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European Journal of Medicinal Chemistry|December 31, 2015
5,7-Disubstituted-[1,2,4]triazolo[1,5-a][1,3,5]triazines as pharmacological tools to explore the antagonist selectivity profiles toward adenosine receptorsStephanie Federico, Antonella Ciancetta, Nicola Porta, et al.Medicinal Research Reviews|November 19, 2011
The A3 adenosine receptor as multifaceted therapeutic target: pharmacology, medicinal chemistry, and in silico approachesSiew Lee Cheong, Stephanie Federico, Gopalakrishnan Venkatesan, et al.Plos One|December 2, 2015
The Influence of the 1-(3-Trifluoromethyl-Benzyl)-1H-Pyrazole-4-yl Moiety on the Adenosine Receptors Affinity Profile of Pyrazolo[4,3-e][1,2,4]Triazolo[1,5-c]Pyrimidine DerivativesStephanie Federico, Sara Redenti, Mattia Sturlese, et al.Journal of Medicinal Chemistry|October 27, 2012
Exploring the directionality of 5-substitutions in a new series of 5-alkylaminopyrazolo[4,3-e]1,2,4-triazolo[1,5-c]pyrimidine as a strategy to design novel human a(3) adenosine receptor antagonistsStephanie Federico, Antonella Ciancetta, Davide Sabbadin, et al.Bioorganic & Medicinal Chemistry Letters|September 19, 2008
Identification of novel protein kinase CK1 delta (CK1delta) inhibitors through structure-based virtual screeningGiorgio Cozza, Alessandra Gianoncelli, Monica Montopoli, et al.ACS Medicinal Chemistry Letters|June 20, 2020
Scaffold Repurposing of in-House Chemical Library toward the Identification of New Casein Kinase 1 δ InhibitorsEleonora Cescon, Giovanni Bolcato, Stephanie Federico, et al.Journal of Chemical Information and Modeling|November 14, 2009
Exploring potency and selectivity receptor antagonist profiles using a multilabel classification approach: the human adenosine receptors as a key studyLisa Michielan, Federico Stephanie, Lothar Terfloth, et al.Journal of Neuroinflammation|July 20, 2019
Ciprofloxacin and levofloxacin attenuate microglia inflammatory response via TLR4/NF-kB pathwayMorena Zusso, Valentina Lunardi, Davide Franceschini, et al.Bioorganic & Medicinal Chemistry|October 16, 2007
Amide bond direction modulates G-quadruplex recognition and telomerase inhibition by 2,6 and 2,7 bis-substituted anthracenedione derivativesGiuseppe Zagotto, Claudia Sissi, Stefano Moro, et al.Frontiers in Cellular Neuroscience|September 20, 2024
CoA synthase plays a critical role in neurodevelopment and neurodegenerationChiara Cavestro, Marco D'Amato, Maria Nicol Colombo, et al.Pageof 31