Showing results (91-100 of 150) with videos related to
Sort By:
Pageof 15
European Journal of Medicinal Chemistry|March 8, 2013
Synthesis and structure-activity relationship studies in serotonin 5-HT(1A) receptor agonists based on fused pyrrolidone scaffoldsAndrea Cappelli, Monica Manini, Salvatore Valenti, et al.Bioorganic Chemistry|June 12, 2019
Bridged bicyclic 2,3-dioxabicyclo[3.3.1]nonanes as antiplasmodial agents: Synthesis, structure-activity relationships and studies on their biomimetic reaction with Fe(II)Sarah D'Alessandro, Gloria Alfano, Luisa Di Cerbo, et al.Journal of Medicinal Chemistry|June 25, 2005
Pyrrolo[1,5]benzoxa(thia)zepines as a new class of potent apoptotic agents. Biological studies and identification of an intracellular location of their drug targetMargaret M Mc Gee, Sandra Gemma, Stefania Butini, et al.Organic & Biomolecular Chemistry|June 2, 2011
Pyrroloquinoxaline hydrazones as fluorescent probes for amyloid fibrilsSandra Gemma, Laura Colombo, Gianluigi Forloni, et al.European Journal of Medicinal Chemistry|September 10, 2025
Developing Type II F508del-CFTR correctors with a protective effect against respiratory virusesFrancesca Barbieri, Maria Grazia Martina, Emanuela Pesce, et al.Antioxidants (Basel, Switzerland)|September 27, 2025
Unveiling Wound Healing Properties of Biostimulated Walnut Kernel Extracts via Epithelial Mesenchymal Transition: Switching a Nutritional Matrix into a Therapeutic RemedyRiccardo Fedeli, Elia Ranzato, Simona Martinotti, et al.ACS Infectious Diseases|October 31, 2019
Screening and Phenotypical Characterization of <i>Schistosoma mansoni</i> Histone Deacetylase 8 (<i>Sm</i>HDAC8) Inhibitors as Multistage Antischistosomal AgentsFulvio Saccoccia, Margherita Brindisi, Roberto Gimmelli, et al.Journal of Medicinal Chemistry|March 18, 2005
Development of molecular probes for the identification of extra interaction sites in the mid-gorge and peripheral sites of butyrylcholinesterase (BuChE). Rational design of novel, selective, and highly potent BuChE inhibitorsGiuseppe Campiani, Caterina Fattorusso, Stefania Butini, et al.Journal of Medicinal Chemistry|May 31, 2011
Selective kainate receptor (GluK1) ligands structurally based upon 1H-cyclopentapyrimidin-2,4(1H,3H)-dione: synthesis, molecular modeling, and pharmacological and biostructural characterizationRaminta Venskutonyte, Stefania Butini, Salvatore Sanna Coccone, et al.European Journal of Pharmacology|July 23, 2013
PBOX-15 induces apoptosis and improves the efficacy of oxaliplatin in human colorectal cancer cell linesGiuseppina Gangemi, Patrizia Gazzerro, Donatella Fiore, et al.Pageof 15