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Journal of Chemical Information and Modeling|October 8, 2014
Combining ligand- and structure-based approaches for the discovery of new inhibitors of the EPHA2-ephrin-A1 interactionDaniele Pala, Riccardo Castelli, Matteo Incerti, et al.Journal of Medicinal Chemistry|December 23, 2016
Metadynamics for Perspective Drug Design: Computationally Driven Synthesis of New Protein-Protein Interaction Inhibitors Targeting the EphA2 ReceptorMatteo Incerti, Simonetta Russo, Donatella Callegari, et al.Langmuir : the ACS Journal of Surfaces and Colloids|March 23, 2011
Adlayers of dimannoside thiols on gold: surface chemical analysisPaul M Dietrich, Tim Horlacher, Pierre-Luc Girard-Lauriault, et al.European Journal of Medicinal Chemistry|September 23, 2022
2-Arylmelatonin analogues: Probing the 2-phenyl binding pocket of melatonin MT1 and MT2 receptorsMichele Mari, Gian Marco Elisi, Annalida Bedini, et al.European Journal of Medicinal Chemistry|January 31, 2020
Optimization of EphA2 antagonists based on a lithocholic acid core led to the identification of UniPR505, a new 3α-carbamoyloxy derivative with antiangiogenetic propertiesMatteo Incerti, Simonetta Russo, Miriam Corrado, et al.Journal of Chemical Information and Modeling|November 1, 2023
Molecular Determinants of EphA2 and EphB2 Antagonism Enable the Design of Ligands with Improved SelectivityLorenzo Guidetti, Alfonso Zappia, Laura Scalvini, et al.Frontiers in Pharmacology|July 13, 2019
Targeting the Eph/Ephrin System as Anti-Inflammatory Strategy in IBDAndrea Grandi, Irene Zini, Simone Palese, et al.Molecules (Basel, Switzerland)|October 25, 2013
Synthesis and structure-activity relationships of amino acid conjugates of cholanic acid as antagonists of the EphA2 receptorSimonetta Russo, Matteo Incerti, Massimiliano Tognolini, et al.European Journal of Medicinal Chemistry|May 18, 2021
Chemical modification of NSC12 leads to a specific FGF-trap with antitumor activity in multiple myelomaRiccardo Castelli, Sara Taranto, Lucia Furiassi, et al.European Journal of Medicinal Chemistry|August 31, 2021
A sulfonyl fluoride derivative inhibits EGFRL858R/T790M/C797S by covalent modification of the catalytic lysineFrancesca Ferlenghi, Laura Scalvini, Federica Vacondio, et al.Pageof 6