We report the first isolation of a previously unknown cannabinoid, cannabizetol (CBGD, 7), from Cannabis sativa extracts, representing the third member of the rare class of methylene-bridged dimeric cannabinoids. The availability of a chemically synthesized standard was crucial for its unequivocal identification, thus confirming the natural occurrence of this new compound. In addition to this structural discovery, we demonstrate that cannabizetol exhibits remarkable antioxidant and skin anti-inflammatory activity, significantly higher than that observed for the known dimeric cannabinoid cannabitwinol (CBDD, 6). These results highlight cannabizetol as a promising bioactive metabolite with potential dermatological applications. To further enable its study, we developed a continuous flow approach to optimize the preparation of these dimers, achieving a substantial reduction in reaction times.

Cannabizetol, a Novel Cannabinoid: Chemical Synthesis, Anti-inflammatory Activity and Extraction from Cannabis sativa L / L. Pozzi, A. Gotti, M. Fumagalli, A. Citarella, V. Fasano, G. Paladino, U. Ciriello, S. Princiotto, F. Annunziata, G. Martinelli, E. Sangiovanni, A. Pinto, M. Dell’Agli, D. Passarella. - In: JOURNAL OF NATURAL PRODUCTS. - ISSN 1520-6025. - (2025), pp. 1-9. [10.1021/acs.jnatprod.5c00826]

Cannabizetol, a Novel Cannabinoid: Chemical Synthesis, Anti-inflammatory Activity and Extraction from Cannabis sativa L

L. Pozzi
Primo
;
A. Gotti
Secondo
;
M. Fumagalli;A. Citarella;V. Fasano;S. Princiotto;F. Annunziata;G. Martinelli;E. Sangiovanni;A. Pinto;M. Dell’Agli;D. Passarella
Ultimo
2025

Abstract

We report the first isolation of a previously unknown cannabinoid, cannabizetol (CBGD, 7), from Cannabis sativa extracts, representing the third member of the rare class of methylene-bridged dimeric cannabinoids. The availability of a chemically synthesized standard was crucial for its unequivocal identification, thus confirming the natural occurrence of this new compound. In addition to this structural discovery, we demonstrate that cannabizetol exhibits remarkable antioxidant and skin anti-inflammatory activity, significantly higher than that observed for the known dimeric cannabinoid cannabitwinol (CBDD, 6). These results highlight cannabizetol as a promising bioactive metabolite with potential dermatological applications. To further enable its study, we developed a continuous flow approach to optimize the preparation of these dimers, achieving a substantial reduction in reaction times.
Cannabinoids; Cannabis sativa; Natural Products; Organic Synthesis; Flow Chemistry; Skin Inflammation
Settore CHEM-05/A - Chimica organica
   Assegnazione Dipartimenti di Eccellenza 2023-2027 - Dipartimento di ECONOMIA, MANAGEMENT E METODI QUANTITATIVI
   DECC23_006
   MINISTERO DELL'UNIVERSITA' E DELLA RICERCA
2025
25-set-2025
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/1184950
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