New phenolic acid compound, preparation method and medical application thereof
A technology of phenolic acids and compounds, which is applied in the field of preparation of phenolic acids and can solve problems such as few
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Embodiment 1
[0027] (1) 1000g of the dried whole herb of Feicai, crushed, heated and ultrasonically extracted with 70% ethanol once (amount of 8L), and recovered the crude extract of the extract under reduced pressure;
[0028] (2) The 70% ethanol crude extract obtained in step (1) is adsorbed by a macroporous resin, and gradient eluted with water, 60% and 90% ethanol-water mixed solvent;
[0029] (3) The 60% ethanol eluate obtained in step (2) is separated by silica gel column chromatography, and is separated by ethyl acetate / methanol 100:1, 100:2, 100:5, 100:8, 100:10, 4:1, 2:1, 1:1 mixed solvent gradient elution;
[0030] (4) step (3) ethyl acetate / methanol 100:3 fraction, carry out high-efficiency liquid phase separation, 250nm detection, flow velocity is 1mL / min, mobile phase is methanol: water=60:40, obtainsedumol A(t R = 7.9 min).
[0031] According to the physical and chemical properties and spectral data of sedumol A, its structure was identified (see the attached NMR spectrum a...
Embodiment 2
[0040] (1) 2000 g of the dried whole herb of Feicai, crushed and extracted twice under reflux with 40% ethanol (amount of 20 L), and the crude extract of the extract was recovered under reduced pressure;
[0041] (2) The 40% ethanol crude extract obtained in step (1) is adsorbed by a macroporous resin, and eluted with water, 10%, 50% and 90% ethanol-water mixed solvent;
[0042] (3) 50% ethanol eluate in step (2), followed by dichloromethane / methanol mixed solvent 100:1, 100:2, 100:3, 100:8, 100:10, 4:1, 2: 1, 1:1 gradient elution;
[0043] (4) The dichloromethane / methanol 100:8 fraction obtained in step (3) adopts high performance liquid phase separation, and 250nm detects, and flow rate is 1mL / min, and mobile phase is methanol: water=60:40, obtains sedumol A ( tR = 7.9 min).
Embodiment 3
[0045] (1) Preparation method of bacterial suspension
[0046] Inoculate Escherichia coli, Staphylococcus aureus, and Bacillus subtilis into the broth and culture at 37°C for 18-24 hours. Add 10ml of sterile distilled water to the sterile test tubes respectively, draw the bacterial solution into the test tubes with a pipette gun, and shake fully for 30 minutes to make a bacterial suspension. Count under a microscope with a hemocytometer. Adjust the bacterial concentration to l05CFU / ml with liquid medium.
[0047] (2) Detection method of minimum inhibitory concentration (MIC) by liquid trace method
[0048]For aseptic operation, add 100 μL of the corresponding liquid medium for detection to each small well of a sterilized 96-well polystyrene culture plate, add 100 μL of the sample to be tested to the first small well, and use a pipette gun to Inhale repeatedly and mix well. Take 100 μL from the first small hole and put it into the second small hole, mix, perform 2-fold prop...
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