A class of furostanol saponins and their applications
A technology of furostanol saponins and compounds, which is applied in the field of furostanol saponins, and can solve problems such as insufficient research on the chemical composition of open arrows
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Embodiment 1
[0026] The extraction and identification of embodiment 1 furostanol saponins
[0027] 1. Extraction of furostanol saponins
[0028] Take 17 kg of open arrow rhizomes, heat and reflux with 60% ethanol to extract 4 times, each time for 4 hours, combine the extracts to recover the solvent under reduced pressure, and obtain the total extract, suspend the total extract with water, and extract with equal volume of ethyl acetate for 4 Next, fat-soluble impurities were removed, and the aqueous layer was separated by D101 macroporous resin column chromatography, and eluted with water, 20% ethanol, 60% ethanol, 80% ethanol, and 95% ethanol respectively to obtain 5 fractions TA, TB, TC, TD, TE. Fraction TC (60% ethanol eluted part) 200g was taken, and the compounds 1, 2 and 6 of the present invention were isolated by silica gel column chromatography, ODS medium and low pressure column chromatography, reverse phase high performance liquid chromatography and other separation methods. Usi...
Embodiment 3
[0113] Embodiment 3 anti-inflammatory test:
[0114] For the anti-inflammatory activity test of the compound of the present invention in vitro, Raw 264.7 (mouse macrophage) cells induced by LPS (lipopolysaccharide) were used to establish an in vitro inflammation model. MTT and Griess experiments were used to investigate the effect of the compound of the present invention on the release of inflammatory mediator NO from Raw 264.7 cells induced by lipopolysaccharide. The anti-inflammatory drug Indomethacin (indomethacin) was used as a positive control.
[0115] 1) MTT experiment
[0116] Raw 264.7 cells were inoculated in a 96-well plate, and after 24 hours of culture, the product to be tested was added, and after another 24 hours of culture, the inhibition rate of the sample on tumor cell proliferation was measured by the MTT method. The cell proliferation inhibition rate was calculated according to the following formula, and the half inhibitory concentration (IC) of the teste...
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