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Apoptosis inducer 17
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Catalog No. T209766
Apoptosisinducer 17 is a hybrid molecule of Curcumin-Piperlongumine that enhances cell cycle arrest and apoptosis (apoptosis) in lung cancer cells by activating the JNK signaling pathway.
Apoptosis inducer 17
Apoptosis inducer 17
Copy Product Info😃Good
Catalog No. T209766
Apoptosisinducer 17 is a hybrid molecule of Curcumin-Piperlongumine that enhances cell cycle arrest and apoptosis (apoptosis) in lung cancer cells by activating the JNK signaling pathway.
| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 10 mg | Inquiry | Inquiry | Inquiry | |
| 50 mg | Inquiry | Inquiry | Inquiry |
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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 | Apoptosisinducer 17 is a hybrid molecule of Curcumin-Piperlongumine that enhances cell cycle arrest and apoptosis (apoptosis) in lung cancer cells by activating the JNK signaling pathway. |
| In vitro | Apoptosis inducer 17 (compound CP; 0.027-60 μM; 72 h) effectively inhibits cell proliferation with IC50 values of 0.021 μM, 0.027 μM, and 0.73 μM for H446, H1299, and SBC-2 cells, respectively. It demonstrates significant colony formation inhibition at 0.03-0.3 μM over 24 hours. JNK-IN-17 induces dose-dependent G2/M phase arrest in H446 and H1299 cells. Additionally, Apoptosis inducer 17 (compound CP; 0.03-0.3 μM; 24 hours) promotes apoptosis in H446 and H1299 cells mediated by caspase activity and activates the JNK signaling cascade. |
| In vivo | Compound CP, administered at 10 mg/kg via intraperitoneal injection twice daily for 15 days, significantly reduced H446 cell growth without causing notable changes in body weight. |
| Formula | C25H27NO7 |
| 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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