Publications by authors named "Simone Lorenzi"

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Use of experimental design to optimize docking performance: the case of LiGenDock, the docking module of LiGen, a new de novo design program.
Claudia Beato, Andrea R Beccari, Carlo Cavazzoni, Simone Lorenzi, Gabriele Costantino

J Chem Inf Model· June 2013

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Biological and biophysical properties of the histone deacetylase inhibitor suberoylanilide hydroxamic acid are affected by the presence of short alkyl groups on the phenyl ring.
Frédérik Oger, Aurélien Lecorgne, Elisa Sala, Vanessa Nardese, Florence Demay, Simone Lorenzi

J Med Chem· March 2010

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Synthesis, enantiomeric resolution, and structure-activity relationship study of a series of 10,11-dihydro-5H-dibenzo[a,d]cycloheptene MT2 receptor antagonists.
Gilberto Spadoni, Annalida Bedini, Giuseppe Diamantini, Giorgio Tarzia, Silvia Rivara, Simone Lorenzi

ChemMedChem· December 2007

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Design and synthesis of N-(3,3-diphenylpropenyl)alkanamides as a novel class of high-affinity MT2-selective melatonin receptor ligands.
Annalida Bedini, Gilberto Spadoni, Giuseppe Gatti, Simone Lucarini, Giorgio Tarzia, Simone Lorenzi

J Med Chem· December 2006

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Dibasic non-imidazole histamine H3 receptor antagonists with a rigid biphenyl scaffold.
Giovanni Morini, Mara Comini, Mirko Rivara, Silvia Rivara, Simone Lorenzi

Bioorg Med Chem Lett· August 2006

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Application of 3D-QSAR in the rational design of receptor ligands and enzyme inhibitors.
Marco Mor, Silvia Rivara, Alessio Lodola, Simone Lorenzi, Fabrizio Bordi

Chem Biodivers· November 2005

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Validation of a histamine H3 receptor model through structure-activity relationships for classical H3 antagonists.
Simone Lorenzi, Marco Mor, Fabrizio Bordi, Silvia Rivara, Mirko Rivara

Bioorg Med Chem· October 2005

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Analysis of structure-activity relationships for MT2 selective antagonists by melatonin MT1 and MT2 receptor models.
Silvia Rivara, Simone Lorenzi, Marco Mor, Pier Vincenzo Plazzi, Gilberto Spadoni

J Med Chem· June 2005

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