Publications by authors named "Sara Cesarini"

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Increased Potency and Selectivity for Group III Metabotropic Glutamate Receptor Agonists Binding at Dual sites.
Chelliah Selvam, Isabelle A Lemasson, Isabelle Brabet, Nadia Oueslati, Berin Karaman, Sara Cesarini

J Med Chem· March 2018

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CoMFA and CoMSIA analyses on 1,2,3,4-tetrahydropyrrolo[3,4-b]indole and benzimidazole derivatives as selective CB2 receptor agonists.
Elena Cichero, Sara Cesarini, Luisa Mosti, Paola Fossa

J Mol Model· September 2010

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CoMFA and CoMSIA analyses on 4-oxo-1,4-dihydroquinoline and 4-oxo-1,4-dihydro-1,5-, -1,6- and -1,8-naphthyridine derivatives as selective CB2 receptor agonists.
Elena Cichero, Sara Cesarini, Luisa Mosti, Paola Fossa

J Mol Model· April 2010

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A virtual screening hit reveals new possibilities for developing group III metabotropic glutamate receptor agonists.
Chelliah Selvam, Nadia Oueslati, Isabelle A Lemasson, Isabelle Brabet, Delphine Rigault, Sara Cesarini

J Med Chem· April 2010

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Acylthiocarbamates as non-nucleoside HIV-1 reverse transcriptase inhibitors: docking studies and ligand-based CoMFA and CoMSIA analyses.
Elena Cichero, Sara Cesarini, Andrea Spallarossa, Luisa Mosti, Paola Fossa

J Mol Model· July 2009

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Parallel synthesis of O-phenoxyethyl and O-adamantyl N-acyl thiocarbamates endowed with antiproliferative activity.
Andrea Spallarossa, Sara Cesarini, Silvia Schenone, Angelo Ranise

Arch Pharm (Weinheim)· June 2009

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Thiocarbamates as non-nucleoside HIV-1 reverse transcriptase inhibitors: docking-based CoMFA and CoMSIA analyses.
Elena Cichero, Sara Cesarini, Paola Fossa, Andrea Spallarossa, Luisa Mosti

Eur J Med Chem· May 2009

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Parallel synthesis, molecular modelling and further structure-activity relationship studies of new acylthiocarbamates as potent non-nucleoside HIV-1 reverse transcriptase inhibitors.
Andrea Spallarossa, Sara Cesarini, Angelo Ranise, Silvia Schenone, Olga Bruno

Eur J Med Chem· May 2009

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6-amino-4-oxo-1,3-diphenyl-2-thioxo-1,2,3,4-tetrahydropyrimidine-5-carbonyl derivatives as a new class of potent inhibitors of Interleukin-8-induced neutrophil chemotaxis.
Sara Cesarini, Andrea Spallarossa, Angelo Ranise, Olga Bruno, Nicoletta Arduino

Bioorg Med Chem· May 2009

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Novel modifications in the series of O-(2-phthalimidoethyl)-N-substituted thiocarbamates and their ring-opened congeners as non-nucleoside HIV-1 reverse transcriptase inhibitors.
Andrea Spallarossa, Sara Cesarini, Angelo Ranise, Olga Bruno, Silvia Schenone

Eur J Med Chem· April 2009

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Computational studies of the binding mode and 3D-QSAR analyses of symmetric formimidoester disulfides: a new class of non-nucleoside HIV-1 reverse transcriptase inhibitor.
Elena Cichero, Sara Cesarini, Andrea Spallarossa, Luisa Mosti, Paola Fossa

J Mol Model· April 2009

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N-acylated and N,N'-diacylated imidazolidine-2-thione derivatives and N,N'-diacylated tetrahydropyrimidine-2(1H)-thione analogues: synthesis and antiproliferative activity.
Sara Cesarini, Andrea Spallarossa, Angelo Ranise, Silvia Schenone, Camillo Rosano

Eur J Med Chem· March 2009

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Parallel one-pot synthesis and structure-activity relationship study of symmetric formimidoester disulfides as a novel class of potent non-nucleoside HIV-1 reverse transcriptase inhibitors.
Sara Cesarini, Andrea Spallarossa, Angelo Ranise, Silvia Schenone, Olga Bruno

Bioorg Med Chem· June 2008

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Thiocarbamates as non-nucleoside HIV-1 reverse transcriptase inhibitors. Part 1: Parallel synthesis, molecular modelling and structure-activity relationship studies on O-[2-(hetero)arylethyl]-N-phenylthiocarbamates.
Sara Cesarini, Andrea Spallarossa, Angelo Ranise, Paola Fossa, Paolo La Colla

Bioorg Med Chem· April 2008

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Thiocarbamates as non-nucleoside HIV-1 reverse transcriptase inhibitors. Part 2: Parallel synthesis, molecular modelling and structure-activity relationship studies on analogues of O-(2-phenylethyl)-N-phenylthiocarbamate.
Sara Cesarini, Andrea Spallarossa, Angelo Ranise, Olga Bruno, Paolo La Colla

Bioorg Med Chem· April 2008

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Crystal structures of HIV-1 reverse transcriptase complexes with thiocarbamate non-nucleoside inhibitors.
Andrea Spallarossa, Sara Cesarini, Angelo Ranise, Marco Ponassi, Torsten Unge

Biochem Biophys Res Commun· January 2008

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A novel potent non-nucleoside reverse transcriptase inhibitor acylthiocarbamate derivative with extensive intramolecular pi-pi interactions.
Angelo Mugnoli, Alberto Borassi, Andrea Spallarossa, Sara Cesarini

Acta Crystallogr C· June 2006

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Structure-based design, parallel synthesis, structure-activity relationship, and molecular modeling studies of thiocarbamates, new potent non-nucleoside HIV-1 reverse transcriptase inhibitor isosteres of phenethylthiazolylthiourea derivatives.
Angelo Ranise, Andrea Spallarossa, Sara Cesarini, Francesco Bondavalli, Silvia Schenone

J Med Chem· June 2005

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