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Maria Novella Romanelli

Showing results (31-40 of 95) with videos related to

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Bioorganic & Medicinal Chemistry Letters|December 15, 2010
Inhibition of P-glycoprotein-mediated Multidrug Resistance (MDR) by N,N-bis(cyclohexanol)amine aryl esters: further restriction of molecular flexibility maintains high potency and efficacyCecilia Martelli, Silvia Dei, Catherine Lambert, et al.
Molecules (Basel, Switzerland)|January 21, 2022
New Histamine-Related Five-Membered N-Heterocycle Derivatives as Carbonic Anhydrase I ActivatorsNiccolò Chiaramonte, Alessio Gabellini, Andrea Angeli, et al.
Scientific Reports|April 29, 2016
Two types of interneurons in the mouse lateral geniculate nucleus are characterized by different h-current densityMichael Leist, Maia Datunashvilli, Tatyana Kanyshkova, et al.
Journal of Medicinal Chemistry|January 29, 2010
Structure-activity relationships studies in a series of N,N-bis(alkanol)amine aryl esters as P-glycoprotein (Pgp) dependent multidrug resistance (MDR) inhibitorsCecilia Martelli, Marcella Coronnello, Silvia Dei, et al.
European Journal of Medicinal Chemistry|January 24, 2017
N-alkanol-N-cyclohexanol amine aryl esters: Multidrug resistance (MDR) reversing agents with high potency and efficacyElisabetta Teodori, Silvia Dei, Marcella Coronnello, et al.
Bioorganic & Medicinal Chemistry|November 6, 2007
Design, synthesis and preliminary pharmacological evaluation of new piperidine and piperazine derivatives as cognition-enhancersElisabetta Martini, Carla Ghelardini, Silvia Dei, et al.
European Journal of Medicinal Chemistry|February 4, 2016
New quinoline derivatives as nicotinic receptor modulatorsDina Manetti, Cristina Bellucci, Silvia Dei, et al.
Medicinal Chemistry (Shariqah (United Arab Emirates))|June 22, 2006
Enantioselective synthesis and preliminary pharmacological evaluation of the enantiomers of unifiram (DM232), a potent cognition-enhancing agentElisabetta Martini, Carla Ghelardini, Carlo Bertucci, et al.
Bioorganic & Medicinal Chemistry|December 31, 2003
Structure-activity relationship studies on unifiram (DM232) and sunifiram (DM235), two novel and potent cognition enhancing drugsSerena Scapecchi, Elisabetta Martini, Dina Manetti, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry|April 28, 2020
Synthesis and carbonic anhydrase activating properties of a series of 2-amino-imidazolines structurally related to clonidine<sup>1</sup>Niccolò Chiaramonte, Soumia Maach, Caterina Biliotti, et al.
Pageof 10

Showing results (31-40 of 95) with videos related to

Sort By:
Pageof 10
Bioorganic & Medicinal Chemistry Letters|December 15, 2010
Inhibition of P-glycoprotein-mediated Multidrug Resistance (MDR) by N,N-bis(cyclohexanol)amine aryl esters: further restriction of molecular flexibility maintains high potency and efficacyCecilia Martelli, Silvia Dei, Catherine Lambert, et al.
Molecules (Basel, Switzerland)|January 21, 2022
New Histamine-Related Five-Membered N-Heterocycle Derivatives as Carbonic Anhydrase I ActivatorsNiccolò Chiaramonte, Alessio Gabellini, Andrea Angeli, et al.
Scientific Reports|April 29, 2016
Two types of interneurons in the mouse lateral geniculate nucleus are characterized by different h-current densityMichael Leist, Maia Datunashvilli, Tatyana Kanyshkova, et al.
Journal of Medicinal Chemistry|January 29, 2010
Structure-activity relationships studies in a series of N,N-bis(alkanol)amine aryl esters as P-glycoprotein (Pgp) dependent multidrug resistance (MDR) inhibitorsCecilia Martelli, Marcella Coronnello, Silvia Dei, et al.
European Journal of Medicinal Chemistry|January 24, 2017
N-alkanol-N-cyclohexanol amine aryl esters: Multidrug resistance (MDR) reversing agents with high potency and efficacyElisabetta Teodori, Silvia Dei, Marcella Coronnello, et al.
Bioorganic & Medicinal Chemistry|November 6, 2007
Design, synthesis and preliminary pharmacological evaluation of new piperidine and piperazine derivatives as cognition-enhancersElisabetta Martini, Carla Ghelardini, Silvia Dei, et al.
European Journal of Medicinal Chemistry|February 4, 2016
New quinoline derivatives as nicotinic receptor modulatorsDina Manetti, Cristina Bellucci, Silvia Dei, et al.
Medicinal Chemistry (Shariqah (United Arab Emirates))|June 22, 2006
Enantioselective synthesis and preliminary pharmacological evaluation of the enantiomers of unifiram (DM232), a potent cognition-enhancing agentElisabetta Martini, Carla Ghelardini, Carlo Bertucci, et al.
Bioorganic & Medicinal Chemistry|December 31, 2003
Structure-activity relationship studies on unifiram (DM232) and sunifiram (DM235), two novel and potent cognition enhancing drugsSerena Scapecchi, Elisabetta Martini, Dina Manetti, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry|April 28, 2020
Synthesis and carbonic anhydrase activating properties of a series of 2-amino-imidazolines structurally related to clonidine<sup>1</sup>Niccolò Chiaramonte, Soumia Maach, Caterina Biliotti, et al.
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