关注
Martin P Schwalm
Martin P Schwalm
在 pharmchem.uni-frankfurt.de 的电子邮件经过验证
标题
引用次数
引用次数
年份
BET bromodomain inhibitors
MP Schwalm, S Knapp
Current opinion in chemical biology 68, 102148, 2022
542022
PROTAC degraders as chemical probes for studying target biology and target validation
V Němec, MP Schwalm, S Müller, S Knapp
Chemical Society Reviews 51 (18), 7971-7993, 2022
352022
Tracking the PROTAC degradation pathway in living cells highlights the importance of ternary complex measurement for PROTAC optimization
MP Schwalm, A Krämer, A Dölle, J Weckesser, X Yu, J Jin, K Saxena, ...
Cell chemical biology 30 (7), 753-765. e8, 2023
232023
Development of the first covalent monopolar spindle kinase 1 (MPS1/TTK) Inhibitor
RA M. Serafim, A da Silva Santiago, MP Schwalm, Z Hu, CV Dos Reis, ...
Journal of Medicinal Chemistry 65 (4), 3173-3192, 2022
162022
A Toolbox for the Generation of Chemical Probes for Baculovirus IAP Repeat Containing Proteins
MP Schwalm, L Berger, M Meuter, J Vasta, C Corona, S Röhm, B Berger, ...
Frontiers in cell and developmental biology 10, 2022
122022
Discovery of a potent and highly isoform-selective inhibitor of the neglected ribosomal protein S6 kinase beta 2 (S6K2)
S Gerstenecker, L Haarer, M Schröder, M Kudolo, MP Schwalm, V Wydra, ...
Cancers 13 (20), 5133, 2021
112021
Crystal structure and inhibitor identifications reveal targeting opportunity for the atypical MAPK kinase ERK3
M Schröder, P Filippakopoulos, MP Schwalm, CA Ferrer, DH Drewry, ...
International journal of molecular sciences 21 (21), 7953, 2020
112020
A chemical probe to modulate human GID4 Pro/N-degron interactions
DDG Owens, MER Maitland, A Khalili Yazdi, X Song, V Reber, ...
Nature Chemical Biology, 1-12, 2024
62024
Development of novel urea-based ATM kinase inhibitors with subnanomolar cellular potency and high kinome selectivity
T Dimitrov, C Anli, AA Moschopoulou, T Kronenberger, M Kudolo, ...
European Journal of Medicinal Chemistry 235, 114234, 2022
62022
Toward effective Atg8‐based ATTECs: Approaches and perspectives
MP Schwalm, S Knapp, VV Rogov
Journal of Cellular Biochemistry, 2023
42023
Development of potent dual BET/HDAC inhibitors via pharmacophore merging and structure-guided optimization
N Bauer, DI Balourdas, JR Schneider, X Zhang, LM Berger, BT Berger, ...
ACS chemical biology 19 (2), 266-279, 2024
32024
Targeting LC3/GABARAP for degrader development and autophagy modulation
MP Schwalm, J Dopfer, A Kumar, FA Greco, N Bauer, F Loehr, J Heering, ...
bioRxiv, 2023.10. 05.560930, 2023
22023
Luciferase-and HaloTag-based reporter assays to measure small-molecule-induced degradation pathway in living cells
MP Schwalm, K Saxena, S Müller, S Knapp
Nature Protocols, 1-41, 2024
12024
Expanding the ligand spaces for E3 ligases for the design of protein degraders
RSZ Saleem, MP Schwalm, S Knapp
Bioorganic & medicinal chemistry, 117718, 2024
12024
Development of Highly Potent and Selective Covalent FGFR4 Inhibitors Based on SNAr Electrophiles
M Schwarz, M Kurkunov, F Wittlinger, R Rudalska, G Wang, MP Schwalm, ...
Journal of medicinal chemistry 67 (8), 6549-6569, 2024
12024
Splice variants of CK1α and CK1α-like: Comparative analysis of subcellular localization, kinase activity and function in the Wnt signaling pathway
T Gybeľ, Š Čada, D Klementová, MP Schwalm, BT Berger, M Šebesta, ...
Journal of Biological Chemistry, 107407, 2024
2024
Thalidomide derivatives degrade BCL-2 by reprogramming the binding surface of CRBN
J Wang, M Heinz, K Han, VJ Shah, S Hasselbeck, MP Schwalm, ...
Cell Reports Physical Science 5 (5), 2024
2024
tracerDB: A crowdsourced fluorescent tracer database for target engagement analysis
M Schwalm, J Dopfer, J Vasta, S Muller, S Knapp, M Robers
2024
High throughput screening for LC3/GABARAP binders utilizing fluorescence polarization assay
MP Schwalm, J Dopfer, S Knapp, VV Rogov
arXiv preprint arXiv:2401.04453, 2024
2024
Development of Highly Potent and Selective FGFR4 Inhibitors Based on SNAr Electrophiles
M Schwarz, M Kurkunov, F Wittlinger, R Rudalska, G Wang, MP Schwalm, ...
2024
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