A kind of alkaloid compound and its preparation method and application
A compound and alkaloid technology, applied in the field of alkaloid compounds and their preparation, can solve the problems of high mortality, failure to improve the survival period of glioma patients, and easy recurrence of glioma, and achieve the effect of broad application prospects
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Embodiment 1
[0031] The acquisition and characterization of the compound of Example 1
[0032] 1. The specific preparation steps of the compound are as follows:
[0033] S1. Preparation of seed culture medium
[0034] S11. Prepare seed medium:
[0035] The components and dosage of the seed medium are: 200 g of potatoes, 20 g of glucose, and 1 L of deionized water. After preparation, they are evenly distributed in five 500 mL Erlenmeyer flasks, and extinguished at 121° C. for 30 minutes.
[0036] S12. Cultivation of seeds: the marine fungus strain Trichobotrys effusa SYSU-MS4729 was inserted into the seed culture medium, placed on a shaker at a temperature of 28° C., and cultivated at a speed of 180 rpm for 120 hours to obtain a seed culture solution.
[0037] S2. Fermentation culture:
[0038] S21. Prepare fermentation medium:
[0039] The components and dosage of the fermentation medium are: 3000 g of rice, 90 g of sea salt, 3 L of deionized water, and extinguished at 121° C. for 30 m...
Embodiment 2
[0057] Example 2 Anti-glioma Activity Test of Compound 1
[0058] The alkaloid compound (compound 1) obtained in Example 1 was subjected to a cytotoxic activity test on two glioma cell lines U251 and SNB19, and the specific steps were as follows:
[0059] 1. Experimental materials
[0060] 1.1 Tetrazole compound (CCK-8): 2-(2-methoxy-4-nitrophenyl)-3-(4-nitrophenyl)-5-(2,4-disulfonic acid benzene) -2H-tetrazole monosodium salt, referred to as CCK-8.
[0061] 1.2 Preparation of target cells: recovery and culture of glioma cell lines U251 and SNB19.
[0062] a. Take out the cryopreservation tubes of human glioma cell lines U251 and SNB19 from the liquid nitrogen tank, quickly place them in a 37°C water bath, shake them continuously to dissolve them quickly, and transfer them into centrifuge tubes aseptically;
[0063] b. Add DMEM complete culture solution to human glioma cell lines U251 and SNB19 respectively to 10 mL, centrifuge at 1000 rpm for 5 min, and discard the superna...
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