Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Silvia Davalli"'
Autor:
Ales Čamra, John Warren, Taylor David, Dinesh Chalasani, Daniele Ragno, Jan Teipel, Tommaso Di Noia, Aurimas Bieliauskas, Elina Zailer-Hafer, Stefano Todisco, Domenico Acquotti, Lorraine M. Bateman, James Donarski, Piero Mastrorilli, Rosa Ragone, Cristina Airoldi, John S. Harwood, Michael Assfalg, Dolores Molero Vilchez, Francesco Longobardi, Magali Martin-Biran, Elisabetta Schievano, Domenico Mallamace, Elisabetta Torregiani, Biagia Musio, Stefania Pontrelli, Paolo Dambruoso, Marina Veronesi, Livio Stevanato, Augusta Caligiani, Erwann Hamon, Maurizio Triggiani, Davide Bertelli, Flaminia Cesare Marincola, Stefano Mammi, Bernd Diehl, Vito Gallo, Daniela Valensin, Bhavaraju Sitaram, Alessandro Barge, Claudia Di Napoli, Elena Sáez Barajas, Pasquale Scapicchio, Emanuela Callone, Antonino Rizzuti, Panteleimon G. Takis, Fabio Bertocchi, Anna Borioni, Cristiano Zuccaccia, Maria Cecilia Rossi, Mario Latronico, Andrea Kobrlová, Luca Goldoni, Nicola Intini, Freddy Thomas, Roberto Gobetto, Renzo Luisi, Ana M. Gil, Pierluigi Mazzei, Julien Wist, Roberto Consonni, Francesca Benevelli, Algirdas Šačkus, Antonio Randazzo, Salvatore Milone, Archimede Rotondo, Roger J. Mulder, Silvia Davalli, Andrea Mele
Nuclear Magnetic Resonance (NMR) is an analytical technique extensively used in almost every chemical laboratory for structural identification. This technique provides statistically equivalent signals in spite of using spectrometer with different har
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d45364f7f7815eab8db34443412307c1
http://hdl.handle.net/10281/263052
http://hdl.handle.net/10281/263052
Autor:
Piero Mastrorilli, Michael Assfalg, Vito Gallo, Rosa Ragone, Palmira Villa-Valverde, Iola F. Duarte, Maurizio Triggiani, Anna Borioni, Biagia Musio, Antonello Pascazio, Francesco Longobardi, Silvia Davalli, Elisabetta Schievano, Silvia Mari, Stefania Pontrelli, Cristiano Garino, Cristina Airoldi, Carlos Cobas, Flaminia Cesare Marincola, Adele Mucci, Andersson Barison, Antonino Rizzuti, Erwann Hamon, Michelle Markus, Panteleimon G. Takis, Francesco Savorani, Luca Casadei, Freddy Thomas, Fabio Sciubba, Domenico Acquotti, Anatoly P. Sobolev, Claudia Di Napoli, Kim Colson, Elena Sáez-Barajas, Francesca Benevelli, Nicola Intini, Gabriele Costantino, Leociley R. A. Menezes, Marco Arlorio, Domenico Mallamace, Mauro Andrea Cremonini, Pasquale Scapicchio, Raffaele Lamanna, Sophie Guyader, Stefano Todisco, Maria Cecilia Rossi, Mario Latronico, Laura Ruth Cagliani, Maren Hegmanns, Fabio Arnesano, Dolores Molero-Vílchez, Stefano Mammi, Roberto Consonni, Salvatore Milone
Publikováno v:
Food analytical methods (2020). doi:10.1007/s12161-019-01664-8
