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Determinants for Tight and Selective Binding of a Medicinal Dicarbene Gold(I) Complex to a Telomeric DNA G-Quadruplex: a Joint ESI MS and XRD Investigation

Angewandte Chemie International Edition, 2016-03, Vol.55 (13), p.4256-4259

International ed. in English, 2016

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Selenolesterase enzyme activity of carbonic anhydrases

Chemical communications (Cambridge, England), 2020-04, Vol.56 (32), p.4444-4447

2020

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Ureidobenzenesulfonamides as Selective Carbonic Anhydrase I, IX, and XII Inhibitors

Molecules (Basel, Switzerland), 2023-11, Vol.28 (23), p.7782

2023

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Diversely N-substituted benzenesulfonamides dissimilarly bind to human carbonic anhydrases: crystallographic investigations of N-nitrosulfonamides

Journal of enzyme inhibition and medicinal chemistry, 2023-12, Vol.38 (1), p.2178430-2178430

2023

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Probing the Efficiency of 13-Pyridylalkyl Berberine Derivatives to Human Telomeric G-Quadruplexes Binding: Spectroscopic, Solid State and In Silico Analysis

International journal of molecular sciences, 2022-11, Vol.23 (22), p.14061

2022

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Development of Praziquantel sulphonamide derivatives as antischistosomal drugs

Journal of enzyme inhibition and medicinal chemistry, 2022-12, Vol.37 (1), p.1479-1494

2022

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Diversely substituted sulfamides for fragment-based drug discovery of carbonic anhydrase inhibitors: synthesis and inhibitory profile

Journal of enzyme inhibition and medicinal chemistry, 2022-12, Vol.37 (1), p.857-865

2022

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Dioxygen, an unexpected carbonic anhydrase ligand

Journal of enzyme inhibition and medicinal chemistry, 2018-01, Vol.33 (1), p.999-1005

2018

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Crystal Structure of a Tetrameric Type II β-Carbonic Anhydrase from the Pathogenic Bacterium Burkholderia pseudomallei

Molecules (Basel, Switzerland), 2020-05, Vol.25 (10), p.2269

2020

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Bacterial β-carbonic anhydrases

The Enzymes, 2024, Vol.55, p.65

Ferraroni, Marta

2024

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Crystal structure and chemical inhibition of essential schistosome host-interactive virulence factor carbonic anhydrase SmCA

Communications biology, 2019-09, Vol.2 (1), p.333-333, Article 333

2019

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Catechol 1,2-dioxygenase from the Gram-positive Rhodococcus opacus 1CP: Quantitative structure/activity relationship and the crystal structures of native enzyme and catechols adducts

Journal of structural biology, 2010-06, Vol.170 (3), p.548-564

2010

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Reaction intermediates and redox state changes in a blue laccase from Steccherinum ochraceum observed by crystallographic high/low X-ray dose experiments

Journal of inorganic biochemistry, 2012-06, Vol.111, p.203-209

2012

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Crystal structure of a blue laccase from Lentinus tigrinus: evidences for intermediates in the molecular oxygen reductive splitting by multicopper oxidases

BMC structural biology, 2007-09, Vol.7 (1), p.60-60, Article 60

2007

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Sulfonamide diuretic azosemide as an efficient carbonic anhydrase inhibitor

Journal of molecular structure, 2022-11, Vol.1268, p.133672, Article 133672

2022

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Crystal structure of the monocupin ring‐cleaving dioxygenase 5‐nitrosalicylate 1,2‐dioxygenase from Bradyrhizobium sp

Acta crystallographica. Section D, Biological crystallography., 2023-07, Vol.79 (7), p.632-640

2023

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Direct and straightforward access to substituted alkyl selenols as novel carbonic anhydrase inhibitors

European journal of medicinal chemistry, 2020-01, Vol.185, p.111811-111811, Article 111811

2020

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Selenols: a new class of carbonic anhydrase inhibitors

Chemical communications (Cambridge, England), 2019-01, Vol.55 (5), p.648-651

2019

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Thioxocoumarins Show an Alternative Carbonic Anhydrase Inhibition Mechanism Compared to Coumarins

Journal of medicinal chemistry, 2016-01, Vol.59 (1), p.462-473

2016

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Famotidine, an Antiulcer Agent, Strongly Inhibits Helicobacter pylori and Human Carbonic Anhydrases

ACS medicinal chemistry letters, 2018-10, Vol.9 (10), p.1035-1038

2018

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The crystal structure of human telomeric DNA complexed with berberine: an interesting case of stacked ligand to G-tetrad ratio higher than 1:1

