PIERSANTI, GIOVANNI

PIERSANTI, GIOVANNI  

Dipartimento di Scienze Biomolecolari (DISB)  

Risultati 1 - 20 di 93 (tempo di esecuzione: 0.023 secondi).
Titolo Data di pubblicazione Autore(i) File
2-n-Butyl- 9-methyl-8-(1,2,3)triazol-2-yl-9H-purin-6-ylamine and Analogues as A2A Adenosine Receptor Antagonists. Design, Synthesis, and Pharmacological Characterization 1-gen-2005 Minetti, P; TINTI M., O; Carminati, P; Castorina, M; DI CESARE M., A; DI SERIO, S; Gallo, G; Ghirardi, O; Giorgi, F; Giorgi, Luca; Piersanti, Giovanni; Bartoccini, Francesca; Tarzia, Giorgio
2-n-butyl-9-methyl-8-(1,2,3)triazol-2yl-9H-purin-6-yl-amine (ST 1535) and analogs as A2a Adenosine receptor antagonists. Design, synthesis and pharmacological characterization 1-gen-2003 Bartoccini, Francesca; Castorina, M.; DI CESARE, M. A.; Gallo, G; Ghirardi, O.; Giorgi, F. GIORGI L.; Minetti, P.; Piersanti, Giovanni; Tarzia, Giorgio; Tinti, M. O.
5-(2-Ethyl-phenyl)-3-(3-methoxy-phenyl)-1H-[1,2,4]triazole (DL-111-IT ) and related compounds induce morphological apoptotic patterns in cultures of human tumor cell lines 1-gen-2003 Burattini, Sabrina; Luchetti, Francesca; Battistelli, Michela; DELLA FELICE, Massimo; Papa, Stefano; Piersanti, Giovanni; Tarzia, Giorgio; Falcieri, Elisabetta
A Versatile Biomimetic Approach to Diindolylmethane Derivatives as Potential Anticancer Agents 1-gen-2012 Lucarini, Simone; Piersanti, Giovanni; Duranti, Andrea; Spadoni, Gilberto
An efficient, economical synthesis of hydroxytyrosol and its protected forms via Baeyer–Villiger oxidation 1-gen-2011 Piersanti, Giovanni; Retini, M; ESPARTERO J., L; Madrona, A; Zappia, Giovanni
Asymmetric Total Synthesis of All Rugulovasine Stereoisomers and Preliminary Evaluation of Their Biological Properties 1-gen-2022 Bartoccini, Francesca; Regni, Alessio; Retini, Michele; Piersanti, Giovanni
Brønsted Acid-Catalyzed Bisindolization of α-amido acetals: Synthesis and Anticancer activity of bis(indolyl)ethanamino derivatives 1-gen-2014 Mari, Michele; Aurora, Tassoni; Lucarini, Simone; Fanelli, Mirco; Piersanti, Giovanni; Spadoni, Gilberto
C3-Alkylation of indoles and oxindoles by alcohols by means of borrowing hydrogen methodology 1-gen-2020 Bartoccini, Francesca; Retini, Michele; Piersanti, Giovanni
The collisional behavior of ESI-generated protonated molecules of some carbamate FAAH inhibitors isosteres and its relationships with biological activity 1-gen-2009 Valitutti, G; Duranti, Andrea; Mor, M; Piersanti, Giovanni; Piomelli, D; Rivara, S; Tontini, Andrea; Tarzia, Giorgio; Traldi, P.
Concise and Convergent Enantioselective Total Syntheses of (+)- and (-)-Fumimycin 1-gen-2019 Retini, Michele; Bartolucci, Silvia; Bartoccini, Francesca; Mari, Michele; Piersanti, Giovanni
Concise catalytic asymmetric synthesis of (R)-4-amino Uhle's ketone 1-gen-2021 Bartoccini, Francesca; Regni, Alessio; Retini, Michele; Piersanti, Giovanni
Conformation by NMR of two tetralin-based receptor ligands 1-gen-2003 Gatti, G.; Piersanti, Giovanni; Spadoni, Gilberto
Correlation between energetics of collisionally activated decompositions, interaction energy and biological potency of carbamates FAAH inhibitors 1-gen-2007 Valitutti, G; Duranti, Andrea; Lodola, A; Mor, M; Piersanti, Giovanni; Piomelli, D; Rivara, S; Tontini, Andrea; Tarzia, Giorgio; Traldi, P.
Cyclohexylcarbamic Acid 3’-or 4’-Substituted Biphenyl-3-yl Esters as Fatty Acid Amide Hydrolase Inhibitors: Synthesis Quantitative Structure–Activity Relationships, and Molecular Modeling Studies 1-gen-2004 Mor, M; Rivara, S; Lodola, A; Plazzi, Pv; Tarzia, Giorgio; Duranti, Andrea; Tontini, Andrea; Piersanti, Giovanni; Kathuria, S; Piomelli, D.
Derivatives of triazoly-imidazopyridine useful as ligands of the adenosine A2a receptor ant their use as medicaments 1-gen-2009 Tarzia, Giorgio; Piersanti, Giovanni; Giorgi, Luca; Patrizia, Minetti; MARIA A., DI CESARE; Grazia, Gallo; Fabrizio, Giorgi
DERIVATIVES OF TRIAZOLYL-IMIDAZOPYRIDINE AND OF THE TRIAZOLYLPURINES USEFUL AS LIGANDS OF THE ADENOSINE A2a RECEPTOR AND THEIR USE AS MEDICAMENTS. 1-gen-2003 Tarzia, Giorgio; Piersanti, Giovanni; P., Minetti; A., DI CESARE; G., Gallo; F., Giorgi; Giorgi, Luca
Derivatizzazione one-pot di indoli per la sintesi di triptofani, pirroloindoline, bis-indoli & co 1-gen-2014 Lucarini, Simone; Piersanti, Giovanni; Duranti, Andrea; Spadoni, Gilberto
Design, SAR and Biological Activity of a New Class of FAAH Inhibitors: Cyclohexyl Carbamic Acid Biphenyl-3-yl Esters 1-gen-2003 Mor, M; Duranti, Andrea; Tontini, Andrea; Piersanti, Giovanni; Tarzia, Giorgio; Rivara, S; Lodola, A; Plazzi, Pv; Calignano, A; Cuomo, V; Kathuria, S; Piomelli, D.
Design, Synthesis and SAR of Alkylcarbamic Acid Aryl Esters, a New Class of Fatty Acids Amide Hydrolase Inhibitors 1-gen-2003 Tarzia, Giorgio; Mor, M; Duranti, Andrea; Tontini, Andrea; Piersanti, Giovanni; Piomelli, D.
Design, Synthesis and Structure–Activity Relationships of Alkylcarbamic Acid Aryl Esters, a New Class of Fatty Acid Amide Hydrolase Inhibitors 1-gen-2003 Tarzia, Giorgio; Duranti, Andrea; Tontini, Andrea; Piersanti, Giovanni; Mor, M; Rivara, S; Plazzi, Pv; Park, C; Kathuria, S; Piomelli, D.