Publication by Weinzinger Lab

19.01.2022

Shared firstauthorship in Front Pharmacol. combines (again) MolTag generations

In a joint effort with the lab of MolTag SAB Marcel Van der Heyden at the University Medical Center Utrecht (NL), MolTag student Theres Friesacher plus MolTag Alumni of the Weinzinger group, namely Xingyu Chen and Eva Plessl showed that a combination of molecular dynamics and inside-out electrophysiology provides the rationale for drug mediated IKATP inhibition, and will be the basis for

1) sreening of additional existing drugs for repurposing to address DEND syndrome, and 

2) rationalized medicinal chemistry to improve IKATP inhibitor efficacy and specificity.

Congratulations to the labs involved!

 
ORIGINAL RESEARCH article; Front. Pharmacol., 14 January 2022 doi.org/10.3389/fphar.2021.814066

Development of IKATP Ion Channel Blockers Targeting Sulfonylurea Resistant Mutant KIR6.2 Based Channels for Treating DEND Syndrome

Marien J. C. Houtman1, Theres Friesacher2, Xingyu Chen2, Eva-Maria Zangerl-Plessl2, Marcel A. G. van der Heyden1 and Anna Stary-Weinzinger2*

1Department of Medical Physiology, Division of Heart and Lungs, University Medical Center Utrecht, Utrecht, Netherlands
2Department of Pharmaceutical Sciences, Division of Pharmacology and Toxicology, University of Vienna, Vienna, Austria

  

 

 

Overview of the KATP channel and the investigated inhibiting compounds.

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