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Flunarizine dihydrochloride

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Catalog No. T0806Cas No. 30484-77-6
Alias R14950, KW-3149, Flunarizine 2HCl

Flunarizine dihydrochloride (R14950) is a selective calcium entry blocker with calmodulin binding properties and histamine H1 blocking activity. Flunarizine dihydrochloride (R14950) is effective in the prophylaxis of migraine, occlusive peripheral vascular disease, vertigo of central and peripheral origin, and as an adjuvant in the therapy of epilepsy.

Flunarizine dihydrochloride

Flunarizine dihydrochloride

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Purity: 99.99%
Catalog No. T0806Alias R14950, KW-3149, Flunarizine 2HClCas No. 30484-77-6
Flunarizine dihydrochloride (R14950) is a selective calcium entry blocker with calmodulin binding properties and histamine H1 blocking activity. Flunarizine dihydrochloride (R14950) is effective in the prophylaxis of migraine, occlusive peripheral vascular disease, vertigo of central and peripheral origin, and as an adjuvant in the therapy of epilepsy.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
500 mg$40In StockIn Stock
1 g$60-In Stock
1 mL x 10 mM (in DMSO)$43In StockIn Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
All TargetMol products are for research purposes only and cannot be used for human consumption. We do not provide products or services to individuals. Please comply with the intended use and do not use TargetMol products for any other purpose.
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Purity:99.99%
Appearance:Solid
Color:White
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Product Introduction

Flunarizine dihydrochloride AI Summary
Flunarizine dihydrochloride shows a broad range of bioactivities. It exhibits binding affinity to opioid receptors with IC50 values of 2410.0 nM (mu), 9480.0 nM (kappa 1), and 3630.0 nM (delta), suggesting its potential as an opioid receptor modulator. It demonstrates antiplasmodial activity against Plasmodium falciparum, with IC50 values between 3981.07 nM and 12589.25 nM, indicating a moderate to potent inhibitory effect on malaria parasites. In addition to its antiplasmodial properties, Flunarizine dihydrochloride shows activity in a wide array of assays, including modulation of Lamin A splicing (IC50: 22387.2 nM), erasure of genomic imprints (IC50: 15848.9 nM), identification of novel anesthetics (IC50: 44668.4 nM), and inhibition of Influenza NS1 Protein Function (IC50: 28183.8 nM). Furthermore, it inhibits various viral and cellular targets, including SARS-CoV-2 3CL-Pro protease by 7.028% at 20 µM, SARS-CoV-2 induced cytotoxicity in Caco-2 and Vero-6 cells, and shows cytotoxicity in HepG2 cells (IC50: 14600.0 nM). Flunarizine dihydrochloride also displays high inhibition of sodium fluorescein uptake in OATP1B1 and OATP1B3-transfected CHO cells at 10 µM concentration, suggesting potential transporter interactions..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Flunarizine dihydrochloride (R14950) is a selective calcium entry blocker with calmodulin binding properties and histamine H1 blocking activity. Flunarizine dihydrochloride (R14950) is effective in the prophylaxis of migraine, occlusive peripheral vascular disease, vertigo of central and peripheral origin, and as an adjuvant in the therapy of epilepsy.
Targets&IC50
Ca2+ channel:68 nM(Ki)
SynonymsR14950, KW-3149, Flunarizine 2HCl
Chemical Properties
Molecular Weight477.42
FormulaC26H28Cl2F2N2
Cas No.30484-77-6
SmilesCl.Fc1ccc(cc1)C(N1CCN(C/C=C/c2ccccc2)CC1)c1ccc(F)cc1.Cl
Relative Density.no data available
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
Ethanol: 2.4 mg/mL (5.03 mM), Sonication is recommended.
DMSO: 50 mg/mL (104.73 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 2 mg/mL (4.19 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
Ethanol/DMSO
1mg5mg10mg50mg
1 mM2.0946 mL10.4730 mL20.9459 mL104.7296 mL
5 mM0.4189 mL2.0946 mL4.1892 mL20.9459 mL
DMSO
1mg5mg10mg50mg
10 mM0.2095 mL1.0473 mL2.0946 mL10.4730 mL
20 mM0.1047 mL0.5236 mL1.0473 mL5.2365 mL
50 mM0.0419 mL0.2095 mL0.4189 mL2.0946 mL
100 mM0.0209 mL0.1047 mL0.2095 mL1.0473 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:
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

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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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