Zobrazeno 1 - 10
of 129
pro vyhledávání: '"Paolo Bovicelli"'
Publikováno v:
ARKIVOC, Vol 2008, Iss 8, Pp 105-115 (2008)
Externí odkaz:
https://doaj.org/article/4d4cf32bf48c475c9f0789171d821c8f
Autor:
Emanuele Lombardo, Cristian Sabellico, Jan Hájek, Veronika Staňková, Tomáš Filipský, Valentina Balducci, Paolo De Vito, Stefano Leone, Eugenia I Bavavea, Ilaria Proietti Silvestri, Giuliana Righi, Paolo Luly, Luciano Saso, Paolo Bovicelli, Jens Z Pedersen, Sandra Incerpi
Publikováno v:
PLoS ONE, Vol 8, Iss 4, p e60796 (2013)
Natural polyphenol compounds are often good antioxidants, but they also cause damage to cells through more or less specific interactions with proteins. To distinguish antioxidant activity from cytotoxic effects we have tested four structurally relate
Externí odkaz:
https://doaj.org/article/ccc1d3729bcb428bba9c051245b910e0
Autor:
Carla Sappino, Mauro Moliterno, Alessandra Mari, Alessandra Ricelli, Lorenza Suber, Giuliana Righi, Matteo Palagri, Chiara Tatangelo, Paolo Bovicelli, Agnese Mantineo
Publikováno v:
Organic & biomolecular chemistry 16 (2018): 1860–1870. doi:10.1039/c8ob00165k
info:cnr-pdr/source/autori:Sappino C.; Mari A.; Mantineo A.; Moliterno M.; Palagri M.; Tatangelo C.; Suber L.; Bovicelli P.; Ricelli A.; Righi G./titolo:New chiral amino alcohol ligands for catalytic enantioselective addition of diethylzincs to aldehydes/doi:10.1039%2Fc8ob00165k/rivista:Organic & biomolecular chemistry/anno:2018/pagina_da:1860/pagina_a:1870/intervallo_pagine:1860–1870/volume:16
Organic & biomolecular chemistry 16 (2018): 1860–1870. doi:10.1039/C8OB00165K
info:cnr-pdr/source/autori:Carla Sappino a, Alessandra Mari a, Agnese Mantineo a, Mauro Moliterno a, Matteo Palagri a, Chiara Tatangelo a, Lorenza Suber b, Paolo Bovicelli c, Alessandra Ricelli c, and Giuliana Righi *c/titolo:New chiral amino alcohol ligands for catalytic enantioselective addition of diethylzincs to aldehydes/doi:10.1039%2FC8OB00165K/rivista:Organic & biomolecular chemistry/anno:2018/pagina_da:1860/pagina_a:1870/intervallo_pagine:1860–1870/volume:16
info:cnr-pdr/source/autori:Sappino C.; Mari A.; Mantineo A.; Moliterno M.; Palagri M.; Tatangelo C.; Suber L.; Bovicelli P.; Ricelli A.; Righi G./titolo:New chiral amino alcohol ligands for catalytic enantioselective addition of diethylzincs to aldehydes/doi:10.1039%2Fc8ob00165k/rivista:Organic & biomolecular chemistry/anno:2018/pagina_da:1860/pagina_a:1870/intervallo_pagine:1860–1870/volume:16
Organic & biomolecular chemistry 16 (2018): 1860–1870. doi:10.1039/C8OB00165K
info:cnr-pdr/source/autori:Carla Sappino a, Alessandra Mari a, Agnese Mantineo a, Mauro Moliterno a, Matteo Palagri a, Chiara Tatangelo a, Lorenza Suber b, Paolo Bovicelli c, Alessandra Ricelli c, and Giuliana Righi *c/titolo:New chiral amino alcohol ligands for catalytic enantioselective addition of diethylzincs to aldehydes/doi:10.1039%2FC8OB00165K/rivista:Organic & biomolecular chemistry/anno:2018/pagina_da:1860/pagina_a:1870/intervallo_pagine:1860–1870/volume:16
A study aimed at the synthesis and structure optimization of new, efficient, optically active β-amino alcohol ligands with a structure suitable for immobilization on magnetite nanoparticles has been carried out. The optimized homogeneous amino alcoh
Publikováno v:
BioFactors. 42:591-599
Negletein has been shown to have therapeutic potential for inflammation-associated diseases, but its effect on neurite outgrowth is still unknown. The present study showed that negletein alone did not trigger PC12 cells to differentiate and extend ne
Publikováno v:
Chirality. 28:387-393
A study of the stereochemical control on the asymmetric dihydroxylation of the double bond of optically active vinyl epoxides and their derivatives (bromo derivatives, azido derivatives, and vinyl aziridines) was carried out and the obtained results
Autor:
Gustavo Portalone, Martina Marini, Paolo Bovicelli, Giuliana Righi, Valerio Isoni, Roberto Dallocchio, Alessandro Dessì, Beatrice Macchi, Antonella Dalla Cort, Matteo Palagri, Ilaria Tirotta, Gianpiero Forte, Caterina Frezza, Romina Pelagalli
