Markus Schweipert
University Of Applied Sciences Darmstadt Haardtring 100 64295 Darmstadt Germany
Darmstadt, HE 64295, Germany
Darmstadt, HE 64295, Germany
Last Updated: 09/26/2026
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Found 20 publications
Exploration of non-hydroxamate based quinoline analogues as HDAC8 inhibitors.
Journal: RSC advances
Published: July 09, 2026
Novel Azaborine-Based Inhibitors of Histone Deacetylases (HDACs).
Journal: Molecules (Basel, Switzerland)
Published: September 05, 2025
Targeted HDAC8 inhibition with non-hydroxamate [1,2,4]triazolo[4,3-a] quinoline compounds.
Journal: Scientific reports
Published: April 04, 2025
The pivotal role of histidine 976 in human histone deacetylase 4 for enzyme function and ligand recognition.
Journal: Bioorganic chemistry
Published: August 16, 2024
Design and synthesis of peptides as stabilizers of histone deacetylase 4.
Journal: Journal of peptide science : an official publication of the European Peptide Society
Published: December 23, 2023
The catalytic domain of free or ligand bound histone deacetylase 4 occurs in solution predominantly in closed conformation.
Journal: Protein science : a publication of the Protein Society
Published: November 09, 2023
Design, Synthesis, and Biological Evaluation of Novel Quinazolin-4(3H)-One-Based Histone Deacetylase 6 (HDAC6) Inhibitors for Anticancer Activity.
Journal: International journal of molecular sciences
Published: May 23, 2023
Continuous enzyme activity assay for high-throughput classification of histone deacetylase 8 inhibitors.
Journal: Exploration of targeted anti-tumor therapy
Published: January 13, 2023
Synthesis and Characterization of Reversible Covalent HDAC4 Inhibitors.
Journal: Methods in molecular biology (Clifton, N.J.)
Published: October 18, 2022
3-Chloro-5-Substituted-1,2,4-Thiadiazoles (TDZs) as Selective and Efficient Protein Thiol Modifiers.
3-Chloro-5-Substituted-1,2,4-Thiadiazoles (TDZs) as Selective and Efficient Protein Thiol Modifiers.
Journal: Chembiochem : a European journal of chemical biology
Published: July 21, 2022
Synthesis and HDAC inhibitory activity of pyrimidine-based hydroxamic acids.
Journal: Beilstein journal of organic chemistry
Published: April 14, 2022
Development and investigation of thiazolidinedione and pyrazoline compounds as antiangiogenic weapons targeting VEGFR-2.
Journal: Future medicinal chemistry
Published: September 28, 2021
Last Updated: 09/26/2026