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Journal of Medicinal Chemistry|February 19, 2016
Development and Pharmacological Characterization of Selective Blockers of 2-Arachidonoyl Glycerol Degradation with Efficacy in Rodent Models of Multiple Sclerosis and PainMargherita Brindisi, Samuele Maramai, Sandra Gemma, et al.Journal of Medicinal Chemistry|January 19, 2024
Development of Potent and Selective Monoacylglycerol Lipase Inhibitors. SARs, Structural Analysis, and Biological CharacterizationStefania Butini, Uwe Grether, Kwang-Mook Jung, et al.Molecules (Basel, Switzerland)|July 3, 2019
Breakthroughs in Medicinal Chemistry: New Targets and Mechanisms, New Drugs, New Hopes-5Arduino A Mangoni, Jean Jacques Vanden Eynde, Josef Jampilek, et al.Journal of Medicinal Chemistry|July 4, 2024
Targeting Relevant HDACs to Support the Survival of Cone Photoreceptors in Inherited Retinal Diseases: Identification of a Potent Pharmacological Tool with In Vitro and In Vivo EfficacyGabriele Carullo, Noemi Orsini, Ilaria Piano, et al.ACS Medicinal Chemistry Letters|November 20, 2020
Spiroindoline-Capped Selective HDAC6 Inhibitors: Design, Synthesis, Structural Analysis, and Biological EvaluationA Prasanth Saraswati, Nicola Relitti, Margherita Brindisi, et al.European Journal of Medicinal Chemistry|November 19, 2018
Structure-activity relationships, biological evaluation and structural studies of novel pyrrolonaphthoxazepines as antitumor agentsMargherita Brindisi, Cristina Ulivieri, Gloria Alfano, et al.European Journal of Medicinal Chemistry|May 13, 2022
Azetidin-2-one-based small molecules as dual hHDAC6/HDAC8 inhibitors: Investigation of their mechanism of action and impact of dual inhibition profile on cell viabilityStefano Federico, Tuhina Khan, Anna Fontana, et al.European Journal of Medicinal Chemistry|March 28, 2022
Design and synthesis of multifunctional microtubule targeting agents endowed with dual pro-apoptotic and anti-autophagic efficacyGiuseppe Campiani, Tuhina Khan, Cristina Ulivieri, et al.Journal of Medicinal Chemistry|July 12, 2021
Harnessing the Role of HDAC6 in Idiopathic Pulmonary Fibrosis: Design, Synthesis, Structural Analysis, and Biological Evaluation of Potent InhibitorsGiuseppe Campiani, Caterina Cavella, Jeremy D Osko, et al.Molecules (Basel, Switzerland)|January 8, 2020
Breakthroughs in Medicinal Chemistry: New Targets and Mechanisms, New Drugs, New Hopes-6Jean Jacques Vanden Eynde, Arduino A Mangoni, Jarkko Rautio, et al.Pageof 15