Literature DB >> 17095219

Evolution of thiazolidine-based blockers of human Kv1.5 for the treatment of atrial arrhythmias.

Chris M Jackson1, Benjamin Blass, Keith Coburn, Laurent Djandjighian, Gina Fadayel, Andrew J Fluxe, Steven J Hodson, John M Janusz, Michael Murawsky, James M Ridgeway, Ronald E White, Shengde Wu.   

Abstract

Blockade of the Kv1.5 ion channel is a potentially atrial-selective avenue for the treatment of atrial fibrillation and atrial flutter. The development and biological evaluation of a series of thiazolidine-based blockers of Kv1.5 is described.

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Year:  2006        PMID: 17095219     DOI: 10.1016/j.bmcl.2006.07.007

Source DB:  PubMed          Journal:  Bioorg Med Chem Lett        ISSN: 0960-894X            Impact factor:   2.823


  2 in total

1.  Crystal structure of (±)-3-[(benzo[d][1,3]dioxol-5-yl)meth-yl]-2-(3,4,5-tri-meth-oxy-phen-yl)-1,3-thia-zolidin-4-one.

Authors:  Rodolfo Moreno-Fuquen; Juan C Castillo; Rodrigo Abonia; Javier Ellena; Carlos A De Simone
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2014-11-05

Review 2.  Challenges Faced with Small Molecular Modulators of Potassium Current Channel Isoform Kv1.5.

Authors:  Zefeng Zhao; Songsong Ruan; Xiaoming Ma; Qian Feng; Zhuosong Xie; Zhuang Nie; Peinan Fan; Mingcheng Qian; Xirui He; Shaoping Wu; Yongmin Zhang; Xiaohui Zheng
Journal:  Biomolecules       Date:  2019-12-19
  2 in total

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