E. Cellupica

Novel Benzohydroxamate-based Potent and Selective Histone Deacetylase 6 (HDAC6) Inhibitors Bearing a Pentaheterocyclic Scaffold: Design, Synthesis and Biological Evaluation.

C. Ripamonti, B. Vergani, E. Galbiati, 2019, Journal of medicinal chemistry.

Vinca alkaloids and analogues as anti-cancer agents: Looking back, peering ahead.

S. Collina, A. Siciliano, Marta Rui, 2018, Bioorganic & medicinal chemistry letters.

Difluoromethyl-1,3,4-oxadiazoles are slow-binding substrate analog inhibitors of histone deacetylase 6 with unprecedented isotype selectivity

B. Vergani, C. Steinkühler, G. Fossati, 2022, The Journal of biological chemistry.

The Importance of the "Time Factor" for the Evaluation of Inhibition Mechanisms: The Case of Selected HDAC6 Inhibitors.

B. Vergani, C. Steinkühler, G. Fossati, 2023, Biology.