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Elisabetta Teodori
Dipartimento di Scienze Farmaceutiche
Università di Firenze
Polo Scientifico
Via U. Schiff 6
Italy
Name/email consistency: high
- N,N-bis(cyclohexanol)amine aryl esters: the discovery of a new class of highly potent inhibitors of transporter-dependent multidrug resistance (MDR). Teodori, E., Dei, S., Martelli, C., Scapecchi, S. Curr. Top. Med. Chem (2010)
- The functions and structure of ABC transporters: implications for the design of new inhibitors of Pgp and MRP1 to control multidrug resistance (MDR). Teodori, E., Dei, S., Martelli, C., Scapecchi, S., Gualtieri, F. Curr. Drug. Targets (2006)
- Exploratory chemistry toward the identification of a new class of multidrug resistance reverters inspired by pervilleine and verapamil models. Teodori, E., Dei, S., Garnier-Suillerot, A., Gualtieri, F., Manetti, D., Martelli, C., Romanelli, M.N., Scapecchi, S., Sudwan, P., Salerno, M. J. Med. Chem. (2005)
- Design, synthesis, and preliminary pharmacological evaluation of 4-aminopiperidine derivatives as N-type calcium channel blockers active on pain and neuropathic pain. Teodori, E., Baldi, E., Dei, S., Gualtieri, F., Romanelli, M.N., Scapecchi, S., Bellucci, C., Ghelardini, C., Matucci, R. J. Med. Chem. (2004)
