24 results on '"Schweipert, Markus"'
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2. Design, synthesis, and biological evaluation of tetrahydroisoquinoline based hydroxamate derivatives as HDAC 6 inhibitors for cancer therapy
3. Synthesis and Characterization of Reversible Covalent HDAC4 Inhibitors
4. Design and synthesis of peptides as stabilizers of histone deacetylase 4
5. Double-edged Swords: Diaryl pyrazoline thiazolidinediones synchronously targeting cancer epigenetics and angiogenesis
6. The catalytic domain of free or ligand bound histone deacetylase 4 occurs in solution predominantly in closed conformation
7. The catalytic domain of free or ligand bound histone deacetylase 4 occurs in solution predominantly in closed conformation
8. Design, Synthesis, and Biological Evaluation of Novel Quinazolin-4(3H)-one-Based Histone Deacetylase 6 (HDAC6) Inhibitors for Anticancer Activity
9. Continuous enzyme activity assay for high-throughput classification of histone deacetylase 8 inhibitors
10. 3‐Chloro‐5‐Substituted‐1,2,4‐Thiadiazoles (TDZs) as Selective and Efficient Protein Thiol Modifiers
11. Synthesis and HDAC inhibitory activity of pyrimidine-based hydroxamic acids
12. Mechanistic Insights into Binding of Ligands with Thiazolidinedione Warhead to Human Histone Deacetylase 4
13. Development and investigation of thiazolidinedione and pyrazoline compounds as antiangiogenic weapons targeting VEGFR-2
14. HDAC4 Inhibitors with Cyclic Linker and Non‐hydroxamate Zinc Binding Group: Design, Synthesis, HDAC Screening and in vitro Cytotoxicity evaluation.
15. Thiazolidinedione “Magic Bullets” Simultaneously Targeting PPARγ and HDACs: Design, Synthesis, and Investigations of their In Vitro and In Vivo Antitumor Effects
16. Multi-target weapons: diaryl-pyrazoline thiazolidinediones simultaneously targeting VEGFR-2 and HDAC cancer hallmarks
17. Permuted 2,4-thiazolidinedione (TZD) analogs as GLUT inhibitors and their in-vitro evaluation in leukemic cells
18. Discovery of novel N-substituted thiazolidinediones (TZDs) as HDAC8 inhibitors: in-silico studies, synthesis, and biological evaluation
19. Discovery of 5-naphthylidene-2,4-thiazolidinedione derivatives as selective HDAC8 inhibitors and evaluation of their cytotoxic effects in leukemic cell lines
20. Kinetically selective and potent inhibitors of HDAC8
21. Multi-target weapons: diaryl-pyrazoline thiazolidinediones simultaneously targeting VEGFR-2 and HDAC cancer hallmarksElectronic supplementary information (ESI) available. See DOI: 10.1039/d1md00125f
22. Kinetically selective and potent inhibitors of HDAC8.
23. Thiazolidinedione “Magic Bullets” Simultaneously Targeting PPARγ and HDACs: Design, Synthesis, and Investigations of their In Vitroand In VivoAntitumor Effects
24. Synthesis and Characterization of Reversible Covalent HDAC4 Inhibitors.
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