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Namodenoson

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Catalog No. T6884Cas No. 163042-96-4
Alias CF-102, 2-Cl-IB-MECA

Namodenoson (2-Cl-IB-MECA) is an adenosine A3 receptor agonist.

Namodenoson

Namodenoson

🥰Excellent
Purity: 98.97%
Catalog No. T6884Alias CF-102, 2-Cl-IB-MECACas No. 163042-96-4
Namodenoson (2-Cl-IB-MECA) is an adenosine A3 receptor agonist.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 mg$31In StockIn Stock
5 mg$72In StockIn Stock
10 mg$122In StockIn Stock
25 mg$247In StockIn Stock
50 mg$397In StockIn Stock
100 mg$597In StockIn Stock
1 mL x 10 mM (in DMSO)$87In 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:98.97%
Appearance:Solid
Color:White
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Product Introduction

Bioactivity
Description
Namodenoson (2-Cl-IB-MECA) is an adenosine A3 receptor agonist.
Targets&IC50
A3 receptor:0.33 nM (Ki)
In vivo
The first infusion of Namodenoson resulted in a rapid fall of the blood pressure to a value which was about 50% of the pre-administration level.The hypotension was short-lasting.After approximately 15 min the blood pressure started to recover and rapidly returned to stable values, which were significantly lower than the blood pressure values in the control group.Administration of the second dose of Namodenoson, at 150 min after the first infusion, did not produce any hypotension at all.The slight increase in the mean arterial pressure during the second infusion was not specific for Namodenoson[1]
Animal Research
Rats were randomly assigned to two treatment groups of 6 animals, which received either two subsequent intravenous infusions of 200 μg/kg 2-chloro-N^6-(3-iodobenzyl)adenosine-5′-N-methylcarboxamide (2-Cl-IB-MECA) during 15 min or two subsequent infusions of the vehicle during 15 min. 2-Cl-IB-MECA was dissolved in dimethylsulfoxide (DMSO) and diluted with a sodium chloride solution to a final 30% (v/v) DMSO solution (a total volume of 765 μl).?Fresh solutions were prepared prior to each experiment.The effect measurements were started at least 45 min prior to the first drug infusion and lasted until 4.5 h after this infusion.?Heart rate and blood pressure were recorded continuously and serial arterial blood samples were drawn for determination of plasma histamine concentrations.?2 h after the first administration the second dose of 2-Cl-IB-MECA (or vehicle) was administered[1].
SynonymsCF-102, 2-Cl-IB-MECA
Chemical Properties
Molecular Weight544.73
FormulaC18H18ClIN6O4
Cas No.163042-96-4
SmilesCNC(=O)[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(NCc3cccc(I)c3)nc(Cl)nc12
Relative Density.2.04 g/cm3 at 20℃
Storage & Solubility Information
StorageIn solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 31 mg/mL (56.91 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 2 mg/mL (3.67 mM), Sonication is recommended.
Please add the solvents sequentially, clarifying the solution as much as possible before adding the next one. Dissolve by heating and/or sonication if necessary. Working solution is recommended to be prepared and used immediately. The formulation provided above is for reference purposes only. In vivo formulations may vary and should be modified based on specific experimental conditions.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM1.8358 mL9.1789 mL18.3577 mL91.7886 mL
5 mM0.3672 mL1.8358 mL3.6715 mL18.3577 mL
10 mM0.1836 mL0.9179 mL1.8358 mL9.1789 mL
20 mM0.0918 mL0.4589 mL0.9179 mL4.5894 mL
50 mM0.0367 mL0.1836 mL0.3672 mL1.8358 mL

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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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μL
2 Enter the in vivo formulation:
% DMSO
%
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Dose Conversion

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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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