TY - JOUR
T1 - Arzanol Inhibits Human Dihydroorotate Dehydrogenase and Shows Antiviral Activity
AU - Alberti, Marta
AU - Tamburello, Martina
AU - Salamone, Stefano
AU - Gallinella, Giorgio
AU - Sanna, Cinzia
AU - Appendino, Giovanni Battista
AU - Lolli, Marco L.
AU - MASSAROTTI, Alberto
AU - POLLASTRO, Federica
AU - MIGGIANO, RICCARDO
PY - 2025
Y1 - 2025
N2 - : Human dihydroorotate dehydrogenase (hDHODH), catalyzing the rate-limiting step of the pyrimidine biosynthesis pathway (PBP), is a drug target extensively investigated for various diseases including cancer, autoimmune disorders, and viral infections. We present evidence that the heterodimeric phloroglucinylpyrone arzanol potently inhibits hDHODH by competing with ubiquinone for binding to the lipophilic patch (LP) of the enzyme. Co-crystallization experiments on the enzyme-arzanol complex provided further insights into the binding pocket of hDHODH, revealing detailed features that could inspire the design of innovative inhibitors. The cellular translation of these enzymatic and biochemical data was validated in antiviral assays on SARS-CoV-2 infected cells. Taken together, these results exemplify the potential of natural products to explore novel areas of the protein druggable space and provide information relevant to multiple critical areas of drug discovery.
AB - : Human dihydroorotate dehydrogenase (hDHODH), catalyzing the rate-limiting step of the pyrimidine biosynthesis pathway (PBP), is a drug target extensively investigated for various diseases including cancer, autoimmune disorders, and viral infections. We present evidence that the heterodimeric phloroglucinylpyrone arzanol potently inhibits hDHODH by competing with ubiquinone for binding to the lipophilic patch (LP) of the enzyme. Co-crystallization experiments on the enzyme-arzanol complex provided further insights into the binding pocket of hDHODH, revealing detailed features that could inspire the design of innovative inhibitors. The cellular translation of these enzymatic and biochemical data was validated in antiviral assays on SARS-CoV-2 infected cells. Taken together, these results exemplify the potential of natural products to explore novel areas of the protein druggable space and provide information relevant to multiple critical areas of drug discovery.
UR - https://iris.uniupo.it/handle/11579/218142
U2 - 10.1021/acs.jnatprod.5c00887
DO - 10.1021/acs.jnatprod.5c00887
M3 - Article
SN - 0163-3864
JO - Journal of Natural Products
JF - Journal of Natural Products
ER -