Department of Life Sciences, University of Modena and Reggio Emilia, Via Giuseppe Campi 103, 41125 Modena, Italy.
LSPCMIB, UMR-CNRS 5068, Université Paul Sabatier-Toulouse III, 118 route de Narbonne, 31062 Toulouse CEDEX 9, France.
Molecules. 2019 Jul 15;24(14):2567. doi: 10.3390/molecules24142567.
Cannabigerol (CBG) and cannabichromene (CBC) are non-psychoactive cannabinoids that have raised increasing interest in recent years. These compounds exhibit good tolerability and low toxicity, representing promising candidates for drug repositioning. To identify novel potential therapeutic targets for CBG and CBC, an integrated ligand-based and structure-based study was performed. The results of the analysis led to the identification of CBG as a low micromolar inhibitor of the Enoyl acyl carrier protein (ACP) reductase (InhA) enzyme.
大麻萜酚(CBG)和大麻色烯(CBC)是非精神活性大麻素,近年来引起了越来越多的关注。这些化合物具有良好的耐受性和低毒性,是药物重新定位的有前途的候选物。为了确定 CBG 和 CBC 的新的潜在治疗靶点,进行了基于配体和基于结构的综合研究。分析结果表明,CBG 是烯酰基辅酶 A 还原酶(InhA)酶的低微摩尔抑制剂。