Follow
Matthias Schmidt
Title
Cited by
Cited by
Year
Regulation of G2/M transition by inhibition of WEE1 and PKMYT1 kinases
M Schmidt, A Rohe, C Platzer, A Najjar, F Erdmann, W Sippl
Molecules 22 (12), 2045, 2017
1662017
Structure-Based Design and Synthesis of Novel Inhibitors Targeting HDAC8 from Schistosoma mansoni for the Treatment of Schistosomiasis
T Heimburg, A Chakrabarti, J Lancelot, M Marek, J Melesina, AT Hauser, ...
Journal of Medicinal Chemistry 59 (6), 2423-2435, 2016
1322016
New 1, 3-dioxolane and 1, 3-dioxane derivatives as effective modulators to overcome multidrug resistance
M Schmidt, J Ungvári, J Glöde, B Dobner, A Langner
Bioorganic & medicinal chemistry 15 (6), 2283-2297, 2007
782007
Structure-based design and biological characterization of selective histone deacetylase 8 (HDAC8) inhibitors with anti-neuroblastoma activity
T Heimburg, FR Kolbinger, P Zeyen, E Ghazy, D Herp, K Schmidtkunz, ...
Journal of Medicinal Chemistry 60 (24), 10188-10204, 2017
752017
Application of docking and QM/MM-GBSA rescoring to screen for novel Myt1 kinase inhibitors
K Wichapong, A Rohe, C Platzer, I Slynko, F Erdmann, M Schmidt, ...
Journal of Chemical Information and Modeling 54 (3), 881-893, 2014
732014
Synthesis and biochemical characterization of new phenothiazines and related drugs as MDR reversal agents
M Schmidt, M Teitge, ME Castillo, T Brandt, B Dobner, A Langner
Archiv der Pharmazie 341 (10), 624-638, 2008
332008
Synthesis, molecular docking and biological characterization of pyrazine linked 2-aminobenzamides as new class I selective histone deacetylase (HDAC) inhibitors with anti …
HS Ibrahim, M Abdelsalam, Y Zeyn, M Zessin, AHM Mustafa, MA Fischer, ...
International Journal of Molecular Sciences 23 (1), 369, 2021
312021
Synthesis, Crystallization Studies, and in vitro Characterization of Cinnamic Acid Derivatives as SmHDAC8 Inhibitors for the Treatment of Schistosomiasis
T Bayer, A Chakrabarti, J Lancelot, TB Shaik, K Hausmann, J Melesina, ...
ChemMedChem 13 (15), 1517-1529, 2018
262018
Design, synthesis, and biological evaluation of dual targeting inhibitors of histone deacetylase 6/8 and bromodomain BRPF1
E Ghazy, P Zeyen, D Herp, M Hügle, K Schmidtkunz, F Erdmann, ...
European journal of medicinal chemistry 200, 112338, 2020
232020
In vitro and in silico studies on substrate recognition and acceptance of human PKMYT1, a Cdk1 inhibitory kinase
A Rohe, F Erdmann, C Bäßler, K Wichapong, W Sippl, M Schmidt
Bioorganic & medicinal chemistry letters 22 (2), 1219-1223, 2012
232012
A Fluorescence Anisotropy–Based Myt1 Kinase Binding Assay
A Rohe, C Henze, F Erdmann, W Sippl, M Schmidt
Assay and drug development technologies 12 (2), 136-144, 2014
212014
Design, synthesis and biological characterization of histone deacetylase 8 (HDAC8) proteolysis targeting chimeras (PROTACs) with anti-neuroblastoma activity
S Darwish, E Ghazy, T Heimburg, D Herp, P Zeyen, R Salem-Altintas, ...
International journal of molecular sciences 23 (14), 7535, 2022
182022
Identification of histone deacetylase 10 (HDAC10) inhibitors that modulate autophagy in transformed cells
P Zeyen, Y Zeyn, D Herp, F Mahmoudi, TZ Yesiloglu, F Erdmann, ...
European Journal of Medicinal Chemistry, 114272, 2022
182022
Computer-aided design, synthesis and biological characterization of novel inhibitors for PKMYT1
A Najjar, C Platzer, A Luft, CA Aßmann, NH Elghazawy, F Erdmann, ...
European Journal of Medicinal Chemistry 161, 479-492, 2019
182019
Synthesis, biological characterisation and structure activity relationships of aromatic bisamidines active against Plasmodium falciparum
B Sauer, TS Skinner-Adams, A Bouchut, MJ Chua, C Pierrot, F Erdmann, ...
European Journal of Medicinal Chemistry 127, 22-40, 2017
162017
First total synthesis of 1, 2-dipalmitoyl-3-(N-palmitoyl-6′-amino-6′-deoxy-α-d-glucosyl)-sn-glycerol—A glycoglycerolipid of a marine alga with a high inhibitor activity …
C Göllner, C Philipp, B Dobner, W Sippl, M Schmidt
Carbohydrate research 344 (13), 1628-1631, 2009
152009
New modified single chained glycolipids. Part 1: synthesis of deoxy and partially O-methylated glycolipids with or without a sulfur containing spacer
M Schmidt, SK Chatterjee, B Dobner, P Nuhn
Chemistry and physics of lipids 114 (2), 139-147, 2002
152002
Identification of PKMYT1 inhibitors by screening the GSK published protein kinase inhibitor set I and II
C Platzer, A Najjar, A Rohe, F Erdmann, W Sippl, M Schmidt
Bioorganic & medicinal chemistry 26 (14), 4014-4024, 2018
142018
Evaluation of potential Myt1 kinase inhibitors by TR-FRET based binding assay
A Rohe, C Göllner, K Wichapong, F Erdmann, GMA Al-Mazaideh, W Sippl, ...
European journal of medicinal chemistry 61, 41-48, 2013
142013
Binding Free Energy (BFE) calculations and Quantitative Structure–Activity Relationship (QSAR) analysis of Schistosoma mansoni histone deacetylase 8 (sm HDAC8) inhibitors
CV Simoben, E Ghazy, P Zeyen, S Darwish, M Schmidt, C Romier, ...
Molecules 26 (9), 2584, 2021
132021
The system can't perform the operation now. Try again later.
Articles 1–20