Synthesis and biological evaluation of PET tracers designed for imaging of calcium activated potassium channel 3.1 (KCa3.1) channels in vivo

Author:

Brömmel Kathrin1,Konken Christian Paul2ORCID,Börgel Frederik1,Obeng-Darko Henry1,Schelhaas Sonja3,Bulk Etmar4,Budde Thomas56,Schwab Albrecht46,Schäfers Michael236,Wünsch Bernhard16ORCID

Affiliation:

1. Institute for Pharmaceutical and Medicinal Chemistry, Westphalian Wilhelms-University Münster, Corrensstraße 48, D-48149 Münster, Germany

2. Department of Nuclear Medicine, University Hospital Münster, Albert-Schweitzer-Campus 1, Building A1, D-48149 Münster, Germany

3. European Institute for Molecular Imaging (EIMI), Westphalian Wilhelms-University Münster, Waldeyerstraße 15, D-48149 Münster, Germany

4. Institute for Physiology II, University Hospital Münster, Robert-Koch-Straße 27b, D-48149 Münster, Germany

5. Institute for Physiology I, University Hospital Münster, Robert-Koch-Straße 27a, D-48149 Münster, Germany

6. Cells-in-Motion Interfaculty Center, Westphalian Wilhelms-University Münster, Waldeyerstraße 15, D-84149 Münster, Germany

Abstract

Expression of the Ca2+ activated potassium channel 3.1 (KCa3.1) channel (also known as the Gàrdos channel) is dysregulated in many tumor entities and has predictive power with respect to patient survival.

Funder

Deutsche Forschungsgemeinschaft

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

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