Browsing by Author Carraro, Fabio

Showing results 1 to 13 of 13
Issue DateTitleAuthor(s)Third Mission
20102-Hydroxypropyl-β-cyclodextrin strongly improves water solubility and anti-proliferative activity of pyrazolo[3,4-d]pyrimidines Src-Abl dual inhibitors.Dreassi, Elena ; Zizzari, ALESSANDRA TANIA; Mori, Mattia ; Filippi, Irene; Belfiore, Amalia; Naldini, Antonella; Carraro, Fabio; Santucci, Annalisa ; Schenone, S; Botta, Maurizio Not applicable
20093D QSAR models built on structure-based alignments of Abl tyrosine kinase inhibitors.Falchi, F; Manetti, Fabrizio ; Carraro, Fabio; Naldini, Antonella; Maga, G; Crespan, E; Schenone, S; Bruno, O; Brullo, C; Botta, Maurizio Not applicable
2010Carborane-Conjugated 2-Quinolinecarboxamide Ligands of the Translocator Protein for Boron Neutron Capture TherapyCappelli, Andrea ; Valenti, S; Mancini, A; Giuliani, Germano ; Anzini, Maurizio ; Altieri, S; Bortolussi, S; Ferrari, C; Clerici, A; Zonta, C; Carraro, Fabio; Filippi, Irene; Giorgi, Gianluca ; Donati, Alessandro ; Ristori, S; Vomero, Salvatore; Concas, A; Biggio, G.Not applicable
2011Design, synthesis, biological activity and ADME properties of pyrazolo[3,4-d]pyrimidines active in hypoxic human leukemia cells: a lead optimization studyRadi, Marco; Dreassi, Elena ; C., Brullo; E., Crespan; Tintori, Cristina; V., Bernardo; Valoti, Massimo; Zamperini, Claudio; H., Daigl; F., Musumeci; Carraro, Fabio; Naldini, Antonella; Filippi, Irene; G., Maga; S., Schenone; Botta, Maurizio Not applicable
2012Downregulation of hypoxia-related responses by novel antitumor histone deacetylase inhibitors in MDAMB231 breast cancer cells.Naldini, Antonella; Filippi, Irene; Cini, Elena ; Rodriquez, M; Carraro, Fabio; Taddei, Maurizio Not applicable
2013Identification of Hck inhibitors as hits for the development of antileukemia and anti-HIV agents.Tintori, Cristina; Laurenzana, Ilaria; La Rocca, F; Falchi, Federico; Carraro, Fabio; Ruiz, A; Esté, Ja; Kissova, M; Crespan, E; Maga, G; Biava, M; Brullo, C; Schenone, S; Botta, Maurizio Not applicable
2007Inhibition of Bcr-Abl phosphorylation and induction of apoptosis by pyrazolo[3,4-d] pyrimidines in human leukemia cellsManetti, Fabrizio ; Pucci, Annalisa; Magnani, M; LOCATELLI G., A; Brullo, C; Naldini, Antonella; Schenone, S; Maga, G; Carraro, Fabio; Botta, Maurizio Not applicable
2011N-[2-Methyl-5-(triazol-1-yl)phenyl]pyrimidin-2-amine as a scaffold for the synthesis of inhibitors of Bcr-Abl.Arioli, F; Borrelli, S; Colombo, F; Falchi, F; Filippi, Irene; Crespan, E; Naldini, Antonella; Scalia, Giusy; Silvani, A; Maga, G; Carraro, Fabio; Botta, Maurizio ; Passarella, D.Not applicable
2004New pyrazolo[3,4-d]pyrimidines endowed with A431 antiproliferative activity and inhibitory properties of Src phosphorylationSchenone, S; Bruno, O; Ranise, A; Bondavalli, F; Brullo, C; Fossa, P; Mosti, L; Menozzi, G; Carraro, Fabio; Naldini, Antonella; Bernini, C; Manetti, Fabrizio ; Botta, Maurizio Not applicable
2006Pyrazolo[3,4-d]pyrimidines as potent antiproliferative and proapoptotic agents toward A431 and 8701-BC cells in culture via inhibition of c-Src phosphorylation.Carraro, Fabio; Naldini, Antonella; Pucci, Annalisa; Locatelli, Ga; Maga, G; Schenone, S; Bruno, O; Ranise, A; Bondavalli, F; Brullo, C; Fossa, P; Menozzi, G; Mosti, L; Modugno, M; Tintori, Cristina; Manetti, Fabrizio ; Botta, Maurizio Not applicable
2004Pyrazolo[3,4-d]pyrimidines Endowed with Antiproliferative Activity on Ductal Infiltrating Carcinoma Cells.Carraro, Fabio; Pucci, Annalisa; Naldini, Antonella; Schenone, S.; Bruno, O.; Ranise, A.; Bondavalli, B.; Brullo, C.; Fossa, P.; Menozzi, G.; Mosti, L.; Manetti, Fabrizio ; Botta, Maurizio Not applicable
2008Structure-Based Optimization of Pyrazolo[3,4-d]pyrimidines as Abl Inhibitors and Antiproliferative Agents toward Human Leukemia Cell Lines.Manetti, Fabrizio ; Brullo, C; Magnani, M; Mosci, F; Chelli, B; Crespan, E; Schenone, S; Naldini, Antonella; Bruno, O; Trincavelli, Ml; Maga, G; Carraro, Fabio; Martini, C; Bondavalli, F; Botta, Maurizio Not applicable
2008Synthesis, biological evaluation and docking studies of 4-amino substituted 1H-pyrazolo[3,4-d]pyrimidines.Schenone, S; Brullo, C; Bruno, O; Bondavalli, F; Mosti, L; Maga, G; Crespan, E; Carraro, Fabio; Manetti, Fabrizio ; Tintori, C; Botta, Maurizio Not applicable