F. Ansideri

发表

Fluorescence polarization-based competition binding assay for c-Jun N-terminal kinases 1 and 2.

F. Boeckler, P. Koch, F. Ansideri, 2017, Analytical biochemistry.

A Diverse and Versatile Regiospecific Synthesis of Tetrasubstituted Alkylsulfanylimidazoles as p38α Mitogen-Activated Protein Kinase Inhibitors

S. Laufer, P. Koch, W. Albrecht, 2018, Molecules.

1-(3′,6′-Dihydroxy-3-oxo-3H-spiro[isobenzofuran-1,9′-xanthen]-5-yl)-3-[4-({4-[1-(4-fluorophenyl)-1H-imidazol-5-yl]pyridin-2-yl}amino)phenyl]thiourea methanol monosolvate

P. Koch, D. Schollmeyer, F. Ansideri, 2016 .

Design, Synthesis and Biological Evaluation of 7-Chloro-9H-pyrimido[4,5-b]indole-based Glycogen Synthase Kinase-3β Inhibitors

S. Laufer, P. Koch, D. Schollmeyer, 2019, Molecules.

Structural Optimization of a Pyridinylimidazole Scaffold: Shifting the Selectivity from p38α Mitogen-Activated Protein Kinase to c-Jun N-Terminal Kinase 3

S. Laufer, F. Boeckler, P. Koch, 2018, ACS omega.

2‐Alkylsulfanyl‐4(5)‐aryl‐5(4)‐heteroarylimidazoles: An Overview on Synthetic Strategies and Biological Activity

P. Koch, F. Ansideri, 2017, Archiv der Pharmazie.

Pyridinylimidazoles as dual glycogen synthase kinase 3β/p38α mitogen-activated protein kinase inhibitors.

A. Poso, S. Laufer, P. Koch, 2019, European journal of medicinal chemistry.

N1-{4-[2-(Methylthio)-1H-imidazol-5-yl]pyridin-2-yl}benzene-1,4-diamine

S. Laufer, P. Koch, Ahmed El-Gokha, 2019, Molbank.

Tri- and Tetrasubstituted Pyridinylimidazoles as Covalent Inhibitors of c-Jun N-Terminal Kinase 3.

S. Laufer, F. Boeckler, Andreas Lange, 2017, Journal of medicinal chemistry.

Fluorescence polarization-based assays for detecting compounds binding to inactive c-Jun N-terminal kinase 3 and p38α mitogen-activated protein kinase.

F. Boeckler, Andreas Lange, P. Koch, 2016, Analytical biochemistry.

Targeting the Gatekeeper MET146 of C-Jun N-Terminal Kinase 3 Induces a Bivalent Halogen/Chalcogen Bond.

Pierre Koch, Andreas Lange, Susanne Hennig, 2015, Journal of the American Chemical Society.

Addressing a Trapped High-Energy Water: Design and Synthesis of Highly Potent Pyrimidoindole-Based Glycogen Synthase Kinase-3β Inhibitors.

S. Knapp, S. Laufer, P. Koch, 2021, Journal of medicinal chemistry.

11th German Conference on Chemoinformatics (GCC 2015)

Timothy Clark, Jonathan W. Essex, Peter Kolb, 2016, J. Cheminformatics.

Pyridinylimidazoles as GSK3β Inhibitors: The Impact of Tautomerism on Compound Activity via Water Networks.

V. Andrisano, S. Laufer, P. Koch, 2019, ACS medicinal chemistry letters.