State Key Laboratory of Bioactive Substance and Function of Natural Medicines, Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100050, China.
J Asian Nat Prod Res. 2024 Feb;26(2):177-188. doi: 10.1080/10286020.2023.2289601. Epub 2024 Jan 2.
Two pairs of new dihydrophenanthro[]furan enantiomers blephebibnols G-H (), one new dihydrophenanthro[]furan derivative blephebibnol I (), along with four known analogues (), were isolated from the tubers of . Their structures including the absolute configurations were determined by the combination of spectroscopic data analysis, ECD and NMR calculations. Compounds , , and showed inhibition of NO production in LPS-stimulated BV-2 cells, with IC values ranging from 4.11 to 14.65 M. Further mechanistic study revealed that suppressed the phosphorylation of p65 subunit to regulate the NF-κB signaling pathway. In addition, some compounds displayed selective cytotoxic activities against HCT-116, HepG2, A549, or HGC27 cancer cell lines with IC values ranging from 0.1 to 8.23 M.
从绵萆薢块茎中分离得到两对新的二氢菲并呋喃对映异构体 blephebibnols G-H (),一个新的二氢菲并呋喃衍生物 blephebibnol I (),以及四个已知类似物 ()。通过光谱数据分析、ECD 和 NMR 计算的组合,确定了它们的结构包括绝对构型。化合物 、 、和 对 LPS 刺激的 BV-2 细胞中的 NO 产生具有抑制作用,IC 值范围为 4.11 至 14.65 μM。进一步的机制研究表明, 抑制 p65 亚基的磷酸化,从而调节 NF-κB 信号通路。此外,一些化合物对 HCT-116、HepG2、A549 或 HGC27 癌细胞系表现出选择性细胞毒性活性,IC 值范围为 0.1 至 8.23 μM。