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Journal of Clinical Medicine|March 14, 2026
Three-Dimensional Postmortem Ultrasound of the Fetal Corneal Volume to Estimate Postmortem IntervalPatricia Ibarra Vilar, Dominique A Badr, Laura De Luca, et al.Molecular Informatics|August 23, 2016
Rational Design, Synthesis and Evaluation of Coumarin Derivatives as Protein-protein Interaction InhibitorsLaura De Luca, Fatima E Agharbaoui, Rosaria Gitto, et al.Bioorganic & Medicinal Chemistry|July 16, 2010
New chloro,fluorobenzylindole derivatives as integrase strand-transfer inhibitors (INSTIs) and their mode of actionStefania Ferro, Laura De Luca, Maria Letizia Barreca, et al.Bioorganic & Medicinal Chemistry|June 20, 2013
Indole derivatives as dual-effective agents for the treatment of neurodegenerative diseases: synthesis, biological evaluation, and molecular modeling studiesMaria Rosa Buemi, Laura De Luca, Alba Chimirri, et al.Bioorganic & Medicinal Chemistry|November 2, 2011
Synthesis and biological profile of new 1,2,3,4-tetrahydroisoquinolines as selective carbonic anhydrase inhibitorsRosaria Gitto, Francesca Maria Damiano, Laura De Luca, et al.Journal of Enzyme Inhibition and Medicinal Chemistry|July 9, 2019
Seeking new approach for therapeutic treatment of cholera disease via inhibition of bacterial carbonic anhydrases: experimental and theoretical studies for sixteen benzenesulfonamide derivativesRosaria Gitto, Laura De Luca, Francesca Mancuso, et al.RSC Medicinal Chemistry|September 21, 2023
Discovery and computational studies of piperidine/piperazine-based compounds endowed with sigma receptor affinityLaura De Luca, Lisa Lombardo, Salvatore Mirabile, et al.Journal of Biological Inorganic Chemistry : JBIC : a Publication of the Society of Biological Inorganic Chemistry|September 2, 2015
Investigation of the salicylaldehyde thiosemicarbazone scaffold for inhibition of influenza virus PA endonucleaseDominga Rogolino, Alessia Bacchi, Laura De Luca, et al.Journal of Enzyme Inhibition and Medicinal Chemistry|July 3, 2020
Synthesis, computational studies and assessment of in vitro inhibitory activity of umbelliferon-based compounds against tumour-associated carbonic anhydrase isoforms IX and XIIFrancesca Mancuso, Laura De Luca, Andrea Angeli, et al.International Journal of Molecular Sciences|May 13, 2023
Leveraging the 3-Chloro-4-fluorophenyl Motif to Identify Inhibitors of Tyrosinase from Agaricus bisporusSalvatore Mirabile, Laura Ielo, Lisa Lombardo, et al.Pageof 19