A kind of new triterpene compound of c3, 4 ring splitting and its preparation method
A technology of triterpene compounds and compounds, applied in the field of medicine, to achieve the effect of novel structure, simple extraction and separation method, and good curative effect
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Embodiment 1
[0036] Embodiment 1: the preparation of formula I compound:
[0037]Using 10 kg of dried medicinal material from the root of Schisandra chinensis as raw material, it was heated and refluxed with 90% ethanol for 3 times, each time for 2 hours, and concentrated to obtain 1500 g of extract-like ethanol extract. The ethanol extract was suspended in water, and extracted 4 times with petroleum ether, 1000 mL each time. Part of the extract extracted from petroleum ether was separated by 200-300 mesh silica gel column chromatography, and gradient eluted with petroleum ether-ethyl acetate (100:1-1:1), wherein the volume ratio of petroleum ether-ethyl acetate was 100: The eluted fraction of 7 was separated by 200-300 mesh silica gel column chromatography, and eluted with petroleum ether-acetone with a volume ratio of 16:1 to obtain the compound of formula I (7 mg).
Embodiment 2
[0038] Embodiment 2: The growth inhibition test of the compound of formula I to human acute promyelocytic leukemia cell line HL-60 in vitro:
[0039] HL-60 cells were cultured in a medium containing 10% heat-inactivated fetal bovine serum, 100 IU / mL penicillin, 100 mg / mL streptomycin and 1 mmol / L L -Glutamine in RPMI1640 medium, 37 °C, 5% CO 2 Incubate in a saturated humidity incubator. Weigh trypan blue, add a small amount of distilled water to grind, add double distilled water to dilute to 4% storage concentration, filter with filter paper, and store at 4 °C. When used, this stock solution was diluted to a working concentration of 0.4% with PBS. Take the above cells (1'10 5 / mL) were inoculated in a 12-well plate, 2 mL per well. Add different concentrations of drugs to prepare a single cell suspension after incubation, take 50 mu L cell suspension added 50 mu 0.4% trypan blue solution in L, mix well, and observe under the microscope within 3 minutes, the dead cells a...
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