I. Vozny

The antibiotic furagin and its derivatives are isoform-selective human carbonic anhydrase inhibitors

C. Supuran, A. Nocentini, R. Žalubovskis, 2020, Journal of enzyme inhibition and medicinal chemistry.

5-Substituted-(1,2,3-triazol-4-yl)thiophene-2-sulfonamides strongly inhibit human carbonic anhydrases I, II, IX and XII: solution and X-ray crystallographic studies.

C. Supuran, K. Tārs, M. Tanc, 2013, Bioorganic & medicinal chemistry.

X-ray crystallographic and kinetic investigations of 6-sulfamoyl-saccharin as a carbonic anhydrase inhibitor.

V. Alterio, A. Di Fiore, G. De Simone, 2015, Organic & biomolecular chemistry.

Symmetric molecules with 1,4-triazole moieties as potent inhibitors of tumour-associated lactate dehydrogenase-A

A. Alafeefy, R. Žalubovskis, M. E. El Shikh, 2017, Journal of enzyme inhibition and medicinal chemistry.

Novel Method for the Preparation of 2H‐1,2,4‐Benzothiadiazin‐3(4H)‐one 1,1‐Dioxides via a Curtius Rearrangement.

D. Borovika, P. Trapencieris, R. Žalubovskis, 2013 .

Synthesis of 6-sulfamoylsaccharin and study of its reactivity in alkylation reactions

P. Trapencieris, R. Žalubovskis, I. Vozny, 2012, Chemistry of Heterocyclic Compounds.

Hydrophobic Substituents of the Phenylmethylsulfamide Moiety Can Be Used for the Development of New Selective Carbonic Anhydrase Inhibitors

C. Supuran, P. Trapencieris, V. Alterio, 2014, BioMed research international.

Synthesis of an 8-Membered Heterocycle from Saccharin and Leakadine

R. Žalubovskis, I. Vozny, A. Mishnev, 2012, Chemistry of Heterocyclic Compounds.