info:cnr-pdr/source/autori:Gallo V, Ragone R, Musio B, Todisco S, Rizzuti A, mMastrorilli P, Pontrelli S, Intini N, Scapicchio P, Triggiani M, Pascazio A, Cobas C, Mari S, Garino C, Arlorio M, Acquotti D, Airoldi C, Arnesano F, Assfalg M, Barison A, Benevelli F, Borioni A, Cagliani LR, Casadei L, Cesare Marincola F, Colson K, Consonni R, Costantino G, Cremonini MA, Davalli S, Duarte I, Guyader S, Hamon E, Hegmanns M, Lamanna R, Longobardi F, Mallamace D, Mammi S, Markus M, Rocha Alencar Menezes L, Milone S, Molero-Vilchez D, Mucci A, Napoli C, Rossi MC, Sáez-Barajas E, Savorani F, Schievano E, Sciubba F, Sobolev A, Takis PG, Thomas F, Villa-Valverde P, Latronico M. A./titolo:Contribution to the harmonization of non-targeted NMR methods for data-driven food authenticity assessment/doi:10.1007%2Fs12161-019-01664-8/rivista:Food analytical methods/anno:2020/pagina_da:/pagina_a:/intervallo_pagine:/volume
info:cnr-pdr/source/autori:Gallo V, Ragone R, Musio B, Todisco S, Rizzuti A, mMastrorilli P, Pontrelli S, Intini N, Scapicchio P, Triggiani M, Pascazio A, Cobas C, Mari S, Garino C, Arlorio M, Acquotti D, Airoldi C, Arnesano F, Assfalg M, Barison A, Benevelli F, Borioni A, Cagliani LR, Casadei L, Cesare Marincola F, Colson K, Consonni R, Costantino G, Cremonini MA, Davalli S, Duarte I, Guyader S, Hamon E, Hegmanns M, Lamanna R, Longobardi F, Mallamace D, Mammi S, Markus M, Rocha Alencar Menezes L, Milone S, Molero-Vilchez D, Mucci A, Napoli C, Rossi MC, Sáez-Barajas E, Savorani F, Schievano E, Sciubba F, Sobolev A, Takis PG, Thomas F, Villa-Valverde P, Latronico M. A./titolo:Contribution to the harmonization of non-targeted NMR methods for data-driven food authenticity assessment/doi:10.1007%2Fs12161-019-01664-8/rivista:Food analytical methods/anno:2020/pagina_da:/pagina_a:/intervallo_pagine:/volume
Spectroscopic non-targeted methods are gaining ever-growing importance in quality control and authenticity assessment of food products because of their strong potential for identification of specific features of the products by data-driven classifier
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::682f6d5e3f6ffb910eb65d4cd40a16f7
http://hdl.handle.net/11577/3316845
http://hdl.handle.net/11577/3316845
Autor:
Thelma A. Pertinhez, Gianluca Paredi, Andrea Mozzarelli, Stefano Bettati, Roberto Benoni, Barbara Campanini, Sara Pellegrino, Francesca Spyrakis, Angelica Pezzotti, Silvia Davalli
Publikováno v:
FEBS letters
590 (2016): 943–953. doi:10.1002/1873-3468.12126
info:cnr-pdr/source/autori:Benoni R, Pertinhez TA, Spyrakis F, Davalli S, Pellegrino S, Paredi GL, Pezzotti A, Bettati S, Campanini B, Mozzarelli A/titolo:Structural insight into the interaction of O-acetylserine sulfhydrylase with competitive, peptidic inhibitors by saturation transfer difference-NMR/doi:10.1002%2F1873-3468.12126/rivista:FEBS letters (Print)/anno:2016/pagina_da:943/pagina_a:953/intervallo_pagine:943–953/volume:590
590 (2016): 943–953. doi:10.1002/1873-3468.12126
info:cnr-pdr/source/autori:Benoni R, Pertinhez TA, Spyrakis F, Davalli S, Pellegrino S, Paredi GL, Pezzotti A, Bettati S, Campanini B, Mozzarelli A/titolo:Structural insight into the interaction of O-acetylserine sulfhydrylase with competitive, peptidic inhibitors by saturation transfer difference-NMR/doi:10.1002%2F1873-3468.12126/rivista:FEBS letters (Print)/anno:2016/pagina_da:943/pagina_a:953/intervallo_pagine:943–953/volume:590
