducer 41
😃Good
Catalog No. T212296Cas No. 3085940-57-1
Apoptosis inducer41 is an apoptosis-inducing agent that prompts cell death through the mitochondrial pathway. It exhibits significant inhibitory effects on MCF-7 cells, with an IC50 of 6.2 μM. Apoptosis inducer41 notably arrests MCF-7 cells in the G2/M phase, increases the accumulation of reactive oxygen species (ROS), and induces mitochondrial membrane potential depolarization. This compound is applicable in breast cancer research.
| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 10 mg | Inquiry | 10-14 weeks | 10-14 weeks | |
| 50 mg | Inquiry | 10-14 weeks | 10-14 weeks |
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Product Introduction
Bioactivity
Chemical Properties
Storage & Solubility Information
| Description | Apoptosis inducer41 is an apoptosis-inducing agent that prompts cell death through the mitochondrial pathway. It exhibits significant inhibitory effects on MCF-7 cells, with an IC50 of 6.2 μM. Apoptosis inducer41 notably arrests MCF-7 cells in the G2/M phase, increases the accumulation of reactive oxygen species (ROS), and induces mitochondrial membrane potential depolarization. This compound is applicable in breast cancer research. |
| In vitro | Apoptosis inducer 41 (Compound 6j) exhibits antiproliferative activity across various cell lines, with IC50 values of 7.1, 40.9, 6.2, and 46.1 μM for MDA-MB-231, MDA-MB-468, MCF-7, and MCF-10A cells, respectively, over a 48-hour period at concentrations of 1-100 μM. In MCF-7 cells, it effectively induces apoptosis through the mitochondrial pathway, causing cell cycle arrest at the G2/M phase at 1-9 μM concentrations over 24-48 hours. Additionally, Apoptosis inducer 41 (1-9 μM, 24 h) generates reactive oxygen species (ROS) and disrupts mitochondrial membrane potential (MMP). |
| Molecular Weight | 721.77 |
| Formula | C39H53BrN4O4 |
| Cas No. | 3085940-57-1 |
| Smiles | C[C@@]12[C@]([C@]3([C@](CC1)([C@]4(C)C(=CC3)C[C@@H](OC(C)=O)CC4)[H])[H])(C[C@]5([C@@]2([C@H](C)[C@@H](CC[C@H](C(NCC6=CN(CC7=CC=C(Br)C=C7)N=N6)=O)C)O5)[H])[H])[H] |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. |
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In Vivo Formulation Calculator (Clear solution)
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:
For example, if the intended dosage is 10 mg/kg for animals weighing 20 g , with a dosing volume of 100 μL per animal, and a total of 10 animals are to be administered, using a formulation of 
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 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.
Preparation of the In Vivo Formulation:
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.
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.
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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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