StructuralStudies of the Dopamine D<sub>4</sub> ReceptorAntagonist Sonepiprazole as an Inhibitor of Human Carbonic Anhydrases

In this study, we provide the first evidence that sonepiprazole, a dopamine D<sub>4</sub> receptor antagonist, acts as a potent inhibitor of human carbonic anhydrases (hCAs). Sonepiprazole exhibited significant inhibitory activity across the panel of catalytically active hCAs, with the exception of hCA IV, and hCA III. The most potent inhibition was observed against the brain-associated isoform hCA VII, with a <i>K</i><sub>I</sub> of 2.9 nM. Insights from X-ray crystallographic structures of the complexes with hCA I, hCA II, and hCA XII revealed that the sulfonamide group of sonepiprazole coordinates the zinc ion in the active site, a typical interaction for this class of inhibitors. Despite the presence of isoform-specific residues at the rim of the active site pocket, these variations seem not to significantly impact the compound overall inhibition potency. These findings highlight a dual functionality of sonepiprazole as both a D<sub>4</sub> receptor antagonist and a carbonic anhydrase inhibitor.

Publication Details

Journal
Figshare
Published
2025-02-10
DOI
https://doi.org/10.1021/acsmedchemlett.5c00034.s001
Primary Topic
Zoonotic diseases and public health
Type
article
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StructuralStudies of the Dopamine D4 ReceptorAntagonist Sonepiprazole as an Inhibitor of Human Carbonic Anhydrases

Figshare
Zoonotic diseases and public health
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StructuralStudies of the Dopamine D4 ReceptorAntagonist Sonepiprazole as an Inhibitor of Human Carbonic Anhydrases

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Abstract

In this study, we provide the first evidence that sonepiprazole, a dopamine D<sub>4</sub> receptor antagonist, acts as a potent inhibitor of human carbonic anhydrases (hCAs). Sonepiprazole exhibited significant inhibitory activity across the panel of catalytically active hCAs, with the exception of hCA IV, and hCA III. The most potent inhibition was observed against the brain-associated isoform hCA VII, with a <i>K</i><sub>I</sub> of 2.9 nM. Insights from X-ray crystallographic structures of the complexes with hCA I, hCA II, and hCA XII revealed that the sulfonamide group of sonepiprazole coordinates the zinc ion in the active site, a typical interaction for this class of inhibitors. Despite the presence of isoform-specific residues at the rim of the active site pocket, these variations seem not to significantly impact the compound overall inhibition potency. These findings highlight a dual functionality of sonepiprazole as both a D<sub>4</sub> receptor antagonist and a carbonic anhydrase inhibitor.

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Clean water and sanitation
Openalex Percentile: Top 40%
Zoonotic diseases and public health
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StructuralStudies of the Dopamine D<sub>4</sub> ReceptorAntagonist Sonepiprazole as an Inhibitor of Human Carbonic Anhydrases · Figshare (2025) | TGRS Research Map | TGRS