Tetrandrine–A molecule of wide bioactivity

N Bhagya, KR Chandrashekar - Phytochemistry, 2016 - Elsevier
Stephania tetrandra and other related species of Menispermaceae form the major source of
the bisbenzylisoquinoline alkaloid–tetrandrine. The plant is extensively referenced in the …

Pharmacology of cardiac potassium channels

J Tamargo, R Caballero, R Gómez… - Cardiovascular …, 2004 - academic.oup.com
Cardiac K+ channels are membrane-spanning proteins that allow the passive movement of
K+ ions across the cell membrane along its electrochemical gradient. They regulate the …

Instability and triangulation of the action potential predict serious proarrhythmia, but action potential duration prolongation is antiarrhythmic

LM Hondeghem, L Carlsson, G Duker - Circulation, 2001 - Am Heart Assoc
Background—Prolongation of action potential duration (APD) is considered a major
antiarrhythmic mechanism (class 2I), but paradoxically, it frequently is also proarrhythmic …

The mechanism of atrial antiarrhythmic action of RSD1235

D Fedida, PMR Orth, JYC Chen, S Lin… - Journal of …, 2005 - Wiley Online Library
Introduction: RSD1235 is a novel drug recently shown to convert AF rapidly and safely in
patients. 1 Its mechanism of action has been investigated in a rat model of ischemic …

Virtual screening on natural products for discovering active compounds and target information

J Shen, X Xu, F Cheng, H Liu, X Luo… - Current medicinal …, 2003 - ingentaconnect.com
Natural products, containing inherently large-scale structural diversity than synthetic
compounds, have been the major resources of bioactive agents and will continually play as …

[HTML][HTML] Cardiac effects and toxicity of chloroquine: a short update

K Mubagwa - International Journal of Antimicrobial Agents, 2020 - Elsevier
There is currently increased interest in the use of the antimalarial drugs chloroquine and
hydroxychloroquine for the treatment of other diseases, including cancer and viral infections …

Characterization of voltage-gated sodium-channel blockers by electrical stimulation and fluorescence detection of membrane potential

CJ Huang, A Harootunian, MP Maher, C Quan… - Nature …, 2006 - nature.com
Voltage-gated ion channels regulate many physiological functions and are targets for a
number of drugs. Patch-clamp electrophysiology is the standard method for measuring …

Drug-induced torsade de pointes: from molecular biology to bedside

J Tamargo - The Japanese journal of pharmacology, 2000 - jstage.jst.go.jp
抄録 A progressively increasing number of cardiac and noncardiac drugs prolong the
ventricular action potential duration (QT interval of the electrocardiogram) and cause a …

Design, Synthesis, and Evaluation of a Novel 4-Aminomethyl-4-fluoropiperidine as a T-Type Ca2+ Channel Antagonist

WD Shipe, JC Barrow, ZQ Yang… - Journal of medicinal …, 2008 - ACS Publications
The novel T-type antagonist (S)-5 has been prepared and evaluated in in vitro and in vivo
assays for T-type calcium ion channel activity. Structural modification of the piperidine leads …

Inhibition of the human ether‐a‐go‐go‐related gene (HERG) potassium channel by cisapride: affinity for open and inactivated states

BD Walker, CB Singleton, JA Bursill… - British journal of …, 1999 - Wiley Online Library
Cisapride is a prokinetic agent which has been associated with QT prolongation, torsades
de pointes and cardiac arrest. The cellular mechanism for these observations is high affinity …