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

نتاج البحث: نشر في مجلةمقالةمراجعة النظراء

25 اقتباسات (Scopus)

ملخص

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.

اللغة الأصليةالإنجليزيّة
رقم المقال5601
دوريةMolecules
مستوى الصوت26
رقم الإصدار18
المعرِّفات الرقمية للأشياء
حالة النشرنُشِر - سبتمبر 2021
منشور خارجيًانعم

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