CHIODINI, GIUSEPPE
CHIODINI, GIUSEPPE
Dipartimento di Scienze Farmaceutiche
3-(Benzodioxan-2-ylmethoxy)-2,6-difluorobenzamides bearing hydrophobic substituents at the 7-position of the benzodioxane nucleus potently inhibit methicillin-resistant Sa and Mtb cell division
2016 V. Straniero, M. Pallavicini, G. Chiodini, C. Zanotto, L. Volontè, A. Radaelli, C. Bolchi, L. Fumagalli, M. Sanguinetti, G. Menchinelli, G. Delogu, B. Battah, C. De Giuli Morghen, E. Valoti
Benzodioxane–benzamides as new bacterial cell division inhibitors
2015 G. Chiodini, M. Pallavicini, C. Zanotto, M. Bissa, A. Radaelli, V. Straniero, C. Bolchi, L. Fumagalli, P. Ruggeri, C. De Giuli Morghen, E. Valoti
SYNTHESIS AND DEVELOPMENT OF NEW ANTIBACTERIAL AGENTS INHIBITORS OF FTSZ
2014 G. Chiodini
Farnesyltransferase inhibitors : CAAX mimetics based on different biaryl scaffolds
2014 V. Straniero, M. Pallavicini, G. Chiodini, P. Ruggeri, L. Fumagalli, C. Bolchi, A. Corsini, N. Ferri, C. Ricci, E. Valoti
6‑Methoxy-7-benzofuranoxy and 6‑Methoxy-7-indolyloxy Analogues of 2‑[2-(2,6-Dimethoxyphenoxy)ethyl]aminomethyl-1,4- benzodioxane (WB4101) : 1 Discovery of a Potent and Selective α1D Adrenoceptor Antagonist
2013 L. Fumagalli, M. Pallavicini, R. Budriesi, C. Bolchi, M. Canovi, A. Chiarini, G. Chiodini, M. Gobbi, P. Laurino, M. Micucci, V. Straniero, E. Valoti
Design, synthesis and biological evaluation of peptidomimetic inhibitors of farnesyltransferase
2012 V. Straniero, G. Chiodini, N. Ferri, M. Zagami, M. Pallavicini, E. Valoti
Affinity and activity profiling of unichiral 8-substituted 1,4-benzodioxane analogues of WB4101 reveals a potent and selective α1B-adrenoceptor antagonist
2012 L. Fumagalli, M. Pallavicini, R. Budriesi, M. Gobbi, V. Straniero, M. Zagami, G. Chiodini, C. Bolchi, A. Chiarini, M. Micucci, E. Valoti
Thiazole- and imidazole-containing peptidomimetic inhibitors of protein farnesyltransferase
2011 C. Bolchi, M. Pallavicini, S.K. Bernini, G. Chiodini, A. Corsini, N. Ferri, L. Fumagalli, V. Straniero, E. Valoti