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EED-IN-5
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Catalog No. T219053 Copy Product Info
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EED-IN-5 is an orally active, EZH2-selective trisubstituted pyridine EED-H3K27me3 inhibitor and immunomodulator with anti-inflammatory properties. It targets EED with an IC50 of 28.21 nM. In mouse models, oral administration of EED-IN-5 leads to preferential and sustained accumulation in lymph nodes. This compound reduces H3K27me3 levels in dendritic cells and inhibits their migration, consequently decreasing the infiltration of specific dendritic cells, macrophages, and T cells into the spinal cord and brain. EED-IN-5 shows hERG inhibition activity, tests negative in Mini-Ames assays, and does not exhibit significant toxicity with long-term high-dose administration. EED-IN-5 is applicable for multiple sclerosis research.
EED-IN-5
| Pack Size | Price | USA Stock | Global Stock | Quantity |
|---|---|---|---|---|
| 10 mg | Inquiry | Inquiry | Inquiry | |
| 50 mg | Inquiry | Inquiry | Inquiry |
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
Storage & Solubility Information
| Description | EED-IN-5 is an orally active, EZH2-selective trisubstituted pyridine EED-H3K27me3 inhibitor and immunomodulator with anti-inflammatory properties. It targets EED with an IC50 of 28.21 nM. In mouse models, oral administration of EED-IN-5 leads to preferential and sustained accumulation in lymph nodes. This compound reduces H3K27me3 levels in dendritic cells and inhibits their migration, consequently decreasing the infiltration of specific dendritic cells, macrophages, and T cells into the spinal cord and brain. EED-IN-5 shows hERG inhibition activity, tests negative in Mini-Ames assays, and does not exhibit significant toxicity with long-term high-dose administration. EED-IN-5 is applicable for multiple sclerosis research. |
| 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
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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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