College of Pharmacy and Research Institute of Pharmaceutical Sciences , Seoul National University , Seoul 08826 , Republic of Korea.
College of Pharmacy and Integrated Research Institute for Drug Development , Dongguk University-Seoul , Gyeonggi-do 10326 , Republic of Korea.
J Nat Prod. 2019 Feb 22;82(2):309-317. doi: 10.1021/acs.jnatprod.8b00748. Epub 2019 Jan 30.
Seven new prenylated flavonoids (1-7) and one new prenylated phenylpropiophenone (8) were isolated from roots and rhizomes of Sophora tonkinensis, along with nine known compounds (9-17). The structures 1-8 were elucidated by spectroscopic data analysis and comparison with reported values. Compounds 8 and 12 (7-methoxyebenosin) showed inhibitory activities against nitric oxide production in lipopolysaccharide-induced RAW264.7 cells, with IC values of 8.1 and 6.2 μM, respectively. They also significantly lowered expression of CSF2, TNF, and IL-1β. Lonchocarpol A (10) and erybraedin D (16) at concentrations of 20 μM downregulated proprotein convertase subtilisin/kexin type 9 (PCSK9) mRNA expression in HepG2 cells. Moreover, erybraedin D (16) inhibited PCSK9 protein synthesis (IC 7.8 μM), while simultaneously activating AMP-activated protein kinase and acetyl-CoA carboxylase.
从越南苦参的根和根茎中分离得到了 7 个新的类黄酮(1-7)和 1 个新的类黄酮苯丙素(8),以及 9 个已知化合物(9-17)。通过光谱数据分析和与报道值的比较,确定了化合物 1-8 的结构。化合物 8 和 12(7-甲氧基埃本辛)对脂多糖诱导的 RAW264.7 细胞中一氧化氮的产生具有抑制活性,IC 值分别为 8.1 和 6.2 μM。它们还显著降低了 CSF2、TNF 和 IL-1β 的表达。Lonchocarpol A(10)和 Erybraedin D(16)在 20 μM 浓度下可下调 HepG2 细胞中前蛋白转化酶枯草溶菌素/克酶 9(PCSK9)mRNA 的表达。此外,Erybraedin D(16)抑制 PCSK9 蛋白合成(IC 7.8 μM),同时激活 AMP 激活的蛋白激酶和乙酰辅酶 A 羧化酶。