Zobrazeno 1 - 10
of 46
pro vyhledávání: '"Anna, Fantinati"'
Autor:
Elena Marchesi, Valentina Gentili, Daria Bortolotti, Lorenzo Preti, Paolo Marchetti, Virginia Cristofori, Anna Fantinati, Roberta Rizzo, Claudio Trapella, Daniela Perrone, Maria Luisa Navacchia
Publikováno v:
ACS Omega, Vol 8, Iss 47, Pp 45078-45087 (2023)
Externí odkaz:
https://doaj.org/article/3e015baece9c4e2fb2c91e2e72a011a0
Autor:
Virginia Cristofori, Davide Illuminati, Chiara Bisquoli, Martina Catani, Greta Compagnin, Giulia Turrin, Claudio Trapella, Anna Fantinati
Publikováno v:
Molecules, Vol 29, Iss 14, p 3267 (2024)
Herein we present the biocatalysed preparation of a mono-N-carbamate-protected precursor of antitumoral Nutlin-3a through enantioselective alkoxycarbonylation of meso-1,2-disubstituted-1,2-diaminoethane using enzyme lipases and dialkyl carbonates as
Externí odkaz:
https://doaj.org/article/59b0a2d3578d4571872fd539124d04e7
Autor:
Davide Illuminati, Anna Fantinati
Publikováno v:
Pharmaceuticals, Vol 17, Iss 5, p 563 (2024)
This Special Issue, which focused on methyl-containing pharmaceuticals, collected different papers and reviews on this topic [...]
Externí odkaz:
https://doaj.org/article/237b05e7b0524a36beeb6abbc40ce5ae
Autor:
Davide Illuminati, Claudio Trapella, Vinicio Zanirato, Remo Guerrini, Valentina Albanese, Chiara Sturaro, Simona Stragapede, Davide Malfacini, Greta Compagnin, Martina Catani, Anna Fantinati
Publikováno v:
Pharmaceuticals, Vol 16, Iss 11, p 1592 (2023)
The enormous influence in terms of bioactivity, affinity, and selectivity represented by the replacement of (L)-2,6-dimethyl tyrosine (Dmt) instead of Phenylalanine (Phe) into Nociceptin/orphanin (N/OFQ) neuropeptide analogues has been well documente
Externí odkaz:
https://doaj.org/article/6b31797137b34faaa6a39005c793b0d6
Publikováno v:
ChemistryOpen, Vol 9, Iss 2, Pp 100-170 (2020)
Abstract The aim of this review is to highlight the rich chemistry of α‐haloamides originally mainly used to discover new C−N, C−O and C−S bond forming reactions, and later widely employed in C−C cross‐coupling reactions with C(sp3), C(s
Externí odkaz:
https://doaj.org/article/5f8eff08c3e645aaa05d6310fb4cb95b
Autor:
Valentina Gentili, Daria Bortolotti, Mascia Benedusi, Andrea Alogna, Anna Fantinati, Anna Guiotto, Giulia Turrin, Carlo Cervellati, Claudio Trapella, Roberta Rizzo, Giuseppe Valacchi
Publikováno v:
PLoS ONE, Vol 15, Iss 2, p e0229613 (2020)
Mucus form H. aspersa muller has been reported to have several therapeutic proprieties, such as antimicrobial activity, skin protection and wound repair. In this study, we have analyzed H. aspersa mucus (Helixcomplex) bio-adhesive efficacy and its de
Externí odkaz:
https://doaj.org/article/004a1ac2274b427288d9452092b5d35d
Publikováno v:
ACS Omega, Vol 3, Iss 7, Pp 8091-8096 (2018)
Externí odkaz:
https://doaj.org/article/bfdb20bda2ed4e47b48099e2c5bb20c3
Autor:
Petra Martini, Alessandra Boschi, Lorenza Marvelli, Licia Uccelli, Stefano Carli, Giuseppe Cruciani, Erika Marzola, Anna Fantinati, Juan Esposito, Adriano Duatti
Publikováno v:
Molecules, Vol 26, Iss 19, p 5954 (2021)
(1) Background: Metal dithiocarbamate compounds have long been the subject of research due to their ease of formation, excellent properties and potential applications. However, manganese complexes with dithiocarbamates, to our knowledge, have never b
Externí odkaz:
https://doaj.org/article/64e3813593444aee8b59213f08f3c658
Autor:
Anna Fantinati, Sara Bianco, Remo Guerrini, Severo Salvadori, Salvatore Pacifico, Maria Camilla Cerlesi, Girolamo Calo, Claudio Trapella
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-7 (2017)
Abstract A diastereoselective synthesis of the title compound as a single E diastereomer has been efficiently accomplished by assembling the featured pyrano-indole scaffold of the spiro[cyclohexane-dihydropyrano[3,4-b]-indole]-amine framework through
Externí odkaz:
https://doaj.org/article/f9793336055c4632b76511f6e3164571
Autor:
Mauro Marastoni, Claudio Trapella, Alessandra Scotti, Anna Fantinati, Valeria Ferretti, Erika Marzola, Gallerani Eleonora, Riccardo Gavioli, Delia Preti
Publikováno v:
Journal of Enzyme Inhibition and Medicinal Chemistry, Vol 32, Iss 1, Pp 865-877 (2017)
The ubiquitin-proteasome system has been largely investigated for its key role in protein degradation mechanisms that regulate both apoptosis and cell division. Because of their antitumour activity, different classes of proteasome inhibitors have bee
Externí odkaz:
https://doaj.org/article/3083672705d5484a8b6e0097fa75b946