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Simona Maria Monti

Showing results (21-30 of 85) with videos related to

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Organic & Biomolecular Chemistry|May 28, 2010
The first example of a significant active site conformational rearrangement in a carbonic anhydrase-inhibitor adduct: the carbonic anhydrase I-topiramate complexVincenzo Alterio, Simona Maria Monti, Emanuela Truppo, et al.
Biology|February 25, 2023
A Combined in Silico and Structural Study Opens New Perspectives on Aliphatic Sulfonamides, a Still Poorly Investigated Class of CA InhibitorsEmma Langella, Davide Esposito, Simona Maria Monti, et al.
Biochemical and Biophysical Research Communications|March 24, 2012
Native expression and purification of hormone-sensitive lipase from Psychrobacter sp. TA144 enhances protein stability and activityGiuseppina Ascione, Donatella de Pascale, Concetta De Santi, et al.
International Journal of Biological Macromolecules|October 25, 2024
Exploring the binding mode of phenyl and vinyl boronic acids to human carbonic anhydrasesDavide Esposito, Simona Maria Monti, Claudiu T Supuran, et al.
Journal of Medicinal Chemistry|March 4, 2017
Discovery of Benzenesulfonamides with Potent Human Carbonic Anhydrase Inhibitory and Effective Anticonvulsant Action: Design, Synthesis, and Pharmacological AssessmentChandra Bhushan Mishra, Shikha Kumari, Andrea Angeli, et al.
Bioorganic & Medicinal Chemistry Letters|May 18, 2010
Carbonic anhydrase inhibitors: crystallographic and solution binding studies for the interaction of a boron-containing aromatic sulfamide with mammalian isoforms I-XVAnna Di Fiore, Simona Maria Monti, Alessio Innocenti, et al.
Bioorganic & Medicinal Chemistry|June 19, 2016
Kinetic and X-ray crystallographic investigations of substituted 2-thio-6-oxo-1,6-dihydropyrimidine-benzenesulfonamides acting as carbonic anhydrase inhibitorsDaniela Vullo, Claudiu T Supuran, Andrea Scozzafava, et al.
Chemical Communications (Cambridge, England)|August 25, 2018
Inhibition of carbonic anhydrases by a substrate analog: benzyl carbamate directly coordinates the catalytic zinc ion mimicking bicarbonate bindingGiuseppina De Simone, Andrea Angeli, Murat Bozdag, et al.
Chemical Reviews|December 19, 2024
Multiple Binding Modes of Inhibitors to Human Carbonic Anhydrases: An Update on the Design of Isoform-Specific Modulators of ActivityKatia D'Ambrosio, Anna Di Fiore, Vincenzo Alterio, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry|July 26, 2017
Insights into the binding mode of sulphamates and sulphamides to hCA II: crystallographic studies and binding free energy calculationsGiuseppina De Simone, Emma Langella, Davide Esposito, et al.
Pageof 9

Showing results (21-30 of 85) with videos related to

Sort By:
Pageof 9
Organic & Biomolecular Chemistry|May 28, 2010
The first example of a significant active site conformational rearrangement in a carbonic anhydrase-inhibitor adduct: the carbonic anhydrase I-topiramate complexVincenzo Alterio, Simona Maria Monti, Emanuela Truppo, et al.
Biology|February 25, 2023
A Combined in Silico and Structural Study Opens New Perspectives on Aliphatic Sulfonamides, a Still Poorly Investigated Class of CA InhibitorsEmma Langella, Davide Esposito, Simona Maria Monti, et al.
Biochemical and Biophysical Research Communications|March 24, 2012
Native expression and purification of hormone-sensitive lipase from Psychrobacter sp. TA144 enhances protein stability and activityGiuseppina Ascione, Donatella de Pascale, Concetta De Santi, et al.
International Journal of Biological Macromolecules|October 25, 2024
Exploring the binding mode of phenyl and vinyl boronic acids to human carbonic anhydrasesDavide Esposito, Simona Maria Monti, Claudiu T Supuran, et al.
Journal of Medicinal Chemistry|March 4, 2017
Discovery of Benzenesulfonamides with Potent Human Carbonic Anhydrase Inhibitory and Effective Anticonvulsant Action: Design, Synthesis, and Pharmacological AssessmentChandra Bhushan Mishra, Shikha Kumari, Andrea Angeli, et al.
Bioorganic & Medicinal Chemistry Letters|May 18, 2010
Carbonic anhydrase inhibitors: crystallographic and solution binding studies for the interaction of a boron-containing aromatic sulfamide with mammalian isoforms I-XVAnna Di Fiore, Simona Maria Monti, Alessio Innocenti, et al.
Bioorganic & Medicinal Chemistry|June 19, 2016
Kinetic and X-ray crystallographic investigations of substituted 2-thio-6-oxo-1,6-dihydropyrimidine-benzenesulfonamides acting as carbonic anhydrase inhibitorsDaniela Vullo, Claudiu T Supuran, Andrea Scozzafava, et al.
Chemical Communications (Cambridge, England)|August 25, 2018
Inhibition of carbonic anhydrases by a substrate analog: benzyl carbamate directly coordinates the catalytic zinc ion mimicking bicarbonate bindingGiuseppina De Simone, Andrea Angeli, Murat Bozdag, et al.
Chemical Reviews|December 19, 2024
Multiple Binding Modes of Inhibitors to Human Carbonic Anhydrases: An Update on the Design of Isoform-Specific Modulators of ActivityKatia D'Ambrosio, Anna Di Fiore, Vincenzo Alterio, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry|July 26, 2017
Insights into the binding mode of sulphamates and sulphamides to hCA II: crystallographic studies and binding free energy calculationsGiuseppina De Simone, Emma Langella, Davide Esposito, et al.
Pageof 9