Teodori E - Search Results

1

MRP1-dependent Collateral Sensitivity of Multidrug-resistant Cancer Cells: Identifying Selective Modulators Inducing Cellular Glutathione Depletion.

Lorendeau D, Dury L, Nasr R, Boumendjel A, Teodori E, Gutschow M, Falson P, Di Pietro A, Baubichon-Cortay H. Lorendeau D, et al. Among authors: teodori e. Curr Med Chem. 2017;24(12):1186-1213. doi: 10.2174/0929867324666161118130238. Curr Med Chem. 2017. PMID: 27855620 Review.

2

Diphenylcyclohexylamine derivatives as new potent multidrug resistance (MDR) modulators.

Dei S, Budriesi R, Sudwan P, Ferraroni M, Chiarini A, Garnier-Suillerot A, Manetti D, Martelli C, Scapecchi S, Teodori E. Dei S, et al. Among authors: teodori e. Bioorg Med Chem. 2005 Feb 15;13(4):985-98. doi: 10.1016/j.bmc.2004.11.043. Bioorg Med Chem. 2005. PMID: 15670906

3

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 MN, Scapecchi S, Sudwan P, Salerno M. Teodori E, et al. J Med Chem. 2005 Nov 17;48(23):7426-36. doi: 10.1021/jm050542x. J Med Chem. 2005. PMID: 16279802

4

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. Teodori E, et al. Curr Drug Targets. 2006 Jul;7(7):893-909. doi: 10.2174/138945006777709520. Curr Drug Targets. 2006. PMID: 16842220 Review.

5

Isomeric N,N-bis(cyclohexanol)amine aryl esters: the discovery of a new class of highly potent P-glycoprotein (Pgp)-dependent multidrug resistance (MDR) inhibitors.

Teodori E, Martelli C, Salerno M, Darghal N, Dei S, Garnier-Suillerot A, Gualtieri F, Manetti D, Scapecchi S, Romanelli MN. Teodori E, et al. J Med Chem. 2007 Feb 22;50(4):599-602. doi: 10.1021/jm0614432. Epub 2007 Jan 26. J Med Chem. 2007. PMID: 17256837

6

N,N-bis(cyclohexanol)amine aryl esters: a new class of highly potent transporter-dependent multidrug resistance inhibitors.

Martelli C, Alderighi D, Coronnello M, Dei S, Frosini M, Le Bozec B, Manetti D, Neri A, Romanelli MN, Salerno M, Scapecchi S, Mini E, Sgaragli G, Teodori E. Martelli C, et al. Among authors: teodori e. J Med Chem. 2009 Feb 12;52(3):807-17. doi: 10.1021/jm8012745. J Med Chem. 2009. PMID: 19140665

7

Structure-activity relationships studies in a series of N,N-bis(alkanol)amine aryl esters as P-glycoprotein (Pgp) dependent multidrug resistance (MDR) inhibitors.

Martelli C, Coronnello M, Dei S, Manetti D, Orlandi F, Scapecchi S, Novella Romanelli M, Salerno M, Mini E, Teodori E. Martelli C, et al. Among authors: teodori e. J Med Chem. 2010 Feb 25;53(4):1755-62. doi: 10.1021/jm9016174. J Med Chem. 2010. PMID: 20104851

8

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. Teodori E, et al. Curr Top Med Chem. 2010;10(17):1715-31. doi: 10.2174/156802610792928031. Curr Top Med Chem. 2010. PMID: 20645921 Review.

9

Design, synthesis, and preliminary biological evaluation of new isoform-selective f-current blockers.

Melchiorre M, Del Lungo M, Guandalini L, Martini E, Dei S, Manetti D, Scapecchi S, Teodori E, Sartiani L, Mugelli A, Cerbai E, Romanelli MN. Melchiorre M, et al. Among authors: teodori e. J Med Chem. 2010 Sep 23;53(18):6773-7. doi: 10.1021/jm1006758. J Med Chem. 2010. PMID: 20795648

10

Inhibition of P-glycoprotein-mediated Multidrug Resistance (MDR) by N,N-bis(cyclohexanol)amine aryl esters: further restriction of molecular flexibility maintains high potency and efficacy.

Martelli C, Dei S, Lambert C, Manetti D, Orlandi F, Romanelli MN, Scapecchi S, Salerno M, Teodori E. Martelli C, et al. Among authors: teodori e. Bioorg Med Chem Lett. 2011 Jan 1;21(1):106-9. doi: 10.1016/j.bmcl.2010.11.059. Epub 2010 Nov 20. Bioorg Med Chem Lett. 2011. PMID: 21145739

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