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Simona Maria Monti

Showing results (41-50 of 84) with videos related to

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Bioorganic & Medicinal Chemistry|December 7, 2016
Discovery of 4-sulfamoyl-phenyl-β-lactams as a new class of potent carbonic anhydrase isoforms I, II, IV and VII inhibitors: The first example of subnanomolar CA IV inhibitorsSrinivas Angapelly, P V Sri Ramya, Andrea Angeli, et al.
Journal of Molecular Biology|March 18, 2008
Gadd45 beta forms a homodimeric complex that binds tightly to MKK7Laura Tornatore, Daniela Marasco, Nina Dathan, et al.
Journal of the American Chemical Society|June 22, 2006
Carbonic anhydrase inhibitors: X-ray and molecular modeling study for the interaction of a fluorescent antitumor sulfonamide with isozyme II and IXVincenzo Alterio, Rosa Maria Vitale, Simona Maria Monti, et al.
Bioorganic & Medicinal Chemistry Letters|January 3, 2012
Dithiocarbamates are strong inhibitors of the beta-class fungal carbonic anhydrases from Cryptococcus neoformans, Candida albicans and Candida glabrataSimona Maria Monti, Alfonso Maresca, Francesca Viparelli, et al.
The Enzymes|October 8, 2025
Fungal α-carbonic anhydrasesKatia D'Ambrosio, Anna Di Fiore, Vincenzo Alterio, et al.
Bioorganic & Medicinal Chemistry Letters|July 16, 2010
Inhibition of the R1 fragment of the cadmium-containing zeta-class carbonic anhydrase from the diatom Thalassiosira weissflogii with anionsFrancesca Viparelli, Simona Maria Monti, Giuseppina De Simone, 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.
Journal of Molecular Biology|November 5, 2019
Biochemical and Structural Insights into Carbonic Anhydrase XII/Fab6A10 ComplexVincenzo Alterio, Markus Kellner, Davide Esposito, et al.
International Journal of Biological Macromolecules|August 13, 2025
Multi-faceted exploration of the novel active γ-carbonic anhydrase PaCAγ1 in the human pathogen Pseudomonas aeruginosaVincenzo Massimiliano Vivenzio, Reygan Braga, Alessandro Bonardi, et al.
Biochimie|October 22, 2013
Structural basis for the rational design of new anti-Brucella agents: the crystal structure of the C366S mutant of L-histidinol dehydrogenase from Brucella suisKatia D'ambrosio, Marie Lopez, Nina A Dathan, et al.
Pageof 9

Showing results (41-50 of 84) with videos related to

Sort By:
Pageof 9
Bioorganic & Medicinal Chemistry|December 7, 2016
Discovery of 4-sulfamoyl-phenyl-β-lactams as a new class of potent carbonic anhydrase isoforms I, II, IV and VII inhibitors: The first example of subnanomolar CA IV inhibitorsSrinivas Angapelly, P V Sri Ramya, Andrea Angeli, et al.
Journal of Molecular Biology|March 18, 2008
Gadd45 beta forms a homodimeric complex that binds tightly to MKK7Laura Tornatore, Daniela Marasco, Nina Dathan, et al.
Journal of the American Chemical Society|June 22, 2006
Carbonic anhydrase inhibitors: X-ray and molecular modeling study for the interaction of a fluorescent antitumor sulfonamide with isozyme II and IXVincenzo Alterio, Rosa Maria Vitale, Simona Maria Monti, et al.
Bioorganic & Medicinal Chemistry Letters|January 3, 2012
Dithiocarbamates are strong inhibitors of the beta-class fungal carbonic anhydrases from Cryptococcus neoformans, Candida albicans and Candida glabrataSimona Maria Monti, Alfonso Maresca, Francesca Viparelli, et al.
The Enzymes|October 8, 2025
Fungal α-carbonic anhydrasesKatia D'Ambrosio, Anna Di Fiore, Vincenzo Alterio, et al.
Bioorganic & Medicinal Chemistry Letters|July 16, 2010
Inhibition of the R1 fragment of the cadmium-containing zeta-class carbonic anhydrase from the diatom Thalassiosira weissflogii with anionsFrancesca Viparelli, Simona Maria Monti, Giuseppina De Simone, 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.
Journal of Molecular Biology|November 5, 2019
Biochemical and Structural Insights into Carbonic Anhydrase XII/Fab6A10 ComplexVincenzo Alterio, Markus Kellner, Davide Esposito, et al.
International Journal of Biological Macromolecules|August 13, 2025
Multi-faceted exploration of the novel active γ-carbonic anhydrase PaCAγ1 in the human pathogen Pseudomonas aeruginosaVincenzo Massimiliano Vivenzio, Reygan Braga, Alessandro Bonardi, et al.
Biochimie|October 22, 2013
Structural basis for the rational design of new anti-Brucella agents: the crystal structure of the C366S mutant of L-histidinol dehydrogenase from Brucella suisKatia D'ambrosio, Marie Lopez, Nina A Dathan, et al.
Pageof 9