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Journal of Medicinal Chemistry|February 27, 2013
Discovery, biological evaluation, and structure-activity and -selectivity relationships of 6'-substituted (E)-2-(benzofuran-3(2H)-ylidene)-N-methylacetamides, a novel class of potent and selective monoamine oxidase inhibitorsLeonardo Pisani, Maria Barletta, Ramon Soto-Otero, et al.Molecules (Basel, Switzerland)|March 22, 2016
Searching for Multi-Targeting Neurotherapeutics against Alzheimer's: Discovery of Potent AChE-MAO B Inhibitors through the Decoration of the 2H-Chromen-2-one Structural MotifLeonardo Pisani, Roberta Farina, Ramon Soto-Otero, et al.Chemmedchem|November 6, 2020
Evaluation of Water-Soluble Mannich Base Prodrugs of 2,3,4,5-Tetrahydroazepino[4,3-b]indol-1(6H)-one as Multitarget-Directed Agents for Alzheimer's DiseaseRosa Purgatorio, Modesto de Candia, Marco Catto, et al.International Journal of Molecular Sciences|October 29, 2025
Investigating Amphoteric 3,4'-Biscoumarin-Based <i>ortho</i>-[(Dialkylamino)methyl]phenols as Dual MAO and ChE InhibitorsAnthi Petrou, Caterina Deruvo, Rosa Purgatorio, et al.Journal of Medicinal Chemistry|March 23, 2011
Homodimeric bis-quaternary heterocyclic ammonium salts as potent acetyl- and butyrylcholinesterase inhibitors: a systematic investigation of the influence of linker and cationic heads over affinity and selectivityAna Conejo-García, Leonardo Pisani, Maria del Carmen Núñez, et al.European Journal of Medicinal Chemistry|June 4, 2019
Investigating 1,2,3,4,5,6-hexahydroazepino[4,3-b]indole as scaffold of butyrylcholinesterase-selective inhibitors with additional neuroprotective activities for Alzheimer's diseaseRosa Purgatorio, Modesto de Candia, Marco Catto, et al.Bioorganic & Medicinal Chemistry|April 1, 2023
Novel thienocycloalkylpyridazinones as useful scaffolds for acetylcholinesterase inhibition and serotonin 5-HT<sub>6</sub> receptor interactionBattistina Asproni, Marco Catto, Giovanni Loriga, et al.Biochemical Pharmacology|July 16, 2017
Potent inhibitors of human LAT1 (SLC7A5) transporter based on dithiazole and dithiazine compounds for development of anticancer drugsLara Napolitano, Mariafrancesca Scalise, Maria Koyioni, et al.RSC Medicinal Chemistry|August 4, 2022
Design, synthesis and biological evaluation of light-driven on-off multitarget AChE and MAO-B inhibitorsMarco Paolino, Mariagrazia Rullo, Samuele Maramai, et al.Journal of Medicinal Chemistry|February 23, 2022
Probing Fluorinated Motifs onto Dual AChE-MAO B Inhibitors: Rational Design, Synthesis, Biological Evaluation, and Early-ADME StudiesMariagrazia Rullo, Marco Cipolloni, Marco Catto, et al.Pageof 12