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
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, Lukas Biermann et al.|Journal of Medicinal Chemistry|2025Cited by 12
A Novel Zinc Binding Group for HDAC6 InhibitionAbigail D. Cragin, David W. Christianson, Finn K. Hansen et al.|The FASEB Journal|2022Cited by 11