Xue Gui-Min, Xue Jin-Feng, Duan Jiang-Jing, Yang Hui-Ying, Sun Yan-Jun, Chen Hui, Zhi Yan-Le, Zhang Zhi-Qiang, Li Rao, Zhu Dong-Rong, Li Guo-Sheng
College of Pharmacy, Henan University of Chinese Medicine, Zhengzhou, 450046, China; Henan Collaborative Innovation Center for Research and Development on the Whole Industry Chain of Yu-Yao, Henan University of Chinese Medicine, Zhengzhou, 450046, China.
College of Pharmacy, Henan University of Chinese Medicine, Zhengzhou, 450046, China.
Phytochemistry. 2025 Nov;239:114608. doi: 10.1016/j.phytochem.2025.114608. Epub 2025 Jul 3.
Six previously undescribed sesquiterpenoids, named achisetaces A-F (1-6), involving a rare C-O-C bridged guaianolide-type sesquiterpenoid (1), along with nine known analogues (7-15), were obtained from the aerial parts of Achillea setacea Waldst. & Kit. The undescribed structures of 1-6 including their absolute configurations were determined through spectroscopic techniques (IR, UV, HRESIMS, 1D and 2D NMR), combined with DP4+ NMR analysis and quantum electronic circular dichroism (ECD) calculations. The inhibitory effects of compounds 1-15 on nitric oxide (NO) production were evaluated in LPS-induced RAW 264.7 cells. Compounds 6 and 10 exhibited significant anti-inflammatory activities with IC values of 1.56 ± 0.32 and 6.89 ± 0.47 μM, respectively. Moreover, a mechanistic study revealed that compound 6 exerted the anti-inflammatory activity by regulating the glycolytic pathway via suppression of PFKFB3 activation.
从绵毛蓍(Achillea setacea Waldst. & Kit.)的地上部分获得了6个新的倍半萜类化合物,命名为蓍草内酯A - F(1 - 6),其中包括一种罕见的C - O - C桥连愈创木烷型倍半萜内酯(1),以及9个已知类似物(7 - 15)。通过光谱技术(红外光谱、紫外光谱、高分辨电喷雾电离质谱、一维和二维核磁共振),结合DP4 +核磁共振分析和量子电子圆二色性(ECD)计算,确定了1 - 6的未知结构及其绝对构型。在脂多糖诱导的RAW 264.7细胞中评估了化合物1 - 15对一氧化氮(NO)产生的抑制作用。化合物6和10表现出显著的抗炎活性,IC50值分别为1.56±0.32和6.89±0.47μM。此外,机理研究表明,化合物6通过抑制PFKFB3激活来调节糖酵解途径,从而发挥抗炎活性。