Mannich-Type Modifications Of (-)-Cannabidiol And (-)-Cannabigerol Leading To New, Bioactive Derivatives

Author:

Lőrincz Eszter Boglárka1,Tóth Gergely1,Spolárics Júlia1,Herczeg Mihály1,Hodek Jan2,Zupko István3,Minorics Renáta3,Ádám Dorottya1,Oláh Attila1,Zouboulis Christos C.4,Weber Jan2,Nagy Lajos1,Ostorházi Eszter5,Bácskay Ildikó1,Borbás Anikó1,Herczegh Pál1,Bereczki Ilona1

Affiliation:

1. University of Debrecen

2. Czech Academy of Sciences

3. University of Szeged

4. Staedtisches Klinikum Dessau

5. Semmelweis University

Abstract

Abstract (‑)-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 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.

Publisher

Research Square Platform LLC

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