O-acetylserine sulfhydrylase (OASS), the enzyme catalysing the last step of cysteine biosynthesis in bacteria, is involved in antibiotic resistance and biofilm formation. Since mammals lack OASS, it is a potential target for antimicrobials. However,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::be08be1dea40b274ce95c82360a10020
http://www.scopus.com/inward/record.url?eid=2-s2.0-84961771312&partnerID=q2rCbXpz
http://www.scopus.com/inward/record.url?eid=2-s2.0-84961771312&partnerID=q2rCbXpz
Autor:
Piero Mastrorilli, Michael Assfalg, Leonardo Tenori, Pierluigi Mazzei, Elisabetta Schievano, Anatoly P. Sobolev, Antonino Rizzuti, Davide Bertelli, Raffaele Lamanna, Cristina Airoldi, Fabio Arnesano, Domenico Mallamace, Cesare Cosentino, Nicola Intini, Roberto Consonni, Ileana Menegazzo, Fabio Sciubba, Salvatore Milone, Roberto Gobetto, Francesca Liguori, Virginia D'Aiuto, Sandra Angelica De Pascali, Mariacristina Valerio, Francesca Benevelli, Maurizio Triggiani, Domenico Acquotti, Silvia Davalli, Luca Rocchigiani, Laura Ruth Cagliani, Vitoantonio Bevilacqua, Adele Mucci, Thelma A. Pertinhez, Luca Casadei, Claudia Di Napoli, Andrea Faccini, Francesco Longobardi, Pasquale Scapicchio, Paolo Fanizzi, Flaminia Cesare Marincola, Mario Latronico, Giuseppe Colafemmina, Vito Gallo
Publikováno v:
Analytical chemistry (Wash.) 87 (2015): 6709–6717. doi:10.1021/acs.analchem.5b00919
info:cnr-pdr/source/autori:Gallo V.; Intini N.; Mastrorilli P.; Latronico M.; Scapicchio P.; Triggiani M.; Bevilacqua V.; Fanizzi P.; Acquotti D.; Airoldi C.; Arnesano F.; Assfalg M.; Benevelli F.; Bertelli D.; Cagliani L.R.; Casadei L.; Cesare Marincola F.; Colafemmina G.; Consonni R.; Cosentino C.; Davalli S.; De Pascali S.A.; D'Aiuto V.; Faccini A.; Gobetto R.; Lamanna R.; Liguori F.; Longobardi F.; Mallamace D.; Mazzei P.; Menegazzo I.; Milone S.; Mucci A.; Napoli C.; Pertinhez T.; Rizzuti A.; Rocchigiani L.; Schievano E.; Sciubba F.; Sobolev A.; Tenori L.; Valerio M./titolo:Performance Assessment in Fingerprinting and Multi Component Quantitative NMR Analyses/doi:10.1021%2Facs.analchem.5b00919/rivista:Analytical chemistry (Wash.)/anno:2015/pagina_da:6709/pagina_a:6717/intervallo_pagine:6709–6717/volume:87
info:cnr-pdr/source/autori:Gallo V.; Intini N.; Mastrorilli P.; Latronico M.; Scapicchio P.; Triggiani M.; Bevilacqua V.; Fanizzi P.; Acquotti D.; Airoldi C.; Arnesano F.; Assfalg M.; Benevelli F.; Bertelli D.; Cagliani L.R.; Casadei L.; Cesare Marincola F.; Colafemmina G.; Consonni R.; Cosentino C.; Davalli S.; De Pascali S.A.; D'Aiuto V.; Faccini A.; Gobetto R.; Lamanna R.; Liguori F.; Longobardi F.; Mallamace D.; Mazzei P.; Menegazzo I.; Milone S.; Mucci A.; Napoli C.; Pertinhez T.; Rizzuti A.; Rocchigiani L.; Schievano E.; Sciubba F.; Sobolev A.; Tenori L.; Valerio M./titolo:Performance Assessment in Fingerprinting and Multi Component Quantitative NMR Analyses/doi:10.1021%2Facs.analchem.5b00919/rivista:Analytical chemistry (Wash.)/anno:2015/pagina_da:6709/pagina_a:6717/intervallo_pagine:6709–6717/volume:87
An interlaboratory comparison (ILC) was organized with the aim to set up quality control indicators suitable for multicomponent quantitative analysis by nuclear magnetic resonance (NMR) spectroscopy. A total of 36 NMR data sets (corresponding to 1260
