Bepridil hydrochloride
Synonym(s):1-Isobutoxy-2-pyrrolidino-3-(N-benzylanilino)propane hydrochloride
- CAS NO.:74764-40-2
- Empirical Formula: C24H37ClN2O2
- Molecular Weight: 421.01578
- MDL number: MFCD00242668
- SAFETY DATA SHEET (SDS)
- Update Date: 2024-03-19 15:37:50
What is Bepridil hydrochloride?
Description
Bepridil (74764-40-2) is a clinically useful calcium channel blocker with antianginal activity.1 It has recently been shown to possess potent activity against SARS-CoV-2 in vitro.2 Bepridil was also able to provide protection from Ebola virus3 and other filoviruses in a mouse model4.
The Uses of Bepridil hydrochloride
Bepridil Hydrochloride is a calcium channel blocker. It also activates mitochondrial ATP-sensitive KATP channelsBepridil Hydrochloride is an antiarrhythmic and antihypertensive agent and used for treating atrial fibrillation.
The Uses of Bepridil hydrochloride
antineoplastic, alkylating agent
What are the applications of Application
Bepridil hydrochloride is a calcium channel protein inhibitor
Definition
ChEBI: The hydrochloride monohydrate of bepridril.
brand name
Bepadin (Medpointe); Vascor (Johnson & Johnson).
General Description
Bepridil hydrochloride,β-[(2-methylpropoxy)methyl]-N-phenyl-N-(phenylmethyl)-1-pyrrolidineethylamine hydrochloride (Vascor), is a secondgenerationalkylamine-type channel blocker, structurallyunrelated to the dihydropyridines. Its actions are less specificthan those of the three prototypical channel blockers,verapamil, diltiazem, and nifedipine. In addition to being aCa2+ channel blocker, it inhibits sodium flow into the hearttissue and lengthens cardiac repolarization, causing bradycardia.Caution should be used if it is given to a patient withhypokalemia. Bepridil hydrochloride is used for stableangina. The drug has a half-life of 33 hours and is highlybound to protein (99%).
Hazard
Moderately toxic by ingestion.
Biochem/physiol Actions
Non-selective calcium channel blocker and class IV antiarrhythmic agent; inhibits Na+-Ca2+ exchange; inhibits growth of brain tumor cells in vitro.
Mechanism of action
In addition to class IV effects, bepridil also shows class I effects. The substance is active against both supraventricular and ventricular arrhythmias , .
References
Hollingshead et al. (1992), A review of its pharmacological properties and therapeutic use in stable angina pectoris; Drugs, 44 835 Vatansever et al. (2021), Bepridil is potent against SARS-CoV-2 in vitro; Proc. Natl. Acad. Sci USA, 118 e2012201118 Johansen et al. (2015), A screen of approved drugs and molecular probes identifies therapeutics with anti-Ebola virus activity; Sci. Transl. Med., 7 290ra89 DeWald et al. (2018), The calcium channel blocker bepridil demonstrates efficacy in the murine model of marburg virus disease; J. Infect. Dis., 218(suppl 5) S588
Properties of Bepridil hydrochloride
Melting point: | 91 ±2° |
storage temp. | Desiccate at RT |
solubility | Soluble in DMSO (up to 25 mg/ml) or ethanol (up to 25 mg/ml) |
form | powder |
color | white |
Stability: | Stable for 1 year from date of purchase as supplied. Solutions in DMSO or ethanol may be stored at -20°C for up to 1 month. |
Safety information for Bepridil hydrochloride
Computed Descriptors for Bepridil hydrochloride
New Products
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