Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Vitale, R."'
Autor:
Daniele Ciceri, Luciano De Petrocellis, Orazio Taglialatela-Scafati, Lolita Arnoldi, Pietro Amodeo, Giuseppina Chianese, Emanuele Benetti, Rosa Maria Vitale, Eric de Combarieu, Aniello Schiano-Moriello, Annalisa Lopatriello, Diego Caprioglio, Daiana Mattoteia, Giovanni Appendino
Publikováno v:
Journal of natural products
83 (2020): 2727–2736. doi:10.1021/acs.jnatprod.0c00668
info:cnr-pdr/source/autori:Chianese, Giuseppina; Lopatriello, Annalisa; Schiano-Moriello, Aniello; Caprioglio, Diego; Mattoteia, Daiana; Benetti, Emanuele; Ciceri, Daniele; Arnoldi, Lolita; De Combarieu, Eric; Vitale, Rosa M.; Amodeo, Pietro; Appendino, Giovanni; De Petrocellis, Luciano; Taglialatela-Scafati, Orazio/titolo:Cannabitwinol, a Dimeric Phytocannabinoid from Hemp, Cannabis sativa L., Is a Selective Thermo-TRP Modulator/doi:10.1021%2Facs.jnatprod.0c00668/rivista:Journal of natural products (Print)/anno:2020/pagina_da:2727/pagina_a:2736/intervallo_pagine:2727–2736/volume:83
83 (2020): 2727–2736. doi:10.1021/acs.jnatprod.0c00668
info:cnr-pdr/source/autori:Chianese, Giuseppina; Lopatriello, Annalisa; Schiano-Moriello, Aniello; Caprioglio, Diego; Mattoteia, Daiana; Benetti, Emanuele; Ciceri, Daniele; Arnoldi, Lolita; De Combarieu, Eric; Vitale, Rosa M.; Amodeo, Pietro; Appendino, Giovanni; De Petrocellis, Luciano; Taglialatela-Scafati, Orazio/titolo:Cannabitwinol, a Dimeric Phytocannabinoid from Hemp, Cannabis sativa L., Is a Selective Thermo-TRP Modulator/doi:10.1021%2Facs.jnatprod.0c00668/rivista:Journal of natural products (Print)/anno:2020/pagina_da:2727/pagina_a:2736/intervallo_pagine:2727–2736/volume:83
Cannabitwinol (CBDD, 3), the second member of a new class of dimeric phytocannabinoids in which two units are connected by a methylene bridge, was isolated from a hemp (Cannabis sativa L.) industrial extract. The structural characterization of cannab
Autor:
Elisabetta Panza, Orazio Taglialatela-Scafati, Rosa Maria Vitale, Pietro Amodeo, Luciano De Petrocellis, Fabio Arturo Iannotti, Giovanni Appendino, Fabrizia De Maio
Publikováno v:
Molecules (Basel, Online) 25 (2020). doi:10.3390/molecules25051119
info:cnr-pdr/source/autori:Iannotti F.A.; De Maio F.; Panza E.; Appendino G.; Taglialatela-Scafati O.; De Petrocellis L.; Amodeo P.; Vitale R.M./titolo:Identification and Characterization of Cannabimovone, a Cannabinoid from Cannabis sativa, as a Novel PPARgamma Agonist via a Combined Computational and Functional Study/doi:10.3390%2Fmolecules25051119/rivista:Molecules (Basel, Online)/anno:2020/pagina_da:/pagina_a:/intervallo_pagine:/volume:25
Molecules, Vol 25, Iss 5, p 1119 (2020)
Molecules
Volume 25
Issue 5
info:cnr-pdr/source/autori:Iannotti F.A.; De Maio F.; Panza E.; Appendino G.; Taglialatela-Scafati O.; De Petrocellis L.; Amodeo P.; Vitale R.M./titolo:Identification and Characterization of Cannabimovone, a Cannabinoid from Cannabis sativa, as a Novel PPARgamma Agonist via a Combined Computational and Functional Study/doi:10.3390%2Fmolecules25051119/rivista:Molecules (Basel, Online)/anno:2020/pagina_da:/pagina_a:/intervallo_pagine:/volume:25
Molecules, Vol 25, Iss 5, p 1119 (2020)
Molecules
Volume 25
Issue 5
Phytocannabinoids (pCBs) are a large family of meroterpenoids isolated from the plant Cannabis sativa. &Delta
9-Tetrahydrocannabinol (THC) and cannabidiol (CBD) are the best investigated phytocannabinoids due to their relative abundance and inte