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0807689ef7a4ba325847494aa53764f9
http://hdl.handle.net/2318/1528415
http://hdl.handle.net/2318/1528415
Autor:
Albert A. Jaxa-Chamiec, Daniele Donati, Silvia Davalli, Fabrizio Micheli, Marilisa Rinaldi, Giorgio Bonanomi, Giovanna Tedesco, Chiara Gallotti, Martyn D. Wood, Silvia Terreni, Marcella Petrone, Graham J. Riley, Federica Damiani, Dieter Hamprecht, Alessandra Pasquarello, Anna Checchia
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 16:3906-3912
Within the continuous quest for the discovery of novel compounds able to treat anxiety and depression, the generation of a pharmacophore model for 5-HT 2C receptor antagonists and the discovery of a new class of potent and selective 5-HT 2C molecules
Publikováno v:
BioNMR in Drug Research, Volume 16
Autor:
M. Dal Cin, Stefano Provera, O. Perini, M. Passarini, Alessio Zaramella, Silvia Davalli, Carla Marchioro
Publikováno v:
Il Farmaco. 57:497-510
Solid phase synthesis (SPS) is a powerful technique to assemble compound libraries in high-throughput parallel and combinatorial synthesis. The widespread applications of these techniques required the development of analytical methods for both struct
Publikováno v:
Magnetic Resonance in Chemistry. 39:38-42
The gradient-enhanced 1H,29Si HMQC experiment was applied to tetra-TMS-α-O-methyl-D-glucopyranose and tetra-TES-α-O-methyl-D-glucopyranose as test samples. All the expected 2J(1H, 29Si) and 3J (1H,29Si) cross peaks were observed, allowing the full
Autor:
Bernardo Pezzati, Maria Pia Catalani, Silvia Davalli, Andrea Bernardelli, Alessandro Mordini, Nicola Pace, Gianna Reginato
Publikováno v:
Tetrahedron: asymmetry (Online) 24 (2013): 75–79. doi:10.1016/j.tetasy.2012.11.015
info:cnr-pdr/source/autori:Reginato, Gianna; Catalani, Maria Pia; Mordini, Alessandro Mordini; Pezzati, Bernardo Pezzati; Bernardelli, Andrea; Davalli, Silvia; Pace, Nicola/titolo:Stereoselective cyclopropanation of chiral 5-substituted dihydro-2H-piperazines/doi:10.1016%2Fj.tetasy.2012.11.015/rivista:Tetrahedron: asymmetry (Online)/anno:2013/pagina_da:75/pagina_a:79/intervallo_pagine:75–79/volume:24
info:cnr-pdr/source/autori:Reginato, Gianna; Catalani, Maria Pia; Mordini, Alessandro Mordini; Pezzati, Bernardo Pezzati; Bernardelli, Andrea; Davalli, Silvia; Pace, Nicola/titolo:Stereoselective cyclopropanation of chiral 5-substituted dihydro-2H-piperazines/doi:10.1016%2Fj.tetasy.2012.11.015/rivista:Tetrahedron: asymmetry (Online)/anno:2013/pagina_da:75/pagina_a:79/intervallo_pagine:75–79/volume:24
The Simmon–Smith cyclopropanation of enantiomerically enriched dehydropiperazines is reported. The reaction is highly stereoselective and allowed us to prepare new, enantiomerically enriched 3-substituted 2,5-diazabicyclo[4.1.0]heptane cores with h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d6b7d8c93e4e65f5370157ef97d885e9
Autor:
T. Rossi, Carla Marchioro, Silvia Davalli, Stanley M. Roberts, Daniele Donati, P. M. Jackson, A. Perboni, S. Proviera
Publikováno v:
ChemInform. 28