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Giuseppina De Simone

Showing results (101-110 of 146) with videos related to

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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 Medicinal Chemistry|September 1, 2006
Carbonic anhydrase inhibitors: Hypoxia-activatable sulfonamides incorporating disulfide bonds that target the tumor-associated isoform IXGiuseppina De Simone, Rosa Maria Vitale, Anna Di Fiore, 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.
Journal of Molecular Biology|November 5, 2019
Biochemical and Structural Insights into Carbonic Anhydrase XII/Fab6A10 ComplexVincenzo Alterio, Markus Kellner, Davide Esposito, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry|August 20, 2019
Exploring benzoxaborole derivatives as carbonic anhydrase inhibitors: a structural and computational analysis reveals their conformational variability as a tool to increase enzyme selectivityEmma Langella, Vincenzo Alterio, Katia D'Ambrosio, 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.
Computational and Structural Biotechnology Journal|August 26, 2022
Biochemical, structural, and computational studies of a γ-carbonic anhydrase from the pathogenic bacterium <i>Burkholderia pseudomallei</i>Anna Di Fiore, Viviana De Luca, Emma Langella, et al.
Biomed Research International|September 27, 2014
Hydrophobic substituents of the phenylmethylsulfamide moiety can be used for the development of new selective carbonic anhydrase inhibitorsGiuseppina De Simone, Ginta Pizika, Simona Maria Monti, et al.
Pageof 15

Showing results (101-110 of 146) with videos related to

Sort By:
Pageof 15
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 Medicinal Chemistry|September 1, 2006
Carbonic anhydrase inhibitors: Hypoxia-activatable sulfonamides incorporating disulfide bonds that target the tumor-associated isoform IXGiuseppina De Simone, Rosa Maria Vitale, Anna Di Fiore, 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.
Journal of Molecular Biology|November 5, 2019
Biochemical and Structural Insights into Carbonic Anhydrase XII/Fab6A10 ComplexVincenzo Alterio, Markus Kellner, Davide Esposito, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry|August 20, 2019
Exploring benzoxaborole derivatives as carbonic anhydrase inhibitors: a structural and computational analysis reveals their conformational variability as a tool to increase enzyme selectivityEmma Langella, Vincenzo Alterio, Katia D'Ambrosio, 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.
Computational and Structural Biotechnology Journal|August 26, 2022
Biochemical, structural, and computational studies of a γ-carbonic anhydrase from the pathogenic bacterium <i>Burkholderia pseudomallei</i>Anna Di Fiore, Viviana De Luca, Emma Langella, et al.
Biomed Research International|September 27, 2014
Hydrophobic substituents of the phenylmethylsulfamide moiety can be used for the development of new selective carbonic anhydrase inhibitorsGiuseppina De Simone, Ginta Pizika, Simona Maria Monti, et al.
Pageof 15