Development of new Kir2.1 channel openers from propafenone analogues

  • Encan Li
  • , Najla Boujeddaine
  • , Marien J.C. Houtman
  • , Renee G.C. Maas
  • , Joost P.G. Sluijter
  • , Gerhard F. Ecker
  • , Anna Stary-Weinzinger
  • , Willem B. van Ham
  • , Marcel A.G. van der Heyden (Corresponding author)

Publications: Contribution to journalArticlePeer Reviewed

Original languageEnglish
Pages (from-to)633-650
Number of pages18
JournalBritish Journal of Pharmacology
Volume182
Issue number3
DOIs
Publication statusPublished - 17 Oct 2024

Funding

We did not preregister this research with an analysis plan in an independent institutional registry. E. Li received financial support from the China Scholarship Council. Funding for the present work was provided by TOP\u2010EVICARE (101138069) of the European Research Council (ERC), Nederlandse Organisatie voor Wetenschappelijk Onderzoek (NWO) TTP HARVEY (2021/TTW/01038252), ZonMW PSIDER (10250022110004), NWO\u2010Take\u2010off 1 VINCI (2023/TTW/01494519) and Health Holland EV\u2010Protect (TKI2306). We thank S. Bendahhou (Universit\u00E9 C\u00F4te d'Azur, Nice, France) for providing Andersen\u2013Tawil Syndrome mutant expression constructs.

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Austrian Fields of Science 2012

  • 301207 Pharmaceutical chemistry

Keywords

  • cardiac pharmacology
  • drug discovery/target validation
  • hiPSC-CMCs
  • ion channels
  • K2.1 channel
  • off-target effects
  • propafenone analogues

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