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International Journal of Molecular Sciences|March 24, 2019
Synthesis of New GABA<sub>A</sub> Receptor Modulator with Pyrazolo[1,5-a]quinazoline (PQ) ScaffoldGabriella Guerrini, Claudia Vergelli, Niccolò Cantini, et al.Journal of Enzyme Inhibition and Medicinal Chemistry|March 21, 2015
Pyrazolo[1,5-a]quinazoline scaffold as 5-deaza analogue of pyrazolo[5,1-c][1,2,4]benzotriazine system: synthesis of new derivatives, biological activity on GABAA receptor subtype and molecular dynamic studyGabriella Guerrini, Giovanna Ciciani, Samuele Ciattini, et al.Journal of Medicinal Chemistry|August 18, 2006
Novel pyrazolopyrimidopyridazinones with potent and selective phosphodiesterase 5 (PDE5) inhibitory activity as potential agents for treatment of erectile dysfunctionMaria Paola Giovannoni, Claudia Vergelli, Claudio Biancalani, et al.Journal of Medicinal Chemistry|July 17, 2007
4-amino-5-substituted-3(2H)-pyridazinones as orally active antinociceptive agents: synthesis and studies on the mechanism of actionMaria Paola Giovannoni, Nicoletta Cesari, Claudia Vergelli, et al.Journal of Medicinal Chemistry|December 22, 2006
Arylpiperazinylalkylpyridazinones and analogues as potent and orally active antinociceptive agents: synthesis and studies on mechanism of actionNicoletta Cesari, Claudio Biancalani, Claudia Vergelli, et al.Archiv Der Pharmazie|February 22, 2003
Novel 3-arylamino- and 3-cycloalkylamino-5, 6-diphenyl-pyridazines active as ACAT inhibitorsLucio Toma, Maria Paola Giovannoni, Claudia Vergelli, et al.Frontiers in Chemistry|October 9, 2020
Novel Sulfonamide Analogs of Sivelestat as Potent Human Neutrophil Elastase InhibitorsLetizia Crocetti, Maria Paola Giovannoni, Niccolò Cantini, et al.Archiv Der Pharmazie|July 30, 2023
Optimization of 4-amino-pyridazin-3(2H)-one as a valid core scaffold for FABP4 inhibitorsGiuseppe Floresta, Letizia Crocetti, Renan Rodrigues de Oliveira Silva, et al.Bioorganic & Medicinal Chemistry|September 13, 2015
Synthesis of five and six-membered heterocycles bearing an arylpiperazinylalkyl side chain as orally active antinociceptive agentsClaudia Vergelli, Giovanna Ciciani, Agostino Cilibrizzi, et al.Bioorganic & Medicinal Chemistry|June 6, 2007
4-Amino-5-vinyl-3(2H)-pyridazinones and analogues as potent antinociceptive agents: Synthesis, SARs, and preliminary studies on the mechanism of actionClaudia Vergelli, Maria Paola Giovannoni, Stefano Pieretti, et al.Pageof 6