Method for extracting dimerized furanone compounds from litsea coreana and application of dimerized furanone compounds
A technology for dimerizing furanones and compounds, which is applied in organic chemistry, drug combination, antineoplastic drugs, etc., and can solve problems such as no reports of dimerizing furanones
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Embodiment 1
[0040] The method for extracting and separating the above-mentioned dimeric furanones from eagle tea includes the following:
[0041] 1) Take 17.81kg of eagle tea leaves from the source of leopard skin camphor, after drying and pulverizing, reflux extraction with 90% methanol for 3 times, each extraction is 3~4h, and the extract is concentrated under reduced pressure to obtain 2020g of methanol extract;
[0042] 2) after the methanol extract in 1) was dispersed in water, extracted 3 times with petroleum ether, ethyl acetate and n-butanol successively, each extraction part was concentrated under reduced pressure to obtain the extract of each part, wherein 889g of ethyl acetate extract was obtained ;
[0043] 3) Separating the ethyl acetate part extract in 2) by silica gel medium pressure column chromatography, using petroleum ether-ethyl acetate in volume ratios of 9:1, 4:1, 3:2, 2:3, 1:4, 1:0 gradient elution, divided into 6 components, numbered Fr.1~Fr.6;
[0044] 4) The th...
Embodiment example 2
[0048] Example 2: MTT assay to detect the cytotoxic effect of the difuranones on HCT-116, SW1990 and OSC-19 cell lines:
[0049] HCT-116, SW1990 and OSC-19 cells in logarithmic growth phase were selected, and the cell concentration was adjusted to 3 × 10 with 10% fetal bovine serum medium. 4 Cells / mL, 100 μL per well, seeded into 96-well flat-bottom cell culture plates, placed at 37°C, 5% CO 2 After culturing in the incubator for 12 h, 100 μL of samples were added, and the concentrations of the samples were 1, 5, 20, 40, and 80 μM, respectively, and five replicate wells were set up. at 37°C, 5%, CO 2Continue to cultivate for 48h in the incubator. Then, 20 μL MTT solution (5 mg / mL) was added to each well to continue culturing for 3 h, and the supernatant was discarded. Finally, add 150 μL DMSO to each well, shake at low speed for 20 min to fully dissolve the crystals, detect the absorbance value at a wavelength of 490 nm, and calculate the cell viability, cell viability=abso...
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