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Giulio Poli

Showing results (61-70 of 102) with videos related to

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Biomolecules|January 28, 2026
Machine Learning-Based Virtual Screening for the Identification of Novel CDK-9 InhibitorsLisa Piazza, Clarissa Poles, Giulia Bononi, et al.
Plos One|June 6, 2018
Rhodanine derivatives as potent anti-HIV and anti-HSV microbicidesCristina Tintori, Giulia Iovenitti, Elisa Rita Ceresola, et al.
Marine Drugs|May 19, 2018
Anticancer Activity of Euplotin C, Isolated from the Marine Ciliate <i>Euplotes crassus</i>, Against Human Melanoma CellsSara Carpi, Beatrice Polini, Giulio Poli, et al.
European Journal of Medicinal Chemistry|February 29, 2016
Synthesis and structure activity relationship investigation of triazolo[1,5-a]pyrimidines as CB2 cannabinoid receptor inverse agonistsMojgan Aghazadeh Tabrizi, Pier Giovanni Baraldi, Emanuela Ruggiero, et al.
International Journal of Molecular Sciences|September 23, 2022
Machine Learning-Based Virtual Screening for the Identification of Cdk5 InhibitorsMiriana Di Stefano, Salvatore Galati, Gabriella Ortore, et al.
Bioorganic Chemistry|June 19, 2019
N-aryl-N'-ureido-O-sulfamates: Potent and selective inhibitors of the human Carbonic Anhydrase VII isoform with neuropathic pain relieving propertiesMurat Bozdag, Giulio Poli, Andrea Angeli, et al.
European Journal of Medicinal Chemistry|December 30, 2018
Continued exploration of 1,2,4-oxadiazole periphery for carbonic anhydrase-targeting primary arene sulfonamides: Discovery of subnanomolar inhibitors of membrane-bound hCA IX isoform that selectively kill cancer cells in hypoxic environmentMikhail Krasavin, Anton Shetnev, Tatyana Sharonova, et al.
Pharmaceuticals (Basel, Switzerland)|July 27, 2022
Novel Potent and Selective Agonists of the GPR55 Receptor Based on the 3-Benzylquinolin-2(1<i>H</i>)-One ScaffoldCostanza Ceni, Michael J Benko, Kawthar A Mohamed, et al.
Future Medicinal Chemistry|January 29, 2025
A series of benzensulfonamide derivatives as new potent carbonic anhydrase IX and XII inhibitorsSusanna Nencetti, Doretta Cuffaro, Lidia Ciccone, et al.
Acta Crystallographica. Section D, Structural Biology|May 28, 2024
An alternative conformation of the N-terminal loop of human dihydroorotate dehydrogenase drives binding to a potent antiproliferative agentMarta Alberti, Giulio Poli, Luca Broggini, et al.
Pageof 11

Showing results (61-70 of 102) with videos related to

Sort By:
Pageof 11
Biomolecules|January 28, 2026
Machine Learning-Based Virtual Screening for the Identification of Novel CDK-9 InhibitorsLisa Piazza, Clarissa Poles, Giulia Bononi, et al.
Plos One|June 6, 2018
Rhodanine derivatives as potent anti-HIV and anti-HSV microbicidesCristina Tintori, Giulia Iovenitti, Elisa Rita Ceresola, et al.
Marine Drugs|May 19, 2018
Anticancer Activity of Euplotin C, Isolated from the Marine Ciliate <i>Euplotes crassus</i>, Against Human Melanoma CellsSara Carpi, Beatrice Polini, Giulio Poli, et al.
European Journal of Medicinal Chemistry|February 29, 2016
Synthesis and structure activity relationship investigation of triazolo[1,5-a]pyrimidines as CB2 cannabinoid receptor inverse agonistsMojgan Aghazadeh Tabrizi, Pier Giovanni Baraldi, Emanuela Ruggiero, et al.
International Journal of Molecular Sciences|September 23, 2022
Machine Learning-Based Virtual Screening for the Identification of Cdk5 InhibitorsMiriana Di Stefano, Salvatore Galati, Gabriella Ortore, et al.
Bioorganic Chemistry|June 19, 2019
N-aryl-N'-ureido-O-sulfamates: Potent and selective inhibitors of the human Carbonic Anhydrase VII isoform with neuropathic pain relieving propertiesMurat Bozdag, Giulio Poli, Andrea Angeli, et al.
European Journal of Medicinal Chemistry|December 30, 2018
Continued exploration of 1,2,4-oxadiazole periphery for carbonic anhydrase-targeting primary arene sulfonamides: Discovery of subnanomolar inhibitors of membrane-bound hCA IX isoform that selectively kill cancer cells in hypoxic environmentMikhail Krasavin, Anton Shetnev, Tatyana Sharonova, et al.
Pharmaceuticals (Basel, Switzerland)|July 27, 2022
Novel Potent and Selective Agonists of the GPR55 Receptor Based on the 3-Benzylquinolin-2(1<i>H</i>)-One ScaffoldCostanza Ceni, Michael J Benko, Kawthar A Mohamed, et al.
Future Medicinal Chemistry|January 29, 2025
A series of benzensulfonamide derivatives as new potent carbonic anhydrase IX and XII inhibitorsSusanna Nencetti, Doretta Cuffaro, Lidia Ciccone, et al.
Acta Crystallographica. Section D, Structural Biology|May 28, 2024
An alternative conformation of the N-terminal loop of human dihydroorotate dehydrogenase drives binding to a potent antiproliferative agentMarta Alberti, Giulio Poli, Luca Broggini, et al.
Pageof 11