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从算盘子叶中分离和纯化环烯醚萜苷。

Iridoid-glycoside isolation and purification from Premna fulva leaves.

机构信息

Guangxi Key Laboratory of Plant Functional Phytochemicals and Sustainable Utilization, Guangxi Institute of Botany, Guangxi Zhuang Autonomous Region and Chinese Academy of Sciences, Guilin, P. R. China.

College of Chemistry and Bioengineering, Guilin University of Technology, Guilin, P. R. China.

出版信息

J Sep Sci. 2023 Jul;46(14):e2300059. doi: 10.1002/jssc.202300059. Epub 2023 Jun 2.

Abstract

Premna fulva Craib, rich in iridoid glycosides, is widely used to treat periarthritis, osteoproliferation, pain, and other diseases. However, no studies have reported effective purification methods for obtaining iridoid glycosides as active materials. This paper describes an efficient strategy for separating iridoid glycosides from Premna fulva leaves using high-speed counter-current chromatography and preparative high-performance liquid chromatography. A two-phase solvent system, ethyl acetate/n-butanol/water (7.5:2.5:10, v/v), was selected for high-speed counter-current chromatography separation. The proposed method effectively separated and purified four iridoid glycosides and four lignans, including three new iridoid glycosides (4-6) and five known compounds (1-3, 7, 8), from Premna fulva leaves, indicating that high-speed counter-current chromatography combined with prep-HPLC can efficiently isolate catalpol derivatives from the genus Premna. Additionally, the in vitro anti-inflammatory activities of all isolated compounds were analyzed using lipopolysaccharide-stimulated RAW 264.7 cells, and the results indicated that six compounds (1 and 3-7) exhibited potential anti-inflammatory activities.

摘要

糙叶树富含有裂环环烯醚萜苷类成分,广泛用于治疗关节炎、骨质增生、疼痛等疾病。然而,目前尚未有研究报道从糙叶树中提取裂环环烯醚萜苷类作为活性物质的有效分离方法。本研究采用高速逆流色谱法(HSCCC)和制备高效液相色谱法(Prep-HPLC),从糙叶树叶子中分离裂环环烯醚萜苷类化合物。选择乙酸乙酯/正丁醇/水(7.5:2.5:10,v/v)两相溶剂体系用于 HSCCC 分离。该方法能够有效地从糙叶树叶子中分离和纯化 4 个裂环环烯醚萜苷类化合物和 4 个木脂素类化合物,包括 3 个新的裂环环烯醚萜苷类化合物(4-6)和 5 个已知化合物(1-3、7、8)。结果表明,高速逆流色谱法结合制备高效液相色谱法可有效地从糙叶树属植物中分离出梓醇衍生物。此外,通过脂多糖刺激的 RAW 264.7 细胞模型对所有分离得到的化合物进行体外抗炎活性分析,结果表明有 6 个化合物(1 和 3-7)具有潜在的抗炎活性。

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