Isopentenyl flavone and application thereof
A technology of prenyl flavonoids and diprenyl quercetin, which is applied in the field of preparation of drugs for the treatment of breast cancer, and can solve problems such as the lack of breast cancer reports of basilica and its compounds
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Embodiment 1
[0016] Dried lobular lotus medicinal material, about 18kg after crushing, reflux extraction twice with 8 times the amount of 95% ethanol, the extraction time is 2 hours and 1 hour respectively, recover the ethanol, concentrate to 70 ℃ and the extract is about 5.2kg with a relative density of 1.10 . Take about 4.8kg, add 10L of distilled water and stir until completely suspended, then extract 5 times with petroleum ether, ethyl acetate, and water-saturated n-butanol in equal volume. The solvent was recovered from the extract under reduced pressure to obtain various extraction fractions. Get 274g of ethyl acetate part, separate through silica gel column (100~200 mesh) chromatography, chloroform-methanol (10:0~0:10) gradient elution, according to TLC test result, in chloroform:methanol is 40:1~ The 30:1 polar site contains 8,2′-diprenylquercetin 3-methyl ether, purified by Sephadex LH-20, eluted with chloroform-methanol (6:4) to give 8,2′-di Prenyl quercetin 3-methyl ether 60mg...
Embodiment 2
[0018] The inhibitory effect of 8,2′-diprenyl quercetin 3-methyl ether on human breast cancer cells was detected by acid phosphatase method.
[0019] Human breast cancer MDA-231 cell line and human breast cancer T47D cell line were cultured in DMEM medium containing 10% newborn bovine serum, 100 U / mL penicillin, and 100 U / mL streptomycin at 37°C and 95% humidity , 5% CO 2 Incubator conditions; conventional 2.5g / L trypsin digestion and passage.
[0020] After digesting the cells in the logarithmic growth phase, make a cell suspension by 1.5×10 3 The density per well was inoculated in a 96-well culture plate. After the cells were completely adhered to the wall after 24 hours of culture, the experimental group was added with different concentrations of compounds; the blank control group was added with DMEM culture medium. In the experiment, set 6 parallel wells for each concentration, discard the medium in the 96-well plate after 24h, 48h, and 72h of action, wash each well with...
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