9h81
From Proteopedia
human carbonic anhydrase I in complex with Sonepiprazole
Structural highlights
FunctionCAH1_HUMAN Reversible hydration of carbon dioxide. Can hydrates cyanamide to urea.[1] Publication Abstract from PubMedIn this study, we provide the first evidence that sonepiprazole, a dopamine D(4) 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 K (I) 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(4) receptor antagonist and a carbonic anhydrase inhibitor. Structural Studies of the Dopamine D(4) Receptor Antagonist Sonepiprazole as an Inhibitor of Human Carbonic Anhydrases.,Angeli A, Ferraroni M, Capasso C, Supuran CT ACS Med Chem Lett. 2025 Feb 10;16(3):483-486. doi: , 10.1021/acsmedchemlett.5c00034. eCollection 2025 Mar 13. PMID:40104783[2] From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine. References
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