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Eliprodil

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Catalog No. T1751Cas No. 119431-25-3
Alias SL-820715

Eliprodil (SL-820715)(SL-820715), a non-competitive NR2B-NMDA receptor antagonist(IC50: 1 uM), less effective for NR2A- and NR2C-containing receptors(IC50> 100 uM). It has been used in trials studying the treatment of Parkinson Disease and Movement Disorders.

Eliprodil

Eliprodil

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Purity: 99.77%
Catalog No. T1751Alias SL-820715Cas No. 119431-25-3
Eliprodil (SL-820715)(SL-820715), a non-competitive NR2B-NMDA receptor antagonist(IC50: 1 uM), less effective for NR2A- and NR2C-containing receptors(IC50> 100 uM). It has been used in trials studying the treatment of Parkinson Disease and Movement Disorders.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
10 mg$33In StockIn Stock
25 mg$64In StockIn Stock
50 mg$119In StockIn Stock
100 mg$178-In Stock
500 mg$427-In Stock
1 mL x 10 mM (in DMSO)$29In StockIn Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Purity:99.77%
Color:White
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Product Introduction

Eliprodil AI Summary
Eliprodil exhibits a range of bioactivities across different biological pathways and receptors. It demonstrates potent competitive antagonist activity at the GluN2B subunit of the NMDA receptor, with a high affinity indicated by a Ki value of 13.0 nM, effectively displacing [3H]ifenprodil. It also shows inhibitory activity against the NMDA responses at NR1A/2B receptors with an IC50 of 1400.0 nM, and exhibits affinity for the alpha-1 adrenergic receptor with an IC50 of 3300.0 nM. In addition, it inhibits voltage-gated K+ currents by 67.0% at 10 µM concentration and has an ED50 of 1.0 mg/kg in the mouse electric shock assay. Additionally, it shows neuroprotective effects in a rat model of focal cerebral ischemia by reducing infarct volume when administered intravenously at 1 mg/kg. Eliprodil also displays antiplasmodial activity against Plasmodium falciparum with IC50 values ranging from 251.19 nM to 2511.89 nM. Furthermore, it shows potential antiviral activity against SARS-CoV-2, inhibiting virus-induced cytotoxicity of VERO-6 cells, although with IC50 values greater than 20000.0 nM. Its diverse range of bioactivities, including modulation of glutamatergic neurotransmission and potential pharmacological effects on various receptors, suggests its importance in therapeutic applications..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Eliprodil (SL-820715)(SL-820715), a non-competitive NR2B-NMDA receptor antagonist(IC50: 1 uM), less effective for NR2A- and NR2C-containing receptors(IC50> 100 uM). It has been used in trials studying the treatment of Parkinson Disease and Movement Disorders.
Targets&IC50
NR2B-NMDA:1 μM
SynonymsSL-820715
Chemical Properties
Molecular Weight347.85
FormulaC20H23ClFNO
Cas No.119431-25-3
SmilesOC(CN1CCC(Cc2ccc(F)cc2)CC1)c1ccc(Cl)cc1
Relative Density.1.205 g/cm3
Storage & Solubility Information
StorageIn solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 6 mg/mL (17.25 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.8748 mL14.3740 mL28.7480 mL143.7401 mL
5 mM0.5750 mL2.8748 mL5.7496 mL28.7480 mL
10 mM0.2875 mL1.4374 mL2.8748 mL14.3740 mL

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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:
TargetMol | Animal experiments For example, if the intended dosage is 10 mg/kg for animals weighing 20 g , with a dosing volume of 100 μL per animal, TargetMol | Animal experiments and a total of 10 animals are to be administered, using a formulation of TargetMol | reagent 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 DMSOTargetMol | reagent 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 DMSOTargetMol | reagent stock solution to 400 μL PEG300TargetMol | reagent 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 ddH2OTargetMol | reagent 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.
All co-solvents required for this protocol, includingDMSO, PEG300/PEG400, Tween 80, SBE-β-CD, and Corn oil, are available for purchase on the TargetMol website.
1 Enter information below:
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2 Enter the in vivo formulation:
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