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Mostra risultati da 1 a 18 di 18
TitoloData di pubblicazioneAutore(i)RivistaEditore
Design, synthesis, antiviral evaluation, and SAR studies of new 1-(phenylsulfonyl)-1H-pyrazol -4-yl-methylaniline derivatives.2019Desideri, N.; Fioravanti, R.; Proietti Monaco, L.; Atzori, E. M.; Carta, A.; Delogu, I.; Collu, G....; and Loddo, RFRONTIERS IN CHEMISTRY
Inhibitors of Yellow Fever Virus replication based on 1,3,5-triphenyl-4,5-dihydropyrazole scaffold: Design, synthesis and antiviral evaluation.2017Fioravanti, R.; Desideri, N.; Carta, A.; Atzori E., M.; Delogu, Ilenia; Collu, Gabriella; Loddo, ...RobertaEUROPEAN JOURNAL OF MEDICINAL CHEMISTRY
A combined in silico/in vitro approach unveils common molecular requirements for efficient BVDV RdRp binding of linear aromatic N-polycyclic systems2016Carta, A; Briguglio, I; Piras, S; Corona, P; Ibba, R; Laurini, E; Fermeglia, M; Pricl, S; Desider...i, N; Atzori, Em; La Colla, P; Collu, G; Delogu, I; Loddo, REUROPEAN JOURNAL OF MEDICINAL CHEMISTRY
Unconventional Knoevenagel-type indoles: Synthesis and cell-based studies for the identification of pro-apoptotic agents2015Spallarossa, Andrea; Caneva, Chiara; Caviglia, Matteo; Alfei, Silvana; Butini, Stefania; Campiani..., Giuseppe; Gemma, Sandra; Brindisi, Margherita; Zisterer, Daniela M.; Bright, Sandra A.; Williams, Clive D.; Crespan, Emmanuele; Maga, Giovanni; Sanna, Giuseppina; Delogu, Ilenia; Collu, Gabriella; Loddo, RobertaEUROPEAN JOURNAL OF MEDICINAL CHEMISTRY
Antiviral activity of benzotriazole derivatives. 5-[4-(Benzotriazol-2-yl)phenoxy]-2,2-dimethylpentanoic acids potently and selectively inhibit Coxsackie Virus B52015Loddo, R; Novelli, F; Sparatore, A; Tasso, B; Tonelli, M; Boido, V; Sparatore, F; Collu, G; Delog...u, I; Giliberti, G; La Colla, PBIOORGANIC & MEDICINAL CHEMISTRY
N-((1,3-Diphenyl-1H-pyrazol-4-yl)methyl)anilines: A novel class of anti-RSV agents2015Fioravanti, R; Desideri, N; Biava, M; Droghini, P; Atzori, EM; Ibba, C; Collu, G; Sanna, G; Delog...u, I; Loddo, RBIOORGANIC & MEDICINAL CHEMISTRY LETTERS
Novel modifications in the series of O-(2-phthalimidoethyl)-N-substituted thiocarbamates and their ring-opened congeners as non-nucleoside HIV-1 reverse transcriptase inhibitors2009SPALLAROSSA A; CESARINI S; RANISE A; BRUNO O; SCHENONE S; LA COLLA P; COLLU G; SANNA G; SECCI B; ...LODDO REUROPEAN JOURNAL OF MEDICINAL CHEMISTRY
Parallel synthesis, molecular modelling and further structure-activity relationship studies of new acylthiocarbamates as potent non-nucleoside HIV-1 reverse transcriptase inhibitors2009SPALLAROSSA A; CESARINI S; RANISE A; SCHENONE S; BRUNO O; BORASSI A; LA COLLA P; PEZZULLO M; SANN...A G; COLLU G; SECCI B; LODDO REUROPEAN JOURNAL OF MEDICINAL CHEMISTRY
Design, synthesis and anti Flaviviridae activity of N6-, 5’,3’-O- and 5’,2’-O-substituted adenine nucleoside analogs2008ANGUSTI A; MANFREDINI S; DURINI E; CILIBERTI N; VERTUANI S; SOLAROLI N; PRICL S; FERRONE M; FERME...GLIA M; LODDO R; SECCI B; VISIOLI A; SANNA T; COLLU G; PEZZULLO M; LA COLLA PCHEMICAL & PHARMACEUTICAL BULLETIN
Synthesis and anti-HIV-1 evaluation of 1,5-disubstituted pyrimidine-2,4-diones2008LOKSHA YM; GLOBISCH D; PEDERSEN EB; LA COLLA P; COLLU G; LODDO RJOURNAL OF HETEROCYCLIC CHEMISTRY
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-phenylthiocarbamate2008CESARINI S; SPALLAROSSA A; RANISE A; BRUNO O; LA COLLA P; SECCI B; COLLU G; AND LODDO RBIOORGANIC & MEDICINAL CHEMISTRY
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 inhibitors2008CESARINI S; SPALLAROSSA A; RANISE A; SCHENONE S; BRUNO O; LA COLLA P; CASULA L; COLLU G; SANNA G;... LODDO RBIOORGANIC & MEDICINAL CHEMISTRY
Synthesis and anti-Picornaviridae in vitro activity of a new class of helicase inhibitors the N,N’-bis[4-(1H(2H)-benzotriazol-1(2)-yl)phenyl]alkyldicarboxamides2007CARTA A; LORIGA M; PIRAS S; PAGLIETTI G; FERRONE M; FERMEGLIA M; PRICL S; LA COLLA P; COLLU G; SA...NNA T.; LODDO RMEDICINAL CHEMISTRY
Synthesis of variously substituted 3-phenoxymethyl quinoxalin-2-ones and quinoxalines capable to potenziate in vitro the antiproliferative activity of anticancer drugs in multi-drug resistant cell lines2006CARTA A; LORIGA M; PIRAS S; PAGLIETTI G; LA COLLA P; BUSONERA B; COLLU GMEDICINAL CHEMISTRY
Aryl nucleoside H-phosphonates. Part 15: Synthesis, properties and, anti-HIV activity of aryl nucleoside 50-a-hydroxyphosphonates2006Szymanska A; Szymczak M; Boryski J; Stawinski J; Kraszewski A; Collu G; Sanna G; Giliberti G; Lod...do R; La Colla PBIOORGANIC & MEDICINAL CHEMISTRY
Synthesis and in vitro evaluation of the anti-viral activity of N-[4-(1H(2H)-benzotriazol-1(2)-yl)phenyl]alkylcarboxamides2006CARTA A; LORIGA G; PIRAS S; PAGLIETTI G; FERRONE M; FERMEGLIA M; PRICL S; LA COLLA P; SECCI B; CO...LLU G; LODDO RMEDICINAL CHEMISTRY
4-Substituted anilino imidazo[1,2-a] and triazolo[4,3-a]quinoxalines. Synthesis and evaluation of in vitro biological activity2006CORONA P; VITALE G; LORIGA M; PAGLIETTI G; LA COLLA P; COLLU G; SANNA G; LODDO REUROPEAN JOURNAL OF MEDICINAL CHEMISTRY
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 derivatives2005Ranise, A; Spallarossa, A; Cesarini, S; Bondavalli, F; Schenone, S; Bruno, O; Menozzi, G; Fossa, ...P; Mosti, L; La Colla, M; Sanna, G; Murreddu, M; Collu, G; Busonera, B; Marongiu, ME; Pani, A; La Colla, P; Loddo, RJOURNAL OF MEDICINAL CHEMISTRY
   
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