[朝鲜蓟茎和叶中的化学成分及其对体外滑膜母细胞增殖的抑制作用]。

Q3 Pharmacology, Toxicology and Pharmaceutics Zhongguo Zhongyao Zazhi Pub Date : 2024-07-01 DOI:10.19540/j.cnki.cjcmm.20240405.203
Jia-Ming Guo, Lin-Xuan Li, Xin-Yi Li, Tian-Yu Wang, En-Ning Zhu, Long-Cheng Cui, Fan Wu, Yan-Ping Liu, Yan-Hui Fu
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引用次数: 0

摘要

采用硅胶、十八烷基硅烷基(ODS)和 Sephadex LH-20 凝胶柱色谱法、制备型高效液相色谱法(Pre-HPLC)以及多种色谱分离技术,系统研究了桑科植物越南冬青(Artocarpus tonkinensis)茎叶中的化学成分。通过分离获得了化合物的光谱数据和理化性质,并与文献报道的化合物进行了比较。结果,从 A. tonkinensis 的茎和叶的 90% 乙醇提取物中分离出 11 种化合物。结果从 A. tonkinensis 茎和叶的 90% 乙醇提取物中分离出 11 种化合物,分别为 artocatonkine(1), 5,6,7,4'-tetramethoxyflavone(2), apigenin-4'-O-β-D-glucoside(3), rayalinol(4), psorachalcone A(5)、4-ketopinoresinol(6), ficusesquilignan B(7), pinnatifidanin AI(8), pinnatifidanin A(9), O-methylmellein(10), and trans-4-hydroxymellein(11).在这些化合物中,化合物 1 是一种新的前酯黄酮,化合物 2-11 则是首次从蒿属植物中分离出来。此外,还对所有化合物 1-11 的抗类风湿性关节炎活性进行了评估,并采用 MTS 法测量了它们对体外滑膜母细胞增殖的抑制作用。活性评价结果表明,黄酮类化合物1-3、5以及木质素化合物8和9具有显著的抗类风湿性关节炎活性,其抑制滑膜母细胞MH7A增殖的IC_(50)值从(6.38±0.06) μmol-L~(-1)到(168.58±0.28)μmol-L~(-1)不等。
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[Chemical constituents from stems and leaves of Artocarpus tonkinensis and their inhibitory effects on proliferation of synovioblasts in vitro].

The chemical constituents from the stems and leaves of Artocarpus tonkinensis in Artocarpus of Moraceae were systematically studied by means of silica gel, octadecylsilyl(ODS), and Sephadex LH-20 gel column chromatographies, as well as preparative high-performance liquid chromatography(Pre-HPLC) and a variety of chromatographic separation techniques. The spectral data and physicochemical properties of the compounds were obtained from separation and compared with those of the compounds reported in the literature. As a result, 11 compounds isolated from the 90% ethanol extract of the stems and leaves of A. tonkinensis were identified as artocatonkine(1), 5,6,7,4'-tetramethoxyflavone(2), apigenin-4'-O-β-D-glucoside(3), rayalinol(4), psorachalcone A(5), 4-ketopinoresinol(6), ficusesquilignan B(7), pinnatifidanin AI(8), pinnatifidanin A(9), O-methylmellein(10), and trans-4-hydroxymellein(11). Among these compounds, compound 1 was a new prenylated flavone, and compounds 2-11 were isolated from the plants belonging to the genus Artocarpus for the first time. Furthermore, all compounds 1-11 were evaluated for their anti-rheumatoid arthritis activities, and the MTS method was used to measure their inhibitory effects on the proliferation of synovioblasts in vitro. The results of activity evaluation showed that flavonoid compounds 1-3, 5, and lignan compounds 8 and 9 displayed significant anti-rheumatoid arthritis activities, showing the IC_(50) values in inhibiting the proliferation of synovioblasts MH7A from(6.38±0.06) μmol·L~(-1) to(168.58±0.28)μmol·L~(-1).

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来源期刊
Zhongguo Zhongyao Zazhi
Zhongguo Zhongyao Zazhi Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (all)
CiteScore
1.50
自引率
0.00%
发文量
581
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