“Photo‐Adrenalines”: Photoswitchable β2‐Adrenergic Receptor Agonists as Molecular Probes for the Study of Spatiotemporal Adrenergic Signaling

Author:

Sink Alexandra1ORCID,Gerwe Hubert1ORCID,Hübner Harald2ORCID,Boivin‐Jahns Valerie3ORCID,Fender Julia3ORCID,Lorenz Kristina34ORCID,Gmeiner Peter2ORCID,Decker Michael1ORCID

Affiliation:

1. Pharmaceutical and Medicinal Chemistry Institute for Pharmacy and Food Chemistry Julius-Maximilians-Universität Würzburg Am Hubland 97074 Würzburg Germany

2. Medicinal Chemistry Department of Chemistry and Pharmacy Friedrich-Alexander-Universität Erlangen-Nürnberg Nikolaus-Fiebiger-Straße 10 91058 Erlangen Germany

3. Institute for Pharmacology and Toxicology Julius-Maximilians-Universität Würzburg Versbacher Straße 9 97078 Würzburg Germany

4. Leibniz-Institut für Analytische Wissenschaften - ISAS-e.V. Bunsen-Kirchhoff-Str. 11 44139 Dortmund Germany

Abstract

Abstractβ2‐adrenergic receptor (β2‐AR) agonists are used for the treatment of asthma and chronic obstructive pulmonary disease, but also play a role in other complex disorders including cancer, diabetes and heart diseases. As the cellular and molecular mechanisms in various cells and tissues of the β2‐AR remain vastly elusive, we developed tools for this investigation with high temporal and spatial resolution. Several photoswitchable β2‐AR agonists with nanomolar activity were synthesized. The most potent agonist for β2‐AR with reasonable switching is a one‐digit nanomolar active, trans‐on arylazopyrazole‐based adrenaline derivative and comprises valuable photopharmacological properties for further biological studies with high structural accordance to the native ligand adrenaline.

Funder

Deutsche Forschungsgemeinschaft

Elitenetzwerk Bayern

Studienstiftung des Deutschen Volkes

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

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