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从三尖杉的嫩枝和叶子中分离鉴定出两种新化合物。

Isolation and identification of two new compounds from the twigs and leaves of Cephalotaxus fortunei.

机构信息

School of Traditional Chinese Materia Medica, Shenyang Pharmaceutical University, Shenyang, China.

Key Laboratory of Computational Chemistry-Based Natural Antitumor Drug Research and Development, Wenhua Road 103, Shenyang, Liaoning Province, 110016, China.

出版信息

J Nat Med. 2019 Jun;73(3):653-660. doi: 10.1007/s11418-019-01308-5. Epub 2019 Apr 11.

DOI:10.1007/s11418-019-01308-5
PMID:30976949
Abstract

Two new compounds, namely 5-hydroxy-7-methoxy-6-methylchromone (1), and sesquiterpene X (6), together with 21 known compounds were isolated from the twigs and leaves of Cephalotaxus fortunei Hook. f. The structures of 1-23 were elucidated on the basis of spectroscopic analysis (1D/2D NMR, HR-ESI-MS and IR) and comparison with literature. The absolute configuration of compound 6 was determined by means of electronic circular dichroism calculation. The in vitro anti-inflammatory activities of all compounds were assayed in RAW 264.7 cells by assessing lipopolysaccharide-induced nitric oxide production. Compounds 1 and 6 exhibited weak effects with percentage inhibitions of 24% and 35.60%, respectively. In addition, compounds 4, 9, and 14 have the potential to be developed as therapeutic agents for inflammatory diseases because of their significant anti-inflammatory activities and high content in C. fortunei.

摘要

从三尖杉的枝叶中分离得到了两个新化合物,分别为 5-羟基-7-甲氧基-6-甲基色酮(1)和倍半萜 X(6),以及 21 个已知化合物。根据光谱分析(1D/2D NMR、HR-ESI-MS 和 IR)和文献比较,确定了 1-23 的结构。通过电子圆二色性计算确定了化合物 6 的绝对构型。通过评估脂多糖诱导的一氧化氮产生,在 RAW 264.7 细胞中测试了所有化合物的体外抗炎活性。化合物 1 和 6 的抑制率分别为 24%和 35.60%,具有较弱的抗炎作用。此外,由于其显著的抗炎活性和在三尖杉中的高含量,化合物 4、9 和 14 具有开发为治疗炎症性疾病的药物的潜力。

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