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MR2938
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Catalog No. T73504Cas No. 1044870-65-6
MR2938 is a potent AChE inhibitor (IC50 = 5.04 μM). MR2938 significantly inhibits the production of NO (IC50 = 3.29 μM). MR2938 inhibits neuroinflammation by blocking the MAPK/JNK and NF-κB signaling pathways and can be used for Alzheimer's disease (AD) research.
MR2938
Copy Product Info😃Good
Catalog No. T73504Cas No. 1044870-65-6
MR2938 is a potent AChE inhibitor (IC50 = 5.04 μM). MR2938 significantly inhibits the production of NO (IC50 = 3.29 μM). MR2938 inhibits neuroinflammation by blocking the MAPK/JNK and NF-κB signaling pathways and can be used for Alzheimer's disease (AD) research.
| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 1 mg | $142 | 35 days | 35 days | |
| 10 mg | $685 | 35 days | 35 days |
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Appearance:Solid
Color:Yellow
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| Description | MR2938 is a potent AChE inhibitor (IC50 = 5.04 μM). MR2938 significantly inhibits the production of NO (IC50 = 3.29 μM). MR2938 inhibits neuroinflammation by blocking the MAPK/JNK and NF-κB signaling pathways and can be used for Alzheimer's disease (AD) research. |
| Targets&IC50 | AChE:5.04 μM, NO:3.29 μM |
| In vitro | MR2938 (0-10 μM, 24 h) can reduce the mRNA levels of pro-inflammatory cytokines IL-1β, TNF-α, IL-6 and CCL2 at 1.25 μM[1]; at a concentration of 10 μM acting for 24 h, it can block the NF-κB signaling pathway in lipopolysaccharide (LPS)-induced BV-2 cells[1]. MR2938 (20 μM) has inhibitory activities against acetylcholinesterase (AChE) and butyrylcholinesterase (BChE), with inhibitory rates of 91.8 ± 2.68% and 38.7 ± 11.7%, respectively[1]. MR2938 (0-10 μM) has little effect on the cell viability of the BV2 cell line[1]. |
| Molecular Weight | 380.44 |
| Formula | C21H24N4O3 |
| Cas No. | 1044870-65-6 |
| Smiles | O=C1N=C(NC=2C=C(OC)C=C(OC)C12)C=3C=CC(=CC3)N4CCN(C)CC4 |
| 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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