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Anna Di Fiore

Showing results (31-40 of 60) with videos related to

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Journal of Inorganic Biochemistry|October 17, 2020
Inhibition of the newly discovered β‑carbonic anhydrase from the protozoan pathogen Trichomonas vaginalis with inorganic anions and small moleculesLinda J Urbański, Andrea Angeli, Vesa P Hytönen, et al.
Bioorganic & Medicinal Chemistry Letters|January 26, 2007
Carbonic anhydrase inhibitors: binding of an antiglaucoma glycosyl-sulfanilamide derivative to human isoform II and its consequences for the drug design of enzyme inhibitors incorporating sugar moietiesAnna Di Fiore, Andrea Scozzafava, Jean-Yves Winum, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry|December 28, 2020
Inhibition of the β-carbonic anhydrase from the protozoan pathogen <i>Trichomonas vaginalis</i> with sulphonamidesLinda J Urbański, Andrea Angeli, Vesa P Hytönen, et al.
The Enzymes|October 8, 2025
Saccharomyces cerevesiae, Candida spp. and Cryptococcus neoformans β-CAsAnna Di Fiore, Martina Buonanno, Davide Esposito, et al.
The Enzymes|October 8, 2025
Fungal α-carbonic anhydrasesKatia D'Ambrosio, Anna Di Fiore, Vincenzo Alterio, et al.
ACS Medicinal Chemistry Letters|May 22, 2020
Looking toward the Rim of the Active Site Cavity of Druggable Human Carbonic Anhydrase IsoformsFrancesca Mancuso, Anna Di Fiore, Laura De Luca, et al.
Bioorganic & Medicinal Chemistry Letters|April 20, 2005
Carbonic anhydrase inhibitors. Zonisamide is an effective inhibitor of the cytosolic isozyme II and mitochondrial isozyme V: solution and X-ray crystallographic studiesGiuseppina De Simone, Anna Di Fiore, Valeria Menchise, et al.
Bioorganic & Medicinal Chemistry Letters|March 25, 2008
Carbonic anhydrase inhibitors: the X-ray crystal structure of ethoxzolamide complexed to human isoform II reveals the importance of thr200 and gln92 for obtaining tight-binding inhibitorsAnna Di Fiore, Carlo Pedone, Jochen Antel, et al.
Bioorganic & Medicinal Chemistry Letters|January 27, 2012
Carbonic anhydrase VII is S-glutathionylated without loss of catalytic activity and affinity for sulfonamide inhibitorsEmanuela Truppo, Claudiu T Supuran, Annamaria Sandomenico, et al.
Bioorganic & Medicinal Chemistry Letters|August 7, 2010
Crystal structure of the C183S/C217S mutant of human CA VII in complex with acetazolamideAnna Di Fiore, Emanuela Truppo, Claudiu T Supuran, et al.
Pageof 6

Showing results (31-40 of 60) with videos related to

Sort By:
Pageof 6
Journal of Inorganic Biochemistry|October 17, 2020
Inhibition of the newly discovered β‑carbonic anhydrase from the protozoan pathogen Trichomonas vaginalis with inorganic anions and small moleculesLinda J Urbański, Andrea Angeli, Vesa P Hytönen, et al.
Bioorganic & Medicinal Chemistry Letters|January 26, 2007
Carbonic anhydrase inhibitors: binding of an antiglaucoma glycosyl-sulfanilamide derivative to human isoform II and its consequences for the drug design of enzyme inhibitors incorporating sugar moietiesAnna Di Fiore, Andrea Scozzafava, Jean-Yves Winum, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry|December 28, 2020
Inhibition of the β-carbonic anhydrase from the protozoan pathogen <i>Trichomonas vaginalis</i> with sulphonamidesLinda J Urbański, Andrea Angeli, Vesa P Hytönen, et al.
The Enzymes|October 8, 2025
Saccharomyces cerevesiae, Candida spp. and Cryptococcus neoformans β-CAsAnna Di Fiore, Martina Buonanno, Davide Esposito, et al.
The Enzymes|October 8, 2025
Fungal α-carbonic anhydrasesKatia D'Ambrosio, Anna Di Fiore, Vincenzo Alterio, et al.
ACS Medicinal Chemistry Letters|May 22, 2020
Looking toward the Rim of the Active Site Cavity of Druggable Human Carbonic Anhydrase IsoformsFrancesca Mancuso, Anna Di Fiore, Laura De Luca, et al.
Bioorganic & Medicinal Chemistry Letters|April 20, 2005
Carbonic anhydrase inhibitors. Zonisamide is an effective inhibitor of the cytosolic isozyme II and mitochondrial isozyme V: solution and X-ray crystallographic studiesGiuseppina De Simone, Anna Di Fiore, Valeria Menchise, et al.
Bioorganic & Medicinal Chemistry Letters|March 25, 2008
Carbonic anhydrase inhibitors: the X-ray crystal structure of ethoxzolamide complexed to human isoform II reveals the importance of thr200 and gln92 for obtaining tight-binding inhibitorsAnna Di Fiore, Carlo Pedone, Jochen Antel, et al.
Bioorganic & Medicinal Chemistry Letters|January 27, 2012
Carbonic anhydrase VII is S-glutathionylated without loss of catalytic activity and affinity for sulfonamide inhibitorsEmanuela Truppo, Claudiu T Supuran, Annamaria Sandomenico, et al.
Bioorganic & Medicinal Chemistry Letters|August 7, 2010
Crystal structure of the C183S/C217S mutant of human CA VII in complex with acetazolamideAnna Di Fiore, Emanuela Truppo, Claudiu T Supuran, et al.
Pageof 6