Flecainide

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Flecainide

CAS No. : 54143-55-4

Biological Activity:Flecainide is a potent and orally active antiarrhythmic agent. Flecainide blocks the cardiac fast inward Na+ current (INa) and the rapid component of the delayed rectifier K+ current. Flecainide prolongs the action potential duration (APD) in ventricular and atrial muscle fibres. Flecainide has the potential for the research of fetal tachycardias[2][3].

Research Area:Cardiovascular Disease

Targets:Sodium Channel|Potassium Channel

Related Screening Libraries:Drug Repurposing Compound Library Plus;FDA-Approved Drug Library Plus;FDA-Approved Drug Library Mini;Bioactive Compound Library Plus;Membrane Transporter/Ion Channel Compound Library;FDA-Approved Drug Library;Drug Repurposing Compound Library;Anti-Cardiovascular Disease Compound Library;Orally Active Compound Library;FDA Approved & Pharmacopeial Drug Library;Anti-Alzheimer’s Disease Compound Library;Neuroprotective Compound Library;Drug-Induced Liver Injury (DILI) Compound Library;Neurodegenerative Disease-related Compound Library;Sodium Channel Blocker Library;Potassium Channel Compound Library;Human Metabolite Library;

Related Small Molecules:Lu AE98134;Kv3 modulator 2;Zandatrigine;Veratridine;Brompheniramine-d6 maleate;Pinacidil;GX-674;AMP-PNP tetralithium;Dibucaine;IK1 inhibitor PA-6;VU590;Sodium Channel inhibitor 2;3-Deoxyaconitine;Domiphen bromide;Mesoridazine benzenesulfonate;Tetrandrine;20(S)-Ginsenoside Rg3;(S)-(+)-Modafinic acid-d5;Tocainide hydrochloride;Ketanserin;Licarbazepine-d4-1;Metaflumizone-d4

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