Melatonin Receptor Agonists: New Options for Insomnia and Depression TreatmentSPADONI, Gilberto; BEDINI, Annalida; RIVARA, Silvia et al.CNS neuroscience & therapeutics (Print). 2011, Vol 17, Num 6, pp 733-741, issn 1755-5930, 9 p.Article

N-(Substituted-anilinoethyl)amides : Design, Synthesis, and Pharmacological Characterization of a New Class of Melatonin Receptor LigandsRIVARA, Silvia; LODOLA, Alessio; GOBBI, Gabriella et al.Journal of medicinal chemistry (Print). 2007, Vol 50, Num 26, pp 6618-6626, issn 0022-2623, 9 p.Article

Synthesis and biological evaluation of new non-imidazole H₃-receptor antagonists of the 2-aminobenzimidazole seriesRIVARA, Mirko; ZULIANI, Valentina; BERTONI, Simona et al.Bioorganic & medicinal chemistry. 2006, Vol 14, Num 5, pp 1413-1424, issn 0968-0896, 12 p.Article

Validation of a histamine H₃ receptor model through structure-activity relationships for classical H₃ antagonistsLORENZI, Simone; MOR, Marco; BORDI, Fabrizio et al.Bioorganic & medicinal chemistry. 2005, Vol 13, Num 19, pp 5647-5657, issn 0968-0896, 11 p.Article

Tandem mass spectrometric data-FAAH inhibitory activity relationships of some carbamic acid O-aryl estersBASSO, Elisa; DURANTI, Andrea; MOR, Marco et al.Journal of mass spectrometry. 2004, Vol 39, Num 12, pp 1450-1455, issn 1076-5174, 6 p.Conference Paper

Structure-Based Virtual Screening of MT₂ Melatonin Receptor: Influence of Template Choice and Structural RefinementPALA, Daniele; BEUMING, Thijs; SHERMAN, Woody et al.Journal of chemical information and modeling. 2013, Vol 53, Num 4, pp 821-835, issn 1549-9596, 15 p.Article

Liquid chromatography-mass spectrometric method for determination of the non-imidazole H₃-receptor antagonist UPR1056 in rat plasmaVACONDIO, Federica; SILVA, Claudia; MORINI, Giovanni et al.Journal of separation science (Print). 2011, Vol 34, Num 14, pp 1656-1663, issn 1615-9306, 8 p.Article

Antidepressant-like activity of the fatty acid amide hydrolase inhibitor URB597 in a rat model of chronic mild stressBORTOLATO, Marco; MANGIERI, Regina A; JIN FU et al.Biological psychiatry (1969). 2007, Vol 62, Num 10, pp 1103-1110, issn 0006-3223, 8 p.Article

Synthesis, antioxidant activity and structure-activity relationships for a new series of 2-(N-acylaminoethyl)indoles with melatonin-like cytoprotective activitySPADONI, Gilberto; DIAMANTINI, Giuseppe; FRANCESCHINI, Davide et al.Journal of pineal research. 2006, Vol 40, Num 3, pp 259-269, issn 0742-3098, 11 p.Article

Synthesis and three-dimensional quantitative structure-activity relationship analysis of H₃ receptor antagonists containing a neutral heterocyclic polar groupRIVARA, Silvia; MOR, Marco; BORDI, Fabrizio et al.Drug design and discovery (Print). 2003, Vol 18, Num 2-3, pp 65-79, issn 1055-9612, 15 p.Article

Dibasic biphenyl H3 receptor antagonists: Steric tolerance for a lipophilic side chainBORDI, Fabrizio; RIVARA, Silvia; BAROCELLI, Elisabetta et al.European journal of medicinal chemistry. 2012, Vol 48, pp 214-230, issn 0223-5234, 17 p.Article

5-Benzylidene-hydantoins: Synthesis and antiproliferative activity on A549 lung cancer cell lineZULIANI, Valentina; CARMI, Caterina; ALFIERI, Roberta R et al.European journal of medicinal chemistry. 2009, Vol 44, Num 9, pp 3471-3479, issn 0223-5234, 9 p.Article

Development and validation of a LC-MS method with electrospray ionization for the determination of the imidazole H₃ antagonist ROS203 in rat plasmaVACONDIO, Federica; SILVA, Claudia; FIONI, Alessandro et al.Journal of pharmaceutical and biomedical analysis. 2008, Vol 46, Num 1, pp 200-205, issn 0731-7085, 6 p.Article

