1. Sematilide

Sematilide (CK-1752) is a selective IKr channel blocker. Sematilide causes a concentration-dependent inhibition of the delayed rectifier K+ current (IC50=25 μM). Sematilide is a class III antiarrhythmic agent.

At equivalent molar concentrations, both the salt and free forms of a compound exhibit comparable biological activity. Nevertheless, the salt form (Sematilide hydrochloride) usually boasts enhanced water solubility and stability.

For research use only. We do not sell to patients.

Sematilide Chemical Structure

Sematilide Chemical Structure

CAS No. : 101526-83-4

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Description

Sematilide (CK-1752) is a selective IKr channel blocker. Sematilide causes a concentration-dependent inhibition of the delayed rectifier K+ current (IC50=25 μM). Sematilide is a class III antiarrhythmic agent[1].

IC50 & Target

IC50: 25 μM (K+ current)[1]

In Vitro

Application of 10, 30, 100 and 300 μM Sematilide causes a concentration-dependent inhibition of the delayed rectifier K+ current (IC50=25 μM)[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

In Vivo

Sematilide (0.3-1.0 mg/kg, intravenously i.v.) is effective in a canine model of arrhythmia[2].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: Mongrel dogs of either sex (10-18 kg body weight)[2]
Dosage: 0.3, 1, 3, and 10 mg/kg
Administration: I.v. infusions
Result: Demonstrated antiarrhythmic effects at 0.3 and 3.0 mg/kg.
Molecular Weight

313.42

Formula

C14H23N3O3S

CAS No.
SMILES

O=C(NCCN(CC)CC)C1=CC=C(NS(=O)(C)=O)C=C1

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Room temperature in continental US; may vary elsewhere.

Storage

Please store the product under the recommended conditions in the Certificate of Analysis.

Purity & Documentation
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Sematilide
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HY-101436
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