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Journal of Medicinal Chemistry|April 5, 2002
Structure-activity relationships in 1,4-benzodioxan-related compounds. 7. Selectivity of 4-phenylchroman analogues for alpha(1)-adrenoreceptor subtypesWilma Quaglia, Maria Pigini, Alessandro Piergentili, et al.European Journal of Medicinal Chemistry|November 15, 2012
Design, synthesis and biological evaluation of 5-hydroxy, 5-substituted-pyrimidine-2,4,6-triones as potent inhibitors of gelatinases MMP-2 and MMP-9Orazio Nicolotti, Marco Catto, Ilenia Giangreco, et al.Bioorganic & Medicinal Chemistry|October 22, 2008
1,3-Dialkyl-8-(hetero)aryl-9-OH-9-deazaxanthines as potent A2B adenosine receptor antagonists: design, synthesis, structure-affinity and structure-selectivity relationshipsAngela Stefanachi, Orazio Nicolotti, Francesco Leonetti, et al.European Journal of Medicinal Chemistry|November 16, 2013
Fine molecular tuning at position 4 of 2H-chromen-2-one derivatives in the search of potent and selective monoamine oxidase B inhibitorsLeonardo Pisani, Marco Catto, Orazio Nicolotti, et al.Molecular Cancer Therapeutics|June 16, 2005
Identification of compounds that inhibit growth of 2-amino-1-methyl-6-phenylimidazo(4,5-b)pyridine-resistant cancer cellsKurtis E Bachman, Jason Sager, Ian Cheong, et al.Future Medicinal Chemistry|October 7, 2015
Docking-based classification models for exploratory toxicology studies on high-quality estrogenic experimental dataDaniela Trisciuzzi, Domenico Alberga, Kamel Mansouri, et al.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.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.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.Pageof 9