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大戟属华美Euphorbia pulcherrima 的三萜类化合物具有抑制破骨细胞生成的作用。

Triterpenoids from Euphorbia pulcherrima with inhibitory effects on osteoclastogenesis.

机构信息

Research Center for Drug Discovery, School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou 510006, People's Republic of China.

Research Center for Drug Discovery, School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou 510006, People's Republic of China; Guangdong Provincial Key Laboratory of New Drug Design and Evaluation, Guangzhou 510006, People's Republic of China.

出版信息

Fitoterapia. 2019 Apr;134:355-361. doi: 10.1016/j.fitote.2019.02.028. Epub 2019 Mar 8.

DOI:10.1016/j.fitote.2019.02.028
PMID:30858048
Abstract

Three new compounds (1-3), euphorimaoid A (1), euphorimaoid B (2), 1α-hydroxy-3β-acetoxy-olean-9,12-diene (3), two firstly isolated natural products 3β-acetyloxy-olean-13(18)-en-12-one (4) and 18,19-epoxyolean-3β-ol acetate (5), together with 13 known compounds (6-18) have been identified from the aerial parts of Euphorbia pulcherrima Willd. Structures of compounds 1-5 were elucidated by comprehensive spectroscopic analysis. The absolute configuration of euphorimaoid A (1) was established using single crystal X-ray diffraction analysis. All the isolates were evaluated for their inhibition of osteoclastogenesis in BMMs. Among them, compounds 7 and 10 showed significantly inhibition in a concentration-dependent manner.

摘要

从美丽泽覃大戟的地上部分分离得到三个新化合物(1-3), euphorimaoid A(1), euphorimaoid B(2),1α-羟基-3β-乙酰氧基-齐墩烷-9,12-二烯(3),两个首次分离得到的天然产物 3β-乙酰氧基-齐墩烷-13(18)-烯-12-酮(4)和 18,19-环氧齐墩烷-3β-醇乙酸酯(5),以及 13 个已知化合物(6-18)。通过综合光谱分析鉴定了化合物 1-5 的结构。通过单晶 X 射线衍射分析确定了 euphorimaoid A(1)的绝对构型。所有分离得到的化合物都评估了其对破骨细胞分化的抑制作用。其中,化合物 7 和 10 表现出明显的浓度依赖性抑制作用。

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