Difluoromethyl-1,3,4-oxadiazoles Are Selective, Mechanism-Based, and Essentially Irreversible Inhibitors of Histone Deacetylase <b>6</b>Beate König, Finn K. Hansen, Abigail D. Cragin et al.|Journal of Medicinal Chemistry|2023Cited by 46
Development of Fluorinated Peptoid-Based Histone Deacetylase (HDAC) Inhibitors for Therapy-Resistant Acute LeukemiaNina Reßing, Finn K. Hansen, Julian Schliehe‐Diecks et al.|Journal of Medicinal Chemistry|2022Cited by 32
Exploring Alternative Zinc-Binding Groups in Histone Deacetylase (HDAC) Inhibitors Uncovers <b>DS-103</b> as a Potent Ethylhydrazide-Based HDAC Inhibitor with Chemosensitizing PropertiesDaniel Stopper, Finn K. Hansen, Matthias U. Kassack et al.|Journal of Medicinal Chemistry|2025Cited by 12