Manfred Jung

Affiliations: 
Albert-Ludwigs-University Freiburg, Freiburg im Breisgau, Baden-Württemberg, Germany 
Area:
Medicinal Chemistry, Chemical Epigenetics
Website:
http://www.pharmazie.uni-freiburg.de/chemie/german/professoren/akjunghp/
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"Manfred Jung"
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Publications

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Wang S, Barthes NPF, Urban S, et al. (2025) Structure-Guided Design of a KMT9 Inhibitor Prodrug with Cellular Activity. Journal of Medicinal Chemistry
Baumann A, Papenkordt N, Robaa D, et al. (2024) Aromatic Amino Acid Hydroxylases as Off-Targets of Histone Deacetylase Inhibitors. Acs Chemical Neuroscience. 15: 4143-4155
Seitz J, Auth M, Prinz T, et al. (2024) Soft drug inhibitors for the epigenetic targets lysine-specific demethylase 1 and histone deacetylases. Archiv Der Pharmazie. e2400450
Colcerasa A, Friedrich F, Melesina J, et al. (2024) Structure-Activity Studies of 1,2,4-Oxadiazoles for the Inhibition of the NAD-Dependent Lysine Deacylase Sirtuin 2. Journal of Medicinal Chemistry
Wang S, Klein SO, Urban S, et al. (2024) Structure-guided design of a selective inhibitor of the methyltransferase KMT9 with cellular activity. Nature Communications. 15: 43
Abdelsalam M, Zmyslia M, Schmidtkunz K, et al. (2023) Design and synthesis of bioreductive prodrugs of class I histone deacetylase inhibitors and their biological evaluation in virally transfected acute myeloid leukemia cells. Archiv Der Pharmazie. e2300536
Sinatra L, Vogelmann A, Friedrich F, et al. (2023) Development of First-in-Class Dual Sirt2/HDAC6 Inhibitors as Molecular Tools for Dual Inhibition of Tubulin Deacetylation. Journal of Medicinal Chemistry. 66: 14787-14814
Helmi YY, Papenkordt N, Rennar G, et al. (2023) Melatonin-vorinostat hybrid ligands show higher histone deacetylase and cancer cell growth inhibition than vorinostat. Archiv Der Pharmazie. e2300149
Kohr M, Papenkordt N, Jung M, et al. (2023) Total synthesis and biological evaluation of histone deacetylase inhibitor WF-3161. Organic & Biomolecular Chemistry
Darwish S, Heimburg T, Ridinger J, et al. (2022) Synthesis, Biochemical, and Cellular Evaluation of HDAC6 Targeting Proteolysis Targeting Chimeras. Methods in Molecular Biology (Clifton, N.J.). 2589: 179-193
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