Cibenzoline is an antiarrhythmic agent that inhibits the KATP channel by directly affecting the pore-forming Kir6.2 subunit rather than the SUR1 subunit. Cibenzoline shows little anticholinergic activity. Cibenzoline markedly reduces LVPG which has a close relationship with myocardial contractility decreasing. Cibenzoline has the potential for hypertrophic obstructive cardiomyopathy research[1][2].
Molekulargewicht:
262.35
CAS Nummer:
[53267-01-9]
Formel:
C18H18N2
Target-Kategorie:
Potassium Channel|||Others
T60428
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