O-derivatization of natural tropolone and β-thujaplicin leading to effective inhibitors of human carbonic anhydrases IX and XII

Herein we report the chemical derivatization of the naturally occurring Tropolone (TRP) and its related compound β-Thujaplicin (β-TJP) as well as their in vitro assessment for inhibition of the physio/pathologically relevant hCAs isoforms I, II, VA; VII, IX and XII to obtain a first set of inhibition data useful for driving selected derivatives towards appropriate biomedical exploitation. The selected compound 17β was characterized for its chemical stability and assessed for its antiproliferative activity on a multiple myeloma model and showed potent pro-apoptotic features jointly with a safe toxicity profile on healthy cells. The binding mode of β-TJP within the hCA II was assessed by means of X-ray crystallography of the hCA II/β-TJP complex and showed almost complete superposition with the hCA II/TRP adduct reported in the literature. The data produced were used to elaborate a binding prediction model of such compounds on the hCAs VA, IX, and XII which are directly connected to important diseases. Overall, the achievements reported in this work are in the sustainment of the exploitation of naturally occurring troponoloid-based structures for biomedical purposes and thus contribute to the field in extending the variety of available chemical features.

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Publication Details

Journal
European Journal of Medicinal Chemistry
Published
2025-03-30
DOI
https://doi.org/10.1016/j.ejmech.2025.117552
Citations
3
Primary Topic
Enzyme function and inhibition
Type
article
Field-Weighted Citation Impact
2.42
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article

O-derivatization of natural tropolone and β-thujaplicin leading to effective inhibitors of human carbonic anhydrases IX and XII

Francesco Melfi, Roberta Torcasio, Clemente Capasso, Emanuela Marchese et al.
3 citations
European Journal of Medicinal Chemistry
Enzyme function and inhibition
2.42
article

O-derivatization of natural tropolone and β-thujaplicin leading to effective inhibitors of human carbonic anhydrases IX and XII

Francesco Melfi, Roberta Torcasio, Clemente Capasso, Emanuela Marchese, Stefano Alcaro, Giosuè Costa, Marta Ferraroni, Claudiu T. Supuran, Francesca Mancuso, Ana Čikoš, Francesca Alessandra Ambrosio, Rosaria Gitto, Simone Carradori, Fabrizio Carta, Nicola Amodio, Ilaria D’Agostino, Gioele Renzi, Josip Rešetar, Andrea Angeli, Daniela Vullo, Chiara Baroni
article en
3 citations

Abstract

Herein we report the chemical derivatization of the naturally occurring Tropolone (TRP) and its related compound β-Thujaplicin (β-TJP) as well as their in vitro assessment for inhibition of the physio/pathologically relevant hCAs isoforms I, II, VA; VII, IX and XII to obtain a first set of inhibition data useful for driving selected derivatives towards appropriate biomedical exploitation. The selected compound 17β was characterized for its chemical stability and assessed for its antiproliferative activity on a multiple myeloma model and showed potent pro-apoptotic features jointly with a safe toxicity profile on healthy cells. The binding mode of β-TJP within the hCA II was assessed by means of X-ray crystallography of the hCA II/β-TJP complex and showed almost complete superposition with the hCA II/TRP adduct reported in the literature. The data produced were used to elaborate a binding prediction model of such compounds on the hCAs VA, IX, and XII which are directly connected to important diseases. Overall, the achievements reported in this work are in the sustainment of the exploitation of naturally occurring troponoloid-based structures for biomedical purposes and thus contribute to the field in extending the variety of available chemical features.

European Journal of Medicinal ChemistryVol. 290
University of Pisa (IT), University of Messina (IT), Magna Graecia University (IT), University of Chieti-Pescara (IT), Institute of Biosciences and Bioresources (IT), Ruđer Bošković Institute (HR), University of Florence (IT)
Openalex Percentile: Top 12%
Enzyme function and inhibition
2.42
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