Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Lavinia Cicione"'
Autor:
Maria Luz Bellido, Eduardo Muñoz, Giovanni Appendino, Zuhal Toker, Federica Pollastro, Giuseppina Chianese, Lavinia Cicione, Hasan Çetin Özen, Orazio Taglialatela-Scafati
Publikováno v:
Journal of Natural Products. 75:453-458
Apart from a large amount (ca. 2.0%) of α-bisabolol β-d-fucopyranoside (2a), the aerial parts of the Mediterranean weed Carthamus glaucus afforded an unusual triglyceride (E-2-crotonyl-1,3- distearolylglycerol, 7), two lipophilic flavonoids (6a,b),
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ebc0a47eb929de1dec469d5f05710d53
https://doi.org/10.1021/np2008973
https://doi.org/10.1021/np2008973
Autor:
Oliver Werz, Julia Bauer, Alberto Minassi, Andreas Koeberle, Giovanni Appendino, Lavinia Cicione, Stefan Laufer
Publikováno v:
European Journal of Organic Chemistry. 2012:772-779
Using the synthesis of the heterodimeric phloroglucinyl pyrone arzanol as a benchmark reaction, a carba-version of the Betti multicomponent reaction has been developed. Capitalizing on the fluorous activation of the phenolic component and the use of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f14873e4b3d06af4ee06ded0988d0a26
https://doi.org/10.1002/ejoc.201101193
https://doi.org/10.1002/ejoc.201101193
Autor:
Francesca Guida, Lavinia Cicione, Federico Corelli, Claudia Mugnaini, Roger G. Pertwee, Teresa Semeraro, Maria De Chiaro, Serena Pasquini, Livio Luongo, Vincenzo Di Marzo, Daniele Bolognini, Maria Grazia Cascio, Sabatino Maione, Pietro Marini, Maria Cristina De Rosa, Alessia Ligresti
Publikováno v:
Journal of medicinal chemistry 53 (2010): 5915–5928.
info:cnr-pdr/source/autori:Pasquini S, Ligresti A, Mugnaini C, Semeraro T, Cicione L, De Rosa M, Guida F, Luongo L, De Chiaro M, Cascio MG, Bolognini D, Marini P, Pertwee R, Maione S, Di Marzo V, Corelli F./titolo:Investigations on the 4-quinolone-3-carboxylic acid motif. 3. Synthesis, structure-affinity relationships, and pharmacological characterization of 6-substituted 4-quinolone-3-carboxamides as highly selective cannabinoid-2 receptor ligands./doi:/rivista:Journal of medicinal chemistry/anno:2010/pagina_da:5915/pagina_a:5928/intervallo_pagine:5915–5928/volume:53
info:cnr-pdr/source/autori:Pasquini S, Ligresti A, Mugnaini C, Semeraro T, Cicione L, De Rosa M, Guida F, Luongo L, De Chiaro M, Cascio MG, Bolognini D, Marini P, Pertwee R, Maione S, Di Marzo V, Corelli F./titolo:Investigations on the 4-quinolone-3-carboxylic acid motif. 3. Synthesis, structure-affinity relationships, and pharmacological characterization of 6-substituted 4-quinolone-3-carboxamides as highly selective cannabinoid-2 receptor ligands./doi:/rivista:Journal of medicinal chemistry/anno:2010/pagina_da:5915/pagina_a:5928/intervallo_pagine:5915–5928/volume:53
A set of quinolone-3-carboxamides 2 bearing diverse substituents at position 1, 3, and 6 of the bicyclic nucleus was prepared. Except for six compounds exhibiting Ki > 100 nM, all the quinolone-3-carboxamides 2 proved to be high affinity CB2 ligands,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f731f5ff70ab14c9c6058d123b03fb17
https://pubmed.ncbi.nlm.nih.gov/20718492
https://pubmed.ncbi.nlm.nih.gov/20718492
Publikováno v:
ChemInform. 41
The reaction of aldehydes with β-dicarbonyls and electron-rich aromatics was investigated to generate in a multicomponent fashion crossed adducts of biological relevance. 4-Hydroxycoumarin, triacetic acid lactone, indole, and a selection of aliphati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::23e16a271ad3f3fccb403fad423cae4c
https://doi.org/10.1002/chin.201003139
https://doi.org/10.1002/chin.201003139
Autor:
Serena Pasquini, Alessia Ligresti, Claudia Mugnaini, Teresa Semeraro, Lavinia Cicione, Maria De Rosa, Francesca Guida, Livio Luongo, Maria De Chiaro, Maria Grazia Cascio, Daniele Bolognini, Pietro Marini, Roger Pertwee, Sabatino Maione, Vincenzo Di Marzo, Federico Corelli
Publikováno v:
Journal of Medicinal Chemistry; Aug2010, Vol. 53 Issue 16, p5915-5928, 14p