Davide Esposito

Naples, Italy

Last Updated: 09/26/2026

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Found 21 publications

1-Aryl-6,7-Dimethoxy-3,4-Dihydroisoquinoline-2(1H)-Sulfonamides as hCA XII Selective Inhibitors: Experimental and Theoretical Studies to Interrogate the Isoform Selectivity.

1-Aryl-6,7-Dimethoxy-3,4-Dihydroisoquinoline-2(1H)-Sulfonamides as hCA XII Selective Inhibitors: Experimental and Theoretical Studies to Interrogate the Isoform Selectivity.

Journal: ChemMedChem

Published: May 22, 2026

Discovery of a Mixed and Prodrug-Like Inhibition Mechanism for Phosphocoumarins and Phosphoquinolinones against Human Carbonic Anhydrases.

Discovery of a Mixed and Prodrug-Like Inhibition Mechanism for Phosphocoumarins and Phosphoquinolinones against Human Carbonic Anhydrases.

Journal: Journal of medicinal chemistry

Published: April 29, 2026

Saccharomyces cerevesiae, Candida spp. and Cryptococcus neoformans β-CAs.

Saccharomyces cerevesiae, Candida spp. and Cryptococcus neoformans β-CAs.

Journal: The Enzymes

Published: October 08, 2025

Salt Stress Mitigation and Field-Relevant Biostimulant Activity of Prosystemin Protein Fragments: Novel Tools for Cutting-Edge Solutions in Agriculture.

Salt Stress Mitigation and Field-Relevant Biostimulant Activity of Prosystemin Protein Fragments: Novel Tools for Cutting-Edge Solutions in Agriculture.

Journal: Plants (Basel, Switzerland)

Published: June 20, 2025

Exploring the binding mode of phenyl and vinyl boronic acids to human carbonic anhydrases.

Exploring the binding mode of phenyl and vinyl boronic acids to human carbonic anhydrases.

Journal: International journal of biological macromolecules

Published: September 03, 2024

Bacterial α-CAs: a biochemical and structural overview.

Bacterial α-CAs: a biochemical and structural overview.

Journal: The Enzymes

Published: September 02, 2024

6-Substituted Triazolyl Benzoxaboroles as Selective Carbonic Anhydrase Inhibitors: In Silico Design, Synthesis, and X-ray Crystallography.

6-Substituted Triazolyl Benzoxaboroles as Selective Carbonic Anhydrase Inhibitors: In Silico Design, Synthesis, and X-ray Crystallography.

Journal: Journal of medicinal chemistry

Published: June 07, 2023

A Combined in Silico and Structural Study Opens New Perspectives on Aliphatic Sulfonamides, a Still Poorly Investigated Class of CA Inhibitors.

A Combined in Silico and Structural Study Opens New Perspectives on Aliphatic Sulfonamides, a Still Poorly Investigated Class of CA Inhibitors.

Journal: Biology

Published: January 16, 2023

Zeta-carbonic anhydrases show CS2 hydrolase activity: A new metabolic carbon acquisition pathway in diatoms?

Zeta-carbonic anhydrases show CS2 hydrolase activity: A new metabolic carbon acquisition pathway in diatoms?

Journal: Computational and structural biotechnology journal

Published: April 16, 2021

2-Mercaptobenzoxazoles: a class of carbonic anhydrase inhibitors with a novel binding mode to the enzyme active site.

2-Mercaptobenzoxazoles: a class of carbonic anhydrase inhibitors with a novel binding mode to the enzyme active site.

Journal: Chemical communications (Cambridge, England)

Published: June 24, 2020

Phenyl(thio)phosphon(amid)ate Benzenesulfonamides as Potent and Selective Inhibitors of Human Carbonic Anhydrases II and VII Counteract Allodynia in a Mouse Model of Oxaliplatin-Induced Neuropathy.

Phenyl(thio)phosphon(amid)ate Benzenesulfonamides as Potent and Selective Inhibitors of Human Carbonic Anhydrases II and VII Counteract Allodynia in a Mouse Model of Oxaliplatin-Induced Neuropathy.

Journal: Journal of medicinal chemistry

Published: May 05, 2020

The non-swapped monomeric structure of the arginine-binding protein from Thermotoga maritima.

The non-swapped monomeric structure of the arginine-binding protein from Thermotoga maritima.

Journal: Acta crystallographica. Section F, Structural biology communications

Published: September 25, 2019

Showing 1-12 of 21

Last Updated: 09/26/2026