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hERGAPDbase: a database documenting hERG channel inhibitory potentials and APD-prolongation activities of chemical compounds
Drug-induced QT interval prolongation is one of the most common reasons for the withdrawal of drugs from the market. In the past decade, at least nine drugs, i.e. terfenadine, astemizole, grepafloxacin, terodiline, droperidol, lidoflazine, sertindole, levomethadyl and cisapride, have been removed fr...
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Formato: | Texto |
Lenguaje: | English |
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Oxford University Press
2011
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3096323/ https://www.ncbi.nlm.nih.gov/pubmed/21586548 http://dx.doi.org/10.1093/database/bar017 |
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author | Hishigaki, Haretsugu Kuhara, Satoru |
author_facet | Hishigaki, Haretsugu Kuhara, Satoru |
author_sort | Hishigaki, Haretsugu |
collection | PubMed |
description | Drug-induced QT interval prolongation is one of the most common reasons for the withdrawal of drugs from the market. In the past decade, at least nine drugs, i.e. terfenadine, astemizole, grepafloxacin, terodiline, droperidol, lidoflazine, sertindole, levomethadyl and cisapride, have been removed from the market or their use has been severely restricted because of drug-induced QT interval prolongation. Therefore, this irregularity is a major safety concern in the case of drugs submitted for regulatory approval. The most common mechanism of drug-induced QT interval prolongation may be drug-related inhibition of the human ether-á-go-go-related gene (hERG) channel, which subsequently results in prolongation of the cardiac action potential duration (APD). hERGAPDbase is a database of electrophysiological experimental data documenting potential hERG channel inhibitory actions and the APD-prolongation activities of chemical compounds. All data entries are manually collected from scientific papers and curated by a person. With hERGAPDbase, we aim to provide useful information for chemical and pharmacological scientists and enable easy access to electrophysiological experimental data on chemical compounds. Database URL: http://www.grt.kyushu-u.ac.jp/hergapdbase/ |
format | Text |
id | pubmed-3096323 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-30963232011-05-17 hERGAPDbase: a database documenting hERG channel inhibitory potentials and APD-prolongation activities of chemical compounds Hishigaki, Haretsugu Kuhara, Satoru Database (Oxford) Original Article Drug-induced QT interval prolongation is one of the most common reasons for the withdrawal of drugs from the market. In the past decade, at least nine drugs, i.e. terfenadine, astemizole, grepafloxacin, terodiline, droperidol, lidoflazine, sertindole, levomethadyl and cisapride, have been removed from the market or their use has been severely restricted because of drug-induced QT interval prolongation. Therefore, this irregularity is a major safety concern in the case of drugs submitted for regulatory approval. The most common mechanism of drug-induced QT interval prolongation may be drug-related inhibition of the human ether-á-go-go-related gene (hERG) channel, which subsequently results in prolongation of the cardiac action potential duration (APD). hERGAPDbase is a database of electrophysiological experimental data documenting potential hERG channel inhibitory actions and the APD-prolongation activities of chemical compounds. All data entries are manually collected from scientific papers and curated by a person. With hERGAPDbase, we aim to provide useful information for chemical and pharmacological scientists and enable easy access to electrophysiological experimental data on chemical compounds. Database URL: http://www.grt.kyushu-u.ac.jp/hergapdbase/ Oxford University Press 2011-05-17 /pmc/articles/PMC3096323/ /pubmed/21586548 http://dx.doi.org/10.1093/database/bar017 Text en © The Author(s) 2011. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/2.5 This is Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.5), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Hishigaki, Haretsugu Kuhara, Satoru hERGAPDbase: a database documenting hERG channel inhibitory potentials and APD-prolongation activities of chemical compounds |
title | hERGAPDbase: a database documenting hERG channel inhibitory potentials and APD-prolongation activities of chemical compounds |
title_full | hERGAPDbase: a database documenting hERG channel inhibitory potentials and APD-prolongation activities of chemical compounds |
title_fullStr | hERGAPDbase: a database documenting hERG channel inhibitory potentials and APD-prolongation activities of chemical compounds |
title_full_unstemmed | hERGAPDbase: a database documenting hERG channel inhibitory potentials and APD-prolongation activities of chemical compounds |
title_short | hERGAPDbase: a database documenting hERG channel inhibitory potentials and APD-prolongation activities of chemical compounds |
title_sort | hergapdbase: a database documenting herg channel inhibitory potentials and apd-prolongation activities of chemical compounds |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3096323/ https://www.ncbi.nlm.nih.gov/pubmed/21586548 http://dx.doi.org/10.1093/database/bar017 |
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