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European Journal of Medicinal Chemistry|August 26, 2023
Discovery of potent pyrrolo-pyrimidine and purine HDAC inhibitors for the treatment of advanced prostate cancerDavide Moi, Davide Bonanni, Silvia Belluti, et al.Bioorganic Chemistry|November 20, 2020
Investigation of the effect of different linker chemotypes on the inhibition of histone deacetylases (HDACs)Pasquale Linciano, Rosaria Benedetti, Luca Pinzi, et al.Chemmedchem|July 20, 2019
2-Phenyloxazole-4-carboxamide as a Scaffold for Selective Inhibition of Human Monoamine Oxidase BMaria L Di Paolo, Michael S Christodoulou, Alessandra M Calogero, et al.Pharmaceutical Research|March 8, 2013
Emerging topics in structure-based virtual screeningGiulio RastelliF1000Research|May 10, 2022
On the development of B-Raf inhibitors acting through innovative mechanismsLuca PinziJournal of Enzyme Inhibition and Medicinal Chemistry|September 29, 2021
Inhibitors of histone deacetylase 6 based on a novel 3-hydroxy-isoxazole zinc binding groupPasquale Linciano, Luca Pinzi, Silvia Belluti, et al.ACS Pharmacology & Translational Science|December 14, 2023
Discovery of a Potent Dual Inhibitor of Aromatase and Aldosterone SynthaseAnnachiara Tinivella, Marta Banchi, Guido Gambacorta, et al.Journal of Chemical Information and Modeling|March 15, 2013
Enrichment factor analyses on G-protein coupled receptors with known crystal structureAndrew Anighoro, Giulio RastelliEuropean Journal of Medicinal Chemistry|July 30, 2025
Design, synthesis, and biological evaluation of chalcone derivatives as selective Monoamine Oxidase-B inhibitors with potential neuroprotective effectsGiorgio Facchetti, Sara Marchese, Valentina Coccè, et al.Future Medicinal Chemistry|September 16, 2016
Exploiting computationally derived out-of-the-box protein conformations for drug designFabiana Caporuscio, Giulio RastelliPageof 10