Natural Products Laboratory, School of Pharmacy, Sungkyunkwan University, Suwon 16419, Republic of Korea.
Laboratory of Pharmacognosy, College of Pharmacy, Gachon University, Incheon 21936, Republic of Korea.
Bioorg Chem. 2018 Apr;77:527-533. doi: 10.1016/j.bioorg.2018.02.006. Epub 2018 Feb 10.
Investigation of the MeOH extract of Betula schmidtii twigs resulted in the isolation and identification of three new triterpenoids (1-3), along with ten known ones (4-13). The structures of new compounds (1-3) were elucidated by spectroscopic methods, including 1D, 2D NMR (H and C NMR, COSY, HSQC, HMBC, and NOESY), HR-MS, and chemical methods. All the isolated compounds were evaluated for their cytotoxicity against A549, SK-OV-3, SK-MEL-2, and HCT-15 cell lines. Compound 11 exhibited potent cytotoxic activities against four cell lines, and compounds 5 and 13 significantly induced nerve growth factor secretion in a C6 rat glioma cell line. Their anti-inflammatory effects were also assessed by measuring nitric oxide production in lipopolysaccharide-activated BV-2 cells. Compounds 7 and 12 displayed potent inhibition of nitric oxide production, without significant cell toxicity.
研究桦木属小枝的甲醇提取物,分离并鉴定了三种新的三萜(1-3),以及十种已知的三萜(4-13)。新化合物(1-3)的结构通过光谱方法阐明,包括 1D、2D NMR(H 和 C NMR、COSY、HSQC、HMBC 和 NOESY)、高分辨率质谱和化学方法。所有分离出的化合物都进行了细胞毒性评估,针对 A549、SK-OV-3、SK-MEL-2 和 HCT-15 细胞系进行了评估。化合物 11 对四种细胞系表现出很强的细胞毒性活性,化合物 5 和 13 显著诱导 C6 大鼠神经胶质瘤细胞系中神经生长因子的分泌。还通过测量脂多糖激活的 BV-2 细胞中的一氧化氮产生来评估它们的抗炎作用。化合物 7 和 12 表现出对一氧化氮产生的强烈抑制作用,而没有明显的细胞毒性。