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European Journal of Medicinal Chemistry|October 6, 2014
Multidrug resistance (MDR) reversers: High activity and efficacy in a series of asymmetrical N,N-bis(alkanol)amine aryl estersSilvia Dei, Marcella Coronnello, Elisa Floriddia, et al.
Journal of Medicinal Chemistry|September 30, 2005
Design, synthesis, and preliminary pharmacological evaluation of a set of small molecules that directly activate gi proteinsDina Manetti, Lorenzo Di Cesare Mannelli, Silvia Dei, et al.
Bioorganic & Medicinal Chemistry|September 30, 2009
Design, synthesis and nootropic activity of new analogues of sunifiram and sapunifiram, two potent cognition-enhancersElisabetta Martini, Alberto Salvicchi, Carla Ghelardini, et al.
Journal of Medicinal Chemistry|March 9, 2011
Synthesis and biological evaluation of 3,7-diazabicyclo[4.3.0]nonan-8-ones as potential nootropic and analgesic drugsElisabetta Martini, Lorenzo Di Cesare Mannelli, Gianluca Bartolucci, et al.
European Journal of Medicinal Chemistry|August 13, 2023
Tetrazole and oxadiazole derivatives as bioisosteres of tariquidar and elacridar: New potent P-gp modulators acting as MDR reversersLaura Braconi, Silvia Dei, Marialessandra Contino, et al.
Molecular Pharmacology|June 14, 2023
Chemical, Pharmacological, and Structural Characterization of Novel Acrylamide-Derived Modulators of the GABAA ReceptorHugo R Arias, Spencer R Pierce, Allison L Germann, et al.
Journal of Medicinal Chemistry|August 28, 2010
Design, synthesis, and preliminary biological evaluation of new isoform-selective f-current blockersMichele Melchiorre, Martina Del Lungo, Luca Guandalini, et al.
Journal of Medicinal Chemistry|October 21, 2022
New Dual P-Glycoprotein (P-gp) and Human Carbonic Anhydrase XII (hCA XII) Inhibitors as Multidrug Resistance (MDR) Reversers in Cancer CellsLaura Braconi, Elisabetta Teodori, Chiara Riganti, et al.
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