Name | Cibenzoline |
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Synonyms |
Cibenzolinum [inn-latin]
UP 33-901 Cibenzolinum Exacor 4,5-dihydro-2-(2,2-diphenylcyclopropyl)-1H-imidazole Cibenzolina Cibenol 2-(2,2-diphenylcyclopropyl)-4,5-dihydro-1 H-imidazole Ro 22-7796 [15N]-Cibenzoline Cifenline |
Description | Cibenzoline is a potent inhibitor of KATP channel with directly affecting the pore-forming Kir6.2 subunit rather than the SUR1 subunit. Cibenzoline is a class Ia antiarrhythmic drug. Cibenzoline has little anticholinergic activity. Cibenzoline markedly attenuate LVPG which has a close relationship with myocardial contractility decreasing. Cibenzoline has the potential for the research of hypertrophic obstructive cardiomyopathy[1][2]. |
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Related Catalog | |
Target |
KATP channel[1] |
References |
Density | 1.17 g/cm3 |
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Boiling Point | 449.2ºC |
Melting Point | 103-104° |
Molecular Formula | C18H18N2 |
Molecular Weight | 262.34900 |
Flash Point | 225.5ºC |
Exact Mass | 262.14700 |
PSA | 24.39000 |
LogP | 2.75870 |
Index of Refraction | 1.655 |
HS Code | 2933290090 |
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~85% 53267-01-9 |
Literature: Gholap, Atul R.; Paul, Vincent; Srinivasan, Kumar V. Synthetic Communications, 2008 , vol. 38, # 17 p. 2967 - 2982 |
Precursor 2 | |
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DownStream 1 | |
HS Code | 2933290090 |
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Summary | 2933290090. other compounds containing an unfused imidazole ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |