A sesquiterpene compound and its preparation method and use
A technology for sesquiterpenoids and compounds, applied in the field of caryophyllene-type new sesquiterpenoids and their preparation, can solve the problems of unsuitability for industrial production and preparation, low yield and the like
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Embodiment 1
[0043] Example 1: R is H and R is CH 3 Preparation of the compound of formula I:
[0044] Pick the spores of the fungus of the genus Ascotrichasp.ZJ-M-5, the preservation number is CGMCCNo.8278, and directly inoculate them into a liquid culture medium for 7 days on a shaker. The culture medium is prepared by distilled water and contains 3% sucrose , NaNO 3 0.3%, KCl0.05%, FeSO 4 ·7H 2 O0.001%, K 2 HPO 4 0.1%, the culture temperature is 28°C, the shaker speed is 180 rpm, the fermentation broth is filtered to remove the mycelia, the filtrate is extracted 3 times with an equal volume of n-butanol, and the n-butanol extract is doubled for 200~ 300 mesh silica gel column chromatographic separation, gradient elution with a volume ratio (5:1-1:1) of petroleum ether-acetone mixed solvent, of which the volume ratio of 3:1 petroleum ether-acetone mixed solvent eluted part, After recrystallization, R is CH 3 The yield of the compound of formula I was 5 mg / L, and the fraction elute...
Embodiment 2
[0045] Embodiment 2: The growth inhibition test of the compound of formula I to human acute promyelocytic leukemia HL-60 cell line, human leukemia K562 cell line and mouse lymphocytic leukemia P388 cell line in vitro:
[0046] HL-60, K562 or P388 cells were cultured in RPMI1640 medium containing 10% heat-inactivated fetal bovine serum, 100IU / mL penicillin, 100μg / mL streptomycin and 1mmol / LL-glutamine at 37°C , 5%CO 2 Incubate in a saturated humidity incubator until the cells are 70%-80% confluent. Weigh trypan blue, add a small amount of distilled water to grind, add double distilled water to dilute to 4% storage concentration, filter with filter paper, and store at 4°C. When used, this stock solution was diluted to a working concentration of 0.4% with PBS. Take HL-60, K562 or P388 cells in 3×10 4 Cells / mL density, 1 mL per well was inoculated in a 24-well plate, and then added different concentrations of drugs (final concentrations were 0.1, 0.5, 1, 3, 10, 30, and 100 μM),...
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