Use of flavone derivates and preparation method thereof
A technology of derivatives and flavonoids, applied in medical preparations containing active ingredients, food preparation, applications, etc., can solve problems such as loss of consciousness, damage, etc., and achieve novel structural effects
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Embodiment 1
[0043] (1) Pulverize 4.2 kg of dried whole herb of Selaginella uncinata (Desv.) Spring, extract by heating and refluxing three times with 60% ethanol 10 times the weight of Selaginella uncinata (Desv.) Spring, 2 hours each time, and combine Extraction solution;
[0044] (2) Remove insoluble matter by filtration, and dry the filtrate under reduced pressure to obtain ethanol extract.
[0045] (3) The ethanol extract was extracted 3 times with equal volumes of ethyl acetate and n-butanol respectively;
[0046] (4) Take the ethyl acetate extract and dry it under reduced pressure in vacuo to obtain the ethyl acetate extract.
[0047](4) The ethyl acetate extract was subjected to open silica gel column chromatography, and the chloroform:methanol ratios were 99:1, 98:2, 97:3, 95:5, 9:1, 8:2, 7:3 , 6:4 solvent gradient elution. Using comprehensive separation methods such as gel Sephadex LH-20 column chromatography, ODS column chromatography, and RP-18 high-performance liquid phase ...
Embodiment 2
[0052] Compounds 1-16 prepared in Example 1 were formulated into liquids with a concentration of 180 μmol / L, 90 μmol / L, and 45 μmol / L respectively as the drug group, and 10% DMSO was used as the control group to protect PC12 cells from hypoxia. test, and calculate the survival percentage of PC12 cells. The experimental results were calculated by Student's ttest, expressed as: mean ± SD. The results are shown in Table 1.
[0053] Table 1 Effects of compounds on PC12 cell hypoxic injury (x±sD)
[0054]
[0055] Note: Compared with the control group * P** P<0.01
[0056] Conclusion: It can be seen from Table 9 that compared with the blank solvent group, compound 1-16 has a strong protective effect on hypoxic PC12 cells at different concentrations, and has anti-hypoxic activity in vitro. It shows that these 16 compounds can be used as anti-hypoxic drugs.
Embodiment 3
[0058] The compounds 1-16 prepared in Example 1 were formulated into liquids with a concentration of 40 mg / mL as the drug group, and 20% DMSO was used as the control group to carry out the airtight hypoxic endurance test in mice, and observe the mice under airtight conditions. The following survival time. The results are shown in Table 2.
[0059] Table 2 Survival of mice under hypoxic conditions (x±SD, n=10)
[0060]
[0061] Note: Compared with the control group * P** P<0.01
[0062] Conclusion: As can be seen from Table 10, compared with the control group, compound 1-16 can significantly improve the survival time of mice under airtight hypoxic conditions, has certain anti-hypoxic activity in vivo, and can be used as an anti-hypoxic drug .
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