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Future Medicinal Chemistry|March 31, 2011
Targeting the DFG-in kinase conformation: a new trend emerging from a patent analysisMauro AngioliniChemistry (Weinheim an Der Bergstrasse, Germany)|February 2, 2002
Conformationally stable and constrained macrocarbocyclic pseudopeptide mimics of beta-hairpin structuresStephen Hanessian, Mauro AngioliniThe Journal of Organic Chemistry|September 13, 2003
Synthesis of functionally diverse and conformationally constrained polycyclic analogues of proline and prolinolStephen Hanessian, Gianluca Papeo, Mauro Angiolini, et al.Pharmaceutical Patent Analyst|November 19, 2013
IP issues facing researchers by Gino D'OcaOrn Almarsson, Mauro Angiolini, Jonathan Baell, et al.Bioorganic & Medicinal Chemistry Letters|July 13, 2010
Structure-based optimization of potent PDK1 inhibitorsMauro Angiolini, Patrizia Banfi, Elena Casale, et al.Bioorganic & Medicinal Chemistry Letters|July 5, 2011
Synthesis and SAR of new pyrazolo[4,3-h]quinazoline-3-carboxamide derivatives as potent and selective MPS1 kinase inhibitorsMarina Caldarelli, Mauro Angiolini, Teresa Disingrini, et al.Journal of Medicinal Chemistry|December 19, 2012
Alkylsulfanyl-1,2,4-triazoles, a new class of allosteric valosine containing protein inhibitors. Synthesis and structure-activity relationshipsPaolo Polucci, Paola Magnaghi, Mauro Angiolini, et al.Pageof 1