A kind of kunlun savinol glycoside compound and its preparation method and application
A compound and related technology, applied in the field of extraction and separation of natural compounds, can solve problems such as carcinogenicity, and achieve the effect of strong DPPH and ABTS free radical scavenging ability
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Embodiment 1
[0030] Embodiment 1, the preparation of compound
[0031] Weigh 5 kg of dried Kunlun chrysanthemum capitulum, mash it with a homogenizer, put it in a 20L volumetric flask, add 10L methanol for extraction, leave it for 24 hours, and extract three times. Use a Buchner funnel to suction filter, place the filter residue in a 20L volumetric flask, and use 2mol·L -1 The NaOH solution was degraded in a water bath at 50°C for 2 hours, neutralized to neutral with hydrochloric acid, extracted with 10L n-butanol, left for 24 hours, and extracted three times. Extract the n-butanol layer, and use a rotary evaporator to concentrate in vacuo at 55° C. to obtain the n-butanol extract.
[0032] The n-butanol extract (152 g) was mixed with 100 g of silica gel in a dry method, then mounted on an atmospheric column equipped with 300 g of silica gel (300-400 mesh), and separated by petroleum ether-acetone-methanol gradient elution. The eluted components were concentrated in vacuum and then detec...
Embodiment 2
[0038] Embodiment 2, the test of antioxidant activity
[0039] 1. Experimental samples and experimental methods
[0040] 1.1 DPPH method.
[0041] Preparation of DPPH solution: Accurately weigh 0.0197g DPPH, adjust the volume to 250ml with absolute ethanol, and obtain a concentration of 2×10 -4 mol L -1 DPPH solution.
[0042] Determination method: Add 2ml DPPH solution to 2ml sample, shake well, keep it in the dark for 30min, measure the absorbance value A at 517nm I ; Replace the sample with 2ml of absolute ethanol for the blank, add 2ml of absolute ethanol to the 2ml sample, shake well and keep it in the dark for 30min, measure the absorbance value A at 517nm J ; Add 2ml of absolute ethanol to 2ml of DPPH solution, shake well, keep it in the dark for 30 minutes, and measure the absorbance A at 517nm C ; The clearance rate is [1-(A I -A J ) / A C ] × 100%. VE solution (20-100μmol L -1 ) as a positive control, and each sample was parallelized three times.
[0043] 1....
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