Publikationen von Sonja Sievers

Ceballos, J.; Schwalfenberg, M.; Karageorgis, G.; Reckzeh, E. S.; Sievers, S.; Ostermann, C.; Pahl, A.; Sellstedt, M.; Nowacki, J.; Carnero Corrales, M. A. et al.; Wilke, J.; Laraia, L.; Tschapalda, K.; Metz, M.; Sehr, D. A.; Brand, S.; Winklhofer, K.; Janning, P.; Ziegler, S.; Waldmann, H.: Synthesis of Indomorphan Pseudo Natural Product Inhibitors of Glucose Transporters GLUT-1 and -3. Angewandte Chemie, International Edition, S. 1 - 28 (2019)

Ceballos, J.; Schwalfenberg, M.; Karageorgis, G.; Reckzeh, E. S.; Sievers, S.; Ostermann, C.; Pahl, A.; Sellstedt, M.; Nowacki, J.; Carnero Corrales, M. A. et al.; Wilke, J.; Laraia, L.; Tschapalda, K.; Metz, M.; Sehr, D. A.; Brand, S.; Winklhofer, K.; Janning, P.; Ziegler, S.; Waldmann, H.: Synthesis of Indomorphan Pseudo Natural Product Inhibitors of Glucose Transporters GLUT‐1 and ‐3. Angewandte Chemie, S. 1 - 28 (2019)

Förster, T.; Shang, E.; Shimizu, K.; Sanada, E.; Schölermann, B.; Hübecker, M.; Hahne, G.; Pascual Lopez-Alberca, M.; Janning, P.; Watanabe, N. et al.; Sievers, S.; Giordanetto, F.; Shimizu, T.; Ziegler, S.; Osada, H.; Waldmann, H.: 2-Sulfonylpyrimidines Target the Kinesin HSET via Cysteine Alkylation. European Journal of Organic Chemistry, S. 1 - 12 (2019)

Nemec, V.; Hylsová, M.; Maier, L.; Flegel, J.; Sievers, S.; Ziegler, S.; Schröder, M.; Berger, B.-T.; Chaikuad, A.; Valcíková, B. et al.; Uldrijan, S.; Drápela, S.; Soucek, K.; Waldmann, H.; Knapp, S.; Paruch, K.: Furo[3,2-b]pyridine: A Privileged Scaffold for Highly Selective Kinase Inhibitors and Effective Modulators of the Hedgehog Pathway. Angewandte Chemie International Edition 58 (4), S. 1062 - 1066 (2019)

Nemec, V.; Hylsová, M.; Maier, L.; Flegel, J.; Sievers, S.; Ziegler, S.; Schröder, M.; Berger, B.-T.; Chaikuad, A.; Valcíková, B. et al.; Uldrijan, S.; Drápela, S.; Soucek, K.; Waldmann, H.; Knapp, S.; Paruch, K.: Furo[3,2-b]pyridine: A Privileged Scaffold for Highly Selective Kinase Inhibitors and Effective Modulators of the Hedgehog Pathway. Angewandte Chemie 131 (4), S. 1074 - 1078 (2019)

Christoforow, A.; Wilke, J.; Binici, A.; Pahl, A.; Ostermann, C.; Sievers, S.; Waldmann, H.: Design, Synthesis and Phenotypic Profiling of Pyrano-Furo-Pyridone Pseudo Natural Products. Angewandte Chemie 131 (41), S. 14857 - 14865 (2019)

Karageorgis, G.; Reckzeh, E. S.; Ceballos, J.; Schwalfenberg, M.; Sievers, S.; Ostermann, C.; Pahl, A.; Ziegler, S.; Waldmann, H.: Chromopynones are pseudo natural product glucose uptake inhibitors targeting glucose transporters GLUT-1 and -3. Nature Chemistry 10, S. 1103 - 1111 (2018)

Spinck, M.; Ecke, M.; Sievers, S.; Neumann, H.: Highly Sensitive Lysine Deacetylase Assay Based on Acetylated Firefly Luciferase. Biochemistry 57 (26), S. 3552 - 3555 (2018)

Klein, A. S.; Brass, H. U. C.; Klebl, D. P.; Classen, T.; Loeschcke, A.; Drepper, T.; Sievers, S.; Jaeger, E.; Pietruszka, J.: Preparation of Cyclic Prodiginines by Mutasynthesis in Pseudomonas putida KT2440. ChemBioChem: A European Journal of Chemical Biology 19, S. 1 - 9 (2018)

