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Sara Cesarini

Research Profile

Chemicals & Drugs

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HIV-1

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Publications

TOP 3
Elena Cichero; Sara Cesarini; Luisa Mosti; Paola Fossa
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
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; Andrea Spallarossa; Luisa Mosti; Paola Fossa
Acylthiocarbamates as non-nucleoside HIV-1 reverse transcriptase inhibitors: docking studies and ligand-based CoMFA and CoMSIA analyses.

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All Publications

2010: Elena Cichero; Sara Cesarini; Luisa Mosti; Paola Fossa
CoMFA and CoMSIA analyses on 1,2,3,4-tetrahydropyrrolo[3,4-b]indole and benzimidazole derivatives as selective CB2 receptor agonists.
Journal of molecular modeling 2010;16(9):1481-98.
2010: Elena Cichero; Sara Cesarini; Luisa Mosti; Paola Fossa
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.
Journal of molecular modeling 2010;16(4):677-91.
2009: Elena Cichero; Sara Cesarini; Andrea Spallarossa; Luisa Mosti; Paola Fossa
Acylthiocarbamates as non-nucleoside HIV-1 reverse transcriptase inhibitors: docking studies and ligand-based CoMFA and CoMSIA analyses.
Journal of molecular modeling 2009;15(7):871-84.
2009: Andrea Spallarossa; Sara Cesarini; Silvia Schenone; Angelo Ranise
Parallel synthesis of O-phenoxyethyl and O-adamantyl N-acyl thiocarbamates endowed with antiproliferative activity.
Archiv der Pharmazie 2009;342(6):344-52.
2009: Sara Cesarini; Andrea Spallarossa; Angelo Ranise; Olga Bruno; Nicoletta Arduino; Maria Bertolotto; Franco Dallegri; Massimiliano Tognolini; Thomas Gobbetti; Elisabetta Barocelli
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.
Bioorganic & medicinal chemistry 2009;17(10):3580-7.
2009: Andrea Spallarossa; Sara Cesarini; Angelo Ranise; Silvia Schenone; Olga Bruno; Alberto Borassi; Paolo La Colla; Margherita Pezzullo; Giuseppina Sanna; Gabriella Collu; Barbara Secci; Roberta Loddo
Parallel synthesis, molecular modelling and further structure-activity relationship studies of new acylthiocarbamates as potent non-nucleoside HIV-1 reverse transcriptase inhibitors.
European journal of medicinal chemistry 2009;44(5):2190-201.
2009: Elena Cichero; Sara Cesarini; Paola Fossa; Andrea Spallarossa; Luisa Mosti
Thiocarbamates as non-nucleoside HIV-1 reverse transcriptase inhibitors: docking-based CoMFA and CoMSIA analyses.
European journal of medicinal chemistry 2009;44(5):2059-70.
2009: Elena Cichero; Sara Cesarini; Andrea Spallarossa; Luisa Mosti; Paola Fossa
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.
Journal of molecular modeling 2009;15(4):357-67.
2009: Andrea Spallarossa; Sara Cesarini; Angelo Ranise; Olga Bruno; Silvia Schenone; Paolo La Colla; Gabriella Collu; Giuseppina Sanna; Barbara Secci; Roberta Loddo
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.
European journal of medicinal chemistry 2009;44(4):1650-63.
2009: Sara Cesarini; Andrea Spallarossa; Angelo Ranise; Silvia Schenone; Camillo Rosano; Paolo La Colla; Giuseppina Sanna; Bernardetta Busonera; Roberta Loddo
N-acylated and N,N'-diacylated imidazolidine-2-thione derivatives and N,N'-diacylated tetrahydropyrimidine-2(1H)-thione analogues: synthesis and antiproliferative activity.
European journal of medicinal chemistry 2009;44(3):1106-18.
2008: Sara Cesarini; Andrea Spallarossa; Angelo Ranise; Silvia Schenone; Olga Bruno; Paolo La Colla; Laura Casula; Gabriella Collu; Giuseppina Sanna; Roberta Loddo
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.
Bioorganic & medicinal chemistry 2008;16(12):6353-63.
2008: Sara Cesarini; Andrea Spallarossa; Angelo Ranise; Olga Bruno; Paolo La Colla; Barbara Secci; Gabriella Collu; Roberta Loddo
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.
Bioorganic & medicinal chemistry 2008;16(7):4173-85.
2008: Sara Cesarini; Andrea Spallarossa; Angelo Ranise; Paola Fossa; Paolo La Colla; Giuseppina Sanna; Gabriella Collu; Roberta Loddo
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.
Bioorganic & medicinal chemistry 2008;16(7):4160-72.
2008: Andrea Spallarossa; Sara Cesarini; Angelo Ranise; Marco Ponassi; Torsten Unge; Martino Bolognesi
Crystal structures of HIV-1 reverse transcriptase complexes with thiocarbamate non-nucleoside inhibitors.
Biochemical and biophysical research communications 2008;365(4):764-70.
2006: Angelo Mugnoli; Alberto Borassi; Andrea Spallarossa; Sara Cesarini
A novel potent non-nucleoside reverse transcriptase inhibitor acylthiocarbamate derivative with extensive intramolecular pi-pi interactions.
Acta crystallographica. Section C, Crystal structure communications 2006;62(Pt 6):o315-7.
2005: Angelo Ranise; Andrea Spallarossa; Sara Cesarini; Francesco Bondavalli; Silvia Schenone; Olga Bruno; Giulia Menozzi; Paola Fossa; Luisa Mosti; Massimiliano La Colla; Giuseppina Sanna; Marta Murreddu; Gabriella Collu; Bernardetta Busonera; Maria Elena Marongiu; Alessandra Pani; Paolo La Colla; Roberta Loddo
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.
Journal of medicinal chemistry 2005;48(11):3858-73.