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Marta Ferraroni

Showing results (91-100 of 112) with videos related to

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Bioorganic & Medicinal Chemistry|May 6, 2008
Muscarinic antagonists with multiple stereocenters: Synthesis, affinity profile and functional activity of isomeric 1-methyl-2-(2,2-alkylaryl-1,3-oxathiolan-5-yl)pyrrolidine sulfoxide derivativesSilvia Dei, Cristina Bellucci, Michela Buccioni, et al.
ACS Medicinal Chemistry Letters|February 19, 2025
Correction to "Study of Chalcogen Aspirin Derivatives with Carbonic Anhydrase Inhibitory Properties for Treating Inflammatory Pain"Elena Lucarini, Vanessa D'Antongiovanni, Luca Antonioli, et al.
Journal of Medicinal Chemistry|January 10, 2023
First-in-Class Dual Hybrid Carbonic Anhydrase Inhibitors and Transient Receptor Potential Vanilloid 1 Agonists Revert Oxaliplatin-Induced NeuropathyAndrea Angeli, Laura Micheli, Fabrizio Carta, et al.
European Journal of Medicinal Chemistry|August 17, 2019
Carbonic anhydrase inhibitors based on sorafenib scaffold: Design, synthesis, crystallographic investigation and effects on primary breast cancer cellsMurat Bozdag, Marta Ferraroni, Carol Ward, et al.
Journal of Medicinal Chemistry|October 8, 2024
Benzoxaborinine, New Chemotype for Carbonic Anhydrase Inhibition: <i>Ex Novo</i> Synthesis, Crystallography, <i>In Silico</i> Studies, and Anti-Melanoma Cell Line ActivitySimone Giovannuzzi, Anna Nikitjuka, Andrea Angeli, et al.
Journal of Medicinal Chemistry|June 15, 2026
Discovery of Subnanomolar and Highly Selective Carbonic Anhydrase II Inhibitors Featuring L-Shaped Scaffolds via Active-Site-Matched Fragment GrowingYitong Wang, Alessio Nocentini, Marta Ferraroni, et al.
Journal of Medicinal Chemistry|February 20, 2007
Synthesis, affinity profile, and functional activity of muscarinic antagonists with a 1-methyl-2-(2,2-alkylaryl-1,3-oxathiolan-5-yl)pyrrolidine structureSilvia Dei, Cristina Bellucci, Michela Buccioni, et al.
European Journal of Medicinal Chemistry|September 10, 2021
Chalcogenides-incorporating carbonic anhydrase inhibitors concomitantly reverted oxaliplatin-induced neuropathy and enhanced antiproliferative actionDamiano Tanini, Simone Carradori, Antonella Capperucci, et al.
European Journal of Medicinal Chemistry|October 31, 2025
Production, crystallographic studies, and functional profiling of γ-carbonic anhydrase from the probiotic Limosilactobacillus reuteri: In vitro and cell-based insightsAlessandro Bonardi, Simone Carradori, Niccolò Paoletti, et al.
RSC Medicinal Chemistry|June 24, 2024
Benzenesulfonamide decorated dihydropyrimidin(thi)ones: carbonic anhydrase profiling and antiproliferative activityHakan Aslan, Gioele Renzi, Andrea Angeli, et al.
Pageof 12

Showing results (91-100 of 112) with videos related to

Sort By:
Pageof 12
Bioorganic & Medicinal Chemistry|May 6, 2008
Muscarinic antagonists with multiple stereocenters: Synthesis, affinity profile and functional activity of isomeric 1-methyl-2-(2,2-alkylaryl-1,3-oxathiolan-5-yl)pyrrolidine sulfoxide derivativesSilvia Dei, Cristina Bellucci, Michela Buccioni, et al.
ACS Medicinal Chemistry Letters|February 19, 2025
Correction to "Study of Chalcogen Aspirin Derivatives with Carbonic Anhydrase Inhibitory Properties for Treating Inflammatory Pain"Elena Lucarini, Vanessa D'Antongiovanni, Luca Antonioli, et al.
Journal of Medicinal Chemistry|January 10, 2023
First-in-Class Dual Hybrid Carbonic Anhydrase Inhibitors and Transient Receptor Potential Vanilloid 1 Agonists Revert Oxaliplatin-Induced NeuropathyAndrea Angeli, Laura Micheli, Fabrizio Carta, et al.
European Journal of Medicinal Chemistry|August 17, 2019
Carbonic anhydrase inhibitors based on sorafenib scaffold: Design, synthesis, crystallographic investigation and effects on primary breast cancer cellsMurat Bozdag, Marta Ferraroni, Carol Ward, et al.
Journal of Medicinal Chemistry|October 8, 2024
Benzoxaborinine, New Chemotype for Carbonic Anhydrase Inhibition: <i>Ex Novo</i> Synthesis, Crystallography, <i>In Silico</i> Studies, and Anti-Melanoma Cell Line ActivitySimone Giovannuzzi, Anna Nikitjuka, Andrea Angeli, et al.
Journal of Medicinal Chemistry|June 15, 2026
Discovery of Subnanomolar and Highly Selective Carbonic Anhydrase II Inhibitors Featuring L-Shaped Scaffolds via Active-Site-Matched Fragment GrowingYitong Wang, Alessio Nocentini, Marta Ferraroni, et al.
Journal of Medicinal Chemistry|February 20, 2007
Synthesis, affinity profile, and functional activity of muscarinic antagonists with a 1-methyl-2-(2,2-alkylaryl-1,3-oxathiolan-5-yl)pyrrolidine structureSilvia Dei, Cristina Bellucci, Michela Buccioni, et al.
European Journal of Medicinal Chemistry|September 10, 2021
Chalcogenides-incorporating carbonic anhydrase inhibitors concomitantly reverted oxaliplatin-induced neuropathy and enhanced antiproliferative actionDamiano Tanini, Simone Carradori, Antonella Capperucci, et al.
European Journal of Medicinal Chemistry|October 31, 2025
Production, crystallographic studies, and functional profiling of γ-carbonic anhydrase from the probiotic Limosilactobacillus reuteri: In vitro and cell-based insightsAlessandro Bonardi, Simone Carradori, Niccolò Paoletti, et al.
RSC Medicinal Chemistry|June 24, 2024
Benzenesulfonamide decorated dihydropyrimidin(thi)ones: carbonic anhydrase profiling and antiproliferative activityHakan Aslan, Gioele Renzi, Andrea Angeli, et al.
Pageof 12