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Author/Creator Ruetz, Stephan

1. In vitro and in vivo characterization of a novel, highly potent p53-MDM2 inhibitor. Issue 20 (1st November 2018)

Authors:
Vaupel, Andrea; Holzer, Philipp; Ferretti, Stephane; Guagnano, Vito; Kallen, Joerg; Mah, Robert; Masuya, Keiichi; Ruetz, Stephan; Rynn, Caroline; Schlapbach, Achim; Stachyra, Thérèse; Stutz, Stefan; Todorov, Milen; Jeay, Sébastien; Furet, Pascal
Journal:
Bioorganic & medicinal chemistry letters
Issue:
Volume 28:Issue 20(2018)
Page Start:
3404
Record Type:
Journal Article
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2. Discovery, X-ray structure and CPP-conjugation enabled uptake of p53/MDM2 macrocyclic peptide inhibitors. Issue 6 (16th September 2021)

Authors:
Schneider, Anselm F. L.; Kallen, Joerg; Ottl, Johannes; Reid, Patrick C.; Ripoche, Sebastien; Ruetz, Stephan; Stachyra, Therese-Marie; Hintermann, Samuel; Dumelin, Christoph E.; Hackenberger, Christian P. R.; Marzinzik, Andreas L.
Journal:
RSC chemical biology
Issue:
Volume 2:Issue 6(2021)
Page Start:
1661
Record Type:
Journal Article
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3. Discovery of a novel class of highly potent inhibitors of the p53–MDM2 interaction by structure-based design starting from a conformational argument. Issue 19 (1st October 2016)

Authors:
Furet, Pascal; Masuya, Keiichi; Kallen, Joerg; Stachyra-Valat, Thérèse; Ruetz, Stephan; Guagnano, Vito; Holzer, Philipp; Mah, Robert; Stutz, Stefan; Vaupel, Andrea; Chène, Patrick; Jeay, Sébastien; Schlapbach, Achim
Journal:
Bioorganic & medicinal chemistry letters
Issue:
Volume 26:Issue 19(2016)
Page Start:
4837
Record Type:
Journal Article
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5. Discovery of dihydroisoquinolinone derivatives as novel inhibitors of the p53–MDM2 interaction with a distinct binding mode. Issue 17 (1st September 2015)

Authors:
Gessier, François; Kallen, Joerg; Jacoby, Edgar; Chène, Patrick; Stachyra-Valat, Thérèse; Ruetz, Stephan; Jeay, Sébastien; Holzer, Philipp; Masuya, Keiichi; Furet, Pascal
Journal:
Bioorganic & medicinal chemistry letters
Issue:
Volume 25:Issue 17(2015)
Page Start:
3621
Record Type:
Journal Article
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