57010-32-9

57010-32-9 structure

Name	Tiapamil hydrochloride
Synonyms	N-[2-(3,4-Dimethoxyphenyl)ethyl]-3-[2-(3,4-dimethoxyphenyl)-1,1,3,3-tetraoxido-1,3-dithian-2-yl]-N-methyl-1-propanaminium chloride 2-(3,4-Dimethoxyphenyl)-N-(2-(3,4-dimethoxyphenyl)ethyl)-N-methyl-1,3-dithiane-2-propanamine 1,1,3,3-tetraoxide hydrochloride dimeditiapramine N-[2-(3,4-Dimethoxyphenyl)ethyl]-3-[2-(3,4-dimethoxyphenyl)-1,1,3,3-tetraoxido-1,3-dithian-2-yl]-N-methylpropan-1-amine hydrochloride (1:1) S3R8JZ9DJH TIAPAMIL HYDROCHLORIDE ANHYDROUS 1,3-Dithiane-2-propanaminium, 2-(3,4-dimethoxyphenyl)-N-[2-(3,4-dimethoxyphenyl)ethyl]-N-methyl-, chloride, 1,1,3,3-tetraoxide (1:1) EINECS 260-511-1

Description	Tiapamil hydrochloride is a calcium channel blocker.
Related Catalog	Signaling Pathways >> Membrane Transporter/Ion Channel >> Calcium Channel Research Areas >> Cardiovascular Disease
Target	Calcium channel[1]
In Vitro	Tiapamil, a new calcium antagonist: hemodynamic effects in patients with acute myocardial infarction. Tiapamil is a new verapamil congener.Without precipitating left ventricular failure, Tiapamil reduced afterload and heart rate and maintained cardiac index while apparently improving diastolic compliance[1]. Tiapamil, a new calcium channel blocking agent with anti-anginal efficacy[2].
References	[1]. Eichler HG, et al. Tiapamil, a new calcium antagonist: hemodynamic effects in patients with acute myocardial infarction. Circulation. 1985 Apr;71(4):779-86. [2]. Khurmi NS, et al. Tiapamil, a new calcium channel blocking agent for the treatment of effort induced chronic stableangina pectoris.