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Novel cbg derivatives can reduce inflammation, pain and obesity

  • Natalya M. Kogan*
  • , Yarden Lavi
  • , Louise M. Topping
  • , Richard O. Williams
  • , Fiona E. McCann
  • , Zhanna Yekhtin
  • , Marc Feldmann
  • , Ruth Gallily
  • , Raphael Mechoulam
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

28 Scopus citations

Abstract

Interest in CBG (cannabigerol) has been growing in the past few years, due to its anti-inflammatory properties and other therapeutic benefits. Here we report the synthesis of three new CBG derivatives (HUM-223, HUM-233 and HUM-234) and show them to possess anti-inflammatory and analgesic properties. In addition, unlike CBG, HUM-234 also prevents obesity in mice fed a high-fat diet (HFD). The metabolic state of the treated mice on HFD is significantly better than that of vehicle-treated mice, and their liver slices show significantly less steatosis than untreated HFD or CBG-treated ones from HFD mice. We believe that HUM-223, HUM-233 and HUM-234 have the potential for development as novel drug candidates for the treatment of inflammatory conditions, and in the case of HUM-234, potentially for obesity where there is a huge unmet need.

Original languageEnglish
Article number5601
JournalMolecules
Volume26
Issue number18
DOIs
StatePublished - 15 Sep 2021

Bibliographical note

Publisher Copyright:
© 2021 by the authors. Licensee MDPI, Basel, Switzerland.

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Anti-inflammatory
  • Cannabigerol
  • Cannabinoid
  • Obesity

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