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Mannich-type modifications of (−)-cannabidiol and (−)-cannabigerol leading to new, bioactive derivatives
- 1.0578610 - ÚOCHB 2024 RIV US eng J - Journal Article
Lőrincz, E. B. - Tóth, G. - Spolárics, J. - Herczeg, M. - Hodek, Jan - Zupkó, I. - Minorics, R. - Ádám, D. - Oláh, A. - Zouboulis, C. C. - Weber, Jan - Nagy, L. - Ostorházi, E. - Bácskay, I. - Borbás, A. - Herczegh, P. - Bereczki, I.
Mannich-type modifications of (−)-cannabidiol and (−)-cannabigerol leading to new, bioactive derivatives.
Scientific Reports. Roč. 13, November (2023), č. článku 19618. ISSN 2045-2322. E-ISSN 2045-2322
R&D Projects: GA MŠMT(CZ) LX22NPO5103
Institutional support: RVO:61388963
Keywords : phytocannabinoids * inflammation * activation
OECD category: Virology
Impact factor: 4.6, year: 2022
Method of publishing: Open access
https://doi.org/10.1038/s41598-023-45565-7
(−)-Cannabidiol (CBD) and (−)-cannabigerol (CBG) are two major non-psychotropic phytocannabinoids that have many beneficial biological properties. However, due to their low water solubility and prominent first-pass metabolism, their oral bioavailability is moderate, which is unfavorable for medicinal use. Therefore, there is a great need for appropriate chemical modifications to improve their physicochemical and biological properties. In this study, Mannich-type reaction was used for the synthetic modification of CBD and CBG for the first time, and thus fifteen new cannabinoid derivatives containing one or two tertiary amino groups were prepared. Thereafter the antiviral, antiproliferative and antibacterial properties of the derivatives and their effects on certain skin cells were investigated. Some modified CBD derivatives showed remarkable antiviral activity against SARS-CoV-2 without cytotoxic effect, while synthetic modifications on CBG resulted in a significant increase in antiproliferative activity in some cases compared to the parent compound.
Permanent Link: https://hdl.handle.net/11104/0347569
File Download Size Commentary Version Access 10.1038s41598-023-45565-7.pdf 2 1.9 MB Publisher’s postprint open-access
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