Claudiu T Supuran

University of Florence

Italy

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Research Interests

Pharmaceutical Chemistry

100%

Biochemistry

40%

Chemical Biology

100%

Heterocyclic Chemistry

90%

Molecular Modeling

70%

Enzyme Engineering

30%

Drug Development

30%

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Articles31

Design and Synthesis of 2-substituted [1,2,4]Triazolo[1,5-a]pyrimidines Tethered with Umbelliferone as Selective Carbonic Anhydrase IX and XII Inhibitors

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Year:

2025

Hybrid and Chimeric Heterocycles for the Inhibition of Carbonic Anhydrases

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2025

Human Carbonic Anhydrase Inhibitors

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2025

Green Synthesis of Sulfonamide Derivatives as Human Carbonic Anhydrase Isoforms I, II, IX, XII Inhibitors and Antioxidants: Comprehensive Insights From Biological Evaluation and In‐Depth In Silico Analysis

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2025

Human carbonic anhydrase modulators: the past, present, and future

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2025

Unveiling the Carbonic Anhydrase Inhibitory Profile of Aprocitentan: Kinetic and Structural Characterization

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2025

Novel Taurinamide‐Based Compounds as Carbonic Anhydrase Inhibitors

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2025

Exploration of 3‐Substituted Benzofuran‐Tethered Sulfamoyl Triazoles as Carbonic Anhydrase Inhibitors: Design, Synthesis, and Biological Evaluation

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2025

Development of a New AMBER Force Field for Cysteine and Histidine Cadmium‐Binding Proteins and Its Validation Through QM/MM MD Simulations

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2025

Unraveling the Potential of Amino-, Acylamino-, and Ureido-Substituted 3H-1,2-Benzoxaphosphepine 2-Oxides toward Nanomolar Inhibitors of Tumor-Associated Carbonic Anhydrases IX and XII

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Year:

2025

Azobenzenesulfonamide Carbonic Anhydrase Inhibitors as New Weapons to Fight Helicobacter pylori: Synthesis, Bioactivity Evaluation, In Vivo Toxicity, and Computational Studies

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2024

A comprehensive investigation of the anion inhibition profile of a β-carbonic anhydrase from Acinetobacter baumannii for crafting innovative antimicrobial treatments

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2024

Cloning, expression, and purification of an α-carbonic anhydrase from Toxoplasma gondii to unveil its kinetic parameters and anion inhibition profile.

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2024

Synthesis, carbonic anhydrase inhibition studies and modelling investigations of phthalimide–hydantoin hybrids

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2024

Physiological modeling of the metaverse of the Mycobacterium tuberculosis β-CA inhibition mechanism

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2024

Hydrogen Sulfide-Releasing Carbonic Anhydrase Inhibitors Effectively Suppress Cancer Cell Growth

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2024

Harnessing Nitric Oxide-Donating Benzofuroxans for Targeted Inhibition of Carbonic Anhydrase IX in Cancer

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2024

Optimization of Ethoxzolamide Analogs with Improved Pharmacokinetic Properties for In Vivo Efficacy against Neisseria gonorrhoeae

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2024

Inhibitory Effect of Two Carbonic Anhydrases Inhibitors on the Activity of Major Cytochrome P450 Enzymes

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2024

Synthesis and Carbonic Anhydrase I, II, IX, and XII Inhibition Studies with a Series of Cyclic Sulfonyl Guanidines

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2024

Discovery of new 6-ureido/amidocoumarins as highly potent and selective inhibitors for the tumour-relevant carbonic anhydrases IX and XII

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2023

Cloning, characterization, and inhibition of the novel β-carbonic anhydrase from parasitic blood fluke, Schistosoma mansoni

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2023

A well-trained and well-organised scientific method is what science is

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2023

Erlotinib-containing benzenesulfonamides as anti-<i>Helicobacter pylori</i> agents through carbonic anhydrase inhibition

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2023

Discovery of sulfonamide-tethered isatin derivatives as novel anticancer agents and VEGFR-2 inhibitors

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Year:

2023

2-((1H-Benzo[d]imidazol-2-yl)amino)benzo[d]thiazole-6-sulphonamides: a class of carbonic anhydrase II and VII-selective inhibitors

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Year:

2023

Antihistamines, phenothiazine-based antipsychotics, and tricyclic antidepressants potently activate pharmacologically relevant human carbonic anhydrase isoforms II and VII

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2023

Aryl derivatives of 3H-1,2-benzoxaphosphepine 2-oxides as inhibitors of cancer-related carbonic anhydrase isoforms IX and XII

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2023

Carbonic anhydrase inhibitory activity of phthalimide-capped benzene sulphonamide derivatives

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2023

Derivatives of 4-methyl-1,2,3-benzoxathiazine 2,2-dioxide as selective inhibitors of human carbonic anhydrases IX and XII over the cytosolic isoforms I and II

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Year:

2023

Development of novel anilinoquinazoline-based carboxylic acids as non-classical carbonic anhydrase IX and XII inhibitors

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Year:

2023

Collaborators17

Daniel Flaherty

Associate Professor

Purdue University

UNITED STATES

Paola Gratteri

Associate Professor

University of Firenze

ITALY

Letizia GIAMPIETRO

Associate Professor

University of Chieti-Pescara

ITALY

Ashok Aspatwar

Adjunct Professor

FINLAND

Fawzy Elbarbry

Professor, Director of Student Success

Pacific University

UNITED STATES

Antonello Mai

Sapienza University of Rome

ITALY

Mattia Mori

Associate Professor

University of Siena

ITALY

Mariangela Agamennone

Associate professor

University of Chieti-Pescara

ITALY

Marta Ferraroni

University of Florence

ITALY

Seppo Parkkila

University of Tampere

FINLAND

Cristina MACCALLINI

Associate Professor

University “G. d’Annunzio” of Chieti-Pescara

ITALY

Ilaria D'Agostino

University of Pisa

ITALY

Gyochang Keum

Professor

University of Science and Technology (UST)

SOUTH KOREA

Dante Rotili

Sapienza University of Rome

ITALY

Andrea Angeli

University of Florence

ITALY

Shoukat Dedhar

Professor

The University of British Columbia

CANADA

Rossella Grande

ITALY

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