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Chemmedchem|October 13, 2011
N-[2-Methyl-5-(triazol-1-yl)phenyl]pyrimidin-2-amine as a scaffold for the synthesis of inhibitors of Bcr-AblFederica Arioli, Stella Borrelli, Francesco Colombo, et al.
Cell Chemical Biology|May 15, 2018
Pharmacological Inhibition of the Ubiquitin Ligase RNF5 Rescues F508del-CFTR in Cystic Fibrosis Airway EpitheliaElvira Sondo, Federico Falchi, Emanuela Caci, et al.
Bioorganic & Medicinal Chemistry Letters|May 25, 2015
From AChE to BACE1 inhibitors: The role of the amine on the indanone scaffoldAngela Rampa, Francesca Mancini, Angela De Simone, et al.
Chemmedchem|October 29, 2015
Multitarget Strategy to Address Alzheimer's Disease: Design, Synthesis, Biological Evaluation, and Computational Studies of Coumarin-Based DerivativesSerena Montanari, Manuela Bartolini, Paolo Neviani, et al.
International Journal of Molecular Sciences|August 3, 2019
Structure-Based Virtual Screening Allows the Identification of Efficient Modulators of E-Cadherin-Mediated Cell-Cell AdhesionAndrea Dalle Vedove, Federico Falchi, Stefano Donini, et al.
Chemmedchem|July 2, 2013
Identification of Hck inhibitors as hits for the development of antileukemia and anti-HIV agentsCristina Tintori, Ilaria Laurenzana, Francesco La Rocca, et al.
ACS Medicinal Chemistry Letters|February 18, 2026
Targeting RAD51-BRCA2 Interaction to Enhance Synthetic Lethality with Olaparib in Pancreatic Cancer: Development of a Novel Phenyl Furan-Quinoline-Carboxylic Acid SeriesGiovanni Ferrandi, Greta Bagnolini, Laura Poppi, et al.
ACS Chemical Biology|August 26, 2017
Synthetic Lethality Triggered by Combining Olaparib with BRCA2-Rad51 DisruptorsFederico Falchi, Elisa Giacomini, Tiziana Masini, et al.
Journal of Medicinal Chemistry|August 8, 2025
Exploration of the Neuromodulatory Properties of Fyn and GSK-3β Kinases Exploiting 7-Azaindole-Based InhibitorsGiambattista Marotta, Francesca Massenzio, Jose Ortega, et al.
Journal of Medicinal Chemistry|July 13, 2023
Innovative Strategy toward Mutant CFTR Rescue in Cystic Fibrosis: Design and Synthesis of Thiadiazole Inhibitors of the E3 Ligase RNF5Irene Brusa, Elvira Sondo, Emanuela Pesce, et al.
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