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Marta Ferraroni

Showing results (41-50 of 112) with videos related to

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Archiv Der Pharmazie|March 18, 2024
Sulfonamide-incorporated bis(α-aminophosphonates) as promising carbonic anhydrase inhibitors: Design, synthesis, biological evaluation, and X-ray crystallographic studiesMarjan Sobati, Morteza Abdoli, Andrea Angeli, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry|May 31, 2022
Development of Praziquantel sulphonamide derivatives as antischistosomal drugsAndrea Angeli, Marta Ferraroni, Fabrizio Carta, et al.
Bioorganic & Medicinal Chemistry|July 22, 2017
1,3-Oxazole-based selective picomolar inhibitors of cytosolic human carbonic anhydrase II alleviate ocular hypertension in rabbits: Potency is supported by X-ray crystallography of two leadsMarta Ferraroni, Laura Lucarini, Emanuela Masini, et al.
European Journal of Medicinal Chemistry|September 8, 2018
Discovery of new 2, 5-disubstituted 1,3-selenazoles as selective human carbonic anhydrase IX inhibitors with potent anti-tumor activityAndrea Angeli, Elena Trallori, Marta Ferraroni, et al.
Chemical Communications (Cambridge, England)|December 19, 2018
Selenols: a new class of carbonic anhydrase inhibitorsAndrea Angeli, Damiano Tanini, Alessio Nocentini, et al.
Chemmedchem|July 20, 2024
Thia- and Seleno-Michael Reactions for the Synthesis of Carbonic Anhydrases InhibitorsAndrea Angeli, Alessio Occhini, Gioele Renzi, et al.
Journal of Molecular Biology|June 24, 2006
Crystal structure of 3-chlorocatechol 1,2-dioxygenase key enzyme of a new modified ortho-pathway from the Gram-positive Rhodococcus opacus 1CP grown on 2-chlorophenolMarta Ferraroni, Marina P Kolomytseva, Inna P Solyanikova, et al.
Chemical Communications (Cambridge, England)|May 1, 2019
Polypharmacology of epacadostat: a potent and selective inhibitor of the tumor associated carbonic anhydrases IX and XIIAndrea Angeli, Marta Ferraroni, Alessio Nocentini, et al.
Bioorganic Chemistry|March 28, 2022
Benzoselenoates: A novel class of carbonic anhydrase inhibitorsDamiano Tanini, Antonella Capperucci, Maria Locuoco, et al.
Journal of Medicinal Chemistry|June 24, 2026
Design and Synthesis of Bendamustine-Carbonic Anhydrase Inhibitors with Antiproliferative Effects in Clear Cell Renal Cell CarcinomaGioele Renzi, Alessandro Tubita, Lorenzo Antonuzzo, et al.
Pageof 12

Showing results (41-50 of 112) with videos related to

Sort By:
Pageof 12
Archiv Der Pharmazie|March 18, 2024
Sulfonamide-incorporated bis(α-aminophosphonates) as promising carbonic anhydrase inhibitors: Design, synthesis, biological evaluation, and X-ray crystallographic studiesMarjan Sobati, Morteza Abdoli, Andrea Angeli, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry|May 31, 2022
Development of Praziquantel sulphonamide derivatives as antischistosomal drugsAndrea Angeli, Marta Ferraroni, Fabrizio Carta, et al.
Bioorganic & Medicinal Chemistry|July 22, 2017
1,3-Oxazole-based selective picomolar inhibitors of cytosolic human carbonic anhydrase II alleviate ocular hypertension in rabbits: Potency is supported by X-ray crystallography of two leadsMarta Ferraroni, Laura Lucarini, Emanuela Masini, et al.
European Journal of Medicinal Chemistry|September 8, 2018
Discovery of new 2, 5-disubstituted 1,3-selenazoles as selective human carbonic anhydrase IX inhibitors with potent anti-tumor activityAndrea Angeli, Elena Trallori, Marta Ferraroni, et al.
Chemical Communications (Cambridge, England)|December 19, 2018
Selenols: a new class of carbonic anhydrase inhibitorsAndrea Angeli, Damiano Tanini, Alessio Nocentini, et al.
Chemmedchem|July 20, 2024
Thia- and Seleno-Michael Reactions for the Synthesis of Carbonic Anhydrases InhibitorsAndrea Angeli, Alessio Occhini, Gioele Renzi, et al.
Journal of Molecular Biology|June 24, 2006
Crystal structure of 3-chlorocatechol 1,2-dioxygenase key enzyme of a new modified ortho-pathway from the Gram-positive Rhodococcus opacus 1CP grown on 2-chlorophenolMarta Ferraroni, Marina P Kolomytseva, Inna P Solyanikova, et al.
Chemical Communications (Cambridge, England)|May 1, 2019
Polypharmacology of epacadostat: a potent and selective inhibitor of the tumor associated carbonic anhydrases IX and XIIAndrea Angeli, Marta Ferraroni, Alessio Nocentini, et al.
Bioorganic Chemistry|March 28, 2022
Benzoselenoates: A novel class of carbonic anhydrase inhibitorsDamiano Tanini, Antonella Capperucci, Maria Locuoco, et al.
Journal of Medicinal Chemistry|June 24, 2026
Design and Synthesis of Bendamustine-Carbonic Anhydrase Inhibitors with Antiproliferative Effects in Clear Cell Renal Cell CarcinomaGioele Renzi, Alessandro Tubita, Lorenzo Antonuzzo, et al.
Pageof 12