Li Han-Fen, Shao Hui-Yan, Huang Ni, Yang Dan, Yang Liu, Kong Qing-Hua, Hu Jiang-Miao
Key Laboratory of Phytochemistry and Natural Medicines, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming 650201, Yunnan, China; University of Chinese Academy of Sciences, Beijing 100049, China.
Key Laboratory of Phytochemistry and Natural Medicines, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming 650201, Yunnan, China.
Bioorg Chem. 2025 Jan;154:108058. doi: 10.1016/j.bioorg.2024.108058. Epub 2024 Dec 13.
Twelve picrotoxane-type sesquiterpenoids were isolated from Dendrobium wardianum, of which dendrowardins K-N (1-4) are new compounds and dendrowardins O and P (9, 10) are new natural products. Notably, the structure of dendrowardin K contains the rarely observed 10,11-γ-lactone ring. The structural configurations of these compounds were determined through comprehensive 1D and 2D nuclear magnetic resonance (NMR), single-crystal X-ray diffraction, and other spectroscopic analyses. Additionally, the hypoglycaemic activities of the picrotoxane-type sesquiterpenes and their analogues were systematically evaluated by determining the antidiabetic activities of these compounds and six others (13-18) obtained from genus Dendrobium. Twelve compounds (1, 2, 4-6, 8, 12, 13 - 15, 17, and 18) significantly improved insulin resistance. Further experiments revealed that compound 6 improved insulin resistance by increasing GLUT-4 expression. The possible mechanism is related to AKT-related pathways, and the effects of treatment with 50 μM compound 6 were comparable to those of the positive control drug metformin. Compounds 4-6 and 13-15, 17 displayed great increases in the secretion of insulin from β-TC-6 cells. On the basis of these findings, the structure-activity relationships (SARs) of picrotoxane-type sesquiterpenoids were discussed for the first time.
从蝴蝶兰中分离出12种印防己毒素型倍半萜类化合物,其中树兰素K-N(1-4)为新化合物,树兰素O和P(9, 10)为新天然产物。值得注意的是,树兰素K的结构包含罕见的10,11-γ-内酯环。通过综合的一维和二维核磁共振(NMR)、单晶X射线衍射和其他光谱分析确定了这些化合物的结构构型。此外,通过测定这些化合物以及从石斛属植物中获得的其他六种化合物(13-18)的抗糖尿病活性,系统评估了印防己毒素型倍半萜及其类似物的降血糖活性。十二种化合物(1, 2, 4-6, 8, 12, 13 - 15, 17, 18)显著改善了胰岛素抵抗。进一步的实验表明,化合物6通过增加GLUT-4表达来改善胰岛素抵抗。可能的机制与AKT相关途径有关,50 μM化合物6的治疗效果与阳性对照药物二甲双胍相当。化合物4-6和13-15、17使β-TC-6细胞的胰岛素分泌大幅增加。基于这些发现,首次讨论了印防己毒素型倍半萜类化合物的构效关系(SARs)。