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European Journal of Medicinal Chemistry|October 6, 2014
Multidrug resistance (MDR) reversers: High activity and efficacy in a series of asymmetrical N,N-bis(alkanol)amine aryl estersSilvia Dei, Marcella Coronnello, Elisa Floriddia, et al.
Biochemical Pharmacology|March 22, 2016
Carbachol dimers as homobivalent modulators of muscarinic receptorsRosanna Matucci, Marta Nesi, Maria Vittoria Martino, et al.
Journal of Medicinal Chemistry|February 20, 2007
Synthesis, affinity profile, and functional activity of muscarinic antagonists with a 1-methyl-2-(2,2-alkylaryl-1,3-oxathiolan-5-yl)pyrrolidine structureSilvia Dei, Cristina Bellucci, Michela Buccioni, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|September 23, 2003
Synthesis, structure and conformation of partially-modified retro- and retro-inverso psi[NHCH(CF3)]Gly peptidesAlessandro Volonterio, Stefano Bellosta, Fabio Bravin, et al.
Bioorganic & Medicinal Chemistry|December 19, 2012
New structure-activity relationship studies in a series of N,N-bis(cyclohexanol)amine aryl esters as potent reversers of P-glycoprotein-mediated multidrug resistance (MDR)Francesca Orlandi, Marcella Coronnello, Cristina Bellucci, et al.
Journal of Medicinal Chemistry|November 26, 2009
Synthesis, affinity profile and functional activity of potent chiral muscarinic antagonists with a pyrrolidinylfuran structureSerena Scapecchi, Marta Nesi, Rosanna Matucci, et al.
European Journal of Pharmacology|June 14, 2020
Carbachol dimers with primary carbamate groups as homobivalent modulators of muscarinic receptorsRosanna Matucci, Cristina Bellucci, Maria Vittoria Martino, et al.
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