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P-gp-IN-35
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Catalog No. T217895 Copy Product Info
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P-gp-IN-35 is an inhibitor of P-glycoprotein (P-gp). It exhibits cytotoxicity against sensitive breast cancer and colorectal cancer cells and can reverse multidrug resistance in breast cancer cells that overexpress P-gp. P-gp-IN-35 is applicable in studies related to multidrug-resistant breast cancer and colorectal cancer.
P-gp-IN-35
Cas No. 1887151-21-4
| Pack Size | Price | USA Stock | Global Stock | Quantity |
|---|---|---|---|---|
| 10 mg | Inquiry | 10-14 weeks | 10-14 weeks | |
| 50 mg | Inquiry | 10-14 weeks | 10-14 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
Chemical Properties
Storage & Solubility Information
| Description | P-gp-IN-35 is an inhibitor of P-glycoprotein (P-gp). It exhibits cytotoxicity against sensitive breast cancer and colorectal cancer cells and can reverse multidrug resistance in breast cancer cells that overexpress P-gp. P-gp-IN-35 is applicable in studies related to multidrug-resistant breast cancer and colorectal cancer. |
| In vitro | P-gp-IN-35 (Compound 4d) significantly inhibits the proliferation of MCF-7, Caco-2, and multidrug-resistant MCF-7/ADR cancer cells, with IC50 values of 8.14, 9.04, and 19.32 μM, respectively, demonstrating selective toxicity towards cancer cells compared to normal HFL-1 and WI-38 lung fibroblasts. At concentrations ranging from 1-100 μM over 48 hours, P-gp-IN-35 dose-dependently reduces P-glycoprotein expression in MCF-7/ADR cells, achieving an inhibition rate of 61.27% at 100 μM and reversing P-gp mediated multidrug resistance with an IC50 of 15.09 μM. Additionally, P-gp-IN-35 inhibits P-glycoprotein efflux pump activity in MCF-7/ADR cells with an IC50 of 47.08 μM. |
| Molecular Weight | 364.78 |
| Formula | C20H13ClN2O3 |
| Cas No. | 1887151-21-4 |
| Smiles | N#CC1=C(OC=2C=3C=C(C=CC3OC(=O)C2C1C=4C=CC=C(Cl)C4)C)N |
| 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.
Dose Conversion
You can also refer to dose conversion for different animals. More Dose Conversion
Tech Support
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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Related Tags: P-gp-IN-35 in vitro | P-gp-IN-35 formula | P-gp-IN-35 molecular weight
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