LIN Zhi-qi, ZHU Hong-bo, ZHOU Tang, WANG Ji, ZHANG Rong-ping, CHEN Xing-long. Study of phenylpropanoids from Tripterygium hypoglaucumJ. Acta Pharmaceutica Sinica, 2024, 59(6): 1730-1740. DOI: 10.16438/j.0513-4870.2023-1268
Citation: LIN Zhi-qi, ZHU Hong-bo, ZHOU Tang, WANG Ji, ZHANG Rong-ping, CHEN Xing-long. Study of phenylpropanoids from Tripterygium hypoglaucumJ. Acta Pharmaceutica Sinica, 2024, 59(6): 1730-1740. DOI: 10.16438/j.0513-4870.2023-1268

Study of phenylpropanoids from Tripterygium hypoglaucum

  • This paper aimed to study phenylpropanoids of Tripterygium hypoglaucum. Twenty-four compounds were isolated from the 70% EtOH extracts of T. hypoglaucum by silica gel column chromatography, reversed phase column chromatography, gel column chromatography, preparative thin layer chromatography, and semi-preparative high performance liquid chromatography. Compounds 1-3 were three new phenylpropionds. Their structures were identified by ultraviolet spectrum, infrared spectroscopy, high resolution electrospray ionization mass spectrometry, and nuclear magnetic resonance data as: threo-2-(4-hydroxy-3-methoxyphenoxy)-3-(4-hydroxy-3-methoxyphenyl)-1, 3-propanedol (1), erythro-2-(4-hydroxy-3-methoxyphenoxy)-3-(4-hydroxy-3-methoxyphenyl)-1, 3-propanediol (2), erythro-3-(4-hydroxy-3, 5-dimethoxyphenyl)-3-ethoxypropane-1, 2-propanediol (3). Compounds 4-6, 9, 14, 15, 18, 19, and 21-24 were obtained from Tripterygium genus for the first time. The cytotoxicity assay of cancer cells suggested that compound 20 displayed cytotoxicity on the breast cancer 4T1 cells whose 50% inhibitory concentration was 125.60 μmol·L-1.
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