Cargando…
Impaired Inactivation of L-Type Ca(2+) Current as a Potential Mechanism for Variable Arrhythmogenic Liability of HERG K(+) Channel Blocking Drugs
The proarrhythmic effects of new drugs have been assessed by measuring rapidly activating delayed-rectifier K(+) current (I(Kr)) antagonist potency. However, recent data suggest that even drugs thought to be highly specific I(Kr) blockers can be arrhythmogenic via a separate, time-dependent pathway...
Autores principales: | Kim, Jae Gon, Sung, Dong Jun, Kim, Hyun-ji, Park, Sang Woong, Won, Kyung Jong, Kim, Bokyung, Shin, Ho Chul, Kim, Ki-Suk, Leem, Chae Hun, Zhang, Yin Hua, Cho, Hana, Bae, Young Min |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4772914/ https://www.ncbi.nlm.nih.gov/pubmed/26930604 http://dx.doi.org/10.1371/journal.pone.0149198 |
Ejemplares similares
-
Improving the hERG model fitting using a deep learning-based method
por: Song, Jaekyung, et al.
Publicado: (2023) -
Ensemble of structure and ligand-based classification models for hERG liability profiling
por: Vittorio, Serena, et al.
Publicado: (2023) -
A structure-based computational workflow to predict liability and binding modes of small molecules to hERG
por: Kalyaanamoorthy, Subha, et al.
Publicado: (2020) -
Gating Charges in the Activation and Inactivation Processes of the hERG Channel
por: Zhang, Mei, et al.
Publicado: (2004) -
Mechanism of C-type inactivation in the hERG potassium channel
por: Li, Jing, et al.
Publicado: (2021)