Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Lucio Ceriani"'
Autor:
Daniele Donati, Andrea Lombardi Borgia, Ettore Perrone, Lucio Ceriani, Chiara Marchionni, Paolo Orsini, Marcella Nesi, Luisa Rusconi, Paola Magnaghi, Marina Fasolini, Nilla Avanzi, G. Canevari, Arturo Galvani, Maristella Colombo, Patrizia Banfi, Elena Ardini, Laura Buffa, Antonella Isacchi, Christian Orrenius, Roberto Bossi, Maria Beatrice Saccardo, Ermes Vanotti, Claudio Fiorelli, Francesco Fiorentini, Maria Menichincheri, Achille Panzeri, Luca Corti, Enrico Pesenti, Eduard R. Felder
Publikováno v:
Journal of Medicinal Chemistry. 59:3392-3408
Anaplastic lymphoma kinase (ALK) is a receptor tyrosine kinase responsible for the development of different tumor types. Despite the remarkable clinical activity of crizotinib (Xalkori), the first ALK inhibitor approved in 2011, the emergence of resi
Autor:
Giuliano Ramella, Angelo Bedeschi, Carlos A. Martinez, Franco Heidempergher, David J. Kucera, Billie J. Kline, Francesco Corcella, Francesco Rossi, Giambattista Ventrella, Daniel R. Yazbeck, Ilaria Candiani, Francesco Caldarelli, Vittorio Pinciroli, Marco Cattaneo, Miriam Auguadro, Lucio Ceriani, Attilio Tomasi, Chiara Marchionni, G. Visentin
Publikováno v:
Organic Process Research & Development. 12:322-338
The multikilogram production of the proline derivative 1, a key intermediate of a HIV protease inhibitor, required the design of a synthetic route able to be safely, effectively, and easily scaled up. Synthesis of the proline skeleton began with cons
Autor:
Nilla Avanzi, Sabrina Cribioli, Paola Gnocchi, Jay Bertrand, Danilo Mirizzi, Daniele Casero, Arturo Galvani, Paola Vianello, Maristella Colombo, Eduard R. Felder, Gabriele Fachin, Achille Panzeri, Lucio Ceriani, G. Canevari, Franco Della Vedova, Dario Ballinari, Cinzia Cristiani, Enrico Pesenti, Marcella Nesi, Tiziano Bandiera, Marina Ciomei, Alessandra Cirla, Maria Gabriella Brasca, Antonella Isacchi, Daniele Donati, Ilaria Motto, Simona Bindi, Marina Fasolini, Davide Carenzi
Publikováno v:
Bioorganicmedicinal chemistry. 22(17)
We report herein the discovery, structure guided design, synthesis and biological evaluation of a novel class of JAK2 inhibitors. Optimization of the series led to the identification of the potent and orally bioavailable JAK2 inhibitor 28 (NMS-P953).
Autor:
Antonella Ciavolella, Lucio Ceriani, Alessia Montagnoli, Eduard R. Felder, Rosita Lupi, Daniele Donati, Gianluca Papeo, Arturo Galvani, Marina Ciomei, Francesco Caprera, Sonia Rainoldi, Dario Ballinari, Antonella Isacchi
Publikováno v:
Cancer Research. 76:1223-1223
Poly(ADP-ribose) polymerase-1 (PARP-1) has a well-established role in the signaling and repair of DNA and is a prominent target in oncology. Inhibition of PARP-1 is synthetically lethal with loss of function of the BRCA1 and BRCA2 tumor suppressor ge
Autor:
Francesco Rossi, Francesco Corcella, Francesco Saverio Caldarelli, Franco Heidempergher, Chiara Marchionni, Miriam Auguadro, Marco Cattaneo, Lucio Ceriani, Giuseppina Visentin, Giambattista Ventrella, Vittorio Pinciroli, Giuliano Ramella, Ilaria Candiani, Angelo Bedeschi, Billie J. Kline, Carlos A. Martinez, Daniel Yazbeck, Attilio Tomasi, David J. Kucera
Publikováno v:
Organic Process Research & Development; Feb2008, Vol. 12 Issue 2, p322-338, 17p
Publikováno v:
Chemistry and Physics of Lipids. 49:97-100
3-Methyl-1,3,5-pentanetriol has been prepared by an improved ozonolysis procedure and some of its diesters have been synthesized. Monooctanoate of the above triol was prepared by enzymatic hydrolysis of dioctanoate (54% yields of isolated product) us