Klein, A. S.; Domröse, A.; Bongen, P.; Brass, H. U. C.; Classen, T.; Loeschcke, A.; Drepper, T.; Laraia, L.; Sievers, S.; Jaeger, K.-E. et al.; Pietruszka, J.: New Prodigiosin Derivatives Obtained by Mutasynthesis in Pseudomonas putida. ACS Synthetic Biology 6 (9), S. 1757 - 1765 (2017)

Sidarovich, A.; Will, C. L.; Anokhina, M. M.; Ceballos, J.; Sievers, S.; Agafonov, D. E.; Samatov, T.; Bao, P.; Kastner, B.; Urlaub, H. et al.; Waldmann, H.; Lührmann, R.: Identification of a small molecule inhibitor that stalls splicing at an early step of spliceosome activation. eLife 6, e23533, S. 1 - 32 (2017)

Gräßle, S.; Susanto, S.; Sievers, S.; Tavsan, E.; Nieger, M.; Jung, N.; Bräse, S.: Synthesis and Investigation of S‑Substituted 2‑Mercaptobenzoimidazoles as Inhibitors of Hedgehog Signaling. ACS Medicinal Chemistry Letters 8 (9), S. 931 - 935 (2017)

Kötzner, L.; Leutzsch, M.; Sievers, S.; Patil, S.; Waldmann, H.; Zheng, Y.; Thiel, W.; List, B.: The Organocatalytic Approach to Enantiopure 2H- and 3H-Pyrroles: Inhibitors of the Hedgehog Signaling Pathway. Angewandte Chemie International Edition 55 (27), S. 7693 - 7697 (2016)

Kötzner, L.; Leutzsch, M.; Sievers, S.; Patil, S.; Waldmann, H.; Zheng, Y.; Thiel, W.; List, B.: Organokatalytische Synthese von enantiomerenreinen 2H- und 3H-Pyrrolen: Inhibitoren des Hedgehog-Signalwegs. Angewandte Chemie 128 (27), S. 7824 - 7828 (2016)

Hackl, M. W.; Lakemeyer, M.; Dahmen, M.; Glaser, M.; Pahl, A.; Lorenz-Baath, K.; Menzel, T.; Sievers, S.; Böttcher, T.; Antes, I. et al.; Waldmann, H.; Sieber, S. A.: Phenyl Esters Are Potent Inhibitors of Caseinolytic Protease P and Reveal a Stereogenic Switch for Deoligomerization. Journal of the American Chemical Society 137 (26), S. 8475 - 8483 (2015)

Samanta, R.; Narayan, R.; Bauer, J. O.; Strohmann, C.; Sievers, S.; Antonchick, A. P.: Oxidative regioselective amination of chromones exposes potent inhibitors of the hedgehog signaling pathway. Chemical Communications 51 (5), S. 925 - 928 (2015)

Götze, S.; Coersmeyer, M.; Müller, O.; Sievers, S.: Histone deacetylase inhibitors induce attenuation of Wnt signaling and TCF7L2 depletion in colorectal carcinoma cells. International Journal of Oncology 45 (4), S. 1715 - 1723 (2014)

Antonchick, A. P.; Lopez Tosco, S.; Parga, J.; Sievers, S.; Schürmann, M.; Preut, H.; Höing, S.; Schöler, H. R.; Sterneckert, J.; Rauh, D. et al.; Waldmann, H.: Highly Enantioselective Catalytic Synthesis of Neurite Growth-Promoting Secoyohimbanes. Chemistry & Biology 20 (4), 1, S. 500 - 509 (2013)

Pahl, A.; Sievers, S.: The Cell Painting Assay as a Screening Tool for the Discovery of Bioactivities in New Chemical Matter. In: Systems Chemical Biology; Methods in Molecular Biology, Vol. 1888, S. 115 - 126. Springer Verlag Humana Press, New York, NY (2019)

Konstantinidis, G.; Sievers, S.; Wu, Y.-W.: Identification of Novel Autophagy Inhibitors via Cell-Based High-Content Screening. In: Methods in Molecular Biology, S. 1 - 9. Springer Verlag, New York (2018)