Application of purslane alkaloid monomeric compound in preparation of anti-tumor medicament
An anti-tumor drug, alkaloid technology, applied in the field of medicine, can solve the problem that the anti-tumor activity has not been reported in literature and so on
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Embodiment 1
[0018] Example 1: Extraction, separation and structural identification of purslane amide B and orange piperonamide.
[0019] Purslane medicinal material (about 100 kg) was purchased, stirred and extracted with absolute ethanol 3 times, each time for 1 hour, and the ethanol was recovered to obtain a black extract. Add 10% sulfuric acid to the extract to dissolve and filter. The pH was adjusted to 10.0 with ammonia water, and a saturated NaCl aqueous solution was added. Dichloromethane was extracted to obtain a dichloromethane layer, which was evaporated to dry to obtain an extract rich in alkaloid extract. The extract of alkaloid extract has undergone repeated silica gel chromatography, Sephadex LH-20, ODS and liquid phase separation methods, combined with physical and chemical properties and modern spectroscopy methods (UV, IR, MS, 1H-NMR, 13C-NMR and 2D- NMR) isolated and identified two monomeric compounds, namely purslane amide B and orange piperonamide.
Embodiment 2
[0020] Example 2: Study on the antitumor activity of purslane amide B and orange piperonamide in vitro.
[0021] The inhibitory activities of purslane amide B and orange piperonamide on human lung adenocarcinoma cells (A549) and human leukemia cell lines (K562) were determined by MTT method.
[0022] (1) Instruments and reagents: RPMI 1640 culture medium and DMEM medium were purchased from Hyclone Company; fetal bovine serum was from Hangzhou Sijiqing; CKX31 inverted microscope (Olympus, Philippines); constant temperature CO2 incubator (Thermo, USA) ); 5810 R desktop high-speed low-temperature centrifuge (Eppendorf, Germany); automatic microplate reader (Biotek Group, USA).
[0023] (2) Cell culture: A549 cells were cultured in DMEM medium (containing 10% fetal bovine serum), K562 were cultured in 1640 medium (containing 10% fetal bovine serum), 37°C, containing 5% CO 2 cultured in a humidified incubator. Passage every 2-3 days. During the experiment, the cells in the logar...
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