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ChemicalBook--->CAS DataBase List--->100678-32-8

100678-32-8

100678-32-8 Structure

100678-32-8 Structure
IdentificationBack Directory
[Name]

Cibenzoline succinate
[CAS]

100678-32-8
[Synonyms]

ole(1:1)
ritmalan
cipralan
Cinobezile
ro22-7796/001
Cibenzoline succinate
cibenzolinesuccinate(1:1)
(+-)-2-(2,2-diphenylcyclopropyl)-2-imidazolinesuccinate(1:1)
4,5-dihydro-2-(2,2-diphenylcyclopropyl)-1h-imidazolsuccinate
4,5-dihydro-2-(2,2-diphenylcyclopropyl)-1h-imidazolesuccinate
2-(2,2-Diphenylcyclopropyl)-4,5-dihydro-1H-imidazole succinate
butanedioicacid,compd.with2-(2,2-diphenylcyclopropyl)-4,5-dihydro-1h-imidaz
2-(2,2-diphenylcyclopropyl)-4,5-dihydro-1h-imidazol(+-)-1h-imidazolbutanedioate(
butanedioicacid,compd.with2-(2,2-diphenylcyclopropyl)-4,5-dihydro-1h-imidazole(1:1)
succinic acid, compound with 2-(2,2-diphenylcyclopropyl)-4,5-dihydro-1H-imidazole (1:2)
2-(2,2-diphenylcyclopropyl)-4,5-dihydro-1H-imidazole succinate, Cibenol, Cipralan, Exacor
[EINECS(EC#)]

634-471-4
[Molecular Formula]

C22H24N2O4
[MDL Number]

MFCD00941423
[MOL File]

100678-32-8.mol
[Molecular Weight]

380.44
Chemical PropertiesBack Directory
[Melting point ]

165°
[storage temp. ]

2-8°C
[solubility ]

H2O: ≥5mg/mL
[form ]

solid
[color ]

white to off-white
Safety DataBack Directory
[Hazard Codes ]

Xn
[Risk Statements ]

22
[WGK Germany ]

3
[RTECS ]

EJ9960100
Hazard InformationBack Directory
[Uses]

Cardiac depressant (anti-arrhythmic).
[Uses]

Cibenzoline Succinate acts as a highly active class I antiarrhythmic agent.
[Definition]

ChEBI: Cibenzoline succinate is a diarylmethane.
[General Description]

Cibenzoline also called (±)-2-(2,2-diphenylcyclopropyl)-2-imidazoline succinate, is generally used in stereo combination of R(+) and S(?) forms. It also exhibits anticholinergic activity.. Cibenzoline is known to improve left ventricular diastolic dysfunction by reducing left ventricular pressure gradient.
[Biochem/physiol Actions]

Cibenzoline is a class IA antiarrhythmic drug. Cibenzoline (μM concentrations) blocks ATP-sensitive K channels in heart and pancreatic cells. Cibenzoline interacts with the channel pore-forming subunit of the K(ATP) channel (Kir6.2) from the cytoplasmic side. Cibenzoline also inhibits the delayed rectifier K current [I(Kr)] in sino-atrial node cells.
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