Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Riccardo, Pasquale"'
Autor:
Tieuli, Sebastiano, Signoretto, Michela, Ghedini, Elena, Carlesso, Anna, Costantini, Antonio, Claudio, Bortolati, Riccardo, Pasquale, Massimiliano, Silvestri, Luca, Frighetto
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3655::d51b367d5a5c40748a74861416d2968a
http://hdl.handle.net/10278/3727347
http://hdl.handle.net/10278/3727347
Autor:
Tieuli, Sebastiano, Signoretto, Michela, Carlesso, Anna, Costantini, Antonio, Zucaro, Rosita, Riccardo, Pasquale, Massimiliano, Silvestri, Luca, Frighetto
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3655::e2f78bdcd5b71feb67a899a841a47db3
http://hdl.handle.net/10278/3721310
http://hdl.handle.net/10278/3721310
Autor:
Armando Gennaro, Giovanni Ribaudo, Raffaele Pezzani, Valeria Pavan, Carla Mucignat-Caretta, Riccardo Pasquale, Marco Crisma, Marco Redaelli, Giuseppe Zagotto, Abdirisak Ahmed Isse
Publikováno v:
European journal of medicinal chemistry 96 (2015): 458–466. doi:10.1016/j.ejmech.2015.04.039
info:cnr-pdr/source/autori:Redaelli, Marco; Mucignat-Caretta, Carla; Isse, Abdirisak Ahmed; Gennaro, Armando; Pezzani, Raffaele; Pasquale, Riccardo; Pavan, Valeria; Crisma, Marco; Ribaudo, Giovanni; Zagotto, Giuseppe/titolo:New naphthoquinone derivatives against glioma cells/doi:10.1016%2Fj.ejmech.2015.04.039/rivista:European journal of medicinal chemistry/anno:2015/pagina_da:458/pagina_a:466/intervallo_pagine:458–466/volume:96
info:cnr-pdr/source/autori:Redaelli, Marco; Mucignat-Caretta, Carla; Isse, Abdirisak Ahmed; Gennaro, Armando; Pezzani, Raffaele; Pasquale, Riccardo; Pavan, Valeria; Crisma, Marco; Ribaudo, Giovanni; Zagotto, Giuseppe/titolo:New naphthoquinone derivatives against glioma cells/doi:10.1016%2Fj.ejmech.2015.04.039/rivista:European journal of medicinal chemistry/anno:2015/pagina_da:458/pagina_a:466/intervallo_pagine:458–466/volume:96
This work was aimed to the development of a set of new naphtoquinone derivatives that can act against glioma. The compounds were tested in order to find out their ability to inhibit the growth of glioma cells, and the results of these assays were cor
Autor:
Giuseppe, Zagotto, Alessandra, Gianoncelli, Claudia, Sissi, Cristina, Marzano, Valentina, Gandin, Riccardo, Pasquale, Giovanni, Capranico, Giovanni, Ribaudo, Manlio, Palumbo
The precise definition of the structural requirements for effective topoisomerase II poisoning by drug molecules is still an elusive issue. In the attempt to better define a pharmacophoric pattern, we prepared several conjugates combining the chemica
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::e70662caafee89a2a98838968e971880
http://hdl.handle.net/11577/2963700
http://hdl.handle.net/11577/2963700
Autor:
Francesca Pizzato, Domenico D'Avella, Riccardo Pasquale, Marco Redaelli, Carla Mucignat-Caretta, Giuseppe Zagotto, Luca Denaro, Giorgio Cozza
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 21:2079-2082
Malignant gliomas continue to demand the search for improved chemotherapeutic solutions. In this work the results of a preliminary in vitro screening performed on a small library of compounds are disclosed. As a result 2-(2,4-dihydroxyphenyl)-8-hydro
Publikováno v:
Energy Environ. Sci.. 3:212-215
An integrated process which generates energy by the combustion of methane in a pure oxygen atmosphere, and produces commercially important cyclic carbonates from the waste carbon dioxide generated during the combustion has been developed.
Publikováno v:
European Journal of Inorganic Chemistry. 2007:3323-3326
Dimetallic aluminium(salen) complexes show exceptionally high catalytic activity for the synthesis of cyclic carbonates from terminal epoxides at ambient temperature and pressure. The process has the potential to contribute towards decreasing atmosph
Autor:
Michael North, Riccardo Pasquale
Publikováno v:
Angewandte Chemie. 121:2990-2992
Autor:
Riccardo Pasquale, Michael North
Publikováno v:
Angewandte Chemie (International Ed. in English)
Three interconnected catalytic cycles account for the title reaction catalyzed by a bimetallic aluminum(salen) complex and Bu(4)NBr. In the first, Bu(4)NBr acts as a nucleophile to activate the epoxide. In the second, Bu(3)N generated in situ serves