| Name | bepridil hydrochloride monohydrate | 
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| Synonyms | 3-isobutoxy-2-pyrrolidino-n-phenyl-n-benzylpropylaminehydrochloridehydrate MFCD00065498 Unii-4W2p15D93m l)-,monohydrochloride,monohydrate angopril Bepridil hydrochloride,N-Benzyl-N-(3-isobutoxy-2-pyrrolidin-1-yl-propyl)anilinehydrochloride | 
| Description | Bepridil hydrochloride hydrate ((±)-Bepridil hydrochloride hydrate) is a non-selective, long-acting Ca+ channel antagonist and Na+, K+ channel inhibitor, with antianginal and type I antiarrhythmic effects. Bepridil hydrochloride hydrate also acts as a cardiac Na+/Ca2+ exchange (NCX1) inhibitor. Bepridil hydrochloride hydrate can be used for the research of cardiovascular disorders[1][2][3][4][5]. | 
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| Related Catalog | |
| Target | Ca2+ | 
| In Vitro | Bepridil hydrochloride hydrate blockades of Ca2+-dependent action potentials in vascular smooth muscle of dog coronary artery[2]. Bepridil hydrochloride hydrate blocks Ca currents and Na currents with IC50s of 0.5 μM and 30 μM, respectively in cultured ventricular cells[4]. Bepridil hydrochloride hydrate decreases IKs under blockade of IKr with E4031 (5 μM), in a concentration-dependent manner[5]. | 
| In Vivo | Bepridil hydrochloride hydrate exhibits a half-life of averages 33±15 hours after single-dose administration[6]. | 
| References | [1]. A Gill, et al. Pharmacology of Bepridil. Am J Cardiol. 1992 Apr 9;69(11):11D-16D. | 
| Melting Point | 91 ±2° | 
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| Molecular Formula | C24H37ClN2O2 | 
| Molecular Weight | 421.01600 | 
| Exact Mass | 420.25400 | 
| PSA | 24.94000 | 
| LogP | 5.50580 | 
| Appearance | powder | white | 
| Storage condition | Desiccate at RT | 
| CHEMICAL IDENTIFICATION
 
 
 
 
 
 
 
 HEALTH HAZARD DATAACUTE TOXICITY DATA
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
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| Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter | 
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| Hazard Codes | Xi | 
| RIDADR | NONH for all modes of transport | 
| WGK Germany | 2 | 
| RTECS | UY1162000 |