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 | |
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 |
Molecular Formula | C26H38ClNO8S2 |
---|---|
Molecular Weight | 592.165 |
Exact Mass | 591.172729 |