p-Aminobenzene-Sulfonamide Derivatives of Substituted Pyrimidines as Human Carbonic Anhydrase Inhibitors

The essential reaction of CO<sub>2</sub> hydration, fundamental to all living organisms, is facilitated by the enzyme carbonic anhydrase (CA, EC 4.2.1.1). This enzyme plays a crucial role in regulating various physiological and pathological processes. A series of heterocyclic benzenesulfonamide derivatives (19 compounds) were evaluated as possible inhibitors of human CAs. Their inhibitory properties were tested against several isoforms such as the cytosolic hCA I and hCA II, as well as the transmembrane isoforms hCA IV, hCA IX and hCA XII. The tested molecules demonstrated notable inhibitory potential, particularly toward hCA II and hCA IV, where five and four compounds, respectively, exhibited greater potency than the reference inhibitor, acetazolamide. Molecular docking simulations were further performed to elucidate the binding interactions of the most active compounds with the human CA II, IV IX and XII isoforms.

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Journal
International Journal of Molecular Sciences
Published
2026-03-17
DOI
https://doi.org/10.3390/ijms27062725
Primary Topic
Enzyme function and inhibition
Type
article
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article

p-Aminobenzene-Sulfonamide Derivatives of Substituted Pyrimidines as Human Carbonic Anhydrase Inhibitors

M. A. Prezent, Samvel N. Sirakanyan, Anthi Petrou, Victor Kartcev et al.
International Journal of Molecular Sciences
Enzyme function and inhibition
article

p-Aminobenzene-Sulfonamide Derivatives of Substituted Pyrimidines as Human Carbonic Anhydrase Inhibitors

M. A. Prezent, Samvel N. Sirakanyan, Anthi Petrou, Victor Kartcev, Andrea Angeli, Athina Geronikaki, Claudiu T. Supuran
article en

Abstract

The essential reaction of CO<sub>2</sub> hydration, fundamental to all living organisms, is facilitated by the enzyme carbonic anhydrase (CA, EC 4.2.1.1). This enzyme plays a crucial role in regulating various physiological and pathological processes. A series of heterocyclic benzenesulfonamide derivatives (19 compounds) were evaluated as possible inhibitors of human CAs. Their inhibitory properties were tested against several isoforms such as the cytosolic hCA I and hCA II, as well as the transmembrane isoforms hCA IV, hCA IX and hCA XII. The tested molecules demonstrated notable inhibitory potential, particularly toward hCA II and hCA IV, where five and four compounds, respectively, exhibited greater potency than the reference inhibitor, acetazolamide. Molecular docking simulations were further performed to elucidate the binding interactions of the most active compounds with the human CA II, IV IX and XII isoforms.

International Journal of Molecular SciencesVol. 27(6)
Aristotle University of Thessaloniki (GR), Institute of Fine Organic Chemistry of Scientific - Technological Center of Organic and Pharmaceutical Chemistry (AM), N.D. Zelinsky Institute of Organic Chemistry (RU), Euroscreen (Belgium) (BE), Istituto Nazionale di Fisica Nucleare, Sezione di Firenze (IT), University of Florence (IT)
Openalex Percentile: Top 19%
Enzyme function and inhibition
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p-Aminobenzene-Sulfonamide Derivatives of Substituted Pyrimidines as Human Carbonic Anhydrase Inhibitors — M. A. Prezent, Samvel N. Sirakanyan, et al. · International Journal of Molecular Sciences (2026) | TGRS Research Map | TGRS