Publikováno v:
Natural product research
32 (2018): 1893–1901. doi:10.1080/14786419.2017.1354191
info:cnr-pdr/source/autori:Righi G.; Pelagalli R.; Isoni V.; Tirotta I.; Marini M.; Palagri M.; Dallocchio R.; Dessì A.; Macchi B.; Frezza C.; Forte G.; Dalla Cort A.; Portalone G.; Bovicelli P./titolo:Synthesis of potential HIV integrase inhibitors inspired by natural polyphenol structures/doi:10.1080%2F14786419.2017.1354191/rivista:Natural product research (Print)/anno:2018/pagina_da:1893/pagina_a:1901/intervallo_pagine:1893–1901/volume:32
32 (2018): 1893–1901. doi:10.1080/14786419.2017.1354191
info:cnr-pdr/source/autori:Righi G.; Pelagalli R.; Isoni V.; Tirotta I.; Marini M.; Palagri M.; Dallocchio R.; Dessì A.; Macchi B.; Frezza C.; Forte G.; Dalla Cort A.; Portalone G.; Bovicelli P./titolo:Synthesis of potential HIV integrase inhibitors inspired by natural polyphenol structures/doi:10.1080%2F14786419.2017.1354191/rivista:Natural product research (Print)/anno:2018/pagina_da:1893/pagina_a:1901/intervallo_pagine:1893–1901/volume:32
Drawing inspiration from the structural features of some natural polyphenols, the synthesis of two different model compounds as potential inhibitors of HIV integrase (IN) has been described. The former was characterised by a diketo acid (DKA) bioisos
Autor:
Alessandro Dessì, Roberto Dallocchio, Beatrice Macchi, Valerio Isoni, Paolo Bovicelli, Caterina Frezza, Ilaria Rossetti, Romina Pelagalli, Ilaria Tirotta, Giuliana Righi
Publikováno v:
Natural product research (Online) 31 (2017): 397–403. doi:10.1080/14786419.2016.1169413
info:cnr-pdr/source/autori:G. Righi, R. Pelagalli, V. Isoni, I. Trotta, R. Dallocchio, A. Dessì, B.Macchi, C. Frezza, I. Rossetti, P. Bovicelli/titolo:Synthesis, molecular modelling and biological evaluation of two new chicoric acid analogs/doi:10.1080%2F14786419.2016.1169413/rivista:Natural product research (Online)/anno:2017/pagina_da:397/pagina_a:403/intervallo_pagine:397–403/volume:31
info:cnr-pdr/source/autori:G. Righi, R. Pelagalli, V. Isoni, I. Trotta, R. Dallocchio, A. Dessì, B.Macchi, C. Frezza, I. Rossetti, P. Bovicelli/titolo:Synthesis, molecular modelling and biological evaluation of two new chicoric acid analogs/doi:10.1080%2F14786419.2016.1169413/rivista:Natural product research (Online)/anno:2017/pagina_da:397/pagina_a:403/intervallo_pagine:397–403/volume:31
Two conformationally constrained compounds similar to chicoric acid but lacking the catechol and carboxyl groups were prepared. In these analogues, the single bond between the two caffeoyl fragments has been replaced with a chiral oxirane ring and bo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c9101327693187be5f240ef719c50fc
http://hdl.handle.net/2108/162631
http://hdl.handle.net/2108/162631
Autor:
Priyanjalee Banerjee, Sasanka Chakrabarti, Shruti Anand, Giuliana Righi, Luciano Saso, Arghyadip Sahoo, Paolo Bovicelli, Anirban Ganguly
Publikováno v:
NeuroMolecular Medicine. 16:787-798
The increased accumulation of iron in the brain in Alzheimer's disease (AD) is well documented, and excess iron is strongly implicated in the pathogenesis of the disease. The adverse effects of accumulated iron in AD brain may include the oxidative s
Publikováno v:
Carbohydrate research. 435
Herein the total synthesis of the pyrrolidine alkaloids 1,4-dideoxy-1,4-imino-d-galactitol and its diastereoisomer 1,4-dideoxy-1,4-imino-d-glucitol is described, starting from a common optically active precursor. The key step in our approach was the
Autor:
Ilaria Tirotta, Carla Sappino, Emanuela Mandic, Paolo Bovicelli, Giuliana Righi, Michela Tomei, Gaia Naponiello, Cristina Marucci
A stereocontrolled, facile and high-yield approach for producing (+)-altroDNJ, has been developed starting from the inexpensive commercial cis 2-butene-1,4-diol. Sharpless epoxidation and a subsequent dihydroxylation were used for the introduction of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2ca6d2e8107a2b1e613e9d6ed765f57d