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Flunarizine

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Catalog No. T21392Cas No. 52468-60-7
Alias Sibelium, Flunarizinum, Flunarizina, Flunarizin

Flunarizine is an orally administered peripheral vasodilator, acting as a dual blocker of voltage-gated Na+/Ca2+ channels and a D2 dopamine receptor antagonist, exhibiting anti-migraine activity.

Flunarizine

Flunarizine

🥰Excellent
Catalog No. T21392Alias Sibelium, Flunarizinum, Flunarizina, FlunarizinCas No. 52468-60-7
Flunarizine is an orally administered peripheral vasodilator, acting as a dual blocker of voltage-gated Na+/Ca2+ channels and a D2 dopamine receptor antagonist, exhibiting anti-migraine activity.
Pack SizePriceAvailabilityQuantity
25 mg$30In Stock
50 mg$42In Stock
100 mg$59In Stock
200 mg$85In Stock
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Product Introduction

Bioactivity
Description
Flunarizine is an orally administered peripheral vasodilator, acting as a dual blocker of voltage-gated Na+/Ca2+ channels and a D2 dopamine receptor antagonist, exhibiting anti-migraine activity.
In vitro
In cultured rat cortical neurons, Flunarizine blocks sodium current (INa) and calcium current (ICa), with half-maximal inhibitory concentrations (IC50) of 0.94 μM and 1.77 μM, respectively [2].
Flunarizine (concentrations 10 μM, 30 μM; exposure time 24 hours) exhibits cytotoxic effects on chromaffin cells [4].
Within the concentration range of 3-10 μM, Flunarizine demonstrates significant cytoprotective effects on chromaffin cells [4].
In vivo
In a lipopolysaccharide (LPS)-induced acute lung injury (ALI) mouse model, preventive administration of Flunarizine (30 mg/kg, intraperitoneal injection) significantly inhibited LPS-induced cell infiltration, protein leakage, and inflammatory cytokine release. Therapeutic administration of flunarizine (30 mg/kg, intraperitoneal injection) also suppressed pulmonary inflammation, but its efficacy was weaker than that of preventive administration [5].
SynonymsSibelium, Flunarizinum, Flunarizina, Flunarizin
Chemical Properties
Molecular Weight404.50
FormulaC26H26F2N2
Cas No.52468-60-7
Relative Density.1.170 g/cm3 (Predicted)
ColorWhite
AppearanceSolid
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
DMSO: 80.00 mg/mL (197.78 mM), Sonication is recommended.
H2O: Insoluble
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.4722 mL12.3609 mL24.7219 mL123.6094 mL
5 mM0.4944 mL2.4722 mL4.9444 mL24.7219 mL
10 mM0.2472 mL1.2361 mL2.4722 mL12.3609 mL
20 mM0.1236 mL0.6180 mL1.2361 mL6.1805 mL
50 mM0.0494 mL0.2472 mL0.4944 mL2.4722 mL
100 mM0.0247 mL0.1236 mL0.2472 mL1.2361 mL

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Please enter your animal experiment information in the following box and click Calculate to obtain the mother liquor preparation method and in vivo formula preparation method:
TargetMol | Animal experimentsFor example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . TargetMol | Animal experiments A total of 10 animals were administered, and the formula you used is 5% TargetMol | reagent DMSO+30% PEG300+5% Tween 80+60% Saline/PBS/ddH2O. So your working solution concentration is 2 mg/mL。
Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSOTargetMol | reagent (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLSaline/PBS/ddH2OTargetMol | reagent mix well and clarify
For Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
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2 Enter the in vivo formulation:
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