Novel diterpenoid alcohol, as well as preparation method and application thereof
A new type of diterpene alcohol technology, applied in the field of preparation of new diterpene alcohols, can solve the problems of extracting monomer compounds that have not been reported yet, and achieve good anti-tumor activity, good inhibitory activity, and rich structure types
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Embodiment 1
[0028] The preparation of embodiment 1 compound
[0029] Weigh 1.5kg of the dried whole herb, extract with 80% ethanol under reflux for 2 hours, the volume ratio of 80% ethanol to Herba Tongjing is 15:1, collect the extract, and add 10 times the volume of 80% ethanol to the remaining samples for reflux extraction for 1 hour , collect the extract; combine the two extracts, filter, combine the filtrate, concentrate under reduced pressure to 2-5 times the volume (v / w), centrifuge at 4000rpm for 5 minutes, and the upper layer is sequentially washed with an equal volume of cyclohexane and chloroform , ethyl acetate, and n-butanol are distributed and extracted, the solvent is recovered, and the extracts of cyclohexane, chloroform, ethyl acetate, and n-butanol are obtained simultaneously.
[0030] The obtained chloroform extract was 20.6g, and a mixed solvent of chloroform-methanol (1:1, V / V) was added to dissolve the extract, and 30g of silica gel was added to mix well, and then p...
Embodiment 2
[0043] Activity test of embodiment 2 compound
[0044] Experimental Materials
[0045] RPMI-1640 medium, calf serum; thiazolyl blue (MTT), dimethyl sulfoxide; penicillin, streptomycin. HL-60 and HO-8910 cell lines were provided by Shanghai Cell Institute of Chinese Academy of Sciences.
[0046] The experimental drug was made by the above method, and the purity was 99.5%.
[0047] experimental method
[0048] HL-60 cells and ovarian cancer cells HO-8910 were cultured in RPMI-1640 medium containing 10% calf serum at 37°C and 5% CO 2 Under normal subculture conditions. Take the cells in the logarithmic growth phase, and use 2×10 5 Cell density per ml was inoculated in a 96-well culture plate, 200 μl per well. The blank control group was added with the same amount of medium without inoculating cells. Each group was added with different concentrations of aspirin B, and the control group was added with 0.5% DMSO, and cultured for 48 hours. Add 50 μl of MTT solution (5 mg / ml)...
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