9-Tetrahydrocannabinol (THC) and cannabidiol (CBD) are the best investigated phytocannabinoids due to their relative abundance and inte
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e0544a5511a5ff04fc924b2c522f8d5e
https://publications.cnr.it/doc/438891
https://publications.cnr.it/doc/438891
Autor:
Deborah H. Charych, Elena Di Matteo, Anna Morena D'Alise, Gabriella Cotugno, Maria De Lucia, Veronica Bignone, Fabio Giovanni Tucci, Guido Leoni, Rosa Bartolomeo, Elisa Scarselli, Elisa Micarelli, Jonathan Zalevsky, Alfredo Nicosia, Linda Nocchi, Francesca Langone, Rosa Maria Vitale, Fulvia Troise, Irene Garzia, Armin Lahm
Publikováno v:
Journal for ImmunoTherapy of Cancer, Vol 9, Iss 11 (2021)
Journal for Immunotherapy of Cancer
Journal for Immunotherapy of Cancer
BackgroundA number of different immune pathways are involved in the effective killing of cancer cells, collectively named as the ‘Cancer Immunity Cycle’. Anti-PD-1 checkpoint blockade (CPB) therapy is active on one of these pathways and reinvigor
Autor:
Jochen Antel, Rosa Maria Vitale, Claudiu T. Supuran, Carlo Pedone, Andrea Scozzafava, Giuseppina De Simone, Pietro Amodeo, Wurl Michael
Publikováno v:
Bioorganic & medicinal chemistry
15 (2007): 4152–4158. doi:10.1016/j.bmc.2007.03.070
info:cnr-pdr/source/autori:Vitale RM; Pedone C; Amodeo P; Antel J; Wurl M; Scozzafava A; Supuran CT; De Simone G/titolo:Molecular modeling study for the binding of zonisamide and topiramate to the human mitochondrial carbonic anhydrase isoform VA/doi:10.1016%2Fj.bmc.2007.03.070/rivista:Bioorganic & medicinal chemistry (Print)/anno:2007/pagina_da:4152/pagina_a:4158/intervallo_pagine:4152–4158/volume:15
15 (2007): 4152–4158. doi:10.1016/j.bmc.2007.03.070
info:cnr-pdr/source/autori:Vitale RM; Pedone C; Amodeo P; Antel J; Wurl M; Scozzafava A; Supuran CT; De Simone G/titolo:Molecular modeling study for the binding of zonisamide and topiramate to the human mitochondrial carbonic anhydrase isoform VA/doi:10.1016%2Fj.bmc.2007.03.070/rivista:Bioorganic & medicinal chemistry (Print)/anno:2007/pagina_da:4152/pagina_a:4158/intervallo_pagine:4152–4158/volume:15
Zonisamide and topiramate are two antiepileptic drugs known to induce weight loss in epilepsy patients. These molecules were recently shown to act as carbonic anhydrase (CA) inhibitors, being presumed that the weight loss may be due to the inhibition
Autor:
Luisa Mengatto, Andrea Cavalli, Anna Berteotti, Romina Vitale, Stefano Ponzano, Tiziano Bandiera, Fabio Bertozzi, Giovanni Bottegoni, Rita Petracca, Daniele Piomelli
Publikováno v:
Ponzano, S; Berteotti, A; Petracca, R; Vitale, R; Mengatto, L; Bandiera, T; et al.(2014). Synthesis, biological evaluation, and 3D QSAR study of 2-methyl-4-oxo-3-oxetanylcarbamic acid esters as N-acylethanolamine acid amidase (NAAA) inhibitors. Journal of Medicinal Chemistry, 57(23), 10101-10111. doi: 10.1021/jm501455s. UC Irvine: Retrieved from: http://www.escholarship.org/uc/item/4058m5gd
© 2014 American Chemical Society. N-(2-Oxo-3-oxetanyl)carbamic acid esters have recently been reported to be noncompetitive inhibitors of the N-acylethanolamine acid amidase (NAAA) potentially useful for the treatment of pain and inflammation. In th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7172cc376699c5581178da5c0d22925a
https://hdl.handle.net/11576/2688382
https://hdl.handle.net/11576/2688382
Autor:
Laura Zaccaro, Benedetto Di Blasio, Carla Isernia, Michele Saviano, Carlo Pedone, Pietro Amodeo, Roberto Fattorusso, Rosa Maria Vitale
Publikováno v:
ChemBioChem
4 (2003): 73–81.
