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桦木科植物华西桦茎枝中的活性三萜类化合物。

Bioactive triterpenoids from twigs of Betula schmidtii.

机构信息

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.

出版信息

Bioorg Chem. 2018 Apr;77:527-533. doi: 10.1016/j.bioorg.2018.02.006. Epub 2018 Feb 10.

Abstract

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.

摘要

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。

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