Search Results - "Spinelli, Lucio"

Expanding the Library of 1,2,4-Oxadiazole Derivatives: Discovery of New Farnesoid X Receptor (FXR) Antagonists/Pregnane X Receptor (PXR) Agonists by Finamore, Claudia, Festa, Carmen, Fiorillo, Bianca, Leva, Francesco Saverio Di, Roselli, Rosalinda, Marchianò, Silvia, Biagioli, Michele, Spinelli, Lucio, Fiorucci, Stefano, Limongelli, Vittorio, Zampella, Angela, De Marino, Simona

“…Compounds featuring a 1,2,4-oxadiazole core have been recently identified as a new chemotype of farnesoid X receptor (FXR) antagonists. With the aim to expand…”
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A label free chemoproteomic-based platform to disclose cannabidiol molecular mechanism of action on chronic myelogenous leukemia cancer cells by Ceccacci, Sara, Corsi, Lorenzo, Spinelli, Lucio, Caroli, Clarissa, Marani, Matilde, Anceschi, Lisa, Mozzicafreddo, Matteo, Pellati, Federica, Monti, Maria Chiara

“…The discovery of the interactome of cannabidiol (CBD), a non-psychoactive cannabinoid from Cannabis sativa L., has been here performed on chronic myelogenous…”
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Expanding the Library of 1,2,4-Oxadiazole Derivatives: Discovery of New Farnesoid X Receptor Agonists by Finamore, Claudia, Festa, Carmen, Fiorillo, Bianca, Leva, Francesco Saverio Di, Roselli, Rosalinda, Marchianò, Silvia, Biagioli, Michele, Spinelli, Lucio, Fiorucci, Stefano, Limongelli, Vittorio, Zampella, Angela, De Marino, Simona

“…Compounds featuring a 1,2,4-oxadiazole core have been recently identified as a new chemotype of farnesoid X receptor (FXR) antagonists. With the aim to expand…”
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Design, Synthesis, and Pharmacological Evaluation of Dual FXR-LIFR Modulators for the Treatment of Liver Fibrosis by Rapacciuolo, Pasquale, Finamore, Claudia, Giorgio, Cristina Di, Fiorillo, Bianca, Massa, Carmen, Urbani, Ginevra, Marchianò, Silvia, Bordoni, Martina, Cassiano, Chiara, Morretta, Elva, Spinelli, Lucio, Lupia, Antonio, Moraca, Federica, Biagioli, Michele, Sepe, Valentina, Monti, Maria Chiara, Catalanotti, Bruno, Fiorucci, Stefano, Zampella, Angela

“…Although multiple approaches have been suggested, treating mild-to-severe fibrosis in the context of metabolic dysfunction associated with liver disease…”
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