Structure-Based Design of Xanthine-Imidazopyridines and -Imidazothiazoles as Highly Potent and In Vivo Efficacious Tryptophan Hydroxylase Inhibitors

Author:

Specker Edgar12ORCID,Wesolowski Radoslaw23,Schütz Anja3,Matthes Susann3,Mallow Keven1,Wasinska-Kalwa Malgorzata1,Winkler Lars4ORCID,Oder Andreas1,Alenina Natalia35ORCID,Pleimes Dirk2,von Kries Jens Peter1,Heinemann Udo3,Bader Michael23567,Nazaré Marc1ORCID

Affiliation:

1. Chemical Biology Platform, Leibniz-Forschungsinstitut für Molekulare Pharmakologie (FMP), Robert-Rössle-Straße 10, 13125 Berlin-Buch, Germany

2. Trypto Therapeutics GmbH, Robert-Rössle Straße 10, 13125 Berlin, Germany

3. Max-Delbrück-Center for Molecular Medicine in the Helmholtz Association (MDC), Robert-Rössle-Straße 10, 13125 Berlin-Buch, Germany

4. Experimental Pharmacology and Oncology GmbH, Robert-Rössle-Straße 10, 13125 Berlin-Buch, Germany

5. German Center for Cardiovascular Research (DZHK), Partner Site Berlin, Potsdamer Straße 58, 10785 Berlin, Germany

6. Charité─Universitätsmedizin Berlin, Charitéplatz 1, 10117 Berlin, Germany

7. University of Lübeck, Institute for Biology, Ratzeburger Allee 160, 23562 Lübeck, Germany

Funder

Bundesministerium für Bildung und Forschung

Bundesministerium für Wirtschaft und Klimaschutz

Helmholtz-Gemeinschaft

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

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