A kind of timasteroid saponin compound and its preparation method and application
A technology of steroidal saponins and compounds, applied in the field of medicine, can solve the problems such as patents or literature reports that have not been found, and achieve the effect of significant anti-tumor activity
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Embodiment 1
[0035] Preparation of Steroidal Saponin Compounds
[0036] Weigh 10kg of dried rhizome of Anemarrhena, put it in an extraction tank, add 50L of 75% ethanol, soak overnight, heat and reflux in a water bath for extraction for 3 hours, filter, and repeat the extraction with 75% ethanol (50L) twice, each time for 3 hours, and combine three times The filtrate was concentrated to obtain extract-like ethanol extract (3.09kg). Suspend the ethanol extract in pure water to obtain a suspension, extract three times successively with equal volumes of petroleum ether, ethyl acetate, and water-saturated n-butanol, and concentrate the extract to obtain three parts of the extract. The n-butanol part extract (600g) is roughly divided by macroporous adsorption resin, and the first gradient elution is carried out with 10%, 30%, 50%, 70%, 95% (v / v) ethanol-water, The eluate from the 70% ethanol part was crudely separated by silica gel column chromatography. Then use 20:1-1:1 (v / v) dichloromethan...
Embodiment 2
[0050] Antitumor activity test of compound I
[0051] 1. Cell lines and reagent materials Human breast cancer cell line MCF-7 and human liver cancer cell line HepG2 are provided by the American Type Culture Collection (ATCC); DMEM medium, RPMI-1640 medium, fetal bovine serum, trypsin, DMSO and MTT et al.
[0052] 2. MTT method to detect cell viability
[0053] Cultivate MCF-7 and HepG2 cell lines with RPMI-1640 medium containing 10% fetal bovine serum, respectively take MCF-7 and HepG2 cell lines in logarithmic growth phase and in good condition, discard the medium, and pre-cool aseptic Wash with PBS three times, then digest with trypsin solution and observe with an inverted biological microscope. After the digestion is completed, the cells are mixed evenly. Spread the MCF-7 and HepG2 cell lines on 96-well plates respectively to ensure that the MCF-7 cell line is 2500 cells / well, and the HepG2 cell line is 2000 cells / well, and the drug concentration is set to 100 μmol / L for ...
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