info:cnr-pdr/source/autori:Vitale, Rosa Maria; Zaccaro, Laura; Di Blasio, Benedetto; Fattorusso, Roberto; Isernia, Carla; Amodeo, Pietro; Pedone, Carlo; Saviano, Michele/titolo:Conformational features of human melanin-concentrating hormone: an NMR and computational analysis/doi:/rivista:ChemBioChem (Print)/anno:2003/pagina_da:73/pagina_a:81/intervallo_pagine:73–81/volume:4
4 (2003): 73–81.
info:cnr-pdr/source/autori:Vitale, Rosa Maria; Zaccaro, Laura; Di Blasio, Benedetto; Fattorusso, Roberto; Isernia, Carla; Amodeo, Pietro; Pedone, Carlo; Saviano, Michele/titolo:Conformational features of human melanin-concentrating hormone: an NMR and computational analysis/doi:/rivista:ChemBioChem (Print)/anno:2003/pagina_da:73/pagina_a:81/intervallo_pagine:73–81/volume:4
The conformational features of human melanin-concentrating hormone (hMCH) [Asp1-Phe2-Asp3-Met4-Leu5-Arg6-cyclo(S[bond]S)(Cys7-Met8-Leu9-Gly10-Arg11-Val12-Tyr13-Arg14-Pro15-Cys16)-Trp17-Gln18-Val19], in water and in a CD(3)CN/H(2)O (1:1 v/v) mixture a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7da79eee36e7a30dc3bf8742a3ceff29
http://hdl.handle.net/11588/166122
http://hdl.handle.net/11588/166122
Autor:
Michele Saviano, Roberto Fattorusso, Ettore Benedetti, Carlo Pedone, Giuseppe Perretta, Rosa Maria Vitale, Laura Zaccaro, Enrico M. Bucci
Publikováno v:
Journal of peptide science
9 (2003): 90–105.
info:cnr-pdr/source/autori:Zaccaro, Laura; Bucci, Enrico; Vitale, Rosa Maria; Perretta, Giuseppe; Fattorusso, Roberto; Benedetti, Ettore; Saviano, Michele; Pedone, Carlo/titolo:Synthetic peptides mimicking the interleukin-6%2Fgp130 interaction: A two-helix bundle system. Design and conformational studies/doi:/rivista:Journal of peptide science (Print)/anno:2003/pagina_da:90/pagina_a:105/intervallo_pagine:90–105/volume:9
9 (2003): 90–105.
info:cnr-pdr/source/autori:Zaccaro, Laura; Bucci, Enrico; Vitale, Rosa Maria; Perretta, Giuseppe; Fattorusso, Roberto; Benedetti, Ettore; Saviano, Michele; Pedone, Carlo/titolo:Synthetic peptides mimicking the interleukin-6%2Fgp130 interaction: A two-helix bundle system. Design and conformational studies/doi:/rivista:Journal of peptide science (Print)/anno:2003/pagina_da:90/pagina_a:105/intervallo_pagine:90–105/volume:9
The objective of our study was to mimic in a typical reductionist approach the molecular interactions observed at the interface between the gp130 receptor and interleukin-6 during formation of their complex. A peptide system obtained by reproducing s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::38c6772a17d839f19e391bdc02f2ed34
http://hdl.handle.net/11588/131094
http://hdl.handle.net/11588/131094