Auflistung nach Autor "Döring, Eva"

Anzeige der Dokumente 1-9 von 9

Design, Synthesis, and Biological Evaluation of Novel Type l1/2 p38 alpha MAP Kinase Inhibitors with Excellent Selectivity, High Potency, and Prolonged Target Residence Time by Interfering with the R-Spine

Walter, Niklas M.; Wentsch-Teltschik, Heike Kristin; Sievers-Engler, Adrian; Bauer, Silke Mona; Döring, Eva; Lämmerhofer, Michael; Laufer, Stefan (2017)
Development, Optimization, and Structure-Activity Relationships of Covalent-Reversible JAK3 Inhibitors Based on a Tricyclic Imidazo[5,4-d]pyrrolo[2,3-b]pyridine Scaffold

Forster, Michael; Dimitrov, Teodor; Holstein, Julia; Gehringer, Matthias; Ghoreschi, Kamran; Döring, Eva; Laufer, Stefan (2018)
From 2-Alkylsulfanylimidazoles to 2-Alkylimidazoles: An Approach towards Metabolically More Stable p38 alpha MAP Kinase Inhibitors

Heider, Fabian Andreas; Haun, Urs; Kudolo, Mark; Sessler, Catharina; Laufer, Stefan; Koch, Pierre; Döring, Eva (2017)
Natural chromones as potential anti-inflammatory agents: Pharmacological properties and related mechanisms

Döring, Eva; Laufer, Stefan (2019)
Pyridinylimidazoles as dual glycogen synthase kinase 3 beta/p38 alpha mitogen-activated protein kinase inhibitors

Heider, Fabian Andreas; Ansideri, Francesco; Tesch, Roberta; Pantsar, Tatu; Haun, Urs; Koch, Pierre; Döring, Eva; Laufer, Stefan; Kudolo, Mark (2019)
Tetra-Substituted Pyridinylimidazoles As Dual Inhibitors of p38 alpha Mitogen-Activated Protein Kinase and c-Jun N-Terminal Kinase 3 for Potential Treatment of Neurodegenerative Diseases

Muth, Felix; Fischer, Sabine; Maier, Julia; Rothbauer, Ulrich; Koch, Pierre; Günther, Marcel Benjamin; Bauer, Silke Mona; Laufer, Stefan; Döring, Eva (2015)
Tri- and Tetrasubstituted Pyridinylimidazoles as Covalent Inhibitors of c-Jun N-Terminal Kinase 3

Muth, Felix; El-Gokha, Ahmed; Ansideri, Francesco; Eitel, Michael; Döring, Eva; Sievers-Engler, Adrian; Lange, Andreas; Böckler, Frank; Lämmerhofer, Michael; Koch, Pierre; Laufer, Stefan (2017)
Trisubstituted Imidazoles with a Rigidized Hinge Binding Motif Act As Single Digit nM Inhibitors of Clinically Relevant EGFR L858R/T790M and L858R/T790M/C797S Mutants: An Example of Target Hopping

Juchum, Michael; Sievers-Engler, Adrian; Laufer, Stefan; Günther, Marcel Benjamin; Döring, Eva; Lämmerhofer, Michael (2017)
Trisubstituted Pyridinylimidazoles as Potent Inhibitors of the Clinically Resistant L858R/T790M/C797S EGFR Mutant: Targeting of Both Hydrophobic Regions and the Phosphate Binding Site

Juchum, Michael; Laufer, Stefan; Günther, Marcel Benjamin; Döring, Eva (2017)

Anzeige der Dokumente 1-9 von 9

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Auflistung nach Autor "Döring, Eva"

Auflistung nach Autor "Döring, Eva"

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