Cyclohexylcarbamic acid 3'- or 4'-substituted biphenyl-3-yl esters as fatty acid amide hydrolase inhibitors: Synthesis, quantitative structure-activity relationships, and molecular modeling studiesMOR, Marco; RIVARA, Silvia; LODOLA, Alessio et al.Journal of medicinal chemistry (Print). 2004, Vol 47, Num 21, pp 4998-5008, issn 0022-2623, 11 p.Article

Synthesis and structure-activity relationships of a series of pyrrole cannabinoid receptor agonistsTARZIA, Giorgio; DURANTI, Andrea; TONTINI, Andrea et al.Bioorganic & medicinal chemistry. 2003, Vol 11, Num 18, pp 3965-3973, issn 0968-0896, 9 p.Article

2-N-acylaminoalkylindoles: Design and quantitative structure-activity relationship studies leading to MT₂-Selective melatonin antagonistsSPADONI, Gilberto; BALSAMINI, Cesarino; PANNACCI, Marilou et al.Journal of medicinal chemistry (Print). 2001, Vol 44, Num 18, pp 2900-2912, issn 0022-2623Article

Epidermal Growth Factor Receptor Tyrosine Kinase Inhibitors: Current Status and Future Perspectives in the Development of Novel Irreversible Inhibitors for the Treatment of Mutant Non-small Cell Lung CancerGALVANI, Elena; ALFIERI, Roberta; PETERS, Godefridus J et al.Current pharmaceutical design (Print). 2013, Vol 19, Num 5, pp 818-832, issn 1381-6128, 15 p.Article

Biphenyl-3-yl alkylcarbamates as fatty acid amide hydrolase (FAAH) inhibitors: Steric effects of N-alkyl chain on rat plasma and liver stabilityVACONDIO, Federica; SILVA, Claudia; TARZIA, Giorgio et al.European journal of medicinal chemistry. 2011, Vol 46, Num 9, pp 4466-4473, issn 0223-5234, 8 p.Article

Bivalent ligand approach on N-{2-[(3-methoxyphenyl)methylamino]ethyl}-acetamide: Synthesis, binding affinity and intrinsic activity for MT₁ and MT₂ melatonin receptorsSPADONI, Gilberto; BEDINI, Annalida; ORLANDO, Pierfrancesco et al.Bioorganic & medicinal chemistry. 2011, Vol 19, Num 16, pp 4910-4916, issn 0968-0896, 7 p.Article

An endocannabinoid mechanism for stress-induced analgesiaHOHMANN, Andrea G; SUPLITA, Richard L; DURANTI, Andrea et al.Nature (London). 2005, Vol 435, Num 7045, pp 1108-1112, issn 0028-0836, 5 p.Article

Analysis of structure-activity relationships for MT₂ selective antagonists by melatonin MT₁ and MT₂ receptor modelsRIVARA, Silvia; LORENZI, Simone; MOR, Marco et al.Journal of medicinal chemistry (Print). 2005, Vol 48, Num 12, pp 4049-4060, issn 0022-2623, 12 p.Article

Design, synthesis, and structure-activity relationships of alkylcarbamic acid aryl esters, a new class of fatty acid amide hydrolase inhibitorsTARZIA, Giorgio; DURANTI, Andrea; TONTINI, Andrea et al.Journal of medicinal chemistry (Print). 2003, Vol 46, Num 12, pp 2352-2360, issn 0022-2623, 9 p.Article

Antinociceptive effects of the N-acylethanolamine acid amidase inhibitor ARN077 in rodent pain modelsSASSO, Oscar; MORENO-SANZ, Guillermo; BERTORELLI, Rosalia et al.Pain (Amsterdam). 2013, Vol 154, Num 3, pp 350-360, issn 0304-3959, 11 p.Article

Nonempirical Energetic Analysis of Reactivity and Covalent Inhibition of Fatty Acid Amide HydrolaseCHUDYK, Ewa I; DYGUDA-KAZIMIEROWICZ, Edyta; LANGNER, Karol M et al.The Journal of physical chemistry. B. 2013, Vol 117, Num 22, pp 6656-6666, issn 1520-6106, 11 p.Article

Functional characterization of gefitinib uptake in non-small cell lung cancer cell linesGALETTI, Maricla; ALFIERI, Roberta R; MOR, Marco et al.Biochemical pharmacology. 2010, Vol 80, Num 2, pp 179-187, issn 0006-2952, 9 p.Article