Literature DB >> 11166255

Screening lead compounds for QT interval prolongation.

R Netzer1, A Ebneth, U Bischoff, O Pongs.   

Abstract

The late detection of cardiotoxic side effects, such as QT prolongation, induced by compounds of pharmacological interest can dramatically impede drug discovery and development projects, and consequently increase their cost. The launch of new drugs with undetected cardiotoxic side effects could have hazardous consequences and could trigger lethal cardiac dysrhythmias in patients. It is desirable, therefore, to test for the potential cardiotoxic side effects of compounds at an early stage of drug development. Electrophysiological test systems and cellular-based fluorometric high-throughput assays are now available for cloned human cardiac ion channels. These test systems are important tools in the preclinical safety evaluation of drugs and newly developed compounds.

Entities:  

Year:  2001        PMID: 11166255     DOI: 10.1016/s1359-6446(00)01602-0

Source DB:  PubMed          Journal:  Drug Discov Today        ISSN: 1359-6446            Impact factor:   7.851


  14 in total

Review 1.  Safety of non-antiarrhythmic drugs that prolong the QT interval or induce torsade de pointes: an overview.

Authors:  Fabrizio De Ponti; Elisabetta Poluzzi; Andrea Cavalli; Maurizio Recanatini; Nicola Montanaro
Journal:  Drug Saf       Date:  2002       Impact factor: 5.606

2.  Microfluidic cell culture and its application in high-throughput drug screening: cardiotoxicity assay for hERG channels.

Authors:  Xiaojing Su; Edmond W K Young; Heather A S Underkofler; Timothy J Kamp; Craig T January; David J Beebe
Journal:  J Biomol Screen       Date:  2010-12-03

3.  A critical assessment of combined ligand- and structure-based approaches to HERG channel blocker modeling.

Authors:  Lei Du-Cuny; Lu Chen; Shuxing Zhang
Journal:  J Chem Inf Model       Date:  2011-10-13       Impact factor: 4.956

Review 4.  The use of pharmacokinetic and pharmacodynamic data in the assessment of drug safety in early drug development.

Authors:  D K Walker
Journal:  Br J Clin Pharmacol       Date:  2004-12       Impact factor: 4.335

Review 5.  KCNH2 pharmacogenomics summary.

Authors:  Connie Oshiro; Caroline F Thorn; Dan M Roden; Teri E Klein; Russ B Altman
Journal:  Pharmacogenet Genomics       Date:  2010-12       Impact factor: 2.089

6.  Modelling of drug-induced QT-interval prolongation: estimation approaches and translational opportunities.

Authors:  Eleonora Marostica; Karel Van Ammel; Ard Teisman; Koen Boussery; Jan Van Bocxlaer; Filip De Ridder; David Gallacher; An Vermeulen
Journal:  J Pharmacokinet Pharmacodyn       Date:  2015-08-11       Impact factor: 2.745

7.  Identifying the translational gap in the evaluation of drug-induced QTc interval prolongation.

Authors:  Anne S Y Chain; Vincent F S Dubois; Meindert Danhof; Miriam C J M Sturkenboom; Oscar Della Pasqua
Journal:  Br J Clin Pharmacol       Date:  2013-11       Impact factor: 4.335

Review 8.  Clinical pharmacology: special safety considerations in drug development and pharmacovigilance.

Authors:  Kwame N Atuah; Dyfrig Hughes; Munir Pirmohamed
Journal:  Drug Saf       Date:  2004       Impact factor: 5.606

9.  PK/PD Modelling of the QT Interval: a Step Towards Defining the Translational Relationship Between In Vitro, Awake Beagle Dogs, and Humans.

Authors:  Eleonora Marostica; Karel Van Ammel; Ard Teisman; David Gallacher; Jan Van Bocxlaer; Filip De Ridder; Koen Boussery; An Vermeulen
Journal:  AAPS J       Date:  2016-04-26       Impact factor: 4.009

10.  Effects of mixed herbal extracts from parched Puerariae radix, gingered Magnoliae cortex, Glycyrrhizae radix and Euphorbiae radix (KIOM-79) on cardiac ion channels and action potentials.

Authors:  Su Jung Park; Kwan Seok Choi; Dong Hoon Shin; Jin Sook Kim; Dae Sik Jang; Jae Beom Youm; Han Choe; Yung E Earm; Sung Joon Kim
Journal:  J Korean Med Sci       Date:  2009-06-12       Impact factor: 2.153

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