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Dimethylamiloride

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Catalog No. T78139Cas No. 1214-79-5

Dimethylamiloride hydrochloride selectively inhibits Na⁺/H⁺ exchangers located in cellular membranes, leading to intracellular H⁺ retention and a reduction in intracellular pH, Dimethylamiloride hydrochloride additionally blocks TRPA1 ion channels with an IC50 of 80 µM, making it a valuable pharmacological tool for studying ion transport, pH homeostasis, sensory signaling, and inflammatory pain mechanisms.

Dimethylamiloride

Dimethylamiloride

😃Good
Purity: 98.90%
Catalog No. T78139Cas No. 1214-79-5
Dimethylamiloride hydrochloride selectively inhibits Na⁺/H⁺ exchangers located in cellular membranes, leading to intracellular H⁺ retention and a reduction in intracellular pH, Dimethylamiloride hydrochloride additionally blocks TRPA1 ion channels with an IC50 of 80 µM, making it a valuable pharmacological tool for studying ion transport, pH homeostasis, sensory signaling, and inflammatory pain mechanisms.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 mg$84-In Stock
5 mg$198-In Stock
10 mg$297-In Stock
25 mg$515-In Stock
50 mg$733-In Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Purity:98.90%
Appearance:Solid
Color:Yellow
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Product Introduction

Bioactivity
Description
Dimethylamiloride hydrochloride selectively inhibits Na⁺/H⁺ exchangers located in cellular membranes, leading to intracellular H⁺ retention and a reduction in intracellular pH, Dimethylamiloride hydrochloride additionally blocks TRPA1 ion channels with an IC50 of 80 µM, making it a valuable pharmacological tool for studying ion transport, pH homeostasis, sensory signaling, and inflammatory pain mechanisms.
In vivo
To assess cardioprotective potential, isolated perfused rat hearts were subjected to an ischemia-reperfusion protocol. The tissue was pretreated with Dimethylamiloride at concentrations ranging from 5 to 20 uM prior to the ischemic event. This pretreatment regimen significantly improved the functional recovery of the heart upon reperfusion and reduced the release of creatine kinase from the tissue [2].
Chemical Properties
Molecular Weight257.68
FormulaC8H12ClN7O
Cas No.1214-79-5
SmilesO=C(NC(=N)N)C1=NC(Cl)=C(N=C1N)N(C)C
Storage & Solubility Information
StorageIn solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 80 mg/mL (310.46 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM3.8808 mL19.4039 mL38.8078 mL194.0391 mL
5 mM0.7762 mL3.8808 mL7.7616 mL38.8078 mL
10 mM0.3881 mL1.9404 mL3.8808 mL19.4039 mL
20 mM0.1940 mL0.9702 mL1.9404 mL9.7020 mL
50 mM0.0776 mL0.3881 mL0.7762 mL3.8808 mL
100 mM0.0388 mL0.1940 mL0.3881 mL1.9404 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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%
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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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