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Flecainide
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Catalog No. T21391Cas No. 54143-55-4
Alias Apocard
Flecainide is an orally administered antiarrhythmic agent acting as a sodium channel blocker and IKr inhibitor, indicated for the treatment of paroxysmal supraventricular tachycardia (PSVT).
Flecainide
🥰Excellent
Purity: 99.896%
Catalog No. T21391Alias ApocardCas No. 54143-55-4
Flecainide is an orally administered antiarrhythmic agent acting as a sodium channel blocker and IKr inhibitor, indicated for the treatment of paroxysmal supraventricular tachycardia (PSVT).
| Pack Size | Price | Availability | Quantity |
|---|---|---|---|
| 5 mg | $40 | In Stock | |
| 10 mg | $64 | In Stock | |
| 25 mg | $119 | In Stock | |
| 50 mg | $197 | In Stock | |
| 100 mg | $297 | In Stock | |
| 200 mg | $373 | In Stock | |
| 1 mL x 10 mM (in DMSO) | $44 | In Stock |
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Purity:99.896%
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Product Introduction
Bioactivity
Chemical Properties
| Description | Flecainide is an orally administered antiarrhythmic agent acting as a sodium channel blocker and IKr inhibitor, indicated for the treatment of paroxysmal supraventricular tachycardia (PSVT). |
| Targets&IC50 | CHO cells:27.1 μM |
| In vitro | Methods: Flecainide (6 μM) was used to treat ventricular myocytes from Casq2-/- mice to observe spontaneous sarcoplasmic reticulum calcium release events and triggered activity. Result: Flecainide significantly suppressed the spontaneous sarcoplasmic reticulum calcium release events and triggered activity induced by adrenergic stimulation.[1] |
| In vivo | Methods: Flecainide (20 mg/kg) was administered intraperitoneally to Casq2-/- mice to observe its inhibitory effect on arrhythmia.
Result: Flecainide completely suppressed adrenaline-induced arrhythmia, including premature ventricular contractions and bidirectional ventricular tachycardia.[1] |
| Synonyms | Apocard |
| Molecular Weight | 414.34 |
| Formula | C17H20F6N2O3 |
| Cas No. | 54143-55-4 |
| Smiles | FC(F)(F)COc1ccc(OCC(F)(F)F)c(c1)C(=O)NCC1CCCCN1 |
| Relative Density. | 1.31g/cm3 |
| Color | White |
| Appearance | Solid |
Storage & Solubility Information
| Storage | keep away from direct sunlight,store under nitrogen | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. | |||||||||||||||||||||||||||||||||||
| Solubility Information | H2O: Insoluble DMSO: 80 mg/mL (193.08 mM), Sonication is recommended. | |||||||||||||||||||||||||||||||||||
Solution Preparation Table | ||||||||||||||||||||||||||||||||||||
DMSO
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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 mother liquor preparation method and in vivo formula preparation method:
For example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . A total of 10 animals were administered, and the formula you used is 5% 
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 DMSO (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.
(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 DMSO main solution, add 300 μLPEG300 mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLSaline/PBS/ddH2O mix well and clarify
main solution, add 300 μLPEG300 mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLSaline/PBS/ddH2O mix well and clarifyFor Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
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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