Cibenzoline succinate

Cibenzoline succinate Structure
CAS No.
100678-32-8
Chemical Name:
Cibenzoline succinate
Synonyms
ritmalan;ole(1:1);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
CBNumber:
CB7255168
Molecular Formula:
C22H24N2O4
Molecular Weight:
380.44
MOL File:
100678-32-8.mol
MSDS File:
SDS
Modify Date:
2023/5/15 10:43:56

Cibenzoline succinate Properties

Melting point 165°
storage temp. 2-8°C
solubility H2O: ≥5mg/mL
form solid
color white to off-white
Stability Light Sensitive

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H302
Precautionary statements  P264-P270-P301+P312-P501
Hazard Codes  Xn
Risk Statements  22
WGK Germany  3
RTECS  EJ9960100

Cibenzoline succinate price More Price(2)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) C1618 Cibenzoline succinate ≥98% (HPLC), solid 100678-32-8 10MG ₹15761.2 2022-06-14 Buy
Sigma-Aldrich(India) C1618 Cibenzoline succinate ≥98% (HPLC), solid 100678-32-8 50MG ₹70827.98 2022-06-14 Buy
Product number Packaging Price Buy
C1618 10MG ₹15761.2 Buy
C1618 50MG ₹70827.98 Buy

Cibenzoline succinate Chemical Properties,Uses,Production

Uses

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

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.

Cibenzoline succinate Preparation Products And Raw materials

Raw materials

Preparation Products

Cibenzoline succinate Suppliers

Global( 32)Suppliers
Supplier Tel Country ProdList Advantage Inquiry
CLEARSYNTH LABS LTD. +91-22-45045900 Hyderabad, India 6351 58 Inquiry
CONIER CHEM AND PHARMA LIMITED +8618523575427 China 49391 58 Inquiry
Career Henan Chemica Co +86-0371-86658258 +8613203830695 China 30253 58 Inquiry
Jilin Chinese Academy of Sciences-yanshen Technology +undefined18143011203 China 42057 58 Inquiry
Jilin Chinese Academy of Sciences-yanshen Technology 18143011203 China 40857 58 Inquiry
Shanghai Haohong Scientific Co., Ltd. 400-400-8210725 China 40041 58 Inquiry
Energy Chemical 021-58432009 400-005-6266 China 44843 58 Inquiry
Sigma-Aldrich 021-61415566 800-8193336 China 51471 80 Inquiry
Mitsubishi Chemical Europe GmbH 49-211-5205410 Germany 1252 58 Inquiry
United States Biological 800.520.3011 or 781.639.5092 United States 6256 80 Inquiry
(+-)-2-(2,2-diphenylcyclopropyl)-2-imidazolinesuccinate(1:1) ole(1:1) ritmalan ro22-7796/001 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 2-(2,2-diphenylcyclopropyl)-4,5-dihydro-1H-imidazole succinate, Cibenol, Cipralan, Exacor Cinobezile Cibenzoline succinate 2-(2,2-diphenylcyclopropyl)-4,5-dihydro-1h-imidazol(+-)-1h-imidazolbutanedioate( 4,5-dihydro-2-(2,2-diphenylcyclopropyl)-1h-imidazolesuccinate 4,5-dihydro-2-(2,2-diphenylcyclopropyl)-1h-imidazolsuccinate butanedioicacid,compd.with2-(2,2-diphenylcyclopropyl)-4,5-dihydro-1h-imidaz butanedioicacid,compd.with2-(2,2-diphenylcyclopropyl)-4,5-dihydro-1h-imidazole(1:1) cibenzolinesuccinate(1:1) cipralan 100678-32-8 C18H18N2C4H6O4 Cell Biology Cell Signaling and Neuroscience BioChemical Voltage-gated Ion Channels Potassium Channel Modulators Ion Channels Monovalent Ion Channels Heterocyclic Compounds