Cibenzoline succinate
![Cibenzoline succinate Structure](CAS/GIF/100678-32-8.gif)
- 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
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 |
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 |
100678-32-8(Cibenzoline succinate)Related Search:
(+-)-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