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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.Journal of Enzyme Inhibition and Medicinal Chemistry|April 8, 2020
6,7-Dimethoxy-2-phenethyl-1,2,3,4-tetrahydroisoquinoline amides and corresponding ester isosteres as multidrug resistance reversersLaura Braconi, Gianluca Bartolucci, Marialessandra Contino, et al.Molecules (Basel, Switzerland)|July 27, 2024
Dual Inhibitors of P-gp and Carbonic Anhydrase XII (hCA XII) against Tumor Multidrug Resistance with Piperazine ScaffoldLaura Braconi, Chiara Riganti, Astrid Parenti, et al.European Journal of Medicinal Chemistry|December 17, 2021
2-(2-Hydroxyethyl)piperazine derivatives as potent human carbonic anhydrase inhibitors: Synthesis, enzyme inhibition, computational studies and antiglaucoma activityNiccolò Chiaramonte, Andrea Angeli, Silvia Sgambellone, et al.European Journal of Medicinal Chemistry|April 5, 2019
Modulation of the spacer in N,N-bis(alkanol)amine aryl ester heterodimers led to the discovery of a series of highly potent P-glycoprotein-based multidrug resistance (MDR) modulatorsSilvia Dei, Laura Braconi, Alfonso Trezza, et al.European Journal of Medicinal Chemistry|September 9, 2019
Design, synthesis and biological evaluation of stereo- and regioisomers of amino aryl esters as multidrug resistance (MDR) reversersElisabetta Teodori, Marialessandra Contino, Chiara Riganti, et al.Pageof 3