Nucleic acids research, 2013-01, Vol.41 (1), p.632-638

2013

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Inhibition of Schistosoma mansoni carbonic anhydrase by the antiparasitic drug clorsulon: X‐ray crystallographic and in vitro studies

Acta crystallographica. Section D, Biological crystallography., 2022-03, Vol.78 (3), p.321-327

2022

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Benzenesulfonamides Incorporating Flexible Triazole Moieties Are Highly Effective Carbonic Anhydrase Inhibitors: Synthesis and Kinetic, Crystallographic, Computational, and Intraocular Pressure Lowering Investigations

Journal of medicinal chemistry, 2016-12, Vol.59 (23), p.10692-10704

2016

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Crystal Structure of the Hydroxyquinol 1,2-Dioxygenase from Nocardioides simplex 3E, a Key Enzyme Involved in Polychlorinated Aromatics Biodegradation

The Journal of biological chemistry, 2005-06, Vol.280 (22), p.21144-21154

2005

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The dopamine D 2 receptors antagonist Veralipride inhibits carbonic anhydrases: solution and crystallographic insights on human isoforms

Chemistry, an Asian journal, 2024-04, Vol.19 (8), p.e202400067

2024

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Determinants for Tight and Selective Binding of a Medicinal Dicarbene Gold(I) Complex to a Telomeric DNA G-Quadruplex: a Joint ESI MS and XRD Investigation

Selenolesterase enzyme activity of carbonic anhydrases

Ureidobenzenesulfonamides as Selective Carbonic Anhydrase I, IX, and XII Inhibitors

Diversely N-substituted benzenesulfonamides dissimilarly bind to human carbonic anhydrases: crystallographic investigations of N-nitrosulfonamides

Probing the Efficiency of 13-Pyridylalkyl Berberine Derivatives to Human Telomeric G-Quadruplexes Binding: Spectroscopic, Solid State and In Silico Analysis

Development of Praziquantel sulphonamide derivatives as antischistosomal drugs

Diversely substituted sulfamides for fragment-based drug discovery of carbonic anhydrase inhibitors: synthesis and inhibitory profile

Dioxygen, an unexpected carbonic anhydrase ligand

Crystal Structure of a Tetrameric Type II β-Carbonic Anhydrase from the Pathogenic Bacterium Burkholderia pseudomallei

Bacterial β-carbonic anhydrases

Crystal structure and chemical inhibition of essential schistosome host-interactive virulence factor carbonic anhydrase SmCA

Catechol 1,2-dioxygenase from the Gram-positive Rhodococcus opacus 1CP: Quantitative structure/activity relationship and the crystal structures of native enzyme and catechols adducts

Reaction intermediates and redox state changes in a blue laccase from Steccherinum ochraceum observed by crystallographic high/low X-ray dose experiments

Crystal structure of a blue laccase from Lentinus tigrinus: evidences for intermediates in the molecular oxygen reductive splitting by multicopper oxidases

Sulfonamide diuretic azosemide as an efficient carbonic anhydrase inhibitor

Crystal structure of the monocupin ring‐cleaving dioxygenase 5‐nitrosalicylate 1,2‐dioxygenase from Bradyrhizobium sp

Direct and straightforward access to substituted alkyl selenols as novel carbonic anhydrase inhibitors

Selenols: a new class of carbonic anhydrase inhibitors

Thioxocoumarins Show an Alternative Carbonic Anhydrase Inhibition Mechanism Compared to Coumarins

Famotidine, an Antiulcer Agent, Strongly Inhibits Helicobacter pylori and Human Carbonic Anhydrases

The crystal structure of human telomeric DNA complexed with berberine: an interesting case of stacked ligand to G-tetrad ratio higher than 1:1

Inhibition of Schistosoma mansoni carbonic anhydrase by the antiparasitic drug clorsulon: X‐ray crystallographic and in vitro studies

Benzenesulfonamides Incorporating Flexible Triazole Moieties Are Highly Effective Carbonic Anhydrase Inhibitors: Synthesis and Kinetic, Crystallographic, Computational, and Intraocular Pressure Lowering Investigations

Crystal Structure of the Hydroxyquinol 1,2-Dioxygenase from Nocardioides simplex 3E, a Key Enzyme Involved in Polychlorinated Aromatics Biodegradation

The dopamine D 2 receptors antagonist Veralipride inhibits carbonic anhydrases: solution and crystallographic insights on human isoforms

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